Representative components of the fly ash (mass fraction, %).
\r\n\tDiagnosis and management of complications while on ECMO therapy and weaning to recovery or advanced therapies will be also discussed.
\r\n\r\n\tChapters focusing on specific patient populations, such as cardiogenic shock, thoracic organ transplantation, trauma, and neonates, Covid-19 syndrome, will provide insight into the particular challenges in dealing with the unusual problems of these very diverse groups.
\r\n\r\n\tThe goal of this book is to provide, thanks to the thorough contributions by known experts in the field, a framework for successful program development. Hopefully, this text will also inspire others to further advance this delicate field.
",isbn:"978-1-80356-549-1",printIsbn:"978-1-80356-548-4",pdfIsbn:"978-1-80356-550-7",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!1,isSalesforceBook:!1,isNomenclature:!1,hash:"254c18981115aeda50bdf71829902141",bookSignature:"Dr. Antonio Loforte",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11718.jpg",keywords:"Heart Failure, Cardiogenic Shock, Respiratory Failure, Circulatory Failure, End-Organ Dysfunction, VA-ECMO, VV ECMO, Central ECMO, ECMO Running, Weaning off ECMO, Adverse Events While on ECMO, Survival on ECMO",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"March 10th 2022",dateEndSecondStepPublish:"April 7th 2022",dateEndThirdStepPublish:"June 6th 2022",dateEndFourthStepPublish:"August 25th 2022",dateEndFifthStepPublish:"October 24th 2022",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"3 months",secondStepPassed:!0,areRegistrationsClosed:!0,currentStepOfPublishingProcess:4,editedByType:null,kuFlag:!1,biosketch:"Dr. Loforte is a dedicated and pioneering researcher in the surgical treatment of advanced heart failure in terms of LVAD, BVAD, ECLS, and TAH adoption in different clinical scenarios. He is a member of several professional organizations including the prestigious STS, ISHLT, ASAIO, EACTS, RHICS, SICCH, SITO, ELSO, and ESOT among others. His bibliography lists over 150 peer-reviewed original articles, 250 abstracts (communications) for international meetings, 20 book chapters, and 8 manuals.",coeditorOneBiosketch:null,coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"42172",title:"Dr.",name:"Antonio",middleName:null,surname:"Loforte",slug:"antonio-loforte",fullName:"Antonio Loforte",profilePictureURL:"https://mts.intechopen.com/storage/users/42172/images/system/42172.jpg",biography:"Dr. Loforte is currently staff surgeon and chair of the Mechanical Circulatory Support (MCS) program at the Department of Cardiothoracic, Transplantation and Vascular Surgery, S. Orsola Hospital, ALMA Mater Studiorum University of Bologna, IRCCS Bologna, Italy. He completed his cardiothoracic surgery recidency at the University of Bologna, S. Orsola Hospital (Italy), at St. Antonius Ziekenhuis, Nieuwegein (the Netherlands) and the Deutsches Herzzentrum Berlin (Germany). He additionally joined the Michael E. DeBakey Department of Surgery, Division of Transplant and Assist Devices, in Houston, Texas, USA.\nDr. Loforte is a member of several professional organizations including the prestigious STS, ISHLT, ASAIO, EACTS, RHICS, SICCH, SITO, ELSO, ESOT among others. His bibliography lists over 150 peer-reviewed original articles, 250 abstracts (communications) for international meetings, 20 book chapters, and 8 manuals. He serves as a reviewer for 25 international journals and is part of the editorial board in 10 of them. He received a ‘European Ph.D. label’ in Organ Transplantation and ten international awards in Europe and USA.",institutionString:"Division of Cardiac Surgery, S. Orsola University Hospital, IRCCS Bologna",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:null}],coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"16",title:"Medicine",slug:"medicine"}],chapters:null,productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},personalPublishingAssistant:{id:"444318",firstName:"Nika",lastName:"Karamatic",middleName:null,title:"Ms.",imageUrl:"https://mts.intechopen.com/storage/users/444318/images/20011_n.jpg",email:"nika@intechopen.com",biography:"As an Author Service Manager, my responsibilities include monitoring and facilitating all publishing activities for authors and editors. From chapter submission and review to approval and revision, copyediting and design, until final publication, I work closely with authors and editors to ensure a simple and easy publishing process. I maintain constant and effective communication with authors, editors and reviewers, which allows for a level of personal support that enables contributors to fully commit and concentrate on the chapters they are writing, editing, or reviewing. I assist authors in the preparation of their full chapter submissions and track important deadlines and ensure they are met. I help to coordinate internal processes such as linguistic review, and monitor the technical aspects of the process. As an ASM I am also involved in the acquisition of editors. Whether that be identifying an exceptional author and proposing an editorship collaboration, or contacting researchers who would like the opportunity to work with IntechOpen, I establish and help manage author and editor acquisition and contact."}},relatedBooks:[{type:"book",id:"6558",title:"Heart Transplantation",subtitle:null,isOpenForSubmission:!1,hash:"fa6adc2ed66fd8de1500ed382fd80f7a",slug:"heart-transplantation",bookSignature:"Antonio Loforte, Andrea Montalto and Cristiano Amarelli",coverURL:"https://cdn.intechopen.com/books/images_new/6558.jpg",editedByType:"Edited by",editors:[{id:"42172",title:"Dr.",name:"Antonio",surname:"Loforte",slug:"antonio-loforte",fullName:"Antonio Loforte"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"6550",title:"Cohort Studies in Health Sciences",subtitle:null,isOpenForSubmission:!1,hash:"01df5aba4fff1a84b37a2fdafa809660",slug:"cohort-studies-in-health-sciences",bookSignature:"R. 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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:"71558",title:"Melting and Dissolving Fly Ash by NaOH for the Removal of Iron, Calcium, and Other Impurities",doi:"10.5772/intechopen.91704",slug:"melting-and-dissolving-fly-ash-by-naoh-for-the-removal-of-iron-calcium-and-other-impurities",body:'Fly ash is a kind of solid waste discharged from power plants and various coal-fired boilers. According to statistics, the amount of fly ash accumulation in China is up to 0.2 billion tons, and it is increasing every year. It is the largest output of ash in industrial waste residue. Fly ash can seriously pollute the environment and cause serious harm to people’s lives, animals and plants, and so on. According to local conditions, timely and effective treatment of fly ash and comprehensive utilization of fly ash have far-reaching significance. It not only saves water, saves soil, and turns waste into treasure but also protects the environment.
At present, fly ash is mainly used as building material. It is used in thermal insulation board, slag cement, wall tile, floor brick, etc. [1]. The utilization ratio of fly ash is large, reaching 67%, but the added value of products is not high. The main representative components of fly ash are silica and alumina, which account for as high as 70%, while the silicon and aluminum are also main ingredients of expensive molecular sieve. Preparing high price molecular sieve with cheap fly ash is an important way to promote the use of additional value. The application of molecular sieve is very wide; can be used for gas or liquid dehydration, drying, separation, and purification; and can also be used as adsorbent, catalyst, and ion exchange agent for various types of reactions in the field of petroleum chemical industry, fine chemical industry, agriculture, and environmental protection. The preparation of molecular sieve with fly ash can not only save raw materials but also can simplify the process and equipment and provide the conditions for large-scale production and wide application of molecular sieves.
The study on the synthesis of molecular sieves with fly ash began from 1985 by Holler and Wrisching [2].
Since then, more and more molecular sieve types [3] have been developed. The domestic and international research on the synthesis of molecular sieve from fly ash is more and more widely and deeply [4].
Yang Liyun et al. recently synthesized zeolite 4A using fly ash fused with synergism of NaOH and Na2CO3 [5]. Asifa Iqbal et al. synthesized and characterized pure phase 4A from coal fly ash [6]. Richa Soni and Dericks Praise Shukia synthesized fly ash-based zeolite-reduced graphene oxide composite and evaluated its property as an adsorbent for arsenic removal [7]. A De Rossi et al. synthesized zeolite by geopolymerization of biomass fly ash and metakaolin [8]. Koshy and Singh described applications of fly ash zeolites for water treatment [9]. Fang et al. synthesized high-quality zeolites from coal fly ash and researched mobility of hazardous elements and environmental applications [10]. Tauanov et al. synthesized coal fly ash-derived zeolites doped with silver nanoparticles for mercury(II) removal from water [11]. Lim et al. prepared quasi-solid-state electrolytes using a coal fly ash-derived zeolite-X and zeolite-A for dye-sensitized solar cells [12]. Collectively, researches on zeolites derived from fly ash focus on applications gradually.
However, fly ash is not pure aluminum silicate. In addition to containing valuable elements of silicon and aluminum, fly ash also contains a considerable part of the iron and calcium and other impurities, leading to impure molecular sieve. The impurities not only are easy to plug in the channels of the molecular sieve but also reduce the exchange capacity, catalytic performance, and cycle performance. The drawbacks have not drawn enough attentions so far. Therefore, it is necessary to pretreat fly ash to remove the impurities such as iron, calcium, and so on before preparing the molecular sieve with fly ash.
Acid leaching of fly ash to remove iron and calcium used to be employed by previous patent literature, as the reaction temperature is below 100°C, the process can not destroy the high-temperature phase such as mullite and quartz, so the high-temperature phase included iron and calcium impurities does not dissolve, this process can only get rid of 60% of iron and calcium, is not complete. We once used carbon reduction-magnetic separation-acid leaching method; although the iron removal efficiency is high, the process is slightly lengthy [13]. Alkali melting method was used in literature, but the following alkali dissolving was not used. The impurities still exist in prepared molecular sieve [14].
A new method, alkali melting, or alkali dissolving, of fly ash, to remove iron, calcium, and other impurities, was proposed in the paper. Firstly, fly ash and NaOH solid were mixed and roasted to convert the mullite and quartz into glass phases. The roasted clinker was leached by NaOH solution to dissolve silicon and aluminum components and to filter out Fe2O3, CaO, and CaSO4 insoluble impurities, etc., so as to obtain purified Na2SiO3 and NaAlO2 solution. The purified solution can be used for the preparation of high pure molecular sieve to improve the performance and the service life.
In this study, the fly ash was gotten from a power plant in Shandong; the main chemical composition is shown in Table 1.
Ingredient | SiO2 | Al2O3 | CaSO4 | MgO | Na2O | Fe2O3 | Others |
---|---|---|---|---|---|---|---|
Percent (%) | 41.36 | 30.45 | 24.75 | 1.15 | 0.26 | 3.70 | 1.66 |
Representative components of the fly ash (mass fraction, %).
The specific steps are as follows. A certain amount of fly ash was weighed, placed in a mortar, and fully ground before putting through a 200 mesh sieve prior to be mixed with NaOH powder with a mass ratio of 1 to 2. The mixture was transferred to a crucible and was roasted at 600°C in a muffle furnace for 2 h. The clinker was then leached with a high concentration of NaOH solution to dissolve the silicon aluminum phase, and the impurities such as iron and calcium are filtered out to obtain a pure solution containing the silicon aluminum phase merely. The contents of Si and Al in the filtrate were analyzed by ICP analyzer, and the dissolution ratios of silicon and aluminum were calculated according to the total amounts. At the same time, the dissolution ratio of fly ash in clinker was also measured. The filtrate was added with hydrochloric acid and the alkalinity (OH/Si) was controlled. A certain proportion of Na2SiO3 solution and the seed crystal directing agent was added to regulate the ratio of silicon and aluminum for a special molecular type. After that, the mixture was stirred evenly, transferred to an autoclave, and crystallized at a certain temperature for a certain time. The derived solid was just a molecular sieve and was filtered and dried, measured by SHIMADZU X-ray diffractometer XRD-6000. Zeolite P was synthesized according to the document [14]. Ion concentration is analyzed by 3600A inductively coupled plasma atomic emission spectrometer made by Keje company in China.
SiO2and Al2O3 existing as quartz and mullite in fly ash have low activity; high-temperature alkali roasting method can greatly increase their activity and improve the efficiency of the fly ash conversion and crystallization synthesis of the molecular sieve. There are commonly two ways to calcine fly ash, one is to add Na2CO3 to calcine at 800°C, and the other is to add NaOH to calcine at 600°C. In the experiment, fly ash and NaOH reacted after roasted in a muffle furnace at 600°C for 2 h. Figure 1 is the contrast diagram of XRD for fly ash before and after calcination with NaOH.
Effect of alkali melting activation on fly ash structure.
From Figure 1, the diffraction peaks of quartz and mullite are strong before calcination, which show the main minerals are quartz and mullite. Quartz and mullite are difficult to react with NaOH at room temperature due to their low activity. Therefore, calcination of fly ash and NaOH at high temperature is necessary and can stimulate its activity. The diffraction pattern of calcined fly ash and NaOH shows that the form of the material is mainly aluminosilicate when calcined at high temperature. At this time, there are few quartz and mullite, and the diffraction peak almost disappeared. This is because as the reaction proceeded, high-temperature roasting destroyed crystal structure, thus releasing the active SiO2 and Al2O3. These substances react with NaOH and generate amorphous aluminosilicate that is able to participate in the zeolite framework structure.
What is more, high-temperature roasting can get rid of the organic impurities in fly ash and amorphous carbon, thereby improving the purity of raw materials. In addition, alkali melting of fly ash provided a large amount of NaOH for the following leaching process since real mass amount of NaOH reacted is equal to the of fly ash according to the experimental result.
Figure 2 shows that the NaOH solution can dissolve alkali melting residue, which includes Na2SiO3 and NaAl(OH)4 derived from mullite, quartz, and other silicon aluminum phases of coal fly ash. Dissolving ratios of Si and Al decrease with increasing mass ratio of solid clinker to alkali solution. The maximum dissolving ratio of Si is 56.6%, while the maximum dissolving ratio of Al is 33.8% under the experimental condition. 100 g of water can dissolve nearly 37 g Na2SiO3; however, 56.6% is not high.
Effect of mass ratio of solid clinker to alkali solution 15% NaOH, 1 h of stirring time, 60°C.
From Figure 3, low leaching temperature is beneficial to high dissolving ratio of Si and Al. Dissolving ratios of Si and Al reach 78.9 and 78.1%, respectively, as the leaching temperature is 20°C. Similar research showed dissolution ratio of Si is 75%, while dissolution ratio of Al is only 25% during alkali leaching from titania slag [15]. Both the dissolving ratios dropped sharply with increasing leaching temperatures because hydrolysis reaction occurred at higher temperatures. H4SiO4 and Al(OH)3 precipitates stayed in solid residues, which led to the low dissolving ratios.
Effect of temperature on dissolving ratio of Si and Al 15% NaOH, NaOH solution clinker mass ratio of 10:1, 1 h of stirring time.
Figure 4 shows higher NaOH concentration is more viable in order to dissolve more Si and Al. When the alkali concentration is increased from 5 to 10%, the dissolution rate of aluminum decreases. The leaching rate fluctuated, just like the acid leaching of titanium-bearing minerals; at present it is thought that the evolution of AlO2− causes the fluctuation because the AlO2− is more soluble than Al(OH)4−, and the general trend is still rising with the increase of NaOH concentration.
Effect of mass ratio of NaOH to solution on dissolving ratio of Si and Al 60°C, NaOH solution to clinker mass ratio of 10:1, 1 h of stirring time.
The possible following reaction occurs when NaOH concentration is larger than 10%.
Thus, insoluble Na2O · Al2O3 · xSiO2 in water dissolved in concentrated NaOH solution. The tendency indicates OH- plays an important role during the process, which takes part in the coordination process. The large amount of use of NaOH causes big cost. Reusing the redundant NaOH solution is significant and economical. The condensation and the seed can make the reuse of NaOH solution possible.
Figure 5 shows Na2O-Al2O3-H2O system phase diagram [16]. The area of OBCO belongs to the dissolving process of Al2O3 into the NaOH solution according to Figure 3. The solubility of Al2O3 in NaOH solution is increasing along the NaOH concentration until 20% (line OB); after the summit of 20% of the solubility, the dissolving ability decreases with the increasing NaOH concentration [line BC]. Therefore, a highly efficient NaOH concentration is around 20%; the number is consistent with our experimental result in Figure 4 where 0.20 mass ratio of NaOH made the highest dissolving ratio of Al. 15% NaOH is used, and NaOH is surplus after the roasting process. Overall, the concentration of NaOH is around 20%.
Na2O-Al2O3-H2O phase diagram.
Figure 6 indicates too long time is disadvantageous for high dissolving ratio of Si and Al. The dissolving ratio decreases with adding stirring time. The tendency is obvious for Al. The dissolving ratio drops steeply during 2 h or so. The gradual decreasing tendency is due to the precipitate of Si and Al. Reducing stirring time is essential so as to get high dissolving ratios of Si and Al. 1 h is enough for the stirring time.
Effect of stirring time on dissolving ratios of Si and Al 60°C, NaOH solution to clinker mass ratio of 10:1.
Figure 7 shows the filtration of slag after alkaline solution filtration. The color of the slag is red, which proves that the slag contains iron oxide, which can be used for carbon reduction to obtain sponge iron for steel-making. The filtered solution can be used for the preparation of the molecular sieve. The molar ratio of Si to Al in the leach solution is adjusted to 4.6; pH drops to 9 by adding HCl solution. Then, the solution is put in an autoclave after aging for 1 h and taken out after crystallization for 16 h at 100°C. The p-type molecular sieve is obtained after filtration, washing, and drying. The cost of raw material and the environmental pollution were reduced because of using fly ash as raw material.
Residue of insoluble clinker after filtration.
The Fe2O3 content of the prepared molecular sieve drops to 0.25% after the alkali treatment from 2.87% by merely acid leaching of fly ash, while the content of CaO drops to 0.066% from 1.18%. The chemical formula of the P molecular sieve prepared is confirmed as Na6Al6Si10O32·12H2O through ICP examination. The purity of the P molecular sieve prepared by the method from coal fly ash is 99.06% (seen in Table 2), while the whiteness level is 96 (seen in Figure 8). Both purity and whiteness level of the molecular sieve can meet the standard of market molecular sieve.
Ingredient | SiO2 | Al2O3 | Na2O | K2O | Fe2O3 | CaO | SO3 |
---|---|---|---|---|---|---|---|
Percent (%) | 58.74 | 25.65 | 14.67 | 0.61 | 0.25 | 0.066 | 0.011 |
Chemical composition of P molecular sieve prepared by fly ash (mass fraction, %).
P molecular sieve prepared by coal fly ash.
Figure 9 shows XRD diagram of the product; there are five characteristic peaks at 2θ = 12.48°, 17.71°, 21.68°, 28.15°, and 33.37°, respectively, and miscellaneous peaks are few, indicating the product is P molecular sieve (
XRD diagram of P molecular sieve prepared by coal fly ash.
At 600°C, the alkali melting activated quartz and mullite in the fly ash into the aluminosilicate glass phase, which can be dissolved in the alkali solution. The optimum conditions of alkali dissolving of clinker were obtained by optimizing experiments, that is, the reaction temperature is 20°C; using 15% NaOH solution, the liquid solid ratio is 10:1, and the stirring time is less than 1 h; the whole dissolution ratio of silicon reaches 78.9%, while that of Al reaches 78.1%. The method provides pure solution for preparing molecular sieves from fly ash. The Fe2O3 content of the prepared molecular sieve through actual verification drops to 0.25% after the alkali treatment from 2.87% by merely acid leaching of fly ash, while the content of CaO drops to 0.066% from 1.18%.
Goats are small ruminants that were among first domesticated farm animals which are into herding from about 10,000 years ago [1]. The acclimatising capacity of goat is peculiar as they can be economically reared in areas ranging from tropics, deserts, temperate to harsh climate of mountains without fluctuation in productivity [2]. Goat is a major supplier of dairy and meat products for rural people and regarded as a “Poor man’s cow” [3].
The world’s goat population has increased by around 55% from 1991 to 2011 whereas cattle population grew only by 9% and sheep population decreased by about 7%. In between these years Goat’s milk (GM) production increased by around 70% [4] which can however be greater because of unreported home consumption of GM in large amount in case of developed countries [5]. The production of GM in world showed an increase of 62% from 1993 to 2013 from 11 to 18 million tons [6]. Except in Antarctic, GM consumption by human is found in all over the world [6]. The contribution of developing countries in goat rearing is noteworthy. Out of total goat population more than 90% alone is maintained by countries in Asia and Africa [7]. Majority of goats including dairy ones in Asia are in the hands of small-scale farmers, among which many of them are poor and landless [8]. The production and consumption pattern of GM and its products has increased in recent decades. Growth in consumption of such milk products is due to their known beneficial effects on human health which are already recognised by the scientific community (Table 1).
Total2 [million head (%)] | Dairy [million head (%)] | Milk [Mt (%)] | Yield3 [L/head] | |||||
---|---|---|---|---|---|---|---|---|
Continent | Sheep | Goats | Sheep | Goats | Sheep | Goats | Sheep | Goats |
Asia | 512 (43.6) | 556 (55.4) | 135 (54.0) | 106 (52.1) | 4.73 (45.6) | 8.04 (52.7) | 35.1 | 76.2 |
Africa | 352 (30.0) | 388 (38.7) | 79 (31.7) | 80 (39.6) | 2.54 (24.5) | 3.93 (25.7) | 32.2 | 48.9 |
Europe | 131 (11.2) | 17 (1.7) | 33 (13.3) | 9 (4.3) | 3.01 (29.0) | 2.54 (16.6) | 90.8 | 290.1 |
America | 84 (7.1) | 38 (3.8) | 3 (1.1) | 8 (4.0) | 0.09 (0.9) | 0.75 (4.9) | 33.0 | 93.4 |
Oceania | 95 (8.1) | 4 (0.4) | <0.1 (0) | <0.1 (0) | <0.01 (0) | <0.01 (0) | — | — |
Total | 1,173 (100) | 1,003 (100) | 250 (100) | 203 (100) | 10.37 (100) | 15.26 (100) | 41.5 | 75.3 |
Total annual milk supply of goat is about 3.4%, sheep milk is 1.4%, camel milk is 0.2%, cow milk is 85% while buffalo contribute 11% [9]. About 80% of total GM supply is only from Asia [3] of which main countries include India, China, Bangladesh, Iran, Pakistan and Turkey [10]. 36.7% of world dairy goats are reared in Indian subcontinent producing 40.7% of the world’s goat milk, with India (60.6%, 129 L/doe), Bangladesh (16.9%, 37 L/doe) and Pakistan (13.3%, 100 L/doe) [11]. Out of 500 breeds of goat only half dozen is raised for milking purpose and about 600–700 million dairy goats are present in the world (Figure 1) [12].
World goat milk production trends from 1916 to 2016 (solid line) and forecast to 2030 by using time series model (dashed line). Source: Ref. [
The major species of milching dairy goat includes Sannen, Anglo-nubian, Toggenburg, British alpine. They produce good quantity of milk. For an instance Toggenburg can produce 7.57 litres of milk per day [13]. Factors like breed, season of kidding, stage of lactation, species, age, parity, colostrums, feed, environmental conditions, length of dry period, disease, body weight etc. can cause change in GM composition [14].
Milk is clean lacteal secretion from mammalians shortly after parturition. GM being highly compatible and nourishing complete natural food, can serve as a substitute for a meal. Its acceptability has increased in recent years which is mainly due to its low fat and capacity to neutralize acids and toxins present in body and also due to higher gross composition than that of cow’s milk. GM has potential that enable tolerating different technological treatments to obtain a product which have ability to satisfy the demand of consumer in terms of health, nutrition, safety and pleasure. Beside qualitative criteria (colour and odour), other aspects should also be given equal importance (milk protein, fat, bacteriology, freezing point, lipolysis, somatic cell count, immunoglobulins, inhibitors etc) for improving the quality of milk [15]. Human milk consumption as defined by the International Congress of Food “milk is the product of the total, full and uninterrupted milking of dairy female in good health, also nourished and not overworked”. It must be collected properly with no colostrum [16].
GM can be consumed as an alternative to cow milk as it is less allergenic [17] and highly digestible [18]. It has been reported by Park (1994) that between 40 and 100% of patients allergic to cow milk proteins can tolerate GM. It is also recommended to pregnant women and infant to fulfil their nutritional requirement at growing stage [19] and also to old and convalescent people [20]. It is immune to several diseases and boost the immunity system of human. It differs from cow and human milk as it shows distinct alkalinity, higher buffering capacity and certain therapeutic values in medicine and human nutrition. The nutritional and health benefits of GM are related to a number of medical problems, the most important being food allergies and a pure substitute for those who are allergic to cow milk (Figure 2) [22].
Goat milk production in the world from 2000 to 2013 (million tons). Source: Ref. [
This review chapter is a compilation of numerous research and review paper. In the course of writing this chapter we have reviewed number of articles, proceedings, magazines, newspaper, bulletin, editorial etc, Solids so that a broad range of information could be collected and presented. So, this is a thorough and detailed information regarding goat milk and its nutritive as well as medicinal values, accordingly which its conclusion has been drawn.
GM because of its specific composition is being considered as a high-quality raw material for manufacturing food of infants along with population with particular needs [23]. Fresh goat milk appears as a white, opaque liquid with a little sweet in taste having no odour in practical life [24]. The Solid content in goat milk ranges from 12 to 18% while protein content in solid lies between 3 and 4.5% in goat milk [25]. Compositional and nutritive value of goat milk can be preserved, enhanced and improved by the aid of processing [26].
The composition and milk yield of goat varies with varying factors such as diet, breed, management, environment, age, stage of lactation, season, plane of nutrition etc. [27]. GM having all the composition in adequate amount is preferred as a high-quality milk and it should be free from pathogens and foreign substances such as antibiotics, antiseptics or residue of pesticides and should not differ from that of cow’s milk in taste and odour. GM is proven to have a better and efficient digestibility, buffering capacity, alkalinity and therapeutic values as compared to human and cow’s milk in human nutrition and medicine [28].
The physical properties like surface tension, viscosity and specific gravity of GM are higher in comparison with cow milk [17]. The fat globules of GM are smaller than bovine milk. The smaller sized fat globules allow dispersion and more homogeneous mixing of fat in milk. The average diameter of globules in GM ranges from 1.5–2 μm while that of cow’s milk ranges from 2.5–3.5 μm [24] which is the reason behind GM to be known as “self homogenised or naturally homogenised milk”. Having smaller fat globules and greater surface area facilitate GM to be more digestible than cow milk as total surface area of globules gets effectively connected with the lipids [29]. Also, lipases in the gut tentatively attack the lipids ester linkages in the short chain fatty acids more readily and rapidly helping in faster digestion of GM [30]. GM is enriched with higher proportion of short and medium chain fatty acids, mostly butyric, palmitic, caproic, capric, caprylic, linolenic, alpha- linolenic, lauric, myristic acid while lower in longer chain fatty acids like oleic and stearic [23]. Among these 3 (Capric, Capryllic and Caproic) have been named after goat because of their predominance in GM [31].
Milk is composed of casein and whey protein where casein (alpha s1, alpha s2, beta and Κ-caseins) represent 80% of proteins while rest part is filled by major whey proteins (alpha-lactoglubulin and alpha-lactalbumin) [32]. The major protein in cow milk is alpha s1 casein while in GM it is beta casein. One of the most representative free amino acid in GM is Taurine [33] which is higher in GM as compared to cow milk [34]. Out of 10 essential amino acids 6 (threonine, isoleucine, lysine, cystine, tyrosine, valine) are found in high amount in GM than in cow milk [35]. Main reason behind the low amount of folic acid in GM is that it contains high concentration of folate binding protein making it unavailable for human to digest and absorb. The heavy fat content and mucus-producing components of cow milk are absent in GM and it is complete source of proteins containing all essential amino acids [36, 37]. Fragments of GM caseins have been found to possess antimicrobial peptides that shows strong activity against gram negative bacteria [38].
The content of Vitamin A in GM is higher than in cow milk as goat convert all beta carotene from foods to Vitamin A (retinol) in milk which is the reason for whiter GM and milk fat [17]. Also, higher casein content is GM promotes the same [39]. It contains 25% more Vitamin B6, 47% more Vitamin A than cow’s milk and it mainly possesses Vitamin A2 [40]. Content of Vitamin D of both GM and cow milk is similar that is mostly needed during infancy (Table 2) [41].
Vitamin | Goat milk | Cow milk |
---|---|---|
Vitamin A (IU) | 185 | 126 |
Vitamin D (IU) | 2.2 | 2.0 |
Thiamine (mg) | 0.068 | 0.045 |
Riboflavin (mg) | 0.21 | 0.16 |
Niacin (mg) | 0.27 | 0.08 |
Pantothenic acid (mg) | 0.31 | 0.32 |
Vitamin B6 (mg) | 0.046 | 0.042 |
Folic acid (ug) | 1.0 | 5.0 |
Biotin (ug) | 1.5 | 2.0 |
Vitamin B12 (ug) | 0.065 | 0.357 |
Vitamin C (mg) | 1.29 | 0.94 |
Major carbohydrate in GM is Lactose whose content is slightly lower in GM than in cow’s milk [42]. Lactose, a valuable nutrient favours intestinal absorption of calcium, phosphorus and also in proper utilisation of vitamin D [31]. It is crucial for milk synthesis and during secretion of milk in the duct system of udder [5]. As compared to cow milk, GM contains surplus amount of lactose derived oligosaccharides. Other carbohydrates that are present in small amount includes oligosaccharides, glycopeptides, glycoproteins and nucleotides [42]. GM oligosaccharides are thought to be exhibiting the anti-inflammatory effects in induced colitis [43]. GM oligosaccharides are especially beneficial for infants due to their prebiotic and anti-infective properties (Table 3) [45].
Component | Cow milk | Goat milk | Human milk |
---|---|---|---|
Protein | 3.58 | 3.52 | 1.63 |
Fat | 4.14 | 4.25 | 3.75 |
Total solids | 13.19 | 13.00 | 12.57 |
Solids not fat | 9.25 | 7.75 | 8.82 |
Lactose | 4.96 | 4.27 | 6.98 |
Ash | 0.71 | 0.86 | 0.21 |
GM contains major and trace minerals that includes Ca, Na, Mg, P, K, Zn, Mn, Se, Cu, Co, Fe which have great health benefits. Percentage of Zn in GM is higher than in cow’s milk that is responsible for maintaining healthy skin, healing of wound, act as antioxidant and eliminate reactive oxygen species via its role as a cofactor for antioxidant enzyme superoxide dismutase (SOD). Mineral content in GM is higher than that of human and cow milk ranging from 0.7 to 0.85% [46]. GM contains 13% more calcium than cow’s milk per serving and 134% more potassium [47]. Selenium content in goat and human milk is higher than that found in cow milk [48]. The Selenium in GM plays a key role in acting as a cofactor for the functioning of glutathione peroxidase (GPX), an antioxidant enzyme which scavenges harmful free radical in body and helps in macrophage activation (Table 4) [49].
Mineral (mg) | Goat milk | Cow milk |
---|---|---|
Ca | 134 | 122 |
P | 121 | 119 |
Mg | 16 | 12 |
K | 181 | 152 |
Na | 41 | 58 |
Cl | 150 | 100 |
S | 28 | 32 |
Fe | 0.07 | 0.08 |
Cu | 0.05 | 0.06 |
Mn | 0.032 | 0.02 |
Zn | 0.56 | 0.53 |
Se | 1.33 | 0.96 |
Because of the highest nutritional value, GM is preferred over cow and buffalo milk [50]. The nutritional and health benefits of GM are directly related to the medical problems that are faced by people of which main being allergies towards milk proteins obtained from cow’s milk [51]. It provides 70 calories per 100 ml. The superior digestibility of GM, its proper fatty acid composition and content of bioactive compounds seem to give those properties to it that help in treating or preventing certain medical conditions. Bioactive peptides derived from milk plays vital role in human health and nutrition. The most vulnerable ones are infants, aged people and pregnant women as their immune system could answer at any time if extra supplement is not administered.
The amount of calcium and phosphate supplied from GM is of much importance to human nutrition. It contains 1.2 g calcium and 1 g phosphate per litre which is higher than that contained in human milk. So, GM offer excess of calcium and phosphorus to human infant that is easily absorbed by them [30]. GM supply adequate amount of Vitamin A and niacin to human infant. Though it supplies excess of thiamine, riboflavin and pantothenic acid [5, 30] it is deficient in terms of Vitamin C, D, B12, pyridoxine and folate [52]. So, these nutrients should be supplied at the time of infant feeding by applying appropriate fortification. American Academy of Paediatrics forbade the use of GM products for infants under one year mainly because they can cause intestinal irritation and anaemia. Infants of such age who are allergic to cow’s milk-based formulas are only fed on goat’s milk formula after properly consulting baby’s doctor or paediatric nutritionist [53].
One of the reasons that consumers are accepting GM and its products in an appreciable manner is due to its nutritive value. It is beneficial in maintaining health, physiological functions, in the nutrition of child and elderly ones [54]. It is reported that it contains off flavour. This is due to the fact that membranes around fat globules in GM are more fragile which may relate to their greater susceptibility in developing off flavour than in cow milk. However, fresh milk obtained under sanitary conditions from properly fed and hygienically managed goats is found to be free from such objectionable flavour and odour [55].
Cow’s milk is reported to be mucus forming for many people but goat milk is not only non-mucus forming but also help in neutralising the mucus. GM has been a viable alternative for those children who are having difficulties in digesting cow’s milk as it is second best option, first being mother’s milk. The composition of goat and human milk is almost similar. Children who drink goat milk tend to remain more satisfied between meals and sleep through the night [56]. 2.5% of infants during first 3 years of their life suffer from cow milk allergy [57] while this percentage rise from 12 to 30% for infants who are less than 3 months old [58]. Not just for infants but also for adults and nursing mother, GM has been good alternative because of its unique properties. GM is rich in vitamins, minerals, trace minerals, enzymes, protein, fatty acids and amino acids (especially tryptophan) that are easily utilised by human body. The greatest advantage of consuming GM by many people lies in the fact that those who cannot digest cow’s milk find it easy in digesting GM without any complications. The reason for this is yet to be known but it is thought that this action in GM is due to lower lactose content (7% less than that of cow milk). There is one fact which says that our body takes 20 minutes to digest GM while it takes 2–3 hours in digesting cow’s milk [56].
Conjugated Linoleic Acid (CLA), an important bioactive component is naturally found in GM which helps in immune response stimulation. Mediators of immunity such as cytokines, prostaglandins, immunoglobulins etc, are modified by the action of CLA. The CLA possess ability to reduce the allergy related immunoglobulin IgE in humans that suggest anti-allergic potential of lipid [38]. The richness of GM in Medium Chain Triglycerides (MCT) helps in improving nutrients absorption and energy production in the body. MCT along with other amino acids exhibits antimicrobial activity [59].
Taurine (free amino acid) performs different roles in human body such as growth and brain development, formation of bile salts, calcium flux modulation, stabilisation of membranes as an osmoregulation by attenuating toxic substances. Its deficiency in human tissues may be the result of cardiomyopathy, epilepsy, lack of growth etc. [60]. In case of animal studies, Taurine is suggested as an important amino acid in alleviating muscle fatigue and can build up exercise capacity during workouts [46].
Amount of Vitamin A contained in GM is similar to human milk which is crucial for innate and adaptive immune responses that also includes cell-mediated immunity and antibody responses as well. Deficiency of this vitamin leads to decreased innate immunity that will affect NK cell function and phagocytic activity. Vitamin D plays an important role in the immune system and help preventing infections, autoimmune diseases, cancer and diabetes. Vitamin C which is present in greater amount in GM than in cow’s milk has shown to affect many aspects of the immune system including regulation of immunity via antiviral and anti-oxidant properties [49].
As compared to cow’s milk GM has higher content of Ca, P, K, Se, chloride, Zn, Cu [61, 62]. Potassium is crucial in acid/base balance and also in the proper functioning of muscles, nerves and kidneys. Chloride maintains fluid balance, blood pH and osmotic pressure. Calcium and phosphorus strengthen the structure of bones, muscles and help in blood coagulation. Selenium is vital in protecting cell against free radicals and also it acts as a major component in preventing dengue fever. Copper helps in metabolism of iron and oxygen and also defence the cell against free radicals [49].
Multivitamins, proteins, minerals (including trace one), fatty acids as well as Lactic acid bacteria in GM help in fighting human against diseases including diarrhoea, vomiting, constipation, gastric discomfort, respiratory disorders and many other [20].
Dengue fever which is transmitted by the bite of
Proteins derived from milk are proved to be precursors of antimicrobial peptides. GM have been reported to have antimicrobial activity of several pathogenic bacteria that are contained in food materials. GM caseins fragments are good source of antimicrobial peptides that are effective against gram negative bacteria [38]. Alpha-S2 Casein (CSN1S2) in GM is studied for its antimicrobial property. The result indicated that this caprine protein has inhibition activity that opposes the pathogenic bacteria by optimal concentration of 5 mg/ml in all bacteria especially Gram positive (
CVD includes diseases that involves heart and blood vessels, veins, coronary heart diseases, high blood pressure, arrhythmias, atherosclerosis etc. Inorder to maintain normal blood pressure and proper heart functioning a good amount of potassium rich food is needed and GM serves for the same. GM supply 498.7 mg of K and 121.5 mg of Na that is sufficient in preventing high blood pressure and protecting against atherosclerosis. Atherosclerosis is likely to occur if people are adopting unhygienic inactive lifestyle (smoking, diet and exercise) and after incidence of dyslipidemia, diabetes, high blood pressure etc. [74]. The Angiotensin converting enzyme (ACE) inhibitory peptides obtained after hydrolysis of GM caseins have shown beneficial effects on blood pressure regulation [75]. Fat in GM reduces total cholesterol levels thereby making it as a food of choice for the prevention of cardiac disorders. GM have selenium and its absence is thought to cause irreversible cardiomyopathy [66]. When excess amount of fat is deposited in the arterial wall and blood vessels then cardiac arrest is common. In case of goat, fat present in its milk and meat is considered as user friendly [76]. The Low-density lipoprotein (LDL) is known as “bad cholesterol” as it transports cholesterol from liver to blood vessels while High-density lipoprotein is “good cholesterol” as it transports cholesterol from vessels to oxidative modification of LDL which suppresses atherosclerosis [74].
The composition of GM exceeds cow’s milk in monounsaturated fatty acids (MUFA), polyunsaturated fatty acids (PUFA) and MCT which have beneficial health effects especially in cardiovascular conditions [23]. Due to anti-inflammatory effects of CLA GM decreases the atherosclerosis incidence [38]. The MCT present in GM includes capric, caproic and caprylic acids which comprises 15% of total milk fat. The higher constituent of MCT in GM helps in lowering cholesterol deposits in the arteries, dissolve and prevent cholesterol deposits in the gallstones. Also, the presence of MCT decrease the synthesis of endogenous cholesterol thus helping to boost the immune system [77]. Capric, caprylic acids and MCT are used in treatment of many diseases including cystic fibrosis, coronary by-pass etc, because of their unique ability to provide energy directly without being deposited in adipose tissues [78]. GM is naturally homogenised while cow’s milk requires homogeniser. When fat globules are forcibly broken down by mechanical homogeniser, an enzyme associated with milk fat i.e., xanthine oxidase become free and can penetrate intestinal wall. When it reaches blood stream via intestinal wall, it can cause tissue scar on the heart and arteries which leads to mechanism causing arteriosclerosis while it is prevented in case of GM [77].
Infants who are suffering from problems like gastrointestinal disturbances, vomiting, colic, constipation and diarrhoea can be treated when they are fed GM. Pasteurised GM is easily tolerated by infants who are suffering from such diseases. GM easily assimilates in human body as chemical composition of GM is almost similar to human one which therefore enhances the bioavailability of nutrients in it. It is reported that GM consumption increases the uptake of Iron and Copper in digestive tract [79]. The readily bioavailable nature of GM has increased its consumption in recent years. The availability of beneficial gut microbes increases when GM is taken. Soft curd formed in fermented milk of goat is easily digested and absorbed [22]. People who are lactose intolerance can also easily digest it because of its small sized fat globules in which the total surface area of globules are effectively connected with lipids and also the fat globules of GM do not clump together as in cow’s milk [29].
GM is the vital source of biorganic sodium, the absence of which causes arthritis. Human stomach stores more sodium than any other organ. The absence of sodium causes digestive discomforts and inhibits stomach from producing needed enzymes leading to bloating and even ulcers. Soft curd in GM can be advantageous for adult humans who are suffering from gastrointestinal disturbances and ulcers [5]. Also, the property of high buffering capacity of GM appears to be fruitful in treating gastric ulcers [52]. The intestinal inflammation and clinical symptoms (diarrhoea and bloody stools) in colitis can be decreased by consuming GM. The presence of oligosaccharides in its milk exhibits anti-inflammatory effect in the management of Inflammatory bowel disease (IBD) [43]. It has been reported in one study of rats infected with colitis when fed GM oligosaccharides reduces and promotes recovery of damaged colonic mucosa due to less severe lesions in colon and production of more favourable gut microbiota [38].
Alpha lactalbumin present in GM is anti-carcinogenic by nature. CLA in GM is full of anti-carcinogenic properties. It is also studied that tumour cells in patients with skin and bladder cancers were killed by alpha lactalbumin. The passive transfer of serum albumin in GM to the blood has an inhibitory effect against growth and development of breast cancerous cells [75].
Proteins are most common antigens that are important for proper body functioning. On the basis of nature, allergies can be acute or chronic that have symptoms ranging from non-life threatening to life threatening. It is recommended as an substitute for patients with cow milk allergy [54]. Eczema, Rhinitis and digestive problems are simple symptoms while bronchospasm, anaphylaxis and urcaria are severe one. GM is less allergenic than cow’s milk. GM is thought to resolves 30–40% of problematic cases of childhood cow milk allergy. Some researches shows that alpha S1 casein in cow’s milk is the reason of cow milk intolerance. It has been found that level of alpha S1 casein in GM is 89% lower than that of cow milk. Therefore, GM is less allergic and improves digestive disorder, colic diseases etc. in people with cow milk sensitivities [80]. Lactose intolerance in many child and adults is caused by the deficiency of lactase enzyme that functions in easing the digestion of lactose. Generally, in case of lactose intolerant individuals, unhydrolyzed lactose passes into the large intestine whereby it is fermented by the aid of microbes which results in the production of hydrogen, methane, carbon-dioxide, SCFA leading to flatulence, diarrhoea as well as abdominal pain [81]. When ulcers worsen it takes a new form i.e., cancer and it is well known that the high buffering capacity of GM prevents gastric ulcers [52].
GM is used as a good alternative to treat mammary, colorectal and colon cancer [82] in case of animal models, as well as in vitro models of human melanoma [83] colorectal and breast cancer [84] because of the known anticarcinogenic properties of CLA [85] which is in surplus amount in it. Lactic Acid Bacteria (LAB) present in goat milk exhibit potential role in combating against cancer [86]. The risk of occurrence of cancer, carcinogenic toxicity and tumour suppression are prevented by LAB present in GM [87]. The bacteria in GM after isolation and microencapsulation can be used as a probiotics to cure cancer [88]. The study of different strains of LAB in GM can strengthen the research of cancer prevention [89].
Se is vital as it plays role in proper functioning of the immune system and thyroid activity as well as participates in spermiogenesis thereby affecting fertility [90]. It is an integral part of the antioxidant capacity of the organism [91]. GM and its products act as immunity booster and prevents from several illness in infants [87]. There is involvement of many cells like T lymphocytes (T-cells), Natural Killer (NK) cells and B-lymphocytes (B-cells) in the innate and adaptive immune response. Even though the structure of Immunoglobulin’s (Ig) are similar, minor differences exist in the main immunological classes (IgG, IgM, IgA, IgD and IgE). The major properties of serum immunoglobulin accounts for IgG and IgA. Several researches have shown immunomodulatory effects of GM in case of both in-vitro and human studies. The release of nitric oxide (NO) from human blood cells exhibits cardio protective effects in the milk consumer and also possesses antibacterial activity which prevents them from infections. Content of sialic acid is higher in GM which acts as an important biological component in playing crucial role in brain development and in boosting infant immunity [92, 93].
Since GM is rich surplus to calcium, proteins, bioactive compounds it can be taken as a “functional and nutraceutical health drink”. The role played by GM in eliminating major health complications including digestive, respiratory, immunological, viral, cardiac, cancer, allergy, osteoporosis, malabsorption, anaemia etc. favours longevity to human life. The contribution of small developing nations in the production of GM should not be neglected rather new technological innovation’s assistance to those nations will uplift the production and contribute to mankind as the consumption of GM has increased in developed nations. The compositional attributes of GM can be raised if goats are provided with ample browsing, adequate temperature and stress-free environment. It should be supplemented with folic acid and can be fortified if consumers find its odour unpleasant.
Goat rearing has several economic returns after its milk, meat, hair etc. are marketed. Goat business can help uplifting the life standard of people in rural areas. The unique properties of GM and its products carve for its more marketing potential. Its nutritional value in treating diseases has broaden its future prospects. If grading up is followed to improve the performance of local breeds of different nations then eventually more milk can be produced that benefits human. That is why more thorough and detailed descriptive research in this field is needed to fight against life taking diseases.
As an Open Access publisher, IntechOpen is dedicated to maintaining the highest ethical standards and principles in publishing. In addition, IntechOpen promotes the highest standards of integrity and ethical behavior in scientific research and peer-review. To maintain these principles IntechOpen has developed basic guidelines to facilitate the avoidance of Conflicts of Interest.
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\\n\\nA Conflict of Interest is a situation in which a person's professional judgment may be influenced by a range of factors, including financial gain, material interest, or some other personal or professional interest. For IntechOpen as a publisher, it is essential that all possible Conflicts of Interest are avoided. Each contributor, whether an Author, Editor, or Reviewer, who suspects they may have a Conflict of Interest, is obliged to declare that concern in order to make the publisher and the readership aware of any potential influence on the work being undertaken.
\\n\\nA Conflict of Interest can be identified at different phases of the publishing process.
\\n\\nIntechOpen requires:
\\n\\nCONFLICT OF INTEREST - AUTHOR
\\n\\nAll Authors are obliged to declare every existing or potential Conflict of Interest, including financial or personal factors, as well as any relationship which could influence their scientific work. Authors must declare Conflicts of Interest at the time of manuscript submission, although they may exceptionally do so at any point during manuscript review. For jointly prepared manuscripts, the corresponding Author is obliged to declare potential Conflicts of Interest of any other Authors who have contributed to the manuscript.
\\n\\nCONFLICT OF INTEREST – ACADEMIC EDITOR
\\n\\nEditors can also have Conflicts of Interest. Editors are expected to maintain the highest standards of conduct, which are outlined in our Best Practice Guidelines (templates for Best Practice Guidelines). Among other obligations, it is essential that Editors make transparent declarations of any possible Conflicts of Interest that they might have.
\\n\\nAvoidance Measures for Academic Editors of Conflicts of Interest:
\\n\\nFor manuscripts submitted by the Academic Editor (or a scientific advisor), an appropriate person will be appointed to handle and evaluate the manuscript. The appointed handling Editor's identity will not be disclosed to the Author in order to maintain impartiality and anonymity of the review.
\\n\\nIf a manuscript is submitted by an Author who is a member of an Academic Editor's family or is personally or professionally related to the Academic Editor in any way, either as a friend, colleague, student or mentor, the work will be handled by a different Academic Editor who is not in any way connected to the Author.
\\n\\nCONFLICT OF INTEREST - REVIEWER
\\n\\nAll Reviewers are required to declare possible Conflicts of Interest at the beginning of the evaluation process. If a Reviewer feels he or she might have any material, financial or any other conflict of interest with regards to the manuscript being reviewed, he or she is required to declare such concern and, if necessary, request exclusion from any further involvement in the evaluation process. A Reviewer's potential Conflicts of Interest are declared in the review report and presented to the Academic Editor, who then assesses whether or not the declared potential or actual Conflicts of Interest had, or could be perceived to have had, any significant impact on the review itself.
\\n\\nEXAMPLES OF CONFLICTS OF INTEREST:
\\n\\nFINANCIAL AND MATERIAL
\\n\\nNON-FINANCIAL
\\n\\nAuthors are required to declare all potentially relevant non-financial, financial and material Conflicts of Interest that may have had an influence on their scientific work.
\\n\\nAcademic Editors and Reviewers are required to declare any non-financial, financial and material Conflicts of Interest that could influence their fair and balanced evaluation of manuscripts. If such conflict exists with regards to a submitted manuscript, Academic Editors and Reviewers should exclude themselves from handling it.
\\n\\nAll Authors, Academic Editors, and Reviewers are required to declare all possible financial and material Conflicts of Interest in the last five years, although it is advisable to declare less recent Conflicts of Interest as well.
\\n\\nEXAMPLES:
\\n\\nAuthors should declare if they were or they still are Academic Editors of the publications in which they wish to publish their work.
\\n\\nAuthors should declare if they are board members of an organization that could benefit financially or materially from the publication of their work.
\\n\\nAcademic Editors should declare if they were coauthors or they have worked on the research project with the Author who has submitted a manuscript.
\\n\\nAcademic Editors should declare if the Author of a submitted manuscript is affiliated with the same department, faculty, institute, or company as they are.
\\n\\nPolicy last updated: 2016-06-09
\\n"}]'},components:[{type:"htmlEditorComponent",content:"In each instance of a possible Conflict of Interest, IntechOpen aims to disclose the situation in as transparent a way as possible in order to allow readers to judge whether a particular potential Conflict of Interest has influenced the Work of any individual Author, Editor, or Reviewer. IntechOpen takes all possible Conflicts of Interest into account during the review process and ensures maximum transparency in implementing its policies.
\n\nA Conflict of Interest is a situation in which a person's professional judgment may be influenced by a range of factors, including financial gain, material interest, or some other personal or professional interest. For IntechOpen as a publisher, it is essential that all possible Conflicts of Interest are avoided. Each contributor, whether an Author, Editor, or Reviewer, who suspects they may have a Conflict of Interest, is obliged to declare that concern in order to make the publisher and the readership aware of any potential influence on the work being undertaken.
\n\nA Conflict of Interest can be identified at different phases of the publishing process.
\n\nIntechOpen requires:
\n\nCONFLICT OF INTEREST - AUTHOR
\n\nAll Authors are obliged to declare every existing or potential Conflict of Interest, including financial or personal factors, as well as any relationship which could influence their scientific work. Authors must declare Conflicts of Interest at the time of manuscript submission, although they may exceptionally do so at any point during manuscript review. For jointly prepared manuscripts, the corresponding Author is obliged to declare potential Conflicts of Interest of any other Authors who have contributed to the manuscript.
\n\nCONFLICT OF INTEREST – ACADEMIC EDITOR
\n\nEditors can also have Conflicts of Interest. Editors are expected to maintain the highest standards of conduct, which are outlined in our Best Practice Guidelines (templates for Best Practice Guidelines). Among other obligations, it is essential that Editors make transparent declarations of any possible Conflicts of Interest that they might have.
\n\nAvoidance Measures for Academic Editors of Conflicts of Interest:
\n\nFor manuscripts submitted by the Academic Editor (or a scientific advisor), an appropriate person will be appointed to handle and evaluate the manuscript. The appointed handling Editor's identity will not be disclosed to the Author in order to maintain impartiality and anonymity of the review.
\n\nIf a manuscript is submitted by an Author who is a member of an Academic Editor's family or is personally or professionally related to the Academic Editor in any way, either as a friend, colleague, student or mentor, the work will be handled by a different Academic Editor who is not in any way connected to the Author.
\n\nCONFLICT OF INTEREST - REVIEWER
\n\nAll Reviewers are required to declare possible Conflicts of Interest at the beginning of the evaluation process. If a Reviewer feels he or she might have any material, financial or any other conflict of interest with regards to the manuscript being reviewed, he or she is required to declare such concern and, if necessary, request exclusion from any further involvement in the evaluation process. A Reviewer's potential Conflicts of Interest are declared in the review report and presented to the Academic Editor, who then assesses whether or not the declared potential or actual Conflicts of Interest had, or could be perceived to have had, any significant impact on the review itself.
\n\nEXAMPLES OF CONFLICTS OF INTEREST:
\n\nFINANCIAL AND MATERIAL
\n\nNON-FINANCIAL
\n\nAuthors are required to declare all potentially relevant non-financial, financial and material Conflicts of Interest that may have had an influence on their scientific work.
\n\nAcademic Editors and Reviewers are required to declare any non-financial, financial and material Conflicts of Interest that could influence their fair and balanced evaluation of manuscripts. If such conflict exists with regards to a submitted manuscript, Academic Editors and Reviewers should exclude themselves from handling it.
\n\nAll Authors, Academic Editors, and Reviewers are required to declare all possible financial and material Conflicts of Interest in the last five years, although it is advisable to declare less recent Conflicts of Interest as well.
\n\nEXAMPLES:
\n\nAuthors should declare if they were or they still are Academic Editors of the publications in which they wish to publish their work.
\n\nAuthors should declare if they are board members of an organization that could benefit financially or materially from the publication of their work.
\n\nAcademic Editors should declare if they were coauthors or they have worked on the research project with the Author who has submitted a manuscript.
\n\nAcademic Editors should declare if the Author of a submitted manuscript is affiliated with the same department, faculty, institute, or company as they are.
\n\nPolicy last updated: 2016-06-09
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Recently, bioinspired systems have been successfully employing biomechanics to develop and improve assistive technology and rehabilitation devices. The research topic "Bioinspired Technology and Biomechanics" welcomes studies reporting recent advances in bioinspired technologies that contribute to individuals\' health, inclusion, and rehabilitation. Possible contributions can address (but are not limited to) the following research topics: Bioinspired design and control of exoskeletons, orthoses, and prostheses; Experimental evaluation of the effect of assistive devices (e.g., influence on gait, balance, and neuromuscular system); Bioinspired technologies for rehabilitation, including clinical studies reporting evaluations; Application of neuromuscular and biomechanical models to the development of bioinspired technology.',coverUrl:"https://cdn.intechopen.com/series_topics/covers/8.jpg",hasOnlineFirst:!1,hasPublishedBooks:!0,annualVolume:11404,editor:{id:"144937",title:"Prof.",name:"Adriano",middleName:"De Oliveira",surname:"Andrade",slug:"adriano-andrade",fullName:"Adriano Andrade",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRC8QQAW/Profile_Picture_1625219101815",biography:"Dr. Adriano de Oliveira Andrade graduated in Electrical Engineering at the Federal University of Goiás (Brazil) in 1997. He received his MSc and PhD in Biomedical Engineering respectively from the Federal University of Uberlândia (UFU, Brazil) in 2000 and from the University of Reading (UK) in 2005. He completed a one-year Post-Doctoral Fellowship awarded by the DFAIT (Foreign Affairs and International Trade Canada) at the Institute of Biomedical Engineering of the University of New Brunswick (Canada) in 2010. Currently, he is Professor in the Faculty of Electrical Engineering (UFU). He has authored and co-authored more than 200 peer-reviewed publications in Biomedical Engineering. He has been a researcher of The National Council for Scientific and Technological Development (CNPq-Brazil) since 2009. He has served as an ad-hoc consultant for CNPq, CAPES (Coordination for the Improvement of Higher Education Personnel), FINEP (Brazilian Innovation Agency), and other funding bodies on several occasions. He was the Secretary of the Brazilian Society of Biomedical Engineering (SBEB) from 2015 to 2016, President of SBEB (2017-2018) and Vice-President of SBEB (2019-2020). He was the head of the undergraduate program in Biomedical Engineering of the Federal University of Uberlândia (2015 - June/2019) and the head of the Centre for Innovation and Technology Assessment in Health (NIATS/UFU) since 2010. He is the head of the Postgraduate Program in Biomedical Engineering (UFU, July/2019 - to date). He was the secretary of the Parkinson's Disease Association of Uberlândia (2018-2019). Dr. Andrade's primary area of research is focused towards getting information from the neuromuscular system to understand its strategies of organization, adaptation and controlling in the context of motor neuron diseases. 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