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POLYMERIZATION OF METHYL METHACRYLATE CHIRAL LIGANDS
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作者 Bin YU Xue Chun LIN +2 位作者 Meng Xian DING Hui Zhen HU Fo Song WANG 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第1期27-30,共4页
Methyl methacrylate was anionically polymerized in the presence of chiral ligands, e. g. (+)-DDB and (-)-Sp. The polymers thus formed were optically inactive due to the instability of the helical chain for the less bu... Methyl methacrylate was anionically polymerized in the presence of chiral ligands, e. g. (+)-DDB and (-)-Sp. The polymers thus formed were optically inactive due to the instability of the helical chain for the less bulky ester group. Isotactic poly(methyl methacrylate) was given when (+)-DDB was used, whereas, a syndiotactic polymer was formed in the presence of (-)-Sp. Accordingly, two different propagation mechanisms were postulated. 展开更多
关键词 DDB LI PMMA POLYMERIZATION OF methyl METHACRYLATE CHIRAL LIGANDS
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PHOTOSENSITIVITY OF Ce (Ⅳ) INITIATED METHYL ACRYLATE POLYMERIZATION
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作者 董建华 杨建清 +1 位作者 丘坤元 冯新德 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 1992年第2期169-175,共7页
The influences of UV light irradiation (313 nm) and diffused daylight on the polymerization of methyl acrylate initiated by the ceric ammonium nitrate without any reducing agent have been studied both in aqueous nitri... The influences of UV light irradiation (313 nm) and diffused daylight on the polymerization of methyl acrylate initiated by the ceric ammonium nitrate without any reducing agent have been studied both in aqueous nitric acid and in pure water. The rate of polymerization was found to be accelerated and the overall activation energy and the induction time were found to be decreased sharply by the UV light irradiation. Under UV light, the rate of polymerization is 8 times as high as the rate in dark. The rate of polymerization was found to attain a maximum with the increase of nitric acid concentration and the rate of polymerization became less sensitive to UV light in the presence of nitric acid whereas the induction period reduced outstandingly. Based on the experimental results, the mechanism is proposed. 展开更多
关键词 Ceric ion initiation PHOTOSENSITIVITY methyl acrylate polymerization
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PHOTOSENSITIVITY OF CERIC ION INITIATED METHYL ACRYLATE POLYMERIZATION
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作者 Jian Hua DONG Jian Qing YANG Kun Yuan QIU Xin De FENG Department of Chemistry,Peking University,Beijing,100871 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第7期565-566,共2页
The polymerization of methyl acrylate was sensitive to UV light. Under UV light,the rate of polymerization is 8 times as high as the rate in dark.The overall activation energy was decreased by the UV light (313nm).A t... The polymerization of methyl acrylate was sensitive to UV light. Under UV light,the rate of polymerization is 8 times as high as the rate in dark.The overall activation energy was decreased by the UV light (313nm).A tentative explanation is given and the mechanism is discussed. 展开更多
关键词 UV NM IV PHOTOSENSITIVITY OF CERIC ION INITIATED methyl ACRYLATE POLYMERIZATION
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Atom Transfer Radical Polymerization of Methyl Methacrylate with α,α-Dichlorotoluene or α,α,α-Trichlorotoluene as Initiator
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作者 Zhi Feng FU Yan SHI +1 位作者 Ming Zhi HUANG Shu Ke JIAO(Department of Polymer Science. Beijing University of Chemical Technology. Beijing 100029) 《Chinese Chemical Letters》 SCIE CAS CSCD 1999年第7期611-614,共4页
The atom transfer radical polymerization (ATRP) of methyl methacrylate using α.α dichlorotoluene or α.α.α-trichlorotoluene as the initiator and CuCl/2.2'-bipyridine complex as the catalyst was investigated. ... The atom transfer radical polymerization (ATRP) of methyl methacrylate using α.α dichlorotoluene or α.α.α-trichlorotoluene as the initiator and CuCl/2.2'-bipyridine complex as the catalyst was investigated. α,α-Dichlorotoluene gave good control of molecular weight with high initiation efficiency and low polydispersity. While α.α.α-trichlorotoluene gave very slow polymerization rate. which could be improved by the addition of Cu (0) to the system. 展开更多
关键词 atom transfer radical polymerization (ATRP) methyl methacrylate INITIATOR
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THE EFFECTS OF N-2-HYDROXYETHYL-N-METHYL-p-TOLUIDINE ON METHYL METHACRYLATE RADICAL POLYMERI-ZATION AND ACRYLONITRILE PHOTOINDUCED POLYMERIZATION
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作者 丘坤元 张璋华 冯新德 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 1992年第3期250-257,共8页
The effects of N-2-hydroxyethyl-N-methyl-p-toluidine (HMT) on MMA polymerization using organic peroxide as an initiator and on AN photoinduced polymerization have been investigated respectively. The kinetics of polyme... The effects of N-2-hydroxyethyl-N-methyl-p-toluidine (HMT) on MMA polymerization using organic peroxide as an initiator and on AN photoinduced polymerization have been investigated respectively. The kinetics of polymerization and the overall activation energy of polymerization were determined. Based on kinetics study and the end group analysis of the polymer obtained by UV spectrum method, the initiation mechanism is proposed. 展开更多
关键词 HMT THE EFFECTS OF N-2-HYDROXYETHYL-N-methyl-p-TOLUIDINE ON methyl METHACRYLATE RADICAL POLYMERI-ZATION AND ACRYLONITRILE PHOTOINDUCED POLYMERIZATION BPO HMA MMA DMT LPO
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Plasma Induced Grafting of PMMA onto Titanium Dioxide Powder 被引量:6
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作者 钟少锋 孟月东 +1 位作者 欧琼荣 徐旭 《Plasma Science and Technology》 SCIE EI CAS CSCD 2005年第4期2955-2958,共4页
Grafting of polymer of methyl methacrylate (PMMA) onto titanium dioxide powder is investigated in this paper. The graft polymerization reaction is induced by dielectric-barrier- discharge produced N2 plasma treatmen... Grafting of polymer of methyl methacrylate (PMMA) onto titanium dioxide powder is investigated in this paper. The graft polymerization reaction is induced by dielectric-barrier- discharge produced N2 plasma treatment of titanium dioxide surfaces. IR, XPS and TGA results show that PMMA is grafted onto the surfaces of titanium dioxide powder. And crystal structure of the titanium dioxide powder observed with XRD spectra is unchanged after plasma graft polymerization. 展开更多
关键词 dielectric barrier discharge PLASMA titanium dioxide graft polymerization polymer of methyl methacrylate (PMMA) surface modification
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