CN107674166B - Hydrogenated styrene thermoplastic elastomer and synthesis method and application thereof - Google Patents

Hydrogenated styrene thermoplastic elastomer and synthesis method and application thereof Download PDF

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CN107674166B
CN107674166B CN201610701403.8A CN201610701403A CN107674166B CN 107674166 B CN107674166 B CN 107674166B CN 201610701403 A CN201610701403 A CN 201610701403A CN 107674166 B CN107674166 B CN 107674166B
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陈健
赵帅
黄旭生
金永辉
陈大魁
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Zhejiang Zhongli Synthetic Material Technology Co ltd
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Abstract

The invention relates to a hydrogenated styrene thermoplastic elastomer, a preparation method and application thereof, wherein the material is obtained by hydrogenating a styrene-isoprene-styrene triblock copolymer. The isoprene soft segment of the hydrogenated styrene thermoplastic elastomer is combined with styrene, so that the melt index of a product and the sensitivity of the viscosity of the product to temperature can be improved, and the hydrogenated styrene thermoplastic elastomer is favorable for being blended with polystyrene. The elastomer is suitable for the fields of adhesives, sealants, coatings, rubber-like compounds (which can replace vulcanized rubber), plastic modifiers, compatilizers, thermosetting resin modifiers, shrink-proofing agents of unsaturated polyester asphalt modifiers and the like.

Description

Hydrogenated styrene thermoplastic elastomer and synthesis method and application thereof
Technical Field
The invention belongs to thermoplastic elastomer materials, and particularly relates to a hydrogenated styrene thermoplastic elastomer, a synthetic method and application thereof.
Background
Thermoplastic elastomers (TPEs) are materials formed by physical network crosslinking between macromolecules, and are characterized in that the TPEs can be processed and plasticized like plastics at high temperature, and the finished products can be used as rubber elastomers at normal temperature. Styrenic thermoplastic elastomers are the thermoplastic elastomers which were first discovered and commercialized, and are one of the most widely used elastomer products today, and mainly include block copolymers synthesized from styrene and isoprene (styrene-isoprene-styrene block copolymer, abbreviated as SIS), block copolymers synthesized from styrene and butadiene (styrene-butadiene-styrene block copolymer, abbreviated as SBS), and hydrogenated products thereof, SEPS, SEBS, and the like. In the 80 s of the 20 th century, the Kuraray company first hydroprocessed SIS to develop SIS series hydrogenated products (including six types of SEPS, SEP and the like) with the brand number of
Figure BDA0001084647150000011
The SIS can greatly improve the performances of heat resistance, oxidation resistance, ozone resistance, ultraviolet irradiation resistance and other oxidation or crosslinking reaction degradation after selective hydrogenation, simultaneously improve the service temperature of the product, and improve the chemical performances of weather resistance, acid and alkali resistance and the like, as well as the wear resistance and the flexibility. The hydrogenated material of SIS has thermoplasticity of non-hydrogenated products and high elasticity of rubber at normal temperature, shows the fluidity of resin at high temperature, and can be directly processed and molded. The above-mentioned properties of the hydrogenated material make it much higher in practical applications than the conventional linear and star-shaped SIS. Currently, commercially available products of the hydrogenation product SEPS of SIS are mainly Kraton G series products from Shell corporation and SEPTON series products from Kuraray corporation in japan. The hydrogenated styrene thermoplastic elastomer material is mainly applied to adhesives, sealants, coatings, rubber-like compounds (which can replace vulcanized rubber), plastic modifiers, compatilizers, thermosetting resin modifiers and unsaturated polyester asphalt modifiersAnd shrink proofing agents.
In the styrene thermoplastic elastomer series, SEBS and SEPS are two hydrogenated styrene thermoplastic elastomers with good performance and low cost, wherein the two ends of the structure are generally polystyrene with the molecular weight of 1-2 ten thousand, and the middle section is generally ethylene/butylene-1 copolymer with the molecular weight of 3-10 thousand or ethylene/propylene copolymer with the molecular weight of 3-10 thousand. Since the solubility parameter difference between polystyrene and olefin copolymer is large, the melt index of hydrogenated styrene thermoplastic elastomer is generally small, and the processing is difficult. In order to adapt to different applications, the design of the molecular structure of the polymer is necessary. For SEBS series, Shell chemical company, from the perspective of polymer design, chemically bonds two Polyisoprene (PI) chains on the SEBS elastic network by anionic polymerization technology, and names the new product SEBS as Kraton GRP-6919. In SEBI, SEBS accounts for 64% of the molecular weight and PI for 36%. There are currently few reports on modifications to the SEPS series.
Disclosure of Invention
An object of the present invention is to provide an isoprene-styrene random polymer, a styrene-isoprene-styrene block copolymer (SIS) and a hydrogenated product thereof (the hydrogenated product of SIS is a hydrogenated-type styrene thermoplastic elastomer).
The other purpose of the invention is to provide a preparation method of the hydrogenated styrene thermoplastic elastomer.
The invention also aims to provide application of the hydrogenated styrene thermoplastic elastomer.
In order to achieve the above object, the present invention provides an isoprene-styrene random polymer, denoted as P1, comprising repeating units represented by formula (I), formula (II), and formula (III):
Figure BDA0001084647150000021
wherein the repeating unit shown in the formula (I) accounts for 5-75 mol% of the sum of the repeating units shown in the formula (I) and the formula (II);
in formula (III), R is an aryl group, preferably a phenyl group.
According to the invention, the recurring units of the formula (I) represent 6 to 70 mol%, more preferably 6.5 to 65 mol%, of the sum of the recurring units of the formulae (I) and (II).
According to the invention, the recurring units of the formula (III) represent 1 to 25 mol%, preferably 2 to 20 mol%, of the sum of the recurring units of the formulae (I), (II) and (III).
According to the present invention, the isoprene-styrene random polymer has a number average molecular weight of 2 to 25 ten thousand as measured by GPC.
The invention further provides a polymer, designated as P2, which is a hydrogenation product of the isoprene-styrene random polymer.
According to the invention, in the hydrogenation product, the degree of hydrogenation of the double bonds in the non-benzene rings is more than 98 mol%, and the degree of hydrogenation of the double bonds in the benzene rings is less than 2 mol%.
According to the invention, the degree of hydrogenation of the double bonds in the benzene rings is 50 to 98 mol% (preferably 50 to 90 mol%) and the degree of hydrogenation of the double bonds in the benzene rings is less than 2 mol%.
The invention further provides a styrene-isoprene-styrene triblock copolymer, which is marked as BP1 and has a structural formula shown as (IV):
Figure BDA0001084647150000022
in the formula (IV), two ends of the triblock copolymer are polystyrene hard sections, and the middle of the triblock copolymer is a polyisoprene soft section; the polyisoprene soft segment comprises repeating units shown as a formula (I), a formula (II) and a formula (III):
Figure BDA0001084647150000031
wherein the repeating unit shown in the formula (I) accounts for 5-75 mol% of the sum of the repeating units shown in the formula (I) and the formula (II);
in formula (III), R is an aryl group, preferably a phenyl group.
According to the invention, the recurring units of the formula (I) represent 6 to 70 mol%, more preferably 6.5 to 65 mol%, of the sum of the recurring units of the formulae (I) and (II).
According to the invention, the recurring units of the formula (III) represent 1 to 25 mol%, preferably 2 to 20 mol%, of the sum of the recurring units of the formulae (I), (II) and (III).
According to the invention, the polystyrene hard blocks constitute from 15 to 50% by weight of the mass of the triblock.
The invention also provides a hydrogenated styrene thermoplastic elastomer, which is a hydrogenated product of the styrene-isoprene-styrene triblock copolymer BP1 and is marked as BP 2.
According to the present invention, in the above thermoplastic elastomer, the degree of hydrogenation of the double bonds in the non-benzene rings is more than 98 mol% (preferably 98.1 to 99.9 mol%), and the degree of hydrogenation of the double bonds in the benzene rings is less than 2 mol%.
According to the present invention, in the above thermoplastic elastomer, the degree of hydrogenation of the double bonds in the non-benzene rings is 50 to 98 mol% (preferably 50 to 90 mol%), and the degree of hydrogenation of the double bonds in the benzene rings is less than 2 mol%.
According to the invention, the thermoplastic elastomer has a number average molecular weight, determined by GPC, of between 4 and 30 ten thousand, preferably between 5 and 25 ten thousand; the molecular weight distribution was about 1.05. The thermoplastic elastomer has a melt index of 0.05-20g/10min at 230 ℃ under the test condition of 2.16 kg.
The invention also provides a preparation method of the hydrogenated styrene thermoplastic elastomer, which comprises the following steps: (1) synthesizing the styrene-isoprene-styrene triblock copolymer with a structural formula shown in a formula (IV) by taking styrene and isoprene as raw materials by adopting an anion polymerization method; (2) hydrogenating the triblock copolymer under the action of a catalyst to prepare the hydrogenated styrene thermoplastic elastomer;
Figure BDA0001084647150000032
in the formula (IV), two ends of the triblock copolymer are polystyrene hard sections, and the middle of the triblock copolymer is a polyisoprene soft section; the polyisoprene soft segment comprises repeating units shown as a formula (I), a formula (II) and a formula (III):
Figure BDA0001084647150000041
wherein the repeating unit shown in the formula (I) accounts for 5-75 mol% of the sum of the repeating units shown in the formula (I) and the formula (II);
in formula (III), R is an aryl group, preferably a phenyl group.
According to the invention, the recurring units of the formula (I) represent 6 to 70 mol%, more preferably 6.5 to 65 mol%, of the sum of the recurring units of the formulae (I) and (II).
According to the invention, the recurring units of the formula (III) represent 1 to 25 mol%, preferably 2 to 20 mol%, of the sum of the recurring units of the formulae (I), (II) and (III).
According to the invention, the polystyrene hard blocks constitute from 15 to 50% by weight of the mass of the triblock.
According to the invention, during the polymerization of the polyisoprene soft block, a polymer microstructure modifier is added to control the content of the repeating unit shown in the formula (I).
According to the present invention, the step (1) specifically includes:
styrene and isoprene are taken as raw materials, butyl lithium is taken as an initiator, and a styrene-isoprene-styrene triblock copolymer is synthesized in a non-polar organic solvent; in order to ensure that the repeating unit represented by the formula (I) accounts for 5-75 mol% of the sum of the repeating units represented by the formula (I) and the formula (II), a polymer microstructure regulator is introduced in the soft-block polymerization process of the polyisoprene.
According to the invention, the polymeric microstructure modifier is selected from tetrahydrofuran, tetrahydrofurfuryl alcohol ethyl ether or N, N-dimethyltetrahydrofurfuryl amine.
According to the invention, the polymeric microstructure modifier is used in an amount of: 0< r < 100. Preferably 0.01< r <10, more preferably 0.05< r < 2. The r represents the molar ratio of the polymer microstructure modifier to the initiator.
According to the invention, the preparation method preferably comprises: (1) firstly, initiating styrene polymerization by using an initiator, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃; then adding a mixture of isoprene and styrene, and polymerizing in the presence of a polymer microstructure regulator, wherein the reaction time is 60-90min and the reaction temperature is 40-80 ℃; finally, adding the rest styrene for polymerization reaction, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃, so as to obtain a triblock polymer; (2) adding a nonpolar organic solvent into the obtained triblock polymer to prepare a solution, adding a hydrogenation catalyst selected from an organic nickel/alkyl aluminum catalyst or a titanocene catalyst, reacting for 1-5 hours at the temperature of 60-90 ℃ and under the condition that the hydrogen pressure is kept at 1.5-2.5MPa, and hydrogenating to obtain the hydrogenated styrene thermoplastic elastomer.
According to the invention, in step (2), the hydrogenation catalyst is selected from an organic nickel/aluminum alkyl catalyst or a titanocene catalyst.
According to the invention, when organic nickel/alkyl aluminum is used as a hydrogenation catalyst, the hydrogenation degree of double bonds in non-benzene rings in the obtained thermoplastic elastomer is more than 98 mol% (preferably 98.1-99.9 mol%), and the hydrogenation degree of double bonds in benzene rings is less than 2 mol%.
According to the invention, when the cyclopentadienyl titanium catalyst is used as the hydrogenation catalyst, the hydrogenation degree of the double bonds in the non-benzene ring in the obtained thermoplastic elastomer is 50-98 mol% (preferably 50-90 mol%), and the hydrogenation degree of the double bonds in the benzene ring is less than 2 mol%.
According to the invention, the butyllithium is selected from n-butyllithium, sec-butyllithium and tert-butyllithium.
According to the invention, the non-polar organic solvent is selected from cycloalkanes. Preferably, the cycloalkane is cyclohexane or cyclopentane. Still preferably, the cyclohexane is cyclohexane containing 30% or less of hexane.
According to the invention, the monomer concentration of styrene during the polymerization of the polystyrene hard block is between 0.1 and 20% by weight (preferably between 0.5 and 2.5% by weight); during the polymerization of the polyisoprene soft block, the monomer concentration of the mixture of isoprene and styrene is 5 to 20 wt% (preferably 6 to 10 wt%), wherein the styrene content in the mixture is 1 to 25 wt%, preferably 2 to 20 wt%.
According to the invention, the organic nickel is selected from nickel naphthenate, alkyl nickel and the like.
The hydrogenated styrene thermoplastic elastomer can be used in the fields of adhesives, sealants, coatings, rubber-like compounds (which can replace vulcanized rubber), plastic modifiers, compatilizers, thermosetting resin modifiers, shrinkage preventives for unsaturated polyester asphalt modifiers and the like.
The invention has the beneficial effects that:
the hydrogenated styrene thermoplastic elastomer provided by the invention has a hydrogenated structure with a specific content of the repeating unit shown in the formula (I), and the elastomer has good compatibility with polypropylene. Furthermore, the introduction of the repeating unit of styrene into the soft segment can improve the melt index of the elastomer and simultaneously improve the sensitivity of the product viscosity to temperature, thereby being beneficial to the blending use of the elastomer and polystyrene.
The invention also provides a method for simply and efficiently preparing the hydrogenated styrene thermoplastic elastomer, products with different hydrogenation degrees are prepared by selecting different catalysts, the method is suitable for different application fields, and the application range of the hydrogenated styrene thermoplastic elastomer is greatly expanded.
Detailed Description
The core purpose of the invention is to provide a hydrogenated styrene thermoplastic elastomer which can improve the melt index of a product and can improve the temperature sensitivity of the viscosity of the product. The styrene-isoprene-styrene triblock copolymer is synthesized by taking styrene and isoprene as raw materials, and the total or partial hydrogenation of polyisoprene in a hydrogenation section is realized on the basis of the design and control of a polyisoprene soft section structure, so that the content of a repeating unit shown in a formula (I) in the triblock copolymer prepared by the invention is obviously improved, and the hydrogenated product has good compatibility with polypropylene. Furthermore, the hydrogenated styrene thermoplastic elastomer prepared by the invention has the advantages that the soft segment is combined with the styrene repeating unit, so that the melt index of the product and the sensitivity of the viscosity of the product to temperature can be improved, and the elastomer and the polystyrene can be favorably blended for use. Specifically, in the styrene-isoprene-styrene triblock copolymer synthesized by the invention, the properties of the polymer are changed and adjusted by controlling the molecular weight of the hard polystyrene segment and the soft polyisoprene segment, the mass percentage of the hard polystyrene segment, the molar percentage of the repeating unit shown in the formula (I), the molar percentage of the repeating unit shown in the formula (III), the hydrogenation degree and the like, so as to prepare a series of products to meet the requirements of different application fields.
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail with reference to specific embodiments below. However, those skilled in the art will recognize that the present invention is not limited to the following examples.
Example 1
Adding styrene, a solvent cyclopentane and an initiator n-butyllithium into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 0.48M, and the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing for 80min at 60 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 120ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.4 ten thousand, and the molecular weight distribution is 1.02; the melt index is 4.35g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 6.98 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 99.1 mol%.
Example 2
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 2.4M, and the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing at 60 ℃ for 70 min; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 120ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.3 ten thousand, and the molecular weight distribution is 1.01; the melt index is 4.54g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 11.33 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 99.3 mol%.
Example 3
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.2M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 1.8M, and the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing at 60 ℃ for 70 min; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 120ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The molecular weight of the obtained hydrogenated polymer is 8.1 ten thousand and the molecular weight distribution is 1.03 through detection; the melt index is 0.53g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of the formula (I) accounts for 10.56 mol% of the sum of the repeating units of the formula (I) and the formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.9 mol%.
Example 4
Adding styrene, a solvent cyclopentane and an initiator n-butyllithium into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.36M, the concentration of the isoprene and the styrene is 8.2 wt% (wherein, the concentration of the styrene is 0.26 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 200ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.8MPa, and carrying out hydrogenation reaction for 2.5h at 75 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 11.2 ten thousand, and the molecular weight distribution is 1.04; the melt index is less than 0.1g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 31.02 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.3 mol%.
Example 5
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.54M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 0.26wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 220ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.8MPa, and carrying out hydrogenation reaction for 2h at 75 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 10.8 ten thousand, and the molecular weight distribution is 1.03; the melt index is less than 0.1g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 45.17 mol% of the sum of the recurring units of formulae (I) and (II); the hydrogenation degree of the non-benzene ring repeating unit in the soft segment after hydrogenation is 98.6 mol%
Example 6
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.54M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 0.65wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2.5h at the temperature of 80 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 11.7 ten thousand, and the molecular weight distribution is 1.04; the melt index is 0.21g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 44.57 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 99.0 mol%.
Example 7
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.54M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 1.0wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.8MPa, and carrying out hydrogenation reaction for 2.5h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 10.5 ten thousand, and the molecular weight distribution is 1.02; the melt index is 0.87g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of the formula (I) accounts for 45.12 mol% of the sum of the repeating units of the formula (I) and the formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.7 mol%.
Example 8
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.54M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 1.5wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2.5h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 10.8 ten thousand, and the molecular weight distribution is 1.03; the melt index is 2.43g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 45.35 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.9 mol%.
Example 9
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 1.5M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 1.0wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 75 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2.5h at 70 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.6 ten thousand, and the molecular weight distribution is 1.02; the melt index is 7.78g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 63.71 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.1 mol%.
Example 10
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 1.5M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 1.5wt percent), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 75 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel isooctanoate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction at 70 ℃ for 2.5h to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.5 ten thousand, and the molecular weight distribution is 1.02; the melt index is 12.01g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 61.58 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.9 mol%.
Example 11
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.6M, the concentration of the isoprene and the styrene is 8.2 wt% (wherein, the concentration of the styrene is 0.65 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2.5h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.6 ten thousand, and the molecular weight distribution is 1.02; the melt index is 5.01g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of the formula (I) accounts for 30.89mol percent of the sum of the repeating units of the formula (I) and the formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 99.5 mol%.
Example 12
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 1.3 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.9M, the concentration of the isoprene and the styrene is 7.4 wt% (wherein, the concentration of the styrene is 0.59 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 1.3 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 200ml of nickel neodecanoate/aluminum alkyl catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction at 65 ℃ for 2.5h to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.7 ten thousand, and the molecular weight distribution is 1.03; the melt index is 5.65g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 43.60 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 99.0 mol%.
Example 13
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 1.6 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.9M, the concentration of the isoprene and the styrene is 6.8 wt% (wherein, the concentration of the styrene is 0.54 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 1.6 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2.5h at 75 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.6 ten thousand, and the molecular weight distribution is 1.01; the melt index is 4.79g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 42.11 mol% of the sum of the recurring units of formulae (I) and (II); the hydrogenation degree of the non-benzene ring repeating unit in the soft segment after hydrogenation is 98.4 mol%
Example 14
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.9M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.9M, the concentration of the isoprene and the styrene is 8.2 wt% (wherein, the concentration of the styrene is 1.0 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 75 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 2.0MPa, and carrying out hydrogenation reaction for 2.5h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 11.5 ten thousand, and the molecular weight distribution is 1.03; the melt index is 0.62g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 60.30 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.9 mol%.
Example 15
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 0.45M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.45M, the concentration of the isoprene and the styrene is 8.2 wt% (wherein, the concentration of the styrene is 0.54 wt%), and polymerizing for 70min at 50 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 75 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 240ml of nickel naphthenate/alkyl aluminum catalyst into the system, keeping the hydrogen pressure at 2.1MPa, and carrying out hydrogenation reaction for 2.5h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 24.3 ten thousand, and the molecular weight distribution is 1.02; the melt index is less than 0.1g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the recurring unit of formula (I) accounts for 55.38 mol% of the sum of the recurring units of formulae (I) and (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 98.0 mol%.
Example 16
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 2.4M, and the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing at 60 ℃ for 70 min; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 0.29g of metallocene titanium catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.5 ten thousand, and the molecular weight distribution is 1.02; the melt index is 4.33g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 12.02 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 67.5 mol%.
Example 17
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 2.4M, and the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing at 60 ℃ for 70 min; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 0.14g of metallocene titanium catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 65 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.4 ten thousand, and the molecular weight distribution is 1.02; the melt index is 4.59g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of the formula (I) accounts for 11.87 mol% of the sum of the repeating units of the formula (I) and the formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 52.3 mol%.
Example 18
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.2M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofuran, isoprene and styrene, wherein the concentration of tetrahydrofuran is 0.4M, the concentration of isoprene and styrene is 8.2 wt% (wherein, the concentration of styrene is 0.26 wt%), and polymerizing at 60 ℃ for 70 min; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 50 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 0.26g of metallocene titanium catalyst into the system, keeping the hydrogen pressure at 1.9MPa, and carrying out hydrogenation reaction for 2h at 68 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 8.2 ten thousand, and the molecular weight distribution is 1.03; the melt index is 2.14g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 7.56 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 88.9 mol%.
Example 19
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding N, N-dimethyl tetrahydrofurfuryl amine, isoprene and styrene, wherein the concentration of the N, N-dimethyl tetrahydrofurfuryl amine is 0.6M, the concentration of the isoprene and the styrene is 8.2wt percent (wherein, the concentration of the styrene is 0.26wt percent), and polymerizing for 70min at 60 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 70 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 0.31g of metallocene titanium catalyst into the system, keeping the hydrogen pressure at 2.0MPa, and carrying out hydrogenation reaction for 2.5h at 71 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.6 ten thousand, and the molecular weight distribution is 1.03; the melt index is 4.17g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 29.74 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 71.8 mol%.
Example 20
Adding styrene, cyclohexane solvent and n-butyllithium initiator into a reactor, wherein the concentration of the styrene is 0.9 wt%, the concentration of the initiator is 1.5M, and polymerizing for 40min at 50 ℃; then adding tetrahydrofurfuryl alcohol ethyl ether, isoprene and styrene, wherein the concentration of the tetrahydrofurfuryl alcohol ethyl ether is 0.9M, the concentration of the isoprene and the styrene is 8.2 wt% (wherein, the concentration of the styrene is 0.26 wt%), and polymerizing for 70min at 60 ℃; finally adding styrene, wherein the concentration of the styrene is 0.9 wt%, and polymerizing for 40min at 75 ℃ to obtain a styrene-isoprene-styrene triblock copolymer;
adding 0.19g of metallocene titanium catalyst into the system, keeping the hydrogen pressure at 2.0MPa, and carrying out hydrogenation reaction for 2.5h at 75 ℃ to obtain the hydrogenated styrene thermoplastic elastomer.
The number average molecular weight of the obtained hydrogenated polymer determined by GPC is 6.5 ten thousand, and the molecular weight distribution is 1.01; the melt index is 5.13g/10min under the test conditions of 230 ℃ and 2.16 kg; in the soft segment, the repeating unit of formula (I) accounts for 43.75 mol% of the sum of the repeating units of formula (I) and formula (II); the degree of hydrogenation of the non-benzene ring repeating units in the soft segment after hydrogenation was 63.8 mol%.
The embodiments of the present invention have been described above. However, the present invention is not limited to the above embodiment. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (48)

1. A preparation method of hydrogenated styrene thermoplastic elastomer, wherein the hydrogenated styrene thermoplastic elastomer is a hydrogenated product of a styrene-isoprene-styrene triblock copolymer, and the structural formula of the styrene-isoprene-styrene triblock copolymer is shown as (IV):
Figure FDA0002667684970000011
in the formula (IV), two ends of the triblock copolymer are polystyrene hard sections, and the middle of the triblock copolymer is a polyisoprene soft section; the polyisoprene soft segment is composed of repeating units shown as a formula (I), a formula (II) and a formula (III):
Figure FDA0002667684970000012
wherein the repeating unit shown in the formula (I) accounts for 42.11-75 mol% of the sum of the repeating units shown in the formula (I) and the formula (II);
in the formula (III), R is aryl; the repeating unit shown in the formula (III) accounts for 1-25 mol% of the sum of the repeating units shown in the formula (I), the formula (II) and the formula (III);
characterized in that the method comprises the following steps:
(1) synthesizing the styrene-isoprene-styrene triblock copolymer with a structural formula shown in a formula (IV) by taking styrene and isoprene as raw materials by adopting an anion polymerization method;
(2) hydrogenating the triblock copolymer under the action of a catalyst to prepare the hydrogenated styrene thermoplastic elastomer;
wherein, in the polymerization process of the polyisoprene soft block, a polymer microstructure regulator is added to control the content of the repeating unit shown in the formula (I), and the dosage of the polymer microstructure regulator is as follows: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator; the polymer microstructure modifier is selected from tetrahydrofurfuryl alcohol ethyl ether or N, N-dimethyl tetrahydrofurfuryl amine.
2. The method according to claim 1, wherein the recurring unit represented by the formula (I) accounts for 42.11 to 70 mol% of the sum of the recurring units represented by the formulae (I) and (II).
3. The method according to claim 2, wherein the recurring unit represented by the formula (I) accounts for 42.11 to 65 mol% of the sum of the recurring units represented by the formulae (I) and (II).
4. The production method according to claim 1, wherein the repeating unit represented by the formula (III) accounts for 2 to 20 mol% of the total of the repeating units represented by the formulae (I), (II) and (III).
5. The method according to claim 1, wherein R is phenyl.
6. The production method according to any one of claims 1 to 5, wherein the polystyrene hard block accounts for 15 to 50 wt% of the mass of the triblock.
7. The process according to claim 1, wherein the degree of hydrogenation of the double bonds in the benzene ring is more than 98 mol% and the degree of hydrogenation of the double bonds in the benzene ring is less than 2 mol%; alternatively, the first and second electrodes may be,
in the thermoplastic elastomer, the degree of hydrogenation of double bonds in non-benzene rings is 50 to 98 mol%, and the degree of hydrogenation of double bonds in benzene rings is less than 2 mol%.
8. The process according to claim 7, wherein the degree of hydrogenation of the double bonds in the benzene ring is 98.1 to 99.9 mol% and the degree of hydrogenation of the double bonds in the benzene ring is less than 2 mol%; alternatively, the first and second electrodes may be,
in the thermoplastic elastomer, the degree of hydrogenation of double bonds in non-benzene rings is 50 to 90 mol%, and the degree of hydrogenation of double bonds in benzene rings is less than 2 mol%.
9. The production process according to claim 1, wherein the thermoplastic elastomer has a number average molecular weight of 4 to 30 ten thousand as measured by GPC; the molecular weight distribution is 1.01, 1.02, 1.03, 1.04 or 1.05.
10. The production method according to claim 9, wherein the number average molecular weight of the thermoplastic elastomer is 5 to 25 ten thousand as measured by GPC.
11. The method according to claim 1, wherein the thermoplastic elastomer has a melt index of 0.05 to 20g/10min at 230 ℃ under a 2.16kg test.
12. The method according to claim 1, wherein the step (1) specifically comprises:
styrene and isoprene are taken as raw materials, butyl lithium is taken as an initiator, and a styrene-isoprene-styrene triblock copolymer is synthesized in a non-polar organic solvent; introducing a polymer microstructure modifier during soft block polymerization of polyisoprene, wherein the content of the repeating unit represented by the formula (I) accounts for 42.11-75 mol% of the sum of the repeating units represented by the formula (I) and the formula (II), and the polymer microstructure modifier is used in an amount that: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator; the polymer microstructure modifier is selected from tetrahydrofurfuryl alcohol ethyl ether or N, N-dimethyl tetrahydrofurfuryl amine.
13. The method of claim 1, comprising: (1) firstly, initiating styrene polymerization by using an initiator, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃; then adding a mixture of isoprene and styrene, and polymerizing in the presence of a polymer microstructure regulator, wherein the reaction time is 60-90min, and the reaction temperature is 40-80 ℃, and the dosage of the polymer microstructure regulator is as follows: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator; the polymer microstructure modifier is selected from tetrahydrofurfuryl alcohol ethyl ether or N, N-dimethyl tetrahydrofurfuryl amine; finally, adding the rest styrene for polymerization reaction, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃, so as to obtain a triblock polymer; (2) adding a nonpolar organic solvent into the obtained triblock polymer to prepare a solution, adding a hydrogenation catalyst selected from an organic nickel/alkyl aluminum catalyst or a titanocene catalyst, reacting for 1-5 hours at the temperature of 60-90 ℃ and under the condition that the hydrogen pressure is kept at 1.5-2.5MPa, and hydrogenating to obtain the hydrogenated styrene thermoplastic elastomer.
14. The production method according to any one of claims 1, 12 or 13, wherein the polymeric microstructure modifier is used in an amount of: 0.05< r <2, said r representing the molar ratio of polymer microstructure modifier to initiator.
15. The method according to claim 1, wherein in the step (2), the hydrogenation catalyst is selected from an organic nickel/aluminum alkyl catalyst or a titanocene catalyst.
16. The preparation method according to claim 13 or 15, wherein when the organic nickel/aluminum alkyl is used as the hydrogenation catalyst, the hydrogenation degree of the double bonds in the non-benzene ring in the obtained thermoplastic elastomer is more than 98 mol%, and the hydrogenation degree of the double bonds in the benzene ring is less than 2 mol%;
when the cyclopentadienyl titanium catalyst is used as a hydrogenation catalyst, the hydrogenation degree of double bonds in non-benzene rings in the obtained thermoplastic elastomer is 50-98 mol%, and the hydrogenation degree of double bonds in benzene rings is less than 2 mol%.
17. The process according to claim 16, wherein, when organic nickel/aluminum alkyl is used as the hydrogenation catalyst, the degree of hydrogenation of the double bonds in the non-benzene ring in the resulting thermoplastic elastomer is 98.1 to 99.9 mol%, and the degree of hydrogenation of the double bonds in the benzene ring is less than 2 mol%;
when the cyclopentadienyl titanium catalyst is used as a hydrogenation catalyst, the hydrogenation degree of double bonds in non-benzene rings in the obtained thermoplastic elastomer is 50-90 mol%, and the hydrogenation degree of double bonds in benzene rings is less than 2 mol%.
18. The method according to claim 12, wherein the butyllithium is selected from the group consisting of n-butyllithium, sec-butyllithium, and tert-butyllithium.
19. The process according to claim 12, wherein the non-polar organic solvent is selected from cycloalkanes.
20. The production method according to claim 19, wherein the cycloalkane is cyclohexane or cyclopentane.
21. The method according to claim 12, wherein the nonpolar organic solvent is selected from cyclohexane containing 30% or less of hexane.
22. The method of claim 1, wherein the monomer concentration of styrene is 0.1-20 wt% during the polymerization of the polystyrene hard segment; in the polymerization process of the polyisoprene soft block, the monomer concentration of the mixture of isoprene and styrene is 5-20 wt%, wherein the content of styrene in the mixture is 1-25 wt%.
23. The method of claim 22, wherein the monomer concentration of styrene is 0.5-2.5 wt% during the polymerization of the polystyrene hard segment; in the polymerization process of the polyisoprene soft block, the monomer concentration of the mixture of isoprene and styrene is 6-10 wt%, wherein the content of styrene in the mixture is 2-20 wt%.
24. The method of claim 13 wherein the organo-nickel is selected from the group consisting of nickel naphthenate and nickel alkyl.
25. The method of claim 1, wherein the elastomer is used for adhesives, sealants, coatings, rubber-like compounds that can replace vulcanized rubber, plastic modifiers, compatibilizers, thermosetting resin modifiers, and shrink proofing agents for unsaturated polyester asphalt modifiers.
26. A preparation method of hydrogenated styrene thermoplastic elastomer is provided, wherein the hydrogenated styrene thermoplastic elastomer is a hydrogenation product of styrene-isoprene-styrene triblock copolymer; the structural formula of the styrene-isoprene-styrene triblock copolymer is shown as (IV):
Figure FDA0002667684970000041
in the formula (IV), two ends of the triblock copolymer are polystyrene hard sections, and the middle of the triblock copolymer is a polyisoprene soft section; the polyisoprene soft segment is composed of repeating units shown as a formula (I), a formula (II) and a formula (III):
Figure FDA0002667684970000042
wherein the repeating unit shown in the formula (I) accounts for 5-75 mol% of the sum of the repeating units shown in the formula (I) and the formula (II);
in the formula (III), R is aryl; the repeating unit shown in the formula (III) accounts for 1-25 mol% of the sum of the repeating units shown in the formula (I), the formula (II) and the formula (III);
in the thermoplastic elastomer, the hydrogenation degree of double bonds in non-benzene rings is more than 98mol percent, and the hydrogenation degree of double bonds in benzene rings is less than 2mol percent;
characterized in that the method comprises the following steps: (1) synthesizing the styrene-isoprene-styrene triblock copolymer with a structural formula shown in a formula (IV) by taking styrene and isoprene as raw materials by adopting an anion polymerization method; (2) hydrogenating the triblock copolymer under the action of a catalyst to prepare the hydrogenated styrene thermoplastic elastomer;
wherein, in the polymerization process of the polyisoprene soft block, a polymer microstructure regulator is added to control the content of the repeating unit shown in the formula (I), and the dosage of the polymer microstructure regulator is as follows: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator;
in the step (2), the hydrogenation catalyst is selected from an organic nickel/alkyl aluminum catalyst; reacting for 1-5 hours at the temperature of 60-90 ℃ and under the condition that the hydrogen pressure is kept at 1.5-2.5MPa, and hydrogenating to obtain the hydrogenated styrene thermoplastic elastomer.
27. The method according to claim 26, wherein the repeating unit represented by the formula (I) accounts for 6 to 70 mol% of the sum of the repeating units represented by the formulae (I) and (II).
28. The method according to claim 27, wherein the repeating unit represented by the formula (I) accounts for 6.5 to 65 mol% of the sum of the repeating units represented by the formulae (I) and (II).
29. The method according to claim 26, wherein the repeating unit represented by the formula (III) accounts for 2 to 20 mol% of the total of the repeating units represented by the formulae (I), (II) and (III).
30. The method of claim 26, wherein R is phenyl.
31. The method of claim 26, wherein the polystyrene hard segments comprise 15 to 50 wt% of the triblock mass.
32. The process according to claim 26, wherein the degree of hydrogenation of the double bonds in the benzene ring is 98.1 to 99.9 mol% and the degree of hydrogenation of the double bonds in the benzene ring is less than 2 mol%.
33. The production method according to claim 26, wherein the thermoplastic elastomer has a number average molecular weight of 4 to 30 ten thousand as measured by GPC; the molecular weight distribution is 1.01, 1.02, 1.03, 1.04 or 1.05.
34. The production method as claimed in claim 33, wherein the thermoplastic elastomer has a number average molecular weight of 5 to 25 ten thousand as measured by GPC.
35. The method of claim 26, wherein the thermoplastic elastomer has a melt index of 0.05-20g/10min at 230 ℃ under a 2.16kg test.
36. The method according to claim 26, wherein the step (1) comprises:
styrene and isoprene are taken as raw materials, butyl lithium is taken as an initiator, and a styrene-isoprene-styrene triblock copolymer is synthesized in a non-polar organic solvent; introducing a polymer microstructure regulator in the soft-block polymerization process of the polyisoprene in order that the repeating unit represented by the formula (I) accounts for 5-75 mol% of the sum of the repeating units represented by the formulas (I) and (II), wherein the polymer microstructure regulator is used in the following amount: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator.
37. The method of claim 26, comprising: (1) firstly, initiating styrene polymerization by using an initiator, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃; then adding a mixture of isoprene and styrene, and polymerizing in the presence of a polymer microstructure regulator, wherein the reaction time is 60-90min, and the reaction temperature is 40-80 ℃, and the dosage of the polymer microstructure regulator is as follows: 0.01< r <10, said r representing the molar ratio of polymer microstructure modifier to initiator; finally, adding the rest styrene for polymerization reaction, wherein the polymerization time is 30-60min, and the polymerization temperature is 40-70 ℃, so as to obtain a triblock polymer; (2) adding a nonpolar organic solvent into the obtained triblock polymer to prepare a solution, adding a hydrogenation catalyst selected from organic nickel/alkyl aluminum catalysts, reacting for 1-5 hours at the temperature of 60-90 ℃ and under the condition of keeping the hydrogen pressure of 1.5-2.5MPa, and hydrogenating to obtain the hydrogenated styrene thermoplastic elastomer.
38. The method of any one of claims 26, 36 or 37, wherein the polymeric microstructure modifier is selected from tetrahydrofuran, tetrahydrofurfuryl alcohol ethyl ether, or N, N-dimethyl tetrahydrofurfuryl amine.
39. The method of any one of claims 26, 36 or 37, wherein the polymeric microstructure modifier is present in an amount of: 0.05< r <2, said r representing the molar ratio of polymer microstructure modifier to initiator.
40. The method of claim 38, wherein the polymeric microstructure modifier is present in an amount of: 0.05< r <2, said r representing the molar ratio of polymer microstructure modifier to initiator.
41. The method according to claim 36, wherein the butyllithium is selected from the group consisting of n-butyllithium, sec-butyllithium, and tert-butyllithium.
42. The method of claim 36, wherein the non-polar organic solvent is selected from cycloalkanes.
43. The production method according to claim 42, wherein the cycloalkane is cyclohexane or cyclopentane.
44. The method according to claim 36, wherein the nonpolar organic solvent is selected from cyclohexane containing 30% or less of hexane.
45. The method of claim 26, wherein the monomer concentration of styrene is 0.1-20 wt% during the polymerization of the polystyrene hard segment; in the polymerization process of the polyisoprene soft block, the monomer concentration of the mixture of isoprene and styrene is 5-20 wt%, wherein the content of styrene in the mixture is 1-25 wt%.
46. The method of claim 45, wherein the monomer concentration of styrene is 0.5-2.5 wt% during the polymerization of the polystyrene hard segment; in the polymerization process of the polyisoprene soft block, the monomer concentration of the mixture of isoprene and styrene is 6-10 wt%, wherein the content of styrene in the mixture is 2-20 wt%.
47. The method of claim 37 wherein the organo-nickel is selected from the group consisting of nickel naphthenate and nickel alkyl.
48. The method of claim 26, wherein the elastomer is used in adhesives, sealants, coatings, rubber-like compounds that can replace vulcanized rubber, plastic modifiers, compatibilizers, thermosetting resin modifiers, and shrink proofing agents for unsaturated polyester asphalt modifiers.
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