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251.
A series of poly [2-(dimethylamino)ethyl methacrylate (DMA)-sodium acrylate (SA)] diblock copolymers were synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization. The polymerization exhibits controlled characters: well-controlled molecular weight, narrow molecular weight distribution, molecular weight increasing with polymerization time. The zwitterionic diblock copolymers show rich solution behaviors. Dynamic light scattering (DLS) indicated the formation of micelles and reverse micelles of copolymers is affected by net charge density of copolymers. Microcalorimetry studies showed that the lower critical solution temperature (LCST) increases with incorporation of hydrophilic segments in buffer. 相似文献
252.
Kyoko Nozaki 《Journal of polymer science. Part A, Polymer chemistry》2004,42(2):215-221
Two examples of asymmetric alternating copolymerization, (1) the alternating copolymerization of α‐olefins (monosubstituted ethenes) with carbon monoxide and (2) the alternating copolymerization of meso‐epoxide with carbon dioxide, are described, and the meaning of chirality in polymer synthesis is emphasized. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 215–221, 2004 相似文献
253.
微波辐照下无皂阳离子聚(St-MMA)高分子纳米粒子的制备和表征 总被引:10,自引:1,他引:10
讨论了微波辐照下 ,以丙酮 水为分散介质 ,利用阳离子型自由基引发剂偶氮二异丁基脒盐酸盐(AIBA)引发苯乙烯 (St)和甲基丙烯酸甲酯 (MMA)共聚 ,合成出表面带正电荷的P(St MMA)共聚物纳米粒子 ,考察了丙酮用量、单体和引发剂浓度对纳米粒子粒径、粒径分布和乳液稳定性的影响 .结果表明 ,丙酮 水的体积比由 0增加到 1 2 6∶1时 ,粒子的平均水化半径从 12 2 2 1nm降低到 2 4 6 8nm ,粒径分布变宽 ,乳液抗电解质稳定性逐渐增强 ;增加引发剂和共聚单体MMA的浓度 ,粒子的水化半径逐渐减小 ,粒径分散系数增大 . 相似文献
254.
Nadine Metz 《European Polymer Journal》2007,43(4):1202-1209
Acetone oxime acrylate has been synthesized as a new active ester monomer. Free radical polymerization yielded a reactive polymer soluble in various organic solvents, such as chloroform, dioxane, DMSO, acetone, methanol, dichloromethane, DMF, and ethanol. Controlled radical polymerization of acetone oxime acrylate was successfully conducted using the RAFT, NMP and Iniferter method. Partly polymer analogous reaction with N-isopropylamine resulted in the reactive copolymer poly(N-isopropylacrylamide-co-acetone oxime acrylate), which featured a lower critical solution temperature (LCST) of 61 °C in water. Further, the reactivity of the copolymer was exemplary proven by complete reaction with ammonia yielding poly(N-isopropylacrylamide-co-acrylamide), which does not possess a LCST. 相似文献
255.
Akikazu Matsumoto Ryuji Kotaki Takayuki Otsu 《Journal of polymer science. Part A, Polymer chemistry》1991,29(12):1707-1715
Bulk polymerization of alkyl N,N-dialkylfumaramates (FAE) and maleamates (MAE) was performed in the presence of a radical initiator. It has been found that FAE is more reactive than MAE when the reactivity of the two geometrical isomers was compared for their homo- and copolymerizations. From investigation on the effect of ester and N-substituents of these monomers, it has been found that the isopropyl ester shows a higher reactivity than the methyl ester and that N-ethyl and n-butyl substitution gives polymers with high molecular weight of more than several thousands. The resulting substituted polymethylenes from FAE and MAE were characterized and compared with each other. The isomerization of MAE to FAE with morpholine as an isomerization catalyst and monomer-isomerization radical polymerization were also investigated. 相似文献
256.
D. Duracher F. Sauzedde A. Elaissari A. Perrin C. Pichot 《Colloid and polymer science》1998,276(3):219-231
Cationic hydrophilic copolymer latexes were synthesized at 70 °C either by batch or two-step emulsifier-free emulsion poly-merization
of styrene (St), N-iso-propylacrylamide (NIPAM), and aminoethylmethacrylate hydro-chloride (AEM) using 2,2′-azobis (2-amidinopropane) dihydrochloride
as initiator. At first, batch polymerization kinetics were followed by gas chromatography (GC), revealing that NIPAM rapidly
homopolymerized, before the polymerization of styrene had started. Particle size analysis by quasi-elastic light scattering
(QELS) and transmission electron microscopy (TEM) showed that monodispersed particles were obtained with the formation of
a poly[NIPAM] rich shell. Adding a small amount of the cationic monomer caused a strong decrease of the particle size without
affecting the size monodispersity. When a shot process was used, a narrow particle size distribution was maintained, provided
that the monomer addition was performed at a relatively high conversion of the first batch step. The poly[NIPAM] rich shell
layer was larger with the shot process, but increasing the amino-containing monomer in the recipe resulted in a dramatic decrease
of the thickness. Combination of transmission, scanning and atomic force microscopy techniques showed that these hydrophilic
particles exhibited odd-shaped structures, the unevenness being dependent upon the performed process. Kinetic data and particle
morphology information were inferred for discussion of the polymerization mechanism of this system.
Received: 21 August 1997 Accepted: 22 October 1997 相似文献
257.
S. Shen E. D. Sudol M. S. El-Aasser 《Journal of polymer science. Part A, Polymer chemistry》1994,32(6):1087-1100
The mechanism for the formation of micron-size polymer particles in the dispersion polymerization of methyl methacrylate was investigated by applying dynamic light scattering to monitor the evolution of the average particle size in the early stages of the polymerization. In addition, the contributions of physically adsorbed stabilizer and graft copolymer were evaluated by measuring the bound, unbound (adsorbed), and free stabilizer, and by determining the amount of added stabilizer required in seeded dispersion polymerizations. Twenty nanometer particles (termed nuclei) were the smallest particles detected and are considered to be formed by aggregation of growing polymer chains precipitating from solution as they exceed their critical chain length. Aggregation of these nuclei with themselves and their aggregates continues until mature and stable particles are formed. This occurs when sufficient stabilizer occupies the particle surface which includes both the polymeric stabilizer [poly(vinylpyrrolidone)] and its graft copolymer which is created in situ. The effects of process variables are discussed based on this mechanistic picture of the dispersion polymerization process. © 1994 John Wiley & Sons, Inc. 相似文献
258.
The interaction of carbenium ion pairs with silica is studied by means of UV-spectroscopy, electrokinetic and adsorption measurements using triphenylmethyl derivatives, (RC6H4)3CX, (X=F, Cl, Br, SCN, OH; R=Cl, I, H, CH3, C(CH3)3, OCH3, N(CH3)2) in interaction with silica particles suspended in 1,2-dichloroethane. The adsorption of triarylmethyl-halides onto silica is accompanied by the heterolytic dissociation of the tertiary carbonhalogen bond. The degree of ionization depends on the basicity of the counter anion and acidity of the cation, respectively. The influences of both concentration and structure of triarylmethyl halides on the zeta-potential are discussed with regard to steric and electronic factor. The zeta-potential values of the adsorbates decrease significantly, as compared with the free silica surface, from a certain triarylmethyl halide concentration where ionization takes place, to a constant level which is characteristic of the carbenium ion pair. These constant zeta-potential values of the adsorbates depend on the basicity of the counter ion and the
p
Hammett constants of the ring substitutents, with exclusion of sterically hindered substituents and salt derivatives, e.g., crystal violet and malachite green. 相似文献
259.
SynthesesandStudiesofPEG┐b┐PNIPABlockPolymersCAOWei-xiao**andZHANGTao(ColegeofChemistryandMolecularEnginering,PekingUniversit... 相似文献
260.
Binyuan Liu Yang Li Boo-gyo Shin Li Zhang Weidong Yan 《Polymer Degradation and Stability》2007,92(5):868-875
The thermal properties and degradation behaviors of poly(norbornene-2,3-dicarboxylic acid dialkyl esters) (PNB-dialkyl esters) (alkyl = Me (PNB-Me), Et (PNB-Et), Pr (PNB-Pr), and Bu (PNB-Bu)) were investigated by thermogravimetric analysis (TGA) in dynamic conditions and by infrared (IR) spectroscopy. The PNB-dialkyl esters show good thermal stability up to 350 °C, and the thermal stability decreases in the order Me > Et > Pr > Bu with the increase in size of side chain. The effect of side-chain size on the thermal degradation behaviors of PNB-dialkyl esters is evidenced by one-step thermal degradation profile for PNB-Me while two-step thermal degradation profile for PNB-Et, PNB-Pr, and PNB-Bu. Transformation is deduced to undergo β-hydrogen elimination and formation of anhydride group in the first stage of thermal degradation reaction according to TGA and IR results for PNB-Et, PNB-Pr, and PNB-Bu. The apparent activation energy and thermal degradation model of PNB-dialkyl esters are estimated by means of Ozawa-Flynn-wall method and Phadnis-Deshpande method, respectively. 相似文献