GB896376A - Partial esters of aliphatic substituted succinic acids and rust inhibiting compositions containing the same - Google Patents
Partial esters of aliphatic substituted succinic acids and rust inhibiting compositions containing the sameInfo
- Publication number
- GB896376A GB896376A GB26449/58A GB2644958A GB896376A GB 896376 A GB896376 A GB 896376A GB 26449/58 A GB26449/58 A GB 26449/58A GB 2644958 A GB2644958 A GB 2644958A GB 896376 A GB896376 A GB 896376A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyhydric alcohol
- alkyl
- diol
- succinic
- anhydride
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000002148 esters Chemical class 0.000 title abstract 10
- 230000002401 inhibitory effect Effects 0.000 title abstract 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Chemical class O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 title abstract 3
- 125000001931 aliphatic group Chemical group 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 235000011044 succinic acid Nutrition 0.000 title 1
- 150000003444 succinic acids Chemical class 0.000 title 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 9
- -1 hydroxycarboxylic acid ester Chemical class 0.000 abstract 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229920005862 polyol Polymers 0.000 abstract 3
- 150000003077 polyols Chemical class 0.000 abstract 3
- 229940014800 succinic anhydride Drugs 0.000 abstract 3
- WVRNUXJQQFPNMN-VAWYXSNFSA-N 3-[(e)-dodec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCC\C=C\C1CC(=O)OC1=O WVRNUXJQQFPNMN-VAWYXSNFSA-N 0.000 abstract 2
- 101100277337 Arabidopsis thaliana DDM1 gene Proteins 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 239000004359 castor oil Substances 0.000 abstract 2
- 235000019438 castor oil Nutrition 0.000 abstract 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 2
- 101150113676 chr1 gene Proteins 0.000 abstract 2
- 150000002009 diols Chemical class 0.000 abstract 2
- 239000000446 fuel Substances 0.000 abstract 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 2
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 abstract 1
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 abstract 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical class ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 abstract 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 1
- RSPWVGZWUBNLQU-FOCLMDBBSA-N 3-[(e)-hexadec-1-enyl]oxolane-2,5-dione Chemical group CCCCCCCCCCCCCC\C=C\C1CC(=O)OC1=O RSPWVGZWUBNLQU-FOCLMDBBSA-N 0.000 abstract 1
- KAYAKFYASWYOEB-ISLYRVAYSA-N 3-[(e)-octadec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCCCCCCCC\C=C\C1CC(=O)OC1=O KAYAKFYASWYOEB-ISLYRVAYSA-N 0.000 abstract 1
- YAXXOCZAXKLLCV-UHFFFAOYSA-N 3-dodecyloxolane-2,5-dione Chemical class CCCCCCCCCCCCC1CC(=O)OC1=O YAXXOCZAXKLLCV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 239000004386 Erythritol Substances 0.000 abstract 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 abstract 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- QMXOFBXZEKTJIK-UHFFFAOYSA-N Glycinol Natural products C1=C(O)C=C2OCC3(O)C4=CC=C(O)C=C4OC3C2=C1 QMXOFBXZEKTJIK-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 abstract 1
- FLISWPFVWWWNNP-BQYQJAHWSA-N dihydro-3-(1-octenyl)-2,5-furandione Chemical group CCCCCC\C=C\C1CC(=O)OC1=O FLISWPFVWWWNNP-BQYQJAHWSA-N 0.000 abstract 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 abstract 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 abstract 1
- 229940009714 erythritol Drugs 0.000 abstract 1
- 235000019414 erythritol Nutrition 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- SAMYCKUDTNLASP-UHFFFAOYSA-N hexane-2,2-diol Chemical compound CCCCC(C)(O)O SAMYCKUDTNLASP-UHFFFAOYSA-N 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000010688 mineral lubricating oil Substances 0.000 abstract 1
- 150000005673 monoalkenes Chemical class 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- 239000003209 petroleum derivative Substances 0.000 abstract 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 239000001384 succinic acid Substances 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical class OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010723 turbine oil Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/143—Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
- C10L1/191—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polyhydroxyalcohols
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
- C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/76—Esters containing free hydroxy or carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/12—Oxygen-containing compounds
- C23F11/128—Esters of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1983—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyesters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2406—Organic compounds containing sulfur, selenium and/or tellurium mercaptans; hydrocarbon sulfides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2406—Organic compounds containing sulfur, selenium and/or tellurium mercaptans; hydrocarbon sulfides
- C10L1/2418—Organic compounds containing sulfur, selenium and/or tellurium mercaptans; hydrocarbon sulfides containing a carboxylic substituted; derivatives thereof, e.g. esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/288—Partial esters containing free carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/084—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/043—Polyoxyalkylene ethers with a thioether group
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
Abstract
Rust-inhibiting compositions comprise a petroleum hydrocarbon having dissolved therein a partial ester of the general formula R11(OH)x-y (-O.CO.CHR1.CHR.COOH)y in which R11 is the residue of a polyhydric alcohol R11(OH)x, one of R and R1 is hydrogen and the other is a C8-18 alkyl or alkenyl group, x is 2, 3 or 4 and y is an integer which is at least 2 but otherwise may be equal to or less than x, the polyhydric alcohol having a carbon chain which may be interrupted by an oxygen, sulphur or tertiary nitrogen atom. The polyhydric alcohol may be a diol, a polyoxyalkylene glycol, glycinol, erythritol, pentaerythritol, castor oil, a triol, a hydroxycarboxylic acid ester of a polyhydric alcohol, a bis-(hydroxy alkyl) sulphide or an N-alkyl or N-alkylol di-alkylol amine; the substituent in the acid radical may be n-octenyl, n-dodecenyl, n-hexadecenyl, n-octadecenyl, or branched dodecenyl or the corresponding alkyl groups. Numerous partial esters are described. The hydrocarbon oil may be a petroleum base such as motor or aviation gasoline, jet fuel, turbine oil, a mineral lubricating oil, or a leaded fuel such as a gasoline containing lead naphthenate.ALSO:The invention comprises partial esters of a substituted succinic acid and a polyhydric alcohol having the general formula R11(OH)x-y (-O.CO.CHR1.CHR.COOH)y in which R11 is the residue of a polyhydric alcohol R11(OH)x, one of the symbols R and R1 is hydrogen and the other a C8-18 alkyl or alkenyl group, x is 2, 3 or 4 and y is an integer which is at least 2 but may otherwise be equal to or less than x, the polyhydric alcohol having a carbon chain which may be interrupted by an oxygen, sulphur or tertiary nitrogen atom. The partial esters may be prepared by heating, at a temperature below that at which water is eliminated, a mono C8-18 alkyl- or alkenyl-substituted succinic anhydride with a polyhydric alcohol R11(OH)x, at least two molar proportions of anhydride being provided for each molar proportion of polyhydric alcohol. The alcohol may be a polyol, an ether thereof, an ester of a polyol with a hydroxycarboxylic acid, a polyhydroxy aliphatic sulphide or a polyhydroxy tertiary amine. Reaction is generally effected at 95 DEG C.-100 DEG C., in the presence if desired of a solvent boiling above 100 DEG C. Saturated alkyl-succinic esters may also be obtained by catalytic hydrogenation of the corresponding alkenyl-succinic esters. The esters have rust-inhibiting properties (see Group III). Examples describe partial esters from (1) branched dodecenyl-succinic anhydride (2 moles) and many diols (1 mole) including ethane-, propane-, butane-, pentane-, hexane- and heptane-diols and isomers thereof, e.g. neopentyl glycol, di- and tri-ethylene glycols, polyethylene glycol 400, polypropylene glycol 425, phenyl ethane diol, a decane diol, 2 : 21-di-hydroxyethyl sulphide, and butene-diol; (2) the same anhydride and a butane-triol, castor oil, triethanolamine, glycerol and pentaerythritol, generally with full esterification of the polyol; (3) n-octenyl-, n-dodecenyl-, n-hexadecenyl or n-octadecenyl succinic anhydride (2 moles) and methyl pentane diol or a butane diol (1 mole); the use of the corresponding alkyl succinic anhydride is mentioned. C8-18 alkenyl succinic anhydrides are prepared by reacting maleic anhydride with a C8-18 mono-olefin, followed by catalytic hydrogenation if the corresponding C8-18 alkyl succinic anhydride is required.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US678525A US3045042A (en) | 1957-08-16 | 1957-08-16 | Acid polyester succinates |
Publications (1)
Publication Number | Publication Date |
---|---|
GB896376A true GB896376A (en) | 1962-05-16 |
Family
ID=24723165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26449/58A Expired GB896376A (en) | 1957-08-16 | 1958-08-18 | Partial esters of aliphatic substituted succinic acids and rust inhibiting compositions containing the same |
Country Status (2)
Country | Link |
---|---|
US (1) | US3045042A (en) |
GB (1) | GB896376A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3287268A (en) * | 1963-11-21 | 1966-11-22 | Exxon Research Engineering Co | Cutting oil containing defoamant |
GB2131820A (en) * | 1982-12-13 | 1984-06-27 | Chevron Res | Nonionic emulsifier and hydrocarbyl substituted succinic anhydride compositions emulsified therewith |
JPS6018584A (en) * | 1983-07-11 | 1985-01-30 | Sanyo Chem Ind Ltd | Rust proof addition agent for fuel oil |
EP0144739A2 (en) * | 1983-11-12 | 1985-06-19 | Henkel Kommanditgesellschaft auf Aktien | Corrosion inhibitor |
US4695401A (en) * | 1982-12-13 | 1987-09-22 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositions therewith |
EP0247653A2 (en) * | 1986-05-27 | 1987-12-02 | EURON S.p.A. | New compounds useful as detergent additives for lubricants and lubricating compositions |
US4849131A (en) * | 1986-06-30 | 1989-07-18 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositions therewith |
US4915786A (en) * | 1982-12-13 | 1990-04-10 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositons therewith |
US5080817A (en) * | 1990-09-18 | 1992-01-14 | Nalco Chemical Company | Corrosion inhibitor for 2-cycle engine oils comprising dodecenyl succinic anhydride-propylene glycol esters |
WO1997045507A1 (en) * | 1996-05-31 | 1997-12-04 | The Associated Octel Company Limited | Fuel additives |
US20150166923A1 (en) * | 2012-07-11 | 2015-06-18 | Idemitsu Kosan Co., Ltd | Lubricating oil composition |
BE1023617B1 (en) * | 2010-11-03 | 2017-05-17 | Afton Chemical Corporation | ADDITIVE FOR DIESEL FUEL |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1271877B (en) * | 1963-04-23 | 1968-07-04 | Lubrizol Corp | Lubricating oil |
US3459733A (en) * | 1964-10-15 | 1969-08-05 | Mobil Oil Corp | Monomeric polyesters of polyhydroxy compounds and process for preparing same |
US3291736A (en) * | 1964-11-20 | 1966-12-13 | Mobil Oil Corp | Grease compositions containing alkyl succinic partial esters |
US3844965A (en) * | 1972-10-05 | 1974-10-29 | Chevron Res | Lubricating oil additives |
US4129508A (en) * | 1977-10-13 | 1978-12-12 | The Lubrizol Corporation | Demulsifier additive compositions for lubricants and fuels and concentrates containing the same |
US4216114A (en) * | 1977-11-18 | 1980-08-05 | Imperial Chemical Industries Limited | Demulsification process |
EP0004426B1 (en) * | 1978-03-23 | 1982-10-06 | Imperial Chemical Industries Plc | Surfactant compositions comprising a blend of two types of polyester and an emulsion of oil in water prepared therewith |
US4664826A (en) * | 1980-10-06 | 1987-05-12 | Exxon Research & Engineering Co. | Metal salt esters of hydrocarbyl substituted succinic acid or anhydride and thio alkanols |
US4702850A (en) * | 1980-10-06 | 1987-10-27 | Exxon Research & Engineering Co. | Power transmitting fluids containing esters of hydrocarbyl succinic acid or anhydride with thio-bis-alkanols |
US4459223A (en) * | 1982-05-05 | 1984-07-10 | Exxon Research And Engineering Co. | Lubricant oil composition with improved friction reducing properties |
US4760170A (en) * | 1985-07-01 | 1988-07-26 | Exxon Research & Engineering Co. | Solution process for preparing metal salt esters of hydrocarbyl substituted succinic acid or anhydride and alkanols |
US4776969A (en) * | 1986-03-31 | 1988-10-11 | Exxon Chemical Patents Inc. | Cyclic phosphate additives and their use in oleaginous compositions |
US4784784A (en) * | 1986-07-17 | 1988-11-15 | Pennzoil Products Company | Succinic acid esters and hydraulic fluids therefrom |
US4689166A (en) * | 1986-07-17 | 1987-08-25 | Pennzoil Product Company | Succinic acid esters and hydraulic fluids thereform |
US4720555A (en) * | 1986-09-12 | 1988-01-19 | Pennzoil Products Company | Hydrocarbyl anhydrides |
US4839068A (en) * | 1987-10-01 | 1989-06-13 | The Lubrizol Corporation | Polysuccinate esters and lubricating compositions comprising same |
US4909952A (en) * | 1989-01-03 | 1990-03-20 | The Lubrizol Corporation | Sulfur-containing polymeric polyesters and additive concentrates and lubricating oils containing same |
US8613799B2 (en) * | 2006-08-22 | 2013-12-24 | Lubrizol Limited | Dispersants |
EP2312019B1 (en) * | 2009-10-01 | 2013-02-27 | Rhein Chemie Rheinau GmbH | Use of anticorrosion additives to protect aluminum and /or aluminum alloys in a finishing process |
WO2011071747A1 (en) | 2009-12-10 | 2011-06-16 | Soane Energy, Llc | Low interfacial tension surfactants for petroleum applications |
US8969612B2 (en) | 2009-12-10 | 2015-03-03 | Soane Energy, Llc | Low interfacial tension surfactants for petroleum applications |
EP3075436B1 (en) * | 2015-04-02 | 2018-08-01 | Afton Chemical Limited | Diesel exhaust fluid solutions and methods of using the same |
WO2022099291A1 (en) * | 2020-11-06 | 2022-05-12 | Exxonmobil Research And Engineering Company | Engine oil lubricant compositions and methods for making same with steel corrosion protection |
CN115678636B (en) * | 2021-07-29 | 2024-05-28 | 中国石油天然气股份有限公司 | Corrosion inhibitor and preparation method and application thereof |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2294259A (en) * | 1938-08-05 | 1942-08-25 | Shell Dev | Capillary-active agent |
US2442672A (en) * | 1941-02-18 | 1948-06-01 | Shell Dev | Rust-preventive hydrocarbon compositions |
US2435619A (en) * | 1944-01-15 | 1948-02-10 | Standard Oil Dev Co | Lubricant compositions |
US2497433A (en) * | 1947-06-11 | 1950-02-14 | Monsanto Chemicals | Alkyl esters of glycol polycarboxylic acid esters |
US2723286A (en) * | 1951-10-06 | 1955-11-08 | Exxon Research Engineering Co | Reduction of acidity in synthetic ester lubes with ethylene carbonate |
US2890210A (en) * | 1956-05-24 | 1959-06-09 | Union Carbide Corp | Compositions comprising epoxides and acid anhydrides |
-
1957
- 1957-08-16 US US678525A patent/US3045042A/en not_active Expired - Lifetime
-
1958
- 1958-08-18 GB GB26449/58A patent/GB896376A/en not_active Expired
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3287268A (en) * | 1963-11-21 | 1966-11-22 | Exxon Research Engineering Co | Cutting oil containing defoamant |
GB2131820A (en) * | 1982-12-13 | 1984-06-27 | Chevron Res | Nonionic emulsifier and hydrocarbyl substituted succinic anhydride compositions emulsified therewith |
US4695401A (en) * | 1982-12-13 | 1987-09-22 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositions therewith |
US4915786A (en) * | 1982-12-13 | 1990-04-10 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositons therewith |
JPH0334519B2 (en) * | 1983-07-11 | 1991-05-22 | Sanyo Chemical Ind Ltd | |
JPS6018584A (en) * | 1983-07-11 | 1985-01-30 | Sanyo Chem Ind Ltd | Rust proof addition agent for fuel oil |
EP0144739A2 (en) * | 1983-11-12 | 1985-06-19 | Henkel Kommanditgesellschaft auf Aktien | Corrosion inhibitor |
EP0144739A3 (en) * | 1983-11-12 | 1985-12-27 | Henkel Kommanditgesellschaft auf Aktien | Corrosion inhibitor |
EP0247653A2 (en) * | 1986-05-27 | 1987-12-02 | EURON S.p.A. | New compounds useful as detergent additives for lubricants and lubricating compositions |
EP0247653A3 (en) * | 1986-05-27 | 1989-05-17 | Euron S.P.A. | New compounds useful as detergent additives for lubricants and lubricating compositions |
US4849131A (en) * | 1986-06-30 | 1989-07-18 | Chevron Research Company | Nonionic emulsifier and substituted succinic anhydride compositions therewith |
US5080817A (en) * | 1990-09-18 | 1992-01-14 | Nalco Chemical Company | Corrosion inhibitor for 2-cycle engine oils comprising dodecenyl succinic anhydride-propylene glycol esters |
WO1997045507A1 (en) * | 1996-05-31 | 1997-12-04 | The Associated Octel Company Limited | Fuel additives |
US6156082A (en) * | 1996-05-31 | 2000-12-05 | The Associated Octel Company Limited | Fuel additives |
BE1023617B1 (en) * | 2010-11-03 | 2017-05-17 | Afton Chemical Corporation | ADDITIVE FOR DIESEL FUEL |
US20150166923A1 (en) * | 2012-07-11 | 2015-06-18 | Idemitsu Kosan Co., Ltd | Lubricating oil composition |
Also Published As
Publication number | Publication date |
---|---|
US3045042A (en) | 1962-07-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB896376A (en) | Partial esters of aliphatic substituted succinic acids and rust inhibiting compositions containing the same | |
US3090753A (en) | Ester oil compositions containing acid anhydride | |
US2575195A (en) | Dibasic acid esters and method for producing them | |
US4609376A (en) | Anti-wear additives in alkanol fuels | |
US4719084A (en) | Mixtures of fatty acid ammonium salts with antifoaming and anticorrosion enhancing polyol fatty acids or salts thereof | |
CN102977945B (en) | Diesel oil lubricity improving agent | |
KR950704453A (en) | MIDDLE PETROLEUM DISTILLATE COMPOSITION CONTAINING A PARAFFIN SETTLING SPEED LIMITER | |
US3123634A (en) | Chzchsocchzchzcoh | |
US2798083A (en) | Synthetic ester lubricants | |
US4048082A (en) | Organic lubricating compositions containing esters of benzotriazole | |
US4631071A (en) | Cold flow improving fuel additive compound and fuel composition containing same | |
GB829337A (en) | Phosphate additives for liquid petroleum hydrocarbon compositions | |
GB1037985A (en) | Alkylbutyrolactone-ª-acetic acids | |
US2559510A (en) | Synthetic lubricants | |
US4459223A (en) | Lubricant oil composition with improved friction reducing properties | |
US3294775A (en) | Reaction products of stabilized rosin amine and organic acid phosphate esters | |
GB795491A (en) | Steam turbine lubricant additives | |
US6165952A (en) | Ashless rust inhibitor lubricant compositions | |
US3148147A (en) | 2, 2-dialkyl-1, 3-propanediol diesters as functional fluids | |
US2759894A (en) | Rust inhibitor | |
US3117089A (en) | Compositions of matter having anti-rust properties | |
US2705724A (en) | Reduction of acidity in synthetic ester lubes with olefin oxides | |
US2742432A (en) | Mineral oil lubricating compositions | |
US2497432A (en) | Antirusting composition | |
US3223636A (en) | Lead corrosion inhibitor |