Nothing Special   »   [go: up one dir, main page]

Yadav et al., 2013 - Google Patents

Selective dehydration of glycerol to acrolein: development of efficient and robust solid acid catalyst MUICaT-5

Yadav et al., 2013

View PDF
Document ID
934199385278067262
Author
Yadav G
Sharma R
Katole S
Publication year
Publication venue
Industrial & Engineering Chemistry Research

External Links

Snippet

Valorization of bioglycerol to industrially relevant products has been targeted worldwide to make biodiesel production cost competitive. Among several bulk chemicals derived from glycerol, synthesis of acrolein/acrylic acid is one route which is favored for which several …
Continue reading at www.academia.edu (PDF) (other versions)

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14Phosphorus; Compounds thereof
    • B01J27/186Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/188Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/02Solids
    • B01J35/10Solids characterised by their surface properties or porosity
    • B01J35/1052Pore diameter
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/0201Impregnation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/02Solids
    • B01J35/10Solids characterised by their surface properties or porosity
    • B01J35/1033Pore volume
    • B01J35/1038Pore volume less than 0.5 ml/g
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/002Catalysts characterised by their physical properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08Heat treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08Silica
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • 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
    • C07C29/60Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of -OH groups, e.g. by dehydration
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves

Similar Documents

Publication Publication Date Title
Yadav et al. Selective dehydration of glycerol to acrolein: development of efficient and robust solid acid catalyst MUICaT-5
Jiang et al. Coking of catalysts in catalytic glycerol dehydration to acrolein
Zhang et al. Dehydration of ethanol to ethylene
Katryniok et al. Recent developments in the field of catalytic dehydration of glycerol to acrolein
Mallesham et al. Production of biofuel additives from esterification and acetalization of bioglycerol over SnO2-based solid acids
Priya et al. Platinum supported on H-mordenite: a highly efficient catalyst for selective hydrogenolysis of glycerol to 1, 3-propanediol
Li et al. Highly efficient process for the conversion of glycerol to acrylic acid via gas phase catalytic oxidation of an allyl alcohol intermediate
Sun et al. Versatile nickel–lanthanum (III) catalyst for direct conversion of cellulose to glycols
Alharbi et al. Dehydration of methanol to dimethyl ether over heteropoly acid catalysts: the relationship between reaction rate and catalyst acid strength
Ciddor et al. Catalytic upgrading of bio‐oils by esterification
Talebian-Kiakalaieh et al. Glycerol for renewable acrolein production by catalytic dehydration
Narkhede et al. Biodiesel production by esterification of oleic acid and transesterification of soybean oil using a new solid acid catalyst comprising 12-tungstosilicic acid and zeolite Hβ
Yan et al. Sustainable production of acrylic acid: catalytic performance of hydroxyapatites for gas-phase dehydration of lactic acid
Li et al. Oxidative dehydration of glycerol to acrylic acid over vanadium-substituted cesium salts of Keggin-type heteropolyacids
Zhang et al. Efficient acrylic acid production through bio lactic acid dehydration over NaY zeolite modified by alkali phosphates
Das et al. Synthesis, characterization, and biofuel application of mesoporous zirconium oxophosphates
Priya et al. Activity and selectivity of platinum–copper bimetallic catalysts supported on mordenite for glycerol hydrogenolysis to 1, 3-propanediol
Ogino et al. Tuning the pore structure and surface properties of carbon-based acid catalysts for liquid-phase reactions
Liu et al. Highly efficient production of acrylic acid by sequential dehydration and oxidation of glycerol
Tao et al. Sustainable production of acrolein: Acidic binary metal oxide catalysts for gas-phase dehydration of glycerol
Zhang et al. Zirconia-based solid acid catalysts for biomass conversion
Yu et al. Ketonization of propionic acid on Lewis acidic Zr-beta zeolite with improved stability and selectivity
CN101289358B (en) Method for synthesizing linear alkylbenzene
Yu et al. Aqueous phase hydrodeoxygenation of phenol over Ni3P-CePO4 catalysts
Poyraz et al. Tungsten-promoted mesoporous group 4 (Ti, Zr, and Hf) transition-metal oxides for room-temperature solvent-free acetalization and ketalization reactions