Preparation and structure characterization of superparamagnetic supported catalyst H3PW12O40/Fe3O4@SiO2 and its application in olefinic alkylation desulfurization
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Preparation and structure characterization of superparamagnetic supported catalyst H3PW12O40/Fe3O4@SiO2 and its application in olefinic alkylation desulfurization
XIONG Xiaolong, LIU Zili, XU Cuixia, et al. Preparation and structure characterization of superparamagnetic supported catalyst H3PW12O40/Fe3O4@SiO2 and its application in olefinic alkylation desulfurization[J]. CIESC Journal, 2014, (3): 921-928. DOI: 10.3969/j.issn.0438-1157.2014.03.022.
DOI:
XIONG Xiaolong, LIU Zili, XU Cuixia, et al. Preparation and structure characterization of superparamagnetic supported catalyst H3PW12O40/Fe3O4@SiO2 and its application in olefinic alkylation desulfurization[J]. CIESC Journal, 2014, (3): 921-928. DOI: 10.3969/j.issn.0438-1157.2014.03.022.DOI:
Preparation and structure characterization of superparamagnetic supported catalyst H3PW12O40/Fe3O4@SiO2 and its application in olefinic alkylation desulfurization
Fe3O4@SiO2 nanocomposite was prepared via modified Stöber method and used as catalyst support. Superparamagnetic supported catalystsprepared by loading H3PW12O40 (HPW) onto Fe3O4@SiO2 support through a wet impregnation method
were used for alkylation reaction
and characterized by X-ray diffraction (XRD)
Fourier transform infrared (FT-IR)
NH3-temperature programmed desorption (TPD)
scanning electron microscope (SEM)
N2-adsorption and vibrating sample magnetometer (VSM). Their physicochemical characterization revealed that HPW had been immobilized and dispersed on Fe3O4@SiO2. Moreover
40%(mass) HPW loading catalyst
been of high magnetization 30.1 emu·g-1
mesoporous structure and the surface area 303.6 m2·g-1
could be considered to be a proper catalyst for olefinic alkylation of thiophenic sulfur (OATS) and they can be easy separated by external magnetic field. In addition
their catalytic activity was also investigated in alkylation reaction of a model mixture of thiophene and 1-octene
and the conversion of thiophene was up to 85.5% after 2 h at 160℃.