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SUPPORTED ZIEGLER-NATTA CATALYSTS FOR ETHYLENE SLURRY POLYMERIZATION AND CONTROL OF MOLECULAR WEIGHT DISTRIBUTION OF POLYETHYLENE 被引量:1
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作者 Vladimir Zakharov Ludmila Echevskaya +4 位作者 Tatiana Mikenas Mikhail Matsko Andrey Tregubov Marina Vanina Marina Nikolaeva 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2008年第5期553-559,共7页
The effect of chemical composition of highly active supported Ziegler-Natta catalysts with controlled morphology on the MWD of PE has been studied.It was shown the variation of transition metal compound in the MgCl_2-... The effect of chemical composition of highly active supported Ziegler-Natta catalysts with controlled morphology on the MWD of PE has been studied.It was shown the variation of transition metal compound in the MgCl_2-supported catalyst affect of MWD of PE produced in broad range:Vanadium-magnesium catalyst(VMC)produce PE with broad and bimodal MWD(M_w/M_n=14-21).MWD of PE,produced over titanium-magnesium catalyst(TMC)is narrow or medium depending on Ti content in the catalyst(M_w/M_n=3.1-4.8).The oxidation ... 展开更多
关键词 Polyethylene(PE) Vanadium magnesium catalyst(VMC) Titanium magnesium catalyst(TMC) Gel permeation chromatographygpc Molecular weight distribution(MWD).
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Thermal aging behavior of high performance poly(vinyl alcohol) hydrogel
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作者 唐启恒 牛润利 +2 位作者 杨荣杰 李晓东 何吉宇 《Journal of Beijing Institute of Technology》 EI CAS 2012年第4期558-563,共6页
The thermal aging behavior of poly ( vinyl alcohol ) ( PVA ) hydrogel was studied at four different temperatures of 40 ℃, 50 ℃, 60 ℃ and 70 ℃ in one year. The samples of PVA hydrogel were closely covered by pl... The thermal aging behavior of poly ( vinyl alcohol ) ( PVA ) hydrogel was studied at four different temperatures of 40 ℃, 50 ℃, 60 ℃ and 70 ℃ in one year. The samples of PVA hydrogel were closely covered by plastic film. The changes of their chemical structures and physical properties during aging were measured through different measurable techniques including tensile testing, gel permeation chromatography ( GPC ), viscosity analysis, and Fourier transform infrared (FTIR) spec- trum. The results showed that the molecular weight of PVA in hydrogel changed little with time and temperature. FTIR spectra of PVA in all the samples were similar to those of the original samples. The tensile strength of PVA hydrogel didn't change until the 330th days. 展开更多
关键词 poly vinyl alcohol) hydrogel thermal aging gel permeation chromatography gpc VISCOMETRY Fourier transform infrared (FTIR) spectrum
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COPPER(0)-MEDIATED RADICAL POLYMERIZATION OF STYRENE AT ROOM TEMPERATURE
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作者 Xiao-fei Zhang Yang Wu +3 位作者 Jun Huang Xue-lang Miao 张正彪 朱秀林 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2013年第4期702-712,共11页
The "living'/controlled radical polymerization (LRP) of styrene (St) at room temperature is rarely reported. In this work, copper(0) (Cu(0))-mediated radical polymerization of St at room temperature was in... The "living'/controlled radical polymerization (LRP) of styrene (St) at room temperature is rarely reported. In this work, copper(0) (Cu(0))-mediated radical polymerization of St at room temperature was investigated in detail. Dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF) as well as a binary solvent, tetrahydrofuravdl,l,l,3,3,3-hexafluoro-2- propanol were used as the solvents, respectively. Methyl-2-bromopropionate and ethyl 2-bromoisobutyrate were used as the initiators, respectively. The polymerization proceeded smoothly with moderate conversions at room temperature. It was found that DMF was a good solvent with the essential features of LRP, while DMSO was a poor solvent with uncontrollable molecular weights. Besides, the match among the initiator, solvent and molar ratios of reactants can modulate the livingness of the polymerization, and the proper selection of ligand was also crucial to a controlled process. This work provided a first example of Cu(0)-mediated radical polymerization of St at room temperature, which would enrich and strength the LRP technique. 展开更多
关键词 Gel permeation chromatography gpc Kinetics (polym.) Cu(0)-mediated radical polymerization Styrene.
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