Pushing the mechanical strength of PolyHIPEs up to the theoretical limit through living radical polymerization

被引:69
作者
Luo, Yingwu [1 ]
Wang, An-Ni [1 ]
Gao, Xiang [1 ]
机构
[1] Zhejiang Univ, Dept Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
国家杰出青年科学基金; 中国国家自然科学基金;
关键词
INTERNAL-PHASE EMULSIONS; IN-OIL EMULSIONS; RAFT POLYMERIZATION; COPOLYMERIZATION; FOAMS; POLYMERS; MONOMERS; KINETICS; SYSTEMS; GROWTH;
D O I
10.1039/c1sm06756g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High internal phase emulsion (HIPE) living polymerization was proposed in current work. Reversible addition-fragmentation chain transfer polymerization (RAFT), one of the living radical polymerization methods, was introduced to the polymerization of HIPE for the preparation of polystyrene PolyHIPEs. Living polymerization changed the crosslinking process giving a highly homogeneous polymeric wall of PolyHIPEs. The resolving of the heterogeneity problem increased the mechanical strength of PolyHIPEs significantly with the Young's modulus reaching the theoretical value of similar to 45 MPa, which was more than 3 times higher than that by the conventional method. Not only the open-cellular structure of PolyHIPEs was maintained but also a higher connectivity was achieved. Both the type and the concentration of RAFT agents were found to have influence on the morphology and mechanical strength of PolyHIPEs.
引用
收藏
页码:1824 / 1830
页数:7
相关论文
共 50 条
[1]   Microcellular polyHIPE polymer supports osteoblast growth and bone formation in vitro [J].
Akay, G ;
Birch, MA ;
Bokhari, MA .
BIOMATERIALS, 2004, 25 (18) :3991-4000
[2]   Highly concentrated emulsions:: Physicochemical principles of formulation [J].
Babak, VG ;
Stébé, MJ .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2002, 23 (1-3) :1-22
[3]   Development of branching in living radical copolymerization of vinyl and divinyl monomers [J].
Bannister, Iveta ;
Billingham, Norman C. ;
Armes, Steven P. ;
Rannard, Steven P. ;
Findlay, Paul .
MACROMOLECULES, 2006, 39 (22) :7483-7492
[4]   POLYHIPE FOAM MATERIALS AS FILTRATION MEDIA [J].
BHUMGARA, Z .
FILTRATION & SEPARATION, 1995, 32 (03) :245-251
[5]   Controlled/living radical polymerization: Features, developments, and perspectives [J].
Braunecker, Wade A. ;
Matyjaszewski, Krzysztof .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (01) :93-146
[6]   Preparation of microporous nickel electrodeposits using a polymer matrix [J].
Brown, IJ ;
Clift, D ;
Sotiropoulos, S .
MATERIALS RESEARCH BULLETIN, 1999, 34 (07) :1055-1064
[7]   Emulsion-derived foams (PolyHIPEs) containing poly(ε-caprolactone) as matrixes for tissue engineering [J].
Busby, W ;
Cameron, NR ;
Jahoda, CAB .
BIOMACROMOLECULES, 2001, 2 (01) :154-164
[8]  
Cameron NR, 1996, ADV POLYM SCI, V126, P163
[9]   Study of the formation of the open cellular morphology of poly(styrene/divinylbenzene) polyHIPE materials by cryo-SEM [J].
Cameron, NR ;
Sherrington, DC ;
Albiston, L ;
Gregory, DP .
COLLOID AND POLYMER SCIENCE, 1996, 274 (06) :592-595
[10]   Thiocarbonylthio compounds (S=C(Z)S-R) in free radical polymerization with reversible addition-fragmentation chain transfer (RAFT polymerization). Effect of the activating group Z [J].
Chiefari, J ;
Mayadunne, RTA ;
Moad, CL ;
Moad, G ;
Rizzardo, E ;
Postma, A ;
Skidmore, MA ;
Thang, SH .
MACROMOLECULES, 2003, 36 (07) :2273-2283