Nominal chemical compositions of the used Al alloys (wt.%).
\\n\\n
IntechOpen was founded by scientists, for scientists, in order to make book publishing accessible around the globe. Over the last two decades, this has driven Open Access (OA) book publishing whilst levelling the playing field for global academics. Through our innovative publishing model and the support of the research community, we have now published over 5,700 Open Access books and are visited online by over three million academics every month. These researchers are increasingly working in broad technology-based subjects, driving multidisciplinary academic endeavours into human health, environment, and technology.
\\n\\nBy listening to our community, and in order to serve these rapidly growing areas which lie at the core of IntechOpen's expertise, we are launching a portfolio of Open Science journals:
\\n\\nAll three journals will publish under an Open Access model and embrace Open Science policies to help support the changing needs of academics in these fast-moving research areas. There will be direct links to preprint servers and data repositories, allowing full reproducibility and rapid dissemination of published papers to help accelerate the pace of research. Each journal has renowned Editors in Chief who will work alongside a global Editorial Board, delivering robust single-blind peer review. Supported by our internal editorial teams, this will ensure our authors will receive a quick, user-friendly, and personalised publishing experience.
\\n\\n"By launching our journals portfolio we are introducing new, dedicated homes for interdisciplinary technology-focused researchers to publish their work, whilst embracing Open Science and creating a unique global home for academics to disseminate their work. We are taking a leap toward Open Science continuing and expanding our fundamental commitment to openly sharing scientific research across the world, making it available for the benefit of all." Dr. Sara Uhac, IntechOpen CEO
\\n\\n"Our aim is to promote and create better science for a better world by increasing access to information and the latest scientific developments to all scientists, innovators, entrepreneurs and students and give them the opportunity to learn, observe and contribute to knowledge creation. Open Science promotes a swifter path from research to innovation to produce new products and services." Alex Lazinica, IntechOpen founder
\\n\\nIn conclusion, Natalia Reinic Babic, Head of Journal Publishing and Open Science at IntechOpen adds:
\\n\\n“On behalf of the journal team I’d like to thank all our Editors in Chief, Editorial Boards, internal supporting teams, and our scientific community for their continuous support in making this portfolio a reality - we couldn’t have done it without you! With your support in place, we are confident these journals will become as impactful and successful as our book publishing program and bring us closer to a more open (science) future.”
\\n\\nWe invite you to visit the journals homepage and learn more about the journal’s Editorial Boards, scope and vision as all three journals are now open for submissions.
\\n\\nFeel free to share this news on social media and help us mark this memorable moment!
\\n\\n\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/237"}},components:[{type:"htmlEditorComponent",content:'
After years of being acknowledged as the world's leading publisher of Open Access books, today, we are proud to announce we’ve successfully launched a portfolio of Open Science journals covering rapidly expanding areas of interdisciplinary research.
\n\n\n\nIntechOpen was founded by scientists, for scientists, in order to make book publishing accessible around the globe. Over the last two decades, this has driven Open Access (OA) book publishing whilst levelling the playing field for global academics. Through our innovative publishing model and the support of the research community, we have now published over 5,700 Open Access books and are visited online by over three million academics every month. These researchers are increasingly working in broad technology-based subjects, driving multidisciplinary academic endeavours into human health, environment, and technology.
\n\nBy listening to our community, and in order to serve these rapidly growing areas which lie at the core of IntechOpen's expertise, we are launching a portfolio of Open Science journals:
\n\nAll three journals will publish under an Open Access model and embrace Open Science policies to help support the changing needs of academics in these fast-moving research areas. There will be direct links to preprint servers and data repositories, allowing full reproducibility and rapid dissemination of published papers to help accelerate the pace of research. Each journal has renowned Editors in Chief who will work alongside a global Editorial Board, delivering robust single-blind peer review. Supported by our internal editorial teams, this will ensure our authors will receive a quick, user-friendly, and personalised publishing experience.
\n\n"By launching our journals portfolio we are introducing new, dedicated homes for interdisciplinary technology-focused researchers to publish their work, whilst embracing Open Science and creating a unique global home for academics to disseminate their work. We are taking a leap toward Open Science continuing and expanding our fundamental commitment to openly sharing scientific research across the world, making it available for the benefit of all." Dr. Sara Uhac, IntechOpen CEO
\n\n"Our aim is to promote and create better science for a better world by increasing access to information and the latest scientific developments to all scientists, innovators, entrepreneurs and students and give them the opportunity to learn, observe and contribute to knowledge creation. Open Science promotes a swifter path from research to innovation to produce new products and services." Alex Lazinica, IntechOpen founder
\n\nIn conclusion, Natalia Reinic Babic, Head of Journal Publishing and Open Science at IntechOpen adds:
\n\n“On behalf of the journal team I’d like to thank all our Editors in Chief, Editorial Boards, internal supporting teams, and our scientific community for their continuous support in making this portfolio a reality - we couldn’t have done it without you! With your support in place, we are confident these journals will become as impactful and successful as our book publishing program and bring us closer to a more open (science) future.”
\n\nWe invite you to visit the journals homepage and learn more about the journal’s Editorial Boards, scope and vision as all three journals are now open for submissions.
\n\nFeel free to share this news on social media and help us mark this memorable moment!
\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:"6863",leadTitle:null,fullTitle:"Electron Microscopy - Novel Microscopy Trends",title:"Electron Microscopy",subtitle:"Novel Microscopy Trends",reviewType:"peer-reviewed",abstract:"TEM and SEM have contributed greatly to the progress of various research fields, which has been accelerated in the last few decades by highly functional electron microscopes and microscopy. In this tide of microscopy, various microscopic methods have been developed to make clear many unsolved problems, e.g. pulse beam TEM, environmental microscopy, correlative microscopy, etc. In this book, a number of reviews have been collected concerning these subjects. We think that the content in each chapter is impressive, and we hope this book will contribute to future advances in electron microscopy, materials science, and biomedicine.",isbn:"978-1-83881-883-8",printIsbn:"978-1-83881-882-1",pdfIsbn:"978-1-83881-884-5",doi:"10.5772/intechopen.73375",price:100,priceEur:109,priceUsd:129,slug:"electron-microscopy-novel-microscopy-trends",numberOfPages:100,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"3ac6c4038d9b6dc73cbde27e43a3841e",bookSignature:"Masashi Arita and Norihito Sakaguchi",publishedDate:"October 2nd 2019",coverURL:"https://cdn.intechopen.com/books/images_new/6863.jpg",numberOfDownloads:5413,numberOfWosCitations:1,numberOfCrossrefCitations:2,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:2,numberOfDimensionsCitationsByBook:0,hasAltmetrics:0,numberOfTotalCitations:5,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"June 13th 2018",dateEndSecondStepPublish:"July 4th 2018",dateEndThirdStepPublish:"September 2nd 2018",dateEndFourthStepPublish:"November 21st 2018",dateEndFifthStepPublish:"January 20th 2019",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"174249",title:"Prof.",name:"Masashi",middleName:null,surname:"Arita",slug:"masashi-arita",fullName:"Masashi Arita",profilePictureURL:"https://mts.intechopen.com/storage/users/174249/images/system/174249.jpeg",biography:"Masashi Arita received the B.S. degree in materials science from Hiroshima University, Hiroshima, Japan, in 1980, and the Ph.D. degree in solid state physics from Eidgenössische Technische Hochschule (ETH) Zurich, Zurich, Switzerland, in 1987. He joined Ciba-Geigy Japan in 1987, where he was engaged in research on crystallography and electrophotography of organic substances. Since joining Nagoya University, Nagoya, Japan, in 1990, he has been engaged in research on crystallography and physical properties of metallic nano particles and ultrathin films. Since 1997, he has been an Associate Professor at the Graduate School of Engineering as well as the Graduate School of Information Science and Technology, Hokkaido University, Sapporo, Japan. His major subject at present is in-situ electron microscopy of electronic devices.",institutionString:"Hokkaido University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"Hokkaido University",institutionURL:null,country:{name:"Japan"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:{id:"262259",title:"Dr.",name:"Norihito",middleName:null,surname:"Sakaguchi",slug:"norihito-sakaguchi",fullName:"Norihito Sakaguchi",profilePictureURL:"https://mts.intechopen.com/storage/users/262259/images/system/262259.jpeg",biography:"Norihito Sakaguchi received the B.S. and M.S. degrees in materials science from Hokkaido University, Sapporo, Japan, in 1994 and 1996, and the Ph.D. degree in materials science from Hokkaido University, Japan, in 1999. He joined Hokkaido University, Sapporo, Japan, in 1999. He has been engaged in research on radiation effects on grain boundaries in metals and alloys. Since 2004, he has been Associate Professor at the Center for Advanced Research of Energy Conversion Materials, Hokkaido University, Sapporo Japan, and moved to the Graduate School of Engineering, Hokkaido University, Sapporo, Japan, in 2010. His major subject at present is nano-analysis using the analytical transmission electron microscopy in metals and semiconductors.",institutionString:"Hokkaido University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"0",totalChapterViews:"0",totalEditedBooks:"0",institution:null},coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1017",title:"Microscopy",slug:"microscopy"}],chapters:[{id:"63863",title:"Ultrafast Electron Microscopy with Relativistic Femtosecond Electron Pulses",doi:"10.5772/intechopen.81405",slug:"ultrafast-electron-microscopy-with-relativistic-femtosecond-electron-pulses",totalDownloads:1129,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"An ultrafast electron microscope (UEM) with a femtosecond temporal resolution is a “dream machine” desired for studies of ultrafast structural dynamics in materials. In this chapter, we present a brief overview of the historical development of current UEMs with nonrelativistic electron pulses to illustrate the need for relativistic-energy electron pulses. We then describe the concept and development of a UEM with relativistic femtosecond electron pulses generated by a radio frequency (RF) acceleration-based photoemission gun. The technique of RF electron gun and physical characteristics of the relativistic electron pulses are described. Demonstrations of UEM images acquired using approximately 100 fs long electron pulses with energies of 3 MeV are presented. 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To obtain direct information about the ATP-coupled myosin head movement, we prepared synthetic myosin filaments (myosin-myosin rod copolymer), in which myosin heads were position-marked with gold particles via antibodies to myosin heads and kept in hydrated, living state in the gas environmental chamber. ATP was applied to the specimen iontophoretically by passing the current to an ATP-containing microelectrode, and the ATP-induced myosin head movement was recorded with an imaging plate system under a magnification of 10,000×, with the following novel findings: (1) In the absence of ATP, myosin heads fluctuate around a definite neutral position. (2) In the absence of actin filaments, myosin heads move away from the bare region of myosin filaments (recovery stroke, average amplitude, 6 nm) on ATP application and return to the neutral position after exhaustion of ATP. (3) In the presence of actin filaments, the ATP-induced myosin head power stroke exhibits two different modes depending on mechanical conditions. (4) Myosin heads determine the direction of ATP-induced movement without being guided by actin filaments.",signatures:"Haruo Sugi, Tsuyosi Akimoto and Shigeru Chaen",downloadPdfUrl:"/chapter/pdf-download/64448",previewPdfUrl:"/chapter/pdf-preview/64448",authors:[null],corrections:null},{id:"64265",title:"Correlative Light-Electron Microscopy (CLEM) and 3D Volume Imaging of Serial Block-Face Scanning Electron Microscopy (SBF-SEM) of Langerhans Islets",doi:"10.5772/intechopen.81716",slug:"correlative-light-electron-microscopy-clem-and-3d-volume-imaging-of-serial-block-face-scanning-elect",totalDownloads:1525,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Correlative light-electron microscopy (CLEM) is a developing technique for combined analysis of immunostaining for various biological molecules coupled with investigations of ultrastructural features of individual cells within a large field of view. This study first introduces a method of CLEM imaging of the same endocrine cells of compact and diffuse Langerhans islets from human pancreatic tissue specimens. The method utilises serial sections obtained from Epon-embedded specimens fixed with glutaraldehyde and osmium tetroxide. Next, serial block-face imaging using scanning electron microscopy (SBF-SEM) is advanced to enable rapid and efficient acquisition of three-dimensional (3D) ultrastructural information from Langerhans islets of mouse pancreas corresponding to the CLEM images. Samples for SBF-SEM observations were postfixed with osmium and stained en bloc and embedded in conductive resins with ketjenblack significantly reduced the charging of samples during SBF-SEM imaging.",signatures:"Sei Saitoh",downloadPdfUrl:"/chapter/pdf-download/64265",previewPdfUrl:"/chapter/pdf-preview/64265",authors:[null],corrections:null},{id:"66502",title:"Transmission Electron Tomography: Intracellular Insight for the Future of Medicine",doi:"10.5772/intechopen.84977",slug:"transmission-electron-tomography-intracellular-insight-for-the-future-of-medicine",totalDownloads:970,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Transmission electron microscopy (TEM) gives a good image for ultra-intracellular organelles in two-dimensional projections, but to get a three-dimensional structural information, we should use the high-voltage transmission electron tomography (TET). The use of TET is important to resolve the questions about the relation between the different cell organelles and their mechanisms of action to correlate structure to function for medical treatment solutions.",signatures:"Abeer A. Abd El Samad",downloadPdfUrl:"/chapter/pdf-download/66502",previewPdfUrl:"/chapter/pdf-preview/66502",authors:[null],corrections:null},{id:"65594",title:"Analytic Analyses of Human Tissues for the Presence of Asbestos and Talc",doi:"10.5772/intechopen.83656",slug:"analytic-analyses-of-human-tissues-for-the-presence-of-asbestos-and-talc",totalDownloads:1002,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"This chapter discusses the historic and current criteria for the analysis of cosmetic talcum powder and the finding the components of the talcum powder in human tissues. It describes how technicians and scientists have looked in the past for these components and how they should be looked at properly today. Within the chapter it has been shown that it can be complicated, especially when the tools and the methods used are not adequate or sensitive enough. It also goes on to describe methods for analysis that are sensitive enough in both mineral analyses and in human tissue. It also defines the terms that are necessary to use for inclusion of structures based on the scientific knowledge we have today not confused with what either industry or their defenders are trying to use to confuse or defend their positions.",signatures:"Ronald E. 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Venkateswarlu",coverURL:"https://cdn.intechopen.com/books/images_new/371.jpg",editedByType:"Edited by",editors:[{id:"58592",title:"Dr.",name:"Arun",surname:"Shanker",slug:"arun-shanker",fullName:"Arun Shanker"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"72",title:"Ionic Liquids",subtitle:"Theory, Properties, New Approaches",isOpenForSubmission:!1,hash:"d94ffa3cfa10505e3b1d676d46fcd3f5",slug:"ionic-liquids-theory-properties-new-approaches",bookSignature:"Alexander Kokorin",coverURL:"https://cdn.intechopen.com/books/images_new/72.jpg",editedByType:"Edited by",editors:[{id:"19816",title:"Prof.",name:"Alexander",surname:"Kokorin",slug:"alexander-kokorin",fullName:"Alexander Kokorin"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"314",title:"Regenerative Medicine and Tissue Engineering",subtitle:"Cells and Biomaterials",isOpenForSubmission:!1,hash:"bb67e80e480c86bb8315458012d65686",slug:"regenerative-medicine-and-tissue-engineering-cells-and-biomaterials",bookSignature:"Daniel Eberli",coverURL:"https://cdn.intechopen.com/books/images_new/314.jpg",editedByType:"Edited by",editors:[{id:"6495",title:"Dr.",name:"Daniel",surname:"Eberli",slug:"daniel-eberli",fullName:"Daniel Eberli"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"57",title:"Physics and Applications of Graphene",subtitle:"Experiments",isOpenForSubmission:!1,hash:"0e6622a71cf4f02f45bfdd5691e1189a",slug:"physics-and-applications-of-graphene-experiments",bookSignature:"Sergey Mikhailov",coverURL:"https://cdn.intechopen.com/books/images_new/57.jpg",editedByType:"Edited by",editors:[{id:"16042",title:"Dr.",name:"Sergey",surname:"Mikhailov",slug:"sergey-mikhailov",fullName:"Sergey Mikhailov"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"50761",title:"Biomass, Abundant Resources for Synthesis of Mesoporous Silica Material",doi:"10.5772/63463",slug:"biomass-abundant-resources-for-synthesis-of-mesoporous-silica-material",body:'\n
The facile discovery of M4IS family of mesoporous silica material is one of the significant breakthroughs in material science in the last two decades. This material with pore diameter between 2 and 50 nm has continued to be a subject of research focus till date, as its potential application in areas such as medicine, catalysis, adsorption, sensing, and photonics continues to rise. This is shown by more than 19,000 literature citations since 1993 along with numerous patents on the subject matter annually. However, the large‐scale commercialization of the numerous research findings and patents in these fields has not been feasible. This may be due to the high cost of reagents (surfactants and silica precursor) combined with environmental concerns occasioned by the high toxicity of majority of the surfactants and precursors system used in the synthesis. Thus, the large‐scale synthesis of cheap and environmentally safe mesoporous silica material is one of the greatest challenges in modern material syntheses.
\nRecently, there have been renewed interests in mesoporous silica‐based material synthesis fueled by the new synthetic approach which lay emphasis on the use of biologically derived materials found in nature or extracted from biomass resources. It is generally believed that the cost and the ecological impacts of these syntheses would be drastically reduced, thus increasing the possibility of commercialization [1] in the nearest future. In addition, these biosynthesized materials often have well‐defined hierarchical structures/network and properties not hitherto seen in those synthesized via utilization of synthetic chemical reagents. Therefore, this chapter provides a critical assessment of the synthetic approach used in the synthesis of mesoporous silica materials with a view to encourage biomass utilization as potential feedstock for the synthesis if scale‐up development of mesoporous silica materials is envisioned at reasonable cost and with relatively less impact on the environment.
\nThe review is organized into four sections. Section 2 reviews the background into the synthesis of mesoporous silica material (MSiM) from commercially sourced reagents (surfactants and silica framework) with a view to provide insight into the effects of choice of reagents on the structure and characteristics of the synthesized materials. While Section 3 focuses on the progress made in the part utilization of biological/biomass materials and the effects on their inclusion on pore size, surface area, and morphology in comparison with materials derived from purely synthetic chemicals. Finally, Section 4 emphasizes on the view to maximize the potential of biomass waste materials in advanced material synthesis.
\nMesoporous materials, an upper pore extension of microporous zeolithic materials, have attracted much attention due their large surface area (>1000 m2/g), pore volume ( app. 1 g/cm3), and narrow pore distribution that can be adjusted between 2 and 50 nm to meet specific needs and functions. The commercial interest in their applications in catalysis, photonics, sensing, chiral separation, and drug delivery are additional incentives to focus on their synthesis. Pioneered by the facile discovery of the M4IS family (including MCM‐41, MCM‐48, and MCM‐50) of mesoporous materials in 1992 [2]. The synthesis of MCM‐41, the first and most popular member of the M4IS family, was facilitated by assembly of long chain cationic surfactant into micelles or lyotropic liquid crystals (LCC) at a specific surfactant concentration in aqueous solution known as
In the report of Beck et al. [2], self‐assembly and electrostatic charge matching between the surfactant and inorganic precursors was believed to be the driving force for the formation of mesostructure. Later, Tanev and Pinnavaia [5] reported a new approach to the synthesis of mesoporous materials via a neutral surfactants‐templating approach which complemented the ionic‐dependent pathways. This approach is based on hydrogen bonding and self‐assembly between neutral amines and neutral inorganic precursor at ambient temperature. Due to weaker repulsive interaction between the neutral surfactant and precursor at the surfactant‐solution interface, structures with thicker framework walls, small scattering sizes, and textural mesoporosities matching with those of materials produced from ionic pathways were obtained. The thicker walls supplied the material with improved thermal and hydrothermal stability and also made the environmentally benign recovery of the template via solvent extraction possible. In addition, the most significant chemical advantage of this approach perhaps is the synthesis of materials that cannot ordinarily be assessed by ionic templating approaches (e.g., alumina). In spite of the obvious advantages of the neutral templating route over the ionic route, the neutral surfactants still suffer from the same negative aspect as the cationic quaternary ammonium surfactants such as high cost and toxicity are therefore not suitable for large‐scale syntheses of mesoporous materials. The original neutral templating approach was extended to obtained phases with increased wall thickness and thermal stability by the use of block copolymers (BCs). BCs such as the polyethylene oxide (PEO) polymeric surfactants were used for the synthesis of disordered worm‐like phases at neutral pH and triblock copolymers under acidic condition to obtain highly ordered 2‐D Santa Barbara Amorphous (SBA). However, despite the low cost of BCs, the surfactant showed poor degradability and toxicity to organisms, thereby hindering its utilization in large‐scale syntheses.
\nSeveral investigations into the synthesis of mesoporous silica materials have concluded that two different mechanisms are involved: (a) On the one hand, it involved the self‐assembly of the surfactant (at high concentration) into a lyotropic crystalline phase (micelles) independent of the crystallization and subsequent polymerization of the silica framework around the preformed micellar aggregates framework. (b) On the other hand, it is also possible to produce this phase at lower surfactant concentration; the cooperative self‐assembly of the surfactant and inorganic species is directed by the aqueous inorganic silica precursor to obtain liquid crystalline phase with hexagonal, cubic, or lamellar shape (Figure 1)
\nFormation of mesoporous materials by surfactant structure directing agents: (a) true liquid‐crystal template mechanism, (b) cooperative liquid‐crystal template mechanism [
A basic condition for the mesophase formation is that there must be an attractive interaction between the template and silica precursor which guarantees the subsequent inclusion of the structure‐directing agent (SDA) in the final material without the occurrence of phase separation. According to Huo et al. [6] these interactions can be classified as follows: (a) under basic conditions, where the silica species are present as anions and cationic quaternary ammonium surfactants are used as the SDA, the synthetic pathway is termed (S+I-). (b) The original synthesis of MCM‐41 is based on this pathway. In the charged reversed phase, under acidic conditions (i.e., below the isoelectronic point of the silica species; pH = 2) where the silica species are positively charged, an anionic SDA (S-) is used to direct the self‐assembly of cationic inorganic silica species (I+) through the S-I+ pathway. (c) To produce an interaction with the cationic surfactant, a mediator ion X- (usually halides) may be added to direct the mesophase formation via the S+X-I-. (d) Conversely, when negatively charged surfactants (S-) are used, it is also possible to work under basic condition whereby a mediator ion M+ (usually alkali ions) can be added to ensure interaction between equally negatively charged species via S-M+I- pathway. Therefore, the interactions in pathways (a)–(d) are predominantly electrostatic in nature. In addition, it is possible for the attractive interactions to be mediated by hydrogen bonds; this is the case when neutral (S0, e.g., long‐chained amine) or nonionic surfactants (N0, e.g., polyethylene oxide) and uncharged silica species (S0I0 or N0I0) or ion pairs (S0H+) (X-Io) pathways are present.
\nDepending on the nature, concentration, and temperature, surfactants in lyotropic systems can form different liquid crystal phases which includes isotropic micellar, cubic micellar, lamellar, or reversed‐phase micellar phases. Therefore, the behavior of surfactants is the key for the controlled synthesis of silica mesostructure. As proposed by Israelachvili et al. [7], the relative stabilities of the different micellar aggregate shapes and the mesophase structures can be predicted from a combination of molecular packing considerations and general thermodynamic principles. He further states that the preferred shape of the self‐assembled surfactant molecules above its CMC depends on the effective mean molecular parameters of the micelle that establish the value of a dimensionless packing parameter
Different processing parameters such as the type of surfactant and precursor among others determine the porosity and morphology of the final material. Mesoporous materials have been largely synthesized from synthetic/commercially sourced surfactants and precursors. However, the high cost, toxicity, and environmental impacts of these reactants and syntheses have led to the search for alternative functional replacements and environmentally benign synthetic routes. Recently, biomass, a renewable resource, has been identified as an abundant source of diverse surfactant materials such as polysaccharides, polypeptides and polyaromatics, and silica frameworks (from rice husk, wheat husk, etc.) that could be applied in silica mineralization. Many biomass materials exhibit hierarchical large‐scale order and self‐assembly properties that can be replicated in a variety of structures; hence, the use of biomass materials as alternative to commercial surfactants and precursors not only yields materials with structural diversities but also holds promise for the synthesis of low‐cost completely biocompatible materials with reduced toxicity and application in areas of human medicine.
\nIn the last few years, several efforts have been made in the production of surfactants with low toxicity and biodegradability; this includes the use of surfactant building blocks (hydrophilic/polar head and hydrophobic tail) derived from renewable resource and the use of surfactants derived from renewable polymer‐ and colloid‐based biomacromolecules such as cellulose and chitosan. With respect to renewable hydrophobic segment of the surfactant, natural fats and oils, which are composed of wide distribution of fatty acids, have been applied in the synthesis of mixtures of surfactants. One of the limitations associated with the use of templates/SDA derived in material synthesis is that they are often obtained in mixtures containing anionic surfactants. The challenge here is that each of the components may interact differently with the silica precursor preventing a suitable organization of the porous network. Moreover, their purification may lead to increase in cost as well as adverse environmental impacts. However, the advantage inherent in this approach is the abundant availability of this sources and their fast biodegradability.
\nCanlas and Pinnavaia [8] reported the utilization of naturally derived oleyl amine surfactants for the synthesis of worm‐like and lamellar mesoporous silica. These structures are similar to those obtained using petroleum‐based alkyl amine surfactant via the S0I0 templating mechanism thus showing that surfactants from renewable source could effectively be used as templates in mesoporous silica synthesis. However, at lower solvent polarity, the surfactant, due to the flexibility of the hydrophobic chain, adopted a hairpin and other extended structures generating mesoporous silica with pore size in the supermicroporous range, thus making them more flexible as templating agents than the alkyl amines. This supermicroporous derivative is believed to offer greater size and shape selection separation and catalysis in comparison to their mesoporous analogues. Oleyl amine is obtained by the transformation of oleic acid derived from tallow fats or vegetable oils such as soya or palm oil. With respect to utilization of hydrophilic segment from renewable resource in generating eco‐friendly surfactants, amino acid derived surfactant from another interesting group of renewable surfactants known for their excellent surface activity, biocompatibility, and low toxicity. Thomas et al. [9] reported the use of surfactant formulations based on glutamic acid and leucine containing a mixture of lauronyl amino acid and fatty acid as SDA for the formation of mixtures of ordered mesoporous silica including lamellar phases. This approach was challenging as the synthesis was carried out at neutral pH and room temperature using organic and inorganic reactants from renewable sources. Measurement of amino acid‐based SDA CMC, surface tension at CMC (ST), foaming capacity, and foaming stability showed that the surfactant mixtures with the longest chain have properties comparable to petroleum‐based surfactants [10]. Sodium N‐dodecyl glycine (C12H25NHCH2COONa) and potassium N‐dodecyl glycine (C12H25NHCH2COOK) amino acid‐based surfactants prepared by reacting coconut oil amine with monochloroacetic acid in alkali medium were used to synthesize mesostructures different from lamellar, more precisely the synthesis of hexagonal and Pm3n cubic structures [11].
\nAnother interesting class of surfactant with polar groups derived from renewable resources is the alkyl glycosides with growing interest due to their liquid crystalline phase‐forming ability, chiral properties, non‐toxicity, and biodegradability. Alkyl glycosides are another class of surfactants with polar head derived from renewable resources. The development of well‐ordered materials using this sugar‐based nonionic surfactant is however limited because the interaction between the weakly charged inorganic silica precursor and the nonionic surfactant are short‐ranged hydrogen bonding often resulting in disordered mesostructure. The deposition of mesostructure silica films via the self‐assembly of commercially available sugar‐based alkyl glycosidic nonionic surfactants, such as n‐octyl β‐d‐glycopyranoside (β‐C8Glc), n‐dodecyl β‐d‐maltopyranoside (β‐C12Mal), and n‐decyl β‐d‐maltopyranoside(β‐C10Mal), in combination with a prehydrolysed silicate, and the effects of size of sugar head group and alkyl chain length on the type of supramolecular assembly of the surfactant have been reported [12]. Although the three alkyl glycoside surfactants were successfully utilized in the sol‐gel processing of crack‐free mesoporous silica films, the hydrogen bonding interactions with the silicate species during the gel formation suppressed the siloxane condensation. β‐C10Mal and β‐C12Mal with bigger maltose head group formed curved mesophases at lower concentrations and lamellar phases at higher concentrations that were stable to template removal by solvent extraction or calcination. β‐C12Mal‐templated and β‐C12Mal‐calcined mesostructure silica film exhibited a significantly higher d spacing (41 Å) than the corresponding β‐C10Mal‐templated silica (30 Å).
\nRenewable biomass wastes generated by agro‐processing and food industries, including polymers and polymer colloids belonging to the polysaccharide family, constitute a potential field of research for obtaining new sustainable surfactants for the design of functional mesostructure. This is due to their availability, non‐competitive use in the food industry, and more importantly, the rich chemical functionality and easy formulations [13]. Various polysaccharide‐based polymers have been used as templates to direct the synthesis of silica; these include chitosan and chitin colloids and cellulose. Chitin, which is found in the exoskeletons of crustaceans, mollusk, and insects in nature, is the second most abundant renewable polysaccharide in nature. However, its use in design of functional material is limited by its poor solubility, but on partial deacetylation, it yields chitosan, a water‐soluble substance furnished with several free amino acid groups. Due to its solubility in acidic media and its rich chemical groups, chitosan has been used for structuring silica‐based materials [13–15]. However, these efforts yielded poorly ordered materials after template removal by calcination.
\nRecently, Alonso and Belamie [16] presented a versatile and novel approach involving the use of chitin colloids (
Cellulose is the most abundant natural biopolymer, which is renewable, biodegradable, and non‐toxic. It is a polysaccharide composed of monomeric anhydroglucose units connected by β‐1,4‐glycosidic bonds. Cellulose also exhibits self‐assembly properties and an inherent structural hierarchy. It is considered as a green alternative to petroleum‐based polymers commonly used as template for the fabrication of mesostructured silica phases. When subjected to acid hydrolysis, cellulose nanocrystals (CNCs), a colloidal suspension, containing the crystalline portion of the polysaccharide, have been reported to assemble into nematic liquid crystalline phase (NLCP), is obtained [21]. This entity, CNC, has been used as a renewable and inexpensive template to cast hybrid mesophase in material synthesis. Dujardin et al. [1] reported a novel synthetic approach to the synthesis of mesoporous silica which involved the sol‐gel mineralization of partially ordered suspension of nematic liquid crystalline CNC template. Removal of the CNC template by calcination at 400oC produced a cracked birefringent silica matrix with pattern mesoporosity consisting of co‐aligned cylindrical pores of approximately 15 and 9 nm diameter and wall thickness, respectively. Significant extension in pore length far beyond the length of individual CNCs were found to be suggestive of both lateral and lengthwise close packing in the nanocrystal bundles of the nematic template.
\nThe versatility of use of cholesteric phase of cellulose derivatives was demonstrated by Thomas and Antonietti [22] with the use of NLCP of hydroxypropyl cellulose for the generation of a porous silica with high surface area devoid of long‐range chiral organization of the template. A freestanding mesoporous silica with high surface area that is a cast of a chiral nematic liquid crystal formed from CNC was reported by Shopsowitz et al. [23]. It was the first material to combine mesoporosity with long‐ranged chiral ordering that showed photonic effects. Recently, mesoporous KIE‐6 (Korea Institute of Energy‐6) was synthesized using crude glycerol waste (CGlW) from biodiesel production. Biodiesel is synthesized through the trans‐esterification of triglycerides from biomass such as palm and jatropha; about 1 million tons of CGlW is generated annually. CGlW (consisting of water and methanol, 40%, and glycerol, soap, and fatty acid methyl ester (FAME), 60%) waste constitutes an environmental problem because it is eliminated by incineration, releasing green house gases into the environment, as the cost for its purification is high. Hence, its use in the synthesis of porous material is a solution to its disposal. The glycerol/silica composite with tunable pore size, pore volume, and specific surface area was synthesized by adding glycerol waste and sulfuric acid into the silica sols at room temperature. However, a pre‐calcination step at 150oC for 2 h was introduced to prevent the escape of the pore‐forming glycerol before the formation of a rigid network by silanol group condensation. Otherwise, glycerol is evaporated before condensation resulting in reduced pore size and volume in the calcined composites. The CGlW template was removed by calcination in air at 550oC for 2 h yielding a 3‐D interconnected worm‐like mesoporous KIE‐6. Properties of mesoporous KIE‐6 such as specific surface area, pore size, and volume, and silica wall thickness were tuned by varying the crude glycerol concentration. Variation in glycerol: silica weight ratio in the composite from 0 through 4.9 to 8.0 yielded composites with increased pore size of 4.7 nm through 7.2 and 10 nm, respectively; pore volume from 0.53 to 1.01cm3/g and stable Brunauer-Emmett-Teller (BET) surface area between 443 and 550 m2/g. In addition, life cycle assessment (LCA) of all the indexes included in the synthetic process from biomass cultivation, through biodiesel production to synthesis of mesoporous material, showed that CO2 emitted during KIE‐6 synthesis was much lower than in other existing routes for mesoporous silica. The reduction was attributed to the utilization of renewable CGlW. A major drawback in this synthetic approach, however, is the inclusion of methanol in the CGlW [24].
\n\nRice, grasses (Germinaecea: bamboo, wheat, maize, and oats), sedges (Cyperaceae), and horsetails (Equisetums) are known to contain high concentration of biogenic silica. Silica is believed to be absorbed from the large abundance of silica in the earth crust released by geological processes as water‐soluble silicic acid, Si(OH)4, which through subsequent polymerization and precipitation are deposited as extracellular deposits on cell walls. This process is known as biosilicification. Biosilicification occurs under mild conditions, generating a variety of complex and hierarchical nanostructures silica frameworks which contributes to cell wall rigidity, photosynthesis efficiency, and increased resistance to pathogenic attacks and diseases [25]. Rice husk (RH), which is currently the main natural silica producer, is a waste generated by rice milling activities and this accounts for 20–25 wt% of the whole dried rice grain. According to the United Nations Food and Agriculture Organization [26], the world rice production in 2014–2015 was estimated to be around 740.2 million tons. Therefore, RH makes up about 20 wt%; rice husk waste is a vast silica source. Due to their characteristic woody and abrasive nature, great bulk, slow biodegradability, and low nutritive properties, efforts made to utilize RHs have been very limited. These involve the pre‐treatment of the RH to increase its surface area, decrease crystallinity of cellulose, eliminate hemicelluloses and break the lignin seal [27]. RH is generally removed by burning to yield particulate rice husk ash. RHA, containing nearly 90% silica and other metallic oxide as impurities, is commonly used raw materials for obtaining highly pure silica [28]. Trace metallic impurities in RHA silica have been found to be responsible for the clustering of primary silica nanoparticles (Nps). These metallic cations such as K+ promote the melting of silica Nps and their concentration are responsible for different degrees of melting and different pore structures and pore sizes (Figure 2) [29]. Several reports on the extraction of pure biogenic nanosilica from RHA have been published [30–33]. However, before its utilization, a preliminary purification step is required to remove its constituent metallic oxides impurities. After calcination to eliminate the organics, metallic impurities such as oxides of alkali metals are removed by leaching with NaOH solution at temperatures between 100 and 200oC for 1 h. Direct recovery of silica by precipitation from the basic solution is achieved by addition of drops of sulfuric acid to the hot basic solution, followed by thermal treatment at 110oC [34]. Several products of commercial interest such as silicon carbide (SiC) used as semiconductors, pozzolan in cement manufacturing, and recently, sodium silicate in the preparation of silica‐based mesoporous materials have been reported [35–42].
\nSEM image of nanoporous silica: (A) 0.20 M K+ pyrolysis at 800oC for 2 h; (B) 0.20 M K+, pyrolysis at 800oC for 4 h; (C) 0.20 M K+, pyrolysis at 800oC for 8 h; (D) 0.50 M K+, pyrolysis at 800oC for 8 h. Effect of K+ on mesoporous silica from bagasse ash [
Siriluk and Yuttapong [42] demonstrated that RHA silica generated from biomass power plant can be used as silica framework for synthesis of MCM‐41‐type material with crystallinity characteristics and porosity similar to those synthesized from commercial silica. Some authors have reported the synthesis MCM‐41‐, MCM‐48‐, and SBA‐15‐type materials on which functional entities were grafted on the surface silanol groups using sodium silicate solutions extracted from RHA [36, 37, 40]; their potential for CO2 and chlorinated volatile organic molecules adsorption was found to be similar to those synthesized from conventional silica sources. Recently, Rahman et al. [43] synthesized mesoporous silica with controlled pore structure from bagasse ash with approximately 656 m2/g surface area and pore diameter 18 nm. Pore structure was influenced by the presence of Na+, template concentration, and pH.
\nSeveral attempts have been made to employ inexpensive, non‐toxic, and renewable biomaterials in synthesizing “
The synthesis of mesoporous silica material from commercially available templates and silica frameworks has made the large‐scale production of this material unrealistic. This is due to high cost and the negative environmental impacts of the reagents and the harsh synthetic conditions. Recently, attempts have been made to utilize alternative reagents from renewable sources and benign synthetic routes. However, these efforts have largely been directed toward the part utilization of renewable biomass materials as reagents at near neutral pH. Although the materials derived showed characteristics and properties that are similar to those synthesized from commercially available reagents, efforts directed to the full utilization of renewable reagents belittle this fact. Therefore, there is need to focus attention on the full utilization of renewable biomass‐generated reagents in the synthesis of MCM. This approach will not only result in the low‐cost production of less toxic materials that will be suitable for various applications but also proffer solutions to the environmental and health threats associated with sustainable biomass waste removal.
\nThis review was facilitated by the collaboration established between Obafemi Awolowo University (OAU) Ile‐Ife and Cape Peninsula University of Technology (CPUT), Cape Town. The authors wish to acknowledge the support of these institutions. TV wishes to acknowledge OAU for providing him a sabbatical position that led to the commencement of this project, while AI acknowledges the support of Joseph Ayo Babalola University for her graduate program.
\nAt high temperatures, wetting of a solid (metal or ceramic) by the molten metallurgical melts is of great technological importance in a variety of metallurgical processes, e.g, hot dipping coating process, brazing process, casting process and sintering process. Each process has the different optimal wetting condition. For the hot dipping coating process, the perfect wettability of base materials by liquid metal is demanded. Two key issues for wetting at high temperatures include the spreading dynamics (wetting behavior) and the final wettability (the degree of wettability). For the former issue, it determined the technological parameters in process; for the latter issue, it would be one of the critical evaluation bases for whether the process can be carried out or not.
The description of wettability since from 1805 in Young’s work [1], has been well developed, as following,
where θ is contact angle for a liquid equilibrium with ideal solid at the point of triple line, σ
The coating process by using a hot dipping method, although a traditional technology with relatively high energy consumption, is also a reliable technology with high efficiency. The quality of coating directly depends on the wetting of base metal by the coating metal. The performance of coating as well as the technological parameters in the coating process is also affected by the trace addition in the alloys which may act on the solid/liquid interface and(or) the liquid/vapor interface. In this chapter, based on the effect of trace elements on the wetting behaviors and the interfacial structures, the wetting mechanism of base metals (steel, Ti6Al4V (TC4) alloy, pure Ti (TA2)) by Al alloys (4043 alloy and 6061 alloy) as well as the formation of precursor film in these systems would be presented in Section 3.
This chapter presents an overview of wetting parameters at high temperatures, wetting mechanism in the isothermal spreading, the effect of trace elements on the formation of interface and the possibility of designed interfacial structures.
At high temperatures, one needs to be careful in the characterization of the wetting of molten metal on the surface of materials (ceramics or metals) with relatively high melting pointing under the quasi-ideal condition.
First, the basic condition is the homogeneous temperature field for wetting should be established.
Second, the average roughness (Ra) of substrate should be obtained before wetting test. Usually, Ra for the metallic substrates after polishing and the monocrystal ceramic substrates are in the range of dozens of nanometers over a distance of 2 mm, Ra for the polycrystal ceramic substrates after polishing are in the range of hundreds of nanometers which depends on the relative density of the polycrystal ceramic substrates.
Third, due to the high sensitivity of metal to oxygen, the oxygen partial pressure in the atmosphere should be controlled, usually in a vacuum of ~10−4 Pa or a dried-deoxidized Ar atmosphere, the oxygen partial pressure was estimated to be lower than 10−14 Pa [2] in such a high vacuum, and the oxygen partial pressure was estimated to be lower than 10−8 Pa [2] in a dried-deoxidized Ar atmosphere.
Once the above conditions were confirmed, and then the various methods for the testing should be considered.
Several methods for the testing at room temperatures, such as sessile drop method, wetting balance method, vertical rod method, tilted plate method, capillary rise method, etc., but the sessile drop method based on the complicated calculation is usually adopted due to the good feasibility. One also should note that the sessile drop method used in more than 90% of wetting studies at high temperatures [3]. The size of drop for testing should refer to its capillary length (i.e., 2σlv/(ρg)1/2, where ρ is the density of liquid and g is the acceleration due to gravity), and thus a drop of volume ~5 μl with a spherical diameter of ~2 mm will be suitable for obtaining of the contact angle. Advancing contact angle is the parameter which the engineers mostly care about, and thus the study of wetting behavior used the advancing contact angle.
To acquire wetting parameters under the quasi-ideal condition, a specific wetting furnace is necessary, as be shown in Figure 1. The whole device mainly includes the controlled heat system, the vacuum system, the inertia gas flow system, the water-cooling system, and the image acquisition and data processing system. The details of this device were shown in Figure 1(a), W, Ta or Mo was used as a heater, and two typical drop transfer modes were used, the modified sessile drop method and the improved sessile drop method.
(a) Schematic diagram for wetting furnace and (b) the designed wetting furnace.
Comparing to the traditional sessile drop method (substrate and metal were heated together), the mentioned two sessile drop methods have a distinct advantage in measurement of initial contact angle and spreading dynamics, particularly for the system with a chemical reaction at elevated temperatures.
To acquire the wetting parameters accurately, a laser backlight source (650 nm in wavelength and 10 mW in power) together with the band-pass filter is necessary for an image acquisition and data processing system. To insure the reliability of obtained data, the drop profiles were captured in two axes, as shown in Figure 1(b). The typical side view of captured drop profile was shown in Figure 2. Before the calculation of contact angle, every pixel in the image was defined as a coordinate value (x and y coordinates), and then the program can seek the boundary between drop and backlight, and thus the pixel coordinate function of drop profile can be extracted. The function was further fitted by several models, i.e., Young-Laplace model, conic model, circle model. The choice of fitting model depends on the symmetry of captured drop profile or the contact angle. If the drop profile is almost axisymmetric, Young-Laplace model is the first choice. If the profile deviates axis symmetry, conic model is the first choice. If the contact angle is less than 5°, conic model or circle model is the first choice. Based on the results of calculation, the detailed wetting parameters can be obtained, i.e., the contact angle, the base diameter, the density, volume and surface tension of liquid.
Typical captured drop profile.
The chemical compositions of the used materials were shown in Tables 1 and 2.
Si | Fe | Cu | Mn | Mg | Zn | Ti | Al | |
---|---|---|---|---|---|---|---|---|
Al 6061 | 0.60 | 0.90 | — | — | 0.90 | 0.25 | 0.15 | Bal. |
Al 4043 | 4.5–6.0 | 0.80 | 0.30 | 0.05 | 0.50 | 0.10 | 0.20 | Bal. |
Nominal chemical compositions of the used Al alloys (wt.%).
Steel | C | Si | Mn | P | S | Fe | |
---|---|---|---|---|---|---|---|
Q235 | 0.12–0.2 | ≤0.3 | 0.3–0.7 | ≤0.045 | ≤0.045 | Bal. | |
Ti alloy | Ti | Fe | Si | C | Al | V | O |
TC4 | Bal. | 0.3 | — | 0.1 | 5.6–5.8 | 3.5–4.5 | 0.2 |
Pure Ti | Ti | Fe | Si | C | N | H | O |
TA2 | Bal. | 0.3 | 0.15 | 0.1 | 0.05 | 0.015 | 0.2 |
Nominal chemical compositions of the used substrates (wt.%).
Based on the wetting characterization, to establish the relationship of wetting behavior and surface/interface evolution, further reveal the wetting mechanism, some necessary micro-analysis were also carried out.
Trace elements in Al alloys, which may act on the surface of drop and/or the solid/liquid interface, and thus the industrial grade Al 4043 alloy and Al 6061 alloy were selected in this work which are of Si addition (~5 wt.%) and of Mg addition (~1 wt.%), respectively. The Si addition may both act on the surface of drop and solid/liquid interface, and the Mg addition may act on the surface of the drop mainly. The metallic substrates were selected as a reactive wetting system, i.e., Al/steel (low-carbon steel), Al/TC4 (Ti6Al4V) and Al/TA2 (TA2 grade pure Ti) systems.
The melting points of Al 4043 alloy and Al 6061 alloy were confirmed by DTA method (STA449-C, NETZSCH, and Germany), are 586 and 582°C, respectively, and thus the isothermal wetting experiments were carried out in a high vacuum (~10−4 Pa) by using improved sessile drop method at the range from 600 to 700°C.
The variations in the contact angle and the normalized contact radius (
Variation in contact angle and normalized contact radius with time, (a) and (b) for 4043 Al/steel, (c) and (d) for 6061 Al/TC4, respectively.
Variation in contact angle and normalized contact radius with time, (a) and (b) for 4043 Al/TC4, (c) and (d) for 6061 Al/TC4, (e) and (f) for 4043 Al/TA2, (g) and (h) for 6061 Al/TA2, respectively.
During spreading, the precursor film (diffusion bond or so called “wetting halo”) was formed at the latter stage of spreading in some specific samples. As shown in Figure 5(a)–(c) are the top-views for the samples after isothermal wetting at 650, 700 and 750°C for Al 4043/steel, and the top-views of (a-1) to (c-1) for Al 6061/steel samples after isothermal wetting at 600, 650 and 700°C. As a consensus, the formation of the precursor film always accompanies the good final wettability, and the larger width of the precursor and the better final wettability. Therefore, the final wettability of Al 6061/steel is better than Al 4043/steel at the same experimental temperature, although the latter has some precursor film at 650 and 700°C, the width of them is very limited (~500–1000 μm). Such a congruent relationship is also suitable for the wetting of metal/ceramic systems [4]. Also, in all Al/TC4 and Al/TA2 (except for Al 6061/TA2 at 600°C which is nonwetting at the final state), the precursor film can be found at the final state after wetting, also can be seen in Hg/Ag system [5] in the study by Be’er et al. However, the formation mechanism is so different from the evaporation-condensation mechanism (suggested by de Gennes [6]) and the surface diffusion mechanism (suggested by Li et al. [7]). Further, the precursor film, in a metal/ceramic system, especially for the melt contain some concentration of the active element, is an adsorbed film. The formation of the film should satisfy some specific conditions, as we reviewed before [4].
Top-view of some typical sessile drop samples of Al/steel after the wetting experiments in vacuum: (a)–(c) for Al 4043 sample at 650, 700 and 750°C; (a-1)–(c-1) for Al 6061 sample at 600, 650 and 700°C.
The sectional views of interfacial structures for Al 6061/steel and Al 4043/steel samples are obviously different after isothermal wetting at the same temperature (at 650°C), as shown in Figures 6(a) and 7(a). Although two types of Fe-Al intermetallics can be found in all the samples (bottom: the continuous Fe2Al5 layer, upper: discontinued FeAl3), the effect of trace elements on the interfacial structures is obvious. In Al 4043/steel, the addition of Si segregated at solid/liquid interface which enhanced the interfacial reaction, so that the barrier of interdiffusion was established. Both Si element distribution map (Figure 6(c)) and the elements line distributions for the corresponding position of Figure 6(b) show Si is incline to segregate at solid/liquid interface rather than surface of liquid. Also, the segregation of Si induced the brittleness of the compact Fe2Al5 layer [8], which induced some continuous and propagating cracks. Actually, some Si was dissolved into the Fe2Al5 phase as a solid solution due to the Si segregation, which can be rewritten as Fe2(Al1−xSix)5, where x is in the range of 0.0625–0.104, as reported by Gupta [9]. Comparing with Al 4043/steel, in the interface of Al 6061/steel, no Mg segregation (even no trace of Mg) can be found in the interface or the bulk of drop due to the high volatility of Mg under the vacuum condition, as shown in Figure 7(a)–(c). The Fe2Al5 reaction layer on steel side is irregular and stretches into the steel side, which is one of the main differences from Al 4043/steel interface. Without the barrier of interdiffusion, the grain boundary as a short-circuit diffused path, Al element prefers to diffuse into the grain boundary, and then reacted with Fe. The X-Ray micro-Diffraction (micro-XRD) pattern of the phases at the surface of the precursor film for Al 6061 sample after isothermal wetting at 700°C in Figure 7(d) shows the precursor film contains Fe2Al5, i.e., the extended reaction layer.
Cross-sectional views of interface structures (Al 4043/steel): (a) at the close of triple line, (b) the central position at interface, (c) Si element distribution map corresponding to the purple rectangle in (b).
Cross-sectional views of interface structures (Al 6061/steel): (a) at the close of triple line, (b) the central position at interface, (c) the typical energy spectrum for the position of yellow cross in (b) and (d) the XRD pattern for the surface of precursor film.
Understanding the reasons caused the wetting, is the benefit of further controlling the manufactured process, which is the prime concern of engineering. In a metallic system, the first obstacle for wetting is the oxide film on the surface of substrate. Protsenko et al. [10] considered the effect of the formation of intermetallic compounds in the wetting with the metallic substrate covered by oxide film. By the formation of IMC by diffusion of reacting components through the thin oxide layer, the oxide film can be disrupted and then in situ a clean surface of intermetallic for wetting can be created. Also, as suggested by Durandet et al. [11], the precipitation of Fe-Al intermetallics is so fast even the contact time of liquid Al and steel as short as 20 ms. Further, the thickness of the IMC layer in this work is larger than the oxide film (in nanoscale), and thus the precipitation of IMC may be a factor for improving wettability. However, the time for spreading cannot correspond to the fast reaction.
The dynamic of IMC precipitation should not be the limited factor for spreading. Although the nonwettable Fe—O oxide film would block wetting, a reduction reaction 2yAl + 3FexOy = yAl2O3 + 3xFe can take place based on the thermodynamic consideration [12], and then Al melts can further react with the fresh surface of Fe. As known, the whole process is limited by the slowest step, and thus the reduction step may be the limited factor for spreading. In Al 6061/steel, although no trace of Mg was observed, the volatilization of Mg cannot be neglected. As suggested by Miller and Pa [13], Mg vapor as a gas flux can reduce Al2O3 in the brazing process of Al alloys. Here, the Fe—O oxide film also can be reduced by Mg vapor due to the more positive formation of Gibbs free energy of Fe—O compounds [12] under the same thermodynamic condition. Based on the result of microstructures, although the precursor film for Al 4043/steel also can be found, it only appears at high experimental temperature with very limited width due to the slight volatility of Al. All the interfacial structures indicate that the formation of the precursor film is related to the volatility of the active element in the specific system. However, the formation mechanism is not the evaporation-condensation mechanism. When the base metal was covered by the thin oxide film, the molten metal would infiltrate under the covered oxide film and then trigger the moving of triple line, and thus the spreading in this stage is also called secondary spreading or wetting, i.e., the formation of precursor film satisfies the subcutaneous infiltration mechanism (as proposed by Zhuang and Lugscheider [14]).
Based on the final wetting states, i.e., nonwetting and wetting states, the typical interfacial structures were selected, as shown in Figures 8, 9, 10. In Figure 8(a) and (b), the precursor with width of several millimeters as well as some Al-Ti intermetallics in the precursor film can be found. The obvious precursor film in Al/TC4 and Al/TA2 (except for the Al/TC4 and Al/TA2 at 600°C which are nonwetting) has the same formation mechanism i.e., so-called “subcutaneous infiltration”. The final wettability was less affected by the oxide film but was determined by the reaction products at the liquid/solid interface. As known, although some residual oxygen in the vacuum chamber could dissolve into Ti due to the high affinity of Ti to oxygen, and then inducing oxidation, however, the diffusion rate for oxygen into the interior of Ti is faster than the oxidation rate so that the oxide film would be thinned or even removed. In Al/TC4 and Al/TA2 systems, both the temperatures and the alloying elements (Si and Mg) caused the different interfacial structures and are responsible for the different final wettability. In Figure 8(d)–(f), the typical cross-sectional view of Al 6061/TC4 after isothermal wetting at 600°C shows the chemical compositions of the granular phase distributed above the reaction layer are closed to Al3Ti. The original concentration of Si in the bulk Al 6061 alloys is only 0.6 at.%, but the concentration of Si in the continuous reaction layer is far beyond that value, as shown in Figure 8(e). The distinct segregation of Si in the reaction layer was formed during wetting. For the nonwetting sample of Al 4043/TC4 (after wetting at 600°C), as shown in Figure 9(a) and (b), the interfacial structures with the virgate phase but no granular phase near triple line and the virgate phase together with granular phase at the center position can be found. Si concentration in the virgate phase is extremely high comparing with the original concentration in bulk Al 4043 alloy, as shown in Figures 9(c)–(e).
(a) Top-view of the microstructures around the triple line for Al 6061/TC4 after isothermal wetting at 600°C; (b) detail of the black rectangle area in (a); cross-sectional view of Al 6061/TC4 (c) near the triple line and (d) at central position of the interfacial microstructures with the elemental line distribution results; (e) and (f) EDS results for the corresponding colored crosses in (d), respectively.
Cross-sectional views for Al 4043/TC4 after isothermal wetting at 600°C: (a) at the triple line; (b) at the center of the interface; (c)–(e) the EDS results for the corresponding cross, circle and triangle in (b).
(a) Top-view of the microstructures at the triple line for Al 4043/TC4 after isothermal wetting at 650°C; (b) detail of the black rectangle area in (a); cross-sectional view of Al 4043/TC4 (c) at the triple line, and (d) at center of the interfacial microstructures with the elemental line distribution results; (e) and (f) EDS results for the corresponding colored crosses in (d), respectively.
For the wetting sample of Al 4043/TC4 which is similar to the interfacial structures in Al 6061/TC4, a precursor film with width of several millimeters was formed. However, such a precursor film contains two layers, as be shown in Figure 10(a) and (b). From the cross-sectional view of the film (Figure 10(c)), the upper layer is the residual Al, which was attracted by the capillary force from the loose reaction layer. At the central position of the interface (Figure 10(d)), the loose continuous layer also can be found, but the virgate phase almost disappeared and only can be found sporadically above the loose layer. Based on the EDS results (Figure 10(e) and (f)), the loose layer may be a continuous Al3Ti layer dissolved with Si as a solid solution. For the sample of Al 4043/TC4 after isothermal wetting at 650°C, the solidified Al was removed by NaOH aqueous solution (1 mol/L), and the macroscopical appearance of the sample and the details for the corresponding positions were shown in Figure 11. The granular phase in Figure 11(b) is corresponding to the loose continuous reaction layer, and the lamellate phase is corresponding to virgate phase in the cross-sectional view of the interface. Further, as shown in Figure 12, the XRD of the phases at the corresponding surface confirmed the granular phase (the loose continuous reaction layer) is Al3Ti, and the lamellate phase is Ti7Al5Si12 (τ1, a solid solution of Al in the TiSi2 phase [15]).
(a) Solidified Al for the sample of Al 4043/TC4 after isothermal wetting at 650°C was removed by NaOH aqueous solution (1 mol/L); (b) and (c) the microstructures for the corresponding positions in (a).
XRD patterns of the phases at the precursor films: for (a) Al 6061 and (b) Al 4043 samples after isothermal wetting at 700°C; (c) the exposed interface of Al 4043/TC4 after isothermal wetting at 650°C through removing of the solidified Al drop using NaOH aqueous solution, and (d) the original surface of TC4.
The formed Ti7Al5Si12 is a metastable phase, once the temperature was above 579°C, a decomposed reaction of Ti7Al5Si12 would take place, i.e.,
Al-Ti-Si partial isothermal section at 700°C for Al rich corner [
Si addition in Al alloys, as known, is a surface-active agent which can decrease the surface tension of the liquid and increase the flowability. However, in Al-Si/steel or Al-Si/Ti system, the interfacial microstructures confirm the affinity of Si to Fe (or Ti) is relatively higher than that of Si to the Al matrix. The Si segregation at the liquid/solid interface satisfies the thermodynamic condition. Such a thermodynamic model also can be used for predicting the segregation of alloying element at the liquid/solid interface. The adsorption energy based on the affinities, which can be described as following [3],
where
where
The calculated
B-M/A | Mg-Al/Fe | Mg-Al/Ti | Mg-Zn/Fe | Mg-Si/Fe | Mg-Cu/Fe | Mg-Ni/Fe | Mg-Si/Ti | Mg-Al/Cu | Mg-Si/Cu | Al-Si/Fe |
---|---|---|---|---|---|---|---|---|---|---|
−149 | −212 | −73 | −133 | 6 | −35 | −249 | −17 | 21 | −20 | |
B-M/A | Al-Zn/Fe | Al-Si/Ti | Al-Si/Cu | Cu-Ag/Si | Ni-Zn/Fe | Al-Cu/Fe | Cu-Si/Fe | Cu-Zn/Fe | Mg-Zn/Ti | Al-Mg/Ti |
43 | −73 | 1.8 | 21 | 70 | 181 | −118 | −42 | −137 | 221 |
All the variation in spreading of Al/steel and Al/Ti indicated the characteristics of reactive wetting, i.e., the typical linear spreading as well as the interfacial reaction. Reaction-limited models of linear spreading and nonlinear spreading for the description of the wetting behavior, as proposed by Eustathopoulos group, were expressed as following,
where
Arrhenius plot of the kinetic constants
Deduced activation energies from the slopes in Figure 14.
The average activation energy of linear stage and nonlinear stage.
In Al/steel system, two types of spreading mode, i.e., the linear spreading in Al 4043/steel and nonlinear spreading in Al 6061/steel, can be found. The activation energy for Al 4043/steel can be deduced from the slopes, is 8 kJ/mol for Al 4043. Also, the activation energy for Al 6061 can be deduced from the fitting result of Eq. (5), is 86 kJ/mol. In the work of wetting and spreading of molten pure Al on the surface of mild steel, studied by Ishida [17], the linear kinetics were also observed, and the activation energy is 21.8 kJ/mol. Obviously, the trace elements in the systems influenced the spreading dynamics, and caused the different activation energies. In Al 4043/steel, the segregation of Si at liquid/solid interface enhanced the reactivity, and then might lead to relatively small activation energy. In Al 6061/steel, the liquid Mg in molten Al 6061 alloy does not react with Fe directly. The moving of the triple depends on the removing of oxide film on the surface of substrate. The reduction of Fe—O oxide film by the Mg in Al 6061 and the formation of Fe-Al intermetallics play a combined action in the removing of oxide film, which can induce the spreading. Two spreading stages for Al 6061 at 700°C also indicate these two reaction mechanisms. Especially for the latter stage, the reduction reaction mechanism may play a major role on the moving of the triple line corresponding to the prolonged precursor film in this stage. Therefore, the apparent activation energy in Al 6061 is so different from Al 4043 and almost an order of magnitude larger.
In Al/TC4 system, such apparent activation energies should relate to the energy change of reaction. As suggested by Chen et al. [18], Gibbs energy changes of reaction per mole of reactants for the formation of Ti7Al5Si12 and Al3Ti in the range of 600–750°C are ~− 48 kJ/mol and ~− 30 kJ/mol, respectively. For the nonlinear stage, Ti7Al5Si12 decomposition may play a dominant role in the change of interface tension corresponding to the apparent activation energy of 10–38 kJ/mol; for the linear stage, the decomposition of Ti7Al5Si12 and the formation of Al3Ti may play the role for the change of interface tension corresponding to the apparent activation energy of 62 kJ/mol. The relatively higher activity of Si in Al 4043 (due to the higher concentration) may slow down the decomposition of Ti7Al5Si12, and then decrease the apparent activation energy. Further, the residual Ti7Al5Si12 beneath the drop and above on Al3Ti reaction layer at the close of the triple line (Figure 11(c)) should be one of the indicators that two reaction mechanisms together played a role on change of interface tension. Also, in Al/TA2 system, the apparent activation energies indicated that the whole wetting process is controlled by the above mechanism. Therefore, the activation energies (47–84 kJ/mol) may be also corresponding to the decomposition of Ti7Al5Si12 and the formation of Al3Ti.
Aluminizing of steel or Ti alloys can increase the ability of anti-corrosion, the service time and the working temperature, significantly. The wetting of Al alloys plays an important role in the aluminizing process, and thus studied in this work. The following conclusions can be drawn:
In Al/steel, the wettability was improved by intermetallic formation which would lead to the replacement of the oxidized surface by a clean surface of an intermetallic compound, also due to the reduction by Al with oxide film; However, the final wettability of pure Ti (TA2) and Ti alloys (TC4) by Al was less affected by the oxide film, but was determined by the reaction products at the liquid/solid interface. Enhanced peritectic reaction of Ti7Al5Si12 caused the different interfacial structures of TA2 and TC4.
The alloying elements in Al 6061 alloy (with Mg addition) and Al 4043 alloy (with Si addition) resulted in distinctly different interfacial structures, the formation of precursor film and spreading dynamics. Mg played a role like gas flux and reduced the oxide film on the surface of substrate. Si segregated at solid/liquid interface which satisfied the thermodynamic model. Such a thermodynamic model also can be used for predicting the element segregation at the interface.
The precursor film in these reactive wetting systems is an extended reaction layer. The formation of it satisfies subcutaneous infiltration mechanism.
The spreading dynamics of these systems can be described by RPC model, and the activation energies are related to the removing of oxide film covered the substrate or the reaction at interface.
This work is supported by National Natural Science Foundation of China (no. 51665031), “Kaiwu” Innovation Team Support Project of Lanzhou Institute of Technology (no. 2018KW-05).
We have no conflicts of interest to declare.
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Recently, two novel domains identified in KHNYN and N4BP1 proteins have shed new light on this research area. Here, I discuss some recent reports that contributed to shed light on the mechanisms underlining the discrimination between ubiquitin and NEDD8. Understanding the details of these molecular mechanisms represents a prominent facet for the identification of new therapeutic targets.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Elena Santonico",authors:[{id:"271923",title:"Dr.",name:"Elena",middleName:null,surname:"Santonico",slug:"elena-santonico",fullName:"Elena Santonico"}]},{id:"65025",doi:"10.5772/intechopen.82883",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1663,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. 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This chapter will present an evolution of the techniques used to identify the proteoforms and the importance of this identification for understanding of biological processes. This chapter highlights the fundamental concepts in the field of top-down mass spectrometry (TDMS), and provides numerous examples for the use of knowledge obtained from the identification of proteoforms. The identification of mutant proteins is one of the emerging areas of proteogenomics and has the potential to recognize novel disease biomarkers and may point to useful targets for identification of therapeutic approaches.",book:{id:"9352",slug:"proteoforms-concept-and-applications-in-medical-sciences",title:"Proteoforms",fullTitle:"Proteoforms - Concept and Applications in Medical Sciences"},signatures:"Jucélia da Silva Araújo and Olga Lima Tavares Machado",authors:[{id:"30130",title:"Dr.",name:"Olga Lima Tavares",middleName:null,surname:"Machado",slug:"olga-lima-tavares-machado",fullName:"Olga Lima Tavares Machado"},{id:"310148",title:"Dr.",name:"Jucelia",middleName:null,surname:"Da Silva Araujo",slug:"jucelia-da-silva-araujo",fullName:"Jucelia Da Silva Araujo"}]},{id:"65025",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1658,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. Torres",authors:[{id:"186645",title:"Dr.",name:"Jorge",middleName:null,surname:"Torres",slug:"jorge-torres",fullName:"Jorge Torres"},{id:"264944",title:"Mr.",name:"Joseph",middleName:null,surname:"Ong",slug:"joseph-ong",fullName:"Joseph Ong"}]},{id:"65109",title:"Ubiquitin Signaling in Regulation of the Start of the Cell Cycle",slug:"ubiquitin-signaling-in-regulation-of-the-start-of-the-cell-cycle",totalDownloads:1559,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"The small protein ubiquitin plays a vital role in virtually all aspects of cellular life. Among the diverse signaling outcomes associated with ubiquitination, the most well-established is the targeted degradation of substrates via the proteasome. During cell growth and proliferation, ubiquitin plays an outsized role in promoting progression through the cell cycle. In particular, ubiquitin-mediated degradation is critically important at transition points where it provides directionality and irreversibility to the cell cycle, which is essential for maintaining genome integrity. Specifically, the boundary between G1 and S-phase is tightly regulated by the ubiquitin proteasome system. Notably, the G1/S boundary represents a major barrier to cell proliferation and is universally dysfunctional in cancer cells, allowing for the unbridled proliferation observed in malignancy. Numerous E3 ubiquitin ligases, which facilitate the ubiquitination of specific substrates, have been shown to control G1/S. In this chapter, we will discuss components in the ubiquitin proteasome system that are implicated in G1/S control, how these enzymes are interconnected, gaps in our current knowledge, and the potential role of these pathways in the cancer cycle and disease proliferation.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Michael James Emanuele and Taylor Paige Enrico",authors:[{id:"264977",title:"Dr.",name:"Michael",middleName:null,surname:"Emanuele",slug:"michael-emanuele",fullName:"Michael Emanuele"},{id:"282200",title:"Ms.",name:"Taylor",middleName:null,surname:"Enrico",slug:"taylor-enrico",fullName:"Taylor Enrico"}]},{id:"60432",title:"Protein-Based Detection Methods for Genetically Modified Crops",slug:"protein-based-detection-methods-for-genetically-modified-crops",totalDownloads:1393,totalCrossrefCites:3,totalDimensionsCites:4,abstract:"The generation of genetically modified (GM) crops is rapidly expanding each and every year around the world. The well-being and quality assessment of these harvests are vital issues with respect to buyers’ interests. This drove the administrative specialists to execute an arrangement of extremely strict strategies for the endorsement to develop and use GMOs and to produce an interest in scientific techniques equipped for identifying GM crops. The GM crops have been added to the effective fuse of various attributes by presenting transgenes, for example, Bacillus thuringiensis (Bt) insecticidal qualities, in various crop species. GM crops give critical financial, natural, well-being and social advantages to both small and large agriculturists. The detection strategies incorporate either DNA-based or protein-based measures. Different immunoassays or catalyst connected immunosorbent tests are delicate and more affordable; however, they need experienced technicians. A very simple method, that is, immunochromatographic (ICS) test, is set up in the world, which is modest, compact and simple to utilize. The ICS is a semiquantitative method for indicative screening and semi-measurement of new remote proteins presented through hereditary change of plants. The strip is the easiest method for the assessment of several Bt crop plants for insecticidal quality.",book:{id:"6635",slug:"protein-protein-interaction-assays",title:"Protein-Protein Interaction Assays",fullTitle:"Protein-Protein Interaction Assays"},signatures:"Kausar Malik, Haleema Sadia and Muhammad Hamza Basit",authors:[{id:"238750",title:"Prof.",name:"Kausar",middleName:null,surname:"Malik",slug:"kausar-malik",fullName:"Kausar Malik"},{id:"243713",title:"Dr.",name:"Haleema",middleName:null,surname:"Sadia",slug:"haleema-sadia",fullName:"Haleema Sadia"},{id:"243714",title:"Mr.",name:"Muhammad Hamza",middleName:null,surname:"Basit",slug:"muhammad-hamza-basit",fullName:"Muhammad Hamza Basit"}]},{id:"60064",title:"Rapid Endosomal Recycling",slug:"rapid-endosomal-recycling",totalDownloads:1304,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"Peripheral membrane proteins are endocytosed by constitutive processes of membrane invaginations, followed by internalization driven by diverse endocytic machinery available at the cell surface. It is believed that after endocytic uptake, cargo proteins proceed either through the endosomal recycling circuit of the cell or travel toward late endosomes for degradation. In this chapter, we analyzed trafficking of seven cargo molecules (transferrin receptor, fully conformed MHC-I, non-conformed MHC-I, cholera-toxin B subunit, CD44, ICAM1, and G-protein-coupled receptor Rae-1) known to use the distinct endocytic route. For that purpose, we developed the software for multicompartment analysis of intracellular trafficking. We demonstrate that all endocytosed molecules are rapidly recycled and propose that the rapid recycling is a constitutive process that should be considered in the analysis of intracellular trafficking of peripheral membrane proteins.",book:{id:"6649",slug:"peripheral-membrane-proteins",title:"Peripheral Membrane Proteins",fullTitle:"Peripheral Membrane Proteins"},signatures:"Hana Mahmutefendić, Gordana Blagojević Zagorac, Senka Maćešić\nand Pero Lučin",authors:[{id:"152008",title:"Prof.",name:"Pero",middleName:null,surname:"Lučin",slug:"pero-lucin",fullName:"Pero Lučin"},{id:"245873",title:"Prof.",name:"Hana",middleName:null,surname:"Mahmutefendić",slug:"hana-mahmutefendic",fullName:"Hana Mahmutefendić"},{id:"245875",title:"Prof.",name:"Gordana",middleName:null,surname:"Blagojević Zagorac",slug:"gordana-blagojevic-zagorac",fullName:"Gordana Blagojević Zagorac"},{id:"245876",title:"Prof.",name:"Senka",middleName:null,surname:"Maćešić",slug:"senka-macesic",fullName:"Senka Maćešić"}]}],onlineFirstChaptersFilter:{topicId:"913",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"81188",title:"Structure- and Design-Based Difficulties in Recombinant Protein Purification in Bacterial Expression",slug:"structure-and-design-based-difficulties-in-recombinant-protein-purification-in-bacterial-expression",totalDownloads:24,totalDimensionsCites:0,doi:"10.5772/intechopen.103958",abstract:"Protein purification is not a simple task. Yet, overexpression at bacterial systems with recombinant modifications brings further difficulties. Adding a tag, an affinity label, and expressing particular domains of the whole protein, especially hydrophobic sections, make purification a challenging process. Protein folding pattern may perturb N- or C-terminal tag and this terminal preference may lead to poor purification yield. Codon optimization, solvent content and type, ionic conditions, resin types, and self-cleavage of recombinant proteins bring further difficulties to protein expression and purification steps. The chapter overviews problems of protein purification through a small peptide overexpression in bacteria (Recombinant anti-SARS Coronavirus 2 (SARS-Cov-2) Spike protein Receptor Binding Domain (RBD) antibody (Clone Sb#14). The chapter also covers troubleshooting at distinct steps and highlights essential points to solve crucial issues of protein purification.",book:{id:"10839",title:"Protein Detection",coverURL:"https://cdn.intechopen.com/books/images_new/10839.jpg"},signatures:"Kubra Acikalin Coskun, Nazlıcan Yurekli, Elif Cansu Abay, Merve Tutar, Mervenur Al and Yusuf Tutar"},{id:"79353",title:"Protein Detection in Clinical Diagnosis and Management of Prevalent Neurodegenerative Diseases and Metabolic Disorders",slug:"protein-detection-in-clinical-diagnosis-and-management-of-prevalent-neurodegenerative-diseases-and-m",totalDownloads:88,totalDimensionsCites:0,doi:"10.5772/intechopen.101051",abstract:"An accurate diagnosis gives leeway to cost-effective treatments. However, many diseases continue to evolve; hence, their etiology is sometimes missed due to the procedures used during diagnosis. Protein-related diseases include proteopathies (proteinopathies) such as neurodegenerative diseases and metabolic disorders like protein-energy malnutrition and some hormonopathies. Hormonopathies are associated with the change in the production of hormones. Diabetes mellitus, a type of hormonopathy, is reviewed in this work alongside neurodegenerative diseases and protein-energy malnutrition. This chapter aims to elucidate more on the diagnosis of these diseases considering the structure and function of their proteins viz-a-viz their deficiencies and hyper-production in man. Their pathogenesis and the principles underlying their diagnosis are further discussed to optimize the management of these diseases among patients.",book:{id:"10839",title:"Protein Detection",coverURL:"https://cdn.intechopen.com/books/images_new/10839.jpg"},signatures:"Ohanube A.K. Goodluck, Obeta M. Uchejeso and Ikeagwulonu R. Chinaza"}],onlineFirstChaptersTotal:2},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:98,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:287,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:107,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:10,numberOfPublishedChapters:103,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:null,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:10,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{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"}}}}]},series:{item:{id:"22",title:"Business, Management and Economics",doi:"10.5772/intechopen.100359",issn:"2753-894X",scope:"\r\n\tThis series will provide a comprehensive overview of recent research trends in business and management, economics, and marketing. 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",coverUrl:"https://cdn.intechopen.com/series/covers/22.jpg",latestPublicationDate:"May 18th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:1,editor:{id:"356540",title:"Prof.",name:"Taufiq",middleName:null,surname:"Choudhry",slug:"taufiq-choudhry",fullName:"Taufiq Choudhry",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000036X2hvQAC/Profile_Picture_2022-03-14T08:58:03.jpg",biography:"Prof. Choudhry holds a BSc degree in Economics from the University of Iowa, as well as a Masters and Ph.D. in Applied Economics from Clemson University, USA. In January 2006, he became a Professor of Finance at the University of Southampton Business School. He was previously a Professor of Finance at the University of Bradford Management School. He has over 80 articles published in international finance and economics journals. His research interests and specialties include financial econometrics, financial economics, international economics and finance, housing markets, financial markets, among others.",institutionString:null,institution:{name:"University of Southampton",institutionURL:null,country:{name:"United Kingdom"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:3,paginationItems:[{id:"86",title:"Business and Management",coverUrl:"https://cdn.intechopen.com/series_topics/covers/86.jpg",isOpenForSubmission:!0,editor:{id:"128342",title:"Prof.",name:"Vito",middleName:null,surname:"Bobek",slug:"vito-bobek",fullName:"Vito Bobek",profilePictureURL:"https://mts.intechopen.com/storage/users/128342/images/system/128342.jpg",biography:"Dr. Vito Bobek works as an international management professor at the University of Applied Sciences FH Joanneum, Graz, Austria. He has published more than 400 works in his academic career and visited twenty-two universities worldwide as a visiting professor. Dr. Bobek is a member of the editorial boards of six international journals and a member of the Strategic Council of the Minister of Foreign Affairs of the Republic of Slovenia. He has a long history in academia, consulting, and entrepreneurship. His own consulting firm, Palemid, has managed twenty significant projects, such as Cooperation Program Interreg V-A (Slovenia-Austria) and Capacity Building for the Serbian Chamber of Enforcement Agents. He has also participated in many international projects in Italy, Germany, Great Britain, the United States, Spain, Turkey, France, Romania, Croatia, Montenegro, Malaysia, and China. Dr. Bobek is also a co-founder of the Academy of Regional Management in Slovenia.",institutionString:"Universities of Applied Sciences FH Joanneum, Austria",institution:null},editorTwo:{id:"293992",title:"Dr.",name:"Tatjana",middleName:null,surname:"Horvat",slug:"tatjana-horvat",fullName:"Tatjana Horvat",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002hXb0hQAC/Profile_Picture_1642419002203",biography:"Tatjana Horvat works as a professor for accountant and auditing at the University of Primorska, Slovenia. She is a Certified State Internal Auditor (licensed by Ministry of Finance RS) and Certified Internal Auditor for Business Sector and Certified accountant (licensed by Slovenian Institute of Auditors). At the Ministry of Justice of Slovenia, she is a member of examination boards for court expert candidates and judicial appraisers in the following areas: economy/finance, valuation of companies, banking, and forensic investigation of economic operations/accounting. At the leading business newspaper Finance in Slovenia (Swedish ownership), she is the editor and head of the area for business, finance, tax-related articles, and educational programs.",institutionString:null,institution:{name:"University of Primorska",institutionURL:null,country:{name:"Slovenia"}}},editorThree:null},{id:"87",title:"Economics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/87.jpg",isOpenForSubmission:!0,editor:{id:"327730",title:"Prof.",name:"Jaime",middleName:null,surname:"Ortiz",slug:"jaime-ortiz",fullName:"Jaime Ortiz",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00002zaOKZQA2/Profile_Picture_1642145584421",biography:"Dr. Jaime Ortiz holds degrees from Chile, the Netherlands, and the United States. He has held tenured faculty, distinguished professorship, and executive leadership appointments in several universities around the world. Dr. Ortiz has previously worked for international organizations and non-government entities in economic and business matters, and he has university-wide globalization engagement in more than thirty-six countries. He has advised, among others, the United Nations Development Program, Inter-American Development Bank, Organization of American States, Pre-investment Organization of Latin America and the Caribbean, Technical Cooperation of the Suisse Government, and the World Bank. Dr. Ortiz is the author, co-author, or editor of books, book chapters, textbooks, research monographs and technical reports, and refereed journal articles. He is listed in Who’s Who in the World, Who’s Who in America, Who’s Who in Finance and Business, Who’s Who in Business Higher Education, Who’s Who in American Education, and Who’s Who Directory of Economists. Dr. Ortiz has been a Fulbright Scholar and an MSI Leadership Fellow with the W.K. Kellogg Foundation. His teaching interests revolve around global economies and markets while his research focuses on topics related to development and growth, global business decisions, and the economics of technical innovation.",institutionString:null,institution:{name:"University of Houston",institutionURL:null,country:{name:"United States of America"}}},editorTwo:null,editorThree:null},{id:"88",title:"Marketing",coverUrl:"https://cdn.intechopen.com/series_topics/covers/88.jpg",isOpenForSubmission:!1,editor:null,editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:1,paginationItems:[{id:"81831",title:"Deep Network Model and Regression Analysis using OLS Method for Predicting Lung Vital Capacity",doi:"10.5772/intechopen.104737",signatures:"Harun Sümbül",slug:"deep-network-model-and-regression-analysis-using-ols-method-for-predicting-lung-vital-capacity",totalDownloads:2,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Decision Science - Recent Advances and Applications",coverURL:"https://cdn.intechopen.com/books/images_new/11604.jpg",subseries:{id:"86",title:"Business and Management"}}}]},overviewPagePublishedBooks:{paginationCount:1,paginationItems:[{type:"book",id:"11392",title:"Leadership in a Changing World",subtitle:"A Multidimensional Perspective",coverURL:"https://cdn.intechopen.com/books/images_new/11392.jpg",slug:"leadership-in-a-changing-world-a-multidimensional-perspective",publishedDate:"May 11th 2022",editedByType:"Edited by",bookSignature:"Muhammad Mohiuddin, Bilal Khalid, Md. Samim Al Azad and Slimane Ed-dafali",hash:"86a6d33cf601587e591064ce92effc02",volumeInSeries:1,fullTitle:"Leadership in a Changing World - A Multidimensional Perspective",editors:[{id:"418514",title:"Dr.",name:"Muhammad",middleName:null,surname:"Mohiuddin",slug:"muhammad-mohiuddin",fullName:"Muhammad Mohiuddin",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000038UqSfQAK/Profile_Picture_2022-05-13T10:39:03.jpg",biography:"Dr. Muhammad Mohiuddin is an Associate Professor of International Business at Laval University, Canada. He has taught at Thompson Rivers University, Canada; University of Paris-Est, France; Osnabruck University of Applied Science, Germany; and Shanghai Institute of Technology and Tianjin University of Technology, China. He has published research in Research Policy, Applied Economics, Review of Economic Philosophy, Strategic Change, International Journal of Logistics, Sustainability, Journal of Environmental Management, Journal of Global Information Management, Journal of Cleaner Production, M@N@GEMENT, and more. He is a member of CEDIMES Institut (France), Academy of International Business (AIB), Strategic Management Society (SMS), Academy of Management (AOM), Administrative Science Association of Canada (ASAC), and Canadian council of small business and entrepreneurship (CCSBE). He is currently the director of the Research Group on Contemporary Asia (GERAC) at Laval University. 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Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. 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Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. 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