Emulsifier-free emulsion copolymerization of styrene (St) and butyl acrylate (BA) in the presence of a cationic functional comonomer, N-dimethyl, N-butyl, Nethyl methacrylate ammonium bromine (DBMA) was carried out using azobis(isobutylamidine hydrochloride) (AIBA) as an initiator. The surface prope
Emulsifier-free emulsion copolymerization of styrene with quaternary ammonium cationic monomers
β Scribed by Zuifang Liu; Huining Xiao; Nicholas Wiseman
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 293 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Emulsifier-free emulsion binary copolymerizations of styrene with four types of quaternary ammonium cationic monomers, diallyldimethylammonium chloride (DADMAC), (3-(methacryloylamino) propyl) trimethyl ammonium chloride (MAPTAC), (2-methacryloyloxy) ethyl) trimethyl ammonium chloride (MATMAC), and vinylbenzyl trimethyl ammonium chloride (VBTMAC), were conducted at 70Β°C. 2, 2'-azobis (2methylpropionamidine) dihydrochloride (V50) and potassium persulphate (KPS) were used as cationic and anionic initiator, respectively. Ternary copolymerizations were also carried out in the presence of acrylamide as a second comonomer. Monomer conversions were followed by ultraviolet spectroscopy and the polymer microparticles were characterized using photon correlation spectroscopy, electrophoresis, colloid titration, and scanning electron microscopy. The results indicated that VBTMAC and MATMAC were highly reactive in the copolymerization with styrene whereas the incorporation of DADMAC was slow. MAPTAC had an intermediate reactivity. Binary copolymerization with VBTMAC, MATMAC, and MAPTAC produced particles smaller in size, but higher in surface-charge density, than styrene homopolymer particles. However, significant agglomerates were detected in the VBTMAC and MATMACcontaining latexes. In contrast, DADMAC-containing polymer particles were almost identical to styrene particles. Continuous nucleation took place in the binary copolymerizations with VBTMAC and with MATMAC when using V50 initiator. In the case of using KPS, VBTMAC-containing particles grew continuously to a mean size much larger than the corresponding particles initiated by V50. The presence of acrylamide reduced DADMAC-containing particle size and diminished the agglomeration in the VBTMAC-and MATMAC-containing latexes. The results were interpreted via particle formation mechanism.
π SIMILAR VOLUMES
The kinetics of emulsifier-free emulsion copolymerization of styrene were investigated in the presence of two amino-containing monomers, aminoethyl methacrylate hydrochloride (AEMH) and vinyl benzyl amine hydrochloride (VBAH), using 2,2azobis(2-amidinopropane) dihydrochloride (V50) as a cationic ini
The colloidal and surface properties of copolymer latex particles prepared by batch emulsifier-free emulsion polymerization of styrene with two different aminocontaining monomers (Amino Ethyl Methacrylate Hydrochloride (AEMH) and Vinyl Benzyl Amine Hydrochloride (VBAH)), and 2,2-azobis(2-amidinoprop
EmulsiΓer-free emulsion copolymerization of styrene (St) and butyl acrylate (BA) in the presence of cationic functional comonomer N,N-dimethyl N-butyl N-methacrylamidino propyl ammonium bromide (DBMPAB) was carried out using azobis(isobutylamidine hydrochloride) (AIBA) as initiator. The surface prop