SU128463A1 - The method of obtaining heat-resistant electrically insulating varnish - Google Patents

The method of obtaining heat-resistant electrically insulating varnish

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Publication number
SU128463A1
SU128463A1 SU635272A SU635272A SU128463A1 SU 128463 A1 SU128463 A1 SU 128463A1 SU 635272 A SU635272 A SU 635272A SU 635272 A SU635272 A SU 635272A SU 128463 A1 SU128463 A1 SU 128463A1
Authority
SU
USSR - Soviet Union
Prior art keywords
electrically insulating
insulating varnish
resistant electrically
obtaining heat
toluene
Prior art date
Application number
SU635272A
Other languages
Russian (ru)
Inventor
К.А. Андрианов
Л.М. Волкова
Д.Я. Жинкин
К.И. Забырина
А.С. Черничкина
Original Assignee
К.А. Андрианов
Л.М. Волкова
Д.Я. Жинкин
К.И. Забырина
А.С. Черничкина
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by К.А. Андрианов, Л.М. Волкова, Д.Я. Жинкин, К.И. Забырина, А.С. Черничкина filed Critical К.А. Андрианов
Priority to SU635272A priority Critical patent/SU128463A1/en
Application granted granted Critical
Publication of SU128463A1 publication Critical patent/SU128463A1/en

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  • Paints Or Removers (AREA)

Description

Известен способ получени  теплостойкого электроизол ционного лака иа основе продуктов совмещени  эпоксидных смол с кремнийорганическими соединени ми.A method of producing heat-resistant electrically insulating varnish based on products combining epoxy resins with organosilicon compounds is known.

Описываемый способ отличаетс  от известного тем, что в качестве кремнийорганического соединени  примен ют продукт согидролиза метил- и фенилхлорсиланов и фениламинометилметилдиэтоксисилана, что повышает цементируюихую способность лака. Способ осуществл ют следующим путем.The described method differs from the known one in that the product of co-hydrolysis of methyl- and phenylchlorosilanes and phenylaminomethylmethyldiethoxysilane is used as the organosilicon compound, which increases the cementing ability of varnish. The method is carried out in the following way.

Пример. Получение фениламинометилметилдиэтоксисилана.Example. Getting phenylaminomethylmethylamine.

В реакционный котел загружают 10 кг хлорметилметилдихлорсилапа и при перемешивании при температуре 20-25° в течение 4 час прибавл ют 5,9 кг абсолютного этилового спирта. Реакционную смесь нагревают при температуре 75-80 при перемещивании 10 час, затем ДJбавл ют 19 кг анилина и продолжают нагревать при температуре 130-140° 15 час, перемешива . После этого продукт охлаждают до 30-35°, добавл ют 10 кг толуола и отфильтровывают образовавщийс  сол нокислый ацилин- От фильтрата отгон ют толуол и анилин до температуры 140-150° (при 35 мм); оставшийс .кубовый остаток представл ет собой фениламинометилметилдиэтоксисилан (70-72% от веса) и продукт частичного его гидролиза.10 kg of chloromethylmethyldichlorosilap are loaded into the reaction kettle and 5.9 kg of absolute ethanol are added with stirring at a temperature of 20-25 ° over 4 hours. The reaction mixture is heated at a temperature of 75-80 with moving for 10 hours, then J is added 19 kg of aniline and continue to be heated at a temperature of 130-140 ° for 15 hours while stirring. After that, the product is cooled to 30-35 °, 10 kg of toluene is added and the hydrochloric acid acylin formed is filtered off. From the filtrate, toluene and aniline are distilled to a temperature of 140-150 ° (at 35 mm); the remaining cubic residue is phenylaminomethylmethyldiethoxysilane (70-72% by weight) and its partial hydrolysis product.

Пример. Получение кремнийорганического полимераВ гидролизер загружают 45 кг воды, 10 кг толуола и при перемещ вании при температуре не 30-40 подают смесь из 2,4 кг диметилднхлорсилана , 1,8 кг метилтрихлорсилана, 5,2 кг фенилтрихлорсилана в 10 кг толуола со скоростью 8-10 . Смесь перемещивают 30 мин иExample. Preparation of organosilicon polymerav hydrolyser loads 45 kg of water, 10 kg of toluene and, when transferred at a temperature of not 30-40, a mixture of 2.4 kg of dimethyl chlorosilane, 1.8 kg of methyltrichlorosilane, 5.2 kg of phenyltrichlorosilane and 10 kg of toluene is fed at a rate of 8 ten . The mixture is moved for 30 minutes and

jvjb i 84B;: - 2 ;;jvjb i 84B ;: - 2 ;;

оставл ют отстаиватьс , отдел   нижний водный cjioii; масл ный слан промывают водо до нейтральной реакции но KOHIO. Промытый и ирофильтропанный продукт повторно загружают в чистый тидролизер, добавл ют 200% от веса продукта воды, обрабатывают раствором соды До рН 7,5 и нрн. перемешивании медленно прибавл ют 0,6 кг фениламинометилметилдиэтокеиеилана . После введени  всего количества амина реакционную смесь перемешивают 40 мин, отдел ют масл ный слой, промывают водой, фильтруют и отгон ют растворитель (50% от веса загруженного маСоЧ нсго сло ). Оставшийс  поллмер охлаждают до темнературы 70°, отфильтровывают через ткань и затем конденсируют при 120-130° с продувкой воздухом. Конец копденсации контролируют по времени желатинизации. Врем  желатииизации составл ет 2-3 мин.. Полнорганосилоксановый лак приготовл ют путем растворени  полученной смолы в толуоле до 50%-пой концентрации. Перед унотргбленнем лак смешивают с 50%-ным спиртотолуольным (1 : 1) раствором смолы ЭД-6 и 50%-ным сниртовЕ1 м раствором тетрабутоксититана из расчета 90% полиоргансилоксанового полимера, 10% ЭД-6 и 1% тетрабутоксититана , счита  на чистые продукты.settle, lower aqueous cjioii; the oil is washed with water until neutral with KOHIO. The washed and microfiltrated product is reloaded into a clean tirrolizer, 200% by weight of water product is added, treated with soda solution until pH 7.5 and nrn. while stirring, 0.6 kg of phenylaminomethylmethyldiethoicieilane is slowly added. After the total amount of amine has been added, the reaction mixture is stirred for 40 minutes, the oil layer is separated, washed with water, filtered and the solvent is distilled off (50% of the weight of the loaded hydrochloric acid layer). The remaining polmer is cooled to a temperaure of 70 °, filtered through a cloth and then condensed at 120-130 ° with air blowing. The end of the condensation is controlled by the gel time. The gelatinization time is 2-3 minutes. The organosiloxane lacquer is prepared by dissolving the resulting resin in toluene to 50% concentration. Before a unbotted bleach, varnish is mixed with a 50% alcohol toluene solution (1: 1) of ED-6 resin and a 50% solution of tetrabutoxy titanium at a rate of 90% polyorganosiloxane polymer, 10% ED-6 and 1% tetrabutoxy titanium, calculated on pure products .

Предмет изобретен и 5гSubject invented and 5g

Способ получени  теплостойкого электроизол ционного лака на основе продуктов совмешени  эноксидных смол с кремнийорганическими соединени ми, отл и ч а ю ш.и и с  тем, что, с целью иовышени  цементирующей способности лака, дл  совмешени  с эпоксидной смолой в качестве кремнийорганического соединени  примен ют продукт согидролиза метил- и фенилхлорсиланов и фениламинометилметилдиэтоксисилана.The method of obtaining heat-resistant electrically insulating lacquer based on products of combining enoxide resins with organosilicon compounds, and with the fact that, in order to improve the cementing ability of varnish, for combining with epoxy resin, the product of organosilicon is used cohydrolysis of methyl- and phenylchlorosilanes and phenylaminomethylmethyldiethoxysilane.

SU635272A 1959-07-30 1959-07-30 The method of obtaining heat-resistant electrically insulating varnish SU128463A1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5362821A (en) * 1990-09-11 1994-11-08 Dow Corning Corporation Epoxy resin with aminofunctional monophenyl polysiloxane
US5431765A (en) * 1994-06-20 1995-07-11 Toray Industries Preparing epoxy resin/aminopolysiloxane/aromatic oligomer composite

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5362821A (en) * 1990-09-11 1994-11-08 Dow Corning Corporation Epoxy resin with aminofunctional monophenyl polysiloxane
US5378532A (en) * 1990-09-11 1995-01-03 Dow Corning Corporation Epoxy resin/aminofunctional polysiloxane fiber-reinforced composite
US5405688A (en) * 1990-09-11 1995-04-11 Dow Corning Corporation Epoxy resin/aminopolysiloxane/aromatic oligomer composite
US5466323A (en) * 1990-09-11 1995-11-14 Toray Industries Preparing epoxy resin/hardener/aminopolysiloxane composite
US5431765A (en) * 1994-06-20 1995-07-11 Toray Industries Preparing epoxy resin/aminopolysiloxane/aromatic oligomer composite

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