US2087578A - Mineral oil composition - Google Patents
Mineral oil composition Download PDFInfo
- Publication number
- US2087578A US2087578A US729901A US72990134A US2087578A US 2087578 A US2087578 A US 2087578A US 729901 A US729901 A US 729901A US 72990134 A US72990134 A US 72990134A US 2087578 A US2087578 A US 2087578A
- Authority
- US
- United States
- Prior art keywords
- gas
- oil
- oil composition
- aromatic
- mineral oil
- 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
Links
- 239000000203 mixture Substances 0.000 title description 15
- 239000002480 mineral oil Substances 0.000 title description 8
- 235000010446 mineral oil Nutrition 0.000 title description 5
- 239000007789 gas Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000035882 stress Effects 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical group N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- -1 nitrogen cyclic compounds Chemical class 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical group CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical group CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 150000001717 carbocyclic compounds Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
- H01B3/22—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils hydrocarbons
Definitions
- This invention pertains to the composition of mineral oils used for electrical purposes, and has for particular purpose to improve the quality of ,cable and condenser oils with regard to their 5 tendency to evolve gas when subjected to electric stress.
- an aromatic mixture such as the Edeleanu extract from a spindle oil
- the addition of 1% of parafilns at approximately the same volatility causes practically no change, while the addition of 1% of more volatile paraflins brings about a considerable evolution of gas.
- My invention consists, therefore, in adding to a suitably refined cable or condenser oil, a relatively more volatile cyclic compound with a com.- pact molecule, in amounts suflicient to give an aromatic nature to the gas phase present or a gas phase which may arise.
- aromatic compounds with a compact molecule may be mentioned those consisting only of carbon and hydrogen, such as benzene, toluene, xylene, anthra- 5Q cene, etc., and also such heterocyclic or nitrogen cyclic compounds as pyridine, picolines, lutidines, collidines, or quinoline and its methyl substituted derivatives.
- a method of insulating electric conductors, as electric cables, carrying high voltages which comprises maintaining around said conductors a mineral oil composition comprising a refined substantially aromatic-free oil suitable for insulating purposes, and a small amount of a relatively more volatile aromatic hydrocarbon having a compact molecule of a molecular weight less than 225, said small amount being effective in inhibiting the formation of gases in said oil composition, and being within the range of from by weight of the refined oil, wherein A is the molecular weight of the aromatic hydrocarbon.
- a method of insulating electric conductors, as electric cables, carrying high voltages which comprises maintaining around said conductors a mineral oil composition comprising a refined substantiallg, aromatic-free oil suitable for insulating purposes, and a small amount of a relatively more volatile liquid sulfur dioxide soluble portion of mineral oil, said portion containing cyclic hydrocarbons having a compact molecule of a molecular weight less than 225, said small amount being efiective in inhibiting the formation of gases in said oil composition, and being within the range of from by weight of the refined oil, wherein A is the average molecular weight of the cyclic com pounds.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Insulating Materials (AREA)
Description
Patented July 20, 1937 UNITED STATES ats'ts is MINERAL on. comrosrrron ware No Drawing. Application June 9, 1934, Serial No. 729,901. in the Netherlands June 16, 1933 2 Giaims.
This invention pertains to the composition of mineral oils used for electrical purposes, and has for particular purpose to improve the quality of ,cable and condenser oils with regard to their 5 tendency to evolve gas when subjected to electric stress.
In modern methods of manufacturing high tension cables having a fibrous insulation impregnated with oil, great care is taken to remove all traces of air in the fibrous layers. The cable to be impregnated is usually first subjected to a very high degree of vacuum, so that a thorough impregnation may be effected with substantially no residual air left in the dielectric.
It has been found, however, that such methods are insufficient to preclude all possibility of gas pockets forming in the dielectric, since gas bubbles may be generated there as a result of the decomposition of the oil itself under the very high electric stresses to which it is subjected. The high field intensities usually prevailing in a high tension cable or condenser may then give rise to glow discharges in the gas pockets, leading to an increase in their number and size and to an ultimate deterioration of the cable or condenser.
It is therefore of the greatest importance to develop a type of oil whose gas-forming tendency under operating conditions would be at a minimum.
It is known that the degree of gas formation depends to a great extent on the nature of the mineral oils. Thus, with two oils having approximately the same flash point but consisting respectively of a substantially parafiinic and of a substantially aromatic mixture of hydrocarbons, the evolution of gas in the aromatic mixture is very considerably lower than that in the paraifinic mixture. 7 I
It is not, however, possible to use aromatic oils in the manufacture of cable wrappings and electric condensers, since the desirable characteristics of these oils with regard to gas formation, are entirely onset by their negative properties, such as their strong tendency to form. sludge and their failure to respond to the action of antioxidants to prevent aging. It has therefore been customary until now to use for these purposes mineral oils which had been subjected to a refining treatment for the removal of aromatic components in order to obtain an oil with the highest possible resistance to oxidation.
I have now discovered that it is possible to obtain an oil composition which although consisting substantially of parafiins and/or naphthenes and 5 possessing therefore the non-oxidizing and nonsludge forming qualities, may be made, through the addition of a very small amount of certain aromatic compounds, to evolve only negligible amounts of gas.
I have found that when a mixture of liquid parafiins is exposed to a high electric stress, a considerable evolution of gas takes place. When 1% of aromatics of the same volatility, such, for example, as an Edeleanu extract of a mineral oil, 5 is added to the mixture, the evolution of the gas remains practically the same. When, however, 1% of more volatile aromatics is added, the gas evolution is considerably reduced.
On the other hand, an aromatic mixture, such as the Edeleanu extract from a spindle oil, gives off only a very small amount of gas when subjected to high electric stresses. The addition of 1% of parafilns at approximately the same volatility causes practically no change, while the addition of 1% of more volatile paraflins brings about a considerable evolution of gas.
These facts prove conclusively that the evolution of gas under the influence of high electric stresses is largely determined by the nature of the most volatile constituents of the oil, which predominate, owing to their relatively high vapor pressure, in the gas bubbles forming in the oil, and probably decompose as a result of the glow discharges.
Moreover, I have found that the rate of gas I formation in hydrocarbon mixtures made according to my invention is lower than the rate of gas formation of either aromatic or paraffinic component used for preparing the mixture.
My invention consists, therefore, in adding to a suitably refined cable or condenser oil, a relatively more volatile cyclic compound with a com.- pact molecule, in amounts suflicient to give an aromatic nature to the gas phase present or a gas phase which may arise.
As examples of such suitable aromatic compounds with a compact molecule may be mentioned those consisting only of carbon and hydrogen, such as benzene, toluene, xylene, anthra- 5Q cene, etc., and also such heterocyclic or nitrogen cyclic compounds as pyridine, picolines, lutidines, collidines, or quinoline and its methyl substituted derivatives.
As stated above, it is necessary to add only very small amounts of these compounds to cable and condenser oils in order to reduce the evolution of gas to a sufiiciently low value. In general, I have found that these amounts should lie between the limits of while particularly satisfactory results are obtained if the quantities of the substances added lie between where A is the molecular weight of the substance added.
The following list gives the percentage by weight, computed according to these formulae, in which some of the above substances may be added to cable and condenser oils:
- Percent Benzene "between" 0.2 and 2 Toluene do 0.3 and 3 Xylene do 0.3 and 3 Anthracene do 1.0 and 5 molecules of carbocyclic or heterocyclic compounds having no side chains, like benzene, naphthalene, pyridine and the like, ortheir substituted derivatives containing one or more methyl groups attached to the cyclic nuclei.
I claim as my invention:
1. A method of insulating electric conductors, as electric cables, carrying high voltages which comprises maintaining around said conductors a mineral oil composition comprising a refined substantially aromatic-free oil suitable for insulating purposes, and a small amount of a relatively more volatile aromatic hydrocarbon having a compact molecule of a molecular weight less than 225, said small amount being effective in inhibiting the formation of gases in said oil composition, and being within the range of from by weight of the refined oil, wherein A is the molecular weight of the aromatic hydrocarbon.
2. A method of insulating electric conductors, as electric cables, carrying high voltages which comprises maintaining around said conductors a mineral oil composition comprising a refined substantiallg, aromatic-free oil suitable for insulating purposes, and a small amount of a relatively more volatile liquid sulfur dioxide soluble portion of mineral oil, said portion containing cyclic hydrocarbons having a compact molecule of a molecular weight less than 225, said small amount being efiective in inhibiting the formation of gases in said oil composition, and being within the range of from by weight of the refined oil, wherein A is the average molecular weight of the cyclic com pounds.
GERRIT WILLEM NEDERBRAGT.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL2087578X | 1933-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2087578A true US2087578A (en) | 1937-07-20 |
Family
ID=19873634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US729901A Expired - Lifetime US2087578A (en) | 1933-06-16 | 1934-06-09 | Mineral oil composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2087578A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2865849A (en) * | 1958-12-23 | Electrical insulating oils and method | ||
| DE1088648B (en) * | 1955-08-12 | 1960-09-08 | Iashellia Res Ltd | Electrical insulating oil |
| US3163705A (en) * | 1959-08-21 | 1964-12-29 | Anaconda Wire & Cable Co | Oil insulated impregnant for high voltage electrical apparatus |
-
1934
- 1934-06-09 US US729901A patent/US2087578A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2865849A (en) * | 1958-12-23 | Electrical insulating oils and method | ||
| DE1088648B (en) * | 1955-08-12 | 1960-09-08 | Iashellia Res Ltd | Electrical insulating oil |
| US3163705A (en) * | 1959-08-21 | 1964-12-29 | Anaconda Wire & Cable Co | Oil insulated impregnant for high voltage electrical apparatus |
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