Developments of modified magnetic nanoparticle -supported heteropolyacid catalytic performances in dibenzothiophene desulfurization
الموضوعات : Iranian Journal of Catalysis
Hossein Salavati
1
(Department of Chemistry, Payame Noor University, 19395-3697, Tehran, Iran.)
Abbas Teimouri
2
(Department of Chemistry, Payame Noor University, 19395-3697, Tehran, Iran.)
Shahnaz Kazemi
3
(Department of Chemistry, Birjand University, 97179-414, Birjand, Iran.)
الکلمات المفتاحية: oxidation, Supported catalyst, Heteropolyacid, Magnetic nanoparticles,
ملخص المقالة :
In this research, Keggin-type polyoxometalate, H5PMoV2O40 (denoted as PMoV) was immobilized on modified NiFe2O4 nanoparticles to produce a magnetically separable catalyst. This catalyst was characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), cyclic voltummetry (CV), energy dispersive X-ray (EDX) and UV-vis diffuse reflectance spectroscopy (UV-DRS). The catalytic activity of synthesized catalyst in oxidation of dibenzothiophene (DBT) to dibenzothiophene sulfone (DBTO2) was investigated using H2O2 as an oxidant and acetonitrile as an extractant. The catalyst could be readily separated from the catalytic system using the magnetic field; and loss of activity was negligible when the catalyst was recovered in five consecutive runs. The effects of main process variables including H2O2 amount (mmol), reaction temperature (°C) and reaction time (min) were analyzed by response surface methodology (RSM) based on the central composite design (CCD). The optimal condition for conversion of DBT was found to be H2O2 2.8 mmol, reaction temperature 42°C and reaction time 57 min for 0.1 g of catalyst dosage. The conversion of DBT to DBTO2 under optimized conditions was 85.9 %. Moreover, the dibenzothiophene sulfone product was characterized by NMR, FT-IR, Mass and GC analysis.
[1] I. Frenanez, N. Khiar, Chem. Rev. 103 (2003) 3651-3701.
[2] Z. Jiang, H. Lü, Y. Zhang, Chin. J. Catal. 32 (2011) 707-715.
[3] D. Xie, Q. He, Y. Su, T. Wang, R. Xu, B. Hu, Chin. J. Catal. 36 (2015) 1205-1213.
[4] F. Yu, R. Wang, Molecules 18 (2013) 13691-13704.
[5] G. Licini, V. Conte, A. Coletti, M. Mba, C. Zonta, Coord. Chem. Rev. 255 (2011) 2345-2357.
[6] S. Ribeiro, A. Barbosa, A. Gomes, M. Pillinger, Fuel Process Technol. 116 (2013) 350-357.
[7] T. Ito, K. Inumaru, M. Misono, Chem. Mater. 13 (2001) 824-831.
[8] D. Long, E. Burkholder, L. Cronin, Chem. Soc. Rev. 36 (2007)105-121.
[9] J. Toufaily, M. Soulard, L. Delmote, Colloids Surf A. 316 (2008) 285-291.
[10] D. Xie, Qihui He, Y. Su, T. Wang, R. Xu, B. Hu, Chin. J. Catal. 36 (2015) 1205-1213.
[11] J. Xiong, W. Zhu, W. Ding, L. Yang, M. Zhang, W. Jiang, Z. Zhao, RSC. Adv. 5 (2015) 16847-16855.
[12] J. Xiong, W. Zhu, H. Li, Y. Xu, W. Jiang, S. Xun, H. Liu, Z. Zhao, AIChE J. 59 (2013) 4696-4699.
[13] Sh. Tangestaninejad, M. Moghadam, V. Mirkhani, I. Mohammadpoor, E. Shams, H. Salavati, Ultrason. Sonochem. 15 (2008) 438-447.
[14] H. Salavati, N. Rasouli, Appl. Surf. Sci. 257 (2011) 4532-4538.
[15] H. Salavati, N. Rasouli, Mater. Res. Bull. 46 (2011) 1853-1859.
[16] Y. Chen, F. Zhang, Y. Fang, X. Zhu, Catal. Commun. 38 (2013) 54-58.
[17] H. Hamadi, M. Kooti, M. Afshari, Z. Ghiasifar, J. Mol. Catal. A 373 (2013) 25-29.
[18] X. Zheng, L.Zhang, J. Li, S. Luo, Chem. Commun. 47 (2011) 12325-12337.
[19] W.P. Wang, H. Yang, T. Xian, J.L. Jiang, Mater. Trans. 53 (2012) 1586-1589.
[20] Z. Zhang, F. Zhang, Q. Zhu, W. Zhao, J. Colloid Interface Sci. 360 (2011) 189-194.
[21] A. Pui, D. Gherca, G. Caria, Dig. J. Nanomater. Biostruct. 6 (2011) 1783-1791.
[22] M.I. Obaidat, B. Issa, Y.O. Haik, J. Nanomater. 5 (2015) 63-89.
[23] O. Veiseh, W. Jonathan, M. Zhang, Adv. Drug Delivery Rev. 62 (2010) 284-304.
[24] V. Haritha, H.M. Meshram, A.B. Rao, Green Sustain. Chem. 5 (2015) 25-30.
[25] S. Sobhani, Z. Pakdin-Parizi, J. Chem. Sci. 125 (2013) 975-979.
[26] S. German, M. Mamoun, Z. Andrei, Chem. Engin. Sci. 6 (2006) 4625-4633.
[27] G. Jianhua, Z. Yuming, Y. Yong, X. Mengwei, China Pet. Process. Petrochem. Technol. 14 (2012) 25-31.
[28] A. Ghosh, K. Sinha, P. Saha, Desalination Water Treat. 51 (2013) 7791-7799.
[29] J. Zhang, Y. Tang, G. Li, C. Hu, Appl. Catal A. 278 (2005) 251-261.
[30] M. Sertkol, Y. Koseoglu, A. Baykal, H. Kavas, A.C. Basaran, J. Magn. Magn. Mater. 321 (2009) 157-162.
[31] M.A. Rezvani, A.F. Shojaei, J. Serb. Chem. Soc. 79 (2014) 1099-1110.
[32] W. Trakarnpruk, K. Rujiraworawut, Fuel Process Technol. 90 (2009) 411-414.
[33] Y. Sasaki, K. Ushimaru, K. Iteya, H. Nakayama, S. Yamaguchi, Tetrahedron Lett. 45 (2004) 9513-9515.
[34] B. Karimi, M. Ghoreishinezhad, J.H. Clark, Org Lett. 7 (2005) 625-628.
