ISSN 1000-6818CN 11-1892/O6CODEN WHXUEU
Acta Phys Chim Sin >> 2006,Vol.22>> Issue(09)>> 1116-1120     doi: 10.3866/PKU.WHXB20060916         中文摘要
Deep Desulfurization by Selective Adsorption on Heteroatom Zeolite Prepared by Secondary Synthesis
TANG Ke;SONG Li-Juan;DUAN Lin-Hai;LI Xiu-Qi;GUI, Jian-Zhou;SUN Zhao-Lin
(College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, P. R. China; College of Petrochemical Engineering, Liaoning University of Petroleum & Chemical Technology, Fushun 113001, P. R. China)
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Gallium atoms had been introduced into the framework of Y zeolite by treatment of zeolites with an aqueous solution of ammonium hexafluoro gallate. At ambient conditions and space velocity of 7 h−1, desulfurization of various model fuel, containing about 500 μg•g−1 sulfur was studied over the synthesized Y zeolite. Every gram adsorbent could adsorb 7.7, 17.4, 14.5 mg sulfur from thiophene, tetrahydrothiophene, 4,6-dimethyldibenzothiophene (4,6-DMDBT), respectively. The charge on S atom of thiophene, 4,6-DMDBT, and tetrahydrothiophene, calculated by using density functional theory (DFT), were −0.159, −0.214, and −0.298 respectively, implying that the S—M bond between the adsorption site and thiophene was much weaker than that between the adsorption site and tetrahydrothiophene or 4,6-DMDBT. The synthesized Y zeolites were evaluated for the adsorptive desulfurization of the FCC gasoline (sulfur content:299 μg•g−1) supplied by the No.2 Refinery in Fushun. After 2.1 mL gasoline being treated in one gram adsorbent, the sulfur content was 54.8 μg•g-1.

Keywords: Isomorphous substitution   Heteroatom Zeolite   Adsorption desulfurization   Model Fuel   DFT  
Received: 2006-03-26 Accepted: 1900-01-01 Publication Date (Web): 2006-09-04
Corresponding Authors: SUN Zhao-Lin Email:

Cite this article: TANG Ke;SONG Li-Juan;DUAN Lin-Hai;LI Xiu-Qi;GUI, Jian-Zhou;SUN Zhao-Lin. Deep Desulfurization by Selective Adsorption on Heteroatom Zeolite Prepared by Secondary Synthesis[J]. Acta Phys. -Chim. Sin., 2006,22 (09): 1116-1120.    doi: 10.3866/PKU.WHXB20060916
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