Ultra-deep adsorptive removal of thiophenic sulfur compounds from FCC gasoline over the specific active sites of CeHY zeolite  

作　　者：Yun Zu Chang Zhang Yucai Qin Xiaotong Zhang Li Zhang Honghai Liu Xionghou Gao Lijuan Song 

机构地区：[1]College of Chemistry and Chemical Engineering,China University of Petroleum(East China),Qingdao 266555,Shandong,China [2]Key Laboratory of Petrochemical Catalytic Science and Technology,Liaoning Shihua University,Fushun 113001,Liaoning,China [3]Lanzhou Petrochemical Research Center,Petrochemical Research Institute,Petro China Company Limited,Lanzhou 730060,Gansu,China

出　　处：《Journal of Energy Chemistry》2019年第12期256-267,共12页能源化学（英文版）

基　　金：financially supported by the National Natural Science Foundation of China (Nos. U1662135 and 21376114, 21076100);by the China National Petroleum Corporation (Grant No. 1001A-01-01-01)

摘　　要：Adsorption desulfurization performance of Na Y,HY and Ce HY zeolites is evaluated in a miniature fixedbed flow by model gasoline containing with thiophene,tetrahydrothiophene,2-methylthiophene,benzothiophene or mixed sulfur compounds.The structural properties of adsorbents are characterized by XRD,N2-adsorption and XPS techniques.Adsorption desulfurization mechanisms of these sulfur compounds over the specific active sites of adsorbents as a major focus of this work,have been systematically investigated by using in situ FT-IR spectroscopy with single and double probing molecules.Desulfurization experimental results show that the Ce HY adsorbent exhibits superior adsorption sulfur capacity at breakthrough point of zero sulfur for ultra-deep removal of each thiophenic sulfur compound,especially in the capture of aromatic 2-methylthiophene(about ca.28.6 mgS/gadsorbent).The results of in situ FT-IR with single probing molecule demonstrate an important finding that high oligomerization ability of thiophene or 2-methylthiophene on the CeHY can promote the breakthrough adsorption sulfur capacity,mainly resulting from the synergy between Br?nsted acid sites and Ce(III)hydroxylated species active sites located in the supercages of Ce HY.Meanwhile,the result of in situ FT-IR with double probing molecules further reveals the essence of oligomerization reactions of thiophene and 2-methylthiophene molecules on those specific active sites.By contrast,the oligomerization reaction of benzothiophene molecules on the active sites of Ce HY cannot occur due to the restriction of cavity size of supercages,but they can be adsorbed on the Br?nsted acid sites via protonation,and on Ce(III)hydroxylated species and extra-framework aluminum hydroxyls species via direct"S-M"bonding interaction.As to the tetrahydrothiophene,adsorption mechanism is similar to that of benzothiophene,except in the absence of protonation.The paper can provide a new design idea of specific adsorption active sites in excellent desulfurization adsorbents for elevatAdsorption desulfurization performance of Na Y, HY and Ce HY zeolites is evaluated in a miniature fixedbed flow by model gasoline containing with thiophene, tetrahydrothiophene, 2-methylthiophene, benzothiophene or mixed sulfur compounds. The structural properties of adsorbents are characterized by XRD, N2-adsorption and XPS techniques. Adsorption desulfurization mechanisms of these sulfur compounds over the specific active sites of adsorbents as a major focus of this work, have been systematically investigated by using in situ FT-IR spectroscopy with single and double probing molecules. Desulfurization experimental results show that the Ce HY adsorbent exhibits superior adsorption sulfur capacity at breakthrough point of zero sulfur for ultra-deep removal of each thiophenic sulfur compound, especially in the capture of aromatic 2-methylthiophene（about ca. 28.6 mgS/gadsorbent）. The results of in situ FT-IR with single probing molecule demonstrate an important finding that high oligomerization ability of thiophene or 2-methylthiophene on the CeHY can promote the breakthrough adsorption sulfur capacity, mainly resulting from the synergy between Br?nsted acid sites and Ce（III） hydroxylated species active sites located in the supercages of Ce HY. Meanwhile, the result of in situ FT-IR with double probing molecules further reveals the essence of oligomerization reactions of thiophene and 2-methylthiophene molecules on those specific active sites. By contrast, the oligomerization reaction of benzothiophene molecules on the active sites of Ce HY cannot occur due to the restriction of cavity size of supercages,but they can be adsorbed on the Br?nsted acid sites via protonation, and on Ce（III） hydroxylated species and extra-framework aluminum hydroxyls species via direct "S-M" bonding interaction. As to the tetrahydrothiophene, adsorption mechanism is similar to that of benzothiophene, except in the absence of protonation. The paper can provide a new design idea of specific adsorption active sites in excellent

关 键 词：CeHY zeolite Active sites Thiophenic sulfur compounds Adsorption desulfurization Oligomerization ability In situ FT-IR spectroscopy 

分 类 号：O64[理学—物理化学]