EP1059643B1 - Composition dielectrique ayant une absorption de gaz amelioree - Google Patents
Composition dielectrique ayant une absorption de gaz amelioree Download PDFInfo
- Publication number
- EP1059643B1 EP1059643B1 EP00401546A EP00401546A EP1059643B1 EP 1059643 B1 EP1059643 B1 EP 1059643B1 EP 00401546 A EP00401546 A EP 00401546A EP 00401546 A EP00401546 A EP 00401546A EP 1059643 B1 EP1059643 B1 EP 1059643B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mixture
- formula
- isomers
- products
- compositions
- 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 claims abstract description 92
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000002480 mineral oil Substances 0.000 claims abstract description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- 235000010446 mineral oil Nutrition 0.000 claims abstract description 7
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical class C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 claims description 2
- GDPISEKNRFFKMM-UHFFFAOYSA-N 1,3-diphenylpropan-2-ylbenzene Chemical class C=1C=CC=CC=1CC(C=1C=CC=CC=1)CC1=CC=CC=C1 GDPISEKNRFFKMM-UHFFFAOYSA-N 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000003921 oil Substances 0.000 abstract description 5
- 239000000047 product Substances 0.000 description 23
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000007789 gas Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000006178 methyl benzyl group Chemical group 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- GTLWADFFABIGAE-UHFFFAOYSA-N 1-chloroethylbenzene Chemical compound CC(Cl)C1=CC=CC=C1 GTLWADFFABIGAE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000926 not very toxic Toxicity 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- -1 transformers 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
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
-
- 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
- the present invention relates to a dielectric composition with mineral oil base for electrical equipment with absorption of improved gas.
- Mineral oils are widely used as oils insulators in various electrical materials such as transformers, capacitors, and cables.
- mineral oils include natural compounds different such as paraffin chains, cyclic compounds saturated naphthenic, aromatic structures whose polyaromatic condensed.
- Aromatic compounds give mineral oils better dielectric properties such as better breakdown voltage or so-called gassing properties.
- the absorption of gas is characteristic of the behavior of a oil under high electric field.
- the oil can either produce more gas in which case it is called “gas-evolving” (gas producer), or absorb hydrogen, it is then called “gas-absorbing” (absorber of gas).
- Condensed polyaromatics are diverse and varied in nature, but most are considered carcinogenic. Also, in order to reduce the polyaromatic content in mineral oils, these undergo a hydrogenation treatment. This treatment however has the disadvantage of making others disappear completely aromatic considered as not very toxic.
- the Applicant has found that the use of small amounts of compounds of the polyarylalkane family made it possible to improve the gas absorption property of mineral oils.
- the compositions (I) may contain product (A) with 2 rings, (methylbenzyl) xylene, and product (A) with 3 rings which is designated by bis (methylbenzyl) xylene.
- compositions (I) usable according to the present invention mention will be made of the polyarylalkane composition sold by ELF ATOCHEM S.A. under the designation JARISOL XX having a content by weight of compounds with 2 and 3 aromatic rings greater than 99%.
- compositions can be obtained by methods described in patents EP 136 230-B1, EP 299 867-B1, EP 384 818-B1, EP 500 435-B1 incorporated in the present invention, by references, which consist of chlorinating toluene or xylene and then to perform a Friedel and Crafts type condensation either on toluene, either on xylene (mixture of isomers), or on a toluene and xylene mixture, either on benzene or on a mixture benzene and toluene.
- the reaction is finished, the or reagents not transformed by distillation then the crude product can be subjected to a dechlorination treatment as described in the patent EP 306 398-81.
- compositions (II) can be obtained by a process described in patent EP 136 230-B1 which consists, in a first step, in reacting chlorine on toluene by radical reaction in the presence of free radical generator at a temperature between 50 ° C and 110 ° C then in a second step, the reaction product from the first step is subjected to a condensation reaction with toluene in the presence of FeCl 3 at a temperature between 50 ° C and 100 ° C.
- compositions (I) can be obtained according to a process described in patent EP 0 50 435-B1 which consists in carrying out the condensation of (methyl) benzyl chloride with xylene in the presence of FeCl 3 .
- the dielectric compositions according to the invention have the advantage of having improved gas behavior (improved gassing).
- the interface between a column of liquid and a volume of hydrogen is subjected to electrical discharges between 2 electrodes placed at different potentials.
- the evolution of the gas volume is monitored as a function of time.
- the gassing expressed in ⁇ l / min, is positive if gas is released and is negative if gas is absorbed.
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Insulating Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9907143A FR2794566B1 (fr) | 1999-06-07 | 1999-06-07 | Composition dielectrique ayant une absorption de gaz amelioree |
| FR9907143 | 1999-06-07 | ||
| FR0001880 | 2000-02-16 | ||
| FR0001880A FR2794567A1 (fr) | 1999-06-07 | 2000-02-16 | Composition dielectrique ayant une absorption de gaz amelioree |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1059643A1 EP1059643A1 (fr) | 2000-12-13 |
| EP1059643B1 true EP1059643B1 (fr) | 2003-07-09 |
Family
ID=26212178
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00401546A Expired - Lifetime EP1059643B1 (fr) | 1999-06-07 | 2000-05-31 | Composition dielectrique ayant une absorption de gaz amelioree |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6391228B1 (enExample) |
| EP (1) | EP1059643B1 (enExample) |
| JP (2) | JP3545993B2 (enExample) |
| KR (1) | KR100375357B1 (enExample) |
| CN (1) | CN1144844C (enExample) |
| AT (1) | ATE244921T1 (enExample) |
| CA (1) | CA2311250C (enExample) |
| DE (1) | DE60003757T2 (enExample) |
| DK (1) | DK1059643T3 (enExample) |
| ES (1) | ES2203405T3 (enExample) |
| FR (1) | FR2794567A1 (enExample) |
| NO (1) | NO20002877L (enExample) |
| TW (1) | TWI257383B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9051419B2 (en) * | 2002-06-14 | 2015-06-09 | Richard H. Hall | Polymer |
| US7531083B2 (en) * | 2004-11-08 | 2009-05-12 | Shell Oil Company | Cycloalkane base oils, cycloalkane-base dielectric liquids made using cycloalkane base oils, and methods of making same |
| US20060100466A1 (en) * | 2004-11-08 | 2006-05-11 | Holmes Steven A | Cycloalkane base oils, cycloalkane-base dielectric liquids made using cycloalkane base oils, and methods of making same |
| KR20140060255A (ko) * | 2010-11-25 | 2014-05-19 | 프리즈미안 에스피에이 | 전압 안정화 열가소성 전기 절연층을 가진 에너지 케이블 |
| FR3008708B1 (fr) * | 2013-07-19 | 2016-09-23 | Arkema France | Composition de fluide dielectrique ou caloporteur |
| CN106675733A (zh) * | 2017-01-05 | 2017-05-17 | 广东美商工业材料有限公司 | 一种应用于油浸式电容的电容油及其制备方法 |
| FR3078711B1 (fr) * | 2018-03-08 | 2020-07-31 | Arkema France | Utilisation d'un melange en tant que fluide dielectrique |
| FR3101477B1 (fr) * | 2019-10-01 | 2021-09-24 | Arkema France | Augmentation de la puissance d’un transformateur |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4914320B1 (enExample) * | 1969-03-31 | 1974-04-06 | ||
| JPS553762B2 (enExample) * | 1973-07-11 | 1980-01-26 | ||
| JPS5078899A (enExample) * | 1973-11-16 | 1975-06-26 | ||
| JPS5086698A (enExample) * | 1973-12-06 | 1975-07-12 | ||
| JPS5086700A (enExample) * | 1973-12-06 | 1975-07-12 | ||
| JPS5086699A (enExample) * | 1973-12-06 | 1975-07-12 | ||
| US4189391A (en) | 1976-05-01 | 1980-02-19 | Nippon Oil Co., Ltd. | Electrical insulating oil compositions |
| DE2632180A1 (de) * | 1976-07-16 | 1978-01-26 | Bp Benzin Und Petroleum Ag | Dielektrische fluessigkeiten fuer die metallbearbeitung durch elektroerosion |
| FR2552423B1 (fr) * | 1983-09-23 | 1985-10-25 | Ugine Kuhlmann | Compositions d'oligomeres de polyarylalcanes et leur procede de fabrication |
| GR850003B (enExample) * | 1984-07-11 | 1985-05-06 | Siemens Ag | |
| FR2643366B1 (fr) * | 1989-02-20 | 1991-09-06 | Atochem | Compositions a base de polyphenylmethanes, leur procede de fabrication et leur application comme dielectrique |
| FR2658655B1 (fr) * | 1990-02-20 | 1994-07-22 | Atochem | Procede de synthese d'oligomeres de (methylbenzyl)xylene et leur application comme dielectrique. |
| FR2658812B1 (fr) * | 1990-02-27 | 1992-05-15 | Atochem | Compositions dielectriques a base de benzyltoluene et de (methylbenzyl) xylene. |
| FR2658813B1 (fr) | 1990-02-27 | 1992-05-15 | Atochem | Composition a base de derives methyles et benzyles du diphenylmethane. son application comme dielectrique. |
| NO177820C (no) * | 1991-11-26 | 1995-11-29 | Atochem Elf Sa | Blanding på basis av benzyltoluener og benzylxylener og deres anvendelse som dielektrika |
| AU4427493A (en) * | 1992-08-03 | 1994-02-10 | Becton Dickinson & Company | Solid phase assay |
| EP0704861B1 (fr) * | 1994-09-30 | 2007-11-07 | Arkema France | Utilisation pour les transformateurs de distribution d'une composition diélectrique à base de polyarylalcanes ayant des propriétés diélectriques améliorées |
| KR101579679B1 (ko) * | 2014-04-22 | 2015-12-22 | 한밭대학교 산학협력단 | 수직형 페럴린 성막 노즐장치 |
-
2000
- 2000-02-16 FR FR0001880A patent/FR2794567A1/fr active Pending
- 2000-05-31 DK DK00401546T patent/DK1059643T3/da active
- 2000-05-31 AT AT00401546T patent/ATE244921T1/de not_active IP Right Cessation
- 2000-05-31 ES ES00401546T patent/ES2203405T3/es not_active Expired - Lifetime
- 2000-05-31 DE DE60003757T patent/DE60003757T2/de not_active Expired - Lifetime
- 2000-05-31 EP EP00401546A patent/EP1059643B1/fr not_active Expired - Lifetime
- 2000-06-06 JP JP2000169594A patent/JP3545993B2/ja not_active Expired - Fee Related
- 2000-06-06 CA CA002311250A patent/CA2311250C/fr not_active Expired - Lifetime
- 2000-06-06 NO NO20002877A patent/NO20002877L/no unknown
- 2000-06-07 KR KR10-2000-0031061A patent/KR100375357B1/ko not_active Expired - Fee Related
- 2000-06-07 CN CNB001217577A patent/CN1144844C/zh not_active Expired - Lifetime
- 2000-06-07 US US09/588,647 patent/US6391228B1/en not_active Expired - Lifetime
- 2000-11-02 TW TW089111062A patent/TWI257383B/zh not_active IP Right Cessation
-
2004
- 2004-02-20 JP JP2004044334A patent/JP2004143468A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NO20002877L (no) | 2000-12-08 |
| KR100375357B1 (ko) | 2003-03-08 |
| FR2794567A1 (fr) | 2000-12-08 |
| NO20002877D0 (no) | 2000-06-06 |
| CA2311250A1 (fr) | 2000-12-07 |
| JP2001055596A (ja) | 2001-02-27 |
| JP3545993B2 (ja) | 2004-07-21 |
| KR20010007272A (ko) | 2001-01-26 |
| DK1059643T3 (da) | 2003-11-03 |
| DE60003757T2 (de) | 2004-05-27 |
| CN1144844C (zh) | 2004-04-07 |
| TWI257383B (en) | 2006-07-01 |
| CA2311250C (fr) | 2007-10-30 |
| JP2004143468A (ja) | 2004-05-20 |
| CN1292402A (zh) | 2001-04-25 |
| US6391228B1 (en) | 2002-05-21 |
| ATE244921T1 (de) | 2003-07-15 |
| EP1059643A1 (fr) | 2000-12-13 |
| ES2203405T3 (es) | 2004-04-16 |
| DE60003757D1 (de) | 2003-08-14 |
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