SU288745A1 - - Google Patents

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Publication number
SU288745A1
SU288745A1 SU1264866A SU1264866A SU288745A1 SU 288745 A1 SU288745 A1 SU 288745A1 SU 1264866 A SU1264866 A SU 1264866A SU 1264866 A SU1264866 A SU 1264866A SU 288745 A1 SU288745 A1 SU 288745A1
Authority
SU
USSR - Soviet Union
Prior art keywords
acetone
soda
potassium permanganate
high purity
anhydrous reagent
Prior art date
Application number
SU1264866A
Other languages
Russian (ru)
Original Assignee
К. В. Вильшау, Н. И. Самсонова , В. Н. Андросова
СПОСОБ очистки АЦЕТОНА
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. В. Вильшау, Н. И. Самсонова , В. Н. Андросова, СПОСОБ очистки АЦЕТОНА filed Critical К. В. Вильшау, Н. И. Самсонова , В. Н. Андросова
Priority to SU1264866A priority Critical patent/SU288745A1/ru
Application granted granted Critical
Publication of SU288745A1 publication Critical patent/SU288745A1/ru

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Description

Изобретение относитс  к способам очистки ацетона.This invention relates to methods for purifying acetone.

Известен способ очистки ацетона путем ректификации .A known method of purification of acetone by distillation.

С целью получени  ацетона высокой стенени чистоты, который может пр-имен тьс  в электровакуумной и полупроводниковой промышленности , предлагают способ, заключающийс  в том, что перед ректификацией ацетон обрабатывают перманганатом кали  в «присутствии безводного основного реагента, например соды. Желательно брать пермаигалат кали  и соду в микроколичествах, например 0,0025 и 0,316 вес. % от вз того ацетона, и рехтифищировать при флегмовом числе не менее 6.In order to obtain high purity acetone, which can be referred to in the electrovacuum and semiconductor industries, a method is proposed that the acetone is treated with potassium permanganate in the presence of an anhydrous basic reagent, for example soda, prior to distillation. It is advisable to take potassium permaigalat and soda in trace amounts, for example, 0.0025 and 0.316 wt. % of acetone taken, and rehashchifirovat when reflux ratio of not less than 6.

При,мер. 500 мл ацетона (395,2 г) загружают в колбу с мешалкой и туда же ввод т 0,01 г иермангаиата кали  и 1,25 г безводной соды. После 15 мин перемешивани  ацетон декантируют и загружают в куб ректификационноп колонны. Ацетон особой чистоты отбирают цри флегмовом числе, равном 6.Example. 500 ml of acetone (395.2 g) were charged into a flask with a stirrer, and 0.01 g of potassium germaniumate and 1.25 g of anhydrous soda were added thereto. After 15 minutes of stirring, the acetone is decanted and rectification columns are loaded into the cube. High purity acetone is taken at a reflux ratio of 6.

Выход целевого продукта составл ет 88,5% от исходного ацетона.The yield of the target product is 88.5% of the starting acetone.

Предмет и з о б р е т е И и  Subject matter

Claims (2)

1. Способ очистки ацетона с применением ректификации, отличающийс  тем, что, с целью получени  ацетона высокой степени чистоты и низкой электропроводности, ацетон перед ректификацией обрабатывают перманганатом кали  в присутствии основного безводного реагента, например соды.1. A method of purifying acetone using rectification, characterized in that, in order to obtain acetone of high purity and low electrical conductivity, acetone is treated with potassium permanganate in the presence of a basic anhydrous reagent, for example, soda, before distillation. 2. Способ по п. 1, отличающийс  тем, что перманганат кали  и основной безводный реагент , например соду, примен ют в микроколичествах , на-иример 6,0025 и 0,316 вес. % от вз того ацетона.2. A method according to claim 1, characterized in that potassium permanganate and a basic anhydrous reagent, for example, soda, are used in trace amounts, an irimer of 6.0025 and 0.316 wt. % of acetone taken.
SU1264866A 1968-08-09 1968-08-09 SU288745A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1264866A SU288745A1 (en) 1968-08-09 1968-08-09

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1264866A SU288745A1 (en) 1968-08-09 1968-08-09

Publications (1)

Publication Number Publication Date
SU288745A1 true SU288745A1 (en) 1973-02-08

Family

ID=20443201

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1264866A SU288745A1 (en) 1968-08-09 1968-08-09

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Country Link
SU (1) SU288745A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001030735A1 (en) * 1999-10-22 2001-05-03 General Electric Company Method for purifying acetone
CN105175236A (en) * 2015-09-25 2015-12-23 江阴润玛电子材料股份有限公司 Ultra-clean high-purity acetone production method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001030735A1 (en) * 1999-10-22 2001-05-03 General Electric Company Method for purifying acetone
US6340777B1 (en) 1999-10-22 2002-01-22 General Electric Company Method for purifying acetone
CN105175236A (en) * 2015-09-25 2015-12-23 江阴润玛电子材料股份有限公司 Ultra-clean high-purity acetone production method

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