[go: up one dir, main page]

Neamtu et al., 2019 - Google Patents

Synthesis and characterization of new solketal alkylesters usable as diesel biobased fuel additives

Neamtu et al., 2019

View PDF
Document ID
4494028288907236004
Author
Neamtu C
Stepan E
Plesu V
Bozga G
Tuluc A
Publication year
Publication venue
Rev. Chim

External Links

Snippet

There are described experimental studies on the esterification of solketal,(the cyclic acetal produced from glycerol and acetone reaction), by transesterification reactions of the-OH group with methyl esters of C3-C10aliphatic acids (propionic, pentanoic, hexanoic, octanoic …
Continue reading at revistadechimie.ro (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/46Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/041,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/061,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having group
    • C07C41/50Preparation of compounds having group by reactions producing groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/03Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters

Similar Documents

Publication Publication Date Title
Cornejo et al. Oxygenated fuel additives from glycerol valorization. Main production pathways and effects on fuel properties and engine performance: A critical review
Nanda et al. Thermodynamic and kinetic studies of a catalytic process to convert glycerol into solketal as an oxygenated fuel additive
da Silva et al. The influence of impurities on the acid-catalyzed reaction of glycerol with acetone
Moens et al. Study of the neutralization and stabilization of a mixed hardwood bio-oil
Royon et al. Ketalization of glycerol to solketal in supercritical acetone
Oprescu et al. Synthesis and testing of glycerol ketals as components for diesel fuel
JP2010538031A (en) Hydroxymethylfurfural ether derived from sugar or HMF and mixed alcohol
US20100212217A1 (en) Hydroxymethylfurfural Ethers from HMF and Olefins
Koberg et al. Optimization of bio-diesel production from oils, cooking oils, microalgae, and castor and jatropha seeds: probing various heating sources and catalysts
FI126782B (en) Process for converting bio-oil
EP2197866A2 (en) Hydroxymethylfurfural ethers from sugars and higher alcohols
Hong et al. Reaction kinetics of glycerol acetal formation via transacetalization with 1, 1-diethoxyethane
Kumar et al. Acetalization of 5-hydroxymethyl furfural into biofuel additive cyclic acetal using protic ionic liquid catalyst-A thermodynamic and kinetic analysis
Mukesh et al. Production of C-14 levulinate ester from glucose fermentation liquors catalyzed by acidic ionic liquids in a solvent-free self-biphasic system
RU2478091C2 (en) Method of producing primary alkyl ethers of glycerol, suitable as biofuel additive, from glycerol
Neamtu et al. Synthesis and characterization of new solketal alkylesters usable as diesel biobased fuel additives
CN105026526B (en) For the method for the integration for preparing the compound that can be used as fuel element
EP3129448B1 (en) Process for preparing cyclic acetals which can be used as fuel components
Pauzi et al. Non‐catalytic esterification of palm fatty acid distillate with 2‐ethyl hexanol for high purity production of biolubricant ester
CN103097372A (en) Process for producing dioxolane
Neamtu et al. Synthesis of new acetals and ketals of glycerol as diesel additives
Salvini et al. Sustainable formation of fatty acid alkyl esters by transesterification of triglycerides with chlorotrimethylsilane
JP2014210800A (en) Process for preparation of primary alkyl glycerol ether useful as biofuel additive from glycerol
Kawale et al. Applications of Glycerol as Green Solvent
EP3297984A1 (en) Process and apparatus for the production of aldehydes starting from 1,2-diols