[go: up one dir, main page]

Sun et al., 2017 - Google Patents

Vapor-phase hydrogenation of levulinic acid and methyl levulinate to γ-valerolactone over non-noble metal-based catalysts

Sun et al., 2017

View PDF
Document ID
7150340803364180469
Author
Sun D
Ohkubo A
Asami K
Katori T
Yamada Y
Sato S
Publication year
Publication venue
Molecular Catalysis

External Links

Snippet

Vapor-phase hydrogenation of levulinic acid (LA) and methyl levulinate (ML) to γ- valerolactone (GVL) was performed over non-noble metal-based catalysts such as Cu/Al 2 O 3, Ni/SiO 2 and Co/SiO 2. The catalytic activity and stability of the Cu-, Ni-and Co-based …
Continue reading at www.sciencedirect.com (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. -COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. -COOH of carboxylic acids or derivatives thereof
    • C07C29/149Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. -COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
    • C07C2523/44Palladium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/15Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
    • C07C29/151Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
    • C07C29/153Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
    • C07C29/156Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/02Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
    • C07C5/08Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon

Similar Documents

Publication Publication Date Title
Sun et al. Vapor-phase hydrogenation of levulinic acid and methyl levulinate to γ-valerolactone over non-noble metal-based catalysts
Duarte et al. Hydrodeoxygenation of 5-hydroxymethylfurfural over alumina-supported catalysts in aqueous medium
Miyazawa et al. Glycerol hydrogenolysis to 1, 2-propanediol catalyzed by a heat-resistant ion-exchange resin combined with Ru/C
West et al. Catalytic conversion of biomass-derived carbohydrates to fuels and chemicals by formation and upgrading of mono-functional hydrocarbon intermediates
Guo et al. Supported Cu catalysts for the selective hydrogenolysis of glycerol to propanediols
Miyazawa et al. Development of a Ru/C catalyst for glycerol hydrogenolysis in combination with an ion-exchange resin
JP5108979B2 (en) Direct and selective production of ethyl acetate from acetic acid using a bimetallic supported catalyst
JP5611252B2 (en) Direct and selective production of ethanol from acetic acid using a platinum / tin catalyst
Akiyama et al. Dehydration–hydrogenation of glycerol into 1, 2-propanediol at ambient hydrogen pressure
CA2732366C (en) Ethanol production from acetic acid utilizing a cobalt catalyst
JP5053458B2 (en) Direct and selective production of acetaldehyde from acetic acid using supported metal catalysts
Baylon et al. Conversion of ethanol to 1, 3-butadiene over Na doped ZnxZryOz mixed metal oxides
Serrano-Ruiz et al. Catalytic upgrading of lactic acid to fuels and chemicals by dehydration/hydrogenation and C–C coupling reactions
Vasiliadou et al. Glycerol transformation to value added C3 diols: reaction mechanism, kinetic, and engineering aspects
Sun et al. Efficient production of propylene in the catalytic conversion of glycerol
Sun et al. Selective hydrogenation of γ-valerolactone to 2-methyltetrahydrofuran over Cu/Al2O3 catalyst
Pirmoradi et al. Continuous hydrogenation of aqueous furfural using a metal-supported activated carbon monolith
Li et al. Nickel and nickel–platinum as active and selective catalyst for the maleic anhydride hydrogenation to succinic anhydride
Madsen et al. Deactivation in continuous deoxygenation of C18-fatty feedstock over Pd/Sibunit
Brainer et al. Wet oxidation of glycerol into fine organic acids: catalyst selection and kinetic evaluation
Auneau et al. Exploring the reaction conditions for Ru/C catalyzed selective hydrogenolysis of xylitol alkaline aqueous solutions to glycols in a trickle-bed reactor
Onyestyák Outstanding efficiency of indium in bimetallic catalysts for hydroconversion of bioacids to bioalcohols
Li et al. Highly active and selective Nickel–Platinum catalyst for the low temperature hydrogenation of maleic anhydride to succinic anhydride and synthesis of succinic acid at 40 C
JPWO2010016462A1 (en) Process for producing glycol and 1-propanol from glycerin
Li et al. Vapor-phase deoxydehydration of 1, 2-propanediol to form propylene over Cu-loaded H3PO4/SiO2-Al2O3 catalyst