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注射氟橡胶胶料的研究 总被引:2,自引:1,他引:1
本文介绍了两种不同门尼粘度很橡胶2601与2605的共用,得到了各项物理机械性能符合GB7040-86,且工艺可行,产品的硫化合格率大于90%的注射胶料。 相似文献
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Fan‐Bao Meng Zheng‐Yan Wang Guo‐Wei Chai Hong‐Guang Wang Ying Chen Bao‐Yan Zhang 《应用聚合物科学杂志》2010,116(4):2384-2395
Several novel side‐chain liquid crystalline (LC) polysiloxanes bearing cholesteryl cinnamate mesogens and trifluoromethyl‐substituted mesogens were synthesized by a one‐step hydrosilylation reaction with poly(methylhydrogeno)siloxane, a cholesteric LC monomer cholesteryl 3‐(4‐allyloxy‐phenyl)‐acryloate and a fluoro‐containing LC monomer 4‐[2‐(3‐trifluoromethyl‐phenoxy)‐acetoxy]‐phenyl 4‐allyloxy‐benzoate. The chemical structures and LC properties of the monomers and polymers were characterized by use of various experimental techniques, such as FTIR, 1H‐NMR, 13C‐NMR, TGA, DSC, POM, and XRD. The temperatures at which 5% weight loss occurred were greater than 300°C for all the polymers, and the residue weight near 600°C increased slightly with increase of the trifluoromethyl‐substituted mesogens in the fluorinated polymer systems. The samples containing mainly cholesteryl cinnamate mesogens showed chiral nematic phase when they were heated and cooled, but the samples containing more trifluoromethyl‐substituted mesogens exhibited chiral smectic A mesophase. The glass transition temperature of the series of polymers increased slightly with increase of trifluoromethyl‐substituted mesogens in the polymer systems, but mesophase–isotropic phase transition temperature did not change greatly. In XRD curves, the intensity of sharp reflections at low angle increased with increase of trifluoromethyl‐substituted mesogens in the fluorinated polymers systems, indicating that the smectic order derived from trifluoromethyl‐substituted mesogens should be strengthened. These results should be due to the fluorophobic effect between trifluoromethyl‐substituted mesogens and the polymer matrix. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
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Abstract: This article presents an improved method to detect d ‐glucosamine hydrochloride in health foods. A simple precolumn derivatization procedure with 7‐flouro‐4‐nitrobenzo‐2‐oxa‐1,3‐diazole (NBD‐F) reagent was employed. The separation of the derivatized d ‐glucosamine hydrochloride (NBD‐d ‐glucosamine hydrochloride) was performed using a mobile phase consisting of acetonitrile, potassium dihydrogen phosphate (0.01 mol/L), and trifluoroacetic acid (350:649.74:0.26, volume ratio) at a flow rate of 1.0 mL/min with the column temperature 35 °C. Under the optimum chromatographic conditions, the peak area of NBD‐d ‐glucosamine hydrochloride compared with its absolute value of the peak area of NBD‐d ‐glucosamine hydrochloride in a standard solution concentration range from 1.0 to 500.0 mg/L showed a good linear calibration (R = 0.9999). Recoveries, at spiked concentrations of 10.0, 40.0, and 500.0 mg/L, varied between 97.2% and 102.6% with relative standard deviations ranging from 0.4% to 1.5%. The present method provides sufficient sensitivity as reflected by the values of limit of detection (LOD) and limit of quantification (LOQ). LOD was determined from the signal‐to‐noise ratios (S/N) of NBD‐d ‐glucosamine hydrochloride peak of at least 3 in the recovery test at 0.02 mg/L, and the estimated LOQ was 0.06 mg/L (S/N = 10). The proposed method was successfully applicable to detect d ‐glucosamine hydrochloride in health foods and drugs containing a variety of complex materials. 相似文献
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二元乙丙橡胶与四丙氟橡胶的并用研究 总被引:1,自引:2,他引:1
将二元乙丙橡胶与四丙氟橡胶并用采用过氧化二异丙苯/三烯丙基异氰脲酸酯作为共硫化体系,测出了不同并用比硫化胶的一些性能,结果表明,并用胶所选用的共硫化体系是成功的,并有和胶性能优良。 相似文献
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