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Transformation of Gaseous Technical Mixture of the Alkanes and Alkenes Into Liquid Fraction Over Ni-HZSM-5 Obtained by Ionic Exchange

机译:通过离子交换获得的Ni-HzSM-5,将烷烃和烯烃的气态化合物转化为液体级分

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Paraffin’s and olefins in the cracked naphtha can be transformed into aromatics and iso-paraffins to reduce the olefins content as well to improve the octane number of the gasoline commercial fraction. In this work Ni-HZSM-5 bifunctional catalyst was prepared by ion exchange with Ni(NO3)2 aqueous solution. The activity of Ni-HZSM-5 (wt.% 1.34% Ni) catalyst prepared by ion exchange method was investigated in the conversion of light hydrocarbons resulted as by-products of petroleum refining process (mixtures of butenes and (normal + iso) butanes as main components). The obtained Ni-based catalyst has been compare with HZSMcatalyst. The conversion experiments have been performed in a fixed-bed stainless-steel reactor (Twin Reactor System Naky) at 450oC, under 4 atm. (over Ni-HZSM-5) and 8 atm. pressure (over HZSM-5), respectively and at a space velocity (WHSV) of 1h-1. The catalytic activity of (Ni-HZSM-5 catalyst) monitored over 10 catalytic tests (with regeneration of catalyst after each test) using a mixtures butanes-butylenes. The catalytic activity and selectivity towards liquid products-BTX aromatic hydrocarbons and oligo(iC5-iC_(10), nC5-nC_(10), > C_(10))-depends on time streaming, composition of butanes-butylenes mixture and pressure. In the first hours of each test the aromatic BTX are the main component of the liquid product (connected with butylenes consume) and after that, the oligo fraction become predominant. The initial aromatization process described as dehydrocyclodimerization of alkanes and alkenes, principally to aromatics BTX and molecular hydrogen, is accompanied by oligomerization, isomerization, cracking and alkylation processes to form finally in the liquid phase product an excessively mixture of iso-and normal-C5-C_(10) and > C_(10) aliphatic hydrocarbons
机译:石蜡中的石蜡和烯烃在裂化的石脑油中可以转化为芳烃和异链烷烃,以减少烯烃含量,也可以改善汽油商业级分的辛烷值。在该工作中,通过与Ni(NO 3)2水溶液的离子交换制备Ni-HzSM-5双官能催化剂。通过离子交换方法制备的Ni-HzSM-5(WT.%1.34%Ni)催化剂的活性在轻质烃的转化中得到了石油精炼方法的副产物(丁烯和(正常+ ISO)丁烷的混合物作为主要成分)。获得的Ni基催化剂与HzsmcaTalyst进行了比较。转化实验已在450℃下的固定床不锈钢反应器(双反应器系统Naky)中进行。 (在Ni-Hzsm-5)和8个ATM。分别和以1H-1的空速(WHSV)的压力(过HZSM-5)。使用混合物 - 丁烯烯酮监测(每次测试后的催化剂再生)的(Ni-HzSM-5催化剂)的催化活性。催化活性和对液体产物-BTX芳烃和寡核苷酸的选择性(IC5-IC_(10),NC5-NC_(10),> C_(10)) - 取决于时间流,丁烯 - 丁基化合物的混合物和压力的组成。在每次测试的第一小时内,芳族BTX是液体产物的主要成分(与丁烯片消耗连接),之后,寡馏分馏分成为主要的。主要是芳族化合物BTX和分子氢的烷烃和烯烃的脱水环化的初始芳族化方法伴随着寡聚化,异构化,裂化和烷基化方法,以在液相产物中形成ISO-and ISO-and-C5-的过量混合物C_(10)和> C_(10)脂族碳氢化合物

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