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Block Copolymer Poly (block + copolymer_poly)
Selected AbstractsNonaqueous dispersion polymerization of styrene in methanol with the ionomer block copolymer poly[(4-methylstyrene)- co -(4-vinyltriethylbenzyl ammonium bromide)]- b -polyisobutene as a stabilizerJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 11 2004Yuhong Ma Abstract The nonaqueous dispersion polymerization of styrene in methanol with poly[(4-methylstyrene)- co -(4-vinyltriethylbenzyl ammonium bromide)]- b -polyisobutene as a stabilizer was investigated. There was no observable inducing period or autoacceleration in the polymerization process. The conversion increased almost linearly with the polymerization time as high as 80%. The average sizes of the obtained polystyrene particles increased, and the size distributions of the polystyrene particles tended to become narrower, with increasing conversion. The mechanism of the dispersion polymerization in the presence of polyisobutene- b -poly[(4-methylstyrene)- co -(4-vinyltriethylbenzyl ammonium bromide)] was nucleation/growth. When the stabilizer/monomer ratio (w/w) was greater than 2.0%, the polystyrene dispersion was stable, and there was no observable polymer particle coagulation taking place during the whole polymerization process. The average diameter of the polymer particles can be mediated through changes in the polymerization conversion, monomer, and stabilizer. Nearly monodispersed polystyrene particles with average diameters of approximately 0.45,2.21 ,m were obtained under optimal conditions. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2678,2685, 2004 [source] Atom transfer radical homo- and block copolymerization of methyl 1-bicyclobutanecarboxylateJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2002Xiao-Ping Chen Abstract A non-olefinic monomer, methyl 1-bicyclobutanecarboxylate (MBC), was successfully polymerized by the controlled/"living" atom transfer radical polymerization (ATRP) technique, resulting in a well-defined homopolymer, PMBC, with only cyclobutane ring units in the polymer chain. An AB block copolymer poly(methyl 1-bicyclobutanecarboxylate)- b -polystyrene (PMBC- b -PS), having an all-ring unit segment, was also synthesized with narrow polydispersity and designed number-average molecular weight in addition to precise end groups. The 1H NMR spectra, glass-transition temperature, and thermal stability of PMBC, PMBC- b -PS, and PS- b -PMBC were investigated. The experimental results showed that the cyclobutane rings in the two block polymers improved their thermal stability. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1929,1936, 2002 [source] Processability and characterization of poly(vinyl chloride)- b -poly(n -butyl acrylate)- b -poly(vinyl chloride) prepared by living radical polymerization of vinyl chloride.JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 4 2006Comparison with a flexible commercial resin formulation prepared with PVC, dioctyl phthalate This work reports the synthesis and processing of a new flexible material based on PVC produced by living radical polymerization. The synthesis was carried out in a two-step process. In the first step the macroinitiator ,, ,-di(iodo)poly(butyl acrylate) [,, ,-di(iodo)PBA] was synthesized in water by single electron transfer/degenerative chain transfer mediated living radical polymerization (SET-DTLRP) catalyzed by Na2S2O4. In the second step this macroinitiator was reinitiated by SET-DTLRP of vinyl chloride (VC), thereby leading to the formation of the block copolymer poly(vinyl chloride)- b -poly(butyl acrylate)- b -poly(vinyl chloride) [PVC- b -PBA- b -PVC]. This new material was processed on a laboratory scale. The DMTA traces showed only a single glass transition temperature, thus indicating that no phase segregation was present. The copolymers were studied with regard to their processing, miscibility, and mechanical properties. The first comparison with commercial formulations made with PVC and dioctyl phthalate (DOP) is presented. J. VINYL ADDIT. TECHNOL., 12:156,165, 2006. © 2006 Society of Plastics Engineers [source] Synthesis and characterization of temperature-sensitive block copolymers from poly(N -isopropylacrylamide) and 4-methyl-,-caprolactone or 4-phenyl-,-caprolactoneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010Ren-Shen Lee Abstract This study synthesizes thermally sensitive block copolymers poly(N -isopropylacrylamide)- b -poly(4-methyl-,-caprolactone) (PNIPA- b -PMCL) and poly(N -isopropylacrylamide)- b -poly(4-phenyl-,-caprolactone) (PNIPA- b -PBCL) by ring-opening polymerization of 4-methyl-,-caprolactone (MCL) or 4-phenyl-,-caprolactone (BCL) initiated from hydroxy-terminated poly(N -isopropylacrylamide) (PNIPA) as the macroinitiator in the presence of SnOct2 as the catalyst. This research prepares a PNIPA bearing a single terminal hydroxyl group by telomerization using 2-hydroxyethanethiol (ME) as a chain-transfer agent. These copolymers are characterized by differential scanning calorimetry (DSC), 1H-NMR, FTIR, and gel permeation chromatography (GPC). The thermal properties (Tg) of diblock copolymers depend on polymer compositions. Incorporating larger amount of MCL or BCL into the macromolecular backbone decreases Tg. Their solutions show transparent below a lower critical solution temperature (LCST) and opaque above the LCST. LCST values for the PNIPA- b -PMCL aqueous solution were observed to shift to lower temperature than that for PNIPA homopolymers. This work investigates their micellar characteristics in the aqueous phase by fluorescence spectroscopy, transmission electron microscopy (TEM), and dynamic light scattering (DLS). The block copolymers formed micelles in the aqueous phase with critical micelle concentrations (CMCs) in the range of 0.29,2.74 mg L,1, depending on polymer compositions, which dramatically affect micelle shape. Drug entrapment efficiency and drug loading content of micelles depend on block polymer compositions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Synthesis of AB-type block copolymers containing benzoxazole and anthracene groups by ATRP and fluorescent propertyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2007Jian-Mei Lu Abstract Two functional monomers, methacrylic acid 4-(2-benzoxazol)-benzyl ester (MABE) containing the benzoxazole group and 4-(2-(9-anthryl))-vinyl-styrene (AVS) containing the anthracene group were synthesized by rational design. The MABE was polymerized via atom transfer radical polymerization (ATRP) using ethyl 2-bromoisobutyrate (EBIB) as initiator in CuBr/N,N,N,,N,,N,-pentamethyldiethylenetriamine (PMDETA) catalyst system; block copolymers poly(MABE- b -AVS) was obtained, which was conducted by using poly(MABE) as macro-initiator, AVS as the second monomer, and CuBr/PMDETA as catalyst. The constitute of two monomers in block copolymers poly(MABE- b -AVS) by ATRP could be adjusted, that is the constitute of the benzoxazole group and the anthracene group could be controlled in AB-type block copolymers. Moreover, the fluorescent properties of homopolymers poly(MABE) and block copolymers poly(MABE- b -AVS) were discussed herein. With the excitation at ,ex = 330 nm, the fluorescent emission spectrum of poly(MABE) solution showed emission at 375 nm corresponding to the benzoxazole-based part; with the same excitation, the fluorescent emission spectrum of poly(MABE- b -AVS) solution showed a broad peek at 330,600 nm when the monomer AVS to the total monomers mole ratio was 0.31, and the fluorescent emission spectrum of poly(MABE- b -AVS) in film state only showed one peak at 525 nm corresponding to the anthracene-based unit that indicated a complete energy transfer from the benzoxazole group to the anthracene group. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3894,3901, 2007 [source] | ||||||||||