Various types of illness due to water.
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Barely three months into the new year and we are happy to announce a monumental milestone reached - 150 million downloads.
\n\nThis achievement solidifies IntechOpen’s place as a pioneer in Open Access publishing and the home to some of the most relevant scientific research available through Open Access.
\n\nWe are so proud to have worked with so many bright minds throughout the years who have helped us spread knowledge through the power of Open Access and we look forward to continuing to support some of the greatest thinkers of our day.
\n\nThank you for making IntechOpen your place of learning, sharing, and discovery, and here’s to 150 million more!
\n\n\n\n\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"5486",leadTitle:null,fullTitle:"Quality Control and Assurance - An Ancient Greek Term Re-Mastered",title:"Quality Control and Assurance",subtitle:"An Ancient Greek Term Re-Mastered",reviewType:"peer-reviewed",abstract:"Quality control and assurance cover a diverse area of modern life and play, undeniably, an important role. This book brings together a collection of international papers that showcase examples of current research and practice in industry and the medical profession. It is hoped that engineers, researchers and scientists will be assisted in their continuous quest for excelling in qualitative aspects. The Ancient Greek word arete means excellence or virtue and defines the highest qualitative state: a man’s effectiveness and skill in goodness (optimum potentiae). Indeed, Ancient Greeks believed that without quality control, specifications are useless and may result to illegitimacy, which in turn may become a threat to society itself.",isbn:"978-953-51-2922-6",printIsbn:"978-953-51-2921-9",pdfIsbn:"978-953-51-6696-2",doi:"10.5772/63135",price:119,priceEur:129,priceUsd:155,slug:"quality-control-and-assurance-an-ancient-greek-term-re-mastered",numberOfPages:228,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"549fefebffcb2f610fb669f6eb86c785",bookSignature:"Leo D. Kounis",publishedDate:"February 22nd 2017",coverURL:"https://cdn.intechopen.com/books/images_new/5486.jpg",numberOfDownloads:19342,numberOfWosCitations:16,numberOfCrossrefCitations:14,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:26,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:56,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"April 26th 2016",dateEndSecondStepPublish:"May 17th 2016",dateEndThirdStepPublish:"August 21st 2016",dateEndFourthStepPublish:"November 19th 2016",dateEndFifthStepPublish:"December 19th 2016",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"111582",title:"Dr.",name:"Leo",middleName:"Dimitrios",surname:"Kounis",slug:"leo-kounis",fullName:"Leo Kounis",profilePictureURL:"https://mts.intechopen.com/storage/users/111582/images/system/111582.jpg",biography:"Leo D. Kounis is the Head of the Department of Communication and Informatics Battalion at the Hellenic Ministry of Defense, Hellenic National Defense General Staff. He obtained his BEng (Hons) degree in Manufacturing Systems Engineering, his MSc in Quality Engineering, and his PhD in Systems Reliability from the University of Hertfordshire, UK. Dr. Kounis has worked as a senior quality engineer in a number of private companies in Greece, and has acted as a part-time lecturer and scientific advisor in academia. His research interests are focused in the area of quality, transportation, and sustainable energy. He has published a number of scientific papers.",institutionString:"Hellenic National Defense General Staff",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"1",totalChapterViews:"0",totalEditedBooks:"3",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"730",title:"Quality Control Management",slug:"engineering-control-engineering-quality-control-management"}],chapters:[{id:"53946",title:"The Evolution of Quality Concepts and the Related Quality Management",doi:"10.5772/67211",slug:"the-evolution-of-quality-concepts-and-the-related-quality-management",totalDownloads:4401,totalCrossrefCites:5,totalDimensionsCites:6,hasAltmetrics:1,abstract:"Enterprises usually adopt some quality practices to control the product quality during the manufacturing process in order to assure the delivery of qualitative good products to customers. The quality practices or quality management systems adopted by industries will further evolve due to the changes of quality concepts as time goes by. This chapter discusses the change of quality concepts and the related revolution of quality management systems in the past century. The quality concepts were gradually changed from the achievement of quality standards, satisfaction of customer needs, and expectations to customer delight. Since merely satisfying customers is not enough to ensure customer loyalty, the enterprises gradually focus on customers’ emotional responses and their delight in order to pursue their loyalty. The emotion of “delight” is composed of “joy” and “surprise,” which can be achieved as the customers’ latent requirements are satisfied. Thus, the concept of “customer delight” and the means to provide the innovative quality so as to meet the unsatisfied customers’ latent needs are elaborated on. Finally, a framework of innovation creation is developed that is based on the mining of customer's latent requirements. This outline will manifest the essential elements of the related operation steps.",signatures:"Ching-Chow Yang",downloadPdfUrl:"/chapter/pdf-download/53946",previewPdfUrl:"/chapter/pdf-preview/53946",authors:[{id:"11862",title:"Prof.",name:"Ching-Chow",surname:"Yang",slug:"ching-chow-yang",fullName:"Ching-Chow Yang"}],corrections:null},{id:"53024",title:"Key Aspects for Implementing ISO/IEC 17025 Quality Management Systems at Materials Science Laboratories",doi:"10.5772/66100",slug:"key-aspects-for-implementing-iso-iec-17025-quality-management-systems-at-materials-science-laborator",totalDownloads:2804,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Implementing a quality management system based on the requirements specified in ISO/IEC 17025 standard at materials science laboratories is challenging, mainly due to two main factors: (i) the high technical complexity degree of some tests used for materials characterization and (ii) the fact that most materials science laboratories provide materials characterization tests and also carry out research and development activities. In this context, this chapter presents key subjects while implementing a quality management system at materials science laboratories and some considerations on strategies for effectively implementing such systems.",signatures:"Rodrigo S. Neves, Daniel P. Da Silva, Carlos E. C. Galhardo, Erlon H.\nM. Ferreira, Rafael M. Trommer and Jailton C. Damasceno",downloadPdfUrl:"/chapter/pdf-download/53024",previewPdfUrl:"/chapter/pdf-preview/53024",authors:[{id:"20571",title:"Prof.",name:"Erlon H.",surname:"Martins Ferreira",slug:"erlon-h.-martins-ferreira",fullName:"Erlon H. Martins Ferreira"},{id:"145815",title:"Dr.",name:"Rodrigo",surname:"De Santis Neves",slug:"rodrigo-de-santis-neves",fullName:"Rodrigo De Santis Neves"},{id:"145816",title:"Dr.",name:"Carlos",surname:"Eduardo Cardoso Galhardo",slug:"carlos-eduardo-cardoso-galhardo",fullName:"Carlos Eduardo Cardoso Galhardo"},{id:"159056",title:"Dr.",name:"Jailton",surname:"Damasceno",slug:"jailton-damasceno",fullName:"Jailton Damasceno"},{id:"191863",title:"Dr.",name:"Daniel",surname:"Fernandes",slug:"daniel-fernandes",fullName:"Daniel Fernandes"},{id:"191865",title:"Dr.",name:"Rafael",surname:"Mello Trommer",slug:"rafael-mello-trommer",fullName:"Rafael Mello Trommer"}],corrections:null},{id:"53144",title:"Youden Two-Sample Method",doi:"10.5772/66397",slug:"youden-two-sample-method",totalDownloads:2398,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The results obtained when testing materials, equipment and procedures are not generally identical. Factors that influence the magnitude of the results are not fully controllable. As such, the interpretation and analysis of results must take into account the variations caused by numerous and random unavoidable causes. Intercomparison exercises are considered of being of importance, as they do allow the examination of the analytical process and their generated results. Youden plot is particularly aimed at interlaboratory comparisons. The raw results provided by the participating laboratories are treated by a statistical method applied by the centre performing the trial. In order to materialize this, two similar materials with small differences in the concentration of the characteristics are required. The advantage of Youden analysis is its ability to separate the random errors with a minimum effort by participants in the design from the point of view of the analytical requirement. This book chapter illustrates the method that has been applied to elaborate on data covering a diverse scientific field: polyunsaturated fatty acids in fat and oils, total blood cholesterol and aspirin in pharmaceutical preparations. Finally, liquid chromatography with tandem mass spectrometry detector has been applied to the determination of an emerging contaminant, methylparaben (MeP), in surface waters.",signatures:"Julia Martín, Nieves Velázquez and Agustin G. Asuero",downloadPdfUrl:"/chapter/pdf-download/53144",previewPdfUrl:"/chapter/pdf-preview/53144",authors:[{id:"190870",title:"Dr.",name:"Agustín G.",surname:"Asuero",slug:"agustin-g.-asuero",fullName:"Agustín G. Asuero"},{id:"190871",title:"Dr.",name:"Julia",surname:"Martín",slug:"julia-martin",fullName:"Julia Martín"},{id:"195055",title:"Dr.",name:"Nieves María",surname:"Velázquez",slug:"nieves-maria-velazquez",fullName:"Nieves María Velázquez"}],corrections:null},{id:"52915",title:"Using Lot Quality Assurance Sampling to Monitor the Prevalence of Abortions and the Quality of Reproductive Health Care in Armenia",doi:"10.5772/66092",slug:"using-lot-quality-assurance-sampling-to-monitor-the-prevalence-of-abortions-and-the-quality-of-repro",totalDownloads:1570,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Monitoring abortion prevalence is essential to plan control efforts. Lot Quality Assurance Sampling (LQAS) is an inexpensive, reliable method for monitoring abortion prevalence and access to quality reproductive health (RH) services. This chapter presents survey results from 2000 in three sites of Armenia (Gyumri, Gavar and Goris) using LQAS principles (i.e., 44%, 95% CI: ±6% of women had an induced abortion in their lifetime, a total abortion rate (TAR) of 2.0 abortions per woman). Modern contraceptive use was lowest in Goris (16%. 95% CI: ±7%) and highest in Gyumri (43%, 95% CI: ±11%). Only 37% (95% CI: ±9%) of women with an induced abortion received family planning information and 21% (95% CI: ±4%) of mothers were counselled about family planning after delivery. While limited access to family planning information and contraceptives is still an issue in Armenia, recently new reproductive health priorities—such as infertility, sex-selective abortions and abortions due to socio-economic difficulties—have become more common and can be investigated using LQAS in both community surveys and health facility assessments. This study demonstrates that measuring national abortion prevalence and access to services mask underlying variations; the awareness of which is essential for health program planning.",signatures:"Joseph J. Valadez and Lusine Mirzoyan",downloadPdfUrl:"/chapter/pdf-download/52915",previewPdfUrl:"/chapter/pdf-preview/52915",authors:[{id:"191876",title:"Prof.",name:"Joseph",surname:"Valadez",slug:"joseph-valadez",fullName:"Joseph Valadez"},{id:"195035",title:"Dr.",name:"Lusine",surname:"Mirzoyan",slug:"lusine-mirzoyan",fullName:"Lusine Mirzoyan"}],corrections:null},{id:"53019",title:"A Framework to Manage Quality of Enterprise Content Management Systems",doi:"10.5772/66199",slug:"a-framework-to-manage-quality-of-enterprise-content-management-systems",totalDownloads:1387,totalCrossrefCites:0,totalDimensionsCites:3,hasAltmetrics:1,abstract:"There is a wide range of enterprise content management (ECM) systems which supports, among other things, document management processes, records management and Web content management. However, each of these systems has many features and some of them can meet organizational needs depending on the scale, sector and workflow of the organization. In addition, it is very common that organizations are unaware of what ECM system best fits their needs, since each company has its particular scope and strategic objectives. This chapter is contextualized within the real project called THOT designed for the Andalusian Public Administration in Spain. The aim of this project is to study in detail ECM systems and propose an objective method to compare them for the specific scope and strategic objective of organizations. Quality evaluation framework (QuEF) has been adapted for this purpose.",signatures:"José González Enríquez, Francisco José Domínguez Mayo, Julián\nAlberto García García, María José Escalona Cuaresma and Manuel\nMejías Risoto",downloadPdfUrl:"/chapter/pdf-download/53019",previewPdfUrl:"/chapter/pdf-preview/53019",authors:[{id:"104846",title:"Dr.",name:"Maria",surname:"Escalona",slug:"maria-escalona",fullName:"Maria Escalona"},{id:"191332",title:"Ph.D.",name:"José",surname:"González",slug:"jose-gonzalez",fullName:"José González"},{id:"191493",title:"Dr.",name:"F.J.",surname:"Domínguez-Mayo",slug:"f.j.-dominguez-mayo",fullName:"F.J. Domínguez-Mayo"},{id:"191494",title:"Dr.",name:"J.A.",surname:"García-García",slug:"j.a.-garcia-garcia",fullName:"J.A. García-García"},{id:"195075",title:"Dr.",name:"M.",surname:"Mejías",slug:"m.-mejias",fullName:"M. Mejías"}],corrections:null},{id:"53267",title:"Exploring the Relationship of Supply Chain Risk Management to Quality Management",doi:"10.5772/65847",slug:"exploring-the-relationship-of-supply-chain-risk-management-to-quality-management",totalDownloads:1524,totalCrossrefCites:4,totalDimensionsCites:4,hasAltmetrics:0,abstract:"This research explores the relationship between an organization's supply chain risk management (SCRM) maturity and quality maturity. SCRM maturity was measured using a survey questionnaire sent to organizations in the USA. Quality maturity was assessed via ISO 9001:2008 certification status as well as through a survey questionnaire of total quality management (TQM) practices for organizations in the USA. The results suggest that ISO 9001:2008 is not related to SCRM maturity, while TQM maturity is related to SCRM maturity. Organizations with more mature TQM programs appear to also have more mature SCRM programs.",signatures:"Tyler Florio",downloadPdfUrl:"/chapter/pdf-download/53267",previewPdfUrl:"/chapter/pdf-preview/53267",authors:[{id:"195084",title:"Mr.",name:"Tyler",surname:"Florio",slug:"tyler-florio",fullName:"Tyler Florio"}],corrections:null},{id:"52958",title:"ALAMEDA Ecosystem: Centering Efforts in Software Testing Development",doi:"10.5772/66043",slug:"alameda-ecosystem-centering-efforts-in-software-testing-development",totalDownloads:2074,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"One of the most important and critical aspects to improve the quality assurance in software is to improve the testing process by utilizing techniques and tools, which will enhance the software testing process, making it more effective and efficient. This chapter presents ALAMEDA ecosystem, a software package that centers its efforts in software testing development and is a result from a real-world project. ALAMEDA provides support to lifecycles focused on the generation, implementation, and testing organization from the earliest stages of software development. In addition, the ecosystem provides an environment of rating the degree of compliance of organizations with the International Standard for Testing ISO/IEC-29119. It is proposed as a tool to use during the various iterations that may occur in an agile software development process.",signatures:"José González Enríquez, Julián Alberto García-García, Francisco José\nDomínguez-Mayo and María José Escalona Cuaresma",downloadPdfUrl:"/chapter/pdf-download/52958",previewPdfUrl:"/chapter/pdf-preview/52958",authors:[{id:"104846",title:"Dr.",name:"Maria",surname:"Escalona",slug:"maria-escalona",fullName:"Maria Escalona"},{id:"191332",title:"Ph.D.",name:"José",surname:"González",slug:"jose-gonzalez",fullName:"José González"},{id:"191493",title:"Dr.",name:"F.J.",surname:"Domínguez-Mayo",slug:"f.j.-dominguez-mayo",fullName:"F.J. Domínguez-Mayo"},{id:"191494",title:"Dr.",name:"J.A.",surname:"García-García",slug:"j.a.-garcia-garcia",fullName:"J.A. García-García"}],corrections:null},{id:"53099",title:"Improving Quality Assurance in Multidisciplinary Engineering Environments with Semantic Technologies",doi:"10.5772/66222",slug:"improving-quality-assurance-in-multidisciplinary-engineering-environments-with-semantic-technologies",totalDownloads:1556,totalCrossrefCites:4,totalDimensionsCites:8,hasAltmetrics:0,abstract:"In multidisciplinary engineering (MDE) projects, for example, automation systems or manufacturing systems, stakeholders from various disciplines, for example, electrics, mechanics and software, have to collaborate. In industry practice, engineers apply individual and highly specialized tools with strong limitation regarding defect detection in early engineering phases. Experts typically execute reviews with limited tool support which make engineering projects defective and risky. Semantic Web Technologies (SWTs) can help to bridge the gap between heterogeneous sources as foundation for efficient and effective defect detection. Main questions focus on (a) how to bridge gaps between loosely coupled tools and incompatible data models and (b) how SWTs can help to support efficient and effective defect detection in context of engineering process improvement. This chapter describes success-critical requirements for defect detection in MDE and shows how SWTs can provide the foundation for early and efficient defect detection with an adapted review approach. The proposed defect detection framework (DDF) suggests different levels of SWT contributions as a roadmap for engineering process improvement. Two selected industry-related real-life cases show different levels of SWT involvement. Although SWTs have been successfully applied in real-life use cases, SWT applications can be risky if applied without good understanding of success factors and limitations.",signatures:"Dietmar Winkler, Marta Sabou and Stefan Biffl",downloadPdfUrl:"/chapter/pdf-download/53099",previewPdfUrl:"/chapter/pdf-preview/53099",authors:[{id:"95798",title:"Dr.",name:"Dietmar",surname:"Winkler",slug:"dietmar-winkler",fullName:"Dietmar Winkler"},{id:"135962",title:"Prof.",name:"Stefan",surname:"Biffl",slug:"stefan-biffl",fullName:"Stefan Biffl"},{id:"196030",title:"Dr.",name:"Marta",surname:"Sabou",slug:"marta-sabou",fullName:"Marta Sabou"}],corrections:null},{id:"53522",title:"The Use of Control Charts in the Study of Bitcoin’s Price Variability",doi:"10.5772/66360",slug:"the-use-of-control-charts-in-the-study-of-bitcoin-s-price-variability",totalDownloads:1638,totalCrossrefCites:0,totalDimensionsCites:2,hasAltmetrics:0,abstract:"The focus of this research is bitcoin’s variability and its comparison with the variability of the EURO/USD exchange rate. Virtual currencies have been evolving in a dynamic way in the last few years. Under 600 different virtual currencies, the most successful was bitcoin. Its adherents saw in it an alternative to the traditional means of payments allowing the performance of real-time transactions at low costs. The accessibility, where no financial infrastructure is ensured or where either limited or no international agreements exist between financial and banking institutions was also an advantage. The opponents perceived this as a temporary curiosity with no future. Time confirmed that bitcoin has gained on popularity and the exchange rate to the main currencies rose in a dynamic way. The analysts, however, underline that the bitcoin is too volatile and unpredictable, so it cannot compete against the main currencies. The aim of this research is to compare the bitcoin (BTC) to US Dollar (USD) exchange rate and Euro to USD exchange rate volatility using control charts. The results have shown that BTC/USD exchange rate volatility is strongly affected by unexpected price jumps during the period (2010–2016), an act that significantly distinguishes it from more stable and predictable EUR/USD exchange rate variability.",signatures:"Beata Szetela",downloadPdfUrl:"/chapter/pdf-download/53522",previewPdfUrl:"/chapter/pdf-preview/53522",authors:[{id:"190806",title:"Ph.D. Student",name:"Beata",surname:"Szetela",slug:"beata-szetela",fullName:"Beata Szetela"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"6235",title:"Quality Management Systems",subtitle:"a Selective Presentation of Case-studies Showcasing Its Evolution",isOpenForSubmission:!1,hash:"a7bb324cdb11307c932cb6a7966a1e00",slug:"quality-management-systems-a-selective-presentation-of-case-studies-showcasing-its-evolution",bookSignature:"Leo D. 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Water, i.e., 2 mol of hydrogen and 1 mol of oxygen or simply called H2O plays a vital role in our everyday life. Without water no one can think of life on earth. About 71% of earth is covered with water. Of that 71% water about 97% resides in oceans and only 3% of water is fresh water (Figure 1a) and of that 3% about 68.7% of freshwater is locked up in icecaps and glaciers (Figure 1b), and it is quite a surprising fact that almost all the remaining fresh water is below the ground. Of all the freshwater on the surface of earth only 0.3% is contained in fresh lakes, and rivers [1].
(a) Water distribution on the earth and (b) freshwater distribution on the earth.
As the population is increasing day by day the water availability per capita is decreasing. So the challenge of limited amount of freshwater and its decreasing per capita availability is an issue of concern but another major challenge is water pollution that has not only environmental impact but also have a major effect on human health. As per the statistics 783 million people do not have access to clean and safe water worldwide [2]. Around 319 million people in Sub-Saharan Africa are without the access to improved reliable drinking water sources. One in nine people worldwide do not have access to safe and clean drinking water. 443 million school days are lost each year due to water-related diseases [3]. In developing countries, as much as 80% of illnesses are linked to poor water and sanitation conditions [4]. 2.6 billion people in the world lack adequate sanitation and which contributes to about 10% of the global disease burden [5]. Half of the world’s hospitals beds are filled with people suffering from a water-related disease [6].
There are various type of illnesses due to water and are summarized in Table 1.
Type of diseases | Source | Example | References |
---|---|---|---|
Water borne | Human or animal waste | Cholera, typhoid, and dysentery, | [7] |
Water washed | Lack of clean water for washing | Skin and eye infections | [8] |
Water based | Organism developed in water and then become parasite | Schistosomiasis | [9] |
Water-related insect vector | Mosquitoes breed in water | Malaria and dengue | [9] |
Various types of illness due to water.
As we have seen that the contaminated water has a very bad impact on human health even some heavy metals that if taken for long time it can cause cancer such as arsenic is considered as one the carcinogenic contaminant in water. After understanding the health issues related to contaminant water there is need to understand the source of contamination and major contaminants that pollute the water.
In recent years, magnetic materials have been potentially used for removal of water pollutants, particularly organic contaminates (dyes, chlorinated hydrocarbons, aromatics), pesticides, as well as heavy metals [10]. There are a large number of techniques available for water treatment for safe drinking water including adsorption, precipitation, solvent extraction, ion exchange, reverse osmosis, membrane separation, evaporation, and photocatalysis. The development of nanoscience and nanotechnology shows their potentiality in removing toxic elements from water bodies with better water treatment process. The design and development of nanomaterials which belong to the size range of 1–100 nm exhibiting unique properties as compared to the bulk materials leads to the enormous improvements in many sectors including, health, manufacturing, electronics, environmental remediation as well. The magnetic nanomaterials (paramagnetic or ferromagnetic or superparamagnetic) with tailored surface chemistry have already expanded their scope of application in water treatment. In this chapter, various processes of drinking water treatment and waste water treatment using advanced magnetic materials in removing toxic metal ions, organic and inorganic solutes, bacteria and viruses has been discussed.
There are many sources of drinking water and the main sources are ground water, lakes, canals, reservoirs, rain water, fog water and sea water. These sources are contaminated in different ways and broadly the source of contamination can be divided in to two categories:
Direct sources or point sources
Indirect sources or non-point sources
Direct sources basically include effluent from industries, treatment plants, refineries, factories, etc. However, indirect sources or non-point sources include the water contamination entering to the water body through a number of processes, e.g., while putting the fertilizers and pesticides to the agricultural field, the elements presents in the chemical percolates down to the groundwater and ultimately pollute the water.
There are various types of water contaminants, however in the following subsections organic contaminants, inorganic contaminants and pathogens are briefly discussed.
Organic contaminants present in drinking water create severe problem on human health. Pollution by organic chemicals in water bodies occurs by various mechanisms. Industrial waste containing various organic chemical contaminants pollutes the water bodies. Volatile organic compounds (VOCs), pesticides, phenolic compounds, phthalates, and nitrogen-containing compounds, are often detected in polluted water [11]. Many of these compounds have been found to be carcinogenic, even in very low concentrations. WHO Guidelines for drinking water quality, levels are set for 28 organic constituents (i.e., microcystin-LR, chlorinated alkanes, chlorinated benzenes and miscellaneous), 33 pesticides, and 9 disinfectant by-products, due to their health effects on humans [12]. It is noteworthy to mention that, occurrence of pharmaceutical and personal care products and perfluoroalkyl acids in aquatic environment has been recognized as emerging issue in environmental chemistry [13].
Inorganic contaminants include metals, salts and other compounds that do not contain carbon. Many of them are naturally occurring and should be considered as an integral part of those waters, e.g., calcium carbonate and bicarbonate in hard water. The metal ions such as Hg(II), Pb(II), Cr(III), Cr(VI), Ni(II), Co(II), Cu(II), Cd(II), Ag(I), As(V) and As(III) are toxic from eco toxicological point of view. Besides, the pollution by the radioactive elements is of major concern looking into their long-term hazardous impacts.
Pathogens such as bacteria, viruses and parasites may be present in very low concentration in drinking water; but cause many infectious diseases and are considered as one of the major risk factors with drinking water safety [14]. The pathogenic microorganisms enter in to water body through sewage discharge as a major source or through the wastewater from industries like slaughterhouses. Water-borne pathogens have been the causes of many disease outbreaks such as diarrhea, cholera, gastro-intestinal illness [15]. The recurrence of water-borne pathogens is due to a number of reasons like heavy water contamination, population explosion, change in potable water treatment methods, globalization of commerce and travel. It has been made possible to detect pathogen based water contamination to a large extent owing to the improved methods for detection and source tracking [16, 17]. The most serious health risk is related with ingestion of water which is contaminated with fecal matter and the discharge of wastewater into various ambient water bodies is what contributes to the multiplication of numbers of such pathogens (bacteria, viruses, protozoa and helminthes) [18].
Water treatment is defined as the removal of the above contaminants using some specific process. In most of the water treatment processes, conventional adsorption process with activated carbon is adopted and the adsorption capacity is substantially decreased in presence of high concentration of organic matters in water where the active sites are mostly occupied by these materials. In recent times, there are various technologies have been employed for the removal of water contaminants such as filtration (ceramic, bio sand, membrane, and activated carbon based filtration), heat and UV radiation, chemical treatment (coagulation-flocculation, chemical disinfection), and desalination (reverse osmosis, distillation). The various techniques in water treatment can categorized into following six classes [19]:
Adsorption
Biotechnology
Catalytic processes
Membrane processes
Ionizing radiation processes
Magnetically assisted processes.
There are specific advantages and disadvantages for a particular process. The nanotech based processes are promising option in current water treatment processes because of their target specificity, ease of separation, high adsorption per unit area, as well as less maintenance.
There has been increased interest in using magnetic materials in water treatment which are basically composed of magnetic core of iron oxides organic compounds, carbon materials, etc. Recently, nanomaterials in different shapes, morphologies, forms, e.g., metal-containing nanoparticles, carbonaceous nanomaterials, zeolites, dendrimers, carbon nanotubes, nanofibers have been used for water purification [20]. However, the difficulty arises in using these materials is the separation of solid materials from liquid and which is more difficult as the particle size decreases in nanoscale. On the other hand, the using of magnetic, particularly the magnetic nanoparticles (MNPs) materials have the advantage of magnetic filtration in separation of solid from liquid and are more efficient [21].
However solid/liquid (S/L) separation is more difficult as the particle size decreases. On the other side, in case of magnetic sorbents based on Fe oxides, the magnetic filtration may be applied for S/L separation. Furthermore, the removal of particles from solution with the use of magnetic fields is more selective and efficient (and often much faster) than centrifugation or filtration (Yauvuz et al.) [21]. Here are the advantages of using MNPs adsorbent for water treatment processes:
Small size and thus high surface to volume ratio
Solid/liquid separation through magnetic filtration is selective, faster than centrifugation and filtration techniques
Reusability
Greater biocompatibility
Magnetic separation
Different types of magnetic materials have been synthesized and designed for development of advanced materials and applied effectively in widespread uses such as biomedicine, magnetic resonance imaging (MRI), catalysis, spintronics, robotics, engineering, environmental remediation, etc. [22] There are different synthesizing methods viz. co-precipitation, solvothermal, hydrothermal, microemulsion, sonochemical, etc. which determine their particle size, distribution, morphology, surface functionality, and magnetic properties and in turn of their various application [22]. Magnetic materials are made from mixtures of metals of iron, cobalt, nickel, and alloys and their oxides (of the type MFe2O4, where M is a metal). Out of these materials, iron (zero valent iron) and its oxides, i.e., usually γ-Fe2O3 (maghemite) and Fe3O4 (magnetite) nanoparticles have attained significant interest in recent years and have been used for water treatment processes. The various composite magnetic materials such as Fe3O4@C [23, 24], Fe@SiO2 [25], Fe3O4@TiO2 [26], Fe3O4@PPO (poly(propylene oxide)), PEO (poly(ethylene oxide) [27], Fe3O4@PDA (polydopamine) [28], Fe3O4@PNIPAM (poly(N-isopropylacrylamide)) [29], Fe3O4@MIPs (molecularly imprinted polymer-encapsulated particles) [30], Fe3O4@CNTs (multi-walled carbon nanotubes) [31], Fe@CS (carbon spheres) [32], Fe/iron oxide-oxyhydroxide/rGO (grapheme) [33], etc. have been used for environmental applications. Singh and his co-workers synthesized a series of magnetic nanocomposites such as CoFe2O4–ZnS [34], Fe3O4@GTPs (green tea polyphenols) [35], Fe3O4–Cr2O3 [36], CoFe2O4-Cr2O3-SiO2 [37] and applied for wastewater treatment.
In addition to their suitable magnetic properties, i.e., ferrimagnetic, ferromagnetic and superparamagnetic (nanoparticle size less than 10 nm), their synthesis procedure is simple and cost-effective and they can be easily functionalized as desired for many applications. The size and shape and magnetism of these magnetic materials can be easily controlled based on their application and thus they can be easily dispersed in liquid medium and their stability can be retained for multiple uses. Moreover, these materials are non-toxic or less toxic, chemically inert, thermally stable as well as biocompatible.
Appearance of water pollution as a global threat demands the development of low-cost and reliable materials for effective waste water remediation. The magnetic materials have been used for clean water technology for both in laboratory as well as field scale [38, 39]. In recent years, iron oxide nanomaterials have been used as adsorbent or immobilizing agent and photocatalyst or the both depending on nature of contaminants in water [40].
Heavy metal contamination in water such as cadmium, zinc, lead, chromium, nickel, copper, vanadium, platinum, silver and titanium due to industrial activities is significantly increasing which is detrimental to human beings and animals. Magnetic nanomaterial adsorbents have been potentially used for removal of metallic ions such as Cr(VI), Cu(II), Co(II),Cd(II), As(V), As(III) and Hg(II) in water [41, 42] which are more effective as compared to micron size particles. The magnetic chelating resin based materials have been used for effective removal of Cu(II), Co(II), and Ni(II) ions [43]. The magnetic hydrogels based on 2-acrylamine-2-methyl-1-propansulfonic acid can be used for removal of many heavy metal ions such Cd(II), Co(II), Fe(II), Pb(II), Ni(II), Cu(II) and Cr(III) from water in repeated cycles [44]. The Cu(II) can also be effectively removed by functionalized mesostructured silica containing magnetite [45]. The acrylate-based polymer composites with magnetite can be used in selective removal of heavy metals from water (selectivity: Cu > Cr > Zn > Ni) [46]. Layered double hydroxide (LDH) prepared from Fe3+ and Ni2+ shows good adsorption of As and subsequent magnetic separation [47]. The magnetic zeolite composites are used for decontamination of heavy metals from water [48]. The composite materials of mesoporous magnetic MCM-41 with aminopropyls are used for selective removal of As(V), and Cr(VI) in presence of Cu(II) [49].
Magnetic nanoparticles are used as an adsorbent for the removal of various dyes and dyes stuff from aqueous solution. Removal of dyes from waste water has become a serious issue of concern because of its harmful impact on human. Dyes basically can be classified in to two categories, i.e., anionic dyes and cationic dyes.
Long et al. [50] synthesized Fe3O4@catechol/polyethylenimine (PEI) nanoparticles and tested for adsorption of three different kind of anionic dyes, i.e., methyl blue, orange G and amaranth and found the maximum adsorption capacities of 344.8, 192.3 and 146.2 mg/g, respectively. Saksornchai et al. [51] synthesized magnetite (Fe3O4) coated with cetyltrimethylammonium bromide (CTAB) and tested for the adsorption of anionic dye Congo red (CR) removal. They found maximum adsorption capacity for CR dye to be 93.46 mg/g. Faraji et al. [52] synthesized triazine-based nitrogen-rich network-modified magnetic nanoparticles were synthesized for the adsorption of methyl orange. Sahraei et al. [53] reported the synthesis of magnetic bio-sorbent hydrogel beads based on modified gum tragacanth/graphene oxide for the removal of heavy metals and dyes from water. They found the adsorption capacity of 101.7 mg/g for Congo red dye. Ge et al. [54] fabricated Fe@MgO magnetic nanocomposites for the removal of heavy metal ions and dye from water. They found that the synthesized nanocomposite showed excellent adsorption capacity of 6947.9 mg/g for methylene orange. Wu et al. [55] fabricated multi-functional magnetic nanoparticle core covered with polyethylenimine (PEI) derived quaternary ammonium compounds (QAC) corona through electrostatic attraction for the removal of dyes and metal ion adsorption. The adsorption results corresponding to synthesized nanoparticle showed the maximum adsorption capacity of 653 mg/g for AF as a representative of dyes. Konicki et al. [56] synthesized Fe@graphite core shell nanocomposite for the removal of anionic dyes from aqueous solution. The synthesized nanoparticles were tested for the adsorption of two anionic dyes namely acid red 88 (AR88) and direct orange 26 (DO26) and the maximum adsorption capacity was found to be 63.7 mg/g and 42.7 for AR88 and DO26, respectively. Zhang et al. [57] synthesized the Fe3O4 nanoparticle modified with 3-glycidoxypropyltrimethoxysilane (GPTMS) and poly-lysine (P-Lys). They found that the synthesized MNPs could effectively remove anionic dyes including methyl blue (MB), orange I (OR-I), amaranth (AM) and acid red 18 (AR-18) from water solution.
Cationic dyes are most toxic because they can easily interact with negatively charged cell membrane surfaces, and also they can enter in to the cells and can concentrate in cytoplasm (Bayramoglu et al.) [58]. Ge et al. [59] have studied the adsorption of cationic dyes such as crystal violet, methylene blue and alkali blue 6B from aqueous solutions by use of polymer-modified magnetic nanoparticles. The cationic dyes could be quickly removed from water solution with high efficiency at pH 5–12. More significantly, the MNP showed high efficiency as a reusable adsorbent for fast and convenient removal of cationic dyes from water solution. Yan et al. [60] have synthesized full biodegradable magnetic adsorbent based on glutamic acid modified chitosan and silica coated Fe3O4 nanoparticles for removal of three different kinds of cationic dyes, methylene blue, crystal violet and cationic light yellow 7GL, from aqueous solutions. Chen et al. [61] have prepared magnetic adsorbent by fabrication of chitosan/polyacrylic acid multilayer onto magnetic Fe3O4 microspheres for removal of adsorption of two cationic dyes, methylene blue and crystal violet from aqueous solution. Amiri et al. [62] synthesized cobalt ferrite silica magnetic nanocomposite for the adsorption of Malachite green dye and found the adsorption capacity of 75.5 mg/g for that dye. Li et al. [63] synthesized wettable magnetic hypercrosslinked microporous nanoparticle for the water treatment. The synthesized nanoparticle consists of microporous organic polymer which combine sodium acrylate functionalized hypercrosslinked polymer with magnetic Fe3O4 nanoparticle to form a hybrid. They tested the synthesized hybrid for the adsorption of Rhodamine B dye and found the maximum adsorption capacity of 216 mg/g. Singh et al. [64] had synthesized the superparamagnetic nanoparticles coated with green tea polyphenol by wet chemical method. They found that the particles have a very high adsorption capacity of (7.25 mg/g) for removal of methylene blue (MB) dye in wastewater treatment. Li et al. [65] synthesized magnetic peach gum bead bio-sorbent for the adsorption of MB dye and found the maximum adsorption capacity of 231.5 mg/g.
The presence of pharmaceuticals such as antibiotics, anticonvulsants, antipyretics drugs, hormones in surface and ground water possesses a major environmental challenge. Their contamination even at trace amount is a serious concern to the aquatic organisms as well.
Attia et al. [66] synthesized magnetic nanoparticles coated zeolite for the adsorption of pharmaceutical compounds from aqueous solution. They found that the synthesized magnetic nanoparticles can remove more that 95% of PPCPs in 10 min. Reddy et al. [67] reviewed spinal ferrite nanoparticles and found that SF and its derivatives can be used for remediation of various pollutants. Nadim et al. [68] Synthesized gallic acid coated magnetic nanoparticles (GA-MNP) and used as a photocatalyst for degradation of meloxicam; a commonly prescribed nonsteroidal anti-inflammatory drug.
Recently, M. Hayasi and his coworker described the use of magnetic poly (styrene-2-acrylamido-2-methyl propanesulfonic acid) (St-AMPS) as adsorbent for removal of the pharmaceuticals viz. ceftriaxone sodium, diclofenac sodium, and atenolol from water [69].
Liu [70] discussed the use of various magnetic nanoparticles (MNPs) in pharmaceutical removal from waste water their recent review which are outlined below (Table 2).
Magnetic materials used | Pharmaceuticals present in water | Processes involved for decontamination | References |
---|---|---|---|
Nano zero-valent iron (nZVI) | Carbamazepine | Adsorption, chemical degradation (Fenton oxidation) | [71] |
Nano zero-valent iron (nZVI) and PEG and zeolite supported nZVI | Amoxicillin, ampicillin | Adsorption | [72] |
Zero valent iron (ZVI) | Carbamazepine | Chemical degradation | [73] |
Diazepam | Chemical degradation | [74] | |
Maghemite (Fe2O3) core confined in a silica porous layer | Atenolol, gemfibrozil, and sulfamethoxazole | Adsorption | [75] |
MFe2O4 (M = Fe, Mn, Co, Zn) | Tetracycline, oxytetracycline, and chlortetracycline | Adsorbent | [76] |
MnFe2O4/(activated carbon)AC | Sulfamethoxazole | Adsorption | [77] |
MgFe2O4/γ-Fe2O3 | Minocycline | Adsorption | [78] |
Fe3O4 MNPs in ultrasound (US)/H2O2 system | Sono-degradation | [79] | |
Fe3O4@α-MnO2 microspheres | Ciprofloxacin | Catalytic degradation | [80] |
Fe-ZnO | Diclofenac | Photocatalytic degradation | [81] |
Magnetic nanomaterials used for removal of pharmaceuticals.
Xu et al. [82] demonstrated that poly-allylamine-hydrochloride (PAAH) stabilized magnetic nanoparticles are powerful tools to remove pathogenic bacteria from drinking water with high efficiency and no significant toxicity was observed in the MNPs treated water. Over 99.5% of the pathogens (four main pathogens viz.
Zhang et al. [83] synthesized magnetic nanoparticle coated with Cu doped MgO through a hydrophilic carbon layer (Fe3O4@C@MgO-Cu). They found its potential application as disinfectant in water purification by examining the antibacterial activity of the Fe3O4@C@MgO-Cu composite toward Gram-negative
Zhang et al. [84] synthesized magnetic poly-N,N′-[(4,5-dihydroxy-1,2-phenylene)bis(methylene)]bisacrylamide) (POHABA)-based core-shell nanostructure on the Fe3O4 core surface (Fe3O4@POHABA). The magnetic nanocomposite, Fe3O4@POHABA can be used in domestic water treatment against bacterial pathogens.
Rana et al. [85] synthesized ferromagnetic Ni-doped ZnO nanoparticles and applied as an antibacterial agent to control the growth of bacterial pathogens. They found the as synthesized material to be very effective against water related bacteria such as
Shukla et al. [86] synthesized the iron oxide nanoparticles coated with chitosan oligosaccharide and used for the removal of pathogenic protozoan cysts, entamoeba cyst (which causes amebiasis) from water. They found that
Zhang et al. [87] synthesized Fe3O4 nanoparticles surrounded with polyethylenimine-derived corona and found to be efficient in capturing the pathogens and heavy metals.
Zhan et al. [88] synthesized the amine-functionalized magnetic nanoparticle (Fe3O4-SiO2-NH2) and used for rapid removal of pathogenic bacteria and viruses. The magnetic materials can be effectively used to capture a wide range of pathogens including various bacteria such as
Park et al. [89] developed a novel magnetic hybrid colloid (MHC) decorated with varying sized Ag nanoparticles. The MHC was prepared as a cluster of superparamagnetic Fe3O4 coated with silica shell. The MHC decorated with the Ag nanoparticle of 30 nm size (Ag30@MHC) exhibited the highest antimicrobial efficacy toward
Magnetic water treatment (MWT) is a new technique which is promising in environmental remediation in addition to its increased application in the area of medicine, agriculture and industrial process. The water molecules acquire unique physicochemical characteristics under the influence of the magnetic fields (MFs). It is a non-chemical method and the water molecules undergo change from their cluster of many loosely bound water molecules into very small, uniform and hexagonally organized clusters of molecules under the magnetic treatment [90]. These features of the magnetized water prevent the polluting agents to enter in to its cluster and also make their easy passage through the cells of plant as well as of animals. Moreover, the MFs have antimicrobial activity on water. Therefore, the magnetized water molecules depict as bio-friendly and eco-friendly compounds to environmental management as well as to plant and animal cells.
While taking sustainability in to consideration there are various factors over which it depends. Important factors include environmental impact on use of MNPs, toxicity associated with the MNPs, reusability, reactivity, adsorption capacity, biocompatibility, stability, etc. For example, uncoated nanoparticles are associated with some toxicity while coating can help them to make non-toxic. Similarly, their regeneration and reusability are the main factors for making them technically more viable and economically sustainable materials for commercial uses.
In this chapter the removal of water pollutants by using magnetic materials of zero valent iron, magnetite (Fe3O4), maghemite (γ-Fe2O3) as adsorbent, photocatalyst and coagulants have been described. The MNPs have been used in removal of water pollutants through their various surface functionalities (e.g., coating with polyphenols, amino acids, sugars, alkaloids, terpenoids, proteins, carbonyl, carboxyl, carbon, polysaccharides, and semiconductors) with desired size and shapes, and magnetic behavior. Looking in to the fast development of magnetic materials in different technological and scientific fields, magnetic nanomaterials appear to be extremely promising for water and wastewater treatment. The waste water treatment methods using these materials are fast, non-toxic, and eco-friendly as compared to the available physic-chemical treatments which make it attractive for materializing commercially. Their magnetic nature makes them attractive for waste water treatment because of their easy separation from aqueous medium after purification and can be reused in repeated treatment cycles. However, research for bulk production, controlling morphology, optimizing surface functionality and their stability, and biocompatibility should be essentially considered prior to commercial application from laboratory scale. Moreover, further studies needs to be addressed to detail mechanism of magnetic nanomaterials in water treatment. The magnetic nanoparticles and their composites with their high surface to volume ratio offer more surfaces for chemical as well as physical adsorption and thus show high reactivity which gives the prospects of using these materials in large scale removal of emerging water pollutants.
The utilization of renewable resources in the field of polymer synthesis has gained a great deal of attention due to the growing public concerns for the environmental concerns and the sustainable development [1, 2]. Epoxidized soybean oil (ESO) is the bio-based product from the epoxidation of soybean oil with hydrogen peroxide and either acetic or formic acid obtained by converting the double bonds into epoxy groups, which is non-toxic and of higher chemical reactivity [3]. It is mainly used as a green plasticizer for many plastics currently [4]. Meanwhile it has also attracted an increasing attention as a green epoxy resin utilizing the reactive epoxy groups into both the monomer synthesis and the polymer preparation due to its low cost, little toxicity, and large production, which imply its great potential in industrial process [5].
ESO can be converted by different kinds of reactions with co-monomers and/or initiators [6]. Permanent network that comes from the directing cross-linking of ESO and hardeners endows ESO with great stability, superior mechanical properties and satisfying chemical resistance, which make the products competitive among a variety of materials. In addition, the chemical modification of ESO has gained more and more attention in recent years. Introducing hydroxyl groups to make polyols for polyurethanes synthesis is one of the most important chemical modification methods [7]. Acrylated epoxidized soybean oil (AESO) obtained by ring opening esterification between acrylic acid and ESO is of high reactivity for thermal and UV initiated polymerization [8, 9]. This chapter reviews the applications of ESO and its derivatives for the preparation of a series of bio-based polymeric materials.
Functional amines are widely used as curing agents for generating epoxy resin. For ESO, a series of amines used as curing agents are listed in Table 1 and the reaction scheme between ESO and amine is shown in Figure 1. Most of the researchers focused on the investigation of the cross-linking process of partially bio-based polymers because of the unsatisfying properties of fully bio-based ones. Three main methods can be applied to improve the properties of ESO-based thermosets, which are using commercial curing agents, adding commercial epoxy resins to ESO, and adding other materials to make composites [10, 11, 12].
No. | Epoxy resin | Hardener |
---|---|---|
1 | ESO | Triethylene glycol diamine (TGD) [13, 14] |
2 | ESO | Triethylenetetramine (TETA) [10, 13, 15, 16, 17, 18] |
3 | ESO | Diethylenetriamine (DETA) [10, 15] |
4 | ESO | Jeffamine D-230 [10] |
5 | ESO | Jeffamine T-403 [10] |
6 | ESO | Jeffamine EDR-148 [10] |
7 | ESO + diglycidyl ether of bisphenol A (DGEBA) | TETA [11, 12, 19] |
8 | ESO + DGEBA | DETA [11, 12] |
9 | ESO + DGEBA | Jeffamine D-230 [11] |
10 | ESO + DGEBA | Jeffamine T-403 [11] |
11 | ESO + DGEBA | Jeffamine EDR-148 [11] |
12 | ESO + DGEBA | Linear polyethylenimine [12] |
13 | ESO, ESO + DGEBA | Dicyandiamide (DICY) [20] |
14 | ESO [21] | Decamethylene diamine, succinic anhydride |
15 | ESO + DGEBA | Isophorone diamine(IPDA) [22] |
Amines for curing ESO and ESO composites.
The curing process between ESO and amine curing agent [
The curing processes of ESO or the mixture of ESO and commercial epoxy resin have been investigated, and some of these systems have been made into composites through adding fibers [10, 11, 12, 14], clay [16, 18] and other reinforcement [19]. Viscoelastic properties, mechanical properties and many other analyses have been studied to evaluate their applicability to be used in industry. The partially bio-based polymers show great potential to replace fully petroleum-based polymers in many areas according to the testing results. Glass-transition (Tg) and viscoelastic properties of amine-cured ESO can be enhanced by increasing the amount of triethylenetetramine (TETA) or triethylene glycol diamine (TGD). TETA endows the polymer with similar viscoelastic properties to a commercial rubber and a higher Tg than TGD does [13]. In this respect, the biopolymers made from ESO and amines have great potential to replace some synthetic rubbers or plastics [13, 14]. Besides, the quasi-static and dynamic compressive properties of the cured products based on ESO and amines and the corresponding composites reinforced by clay have also been investigated to develop compressive one-dimensional stress-strain material models [15, 16]. Solid freeform fabrication method has been applied to the preparation of ESO-based composites and proved to be a suitable method for this kind of curing system [10, 11, 12]. ESO/TETA/clay composites show controllable biodegradability, low cost, good thermal and mechanical properties, and these properties indicates that the composites may work as alternative to petroleum-based polymers in the field of insulation materials and coating materials [18]. For clay-reinforced composites based on commercial epoxy resin the addition of ESO can enhance the impact strengths [22]. More interestingly, the product from ESO and TETA can be made into an ion-exchange resin through hydrolysis [17]. Usually, epoxy groups in the internal of the long aliphatic chain exhibits much poorer reactivity than those terminal epoxy groups. Due to this fact, the reported curing processes of ESO usually needs higher temperature and longer time than commercial petroleum-based epoxy resin, such as bisphenol A epoxy resin. However, the combination of the hardener, dicyandiamide (DICY), and the accelerator, carbonyldiimidazole (CDI), can make the gelation of ESO occur within 13 min at 190°C [20]. Moreover, the gelation of the mixture of ESO and DGEBA is achieved with the aid of DICY and CDI within 3 min at 160°C [20].
Fully or high bio-based polymers are also attractive to researchers owing to people’s strong attention to environment concerns. A series of fully bio-based elastomers have been synthesized through the ring-opening reaction between ESO and a bio-based amine hardener, decamethylene diamine, and they can be cross-linked by further reaction with another bio-based anhydride hardener, succinic anhydride [21]. These fully bio-based elastomers have great potential to replace some petroleum-based rubbers in engineering because of their good damping property, low water absorption and weak degradability in phosphate buffer solution [21].
Anhydrides, which are less toxic than amines, are another kind of mainly-used hardeners (Table 2). The structure of anhydride-cured ESO is shown in Figure 2.
No. | Epoxy resin | Hardener |
---|---|---|
1 | ESO | Maleopimaric acid (MPA) [24, 25] |
2 | ESO | Methyltetrahydrophthalic anhydride (MTHPA) [34, 35] |
3 | ESO + DGEBA | MTHPA [22, 36] |
4 | ESO [37, 38, 39, 40], ESO + DGEBA [41, 42] | Methylhexahydropthalic anhydride (MHHPA) |
6 | ESO | Maleic anhydride (MAL) [43, 44] |
7 | ESO | Phthalic anhydride [45] |
8 | ESO | Nadic methyl anhydride [46] |
9 | ESO | maleinized polybutadiene (MMPBD) [47] |
10 | ESO [30] | terpene-based acid anhydride (TPAn), maleinated linseed oil, hexahydrophthalic anhydride |
11 | ESO [44] | hexahydrophthalic anhydride (CH), MAL, succinic anhydride (SUC), dodecenylsuccinic anhydride (DDS) |
12 | ESO [26, 27, 28, 33], ESO + DGEBA [48] | Sebacic acid |
13 | ESO [33] | Adipic acid, 1,12-dodecanedicarboxylic acid, sebacic acid |
14 | ESO [32] | Citric acid, carboxylic acid functionalized MWCNTs |
15 | ESO [49], ESO + epoxidized linseed oil (ELO) [50] | Carboxyl-terminated polyester |
16 | ESO | Dicarboxyl terminated oligomeric poly(butylene succinate) [51] |
17 | ESO | Dicarboxyl-terminated polymide1010 oligomers [23] |
18 | ESO + ELO | Phosphorylated castor oil [31] |
Anhydride and acid for curing ESO and ESO composites.
The curing process between ESO and dicarboxylic acids or anhydrides [
The investigation of green anhydride curing agents is one of the research priorities. Maleopimaric acid (MPA), which comes from rosin acid, has been used for ESO curing to obtain new polymeric thermosets with a high bio-based content [24, 25]. The total heat release is only 31.7 kJ/mol epoxy group. Compared with its petroleum-based analogues, MPA endows the polymer with larger breaking elongation, higher storage modulus and better thermal stability. Sebacic acid is another bio-based curing agent for ESO in lab. A fully bio-based composite with highly improved thermal and mechanical properties can be produced through interaction between sebacic-cured ESO and PLA [26, 27]. What’s more, sebacic acid-cured ESO can be applied in the field of superhydrophobic materials to make a sustainable and biodegradable superhydrophobic material [28, 29]. Other bio-based chemicals, such as terpene [30], vegetable oils [30, 31] and citric acid [32], are all the optional raw material for green curing agents. A terpene-based acid anhydride has been found to endow ESO with higher Tg, higher tensile strength and greater modulus than maleinated linseed oil and hexahydrophthalic anhydride do [30]. But maleinated linseed oil makes the thermoset easier to biodegrade [30]. Biodegradable and biocompatible elastomers, which may be competitive in the field of implantable materials, can be obtained by curing ESO and Epoxidized linseed oil (ELO) with phosphorylated castor oil [31]. Carboxylic acid functionalized MWCNTs are always used as the filler for fully bio-based ESO/citric acid system [32]. The produced composites with good mechanical properties and high bio-based content may be applied in the field of industry [32]. Physical tests of fully sustainable polymers obtained from curing ESO with different dicarboxylic acids show the decreases of Tg and elongation at break, and the increases of tensile strength and Young’s modulus with the increasing of chain-length of the curing agents [33]. In this respect, besides bio-based micromolecular chemicals, bio-based dicarboxyl-terminated polymers are also able to work as green curing agents for ESO to make fully bio-based polymers [23]. Polymer curing agents with long chain length can avoid the short, brittle and amorphous cross-link structures which may be the reason for the poor performance of ESO-based thermosets [23].
Like the situation occurring in amine-cured systems, anhydride-cured ESO with a high bio-based content usually cannot exhibit excellent properties as petroleum-based polymers do. In order to overcome this deficiency, ESO usually works together with some petroleum-based chemicals. For this kind of complicated reaction systems, many factors are worth investigations. We are going to discuss this kind of reaction systems in terms of the properties of epoxides, the addition of commercial curing agents, the influence of the catalysts and the incorporation of fillers.
The internal epoxy rings in ESO exhibits lower reactivity than terminal ones do and the epoxy equivalent weight of ESO is usually higher than commercial epoxy resins. The addition of ESO in the mixture of DGEBA and ESO results in the increase of peak exothermic temperature, and activation energy and the decrease of enthalpy of reaction [36, 48]. Tensile strength, modulus, fracture toughness, impact strength, storage modulus (E′) in the glassy state and Tg of the cured products decrease because of the addition of ESO [36, 41]. Besides, the thermal and mechanical properties of the cured products has a positive correlation with the epoxide content of ESO [35].
Aside from the alteration of epoxides, the properties of the cured products can be enhanced with the aid of commercial curing agents. Bio-based foams based on methyltetrahydrophthalic anhydride (MTHPA)-cured ESO show similar mechanical properties to synthetic epoxy foams and the contents of ESO can be larger than 55 wt%, which indicates that this kind of green foams can be valuable alternative for commercial epoxy foams [34]. Polymers with anhydride groups [47] and dicarboxylic acids [49, 50, 51] are also able to work as curing agents for ESO. The carboxylic acid-terminated polyesters can work with ESO to produce green pressure-sensitive adhesives, which are environmentally friendly [50], thermal stable and with flame retardance [49]. In this kind of curing systems, the molecular weight of the polymer curing agents obviously have a great influence on the curing process and the physical properties of the cured bio-based products [51]. One of the remarkable advantages of bio-based polymers is their potential biodegradability. Lower crosslink density usually means higher biodegradability for ESO-based thermosets [40]. The cross-link density of the cured product reaches maximum at stoichiometric ratio between ESO and hardener [45].
Not only the properties of the main reactants, but the loading and type of the catalyst have a great influence on the on the curing process [38] final polymers [39]. The curing kinetics of ESO/methyl hexahydrophthalic anhydride (MHHPA) system show a significantly autocatalytic characteristic and ESO with 1.5 phr (parts per hundreds of resin) of 2-ethyl-4-methylimidazole (EMI) catalyst is a recommended composition for ESO/MHHPA system to be cured effectively at relative low temperature and short time [38].
ESO-based thermosets can also be used as good matrixes for organoclays [22, 35], organo-montmorillonite clay [37], proteins [46], regenerated cellulose [30] and other fillers. These works show that the thermal and mechanical properties of the composites can be improved significantly with the addition of different fillers.
Besides adding curing agents, ESO can also be cross-linked only by initiators, as shown in Figure 3. Fluoroantimonic acid hexahydrate (HSbF6·6H2O) [6] and boron trifluoride diethyl etherate (BF3·OEt2) [52, 53, 54] are commonly employed to initiate the ring-opening polymerization of ESO. As the special macromolecular structure and mechanical properties, the products have the potential to be made into hydrogels and applied in the areas of personal and health care [6, 53]. Besides, the cross-linked ESO initiated by BF3·OEt2 can be used to synthesize bio-based surfactants, which can help produce microbubbles effectively [54] and may take the place of petroleum-based detergents and surfactants [55].
Chain-growth polymerization of ESO under initiators [
Besides the curing, introducing hydroxyl groups is one of the most important chemical modification of ESO. Hydroxyl groups are functional groups that can be compatible with matrixes through hydrogen bonding or can be able to covalently bond with matrixes using some active chemicals [56].
Bio-based polyols with two or more hydroxyl groups can be synthesized from ESO by epoxy ring opening applying different approaches (see Figure 4). Ring opening reagents mainly include in mono-functional amines, alcohols (such as methanol, ethylene glycol, propylene glycol or butanol), acids (such as acrylic acid, acetic acid, phosphoric acid, fatty acids, carboxylic acid, hexanoic acids, or octanoic acids), thioethers or ketones [57, 58, 59, 60, 61, 62, 63, 64]. Lewis acid is known as a kind of useful initiator for the hydroxyl reaction with epoxides. ESO-based polyether polyols are capable to be prepared by Lewis acids catalyzing ring opening with propylene glycol [60]. After that, the ESO-based polyether polyols with higher molecular weight can be cured with phenolic, melamine and other conventional crosslinkers to give reasonable film properties [65]. Besides, ESO phosphate ester polyols have been synthesized by using super phosphoric acid phosphorylated ESO, which is able to be incorporated in bake coatings with excellent performance [62]. A series of methoxylated soybean oil polyols (MSOLs) have been prepared with different hydroxyl functionalities by the ring opening of ESO with methanol [66]. These polyols have been applied to synthesize the environmentally friendly vegetable-oil-based polyurethane dispersions (PUDs) with very promising properties. Thioglycolic acid (TGA) bearing thiol and carboxylic acid as two different functional groups, glycolic acid (GA) containing hydroxyl and carboxyl functionality and methyl ester of thioglycolic acid (TGAME) have been also used as ring opening agents of ESO to synthesize novel bio-based polyols [57, 67]. Using TGA and GA, the epoxy rings are opened by the carboxylic acid group, while the epoxy rings are opened by the thiol group primarily when using TGAME. In addition, polyols obtained by ring opening with TGA have higher molecular weight comparing to GA and TGAME. That is because some of the thiol groups of TGA initially remain intact and then are involved in ring opening of other epoxy groups resulting in chain coupling [57, 67].
Epoxy ring opening reactions with various ring opening reagents [
There are some side reactions occurring during the ring-opening of ESO epoxide groups, and these side reactions often depend on reaction parameters [68, 69]. A substantial degree of oligomerization due to oxirane-oxirane, and oxirane-hydroxyl reaction will take place in the presence of phosphoric acid. It is possible to synthesize ESO-based polyols having varying hydroxyl content and phosphate-ester functionality by controlling the type and amount of polar solvent and phosphoric acid content [70]. Inter-esterification or intermolecular ether formation are also observed as side reactions, depending on the molar proportion of the hydrogen donor [68]. Different catalysts for the ring opening of the epoxide groups in ESO have been evaluated in many works. The most common catalysts are sulfuric acid, p-toluenesulfonic acid, perchloric acid, tetrafluoroboric acid (HBF4) and activated clays. HBF4 have been found to produce polyols with a higher OH content, and lower viscosity than other catalysts in the ring opening reaction of ESO with methanol [69]. And, triflic acid is a very effective catalyst for preparing ESO polyether polyols [60]. As alcohol concentration relative to ESO is reduced, higher molecular weight polyether polyols can be produced in a controlled way [60].
Currently, vegetable oils-based polyols are gradually replacing petroleum-based hydroxyl for preparing PUs, which are considered as sustainable and environmentally friendly polymers from biomass industry [5]. ESO based polyols can be co-polymerized with some commercial isocyanates, such as toluene di-isocyanate (TDI), methylene-4,49-diphenyldiisocyanate (MDI) or others, to obtain bio-based PUs with useful properties, including enhanced hydrolytic and thermal stability, as shown in Figure 5.
Synthesis of soybean-oil-based PUs [
The structure-property relationships between ESO based polyols and PUs have been extensively investigated. Several factors have important influences on the properties of the PUs, such as chemical structure of the segment, chemical composition, hydroxyl group position, hydroxyl values of polyols and cross-linking densities of the PUs networks [71]. The structure and properties of PUs prepared from halogenated as well as non-halogenated soybean polyols with commercial isocyanates have been studied which shows that brominated polyols and their corresponding PUs have the highest densities and Tg while their thermal stabilities are lowest. Chlorinated polyols have comparable glass transition and strength to brominated polyols, somewhat higher than the methoxy-containing and hydrogenated polyols [69]. Besides, the NCO/OH mole ratios also show effects on the properties of the PUs networks that the cross-linking densities, Tg, and tensile strengths deteriorate as the NCO/OH ratios decrease and glassy polymers can be produced when the NCO/OH ratio is between 0.8 and 1.05 [72]. The studies on polyurethane resins from a blend of glycerol and polyol show that the increasing of Tg caused by the incorporation of glycerol into soy polyols obviously enhances the rigidity of PUs [73]. The polyurethanes elastomers synthesized from ESO based polyols obtained by ring opening with Ricinoleic acid (RA) and sebacic acid with citric acid as the cross-linker display biocompatibility and biodegradability and are very suitable for bone tissue engineering [74].
Furthermore, ESO is able to be effectively converted to carbonated soybean oil (CSBO) containing five-membered cyclic carbonates by reacting with carbon dioxide in the presence of tetra-butylammonium bromide at 110°C in high yield [75]. Then, CSBO can easily react with diamines to give the corresponding non-isocyanate polyurethane networks(NIPUs), and the thermal and mechanical properties of NIPUs can be well adjusted and controlled by changing the CSBO/amine ratio [76].
AESO is commercially-manufactured derivative of ESO and has been extensively used in coatings, resins and composites. The acid-catalyzed synthesis process of AESO is shown in Figure 6. The acid catalyst promotes the formation of an oxonium ion, which can be stabilized by local epoxide group. And the ring-opening reaction happened between acrylic acid and the oxonium ion. Inhibitor is needed in this reaction to prevent polymerization of vinyl groups. The acrylation reaction has a first-order dependence on the concentration of epoxy groups, but the rate constant increases with the decreasing of epoxides per fatty acid due to steric hindrance and the stabilization effect of local epoxide group on oxonium groups [77].
Mechanism of AESO synthesis [
Through reversible addition-fragmentation chain transfer (RAFT) polymerization, AESO can be made into a hyper-branched bio-based polymer without macro-gelation [8, 79]. The conversion of vinyl is usually over 50%, which indicates that it is possible for multifunctional renewable feed stocks to be made into bio-based thermoplastics polymers at a high conversion without gelation [8].
Most of the researches focused on the cross-linking reaction of AESO through free radical polymerization. Like the ESO, the cross-linked homopolymers from AESO also have the shortage that the polymers exhibit poor mechanical properties [80]. One of the common methods used to enhance its mechanical properties is adding reinforcements to make polymer composites. There are many polar groups in the structure of AESO, including C〓O, ▬OH and epoxy groups. These polar groups provide the possibility for the formation of hydrogen bonds between AESO and fillers [80]. Thermoplastic polyurethane [81], microcrystalline cellulose (MCC) [80] and cellulose fiber [82] are the common reinforcements worth investigation for poly(acrylated epoxidized soybean oil)(PAESO). The interaction between PAESO and polyurethane can be enhanced by the formation of hydrogen bonds between hydrophilic functional groups from both of the two components which give rise to the result of improving the toughness and increasing the elongation of PAESO [81]. As a green filler, microcrystalline cellulose will increase the density, hardness, flexural strength and modulus of the material without decreasing the bio-based content [80]. Cellulose-reinforced PAESO can also be successfully made into bio-based foams with enhanced mechanical properties, which shows the great potential to replace petroleum-based foams [82].
Another common way to adjust the properties of AESO-based materials is the incorporation of co-monomers. Styrene [83, 84, 85, 86], N-vinyl-2-pyrrolidone (NVP) [64, 87], 3-isopropenyldimethylbenzyl isocyanate (TMI) [88], isocyanatoethyl methacrylate (IEM) [88], 1,6-hexanediol diacrylate [89], divinylbenzene [86, 89] and unsaturated polyester [90, 91, 92, 93, 94] are widely used as co-monomers for AESO. The diblock copolymers based on AESO and styrene are able to work as an additive for asphalt to modify the rheological performance so that the corresponding stiffness, elasticity and rutting resistance of the asphalt can be substantially improved [83]. The copolymer based on AESO and styrene can also be reinforced by natural fibers [84] and denim [85] to obtain bio-based composites for structural applications, such as roof structure and safety helmets. Due to the toxicity of styrene, styrene-free polymers become more attractive recently. NVP is an alternative to styrene in the synthesis of copolymer based on AESO, and the corresponding hemp fibers (HFs) composites exhibit superior static and dynamic mechanical properties [64]. As both AESO and HFs contains ▬OH groups in their structures, the addition of isophorone diisocyanate, whose isocyanate groups can react with ▬OH groups, to the AESO/HFs/NVP system can improve the properties by working as both a cross-linker and a coupling agent [87]. Accordingly, TMI and IEM bringing both C〓C double bonds and isocyanate groups into the reaction systems may also be good co-monomers for AESO/HFs system. Besides the free radical polymerization of vinyl groups, the reactions between isocyanate groups and the ▬OH groups of AESO and HFs also occurred at the same time in this bio-based polymer composite systems [88]. Consequently, the crosslinking density and interfacial reaction between reinforcement and the matrix can be improved significantly, leading to the enhancement of storage modulus, Tg and water resistance. As a nonvolatile and nonhazardous chemical, AESO is a suitable replacement for styrene in unsaturated polyester (UPE) resin to obtain hybrid polymer networks [90, 91, 92, 93, 94]. The UPE with unsaturated sites works as the co-monomer for AESO, and the final products usually exhibit comparable properties to correspondingly styrene-based products. The combination of a variety of co-monomers may provide AESO based copolymers with more possibilities. The thermosets based on the combination of AESO, styrene and divinylbenzene can be the potential replacements for commercial electronic materials [86]. The combination of AESO, 1,6-hexanediol diacrylate and divinylbenzene is able to make into the matrix for bacterial cellulose nanocomposite foams and the properties of the composites can be tailored by adjusting the compositions [89].
Although petroleum-based co-monomers can bring excellent properties, the decrease of the bio-based content is still not expected. Functional bio-based co-monomers are desired in consequence. Isosorbide can be used to synthesize a bio-based co-monomer for AESO through the reaction with methacrylate anhydride [95]. The product, isosorbide-methacrylate (IM), which has stiff structure, endows the bio-based networks with ideal thermal and mechanical properties. Similarly, rosin is also a bio-based raw material with a rigid molecular structure. Its derivative, N-dehydroabietic acrylamide (DHA-AM), can enhance the storage modulus, Tg, thermal stability, tensile strength and hydrophobicity of AESO/DHA-AM thermosets [96]. Methacrylated lauric acid (MLAU) is another bio-based reactive diluent for AESO. The mixture exhibits a suitable viscosity for liquid molding techniques to get AESO based thermoset specimens with low densities and Tg around room temperature [97].
AESO has been widely applied in the UV curing systems for their lower volatility and relatively higher reactivity of C〓C bonds which are able to conduct free-radical polymerization in the presence of functional initiator. In general, residual internal stress in the UV-curing coating film often leads to poor adhesion with substrate. AESO can be used to synthesize cured films with reduced internal stress and its flexible triglyceride structure can improve adhesion [9]. UV-curable materials based on AESO have been found many applications like coatings, adhesives and composite materials [98]. As petroleum-based fiber composites often swell after water absorption resulting in deterioration of mechanical properties, the dried distillers grains (DDGS)-flax mat coated with AESO polymerized by UV light with the initiation of irgacure 819 shows improved water resistance property [99]. Besides, AESO-based UV-cured PUDs with higher functionality can be used in textiles printing. Different content of AESO based UV-curable PUDs pigment prints adhesive have been successfully synthesized with isophorone diisocyanate (IPDI), poly(caprolactone glycol) and 2-hydroxyethyl methacrylate, and all UV-curing films have excellent thermal stability [98]. With the increasing of AESO content, the color strength of printed fabrics can be enhanced correspondingly. Conversely, the increasing of UV radiation time shows positive impact on the color fastness [100]. UV-curable, AESO-based organic shape-stabilized phase change materials also can be obtained by UV technique with enhanced thermal performance, decreased melting and freezing temperature, which verify the promising application of UV-curable material for thermal energy storage [100].
However, the existing of soft long aliphatic chains usually results in low mechanical or thermal properties and some rigid compounds are often added as the co-monomers to improve the performances of AESO-based UV-curable materials. Acrylate acid is one of the most common-used petroleum-based rigid compounds. The performances of AESO-based UV curable coating materials by using petroleum-based hyper-branched acrylates (HBAs) as co-photo-polymerization monomer, using acrylated sucrose (AS) as tougheners and using tetra-hydrofurfural acrylate (THFA) as reactive diluents show the increased coating hardness, adhesion, modulus, solvent resistance and glass transition temperature [101]. Nowadays, many researchers are devoted to exploit bio-based co-monomers to develop high bio-based content UV-curable coatings. Monomer acrylated betulin (AB) synthesized from botulin [102], unsaturated monomer (named IG) synthesized from itaconic acid and glycidyl methacrylate [103], monomers (named EM2G and EM3G) synthesized from eugenol via a thiol-ene reaction and epoxide ring-opening reaction [104] have been all evaluated to be successfully used with AESO matrix polymer and have great potential to improve the properties of UV curable coating. Coating films containing AB from 5 to 10 wt% contents have better modulus of elasticity, tensile strength, abrasion resistance and hardness, higher Tg and lower strain at break value, while the transmittance of the cured films is reduced with increasing AB loading, especially for wavelengths below 650 nm. In comparison, the polycyclic structure of betulin imposes a more rigid structure on AESO matrix polymer to enhance the applied performance [102]. In the presence of irgacure 184 as initiator, a series of UV-cured coatings without any solvent can be successfully prepared with IG (EM2G or EM3G) and AESO, and EM2G and EM3G show higher reactivity when copolymerized with AESO. The introduction of IG, EM2G and EM3G in the UV-curing system results in significantly improved mechanical and thermal properties as well as coating performances such as hardness, flexibility, adhesion, solvent resistance [103, 104].
ESO is initially used as a plasticizer in industry for poly(vinyl chloride) chlorinated (PVC) rubber, and poly(vinyl alcohol) (PVA) emulsions to improve stability and flexibility [105, 106], and ESO is also considered to be potential nontoxic biocompatible plasticizers for poly(3-hydroxybutyrate) (PHB) and polylactic acid (PLA) when combined with other plasticizers [107, 108, 109]. Moreover, it is an interesting trend to prepare composites of ESO or its homo-polymers with other materials because of their special properties. A double network composites with ESO and a di-hydrocoumarin derived network can been synthesized with toughening effect, which make the ESO-based polymer possible to be applied in the fields of coatings and films [110]. The composites of cross-linked ESO and acrylic monolith [111] or poly(lactic acid) [112] apparently exhibit much larger Young’s modulus and tensile strength than ESO homo-polymer and can work as shape memory materials, which makes ESO a potential component for manufacture of intelligent polymer materials.
Interestingly, the long chain alkane fatty acid residues in ESO can give the composites hydrophobicity, so cross-linked ESO can also work as a water-resistant film for paper that the obtained composites may be competitive in the field of packaging considering their good properties [113]. An efficient method has been reported for the formation of cellulose-based materials grafting with poly epoxidized soybean oil (PESO) with controllable hydrophobic properties [114] 1–2. A kind of PESO coated paper composites with good water-resistant property have been obtained via in situ polymerization of ESO on the surface of the paper cellulose fibers [113].
This chapter summarizes the most recent advances in the application of ESO and its derivatives for preparation of bio-based polymeric materials. The multiple reactive epoxy groups from triglycerides of unsaturated fatty acids imply its great potential in the bio-based polymer preparation fields with controllable biodegradability, thermal and mechanical properties. ESO can crosslink directly with variety curing agents to form permanent network, or to introducing reactive function groups by chemical modifications. Two most important modifications are introducing hydroxyl groups and esterification to produce acrylates. Based on these, varieties of new polymeric materials have been prepared recently from ESO and derivatives that exhibit industrially viable thermos-physical and mechanical properties and thus may find many possible applications. It is believed that ESO based compounds will gain continuously strong interest and allow new developments both in academic and industrial points of view.
The authors are grateful to the National Key Research and Development Program of China (Grant no. 2016YFB0302701), the National Natural Science Foundation of China (Grant no. 21676083), the Shanghai Rising-Star Program (Grant no. 16QB140130), the Fundamental Research Funds for the Central Universities, and the 111 Project (B08021).
The authors have declared that no conflict of interest exists.
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All published Book Chapters are licensed under a Creative Commons Attribution 3.0 Unported License. Monographs are licensed under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) license granted to all others. Our Copyright Policy aims to guarantee that original material is published while at the same time giving significant freedom to our Authors. IntechOpen upholds a flexible Copyright Policy meaning that there is no copyright transfer to the publisher and Authors hold exclusive copyright to their work.
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