共查询到20条相似文献,搜索用时 90 毫秒
1.
2.
3.
本文叙述了玻纤增强不饱和聚酯模塑料SMC制造配方、设备、复合及增稠等制备工艺,还阐述了SMC压塑成型三要素及制品性能。 相似文献
4.
第1部分 SMC/BMC:基础研究(Ⅰ) 1—A 影响表面平滑度的因素及不饱和聚酯和玻璃纤维的作用 1—B SMC模塑件中针孔主要成因的研究 1—C 优化SMC工艺条件改善产品表面质量 1—D 不饱和聚酯混合物的低收缩机理研 相似文献
5.
6.
有机累托石改性不饱和聚酯/玻璃纤维复合材料的研究 总被引:2,自引:0,他引:2
采用有机累托石改性不饱和聚酯,以改性的不饱和聚酯为基体,以两种玻璃布(EW210、CWR400-90)为增强材料,以两个不同凝胶时间的不饱和聚酯树脂体系制备三种有机累托石改性的不饱和聚酯磁璃纤维复合材料(UPB1、UPB2、UPB3)。测试了不饱和聚酯/玻璃纤维的力学性能;研究了复合材料的耐湿热性及耐介质性能;利用扫描电镜及透射电镜分析了复合材料的增强机理。结果表明,采用有机累托石改性不饱和聚酯所制备的不饱和聚酯/玻璃纤维复合材料的综合力学性能优于纯不饱和聚酯/玻璃纤维复合材料。 相似文献
7.
8.
聚酯预浸料复合SMC工艺及其应用 总被引:1,自引:0,他引:1
对以SMC为基础,添加以不饱和聚酯预浸材料作为加强层,形成的复合SMC材料进行了研究,介绍了采用的工艺流程和成型方法;以0.4mm的无碱玻璃布作为加强层增强材料,制作预浸布,以1∶1的体积比与SMC材料复合,采用复合SMC工艺成型的制品机械性能与常规SMC和采用聚酯作为树脂基体的RTM制品性能比较,拉伸强度达到180MPa,弯曲强度达到262MPa,冲击强度达到246kJ/m2,性能优势明显。 相似文献
9.
PF—SMC的性能、成型方法及其应用 总被引:1,自引:0,他引:1
PF—SMC(酚醛树脂片状模塑料)具有与UP—SMC(不饱和聚酯片状模塑料)基本相同的机械性能。但PF—SMC受热下的机械性能、阻燃和热稳定性更优于UP—SMC,已被广泛地应用于宇航、建筑、运输业等领域。 相似文献
10.
11.
乙烯酮(双乙烯酮)是十分重要的化工中间体,其下游产品较多。江苏某化工厂开发生产乙烯酮(双乙烯酮)下游产品三十多个,年生产规模三万多吨,是国内以乙烯酮(双乙烯酮)为中间体生产精细化学品的综合骨干企业。针对乙烯酮(双乙烯酮)下游产品废水特点,该厂结合企业实际,开展了产品优化,结构调整,清洁生产,资源循环利用,节水降耗等工作,从源头削减了污染物的生产。同时投资二千多万元新建预处理装置三套,6000m3/d废水生化处理装置一套,使全厂乙烯酮(双乙烯酮)下游产品的废水得到了有效的治理。 相似文献
13.
14.
D. G. Gordeev L. F. Gudarenko M. V. Zhernokletov V. G. Kudel’kin M. A. Mochalov 《Combustion, Explosion, and Shock Waves》2008,44(2):177-189
A semi-empirical equation of state for metals is described. Its capabilities are demonstrated by the example of the equation
of state for aluminum. New experimental data are presented on the location of the isentrope of aluminum for unloading from
the state at p = 229.71 GPa on the shock adiabat to an aerogel (SiO2) of density 0.08 g/cm3.
__________
Translated from Fizika Goreniya i Vzryva, Vol. 44, No. 2, pp. 61–75, March–April, 2008. 相似文献
15.
16.
Jorge Marcelo Romero Soledad Bustillo Hugo Enrique Ramirez Maisuls Nelly Lidia Jorge Manuel Eduardo Gómez Vara Eduardo Alberto Castro Alicia H. Jubert 《International journal of molecular sciences》2007,8(7):688-694
A thermochemical rather simple experimental technique is applied to determine the enthalpy of formation of Diperoxide of ciclohexanone. The study is complemented with suitable theoretical calculations at the semiempirical and ab initio levels. A particular satisfactory agreement between both ways is found for the ab initio calculation at the 6–311G basis This set level. Some possible extensions of the present procedure are pointed out. 相似文献
17.
18.
19.
The objective of the study was to explore the effect of the degree of deacetylation (DD) of the chitosan used on the degradation rate and rate constant during ultrasonic degradation. Chitin was extracted from red shrimp process waste. Four different DD chitosans were prepared from chitin by alkali deacetylation. Those chitosans were degraded by ultrasonic radiation to different molecular weights. Changes of the molecular weight were determined by light scattering, and data of molecular weight changes were used to calculate the degradation rate and rate constant. The results were as follows: The molecular weight of chitosans decreased with an increasing ultrasonication time. The curves of the molecular weight versus the ultrasonication time were broken at 1‐h treatment. The degradation rate and rate constant of sonolysis decreased with an increasing ultrasonication time. This may be because the chances of being attacked by the cavitation energy increased with an increasing molecular weight species and may be because smaller molecular weight species have shorter relaxation times and, thus, can alleviate the sonication stress easier. However, the degradation rate and rate constant of sonolysis increased with an increasing DD of the chitosan used. This may be because the flexibilitier molecules of higher DD chitosans are more susceptible to the shear force of elongation flow generated by the cavitation field or due to the bond energy difference of acetamido and β‐1,4‐glucoside linkage or hydrogen bonds. Breakage of the β‐1,4‐glucoside linkage will result in lower molecular weight and an increasing reaction rate and rate constant. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3526–3531, 2003 相似文献
20.
A perturbation viscometer is a differential capillary viscometer that measures the logarithmic viscosity gradient of the viscosity-composition curve for gas mixtures. Measurements are made at different gas mixture compositions. Integration of the logarithmic viscosity gradients measured over the full composition range gives the mixture viscosity relative to the viscosity of one of the pure components of the gas mixture. This method is attractive because, for measurements of equal precision, integration of the gradients is potentially an order of magnitude more precise than measurement of the viscosities directly. It can also work at high and low temperatures and perhaps high pressures.The perturbation viscometer has been used to make measurements on ideal gas mixtures at ambient and elevated temperatures. The situation is more complicated when the gas mixtures are non-ideal. Extra effects due to density differences, molar volume change on mixing and differential thermal expansion may be measured in addition to the desired viscosity change producing systematic errors in the results. Thus, a more sophisticated apparatus is required. The standard perturbation viscometer has been modified to separate out the extra effects to permit measurement of the true change in viscosity. In addition, the theoretical operation of the modified apparatus has been revised to account for the design changes to permit calculation of the viscosity-composition profiles from the results.The apparatus has been tested using helium-HFC-125 mixtures and two new viscosity-composition profiles are presented for these mixtures at 23 and . Internal consistency tests have been used to confirm that the data produced are of high quality with an estimated uncertainty in the viscosity ratio data at of 0.9% and at of 1.5%. 相似文献