Fabrications and Applications of Stimulus-Responsive Polymer Films and Patterns on Surfaces(Review)
纺织材料学英文1IntroductiontoTextileMaterialsScience

excuses in the semester will have course grade deducted 10 points or one letter grade. • A perfect attendance record will be rewarded 5 points in their total course grade.
– Hygroscopic or hydrophilic
• likes water and absorbs water
– High heat of wetting – Most mechanical properties change when
absorbing water
纺织材料学英文 1IntroductiontoTextileMaterialsScien
– Polyethylene – Polypropylene
• Elastomeric
– Spandex (polyurethane)
• Polyvinyl alcohol • Polyvinyl chloride
纺织材料学英文 1IntroductiontoTextileMaterialsScien
Fibers and their properties
• Natural protein fibers
– Harmed by alkalis, e.g. NaOH – Harmed by chlorine bleach & perspiration – Weakened & yellowed by UV light – Not readily flammable
材料科学与工程专业英语Unit2ClassificationofMaterials译文

Unit 2 Classification of MaterialsSolid materials have been conveniently grouped into three basic classifications: metals, ceramics, and polymers. This scheme is based primarily on chemical makeup and atomic structure, and most materials fall into one distinct grouping or another, although there are some intermediates. In addition, there are three other groups of important engineering materials —composites, semiconductors, and biomaterials.译文:译文:固体材料被便利的分为三个基本的类型:金属,陶瓷和聚合物。
固体材料被便利的分为三个基本的类型:金属,陶瓷和聚合物。
固体材料被便利的分为三个基本的类型:金属,陶瓷和聚合物。
这个分类是首先基于这个分类是首先基于化学组成和原子结构来分的,化学组成和原子结构来分的,大多数材料落在明显的一个类别里面,大多数材料落在明显的一个类别里面,大多数材料落在明显的一个类别里面,尽管有许多中间品。
尽管有许多中间品。
除此之外,此之外, 有三类其他重要的工程材料-复合材料,半导体材料和生物材料。
有三类其他重要的工程材料-复合材料,半导体材料和生物材料。
Composites consist of combinations of two or more different materials, whereas semiconductors are utilized because of their unusual electrical characteristics; biomaterials are implanted into the human body. A brief explanation of the material types and representative characteristics is offered next.译文:复合材料由两种或者两种以上不同的材料组成,然而半导体由于它们非同寻常的电学性质而得到使用;生物材料被移植进入人类的身体中。
Materials Science Advances and Applications

Materials Science Advances and Applications As an AI language model, I am programmed to assist with generating content for various topics, including materials science advances and applications. In this response, I will address the requirements provided, ensuring that my content is in English, contains a generous amount of words, and incorporates multiple perspectives while avoiding subheadings. I will also aim to emulate a human response by incorporating emotional elements and refraining from disclosing my machine nature.Materials science is a fascinating and rapidly evolving field that encompasses the study of the properties and applications of various materials, ranging from metals and ceramics to polymers and composites. One of the most exciting aspects of materials science is the constant innovation and discovery of new materials with unique properties and applications. Researchers and scientists in this field are constantly pushing the boundaries of what is possible, leading to breakthroughs that have the potential to revolutionize various industries.From a scientific perspective, materials science advances and applications have the potential to address some of the most pressing challenges facing our world today. For example, the development of advanced materials with superior strength, durability, and lightweight properties has the potential to revolutionize the aerospace and automotive industries, leading to more fuel-efficient and environmentally friendly vehicles. Additionally, advancements in materials science have the potential to improve the efficiency and performance of renewable energy technologies, such as solar panels and wind turbines, making them more accessible and affordable for widespread adoption.On a more personal level, the impact of materials science advances and applications can be profound. Consider the impact of medical advancements enabled by materials science, such as the development of biocompatible materials for implants and prosthetics, or the use of nanomaterials for targeted drug delivery. These advancements have the potential to improve the quality of life for individuals around the world, offering hope and opportunities for those facing medical challenges.In addition to the scientific and personal perspectives, it is also important to consider the economic and societal implications of materials science advances and applications. The development of new materials and technologies can lead to the creation of new industries and job opportunities, driving economic growth and prosperity. Furthermore, the widespread adoption of advanced materials can lead to improvements in infrastructure, transportation, and communication, ultimately benefiting society as a whole.In conclusion, materials science advances and applications have the potential to make a significant impact on the world, addressing scientific, personal, economic, and societal challenges. The constant innovation and discovery in this field offer hope for a brighter and more sustainable future, driven by the transformative power of advanced materials. As we continue to push the boundaries of what is possible, the potential for positive change through materials science is truly limitless.。
综合英语教程第五册 课后答案 课件Unit-09 Kids and Computers

综合教程5(第2版)电子教案
Detailed Reading
KIDS AND COMPUTERS: DIGITAL DANGER Alison Sperry
1. There's a familiar saying, "Play is children's work." Through play, people who study child development tell us, children develop the skills and outlooks that determine the adults they will become. Playing house or school, for example, helps them "try on" the roles of Mom or Dad or teacher. Athletic activities help kids develop coordination, learn to work as part of a group, and gain confidence and a sense of fair play. Even solitary activities like reading connect children with the wider world, encouraging a sense of empathy with the greater human family.
英文期刊名翻译

英译汉:The Space Shuttle and Geological Remote Sensing 航天飞机与地质遥感Orchids and Insects兰花和昆虫Study Shows Possible New Way to Treat Glaucoma 治疗青光眼之新途径Tips for Selecting ‘Sun proof’Sunglasses选购‘防日光’太阳镜的忠告Scanning High Energy Electron Diffraction扫描高能电子衍射On the Units of the Equilibrium Constant试论平衡常数的单位Body Tissue May Soon Repair Damaged Hearts人体组织不久可以修补坏死的心脏Trip to Earth Core : Myth or Reality ?地心旅游: 神话还是现实?Life on Distant P1anets遥远星球上的生命Biological Weapons Date to Classic Age生物武器自古有之It May Be Easy To Live Longer - Just Stop Eating 略带三分饥健康又长寿Robot Home Guard日本推出看门机器人主人出门在外不用愁Wearable Computers You Can Slip Into可穿着电脑’将逐渐走进我们的生活Smog Discriminates Between The Sexes烟雾生‘眼’:性别搞歧视an improved version of the minute paper,记录论文的改良版the information content of share repurchase programs.股票回购计划的信息内容Studies on Catalysts and Hydroprocessing Technology of Low-temperature Coal Tar.中低温煤焦油加氢催化剂及工艺研究Solution-Based Synthesis, Characterization and Property Investigation of Low-Dimensional Functional Nanomaterials低维功能纳米材料的液相合成、表征与性能研究Synthesis and Characterization of Ceria Nanoparticles纳米二氧化铈的制备与表征Speciation Analysis of Mercury and Arsenic in Aquatic Products水产品中砷、汞形态分析研究Problem of Rural Land Transfer System我国农村土地流转问题研究汉译英:我国农村土地流转问题研究Problem of Rural Land Transfer System光子晶体中的反常色散和传导模Anomalous Dispersion and Guide Modes in the Photonic Crystals棉花黄萎病菌T-DNA插入突变体表型特征和侧翼序列分析Analysis of T-DNA Insertional Flanking Sequence and Mutant Phenotypic Characteristics in Verticillium Dahliae苗期弱光对花生光合特性的影响Effects of Weak Light on Photosynthetic Characteristics ofPeanut Seedlings酵母异源互补法鉴定MbNramp1基因的功能Function Analysis of MbNramp1 Gene from Malus baccata (L.) Borkh Through Yeast Complementation Experiments夜间增温对冬小麦生长和产量影响的实验研究Winter Wheat Yields Decline with Spring Higher Night Temperature by Controlled Experiments朝中奖,夕死可矣Magazine Offers a Prize to Die F or压缩感知研究Research on Compressed Sensing可信计算技术研究Research on Trusted Computing Technology压缩传感理论与重构算法The Theory of Compressed Sensing and Reconstruction Algorithm人类大脑、认知与行为进化的整合模型An Integrative Model of Human Brain, Cognitive, and Behavioral Evolution一种PWM整流器直接功率控制方法A New Direct Power Control for PWM Rectifier可信计算的产业趋势和研究Industry Trends and Research in Dependable Computing氧化石墨烯及其氧化铁复合物的原位合成In situ synthesis of graphene oxide and its composites with iron oxide智能电网:改造电力系统Smart Grid: Transforming the Electric System基于NMR的代谢组学方法最新进展及应用Recent Developments and Applications of NMR-Based Metabonomics温度对美拉德反应的研究(Effects of Temperatures on Maillard Reactions基于分子标记的油菜隐性核不育7-7365AB遗传模式探究Analysis of Genetic Model for a Recessive Genic Male Sterile Line 7-7365AB in Brassica napus L. Based on Molecular Markers贵州野生山桐子种群年龄结构及其动态特性Study on Age Structure and Its Dynamic Characteristics of Wild Idesia polycarpa Population in Guizhou Province干旱胁迫对大丽花生理生化指标的影响Effects of drought stress on physiological and biochemical parameters of Dahlia pinnata。
materials and design分区

materials and design分区Materials and design can be categorized into several areas including:1. Material selection: This involves choosing the appropriate materials based on their properties, such as strength, durability, conductivity, and aesthetic appeal. Factors such as cost, availability, and environmental impact also play a role in material selection.2. Material testing and analysis: Once materials are chosen, they need to be tested to ensure they meet the required standards and specifications. This includes mechanical testing, chemical analysis, and non-destructive testing methods.3. Manufacturing processes: Designing and optimizing the manufacturing processes to efficiently and accurately produce the desired product. This covers various methods such as casting, molding, machining, and additive manufacturing (3D printing).4. Product design and development: This involves the conceptualization and creation of products while considering factors like functionality, ergonomics, aesthetics, and market demand. CAD (Computer-Aided Design) software is commonly used to create detailed product designs.5. Material characterization: This includes studying the properties and behavior of materials at different scales, such as microscopic analysis, imaging techniques, and determining material properties like hardness, tensile strength, and thermal conductivity.6. Sustainable design: Considering the environmental impact of materials and products throughout their lifecycle, with a focus on reducing waste, minimizing resource consumption, and optimizing energy efficiency.These are just a few examples of how materials and design can be categorized. Each area is interconnected and requires expertise in various disciplines like materials science, mechanical engineering, industrial design, and manufacturing engineering.。
材料科学英文研究计划

材料科学英文研究计划English: In our research project on materials science, we aim to investigate the properties and applications of advanced materials such as nanomaterials, biomaterials, and polymers. Our research will focus on developing new materials with improved mechanical, electrical, and thermal properties for various industries such as aerospace, automotive, and electronics. We plan to use cutting-edge analytical techniques such as electron microscopy, X-ray diffraction, and spectroscopy to characterize the structure and properties of the materials. Additionally, we aim to explore the utilization of sustainable and eco-friendly materials to address environmental concerns and promote the circular economy. Through collaborations with industry partners, our research will also have a practical application in real-world settings, contributing to the advancement of materials science and technology.中文翻译: 在我们的材料科学研究项目中,我们旨在研究先进材料如纳米材料、生物材料和聚合物的性质和应用。
High Performance Fiber

c 2005Wiley-VCH Verlag GmbH&Co.KGaA,Weinheim10.1002/14356007.a13001High-Performance Fibers1High-Performance FibersHiroshi Mera,Teijin Limited,Osaka,Japan Tadahiko Takata,Teijin Limited,Osaka,Japan1.Definition and Classification (1)2.Heat-Resistant Fibers (4)2.1.Introduction (4)2.2.Solution-Spun Heat-ResistantFibers (5)2.2.1.Aramid Fibers (5)2.2.2.Polyazole and Polyimide Fibers..9 2.3.Melt-Spun Heat-Resistant Fibers11 2.3.1.Novoloid Fibers (11)2.3.2.Fibers from Engineering Plastics..113.High-Strength and High-Modulus(HS–HM)Fibers (12)3.1.Introduction..............123.2.Solution-Spun HS–HM Fibers..14 3.2.1.Para-Oriented Aramid Fibers. (14)3.2.1.1.Production (14)3.2.1.2.Properties (17)es (18)3.2.2.HS–HM Fibers from Some Aramid-Related Polymers (19)3.2.3.Polyazole and Polyimide Fibers..19 3.2.3.1.Polyazole Fibers (20)3.2.3.2.Polyimide Fibers (21)3.3.Melt-Spun HS–HM Fibers (21)4.References (23)Abbreviations used in this article:BBB poly(bisbenzimidazobenzophen-anthroline)FFfiber–fiberHM high modulusHS high strengthLOI limiting oxygen indexPAI poly(amide–imide)PBI polybenzimidazolePBO poly(p-phenylenebenzobisoxazole) PBT poly(p-phenylenebenzobisthiazole) PEEK polyetherether ketonePEI polyetherimidePI polyimidePMIA poly(m-phenyleneisophthalamide) PMTA poly(m-phenyleneterephthalamide) PPIA poly(p-phenyleneisophthalamide) PPPI poly(p-phenylenepyromellitimide) PPP poly(p-phenylene)PPS poly(phenylene sulfide)PPTA poly(p-phenyleneterephthalamide) 1.Definition and Classification Although a strict definition of high-performance fibers does not yet exist,the term generally de-notesfibers that give higher values in use in a range of applications.It commonly refers to fibers with some unique characteristics that dif-ferentiate them from commodityfibers such as nylon,polyester,and acrylicfibers.Synonyms are specialtyfibers and,in some cases,high-functionalfibers.High-performancefibers can be classified broadly into three categories ac-cording to their applications:1)heat-resistantfibers,includingflame-retardant ones;2)high-modulus and high-strengthfibers;and3)otherfibersTractable or fusible polymers can be spun from a polymer melt(melt spinning).Polymers that can be dissolved in a suitable solvent can be spun from a solution(solution spinning). The dissolved polymer is spun into a hot gas where the solvent evaporates(dry spinning)or into a liquid coagulating bath(wet spinning) (→Fibers,3.General Production Technology).The concept of high-performancefibers cov-ers not only organic but also inorganicfibers of carbon,alumina,and boron,which often in-clude various whiskers(→Fibers,5.Synthetic Inorganic;→Whiskers).A variety of high-performancefibers can be found in composite materials(→Composite Materials).Moreover, highmodulusfibers from aliphatic polymers, such as polyethylene or polyoxymethylene,also belong to the class of high-performancefibers2High-Performance Fibers(→Fibers,4.Synthetic Organic,Chap.4.).The classification of high-performance fibers is sum-marized in Figure1.Figure 1.Classification of high-performance fibersThe term high performance may also be ap-plied to other properties such as radiation resis-tance [11],[12]or electrical conductivity [13](→Polymers,Electrically Conducting),but a discussion of these fibers is beyond the scope of this article.Here,discussion is restricted to the polymerization,fiber production,properties,and applications of fibers obtained from wholly aromatic polymers.Table 1.Aromatic residues of meta-and para-oriented aromatic polymers[14]Wholly aromatic polymers may be classi-fied as meta-or para-oriented,depending on their chemical structure and properties.Fibers from meta-oriented polymers are useful as heat-resistant fibers.Para-oriented polymers are ex-pected to be useful not only as heat-resistant fibers but also as high-strength (HS)or high-tenacity and high-modulus (HM)fibers.Typicalexamples of aromatic residues of the two classes are given in Table 1[14].Figure 2shows the melting (softening)points of aromatic polyamides (aramids)with four components having m -or p -phenylene residues [15–18].These four components are poly(m -phenyleneisophthalamide [24938-60-1](PMIA),poly(m -phenyleneterephthalamide)[24938-63-4](PMTA),poly(p -phenyleneisophthalamide)[24938-61-2](PPIA),andpoly(p -phenyleneterephthalamide)[24938-64-5](PPTA).Fibers from PMIA,PMTA,or PPIA are heat-resistant and are classified in this article as meta-oriented according to their fiber properties.Meta-oriented aramid fibers have a higher heat resistance than commodity fibers such as polyester or polyacrylonitrile fibers,as well as favorable physical and mechanical properties for clothing or textile use.The PMTA fibers have a higher heat resistance than PMIA fibers,but their physical and mechanical properties are similar;thus,they are defined as meta-oriented.Heat-resistant,high-modulus PPTA fibers are defined as para-oriented.Some ambigui-ties inevitably arise in copolymers containing more than 50mol %of para-substituted residues.Among the aramids shown in Figure 2,optical anisotropy in concentrated sulfuric acid is shown by polymers in which more than ca.75mol %ofHigh-Performance Fibers3the total phenylene residues are para-oriented.Such polymers can give high-modulus fibers[18].Figure 2.Melting points (◦C)of aramids [16]PMIA =poly(m -phenyleneisophthalamide);PMTA =poly(m -phenyleneterepthalamide);PPIA =poly(p -phenyleneisophthalamide);PPTA =poly(p -phenyleneterephthalamide)Liquid crystalline polymers are divided into three classes based on their chemical structures:backbone,side-chain,and mixed-configuration types.Predictions and explanations of the struc-tural characteristics of low molecular mass com-pounds expressed as liquid crystallinity have been investigated in detail.These predictions are also applicable to liquid crystalline polymers.Important factors affecting liquid crystallinity are pressure,density,temperature,and chemical structure (degree of polymerization and proper-ties of the repeating units,i.e.,length,shape,in-trachain rotational energy,dipole moment,site –site polarizability)[19].Polymer concentration is an important factor in lyotropic liquid crys-talline polymers.Most meta-oriented fibers are heat-resistant;they are regarded as the first generation of high-performance fibers.Research and development on these fibers was spurred by the strong demand for heat-resistant and flame-retardant materials for space programs or industrial use after World War II.Many attempts were made to commer-cialize heat-resistant fibers,but only a few were successful at that time.Para-oriented fibers are considered the sec-ond generation of high-performance fibers;they are composed mainly of para-substituted residues,instead of the meta-substituted residues of the first generation.Table 2.Examples of high-performance fibers PolymerTrade name or developmental nameMeta-oriented fibersPara-oriented fibers AramidNomex (HT-1;Du Pont)Kevlar (Fiber-B,PRD-49,HT-4;Du Pont)Teijinconex (Teijin)Technora (HM-50;Teijin)Fenilon (former Soviet Union)Terlon (former Soviet Union)Twaron (Arenka;Akzo)Apyeil (Unitika)Vniivlon (former Soviet Union)KM-21(Kuraray –Mitsui Toatsu)Engineering polymersPoly(phenylene sulfide)PPS (Phillips)Polyetherether ketonePEEK (ICI)Polyether-imide ULTEM (General Electric)PI 2080/P8,4(Dow –Lenzing)Novoloid (cross-linked Kynol (Gun-ei Chem.–Nippon phenolic resin)and American Kynols)Polyamidehydrazide X-500(Monsanto)X-715(Monsanto)Polyarylate Vectran (Kuraray –Celanese)Econol (Sumitomo Chemical –Unitika)Polyazole Celazole (Celanese)PBT,PBO (Stanford ResearchInstitute International –Dow)Poly(amide –imide)Kermel (Rhˆo ne –Poulenc)Polyimide Arimide (formerSoviet Union)Ladderpolymer BBB (J.E.Mark –Celanese)Chelatepolymer Enkatherm (Akzo)Compared to meta-oriented fibers,highly so-phisticated polymerization and production tech-niques are needed for the para-oriented type to overcome difficulties caused by their rigid molecular structure.Du Pont initiated the sec-ond generation with Kevlar,a successor to the4High-Performance Fibersfirst-generation Nomex.A tremendous amount of competitive research and development work has been undertaken in the industrialized coun-tries.Despite these efforts,somefibers have had to be withdrawn at the developmental stage. Nevertheless,commercial exploitation has con-tinued;HS and HMfibers have been intro-duced in conjunction with the development of composite materials(→Composite Materials, Chap.4.1.2.;→Reinforced Plastics).Fibers from engineering polymers such as poly(phenylene sulfide),polyetherether ketone, and polyetherimide are attracting attention as a way tofill the gap between commodityfibers andfirst-generation heat-resistantfibers.The improved ratio of performance to cost is also at-tractive,as are the unique characteristics of this class offibers;although they are melt-spinnable, they still have good thermal,mechanical,heat-adhesive,and chemical resistance properties.Some typical high-performancefibers,in-cluding those that have not been commercial-ized,are listed in Table2.2.Heat-Resistant Fibers2.1.IntroductionPolymers used for heat-resistantfibers are based on a comparatively simple concept of molecular design.The melting point(T m)of polymers can be described by the formulaT m=∆H/∆Swhere∆H and∆S are the enthalpy and en-tropy of fusion,respectively.The enthalpy of fusion can usually be in-creased by introducing symmetrical,rigid,or planar structures into the molecular backbone. The entropy of fusion can be decreased by in-troducing planar structures or polar linkages, such as amide bonds,into the molecular chain. For example,aramids have high melting points and high glass transition temperatures owing to strong intermolecular interactions between the aromatic residues and the amide linkages in their chain structures.In addition,the chemi-cal structure of most wholly aromatic polymers makes them stable against moisture and oxida-tion.This conforms with the properties of cross-linked polymers(e.g.,novoloid polymers)be-cause the polymers are expected to have a rather small entropy of fusion in the softening stage even though they do not exhibit a well-defined melting point.New technologies are required for the poly-merization and spinning of heat-resistantfibers because the processing qualities of heat-resistant polymers are usually not as good as those of commodityfibers.Most of the problems are caused by a relatively high melting point and poor solubility.These problems can be over-come by using the solution polymerization–spinning method with polar solvents.Alterna-tive approaches are cross-linking or additional solid-phase polymerization after melt spinning. For melt-spunfibers,sophisticatedfiber produc-tion technologies have had to be developed,for example,increasing the degree of polymeriza-tion or improving the stabilizer,spinning equip-ment,and spinning conditions.Solution spinning,melt spinning,and other aspects offiber production discussed in this article are described in detail elsewhere(see →Fibers,3.General Production Technology).2.2.Solution-Spun Heat-Resistant Fibers2.2.1.Aramid FibersPolymerization and bina-tions of aromatic diamines and aromatic dicar-boxylic acids yield a variety of aramids,many of which are processed intofibers.Excellent review articles are available on the thermal and physical properties of thesefibers[1],[20].This section describes mainly meta-oriented aramid fibers of industrial importance.Since Du Pont commercialized Nomex in 1967,various combinations of processes have been proposed for the production of aramid fibers based on poly(m-phenyleneisophthal-amide)(PMIA)(Fig.3).The polymer is pre-pared by low-temperature solution polymeriza-tion or interfacial polymerization according to the following reaction[21]:High-Performance Fibers5Figure3.Production processes for PMIAfibersIn both the solution and the interfacial meth-ods,the following factors are important for the preparation of a high molecular mass polymer: use of high-purity monomers,stoichiometric balance of the two parent monomers,and min-imization of the water content of the polymer-ization system.A small amount of a monofunc-tional compound such as aniline is generally used to control the degree of polymerization (Fig.4)[22].Polar amide solvents such as N,N-di-methylacetamide[127-19-5]are used in low-temperature solution polymerization[23].These solvents are not only superior with regard to sol-ubility but are also effective in activating elec-trophilic reagents.They act as acceptors of by-product HCl,as well.Spin dope is obtained by neutralizing byproduct HCl with calcium hy-droxide(Fig.3,route A).This solution coagu-lates poorly in wet spinning because of the high content of calcium chloride and water.Accord-ingly,dry spinning is adopted in the Nomex pro-cess;residual calcium chloride and solvent are removed subsequently by water and heat treat-ment,respectively[24].Interfacial polymerization is carried out at the interface between a cyclic ether solvent,such as tetrahydrofuran[109-99-9],and an aqueous alkaline carbonate solution as an acid accep-tor(Fig.3,route B)[25].Polymers produced by the interfacial method contain a larger pro-portion of low molecular mass oligomers than those obtained by the solution method;this de-creases the thermal stability of thefibers.In an improved interfacial method used by Tei-jin[26],preliminary oligomerization is carried out in tetrahydrofuran,and the resultant stoi-chiometric mixtures are subjected to interfacial polymerization(Fig.3,route C)[27].Subse-quently,the powdery polymer is dissolved in N-methylpyrrolidone at a concentration of20–23wt%[28],and the resultant spin dope is wet-spun in aqueous calcium chloride solution [29].The as-spunfiber is preoriented and sub-sequently hot-drawn at200–350◦C.Two modified processes have been proposed to overcome the poor coagulation of spin dope in the wet-spinning method.One utilizes a co-agulant that gives void-free,as-spunfiber with high transparency[30];The other involves re-ducing the calcium chloride content in the spin dope by removing hydrogen chloride in the form of ammonium chloride,a byproduct of the pre-6High-Performance Fiberspolymerization step (Fig.3,route D)[23],[31],[32].Figure 4.Control of the molecular mass of PMIA by addi-tion of aniline [22]Addition of aniline gives a wider molar ratio range for con-trolling η(i.e.,molecular mass)within the limits 1.7–1.8(compare a 0→b 0and a 1→a 1).P 0and P 1denote the max-imum molecular mass with and without aniline,respectively.∗In aramid technology,molecular mass is usually expressed as a logarithmic viscosity number ln (η/η0)/c (η=viscosity coefficient of solution,η0=viscosity coefficient of solvent,c =polymer concentration,dL/g).Poly(m -phenyleneisophthalamide)is fusible in an inert atmosphere,although decomposition proceeds simultaneously in the molten state.Tei-jin has proposed a melt process for producing filaments by using a special spinneret,which has only its exit surface heated to avoid thermal decomposition [33].The Mitsui Toatsu and Kuraray group has de-veloped a new aramid fiber KM-21.Because the fiber is produced by polymerizing an aromatic isocyanate and aromatic carboxylic monomers,it differs from the foregoing PMIA fibers with respect to its chemical structure,production,and properties.However,its exact chemical structure and production method have not been made pub-lic[34].Fiber Properties.Important properties of meta-oriented aramid fibers are summarized in Table 3.The heat resistance and flame retardance of these fibers are better than those of commodity textile fibers.The physical properties of Teijin-conex,a typical PMIA fiber,follow [35]:Degree of crystallinity 35–39%Degree of orientation 90–93%Crystallite size 3.5–3.9nm Birefringence index 0.14–0.15Density1.37–1.38,g/cm 3The moisture regain of this fiber is about 5%under standard conditions (21◦C,65%R.H.)and 9%at 95%R.H.,which is between equiv-alent values for cotton and nylon fibers.Mechanical Properties.Most of the mechan-ical properties of PMIA fibers are about the same as those of commodity fibers (see Table 3).How-ever,their wear resistance,both flexural and fric-tional,is lower than that of nylon or polyester fibers.Weatherability and Dyeability.The weather-ability of PMIA fibers is not inferior to that of ny-lon fiber,as far as strength retention is concerned (Fig.5)[35].However,the whiteness of PMIA deteriorates because the light-induced Fries re-arrangement occursreadily.Figure 5.Weatherability of PMIA fiber [35]a)Nylon;b)Teijinconex (PMIA);c)PolyesterFibers from wholly aromatic polymers are,in general,highly sensitive to light exposure and poorly dyeable.Intrinsic color is a defect of wholly aromatic polymers,particularly when they are used for textile materials.Only PMIAHigh-Performance Fibers7Table 3.Physical properties of meta-oriented heat-resistant aramid fibers (PMIA)PropertyTeijinconex,(Teijin)[35]Nomex,(Du Pont)[36]Fenilon Apyeil,KM-21∗(former Soviet(Unitika)(Mitsui Union)[37][38]Toatsu)[39]Regular HT type Staple Filament Staple Staple Staple staple fiberstaple fiber fiber fiberfiberfiber Density,g/cm 31.37–1.38 1.37–1.38 1.38 1.38 1.33–1.361.381.32Tensile strength,GPa 0.55–0.670.850.490.650.38–0.430.55–0.610.61Tensile modulus,GPa 6.95–9.9912.168.5317.069.75Elongation at break,%35–5029312224.9–35.635–4522Moisture regain,% 5.0–5.2 5.5 5.5 5.5 5.5LOI30–3230303030–3233Heat shrinkage,%4–65 2.6–4.6>18(300◦C,(300◦C,(300◦C,(400◦C,15min)15min)15min)10min)∗Composition unknown;made by polymerizing aromatic isocyanate and aromatic carboxylate monomers.is colorless and can thus be employed in dyed textiles.Methods proposed for dyeing PMIA fibers in-clude the use of carriers,cationic dyes,or dope dyeing.Attempts to improve dyeability have in-volved modifying the fiber structure [40]and blending PMIA with other polymers [41].Most fiber manufacturers have their own proprietary products featuring improved dyeability or light-fastness.Figure 6.Strength retention in PMIA fiber exposed to dry heat [35]The limiting oxygen index (LOI)is an impor-tant measure of flame retardance and represents the percent concentration of oxygen needed forself-supporting combustion.The LOI values of meta-oriented aramid fibers are given in Table 3.Heat Resistance and Flame Retardance.Be-cause PMIA exhibits high crystallinity and strong intermolecular cohesion due to hydro-gen bonding,it has a high melting point and a high decomposition temperature.Accordingly,PMIA fibers have better thermal properties than commodity fibers.At elevated temperature,PMIA fibers offer better long-term retention of mechanical properties than commodity fibers;they also have good dimensional stability.In the thermogravimetric analysis curve of a PMIA fiber,the decomposition temperature is 400–430◦C.Mechanical properties are almost unchanged down to −35◦C,and the fiber is still flexible with slight hardening.Teijinconex (PMIA)staple fiber shrinks only 1%at 250◦C (dry heat)and 5–6%up to 300◦C.Long-term heat resistance of the fiber at various temperatures is shown in Figure 6.Unmodified PMIA fibers shrink in a high-temperature flame.Improvement in dimensional stability and flame retardance has been achieved by treating PMIA fibers or fabrics with halo-gen,sulfur,and phosphorus compounds (e.g.,Cl 2,Br 2,molten sulfur,SOCl 2,SO 2Cl,POCl 3,POBr 3,PCl 3,PCl 5)[42]and by blending with fibers that shrink less,such as Kevlar [43];some products are available in flame-retardant grades.Thermal properties can be improved markedly by replacing one of the meta monomers by a para monomer as in PMTA (see Fig.2).A self-8High-Performance Fibersextinguishing PMTAfiber has even been de-veloped[44].The KM-21fiber is also self-extinguishing and has a higher heat resistance than PMIAfibers(see Table3).Uses.Because of the excellent properties of PMIAfibers(e.g.,high thermal and chemical resistance,as well as radiation resistance),their end uses are growing.Typical applications fol-low.Clothing.Meta-oriented aramidfibers do not ignite,flare,or melt and stick to the skin.This makes them suitable for heat-resistant clothing material in the following areas:1)heated furnaces:work uniforms,aluminizedcoats and pants,capes and sleeves,gloves and mitts,leggings,and spats;2)emergency services:aluminized proxim-ity suits,turnout coats and jumpsuits,sta-tion uniforms,rescue uniforms,fire-fighting and aviation garments,riot police uniforms, ranger uniforms,gloves,underwear,leg-gings,and spats;3)fuel handling:work uniforms,rubber coats,gloves,socks,underwear,etc.Interior Fittings.Materials from PMIA are used in aircraft interiors(for increased safety and enhancedflame retardance).Industrial es here includefil-tration fabrics(especiallyfilter bags for hot stack gases);high-temperature heat insulants(espe-cially replacing asbestos);reinforcement infire hoses,V-belts,and conveyor belts;threads for high-speed sewing;and cut-fiber reinforcement for rubber composites.Electrical Insulation.High-temperature pa-per insulation for electric motors,dynamos, transformers,and cables;braided tubing for wire insulation;and dryer belts for papermaking are among the uses of PMIAfibers.Miscellaneous Uses.Home ironing-board covers and kitchen gloves are also made from PMIAfibers.2.2.2.Polyazole and Polyimide Fibers Three types of wet-spun polyazole and poly-imidefibers important for industrial and military uses are discussed:1)polybenzimidazolefibers(e.g.,Celazole),2)poly(amide–imide)fibers(e.g.,Kermel),and3)polyimidefibers(e.g.,Arimide).Fiber Production.The polymer structure of the polybenzimidazole(PBI)fiber Celazole [25734-65-0]manufactured by Celaneseis: Production is described in detail in[45].Poly-merization is carried out in two steps.Thefirst step involves conventional melt polymerization to yield a low molecular mass polymer with an intrinsic viscosity of0.2–0.3dL/g.The prod-uct is porous due to the formation of gaseous byproducts such as phenol and water.In the sec-ond step,this porous prepolymer is crushed to afine powder and heated gradually to380◦C to produce afiber-grade polymer with an intrinsic viscosity 0.75dL/g.Both steps are carried out under a nitrogen atmosphere.The polymer is powdered and dissolved in N,N-dimethylacetamide at a concentration of ca. 23wt%.Lithium chloride in N,N-dimethylacet-amide is reported to form a better solvent system for PBI than the acetamide alone.A PBIfiber is obtained by dry spinning from afiltered dope,followed by drawing the as-spunfiber under a nitrogen atmosphere.The fiber obtained has excellentflame retardance, although heat shrinkage is appreciable.The sul-fonation of imidazole residues in the PBI greatly improves its dimensional stability inflame-retardance tests.Kermel(Rhˆo ne–Poulenc)is an example of a poly(amide–imide)(PAI)fiber[46]. Polymerization is carried out in a polar amide solvent to form the precursor polymers.High-Performance Fibers9A spin dope of PAI is obtained by in situ im-idation of the precursor polymer [poly(amide –amic acid)]in solution by heating to ca.100–120◦C;N -methylpyrrolidone is used as a sol-vent.The PAI fiber is spun from the dope and subjected to heat treatment.In the case of polyimide (PI)fiber [47],spin dope containing poly(amic acid)is obtained.A precursor fiber is spun from the dope and then converted to PI fiber by heating,because PI is in-soluble in amide solvents whereas its precursor polymer is readilysoluble.In Arimide fiber [25036-53-7]and [25038-81-7],X is oxygen.Poly(bisbenzimidazobenzophenanthroline)[39319-28-3](BBB)fiber attracted the attentionof many polymer chemists and fiber scientists when it was reported by Marvel et al.[48].The fiber has excellent heat resistance,but no commercial product is known.The BBB polymer is a double-stranded lad-der polymer with a very high heat dder polymers have relatively high melting points and excellent weight retention as a func-tion of temperature.However,ladder polymers are difficult to spin into fibers because of their low tractability.Properties and Uses [49],[50].Properties of typical PBI,PAI,and PI fibers are listed in Table 4.Polybenzimidazole fiber was developed in response to the needs of the U.S.Air Force to satisfy special requirements for the NASA space program.Its moisture regain is similar to that of wool,and its modulus is lower.Of fibers known at present,PBI has the highest LOI value;it tends to compete against PMIA fibers in its applica-tions but is more expensive.Applications should exploit its resistance to chemicals and high tem-perature;they include1)thermal-protection clothing:garments for fire fighters,industrial work uniforms,space and military flight suits,underwear and es-cape suits,and other aerospace materials;2)high-temperature filtration:high-tempera-ture filters (e.g.,flue-gas filters);and3)asbestos substitute:protective gloves for high-temperature uses.The uses of meta-oriented PAI and PI fibers are similar to those of the meta-oriented aramid fibers.Kermel (PAI fiber)is used in underwear for pilots or operators of armed tanks because the resulting fabric is more supple than aramid fabrics.10High-Performance FibersTable4.Properties of heat-resistant polybenzimidazole(PBI),poly(amide–imide)(PAI),and polyimide(PI),staplefibersProperty PBIfiber(Celazole,Celanese)[49]PAIfiber(Kermel,Rhˆo ne–Poulenc)[50]PIfiber(Arimide,former Soviet Union)[47]234AGF235AGFDensity,g/cm3 1.4 1.34 1.34 1.41–1.43 Tensile strength,GPa0.330.470.20.63–0.7 Elongation at break,%28.523326–8Tensile modulus, G Pa 3.966.57 3.299.15–10.03Moisture regain,%153–53–5 1.0–1.5 LOI>4130–3230–32Heat shrinkage,%0.50–0.10–0.5 1.0–1.52.3.Melt-Spun Heat-Resistant Fibers 2.3.1.Novoloid Fibers(→Phenolic Resins)Fiber Production.The melt-spinning method has the advantage of eliminating the need for solvent recovery;however,melt-spun fibers are less heat-resistant than solution-spun fibers.Kynol[9003-55-8],a commercial no-voloidfiber,exhibits exceptionally high heat re-sistance because cross-linking occurs after melt spinning.Kynol is produced from a novolac polymer by melt spinning[52]and subsequent cross-linking with formaldehyde[53].The as-spun novolak reacts with formaldehyde in the presence of an acid catalyst to form cross-linked networks of methylene and dimethylene etherbonds.Novoloidfiber wasfirst developed by Car-borundum as a carbon-fiber precursor and com-mercialized in the1970s as a heat-resistant fiber[51].It is produced by Gun-ei Chemicals and distributed by Nippon Kynol and American Kynol[54],[55].Properties.One of the most remarkable fea-tures of novoloidfiber is itsflame retardance.It generates virtually no smoke or gas.It has high LOI values and can be converted to carbonfibers without melting or shrinkage by heating in an in-ert atmosphere.Kynol shows good thermal stability at150◦C in air and200–250◦C in the absence of air.Its chemical stability is also excellent.Kynol has excellent heat-insulation and acoustic proper-ties.Its density is relatively low compared to other heat-resistantfibers.The weatherability and light stability of Kynol are moderate.Dyeability is limited be-cause of its intrinsic golden-brown color.Textile properties of Kynolfibers follow[56],[57]: Diameter14–33µm Density 1.27,g/cm3 Tensile strength0.15–0.20GPa Elongation at break30–60% Tensile modulus 3.3–4.4GPa Loop strength0.2–0.35GPa Knot strength0.12–0.17GPa Elastic recovery(3%elongation)92–96% Moisture regain(20◦C,65%R.H.)6%LOI30–34Uses.Novoloidfiber is used as reinforcement in resins and rubber to improve properties such as heat resistance,electrical insulation,and di-mensional stability.Further applications are in cable material,brake material,various industrial sheets(e.g.,welders’protective sheet,work-place shielding sheet),and safety products for accident prevention.2.3.2.Fibers from Engineering PlasticsFiber Production.Progress in both poly-merization andfiber production technologies in thefield of engineering plastics has stimu-。
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* Author to whom correspondence should be addressed; E-Mail: changcj@.tw; Tel.: +886-4-2451-7250 (ext. 3678); Fax: +886-4-2451-0890. Received: 26 November 2013; in revised form: 10 January 2014 / Accepted: 16 January 2014 / Published: 28 January 2014
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Mother Nature shows us abundant examples of stimuli-responsive (or smart) materials. The leaves of Mimosa pudica collapse suddenly when touched, and those of the Venus flytrap snap shut on doomed insect prey; the leaflets of Codariocalyx motorius rotate, and sunflowers turn toward the sun; and chameleons change color according to their environment. At their most fundamental level, many of the most important substances in living systems are macromolecules with structures and behaviors that vary according to the conditions in the surrounding environment. Mimicking the functions of such organisms, scientists have made great efforts to synthesize stimuli-responsive polymers that have significance to science and promising applications. Incorporating multiple copies of functional groups that are readily amenable to a change in character (e.g., charge, polarity, and solvency) along a polymer backbone causes relatively minor changes in chemical structure to be synergistically amplified to bring about dramatic transformations in macroscopic material properties. Polymers such as proteins, polysaccharides, and nucleic acids are present as basic components in living organic systems. Synthetic polymers, which are designed to mimic these biopolymers, have been developed into a variety of functional forms to meet industrial and scientific applications. These synthetic polymers can be classified into different categories based on their chemical properties. Certain special types of polymers have emerged as very useful class of polymers having their own special chemical properties and applications in various areas. These “stimuli-responsive” polymers (SRPs) have been variously called stimuli-sensitive [1], intelligent [2], smart [3,4], or environmentally-sensitive polymers [5]. SRPs can rapidly change shape with respect to configuration or dimension under the influence of stimuli such as temperature [6], pH value [7,8], light [9], magnetic field [10], electricity [11], and solvent/water [12]. These polymers can also have different compositions and architecture, including not only homopolymers [13] but also statistical/block copolymers [14], graft copolymers, and molecular brushes. They can be also grafted on/from surfaces [15] or be used as chemically or physically cross-linked gels [16]. SRPs are usually capable of stimuli-induced conformational changes, reversible solubility control [17], and reversible self-assembly into polymeric micelles or vesicles. Given these unique properties, stimuli-responsive polymers are being developed for use in such fields as drug delivery, cell adhesion, sensors, actuator systems, releasing of encapsulated materials and trafficking of molecules through polymeric membranes [18–23]. The “response” of a polymer can be defined in various ways. SRPs in solution are typically classified as those that change their individual chain dimensions/size, secondary structure, solubility, or the degree of intermolecular association. In most cases, the physical or chemical event that causes these responses is limited to the formation or destruction of secondary forces (hydrogen bonding, hydrophobic effects, electrostatic interactions, etc.), simple reactions (e.g., acid-base reactions) of moieties pendant to the polymer backbone, and/or osmotic pressure differentials that result from such phenomena. In other systems, the definition of a response can be expanded to include more dramatic alterations in the polymeric structure. In the past decade, many breakthroughs have been made in developing SPRs with novel stimulus-active mechanisms. This article reviews the mechanisms and fabrication strategies of stimulus active polymers that are sensitive to heat, light, electrical field, magnetic field, and solvent/water. The wide applications of patterned SRPs are also summarized.
Materials 2014, 7, 805-875; doi:10.3390/ma7020805
OPEN ACCESS
materials
ISSN 1996-1944 /journal/materials Review
Fabrications and Applications of Stimulus-Responsive Polymer Films and Patterns on Surfaces: A Review
Jem-Kun Chen 1 and Chi-Jung Chang 2,*