NO152582B - INSECTICID AGENT CONTAINING AS ACTIVE COMPONENT ONE OR MORE 3-SUBSTITUTED 2,2-DIMETHYL-CYCLOPROPANCARBOXYL ACID ESTERS - Google Patents
INSECTICID AGENT CONTAINING AS ACTIVE COMPONENT ONE OR MORE 3-SUBSTITUTED 2,2-DIMETHYL-CYCLOPROPANCARBOXYL ACID ESTERS Download PDFInfo
- Publication number
- NO152582B NO152582B NO790621A NO790621A NO152582B NO 152582 B NO152582 B NO 152582B NO 790621 A NO790621 A NO 790621A NO 790621 A NO790621 A NO 790621A NO 152582 B NO152582 B NO 152582B
- Authority
- NO
- Norway
- Prior art keywords
- capacitor
- paper
- insecticid
- substituted
- active component
- Prior art date
Links
- 239000003795 chemical substances by application Substances 0.000 title description 7
- 239000002253 acid Substances 0.000 title 1
- 150000002148 esters Chemical class 0.000 title 1
- 239000003990 capacitor Substances 0.000 claims description 22
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 6
- 229920001131 Pulp (paper) Polymers 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 239000011888 foil Substances 0.000 claims description 2
- 238000005470 impregnation Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- -1 3-SUBSTITUTED 2,2-DIMETHYL CYCLOPROPANE CARBOXYLIC ACID Chemical class 0.000 abstract 1
- 239000000356 contaminant Substances 0.000 description 4
- 238000011109 contamination Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/40—Unsaturated compounds containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Indole Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
INSECTICID MIDDEL INNEHOLDENDE SOM AKTIV KOMPONENT EN ELLER FLERE 3-SOBSTITUERTE 2,2-DIMETHYL-CYCLOPROPANCARBOXYLSYREESTERE.INSECTICID CONTAINING AS ACTIVE COMPONENT ONE OR MORE 3-SUBSTITUTED 2,2-DIMETHYL CYCLOPROPANE CARBOXYLIC ACID RESIDENTS.
Description
Anordning ved kondensatorer. Device for capacitors.
Oppfinnelsen vedrører en anordning ved kondensatorer som omfatter konden-satorelement eller av kondensatorelementer oppbyggete kondensatorelementgrupper, hvilke elementer eller elementgrupper er anbragt i en med impregneringsvæske fylt beholder, idet elementenes aktive deler består av aluminiumfolier adskilt av kondensatorpapir inneholdende aluminiumoksyd, hvilke papir utgjør kondensatorens dielektrikum. The invention relates to a device for capacitors comprising capacitor elements or capacitor element groups made up of capacitor elements, which elements or element groups are placed in a container filled with impregnation liquid, the active parts of the elements consisting of aluminum foils separated by capacitor paper containing aluminum oxide, which paper constitutes the capacitor's dielectric.
Som dielektrikum i kondensatorer an-vendes som regel kondensatorpapir med aluminiumoksyd. Oksydets oppgave er å binde forurensninger og derved minske ta-pene, spesielt ved høyere temperatur. Dette er av stor betydning for moderne kondensatorer med høy volumeffekt. Oksydpapiret har imidlertid en betydelig ulempe, som på en avgjørende måte kan minske dets an-vendelse. Forurensninger som stammer fra beholderen kan nemlig trenge inn i kon-densatorelementet og absorberes av oksydpapiret. Derved vil egenskapene for dielek-trikumet endres. Capacitor paper with aluminum oxide is usually used as a dielectric in capacitors. The oxide's task is to bind contaminants and thereby reduce losses, especially at higher temperatures. This is of great importance for modern capacitors with a high volume effect. However, the oxide paper has a significant disadvantage, which can decisively reduce its use. Contamination originating from the container can in fact penetrate into the condenser element and be absorbed by the oxide paper. Thereby, the properties of the dielectric material will change.
Hensikten med oppfinnelsen er å til-veiebringe en anordning med hvis hjelp disse ulemper kan unngås. Anordningen kjennetegnes ved at hvert kondensator-element resp. kondensatorelementgruppe helt omsluttes av et isolerende hus, som omfatter isolasjonspapir oppblandet med aluminiumoksyd, som ved papirfremstillin-gen er blitt innblandet i papirmassen i en mengde av omkring 2—3 %. The purpose of the invention is to provide a device with the help of which these disadvantages can be avoided. The device is characterized by the fact that each capacitor element or capacitor element group is completely enclosed by an insulating housing, which comprises insulating paper mixed with aluminum oxide, which has been mixed into the paper pulp during paper production in an amount of around 2-3%.
En kondensator av det slag som her A capacitor of the kind here
betraktes består vanligvis av en elementpakke bygget opp av flere kondensatorelementer. Denne elementpakke er inne-sluttet i en beholder, vanligvis av plate-materiale. Elementpakken er impregnert med et impregneringsmiddel og hele beholderen er dessuten fylt med dette impregneringsmiddel. Det finnes da dels en fri mengde impregneringsmiddel på grunn av at elementpakken ikke helt kan fylle beholderen, dels en bundet mengde i elementpakken. Under drift vil det nu skje en kontinuerlig utveksling mellom fritt og bundet impregneringsmiddel. Det frie impregneringsmiddel fører da med seg forurensninger fra beholderen inn i dielektrikum hvor forurensningene absorberes av oksydpartiet. Dette kan litt etter litt foran-ledige store lokale konsentrasjoner av forurensninger i dielektrikum, og vesentlig re-dusere gj ennomslagsholdf astheten. considered usually consists of an element package built up of several capacitor elements. This element package is enclosed in a container, usually made of plate material. The element package is impregnated with an impregnating agent and the entire container is also filled with this impregnating agent. There is then partly a free amount of impregnating agent due to the fact that the element pack cannot completely fill the container, and partly a bound amount in the element pack. During operation, there will now be a continuous exchange between free and bound impregnating agent. The free impregnating agent then carries with it contaminants from the container into the dielectric where the contaminants are absorbed by the oxide portion. Little by little, this can lead to large local concentrations of contaminants in the dielectric, and significantly reduce the breakdown strength.
Ved hjelp av anordningen ifølge oppfinnelsen hindres altså denne prosess ved rundt elementpakken å anbringe en isolerende kappe som omfatter isolasjonspapi-ret i hvilket er innblandet passende meng-der aluminiumoksyd. De forurensninger som det frie impregneringsmiddel medfører absorberes av papiret i isolasjonskappen, og kan derfor ikke trenge inn i dielektrikum og påvirke dettes egenskaper. With the aid of the device according to the invention, this process is therefore prevented by placing an insulating jacket around the element package which includes the insulating paper into which appropriate amounts of aluminum oxide have been mixed. The contamination caused by the free impregnating agent is absorbed by the paper in the insulation jacket, and therefore cannot penetrate the dielectric and affect its properties.
Claims (1)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2071478A IT1095450B (en) | 1978-02-28 | 1978-02-28 | 3-Poly:fluoro-propyl cyclopropane-carboxylate ester derivs. - with insecticidal and acaricidal activities |
| IT20713/78A IT1095449B (en) | 1978-02-28 | 1978-02-28 | NEW PYRETROIDS |
| IT3131078A IT1160403B (en) | 1978-12-27 | 1978-12-27 | 3-Poly:fluoro-propyl cyclopropane-carboxylate ester derivs. - with insecticidal and acaricidal activities |
| IT1970379A IT1166603B (en) | 1979-01-30 | 1979-01-30 | 3-Poly:fluoro-propyl cyclopropane-carboxylate ester derivs. - with insecticidal and acaricidal activities |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO790621L NO790621L (en) | 1979-08-29 |
| NO152582B true NO152582B (en) | 1985-07-15 |
| NO152582C NO152582C (en) | 1985-10-23 |
Family
ID=27452781
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO790621A NO152582C (en) | 1978-02-28 | 1979-02-23 | INSECTICID AGENT CONTAINING AS ACTIVE COMPONENT ONE OR MORE 3-SUBSTITUTED 2,2-DIMETHYL-CYCLOPROPANCARBOXYL ACID ESTERS |
| NO792716A NO153098C (en) | 1978-02-28 | 1979-08-21 | 3-SUBSTITUTED 2,2-DIMETHYL-CYCLOPROPANCARBOXYL ACIDES AND LOWER ALKYLESTERS THEREOF USE AS OUTSIDE MATERIALS IN THE PREPARATION OF PYRETHROIDS WITH INSECTICID EFFECT |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO792716A NO153098C (en) | 1978-02-28 | 1979-08-21 | 3-SUBSTITUTED 2,2-DIMETHYL-CYCLOPROPANCARBOXYL ACIDES AND LOWER ALKYLESTERS THEREOF USE AS OUTSIDE MATERIALS IN THE PREPARATION OF PYRETHROIDS WITH INSECTICID EFFECT |
Country Status (28)
| Country | Link |
|---|---|
| JP (1) | JPS54130537A (en) |
| AR (1) | AR241108A1 (en) |
| AU (1) | AU531296B2 (en) |
| BE (1) | BE874515A (en) |
| BG (3) | BG48921A3 (en) |
| BR (1) | BR7901221A (en) |
| CA (1) | CA1237439A (en) |
| CH (1) | CH638485A5 (en) |
| DD (2) | DD148767A5 (en) |
| DE (1) | DE2907609A1 (en) |
| DK (1) | DK161830C (en) |
| ES (1) | ES478426A1 (en) |
| FR (1) | FR2442826A1 (en) |
| GB (1) | GB2015519B (en) |
| GR (1) | GR72544B (en) |
| HU (1) | HU185607B (en) |
| IL (1) | IL56739A0 (en) |
| IN (1) | IN150228B (en) |
| KE (1) | KE3293A (en) |
| LU (1) | LU80981A1 (en) |
| MX (1) | MX5698E (en) |
| NL (1) | NL7901460A (en) |
| NO (2) | NO152582C (en) |
| NZ (1) | NZ189791A (en) |
| PL (1) | PL135350B1 (en) |
| PT (1) | PT69283A (en) |
| RO (1) | RO77772A (en) |
| YU (1) | YU48279A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2831193A1 (en) * | 1978-07-15 | 1980-01-24 | Bayer Ag | FLUORALKENYL-SUBSTITUTED CYCLOPROPANCARBONIC ACID ESTERS AND THEIR USE AS INSECTICIDES |
| DE2965744D1 (en) * | 1978-10-27 | 1983-07-28 | Ici Plc | Process for separating optical isomers of substituted cyclopropane carboxylic acids; amine salts of substituted cyclopropane carboxylic acids; a substituted cyclopropane carboxylic acid |
| DE2919820A1 (en) * | 1979-05-16 | 1980-11-20 | Bayer Ag | FLUOR-SUBSTITUTED OXYALKENYL-CYCLOPROPANCARBONIC ACID ESTERS, METHODS FOR THE PRODUCTION THEREOF AND THEIR USE AS INSECTICIDES AND ACARICIDES |
| EP0022608B1 (en) * | 1979-07-13 | 1983-07-06 | Imperial Chemical Industries Plc | Process for the preparation of cyclopropane carboxylic acid esters |
| IT1131883B (en) * | 1980-07-02 | 1986-06-25 | Montedison Spa | INTERMAEDI PROCESS FOR STEREOSELECTIVE SYNTHESIS OF CYCLOPROPANCARBOXYLATES FOR PYRETROIDS |
| IL83606A (en) * | 1986-08-27 | 1992-03-29 | Montedison Spa | Esters of 3-(3-substituted-3,3-difluoro-1-propenyl)2,2-dimethyl-cyclopropanecarboxylic acid,their preparation and their use as insecticides and acaricides |
| DE3900275A1 (en) * | 1989-01-07 | 1990-07-12 | Basf Ag | SUBSTITUTED CYCLOPROPANCARBONIC ACID PROPARGYL ESTERS, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING Pests |
| FR2687152A1 (en) * | 1992-02-07 | 1993-08-13 | Roussel Uclaf | NOVEL PYRETHRINOUID ESTERS DERIVED FROM FURANIC OR THIOPHENIC ALCOHOL, PROCESS FOR THEIR PREPARATION AND THEIR USE AS PESTICIDES |
| US6072074A (en) * | 1998-05-08 | 2000-06-06 | Sumitomo Chemical Company Limited | Process for producing 3-propynyl-2-2-dimethylcycloprophane-carboxylic acid and its lower akyl esters |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS515450B1 (en) | 1971-06-29 | 1976-02-20 | ||
| DE2326077C2 (en) | 1972-05-25 | 1985-12-12 | National Research Development Corp., London | Unsaturated cyclopropanecarboxylic acids and their derivatives, their preparation and insecticides containing them |
| JPS5283720A (en) * | 1976-01-01 | 1977-07-12 | Kuraray Co Ltd | Substituted cyclopropanecarboxylic acid derivatives, and insecticides and acaricides containing a-substituted cyclopropanecarboxylic acid deri vatives |
| US4130655A (en) * | 1976-07-12 | 1978-12-19 | Ciba-Geigy Corporation | Pesticidal 2,2-dimethyl-3-isobutyl-cyclopropionates |
| DE2638356A1 (en) * | 1976-08-26 | 1978-03-02 | Bayer Ag | METHOD FOR PRODUCING VINYL-SUBSTITUTED CYCLOPROPANCARBONIC ACID ESTERS |
| US4183948A (en) * | 1977-01-24 | 1980-01-15 | Imperial Chemical Industries Limited | Halogenated esters |
| GB2008572B (en) * | 1977-11-28 | 1982-01-27 | Ici Ltd | Manufacture of esters |
| IN150399B (en) * | 1978-01-20 | 1982-09-25 | Fmc Corp |
-
1979
- 1979-02-06 BG BG044136A patent/BG48921A3/en unknown
- 1979-02-06 BG BG044135A patent/BG48333A3/en unknown
- 1979-02-23 DK DK080379A patent/DK161830C/en not_active IP Right Cessation
- 1979-02-23 NO NO790621A patent/NO152582C/en unknown
- 1979-02-23 NL NL7901460A patent/NL7901460A/en not_active Application Discontinuation
- 1979-02-23 BR BR7901221A patent/BR7901221A/en unknown
- 1979-02-26 GR GR58472A patent/GR72544B/el unknown
- 1979-02-26 BG BG042659A patent/BG48931A3/en unknown
- 1979-02-26 IN IN173/CAL/79A patent/IN150228B/en unknown
- 1979-02-26 PT PT69283A patent/PT69283A/en unknown
- 1979-02-26 IL IL56739A patent/IL56739A0/en not_active IP Right Cessation
- 1979-02-27 GB GB7906851A patent/GB2015519B/en not_active Expired
- 1979-02-27 DD DD79218658A patent/DD148767A5/en not_active IP Right Cessation
- 1979-02-27 YU YU00482/79A patent/YU48279A/en unknown
- 1979-02-27 CA CA000322525A patent/CA1237439A/en not_active Expired
- 1979-02-27 PL PL1979213760A patent/PL135350B1/en unknown
- 1979-02-27 CH CH194279A patent/CH638485A5/en unknown
- 1979-02-27 HU HU79MO1039A patent/HU185607B/en unknown
- 1979-02-27 ES ES478426A patent/ES478426A1/en not_active Expired
- 1979-02-27 AU AU44631/79A patent/AU531296B2/en not_active Expired
- 1979-02-27 DE DE19792907609 patent/DE2907609A1/en active Granted
- 1979-02-27 FR FR7904952A patent/FR2442826A1/en active Granted
- 1979-02-27 DD DD79211259A patent/DD142281A5/en not_active IP Right Cessation
- 1979-02-28 MX MX797764U patent/MX5698E/en unknown
- 1979-02-28 NZ NZ189791A patent/NZ189791A/en unknown
- 1979-02-28 LU LU80981A patent/LU80981A1/en unknown
- 1979-02-28 BE BE0/193748A patent/BE874515A/en not_active IP Right Cessation
- 1979-02-28 AR AR275649A patent/AR241108A1/en active
- 1979-02-28 JP JP2204779A patent/JPS54130537A/en active Granted
- 1979-02-28 RO RO79101065A patent/RO77772A/en unknown
- 1979-08-21 NO NO792716A patent/NO153098C/en unknown
-
1983
- 1983-06-08 KE KE3293A patent/KE3293A/en unknown
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