US2664436A - Lubricating oil composition of high viscosity and method for preparing same - Google Patents
Lubricating oil composition of high viscosity and method for preparing same Download PDFInfo
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- US2664436A US2664436A US199572A US19957250A US2664436A US 2664436 A US2664436 A US 2664436A US 199572 A US199572 A US 199572A US 19957250 A US19957250 A US 19957250A US 2664436 A US2664436 A US 2664436A
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- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/40—Six-membered ring containing nitrogen and carbon 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
-
- 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
- C10M2215/22—Heterocyclic nitrogen 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
-
- 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
- C10M2215/30—Heterocyclic compounds
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Definitions
- the presentinventicn is directed to a lubricating oil composition. More particularly, the invention directed to a method of preparing a lubricating-oil compo "tion having a high. viscosity and a low he. .lization value.
- a high viscosity lubricating oil composition having a low neutralization value is prepared by formins a mixture of an olefinic lubricating'oil polymer having lubricating oil characteristics and an amount in the range between 0.1% and5% by The mixture is then "subjected'to oxidizing conditions at an elevated temperature' for a time sufficient to'form an oxidized product.
- Theoxidizedproduct is appreciatecl'in viscosity by formation of oxidized bodies but the oxidized product has a relatively low neutralization value indicating that the oxidized bodies are not acidic in nature.
- the quinoline employed in the practice of the present invention may be used as stated in an amount in the range between 0.1% and 5% by Weight witha preferred range from 0.5% to3% by weight. An amount which givesvery satisfactory results is 2% by weight.
- the olefinic lubricating oil polymeremployed in the practice of the present invention may be obtained by polymerizing alpha olefins to produce polymers in the lubricating oil boiling range and having lubricating oil characteristics.
- Such polymers may be produced by polymerizing alpha olefins boiling in the range between 190 and 400 F. in the presence of a Friedel-Crafts catalyst'at a'temperature of about 75 to'200 F.
- Olefins which may be polymerized to produce lubricating oil polymers are the alpha olefins having from 5 to carbon atoms in the molecule including pentene-l, hexene-l, hep-tene-l, octene-l, nonene-l, and decene-l.
- a convenient source of alpha olefins is the naphtha fraction produced in the Fischer-Tropsch synthesis when employing a promoted iron catalyst.
- the olefinic lubricating oil polymer will ordinarily be employed in an amount in the range between 95% and 99.9% by weight with a preferred range being from 97% to 99.5% by weight.
- the mixture may be oxidized at a temperature in the range from 300 to 600 F.
- the oxidation time may range from about minutes up to about 16 hours.
- Air is a suitable source of oxygen but other sources may be used.
- compositions were made up which various-additives were admixed with an olefinic lubricating oil polymer. . The admixtures were then oxidized at 375 F. and the oxidized mixture then tested for per cent increase in viscosity at 210 F., for neutralization value and for sludge formation. The'results of these tests are pre- 7 sented in the following table:
- the oxidation of the naphthenic mineral oil in the method of the present invention was carried out as follows in a 200 cc. glass threenecked round bottom flask.
- the central neck of this flask is 5 cm. long and has an inside diameter of 3 cm.
- the flask has two opposed side necks which are 6 cm. long and 1.5 cm. inside diameter, and are situated at a 30 angle with the central neck, perpendicular to the surface of the spherical flask.
- the stirrer is a glass rod 0.5 cm. in diameter, entering the flask through a glass tube bearing held in place by a rubber stopper in the central neck, with two glass blades 1.0 cm. long by 0.7 cm.
- the stirrer is driven by a 1750 R. P. M. motor connected to the stirrer by a rubber tubing coupling.
- the blades of the stirrer are situated about 0.5 cm. from the bottom of the flask and spin in such a direction that their propeller-like action circulates the oil to the bottom of the flask, up along the sides of the flask, back to the center of the flask, and down to the stirrer blades again. A considerable amount of air is sucked down with the descending oil and intimately contacted with it by the action of the stirrer.
- a thermometer well 5 cm. long and 1.0 cm.
- inside diameter is situated in one side of the flask equidistant from the two side arms.
- the flask is about two-thirds immersed in an oil bath maintained at 375 F.
- the temperature of the oil in the flask is usually 5 to F. below the temperature of the oil bath.
- the oxidation operation is carried out in the specially constructed flask by stirring 100 cc. of the sample in the presence of air for sixteen hours at 375 F. At the end of that time the flask is removed from the oil bath and tests obtained on the oxidized oil.
- the oxidation operation was carried out for 16 hours at 375 F.
- the operation to appreciate the viscosity may be conducted at a lower temperature for a longer period of time or at a higher temperature for a shorter period of time.
- the oxidation may be carried out at a temperature in the range from 300 to 600 F. and for a time ranging from about 30 minutes up to 16 hours.
- While the neutralization value of the oxidized product in accordance with the present invention is low it may be desirable to decrease the neutralization value even further. This may be done by contacting the oxidized product with an adsorbent material, such as a contact clay.
- An-- other way of lowering a neutralization value is to neutralize the organic acidic material with an alkaline material, such as a solution of sodium hydroxide or sodium carbonate.
- the oxidized product of the present invention may suitably be used as a compounding oil and may find particular usage as a component of steam cylinder lubricant or as the hydrocarbon component in grease manufacture.
- a method for increasing the viscosity of an olefinic lubricating oil polymer having lubrieating oil characteristics which comprises oxidizing the polymer at a temperature in the range from 300 to 600 F. in the presence of an oxidation promoter consisting of an amount no less than 0.1% by weight of quinoline to form an oxidized product having a substantially increased viscosity and a low neutralization value and recovering said product.
- a method for forming a high viscosity lubricating oil which comprises forming a mixture of a lubricating oil polymer of an alpha olefin having from 5 to 10 carbon atoms in the molecule and an oxidation promoter consisting of an amount no less than 0.1% by weight of quino line, oxidizing the mixture at a temperature in the range from 300 to 600 F. to form an oxidized product having a substantially increased viscosity and a low neutralization value and recovering said product.
- a method for producing a high viscosity lubricating oil which comprises forming a mixture of a lubricating oil polymer of an alpha olefin having from 5 to 10 carbon atoms in the molecule and an oxidation promoter consisting of an amount in the range from 0.1% to 5% by weight of quinoline, oxidizing the mixture in the presence of air at a temperature in the range from 300 to 600 F. for a time in the range from 30 minutes to 16 hours to form an oxidized prod not having a substantially increased viscosity and a low neutralization value, and recovering said product.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
' weight of quinoline.
Patented Dec. 29, 1953 LUBRIC'ATING OIL COMPOSITION OFHIGH VISCO;5311? AND. .ME
.ING SAME Raymond L. --Heinrich, Baytown, Tex.,
fby mesne assignments, to
THGD FOR PREPAR- assignor, Standard Oil Development CompanmElizabeth -N. 'J., a corporation of Delaware No Drawing. Application 'December"6,"1950, .SerialNo. 199,572
:4 Claims. -(o1. 260-451) The presentinventicn is directed to a lubricating oil composition. More particularly, the invention directed to a method of preparing a lubricating-oil compo "tion having a high. viscosity and a low he. .lization value.
In accordance with the present invention a high viscosity lubricating oil composition having a low neutralization value is prepared by formins a mixture of an olefinic lubricating'oil polymer having lubricating oil characteristics and an amount in the range between 0.1% and5% by The mixture is then "subjected'to oxidizing conditions at an elevated temperature' for a time sufficient to'form an oxidized product. Theoxidizedproduct is appreciatecl'in viscosity by formation of oxidized bodies but the oxidized product has a relatively low neutralization value indicating that the oxidized bodies are not acidic in nature. a
The quinoline employed in the practice of the present invention may be used as stated in an amount in the range between 0.1% and 5% by Weight witha preferred range from 0.5% to3% by weight. An amount which givesvery satisfactory results is 2% by weight.
The olefinic lubricating oil polymeremployed in the practice of the present invention may be obtained by polymerizing alpha olefins to produce polymers in the lubricating oil boiling range and having lubricating oil characteristics. Such polymers may be produced by polymerizing alpha olefins boiling in the range between 190 and 400 F. in the presence of a Friedel-Crafts catalyst'at a'temperature of about 75 to'200 F. Olefins which may be polymerized to produce lubricating oil polymers are the alpha olefins having from 5 to carbon atoms in the molecule including pentene-l, hexene-l, hep-tene-l, octene-l, nonene-l, and decene-l. A convenient source of alpha olefins is the naphtha fraction produced in the Fischer-Tropsch synthesis when employing a promoted iron catalyst. The olefinic lubricating oil polymer will ordinarily be employed in an amount in the range between 95% and 99.9% by weight with a preferred range being from 97% to 99.5% by weight.
In oxidizing a mixture of clefinic lubricating oil polymer having lubricating oil characteristics and quinoline, the mixture may be oxidized at a temperature in the range from 300 to 600 F. The oxidation time may range from about minutes up to about 16 hours. Air is a suitable source of oxygen but other sources may be used.
In order to illustrate the invention further, a number of compositions were made up which various-additives were admixed with an olefinic lubricating oil polymer. .The admixtures were then oxidized at 375 F. and the oxidized mixture then tested for per cent increase in viscosity at 210 F., for neutralization value and for sludge formation. The'results of these tests are pre- 7 sented in the following table:
Table Tests on oxidized oils .Olefin polymer 1 Oxidation promoter Weight pg rccnt Percent New roincrease tra-liza- Sludge meter 21 3 62 tion formation R value None 11. 6 None. Beta-naphthol 1. O 16. 2 o. Dicthanol su1fide 2.0 8. 4 Moderate Hydroquinone... 1.0 14.0 None.
Do -2. 0 8. 4 D0. Dibenzyl p-amino phenol... 2. 0 11. 8 Heavy. Sulfur monochloride ,1. 0 7. 7 None. Quinolinc 2. 0 1. 4 Do. Lauryl mercaptan 1. 0 6. 2 Do.
. 2.0 2. 8 Do. Commercial -metal deacti 1.0 20. 2 Do.
vator. V p-Tolucne sulfonyl amide 2. 0 1. 5 I cry lice vy Benzene sulfonyl amide '2. 0 0.9 Do.
Prepared by A1013 catalyzed polymerization of octenc-l, 47.7 vis. 210 F. SSU, viscosity-index.
2 Extremely viscous material, too viscous for SSU viscosity determination.
. twill be seen from the foregoing results that of 1c additives added to the olefinic polymer only quinoline increased the viscosity while yet maintaining a low neutralization value. High neutralization values are indicative of high acid contents which .are undesirable in lubricating oil. These datashow that the viscosity of an olefinic polymer may be varied by varying the amount of the quinoline toproduce nearly any desired viscosity while yet allowing the production of a lubricating oil having a low neutralization value and in which is not formed any substantial amount of sludge.
The oxidation of the naphthenic mineral oil in the method of the present invention was carried out as follows in a 200 cc. glass threenecked round bottom flask. The central neck of this flask is 5 cm. long and has an inside diameter of 3 cm. The flask has two opposed side necks which are 6 cm. long and 1.5 cm. inside diameter, and are situated at a 30 angle with the central neck, perpendicular to the surface of the spherical flask. The stirrer is a glass rod 0.5 cm. in diameter, entering the flask through a glass tube bearing held in place by a rubber stopper in the central neck, with two glass blades 1.0 cm. long by 0.7 cm. wide welded to opposite sides of the bottom end of the glass rod at a 30 angle with the vertical. The stirrer is driven by a 1750 R. P. M. motor connected to the stirrer by a rubber tubing coupling. The blades of the stirrer are situated about 0.5 cm. from the bottom of the flask and spin in such a direction that their propeller-like action circulates the oil to the bottom of the flask, up along the sides of the flask, back to the center of the flask, and down to the stirrer blades again. A considerable amount of air is sucked down with the descending oil and intimately contacted with it by the action of the stirrer. A thermometer well 5 cm. long and 1.0 cm. inside diameter is situated in one side of the flask equidistant from the two side arms. During the oxidation the flask is about two-thirds immersed in an oil bath maintained at 375 F. The temperature of the oil in the flask is usually 5 to F. below the temperature of the oil bath.
The oxidation operation is carried out in the specially constructed flask by stirring 100 cc. of the sample in the presence of air for sixteen hours at 375 F. At the end of that time the flask is removed from the oil bath and tests obtained on the oxidized oil.
While the oxidation operation was carried out for 16 hours at 375 F., the operation to appreciate the viscosity may be conducted at a lower temperature for a longer period of time or at a higher temperature for a shorter period of time. For example, the oxidation may be carried out at a temperature in the range from 300 to 600 F. and for a time ranging from about 30 minutes up to 16 hours.
The neutralization value which is used as a method of test is described in A. S. T. M. Standards for Petroleum Products and Lubricants prepared by A. S. T. M. Committee D-2, November 1948, and designated Tentative Method of Test for Neutralization Value (Acid and Base Numbers) by Color Indicator Titration, A. S. T. M. designation: 974-48T.
While the neutralization value of the oxidized product in accordance with the present invention is low it may be desirable to decrease the neutralization value even further. This may be done by contacting the oxidized product with an adsorbent material, such as a contact clay. An-- other way of lowering a neutralization value is to neutralize the organic acidic material with an alkaline material, such as a solution of sodium hydroxide or sodium carbonate.
The oxidized product of the present invention may suitably be used as a compounding oil and may find particular usage as a component of steam cylinder lubricant or as the hydrocarbon component in grease manufacture.
The nature and objects of the present inven tion having been completely described and illustrated, what I wish to claim as new and usefu1 and to secure by Letters Patent is:
l. A method for increasing the viscosity of an olefinic lubricating oil polymer having lubrieating oil characteristics which comprises oxidizing the polymer at a temperature in the range from 300 to 600 F. in the presence of an oxidation promoter consisting of an amount no less than 0.1% by weight of quinoline to form an oxidized product having a substantially increased viscosity and a low neutralization value and recovering said product.
2. A method for forming a high viscosity lubricating oil which comprises forming a mixture of a lubricating oil polymer of an alpha olefin having from 5 to 10 carbon atoms in the molecule and an oxidation promoter consisting of an amount no less than 0.1% by weight of quino line, oxidizing the mixture at a temperature in the range from 300 to 600 F. to form an oxidized product having a substantially increased viscosity and a low neutralization value and recovering said product.
3. A method for forming a high viscosity lubricating oil which comprises forming a mixture of a lubricating oil polymer of octene-l having lubricating oil characteristics and an oxidation promoter consisting of 2% by weight or quinoline, oxidizing the mixture at a temperature of about 375 F. for a time sufiicient to form an oxidized product having a substantially in-= creased viscosity and a 10W neutralization value and recovering said product.
4. A method for producing a high viscosity lubricating oil which comprises forming a mixture of a lubricating oil polymer of an alpha olefin having from 5 to 10 carbon atoms in the molecule and an oxidation promoter consisting of an amount in the range from 0.1% to 5% by weight of quinoline, oxidizing the mixture in the presence of air at a temperature in the range from 300 to 600 F. for a time in the range from 30 minutes to 16 hours to form an oxidized prod not having a substantially increased viscosity and a low neutralization value, and recovering said product.
RAYMOND L. HEINRICH.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 1,762,688 Hofmann June 10, 1930 2,330,239 Prutton Sept. 28, 1943 2,475,605 Prutton et a1 July 12, 1949 2,500,162 Seger et al Mar. 14, 1950 2,508,016 Doyle et a1. May 16, 1950
Claims (1)
1. A METHOD FOR INCREASING THE VISCOSITY OF AN OLEFINIC LUBRICATING OIL POLYMER HAVING LUBRICATING OIL CHARACTERISTICS WHICH COMPRISES OXIDIZING THE POLYMER AT A TEMPERATURE IN THE RANGE FROM 300* TO 600* F. IN THE PRESENCE OF AN OXIDATION PROMOTER CONSISTING OF AN AMOUNT NO LESS THAN 0.1% BY WEIGHT OF QUINOLINE TO FORM AN OXIDIZED PRODUCT HAVING A SUBSTANTIALLY INCREASED VISCOSITY AND A LOW NEUTRALIZATION VALUE AND RECOVERING SAID PRODUCT.
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US199572A US2664436A (en) | 1950-12-06 | 1950-12-06 | Lubricating oil composition of high viscosity and method for preparing same |
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US199572A US2664436A (en) | 1950-12-06 | 1950-12-06 | Lubricating oil composition of high viscosity and method for preparing same |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4186077A (en) * | 1978-06-22 | 1980-01-29 | Ashland Oil, Inc. | Oxidation of hydrocarbon waxes in the presence of amine oxides |
US4198285A (en) * | 1978-06-22 | 1980-04-15 | Ashland Oil, Inc. | Oxidation of hydrocarbon waxes in the presence of sulfobetaines |
US11345873B2 (en) | 2019-08-14 | 2022-05-31 | Valvoline Licensing And Intellectual Property Llc | Lubricant composition containing ashless TBN molecules |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1762688A (en) * | 1927-03-18 | 1930-06-10 | Ig Farbenindustrie Ag | Oxidizing paraffins, waxes, and the like |
US2330239A (en) * | 1940-11-25 | 1943-09-28 | Lubri Zol Corp | Lubricant |
US2475605A (en) * | 1944-03-25 | 1949-07-12 | Lubrizol Corp | Process of producing predominantly lower oxidation products from hydrocarbons |
US2500162A (en) * | 1948-09-02 | 1950-03-14 | Socony Vacuum Oil Co Inc | Method of preparing viscous oils by the thermal condensation of short chain monoolkfins with long chain monoolefins |
US2508016A (en) * | 1950-05-16 | Lubricating oil foe use in rolling |
-
1950
- 1950-12-06 US US199572A patent/US2664436A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2508016A (en) * | 1950-05-16 | Lubricating oil foe use in rolling | ||
US1762688A (en) * | 1927-03-18 | 1930-06-10 | Ig Farbenindustrie Ag | Oxidizing paraffins, waxes, and the like |
US2330239A (en) * | 1940-11-25 | 1943-09-28 | Lubri Zol Corp | Lubricant |
US2475605A (en) * | 1944-03-25 | 1949-07-12 | Lubrizol Corp | Process of producing predominantly lower oxidation products from hydrocarbons |
US2500162A (en) * | 1948-09-02 | 1950-03-14 | Socony Vacuum Oil Co Inc | Method of preparing viscous oils by the thermal condensation of short chain monoolkfins with long chain monoolefins |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4186077A (en) * | 1978-06-22 | 1980-01-29 | Ashland Oil, Inc. | Oxidation of hydrocarbon waxes in the presence of amine oxides |
US4198285A (en) * | 1978-06-22 | 1980-04-15 | Ashland Oil, Inc. | Oxidation of hydrocarbon waxes in the presence of sulfobetaines |
US11345873B2 (en) | 2019-08-14 | 2022-05-31 | Valvoline Licensing And Intellectual Property Llc | Lubricant composition containing ashless TBN molecules |
US11597891B2 (en) | 2019-08-14 | 2023-03-07 | Valvoline Licensing And Intellectual Property Llc | Lubricant composition containing Ashless TBN molecules |
US11674104B2 (en) | 2019-08-14 | 2023-06-13 | Vgp Ipco Llc | Lubricant composition containing ashless TBN molecules |
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