1977
DOI: 10.1021/i360063a009
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Break-in Behavior of a Tungsten Oxide on Silica Catalyst in Propylene Disproportionation

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Cited by 14 publications
(5 citation statements)
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“…As can be seen in Fig. 3, there is an approximately 1.5 h break-in period as reported in previous studies [43,50,51]. Thomas et al [43] observed such a period on WO 3 /SiO 2 catalyst, which is attributed to the gradual formation of the active W-carbene species on the catalyst.…”
Section: Benchmarking Experiments With Wo 3 -Impregnated Silicas As Csupporting
confidence: 80%
“…As can be seen in Fig. 3, there is an approximately 1.5 h break-in period as reported in previous studies [43,50,51]. Thomas et al [43] observed such a period on WO 3 /SiO 2 catalyst, which is attributed to the gradual formation of the active W-carbene species on the catalyst.…”
Section: Benchmarking Experiments With Wo 3 -Impregnated Silicas As Csupporting
confidence: 80%
“… 9 Many factors affect catalytic activity including the content of tungsten oxide loading, 10 oxidation state of tungsten species, 11 conditions of preparation, 12–14 properties of support, 8,15 and pretreatment conditions. 16,17 Experimental studies have reported that the tetrahedral tungsten oxide species are the active sites for metathesis 2,18 and that WO 3 crystals are not active in metathesis and catalyst sites should be contained in the amorphous surface. 19 …”
Section: Introductionmentioning
confidence: 99%
“…yield of detergent-range alkenes Y C 2 [%] yield of ethylene Y C 3 [%] yield of propylene Figure 9. C 10 -C 16 yield surface plots of feed composition and space time at a fixed temperature of 440°C; feed composition and temperature at a fixed space time of 300 g min mol -1 ; space time and temperature at a fixed feed composition of 70 mol % 1-hexene for (a) standard 8 wt % WO 3 /SiO 2 , (b) 0.1 wt % K-doped, and (c) 0.5 wt % K-doped catalysts.…”
Section: Discussionmentioning
confidence: 99%
“…The reaction involves the formal cleavage of the carbon double bonds in two alkene molecules followed by the redistribution of the alkyl fragments: 2CH 2 =CH(CH 2 ) n CH 3 CH 3 (CH 2 ) n CH=CH(CH 2 ) n CH 3 + CH 2 =CH 2 The primary reaction products include ethylene and a longchain alkene with symmetrical internal placement of the double bond. Synthetic fuel processing plants produce large volumes of linear and branched terminal alkenes within the C 4 -C 8 range.…”
Section: Introductionmentioning
confidence: 99%
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