Catalytic hydrogenation to remove gas from x-ray tube cooling oil

Information

  • Patent Grant
  • 6632970
  • Patent Number
    6,632,970
  • Date Filed
    Wednesday, December 29, 1999
    25 years ago
  • Date Issued
    Tuesday, October 14, 2003
    21 years ago
Abstract
The present invention deals with the catalytic hydrogenation of fluid used to cool and dielectrically insulate an x-ray generating device within an x-ray system. According to the present invention, a method and apparatus are provided for hydrogenating fluid that has been exposed to x-rays to reduce the amount of H2 gas, free hydrogen atoms and unsaturated molecules in the fluid. The method comprises exposing the fluid within the x-ray system to a catalytically effective amount of catalyst. The catalyst operates in temperatures in the range of about 10-300° C. and pressures in the range of about 0.1-30 atmospheres. The catalyst may comprise a solid, non-soluble catalyst, a soluble catalyst, or a combination of both. A suitable solid, non-soluble catalyst comprises Group VIII elements and their compounds. Group VIII elements comprise iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium and platinum. The catalytically effective amount of solid catalyst ranges from about 1-100 cm2 of surface area of solid catalyst per liter of fluid. Additionally, a suitable soluble catalyst may be added to the fluid and may comprise tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution such as HRu(C2H4)(C6H4PPh2)(PPh3)2), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds. A catalytically effective amount of soluble catalyst may comprise from about 0.01-1 gram per liter of fluid. The fluid may comprise about 99.7% hydrocarbon, about 0.1% soluble catalyst, and the remainder comprising conditioning additives. The hydrocarbon preferably comprises about 99.7% hydrogenated light naphthenic petroleum distillates.
Description




FIELD OF THE INVENTION




The present invention relates to dielectric fluid for cooling and electrically insulating x-ray tubes, and more particularly, to a system and method for catalytic hydrogenation of x-ray tube dielectric fluid that is subject to chemical breakdown due to exposure to x-ray radiation.




BACKGROUND




A dielectric oil is typical fluid used to cool and electrically insulate an x-ray tube. The dielectric oil is subject to chemical breakdown, however, upon exposure to x-ray radiation. After exposure to x-rays, the dielectric oil comprises unsaturated hydrocarbon molecules, free hydrogen atoms, and H


2


gas. The formation of the H


2


gas is disadvantageous as it may reduce the electrical insulating characteristics of the dielectric oil and may interfere with the transmission of the x-rays. Thus, it is desirable to reduce and/or eliminate the formation of H


2


gas in the x-ray tube dielectric fluid.




Typically, an x-ray beam generating device, referred to as an x-ray tube, comprises dual electrodes of an electrical circuit in a vacuum chamber within a cylindrical vacuum vessel envelope. The vacuum vessel envelope typically comprises a glass tube or a cylinder made of metal. One of the electrodes is a cathode assembly which is positioned in a spaced relationship to a rotating, disc-shaped target that comprises the anode assembly. Upon energization of the electrical circuit connecting the electrodes, the cathode assembly produces a supply of electrons which are accelerated and focused to a thin beam. The thin beam of very high velocity electrons is directed parallel to the axis of the vacuum vessel envelope to strike a section of the rotating target anode. The kinetic energy produced by the beam of electrons striking the surface of the section of the target anode, which comprises a material such as a refractory metal, is converted to electromagnetic waves of very high frequency. These high frequency electromagnetic waves are x-rays. The surface of the target anode is typically angled, which helps to direct the x-rays out the side of the vacuum vessel envelope. After exiting the vacuum vessel envelope, the x-rays are directed to penetrate an object, such as human anatomical parts for medical examination and diagnostic procedures. Further, industrial x-ray tubes may be used, for example, to inspect metal parts for cracks or for inspecting the contents of luggage at airports.




The x-ray generating device is ordinarily surrounded by a casing filled with a circulating fluid, which helps to minimize the operating temperature of the x-ray tube by absorbing heat. Dielectric fluid for x-ray generating devices typically operates at temperatures in the range of about 20-70° C. This very high operating temperature is the result of the thermal energy transferred from the tube to the fluid due to the high electric current required to generate and accelerate the electrons, the kinetic energy produced by the electrons hitting the target, and the x-rays themselves. Dielectric oil is typically the fluid utilized to carry the heat away from the x-ray tube, as dielectric oil can absorb and carry away a large amount of thermal energy.




The circulating fluid used to cool the x-ray tube additionally has dielectric properties that electrically insulate the tube. A typical x-ray tube utilizes a tremendous amount of energy to generate x-rays. A typical x-ray tube may require from about 120,000 to 140,000 volts and from about 40-400 milliamps, which produces up to about 40 kilowatts of power. Whereas this very high electrical charge exists within the x-ray tube, the casing is at ground potential. Without an electrical insulator between the tube and the casing, the electrical charge within the tube would tend to arc to the casing, similar to lightning arcing from the clouds to the earth. So, if there is a bad dielectric insulator around the tube, the voltage can break through the tube and ground to the casing. The break through of the voltage can result not only in the charring of the circulating dielectric, but also in the cracking of the vacuum envelope of the tube. Thus, the dielectric properties of the circulating fluid must be maintained to insure the reliability of the x-ray tube.




The dielectric properties of the circulating fluid, however, are negatively affected by the x-rays generated by the tube. The x-ray radiation breaks chemical bonds within the dielectric fluid. Typically, the x-ray radiation breaks carbon-carbon (C—C) and carbon-hydrogen (C—H) bonds, resulting in the release of hydrogen atoms. The free hydrogen atoms combine into diatomic hydrogen or H


2


, which is a gas that forms bubbles within the circulating dielectric fluid. As the amount of H


2


in the dielectric fluid increases, the size of the bubbles can increase and displace the dielectric fluid. The high voltage within the x-ray tube can then arc across the bubble and short out on the casing. Thus, the formation of gas bubbles caused by the break down of the dielectric fluid by the x-ray radiation inhibits the electrical insulating properties of the dielectric fluid, possibly leading to high voltage arcing and the failure of the x-ray tube.




Many sources of gas within the dielectric fluid can be removed by vacuum treating the fluid prior to its use. In this case, however, the gas is produced during the x-ray generating process. As such, vacuum treating the dielectric fluid prior to its use will not eliminate this problem. Thus, there is a need for a method to eliminate the gas produced within the dielectric fluid during the x-ray process.




SUMMARY OF THE INVENTION




According to the present invention, a method for hydrogenating a dielectric fluid comprising a hydrocarbon that upon exposure to x-rays releases hydrogen atoms, comprises exposing the dielectric fluid to an effective amount of a catalyst system that promotes the recombination of the hydrogen atoms with the hydrocarbon. The dielectric fluid is employed as a cooling element for an x-ray generating device, and preferably comprises hydrogenated napthacene. The catalyst system operates in temperatures in the range of about 10-300° C. and pressures in the range of about 0.1-30 atmospheres. The catalyst system may comprise either a solid, non-soluble catalyst or a soluble catalyst.




A suitable solid catalyst may comprise a Group VIII element or a compound of a Group VIII element. The effective amount of solid catalyst is at least 1 cm


2


surface area per liter of the dielectric fluid up to about 100 cm


2


, and preferably 10 cm


2


surface area per liter of the dielectric fluid. The solid catalyst may comprise an element selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum, or more preferably solid catalyst comprises at least one of palladium and platinum.




A suitable soluble catalyst is in solution with the dielectric fluid, wherein the effective amount of soluble catalyst is at least 0.01 gram per liter of the dielectric fluid up to about 1 gram per liter of dielectric fluid. The soluble catalyst may comprise tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution such as HRu(C


2


H


4


)(C


6


H


4


PPh


2


)(PPh


3


)


2


), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds.




In another embodiment, a system for hydrogenating dielectric fluid subject to the formation of hydrogen gas and unsaturated hydrocarbons due to x-ray exposure from an x-ray generating device, comprises an effective amount of a catalyst system positioned within the x-ray generating device to interact with the dielectric fluid for promoting the reaction of the hydrogen gas with the unsaturated hydrocarbons within the dielectric fluid to reduce the amount of hydrogen gas in the dielectric fluid. The hydrogenating system preferably comprises an x-ray system. The catalyst system operates in temperatures in the range of about 10-300° C. and pressures in the range of about 0.1-30 atmospheres. The catalyst system may comprise a solid catalyst or a soluble catalyst. A suitable solid catalyst comprises a Group VIII element or a compound of a Group VIII element. The solid catalyst may comprise an element selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum, or more preferably solid catalyst comprises at least one of palladium and platinum. The effective amount of solid catalyst is at least 1 cm


2


surface area per liter of the dielectric fluid up to about 100 cm


2


, and preferably 10 cm


2


surface area per liter of the dielectric fluid. A suitable soluble catalyst is in solution with the dielectric fluid, wherein the effective amount of catalyst is at least 0.01 gram per liter of the dielectric fluid up to about 1 gram per liter of dielectric fluid. The soluble catalyst may comprise tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution such as HRu(C


2


H


4


)(C


6


H


4


PPh


2


)(PPh


3


)


2


), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds.




In yet another embodiment, an x-ray system, comprises an x-ray generating device for producing x-rays, a dielectric fluid circulated about the device to cool and electrically insulate the device, wherein the fluid comprises a hydrocarbon that upon exposure to the x-rays releases hydrogen atoms, and an effective amount of a catalyst system, in communication with the dielectric fluid, that promotes the recombination of the hydrogen atoms with the hydrocarbon. The catalyst system operates in temperatures in the range of about 10-300° C. and pressures in the range of about 0.1-30 atmospheres. The catalyst system may comprise a solid catalyst or a soluble catalyst. A suitable solid catalyst comprises a Group VIII element or a compound of a Group VIII element. The solid catalyst may comprise an element selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum, or more preferably solid catalyst comprises at least one of palladium and platinum. The effective amount of solid catalyst is at least 1 cm


2


surface area per liter of the dielectric fluid up to about 100 cm


2


, and preferably 10 cm


2


surface area per liter of the dielectric fluid. A suitable soluble catalyst is in solution with the dielectric fluid, wherein the effective amount of catalyst is at least 0.01 gram per liter of the dielectric fluid up to about 1 gram per liter of dielectric fluid. The soluble catalyst may comprise tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution such as HRu(C


2


H


4


)(C


6


H


4


PPh


2


)(PPh


3


)


2


), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds.




Finally, the present invention discloses a dielectric fluid comprising a hydrocarbon component, a hydrogenating catalyst system, and wherein the dielectric fluid is suitable for use as a cooling element for an x-ray generating device. The dielectric fluid further comprises about 99.7% hydrocarbon, about 0.1% catalyst system, and the remainder comprising conditioning additives. The hydrocarbon comprises about 99.7% hydrogenated light naphthenic petroleum distillates. The hydrogenating catalyst system comprises tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution such as HRu(C


2


H


4


)(C


6


H


4


PPh


2


)(PPh


3


)


2


), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a plan view of a representative x-ray system having an x-ray generating device or x-ray tube positioned therein;





FIG. 2

is a sectional view with parts removed of the x-ray system of

FIG. 1

including the x-ray generating device;





FIG. 3

is a sectional view taken along line


3





3


in

FIG. 1

; and





FIG. 4

is a perspective view of a fluid hose with portions removed exposing the solid catalyst.











DETAILED DESCRIPTION OF THE INVENTION




According to one aspect of the present invention, a method of hydrogenating a dielectric fluid, comprising a hydrocarbon that upon exposure to x-rays releases hydrogen atoms, comprises exposing the dielectric fluid to an effective amount of a catalyst system that promotes the recombination of the hydrogen with the dielectric fluid.




In another aspect of the present invention, a system for hydrogenating dielectric fluid subject to the formation of hydrogen gas and unsaturated hydrocarbons due to x-ray exposure in a x-ray generating device, comprises an effective amount of a catalyst system positioned within the x-ray generating device to interact with the dielectric fluid for promoting the reaction of the hydrogen gas with the unsaturated hydrocarbons within the dielectric fluid to reduce the amount of hydrogen gas in the dielectric fluid.




In a further aspect of the present invention, an x-ray system comprises an x-ray generating device for producing x-rays, a dielectric fluid circulated about the device to cool and electrically insulate the device, where the fluid comprises a hydrocarbon that upon exposure to x-rays releases hydrogen atoms, and an effective amount of a catalyst system, in communication with the dielectric fluid, that promotes the recombination of the hydrogen atoms with the hydrocarbon.




In yet another aspect of the invention, a dielectric fluid comprises a hydrocarbon component, a hydrogenating catalyst, and the dielectric fluid is suitable for use as a cooling element for an x-ray generating device. The dielectric fluid may comprise about 99.7% hydrocarbon, about 0.1% catalyst system, and the remainder comprising conditioning additives. Further, the hydrocarbon may comprise about 99.7% hydrogenated light naphthenic petroleum distillates and the catalyst may comprise tris(triphenylphosphine) rhodium (I) chloride.




Referring to

FIGS. 1 and 2

, the present invention is typically utilized in an x-ray system


20


. A typical x-ray system


20


comprises a fluid pump


22


, an anode end


24


, a cathode end


26


, a center section


28


positioned between the anode end and cathode end, which contains an x-ray generating device or x-ray tube


30


(FIG.


2


). The x-ray generating device


30


is enclosed in a fluid chamber


32


within lead-lined casing


34


(FIG.


2


). Chamber


32


is typically filled with fluid


36


, such as a dielectric fluid, but other fluids may be utilized. Fluid


36


circulates through system


20


to cool x-ray generating device


30


and also to insulate casing


34


from the high electrical charges within vacuum vessel envelope


38


of the device. A radiator


40


for cooling fluid


36


is positioned to one side of center section


28


and may have operatively connected fans


42


and


44


for providing cooling air flow over the radiator as the hot fluid


36


circulates through it. Pump


22


is provided to circulate fluid


36


through system


20


, fluid hoses


45


and through radiator


40


, etc. Electrical connections are provided in anode receptacle


46


and cathode receptacle


48


(

FIG. 2

) for energizing system


20


.




Referring to

FIG. 2

, x-ray system


20


comprises casing


34


preferably made with aluminum and lined with lead to block x-ray passage. X-ray generating device or x-ray tube


30


within system


20


typically comprises a cathode assembly


50


and a rotating, disc-like target anode assembly


52


within a vacuum chamber


54


in a vacuum vessel envelope


38


. A stator


56


is positioned outside vacuum vessel envelope


38


inside lead-lined casing


34


relative to rotating disc-like target anode assembly


52


. Upon energization of the electrical circuit connecting cathode assembly


50


and anode assembly


52


, a stream of electrons


58


are directed and accelerated toward the anode assembly. The stream of electrons


58


strikes the surface of anode assembly


52


and produces high frequency electromagnetic waves or x-rays


60


. X-rays


60


are directed through vacuum chamber


54


and out of vacuum vessel envelope


38


through transmissive window


62


. Alternatively, if vacuum vessel envelope


38


is glass, Pyrex or a material with low attenuation of diagnostic levels of radiation (≧60,000 electronvolts), then no separate window


62


is required (not shown). The x-rays


60


proceed through fluid


36


between x-ray generating device


30


and casing


34


and through window


64


, which comprises an x-ray transmissive material, such as beryllium. Window


64


is operatively formed in casing


34


relative to transmissive window


62


in vacuum vessel envelope


38


. Thus, x-rays


60


are emitted from system


20


toward an object.




Vacuum vessel envelope


38


is constructed of a material that is able to structurally handle the loads generated by vacuum chamber


54


and rotating anode assembly


52


in a high temperature environment. Vacuum vessel envelope


38


is formed using well-known manufacturing methods, and as mentioned above, may be formed of x-ray transmissive material such as glass or Pyrex, or a non-x-ray transmissive material such as stainless steel or copper. Vacuum vessel envelope


38


must be able to withstand the high temperatures of the x-ray generating device


30


environment. For example, anode


52


operates from about 500-1800° C., cathode


50


up to about 600° C. and vacuum vessel envelope


38


operates up to about 120° C. Vacuum vessel envelope


38


is heated by the operating temperatures within chamber


54


, and further by absorption of x-rays


60


, deflected electrons and lower energy electromagnetic waves (not shown) within the vacuum chamber that have not attained enough energy to become x-rays.




Fluid


36


is typically a dielectric fluid capable of electrically insulating casing


34


from the very high voltages and currents within x-ray tube


30


and also capable of cooling the tube. Fluid


36


provides electrical insulation from voltages which may range from about 80 KV to 160 KV and currents which may range from about 250 to 400 mA. Additionally, fluid


36


is capable of cooling x-ray tube


30


and maintaining the tube at a predetermined operating temperature by absorbing heat from the x-ray generation process. Such dielectric fluids may comprise hydrogenated naphthacene compounds, as well as other hydrogenated polyaromatic compounds.




As x-rays


60


pass through fluid


36


, the radiation from the x-rays tends to cause a chemical breakdown of the fluid molecule. Exposure to x-rays


60


tends to break the carbon-carbon (C—C) bonds and carbon-hydrogen (C—H) bonds, producing an unsaturated molecule and free hydrogen atoms which tend to form H


2


gas. By way of example for a fluid


36


comprising hydrogenated naphthacene compounds, it is believed the reaction proceeds as follows:











Results in:











The chemical breakdown of the hydrogenated napthacene is problematic because the H


2


gas produces bubbles within fluid


36


and displaces the fluid. The bubbles and fluid displacement reduce the effectiveness of fluid


36


as an electrical insulator, as the electricity may arc through the bubbles to casing


34


. Additionally, fluid


36


cannot be pre-treated, such as by vacuum treating, to eliminate the H


2


gas as the gas forms during the operation of system


40


.




The present invention provides a system and method for advantageously recombining the free hydrogen atoms and H


2


gas with the unsaturated molecule produced by exposure to x-ray radiation. A hydrogenation catalyst system


66


is introduced into x-ray system


20


to interact with fluid


36


. Catalyst system


66


drives a reaction between the unsaturated molecule and the free hydrogen atoms and H


2


gas, resulting in decreasing the amount of unsaturated molecules, free hydrogen atoms and H


2


gas in fluid


36


. By way of example for a fluid


36


comprising hydrogenated naphthacene compounds, it is believed the reaction proceeds as follows:











Results in:











Thus, catalyst system


66


provides a means for returning the free hydrogen atoms to the molecules comprising fluid


36


, thereby reversing the formation of the H


2


gas and improving the dielectric properties of the fluid.




The present invention is capable of driving the reaction at temperatures in the range of about 10-300° C. and pressures in the range of about 0.1-30 atmospheres. Catalyst


66


thereby advantageously is able to reduce and eventually substantially eliminate H


2


gas within fluid


36


at all levels of operating temperatures as well as at ambient when x-ray tube


30


is inactive.




Catalyst system


66


may be provided either in solution with fluid


36


, or as a solid, non-soluble material, or as some combination of both. Referring to

FIGS. 3 and 4

, solid catalyst


68


is provided within hose


45


within the fluid circulation system, comprising pump


22


and radiator


40


. Solid catalyst


68


may comprise a filter-like mesh of strands of the catalyst material. Alternatively, depending on the reaction conditions, solid catalyst


68


may form a lining of the circulation system, such as by a deposition process, or the solid catalyst may be contained within the system whereby fluid


36


circulates over the solid catalyst. A suitable solid catalyst


68


preferably comprises Group VIII elements and their compounds. Group VIII elements comprise iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium and platinum. Fluid


36


, comprising the unsaturated hydrocarbons and hydrogen atoms and H


2


gas, interacts with the surface of solid catalyst


68


, resulting in the recombination of hydrogen with the unsaturated hydrocarbon thereby reducing the amount of H


2


gas in fluid


36


.




When using the solid catalyst


68


, a catalytically effective amount of the solid catalyst may comprise from about 1-100 cm


2


, preferably about 10 cm


2


, of surface area of catalyst per liter of fluid


36


. As one skilled in the art will recognize, the range of the effective amount of solid catalyst


68


varies depending upon the type of catalyst used and the type of fluid


36


. In this embodiment, solid catalyst


68


may comprise rolled foil, shredded and plated metal, plated lining in casing


34


or within radiator


40


, pump


22


or other fluid circulating components. Further, solid catalyst


68


may be a solid material in a porous container, plated metal on a screen or other filter-like device that fluid


36


may circulate through, or other similar devices which would be obvious to one skilled in the art in view of this disclosure.




Alternatively, catalyst system


66


may be provided as a soluble catalyst


70


in solution with fluid


36


. For example, a suitable soluble catalyst


70


may comprise tris(triphenylphosphine) rhodium (I) chloride added to fluid


36


. Other examples of soluble catalyst


70


in solution with fluid


36


include precious metals in solution such as HRu(C


2


H


4


)(C


6


H


4


PPh


2


)(PPh


3


)


2


), Wilkinson's catalyst which comprises a rhodium, chromium, phosphorus triphenyl chloride compound, and other similar compounds. A catalytically effective amount of soluble catalyst


70


may comprise from about 0.01-1 gram per liter of fluid


36


. The dielectric fluid may comprise about 99.7% hydrocarbon, about 0.1% soluble catalyst


70


, and the remainder comprising conditioning additives. Preferably, the hydrocarbon may comprise about 99.7% hydrogenated light naphthenic petroleum distillates and the catalyst may comprise tris(triphenylphosphine) rhodium (I) chloride. As one skilled in the art will recognize, however, the range of the effective amount of soluble catalyst


70


varies depending upon the type of catalyst used and the type of fluid


36


.




One advantageous feature of the present invention provides for decreasing the amount of unsaturated molecules, free hydrogen atoms and H


2


gas in fluid


36


both at operating temperatures of the fluid and at ambient temperature, such as when system


20


is idle. When the capability of hydrogenating fluid


36


at ambient temperatures is desired, solid catalyst


68


is preferably palladium, but may comprise platinum, rhodium, iridium, osmium and ruthenium. Similarly, the various soluble catalysts


70


discussed above also are active and drive the desired reaction at ambient temperature. This range of activity beneficially allows the hydrogenation of fluid


36


to occur at low level temperatures where typical commercial hydrogenation catalysts, such as nickel and its compounds, cannot be used.




Thus, the present invention advantageously provides a method and apparatus for catalytic hydrogenation of radiation-damaged fluid


36


used to cool and electrically insulate x-ray tube


30


in x-ray system


20


.




Although the invention has been described with reference to these preferred embodiments, other embodiments can achieve the same results. Variations and modifications of the present invention will be apparent to one skilled in the art and the following claims are intended to cover all such modifications and equivalents.



Claims
  • 1. In an x-ray generation system, a method for hydrogenating a dielectric fluid comprising a hydrocarbon that upon exposure to x-rays releases hydrogen atoms, comprising:exposing the dielectric fluid in the x-ray generation system to an effective amount of catalyst, operative independent of x-ray energy, that promotes the recombination of the hydrogen atoms with the hydrocarbon, wherein the effective amount of the catalyst comprises at least one of: (1) at least 1 cm2 surface area of a solid catalyst per liter of the dielectric fluid, and (2) at least 0.01 gram of a soluble catalyst per liter of the dielectric fluid.
  • 2. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the dielectric fluid is employed as a cooling element for the x-ray generating system.
  • 3. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the dielectric fluid comprises hydrogenated napthacene.
  • 4. A method of hydrogenating dielectric fluid as recited in claim 1, wherein exposing the dielectric fluid to the catalyst occurs at temperatures in the range of about 10° C.-300° C. and pressures in the range of about 0.1 atmospheres-30 atmospheres.
  • 5. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the catalyst comprises at least one of the following: a Group VIII element and a compound of a Group VIII element.
  • 6. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the effective amount of catalyst comprises about 1 cm2 surface area per liter of the dielectric fluid up to about 100 cm2 surface area per liter of the dielectric fluid.
  • 7. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the catalyst comprises at least one of iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium and platinum.
  • 8. A method of hydrogenating dielectric fluid as recited in claim 6, wherein the catalyst comprises at least one of palladium and platinum.
  • 9. A method of hydrogenating dielectric fluid as recited in claim 1, wherein the catalyst is in solution with the dielectric fluid.
  • 10. A method of hydrogenating dielectric fluid as recited in claim 9, wherein the effective amount of catalyst comprises about 0.01 gram per liter of the dielectric fluid up to about 1 gram per liter of the dielectric fluid.
  • 11. A method of hydrogenating dielectric fluid as recited in claim 9, wherein the catalyst comprises at least one of the following: tris(triphenylphosphine) rhodium (I) chloride, precious metals in solution, and Wilkinson's catalyst.
  • 12. A method of hydrogenating dielectric fluid as recited in claim 1, further comprising circulating the dielectric fluid through a mesh, wherein the mesh comprises the catalyst.
Parent Case Info

The present invention is a divisional application of U.S. patent application Ser. No. 09/108,452 filed Jul. 1, 1998, now U.S. Pat. No. 6,123,456.

US Referenced Citations (6)
Number Name Date Kind
2326324 Berger et al. Aug 1943 A
3036010 Freier et al. May 1962 A
4469849 Murrer et al. Sep 1984 A
5086449 Furbee et al. Feb 1992 A
5222118 Gerth Jun 1993 A
5357555 Gerth Oct 1994 A
Foreign Referenced Citations (4)
Number Date Country
4414687 Nov 1995 DE
4414688 Nov 1995 DE
62-274599 Nov 1989 JP
9-45492 Feb 1997 JP