US3094488A - Radiation resistant mineral oils - Google Patents

Radiation resistant mineral oils Download PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
ultraviolet light
gamma radiation
oils
oil
radiation
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
Application number
US854567A
Inventor
Beerbower Alan
John L Murray
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Exxon Research and Engineering Co filed Critical Exxon Research and Engineering Co
Priority to US854567A priority Critical patent/US3094488A/en
Priority to GB35674/60A priority patent/GB952859A/en
Priority to FR843637A priority patent/FR1273292A/en
Application granted granted Critical
Publication of US3094488A publication Critical patent/US3094488A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/022Well-defined aliphatic compounds saturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/04Well-defined cycloaliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/024Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/044Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/284Esters of aromatic monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/042Alcohols; Ethers; Aldehydes; Ketones
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/221Six-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/32Light 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.

Landscapes

  • 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.
US854567A 1959-11-23 1959-11-23 Radiation resistant mineral oils Expired - Lifetime US3094488A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (15)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
KR102205672B1 (en) Biogenic low viscosity insulating oil
GB1061904A (en) Improvements in or relating to compositions containing metal deactivators
US3839210A (en) Antioxidant composition comprising a synergistic mixture of a phenol, amine and sulfone
Broadhurst Use and replaceability of polychlorinated biphenyls.
SE8202932L (en) ABSORPTION AGENTS FOR ORGANIC LIQUIDS, IN PARTICULAR OIL, WHICH ARE NOT DAMAGE EXPLOSIVE AND LOW FIRE RISK
US3094488A (en) Radiation resistant mineral oils
US3028334A (en) Lubricants resistant to atomic radiation
US2883331A (en) Inhibited reactor coolants and use thereof
US2431008A (en) Cooling fluid
US2921891A (en) Reactor coolant-moderator
US2982730A (en) Radiation resistant lubricating oil
US3083160A (en) Grease compositions
Mahoney et al. Meta-linked polyphenyl ethers as high-temperature radiation-resistant lubricants
US3003937A (en) Lubricants
GB1470870A (en) Insecticidal compositions
US4753741A (en) Super highly radiation-resistant grease
US3249542A (en) Radiation resistant lubricating oil
US3115467A (en) Method of inhibiting irradiation-induced viscosity increase of organic fluids
US3203906A (en) Bituminous shielding composition
US2943056A (en) Constant viscosity radiation resistant lubricant and method of using same
US4275253A (en) Radiation resistant oil and method of lubricating for atomic power facilities
US3115462A (en) Method of inhibiting irradiation-induced viscosity increase of organic fluids
US3155618A (en) Lubricant
BE449614A (en)
US2909487A (en) Nuclear reactor coolant