Te-promoted (1%) vanadium phosphate catalyst (VPDTe) was prepared via VOPO4·2H2O by calcining its precursor VOHPO4·0.5H2O in a flow of n-butane/air.VPDTe catalyst has resulted a higher existence of V5+ ...Te-promoted (1%) vanadium phosphate catalyst (VPDTe) was prepared via VOPO4·2H2O by calcining its precursor VOHPO4·0.5H2O in a flow of n-butane/air.VPDTe catalyst has resulted a higher existence of V5+ phase with V5+/V4+ ratio of 0.23.SEM micrographs show that Te addition altered the arrangement of the platelets from "rose-like" clusters to layer with irregular shape.Te addition has also markedly lowered the reduction activation energies of the vanadium phosphate catalyst as revealed by TPR profile.The amount of active oxygen species associated with V4+ phase of the Te promoted catalyst was significantly higher than those of the unpromoted catalyst.These observations suggest that high mobility and availability of reactive oxygen species contributed to the enhancement of n-butane conversion up to 80% at 673 K,while only 47% over unpromoted catalyst (2400 h^-1,1.7% n-butane in air).展开更多
A novel pH gradient methodology was used to synthesise a series of Cu–ZrO2 catalysts containing different quantities of Cu and Zr.All of the catalysts were highly selective to the desired product,γ-valerolactone, an...A novel pH gradient methodology was used to synthesise a series of Cu–ZrO2 catalysts containing different quantities of Cu and Zr.All of the catalysts were highly selective to the desired product,γ-valerolactone, and are considerably more stable than Cu–ZrO2 catalysts prepared by other co-precipitation methods for this reaction.Characterisation and further investigation of these catalysts by XRD, BET, SEM and XPS provided insight into the nature of the catalytic active site and the physicochemical properties that lead to catalyst stability.We consider the active site to be the interface between Cu/CuOxand ZrOx and that lattice Cu species assist with the dispersion of surface Cu through the promotion of a strong metal support interaction.This enhanced understanding of the active site and roles of lattice and surface Cu will assist with future catalyst design.As such, we conclude that the activity of Cu–ZrO2 catalysts in this reaction is dictated by the quantity of Cu–Zr interface sites.展开更多
The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy i...The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy is dependent on using a platinumdivinyltetramethyldisiloxane complex(Pt^(0)-DVTMS)as the precursor,which we demonstrate can be removed through a H_(2)-treatment under mild conditions.This,in turn,allowed for the synthesis of catalysts with well dispersed Pt particles.The presence of FeO_(x) species also aided Pt dispersion;when coated onto SBA-15,FeO_(x) strongly interacted with dissociated Pt species,inhibiting both Pt aggregation and metal leaching.Using cinnamaldehyde as a modelα,β-unsaturated aldehyde,it was demonstrated that this catalyst was highly selective towards the unsaturated alcohol and no obvious loss in activity was observed over five recycles.This catalyst was determined to be significantly more effective than an analogous catalyst prepared using chloroplatinic acid as a precursor,evidencing the importance of using the Pt0-DVTMS precursor.We corroborate the excellent catalytic performance to highly dispersed Pt-species,whereby Pt0 and Pt^(2+) play a critical role in activating H_(2) and the C=O bond.This research demonstrates that the Pt precursor can have a significant impact on the physicochemical properties and thus,the performance of the final catalyst.It also evidences how metal support interactions can dramatically influence selectivity in such hydrogenation reactions.This novel catalyst preparation protocol,using a DVTMS ligand for Pt impregnation,offers a facile approach to the design of multi-component heterogeneous catalysts.展开更多
A dual-templating method was used to synthesize a series of hierarchical carbon supports containing different proportions of spherical macropores(ca.200 nm in diameter)and mesoporous channels(ca.4 nm in diameter).Thes...A dual-templating method was used to synthesize a series of hierarchical carbon supports containing different proportions of spherical macropores(ca.200 nm in diameter)and mesoporous channels(ca.4 nm in diameter).These and some other conventional carbon materials were subsequently impregnated with Ni and tested for the conversion of glycerol.The hierarchical catalysts exhibited a significantly higher conversion(96%)and selectivity(77%)to 1,2-propanediol,and the specificity selectivity coefficient(6.1)towards 1,2-propanediol against lactic acid was three times higher than that observed over a conventional Ni/Cmnicro catalyst(2.1).The enhanced performance of these materials,compared with the Ni nanoparticles supported on conventional carbon supports,was attributed to their high surface areas(>1110 m^2·g^-1)and large pore volumes(ca.0.4 cm^3·g^-1)permitting greater accessibility of substrate and/or intermediates to Ni active sites.Given that the concentration of accessible Ni sites in these materials is higher,a competitive benzilic-acid-rearrangement reaction to produce lactic acid was suppressed,leading to an enhanced hydrogenation selectivity to 1,2-propanediol.This study evidences the potential benefits,which can be established from utilizing hierarchical support materials in the valorization of biomass.展开更多
Processes for the isomerization of light alkanes have been commercialized;however,the isomerization of paraffins(C_(n)H_(2n+2),n≥7)remains a challenge.On mesoporous tungsten-zirconia catalyst supported Pt catalysts(P...Processes for the isomerization of light alkanes have been commercialized;however,the isomerization of paraffins(C_(n)H_(2n+2),n≥7)remains a challenge.On mesoporous tungsten-zirconia catalyst supported Pt catalysts(Pt/WZrOx),initial isomerization productivity of 5249 moli-C7/molPt/h was obtained for n-heptane reforming at 275°C and 5 bar of hydrogen.展开更多
文摘Te-promoted (1%) vanadium phosphate catalyst (VPDTe) was prepared via VOPO4·2H2O by calcining its precursor VOHPO4·0.5H2O in a flow of n-butane/air.VPDTe catalyst has resulted a higher existence of V5+ phase with V5+/V4+ ratio of 0.23.SEM micrographs show that Te addition altered the arrangement of the platelets from "rose-like" clusters to layer with irregular shape.Te addition has also markedly lowered the reduction activation energies of the vanadium phosphate catalyst as revealed by TPR profile.The amount of active oxygen species associated with V4+ phase of the Te promoted catalyst was significantly higher than those of the unpromoted catalyst.These observations suggest that high mobility and availability of reactive oxygen species contributed to the enhancement of n-butane conversion up to 80% at 673 K,while only 47% over unpromoted catalyst (2400 h^-1,1.7% n-butane in air).
基金financially supported by the European Union FP7 NMP project NOVACAM (Novel cheap and abundant EU-Japan604319)
文摘A novel pH gradient methodology was used to synthesise a series of Cu–ZrO2 catalysts containing different quantities of Cu and Zr.All of the catalysts were highly selective to the desired product,γ-valerolactone, and are considerably more stable than Cu–ZrO2 catalysts prepared by other co-precipitation methods for this reaction.Characterisation and further investigation of these catalysts by XRD, BET, SEM and XPS provided insight into the nature of the catalytic active site and the physicochemical properties that lead to catalyst stability.We consider the active site to be the interface between Cu/CuOxand ZrOx and that lattice Cu species assist with the dispersion of surface Cu through the promotion of a strong metal support interaction.This enhanced understanding of the active site and roles of lattice and surface Cu will assist with future catalyst design.As such, we conclude that the activity of Cu–ZrO2 catalysts in this reaction is dictated by the quantity of Cu–Zr interface sites.
基金the National Natural Science Foundation(Nos.U1910202 and 21978194)the Key Research and Development Program of Shanxi Province(No.202102090301005)the Fund for Shanxi“1331 Project”.
文摘The chemoselective hydrogenation ofα,β-unsaturated aldehydes is a key strategy for the synthesis of fine chemicals.Herein,we developed an efficient method of depositing Pt particles on FeO_(x)/SBA-15.This strategy is dependent on using a platinumdivinyltetramethyldisiloxane complex(Pt^(0)-DVTMS)as the precursor,which we demonstrate can be removed through a H_(2)-treatment under mild conditions.This,in turn,allowed for the synthesis of catalysts with well dispersed Pt particles.The presence of FeO_(x) species also aided Pt dispersion;when coated onto SBA-15,FeO_(x) strongly interacted with dissociated Pt species,inhibiting both Pt aggregation and metal leaching.Using cinnamaldehyde as a modelα,β-unsaturated aldehyde,it was demonstrated that this catalyst was highly selective towards the unsaturated alcohol and no obvious loss in activity was observed over five recycles.This catalyst was determined to be significantly more effective than an analogous catalyst prepared using chloroplatinic acid as a precursor,evidencing the importance of using the Pt0-DVTMS precursor.We corroborate the excellent catalytic performance to highly dispersed Pt-species,whereby Pt0 and Pt^(2+) play a critical role in activating H_(2) and the C=O bond.This research demonstrates that the Pt precursor can have a significant impact on the physicochemical properties and thus,the performance of the final catalyst.It also evidences how metal support interactions can dramatically influence selectivity in such hydrogenation reactions.This novel catalyst preparation protocol,using a DVTMS ligand for Pt impregnation,offers a facile approach to the design of multi-component heterogeneous catalysts.
文摘A dual-templating method was used to synthesize a series of hierarchical carbon supports containing different proportions of spherical macropores(ca.200 nm in diameter)and mesoporous channels(ca.4 nm in diameter).These and some other conventional carbon materials were subsequently impregnated with Ni and tested for the conversion of glycerol.The hierarchical catalysts exhibited a significantly higher conversion(96%)and selectivity(77%)to 1,2-propanediol,and the specificity selectivity coefficient(6.1)towards 1,2-propanediol against lactic acid was three times higher than that observed over a conventional Ni/Cmnicro catalyst(2.1).The enhanced performance of these materials,compared with the Ni nanoparticles supported on conventional carbon supports,was attributed to their high surface areas(>1110 m^2·g^-1)and large pore volumes(ca.0.4 cm^3·g^-1)permitting greater accessibility of substrate and/or intermediates to Ni active sites.Given that the concentration of accessible Ni sites in these materials is higher,a competitive benzilic-acid-rearrangement reaction to produce lactic acid was suppressed,leading to an enhanced hydrogenation selectivity to 1,2-propanediol.This study evidences the potential benefits,which can be established from utilizing hierarchical support materials in the valorization of biomass.
基金support from the Natural Science Foundation of China(nos.21725301,21932002,22005007,and 21821004)the National Key R&DProgram of China(no.2017YFB0602200)and the Chinese Postdoctoral Science Foundation(no.8206300246).B.Z.gratefully acknowledges the support of the Boya Postdoctoral Fellowship of Peking University(2019–2020)and the Junior Fellowship of Beijing National Laboratory of Molecular Science(BMS Junior Fellow,2020–2023).D.M.acknowledges support from the Tencent Foundation through the XPLORER PRIZE and the support from OSSO state key lab。
文摘Processes for the isomerization of light alkanes have been commercialized;however,the isomerization of paraffins(C_(n)H_(2n+2),n≥7)remains a challenge.On mesoporous tungsten-zirconia catalyst supported Pt catalysts(Pt/WZrOx),initial isomerization productivity of 5249 moli-C7/molPt/h was obtained for n-heptane reforming at 275°C and 5 bar of hydrogen.