Lubricants from chemically modified vegetable oils

This work reports laboratory results obtained from the production of polyols with branched ether and ester compounds from epoxidized vegetable oils pertaining to annual, temperate climate crops (soybean, sunflower and high-oleic sunflower oils), focusing on their possible use as components of lubric...

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Autores principales: Campanella, A., Rustoy, E., Baldessari, A., Baltanás, M.A.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_09608524_v101_n1_p245_Campanella
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spelling todo:paper_09608524_v101_n1_p245_Campanella2023-10-03T15:53:53Z Lubricants from chemically modified vegetable oils Campanella, A. Rustoy, E. Baldessari, A. Baltanás, M.A. Lubricants Oxirane ring-opening Polyol derivatives Vegetable oils Acid media Aliphatic alcohol Base stock Chemically modified Epoxidized vegetable oil Experimental data Glacial acetic acid Long-term storage Oleic sunflower Opening reactions Organic phase Oxirane ring-opening Polyol derivatives Polyols Rheological technique Short reaction time Synthesis temperatures Temperate climate Aromatic hydrocarbons Chemical modification Climatology Esters Ethanol Ethers Lubricating oils Methanol Synthesis (chemical) Vegetable oils acetic acid alcohol alkanol epoxide ester derivative ether derivative lubricating agent methanol polyol sunflower oil vegetable oil acetic acid nuclear magnetic resonance rheology vegetable oil viscosity article chemical modification chemical reaction priority journal synthesis temperature viscosity Computer Simulation Lubricants Lubrication Materials Testing Models, Chemical Plant Oils Viscosity Glycine max Helianthus This work reports laboratory results obtained from the production of polyols with branched ether and ester compounds from epoxidized vegetable oils pertaining to annual, temperate climate crops (soybean, sunflower and high-oleic sunflower oils), focusing on their possible use as components of lubricant base stocks. To this end, two different opening reactions of the epoxide ring were studied. The first caused by the attack with glacial acetic acid (exclusively in a single organic phase) and the second using short-chain aliphatic alcohols, methanol and ethanol, in acid media. Both reactions proceed under mild conditions: low synthesis temperature and short reaction times and with conversions above 99%. Spectroscopic (NMR), thermal (DSC) and rheological techniques were used to characterize the oils, their epoxides and polyols, to assess the impact of the nature of the vegetable oil and the chemical modifications introduced, including long-term storage conditions. Several correlations were employed to predict the viscosity of the vegetable oils with temperature, and good agreement with the experimental data was obtained. © 2009 Elsevier Ltd. All rights reserved. Fil:Rustoy, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_09608524_v101_n1_p245_Campanella
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Lubricants
Oxirane ring-opening
Polyol derivatives
Vegetable oils
Acid media
Aliphatic alcohol
Base stock
Chemically modified
Epoxidized vegetable oil
Experimental data
Glacial acetic acid
Long-term storage
Oleic sunflower
Opening reactions
Organic phase
Oxirane ring-opening
Polyol derivatives
Polyols
Rheological technique
Short reaction time
Synthesis temperatures
Temperate climate
Aromatic hydrocarbons
Chemical modification
Climatology
Esters
Ethanol
Ethers
Lubricating oils
Methanol
Synthesis (chemical)
Vegetable oils
acetic acid
alcohol
alkanol
epoxide
ester derivative
ether derivative
lubricating agent
methanol
polyol
sunflower oil
vegetable oil
acetic acid
nuclear magnetic resonance
rheology
vegetable oil
viscosity
article
chemical modification
chemical reaction
priority journal
synthesis
temperature
viscosity
Computer Simulation
Lubricants
Lubrication
Materials Testing
Models, Chemical
Plant Oils
Viscosity
Glycine max
Helianthus
spellingShingle Lubricants
Oxirane ring-opening
Polyol derivatives
Vegetable oils
Acid media
Aliphatic alcohol
Base stock
Chemically modified
Epoxidized vegetable oil
Experimental data
Glacial acetic acid
Long-term storage
Oleic sunflower
Opening reactions
Organic phase
Oxirane ring-opening
Polyol derivatives
Polyols
Rheological technique
Short reaction time
Synthesis temperatures
Temperate climate
Aromatic hydrocarbons
Chemical modification
Climatology
Esters
Ethanol
Ethers
Lubricating oils
Methanol
Synthesis (chemical)
Vegetable oils
acetic acid
alcohol
alkanol
epoxide
ester derivative
ether derivative
lubricating agent
methanol
polyol
sunflower oil
vegetable oil
acetic acid
nuclear magnetic resonance
rheology
vegetable oil
viscosity
article
chemical modification
chemical reaction
priority journal
synthesis
temperature
viscosity
Computer Simulation
Lubricants
Lubrication
Materials Testing
Models, Chemical
Plant Oils
Viscosity
Glycine max
Helianthus
Campanella, A.
Rustoy, E.
Baldessari, A.
Baltanás, M.A.
Lubricants from chemically modified vegetable oils
topic_facet Lubricants
Oxirane ring-opening
Polyol derivatives
Vegetable oils
Acid media
Aliphatic alcohol
Base stock
Chemically modified
Epoxidized vegetable oil
Experimental data
Glacial acetic acid
Long-term storage
Oleic sunflower
Opening reactions
Organic phase
Oxirane ring-opening
Polyol derivatives
Polyols
Rheological technique
Short reaction time
Synthesis temperatures
Temperate climate
Aromatic hydrocarbons
Chemical modification
Climatology
Esters
Ethanol
Ethers
Lubricating oils
Methanol
Synthesis (chemical)
Vegetable oils
acetic acid
alcohol
alkanol
epoxide
ester derivative
ether derivative
lubricating agent
methanol
polyol
sunflower oil
vegetable oil
acetic acid
nuclear magnetic resonance
rheology
vegetable oil
viscosity
article
chemical modification
chemical reaction
priority journal
synthesis
temperature
viscosity
Computer Simulation
Lubricants
Lubrication
Materials Testing
Models, Chemical
Plant Oils
Viscosity
Glycine max
Helianthus
description This work reports laboratory results obtained from the production of polyols with branched ether and ester compounds from epoxidized vegetable oils pertaining to annual, temperate climate crops (soybean, sunflower and high-oleic sunflower oils), focusing on their possible use as components of lubricant base stocks. To this end, two different opening reactions of the epoxide ring were studied. The first caused by the attack with glacial acetic acid (exclusively in a single organic phase) and the second using short-chain aliphatic alcohols, methanol and ethanol, in acid media. Both reactions proceed under mild conditions: low synthesis temperature and short reaction times and with conversions above 99%. Spectroscopic (NMR), thermal (DSC) and rheological techniques were used to characterize the oils, their epoxides and polyols, to assess the impact of the nature of the vegetable oil and the chemical modifications introduced, including long-term storage conditions. Several correlations were employed to predict the viscosity of the vegetable oils with temperature, and good agreement with the experimental data was obtained. © 2009 Elsevier Ltd. All rights reserved.
format JOUR
author Campanella, A.
Rustoy, E.
Baldessari, A.
Baltanás, M.A.
author_facet Campanella, A.
Rustoy, E.
Baldessari, A.
Baltanás, M.A.
author_sort Campanella, A.
title Lubricants from chemically modified vegetable oils
title_short Lubricants from chemically modified vegetable oils
title_full Lubricants from chemically modified vegetable oils
title_fullStr Lubricants from chemically modified vegetable oils
title_full_unstemmed Lubricants from chemically modified vegetable oils
title_sort lubricants from chemically modified vegetable oils
url http://hdl.handle.net/20.500.12110/paper_09608524_v101_n1_p245_Campanella
work_keys_str_mv AT campanellaa lubricantsfromchemicallymodifiedvegetableoils
AT rustoye lubricantsfromchemicallymodifiedvegetableoils
AT baldessaria lubricantsfromchemicallymodifiedvegetableoils
AT baltanasma lubricantsfromchemicallymodifiedvegetableoils
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