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931.
Filled covulcanizates of elastomer blend comprising natural rubber (NR) and ethylene‐propylene‐diene rubber (EPDM) of commercial importance were successfully prepared by using a multifunctional rubber additive; namely, bis(diisopropyl)thiophosphoryl disulfide (DIPDIS). A Two‐stage vulcanization technique further improved the physicochemical properties of the blend vulcanizates by restricting, through the formation of polar rubber bound intermediates, the migration of curative and filler from lower to highly unsaturated rubber. Scanning electron microscopy studies indicate homogeneity and coherency in the morphology of the two‐stage vulcanizates. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1001–1010, 2002; DOI 10.1002/app.10361  相似文献   
932.
The reactive compatibilization of syndiotactic polystyrene (sPS)/oxazoline‐styrene copolymer (RPS)/maleic anhydride grafted ethylene‐propylene copolymer (EPR‐MA) blends is investigated in this study. First, the miscibility of sPS/RPS blends is examined by thermal analysis. The cold crystallization peak (Tcc) moved toward higher temperature with increased PRS, and, concerning enthalpy relaxation behaviors, only a single enthalpy relation peak was found in all aged samples. These results indicate that the sPS/RPS blend is miscible along the various compositions and RPS can be used in the reactive compatibilization of sPS/RPS/EPR‐MA blends. The reactive compatibilized sPS/RPS/EPR‐MA blends showed finer morphology than sPS/EPR‐MA physical blends and higher storage modulus (G') and complex viscosity (η*) when RPS contents were increased. Moreover, the impact strength of sPS/RPS/EPR‐MA increased significantly compared to sPS/EPR‐MA blend, and SEM micrographs after impact testing show that the sPS/RPS/EPR‐MA blend has better adhesion between the sPS matrix and the dispersed EPR‐MA phase. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2084–2091, 2002  相似文献   
933.
The attachment of anticancer agents to polymers is a promising approach towards reducing the toxic side‐effects and retaining the potent antitumour activity of these agents. A new tetrahydrophthalimido monomer containing 5‐fluorouracil (ETPFU) and its homopolymer and copolymers with acrylic acid (AA) and with vinyl acetate (VAc) have been synthesized and spectroscopically characterized. The ETPFU contents in poly(ETPFU‐co‐AA) and poly(ETPFU‐co‐VAc) obtained by elemental analysis were 21 mol% and 20 mol%, respectively. The average molecular weights of the polymers determined by gel permeation chromatography were as follows: Mn = 8900 g mol?1, Mw = 13 300 g mol?1, Mw/Mn = 1.5 for poly(ETPFU); Mn = 13 500 g mol?1, Mw = 16 600 g mol?1, Mw/Mn = 1.2 for poly(ETPFU‐co‐AA); Mn = 8300 g mol?1, Mw = 11 600 g mol?1, Mw/Mn = 1.4 poly(ETPFU‐co‐VAc). The in vitro cytotoxicity of the compounds against FM3A and U937 cancer cell lines increased in the following order: ETPFU > 5‐FU > poly(ETPFU) > poly(ETPFU‐co‐AA) > poly(ETPFU‐co‐VAc). The in vivo antitumour activities of all the polymers in Balb/C mice bearing the sarcoma 180 tumour cell line were greater than those of 5‐FU and monomer at the highest dose (800 mg kg?1). © 2002 Society of Chemical Industry  相似文献   
934.
We used three kinds of alkyl diallyl ammonium salts (methyl, ethyl, and propyl) in combination with dimethyloldihydroxyethyleneurea (DMDHEU) as crosslinking agents. The nitrogen content, dry crease recovery angle (DCRA), moisture regain, and wicking height for the DMDHEU/alkyl diallyl ammonium salts were in the order of ? CH3 > ? C2H5 > ? C3H7, but the wet crease recovery angle (WCRA) and tensile strength retention (TSR) were in the opposite order at the same resin concentration. For the same DCRA and TSR, the WCRA values for only DMDHEU were lower than those for DMDHEU/alkyl diallyl ammonium salts, and the WCRA values for DMDHEU/alkyl diallyl ammonium salts were in the order of ? C3H7 > ? C2H5 > ? CH3. Both the ? OH group of the cellulose and DMDHEU could react with the vinyl or epoxy groups of the alkyl diallyl ammonium salts during the pad–dry–cure process. The surface migration for DMDHEU/alkyl diallyl ammonium salts was in the order of ? CH3 > ? C2H5 > ? C3H7. Fabrics treated with DMDHEU/alkyl diallyl ammonium salts showed good antibacterial properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1662–1669, 2003  相似文献   
935.
论述恒压源与恒流源两种高压直流电源的工作原理和技术特点.对两种电源常见故障的原因进行分析,提出相应的解决方法。介绍两种电源在230kt/a诺兰达炉冶炼烟气和270kt/a转炉冶炼烟气制酸装置的电除雾器中的使用情况.  相似文献   
936.
有毒化学品和有害废物对环境的污染及对人体健康的危害是中国环境保护面临的重大问题。本文概述了中国处理有毒化学品和有害废物的国家政策,化学工业有毒化学品和有害废物安全与控制的现状,并指出存在的问题及优先改进的领域。  相似文献   
937.
丙酸的合成与应用   总被引:5,自引:0,他引:5  
介绍了丙酸的各种合成方法、工艺流程及国内外丙酸的生产和应用概况,分析了各种方法的优缺点,对我国发展丙酸生产提出了建议。  相似文献   
938.
A new series of aromatic copolyesters containing siloxane linkages were prepared by the melt polymerization of bisphenol A (BPA) with eugenol end‐capped siloxane (EuSi), diphenyl terephthalate (DPT), and diphenyl isophthalate (DPI) in varying ratio in the temperature range 220–290°C under reduced pressure in the presence of dibutyl tin dilaurate (DBTL) catalyst. The siloxane copolyesters prepared were characterized by FTIR, 1H‐NMR spectroscopy, solution viscosity, thermogravimetric analysis, differential scanning calorimetry, and X‐ray diffraction. The effect of incorporation of eugenol end‐capped siloxane was studied on the properties of BPA/DPI/DPT copolyesters. The glass‐transition temperature of copolyester was decreased from 184 to 70°C by incorporation of 20% of eugenol end‐capped siloxane. All copolyesters were found to be soluble in commonly used aprotic polar solvents and had film‐forming properties. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3222–3228, 2006  相似文献   
939.
本文用失重法和慢应变率法确定16Mn钢在3%氯化钠水溶液中适宜阴极保护电位区间,用扫描电镜观察慢应变拉伸断口形貌。结果表明:16Mn钢在3%氯化钠水溶液中适宜阴极保护电位区间是:-775mVSCE——-900mVSCE。阴极过保护电位下,16Mn钢将发生以沿晶脆断为特征的氢脆,而且保护电位越负,其氢脆敏感性越大。  相似文献   
940.
通过田间试验探讨了复合改良制剂、草炭、风化煤等腐植酸类物质施用对盐碱化中低产田土壤理化性质及生长作物的影响,结果表明:复合改良制剂、草炭、风化煤施用对土壤理化性质均有积极的影响,与对照相比达到显著水平。玉米产量的方差分析表明,复合改良制剂处理与草炭、风化煤等处理差异显著,与对照差异极显著,增产率均达到30.67%以上。  相似文献   
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