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121.
Hybrid precursors were assembled with cerium coordination polymers, polyethyl glycohol (PEG), SrCO3 and other functional components using a modified in-situ chemical polymeric gel technology. The hybrid precursors were calcinated to achieve the Sr2CeO4 phosphors, whose particle sizes were in the range of micrometer by XRD and SEM. The photoluminescence spectra indicate that the phosphors present a strong blue emission. 相似文献
122.
123.
Heather J. Avens 《Polymer》2008,49(22):4762-4768
Surface modification by surface-mediated polymerization necessitates control of the grafted polymer film thicknesses to achieve the desired property changes. Here, a microarray format is used to assess a range of reaction conditions and formulations rapidly in regards to the film thicknesses achieved and the polymerization behavior. Monomer formulations initiated by eosin conjugates with varying concentrations of poly(ethylene glycol) diacrylate (PEGDA), N-methyldiethanolamine (MDEA), and 1-vinyl-2-pyrrolidone (VP) were evaluated. Acrylamide with MDEA or ascorbic acid as a coinitiator was also investigated. The best formulation was found to be 40 wt% acrylamide with MDEA which yielded four to eightfold thicker films (maximum polymer thickness increased from 180 nm to 1420 nm) and generated visible films from fivefold lower eosin surface densities (2.8 versus 14 eosins/μm2) compared to a corresponding PEGDA formulation. Using a microarray format to assess multiple initiator surface densities enabled facile identification of a monomer formulation that yields the desired polymer properties and polymerization behavior across the requisite range of initiator surface densities. 相似文献
124.
125.
详细研究了以乙酸乙酯和环己烷为溶剂,丙烯酸为单体,BPO,LPO,AIBN为引发剂,聚烯基多醚为交联剂,合成增稠能力强、透明度高的聚丙烯酸树脂。于混和溶剂存在下制得的聚合物,消除了以往由二氯甲烷为溶剂的反应介质中所得产品的毒性,可广泛应用于医药及日用化工等行业。 相似文献
126.
水溶性聚偶氮酯的研究 总被引:1,自引:0,他引:1
用Pinner合成方法制备了用PEG400封端的水溶性聚偶氮酯,并表征了其结构;研究了热分解反应动力学及用于乳液聚合的动力学。结果表明,该种引发剂具有引发速度快、热分解机理简单和具有辅助乳化作用等优点。 相似文献
127.
W. Harmon Ray 《加拿大化工杂志》1991,69(3):626-629
A brief review of addition polymerization processes is presented with a summary of the key characteristics classified by kinetic mechanism (free-radical, anionic, cationic, group transfer, or Ziegler–Natta), phase behavior, and reactor type. A practical approach to modelling in the industrial R & D environment is discussed in terms of a CAD package for polymerization processes. 相似文献
128.
The effects of temperature, initiator, and accelerator levels on the curing of an epoxy bisphenol‐A vinyl ester resin Derakane® 411‐45 (formulated with styrene) were investigated by gel‐time and exotherm‐peak measurements on bulk samples. It was observed that the gel time was reduced as the initiator or accelerator ratio increased. Except at higher contents of the accelerator, a small kinetic plateau was seen in the gel curve and a shift of the maximum exotherm toward high temperatures in the DSC curves. This was explained by the dual role played by the accelerator species. A regression analysis of all gel‐time data showed a dependence of 3/2 order in the accelerator and first order in the initiator concentrations. Thus, for this polymerization initiation system, the gel time can be predicted for any initiator and cobalt levels and at any temperature within the ranges studied. The effect of the initiator on the unreacted styrene and vinyl ester was also examined. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1146–1154, 2002; DOI 10.1002/app.10403 相似文献
129.
Radiation polymerization of acrylonitrile in a viscous system with styrene was performed at ambient temperature by using γ‐rays. It is found that the overall rate of polymerization was accelerated after critical conversion due to the gel effect. As the molar fraction of styrene in monomer feed (fSt) is increased, both the total polymer conversion and molar fraction of acrylonitrile in the copolymer feed (FAN) were decreased. The monomer reactivity ratios for acrylonitrile and styerne were determined to be r1 (AN) = 0.25 and r2 (St) = 2.0, respectively. The copolymers obtained were characterized by Fourier transformed infrared spectra (FTIR), X‐ray diffraction (XRD), scanning electron microscopy (SEM), 1H‐NMR, and pyrolysis mass spectrometry (PMS). It was found that the slight addition of styrene to acrylonitrile strongly changes crystallinity, morphology, and thermal decomposition of the resulting polymer. 1H‐NMR measurment of AN/St copolymer showed the appearance of aromatic proton signals and shifted the resonance of the methylene proton to lower chemical shifts. The mass spectra of AN/St copolymers showed fragments of pyrolysates corresponding to oligonitriles with styrene end groups. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 268–275, 2002; DOI 10.1002/app.10324 相似文献
130.
高分子量阴离子型聚丙烯酰胺的制备 总被引:7,自引:0,他引:7
介绍了聚丙烯酰胺的品种、性能及用途;研究了以丙烯酸为共聚单体,采用反相乳液聚合制备高分子量阴离子型聚丙烯酰胺胶乳的原理和方法;分析讨论了原料纯度、乳化剂和引发剂种类及操作条件等因素对产品性能的影响. 相似文献