2015
DOI: 10.1016/j.fuel.2015.01.064
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Direct synthesis of mesoporous H 3 PMo 12 O 40 /SiO 2 and its catalytic performance in oxidative desulfurization of fuel oil

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Cited by 95 publications
(36 citation statements)
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References 28 publications
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“…This phenomenon was also observed by impregnating the heteropolyacid H 3 PW 12 O 40 onto MCM-41 [39] and PMA on mesoporous silica. [40] No crystal diffraction peaks of the MoO 3 phase in PMA/SiO 2 -(E) were found in the XRD patterns despite the fact that it is reflectedi nt he Raman spectra by the band at ñ = 825 cm À1 .T his may be due to the low contentofformed MoO 3 in PMA/SiO 2 -(E) and due to af inely dispersed, small particulate molybdenum oxide structure. According to XRD literature data [41] the most intense diffraction patterns from crystalline molybdenum oxide become noticeable when the Mo loading level of MoO 3 on SiO 2 is increasedt o20wt%.…”
Section: Resultsmentioning
confidence: 93%
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“…This phenomenon was also observed by impregnating the heteropolyacid H 3 PW 12 O 40 onto MCM-41 [39] and PMA on mesoporous silica. [40] No crystal diffraction peaks of the MoO 3 phase in PMA/SiO 2 -(E) were found in the XRD patterns despite the fact that it is reflectedi nt he Raman spectra by the band at ñ = 825 cm À1 .T his may be due to the low contentofformed MoO 3 in PMA/SiO 2 -(E) and due to af inely dispersed, small particulate molybdenum oxide structure. According to XRD literature data [41] the most intense diffraction patterns from crystalline molybdenum oxide become noticeable when the Mo loading level of MoO 3 on SiO 2 is increasedt o20wt%.…”
Section: Resultsmentioning
confidence: 93%
“…The TEM data shows that H 3+ +x PMo 12Àx 40 .T he average particles ize is around 2.6 nm for the fresh catalyst and around2 .1 nm for the catalyst after reaction (Figure 4).…”
Section: Resultsmentioning
confidence: 96%
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“…The FT‐IR spectrum of TBA‐Si 2 W 18 Mn 4 showed strong bands at 961, 885 and 736 cm − 1 due to the characteristic absorption of W─O terminal (W&dbond;O t ) and W─O bridging groups (W─O b ─W and W─O c ─W), respectively (Fig. c) . The peaks at 1397 and 1493 cm −1 are assigned to C─H scissoring vibrations of CH 3 ─N + .…”
Section: Resultsmentioning
confidence: 95%
“…To increase their selectivity, catalytic activity and/or stereochemistry in synthetic organic reactions, Lewis acids are further tuned through combination with different ligands to form new custom-designed catalysts based on metal complexes and/or metal salts (Popa et al, 2006;Bordoloi et al, 2007;Rao et al, 2010). The interest in using such catalysts with Lewis acid character for synthetic organic chemistry lies in their versatility in a wide range of reactions, including Diels-Alder cycloadditions, Friedel-Crafts alkyl- ISSN 2053ISSN -2296 # 2018 International Union of Crystallography ations/acylations, aldol condensations, Michael additions, chain isomerizations, or oxidations such as epoxidation and dehydrogenation (Boon et al, 1986;Wang et al, 2001;Pizzio et al, 2003;Chang et al, 2010;Qiu et al, 2015).…”
Section: Introductionmentioning
confidence: 99%