GB866502A - Manufacture of metal salts of dialkyl dithiophosphoric acids - Google Patents
Manufacture of metal salts of dialkyl dithiophosphoric acidsInfo
- Publication number
- GB866502A GB866502A GB40509/58A GB4050958A GB866502A GB 866502 A GB866502 A GB 866502A GB 40509/58 A GB40509/58 A GB 40509/58A GB 4050958 A GB4050958 A GB 4050958A GB 866502 A GB866502 A GB 866502A
- Authority
- GB
- United Kingdom
- Prior art keywords
- range
- alkanols
- maintaining
- water content
- mixture
- 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
- 150000003839 salts Chemical class 0.000 title abstract 7
- 229910052751 metal Inorganic materials 0.000 title abstract 5
- 239000002184 metal Substances 0.000 title abstract 5
- 239000002253 acid Substances 0.000 title abstract 4
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 150000007513 acids Chemical class 0.000 title 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 8
- 239000000203 mixture Substances 0.000 abstract 8
- 239000004215 Carbon black (E152) Substances 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 229930195733 hydrocarbon Natural products 0.000 abstract 6
- 150000002430 hydrocarbons Chemical class 0.000 abstract 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 230000003472 neutralizing effect Effects 0.000 abstract 5
- 239000003921 oil Substances 0.000 abstract 5
- 239000011701 zinc Substances 0.000 abstract 5
- 229910052725 zinc Inorganic materials 0.000 abstract 5
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 abstract 4
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 abstract 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 4
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 abstract 4
- 239000011541 reaction mixture Substances 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 239000003085 diluting agent Substances 0.000 abstract 3
- 238000001035 drying Methods 0.000 abstract 3
- 238000001914 filtration Methods 0.000 abstract 3
- 229910003480 inorganic solid Inorganic materials 0.000 abstract 3
- 239000010687 lubricating oil Substances 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- 238000002791 soaking Methods 0.000 abstract 3
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 239000000654 additive Substances 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052788 barium Inorganic materials 0.000 abstract 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011575 calcium Substances 0.000 abstract 2
- 229910052791 calcium Inorganic materials 0.000 abstract 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 abstract 2
- 239000010941 cobalt Substances 0.000 abstract 2
- 229910017052 cobalt Inorganic materials 0.000 abstract 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 2
- 239000012141 concentrate Substances 0.000 abstract 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 2
- 230000005484 gravity Effects 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 2
- 229910052742 iron Inorganic materials 0.000 abstract 2
- 229910052749 magnesium Inorganic materials 0.000 abstract 2
- 239000011777 magnesium Substances 0.000 abstract 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 2
- 150000002736 metal compounds Chemical class 0.000 abstract 2
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 abstract 2
- -1 polybutylene Polymers 0.000 abstract 2
- 229920001748 polybutylene Polymers 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- OKENIJHKINGHGK-UHFFFAOYSA-N 4-methylpentan-2-ol propan-2-ol Chemical compound CC(O)CC(C)C.C(C)(C)O OKENIJHKINGHGK-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- 239000004435 Oxo alcohol Substances 0.000 abstract 1
- FQNGWRSKYZLJDK-UHFFFAOYSA-N [Ca].[Ba] Chemical compound [Ca].[Ba] FQNGWRSKYZLJDK-UHFFFAOYSA-N 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- XOIXUOQWXVZBRQ-UHFFFAOYSA-N barium;2-nonylphenol Chemical compound [Ba].CCCCCCCCCC1=CC=CC=C1O XOIXUOQWXVZBRQ-UHFFFAOYSA-N 0.000 abstract 1
- 235000011132 calcium sulphate Nutrition 0.000 abstract 1
- 239000001175 calcium sulphate Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- YOCUPQPZWBBYIX-UHFFFAOYSA-N copper nickel Chemical compound [Ni].[Cu] YOCUPQPZWBBYIX-UHFFFAOYSA-N 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 229940035429 isobutyl alcohol Drugs 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 238000000638 solvent extraction Methods 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/17—Esters of thiophosphoric acids with hydroxyalkyl compounds without further substituents on alkyl
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- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
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- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/081—Inorganic acids or salts thereof containing halogen
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
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- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
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- C10M2201/084—Inorganic acids or salts thereof containing sulfur, selenium or tellurium
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- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- 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
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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- C10M2225/041—Hydrocarbon polymers
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- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
-
- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/16—Groups 8, 9, or 10
-
- 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
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/042—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/044—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
Abstract
Metal salts of dialkyl (or dicycloalkyl) dithiophosphoric acid suitable for use us additives for lubricants (see Group III) are obtained by reacting phosphorus pentasulphide with at least one alkanol or cycloalkanol having up to 14 carbon atoms at a temperature in the range of 160 DEG to 200 DEG F. for a time in the range of 1 to 6 hours while maintaining the specific gravity of the reaction mixture in the range of 1,015 to 1,035 at 78 DEG F. to obtain a dark coloured reaction mixture and separating solids therefrom, neutralising the purified dark product with a basic inorganic metal compound at a temperature in the range of 140 to 200 DEG F., heat soaking the dialkyl (or dicycloalkyl) dithiophosphoric acid salt so obtained at a temperature in the range of 150 DEG to 200 DEG F. for 1 to 4 hours, while maintaining the water content thereof at from 0,5 to 4 weight per cent and the pH at from 6,0 to 6,6 then separating substantially completely inorganic solids from the heat soaked acid salt by filtering while maintaining the water content at from 0,5 to 4 weight per cent., and drying the purified acid salt to a water content not exceeding one weight per cent. Specified alcohols are methanol, ethanol, butanol, isobutanol, isopropanol, cyclohexanol, methyl isobutyl carbinol, 2-ethyl hexanol, methyl cyclohexanol and primary branched chain alkanols such as C5, C7 or C13 "Oxo" alcohols and mixtures of alkanols having from 3 to 14 carbon atoms may be used and especially a mixture of two alkanols having from 3 to 6 carbon atoms. Suitable mixtures are isopropanol-methyl isobutyl carbinol, and isobutyl alcohol-primary amyl alcohol. The neutralising agent is preferably an oxide or hydroxide of a suitable metal, e.g. zinc, magnesium, calcium, aluminium, manganese, iron, cobalt, nickel, copper, barium, or lead. A diluent oil e.g. a hydrocarbon distillate oil is preferably used after the neutralisition and heat soaking steps and prior to the filtration to remove inorganic solids. An example is given for the production of a zinc dialkyl dithiophosphate from a mixture of methyl isobutyl carbinol (70% wt.) and isopropanol (30% wt.) using zinc oxide as the neutralising agent. The final drying step may be effected by stripping with an inert gas e.g. nitrogen, by azeotroping with benzene or isobutyl alcohol or by entrainment with a light hydrocarbon, e.g. hexane.ALSO:An additive for lubricating oils comprises a metal salt of a dialkyl or dicycloalkyl dithiophosphoric acid obtained by reacting phosphorus pentasulphide with at least one alkanol or cycloalkanol having up to 14 carbon atoms at a temperature in the range of 160 DEG to 200 DEG F. for a time of 1 to 6 hours while maintaining the specific gravity of the reaction mixture in the range of 1.015 to 1.035 at 78 DEG F. to obtain a dark coloured reaction mixture, cooling the latter and separating solids therefrom, neutralising the purified dark product with a basic inorganic metal compound at from 140 DEG to 200 DEG F., heat soaking the dialkyl dithiophosphoric acid salt at from 150 DEG to 200 DEG F. for 1 to 4 hours while maintaining its water content at from 0.5 to 4% weight and the pH in the range of 6.0 to 6.6 then separating substantially completely inorganic solids from the heat soaked acid salt by filtering, preferably after the addition of a diluent oil, e.g. a hydrocarbon diluent oil, while maintaining the water content at from 0.5 to 4% weight and drying the purified salt to a water content not exceeding 1% weight (see Group IV(b)). Specified alkanols and cycloalkanols are methanol, ethanol, butanol, isobutanol, isopropanol, cyclohexanol, methyl isobutyl carbinol, 2-ethyl hexanol, methyl cyclohexanol and C5, C7 and C13 oxo alcohols. Mixtures of C3-C14 alkanols and especially a mixture of two alkanols having from 3 to 6 carbon atoms may also be used. The neutralising agent is preferably an oxide or hydroxide of a suitable metal, e.g. zinc, magnesium, calcium, aluminium, manganese, iron, cobalt, nickel copper, barium or lead. In an example a concentrate of a zinc dialkyl dithiophosphate in a hydrocarbon distillate oil, said concentrate being obtained as above from a mixture of methyl isobutyl carbinol (70% wt.) and isopropanol (30% wt.) is added to a hydrocarbon lubricating oil (derived from a mid-continent crude by solvent extraction) and a methacrylate type viscosity index improver, a barium-calcium sulphurised phenate, calcium sulphate and a phosphosulphurised pinene are also added. In another example the zinc dialkyl dithiophosphate is added to a mixed hydrocarbon lubricating oil and a polybutylene type viscosity index improver, a phosphosulphurised polybutylene neutralised with a basic barium nonyl phenol sulphide-sulphonate mixture and a chlorinated wax-naphthalene condensate also added.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US866502XA | 1958-01-07 | 1958-01-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB866502A true GB866502A (en) | 1961-04-26 |
Family
ID=22199959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40509/58A Expired GB866502A (en) | 1958-01-07 | 1958-12-16 | Manufacture of metal salts of dialkyl dithiophosphoric acids |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1119854B (en) |
| FR (1) | FR1218677A (en) |
| GB (1) | GB866502A (en) |
| NL (2) | NL111965C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3277003A (en) * | 1964-02-17 | 1966-10-04 | Phillips Petroleum Co | Lubricating oils containing amine oxides |
| US5178782A (en) * | 1985-03-12 | 1993-01-12 | The Lubrizol Corporation | Metal salts of mixed aromatic/aliphatic phosphorodithioic acids |
| EP1529829A1 (en) * | 2003-11-06 | 2005-05-11 | Afton Chemical Corporation | Process for producing zinc dialkyldithiophosphates exhibiting improved seal compatibility properties |
| CN107955034A (en) * | 2017-10-25 | 2018-04-24 | 江苏腾龙生物药业有限公司 | A kind of preparation process of Rogor active compound |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL85589C (en) * | 1951-03-29 |
-
0
- NL NL234911D patent/NL234911A/xx unknown
- NL NL111965D patent/NL111965C/xx active
-
1958
- 1958-12-16 GB GB40509/58A patent/GB866502A/en not_active Expired
- 1958-12-19 DE DEE16906A patent/DE1119854B/en active Pending
- 1958-12-31 FR FR783082A patent/FR1218677A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3277003A (en) * | 1964-02-17 | 1966-10-04 | Phillips Petroleum Co | Lubricating oils containing amine oxides |
| US5178782A (en) * | 1985-03-12 | 1993-01-12 | The Lubrizol Corporation | Metal salts of mixed aromatic/aliphatic phosphorodithioic acids |
| EP1529829A1 (en) * | 2003-11-06 | 2005-05-11 | Afton Chemical Corporation | Process for producing zinc dialkyldithiophosphates exhibiting improved seal compatibility properties |
| US7368596B2 (en) | 2003-11-06 | 2008-05-06 | Afton Chemical Corporation | Process for producing zinc dialkyldithiophosphates exhibiting improved seal compatibility properties |
| US7592490B2 (en) | 2003-11-06 | 2009-09-22 | Afton Chemical Corporation | Process for producing zinc dialkyldithiophosphates exhibiting improved seal compatibility properties |
| CN107955034A (en) * | 2017-10-25 | 2018-04-24 | 江苏腾龙生物药业有限公司 | A kind of preparation process of Rogor active compound |
| CN107955034B (en) * | 2017-10-25 | 2020-05-12 | 江苏腾龙生物药业有限公司 | Preparation process of raw dimethoate |
Also Published As
| Publication number | Publication date |
|---|---|
| NL234911A (en) | |
| DE1119854B (en) | 1961-12-21 |
| NL111965C (en) | |
| FR1218677A (en) | 1960-05-12 |
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