Crosslinkable surfactants based on linoleic acid-functionalized block copolymers of ethylene oxide and ε-caprolactone for the preparation of stable PMMA latices

被引:20
作者
Tan, BH
Grijpma, DW
Nabuurs, T
Feijen, J
机构
[1] Univ Twente, Fac Sci & Technol, Inst Biomed Technol, BMTI, NL-7500 AE Enschede, Netherlands
[2] Univ Twente, Fac Sci & Technol, Dept Polymer Chem & Biomat, NL-7500 AE Enschede, Netherlands
[3] NeoResins Bv, NL-5410 AC Waalwijk, Netherlands
关键词
crosslinkable surfactants; block copolymers; emulsion polymerization;
D O I
10.1016/j.polymer.2004.11.070
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic diblock and triblock copolymers consisting of poly(ethylene oxide) (PEO) as (central) hydrophilic segment and poly(epsilon-caprolactone) (PCL) as hydrophobic segment(s) were prepared by ring opening polymerization. The length of the PEO segment was kept constant (x(n) = 45), whereas the length of the PCL block(s) was either 6 or 10 units for diblock copolymers and 3 or 5 units at each end for the triblock copolymers. These block copolymers were end-functionalized by esterification with linoleic acid (LA), which contains reactive double bonds. The autoxidative behavior of PEO45-(CL3-LA)(2) functionalized triblock copolymers was investigated by exposure of films to air at ambient conditions. Ninety percent of the double bonds had disappeared in 15 d and a crosslinked structure was obtained after 30 d. Critical micelle concentrations (CMC) of the crosslinkable surfactants were in the range of 0.08-0.19 mmol/l for the diblock copolymer and of 0.19-0.26 mmol/l for the triblock copolymer. The surface tension of aqueous surfactant solutions at the CMC (gamma(CMC)) (25 degreesC) varied from 47.1 to 51.4 mN/m for the diblock and from 45.6 to 48.1 mN/m for the triblock systems. For both systems CMC and gamma(CMC) increase with increasing RLB values. These surfactants were used in PMMA latex preparations. The latices of PMMA prepared with LA-functionalized diblock and triblock copolymers yielded narrow particle size distributions and particle sizes of 180 and 370 nm, respectively, whereas latices prepared with SDS had a particle size of 90 nm. After extraction of the latex particles with methanol, the amounts of the unextractable (either buried or copolymerized) LA-functionalized diblock and triblock copolymers found in extracted PMMA latex particles were 10 and 24% of the initial amount of surfactant added respectively. Control experiments with a stearic acid (SA) containing diblock copolymer showed that the amount of buried surfactant in PMMA latices was 6.5%. By comparing the overall latex characteristics and stability (shelf stability, freeze-thaw testing and addition of electrolyte solutions and ethanol) it was concluded that an LA-functionalized diblock copolymer (MPEO45-CL10-LA) gave better stabilization of PMMA latices than an LA-functionalized triblock copolymer of comparable composition and HLB value. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1347 / 1357
页数:11
相关论文
共 43 条
[1]   Distribution of surfactants near acrylic latex film surfaces:: A comparison of conventional and reactive surfactants (surfmers) [J].
Aramendia, E ;
Mallégol, J ;
Jeynes, C ;
Barandiaran, MJ ;
Keddie, JL ;
Asua, JM .
LANGMUIR, 2003, 19 (08) :3212-3221
[2]  
Asua JM, 1998, ACTA POLYM, V49, P671, DOI 10.1002/(SICI)1521-4044(199812)49:12<671::AID-APOL671>3.0.CO
[3]  
2-L
[4]  
BECHER P, 2002, EMULSIONS THEORY PRA
[5]  
BUECKMANN AJP, 2002, INT WAT HIGH SOL POW
[6]  
BUECKMANN AJP, 2001, NUER C CREAT ADV COA
[7]   Application of a non-ionic amphiphilic maleic diester as polymerizable surfactant in free-radical emulsion polymerization [J].
Bui, CO ;
Lassau, C ;
Charleux, B ;
Vairon, JP ;
Tintiller, P ;
Le Hen-Ferrenbach, C .
POLYMER BULLETIN, 1999, 42 (03) :287-294
[8]   Nonionic reactive surfactants. I. Synthesis and characterization [J].
Dufour, M ;
Guyot, A .
COLLOID AND POLYMER SCIENCE, 2003, 281 (02) :97-104
[9]  
GONI AM, 1999, POLYMER, V40, P1067
[10]  
Guyot A, 1999, ACTA POLYM, V50, P57, DOI 10.1002/(SICI)1521-4044(19990201)50:2/3<57::AID-APOL57>3.0.CO