Present and Future of Thermoplastic Elastomers As Environmentally Friendly Organic Materials

被引:0
作者
Choi, Eun Ji [1 ]
Yoon, Ji Hwan [1 ]
Jo, Jung Kyu [1 ]
Shim, Sang Eun [2 ]
Yun, Ju Ho [3 ]
Kim, Il [1 ]
机构
[1] Pusan Natl Univ, WCU Ctr Synthet Polymer Bioconjugate Hybrid Mat, Dept Polymer Sci & Engn, Busan 609735, South Korea
[2] Inha Univ, Dept Chem Engn, Incheon 402751, South Korea
[3] Korea Automot Technol Inst, Enviromental Mat & Components R&D Ctr, Chonan Si 330912, Chungnam, South Korea
来源
ELASTOMERS AND COMPOSITES | 2010年 / 45卷 / 03期
关键词
thermoplastic elastomers; history; preparation; properties; applications; processing;
D O I
暂无
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Much interest on the thermoplastic elastomers (TPEs) has recently been attracted in commercial fields as well as scientific and applied researches. The TPEs have their own characteristic area especially in relation with block copolymers as well as many other polymeric materials, since they show interesting features displayed by the conventional vulcanized rubber, and at the same time, by the thermoplastics. In addition, they are characterized by a set of interesting properties inherent to block and graft copolymers, variety of blends and vulcanized materials. The importance of TPE as organic materials can be evaluated by the number of published reports (papers, patents, technical reports, etc). The input of the concept 'thermoplastic elastomer' to SciFinderScholar yields 18,508 results between 1939 and July 10, 2010, and the number increased exponentially after the mid of 1990. For the suitable introduction of the TPE, historic, scientific, technical and commercial considerations should be taken into account. This review article starts with a brief discussion on historical considerations, followed by a introduction of the main preparations and analytical techniques utilized in chemical, structural, and morphological studies. The properties, processing tools, the position among organic materials, and applications of TPEs are also briefly reviewed. Finally, the most probable trends of their future development are discussed in a short final remarks.
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页码:170 / 187
页数:18
相关论文
共 74 条
[11]   UBER NEUARTIGE HOCHELASTISCHE STOFFE VULCOLLAN .6. MITTEILUNG UBER POLYURETHANE [J].
BAYER, O ;
MULLER, E ;
PETERSEN, S ;
PIEPENBRINK, HF ;
WINDEMUTH, E .
ANGEWANDTE CHEMIE, 1950, 62 (03) :57-66
[12]   Synthesis and characterization of poly(copolyethers-block-polyamides). I. Structural study of polyether precursors [J].
Boulares, A ;
Tessier, M ;
Marechal, E .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 1998, A35 (06) :933-953
[13]   Polyisobutylene based thermoplastic elastomers:: VI.: Poly(α-methylstyrene-b-isobutylene-6-b-α-methylstyrene) triblock copolymers by coupling of living poly(α-methylstyrene-b-isobutylene) diblock copolymers [J].
Cao, XY ;
Sipos, L ;
Faust, R .
POLYMER BULLETIN, 2000, 45 (02) :121-128
[14]   NEW HIGH-TEMPERATURE THERMOPLASTIC ELASTOMERS [J].
CHEN, AT ;
NELB, RG ;
ONDER, K .
RUBBER CHEMISTRY AND TECHNOLOGY, 1986, 59 (04) :615-622
[15]   Blends of thermoplastic polyurethane and polyether-polyimide: preparation and properties [J].
Chen, JN ;
Zhang, JF ;
Zhu, TY ;
Hua, ZC ;
Chen, QM ;
Yu, XH .
POLYMER, 2001, 42 (04) :1493-1500
[16]  
Christ RE, 1943, US patent, Patent No. [2,333,639, 2333639]
[17]   SYNTHESIS AND PROPERTIES OF POLY(AMIDE-BLOCK-ETHER) BLOCK COPOLYCONDENSATES .3. REACTION OF POLYCONDENSATION OF DICARBOXYLIC OMEGA, OMEGA'-POLYAMIDE-11 AND DIHYDROXY-OMEGA, OMEGA' POLYOXYETHYLENE - DETERMINATION OF RATE CONSTANT AND ACTIVATION-ENERGY CONSTANT [J].
DELEENS, G ;
FOY, P ;
MARECHAL, E .
EUROPEAN POLYMER JOURNAL, 1977, 13 (05) :353-360
[18]   Synthesis and characterization of novel nylon 6-b-polyimide-b-nylon 6 copolymers [J].
Ding, H ;
Harris, FW .
PURE AND APPLIED CHEMISTRY, 1995, 67 (12) :1997-2004
[19]  
Fakirov S, 2005, HANDBOOK OF CONDENSATION THERMOPLASTIC ELASTOMERS, P1, DOI 10.1002/3527606610
[20]   Synthesis of linear and star-shaped block copolymers of isobutylene and methacrylates by combination of living cationic and anionic polymerizations [J].
Feldthusen, J ;
Ivan, B ;
Muller, AHE .
MACROMOLECULES, 1998, 31 (03) :578-585