A FAST CATALYST SYSTEM FOR THE RING-OPENING POLYMERIZATION OF CYCLOSILOXANES

被引:93
作者
MOLENBERG, A [1 ]
MOLLER, M [1 ]
机构
[1] UNIV ULM,D-89069 ULM,GERMANY
关键词
D O I
10.1002/marc.1995.030160606
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Methanol, in combination with a non-ionic phosphazene base, was used to initiate the polymerization of octamethylcyclotetrasiloxane. In bulk, an instantaneous and large increase in viscosity was observed upon addition of the initiator. In toluene solution, the equilibrium state was reached in approximately 1 min. In addition to its high polymerization rate, another advantage of this system, as compared with e. g. alkali metal hydroxides, is that it is homogeneous.
引用
收藏
页码:449 / 453
页数:5
相关论文
共 9 条
[1]   DILUTION EFFECTS ON DIMETHYLSILOXANE RING-CHAIN EQUILIBRIA [J].
CARMICHAEL, JB ;
GORDON, DJ ;
ISACKSON, FJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (07) :2011-+
[2]  
Chojnowski J., 1993, SILOXANE POLYM, P1
[3]   KINETICS OF THE POLYMERIZATION OF A CYCLIC DIMETHYLSILOXANE [J].
GRUBB, WT ;
OSTHOFF, RC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (06) :1405-1411
[4]   THE MECHANISM OF THE BASE-CATALYZED REARRANGEMENT OF ORGANOPOLYSILOXANES [J].
HURD, DT ;
OSTHOFF, RC ;
CORRIN, ML .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (01) :249-252
[5]   PERALKYLATED POLYAMINOPHOSPHAZENES - EXTREMELY STRONG, NEUTRAL NITROGEN BASES [J].
SCHWESINGER, R ;
SCHLEMPER, H .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1987, 26 (11) :1167-1169
[6]  
Schwesinger R., 1990, NACHR CHEM TECH LAB, V38, P1214
[7]  
Schwesinger R., 1987, ANGEW CHEM, V99
[8]  
Semlyen J. A., 1976, ADV POLYM SCI, V21, P41
[9]  
SEMLYEN JA, 1993, SILOXANE POLYM, P135