US2977554A - Dielectric liquid and apparatus utilizing same - Google Patents
Dielectric liquid and apparatus utilizing same Download PDFInfo
- Publication number
- US2977554A US2977554A US405103A US40510354A US2977554A US 2977554 A US2977554 A US 2977554A US 405103 A US405103 A US 405103A US 40510354 A US40510354 A US 40510354A US 2977554 A US2977554 A US 2977554A
- Authority
- US
- United States
- Prior art keywords
- liquid
- core piece
- naphthalene
- transformer
- tertiary
- 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
- 239000007788 liquid Substances 0.000 title claims description 28
- 238000009835 boiling Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 10
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000003989 dielectric material Substances 0.000 claims description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 18
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 13
- 238000004804 winding Methods 0.000 description 12
- QPUYECUOLPXSFR-UHFFFAOYSA-N alpha-methyl-naphthalene Natural products C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 125000000217 alkyl group Chemical group 0.000 description 8
- -1 alkyl naphthalene Chemical group 0.000 description 8
- 229940075566 naphthalene Drugs 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000002826 coolant Substances 0.000 description 5
- 229910000286 fullers earth Inorganic materials 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- URGSMJLDEFDWNX-UHFFFAOYSA-N 1-butylnaphthalene Chemical group C1=CC=C2C(CCCC)=CC=CC2=C1 URGSMJLDEFDWNX-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 125000005233 alkylalcohol group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000012809 cooling fluid Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- GOQBFDVVKDFHPN-UHFFFAOYSA-N 1,2-ditert-butylnaphthalene Chemical compound C1=CC=CC2=C(C(C)(C)C)C(C(C)(C)C)=CC=C21 GOQBFDVVKDFHPN-UHFFFAOYSA-N 0.000 description 1
- SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical group CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 description 1
- MZOGBVZHJWAQSG-UHFFFAOYSA-N 1-octylnaphthalene Chemical class C1=CC=C2C(CCCCCCCC)=CC=CC2=C1 MZOGBVZHJWAQSG-UHFFFAOYSA-N 0.000 description 1
- FDHDUXOBMHHFFJ-UHFFFAOYSA-N 1-pentylnaphthalene Chemical group C1=CC=C2C(CCCCC)=CC=CC2=C1 FDHDUXOBMHHFFJ-UHFFFAOYSA-N 0.000 description 1
- SPLGZANLVHBDCC-UHFFFAOYSA-N 1-tert-butylnaphthalene Chemical compound C1=CC=C2C(C(C)(C)C)=CC=CC2=C1 SPLGZANLVHBDCC-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000000110 cooling liquid Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
- 150000005377 tertiary alkyl halides Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F27/00—Details of transformers or inductances, in general
- H01F27/08—Cooling; Ventilating
- H01F27/10—Liquid cooling
- H01F27/12—Oil cooling
- H01F27/125—Cooling by synthetic insulating and incombustible liquid
-
- 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 relates to an improved dielectric liquid; more particularly, the invention relates to a liquid-cooled transformer utilizing an improved liquid dielectric material as the coolant.
- the transformer consists of a liquid-tight housing or tank 3 fitted with a removable cover 7 provided with a pair of external terminals 4 and 5. Extending vertically with respect to the tank 3 are a plurality of cooling conduits 9 through which cooling fluid circulates. Positioned on the interior of the tank 3 is a core piece 1 and a plurality of electrical windings 2 in accordance with conventional transformer construction. The core piece 1 and windings 2 are immersed in a dielectric liquid 6 which will be described in more detail hereinafter.
- the dielectric fluid 6 is a monotertiary alkyl naphthalene or a monotertiary alkyl methyl naphthalene wherein the tertiary alkyl group contains from 4 to 8 carbon atoms. While monotertiary butyl naphthalene is the preferred dielectric liquid, the other liquids in the class defined above are also satisfactory.
- the naphthalene derivatives of this invention are not new to the art. They may be prepared by reacting naphthalene or methyl naphthalene with the appropriate tertiary alkyl alcohol in the presence of aluminum chloride according to the method of Trukervank and Vichrova [1. Gen. Chem.
- Larsen Patent 2,436,110 discloses an electric cable in which polytertiary alkyl naphthalenes are used as a dielectric material.
- Example 1 of the Larsen patent describes the preparation of octyl naphthalenes and refers to a light fraction boiling fro-m 178 to 193 C. at 3 millimeters mercury pressure and a heavier fraction boiling in the range from 193 to 205 C. at 3 millimeters mercury pressure.
- Larsen uses the heavier fraction as his impregnant. In the present invention it is the portion corresponding to one of Larsens light fractions, which Larsen describes as having a fairly low dielectric strength which is utilized.
- the material of the present invention has a boiling range of l14-120 C. at 3 mm. Hg pressure and it is characterized by a dielectric strength in excess of 53 kv.
- Vhile aluminum choride has been the best catayst used in the reaction, aiurninum bromide, ferric chloride, and other Friedel-Crafts catalysts'are satisfactory.
- the product produced in accordance with this invention usually consists of an isomeric mixture in which the [3 isomer predominates. Where the starting material is methyl naphthalene the final product is a mixture of a number of monoalkyl isomers.
- the dielectric liquids of this invention are characterized by having a boiling range of about 260 to 360 C. at atmospheric pressure, corresponding to 110 to 175 C. at 3 millimeters Hg pressure, a pour point ranging from 0 C. to 40 C., and superior resistance to oxidation. Tests have indicated that the liquids of this invention possess sufficient oxidation stability to enable them to remain essentially unchanged after many years of use under normal operating conditions. The factthat these liquids are not at all decomposed by distillation at atmospheric pressure is a further indication of their oxidation stability.
- the oxidation stability of the liquids of this invention enables transformers to operate satisfactorily at a higher operating temperature.
- the maintenance of a liquid temperature of C. is readily feasible.
- a trans- I former having incorporated therein the dielectric liquids of this invention will have a higher kva. rating than the same size transformer using conventional dielectric liquids.
- a transformer comprising a core piece, a primary winding on said core piece, a secondary winding on said core piece, a liquid-tight housing encasing said windings and core piece, and a liquid in said housing surrounding said windings and core piece, said liquid having a boiling point below C. at a pressure of 3 mm. of mercury and consisting essentially of a compound of the structure wherein R is selected from the group consisting of hydrogen and a methyl group and R is a tertiary alkyl group containing from 4 t0 8 carbon atoms.
- a transformer comprising a core piece, a plurality of windings positioned on said core piece, a liquid-tight container encasing said windings and core piece, a liquid in said container contacting said core piece and windings, said liquid having a boiling point below 150 C. at a pressure of 3 mm. of mercury and consisting essentially of a compound of the structure:
- R is selected from the group consisting of hydrogen and a methyl group and R is a tertiary alkyl group containing from 4 to 8 carbon atoms
- means for I wherein R is, selected from the group consisting of hy drogen and a methyl group and R is a tertiary alkyl wherein R is selected from the group consisting of hydrogen and a methyl group and R is a tertiary alkyl group containing 4 to 8 carbon atoms, said material having a boiling point below 150 C. at a pressure of 3 mm. of mercury.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Power Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Combustion & Propulsion (AREA)
- Organic Insulating Materials (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US405103A US2977554A (en) | 1954-01-20 | 1954-01-20 | Dielectric liquid and apparatus utilizing same |
JP296455A JPS332388B1 (en:Method) | 1954-01-20 | 1955-01-20 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US405103A US2977554A (en) | 1954-01-20 | 1954-01-20 | Dielectric liquid and apparatus utilizing same |
Publications (1)
Publication Number | Publication Date |
---|---|
US2977554A true US2977554A (en) | 1961-03-28 |
Family
ID=23602290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US405103A Expired - Lifetime US2977554A (en) | 1954-01-20 | 1954-01-20 | Dielectric liquid and apparatus utilizing same |
Country Status (2)
Country | Link |
---|---|
US (1) | US2977554A (en:Method) |
JP (1) | JPS332388B1 (en:Method) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2245721A (en) * | 1938-07-26 | 1941-06-17 | Colgate Palmolive Peet Co | Organic reactions in sulphur dioxide |
US2390835A (en) * | 1940-04-30 | 1945-12-11 | Du Pont | Method of alkylating aromatic compounds |
US2436110A (en) * | 1943-01-11 | 1948-02-17 | Shell Dev | Electric cable impregnated with tertiary alkyl naphthalenes |
US2572808A (en) * | 1948-09-18 | 1951-10-23 | Monsanto Chemicals | Dielectric with n, n'-1-3 dimorpholino isopropanol as scavenger |
-
1954
- 1954-01-20 US US405103A patent/US2977554A/en not_active Expired - Lifetime
-
1955
- 1955-01-20 JP JP296455A patent/JPS332388B1/ja active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2245721A (en) * | 1938-07-26 | 1941-06-17 | Colgate Palmolive Peet Co | Organic reactions in sulphur dioxide |
US2390835A (en) * | 1940-04-30 | 1945-12-11 | Du Pont | Method of alkylating aromatic compounds |
US2436110A (en) * | 1943-01-11 | 1948-02-17 | Shell Dev | Electric cable impregnated with tertiary alkyl naphthalenes |
US2572808A (en) * | 1948-09-18 | 1951-10-23 | Monsanto Chemicals | Dielectric with n, n'-1-3 dimorpholino isopropanol as scavenger |
Also Published As
Publication number | Publication date |
---|---|
JPS332388B1 (en:Method) | 1958-04-08 |
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