硫酸盐处理的纳米结构双功能氧化锆催化剂在正庚烷加氢异构化反应中的催化行为的实验和动力学研究

IF 2.8 Q2 ENGINEERING, CHEMICAL
Mohammed Khalil, B. Al-Zaidi, Zaidoon M. Shakor, S. Hussein, Ali Al-Shathr
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引用次数: 0

摘要

在本研究中,对单功能的ZrO2纳米材料进行硫处理,并负载两种不同比例的铂金属(即0.5 wt%和1 wt%),生成酸性双功能Pt/SZrO2纳米催化剂,以同时提高催化活性和选择性。这项工作的目的是确定最少量的昂贵的铂金属可以添加到催化剂中,以实现酸性和金属位点之间的适当平衡。因此,在整个反应过程中可以防止超酸性纳米催化剂的快速失活和零辛烷正庚烷链的快速裂解。这可以通过在5bar的压力下加速加氢异构反应来实现,以达到在燃料中产生所需多支化合物的最高选择性。采用XRD、SEM、EDX、BET和FTIR等表征技术对催化剂的物理性能进行了评价。与其他测试温度相比,在230℃时获得了最佳反应产物。制备的催化剂表面反应产物的转化率、选择性和产率依次为:0.5 wt% Pt/SZrO2 > 1 wt% Pt/SZrO2 > 0.5 wt% Pt/ZrO2 > 1 wt% Pt/ZrO2 > SZrO2 > ZrO2。0.5 wt% Pt/SZrO2催化剂表面的转化率、选择性和产率最高,分别为69.64、81.4和56.68 wt%,母体ZrO2催化剂表面的转化率、选择性和产率最低,分别为43.9、61.1和26.82 wt%。对加氢异构化、加氢/脱氢和加氢裂化反应的动力学模型和表观活化能进行了计算,结果表明:加氢异构化反应<加氢/脱氢反应<加氢裂化反应。活性最强、选择性最高的0.5% Pt/SZrO2纳米催化剂表面的表观活化能最低,为123.39 kJ/mol。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental and Kinetic Study of the Catalytic Behavior of Sulfate-Treated Nanostructured Bifunctional Zirconium Oxide Catalysts in n-Heptane Hydroisomerization Reactions
In this study, a mono-functional ZrO2 nanomaterial was treated with sulfur and loaded with two different percentages of platinum metals (i.e., 0.5 and 1 wt%) to generate an acidic bi-functional Pt/SZrO2 nanocatalyst for the purpose of increasing the catalytic activity and selectivity together. This work aims to determine the least amount of the costly platinum metal that can be added to the catalyst to achieve the appropriate balance between the acidic and metallic sites. Both rapid deactivation of the super-acid nanaocatalyst and fast cleavage of the zero-octane n-heptane chain can consequently be prevented throughout the reaction. This can be achieved by accelerating the hydroisomerization reactions at a pressure of 5 bar to reach the highest selectivity towards producing the desired multi-branched compound in fuel. Several characterization techniques, including XRD, SEM, EDX, BET, and FTIR, have been used to evaluate the physical properties of the catalysts. The best reaction product was obtained at 230 °C compared to the other tested temperatures. The conversion, selectivity, and yield of reaction products over the surfaces of the prepared catalysts followed this order: 0.5 wt% Pt/SZrO2 > 1 wt% Pt/SZrO2 > 0.5 wt% Pt/ZrO2 > 1 wt% Pt/ZrO2 > SZrO2 > ZrO2. The highest conversion, selectivity, and yield values were obtained on the surface of the 0.5 wt% Pt/SZrO2 catalyst, which are 69.64, 81.4 and 56.68 wt%, respectively, while the lowest values were obtained on the surface of the parent ZrO2 catalyst, which are 43.9, 61.1 and 26.82, respectively. The kinetic model and apparent activation energies were also implemented for each of the hydroisomerization, hydrogenation/dehydrogenation, and hydrocracking reactions, which track the following order: hydroisomerization < hydrogenation/dehydrogenation < hydrocracking. The lowest apparent activation energy value of 123.39 kJ/mol was found on the surface of the most active and selective 0.5% Pt/SZrO2 nanocatalyst.
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来源期刊
ChemEngineering
ChemEngineering Engineering-Engineering (all)
CiteScore
4.00
自引率
4.00%
发文量
88
审稿时长
11 weeks
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