US2058343A - Petroleum product and method of making same - Google Patents
Petroleum product and method of making same Download PDFInfo
- Publication number
- US2058343A US2058343A US46870A US4687035A US2058343A US 2058343 A US2058343 A US 2058343A US 46870 A US46870 A US 46870A US 4687035 A US4687035 A US 4687035A US 2058343 A US2058343 A US 2058343A
- Authority
- US
- United States
- Prior art keywords
- oils
- oil
- lubricating
- compounds
- cadmium
- 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 - Lifetime
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- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000003209 petroleum derivative Substances 0.000 title 1
- 239000003921 oil Substances 0.000 description 62
- 239000010687 lubricating oil Substances 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- 230000001050 lubricating effect Effects 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 230000007797 corrosion Effects 0.000 description 12
- 238000005260 corrosion Methods 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- -1 cadmium-silver Chemical class 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 7
- 239000000956 alloy Substances 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000000314 lubricant Substances 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- 239000010705 motor oil Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 229910052793 cadmium Inorganic materials 0.000 description 6
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 6
- 230000002401 inhibitory effect Effects 0.000 description 6
- 238000007670 refining Methods 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 6
- 238000011105 stabilization Methods 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000011133 lead Substances 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910001316 Ag alloy Inorganic materials 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 229910000978 Pb alloy Inorganic materials 0.000 description 2
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000002542 deteriorative effect Effects 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000010723 turbine oil Substances 0.000 description 2
- 239000010913 used oil Substances 0.000 description 2
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 1
- 229910000897 Babbitt (metal) Inorganic materials 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000357293 Leptobrama muelleri Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000727 fraction Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 150000003739 xylenols Chemical class 0.000 description 1
Classifications
-
- 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
- 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
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
-
- 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
- C10N2040/135—Steam engines or turbines
-
- 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
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
-
- 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
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
Definitions
- This invention is directed to the stabilization of hydrocarbon oils of higher boiling points against the deteriorating effects of oxidation.
- Highly refined oils of the non-sludging types such as the white oils, turbine oils and the like, must be able to withstand the conditions of their use without the formation of acidic constituents of a corrosive or otherwise damaging nature.
- This invention contemplates the stabilization of such oils.
- Moderately refined oils of the nature of many lubricant fractions must likewise be able to withstand the conditions of their use without the formation of sludges, loss of color, or development of oxidation products corrosive to commonly used metals, as for instance to copper.
- This invention likewise contemplates the stabilization of such moderately refined oils.
- this invention is directed to the stabilization against deterioration due to oxidation reactions of any petroleum fractions of a light lubricant nature or heavier, from the lightest spindle oils, through the various classes of moderately, refined oils of higher viscosity, and inclusive of the highly refined oils such as turbine oils, white oils and the like.
- This invention has for an important object the preparation of oils falling within the above classes which are stable against oxidation and capable of meeting the normal conditions of their use without the formation of gummy material, sludges,
- An object of this invention is to provide an additive reagent or ingredient capable of inhibiting the corrosive properties of these oils.
- the production of solvent refined oils of low corrosive properties under conditions of automotive use is a major object of this invention, as well as the method of production of such oils which couple high viscosity index with low tendency to corrosion.
- hydrocarbon oils of the classes defined above can be stabilized in the respects above indicated by the addition thereto of small amounts of compounds selected from the class of aryl phosphites, having the general formula (AlO)3P in which Ar designates an aryl radical, as for instance (3635, or CHaCeHs.
- aryl phosphites which are suitable for the uses of this invention are as follows: Compounds of the general formula where one or more of the R's is a radical selected from the group consisting of where the R's are radicals selected from the group consisting of hydrogen, alkyl, hydroxy, halogen, aryl (such as phenyl and hydroxy phenyl), alkaryl, alkoxy, nitro, and amino and substituted amino (as phenyl or benzyl substituted).
- R's are radicals selected from the group consisting of hydrogen, alkyl, hydroxy, halogen, aryl (such as phenyl and hydroxy phenyl), alkaryl, alkoxy, nitro, and amino and substituted amino (as phenyl or benzyl substituted).
- R's are radicals selected from the group consisting of hydrogen, alkyl, hydroxy, halogen, aryl (such as phenyl and hydroxy phenyl), alkaryl,
- R is alkyl, it may range from a short alkyl such as methyl to very long alkyls corresponding for example to paraffin wax.
- phosphites of the type defined wherein the R is derived from hydroquinone, hydroxy diphenyl, guiacol, xylenol
- R is derived from hydroquinone, hydroxy diphenyl, guiacol, xylenol
- P013 a molecule of phosphorous trichloride
- three molecular amounts of phenol may be mixed with one molecular amount of phosphorous trichloride, and heated to about C. until the evolution of HCl gas ceases, indicating completion of the reaction.
- the reaction mixture may then be heated to about C. under a pressure of 1 mm. mercury to free it completely of HCl gas and the like.
- the product may be fractionally distilled under the same pressure. to yield a distiliate boiling from 205 to 215 C; at 2 mm. mercury, and consisting substantially of triphenylphosphite. (B. P. 209-210 C. at 2 mm. Hg). 5 Similar methods of preparation may be used for preparation of homologues, for example using ortho-cresol as starting ingredient for the production of triorthocresylphosphite. These compounds are clear oils of light color and are freely l0 miscible with hydrocarbon oils. When so mixed they do not darken nor deepen the color of the oils and show no tendency to separate under the normal conditions of storage and use.
- Moderately refined oils when subjected to ox- 5 idizing conditions in the absence of an effective inhibitor, yield both acidic compounds and sludges, tending to darken in color and to become corrosive.
- the inhibitory efiect of the arylphosphites may We demonstrated by the following exemplary test data. In these tests a moder-' ately refined hydrocarbon oil having a Saybolt viscosity of 152 seconds at 100 F. and a flash point of 385 F. was heated for three days at 230 F. in the presence of copper with exposure to air.
- the following table shows color. color after aging, and neutralization number of aged oil for an oil blank, and for oils containing stated amounts of triphenylphosphite and of triorthocresyl phosphite.
- Oils of the motor oil classes are also prone to oxidation with the formation of corrosive acidic 60 compounds, sludges, and the like.
- the arylphosphites contemplated by this invention are capable of effecting an inhibitive action in these oils as well, as is demonstrated by the following tests. 7 In these tests, 30 grams of oil were heated to 347 F. for 22 hours. Suspended in the oil was a carefully weighed piece of cadmium-silver alloy bearing metal. A jet of air (2000 ml. per hour) was so directed into the oil as to strike the metal. 7 Tests were run on an oil blank and on oil containing various percentages of the several aryl phosphites listed in the table. The oil used was a solvent refined motor oil of SAE 20 grade, viscosity 56 seconds Saybolt at 210 F. The loss i weight of the metal and the neutralization number of the used oil are reported.
- arylphosphites of this invention are quite effective in protection of moderately refined lubricants of the nature of motor oils against oxidation and specifically against corrosion of bearing metals of the cadmium-silver type.
- the amount of oxidized material extractable by means of alcoholic sodium hydroxide reported as tar is indicative of the degree of oxidation.
- the tests reported include an oil blank and the oil inhibited with triphenylphosphite, a tricresylphosphite, and tribetanaphthylphosphite.
- the amount of the stabilizing ingredient to be used will vary with the nature of the oil to be stabilized and with the use to which it will be put. In general, effective stabilization will be obtained in the oils of the class herein discussed with not in excess of 2% of arylphosphites, usually not more than 1%. For most common uses, effective stabilization may be had with from 0.05% to 0.50% of these compounds.
- hydrocarbon oils of relatively high boiling point or the equivalent thereof is used, it is intended to mean any and include all hydrocarbon mineral oil products normally used as lubricants or for electrical insulating purposes. It includes oils with an S. U. V. of 50 seconds at 100 F. or higher, or a flash point greater than 200 F. (Cleveland open cup). This term, in effect, is used in contradistinction of gasolines, kerosenes, and the like.
- a method of lubricating bearing surfaces in internal combustion engines when subjected to conditions of operation which comprises maintaining between bearing surfaces, one of which is an alloy formed chiefly of a metal selected from the class consisting of cadmium and copper, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but sufficient proportion substantially. to retard the corrosion.
- a method of lubricating bearing surfaces in internal combustion engines when subjected to conditions of operation which comprises maintaining between bearing surfaces, one of which is an alloy formed chiefly of a metal selected from the class consisting of cadmium and copper, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein from 0.1% to 1.0% of aryl phosphite suflicient substantially to retard the corrosion.
- a method of lubricating bearing surfaces which comprises maintaining between bearing surfaces, one of which is an alloy selected from the class consisting of cadmium-silver, cadmiumnickel, and copper-lead alloys, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but suflicient proportion substantially to retard the corrosiou.
- a method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but suflicient proportion to substantially retard the corrosion.
- a method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend tocorrode the aforesaid surface, and maintaining the efiectiveness of the lubricating oil by incorporating therein tribetanaphthyl phosphite in a small but sufficient proportion to substantially retard the corrosion.
- a method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the effectiveness of the lubricating oil by incorporating therein a compound or the general formula FCC-R I ⁇ O-R where the R's are radicals selected from the group consisting of and r retard the corrosion.
- a method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricatingoil which initially produces an efie'ctive lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the efiectiveness oi the lubricating oil by incorporating therein a compoundof the general formula /OR PIC-R 0-11 in which the R's are identical and each consists of a radical oi the general formula l small but sufiicient proportion to substantially retard the corrosion.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Oct. 20, 1936 UNITED STATES PATENT OFFICE Robert O. Moran,
Wenonah, and William L.
Ever: andEverett W. Fuller, Woodbury, N. J., assignors to Socony-Vacuum Oil Company, Incorporated, New York, N. Y., a corporation of New York No Drawing. Application October 26, 1935, Serial No. 46,870
7 Claims. (01. 87-9) This invention is directed to the stabilization of hydrocarbon oils of higher boiling points against the deteriorating effects of oxidation. Highly refined oils of the non-sludging types, such as the white oils, turbine oils and the like, must be able to withstand the conditions of their use without the formation of acidic constituents of a corrosive or otherwise damaging nature. This invention contemplates the stabilization of such oils. Moderately refined oils of the nature of many lubricant fractions must likewise be able to withstand the conditions of their use without the formation of sludges, loss of color, or development of oxidation products corrosive to commonly used metals, as for instance to copper. This invention likewise contemplates the stabilization of such moderately refined oils. In short, this invention is directed to the stabilization against deterioration due to oxidation reactions of any petroleum fractions of a light lubricant nature or heavier, from the lightest spindle oils, through the various classes of moderately, refined oils of higher viscosity, and inclusive of the highly refined oils such as turbine oils, white oils and the like.
This invention has for an important object the preparation of oils falling within the above classes which are stable against oxidation and capable of meeting the normal conditions of their use without the formation of gummy material, sludges,
materials of an acidic or corrosive nature, and/or darker color. It also has for an object the provision of a class of stabilizing materials not heretofore known to be effective for that purpose.
Recent changes in automotive engine design, tending toward higher bearing pressures, higher rotative speeds, higher engine temperatures, and the like, have occasioned departure from the use of the usual bearing metals such as babbit. The newer bearing metals are of different nature, and while harder, are in general more susceptible to destructive agencies of a corrosive nature. cal of these newer bearings are those composed of a cadmium-silver alloy supported upon a steel back, which are now widely installed in certain makes of automobiles. Others of these relatively new bearing metals which may be mentioned are cadmium-nickel and copper-lead alloys.
These changes in engine design have been concurrent with marked advances in methods of refining lubricant oils for automotive use. The demand for oils having lesser changes in viscosity with temperature change; i. e., higher viscosity index (VI), has been met by refining lubricants intended for motor oils by certain solvent refining or solvent extraction processes, wherein ad- 5 vantage is taken of the selective solvent power for hydrocarbons of various types which is possessed by certain liquid reagents, for example, dichlorodiethylether, cresylic acid, phenol, chloraniline, chlorophenol, phenetidine, benzyl alcohol, nitrol0 benzene, benzonitrile, furfural, aniline, benzyl acetate, liquid sulfur dioxide, mixtures of liquid sulfur dioxide or aniline with benzol, and the like. These solvent refining processes are operated to concentrate in the desired lubricant frac tion those compounds of a paraflinic nature possessed of.the ability to suffer only a small change of viscosity upon change of temperature, and to reject the compounds of naphthenic nature which do sufier such change of viscosity to 20 a more marked degree. These refining processes have enabled supply of an oil of quite desirable general characteristics, definitely far superior to any oil previously produced from mixed base or as'phaltic crudes, and superior to a like, though 25 lesser, degree over oils previously produced from paraflin base crudes.
It has been found that the solvent refined motor oils referred to above are for some reason definitely corrosive to the newer bearing metals under nor- 30 mal conditions of automotive use, sometimes resulting in bearing failure after only a few thousand miles of normal driving. It is further known that the same reaction, -viz., corrosion of alloy bearing metals such as cadmium-silver, also oc- 3 curs in good parafiinic base oils which have not been subjected to solvent refining. The higher the VI of the lubricating oil, the more pronounced is the tendency to corrosion of the kind referred to above. Generally speaking, the problem is encountered in oils having a VI of '75 or higher, and becomes imporant in oils having a VI of to or higher, and very important in oils of VI or higher. 45
It is an important object of this invention to provide means for satisfactorily inhibiting or preventing this corrosion from taking place to a serious degree. It is an object of this invention to alter or modify a highly refined motor oil, 50
normally corrosive, by the use of an additive ingredient capable of substantially inhibiting this corrosion. It is an object to provide a substantially non-corrosive motor oil of high VI. An object of this invention is to provide an additive reagent or ingredient capable of inhibiting the corrosive properties of these oils. The production of solvent refined oils of low corrosive properties under conditions of automotive use is a major object of this invention, as well as the method of production of such oils which couple high viscosity index with low tendency to corrosion.
We have found that hydrocarbon oils of the classes defined above can be stabilized in the respects above indicated by the addition thereto of small amounts of compounds selected from the class of aryl phosphites, having the general formula (AlO)3P in which Ar designates an aryl radical, as for instance (3635, or CHaCeHs. The aryl phosphites which are suitable for the uses of this invention are as follows: Compounds of the general formula where one or more of the R's is a radical selected from the group consisting of where the R's are radicals selected from the group consisting of hydrogen, alkyl, hydroxy, halogen, aryl (such as phenyl and hydroxy phenyl), alkaryl, alkoxy, nitro, and amino and substituted amino (as phenyl or benzyl substituted). Of the above defined classes of compounds, those at present preferred for the uses of this invention are those wherein all three R's are radicals of either type (a) or (b) defined above, and wherein the Rs are either hydrogen or alkyl. Examples of specific materials which we have found especially suitable for the uses of this invention are triphenyl phosphite, tricresyl phosphites and tribetanaphthyl phosphite. Where R is alkyl, it may range from a short alkyl such as methyl to very long alkyls corresponding for example to paraffin wax. Other examples which may be mentioned of suitable compounds selected from the above defined classes are phosphites of the type defined wherein the R is derived from hydroquinone, hydroxy diphenyl, guiacol, xylenol These preferred compounds may be generally described as the reaction products resulting from the reaction of trimolecular amounts of phenol or substituted phenol as defined above with a molecule of phosphorous trichloride (P013). As an example of this preparation, three molecular amounts of phenol may be mixed with one molecular amount of phosphorous trichloride, and heated to about C. until the evolution of HCl gas ceases, indicating completion of the reaction. The reaction mixture may then be heated to about C. under a pressure of 1 mm. mercury to free it completely of HCl gas and the like.
If it is desired, the product may be fractionally distilled under the same pressure. to yield a distiliate boiling from 205 to 215 C; at 2 mm. mercury, and consisting substantially of triphenylphosphite. (B. P. 209-210 C. at 2 mm. Hg). 5 Similar methods of preparation may be used for preparation of homologues, for example using ortho-cresol as starting ingredient for the production of triorthocresylphosphite. These compounds are clear oils of light color and are freely l0 miscible with hydrocarbon oils. When so mixed they do not darken nor deepen the color of the oils and show no tendency to separate under the normal conditions of storage and use.
Moderately refined oils, when subjected to ox- 5 idizing conditions in the absence of an effective inhibitor, yield both acidic compounds and sludges, tending to darken in color and to become corrosive. The inhibitory efiect of the arylphosphites may We demonstrated by the following exemplary test data. In these tests a moder-' ately refined hydrocarbon oil having a Saybolt viscosity of 152 seconds at 100 F. and a flash point of 385 F. was heated for three days at 230 F. in the presence of copper with exposure to air. The following table shows color. color after aging, and neutralization number of aged oil for an oil blank, and for oils containing stated amounts of triphenylphosphite and of triorthocresyl phosphite. 30
Table I.-Moderately refined oils Co or (Lovibond) Before After aging a n Oil alone 50 Oil+0.05% triphenylphosphite Oil-+0.10% triphenylphosphite Oil+0. 10% triorthocresylphosphite.
raw-
It is thus evident that quite minute amounts of 55 these compounds are capable of effectively protecting oils of this kind from the deteriorating effects of oxidation.
- Oils of the motor oil classes are also prone to oxidation with the formation of corrosive acidic 60 compounds, sludges, and the like. The arylphosphites contemplated by this invention are capable of effecting an inhibitive action in these oils as well, as is demonstrated by the following tests. 7 In these tests, 30 grams of oil were heated to 347 F. for 22 hours. Suspended in the oil was a carefully weighed piece of cadmium-silver alloy bearing metal. A jet of air (2000 ml. per hour) was so directed into the oil as to strike the metal. 7 Tests were run on an oil blank and on oil containing various percentages of the several aryl phosphites listed in the table. The oil used was a solvent refined motor oil of SAE 20 grade, viscosity 56 seconds Saybolt at 210 F. The loss i weight of the metal and the neutralization number of the used oil are reported.
Table II Loss in weight N. N. of of metal used oils mgs.
83f?? 'H""I"H"'HEB 8 f? a trip eny p osp l Oil+0 tripbenylphosphi 0 0.8 01l+0 tripheny1phbsph1te. l 0. 5 O1l+0 25% triorthocresylphosphlte l 0. 6 Oil+0.10% trlorthocresylphosphlte" 0 0. 4 Oil alone 69 2. 3 Oil+0.10% of a phosphite made from a mixture of o-m-p cresols 2 0. 4 Oil alone 23 l. 0 0il+0.l0% tribetanaphthylphosphite 0 0. 4 Oil alone 19 l. 6 0il+ 0.l0% triphospbite oi hydroqulnona.-. 8 0. 4
From these results it is seen that arylphosphites of this invention are quite effective in protection of moderately refined lubricants of the nature of motor oils against oxidation and specifically against corrosion of bearing metals of the cadmium-silver type.
Highly refined oils of the non-sludging or white oil type and of the transformer oil type are likewise subjected to conditions of use wherein the formation of acidic or corrosive products of oxidation is detrimental. A convenient method of testing the efiect of inhibitive compounds in such cases is the so-called German tar test. In this test, as reported below, an oil that had been highly refined by successive treatments with 98% sulfuric acid and 104% sulfuric acid, and having in finished form a specific gravity of 0.885, a viscosity of 66 seconds Saybolt at 104 F. and a flash point of 320 F., was oxidized at 248 F. by bubbling oxygen gas through it for '70 hours. The amount of oxidized material extractable by means of alcoholic sodium hydroxide reported as tar is indicative of the degree of oxidation. The tests reported include an oil blank and the oil inhibited with triphenylphosphite, a tricresylphosphite, and tribetanaphthylphosphite.
From the above data it is apparent that these compounds are competent stabilizers for the oils of the more highly refined classes as well.
The amount of the stabilizing ingredient to be used will vary with the nature of the oil to be stabilized and with the use to which it will be put. In general, effective stabilization will be obtained in the oils of the class herein discussed with not in excess of 2% of arylphosphites, usually not more than 1%. For most common uses, effective stabilization may be had with from 0.05% to 0.50% of these compounds.
In the claims, where the term "hydrocarbon oils of relatively high boiling point" or the equivalent thereof is used, it is intended to mean any and include all hydrocarbon mineral oil products normally used as lubricants or for electrical insulating purposes. It includes oils with an S. U. V. of 50 seconds at 100 F. or higher, or a flash point greater than 200 F. (Cleveland open cup). This term, in effect, is used in contradistinction of gasolines, kerosenes, and the like.
We claim:
1. A method of lubricating bearing surfaces in internal combustion engines when subjected to conditions of operation which comprises maintaining between bearing surfaces, one of which is an alloy formed chiefly of a metal selected from the class consisting of cadmium and copper, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but sufficient proportion substantially. to retard the corrosion.
2. A method of lubricating bearing surfaces in internal combustion engines when subjected to conditions of operation which comprises maintaining between bearing surfaces, one of which is an alloy formed chiefly of a metal selected from the class consisting of cadmium and copper, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein from 0.1% to 1.0% of aryl phosphite suflicient substantially to retard the corrosion.
3. A method of lubricating bearing surfaces which comprises maintaining between bearing surfaces, one of which is an alloy selected from the class consisting of cadmium-silver, cadmiumnickel, and copper-lead alloys, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid alloy, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but suflicient proportion substantially to retard the corrosiou.
4. A method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the effectiveness of the lubricating oil by incorporating therein aryl phosphite in a small but suflicient proportion to substantially retard the corrosion.
5. A method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend tocorrode the aforesaid surface, and maintaining the efiectiveness of the lubricating oil by incorporating therein tribetanaphthyl phosphite in a small but sufficient proportion to substantially retard the corrosion.
6. A method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricating oil which initially produces an effective lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the effectiveness of the lubricating oil by incorporating therein a compound or the general formula FCC-R I \O-R where the R's are radicals selected from the group consisting of and r retard the corrosion.
7. A method of lubricating bearing surfaces which comprises maintaining between the bearing surfaces, one of which contains a characterizing proportion of cadmium, silver, nickel, copper or lead, a film of lubricatingoil which initially produces an efie'ctive lubricating action but which would normally tend to corrode the aforesaid surface, and maintaining the efiectiveness oi the lubricating oil by incorporating therein a compoundof the general formula /OR PIC-R 0-11 in which the R's are identical and each consists of a radical oi the general formula l small but sufiicient proportion to substantially retard the corrosion.
ROBERT c. MORAN. WILLIAM L. EvERs. EVERETT w. FULLER.
CERTIFICATE OF CORRECTION.
Patent No. 2,058,343. I October 20. 1936;
ROBERT c. MORAN, ET AL.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 2, first column, lines 29 and 49, for "R's" read Rs; lines 42 and '51, for "R's" read B's; and second column, line 45, in the heading to the table, for "Co or" read Color; page 4, first column, line '7, claim 6, and second column, line 13, claim 7,. for "R's" read Rs; same page, first column, line 22, claim 6, and second column, line 21, claim '7, for "R's read B's; and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 23rd day of February, A. D. 1937.
Henry Van Arsdale (Seal) Acting Commissioner of Patents.
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US46870A US2058343A (en) | 1935-10-03 | 1935-10-26 | Petroleum product and method of making same |
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US43328A US2058342A (en) | 1935-10-03 | 1935-10-03 | Petroleum lubricant product and method of making same |
US46870A US2058343A (en) | 1935-10-03 | 1935-10-26 | Petroleum product and method of making same |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2643962A (en) * | 1950-04-17 | 1953-06-30 | Johnson & Co A | Treatment of electric apparatus intended to contain oil |
US2790014A (en) * | 1953-12-01 | 1957-04-23 | Monsanto Chemicals | Stabilized hydrocarbons |
US3071548A (en) * | 1959-12-14 | 1963-01-01 | Universal Oil Prod Co | Stabilization of organic substances |
US3280031A (en) * | 1963-12-31 | 1966-10-18 | Mobil Oil Corp | High temperature lubricating oils |
US4321218A (en) * | 1978-01-10 | 1982-03-23 | Ciba-Geigy Corporation | Phosphite stabilizer |
US4415686A (en) * | 1982-11-24 | 1983-11-15 | The B. F. Goodrich Company | Sterically hindered phenyl bis(naphthyl)phosphites and compositions thereof |
US4444929A (en) * | 1982-11-24 | 1984-04-24 | The B. F. Goodrich Company | Unsymmetrical phosphite-phenolic isocyanurate stabilizer combinations |
US4495320A (en) * | 1983-05-27 | 1985-01-22 | The B. F. Goodrich Company | 3,6-Di-t-butyl-2-naphthyl catechol phosphite and compositions thereof |
US4520151A (en) * | 1982-04-02 | 1985-05-28 | The B. F. Goodrich Company | Tris (3,6-di-t-butyl-2-naphthyl) phosphite and compositions thereof |
US4656302A (en) * | 1985-03-08 | 1987-04-07 | Koppers Company, Inc. | Tris-(3-hydroxy-4,6-di-t-alkylphenyl) phosphites |
-
1935
- 1935-10-26 US US46870A patent/US2058343A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2643962A (en) * | 1950-04-17 | 1953-06-30 | Johnson & Co A | Treatment of electric apparatus intended to contain oil |
US2790014A (en) * | 1953-12-01 | 1957-04-23 | Monsanto Chemicals | Stabilized hydrocarbons |
US3071548A (en) * | 1959-12-14 | 1963-01-01 | Universal Oil Prod Co | Stabilization of organic substances |
US3280031A (en) * | 1963-12-31 | 1966-10-18 | Mobil Oil Corp | High temperature lubricating oils |
US4321218A (en) * | 1978-01-10 | 1982-03-23 | Ciba-Geigy Corporation | Phosphite stabilizer |
US4520151A (en) * | 1982-04-02 | 1985-05-28 | The B. F. Goodrich Company | Tris (3,6-di-t-butyl-2-naphthyl) phosphite and compositions thereof |
US4415686A (en) * | 1982-11-24 | 1983-11-15 | The B. F. Goodrich Company | Sterically hindered phenyl bis(naphthyl)phosphites and compositions thereof |
US4444929A (en) * | 1982-11-24 | 1984-04-24 | The B. F. Goodrich Company | Unsymmetrical phosphite-phenolic isocyanurate stabilizer combinations |
US4495320A (en) * | 1983-05-27 | 1985-01-22 | The B. F. Goodrich Company | 3,6-Di-t-butyl-2-naphthyl catechol phosphite and compositions thereof |
US4656302A (en) * | 1985-03-08 | 1987-04-07 | Koppers Company, Inc. | Tris-(3-hydroxy-4,6-di-t-alkylphenyl) phosphites |
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