US3094488A - Radiation resistant mineral oils - Google Patents
Radiation resistant mineral oils Download PDFInfo
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- US3094488A US3094488A US854567A US85456759A US3094488A US 3094488 A US3094488 A US 3094488A US 854567 A US854567 A US 854567A US 85456759 A US85456759 A US 85456759A US 3094488 A US3094488 A US 3094488A
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- ultraviolet light
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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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- 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
- C10M2203/02—Well-defined aliphatic compounds
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- 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
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
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- 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
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/024—Well-defined aliphatic compounds unsaturated
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- 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
- C10M2203/04—Well-defined cycloaliphatic compounds
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/044—Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/046—Hydroxy ethers
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/284—Esters of aromatic monocarboxylic acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/285—Esters of aromatic polycarboxylic acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/022—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/042—Alcohols; Ethers; Aldehydes; Ketones
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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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
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- 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
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- 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
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- 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
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
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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
- 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
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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
- 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
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- 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
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- 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
- C10N2030/32—Light or X-ray resistance
Definitions
- the present invention relates to the preparation of radiation resistant mineral oils. More particularly the invention relates to novel compositions of matter involvingwhite mineral oils or lubricating oils which have added to them certain materials that tend to minimize deterioration of such oils when subjected to gamma radiation.
- White mineral oils in particular are subject to such damage which limits their usefulness in radiation-proof windows and the like.
- mineral oils such as white oils or lubricating oils are used in close association with varying degrees of intensity of gamma radiation; for example, oils are required in nuclear power plants, in turbines, control rod mechanisms, food sterilization by radiation, space ship lubrication and the like.
- the mechanisms employed in connection with or in the presence of intense gamma radiation require lubrication but heretofore it has been a problem to devise an oil which will withstand the radiation and will not become rancid and break down under such radiation.
- oils can be protected to the extent that their deterioration by gamma radiation is minimized.
- To produce mineral oil compositions which stand up well in the presence of gamma radiation requires the use of protective additives. If there is added to the oils one or more liquid scintillation phosphors either alone or admixed with a compound capable of absorbing ultraviolet light, this can be achieved.
- Ordinary white mineral oil shows radiation damage when subjected to even low doses of gamma radiation, i.e. of the order of less than 10 roentgens and becomes seriously deteriorated at 10 roentgens.
- Ordinary highly refined mineral lubricating oils tend to break down between 10 and 10 roentgens.
- White mineral oils treated in accordance with the present invention are able to withstand 2.3 X 10 roentgens at roentgens per hour without being substantially changed in any detectable respect, and highly refined lubricating oils are improved in proportion to their original resistance.
- Liquid scintillation phosphors are employed in producing the compositions of the present invention. These compounds are described in considerable detail in Nucleonics, December 1955, pp. 38-41, see particularly the tables appearing on pps. 40 and 41. As stated in the article, the liquid scintillation phosphors are selected from the group consisting of aromatic hydrocarbons, furans, pyrroles, oxazoles, 1,3,4-oxadiazoles, pyridines, indoles, and benzoxazoles. These compounds may have substituent groups attached to them, such as methyl, methoxyl, fluoro, and chloro. The specific compounds therein disclosed are incorporated into this description by express reference and are made a part hereof.
- the mineral oils to which the phosphors are added are those mineral oils which are customarily employed as white oils for look windows in nuclear reactor installations or in hot cell installations operating in the presence of radioactive materials and for lubricating oils of the general type employed for lubricating conveyors, nu-
- the lubricating oils are highly refined and are one of three types.
- Oleum treated naphthenic or paraffinic lubricating oils for example, white mineral oils of the USP and National Formulary grades, or technical white oils meeting less exacting specifications.
- Phenol extracted lubricating oils such as turbine oils, motor oils and other lubricants from which the major portion of aromatic compounds have been removed.
- a liquid scintillation phosphor or a mixture of scintillation phosphors is sufficient to minimize the deterioration of the oil due to gamma radiation.
- greater quantities of phosphors may be employed; for example, up to about 0.5% by weight, but effective concentrations are generally attained without using as much as 0.5% of the phosphors.
- an ultraviolet compound capable of absorbin-g ultraviolet light may also be added to the mineral oil composition.
- a primary solute liquid scintillation phosphor
- the function of an ultraviolet light absorber is merely that a fluoroescent material is maintained in the solution in order to get a more favorable wave length (such as visible or infra-red radiation) so that the energy of the gamma radiation is dissipated in the form of low energy photons and is therefore unable to seriously break down or deteriorate the structure of the oil molecules.
- the phosphor serves to convert ionizing radiation of either the beta or gamma form to ultraviolet light.
- the presence of the ultraviolet light absorber although it contributes little to this primary system, does effectively remove the secondary eifects of the ultraviolet and hence, although it is not necessary, the presence of an ultraviolet light absorber is in most instances a desirable addition to the composition.
- the above discussion is, of course, theoretical and there is no intention of limiting the invention to that theory.
- Any conventional compound having the ability of absorbing ultraviolet light may be employed.
- any conventional compound having the ability of absorbing ultraviolet light may be employed.
- such compounds which may be used, the following are disclosed:
- the compounds capable of absorbing ultraviolet light are present in the compositions in about the same quantities, i.e. from about 75 p.p.m. to about 1,000 p.p.m. and may be present if desired up to about 0.5% of the composition, but here again such large amounts are unnecessary in ordinary circumstances in order to ac aces res complish a minimizing of deterioration of the mineral oil due to gamma radiation.
- a gamma radiation resistant composition comprising a major proportion of mineral oil, about 75 parts per million to 0.5 Wt. percent of an oil-soluble liquid scintillation phosphor capable of absorbing gamma radiation and converting said gamma radiation into ultraviolet light, when said oil is subjected to gamma irradiation, and about 75 parts per million to 0.5 Wt. percent of an ultraviolet light absorber capable of absorbing said ultraviolet light emitted by said phosphor and converting said absorbed ultraviolet light into low energy photons substantially harmless to said composition.
- composition according to claim 1 wherein said mineral oil is a lubricating oil.
- a gamma radiation resistant composition comprising a major proportion of mineral oil, about 75 parts per million to 0.5 wt. percent of oil soluble liquid scintillation phosphor capable of absorbing high energy gamma radiation and converting said gamma radiation into ultraviolet light, said phosphor being selected from the group consisting of aromatic hydrocarbons, furans, pyrroles, oxazoles, 1,3,4-oxadiazoles, pyr-ridines, indoles, and benzoxazoles, and 75 parts per million to 0.5 Wt. percent of an ultraviolet light absorber capable of absorbing ultraviolet light emitted by said phosphor to thereby convert said ultraviolet light into low energy photons substantially harmless to said mineral oil.
- composition according toclaim 3 wherein said liquid scintillation phosphor is 2,5-diphenyl oxazole.
- liquid scintillation phosphor is 1,1,4,4-tetraphenyl-1,3- butadiene.
- a composition according to claim 3 wherein said liquid scintillation phosphor is 2,5-diphenyl oxazole and said compound capable of absorbing ultraviolet light is 2,2(-dihydroXy-4-rnethoxy benzophenone.
- composition according to claim 3 wherein said liquid scintillation phosphor is itetraphenyl butadiene and said compound capable of absorbing ultraviolet light is 2,2-dihydroXy-4-methoxy benzophenone.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Description
United States Patent 3,094,488 RADIATION RESISTANT MINERAL OILS Alan Beerbower and John L. Murray, Westfield, N.J., as-
signors to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Nov. 23, 1959, Ser. No. 854,567 '7 Claims. (Cl. 252-51.5)
The present invention relates to the preparation of radiation resistant mineral oils. More particularly the invention relates to novel compositions of matter involvingwhite mineral oils or lubricating oils which have added to them certain materials that tend to minimize deterioration of such oils when subjected to gamma radiation.
Oils in general deteriorate when subjected to intense gamma radiation. White mineral oils in particular are subject to such damage which limits their usefulness in radiation-proof windows and the like. There are many situations in present technology where mineral oils such as white oils or lubricating oils are used in close association with varying degrees of intensity of gamma radiation; for example, oils are required in nuclear power plants, in turbines, control rod mechanisms, food sterilization by radiation, space ship lubrication and the like. The mechanisms employed in connection with or in the presence of intense gamma radiation require lubrication but heretofore it has been a problem to devise an oil which will withstand the radiation and will not become rancid and break down under such radiation.
It has now been discovered that such oils can be protected to the extent that their deterioration by gamma radiation is minimized. To produce mineral oil compositions which stand up well in the presence of gamma radiation requires the use of protective additives. If there is added to the oils one or more liquid scintillation phosphors either alone or admixed with a compound capable of absorbing ultraviolet light, this can be achieved. Ordinary white mineral oil shows radiation damage when subjected to even low doses of gamma radiation, i.e. of the order of less than 10 roentgens and becomes seriously deteriorated at 10 roentgens. Ordinary highly refined mineral lubricating oils tend to break down between 10 and 10 roentgens. White mineral oils treated in accordance with the present invention are able to withstand 2.3 X 10 roentgens at roentgens per hour without being substantially changed in any detectable respect, and highly refined lubricating oils are improved in proportion to their original resistance.
Liquid scintillation phosphors are employed in producing the compositions of the present invention. These compounds are described in considerable detail in Nucleonics, December 1955, pp. 38-41, see particularly the tables appearing on pps. 40 and 41. As stated in the article, the liquid scintillation phosphors are selected from the group consisting of aromatic hydrocarbons, furans, pyrroles, oxazoles, 1,3,4-oxadiazoles, pyridines, indoles, and benzoxazoles. These compounds may have substituent groups attached to them, such as methyl, methoxyl, fluoro, and chloro. The specific compounds therein disclosed are incorporated into this description by express reference and are made a part hereof.
The mineral oils to which the phosphors are added are those mineral oils which are customarily employed as white oils for look windows in nuclear reactor installations or in hot cell installations operating in the presence of radioactive materials and for lubricating oils of the general type employed for lubricating conveyors, nu-
3,094,488 Patented June 18, 1963 clear control rods, and the various types of machinery in which friction must be controlled and which are subject to radioactive radiation as heretofore set forth.
In general, the lubricating oils are highly refined and are one of three types.
(1) Oleum treated naphthenic or paraffinic lubricating oils, for example, white mineral oils of the USP and National Formulary grades, or technical white oils meeting less exacting specifications.
(2) Phenol extracted lubricating oils such as turbine oils, motor oils and other lubricants from which the major portion of aromatic compounds have been removed.
(3) The hydrogenated and therefore fully saturated lubricating oils such as super-refined semi-white oils used in aviation jet engines.
In general, between about p.p.m. and about 1,000 p.p.m. (0.1%) of a liquid scintillation phosphor or a mixture of scintillation phosphors is suficient to minimize the deterioration of the oil due to gamma radiation. However, if desired, greater quantities of phosphors may be employed; for example, up to about 0.5% by weight, but effective concentrations are generally attained without using as much as 0.5% of the phosphors.
Additionally, an ultraviolet compound capable of absorbin-g ultraviolet light may also be added to the mineral oil composition. A primary solute (liquid scintillation phosphor) is believed to draw ofl? excitation energy from the mineral oil component which the latter receives by reason of its absorption of the gamma radiation and conversion of the energy to the longer wave length ultraviolet radiation. The function of an ultraviolet light absorber is merely that a fluoroescent material is maintained in the solution in order to get a more favorable wave length (such as visible or infra-red radiation) so that the energy of the gamma radiation is dissipated in the form of low energy photons and is therefore unable to seriously break down or deteriorate the structure of the oil molecules. The phosphor serves to convert ionizing radiation of either the beta or gamma form to ultraviolet light. The presence of the ultraviolet light absorber, although it contributes little to this primary system, does effectively remove the secondary eifects of the ultraviolet and hence, although it is not necessary, the presence of an ultraviolet light absorber is in most instances a desirable addition to the composition. The above discussion is, of course, theoretical and there is no intention of limiting the invention to that theory.
Any conventional compound having the ability of absorbing ultraviolet light may be employed. As examples of such compounds which may be used, the following are disclosed:
Z-hydroxy, 4-methoxy benzophenone 2,2-dihydroxy 4-methoxy benzophenone 2,2'-dihydroxy 4,4-dimethoxy benzophenone 4-tertiary butyl phenyl salicylate 2,4-dibenzoyl resorcinol 5-chloro 2-hydr0xy benzophenone As in the case of the liquid scintillation phosphor addition, the compounds capable of absorbing ultraviolet light are present in the compositions in about the same quantities, i.e. from about 75 p.p.m. to about 1,000 p.p.m. and may be present if desired up to about 0.5% of the composition, but here again such large amounts are unnecessary in ordinary circumstances in order to ac aces res complish a minimizing of deterioration of the mineral oil due to gamma radiation.
Example Blend Composition Additive Class Deterioration in Odor 1 No additives Bzizdly deteriorated- 2 75 p.p.m. 2,2-Dihy- U.V Do.
droxyt-methoxy Benzophenone.
3 75 ppm. 2,5-Di- LSP Mild deterioration.
phenyl Oxazole.
4 75 p.p.m. Tetra LSP Do.
phenyl Butadiene.
5 50% #2, 50% #3 U.V.+LSP Almost unchanged.
6 50% #2, 50% #4 U.V.+LSP Do.
7 10 ppm. Ditert Antioxidant..- Worse than #1- butyl p-cresol. Rancid.
Having now thus fully described and illustrated the character of the invention, what is desired to be secured by the Letters Patent is:
What is claimed is:
1. A gamma radiation resistant composition comprising a major proportion of mineral oil, about 75 parts per million to 0.5 Wt. percent of an oil-soluble liquid scintillation phosphor capable of absorbing gamma radiation and converting said gamma radiation into ultraviolet light, when said oil is subjected to gamma irradiation, and about 75 parts per million to 0.5 Wt. percent of an ultraviolet light absorber capable of absorbing said ultraviolet light emitted by said phosphor and converting said absorbed ultraviolet light into low energy photons substantially harmless to said composition.
2. A composition according to claim 1, wherein said mineral oil is a lubricating oil.
3. A gamma radiation resistant composition comprising a major proportion of mineral oil, about 75 parts per million to 0.5 wt. percent of oil soluble liquid scintillation phosphor capable of absorbing high energy gamma radiation and converting said gamma radiation into ultraviolet light, said phosphor being selected from the group consisting of aromatic hydrocarbons, furans, pyrroles, oxazoles, 1,3,4-oxadiazoles, pyr-ridines, indoles, and benzoxazoles, and 75 parts per million to 0.5 Wt. percent of an ultraviolet light absorber capable of absorbing ultraviolet light emitted by said phosphor to thereby convert said ultraviolet light into low energy photons substantially harmless to said mineral oil.
4. A composition according toclaim 3 'wherein said liquid scintillation phosphor is 2,5-diphenyl oxazole.
5. A composition according to claim 3 wherein said liquid scintillation phosphor is 1,1,4,4-tetraphenyl-1,3- butadiene.
6. A composition according to claim 3 wherein said liquid scintillation phosphor is 2,5-diphenyl oxazole and said compound capable of absorbing ultraviolet light is 2,2(-dihydroXy-4-rnethoxy benzophenone.
7. A composition according to claim 3 wherein said liquid scintillation phosphor is itetraphenyl butadiene and said compound capable of absorbing ultraviolet light is 2,2-dihydroXy-4-methoxy benzophenone.
References Cited in the file of this patent UNITED STATES PATENTS 1,768,910 Ihrig July 1, 1930 1,962,564 Kuhrrnann et a1 June 12, 1934 2,094,202 Bennett et a1 Sept. 28, 1937 2,160,293 Shoemaker et a1. May 30, 1939 2,191,089 Barth Feb. 20, 1940 2,198,961 Dietrich Apr. 30, 1940 2,221,380 Horsch Nov. 12, 1940 2,231,248 Bowden Feb. 11, 1941 2,363,880 Lieber et al. Nov. 28, 1944 2,427,766 Diamond Sept. 23, 1947 2,554,687 Thompson et a1 May 29, 1951 2,853,521 Hardy et al Sept. 23, 1958 2,982,730 Barry May 2, 1961 FOREIGN PATENTS 784,793 Great Britain Oct. 16, 1957 809,360 Great Britain Feb. 25, 1959 OTHER REFERENCES Progress Report 2 on Fluorescence and Conductivity Phenomena, July 1950, US. Signal Corps. (SCEL), Fort Monmouth, N1, research by Physics Dept, New York University under Contract No. DA-36-039 sit-35, re produced by Central Air Documents Oifice, Wright Patterson Air Force Base, Dayton, Ohio, ATI 'No. 90,866, 82 pp., p. 33.
Progress Report 4 on Fluorescence and Conductivity Phenomena, May 1951, US. Signal Corps. (SCEL), Fort Monmouth, N.l., research by Physics Dept, New York University under Contract No. DA-36039 so-35, reproduced by Central Air Documents Oflice, Wright- Patterson Air Force Base, Dayton, Ohio, ATI No. 108,168, 66 pp. p. 16.
Claims (1)
1. A GAMMA RADIATION RESISTANT COMPOSITION COMPRISING A MAJOR PROPORTION OF MINERAL OIL, ABOUT 75 PARTS PER MILLION TO 0.5 WT. PERCENT OF AN OIL-SOLUBLE LIQUID SCINTILLATION PHOSPHOR CAPABLE OF ABSORBING GAMMA RADIATION AND CONVERTING SAID GAMMA RADIATION INTO ULTRAVIOLET LIGHT, WHEN SAID OIL IS SUBJECTED TO GAMMA IRRADIATION, AND ABOUT 75 PARTS PER MILLION TO 0.5 WT. PERCENT OF AN ULTRAVIOLET LIGHT ABSORBER CAPABLE OF ABSORBING SAID ULTRAVIOLET LIGHT EMITTED BY SAID PHOSPHOR AND CONVERTING SAID ABDORBED ULTRAVIOLET LIGHT LOW ENERGY PHOTONS SUBSTANTIALLY HARMLESS TO SAID COMPOSITION.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US854567A US3094488A (en) | 1959-11-23 | 1959-11-23 | Radiation resistant mineral oils |
GB35674/60A GB952859A (en) | 1959-11-23 | 1960-10-18 | Radiation resistant mineral oils |
FR843637A FR1273292A (en) | 1959-11-23 | 1960-11-10 | Mineral oils resistant to gamma radiation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US854567A US3094488A (en) | 1959-11-23 | 1959-11-23 | Radiation resistant mineral oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US3094488A true US3094488A (en) | 1963-06-18 |
Family
ID=25319057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US854567A Expired - Lifetime US3094488A (en) | 1959-11-23 | 1959-11-23 | Radiation resistant mineral oils |
Country Status (3)
Country | Link |
---|---|
US (1) | US3094488A (en) |
FR (1) | FR1273292A (en) |
GB (1) | GB952859A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3282842A (en) * | 1964-03-06 | 1966-11-01 | Mobil Oil Corp | Lubricating oil compositions |
US4275253A (en) * | 1973-03-29 | 1981-06-23 | Kureha Kagaku Kogyo Kabushiki Kaisha | Radiation resistant oil and method of lubricating for atomic power facilities |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1768910A (en) * | 1927-06-22 | 1930-07-01 | Harry K Ihrig | Oil-composition |
US1962564A (en) * | 1930-09-30 | 1934-06-12 | Ig Farbenindustrie Ag | Fluorescent hydrocarbon |
US2094202A (en) * | 1935-02-04 | 1937-09-28 | Mid Continent Petroleum Corp | Lubricant |
US2160293A (en) * | 1936-12-05 | 1939-05-30 | Standard Oil Co | Lubricant |
US2191089A (en) * | 1936-05-05 | 1940-02-20 | Sinclair Refining Co | Art of refining |
US2198961A (en) * | 1938-04-05 | 1940-04-30 | Du Pont | Lubricant |
US2221380A (en) * | 1938-01-25 | 1940-11-12 | Socony Vacuum Oil Co Inc | Method of renovating used oil and system containing same |
US2231248A (en) * | 1936-11-05 | 1941-02-11 | Bowden Frank Philip | Lubricant |
US2363880A (en) * | 1942-01-01 | 1944-11-28 | Standard Oil Dev Co | Lubricants |
US2427766A (en) * | 1944-08-05 | 1947-09-23 | Shell Dev | Compounded lubricating oil |
US2554687A (en) * | 1948-01-29 | 1951-05-29 | Universal Oil Prod Co | Stabilization of organic compounds |
GB784793A (en) * | 1954-01-29 | 1957-10-16 | Exxon Research Engineering Co | Improvements in or relating to lubricants resistant to atomic radiation |
US2853521A (en) * | 1956-06-20 | 1958-09-23 | American Cyanamid Co | Hydroxylated benzophenone ethers |
GB809360A (en) * | 1957-08-16 | 1959-02-25 | Shell Res Ltd | Oil compositions having increased stability towards free radicals |
US2982730A (en) * | 1957-05-03 | 1961-05-02 | Socony Mobil Oil Co Inc | Radiation resistant lubricating oil |
-
1959
- 1959-11-23 US US854567A patent/US3094488A/en not_active Expired - Lifetime
-
1960
- 1960-10-18 GB GB35674/60A patent/GB952859A/en not_active Expired
- 1960-11-10 FR FR843637A patent/FR1273292A/en not_active Expired
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1768910A (en) * | 1927-06-22 | 1930-07-01 | Harry K Ihrig | Oil-composition |
US1962564A (en) * | 1930-09-30 | 1934-06-12 | Ig Farbenindustrie Ag | Fluorescent hydrocarbon |
US2094202A (en) * | 1935-02-04 | 1937-09-28 | Mid Continent Petroleum Corp | Lubricant |
US2191089A (en) * | 1936-05-05 | 1940-02-20 | Sinclair Refining Co | Art of refining |
US2231248A (en) * | 1936-11-05 | 1941-02-11 | Bowden Frank Philip | Lubricant |
US2160293A (en) * | 1936-12-05 | 1939-05-30 | Standard Oil Co | Lubricant |
US2221380A (en) * | 1938-01-25 | 1940-11-12 | Socony Vacuum Oil Co Inc | Method of renovating used oil and system containing same |
US2198961A (en) * | 1938-04-05 | 1940-04-30 | Du Pont | Lubricant |
US2363880A (en) * | 1942-01-01 | 1944-11-28 | Standard Oil Dev Co | Lubricants |
US2427766A (en) * | 1944-08-05 | 1947-09-23 | Shell Dev | Compounded lubricating oil |
US2554687A (en) * | 1948-01-29 | 1951-05-29 | Universal Oil Prod Co | Stabilization of organic compounds |
GB784793A (en) * | 1954-01-29 | 1957-10-16 | Exxon Research Engineering Co | Improvements in or relating to lubricants resistant to atomic radiation |
US2853521A (en) * | 1956-06-20 | 1958-09-23 | American Cyanamid Co | Hydroxylated benzophenone ethers |
US2982730A (en) * | 1957-05-03 | 1961-05-02 | Socony Mobil Oil Co Inc | Radiation resistant lubricating oil |
GB809360A (en) * | 1957-08-16 | 1959-02-25 | Shell Res Ltd | Oil compositions having increased stability towards free radicals |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3282842A (en) * | 1964-03-06 | 1966-11-01 | Mobil Oil Corp | Lubricating oil compositions |
US4275253A (en) * | 1973-03-29 | 1981-06-23 | Kureha Kagaku Kogyo Kabushiki Kaisha | Radiation resistant oil and method of lubricating for atomic power facilities |
Also Published As
Publication number | Publication date |
---|---|
GB952859A (en) | 1964-03-18 |
FR1273292A (en) | 1961-10-06 |
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