SU126265A1 - Method for producing ion exchange resins - Google Patents

Method for producing ion exchange resins

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Publication number
SU126265A1
SU126265A1 SU627430A SU627430A SU126265A1 SU 126265 A1 SU126265 A1 SU 126265A1 SU 627430 A SU627430 A SU 627430A SU 627430 A SU627430 A SU 627430A SU 126265 A1 SU126265 A1 SU 126265A1
Authority
SU
USSR - Soviet Union
Prior art keywords
exchange resins
ion exchange
producing ion
copolymer
acenaphthylene
Prior art date
Application number
SU627430A
Other languages
Russian (ru)
Inventor
М.И. Иткина
А.Б. Пашков
В.С. Титов
Original Assignee
М.И. Иткина
А.Б. Пашков
В.С. Титов
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 М.И. Иткина, А.Б. Пашков, В.С. Титов filed Critical М.И. Иткина
Priority to SU627430A priority Critical patent/SU126265A1/en
Application granted granted Critical
Publication of SU126265A1 publication Critical patent/SU126265A1/en

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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Известен способ получени  катионообменных смол на основе продуктов сульфировани  сополимера аценафтилена и дивинилбензола.A known method of producing cation exchange resins based on the products of sulfonation of the copolymer of acenaphthylene and divinylbenzene.

Описываемый способ получени  ионообменных смол по сравнению с известным способом позвол ет получать анионообменные смолы путем хлорметилировани  сополимера аценафтилена с дивинилбензолом в присутствии катализатора Фридел -Крафтса с дальнейшим аминированием органическими аминами, например, триметиламином.The described method for the preparation of ion exchange resins, in comparison with the known method, makes it possible to obtain anion exchange resins by chloromethylation of a copolymer of acenaphthylene with divinylbenzene in the presence of a Friedel Crafts catalyst with further aminating with organic amines, for example, trimethylamine.

Пример 1. В реактор загружают 152 г сополимера аценафтилена с дивинилбензолом в виде гранулированного порон1ка и 300 г дихлорэтана . Смесь выдерживают 2-4 час. до достаточного набухани  сололимера , после чего в колбу ввод т 136-137 г катализатора (хлористого цинка ) и 402-403 г хлорметилового эфира. При работающей мешалке смесь подогревают до 55-57 в течение 3 час. По окончании реакции хлорметилировани , хлорметилированный сополимер отфильтровывают, промывают 5% сол ной кислотой и далее водой до нейтральной реакции. Содержание хлора в ородукте около 18%. Затем берут 200 г хлорметилированного продукта и заливают в реакторе 500 г бензола дл  набухани  в течение примерно суток. К смеси затем добавл ют 440 мл 35Vo-HOго водного раствора триметиламина и смесь нагревают при 60° в течение 6 час. Полученный сильноосновной анионит отфильтровывают и промывают . Анионит имеет следуюш,ие характеристики: Статическа  обменна  емкость в мг экв1гExample 1. 152 g of copolymer of acenaphthylene with divinylbenzene in the form of granulated poron1 and 300 g of dichloroethane are loaded into the reactor. The mixture is kept for 2-4 hours. until the sololimer swells sufficiently, after which 136-137 g of catalyst (zinc chloride) and 402-403 g of chloromethyl ether are introduced into the flask. With the stirrer running, the mixture is heated to 55-57 for 3 hours. At the end of the chloromethylation reaction, the chloromethylated copolymer is filtered off, washed with 5% hydrochloric acid and then with water until neutral. The chlorine content in the product is about 18%. Then, 200 g of chloromethylated product is taken and 500 g of benzene is poured in the reactor for swelling for about a day. To the mixture is then added 440 ml of a 35Vo-HCO aqueous solution of trimethylamine and the mixture is heated at 60 ° for 6 hours. The obtained strongly basic anion exchange resin is filtered and washed. Anion exchanger has the following characteristics: Static exchange capacity in mg EQ1 g

по 0,1 н ,00.1 n, 0

То же, по 0,1 н NaCl-3,7The same, for 0.1 n NaCl-3,7

Удельный объем в мл/гSpecific volume in ml / g

в 0,1 н НС1-3,20.1 n HC1-3.2

в 0,1 и NaCl,-3,3in 0.1 and NaCl, -3.3

в воде-3,8in water is 3.8

№ 126265No. 126265

Пример 2. Синтез провод т так же, как описано в примере 1, но вместо триметиламина берут 400 мл 20% водного диметиламина и врем  аминировани  при температуре 60 увеличивают до 10-12 час.Example 2. The synthesis was carried out as described in Example 1, but instead of trimethylamine, 400 ml of 20% aqueous dimethylamine was taken and the time of amination at 60 was increased to 10-12 hours.

Предмет изобретени Subject invention

Способ получени  ионообменных смол по авт. св. № 105382, отличающийс  тем, что, с целью получени  анионообменных смол, сополимер аценафтилена с дивинилбензолом подвергают хлорметилированию в присутствии катализатора Фридел -Крафтса, а затем аминируют органическими аминами, например, триметиламином.The method of obtaining ion exchange resins according to ed. St. No. 105382, characterized in that, in order to obtain anion exchange resins, the copolymer of acenaphthylene with divinylbenzene is subjected to chloromethylation in the presence of a Friedel-Crafts catalyst, and then aminated with organic amines, for example, trimethylamine.

SU627430A 1959-05-07 1959-05-07 Method for producing ion exchange resins SU126265A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU627430A SU126265A1 (en) 1959-05-07 1959-05-07 Method for producing ion exchange resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU627430A SU126265A1 (en) 1959-05-07 1959-05-07 Method for producing ion exchange resins

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
SU105382 Addition

Publications (1)

Publication Number Publication Date
SU126265A1 true SU126265A1 (en) 1959-11-30

Family

ID=48397578

Family Applications (1)

Application Number Title Priority Date Filing Date
SU627430A SU126265A1 (en) 1959-05-07 1959-05-07 Method for producing ion exchange resins

Country Status (1)

Country Link
SU (1) SU126265A1 (en)

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