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1.
廖畅生 《赣南师范学院学报》1992,(Z1)
以江西省各地高岭土作原料,用水热合成法制备了优良的新型洗涤剂助剂4A分子筛,产品的钙交换能力达到302mgcaco_3/g绝干分子筛,相对白度97,平均粒径4.04um,同时讨论了高岭土的脱色,合成过程的控制因素,并对产物进行了表征。 相似文献
2.
贾静娴 《唐山师范学院学报》2002,24(5):30-31
介绍了国内外洗涤助剂的发展状况,传统洗涤助剂磷酸盐被限制,沸石类助剂有局限,层状硅酸钠以优良的洗涤性能,环保无污染的特点,成为洗涤工业的新宠。 相似文献
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分两步法合成了低硅Beta分子筛,并以丙烯酸与异戊醇酯化反应作探针反应考察了低硅Beta分子筛的酸性能。结果表明:所合成的Beta分子筛具有独特的结构和酸性特征,反应温度140℃,反应时间2.5 h的条件下,丙烯酸的转化率可达76%。 相似文献
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采用产自云南文山的天然沸石矿作为试验材料,通过水洗、稀硫酸溶液浸渍和饱和氯化钠溶液浸渍三种方法活化改性处理;X衍射实验结果显示,样品中的基本成分钠红沸石保持不变;脱氮试验结果显示,饱和氯化钠溶液浸渍后的样品效果最佳,稀硫酸溶液浸渍的样品的效果次之,水洗后的样品的效果最差。 相似文献
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研究具有天然纳米孔道结构的沸石矿物材料的调湿性能,用酸活化和热活化的改性方法调控其显微结构,对改性工艺参数进行优选,得到性能较好的沸石调湿材料. 相似文献
7.
廖畅生 《赣南师范学院学报》1990,(Z1)
以三乙醇胺作模板剂,用水热法合成了MnCoAPO-5分子筛。用X射线衍射,电子探针,红外光谱等方法进行了结构研究,并测定了其晶胞参数和化学组成,同时对此分子筛的晶体形貌,热稳定性,吸附性能和比表面等进行了研究。证明锰和钴同时进入AlPO-5分子筛骨架而未改变结构类型。 相似文献
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Para-tert-butyl phenol (p-TBP) and 2,4-di-tert-butyl phenol ( 2,4-DTBP) are wi.dely used for the preparation of antioxidants. Zeolite catalysts showed good performance for the synthesis of p-TBP and 2,4-DTBP. In this work, zeolite H-mordenite (HM) catalyst was prepared and the alkylation of phenol with tert-butyl alcohol over zeolite HM catalyst was investigated at different reaction conditions. It is found that increasing temperature enhances the selectivity to p-TBP and the optimum reaction temperature for phenol conversion is 438 K. Increasing flow rate decreases phenol conversion apparently while the selectivity to p-TBP has a little increase. The suitable tert-butyl alcohol/phenol molar ratio is 2. Lower alcohol/phenol molar ratios are beneficial to p-TBP while higher ones are helpful for producing 2,4-DTBP. 相似文献
9.
ZHANG Hong-jing LONG Teng-rui CAO Yan-xiao 《重庆大学学报(英文版)》2006,5(3):152-156
1 Introduction ? The biological aerated filter technique has developed rapidly since 1980s, and is widely used in municipal sewage treatment. It has been used in the primary and secondary treatment processes due to its desirable economical efficiency and … 相似文献
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The OXZEO (oxide−zeolite) bifunctional catalyst concept has enabled selective syngas conversion to a series of value-added chemicals and fuels such as light olefins, aromatics and gasoline. Herein we report for the first time a dynamic confinement of SAPO-17 cages on the selectivity control of syngas conversion observed during an induction period. Structured illumination microscopy, intelligent gravimetric analysis, UV-Raman, X-ray diffraction, thermogravimetry and gas chromatography-mass spectrometer analysis indicate that this is attributed to the evolution of carbonaceous species as the reaction proceeds, which gradually reduces the effective space inside the cage. Consequently, the diffusion of molecules is hindered and the hindering is much more prominent for larger molecules such as C4+. As a result, the selectivity of ethylene is enhanced whereas that of C4+ is suppressed. Beyond the induction period, the product selectivity levels off. For instance, ethylene selectivity levels off at 44% and propylene selectivity at 31%, as well as CO conversion at 27%. The findings here bring a new fundamental understanding that will guide further development of selective catalysts for olefin synthesis based on the OXZEO concept. 相似文献