Putra et al., 2018 - Google Patents
In-situ glycerol aqueous phase reforming and phenol hydrogenation over Raney Ni®Putra et al., 2018
- Document ID
- 16546761108694161121
- Author
- Putra R
- Trajano H
- Liu S
- Lee H
- Smith K
- Kim C
- Publication year
- Publication venue
- Chemical Engineering Journal
External Links
Snippet
In-situ glycerol aqueous phase reforming and phenol hydrogenation (IGAPH) was conducted with Raney Ni® at 180–240° C for phenol to glycerol ratios from 0 to 4.88. Thermodynamic analysis of the complex IGAPH reaction system revealed the need to …
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine 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OCC(O)CO 0 title abstract description 567
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/15—Preparation 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
- C07C29/151—Preparation 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
- C07C29/153—Preparation 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
- C07C29/156—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/60—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation 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
- C07C29/136—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/207—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4012—Pressure
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Xiong et al. | An in situ reduction approach for bio-oil hydroprocessing | |
Long et al. | SO3H-functionalized ionic liquid: Efficient catalyst for bagasse liquefaction | |
Vasiliadou et al. | Glycerol transformation to value added C3 diols: reaction mechanism, kinetic, and engineering aspects | |
Ma et al. | Selective conversion of furfural to cyclopentanol over cobalt catalysts in one step | |
Zeng et al. | In situ hydrodeoxygenation of phenol with liquid hydrogen donor over three supported noble-metal catalysts | |
Xu et al. | Alcohol-assisted hydrodeoxygenation as a sustainable and cost-effective pathway for biomass derivatives upgrading | |
Madenoğlu et al. | Simultaneous effect of temperature and pressure on catalytic hydrothermal gasification of glucose | |
Wang et al. | Synthesis of renewable diesel with 2-methylfuran and angelica lactone derived from carbohydrates | |
Hirano et al. | Selective transformation of glucose into propylene glycol on Ru/C catalysts combined with ZnO under low hydrogen pressures | |
Xu et al. | In-situ hydrogenation of model compounds and raw bio-oil over Ni/CMK-3 catalyst | |
Boscagli et al. | Reactivity of platform molecules in pyrolysis oil and in water during hydrotreatment over nickel and ruthenium catalysts | |
Chen et al. | Improved catalytic upgrading of simulated bio-oil via mild hydrogenation over bimetallic catalysts | |
Keskiväli et al. | One-step Pd/C and Eu (OTf) 3 catalyzed hydrodeoxygenation of branched C11 and C12 biomass-based furans to the corresponding alkanes | |
Therdthianwong et al. | Hydrogen production from bioethanol reforming in supercritical water | |
Pairojpiriyakul et al. | Hydrogen production from supercritical water reforming of glycerol in an empty Inconel 625 reactor | |
Park et al. | Total chemocatalytic cascade conversion of lignocellulosic biomass into biochemicals |