Effect of LiClO4 on radical polymerization of methyl methacrylate
β Scribed by Makiko Seno; Nobuyuki Matsumura; Hiroyuki Nakamura; Tsuneyuki Sato
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 203 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The effect of LiClO 4 on the polymerization of methyl methacrylate (MMA) with dimethyl 2,2-azobisisobutyrate (MAIB) was investigated at 50ΠC in methyl ethyl ketone. The polymerization proceeded homogeneously even at [LiClO 4 ] as high as 3.00 mol/L. The polymerization rate (R p ) and the molecular weight of the resulting polymer profoundly increased with increasing [LiClO 4 ]. R p at 3.00 mol/L [LiClO 4 ] was 12 times that in the absence of LiClO 4 . The rate equation depended on the presence or absence of LiClO 4 : R p Γ k[MAIB] 0.5 [MMA] 1.5 in the presence of 3.00 mol/L [LiClO 4 ] and R p Γ k[MAIB] 0.5 [MMA] 1.0 in the absence of LiClO 4 . The overall activation energies of polymerization were 38.5 kJ/mol in the presence of 3.00 mol/L [LiClO 4 ] and 77.4 kJ/ mol in the absence of LiClO 4 , respectively. The tacticities of resulting poly(MMA) were insensitive to the presence of LiClO 4 . In the copolymerization of MMA and styrene, Q and e values of MMA increased with increasing [LiClO 4 ], leading to enhanced alternating copolymerizability.
π SIMILAR VOLUMES
Living radical polymerization of methyl methacrylate (MMA) through the use of benzyl diethyl dithiocarbamate (BDC) was studied. The aim was to investigate the role of the concentration, BDC-to-MMA mol ratio, and reaction time upon the molecular weight, polydispersity, and conversion of the product.
The effect of LiClO 4 on the polymerization of di-2-[2-(2-methoxyethoxy)ethoxy]ethyl itaconate (DMEI) with dimethyl 2,2-azobisisobutyrate (MAIB) was investigated in methyl ethyl ketone (MEK) kinetically and by ESR. The polymerization rate (R p ) at 50ΠC, where the concentrations of DMEI and MAIB wer
Five binary formulations were prepared from methyl methacrylate (MMA) and methacrylic acid (MAA) monomers, and six ternary formulations were prepared from polysols of 30% wt polymethyl methacrylate (PMMA)/MMA and MAA. Using thermal analyses (DSC and TGA) the polymerization kinetics, condition of pos