Polymerization rate and mechanism of ultrasonically initiated emulsion polymerization of n-butyl acrylate

被引:91
作者
Xia, HS
Wang, Q [1 ]
Liao, YQ
Xu, X
Baxter, SM
Slone, RV
Wu, SG
Swift, G
Westmoreland, DG
机构
[1] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
[2] Rohm & Haas Co, Res Labs, Spring House, PA 19477 USA
关键词
ultrasonic irradiation; emulsion polymerization rate; n-butyl acrylate;
D O I
10.1016/S1350-4177(01)00118-3
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
The factors affecting the induction period and polymerization rate in ultrasonically initiated emulsion polymerization of n-butyl acrylate (BA) were investigated. The induction period takes only an instant in ultrasonically initiated emulsion polymerization of BA without any added initiator by enhancing the N-2 flow rate. Increasing temperature, power output and SDS concentration, decreasing the monomer concentration results in further decreasing induction period and enhanced polymerization rate. Under optimized reaction conditions the conversion of BA reaches 92% in 11 min. The polymerization rate can be controlled by varying reaction parameters, The apparatus of ultrasonically initiated semi-continuous and continuous emulsion polymerization were set up and the feasibility was first studied. Based on the experimental results, a free radical polymerization mechanism for ultrasonically initiated emulsion polymerization was proposed. including the sources of the radicals, the process of radical formation, the locus of polymerization and the polymerization process. Compared with conventional emulsion polymerization, where the radicals come from thermal decomposition of a chemical initiator, ultrasonically initiated emulsion polymerization has attractive features such as no need for a chemical initiator, lower reaction temperature, faster polymerization rate, and higher molecular weight of the polymer prepared. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:151 / 158
页数:8
相关论文
共 21 条
[11]   THE CHEMICAL EFFECTS PRODUCED BY ULTRASONIC WAVES [J].
LINDSTROM, O ;
LAMM, O .
JOURNAL OF PHYSICAL AND COLLOID CHEMISTRY, 1951, 55 (07) :1139-1146
[12]   ANALYSIS OF ULTRASONICALLY INDUCED FREE-RADICALS IN THE EMULSION POLYMERIZATION SYSTEM BY GC-MS [J].
LIU, YB ;
CHOU, HC ;
STOFFER, JO .
JOURNAL OF APPLIED POLYMER SCIENCE, 1994, 53 (02) :247-254
[13]   ENHANCEMENT OF CHEMICAL-REACTIVITY BY POWER ULTRASOUND - AN ALTERNATIVE INTERPRETATION OF THE HOT-SPOT [J].
LORIMER, JP ;
MASON, TJ ;
FIDDY, K .
ULTRASONICS, 1991, 29 (04) :338-343
[14]   CHEMICAL EFFECTS OF ULTRASOUND ON AQUEOUS-SOLUTIONS - FORMATION OF HYDROXYL RADICALS AND HYDROGEN-ATOMS [J].
MAKINO, K ;
MOSSOBA, MM ;
RIESZ, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (08) :1369-1377
[15]  
Mason TJ, 1988, SONOCHEMISTRY THEORY
[16]   CAVITATION PRODUCED BY ULTRASONICS [J].
NOLTINGK, BE ;
NEPPIRAS, EA .
PROCEEDINGS OF THE PHYSICAL SOCIETY OF LONDON SECTION B, 1950, 63 (369) :674-685
[17]   POLYMERIZATION OF METHYL-METHACRYLATE INITIATED BY ULTRASOUND [J].
PRICE, GJ ;
NORRIS, DJ ;
WEST, PJ .
MACROMOLECULES, 1992, 25 (24) :6447-6454
[18]  
SHEN Y, 1985, J MACROMOL SCI CHEM, V22, P455
[19]   SONOCHEMISTRY [J].
SUSLICK, KS .
SCIENCE, 1990, 247 (4949) :1439-1445
[20]   THE SONOCHEMICAL HOT-SPOT [J].
SUSLICK, KS ;
HAMMERTON, DA ;
CLINE, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (18) :5641-5642