Preparation and characterization of crosslinked polyurethane-block-poly(trifluoropropylmethyl)siloxane elastomers with potential biomedical applications

被引:14
作者
Shi, Zhendong [1 ]
机构
[1] Wuyi Univ, Sch Text & Clothing, Jiangmen 529020, Guangdong, Peoples R China
关键词
polyurethane; poly(trifluoropropylmethyl)siloxane polyurethane diol; crosslink density; -bis(3-aminopropyldiethoxylsilane); poly(trifluoropropylmethyl)siloxane; HYDROXYL TERMINATED POLYBUTADIENE; THERMAL-DEGRADATION; POLYURETHANE; BIOSTABILITY; ADHESION;
D O I
10.1002/pi.4428
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of crosslinked polyurethane-block-poly(trifluoropropylmethyl)siloxane elastomers were prepared via two steps. First, poly(trifluoropropylmethyl) siloxane polyurethane (FSPU) prepolymers were synthesized with alpha,omega-bis(3-amino propyldiethoxylsilane) poly(trifluoropropylmethyl) siloxane (APFS) and toluenediisocyanate (TDI) and then capped with butanediol to generate the macromolecular FSPU diol extender. Second, polyurethane prepolymers synthesized from poly(tetramethylene oxide) and TDI were reacted with FSPU diol extenders with different ratios. The copolymers formed films through moisture curing and were characterized by Fourier transform infrared spectroscopy, DSC, dynamic mechanical analysis, TGA, mechanical testing etc. It is found that the equivalent ratio of reactants gives rise to a high molecular weight of copolymers and that low molecular weight APFS in the copolymers can form a certain number of silicon-oxygen crosslinks resulting from silicon alkoxy to produce higher tensile strength elastomers. The material thus has higher thermal stability and a more stable surface performance. The copolymers are then good candidates for biomedical applications. (C) 2013 Society of Chemical Industry
引用
收藏
页码:1351 / 1357
页数:7
相关论文
共 28 条
[1]   Low-modulus siloxane-polyurethanes. Part II. Effect of chain extender structure on properties and morphology [J].
Adhikari, R ;
Gunatillake, PA ;
McCarthy, SJ ;
Bown, M ;
Meijs, GF .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 87 (07) :1092-1100
[2]   Evaluation of Adhesion Strength, Flammability, Degradation of HBCD-Containing Polyurethane and Adhesives [J].
Amrollahi, M. ;
Sadeghi, G. Mir Mohamad .
JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 110 (06) :3538-3543
[3]  
[Anonymous], 1989, Polymer Handbook
[4]   COHESIVE ENERGY DENSITIES OF POLYMERS .1. COHESIVE ENERGY DENSITIES OF RUBBERS BY SWELLING MEASUREMENTS [J].
BRISTOW, GM ;
WATSON, WF .
TRANSACTIONS OF THE FARADAY SOCIETY, 1958, 54 (11) :1731-1741
[5]  
Capone C D, 1992, J Biomater Appl, V7, P108, DOI 10.1177/088532829200700202
[6]  
FLORY PJ, 1953, PRINCIPLES POLYM CHE, P579
[7]   THERMAL-DEGRADATION OF POLYURETHANE FROM 1,4-BUTANEDIOL AND METHYLENE BIS(4-PHENYL ISOCYANATE) [J].
GRASSIE, N ;
ZULFIQAR, M .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1978, 16 (07) :1563-1574
[8]   Synthesis, characterization and platelet adhesion of segmented polyurethanes grafted phospholipid analogous vinyl monomer on surface [J].
Korematsu, A ;
Takemoto, Y ;
Nakaya, T ;
Inoue, H .
BIOMATERIALS, 2002, 23 (01) :263-271
[9]   STEREOREGULARITY IN POLY[METHYL(3,3,3-TRIFLUOROPROPYL)SILOXANE] [J].
KUO, CM ;
SAAM, JC ;
TAYLOR, RB .
POLYMER INTERNATIONAL, 1994, 33 (02) :187-195
[10]  
Liu FQ, 1995, POLYM PHYS, P108