SU865130A3 - Thermoplastic mouldable composition - Google Patents

Thermoplastic mouldable composition Download PDF

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Publication number
SU865130A3
SU865130A3 SU772554603A SU2554603A SU865130A3 SU 865130 A3 SU865130 A3 SU 865130A3 SU 772554603 A SU772554603 A SU 772554603A SU 2554603 A SU2554603 A SU 2554603A SU 865130 A3 SU865130 A3 SU 865130A3
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USSR - Soviet Union
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polystyrene
thermoplastic
compositions
radial teleblock
mouldable composition
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SU772554603A
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Russian (ru)
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Фан Ли Джим (Младший)
Филип Шанк Чарльз
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Дженерал Электрик Компани (Инофирма)
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C08G81/021Block or graft polymers containing only sequences of polymers of C08C or C08F
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C08G81/021Block or graft polymers containing only sequences of polymers of C08C or C08F
    • C08G81/022Block or graft polymers containing only sequences of polymers of C08C or C08F containing sequences of polymers of conjugated dienes and of polymers of alkenyl aromatic compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/08Polyethers derived from hydroxy compounds or from their metallic derivatives
    • C08L71/10Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
    • C08L71/12Polyphenylene oxides
    • C08L71/123Polyphenylene oxides not modified by chemical after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/08Polyethers derived from hydroxy compounds or from their metallic derivatives
    • C08L71/10Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
    • C08L71/12Polyphenylene oxides

Abstract

Thermoplastic compositions moldable to articles of high impact strength are disclosed which comprise an intimate admixture of a polyphenylene ether resin, a styrene resin, and a radial teleblock copolymer comprising a vinyl aromatic compound, a saturated rubber, and a coupling agent. Also included within the scope of this invention are reinforced and flame-retardant compositions of said thermoplastic materials.

Description

1one

Изобретение относитс  к композици м простых полиэфиров, а именно к термопластичным формовочным композици м на основе полифениленэфирных смол, и может быть использовано в химической промышленности.This invention relates to polyether compositions, namely thermoplastic molding compositions based on polyphenylene ether resins, and can be used in the chemical industry.

Известна термопластична  формовочна  композици  на основе смеси полифениленэфирных смол и различных наполнителей , красителей Г13 Known thermoplastic molding composition based on a mixture of polyphenylene ether resins and various fillers, dyes G13

. Недостатком этой композиции  вл ютс  относительйо низкие физико-механические показатели, в частности , ударопрочность.. The disadvantage of this composition is relatively low physical and mechanical properties, in particular, impact resistance.

Наиболее близкой к предлагаемому изобретению по технической .сущности  вл етс  термопластична  формовочна  композици , содержаща  поли-(2,б-диметил-1 ,4-фениленовый) -эфир и полистирольную смолу, выбранную из группы , состо щей из полистирола, и модифицированного бутадиеновым каучуком полистирола С23 .Closest to the proposed invention in technical terms is a thermoplastic molding composition containing a poly (2, b-dimethyl-1, 4-phenylene) ether and a polystyrene resin selected from the group consisting of polystyrene and modified with butadiene rubber polystyrene C23.

НедостаткЬм зтой композиции  вл етс  также относительно низка  ударопрочность .The disadvantage of this composition is also relatively low impact resistance.

Цель изобретени  - повышение ударопрочности композиции.The purpose of the invention is to increase the impact strength of the composition.

Цель достигаетс  тем, что термопластична  формовочна  композици .The goal is achieved by the thermoplastic molding composition.

содержаща  поли-(2,б-диметил-1 ,4-фениленовый )эфир и полистйрольную смолу , выбранную из группы, состо щей из полистирола и модифицированного бутадиеновым каучуком полистирола, дополнительно содержит гидрированный радиальный телеблочный блок-сополимер стирола и бутадиена при следующем соотношении компонентов, вес.ч.: containing poly (2, b-dimethyl-1, 4-phenylene) ether and a polystyrene resin selected from the group consisting of polystyrene and polystyrene modified with butadiene rubber, further contains a hydrogenated radial teloblochny block copolymer of styrene and butadiene in the following ratio of components , weight:

10 Поли-(2,б-диметил-1,4фениленЬвый )эфир 5,0-55 Полистирольна  смола 30-42 Гидрированный радиальный телеблочный блок15 сополимер8-15 Предпочтительны стирольными смолами  вл ютс  гомополистирол и модифицированные каучуком полистирольные смолы с высокой ударной проч20 ностью, т.е. смолы, которые модифицированы натуральными или сиитетичео кими полимерными материалами, ведущими себ  при комнатной температуре (например 20-25с) как эластомеры, 10 Poly- (2, b-dimethyl-1,4phenylene) ether 5.0-55 Polystyrene resin 30-42 Hydrogenated radial teloblok block15 copolymer8-15 Preferred styrene resins are homopolystyrene and rubber-modified polystyrene resins with high impact strength, t . resins that are modified with natural or synthetic polymeric materials that conduct themselves as elastomers at room temperature (for example, 20-25 seconds),

25 в частности полистирольиые смолы,со .держащие полибутадиен или каучукоподобные стирол-бутадиеновые сополимеры .25 in particular polystyrene resins containing polybutadiene or rubbery styrene-butadiene copolymers.

Целесообразным полистиролом с вы 30 сокой ударной прочностью  вл етс A suitable polystyrene with a high impact strength is 30

продукт FG-834, выпускаемый фирмой Фостергрант Ко., который представл ет собой модифицированный каучуком полистирол с высокой ударной прочностью , содержащий приблизительно 8% полибутадиенового каучука. Предпочтительным низкомолекул рным гомополистиролом  вл етс  .продукт KPTL-5, которглй в виде технического продукта выпускаетс  фирмой Арко полимере, Инк, средний молекул рный вес которого приблизительно 40 000. Предпочтительный гомополистирол с.относительно высоким молекул рным весом представл ет собой продукт DYL-8G, средний мс лекул рный вес которого примерно iso 000, также выпускаемый фирмой Арко.FG-834, manufactured by Fostergrant Co., which is a rubber-modified high impact polystyrene containing approximately 8% polybutadiene rubber. A preferred low molecular weight homopolystyrene is KPTL-5 product, which is commercially available from Arco Polymer, Inc., with an average molecular weight of approximately 40,000. Preferred homopolystyrene with a relatively high molecular weight is DYL-8G, The average MS medical weight is about iso 000, also produced by Arco.

Радиальные телеблочные блок-сополимеры представл ют собой технически доступные продукты. Их получают сополимеризацией со стиролом в прису.тствии металлоорганического инициатора , например н-бут-иллити , с получением сополимеров, которые содержат активный металлический атом, в частности литий, на одном конце каждой из полимерных цепей. Эти полимеры с наход щимис  на концах молекул металлическими атомами затем используют дл  реакции с агентом реакции сочетани , молекулы которого содержат по меньшей мере три активных участка, приемлемых дл  реакции со св з ми углерод-металлический атом в полимерных цеп х и замещени  металлических атомов цепей. Это приводит к образованию полимеров, которые имеют относительно длинные ответвлени , отход щие в виде лучей от кольца, образованного полифункциональным агентом реакции сочетани .Radial teleblock block copolymers are technically available products. They are obtained by copolymerization with styrene in the presence of an organometallic initiator, such as n-butylity, to produce copolymers that contain an active metallic atom, in particular lithium, at one end of each of the polymer chains. These polymers with metal atoms at the ends of the molecules are then used to react with a coupling reaction agent, the molecules of which contain at least three active sites that are suitable for reacting with the carbon-metal atom in the polymer chains and replacing the metal atoms of the chains. This leads to the formation of polymers that have relatively long branches, which come in the form of beams from the ring formed by the polyfunctional coupling agent.

Агентыреакции сочетани  дл  радйальнйх телеблочных сополимеров можно выбрать из класса полиэпоксидов, полиизоцианатов, полииминов, полиальдегидов , поликетонов, полиангидридов сложных полиэфиров, полигалогенидовCombination reaction agents for radial teleblock copolymers can be selected from the class of polyepoxides, polyisocyanates, polyimines, polyaldehydes, polyketones, polyesters polyanhydrides, polyhalides

и т .п.etc.

Гидрогенизацию радиальных телеблочных блок-сополимеров с получением гидрогенизованных радиальных телеблочных блок-сополимеров можно проводить .любым известным способом.The hydrogenation of radial teleblock block copolymers to produce hydrogenated radial teleblock block copolymers can be carried out by any known method.

Молекул рный вес гидрогенизованного радиального телеблочного блок-сополимера и количественные соотношени  между его сомономерами могут измен тьс  в широком интервале. В предпочтительных вариантах молекул рный вес гидрогенизованного радиального телеблочного сополимера находитс  в, интервале приблизительно 75 000 350 000, он содержит 1 - 45 вес.% звеньев винилового ароматического соединени  и 99 - 55 в. % насыщенного каучука в пересчете на весовое количество радиального телеблочного сополимера. Количество агента сочетани  в сополимере зависит от конкретного используемого агента и количесхва металлоорганического инициатора. Обычно использую,т относительно малые количества агента сочетани , например 0,1 -1 вес. ч. на каждые 100 вес.ч. используемой смолы.The molecular weight of the hydrogenated radial teleblock block copolymer and the quantitative ratios between its comonomers can vary over a wide range. In preferred embodiments, the molecular weight of the hydrogenated radial teleblock copolymer is in the range of about 75,000 to 350,000, it contains 1 to 45 wt.% Of the vinyl aromatic units and 99 to 55 in. % saturated rubber in terms of the weight amount of the radial teleblock copolymer. The amount of coupling agent in the copolymer depends on the specific agent used and the amount of organometallic initiator. I usually use relatively small amounts of a combination agent, e.g. 0.1-1 wt. hours for every 100 weight.h. used resin.

Предлагаемые композиции могут включать в себ  другие компоненты, в частности агенты, придающие огнестойкость , наполнители, вещества дл  улучшени  технологических свойст пигменты, стабилизаторы и другие средства, добавл емые дл  тех же целей . Можно использовать армирующие наполнители в количестве, достаточном дл  сообщени  улучшени  прочностных свойств,в частности алюминий, железо, никель и т.п., а также неметаллические армирующие агенты, в частности угольные -волокна, силикаты , в частности игольчатый силикат кальци , асбест, двуокись титана, титанат кали  и титанатные нитевидные кристаллы, стекл нные чешуйки, стекловолокно и т.п.The proposed compositions may include other components, in particular, flame retardants, fillers, substances to improve the technological properties of pigments, stabilizers and other agents added for the same purpose. It is possible to use reinforcing fillers in an amount sufficient to impart an improvement in the strength properties, in particular aluminum, iron, nickel, etc., as well as non-metallic reinforcing agents, in particular carbon fiber, silicates, in particular calcium needle silicate, asbestos, dioxide titanium, potassium titanate and titanate filamentous crystals, glass flakes, glass fibers, and the like.

Предлагаютс  также огнестойкие, композиции,которые содержат придающие огнестойкость добавки, относ щиес  к классу галоидированных органических соединений в смеси с соединени ми сурьмы, элементарным фосфором или соединени ми фосфора, или же соединени ми, в молекулах кот.орых имеютс  св зи фосфор-азот, или смесь двух или большего числа вышеперечисленных компонентов.Flame retardant compositions that contain flame retardant additives belonging to the class of halogenated organic compounds in mixture with antimony compounds, elemental phosphorus or phosphorus compounds, or compounds in molecules that have phosphorus-nitrogen bonds, are also proposed. or a mixture of two or more of the above components.

Claims (2)

1. Патент Великобритании № 930993, кл. 2(5)R, опублик. 1963.1. Patent of Great Britain No. 930993, cl. 2 (5) R, pub. 1963. 2. Патент США 3383435, кл. 260-874, опублик. 1968 (прототип ) . ;2. US patent 3383435, cl. 260-874, published. 1968 (prototype). ;
SU772554603A 1976-12-20 1977-12-19 Thermoplastic mouldable composition SU865130A3 (en)

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US75202476A 1976-12-20 1976-12-20

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JP (1) JPS5394540A (en)
AU (1) AU513181B2 (en)
BR (1) BR7708529A (en)
CA (1) CA1119742A (en)
DD (1) DD133962A5 (en)
DE (1) DE2750242A1 (en)
FR (1) FR2374378A1 (en)
GB (1) GB1559052A (en)
IT (1) IT1088289B (en)
MX (1) MX146397A (en)
NL (1) NL7712660A (en)
SU (1) SU865130A3 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55145752A (en) * 1979-05-01 1980-11-13 Asahi Chem Ind Co Ltd Aromatic polyether resin composition
GB2060656A (en) * 1979-10-15 1981-05-07 Gen Electric Self-extinguishing polyphenylene oxide/plasticizer blends
US4309514A (en) * 1979-11-30 1982-01-05 General Electric Company Molding compositions comprising polyphenylene ether and hydrogenated radial block copolymer of vinyl aromatic compound and diene rubber
US4313864A (en) * 1980-01-21 1982-02-02 General Electric Company Polyphenylene oxide/plasticizer/hydrogenated radial teleblock copolymer blends
JPS571733A (en) * 1980-06-06 1982-01-06 Asahi Chem Ind Co Ltd Injection-molded form of polyphenylene ether resin having good appearance
US4423189A (en) * 1981-10-28 1983-12-27 General Electric Company Compositions of a polyphenylene ether resin, low molecular weight polystyrene and a block copolymer
US4383082A (en) * 1981-12-01 1983-05-10 General Electric Company Polyphenylene ether resin compositions containing polyolefin in high amount
DE3219048A1 (en) * 1982-05-21 1983-11-24 Basf Ag, 6700 Ludwigshafen THERMOPLASTIC MOLDS
DE3434978A1 (en) * 1984-09-24 1986-04-03 Basf Ag, 6700 Ludwigshafen THERMOPLASTIC MOLDS
ES2059446T3 (en) * 1987-07-16 1994-11-16 Asahi Chemical Ind COMPOSITION OF A SPECIFIC HYDROGENATED BLOCK COPOLYMER AND PROCESS FOR ITS MANUFACTURE.
US5234994A (en) * 1988-11-01 1993-08-10 Asani Kasei Kogyo Kabushiki Kaisha Thermoplastic polymer composition
EP0476366A3 (en) * 1990-09-18 1992-09-30 General Electric Company Polyphenylene ether compositions of improved melt strength

Family Cites Families (4)

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US3281383A (en) * 1962-08-09 1966-10-25 Phillips Petroleum Co Branched polymers prepared from monolithium-terminated polymers and compounds having at least three reactive sites
US3696088A (en) * 1970-09-11 1972-10-03 Phillips Petroleum Co Hydrogenation process
JPS4830151A (en) * 1971-08-21 1973-04-20
DE2434848C2 (en) * 1973-08-13 1986-09-04 General Electric Co., Schenectady, N.Y. Thermoplastic mass

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AU513181B2 (en) 1980-11-20
FR2374378A1 (en) 1978-07-13
JPS5394540A (en) 1978-08-18
CA1119742A (en) 1982-03-09
NL7712660A (en) 1978-06-22
BR7708529A (en) 1978-08-08
FR2374378B1 (en) 1983-10-28
IT1088289B (en) 1985-06-10
DD133962A5 (en) 1979-01-31
DE2750242C2 (en) 1989-02-09
AU3170277A (en) 1979-06-28
DE2750242A1 (en) 1978-06-22
GB1559052A (en) 1980-01-16
MX146397A (en) 1982-06-23

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