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环氧树脂/纳米介孔分子筛复合材料的制备及性能研究 总被引:5,自引:3,他引:2
通过溶液共混法制备出环氧树脂(EP)/纳米介孔分子筛MCM-41(with template)(以下简称MCM-41)复合材料。研究了不同的MCM-41粒子含量对其在EP中的分散性和EP/MCM-41复合材料拉伸性能的影响。结果表明,这种具有独特的有机-无机复合结构的MCM-41直接用作填料时,能与EP形成新型网络复合结构,当MCM-41粒子的用量为1.5~2.5份时,它能均匀地分散在EP基体中,有效地提高EP/MCM-41复合材料的拉伸性能。 相似文献
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利用水热合成法制备得到纳米介孔分子筛MCM-48,并研究了其对果胶酶的吸附固载性能和吸附条件及过程特点,测定了固载果胶酶的活性。动力学研究表明,MCM-48与果胶酶间的吸附符合准二阶动力学方程。热力学计算表明,该吸附过程ΔH=-68.94kJ/mol,ΔS=-197.90J·mol~(-1)·K~(-1),说明MCM-48对于果胶酶的吸附是一个放热的、熵减的吸附过程。通过对比游离酶(酶活力14 569U)和固定化果胶酶(酶活力13 345U)的酶活力,说明固载在MCM-48中的果胶酶依然具有良好的活性,这对于保持果胶酶的天然结构以及生物活性非常有益。 相似文献
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介孔分子筛催化剂作为一类新型催化材料,与传统的质子酸催化剂相比,其优点突出,已应用于炼油技术、化工和精细化学品的合成领域,文章对介孔分子筛的应用进展进行了综述并展望了微孔—介孔复合分子筛的发展远景,同时指出了存在的问题和不足。 相似文献
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MCM-41介孔分子筛改性研究进展 总被引:1,自引:0,他引:1
介绍了有序介孔材料的定义和分类,MCM-41介孔分子筛、合成方法和形成机理,针对其MCM-41目前存在的一些问题,综述了国内外对MCM-41介孔分子筛最新的改性研究进展。 相似文献
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Nylon 66/mesoporous molecular sieve (pore diameter: 2.7 nm) composites were prepared by annealing mixtures of nylon 66 and mesoporous molecular sieve (FSM) powders under high pressures and high temperature (FSM content: 0–60 wt %; pressure: 0.5–30 MPa; temperature: 300°C; time: 1 h). X‐ray diffraction and TEM measurements indicated the presence of the pores of FSM in the composite. Above 2 MPa, nylon 66 was charged in the pores of FSM. The fraction of the charged nylon 66 increased with pressure and was independent of the FSM content (pressure: 2–30 MPa; fraction of charged nylon 66: 54–66%). The infrared spectrum of the composite showed the bands based on Si O, C H, N H, CO. DSC measurement indicated that the heat of fusion of nylon 66 crystallite in the FSM pores was low compared with that of nylon 66. The composites prepared above 2 MPa were found to be superior in storage modulus to nylon 66. The modulus increased with an increase in the fraction of charged nylon 66 and the amount of FSM. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 3254–3258, 1999 相似文献
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A titanium-containing redox material with disordered wormhole-like mesoporous structure was prepared using microwave heating. Substantially accelerated crystallization was achieved using microwave heating compared with the conventional oven heating. Development of the mesopore structure was confirmed by XRD, TEM, and N2 physisorption. Incorporation of titanium into the mesopore structure was confirmed by UV-vis spectroscopy. A laser light particle size analyzer showed that smaller particle size and narrower particle size distribution were obtained with microwave heating than with oven-heated hydrothermal synthesis. These mesoporous titanosilicates were equally active as catalysts for liquid-phase oxidation of 2,6-di-tert-butylphenol with hydrogen peroxide as an oxidant. This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
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介绍了MCM-41介孔分子筛的优点,主要表现在具有较大的比表面积,孔体积与孔径和可调变等。综述了MCM-41介孔分子筛的合成方法与改性研究现状,阐述了MCM-41介孔分子筛的应用研究进展。 相似文献
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在水热体系中研究了以阳离子表面活性剂为主,阴离子表面活性剂、非离子表面活性剂、中性伯胺等为辅的混合表面活性剂对合成锆掺杂介孔分子筛的影响,考察了水/SiO2摩尔比、晶化温度、晶化时间及混合表面活性剂/SiO2摩尔比对所制分子筛结构的影响,对优化条件下合成的样品进行了表征. 结果表明,锆掺杂介孔分子筛的最佳合成体系为阴阳离子表面活性剂混合体系,最佳合成配方为水/SiO2摩尔比58,混合表面活性剂/SiO2摩尔比0.15, 100℃下晶化48 h. 最佳条件下合成的样品在小角区域有一个明显的衍射峰,表明其具有一定的长程有序性,晶面间距d=9.71 nm,平均孔径为5.55 nm,壁厚4.16 nm,具有三维蠕虫状孔道结构,吸附亚甲基蓝、罗丹明B与甲基橙的混合溶液时,对亚甲基蓝的吸附选择性较好,吸附率达90.24%. 相似文献
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The nonisothermal and isothermal degradation processes of poly(ethylene terephthalate)/mesoporous molecular sieve (PET/MMS)
composites synthesized by insitu polymerization were studied by using thermogravimetric analysis in nitrogen. The nonisothermal
degradation of the composite is found to be the first-order reaction. An isoconversional procedure developed by Ozawa is used
to calculate the apparent activation energy (E), which is an average value of about 260 kJ/mol with the weight conversion from 0% to 30%, and is higher than that of neat
PET. Isothermal degradation results are confirmed with the nonisothermal process, in which PET/MMS showed higher thermal stability
than neat PET. The polymer in mesoporous channels has more stability due to the protection of the inorganic pore-wall. These
results indicate that mesoporous MMS in PET/MMS composites improve the stability of the polymer.
Translated from Polymer Materials Science and Engineering, 2006, 22(1): 64–67 [译自: 高分子材料与工程] 相似文献