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Understanding the catalytic performance and deactivation behaviour of second-promoter doped Pt/WO_(χ)/γ-Al_(2)O_(3) catalysts in the glycerol hydrogenolysis for selective and cleaner production of 1,3-propanediol
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作者 Rafik Rajjak Shaikh Sittichai Damruang +2 位作者 Rais Ahmad Khan Supareak Praserthdam Piyasan Praserthdam 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第7期486-507,共22页
The selective aqueous-phase glycerol hydrogenolysis is a promising reaction to produce commercially useful 1,3-propanediol(1,3-PDO).The Pt-WOx bifunctional catalyst can catalyse the glycerol hydrogenol-ysis but the ca... The selective aqueous-phase glycerol hydrogenolysis is a promising reaction to produce commercially useful 1,3-propanediol(1,3-PDO).The Pt-WOx bifunctional catalyst can catalyse the glycerol hydrogenol-ysis but the catalyst deactivation via sintering,metal leaching,and coking can predominantly occur in the aqueous phase reaction.In this work,the effect of reaction temperature,pressure and second promoter(Cu,Fe,Rh,Mn,Re,Ru,Ir,Sn,B,and P)on catalytic performance and deactivation behaviour of Pt/WOx/-Al2O3 was investigated.When doped with Rh,Mn,Re,Ru,Ir,B,and P,the second promoter boosts catalytic activity by promoting great dispersion of Pt on support and increasing Pt surface area.The increased Bronsted acid sites lead to selective synthesis of 1,3-PDO than 1,2-propanediol(1,2-PDO).The characterization studies of fresh and spent catalysts reveal that the main cause of catalyst deactivation is the Pt sintering,as interpreted based on XRD,CO chemisorption,and TEM analyses.The Pt sintering is affected depending on the second promoter that can either or reduce the interaction between Pt,WO_(χ)/γ and Al_(2)O_(3).As an electron acceptor of Pt in Pt/WO_(χ)/γ-Al_(2)O_(3),Re and Mn as second promoters resulted in increased Pt^(2+) on the catalytic surface,which strengthens the contact between Pt andγ-Al_(2)O_(3) and WO_(χ),resulting in a decrease in Pt sintering.The metal leaching and coking are not affected by the presence of second promoter.The catalyst modified with a second promoter possesses improved catalytic activity and 1,3-PDO production,however the stability continues to remain a challenge.The present work unrav-elled the determining parameters of catalytic activity and deactivation,thus providing a promising pro-tocol toward effective catalysts for glycerol hydrogenolysis. 展开更多
关键词 glycerol hydrogenolysis 1 3-PROPANEDIOL Metal-support interaction Second promoter Liquid phase Catalyst deactivation
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Hydrogenolysis of glycerol over HY zeolite supported Ru catalysts
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作者 Shaohua Jin Zihui Xiao +2 位作者 Chuang Li Christopher T.Williams Changhai Liang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2014年第2期185-192,共8页
An enhanced active and selective catalyst consisting of ruthenium supported on dealuminated HY zeolite has been prepared by a wet im- pregnation method. It was found that BET surface area of Ru/HY catalysts significan... An enhanced active and selective catalyst consisting of ruthenium supported on dealuminated HY zeolite has been prepared by a wet im- pregnation method. It was found that BET surface area of Ru/HY catalysts significantly increases after HC1 treatment. This treatment also increases the concentration of strong acid sites in the catalyst. The hydrogenolysis of glycerol over 5 wt% Ru/HY catalyst was investigated at 190-220℃ , an initial H2 pressure of 3-6 MPa, and in 20 wt% glycerol aqueous solution, The results indicate that HC1 treated Ru/HY catalyst shows higher activity compared with the untreated Ru/HY catalyst, and that the glycerol hydrogenolysis efficiency is influenced by the porosity and acidity of the support. A selectivity to 1,2-PDO of 81.3% at a glycerol conversion of 60.1% under 3 MPa H2 pressure and 220 ℃ for 10 h was achieved over the modified Ru/HY catalyst with a 1.0 mol/L HC1 treatment. It has also been shown that a longer reaction time, a higher temperature and a higher H2 pressure have the positive effects on the glycerol hydrogenolysis efficiency of the enhanced Ru/HY. 展开更多
关键词 RUTHENIUM HY zeolite IMPREGNATION MODIFICATION glycerol hydrogenolysis
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