SU427958A1 - METHOD OF OBTAINING WATER SOLUBLE COPOLYMERS - Google Patents

METHOD OF OBTAINING WATER SOLUBLE COPOLYMERS

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Publication number
SU427958A1
SU427958A1 SU1756814A SU1756814A SU427958A1 SU 427958 A1 SU427958 A1 SU 427958A1 SU 1756814 A SU1756814 A SU 1756814A SU 1756814 A SU1756814 A SU 1756814A SU 427958 A1 SU427958 A1 SU 427958A1
Authority
SU
USSR - Soviet Union
Prior art keywords
water soluble
acid
copolymers
obtaining water
soluble copolymers
Prior art date
Application number
SU1756814A
Other languages
Russian (ru)
Inventor
А. Б. Кучкаров А. Б. Аловитдинов изобретени У. Кочкарова
Original Assignee
Ташкентский Политехнический Институт
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Application filed by Ташкентский Политехнический Институт filed Critical Ташкентский Политехнический Институт
Priority to SU1756814A priority Critical patent/SU427958A1/en
Application granted granted Critical
Publication of SU427958A1 publication Critical patent/SU427958A1/en

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Description

II

1one

Известен способ .получени  водорастворимых сополимеров путем взаимодействи  N-ви11ил пирролидона с с ,-фенил1винилфосф,иповой кислотой в pacTiBope при xeMineipaType 50 -100° С в присутствии ди-нитрила азоизомасл ной кислоты. Получаемые сополимеры обладают повыше«ной термо- и огнестойкостью .The known method is to obtain water-soluble copolymers by reacting N-vi11yl-pyrrolidone with-phenyl 1-vinyl phosphate, ipic acid in pacTiBope at xeMineipaType 50-100 ° C in the presence of azo-isobutyric acid di-nitrile. The resulting copolymers have higher thermal and fire resistance.

С целью получени  новых сополимеров, обладающих .повышенной хИМической стойкостью и комллемсообразующей опособ|Ностью предлагаетс  в качестве сомоно меров а-фенилвИНилфосфиновой кислоты использовать амиды а.криловой или метакрилавой кислот.In order to obtain new copolymers possessing increased chemical resistance and complexing agent, Nostie proposes to use amides of acrylic acid or methacrylate acid as co-monomers of a-phenylvinyl-vinylphosphinic acid.

Процесс осуществл етс  в орга ическомThe process is carried out in an organic

растворителе, иашример днсксане, .при телгпературе пор дка 80°С в инертной атмосфере.solvent, iashrimer dnskane, at a temperature of about 80 ° C in an inert atmosphere.

Получаемые соеолимеры можно использовать в качестве термостойких и химически СТОЙ1КИХ веществ, а также как ко.мплексообразующие и экстрагирующие .полимерные агенты и водорастворимые полизлектролиты дл  осветлени  промышленных растворов.The resulting co-polymers can be used as heat-resistant and chemically resistant substances, as well as complex-forming and extracting polymeric agents and water-soluble poly-electrolytes to clarify industrial solutions.

Сополимеры легко растворимы в воде и органи1Чбаких растворител х и в отличие от сополимеров, полученных известным способом, их растворы не кетоенолизируют.The copolymers are readily soluble in water and organic solvents and, unlike copolymers prepared in a known manner, their solutions are not ketoenolized.

Объемна  емкость сополимеров колеблетс  от 4,2 до 5,6 .1;г же по КОН. 3 Пример. Сололимеризацию а-фенилвинилфосфиновой кислоты (сс-ФВК - т. пл. С) с акриламидом (или -метакриламидом ) Лрн различныхюоотношени х моломеpoiB в исходной смеси ведут в заоа иных aiM-5 пулах в атмосфере азота илйции1рованием азонитрилом изомасл ной кислоты (1% от общего веса мо1вомер:ов) прн 80° С в среде дноксала . Отношение общего веса моно1меров к весу растворител  1:1.Ю Врем  сополи1мериза.ции зависит от соотношени  исходных камтонентов (см. таблицу ). Очищенные сополимеры алализируют. 4 П-ре д.мет изобретени  Опэсоб ползчени  водорастворИ.мых соиолимеров лутем взаимодействи  а-фенил1винилфо/сфил-овой кислоты с виниламидом при нагреваиии в растворе IB ирисутютвии дииитрила азоизамасл лой кислоты, отличающийс  тем, что, с получени  соиолнмерое, обладаюш .их повышенной химической стойздастью и комшлбысоо-бразующей способностью, в качестве винила1Мида используют амид акриловой или метакриловой кислоты.The volumetric capacity of the copolymers ranges from 4.2 to 5.6 .1; the same for KOH. 3 Example. Solimerization of a-phenyl vinylphosphinic acid (cc-PVC; t. C) with acrylamide (or methacrylamide) LDH of different molomeroib ratios in the initial mixture is carried out in a different aiM-5 pool in a nitrogen atmosphere or treated with azo- nitrile isomeric acid; the total weight of the model: s) prn 80 ° C in the environment of the dnixal. The ratio of the total weight of monomers to the weight of the solvent is 1: 1. The copolymerisation time depends on the ratio of the initial camotants (see table). Purified copolymers are alalized. 4 P-re d.me. of the invention for creeping water-soluble soiolimers by reacting a-phenylvinylfoil / sphylic acid with vinylamide upon heating in solution IB and dissolving dioitrile of azo-butyric acid, characterized in that, with the production of hearth. chemical resistance and complexing ability, as the vinyl 1Mide use amide of acrylic or methacrylic acid.

SU1756814A 1972-03-07 1972-03-07 METHOD OF OBTAINING WATER SOLUBLE COPOLYMERS SU427958A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1756814A SU427958A1 (en) 1972-03-07 1972-03-07 METHOD OF OBTAINING WATER SOLUBLE COPOLYMERS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1756814A SU427958A1 (en) 1972-03-07 1972-03-07 METHOD OF OBTAINING WATER SOLUBLE COPOLYMERS

Publications (1)

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SU427958A1 true SU427958A1 (en) 1974-05-15

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5439999A (en) * 1993-03-24 1995-08-08 Albright & Wilson Limited Bulk polymerisation process and product

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5439999A (en) * 1993-03-24 1995-08-08 Albright & Wilson Limited Bulk polymerisation process and product

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