CN101475673A - Transparent phenylethylene-dialkene star shaped copolymer and continuous preparation thereof - Google Patents

Transparent phenylethylene-dialkene star shaped copolymer and continuous preparation thereof Download PDF

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CN101475673A
CN101475673A CNA2009100954663A CN200910095466A CN101475673A CN 101475673 A CN101475673 A CN 101475673A CN A2009100954663 A CNA2009100954663 A CN A2009100954663A CN 200910095466 A CN200910095466 A CN 200910095466A CN 101475673 A CN101475673 A CN 101475673A
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phenylethylene
dialkene
polymerization
star shaped
transparent
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CN101475673B (en
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周赞斌
程国丽
冯震
高碧波
高书峰
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ZHEJIANG SANBO POLYMERS CO Ltd
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ZHEJIANG SANBO POLYMERS CO Ltd
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Abstract

The invention discloses a transparent styrene-diolefin star copolymer and a continuous preparation method thereof. The copolymer has the following structure: (PS-PB-PB/PS-PS) n-R or (PS-PB-PB/PS) n-R, wherein PS represents a polystyrene block, PB represents a polydiolefin block, PB/PS represents a styrene-diolefin random copolymer block, and R represents the core of the star structure. The invention also discloses the continuous preparation method for the copolymer. The preparation method has a high monomer conversion rate above 99.999 percent. The preparation method is characterized by low production cost, short reaction time, high yield, low operating cost, simple maintenance, no leakage of unconverted monomers and solvents during the production, reutilization, safety and environmental protection, and wide application range.

Description

Transparent phenylethylene-dialkene star shaped copolymer and continuous preparation method thereof
Technical field
The present invention relates to a kind of transparent phenylethylene-dialkene star shaped copolymer and continuous preparation method thereof.
Background technology
Phenylethylene resin series is one of five big universal synthetic resins, generally is only second to PE, PVC and PP by output and occupies the 4th.Polystyrene (PS), nineteen twenty-five, Germany I.G.Farben industrial took to cinnamic industrial production development, and nineteen thirty is realized suitability for industrialized production.China began to prepare production equipment in 1958, had started the industrial production of Chinese polystyrene resin.The phenylethylene resin series early stage of development, only produce general purpose polystyrene.Its matter is hard and crisp, physical strength is not high, thermotolerance is relatively poor, and inflammable.People have done a large amount of improvements for this reason, and having formed with high-impact polystyrene (HIPS), Expandable Polystyrene (EPS) (EPS), styrene-butadiene copolymer (K-Resin) etc. is the huge phenylethylene resin series system of representative.
Nineteen fifty-two Amos etc. develops a kind of technology of new production toughness polystyrene resin, its ultimate principle is to stir in polymerization process, thereby make rubber become dispersed particle rather than external phase, the toughness polystyrene of Sheng Chaning is exactly so-called high-impact polystyrene (HIPS) like this, HIPS removes has the advantages such as rigidity, processing characteristics and tint permanence of general purpose polystyrene, the introducing of rubber is risen its shock strength significantly, but performance index such as tensile strength, hardness, gloss descend, and have also lost certain transparency simultaneously.Because HIPS all adopts the radical polymerization mode to produce, and always has the small amounts of styrene monomer in the finished product, styrene monomer is poisonous, so its range of application just is subjected to certain restriction.
K-Resin is by the breadboard chemist AlonzoKitchen invention of Phillips oil research and development, the pilot plant of first resin was built in 1967, begin commodity production in the Borger of Texas SBC factory in October, 1972, and up to the present the yearly capacity in the world may surpass 500,000 tons.K-Resin is known as the transparent anti-impact resin of butylbenzene again, it is a butadiene-styrene block copolymer, its main characteristic is high transparent, high impact properties and nontoxicity, it is the modified product of general purpose polystyrene, not only keep the transparency of general purpose polystyrene excellence and good processibility, and overcome deadly defects such as the fragility of general purpose polystyrene and environmental stress crack resistance difference.With some other shock proof transparent material: polycarbonate, rhodia, synthetic glass or modified organic glass are compared, though the shock strength of the transparent anti-impact resin of butylbenzene not as they, the very big advantage of tool on cost, processing characteristics.Therefore, it is widely used for fields such as food product pack, medical treatment product, toy for children, office appliance.The weight percentage of divinyl is generally 20-35% among the K-Resin, though it has overcome shortcomings such as the fragility of general purpose polystyrene and environmental stress crack resistance, but compare its rigidity loss with general purpose polystyrene bigger, application in some field is unsatisfactory, therefore in the long-term inflexible Application Areas of needs, K-Resin can not replace general purpose polystyrene fully.
Summary of the invention
The object of the present invention is to provide a kind of transparent phenylethylene-dialkene star shaped copolymer and continuous preparation method thereof, monomer conversion of the present invention is very high,〉99.999%, production cost is low, is easy to be accepted by market the continuous processing production technique, has the reaction times weak point, output is big, and running cost is low, safeguards simple, unconverted monomer and solvent do not have leakage in the production process, can recycle safety and environmental protection, the characteristics of applied range.
In order to achieve the above object, technical scheme of the present invention is:
A kind of transparent phenylethylene-dialkene star shaped copolymer is characterized in that this multipolymer has following structure: (PS-PB-PB/PS-PS) n-R or (PS-PB-PB/PS) n-R.Wherein, PS is that polystyrene block, PB are that polydiolefin block, PB/PS are the phenylethylene-dialkene block of random copolymer, and R is " nuclear " of star structure.The molecular-weight average of phenylethylene-dialkene star shaped copolymer is 8 * 10 4-8 * 10 6, 3-10 bar " arm " is arranged, i.e. n=3-10.The weight percentage of diolefine is 0.1-19.9% in the phenylethylene-dialkene star shaped copolymer, and the weight ratio of vinylbenzene and diolefine is 99.9:0.1-80.1:19.9, and its mist degree is less than 3%, and transparency is greater than 85%.
Described diolefine is 1,3-butadiene and 2-methyl isophthalic acid, one or both in the 3-butadiene.
The phase farmland of described polymer P B block is of a size of 100-400nm, phase farmland size is the size of system polydiolefin phase structure that block forms, that can observe in the photo of electron microscope or atomic force microscope arrives, its size also can be clear and definite measure, its size directly has influence on the transparency of polymkeric substance.
The continuous preparation method of described transparent phenylethylene-dialkene star shaped copolymer, comprise the steps: that phenylethylene-dialkene star shaped copolymer adopts the negatively charged ion continuous polymerization method, at first the monomer styrene with liquid state carries out one-step polymerization with being pumped in the flow reactor; Treat that one section monomer conversion reaches 95% and adds diolefine when above and carry out two sections polymerizations; , added diolefine and cinnamic mix monomer and carry out polymerization greater than 95% o'clock at two sections monomer conversions, make it contain the PB/PS block; If need, can continue to add vinylbenzene and carry out polymerization; Add coupling agent at last, form the molecular structure of star.The weight percent that makes diolefine in the polymkeric substance in the polymerization process is 0.1-19.9%, add catalyzer in the polymerization process, polymerization ends and adds terminator, monomer or monomer solution exist with liquid state all the time in whole polymerization process, and polymkeric substance exists with fusion, solution, slurry or solid state, after polyreaction finished, final reacting product directly entered recovery system and carries out MONOMER RECOVERY, and the polymkeric substance that obtains carries out obtaining phenylethylene-dialkene star shaped copolymer after the subsequent disposal.
Described negatively charged ion continuous polymerization method is a kind of in solution polymerization and the mass polymerization.
Described solution polymerization is meant that adding a certain amount of solvent in monomer carries out premix, and solvent and monomeric volume ratio are 100:1-1:100, and reacted final product needs solvent is reclaimed after entering recovery system.
The solvent that described and monomer carry out premix is one or more of ethylene dichloride, hexanaphthene, normal hexane, benzene,toluene,xylene, hexane, tetrahydrofuran (THF), acetone, heptane, sherwood oil, dioxolane, dioxane, dioxy seven rings and three oxygen, eight rings.
Catalyzer in the described polymerization process is a lithium alkylide.
The polymerization time of described polyreaction is 0.5-120min, polymeric reaction temperature is-and 20-200 ℃.
Described flow reactor adopts continuous tubular reactor, forward to carry single screw extrusion machine, oppositely carry single screw extrusion machine, forward to carry reciprocating type single screw extrusion machine, oppositely carry reciprocating type single screw extrusion machine, forward to carry in the same way with Heterodromy double-screw extruder, oppositely carry and carry four screw extruder with Heterodromy double-screw extruder, forward in the same way and oppositely carry a kind of in the four screw extruder, and its length-to-diameter ratio is 10-200.
Beneficial effect of the present invention is: transparent phenylethylene-dialkene star shaped copolymer of the present invention possesses the rigidity of general purpose polystyrene and the toughness of HIPS, have low haze similar and high transparent again, filled up the blank of present phenylethylene resin series Application Areas to K-Resin; And styrene monomer residual employing anionoid polymerization, monomer conversion very high (〉 99.999%), so in the product is extremely low; The more important thing is that production cost is low, be easy to be accepted by market.What the present invention adopted is flow reactor continuous processing production technique, and this technological reaction time is short, and output is big, and running cost is low, safeguards that simply unconverted monomer and solvent do not have leakage in the production process, can recycle safety and environmental protection.Phenylethylene-dialkene star shaped copolymer applied range of the present invention can be widely used in stationery, clothes rack capable, vehicle lampshade, hard food holds and fields such as packing box, medical device, toy, artwork ornaments.
Embodiment
Embodiment 1
The working temperature that with length-to-diameter ratio is 200 reverse conveying four screw extruder is controlled at 200 ℃, and rotating speed is controlled to be 30r/min.The monomer styrene of liquid state carries out one-step polymerization with being pumped in the reverse conveying four screw extruder; Treat that one section monomer conversion reaches 95% and adds 1,3-butadiene when above and carry out two sections polymerizations; Two sections monomer conversions added 1,3-butadiene greater than 95% o'clock and carry out three stage polymerization with cinnamic mix monomer, added vinylbenzene then and carried out four sections polymerizations, added coupling agent at last, the molecular structure of formation 3 " arm " star.The weight ratio of vinylbenzene and 1,3-butadiene is in the polymerization process: 80.1:19.9.Then by adopt German Bruker nuclear magnetic resonance analyser ( 1H NMR) measure diene content, the weight percent that obtains 1,3-butadiene in the final polymkeric substance is 19.9%, and is as shown in table 1, and table 1 is the basic parameter table of polymkeric substance of the present invention; Add the catalyzer lithium alkylide in the polymerization process, total polymerization time is 60min.All added a certain amount of solvents tetrahydrofurane in above-mentioned arbitrary process monomer and carried out premix, solvent and monomeric volume ratio are 1:100.Polymeric reaction temperature is 200 ℃.Polymerization ends and adds terminator water.Monomer solution exists with liquid state all the time in whole polymerization process, and polymkeric substance exists with solution state.What carried out this moment is solution anionoid polymerization.After polyreaction finishes, final reacting product directly enters the recovery that recovery system is carried out monomer and solvent, the polymkeric substance that obtains carries out obtaining transparent phenylethylene-dialkene star shaped copolymer after the subsequent disposal, adopts U.S. Waters gel permeation chromatograph (GPC) to measure its molecular-weight average to be: 8 * 10 4The phase farmland dimension measurement that adopts U.S. NanoScope III atomic force microscope (AFM, percussion mode) to carry out the PB block is: 400nm.
Embodiment 2
With length-to-diameter ratio is that 140 forward carries the working temperature of single screw extrusion machine to be controlled at-10 ℃, and rotating speed is controlled to be 30r/min.The monomer styrene of liquid state carries out one-step polymerization with being pumped in the forward conveying single screw extrusion machine; Treat that one section monomer conversion reaches 95% and adds the 2-methyl isophthalic acid when above, the 3-divinyl carries out two sections polymerizations; Two sections monomer conversions added the 2-methyl isophthalic acid greater than 95% o'clock, and 3-divinyl and cinnamic mix monomer carry out three stage polymerization, add coupling agent at last, form the molecular structure of 10 " arm " star.Vinylbenzene and 2-methyl isophthalic acid in the polymerization process, the weight ratio of 3-divinyl is: 88.0:12.0.Then by adopt German Bruker nuclear magnetic resonance analyser ( 1H NMR) measure diene content, obtain 2-methyl isophthalic acid in the final polymkeric substance, the weight percent of 3-divinyl is 12%, and is as shown in table 1, and table 1 is the basic parameter table of polymkeric substance of the present invention; Add the catalyzer lithium alkylide in the polymerization process, total polymerization time is 20min.Polymeric reaction temperature is-10 ℃.Polymerization ends and adds terminator methyl alcohol.Monomer exists with liquid state all the time in whole polymerization process, and polymkeric substance exists with molten state.What carried out this moment is the body anionic polymerization.After polyreaction finishes, final reacting product directly enters the recovery that recovery system is carried out monomer and solvent, the polymkeric substance that obtains carries out obtaining transparent phenylethylene-dialkene star shaped copolymer after the subsequent disposal, adopts U.S. Waters gel permeation chromatograph (GPC) to measure its molecular-weight average to be: 2 * 10 5The phase farmland dimension measurement that adopts U.S. NanoScope III atomic force microscope (AFM, percussion mode) to carry out the PB block is: 200nm.
Embodiment 3
The working temperature that with length-to-diameter ratio is 10 the reciprocating type single screw extrusion machine of reverse conveying is controlled at 80 ℃, and rotating speed is controlled to be 30r/min.The monomer styrene of liquid state carries out one-step polymerization with being pumped in the reciprocating type single screw extrusion machine of reverse conveying; Treat that one section monomer conversion reaches 95% and adds 1,3-butadiene when above and carry out two sections polymerizations; Two sections monomer conversions added 1,3-butadiene greater than 95% o'clock and carry out three stage polymerization with cinnamic mix monomer, added coupling agent at last, the molecular structure of formation 5 " arm " star.The weight ratio of vinylbenzene and 1,3-butadiene is in the polymerization process: 92.0:8.0, then by adopt German Bruker nuclear magnetic resonance analyser ( 1HNMR) measure diene content, the weight percent that obtains 1,3-butadiene in the final polymkeric substance is 8%, and is as shown in table 1, and table 1 is the basic parameter table of polymkeric substance of the present invention; Add the catalyzer lithium alkylide in the polymerization process, total polymerization time is 75min.All added a certain amount of solvent dioxane in above-mentioned arbitrary process monomer and carried out premix, solvent and monomeric volume ratio are 20:100.Polymeric reaction temperature is 80 ℃.Polymerization ends and adds terminator ethanol.Monomer solution exists with liquid state all the time in whole polymerization process, and newly-generated polymkeric substance and monomer and solvent can not mix when temperature is high, so polymkeric substance exists with slurry state.What carried out this moment is solution anionoid polymerization.After polyreaction finishes, final reacting product directly enters the recovery that recovery system is carried out monomer and solvent, the polymkeric substance that obtains carries out obtaining transparent phenylethylene-dialkene star shaped copolymer after the subsequent disposal, adopts U.S. Waters gel permeation chromatograph (GPC) to measure its molecular-weight average to be: 6 * 10 6The phase farmland dimension measurement that adopts U.S. NanoScope III atomic force microscope (AFM, percussion mode) to carry out the PB block is: 180nm.
Embodiment 4
The working temperature of continuous tubular reactor is controlled at 0 ℃, and material flow is controlled to be 3m/min.The monomer styrene of liquid state carries out one-step polymerization with being pumped in the continuous tubular reactor; Treat that one section monomer conversion reaches 95% and adds 1,3-butadiene when above and carry out two sections polymerizations; Two sections monomer conversions added 1,3-butadiene greater than 95% o'clock and carry out three stage polymerization with cinnamic mix monomer, added vinylbenzene then and carried out four sections polymerizations, added coupling agent at last, the molecular structure of formation 4 " arm " star.The weight ratio of vinylbenzene and 1,3-butadiene is in the polymerization process: 99.9:0.1.Then by adopt German Bruker nuclear magnetic resonance analyser ( 1H NMR) measure diene content, the weight percent that obtains 1,3-butadiene in the final polymkeric substance is 0.1%, and is as shown in table 1, and table 1 is the basic parameter table of polymkeric substance of the present invention; Add the catalyzer lithium alkylide in the polymerization process, total polymerization time is 10min.Polymeric reaction temperature is 0 ℃.Polymerization ends and adds terminator water.Monomer exists with liquid state all the time in whole polymerization process, and polymkeric substance exists with molten state.What carried out this moment is the body anionic polymerization.After polyreaction finishes, final reacting product directly enters the recovery that recovery system is carried out monomer and solvent, the polymkeric substance that obtains carries out obtaining transparent phenylethylene-dialkene star shaped copolymer after the subsequent disposal, adopts U.S. Waters gel permeation chromatograph (GPC) to measure its molecular-weight average to be: 8 * 10 6The phase farmland dimension measurement that adopts U.S. NanoScope III atomic force microscope (AFM, percussion mode) to carry out the PB block is: 100nm.
Embodiment 5
Embodiment 1-4 is compared with the fundamental property of general PS, HIPS and K-Resin.Wherein tensile yield strength and elongation at break all adopt American I nstra universal testing machine to measure, and the Izod shock strength adopts the Taiwan HK-5047 of remittance section type shock strength machine to measure.Shao's formula hardness adopts outstanding grace LX-D type duroplasts Shao formula sclerometer to measure.Transparence adopts DRK122 type photoelectricity haze meter to measure.As shown in table 2, table 2 is polymkeric substance of the present invention, PS, HIPS and K-Resin fundamental property test result; Transparent phenylethylene-dialkene star shaped copolymer tensile yield strength of the present invention as can be seen from Table 2 all is higher than K-Resin, and wherein high molecular weight products (6 * 10 6With 8 * 10 6) tensile yield strength in addition surpassed general PS and HIPS; Elongation at break and Izod shock strength are between general PS and K-Resin; Shao's formula hardness is a little less than general PS, and suitable in K-Resin; Transparence and general PS and K-Resin are suitable substantially, and far above HIPS.This shows that transparent phenylethylene-dialkene star shaped copolymer of the present invention possesses the rigidity of general purpose polystyrene, have low haze similar and high transparent again, filled up the blank of present phenylethylene resin series Application Areas to K-Resin.
Table 1
Basic parameter Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4
Molecular-weight average 80,000 20,0000 600,0000 800,0000
Diene content (wt) % 19.9 12.0 8.0 0.1
The diolefine kind 1,3-butadiene The 2-methyl isophthalic acid, the 3-divinyl 1,3-butadiene 1,3-butadiene
The bar number of " arm " in the molecule 3 10 5 4
Synthetic catalyst Lithium alkylide Lithium alkylide Lithium alkylide Lithium alkylide
Table 2
Test event Testing standard Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4 General PS HIPS K-Resin
Tensile yield strength (MPa) ASTM-D638 26 30 50 70 46 31 23.7
Elongation at break (%) ASTM-D638 25 20 8 2 2 23 30
Izod shock strength (J/m) ASTM-D256 31 27 25 23 19.7 64 30
Shao's formula hardness (D) ASTM-D2440 65 65 67 72 72 70 64
Transparence (%) ASTM-D1003 87 90 91 93 92 65 90

Claims (10)

1, a kind of transparent phenylethylene-dialkene star shaped copolymer is characterized in that this multipolymer has following structure: (PS-PB-PB/PS-PS) n-R or (PS-PB-PB/PS) n-R; Wherein, PS is that polystyrene block, PB are that polydiolefin block, PB/PS are the phenylethylene-dialkene block of random copolymer, and R is " nuclear " of star structure; The molecular-weight average of phenylethylene-dialkene star shaped copolymer is 8 * 10 4-8 * 10 6, 3-10 bar " arm " is arranged, i.e. n=3-10; The weight percentage of diolefine is 0.1-19.9% in the phenylethylene-dialkene star shaped copolymer, and the weight ratio of vinylbenzene and diolefine is 99.9:0.1-80.1:19.9, and its mist degree is less than 3%, and transparency is greater than 85%.
2, transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 1 is characterized in that: described diolefine is 1,3-butadiene and 2-methyl isophthalic acid, one or both in the 3-butadiene.
3, transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 1 is characterized in that: the phase farmland of described polymer P B block is of a size of 100-400nm.
4, a kind of continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 1, it is characterized in that: phenylethylene-dialkene star shaped copolymer adopts the negatively charged ion continuous polymerization method, and at first the monomer styrene with liquid state carries out one-step polymerization with being pumped in the flow reactor; Treat that one section monomer conversion reaches 95% and adds diolefine when above and carry out two sections polymerizations; , added diolefine and cinnamic mix monomer and carry out polymerization greater than 95% o'clock at two sections monomer conversions, make it contain the PB/PS block; If need, can continue to add vinylbenzene and carry out polymerization; Add coupling agent at last, form the molecular structure of star; The weight percent that makes diolefine in the polymkeric substance in the polymerization process is 0.1-19.9%, add catalyzer in the polymerization process, polymerization ends and adds terminator, monomer or monomer solution exist with liquid state all the time in whole polymerization process, and polymkeric substance exists with fusion, solution, slurry or solid state, after polyreaction finished, final reacting product directly entered recovery system and carries out MONOMER RECOVERY, and the polymkeric substance that obtains carries out obtaining phenylethylene-dialkene star shaped copolymer after the subsequent disposal.
5, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 4 is characterized in that: described negatively charged ion continuous polymerization method is a kind of in solution polymerization and the mass polymerization.
6, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 5, it is characterized in that: described solution polymerization is meant that adding a certain amount of solvent in monomer carries out premix, solvent and monomeric volume ratio are 100:1-1:100, need solvent is reclaimed after reacted final product enters recovery system.
7, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 6 is characterized in that: the solvent that described and monomer carry out premix is one or more of ethylene dichloride, hexanaphthene, normal hexane, benzene,toluene,xylene, hexane, tetrahydrofuran (THF), acetone, heptane, sherwood oil, dioxolane, dioxane, dioxy seven rings and three oxygen, eight rings.
8, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 4, it is characterized in that: the catalyzer in the described polymerization process is a lithium alkylide.
9, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 4, it is characterized in that: the polymerization time of described polyreaction is 0.5-120min, polymeric reaction temperature is-20-200 ℃.
10, the continuous preparation method of transparent phenylethylene-dialkene star shaped copolymer as claimed in claim 4, it is characterized in that: described flow reactor adopts continuous tubular reactor, forward is carried single screw extrusion machine, oppositely carry single screw extrusion machine, forward is carried reciprocating type single screw extrusion machine, oppositely carry reciprocating type single screw extrusion machine, forward is carried in the same way and Heterodromy double-screw extruder, oppositely carry in the same way and Heterodromy double-screw extruder, forward is carried four screw extruder and is oppositely carried a kind of in the four screw extruder, and its length-to-diameter ratio is 10-200.
CN2009100954663A 2009-01-15 2009-01-15 Transparent phenylethylene-dialkene star shaped copolymer and continuous preparation thereof Expired - Fee Related CN101475673B (en)

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WO2016127353A1 (en) * 2015-02-12 2016-08-18 浙江三博聚合物有限公司 Hydrogenated styrene thermoplastic elastomer and preparation method therefor
CN106397696A (en) * 2016-08-31 2017-02-15 广东众和化塑有限公司 SBS elastomer simultaneously having high transmittance, high twisting resistance and high foaming efficiency, and production method thereof
CN110621739A (en) * 2017-03-16 2019-12-27 英力士苯领集团股份公司 High-softness, non-stick and transparent styrene thermoplastic elastomer composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016127353A1 (en) * 2015-02-12 2016-08-18 浙江三博聚合物有限公司 Hydrogenated styrene thermoplastic elastomer and preparation method therefor
CN106397696A (en) * 2016-08-31 2017-02-15 广东众和化塑有限公司 SBS elastomer simultaneously having high transmittance, high twisting resistance and high foaming efficiency, and production method thereof
CN106397696B (en) * 2016-08-31 2019-03-22 广东众和化塑有限公司 It is a kind of to be provided simultaneously with high saturating, highly resistance tortuosity and SBS elastomer of high-foaming efficiency and preparation method thereof
CN110621739A (en) * 2017-03-16 2019-12-27 英力士苯领集团股份公司 High-softness, non-stick and transparent styrene thermoplastic elastomer composition
CN110621739B (en) * 2017-03-16 2022-12-27 英力士苯领集团股份公司 High-softness, non-stick and transparent styrene thermoplastic elastomer composition

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