Sulfided NiMo/Clinoptilolite Catalysts for Selective Sulfur Removal from Naphtha Stream without Olefin Hydrogenation

Cristina Farías Rosales, R. Guil-López, M. Faraldos, Rafael Maya Yescas, Trino Armando Zepeda, B. Pawelec, R. Huirache-Acuña
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引用次数: 1

Abstract

The natural clinoptilolite zeolite has been modified by acid leaching with HNO3 in order to obtain economic material for supporting NiMoS hydrotreating catalysts. The most optimized zeolite material was obtained by leaching with HNO3 at 80°C during 24 h. The bimetallic NiMo catalysts prepared by wet impregnation of a zeolite support, followed by calcination and sulfidation, were characterized by several physico-chemical techniques and tested in the hydrodesulfurization (HDS) of 3-methyl-thiophene (3-MT) model feed at atmospheric H2 pressure and T = 280°C. For all catalysts, the 3-MT transformation mainly occurs via direct desulfurization reaction route being diminished the catalyst hydrogenation function. This was linked with the formation of highly stacked layers of MoS2 particles having a low amount of “brim sites,” as demonstrated by HRTEM. The cause of the best performance of Ni-Mo(H)/Z-1 sulfide catalyst in the HDS of 3-MT can be the presence of K impurities on the support surface which forces the formation of highly stacked layers of MoS2 particles.
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硫化镍/斜沸石催化剂在石脑油不加氢选择性脱硫中的应用
采用HNO3酸浸法对天然斜沸石沸石进行了改性,以获得经济的NiMoS加氢催化剂载体材料。采用沸石载体湿浸渍、煅烧、硫化法制备的双金属NiMo催化剂,在常压H2、温度为280℃条件下对3-甲基噻吩(3-MT)模型进料加氢脱硫(HDS)进行了实验研究。所有催化剂的3-MT转化主要通过直接脱硫反应途径进行,催化剂的加氢功能减弱。正如HRTEM所证明的那样,这与具有少量“边缘位置”的高度堆叠的二硫化钼颗粒层的形成有关。Ni-Mo(H)/Z-1硫化物催化剂在3-MT的HDS中表现出最佳性能的原因可能是K杂质在载体表面的存在,迫使MoS2颗粒形成高度堆叠的层。
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