SU979442A1 - Polymeric composition - Google Patents
Polymeric composition Download PDFInfo
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- SU979442A1 SU979442A1 SU813294971A SU3294971A SU979442A1 SU 979442 A1 SU979442 A1 SU 979442A1 SU 813294971 A SU813294971 A SU 813294971A SU 3294971 A SU3294971 A SU 3294971A SU 979442 A1 SU979442 A1 SU 979442A1
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- SU
- USSR - Soviet Union
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- weight
- block copolymer
- prepared
- tested
- stabilizer
- Prior art date
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- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Description
Изобретение относитс к получению полимерных композиций на основе блоксополимера изопрена со стиролом и может быть использовано в производстве полимерных изделий, устойчивых к действию света.The invention relates to the preparation of polymer compositions based on isoprene block copolymer with styrene and can be used in the manufacture of polymer products that are resistant to the action of light.
Известна композици на основе карбоцепинх полимеров, содержаща в качестве стабилизирующей добавки производные 2,2,6,6-тетраметилпиперидилен-4-уксусной кислотьт fl.A known composition based on carbocepine polymers containing 2,2,6,6-tetramethylpiperidylene-4-acetic acid fl. As a stabilizing additive.
Однако указанна композици характеризуетс ; недостаточной светостойкостью , а синтез стабилизирующих добавок нетехнологичен, поскольку включает много стадий и св зан с применением малодоступных реагентов.However, said composition is characterized; insufficient light fastness, and the synthesis of stabilizing additives is not technological, since it involves many stages and is associated with the use of inaccessible reagents.
Наиболее близкой к предлагаемой по технической сущности и получаемо му эффекту вл етс полимерна KQMпозици на основе карбодепных полимеров f в том числе блок-сополимера изопрена со стиролом, содержаща в качестве стабилизирующей добавки . производные 2,2,6,6-тетраметилпипе- ридил-4-Уксусной кислоты f2.Closest to the proposed technical essence and the effect obtained is a polymer KQM position based on carbodepous polymers f including a block copolymer of isoprene with styrene, containing as a stabilizing additive. 2,2,6,6-tetramethylpiperidyl-4-acetic acid derivatives f2.
Указанна композици также характеризуетс недостаточной светостойкостью а синтез стабилизируюг их добавок нетехнологичен.This composition is also characterized by insufficient lightfastness, and the synthesis of the stabilization of their additives is not technological.
Цель изобретени - повыиение светостойкости .The purpose of the invention is to increase the light resistance.
Поставленна цель достигаетс тем, что полимерна композици , включюща блок-сополимер изопрена со стиролом. и стабилизируюидую добавку - производное тетраметилпиперидинкарбоновой кислоты, содержит в качестве стабилизирующей добавки соединение общей This goal is achieved in that a polymer composition comprising an isoprene block copolymer with styrene. and a stabilizing additive, a derivative of tetramethylpiperidinecarboxylic acid, contains as a stabilizing additive a compound of the total
10 формулы10 formulas
ОABOUT
NЛг15NLg15
.CHjCHaR.CHjCHaR
HjCvJ ,Hjcvj
2020
О или Oh or
где X У Н или 6}where X Y N or 6}
или CN or CN
R СООСН,R COOCH,
при следующем соотношении компонек25 тов, вес,ч.:with the following ratio of components, weight, hours:
Блок-сополимер изопренаIsoprene block copolymer
со стиролом100with styrene 100
Стабилизирующа добавка, 30 указанна вьлче 0,2-1 Синтез предлагаемых стабилизирующих добавок прост и включает легко доступные реагенты, Дл синтеза эти соединений триацетонамин или 2,2,6, -тетраметил-4-оксопиперидин-1-оксил обрабатывают вторичным циклическим амином, а продукт реакции алкилируют эфирами акриловой кислоты или ак рилонитрилом. Пример, Раствор ют 1,5 г блок-сополимера изопрена со стироло ( марка ИСТ-30) и 15 мг (1 вес.ч.) ,соединени 1 таблица) в 10 мл хлороформа . Раствор перемешивают и нан с т на нат нутую целлофановую пленку . После испарени растворител и отслаивани подложки водой получают пленку толщиной л 2 мм. Полученную пленку облучают светом ртутной лампы ДРМ-120 с длиной волны свыше ЗОО нм. В качестве характеристики светостойкости используют величину индукционного периода образовани гидроксильных групп, поглощающих в област х 3450 нм. П р и м е р 2. Аналогично примеру 1 готов т и испытывают пленки блок-сополимера, содержащего в качестве стабилизатора 1 вес.ч. соеди нени 2 (таблица). П р и м е р 3. Аналогично примеру 1 готов т и испытывают пленку блок-сополимера, содержащего в качестве стабилизатора 1 вес.ч, соеди нени 3 (таблица).A stabilizing additive, 30 indicated greater than 0.2-1. The synthesis of the proposed stabilizing additives is simple and includes easily available reagents. To synthesize these compounds, triacetonamine or 2,2,6, -tetramethyl-4-oxopiperidin-1-oxyl is treated with a secondary cyclic amine, and the reaction product is alkylated with acrylic esters or acrylonitrile. Example: 1.5 g of isoprene block copolymer with styrene (grade EAST-30) and 15 mg (1 part by weight), compound 1 table are dissolved in 10 ml of chloroform. The solution is mixed and coated with a tensioned cellophane film. After evaporation of the solvent and peeling of the substrate with water, a film 2 mm thick is produced. The resulting film is irradiated with light of a DRM-120 mercury lamp with a wavelength in excess of AOO nm. As a lightfastness characteristic, the value of the induction period for the formation of hydroxyl groups absorbing in the regions of 3450 nm is used. EXAMPLE 2 Analogously to Example 1, films of a block copolymer containing 1 weight.h. as stabilizer are prepared and tested. Connect n 2 (table). EXAMPLE 3 Analogously to Example 1, a block copolymer film containing 1 weight.h, compound 3 (table) as a stabilizer is prepared and tested.
СветостабилизаторLight stabilizer
СоединениеCompound
Этиловый эфир (2,2,6,6-тетраметил-4-Ы-морфолино-1 ,2,5,6-тетрагидропиперидил-5 )-3-пропионовой кислотыEthyl ester (2,2,6,6-tetramethyl-4-Y-morpholino-1, 2,5,6-tetrahydropiperidyl-5) -3-propionic acid
Этиловый эфир (2,2,6,6-тетраметил-4-М-пиперидино-1 ,2,5,6-тетрагидропиперидил-5 )-3-пропивновой кислотыEthyl ester (2,2,6,6-tetramethyl-4-M-piperidino-1, 2,5,6-tetrahydropiperidyl-5) -3-propivnova acid
Метиловый эфир (2, 2,6 ,6-тeтpaмeтил-4-N-мopфoлинo-l ,2,5,6-тетрагидропиперидил-5 )-3-пропионовой кислоты АMethyl ester of (2, 2,6, 6-tetramethyl-4-N-morpholino-l, 2,5,6-tetrahydropiperidyl-5) -3-propionic acid A
Этиловый эфир (2,2,6,6-тeтpaмeтил-l-oкcил-4-N-мopфoлинo-l , 2,5.,6-тетрагидропиперидил-5 )-3-пропионовой кислотыEthyl ester of (2,2,6,6-tetramethyl-1-oxyl-4-N-morpholino-1, 2.5., 6-tetrahydropiperidyl-5) -3-propionic acid
Нитрил (2,2,6,6-тетраиетил-4-Ы-морфолино-1 ,2,5,6-тетрагидропиперидил-5)-3-пропионовой кислотыNitrile (2,2,6,6-tetraietil-4-Y-morpholino-1, 2,5,6-tetrahydropiperidyl-5) -3-propionic acid
Нитрил (2,2,6,6-тетраметил-1-оксил-4-Ы-морфолино-1 ,2,5,6-твтрагидропиперидил-5) -3-пропионоврй кислотыNitrile (2,2,6,6-tetramethyl-1-oxyl-4-A-morpholino-1, 2,5,6-tvtrahydropiperidyl-5) -3-propionic acid
Этиловый эфир 2,2,6,6-тетраметилпиперидил-4-уксусноЯ кислоты (прототип)Ethyl ester 2,2,6,6-tetramethylpiperidyl-4-acetic acid (prototype)
2-(2-Окси-5-метилфенил)бензотриазол Без добавки2- (2-Oxy-5-methylphenyl) benzotriazole Without additive
Индукционный период, чInduction period, h
4949
4545
44 80 2844 80 28
5757
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU813294971A SU979442A1 (en) | 1981-05-29 | 1981-05-29 | Polymeric composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU813294971A SU979442A1 (en) | 1981-05-29 | 1981-05-29 | Polymeric composition |
Publications (1)
Publication Number | Publication Date |
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SU979442A1 true SU979442A1 (en) | 1982-12-07 |
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SU813294971A SU979442A1 (en) | 1981-05-29 | 1981-05-29 | Polymeric composition |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4548973A (en) * | 1984-08-27 | 1985-10-22 | Olin Corporation | Selected 2,2,6,6-tetramethyl-4-piperidinyl derivatives and their use as light stabilizers |
-
1981
- 1981-05-29 SU SU813294971A patent/SU979442A1/en active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4548973A (en) * | 1984-08-27 | 1985-10-22 | Olin Corporation | Selected 2,2,6,6-tetramethyl-4-piperidinyl derivatives and their use as light stabilizers |
EP0173050A2 (en) * | 1984-08-27 | 1986-03-05 | Olin Corporation | Selected 2,2,6,6-tetramethyl-4-piperidinyl derivatives and their use as light stabilizers |
EP0173050A3 (en) * | 1984-08-27 | 1988-05-25 | Olin Corporation | Selected 2,2,6,6-tetramethyl-4-piperidinyl derivatives and their use as light stabilizers |
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