Analysis data for Fe3O4 nanoparticles, energy dispersive.
\\n\\n
Dr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\\n\\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\\n\\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\\n\\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\\n\\nThank you all for being part of the journey. 5,000 times thank you!
\\n\\nNow with 5,000 titles available Open Access, which one will you read next?
\\n\\nRead, share and download for free: https://www.intechopen.com/books
\\n\\n\\n\\n
\\n"}]',published:!0,mainMedia:null},components:[{type:"htmlEditorComponent",content:'
Preparation of Space Experiments edited by international leading expert Dr. Vladimir Pletser, Director of Space Training Operations at Blue Abyss is the 5,000th Open Access book published by IntechOpen and our milestone publication!
\n\n"This book presents some of the current trends in space microgravity research. The eleven chapters introduce various facets of space research in physical sciences, human physiology and technology developed using the microgravity environment not only to improve our fundamental understanding in these domains but also to adapt this new knowledge for application on earth." says the editor. Listen what else Dr. Pletser has to say...
\n\n\n\nDr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\n\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\n\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\n\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\n\nThank you all for being part of the journey. 5,000 times thank you!
\n\nNow with 5,000 titles available Open Access, which one will you read next?
\n\nRead, share and download for free: https://www.intechopen.com/books
\n\n\n\n
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"8834",leadTitle:null,fullTitle:"Managing Wildlife in a Changing World",title:"Managing Wildlife in a Changing World",subtitle:null,reviewType:"peer-reviewed",abstract:"The declining trends of wildlife habitats and species populations are obvious consequences of the socio-economic, political, ecological, and technological changes occurring globally. Along with human population growth, there is a growing wave of wildlife diseases, invasive alien species, human-wildlife conflicts, climate change, poaching, infrastructure development, and economic options that are ecologically damaging. These changes have implications on the management of wildlife resources. Managing Wildlife in a Changing World draws experiences from different parts of the world on status, challenges, and efforts of reversing the current negative trends on wildlife habitats and species in the face of these changes. This book is useful for academicians, researchers, policy makers, conservation practitioners, students, and other interested readers.",isbn:"978-1-83880-976-8",printIsbn:"978-1-83880-975-1",pdfIsbn:"978-1-83880-977-5",doi:"10.5772/intechopen.81141",price:119,priceEur:129,priceUsd:155,slug:"managing-wildlife-in-a-changing-world",numberOfPages:154,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"a27827009edc70af81e12c10aa3e51dd",bookSignature:"Jafari R. Kideghesho",publishedDate:"December 8th 2021",coverURL:"https://cdn.intechopen.com/books/images_new/8834.jpg",numberOfDownloads:1725,numberOfWosCitations:0,numberOfCrossrefCitations:1,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:8,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:9,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"May 15th 2020",dateEndSecondStepPublish:"June 5th 2020",dateEndThirdStepPublish:"August 4th 2020",dateEndFourthStepPublish:"October 23rd 2020",dateEndFifthStepPublish:"December 22nd 2020",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"280695",title:"Prof.",name:"Jafari R.",middleName:null,surname:"Kideghesho",slug:"jafari-r.-kideghesho",fullName:"Jafari R. Kideghesho",profilePictureURL:"https://mts.intechopen.com/storage/users/280695/images/system/280695.png",biography:"Professor Jafari R. Kideghesho was born in Ugweno, Kilimanjaro in Northern Tanzania. He obtained his BSc in Agriculture from Sokoine University of Agriculture (SUA), Tanzania, in 1993; an MSc in Conservation Biology from Kent University, UK, in 1996; and a Ph.D. from Norwegian University of Science and Technology, in 2006. He started his career in wildlife management at the College of African Wildlife Management, Mweka, where he taught for six years before joining SUA in 1999. He served as a deputy director of the Wildlife Division in Tanzania’s Ministry of Natural Resources and Tourism for two years (2012–2014). Dr. Kideghesho has been an active supporter of academic efforts within and outside Tanzania through teaching and serving as an external examiner at different universities. He has published more than fifty scientific articles in reputable journals and is an author and editor of numerous books. Currently, he is the rector at the College of African Wildlife Management, Mweka, Kilimanjaro.",institutionString:"College of African Wildlife Management",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"College of African Wildlife Management",institutionURL:null,country:{name:"Tanzania"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"130",title:"Environmental Management",slug:"environmental-sciences-environmental-management"}],chapters:[{id:"78486",title:"Introductory Chapter: Managing Wildlife in a Changing World - Trends, Drivers and the Way Forward",doi:"10.5772/intechopen.98851",slug:"introductory-chapter-managing-wildlife-in-a-changing-world-trends-drivers-and-the-way-forward",totalDownloads:98,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Jafari R. Kideghesho",downloadPdfUrl:"/chapter/pdf-download/78486",previewPdfUrl:"/chapter/pdf-preview/78486",authors:[{id:"175015",title:"Associate Prof.",name:"Jafari",surname:"Kideghesho",slug:"jafari-kideghesho",fullName:"Jafari Kideghesho"}],corrections:null},{id:"73394",title:"Conserving Freshwater Biodiversity in an African Subtropical Wetland: South Africa’s Lower Phongolo River and Floodplain",doi:"10.5772/intechopen.93752",slug:"conserving-freshwater-biodiversity-in-an-african-subtropical-wetland-south-africa-s-lower-phongolo-r",totalDownloads:445,totalCrossrefCites:0,totalDimensionsCites:5,hasAltmetrics:0,abstract:"Freshwater biodiversity is under constant threat from a range of anthropogenic stressors. Using South Africa’s Phongolo River and floodplain (PRF) as a study case, the aim of this chapter is to provide an overview of the conservation and management of freshwater biodiversity in a highly diverse subtropical ecosystem. The PRF is the largest floodplain system in South Africa which is severely threatened by irregularly controlled flood releases from a large upstream dam, prolonged drought, deteriorating water quality, organic pollutants and the increasing dependence of the local communities. Based on a decade of survey of the PRF conducted from 2010 to 2020, this chapter highlights the current diversity of aquatic organisms (invertebrates, fishes, frogs and their parasitic fauna), followed by an overview of their biological and physical stressors. The current challenges in the management of the aquatic biodiversity of this region and a way forward to conservation strategies are also addressed in this chapter.",signatures:"Aline Angelina Acosta, Edward C. Netherlands, Francois Retief, Lizaan de Necker, Louis du Preez, Marliese Truter, Reece Alberts, Ruan Gerber, Victor Wepener, Wynand Malherbe and Nico J. Smit",downloadPdfUrl:"/chapter/pdf-download/73394",previewPdfUrl:"/chapter/pdf-preview/73394",authors:[{id:"323315",title:"Dr.",name:"Aline",surname:"Acosta",slug:"aline-acosta",fullName:"Aline Acosta"},{id:"323318",title:"Dr.",name:"Lizaan",surname:"De Necker",slug:"lizaan-de-necker",fullName:"Lizaan De Necker"},{id:"323319",title:"Dr.",name:"Wynand",surname:"Malherbe",slug:"wynand-malherbe",fullName:"Wynand Malherbe"},{id:"323320",title:"MSc.",name:"Marliese",surname:"Truter",slug:"marliese-truter",fullName:"Marliese Truter"},{id:"323321",title:"Prof.",name:"Louis",surname:"Du Preez",slug:"louis-du-preez",fullName:"Louis Du Preez"},{id:"323322",title:"Dr.",name:"Edward C.",surname:"Netherlands",slug:"edward-c.-netherlands",fullName:"Edward C. Netherlands"},{id:"323323",title:"Dr.",name:"Ruan",surname:"Gerber",slug:"ruan-gerber",fullName:"Ruan Gerber"},{id:"323325",title:"Prof.",name:"Francois",surname:"Retief",slug:"francois-retief",fullName:"Francois Retief"},{id:"323326",title:"Dr.",name:"Reece",surname:"Albert",slug:"reece-albert",fullName:"Reece Albert"},{id:"323327",title:"Prof.",name:"Victor",surname:"Wepener",slug:"victor-wepener",fullName:"Victor Wepener"},{id:"323328",title:"Prof.",name:"Nico J.",surname:"Smit",slug:"nico-j.-smit",fullName:"Nico J. Smit"}],corrections:null},{id:"79397",title:"The Predicament of Macaque Conservation in Malaysia",doi:"10.5772/intechopen.101136",slug:"the-predicament-of-macaque-conservation-in-malaysia",totalDownloads:149,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Macaques are commonly found in Malaysia, with the current existing three species placed between endangered to least concern status under the IUCN Red List, namely the stump-tailed macaque (Macaca arctoides), pig-tailed macaque (Macaca nemestrina), and the notorious long-tailed macaque (Macaca fascicularis). The species classified under the endangered and vulnerable group are facing threats mainly from the loss of habitat. Conversely, species that are categorized as least concerned are often cited at the top of human-wildlife conflicts reports in various countries, although they too are facing pressure from habitat loss. There are different methods employed to control the fast-growing population of these species, calling for different levels of investment in terms of resources. It is of great interest to understand the disparities between these species, as they are able to adapt to environmental changes and some find ways to survive in alternative localities, including urban areas. The proximity of macaques to human dwellings raises a public health concern through the transmission of zoonotic diseases. More scientific studies are imperative in order to further understand the needs of these animals for continued survival and co-existence with humans and other animals in the ecosystem. Urgent efforts must be taken to preserve the macaque’s natural habitats while creating the public awareness on the predicament of these species. The focus should be on human-wildlife conflicts todispute the existing false impression that all macaques are on equal ground and abundance in numbers.",signatures:"Siew Shean Choong, Mimi Armiladiana Mohamad, Li Peng Tan and Ruhil Hayati Hamdan",downloadPdfUrl:"/chapter/pdf-download/79397",previewPdfUrl:"/chapter/pdf-preview/79397",authors:[{id:"332287",title:"Dr.",name:"Siew Shean",surname:"Choong",slug:"siew-shean-choong",fullName:"Siew Shean Choong"},{id:"426575",title:"Dr.",name:"Mimi Armiladiana",surname:"Mohamad",slug:"mimi-armiladiana-mohamad",fullName:"Mimi Armiladiana Mohamad"},{id:"426643",title:"Dr.",name:"Li Peng",surname:"Tan",slug:"li-peng-tan",fullName:"Li Peng Tan"},{id:"426644",title:"Dr.",name:"Ruhil Hayati",surname:"Hamdan",slug:"ruhil-hayati-hamdan",fullName:"Ruhil Hayati Hamdan"}],corrections:null},{id:"73864",title:"Diseases as Impediments to Livestock Production and Wildlife Conservation Goals",doi:"10.5772/intechopen.94467",slug:"diseases-as-impediments-to-livestock-production-and-wildlife-conservation-goals",totalDownloads:95,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Disease outbreaks, epidemics or pandemics have been of importance for human and animal health worldwide and sparked enormous public interest. These outbreaks might be caused by known endemic pathogens or by emerging or re-emerging pathogens. Wildlife are the major reservoirs and responsible for most of these outbreaks. They play significant role in the transmission of several livestock diseases and pathogen spill-over may occur in complex socio-ecological systems at the wildlife-domestic animal interface which have been seldom studied. Interspecific pathogen spill-over at the wildlife-livestock interface have been of growing concern in the scientific community over the past years due to their impact on wildlife, livestock and human health. In this section the epidemiology of some viral infections (Foot and Mouth Disease and rabies), bacterial infections (Tuberculosis and brucellosis) and parasites (haemo and endo-parasites) at the wildlife-livestock interface and potential impacts to livestock production and conservation goal is described.",signatures:"Y.J. Atuman, C.A. Kudi, P.A. Abdu, O.O. Okubanjo and A. Abubakar",downloadPdfUrl:"/chapter/pdf-download/73864",previewPdfUrl:"/chapter/pdf-preview/73864",authors:[{id:"321985",title:"Ph.D.",name:"Yakubu Joel",surname:"Atuman",slug:"yakubu-joel-atuman",fullName:"Yakubu Joel Atuman"},{id:"329216",title:"Prof.",name:"Caleb",surname:"Kudi",slug:"caleb-kudi",fullName:"Caleb Kudi"},{id:"329217",title:"Prof.",name:"P.A.",surname:"Abdu",slug:"p.a.-abdu",fullName:"P.A. Abdu"}],corrections:null},{id:"74028",title:"Retracted: Interlinks between Wildlife and Domestic Cycles of Echinococcus spp. in Kenya",doi:"10.5772/intechopen.94612",slug:"retracted-interlinks-between-wildlife-and-domestic-cycles-of-em-echinococcus-em-spp-in-kenya",totalDownloads:255,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Effective conservation and management of wildlife in the current changing world, call for incorporation of infectious zoonotic diseases surveillance systems, among other interventions. One of such diseases is echinococcosis, a zoonotic disease caused by Echinococcus species. This disease exists in two distinct life cycle patterns, the domestic and wildlife cycles. To investigate possible inter-links between these cycles in Kenya, 729 fecal samples from wild carnivores and 406 from domestic dogs (Canis lupus familiaris) collected from Maasai Mara and Samburu National Reserves were analyzed. Taeniid eggs were isolated by zinc chloride sieving-flotation method and subjected to polymerase chain reaction of nicotinamide adenine dehydrogenase subunit 1 (NAD1). Subsequent amplicons were sequenced, edited and analyzed with GENtle VI.94 program. The samples were further subjected to molecular identification of specific host species origin. All sequences obtained were compared with those in Gene-bank using Basic Local Alignment Search Tool (BLAST). The study found that there were 74 taeniid positive samples, 53 from wild carnivores and 21 from domestic dogs. In wildlife, mixed infections with Echinococcus and Taenia species were identified and these included E. granulosus sensu stricto, E. felidis, T. canadensis G6/7, Taenia hydatigena, T. multiceps, and T. saginata. Domestic dogs harbored Echinococcus and Taenia species similar to wild carnivores including E. granulosus G1–3, E. felidis, T. multiceps, T. hydatigena, and T. madoquae. Taenia species of nine taeniid eggs were not identified. Majority of genotypes were found in hyena (Crocuta crocuta) fecal samples. Distribution of Echinococcus and Taenia spp. varied with hosts. Mixed infections of Echinococcus spp, T. multiceps and T. hydatigena in a single animal were common. There seemed to be existence of interactions between the two cycles, although public health consequences are unknown. The presence of T. saginata in hyena suggests scavenging of human fecal matter by the animal. In addition, presence of T. multiceps, T hydatigena, T madoquae and T. saginata in the two cycles suggested possible human exposure to these parasites. The results are important in drawing up of strategies and policies towards prevention and control of Echinococcosis and other Taenia related parasitic infections, especially in endemic areas given their potential risk to public and socio- economic livelihood.",signatures:"Dorothy Kagendo, Eric Muchiri, Peter Gitonga and Esther Muthoni",downloadPdfUrl:"/chapter/pdf-download/74028",previewPdfUrl:"/chapter/pdf-preview/74028",authors:[{id:"189056",title:"Ph.D. Student",name:"Dorothy",surname:"Kagendo",slug:"dorothy-kagendo",fullName:"Dorothy Kagendo"},{id:"194332",title:"Prof.",name:"Eric",surname:"Muchiri",slug:"eric-muchiri",fullName:"Eric Muchiri"},{id:"194336",title:"BSc.",name:"Peter",surname:"Gitonga",slug:"peter-gitonga",fullName:"Peter Gitonga"},{id:"194342",title:"BSc.",name:"Esther",surname:"Muthoni",slug:"esther-muthoni",fullName:"Esther Muthoni"}],corrections:null},{id:"76660",title:"Wildlife Management Areas in Tanzania: Vulnerability and Survival Amidst COVID-19",doi:"10.5772/intechopen.97396",slug:"wildlife-management-areas-in-tanzania-vulnerability-and-survival-amidst-covid-19",totalDownloads:280,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The establishment of Wildlife Management Areas (WMAs) has been adopted as intervention to safeguard the wildlife and their habitats outside the core protected areas in Tanzania. Along with their conservation role, WMAs provide an opportunity for local communities to derive economic benefits from wildlife-based enterprises on their land. WMAs primarily rely on revenues generated from photographic and hunting tourism to support operational activities and create incentives for the local communities to conserve wildlife resources. The current global travel restrictions and lockdown caused by an outbreak of COVID-19 pandemic have reduced a vital funding source for WMAs. This, therefore, undermines the ability to manage the wildlife resources and reward communities for the opportunity cost of their land and other costs associated with coexisting with wildlife. This chapter examines the extent to which the decline of tourism revenues as a result of the outbreak of COVID-19 pandemic has affected WMAs as a framework for local communities to manage and benefit from wildlife. Data were collected through semi-structured interviews on five WMAs in Northern Tanzania that were purposively selected based on their ability to generate a significant amount of revenues from tourism. Findings show that the decline of tourism revenues triggers unprecedented adverse effects on the conservation of wildlife resources within WMAs. Livelihood of the local communities is also affected due to loss of employment opportunities and drop-off of tourism income obtained from the sales of local goods to the tourists and tourist hotels. We recommend the creation of local mechanisms for revenue acquisition that are more resilient to global shocks, diversifying revenue-generating options within WMAs, and putting in place the right funding model that would warrant WMAs sustainability.",signatures:"Rehema Abeli Shoo, Elizabeth Kamili Mtui, Julius Modest Kimaro, Neema Robert Kinabo, Gladys Joseph Lendii and Jafari R. Kideghesho",downloadPdfUrl:"/chapter/pdf-download/76660",previewPdfUrl:"/chapter/pdf-preview/76660",authors:[{id:"280695",title:"Prof.",name:"Jafari R.",surname:"Kideghesho",slug:"jafari-r.-kideghesho",fullName:"Jafari R. Kideghesho"}],corrections:null},{id:"78612",title:"A Step Change in Wild Boar Management in Tuscany Region, Central Italy",doi:"10.5772/intechopen.100012",slug:"a-step-change-in-wild-boar-management-in-tuscany-region-central-italy",totalDownloads:165,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"In this chapter, reducing the high-density populations of wild boars in an Italian’s Tuscany region is addressed as a measure of controlling crop damage and road accidents. The issue is usually tackled from a technical and rarely sociological point of view, making the proposed and implemented solutions less effective. The results presented in these chapter highlight the importance of awareness of the social context when the technical choices are applied. The management of ungulates creates economic interests that oppose changes that shift the economic balance, even when the actions taken are for the benefit of the entire community’. In the previous decades, the wild boar populations have increased considerably in Italy in the Tuscany region. As a consequence of this phenomenon, damage to crops and road accidents has increased. In 2016, the Tuscany region enacted a law to change the management of ungulates by promoting individualism in unsustainable harvest rate areas, allowing shooting wild boar with stalking and selling the meat and maintaining a corporate approach in sustainable harvest rate areas. In three years of enforcing the law, damage to crops and road accidents have decreased significantly and meet supply chain has started. On the other hand, a strong reaction against this Law by wild boar drive hunters emerged. The region is, consequently, faced with an emblematic case where political intervention in future is inevitable in order to mediate between long-term results and short-term consensus.",signatures:"Paolo Banti, Vito Mazzarone, Luca Mattioli, Marco Ferretti, Andrea Lenuzza, Rocco Lopresti, Marco Zaccaroni and Massimo Taddei",downloadPdfUrl:"/chapter/pdf-download/78612",previewPdfUrl:"/chapter/pdf-preview/78612",authors:[{id:"272715",title:"Dr.",name:"Marco",surname:"Ferretti",slug:"marco-ferretti",fullName:"Marco Ferretti"},{id:"328644",title:"Dr.",name:"Marco",surname:"Zaccaroni",slug:"marco-zaccaroni",fullName:"Marco Zaccaroni"},{id:"328645",title:"Dr.",name:"Vito",surname:"Mazzarone",slug:"vito-mazzarone",fullName:"Vito Mazzarone"},{id:"328646",title:"Dr.",name:"Luca",surname:"Mattioli",slug:"luca-mattioli",fullName:"Luca Mattioli"},{id:"328647",title:"Dr.",name:"Andrea",surname:"Lenuzza",slug:"andrea-lenuzza",fullName:"Andrea Lenuzza"},{id:"328648",title:"Dr.",name:"Paolo",surname:"Banti",slug:"paolo-banti",fullName:"Paolo Banti"},{id:"328649",title:"Mr.",name:"Massimo",surname:"Taddei",slug:"massimo-taddei",fullName:"Massimo Taddei"},{id:"337449",title:"Dr.",name:"Rocco",surname:"Lopresti",slug:"rocco-lopresti",fullName:"Rocco Lopresti"}],corrections:null},{id:"74177",title:"Managing Invasive Alien Species by the European Union: Lessons Learnt",doi:"10.5772/intechopen.94548",slug:"managing-invasive-alien-species-by-the-european-union-lessons-learnt",totalDownloads:238,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:0,abstract:"The contribution concentrates on the fight against invasive alien species within the European Union (EU), which groups 27 States. In 2014, the EU adopted a regulation to identify and manage invasive alien species. This regulation and its monitoring are discussed in detail, in order to see, what lessons can be learnt from the cooperation and concertation of the different states.",signatures:"Ludwig Krämer",downloadPdfUrl:"/chapter/pdf-download/74177",previewPdfUrl:"/chapter/pdf-preview/74177",authors:[{id:"321981",title:"Mr.",name:"Ludwig",surname:"Krämer",slug:"ludwig-kramer",fullName:"Ludwig Krämer"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"7477",title:"Advances in Environmental Monitoring and Assessment",subtitle:null,isOpenForSubmission:!1,hash:"23d6e3704efd9ff5940bbbefc54d3b86",slug:"advances-in-environmental-monitoring-and-assessment",bookSignature:"Suriyanarayanan Sarvajayakesavalu",coverURL:"https://cdn.intechopen.com/books/images_new/7477.jpg",editedByType:"Edited by",editors:[{id:"237021",title:"Dr.",name:"Suriyanarayanan",surname:"Sarvajayakesavalu",slug:"suriyanarayanan-sarvajayakesavalu",fullName:"Suriyanarayanan Sarvajayakesavalu"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"1591",title:"Infrared Spectroscopy",subtitle:"Materials Science, Engineering and Technology",isOpenForSubmission:!1,hash:"99b4b7b71a8caeb693ed762b40b017f4",slug:"infrared-spectroscopy-materials-science-engineering-and-technology",bookSignature:"Theophile Theophanides",coverURL:"https://cdn.intechopen.com/books/images_new/1591.jpg",editedByType:"Edited by",editors:[{id:"37194",title:"Dr.",name:"Theophile",surname:"Theophanides",slug:"theophile-theophanides",fullName:"Theophile Theophanides"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3161",title:"Frontiers in Guided Wave Optics and Optoelectronics",subtitle:null,isOpenForSubmission:!1,hash:"deb44e9c99f82bbce1083abea743146c",slug:"frontiers-in-guided-wave-optics-and-optoelectronics",bookSignature:"Bishnu Pal",coverURL:"https://cdn.intechopen.com/books/images_new/3161.jpg",editedByType:"Edited by",editors:[{id:"4782",title:"Prof.",name:"Bishnu",surname:"Pal",slug:"bishnu-pal",fullName:"Bishnu Pal"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3092",title:"Anopheles mosquitoes",subtitle:"New insights into malaria vectors",isOpenForSubmission:!1,hash:"c9e622485316d5e296288bf24d2b0d64",slug:"anopheles-mosquitoes-new-insights-into-malaria-vectors",bookSignature:"Sylvie Manguin",coverURL:"https://cdn.intechopen.com/books/images_new/3092.jpg",editedByType:"Edited by",editors:[{id:"50017",title:"Prof.",name:"Sylvie",surname:"Manguin",slug:"sylvie-manguin",fullName:"Sylvie Manguin"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"371",title:"Abiotic Stress in Plants",subtitle:"Mechanisms and Adaptations",isOpenForSubmission:!1,hash:"588466f487e307619849d72389178a74",slug:"abiotic-stress-in-plants-mechanisms-and-adaptations",bookSignature:"Arun Shanker and B. 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\r\n\tWe are living in a society where automation in each electrical appliance/instrument is a great demand. We wish to have automatic devices/gadgets/instruments with no or minimal intervention from humans in their daily operation. Then only, these devices can qualify to call it is smart instruments. To fulfill this, one of the major requirements is to come up with highly sensitive, long-lasting, low-cost smart sensors. On the other hand, the healthcare industry demands low-cost, Lab-on-chip type biosensors for simple and rapid detection of various biomolecules or biogases. A sensor is an analytical device that detects the change in the environment and responds to some output in terms of a measurable analog resistance/voltage/current converted into a human-readable display or transmitted for further processing. In the last two decades, a significant amount of research has been devoted to the development of various types of gas sensors using different nanomaterials in the electronic and healthcare industry.
\r\n\r\n\tThis book aims to provide the reader (research scholars, scientists, and engineers working in the field of sensors) an overview of the recent advances made in the development of various gas sensors for the electronic and healthcare industries for the betterment of the human lifestyle. Also, this book will intend to address existing challenges and a few future directions of research for easy integration and cost-effective fast sensing of such
\r\n\tgas sensors.
Magnetic nanofluids, known also as ferrofluids or magnetic liquids, are stable colloidal suspensions of superparamagnetic nanoparticles such as γ-Fe2O3, α-Fe2O3, Fe3O4, CoFe2O4, Mn1−
Besides the well-known application of ferrofluids in sealing and lubrication, recent developments envisaged their potential in fields like actuation [22, 23], medicine [1, 16], biotechnology [14, 24], as cooling fluids [25–29] or as liquid core in power transformers [30, 31]. The applications in medicine and biotechnology require from the magnetic nanofluid to be biocompatible. Therefore, water-based magnetic nanofluids are the candidates for magnetic hyperthermia for cancer treatment and targeted drug delivery, as well magnetic separation for purification of cells, proteins or else. The applications envisaged in electrical engineering require from the proposed magnetic nanofluid to also have good thermal and insulating properties. These conditions can be fulfilled by the transformer oil-based magnetic nanofluids.
This chapter is addressing the application of a Fe3O4 magnetic nanofluid based on transformer oil, as cooling and insulating fluid of a power transformer. Thus, the preparation procedure and the characterization of structural, magnetic, rheological, thermal and electrical properties are presented. The mathematical model applied to the problem is introduced, and the numerical results for two power transformers are discussed. The use of this Fe3O4 magnetic nanofluid in a micro-actuation application is also presented.
The materials used for the synthesis of nanofluid with colloidal magnetic Fe3O4 nanoparticles we can mention: hexahydrated ferric chloride (FeCl3x6H2O) of 99% purity obtained from Merck Germany; ferrous sulfate sheptahydrate (FeSO4x7H2O) of 98% purity purchased from Chimopar, Romania; sodium hydroxide (NaOH) of 99% purity and oleic acid (C18H34O2) of 99% purity provided by Riedel de Haen. Other chemicals were of analytic grade. The reagents were used without further purification. All solutions were prepared with deionized water.
The transformer oil-based ferrofluid with Fe3O4 nanoparticles was synthesized by chemical co-precipitation method [23], using FeCl3×6H2O and FeSO4×7H2O with a molar ratio of Fe2+/Fe3+ = 1:2, dissolved in 300 ml of water and treated with NaOH 10%. The mixture was stirred at 80°C for 1 h. The resulting black color precipitate of Fe3O4 was washed with deionized water and magnetically decanted until a pH of 7 was reached. Then, 10 ml of HCl 0.1 N was added to the Fe3O4 precipitate for peptization. The mixture was washed and decanted again until pH 7, dried at 90°C and treated with acetone for water removal. A small part of the obtained powder was analyzed [X-ray diffraction, scanning electron microscopy (SEM) and elemental analysis EDX] for structural properties. The remaining part of the powder was treated with 2 ml of oleic acid as surfactant, and with 5 ml of toluene and heated at 90°C for toluene removal. Finally, the mixture was dispersed in 50 ml of UTR 40 transformer oil, under strong stirring for 20 h in order to obtain the magnetic nanofluid. Figure 1 schematically presents the transformer oil-based magnetic nanofluid of Fe3O4 synthesis.
Transformer oil-based magnetic nanofluid of Fe3O4 synthesis.
The Fe3O4 powder was structurally characterized by X-ray diffraction using a diffractometer D8 ADVANCE type X Bruker-AXS in conditions: Cu-Kα radiation (
The XRD pattern of the powder is presented in Figure 2 and shows the peaks corresponding to the Fe3O4 highlighted by “hkl” Miller indices (220), (311), (400), (422), (511) and (440), [2, 4], which denote a spinel structure with lattice parameter
The Fe3O4 XRD pattern of the Fe3O4 nanoparticles.
where
The morphology of the sample was studied by SEM using a Carl Zeiss SMT FESEM-FIB Auriger type scanner. The elemental analysis (energy-dispersive X-ray spectroscopy EDX) was performed with an energy dispersive probe of Inca Energy 250 type Oxford Instruments LTD England coupled to SEM.
The topology of the Fe3O4 powder analyzed by scanning electron microscopy evidenced two types of surface: smooth surface and rough surface (fracture). A crystalline structure of the material was found for the first type of surface, which is composed of crystallites having average sizes between 10 and 30 nm (Figure 3) in good agreement with the diffraction analysis. For the second type of surface, a structure of acicular type agglomerates was found (Figure 4).
The SEM image for the first structure.
The SEM image for the second structure.
The elemental analysis confirms the presence of Fe3O4 (Figure 5) and shows that the resulting black powder contains 70.14%Fe, 24.96% O, 4.16% C and 0.74% Cl (Table 1). The presence of the Fe3O4 is exhibited by elemental Fe-peaks of about 6.45 and 0.75 keV. The high percentage of oxygen is related to its existence in the iron oxide.
Element | Weight (%) | Atomic (%) |
---|---|---|
C K | 4.16 | 10.89 |
O K | 24.96 | 49.01 |
Cl K | 0.74 | 0.66 |
Fe K | 70.14 | 39.45 |
Totals | 100.00 | 100.00 |
Analysis data for Fe3O4 nanoparticles, energy dispersive.
The elemental analysis for Fe3O4 powder: (a) the SEM image and (b) the elemental energy dispersive X-ray analysis.
The SEM image (Figure 5a) and the elemental energy dispersive X-ray analysis (Figure 5b) confirms the data determined by X-ray diffraction. The content of C and Cl represents the little impurities.
The full magnetization curve and the hysteresis loop of the transformer oil-based magnetic nanofluid (MNF/UTR 40), with a solid volume fraction of the dispersed magnetite particles of 1.67%, were measured at room temperature (25°C), using a vibrating sample magnetometer—VSM 880—ADE Technologies USA, in the magnetic field range of 0–950 kA/m.
The magnetization M measured at the maximum value of the applied magnetic field, approx. 900 kA/m, is considered to be the nominal magnetization of the investigated sample. Also, the absence of hysteresis loop area indicates a specific behavior of soft magnetic material (Figure 6) with the magnetic characteristics shown in Table 2.
Sample | ||||||
---|---|---|---|---|---|---|
MNF/UTR 40 | 50 | 3.98 | – | – | 0.96 | 1.67 |
Physical properties of MNF/UTR 40 sample.
Hysteresis loop and full magnetization curve of the transformer oil-based magnetic fluid sample shows specific behavior of soft magnetic materials: (a) hysteresis loop for UTR 40-based MNF sample and (b) full magnetization curve for UTR 40-based MNF sample.
In Table 2,
According to Shliomis [32], the magnetic behavior of a diluted magnetic nanofluid
with
representing the Langevin parameter. Herein
In low magnetic fields
On the other hand, in the region of intense magnetic fields
where
In fact, in real ferrofluids, the dimensional polydispersity of the magnetic particles is a characteristic that cannot be neglected and, in the absence of inter-particle interactions, an accurate expression of magnetization is obtained [34],
where
(a) TEM image of mono-layer covered magnetite nanoparticles with oleic acid and stably dispersed in hexane; (b) dimensional distribution of the magnetic particles physical diameters is well approximated by the log-normal distribution function.
with
Another important aspect regarding the magnetization evaluation that should be considered is the dependence of the dispersed nanoparticles magnetic moments with their magnetic diameters [36, 37]. Here,
with
The linear dependence of the initial magnetic susceptibility versus magnetic particle concentration in low fields, rel. (4), and the asymptotic variation in magnetization in intense magnetic fields, rel. (5), form the basic instruments of magnetogranulometric analysis, in order to determine the mean magnetic diameter of the dispersed magnetic particles,
and standard deviation
where the dimensional distribution parameters are evaluated first,
and
The expression of the dimensional distribution parameters was obtained from rel. (8), considering the above presented limit cases and evaluating the initial magnetic susceptibility and saturation magnetization, respectively.
In the linear region of small magnetic fields
Sample | ||||||
---|---|---|---|---|---|---|
MNF/UTR 40 | 0.11 | 0.99467 | 4.24 | 53.23 | 34.72 | 0.98580 |
Initial magnetic susceptibility and saturation magnetization of the transformer oil-based magnetic fluid sample.
Obtaining
Magnetogranulometric analysis of the MNF/UTR 40 sample has revealed a mean magnetic diameter of the magnetite particles of
a value of 8.12 nm was determined for the mean physical diameter. Furthermore, a thickness of 1.9 nm of the oleic acid monolayer cover of magnetite particles
Main results obtained through magnetogranulometric analysis of the MNF/UTR 40 sample are summarized in Table 4.
Sample | |||||||
---|---|---|---|---|---|---|---|
MNF/UTR 40 | 6.12 | 0.33 | 4.50 | 6.46 | 2.18 | 8.12 | 11.92 |
Main properties of MNF/UTR 40 sample obtained through magnetogranulometric analysis, including the log-normal distribution parameters values.
Rheological investigations, carried out with an Anton Paar Physica MCR 300 rheometer using a double-gap concentric cylinder geometry, consisted of measuring the dynamic viscosity curves of the samples in the absence of the magnetic field. The shear rate,
Viscosity curves showed that the Newtonian behavior of the carrier (UTR 40) (a) is preserved throughout the temperature range, also for the magnetic nanofluid (MNF/UTR 40), (b) that contains a small amount of the di
This behavior indicates the absence of the magnetic particle interactions, that is, a very good stability of the sample, mainly due to the efficient steric stabilization. An Arrhenius-type relationship describes the sample viscosity behavior with temperature,
where
Considering a shear rate of 100 s−1, rel. (16) was used to fit the dependence
Arrhenius type dependence of the samples dynamic viscosity with temperature: (a) carrier liquid UTR 40 and (b) transformer oil-based magnetic nanofluid MNF/UTR 40.
In Table 5, it can be observed that the value of the viscous flow activation energy does not change after dispersing a small amount of surfacted magnetite particles in the carrier liquid. It can be concluded that the adding of small volume fractions of surfacted magnetite particles in a carrier liquid
Sample | ||
---|---|---|
MNF/UTR 40 | 1.67 | 28.27 × 103 |
UTR 40 | – | 28.38 × 103 |
Viscous flow activation energy of the carrier liquid (UTR 40) and the magnetic nanofluid (MNF/UTR 40).
The addition of metallic nanoparticles (magnetic or non-magnetic) or non-metallic (e.g., diamond nanoparticles) in transformer oils in order to improve their cooling performances is a solution that was demonstrated by several patents and associated research works (e.g. [39–45]). This paragraph analyzes the thermal properties of the magnetic nanofluid, which was tested for use as cooling and insulating medium in power transformers.
Determination of the effective thermal properties that characterize the cooling fluids in our study as well as their modeling using analytical formulae is representing a main problem of the topic in discussion. Irrespective of the considered approach, either theoretical or experimental, a representative element of the studied medium has to be chosen. It has to be underlined that the determination of the properties of heterogeneous materials has to be made by complying with the request of representativeness of the studied volume, that is, the considered volume of the heterogeneous material must be sufficiently large in order to be statistically representative irrespective of the type of the carried out experiment [46, 47].
The main properties that are influencing the thermal behaviour of a material are the heat capacity, thermal conductivity, density, thermal expansion coefficient and thermal diffusivity (a property that depends on the first three). Various experimental studies determined that the effective properties of nanofluids (magnetic or non-magnetic) are dependent on the following characteristics of their components [25, 48–50]: the thermo-physical properties of the carrier fluid, nanoparticles and surfactant; nanoparticles volume fraction, size distribution, mean diameter and shape; temperature; magnetic field (in the case of magnetic nanoparticles).
A review of the reference literature regarding the main properties of the transformer oil-based fluids and their dependence with the temperature outlined the followings: specific heat is increasing as linear function with temperature; thermal conductivity is decreasing as a quasi-linear function with temperature especially for transformer oils; dynamic viscosity is decreasing with the increasing temperature; the dielectric constant has relatively low values and decreases with the increasing temperature [51–53].
The thermal conductivity of magnetic nanofluids can be described as a function of several parameters, among the most important are the thermal conductivities of the carrier liquid and magnetic nanoparticles and their dependence on temperature and pressure, the volume fraction, the shape and the size distribution of the nanoparticles. The interfacial thermal resistance between the nanoparticles and the surrounding liquid is also considered. It has been proved numerically and experimentally that an applied magnetic field can affect the thermal conductivity of a magnetic nanofluid due to the consequent ordering of magnetic dipoles of the nanoparticles along the field lines [25, 54].
There are many Maxwell-type models developed for the thermal conductivity of mixtures (also named effective thermal conductivity—ETC), either solid matrix—solid filler or liquid carrier and dispersed nanoparticles that are based on the Maxwell model, which is recommended for low volume fraction of the filler/nanoparticles and considers that the nanoparticles are identical, spherical and non-interacting. The Holotescu-Stoian model, developed initially for the solid matrix—solid filler mixture and presented in Refs. [55, 56], introduced for the first time the filler particle size distribution in the Maxwell model. The expression for the effective thermal conductivity of the Holotescu-Stoian model, rel. (17), in the case of a magnetic nanofluid is [57],
where
with
with
The relationship between physical (geometrical) diameter
This model, confirmed by the experimental data [57], was applied to determine the thermal conductivity of the analyzed magnetic nanofluid sample. The results (at room temperature) are given in Table 6, and we observe that the addition of magnetite nanoparticles alone is increasing the thermal conductivity of the magnetic nanofluid. The transformer oil thermal conductivity is decreasing with the increasing temperature, thus the cooling performance can be diminished at normal operating conditions in power transformers (and other electrical equipments). We can conclude that the addition of the magnetite nanoparticles can counteract this disadvantage. Moreover, during the operation of a power transformer, for instance, the magnetic field is acting on the magnetic nanofluid, influencing its physical properties, and generating the magneto-convection that can enhance the heat transfer, as shown in the next section.
Property/sample | UTR | NP | MNF_UTR | ΔX/XUTR |
---|---|---|---|---|
0.127 | 1.39 | 0.135 | +6.29% | |
1910.1 | 0.892 | 1867.8 | −2.2% | |
7.15 × 10−4 | 1.2 × 10−4 | 6.44 × 10−4 | −9.94% |
Thermal expansion coefficients.
The specific heat of the magnetic nanofluid, at constant pressure, was determined using the following mixture formula [58]
where the transformer oil specific heat was determined by using
and the specific heat of the magnetite by using [59],
where T (K) is the absolute temperature of the solid and
The numerical results obtained for the magnetic nanofluid specific heat indicate a slightly decrease compared to that of the carrier liquid. In what it concerns the effect of an applied magnetic field on the specific heat capacity of a magnetic nanofluid, for a certain range of temperature, the reference literature indicates the influence of the nanoparticles volume fraction and nanofluid composition (carrier liquid and nanoparticles). Also, the magnitude and the applied field orientation relative to the gravitational field (as the experiments were conducted in gravitational field) should be considered. Korolev et al. [60] analyzed the influence of an applied magnetic field (oriented perpendicularly on gravity) on a transformer oil-based magnetic nanofluid with magnetite nanoparticles, having a solid volume fraction of 7.4%, in the temperature range from 15 to 80°C. The experiment showed that, for a certain temperature, the specific heat capacity has a maximum in the investigated range of the applied magnetic field, which, according to the authors, indicates the presence of a magneto-caloric effect.
Similarly, to determine the thermal expansion coefficient of the magnetic nanofluid, a corresponding mixing formula was used [61],
where
The results of the calculations, summarized in Table 6, give the thermal properties at room temperature. We observe that the analyzed thermal properties have a diverging behavior. While the thermal expansion coefficient and specific heat are decreasing, the thermal conductivity is increasing. The last column is indicating the relative variation compared to the corresponding property of the carrier liquid (transformer oil).
To determine the potential performance of the magnetic nanofluid for heat transfer, we considered the figure-of-merit (FOM), as defined for natural convection [64],
where
The results obtained for the FOM of the carrier liquid and the magnetic nanofluid, using the properties determined above, are presented in Table 7. The comparison of the relative increase of FOM indicates that the addition of nanoparticles is advantageous for both laminar and turbulent flow.
Property/sample | UTR | MNF_UTR | ΔX/XUTR |
---|---|---|---|
FOM, | 18.61 | 19.57 | +5.15% |
FOM, | 91.85 | 96.25 | +4.8% |
FOM results, obtained for the carrier liquid and for the magnetic nanofluid.
As underlined above, the use of a magnetic nanofluid in electrical engineering applications imposes restrictions regarding its insulating properties. Transformer oils are known to be electrical insulators so they are an appropriate carrier liquid for a magnetic nanofluid used in such applications. If the magnetic nanoparticles volume fraction is kept in certain limits, the magnetic nanofluid preserves its insulating properties within the required limits, too [49, 50].
We estimated the effective electric permittivity of the magnetic nanofluid
with
The results are presented in Table 8, along with the relative difference between the values corresponding to the transformer oil and magnetic nanofluid,
Property/sample | UTR | NP | MNF_UTR | Δ |
---|---|---|---|---|
2.2 × | 81 × | 2.26 × | 2.85% |
Effective electric permittivity of the Fe3O4 transformer oil-based magnetic nanofluid.
We observed that for the current volume fraction of magnetic nanoparticles, the insulating properties of the magnetic nanofluid remain very close to those of the carrier liquid (UTR 40). In what concerns the effect of working temperatures in the power transformer, experimental studies showed that electrical permittivity decreases with increasing temperature in the case of transformer oils [51].
A colloidal Fe3O4 specific nanofluid dispersed in oil transformer UTR 40, named MNF/UTR 40, is utilized in a number of technologically relevant applications where external magnetic fields are used to adjust their flow. A mathematical model and numerical simulation results are useful for investigating the heat transfer properties of the magnetic nanofluid. Based on this study, it was built and tested the experimental model: low power, medium voltage, single-phased transformer type TMOf-24-5” (Figure 18) and low power, medium voltage, single-phased transformer type TMOf2-36kV-40 kVA (Figure 19). First of all, it was used for the transformer the transformer oil UTR 40 as cooling and insulating liquid. After that, this oil was drained and the experimental model was filled with magnetic nanofluid based on transformer oil MNF/UTR 40. The MNF/UTR 40 specific nanofluid has been shown to provide both thermal and dielectric benefits to transformers, and can be utilized to improve cooling by enhancing fluid circulation within transformer windings, to increase transformer capacity to withstand lightning impulses, while also minimizing the effect of moisture on typical insulating fluids. Magnetic nanofluid flow may be influenced by external magnetic fields, and the retention force of a magnetic nanofluid can be adjusted by changing either the magnetization of the fluid or the magnetic field in the region. Opposite to usual magnetic fluids, the magnetizable nanofluids destined to heat transfer should have a low concentration of magnetic nanoparticles in order to make them competitive with the non-magnetic fluids.
The 2D simplified model and the FEM mesh made of triangular elements: (a) computational domain and (b) detailed view—windings, iron core, case.
Magnetic field, temperature and flow fields for mono-phased transformer of low power and medium voltage, type TMOf-24-5, (a) Heat transfer and thermal flow—upper part, (b) detail—temperature, buoyancy flow, (c) heat transfer and thermal flow—bottom part and (d) magnetic field.
Magnetic field and body forces when the coolant is a magnetic nanofluid, MNF/UTR 40: (a) detail (top)—magnetic body forces, (b) detail (top)—buoyancy forces, (c) detail (bottom)—magnetic body forces, (d) detail (bottom)—buoyancy forces.
2D, axial model - magnetic flux density field, temperature distribution, and flow field for the horizontal design TMOf-24-5 type transformer: (a) the coolant is regular UTR 40 transformer oil and (b) the coolant is a magnetic nanofluid, MNF/UTR 40.
2D, axial model - magnetic flux density field, temperature distribution, and flow field for the vertical design TMOf 2-36kV-40kVA type transformer: (a) the coolant is regular UTR 40 transformer oil and (b) the coolant is a magnetic nanofluid, MNF/UTR 40.
The aggregate active parts, core and windings [
Magnetic cores and the core rolling device [
Several simplifying assumptions aimed and keeping the physical system within approachable software and hardware limits are requested and 2D models are best candidates, providing numerical simulation relevant results, of satisfactory accuracy. Following this path, we consider a 2D, Cartesian cross-sectional model, as shown in Figure 11.
The heat transfer and transport processes under the influence of the magnetic field for two prototypes electric transformer: low power mono-phased transformer (24 kVA), at medium voltage (20/√3//0,4/√3kV), TMOf-24-5 and low power mono-phased transformer (40 kVA), at medium voltage (30/√3//0,4/√3kV), prototype TMOf 2-36kV-40 kVA, are described by the following set of coupled partial differential equations [44]:
electromagnetic field—quasi-steady, harmonic diffusion,
momentum balance (Navier-Stokes),
mass conservation (incompressible flow),
heat transfer (energy equation),
Here:
The magnetic field magnetizes the magnetic nanofluid, and the corresponding body force term adds to the gravitational, thermal flow of the magnetic nanofluid coolant. The flow structure is the result of the two competing forces: thermal force and magnetic force. In this study, we deal with a super-paramagnetic magnetic nanofluid where the influence of the coercive magnetic field intensity,
The magnetic field produced by the electrical current in the coil magnetizes the fluid and is responsible for the magnetic body forces that influence the thermally induced flow. The magnetization of the magnetic fluid is approximated here by the analytic formula
with
The strategy that we used in the numerical simulation consists of solving for the magnetic field first, and then using the active power thus obtained as heat source in the heat transfer and flow parts of the problem. The obtained solutions are steady state [65] for heat transfer and flow and quasi-steady (harmonic) for the electromagnetic field.
The main dimensions (windings, iron core, case sizes) are those of the single-phased transformer considered in our study. The amperturns of the windings correspond to the nominal working point, when the iron core exhibits lower levels of magnetization—the amperturns are compensated.
Numerical simulation of the mono-phased transformer of low power and medium voltage type TMOf-24-5 evidenced that the convective heat transfer in the channels between the windings and between the windings and core (3–5 mm) is less important in the overall process, therefore it was discarded, and only conduction heat transfer was accounted for in these areas. Figure 12 shows simulation results for a non-magnetic, regular cooling fluid—the temperature field (surface color map, Figure 12a–d), the thermal flow (streamlines and velocity vectors, Figure 12a–c), magnetic flux density (Figure 12d, surface color map, iso-lines of magnetic vector field). Apparently, the thermal flow exhibits two minor recirculation areas—in the upper and lower part of the windings, by the top and bottom covers—trapped within a larger recirculation cell that develops by the lateral wall. For the heat transfer part of the problem, we assumed a convection (Robin) type boundary condition (the ambient temperature was assumed to be
The iron core, although less magnetized in this particular regime (compensated primary and secondary amperturns), plays a crucial role in the heat transfer problem.
When a colloidal Fe3O4 specific nanofluid MNF/UTR 40 is utilized as a coolant, magnetic body forces add to the thermal, gravitational body forces. Figure 13 displays the magnetic field and forces (magnetic and thermal). Apparently, the magnetic forces contribute differently to the overall convection flow: in the upper part of the cell they add to the buoyancy forces, whereas in the lower part they are opposite. However not unexpected, Eq. rel. (33), another important finding is the effect that the en-parts of the windings and the iron core have: these are regions of high gradient magnetic field strength, and it is here that the body magnetization forces are significant. The orientation of the magnetic forces versus the thermal forces is an important factor in providing an optimal design. We observe that the thermal gravitationally driven forces and the magnetic forces act concurrently in this plane, their combined effect being greater at the left and right end regions. Similarly, the heat transfer direction is from the hotter regions (core and windings) to the case, but with enhanced convection and increased heat removal efficiency. Comparing the two cooling options, that is, specific nanofluid MNF/UTR 40 (Figure 14b) versus regular coolant UTR 40 (Figure 14a) apparently the MNF/UTR 40 may do better in cooling the transformer. This essentially means a lower hot spot temperature by approximately 10° in this model and a more uniform temperature distribution. These results suggest that the vertical design of the low-power mono-phased transformer (40 kVA), at medium voltage (30/√3//0,4/√3kV) prototype TMOf 2-36kV-40kVA (Figure 15) may be advisable [66, 67]. This prototype TMOf 2-36kV-40kVA realized in compliance with the constructive solutions with characteristics specific for the aimed purpose presents the following advantages: reduced weight and dimensions in comparison with the current power transformers that have the same rated voltage and rated power, following the intensification of the cooling effect in the presence of the specific nanofluid MNF/UTR 40 (Figure 15b). The number of convection zones is greater when the coolant is magnetic nanofluid MNF/UTR 40 (Figure 15b) as compared to the regular coolant, that is, the UTR 40 transformer oil (Figure 15a). Also, because of the execution form of the magnetic circuit and of the metallic construction (tank-bottom-lid), the construction of the power transformer in the aggregate is realized with a smaller consumption of the main materials: copper, magnetic steel sheet and the specific nanofluid MNF/UTR 40 are included.
The low-power mono-phased transformer (40 kVA), at medium voltage (30/√3//0,4/√3kV), prototype vertical design TMOf 2-36kV-40kVA type transformer has the active part (Figures 16 and 17), magnetic iron core with the high voltage (HV) and low voltage (LV) windings fixed in a finned metallic tank constituted from two parts air-proof assembled through a soldering that is soft and capable of elastic deformation for the taking-over of the variation with temperature of the cooling liquid volume (Figure 19). The magnetic circuit is coating type, constituted of two identical cores of rectangular shape (flat-core), back to back disposal (Figure 17). The aggregate active parts (Figure 16) are the magnetic core with the high voltage and low voltage windings, fixed on a metallic lid with their axes in a vertical position, the most convenient situation for the heat transfer enhancement by the nanoparticles in the presence of the electromagnetic field. With a view to performing comparative tests related to the use of magnetic nanofluid MNF/UTR 40 as cooling and insulating fluid transformers and regular UTR 40 transformer oil cooling, the mono-phased transformer of low power and medium voltage, the horizontal design TMOf-24-5 type transformer (Figure 18) and mono-phased transformer of low power and medium voltage the vertical design TMOf 2-36kV-40kVA type transformer (Figure 19) has been achieved [44]. The numerical simulation results show that the direction of the magnetizing force in comparison with the gravitational thermal force is an important element in assuring of an optimal heat transfer. Both numerical simulations as well as laboratory measurements [65–67] confirm the following aspects: about the usage of a magnetic nanofluid MNF/UTR 40 as cooling and insulating fluid for transformers, this provides for magnetization body forces that add to the thermal, gravitational forces. In the vertical layout of the transformer, these forces act concurrently with the thermal flow, and the overall effect is the enhancement of the heat transferred from the aggregate active parts (core and windings) to the ambient.
Mono-phased transformer of low power and medium voltage, the horizontal design TMOf-24-5 type transformer.
Mono-phased transformer of low power and medium voltage, the vertical design TMOf 2-36kV-40kVA type transformer [
In both cases, first of all, the regular UTR 40 transformer oil as cooling and insulating fluid was used for the transformers. After that, this oil was drained and the transformers were filled with magnetic nanofluid MNF/UTR 40 as cooling and insulating fluid.
Figures 20 and 21 show the temperature on the surface of the ribbed tank when magnetic nanofluid MNF/UTR 40 is used for the vertical design TMOf 2-36kV-40kVA type transformer after 1 h of operation. Monitoring of the temperature was achieved with the thermographic camera, FLUKE Ti 20. The temperature does not exceed the value of 54°C. Magnetic nanofluid MNF/UTR 40 provides also the increase of the transformer’s capacity to sustain over-voltages and withstand better to degradation in time due to humidity, as compared to the regular UTR 40 transformer oil coolant. Thus, transformers with reduced dimensions and higher efficiency with loading capacity and extended life duration may be designed.
Temperature distribution by thermographic imaging-the tank- for mono-phased transformer of low power and medium voltage, type TMOf2-36kV-40 kVA, after 1 h of operation.
3D characteristic of the temperature depending on the
Based on the afore described magnetic nanofluid, we can make a microactuator whose operation complies with the principle of Pulse Width Modulation (PWM) [23, 68]. The output PWM rectangular pulse form for a pulse duty factor of 14% is presented in Figure 22. The PWM generator discharges on the microactuator magnetic nanofluid impedances, two windings L1 and L2 (Figure 23). The electromagnetic force developed by the microactuator and implicitly the movement of the magnetic nanofluid depends mainly on the windings excitation voltage pulse duty factor
The output PWM rectangular pulse form, for a pulse duty factor of 14%.
The microactuator with magnetic nanofluid during testing [
The authors express special thanks to Prof. Alexandru Mihail Morega, corresponding Member of the Romanian Academy, for valuable results concerning the numerical simulations. The research was performed with the support of UEFISCDI, PNCDI II Programme—Joint Applied Research Projects, Romania, Contract 63/2014, Environment energy harvesting hybrid system by photovoltaic and piezoelectric conversion, DC/DC transformation with MEMS integration and adaptive storage. Also, the numerical simulations were conducted in the Laboratory for Multiphysics Modeling, at UPB, with the support of the PNCDI-II “Parteneriate” Contract 21-043/2008.
Hepatitis B virus (HBV) is a partially double-stranded viral agent with a circular deoxyribose nucleic acid (DNA) that replicates by reverse transcription. HBV infection is a hepatocyte infection that is globally considered as a public health concern [1, 2, 3]. There are more than 2 billion persons infected with HBV living today worldwide with 260 million estimated to be chronically infected with the infection and having a carrier rate varying from 9 to 20% in Sub-Saharan Africa (SSA) [4, 5, 6]. Annually, there are close to 900,000 HBV-related deaths, mainly due to cirrhosis or hepatocellular carcinoma (HCC). The viral infection is the fourth most common vaccine preventable infection among travelers returning home ill after enteric fever, acute hepatitis A, and influenza [7, 8]. This viral agent can cause both acute and chronic infections. Many infected persons show no symptoms during the initial stage of the infection. Typically, the viral agent has an incubation period of 90 days (range, 60–150 days). The acute HBV infection that is acquired newly only shows symptoms rarely. Signs and symptoms of the viral infection differs with age; most children aged under 5 years old and newly infected immunosuppressed adults often show no symptoms, while about 30–50% of people that are more than 5 years of age are usually symptomatic [7]. When present, the typical signs and symptoms of acute infection include malaise, fatigue, poor appetite, nausea, vomiting, abdominal pain, fever, dark urine, light color (clay-colored) stool, joint pain, and jaundice [8]. The overall case fatality ratio of acute infection due to HBV is approximately 1% [9]. People infected with HBV are susceptible to infection with hepatitis D virus; coinfection increases the risk of fulminant hepatitis and rapidly progressive liver disease [10]. Transmission of HBV is mainly through percutaneous or mucosal exposure to HBV-infected blood or bodily fluids including saliva or semen [2]. There are reports of transmission via sexual contact and contaminated medical equipment and through sharing of infected needles and injecting apparatus [11].
The prevalence of chronic HBV infection is ≥2%, such as in the western Pacific and African regions; expatriates, missionaries, and long-term development workers may be at increased risk for HBV infection in such countries [7, 8]. Serologic markers specific for the viral agent are necessary to diagnose HBV infection and for appropriate clinical management [12]. These markers can differentiate between acute, resolving, and chronic infections. Polymerase chain reaction (PCR) method can further be use to qualitatively or quantitatively detect the amount of HBV DNA in patients’ specimen after checking the markers of the virus [13]. All travelers should be screened for HBV infection markers, so that they would not be at risk of acquiring the virus during their stay [7].
Hepatitis B virus belongs to the family of
Morphology of hepatitis B virus [
The cardinal feature of HBV replication cycle is the replication of the DNA genome by reverse transcription, when virions bind susceptible cell-surface receptors and IgA receptors on liver cells following of RNA intermediate [18, 20]. The viral genome is transported into the nucleus, and it is then converted into a covalently closed circular double-stranded HBV DNA (cccDNA) molecule which acts as the transcriptional template for the host RNA polymerase II machinery that synthesizes polyadenylated and four capped mRNAs which encode the envelope structural proteins, viral core and the precore; polymerase; and X non-structural viral proteins [20]. A 3.5-kb genome length RNA is one of the major HBV transcripts which is translated to synthesize the viral core and polymerase proteins and also plays role as a pregenomic RNA that is encapsidated with the polymerase by the core protein in the cytoplasm of the liver cells. The replication of the viral agent usually happens entirely within these capsids by reverse transcription of the pregenomic RNA to synthesize a single-strand DNA copy that serves as the template for the second strand DNA produced, synthesizing a circular double-stranded DNA [21]. The viral capsids that contain the double-stranded DNA traffic either to the nucleus where amplification occurs or the viral cccDNA genome to stabilize intranuclear pool of transcriptional templates or to the endoplasmic reticulum, where they acquire the viral envelope proteins, bud into the lumen, and exit the cell as virions that can infect other cells [22, 23].
Hepatitis B virus gets entry into the bloodstream and targets the liver cells [24]. The hepatocytes which are infected are distended, and the cytoplasm assumes a ground appearance that is glassy. The virus is not cytopathic, and injury of the liver in HBV chronic infection is due to immunological responses [8, 25]. Although, the virus has a long incubation period of 45–180 days, replication starts few days after infection. The infection can be acute, an unexpected sickness with a mild-to-severe course followed by comprehensive resolve [26]. On the other hand, if the cell-mediated immune reaction is feeble, the infection does not resolve, and chronic hepatitis arises with an extended course of active disease or silent asymptomatic infection [27].
About 30–80% adults of acute HBV infection shows symptoms (1% fulminant hepatitis), whereas less than 1 year old children shows no symptoms [28]. Symptoms of HBV infection include malaise, dark urine, fever, nausea, jaundice, pale stools, right upper quadrant pain, and anorexia. The risk of chronic infection of HBV is hinged on the duration of acquisition [26]. About 90% of infected neonates, 30–50% of children aged 1–4 years, and 1–10% of acutely infected adults result to persistent infection. There are approximately 15–40% with persistent infection that leads to advanced liver disease, cirrhosis, and/or HCC [8, 29].
Transmission of HBV in travelers is through percutaneous or mucosal exposure to HBV-infected blood or bodily fluids including saliva or semen [30, 31]. There are reports of transmission via sexual contact, contaminated blood and its products, and contaminated medical equipment and through sharing of infected needles and injecting apparatus [31, 32].
In SSA, the viral infection, is often disseminated through perinatal and horizontal route, while in the developed regions, most infections occur in adults of younger ages through injecting drug use or high-risk sexual behavior (e.g., bisexuals and homosexuals) [8, 33]. HBV infection is known to be transmitted from the mother to child and it is a thing of worry [34, 35]. Every year, about 25,000 infants are born to HBV-diagnosed mothers in the United States, and approximately 1000 mothers transmit HBV to their infants. This means that about 90% of HBV-infected newborns will eventually develop to chronic infection, and up to 25% of those infected at birth will eventually die prematurely due to HBV-related complications. Therefore, the standard care for pregnant women includes an HBV testing during each pregnancy, to prevent HBV-positive pregnant women from transmitting the viral agent to her unborn child [34, 35].
Inadequate infection control in healthcare settings also constitutes to a significant mode of HBV transmission. That is why immigrants from many countries are recommended to be tested for HBV [12]. Transmission by blood transfusion is now rare, whereas before screening of donor blood, it was not uncommon [32]. Cord blood is usually negative for the serological markers of HBV, but occasionally intrauterine infection might happen. Fetal blood sampling might enhance this risk, but amniocentesis does not appear to increase the chances of intrauterine transmission [36]. Infection presumably occurs at or soon after birth. It perhaps occurs through breast (feeding) milk, as it is known to carry the virus. Transmission could occur if there was an in apparent breach in the mucosa of the mouth or during teething [37]. Among adults, high-risk sexual activity is one of the most frequent routes of transmission for HBV [38]. Historically, male homosexual contacts have been associated with a high risk for the viral infection [38]. Sexual transmission accounts for a majority of the transmission occurring in adult life [38]. More recently, heterosexual transmission is reported to be the most common cause of acute HBV infection in adults [39]. Transmission may also continue to occur in healthcare settings. It is a result of nonadherence to isolation guidelines in a hemodialysis unit, or direct person-person exposure (e.g., surgeon-to-patient or dentist-to-patient) may transmit the virus [40]. Sharing of clothes and bed spaces could pose jeopardy because the virus could be found in saliva, tears, urine, breast milk, and any other body fluid [13]. Other possible means of transmission include an infected parent kissing the cut finger or scraped knee of his child and sharing of personal items of personal hygiene such as toothbrushes between parents and children [3].
There is insufficient information that depicts predisposing factors to travelers; however, there is scarcity of public reports of HBV infection in travelers, and there is low risk for travelers who are not engaged in high-risk behaviors [7]. The risk of the viral infection might increase in countries/regions that have a 2% prevalence of chronic HBV infection, such as in the African and Western Pacific regions; missionaries, long-term community development workers, and expatriates might be at high risk for the viral agent in such areas [41]. Travelers should take note on how the virus is acquired and take precautionary measures to mitigate transmission. The risk of injury due to accident is much higher for travelers than for people in their own environment. These injuries may involve medical attention that will require injections, IVs, or blood transfusions, thereby enhancing the risk of HBV exposure [7]. Older aged travelers, especially those with heart problems, may also require medical treatments that will require the same risks of exposure.
The global prevalence of HBV indicated by the proportion of chronic HBV carriers in the population that is seropositive for the hepatitis B surface antigen (HBsAg) varies strongly between different geographical regions [12]. The virus endemicity level is different from one nation to another. The level is mostly lowered in the Western Europe, the United States, Canada, and some South American and Northern African countries (with an HBsAg chronic carrier rate < 2%); intermediate (i.e., 2–8%) in Eastern Europe, Central Asia, and some Eastern Asian countries; and high (above 8%) in Alaska, Sub-Saharan African countries, and some Asian countries [12, 42]. Infection with HBV is considered among the commonest immunization preventable infections among immigrants [12, 43]. The prevalence of the virus in travelers is associated with the status of the traveler’s immunity, the duration of travel, and the level of HBV endemicity in the destination country. More so, there are peculiar populations of travelers that might be of higher risk of HBV acquisition which includes those visiting relatives and friends, the expatriates, dental surgery and medical procedure travelers, and those casual sex engagers [7]. Empirical information posited that travelers seeking urgent, unforeseen medical attention are common which makes travelers at risk of the viral agent [44]. There is paucity of empirical evidence to quantify the risk travelers might also be exposed to HBV through activities that involve tattooing, piercings, and acupuncturing [7].
Coppola et al. [42] reported HBsAg seropositivity of 9.6% among undocumented refugees and immigrants in Southern Italy. The study showed that male sex, SSA origin, low level of schooling, and minor parenteral risks for acquiring HBV infection (acupuncture, tattoo, piercing, or tribal practices) were independently associated with ongoing or past HBV infection [42]. A study in Thailand among international backpackers reported that 25% of its population had engaged in casual sex, while traveling and about half of the population did not often use condom [45]. The risk of HBV infection from sex without protection increase with the number of sex partners, and the incidence of unprotected sex was higher among the singles based on a study carried out on Dutch travelers to tropical and subtropical regions [46]. A study among Australian travelers reported that about half of them had indulged in at least one activity with an HBV risk during their last overseas trip to Southeast or East Asia [47]. Travelers without immunity for the virus traveling to high HBV prevalence countries like Nigeria might be at risk of acquiring the infection due to the many potential accidental and uncontrollable exposures during travel. A Netherlands study reported that 9% of all HBV cases between 1992 and 2003 were travel-related with an estimated incidence of HBV infection of 4.5 per 100,000 travelers [48]. In a study carried out between 1997 and 2007, HBV infection was reported in 51 cases of a cohort of ill travelers presenting to GeoSentinel clinics [49]. The study also found out that male sex and older age are associated with HBV acquisition statistically. Findings among travelers have shown that new sexual partners and unprotected sex are common, especially where there is excessive alcohol intake environment [44, 50, 51]. In countries with high HBV endemicity, the monthly estimated incidence of the infection ranges from 25 per 100,000 for symptomatic infections to 80–420 per 100,000 for all HBV infections in susceptible expatriates residing in such country [52]. Development/aid workers, volunteers, and missionaries pose greater risk of the infection due to extension of travel stay and local community close contact [7]. The prevalence of anti-HBc antibody was 5%, doubling that of the general population in a Swedish expatriate’s population. Short duration of travel stay will obviously lower the risk of the infection [53]. Nielsen et al. reported that the incidence per month of HBV infection was 10.2 per 100,000 with 62% of cases traveling for less than 4 weeks [54]. Most research is hinged on travelers becoming sick after travel before testing to occur, so this tends to underestimate the incidence of the viral infection [7, 49].
Many cross-sectional research have find out that travelers have reduced baseline understanding on infections related to travels and put themselves in jeopardy to HBV infection through their actions while in foreign land [47, 55]. Nielsen et al. reported that 5% of short-term and 5% nonimmune travelers were under a great risk of getting infected with HBV via tattooing, injections, and operation activities [44]. About 41% high-risk endeavors were reported among travelers in more than 6 months with most of the endeavors being unintentional and involuntary [44]. In a retrospective study among Australian travelers, 281 (56%) had visited a country with medium to high prevalence of HBV, of whom only 43% had been vaccinated and 162 (33%) undertook activities associated with potential HBV exposure [55]. Medical tourism and transplantation of organs have been identified several times as predictors for the viral agent, which highlights that checking for transmissible infection cannot be guaranteed universally [56, 57]. A study among Australian patients finds out that 2 of 16 who traveled overseas for commercial kidney transplantation developed fulminant hepatitis related to HBV infection and died [58]. Significantly high-incidence rate of HBV infection was reported among patients receiving renal transplantations in India than in Saudi Arabia [59].
Hepatitis B virus until now has been reported to have 10 genotypes (A–J) with identified peculiar distribution based on regions to its high degree of genetic heterogeneity [5, 60, 61, 62]. HBV genotyping is significant in diverse ways. First, it provides global data on the genotypic distribution of the virus including phylogenetic and phylogeographic evidence. Second, it justifies the relationship between the viral strain and course of disease. It makes us understand the role of human migration on the evolution of the virus [63, 64].
One of the three genotypes A, D, and E is predominantly circulating in Africa depending on the country. Genotype A is found in the Southern and Eastern regions, and genotype D is predominantly circulating in the Northern Africa region. Genotype E is more in most of SSA regions including Nigeria; this report excludes Uganda and Cameroon which are predominant with the A genotype [5, 60, 64, 65]. Genotype A is prevalent in Europe and Southeast Asia, including the Philippines [43, 66]. Genotypes B and C are predominant in Asia [67]; genotype D is common in the Mediterranean area, the Middle East, and India; genotype F is common in Central and South America [66]. Genotype G has been identified in Germany and France [67]. Genotype I has been detected in Laos, Vietnam, and China [68, 69], while the newest genotype J was identified in the Ryukyu Island in Japan [70, 71].
HBsAg is the standard diagnostic marker used to screen for HBV infection in travelers. A positive test depicts an acute or chronic infection [2]. Quantifying HBsAg (qHBsAg) is also an essential tool in staging of HBV infection and predicting responses to HBV treatment. This tool depend on both viral and host factors, such as genotype, preS/S gene variability, and hepatic disease stage [72]. The presence of hepatitis B envelope antigen (HBeAg) indicates that the virus is actively replicating and typically correlates with higher levels of HBV DNA. Immunoglobulin (Ig) G and IgM to hepatitis B core antigen indicates either that the individual has previously been infected or has an ongoing infection. IgG anti hepatitis B core (IgG anti-HBc) will often persists for life. The presence of anti-HBs shows that the individual has obtained immunity either from infection or vaccination [3, 6].
Touching upon the technical procedures behind the tests, tests for serological markers are carried out using different techniques, based on resources availability. Chemiluminescent microparticle immunoassay (CMIA) is one of those qualitative tests that detect the viral antigen in blood or serum. The technique has a high specificity and sensitivity and is based on the antigenic features (e.g., HBsAg or HBeAg) binding to commercially synthesized antibodies (anti-HB) with chemiluminescence [73]. The light produced in a chemiluminescent reaction can be measured. This method is more sensitive than the enzyme-linked immunosorbent assay (ELISA) [73].
Polymerase chain reaction (PCR) is an advanced technique to detect HBV. It amplifies the nucleic acid and greatly enhances the amount of DNA [3]. This method can qualitatively or quantitatively detect the amount of HBV DNA in patients’ specimen, which reflects the replicative condition of the virus. To monitor and manage HBV infection, then a quantitative detection method is the technique of choice [73]. ALT levels are measured to help determine liver inflammation. ALT is an enzyme that is normally found in the liver, but also present in other body tissue, that is discharged into the circulation system as a consequence to hepatocellular injury [26]. ALT plays a role in characterization of HBV infection phases in synergy with HBV DNA [74]. Different noninvasive diagnoses such as aspartate aminotransferase (AST), platelet ratio index (APRI), and transient elastography (FibroScan) still exist. APRI is an index to determine the hepatic fibrosis based on a formula derived from platelet and AST concentrations [3]. FibroScan measures grade of liver fibroses through the detection of liver stiffness. Both methods are recommended by WHO to evaluate cirrhosis presence, but while FibroScan is preferred in a context where availability and cost is not an issue, APRI is used in settings with limited resources. Liver biopsy has been used to assess degree of necroinflammation and fibrosis degrees. However, the method has diverse demerits and constraints [6, 75].
All travelers should be screened for HBV infection markers, so that they will not be at risk of acquiring the virus during stay [74]. Recently updated guidelines also recommend that pregnant women with chronic HBV be referred to a specialist and considered for HBV treatment to further reduce the chance of transmitting the virus [3]. In infants born to HBsAg-positive mothers, the risk of mother-to-child transmission is significantly greater if the mother is positive for HBeAg, has a high viral load, and/or is infected with HIV [33]. Such infants should be given both vaccine and HBIgG (0.5 ml) within 12 hours of delivery. The infants should be evaluated for HBsAg, anti-HBs, and anti-HBc at age 12 months. The presence of anti-HBs depicts vaccine-induced immunity, and detection of both anti-HBs and anti-HBc shows immunoprophylaxis-modified infection, whereas the presence of HBsAg indicates prophylaxis failure [15, 76, 77].
Individuals who have not received the HBV vaccination and are exposed to the virus (through needle stick injury, splashing, or sexual exposure to partners infected with the viral agent) should be vaccinated with HBIG (0.04–0.07 ml/kg) as soon as possible after exposure. Immunization for the newborn babies should start immediately with the initial shot given at a site that is not similar with that for HBIG; an accelerated four dose immunization schedule (0, 1, 2, and 12 months) is required in the maternal-fetal transmission scenario [8, 77]. HBV can also be prevented by avoiding contact with contaminated blood and blood products and unprotected sexual exposure. Using condoms has also been shown to reduce the chance of sexually transmitted infections [8].
Several reasons why people did not opt for pre-travel vaccinations include traveler’s pre-knowledge regarding the prevention of diseases during overseas travel, the limited number of healthcare settings that gives immunization, and that some countries have not yet approved the number of vaccines a traveler needs [9, 31].
There are commercially hepatitis B vaccines available currently, for example, recombinant HBV vaccine (Engerix-B®, GlaxoSmithKline, and Recombivax HB®, Merck & Co., Inc.) and the HAV and HBV combined vaccine (Twinrix®, GlaxoSmithKline) [78]. The complete HBV vaccination requires three shots of vaccine. The normal timeline of the three intramuscular injections is to have the second and third injections given 1 and 6 months after the first dose. An accelerated schedule (doses on days 0, 7, and 21 and then a post-travel dose at 12 months) might be required if there is an inadequate time for immunization prior to travel [79, 80]. An HBV vaccine can also be used to treat persons who have been exposed to the virus, in order to prevent disease development [31].
The prevalence of HBV differs between countries and regions, and therefore the number of persons acquiring protective immunity from a previous HBV infection also changes. Therefore, the recommendation of its vaccination should be hinged on likelihood of infection during travel and evidence of previous immunization or recovery from previous infection [74]. In those travelers without evidence of previous HBV immunity, HBV vaccination is recommended in those with HBV exposure risks and traveling to HBV endemic regions [78]. The CDC has recommend HBV vaccination to all persons without evidence of immunization before traveling to areas with intermediate and high prevalence of chronic hepatitis B and, irrespective of the traveler’s destination, and based on the traveler’s potential risky activities and exposures [11, 81]. High-risk activities might include unprotected sex with a new partner, getting a tattoo or piercing, or having any medical procedures like surgery [11, 81]. Studies have reported that only 19% of all American travelers and 30% of American travelers planning high-risk activities had received a completed HBV vaccination before departure irrespective of the recommendation made by the CDC [79]. This finding is in consonance with information from Europe that only 15% of international travelers to HBV endemic regions receive a completed HBV vaccination before travel [79]. There is often a very low immunity of HBV to travelers from low endemic regions and those born before the EPI schedules [82, 83]. Obviously, there are no recommendations for HBV serologic examination of international travelers currently. This might be because of the large population of international travelers, thus making it impossible to screen all for the virus. Reports have it that only 3.4–3.9% of the population in low endemic countries will have evidence of the HBV serologic markers prior infection [82, 83]. Vaccination of those populations should be considered when long-term travel is arranged to countries where HBV prevalence is intermediate or hyperendemic [31].
There are several antiviral treatments available for chronic HBV infection, and everyone with chronic HBV should be linked to care, considered for treatment, and checked for liver damage and liver cancer regularly [84]. Therapy of HBV reduces the amount of virus in the system and lowers the chance of developing to serious liver disease and liver cancer. However, most people cannot be cured of the viral agent, and as such therapy is recommended to continue for life [85, 86].
Worthy of note is the fact that there are currently two main antiviral drugs for the treatment of chronic HBV infection [87]. They are nucleos(t)ide analogues (NA) and interferon (IFN) including normal IFNs and pegylated IFNs (Peg-IFNs). NA gives a direct antiviral effect by stopping DNA polymerase. It is usually given orally. There are six types of NAs as approved for treatment of HBV by the WHO: Lamivudine (LAM), Adefovir (ADV), Telbivudine (TBV), Entecavir (ETV), Tenofovir disoproxil fumarate (TDF), and Tenofovir alafenamide (TAF). IFNs, especially the Peg-IFNs, have a suppressed antiviral effect than the NA therapy, but its persistent effect can be achieved with a finite therapy. It is usually given via subcutaneous injection. There are reports of combination therapy of NA + NA and Peg-IFN + NA [86, 87].
There are serious ongoing clinical trials for the development of more effective treatments and a cure for HBV infection [3, 6].
Early screening and treatment will help mitigate frequent transmission of the viral agent and curb morbidities and mortalities in infected persons [85]. The first line should be to give the exact medical advice and start antiviral treatment, if available. Sadly, undergoing this step is often a problem in developing regions where there is lack of access to good healthcare facilities, and antiviral treatment is often exorbitant [6, 86].
Advocacy of immunization exercise for HBV infection should be key in eliminating the viral agent worldwide which is central to WHO’s agenda [6, 10]. To maximize implementation of the WHO agenda, provision of technical guidance and support to reduce transmission of the disease such as adhering to safer blood transfusion and disposable needles among others. The virus vaccine is very effective in preventing disease progression. It has been reported that only 27% of newborn babies had receive a birth dose of hepatitis B vaccine globally [86]. Birth dose vaccination of the viral agent is fundamental to halting mother-to-child transmission as late immunization is not fully effective in destroying the chain of mother-to-child transmission. Coordination between maternal health services and immunization should be effectively established [88].
Self-protection measures are one of the pre-travel counseling given to potential travelers to HBV and other blood-borne pathogen endemic regions [7, 8, 43]. Persons should be guided from contaminated items or equipment used in medical or cosmetic procedures, blood products, injection drug use or any exercise that involve piercing the skin or mucosa, or unprotected sexual activity. Travelers should be advised properly against the use of equipment that is not properly sterilized or disinfected on medical or beautification tourism (such as tattooing or piercing) [8]. The viral agent can be disseminated to others if tools are not sterile or if personnel do not follow proper infection control protocols [89].
Educational awareness and programs that will be targeted towards HBV awareness lowers transmission of the infection [90, 91]. There is a large pool of persons suffering from chronic HBV infection in Sub-Saharan Africa that are not aware of their situation. Educational awareness and implementation of local health measures are pertinent in eradicating the scourge of the infection [2]. These should include training local communities on how to perform safe blood transfusion and establishing efficient screening methods for transfusion of donated bloods. Health education programs should include administration of safe injections (intravenous drug users and healthcare settings) and implementation of safer sex practices (especially the use of condoms). More so, occupational safety trainings should be advocated for health workers [92]. It is also worthy to note that effective communication and emphasizing the role of the virus testing, follow-up visits, and monitoring therapy will help eliminate HBV infection [43].
Enhancing the socioeconomic conditions of a particular population has shown reduction in the rate of HBV infection. Government and non-governmental organization (NGO) bodies should ensure that there is a universal access to portable water and encourage food handling that is safe and hygienic [92]. They should also implement good sanitation systems. Safe disposal practice of medical waste should be advocated in the health settings [43].
There are ongoing development of two novel anti-HBV drugs, namely, Besifovir and Myrcludex-B that will soon be in the market [3]. The infection is one of those preventable infections by immunization in travelers. Therefore, travelers should often be screened and immunized for HBV infection before traveling to endemic countries because immigrants and/or travelers who have the viral infection pose a great risk of HCC and death. They as well serve as transmitters of the viral agent to those not infected when returned from travel. Continuous health surveillance and strict checking of migrants to ascertain previous vaccination evidence will go a long way in mitigating the infection across travelers. There is no single measure strong enough to curb viral hepatitis epidemics, but having a global vision and implementing multiple strategies will go a long way towards eliminating HBV infection and other global disease burden in 2030.
IntechOpen implements a robust policy to minimize and deal with instances of fraud or misconduct. As part of our general commitment to transparency and openness, and in order to maintain high scientific standards, we have a well-defined editorial policy regarding Retractions and Corrections.
",metaTitle:"Retraction and Correction Policy",metaDescription:"Retraction and Correction Policy",metaKeywords:null,canonicalURL:"/page/retraction-and-correction-policy",contentRaw:'[{"type":"htmlEditorComponent","content":"IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
\\n\\n1. RETRACTIONS
\\n\\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\\n\\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\\n\\nPublishing of a Retraction Notice will adhere to the following guidelines:
\\n\\n1.2. REMOVALS AND CANCELLATIONS
\\n\\n2. STATEMENTS OF CONCERN
\\n\\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\\n\\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\\n\\n3. CORRECTIONS
\\n\\nA Correction will be issued by the Academic Editor when:
\\n\\n3.1. ERRATUM
\\n\\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\\n\\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n3.2. CORRIGENDUM
\\n\\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n4. FINAL REMARKS
\\n\\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\\n\\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\\n\\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\\n\\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\\n\\nPolicy last updated: 2017-09-11
\\n"}]'},components:[{type:"htmlEditorComponent",content:'IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
\n\n1. RETRACTIONS
\n\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\n\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\n\nPublishing of a Retraction Notice will adhere to the following guidelines:
\n\n1.2. REMOVALS AND CANCELLATIONS
\n\n2. STATEMENTS OF CONCERN
\n\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\n\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\n\n3. CORRECTIONS
\n\nA Correction will be issued by the Academic Editor when:
\n\n3.1. ERRATUM
\n\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\n\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n3.2. CORRIGENDUM
\n\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n4. FINAL REMARKS
\n\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\n\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\n\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\n\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\n\nPolicy last updated: 2017-09-11
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I am also a member of the team in charge for the supervision of Ph.D. students in the fields of development of silicon based planar waveguide sensor devices, study of inelastic electron tunnelling in planar tunnelling nanostructures for sensing applications and development of organotellurium(IV) compounds for semiconductor applications. I am a specialist in data analysis techniques and nanosurface structure. I have served as the editor for many books, been a member of the editorial board in science journals, have published many papers and hold many patents.",institutionString:null,institution:{name:"Sheffield Hallam University",country:{name:"United Kingdom"}}},{id:"12392",title:"Mr.",name:"Alex",middleName:null,surname:"Lazinica",slug:"alex-lazinica",fullName:"Alex Lazinica",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/12392/images/7282_n.png",biography:"Alex Lazinica is the founder and CEO of IntechOpen. 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Čepička",authors:[{id:"103948",title:"Dr.",name:"Ivan",middleName:null,surname:"Cepicka",slug:"ivan-cepicka",fullName:"Ivan Cepicka"},{id:"103954",title:"MSc.",name:"Tomas",middleName:null,surname:"Panek",slug:"tomas-panek",fullName:"Tomas Panek"}]},{id:"28888",doi:"10.5772/35101",title:"Genotyping Techniques for Determining the Diversity of Microorganisms",slug:"genotyping-techniques-for-determining-the-diversity-of-microorganisms",totalDownloads:6449,totalCrossrefCites:3,totalDimensionsCites:13,abstract:null,book:{id:"2253",slug:"genetic-diversity-in-microorganisms",title:"Genetic Diversity in Microorganisms",fullTitle:"Genetic Diversity in Microorganisms"},signatures:"Katarzyna Wolska and Piotr Szweda",authors:[{id:"102977",title:"Dr.",name:"Katarzyna",middleName:null,surname:"Wolska",slug:"katarzyna-wolska",fullName:"Katarzyna Wolska"},{id:"117528",title:"Dr.",name:"Szweda",middleName:null,surname:"Piotr",slug:"szweda-piotr",fullName:"Szweda Piotr"}]},{id:"71577",doi:"10.5772/intechopen.91886",title:"Single Nucleotide Polymorphisms (SNPs) in Plant Genetics and Breeding",slug:"single-nucleotide-polymorphisms-snps-in-plant-genetics-and-breeding",totalDownloads:1488,totalCrossrefCites:8,totalDimensionsCites:10,abstract:"Recent advances in genome technology revealed various single nucleotide polymorphisms (SNPs), the most common form of DNA sequence variation between alleles, in several plant species. The discovery and application of SNPs increased our knowledge about genetic diversity and a better understanding on crop improvement. Natural breeding process which takes an agelong time during collecting, cultivating, and domestication has been accelerated by detecting dozens of SNPs on various species using advanced biotechnological techniques such as next-generation sequencing. This will result in the improvement of economically important traits. Therefore, we would like to focus on the discovery, current technologies, and applications of SNPs in breeding. The chapter covers the following topics: (1) introduction, (2) application of SNPs, (3) techniques to detect SNPs, (4) importance of SNPs for crop improvement, and (5) conclusion.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Hande Morgil, Yusuf Can Gercek and Isil Tulum",authors:null}],mostDownloadedChaptersLast30Days:[{id:"75504",title:"Introductory Chapter: Genetic Variation - The Source of Biological Diversity",slug:"introductory-chapter-genetic-variation-the-source-of-biological-diversity",totalDownloads:420,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"9743",slug:"genetic-variation",title:"Genetic Variation",fullTitle:"Genetic Variation"},signatures:"Rafael Trindade Maia and Magnólia de Araújo Campos",authors:[{id:"212393",title:"Prof.",name:"Rafael",middleName:"Trindade",surname:"Trindade Maia",slug:"rafael-trindade-maia",fullName:"Rafael Trindade Maia"},{id:"344747",title:"Associate Prof.",name:"Magnólia",middleName:"De Araújo",surname:"de Araújo Campos",slug:"magnolia-de-araujo-campos",fullName:"Magnólia de Araújo Campos"}]},{id:"73657",title:"Potential of Mutation Breeding to Sustain Food Security",slug:"potential-of-mutation-breeding-to-sustain-food-security",totalDownloads:741,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"Mutation is a sudden heritable change in the genetic material of living organism. Spontaneous mutation, the natural process that develops new allele copies of a gene was the only source of genetic diversity until the 20th century. Besides, mutations can also be induced artificially using physical or chemical mutagens. Chemical mutations received popularity due to its efficiency in creating gene mutations contrary to chromosomal changes. Mutation has played a vital role in the improvement of crop productivity and quality, resultantly > 3,000 varieties of 175 plant species have been developed either through direct or indirect induced mutation breeding approaches worldwide. The advances in plant breeding also achieved through molecular marker technology. The in vitro mutagenesis, heavy-ion beam, and space mutation breeding are being efficiently used to create genetic variability to improve various complicated traits in crop plants. In mutation breeding, TILLING (Targeting Induced Local Lesions in Genomes), a more advanced molecular technique is being used to identify specific sequential genomic changes in mutant plants. Therefore, the mutation breeding in combination with molecular techniques could be an efficient tool in plant breeding programs. This chapter will discuss and review the mutation breeding application for the improvement of crop productivity and environmental stresses.",book:{id:"9743",slug:"genetic-variation",title:"Genetic Variation",fullTitle:"Genetic Variation"},signatures:"Arain Saima Mir, Meer Maria, Sajjad Muhammad and Sial Mahboob Ali",authors:[{id:"329068",title:"Dr.",name:"Arain Saima Mir",middleName:null,surname:"Saima Mir",slug:"arain-saima-mir-saima-mir",fullName:"Arain Saima Mir Saima Mir"},{id:"330046",title:"Ms.",name:"Meer",middleName:null,surname:"Maria",slug:"meer-maria",fullName:"Meer Maria"},{id:"330047",title:"Dr.",name:"Sajjad",middleName:null,surname:"Muhammad",slug:"sajjad-muhammad",fullName:"Sajjad Muhammad"},{id:"330048",title:"Dr.",name:"Sial",middleName:null,surname:"Mahboob Ali",slug:"sial-mahboob-ali",fullName:"Sial Mahboob Ali"}]},{id:"65713",title:"Introductory Chapter: Population Genetics - The Evolution Process as a Genetic Function",slug:"introductory-chapter-population-genetics-the-evolution-process-as-a-genetic-function",totalDownloads:2336,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"6974",slug:"integrated-view-of-population-genetics",title:"Integrated View of Population Genetics",fullTitle:"Integrated View of Population Genetics"},signatures:"Rafael Trindade Maia and Magnólia de Araújo Campos",authors:[{id:"212393",title:"Prof.",name:"Rafael",middleName:"Trindade",surname:"Trindade Maia",slug:"rafael-trindade-maia",fullName:"Rafael Trindade Maia"}]},{id:"71577",title:"Single Nucleotide Polymorphisms (SNPs) in Plant Genetics and Breeding",slug:"single-nucleotide-polymorphisms-snps-in-plant-genetics-and-breeding",totalDownloads:1492,totalCrossrefCites:8,totalDimensionsCites:10,abstract:"Recent advances in genome technology revealed various single nucleotide polymorphisms (SNPs), the most common form of DNA sequence variation between alleles, in several plant species. The discovery and application of SNPs increased our knowledge about genetic diversity and a better understanding on crop improvement. Natural breeding process which takes an agelong time during collecting, cultivating, and domestication has been accelerated by detecting dozens of SNPs on various species using advanced biotechnological techniques such as next-generation sequencing. This will result in the improvement of economically important traits. Therefore, we would like to focus on the discovery, current technologies, and applications of SNPs in breeding. The chapter covers the following topics: (1) introduction, (2) application of SNPs, (3) techniques to detect SNPs, (4) importance of SNPs for crop improvement, and (5) conclusion.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Hande Morgil, Yusuf Can Gercek and Isil Tulum",authors:null},{id:"71702",title:"Single-Nucleotide Polymorphisms in Inflammatory Bowel Disease",slug:"single-nucleotide-polymorphisms-in-inflammatory-bowel-disease",totalDownloads:975,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Inflammatory bowel disease (IBD) mainly includes ulcerative colitis (UC) and Crohn’s disease (CD). Both conditions are characterized by chronic inflammation of the gastrointestinal tract, with alternating periods of relapse and remission. Both forms of IBD involve an uncontrolled inflammatory process in the intestines, leading to worsening quality of life and requiring long-term medical and/or surgical intervention. Epidemiological and clinical studies suggest that the pathogenesis of inflammatory bowel disease is strongly linked to genetic predisposition. CD and UC are considered polygenic diseases in which familial clustering is observed in 5–10% of patients. Among genetic factors associated with IBD development, it has been found that many single nucleotide polymorphisms are associated with susceptibility to IBD progression. SNP can affect the production or function of a protein and thus affect the development of the disease. However, although the overall role of genes involved in the development of IBD is already in most cases known, as of today it is unclear how the SNPs in these genes affect cellular function, or how such changed cellular functions would contribute to the development of IBD. In the present work several selected polymorphisms in genes involved in IBD development are discussed.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Ewa Dudzińska",authors:null}],onlineFirstChaptersFilter:{topicId:"61",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:87,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:99,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:289,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:139,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:0,numberOfUpcomingTopics:2,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!1},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:108,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:104,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:0,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!1},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:12,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}},{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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While a daunting task, learning is facilitated by identifying common and effective signaling pathways mediated by a variety of factors employed by nature to preserve and sustain homeostatic life. \r\nAs a leading example, the cellular interaction between intracellular concentration of Ca+2 increases, and changes in plasma membrane potential is integral for coordinating blood flow, governing the exocytosis of neurotransmitters, and modulating gene expression and cell effector secretory functions. 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His primary area of interest is physiology and pathophysiology of the gastrointestinal (GI) tract, with the major focus on the mechanism of GI mucosal defense, protection, and ulcer healing. He was a postdoctoral NIH fellow at the University of California and the Gastroenterology VA Medical Center, Irvine, Long Beach, CA, USA, and at the Gastroenterology Clinics Erlangen-Nuremberg and Munster in Germany. He has published 290 original articles in some of the most prestigious scientific journals and seven book chapters on the pathophysiology of the GI tract, gastroprotection, ulcer healing, drug therapy of peptic ulcers, hormonal regulation of the gut, and inflammatory bowel disease.",institutionString:null,institution:{name:"Jagiellonian University",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"10",title:"Animal Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/10.jpg",isOpenForSubmission:!0,annualVolume:11406,editor:{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. 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From\r\n1964 to 1974, he worked as Assistant in Biochemistry at the School of MedicineUniversidad Nacional de La Plata, Argentina. From 1974 to 1976, he was a Fellowof the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor oBiochemistry at the Universidad Nacional de La Plata, Argentina. He is Member ofthe National Research Council (CONICET), Argentina, and Argentine Society foBiochemistry and Molecular Biology (SAIB). His laboratory has been interested for manyears in the lipid peroxidation of biological membranes from various tissues and different species. Professor Catalá has directed twelve doctoral theses, publishedover 100 papers in peer reviewed journals, several chapters in books andtwelve edited books. Angel Catalá received awards at the 40th InternationaConference Biochemistry of Lipids 1999: Dijon (France). W inner of the Bimbo PanAmerican Nutrition, Food Science and Technology Award 2006 and 2012, South AmericaHuman Nutrition, Professional Category. 2006 award in pharmacology, Bernardo\r\nHoussay, in recognition of his meritorious works of research. Angel Catalá belongto the Editorial Board of Journal of lipids, International Review of Biophysical ChemistryFrontiers in Membrane Physiology and Biophysics, World Journal oExperimental Medicine and Biochemistry Research International, W orld Journal oBiological Chemistry, Oxidative Medicine and Cellular Longevity, Diabetes and thePancreas, International Journal of Chronic Diseases & Therapy, International Journal oNutrition, Co-Editor of The Open Biology Journal.",institutionString:null,institution:{name:"National University of La Plata",institutionURL:null,country:{name:"Argentina"}}},editorTwo:null,editorThree:null},{id:"12",title:"Human Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/12.jpg",isOpenForSubmission:!0,annualVolume:11408,editor:{id:"195829",title:"Prof.",name:"Kunihiro",middleName:null,surname:"Sakuma",slug:"kunihiro-sakuma",fullName:"Kunihiro Sakuma",profilePictureURL:"https://mts.intechopen.com/storage/users/195829/images/system/195829.jpg",biography:"Professor Kunihiro Sakuma, Ph.D., currently works in the Institute for Liberal Arts at the Tokyo Institute of Technology. He is a physiologist working in the field of skeletal muscle. He was awarded his sports science diploma in 1995 by the University of Tsukuba and began his scientific work at the Department of Physiology, Aichi Human Service Center, focusing on the molecular mechanism of congenital muscular dystrophy and normal muscle regeneration. His interest later turned to the molecular mechanism and attenuating strategy of sarcopenia (age-related muscle atrophy). 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Additionally, to understand how to maintain and improve physical function in older adults, to conduct studies about the mechanism of sarcopenia and determine when possible interventions are needed.",institutionString:null,institution:{name:"Ritsumeikan University",institutionURL:null,country:{name:"Japan"}}}},{id:"13",title:"Plant Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/13.jpg",isOpenForSubmission:!0,annualVolume:11409,editor:{id:"332229",title:"Prof.",name:"Jen-Tsung",middleName:null,surname:"Chen",slug:"jen-tsung-chen",fullName:"Jen-Tsung Chen",profilePictureURL:"https://mts.intechopen.com/storage/users/332229/images/system/332229.png",biography:"Dr. Jen-Tsung Chen is currently a professor at the National University of Kaohsiung, Taiwan. He teaches cell biology, genomics, proteomics, medicinal plant biotechnology, and plant tissue culture. Dr. Chen\\'s research interests include bioactive compounds, chromatography techniques, in vitro culture, medicinal plants, phytochemicals, and plant biotechnology. He has published more than ninety scientific papers and serves as an editorial board member for Plant Methods, Biomolecules, and International Journal of Molecular Sciences.",institutionString:"National University of Kaohsiung",institution:{name:"National University of Kaohsiung",institutionURL:null,country:{name:"Taiwan"}}},editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:17,paginationItems:[{id:"81791",title:"Self-Supervised Contrastive Representation Learning in Computer Vision",doi:"10.5772/intechopen.104785",signatures:"Yalin Bastanlar and Semih Orhan",slug:"self-supervised-contrastive-representation-learning-in-computer-vision",totalDownloads:12,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Pattern Recognition - New Insights",coverURL:"https://cdn.intechopen.com/books/images_new/11442.jpg",subseries:{id:"26",title:"Machine Learning and Data Mining"}}},{id:"79345",title:"Application of Jump Diffusion Models in Insurance Claim Estimation",doi:"10.5772/intechopen.99853",signatures:"Leonard Mushunje, Chiedza Elvina Mashiri, Edina Chandiwana and Maxwell Mashasha",slug:"application-of-jump-diffusion-models-in-insurance-claim-estimation-1",totalDownloads:2,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Data Clustering",coverURL:"https://cdn.intechopen.com/books/images_new/10820.jpg",subseries:{id:"26",title:"Machine Learning and Data Mining"}}},{id:"81557",title:"Object Tracking Using Adapted Optical Flow",doi:"10.5772/intechopen.102863",signatures:"Ronaldo Ferreira, Joaquim José de Castro Ferreira and António José Ribeiro Neves",slug:"object-tracking-using-adapted-optical-flow",totalDownloads:10,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Information Extraction and Object Tracking in Digital Video",coverURL:"https://cdn.intechopen.com/books/images_new/10652.jpg",subseries:{id:"24",title:"Computer Vision"}}},{id:"81558",title:"Thresholding Image Techniques for Plant Segmentation",doi:"10.5772/intechopen.104587",signatures:"Miguel Ángel Castillo-Martínez, Francisco Javier Gallegos-Funes, Blanca E. 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