共查询到19条相似文献,搜索用时 125 毫秒
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催化裂化汽油在多元沸石基催化剂上加氢改质研究 总被引:1,自引:0,他引:1
采用浸渍法分别制备了以丝光沸石(HM)、Hβ和HZSM-5及其组合为载体的沸石基Ni-Mo-P催化剂,考察了载体组成对催化裂化汽油加氢改质反应性能的影响。结果表明,由适宜比例的三者组合得到的沸石基Ni-Mo-P催化剂具有良好的加氢异构化、脱硫、芳构化活性及稳定性,可在催化裂化汽油脱硫降烯烃的同时保证产品的辛烷值不降低。考察了工艺条件对三元沸石基Ni-Mo-P催化剂反应性能的影响。在温度300 ℃、氢油体积比350、液相体积空速2.5 h-1和反应压力1.5 MPa反应条件下,催化裂化汽油异构烷烃收率、芳烃收率、脱硫率及液相收率分别达41.9%、31.7%、51.0%和98.3% 。 相似文献
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R. D. Wragg P. G. Ashmore J. A. Hockey 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1972,22(6):759-768
The heterogeneously-catalysed oxidation of hydrocarbons over oxide catalysts is reviewed. The first section of the paper deals in a general way with the structural features of hydrocarbons and relates these to the selective oxidation products which may be obtained from them. The interaction of oxygen and hydrocarbons with oxides is also considered in a general context and the kinetics of heterogeneous oxidation of hydrocarbons are discussed. The second section of the paper deals in more detail with the selective oxidation of aromatic hydrocarbons with particular reference to vanadium oxide containing catalysts. Finally, an account is given of the selective oxidation of monoalkenes to 1,3 conjugated systems and ketones over mixed oxide catalysts. The information available is considered throughout with a view to revealing those features of such systems which give rise to the selectivity. 相似文献
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分子筛催化剂上催化裂化汽油掺混甲醇的改质研究 总被引:1,自引:1,他引:0
以实现甲醇制取低碳烯烃转化工艺和FCC汽油降烯烃工艺的有效组合为目的,在固定床微型反应装置上,使用SAPO-34、ZSM-5、DOCO以及分子筛组合催化剂,对FCC汽油掺混甲醇改质进行了研究。主要对反应温度、空速和混炼比等影响因素进行了考察。结果表明,SAPO-34分子筛上甲醇制取低碳烯烃效果较好,高烯烃含量汽油在SAPO-34分子筛上的氢转移和芳构化效果显著,ZSM-5分子筛上的芳构化反应效果和DOCO的异构化反应效果较显著,甲醇转化与汽油转化反应间的相互协同作用,既有利于甲醇转化成低碳烯烃又能提高汽油降烯烃转化深度。适宜的混炼条件:反应温度400℃,m(甲醇):m(汽油)=0.05,空速3h~(-1),组合催化剂上,产物汽油中烯烃含量较FCC粗汽油下降23%以上。 相似文献
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通过可控液相沉积制备具有超顺磁性能的介孔核-壳结构Fe3O4@nSiO2@mSiO2-Al2O3和H3P12W40/Fe3O4@nSiO2@mSiO2-Al2O3催化剂。以噻吩和异戊烯组成的模拟汽油烷基化反应作为探针反应,考察催化脱硫性能,并采用FT-IR、N2等温吸附-脱附、NH3-TPD、VSM和SEM等方法对催化剂进行表征。结果表明,Fe3O4@nSiO2@mSiO2-Al2O3催化剂是具有超顺磁性和介孔结构特征的固体酸催化剂,其饱和磁化强度为46.3 emu·g-1,低矫顽力为零,比表面积为342.6 m2·g-1。模拟汽油在Fe3O4@nSiO2@mSiO2-Al2O3催化剂上170 ℃反应2 h,噻吩转化率为72.2%,负载质量分数40%的磷钨酸后,噻吩转化率达96.9%,催化活性、选择性和催化剂寿命均提高。 相似文献
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新型MCM-22/MCM-41复合分子筛上FCC汽油降烯烃芳构化反应 总被引:1,自引:0,他引:1
采用纳米组装法合成MCM-22/MCM-41微孔/介孔复合分子筛,分别以H-MCM-22和H-MCM-22/MCM-41为催化剂,在固定床微反装置上对FCC汽油进行降烯烃芳构化的对比考察。结果表明,在反应时间2 h内,与MCM-22相比, MCM-22/MCM-41具有高的芳构化性能和持久的初始活性,复合分子筛汽油改质的产物中,芳烃体积分数由28.58%上升至51.1%,烯烃体积分数由34.04%降至5.8%。探讨了新型H-MCM-22/MCM-41复合分子筛用于FCC汽油改质的操作条件以及催化剂失活再生性能。结果表明,最佳反应条件为:反应温度400 ℃,压力2 MPa,空速3 h-1。失活催化剂经过两次再生,降烯烃芳构化性能基本不变。 相似文献
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Karishma Irani William S. Epling Richard Blint 《Applied catalysis. B, Environmental》2009,92(3-4):422-428
The effect of propylene concentration on NO oxidation as a function of temperature and position over a model Pt-Pd/Al2O3 diesel oxidation catalyst was investigated. Propylene had an apparent inhibition effect on NO oxidation. This apparent inhibition is a result of NO2, as the NO oxidation product, acting as an oxidant in the reaction with propylene. This was verified with experiments that included NO2, and a resulting significant temperature decrease in the onset of NO2 reduction when propylene was present. Furthermore, increasing amounts of propylene further decreased the NO2 reduction temperature. Similar results were observed with m-xylene and dodecane addition as well. The results also demonstrate that NO2 was consumed preferentially relative to O2 during hydrocarbon oxidation. With low inlet levels of O2, the addition of NO2 apparently inhibited propylene oxidation after the onset of NO2 reduction. This subsequent inhibition was due to the NO formed, demonstrating that propylene results in reduced NO2 outlet levels while NO inhibits propylene oxidation. 相似文献
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The effect of various metal additives on the catalytic performance of carbon during the selective reduction of NO with methanol has been studied in the absence and in the presence of gas-phase oxygen. The mechanism of this reaction in the use of carbon-supported catalysts was studied by means of in situ FTIR combined with the measurements of catalytic activity. In the absence of oxygen, NO is adsorbed in a very small amount on the surface of carbon. The reaction of NO with the products of the methanol decomposition, results in the formation of adsorbed isocyanate (NCO) species at 2229 cm−1. Formation of gaseous NH3 as a product of the reaction between NO and methanol was observed. Oxygen-containing surface functional groups of carbon effectively promotes the reduction of NO with methanol. IR spectroscopic results of this study show that in the presence of O2 nitric oxide is catalytically oxidized to nitrogen dioxide, which is chemisorbed on the surface of carbon. The surface nitrogen species were identified by FTIR spectroscopy. 相似文献