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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received September 24, 2012
Accepted October 26, 2013
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Photocatalytic oxidative desulfurization of dibenzothiophene catalyzed by amorphous TiO2 in ionic liquid

School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China 1School of the Environment, Jiangsu University, Zhenjiang 212013, P. R. China
lihm@ujs.edu.cn
Korean Journal of Chemical Engineering, February 2014, 31(2), 211-217(7), 10.1007/s11814-013-0224-3
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Abstract

Three types of TiO2 were synthesized by a hydrolysis and calcination method. The catalysts were characterized by X-ray powder diffraction (XRD), diffuse reflectance spectrum (DRS), Raman spectra, and X-ray photoelectron spectroscopy (XPS). The XRD and Raman spectra indicated that amorphous TiO2 was successfully obtained at 100 ℃. The results indicated that amorphous TiO2 achieved the highest efficiency of desulfurization. The photocatalytic oxidation of dibenzothiophene (DBT), benzothiophene (BT), 4,6-dimethyldibenzothiophene (4,6-DMDBT) and_x000D_ dodecanethiol (RSH) in model oil was studied at room temperature (30 ℃) with three catalysts. The system contained amorphous TiO2, H2O2, and [Bmim]BF4 ionic liquid, ultraviolet (UV), which played vitally important roles in the photocatalytic oxidative desulfurization. Especially, the molar ratio of H2O2 and sulfur (O/S) was only 2 : 1, which corresponded to the stoichiometric reaction. The sulfur removal of DBT-containing model oil with amorphous TiO2 could reach 96.6%, which was apparently superior to a system with anatase TiO2 (23.6%) or with anatase - rutile TiO2 (18.2%). The system could be recycled seven times without a signicant decrease in photocatalytic activity.

References

Ko NH, Lee JS, Huh ES, Lee H, Jung KD, Kim HS, Cheong M, Energy Fuels, 22(3), 1687 (2008)
Lin F, Wang DE, Jiang ZX, Ma Y, Li J, Li RG, Li C, Energy Environ. Sci., 5, 6400 (2012)
Li FT, Liu Y, Sun ZM, Zhao Y, Liu RH, Chen LJ, Zhao DS, Catal. Sci. Technol., 2, 1455 (2012)
Lokhande CD, Lee EH, Jung KD, Joo OS, J. Mater. Sci., 39(8), 2915 (2004)
Shiraishi Y, Hirai T, Komasawa I, J. Chem. Eng. Jpn., 35(12), 1305 (2002)
Thu HTV, Thu TTN, Phuong HTN, Do MH, Au HT, Nguyen TB, Nguyen DL, Park JS, Mater. Res. Bull., 47(2), 308 (2012)
Li FT, Liu RH, Sun ZM, China Petrol. Process. Petrochem. Technol., 53 (2008)
RE Demaray, HM Zhang, M Narasimhan, V Milonopoulou, US Patent, 20,040,259,305 A1 (2004)
Zhang ZY, Maggard PA, J. Photochem. Photobiol. A, 186, 8 (2007)
Senevirathna MKI, Pitigala PKDDP, Tennakone K, J. Photochem. Photobiol. A: Chem., 171, 257 (2005)
Zhu WSA, Li HM, Gu QQ, Wu PW, Zhu GP, Yan YS, Chen GY, J. Mol. Catal. A-Chem., 336(1-2), 16 (2011)
Ding YX, Zhu WS, Li HM, Jiang W, Zhang M, Duan YQ, Chang YH, Green Chem., 13, 1210 (2011)
Zhu WS, Zhang JT, Li HM, Chao YH, Jiang W, Yin S, Liu H, RSC Adv., 2, 658 (2012)
Cai TJ, Liao YC, Peng ZS, Long YF, Wei ZY, Deng Q, J. Environ. Sci., 21, 997 (2009)
Tayade RJ, Surolia PK, Kulkarni RG, Jasra RV, Sci. Technol. Adv. Mater., 8, 455 (2007)
Chen YF, Lee CY, Yeng MY, Chiu HT, J. Cryst. Growth, 247(3-4), 363 (2003)
Kumar PM, Badrinarayanan S, Sastry M, Thin Solid Films, 358(1-2), 122 (2000)
Davidson RS, Morrison CL, Abraham J, J. Photochem., 24, 27 (1984)
Zou J, Gao JC, Xie FY, J. Alloy. Compd., 497, 420 (2010)
Yoshitake H, Abe D, Micropor. Mesopor. Mater., 119, 267 (2009)
McCafferty E, Wightman JP, Surf. Interface Anal., 26, 549 (1998)
Anpo M, Yamashita H, Ikeue K, Fujii Y, Zhang SG, Ichihashi Y, Park DR, Suzuki Y, Koyano K, Tatsumi T, Catal. Today, 44(1-4), 327 (1998)
Muruganandham M, Swaminathan M, J. Hazard. Mater., 135(1-3), 78 (2006)
Matsuzawa S, Tanaka J, Sato S, Ibusuki T, J. Photochem. Photobiol. A: Chem., 149, 183 (2002)
Zhao DS, Liu R, Wang JL, Liu BY, Energy Fuels, 22(2), 1100 (2008)
Zhang J, Zhao DS, Yang LY, Li YB, Chem. Eng. J., 156(3), 528 (2010)
Xu JH, Zhao S, Chen W, Wang M, Song YF, Chem. Eur. J., 18, 4775 (2012)
Otsuki S, Nonaka T, Takashima N, Qian WH, Ishihara A, Imai T, Kabe T, Energy Fuels, 14(6), 1232 (2000)
Zhu WS, Li HM, Jiang X, Yan YS, Lu JD, He LN, Xia JX, Green Chem., 10, 641 (2008)

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