CN1242380A - Seven block co-polymer of butadiene, isoprene and styrene, and method for prepn. of same - Google Patents
Seven block co-polymer of butadiene, isoprene and styrene, and method for prepn. of same Download PDFInfo
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- CN1242380A CN1242380A CN 99111139 CN99111139A CN1242380A CN 1242380 A CN1242380 A CN 1242380A CN 99111139 CN99111139 CN 99111139 CN 99111139 A CN99111139 A CN 99111139A CN 1242380 A CN1242380 A CN 1242380A
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Abstract
The present invention relates to a kind of butadiene, isoprene, styrene heptablock copolymer and its preparation method. Said block copolymer includes the following two kinds of symmetrical structure: S-IS-I-B-I-IS-S, in which S is polystyrene block, B is polybutadiene block, I is polyisoprene block, IS is isoprene and styrene ladder copolymer block, in which the styrene content is 10%-50% (wt%), isoprene content is 10%-75% (wt%) and butadiene content is 10%-75% (wt%).
Description
The present invention relates to a class divinyl, isoprene, vinylbenzene seven segmented copolymers and preparation method thereof, this based block copolymer has following symmetrical structure: S-IS-I-B-I-IS-S, wherein: S is a polystyrene block, B is a polybutadiene block, I is a polyisoprene blocks, and IS is isoprene, the trapezoidal copolymer block of vinylbenzene.
Usually based on divinyl, isoprene, three kinds of monomeric segmented copolymers of vinylbenzene SBS, SIS are arranged; SBS is a divinyl, (wherein: B is a polybutadiene block to styrene triblock copolymer; S is a polystyrene block); SIS is isoprene, styrene triblock copolymer (wherein: I is a polyisoprene blocks, and S is a polystyrene block).With the bifunctional lithium alkylide is initiator, change the order of addition(of ingredients) of divinyl, isoprene, styrene monomer, can obtain the segmented copolymer of different structure, this based block copolymer comprises following symmetrical structure: (1) S-I-BI-B-BI-I-S (divinyl and isoprene once add, vinylbenzene list add); (2) S-I-B-I-S (divinyl, isoprene, vinylbenzene add in proper order); (3) S-B-I-B-S (isoprene, divinyl, vinylbenzene add in proper order); When the divinyl list adds, isoprene and vinylbenzene add fashionablely simultaneously, can make S-IS-I-B-I-IS-S; Wherein: S is a polystyrene block, and B is a polybutadiene block, and I is a polyisoprene blocks, and BI is divinyl, the trapezoidal copolymer block of isoprene, and IS is isoprene, the trapezoidal copolymer block of vinylbenzene.
The objective of the invention is to prepare a class based on divinyl, isoprene, three kinds of monomeric polynary segmented copolymers of vinylbenzene, this based block copolymer is the broad-spectrum thermoplastic elastic material of a class with the performance of SBS and SIS excellence.Hydrogenation S-IS-I-B-I-IS-S can be used for preparing heat-sensitive glue and pressure sensitive adhesive, has the advantage that general SBS, SIS can't compare.
Technical characterictic of the present invention is the B section among the common SBS, I section among the SIS are replaced divinyl, two kinds of monomers of isoprene by common a kind of monomer, and I section, B section and trapezoidal copolymer block IS exist simultaneously.
Prepared divinyl, isoprene, vinylbenzene seven segmented copolymers of the present invention have following symmetrical structure: S-IS-I-B-I-IS-S.The number-average molecular weight of segmented copolymer (Mn) general range is 5 * 10
4-35 * 10
4, optimum range is 10 * 10
4-25 * 10
4The general range of monomer styrene consumption is 10%-45% (weight percent, below identical), and optimum range is 20%-40%; The general range of isoprene consumption is 10%-75%, and optimum range is 20%-50%; The general range of divinyl consumption is 10%-75%, and optimum range is 20%-50%.1.2-the polybutadiene content general range is 6%-35% (weight percent, below identical), optimum range is 10%-20%; 3.4-polyisoprene content general range is 6%-35% (weight percent, below identical), optimum range is 10%-20%.
Divinyl involved in the present invention, isoprene, seven segmented copolymer preparation methods are as follows for vinylbenzene: once join divinylic monomer in the reactor by monomer ratio in the non-polar hydrocarbon kind solvent, monomer concentration is 10%-20% (weight percent), the non-polar hydrocarbon kind solvent is selected from a kind of varsol in nonpolar aromatic hydrocarbons and the nonpolar fatty hydrocarbon or the mixture of several varsols, generally be selected from: benzene, toluene, ethylbenzene, dimethylbenzene, pentane, hexane, heptane, octane, hexanaphthene, Mixed XYLENE, raffinate oil, open stirring, after reaching kick off temperature, the initiation reaction temperature is 30 ℃-80 ℃, adding the bifunctional lithium alkylide is initiator, the consumption of bifunctional alkyl lithium initiator is decided according to the size of multipolymer number-average molecular weight, and the number-average molecular weight scope of segmented copolymer is generally 5 * 10
4-35 * 10
4The bifunctional alkyl lithium initiator is selected from the mixture of a kind of bifunctional alkyl lithium initiator or several bifunctional alkyl lithium initiators, generally be selected from two lithiums of two haloalkane hydro carbons and the two lithiums of oligopolymer thereof, the two lithiums of naphthalene class, two lithiums of diene hydro carbons and the two lithiums of oligopolymer thereof, after the divinyl total overall reaction finishes, once join isoprene and styrene monomer in the reactor by monomer ratio again, begin to prepare I, IS, the S block, after isoprene and vinylbenzene total overall reaction are finished, add anti-aging agent (1010 with weight ratio 1: 1 mix with 2.6.4), adopt traditional method that the polymkeric substance glue is carried out aftertreatment, carry out analytical test behind the product drying, obtain S-IS-I-B-I-IS-S seven segmented copolymers.
Non-polar organic solvent used in the present invention is selected from a kind of varsol in nonpolar aromatic hydrocarbons and the nonpolar fatty hydrocarbon or the mixture of several varsols, generally be selected from: benzene, toluene, ethylbenzene, dimethylbenzene, pentane, hexane, heptane, octane, hexanaphthene, BTX aromatics (as: Mixed XYLENE), mixing-in fat hydrocarbon (as: raffinating oil), preferably from: hexane, hexanaphthene, raffinate oil.
Initiator used in the present invention is the bifunctional alkyl lithium initiator, be selected from the mixture of a kind of bifunctional alkyl lithium initiator or several bifunctional alkyl lithium initiators, as: two lithiums of two haloalkane hydro carbons and the two lithiums of oligopolymer thereof, as: LiRLi, Li (DO) nR (DO) nLi, wherein: R is that carbonatoms is the alkyl of 4-10, and DO is that carbonatoms is a kind of conjugated diene of 4-8 or the mixture of several conjugated dienes, with 1, the 3-divinyl, isoprene is good, n is the oligomerisation degree, and n is generally 2-8, is good with 3-6, two lithiums of two haloalkane hydro carbons and the two lithiums of oligopolymer thereof are selected from: 1,4-two lithium butane, 1,2-two lithiums-1,2-diphenylethane, 1,4-two lithiums-1,1,4,4-tetraphenyl butane, 1,4-dimethyl-1,4-diphenyl butane two lithiums, polyisoprene two lithium oligopolymers, polyhutadiene two lithium oligopolymers; The two lithiums of naphthalene class are selected from: naphthalene lithium, alpha-methyl-naphthalene lithium; Two lithiums of diene hydro carbons and the two lithiums of oligopolymer thereof are selected from: 1,1 '-(1, the 3-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] two lithiums, 1,1 '-(1, the 3-penylene)-two two lithiums of [3-methyl isophthalic acid-(4-tolyl) amyl group] butadiene oligomer, 1,1 '-(1, the 3-penylene)-two two lithiums of [3-methyl isophthalic acid-(4-tolyl) amyl group] isoprene oligopolymer, 1,1 '-(1, the 4-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] two lithiums, the two lithiums of 1,1 '-(1, the 4-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] butadiene oligomer, 1, the two lithiums of 1 '-(1, the 4-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] isoprene oligopolymer.
Further specify the present invention below in conjunction with embodiment, but and the scope of unrestricted claim protection of the present invention.Embodiment 1
In 5 liters of stainless steel cauldrons that have a stirring, add 3.5 liters of hexanaphthenes, 105 gram divinyl, be warmed up to 50 ℃, add bifunctional alkyl lithium initiator 1, the two lithiums in 1 '-(1, the 3-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group], the multipolymer number-average molecular weight is 15 * 10
4The isoprene polymerization reaction is all finished when polyreaction proceeds to 30 minutes, add 140 gram isoprene and 105 gram vinylbenzene again, continue reaction 60 minutes, after the reaction of isoprene and styrene polymerization is all finished, add anti-aging agent (1010 with weight ratio 1: 1 mixes with 2.6.4) 3.5 and restrain, the employing traditional method is carried out the glue aftertreatment, classical way specimen structure and mechanical property are adopted in dry back, and the result is as shown in table 1.Embodiment 2-7
Polymerization process and processing condition are with embodiment 1, and just vinylbenzene, isoprene, divinylic monomer proportioning difference have prepared S-IS-I-B-I-IS-S seven segmented copolymers, and polymerization process condition, product structure transitivity test result are respectively shown in 2-7 in the table 1.Table 1 polymerization process condition and product rerum natura
Annotate: S is a styrene content, and I is an isoprene content, and B is a butadiene content, and S/I/B is vinylbenzene, isoprene, divinylic monomer proportioning.
| Embodiment | ????1 | ????2 | ????3 | ????4 | ????5 | ????6 | ????7 |
| ??S(g) | ????105 | ????105 | ????105 | ????140 | ????140 | ????70 | ????70 |
| ??I(g) | ????140 | ????105 | ????70 | ????105 | ????70 | ????140 | ????105 |
| ??B(g) | ????105 | ????140 | ????175 | ????105 | ????140 | ????140 | ????175 |
| ??S/I/B | ????3/4/3 | ????3/3/4 | ????3/2/5 | ????4/3/3 | ????4/2/4 | ????2/4/4 | ????2/3/5 |
| Tensile strength (MPa) | ????16.5 | ????17.0 | ????18.8 | ????22.0 | ????20.7 | ????14.6 | ????15.8 |
| Elongation at break (%) | ????1280 | ????1250 | ????1050 | ????1060 | ????980 | ????1480 | ????1250 |
Claims (15)
1. a class divinyl, isoprene, vinylbenzene seven segmented copolymers, it is characterized in that this multipolymer has following symmetrical structure: S-IS-I-B-I-IS-S, wherein: S is a polystyrene block, B is a polybutadiene block, I is a polyisoprene blocks, IS is isoprene, the trapezoidal copolymer block of vinylbenzene, monomer styrene content is 10%-50% (weight percent), the monomer isoprene content is 10%-75% (weight percent), and the monomer butadiene content is 10%-75% (weight percent).
2. segmented copolymer according to claim 1, wherein the number-average molecular weight of segmented copolymer is 5 * 10
4-50 * 10
4
3. segmented copolymer according to claim 2, wherein the number-average molecular weight of segmented copolymer is 10 * 10
4-30 * 10
4
4. segmented copolymer according to claim 1, monomer styrene content are 20%-40% (weight percent).
5. segmented copolymer according to claim 1, monomer isoprene content are 20%-50% (weight percent).
6. segmented copolymer according to claim 1, monomer butadiene content are 20%-50% (weight percent).
7. segmented copolymer according to claim 1, in the polyhutadiene 1, the 2-structural content is not more than 35% (weight percent), and in the polyisoprene 3, the 4-structural content is not more than 35% (weight percent).
8. segmented copolymer according to claim 7, in the polyhutadiene 1, the 2-structural content is not more than 20% (weight percent), and in the polyisoprene 3, the 4-structural content is not more than 20% (weight percent).
9. a class divinyl, isoprene, the preparation method of vinylbenzene seven segmented copolymer S-IS-I-B-I-IS-S, it is characterized in that: in the non-polar hydrocarbon kind solvent, once join divinylic monomer in the reactor by monomer ratio, divinylic monomer content is 10%-75% (weight percent), monomer concentration is 10%-20% (weight percent), the non-polar hydrocarbon kind solvent is selected from a kind of varsol in nonpolar aromatic hydrocarbons and the nonpolar fatty hydrocarbon or the mixture of several varsols, open stirring, after reaching kick off temperature, the initiation reaction temperature is 30 ℃-80 ℃, adding the bifunctional lithium alkylide is initiator, the consumption of bifunctional alkyl lithium initiator is decided according to the size of multipolymer number-average molecular weight, and the number-average molecular weight of segmented copolymer is 5 * 10
4-50 * 10
4The bifunctional alkyl lithium initiator is selected from two lithiums of two haloalkane hydro carbons and the two lithiums of oligopolymer thereof, the two lithiums of naphthalene class, a kind of bifunctional alkyl lithium initiator in two lithiums of diene hydro carbons and the two lithiums of oligopolymer thereof or the mixture of several bifunctional alkyl lithium initiators, after polymerizing butadiene is all finished, once join isoprene and styrene monomer in the reactor by monomer ratio again, isoprene content is 10%-75% (weight percent), styrene content is 10%-50% (weight percent), begin to prepare I, IS, the S block, after isoprene and styrene polymerization are all finished, add anti-aging agent, anti-aging agent is four [3-(3 ' 5 '-di-t-butyl-4 '-hydroxy phenyl) propionic acid] pentaerythritol ester and 2, the 6-di-tert-butyl-4-methy phenol mixes with weight ratio at 1: 1, aging inhibitor dosage is calculated with 1% of polymer weight, adopt traditional method that the polymkeric substance glue is carried out aftertreatment, carry out analytical test behind the product drying, obtain S-IS-I-B-I-IS-S seven segmented copolymers.
10. method according to claim 9, two lithiums of wherein two haloalkane hydro carbons and the two lithiums of oligopolymer thereof are selected from: LiRLi, Li (DO) nR (DO) nLi, R is that carbonatoms is the alkyl of 4-10, DO is that carbonatoms is a kind of conjugated diene of 4-8 or the mixture of several conjugated dienes, n is the oligomerisation degree, and n is 2-8.
11. method according to claim 10, wherein conjugated diene is preferably from divinyl, isoprene, and oligomerisation degree n is 3-6.
12. method according to claim 9, wherein two lithiums of diene hydro carbons and oligopolymer dilithium initiator thereof are selected from: 1,1 '-(1, the 3-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] two lithiums, 1,1 '-(1, the 3-penylene)-two two lithiums of [3-methyl isophthalic acid-(4-tolyl) amyl group] butadiene oligomer, 1,1 '-(1, the 3-penylene)-two two lithiums of [3-methyl isophthalic acid-(4-tolyl) amyl group] isoprene oligopolymer, 1,1 '-(1, the 4-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] two lithiums, 1,1 '-(1, the 4-penylene)-two two lithiums of [3-methyl isophthalic acid-(4-tolyl) amyl group] butadiene oligomer, the two lithiums of 1,1 '-(1, the 4-penylene)-two [3-methyl isophthalic acid-(4-tolyl) amyl group] isoprene oligopolymer.
13. method according to claim 9, wherein the two lithiums of naphthalene class are selected from: naphthalene lithium, alpha-methyl-naphthalene lithium.
14. method according to claim 9, wherein the non-polar hydrocarbon kind solvent is selected from: benzene, toluene, ethylbenzene, dimethylbenzene, pentane, hexane, heptane, octane, hexanaphthene, Mixed XYLENE, raffinate oil.
15. method according to claim 14, wherein the non-polar hydrocarbon kind solvent is selected from: hexane, hexanaphthene, raffinate oil.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN99111139A CN1108322C (en) | 1999-07-28 | 1999-07-28 | Seven block co-polymer of butadiene, isoprene and styrene, and method for prepn. of same |
| US09/627,105 US6372853B1 (en) | 1999-07-28 | 2000-07-27 | Butadiene/isoprene/monovinyl aromatic monomer heptablock copolymers and method for the preparation thereof |
| EP00949042A EP1211272B1 (en) | 1999-07-28 | 2000-07-28 | Butadiene/isoprene/aromatic vinyl hydrocarbon sevenblock copolymer and the preparing method thereof |
| KR1020027001190A KR100622112B1 (en) | 1999-07-28 | 2000-07-28 | Butadiene/isoprene/aromatic vinyl hydrocarbon sevenblock copolymer and the preparing method thereof |
| JP2001514016A JP4380958B2 (en) | 1999-07-28 | 2000-07-28 | Heptablock copolymer of butadiene / isoprene / monovinyl aromatic monomer and process for producing the same |
| DE60036387T DE60036387T2 (en) | 1999-07-28 | 2000-07-28 | BUTADIENE / ISOPRENE / AROMATIC VINYL CARBON DIOXIDE SEPARATE COPOLYMER AND ITS PRODUCTION PROCESS |
| AU62576/00A AU6257600A (en) | 1999-07-28 | 2000-07-28 | Butadiene/isoprene/aromatic vinyl hydrocarbon sevenblock copolymer and the preparing method thereof |
| PCT/CN2000/000214 WO2001009212A1 (en) | 1999-07-28 | 2000-07-28 | Butadiene/isoprene/aromatic vinyl hydrocarbon sevenblock copolymer and the preparing method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN99111139A CN1108322C (en) | 1999-07-28 | 1999-07-28 | Seven block co-polymer of butadiene, isoprene and styrene, and method for prepn. of same |
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| Publication Number | Publication Date |
|---|---|
| CN1242380A true CN1242380A (en) | 2000-01-26 |
| CN1108322C CN1108322C (en) | 2003-05-14 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN99111139A Expired - Fee Related CN1108322C (en) | 1999-07-28 | 1999-07-28 | Seven block co-polymer of butadiene, isoprene and styrene, and method for prepn. of same |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1266916A4 (en) * | 2000-02-17 | 2004-03-31 | China Petroleum & Chemical | Multiblock copolymer the preparing method thereof |
| CN102719207A (en) * | 2012-06-27 | 2012-10-10 | 广州市豪特粘接材料有限公司 | Hot melt adhesive |
| CN106146769A (en) * | 2015-04-24 | 2016-11-23 | 中国石油化工股份有限公司 | Block copolymer of bromination as fire retardant and preparation method thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0058952B1 (en) * | 1981-02-20 | 1984-08-22 | Asahi Kasei Kogyo Kabushiki Kaisha | A film, sheet or tube of a block copolymer or a composition containing the same |
| CA2028410C (en) * | 1990-01-02 | 1996-09-17 | William J. Trepka | Tapered block styrene/butadiene copolymers |
-
1999
- 1999-07-28 CN CN99111139A patent/CN1108322C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1266916A4 (en) * | 2000-02-17 | 2004-03-31 | China Petroleum & Chemical | Multiblock copolymer the preparing method thereof |
| CN102719207A (en) * | 2012-06-27 | 2012-10-10 | 广州市豪特粘接材料有限公司 | Hot melt adhesive |
| CN102719207B (en) * | 2012-06-27 | 2013-11-13 | 广州市豪特粘接材料有限公司 | Hot melt adhesive |
| CN106146769A (en) * | 2015-04-24 | 2016-11-23 | 中国石油化工股份有限公司 | Block copolymer of bromination as fire retardant and preparation method thereof |
| CN106146769B (en) * | 2015-04-24 | 2018-09-04 | 中国石油化工股份有限公司 | Brominated block copolymer and preparation method thereof as fire retardant |
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| Publication number | Publication date |
|---|---|
| CN1108322C (en) | 2003-05-14 |
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