Selective acetylene removal from ethylene-rich feed by cross-metathesis over supported WO3 catalysts

被引:3
|
作者
Promchana, Pratya [1 ,2 ]
Choojun, Kittisak [1 ,2 ]
Limphirat, Wanwisa [3 ]
Poo-arporn, Yingyot [3 ]
Sooknoi, Tawan [1 ,2 ]
机构
[1] King Mongkuts Inst Technol Ladkrabang, Sch Sci, Dept Chem, Chalongkrung Rd, Bangkok 10520, Thailand
[2] King Mongkuts Inst Technol Ladkrabang, Sch Sci, Catalyt Chem Res Unit, Chalongkrung Rd, Bangkok 10520, Thailand
[3] Synchrotron Light Res Inst, 111 Univ Ave, Muang Dist 30000, Nakhon Ratchasi, Thailand
关键词
Cross; -metathesis; Acetylene removal; Ethylene; Tungsten oxide; Silica; TUNGSTEN-OXIDE CATALYSTS; DIELS-ALDER REACTION; SURFACE; CRACKING; POLYMERIZATION; ENVIRONMENT; CLUSTERS; PROPENE; NAPHTHA; 1,3-BUTADIENE;
D O I
10.1016/j.apcata.2022.118972
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Acetylene in ethylene-rich feed can be removed via acetylene/ethylene cross-metathesis over WO3-supported catalysts at 450 degrees C, yielding 1,3-butadiene with cyclohexene as a minor product. The catalyst must be treated with ethylene at 600 degrees C to generate a genuinely active site of tungsten (IV) alkylidene species (W=CH2). The H2 treatment decreases surface W--O concentration, and hence the activity. Raman spectroscopy shows that active single-site WO3 species, including mono oxo-WO3 ((O=)W(O-Si)3 and (O=)W(O-Si)4) and dioxo-WO3 species (O=)2W(O-Si)2) were generated in 2%WO3/SiO2, while the WO3 cluster and bulk WO3 exist in 3-5%WO3/SiO2 and 7%WO3/SiO2, respectively. The 5%WO3/NaX and 5%WO3/NaY provide lower activity due to coke forma-tion over the acid sites. With high surface area and confined surface silanol of 5%WO3/MCM-41% and 5%WO3/ SBA-15, in situ TR-EXAFS evidences the formation of only O--W(O-Si)3. This species provides an isolated W=CH2 site with relatively higher activity and is less prone to coke formation than the WO3 cluster in 5%WO3/SiO2.
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页数:11
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