SU865130A3 - Thermoplastic mouldable composition - Google Patents
Thermoplastic mouldable composition Download PDFInfo
- 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
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- polystyrene
- thermoplastic
- compositions
- radial teleblock
- mouldable composition
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions 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
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular 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
- C08G81/021—Block or graft polymers containing only sequences of polymers of C08C or C08F
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular 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
- C08G81/021—Block or graft polymers containing only sequences of polymers of C08C or C08F
- C08G81/022—Block 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions 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
- C08L51/04—Compositions 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08L71/12—Polyphenylene oxides
- C08L71/123—Polyphenylene oxides not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08L71/12—Polyphenylene oxides
Abstract
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75202476A | 1976-12-20 | 1976-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU865130A3 true SU865130A3 (en) | 1981-09-15 |
Family
ID=25024524
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU772554603A SU865130A3 (en) | 1976-12-20 | 1977-12-19 | Thermoplastic mouldable composition |
Country Status (12)
Country | Link |
---|---|
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)
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
-
1977
- 1977-11-10 DE DE19772750242 patent/DE2750242A1/en active Granted
- 1977-11-17 NL NL7712660A patent/NL7712660A/en not_active Application Discontinuation
- 1977-11-18 GB GB48047/77A patent/GB1559052A/en not_active Expired
- 1977-11-25 IT IT30048/77A patent/IT1088289B/en active
- 1977-12-02 CA CA000292241A patent/CA1119742A/en not_active Expired
- 1977-12-16 DD DD77202721A patent/DD133962A5/en unknown
- 1977-12-16 JP JP15232177A patent/JPS5394540A/en active Pending
- 1977-12-16 MX MX171781A patent/MX146397A/en unknown
- 1977-12-19 FR FR7738187A patent/FR2374378A1/en active Granted
- 1977-12-19 AU AU31702/77A patent/AU513181B2/en not_active Expired
- 1977-12-19 SU SU772554603A patent/SU865130A3/en active
- 1977-12-20 BR BR7708529A patent/BR7708529A/en unknown
Also Published As
Publication number | Publication date |
---|---|
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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