共查询到18条相似文献,搜索用时 78 毫秒
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采用水热法合成出n(Si)/n(Al)=25的Al-MCM-48介孔分子筛,并用NH4NO3溶液处理得到H型的H-Al-MCM-48介孔分子筛。采用XRD、N2吸附–脱附、TEM等手段对样品进行了表征,并研究了样品对苯酚与叔丁醇烷基化反应催化性能。结果表明,合成的Al-MCM-48样品具有高度有序的立方介孔结构,H-Al-MCM-48的介孔有序性和比表面积有所降低,但样品仍具有MCM-48的立方结构。H-Al-MCM-48在苯酚与叔丁醇的烷基化反应中显示出良好的催化活性,在反应温度为140℃时苯酚的转化率高达98.9%。 相似文献
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采用水热法合成出不含镍和含镍的硅基介孔分子筛.利用XRD、FT-IR、TPR、TEM和比表面孔径测定等手段对样品进行了表征.结果表明:合成出有序性好的介孔分子筛(MCM-41),550 ℃焙烧可以将模板剂有效去除,所合成介孔分子筛负载Pt后介孔有序性降低,但是介孔结构仍然存在.苯催化加氢反应研究表明:不含Ni的介孔分子筛不具有加氢活性,当将其负载Pt后具有苯加氢催化活性;含Ni介孔分子筛本身具有苯加氢活性,含Ni介孔分子筛负载Pt后苯加氢催化活性有较大的提高,所有样品的环己烷选择性都接近100 %,说明含Ni介孔分子筛可以直接作为苯加氢反应的催化剂或作为苯加氢催化剂良好的载体. 相似文献
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采用嫁接法制备了Al-SBA-15介孔分子筛,并对硅铝比、焙烧温度等影响产物的制备因素进行了考察。通过XRD,BET,FT-IR,NH3-TPD等分析手段对所得样品进行了分析。将所得产物Al-SBA-15与SBA-15在相同条件下进行了吸附脱除碱性氮化物对比实验。结果表明:Al-SBA-15保留了SBA-15高度有序的二维六方介孔结构。AlSBA-15具有比SBA-15更好的吸附脱氮能力,在焙烧温度550℃、硅铝比(原子比)为50的条件下,Al-SBA-15(50)介孔分子筛最高脱氮率为68.02%,此时饱和吸附量为30.6 mg/g。 相似文献
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以正硅酸乙酯(TEOS)为硅源,十六烷基三甲基溴化铵(CTABr)为模板剂,三氯化铝为铝源在室温条件下合成了介孔硅铝分子筛A1-MCM-41。采用红外光谱(IR)、X射线衍射(XRD)、低温氮吸附等温线等方法对分子筛进行了结构表征。评价结果表明,A1-MCM-41分子筛对桥式四氢双环戊二烯(endo-TCD)具有良好的催化异构化性能。 相似文献
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以阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)作为模板剂,正硅酸乙酯(TEOS)作为硅源,在强碱性条件下,加入过渡金属氧化物偏钨酸铵合成得到WSiOx介孔分子筛,使用乙酰丙酮作为助剂,考察其对孔结构的影响,通过X射线衍射仪(XRD)、N2吸附-脱附、原位红外(FT-IR)、扫描电镜(SEM)表征手段对合成出的WSiOx上分子筛的结构性能进行研究.随着W质量分数的增加,介孔特征衍射峰的有序度增加,质量分数大于6%后有序度下降;W的加入没有破坏介孔分子筛的骨架结构.最后的结果得到,最佳W质量分数为5%,模板剂质量分数为1.8%,乙酰丙酮质量分数为9%.平均孔径为4.68 nm,比表面积为966 m2/g. 相似文献
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在强酸性和水热条件下以硅酸钠(Na2SiO3·9H2O)为硅源合成表面含磺酸基的介孔分子筛催化剂SBA-15-SO3H。XRD结果表明,该分子筛具有规则的六方立柱形介孔结构。SBA-15-SO3H用于叔丁醇和乙醇合成乙基叔丁基醚(ETBE)的醚化反应研究,分别考察了反应温度、原料配比和反应时间等因素对醚化反应的影响。最佳操作条件为:温度120 ℃,n(乙醇)∶n(叔丁醇)=2∶1,反应时间5 h,m(催化剂) ∶m(原料)=1∶10。在此条件下,叔丁醇的转化率为62.83%。 相似文献
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钛硅分子筛TS-1的合成改性及其催化功能 总被引:1,自引:0,他引:1
钛硅分子筛TS-1由于其优异的催化氧化性能而受到极大关注,TS-1的制备及基础研究是催化领域的一个热点。本文重点综述了近年来钛硅分子筛催化材料的合成、改性及其催化应用的研究进展,包括钛硅分子筛(TS-1)的水热合成方法和同晶取代合成法、改性、成型与负载以及钛硅分子筛催化氧化功能和酸催化功能的研究。 相似文献
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Chemical modification (CM) and deposition-precipitation (DP) methods were used for the dispersion of active Au nanoparticles on mesoporous silica materials in this work. XRD, TEM, N2 adsorption isotherms and UV-Vis absorption spectra were used to characterize in detail Au-SBA-15 materials prepared by the two methods. The analysis results showed that high loading (1.7%, by mass) and uniform Au nanoparticles (approximately 3 nm) were dispersed in the channels of mesoporous SBA-15 by the CM method. While for the DP method, most of Au nanoparticles with the size of 10—15nm were aggregated outside of the channels of SBA-15 and the actual loading of Au was only 0.38% (by mass). 相似文献
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Li Qiang Dou Tao Zhang Ying Li Yuping Wang Shan Sun Famin 《Frontiers of Chemical Engineering in China》2007,1(1):1-5
Mesoporous aluminosilicate MCM-48 containing zeolite secondary building units in the pore wall has been synthesized in alkaline
media with a two-step procedure. The aluminosilicate precursors comprising zeolite secondary building units were first synthesized
by carefully controlling reaction conditions and then were assembled using co-templates of gemini surfactant [C18H37N(CH3)2(CH2)3-N(CH3)2C18H37]2+ (18-3-18) and triethanolamine (TEA). X-ray Diffraction (XRD) patterns of the as-made samples indicated that highly ordered
mesostructured MCM-48 was formed. Transmission Electron Microscopy (TEM) images further verified the formation of MCM-48 with
uniform cubic pore channel system having the pore opening diameter of about 25 ?. Compared with the conventionally synthesized
MCM-48, the as-synthesized MCM-48 sample showed an adsorption band at 520–600 cm−1 in its FT-IR spectrum, which was assigned to five-membered ring vibration from zeolite structure. This suggested the presence
of zeolite building units in the pore wall. N2 adsorption data showed that the material had a much higher specific surface area (1 200 m2/g) than the conventional MCM-48(1 100 m2/g). Finally, the catalytic performance of the as-made MCM-48 was evaluated by hydrogenation dealkylation reaction of heavy
aromatic hydrocarbons. Catalytic results showed that the as-made MCM-48 catalyst exhibited higher conversion than the conventional
MCM-48 catalyst. The as-made mesostructured MCM-48 may have a potential catalytic application in the conversion of bulky molecules.
Translated from Journal of Fuel Chemistry and Technology, 2006, 34(1): 105–108 [译自: 燃料化学学报] 相似文献
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The development of ordered mesoporous solids is revised. Acid, base, and redox catalytic properties are presented together
with their application for a series of organic reactions of fundamental and practical interest. Finally it is explained that
it is possible to make use of the high surface and regular porosity of MCM–41 to prepare supported metals, and bifunctional
catalysts. The above properties together with the presence of a large number of surface silanol groups allow the grafting
of catalytically active transition metal complexes.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
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