CN113278119B - Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof - Google Patents

Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof Download PDF

Info

Publication number
CN113278119B
CN113278119B CN202110772697.4A CN202110772697A CN113278119B CN 113278119 B CN113278119 B CN 113278119B CN 202110772697 A CN202110772697 A CN 202110772697A CN 113278119 B CN113278119 B CN 113278119B
Authority
CN
China
Prior art keywords
hydrogenation
polymerization reaction
reaction
stage polymerization
kettle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202110772697.4A
Other languages
Chinese (zh)
Other versions
CN113278119A (en
Inventor
黎广贞
谢宝东
杨寿盛
郑岩
张海涛
李才亮
王平
舒畅
刘敏
张先汉
袁兴有
车国桥
严莹珞
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Zhonghe High Tech Co ltd
Original Assignee
Guangdong Zhonggao Technology Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangdong Zhonggao Technology Co ltd filed Critical Guangdong Zhonggao Technology Co ltd
Priority to CN202110772697.4A priority Critical patent/CN113278119B/en
Publication of CN113278119A publication Critical patent/CN113278119A/en
Application granted granted Critical
Publication of CN113278119B publication Critical patent/CN113278119B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/04Reduction, e.g. hydrogenation

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

The invention provides a hydrogenated styrene-butadiene block copolymer, a preparation method and application thereof, wherein the preparation method comprises the following steps: (1) preparing a base adhesive by utilizing a three-stage polymerization reaction, and then introducing hydrogen to terminate the polymerization reaction; (2) mixing titanocene dichloride and n-butyl lithium, and performing an aging reaction to obtain a hydrogenation catalyst; (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2), and introducing hydrogen to carry out hydrogenation reaction to prepare a hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of more than or equal to 98%; wherein, the step (1) and the step (2) are not in sequence; and (4) adopting recycle hydrogen at the later stage of the hydrogenation reaction in the step (3). The preparation method provided by the invention avoids the use of co-catalyst phthalates in the hydrogenation process, and adopts recycle hydrogen in the later stage of the hydrogenation reaction, so that the contact area of the hydrogenation catalyst and hydrogen is increased, the hydrogenation degree of the obtained product is improved, and the preparation process is simplified.

Description

Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof
Technical Field
The invention belongs to the technical field of copolymers, relates to a hydrogenated styrene-butadiene block copolymer, and particularly relates to a hydrogenated styrene-butadiene block copolymer and a preparation method and application thereof.
Background
Hydrogenated styrene-butadiene block copolymers (SEBS) are novel thermoplastic elastomers prepared by selective hydrogenation of the unsaturated double bonds in styrene-butadiene block copolymers (SBS). After hydrotreating, unsaturated double bonds on the molecular chain of the SEBS product are greatly reduced, and the performance is obviously improved compared with SBS. The SEBS has thermoplasticity of SBS and high elasticity of rubber at normal temperature, shows fluidity of resin at high temperature and can be directly processed and molded. The SEBS main chain has high saturation, so that the SEBS main chain has better stability, heat resistance, oxidation resistance, weather resistance and solvent resistance than SBS, and has wider application range.
CN 106749783a discloses a curable crosslinked liquid rubber and a preparation method thereof, wherein the preparation method comprises the following steps: adding cyclohexane and tetrahydrofuran into a high-pressure reaction kettle, stirring and heating; then adding styrene, and injecting n-butyl lithium/cyclohexane solution by using an injector; after the temperature is raised, butadiene is pressed in from a metering tank, then styrene is added from an injection, the reaction liquid is pressed into a hydrogenation kettle, hydrogen is introduced, and the reaction is stopped; after half an hour, adding methyl o-methylbenzoate and a catalyst titanocene dichloride, introducing hydrogen, controlling the pressure, and supplementing methyl o-methylbenzoate every 1 hour; and discharging after the reaction is finished, filtering, adding ethanol for washing and separating, and evaporating to remove the solvent to obtain the hydrogenated polystyrene/butadiene/styrene liquid rubber with different polystyrene chain segment ratios. However, the preparation method provided by the invention is complicated in process, and the limited-use substance methyl o-methylbenzoate is adopted, so that certain harm is caused to the environment, and the hydrogenation degree of the product needs to be further improved.
Therefore, how to provide a preparation method of the hydrogenated styrene-butadiene block copolymer avoids using limited substances, further improves the hydrogenation degree of the product and simplifies the preparation process, and becomes a problem which needs to be solved by technical personnel in the field at present.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a hydrogenated styrene-butadiene block copolymer, a preparation method and application thereof.
In order to achieve the purpose, the invention adopts the following technical scheme:
in a first aspect, the present invention provides a method for preparing a hydrogenated styrene-butadiene block copolymer, the method comprising the steps of:
(1) preparing a base adhesive by utilizing a three-stage polymerization reaction, and then introducing hydrogen to terminate the polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium, and carrying out an aging reaction to obtain a hydrogenation catalyst;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2), and introducing hydrogen to carry out hydrogenation reaction to prepare the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of more than or equal to 98%.
Wherein, the step (1) and the step (2) are not in sequence; and (4) adopting recycle hydrogen at the later stage of the hydrogenation reaction in the step (3).
According to the preparation method provided by the invention, before hydrogenation reaction, titanocene dichloride and n-butyl lithium are mixed for aging reaction, then the obtained hydrogenation catalyst is mixed with a basic glue phase for subsequent hydrogenation reaction, compared with the conventional method that n-butyl lithium is added firstly and then hydrogen is terminated, titanocene dichloride and phthalate substances are added for hydrogenation reaction, the stability of the hydrogenation catalyst is improved, and the use of co-catalyst phthalate in the hydrogenation process is avoided; in addition, the invention adopts the circulating hydrogen in the later stage of the hydrogenation reaction, increases the contact area of the hydrogenation catalyst and the hydrogen, improves the hydrogenation degree of the obtained product and simplifies the preparation process.
Preferably, the three-stage polymerization reaction in step (1) is specifically: adding styrene and an initiator into a system of a nonpolar hydrocarbon solvent to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; and after the second-stage polymerization reaction is finished, adding styrene into the system to perform a third-stage polymerization reaction.
Preferably, the initiator comprises n-butyllithium and/or sec-butyllithium.
Preferably, the non-polar hydrocarbon solvent comprises cyclohexane and/or n-hexane.
Preferably, the initiation temperature of the three-stage polymerization reaction in step (1) is 55-65 ℃, for example 55 ℃, 56 ℃, 57 ℃, 58 ℃, 59 ℃, 60 ℃, 61 ℃, 62 ℃, 63 ℃, 64 ℃ or 65 ℃, but is not limited to the recited values, and other values not recited in the range of the values are also applicable.
Preferably, the glue solution content of the base glue in step (1) is 8-15wt%, for example 8 wt%, 9 wt%, 10 wt%, 11 wt%, 12 wt%, 13 wt%, 14 wt% or 15wt%, but not limited to the recited values, and other values not recited in the range of the recited values are also applicable.
Preferably, the molecular weight of the base gum in step (1) is 30000-200000, such as 30000, 40000, 60000, 80000, 100000, 120000, 140000, 160000, 180000 or 200000, but not limited to the recited values, and other non-recited values within the range of values are equally applicable.
In the present invention, the base rubber obtained in step (1) is not particularly limited as long as it can satisfy the requirement that the solid content of the rubber solution is 8-15wt% and the molecular weight is 30000-200000.
Preferably, the three-stage polymerization reaction in the step (1) is performed in a polymerization kettle, and hydrogen is introduced to terminate the polymerization reaction after the obtained base rubber is transferred into a hydrogenation kettle.
Preferably, the aging reaction in step (2) is carried out in an aging kettle.
Preferably, the titanocene dichloride of step (2) is used in an amount of 0.2-0.3mmol per 100g of base gum, which may be, for example, 0.2mmol per 100g of base gum, 0.22mmol per 100g of base gum, 0.24mmol per 100g of base gum, 0.26mmol per 100g of base gum, 0.28mmol per 100g of base gum or 0.3mmol per 100g of base gum, but is not limited to the values listed, and other values not listed in this range of values are equally applicable.
Preferably, the molar ratio Li/Ti of titanocene dichloride and n-butyllithium in step (2) is 10 to 15, and may be, for example, 10, 10.5, 11, 11.5, 12, 12.5, 13, 13.5, 14, 14.5 or 15, but is not limited to the recited values, and other values not recited in this range are also applicable.
Preferably, the temperature of the aging reaction in step (2) is 25 to 75 ℃, for example 25 ℃, 30 ℃, 35 ℃, 40 ℃, 45 ℃, 50 ℃, 55 ℃, 60 ℃, 65 ℃, 70 ℃ or 75 ℃, but is not limited to the recited values, and other unrecited values within the range of the recited values are equally applicable.
Preferably, the hydrogenation reaction in step (3) is carried out in a hydrogenation kettle.
Preferably, the hydrogenation in step (3) is carried out at a hydrogenation temperature of 70-80 deg.C, such as 70 deg.C, 71 deg.C, 72 deg.C, 73 deg.C, 74 deg.C, 75 deg.C, 76 deg.C, 77 deg.C, 78 deg.C, 79 deg.C or 80 deg.C, but not limited to the recited values, and other values not recited in the recited values are also applicable.
Preferably, the hydrogenation pressure in the hydrogenation reaction in step (3) is 1 to 2.5MPa, and may be, for example, 1MPa, 1.1MPa, 1.3MPa, 1.5MPa, 1.7MPa, 1.9MPa, 2MPa, 2.1MPa, 2.3MPa or 2.5MPa, but is not limited to the values listed, and other values not listed in the range of the values are also applicable.
Preferably, the hydrogenation time of the hydrogenation reaction in step (3) is 90-180min, such as 90min, 100min, 110min, 120min, 130min, 140min, 150min, 160min, 170min or 180min, but is not limited to the recited values, and other values not recited in the range of the values are also applicable.
Preferably, the latter stage of the hydrogenation reaction in the step (3) specifically refers to the reaction stage after the hydrogenation temperature reaches a peak value.
As a preferred technical solution of the first aspect of the present invention, the preparation method comprises the steps of:
(1) preparing a base adhesive with 8-15wt% of solid glue solution and molecular weight of 30000-200000 in a polymerization kettle by utilizing three-stage polymerization with initiation temperature of 55-65 ℃, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and an initiator into a system of a nonpolar hydrocarbon solvent to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction; the initiator comprises n-butyllithium and/or sec-butyllithium, and the non-polar hydrocarbon solvent comprises cyclohexane and/or n-hexane;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 10-15, and carrying out an aging reaction at the temperature of 25-75 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.2-0.3mmol/100g of base glue;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 70-80 ℃, the hydrogenation pressure of 1-2.5MPa and the hydrogenation time of 90-180min to obtain the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of more than or equal to 98%.
Wherein, the step (1) and the step (2) are not in sequence; and (4) adopting recycle hydrogen after the hydrogenation temperature reaches a peak value in the hydrogenation reaction in the step (3).
In a second aspect, the present invention provides a hydrogenated styrene-butadiene block copolymer prepared by the preparation method according to the first aspect.
In a third aspect, the present invention provides a use of the hydrogenated styrene-butadiene block copolymer according to the first aspect for a polymeric film, a toy or a medical article.
Compared with the prior art, the invention has the beneficial effects that:
(1) before the hydrogenation reaction, the preparation method provided by the invention firstly mixes the cyclopentadienyl titanium dichloride and the n-butyl lithium to carry out an aging reaction, then mixes the obtained hydrogenation catalyst with the basic glue phase to carry out a subsequent hydrogenation reaction, compared with the conventional method that the n-butyl lithium is firstly added and then the hydrogen is terminated, and then the cyclopentadienyl titanium dichloride and the phthalate are added to carry out the hydrogenation reaction, the stability of the hydrogenation catalyst is improved, and the use of a cocatalyst of phthalate in the hydrogenation process is avoided;
(2) the invention adopts the circulating hydrogen in the later stage of the hydrogenation reaction, increases the contact area of the hydrogenation catalyst and the hydrogen, improves the hydrogenation degree of the obtained product and simplifies the preparation process.
Detailed Description
The technical solution of the present invention is further explained by the following embodiments.
Example 1
This example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, the method comprising the steps of:
(1) preparing a base adhesive with 12 wt% of solid glue solution and 120000 molecular weight by utilizing three-stage polymerization reaction at the initiation temperature of 60 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and n-butyllithium into a cyclohexane system, and carrying out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 12, and performing an aging reaction at the temperature of 50 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.25mmol/100g of base adhesive;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 75 ℃, the hydrogenation pressure of 2MPa and the hydrogenation time of 140min to prepare the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of 99%.
Wherein, the hydrogenation reaction in the step (3) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Example 2
This example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, comprising the steps of:
(1) preparing a base adhesive with 10 wt% of solid glue solution and 100000 molecular weight by utilizing three-stage polymerization reaction at the initiation temperature of 58 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and sec-butyl lithium into a normal hexane system to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 11, and carrying out an aging reaction at the temperature of 40 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.25mmol/100g of base rubber;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at a hydrogenation temperature of 72 ℃, a hydrogenation pressure of 1.8MPa and a hydrogenation time of 120min to obtain the hydrogenated styrene-butadiene block copolymer with a hydrogenation degree of 98%.
Wherein, the hydrogenation reaction in the step (3) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Example 3
This example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, the method comprising the steps of:
(1) preparing a base adhesive with 14 wt% of solid glue solution and 180000 molecular weight by utilizing three-stage polymerization reaction at the initiation temperature of 62 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and n-butyllithium into a system of n-hexane for carrying out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 14, and carrying out an aging reaction at the temperature of 60 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.25mmol/100g of base adhesive;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at a hydrogenation temperature of 78 ℃, a hydrogenation pressure of 2.2MPa and a hydrogenation time of 160min to obtain the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of 98%.
Wherein, the hydrogenation reaction in the step (3) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Example 4
This example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, comprising the steps of:
(1) preparing a base adhesive with 8 wt% of solid glue solution and 30000 molecular weight in a polymerization kettle by utilizing three-stage polymerization reaction with the initiation temperature of 55 ℃, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and sec-butyl lithium into a cyclohexane system to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyl lithium in an aging kettle according to the Li/Ti molar ratio of 10, and performing an aging reaction at the temperature of 25 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.2mmol/100g of base adhesive;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 70 ℃, the hydrogenation pressure of 1MPa and the hydrogenation time of 180min to prepare the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of 98%.
Wherein, the hydrogenation reaction in the step (3) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Example 5
This example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, the method comprising the steps of:
(1) preparing a base adhesive with 15wt% of solid content of adhesive liquid and 200000 molecular weight by using a three-stage polymerization reaction at the initiation temperature of 65 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and n-butyllithium into a system of n-hexane for carrying out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 15, and carrying out an aging reaction at the temperature of 75 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.3mmol/100g of base adhesive;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at a hydrogenation temperature of 80 ℃, a hydrogenation pressure of 2.5MPa and a hydrogenation time of 90min to prepare the hydrogenated styrene-butadiene block copolymer with a hydrogenation degree of 98%.
Wherein, the hydrogenation reaction in the step (3) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Comparative example 1
This comparative example provides a method of preparing a hydrogenated styrene-butadiene block copolymer, the method comprising the steps of:
(1) preparing a base adhesive with 12 wt% of solid glue solution and 120000 molecular weight by utilizing three-stage polymerization reaction at the initiation temperature of 60 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and n-butyllithium into a cyclohexane system, and carrying out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing the base glue obtained in the step (1) and n-butyllithium in a hydrogenation kettle, and stopping introducing hydrogen; then adding titanocene dichloride and methyl o-methylbenzoate, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 75 ℃, the hydrogenation pressure of 2MPa and the hydrogenation time of 140min to prepare a hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of 98%; the mol ratio of the n-butyllithium to the titanocene dichloride is 12 according to Li/Ti, and the using amount of the titanocene dichloride is 0.25mmol/100g of base rubber.
Wherein, the hydrogenation reaction in the step (2) adopts recycle hydrogen after the hydrogenation temperature reaches a peak value.
Compared with example 1, the comparative example adopts the substance of o-methyl benzoate with limited use, and although hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of more than or equal to 98 percent can be prepared, the comparative example does not meet the requirement of environmental protection.
Comparative example 2
The present comparative example provides a method for preparing a hydrogenated styrene-butadiene block copolymer, comprising the steps of:
(1) preparing a base adhesive with 12 wt% of solid content of adhesive liquid and 120000 molecular weight by utilizing three-stage polymerization reaction at the initiation temperature of 60 ℃ in a polymerization kettle, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and n-butyllithium into a cyclohexane system, and carrying out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 12, and performing an aging reaction at the temperature of 50 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.25mmol/100g of base rubber;
(3) and (3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 75 ℃, the hydrogenation pressure of 2MPa and the hydrogenation time of 140min to prepare the hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of 97%.
Compared with the example 1, the comparative example does not adopt recycle hydrogen in the later stage of the hydrogenation reaction, and the contact area of the hydrogenation catalyst and hydrogen is reduced, so that the hydrogenation degree of the obtained product is reduced to a certain extent.
Therefore, according to the preparation method provided by the invention, before the hydrogenation reaction is carried out, titanocene dichloride and n-butyl lithium are mixed for an aging reaction, then the obtained hydrogenation catalyst is mixed with the basic glue for a subsequent hydrogenation reaction, compared with the conventional method that n-butyl lithium is added firstly and then hydrogen is terminated, titanocene dichloride and phthalate substances are added for the hydrogenation reaction, the stability of the hydrogenation catalyst is improved, and the use of co-catalyst phthalate in the hydrogenation process is avoided; in addition, the invention adopts the circulating hydrogen in the later stage of the hydrogenation reaction, increases the contact area of the hydrogenation catalyst and the hydrogen, improves the hydrogenation degree of the obtained product and simplifies the preparation process.
The above-mentioned embodiments are intended to illustrate the objects, technical solutions and advantages of the present invention in further detail, and it should be understood that the above-mentioned embodiments are only exemplary embodiments of the present invention, and are not intended to limit the present invention, and any modifications, equivalents, improvements and the like made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (10)

1. A method for producing a hydrogenated styrene-butadiene block copolymer, comprising the steps of:
(1) preparing a base adhesive with the solid content of the adhesive liquid of 8-15wt% by utilizing three-stage polymerization reaction, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and an initiator into a system of a nonpolar hydrocarbon solvent to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction;
(2) mixing titanocene dichloride and n-butyllithium according to the Li/Ti molar ratio of 10-15, and carrying out aging reaction to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.2-0.3mmol/100g of base glue;
(3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2), and introducing hydrogen to carry out hydrogenation reaction at a hydrogenation temperature of 70-80 ℃, a hydrogenation pressure of 1-2.5MPa and a hydrogenation time of 90-180min to prepare a hydrogenated styrene-butadiene block copolymer with a hydrogenation degree of more than or equal to 98%;
wherein, the step (1) and the step (2) are not in sequence; and (4) adopting recycle hydrogen after the hydrogenation temperature reaches a peak value in the hydrogenation reaction in the step (3).
2. The method of claim 1, wherein the initiator comprises n-butyllithium and/or sec-butyllithium.
3. The method according to claim 1, wherein the nonpolar hydrocarbon solvent comprises cyclohexane and/or n-hexane.
4. The method according to claim 1, wherein the initiation temperature of the three-stage polymerization in the step (1) is 55 to 65 ℃.
5. The method as claimed in claim 1, wherein the molecular weight of the base gum in step (1) is 30000-200000.
6. The preparation method according to claim 1, wherein the three-stage polymerization reaction in step (1) is carried out in a polymerization kettle, and the obtained base rubber is transferred into a hydrogenation kettle and then hydrogen is introduced to terminate the polymerization reaction.
7. The method for preparing according to claim 1, wherein the aging reaction of step (2) is carried out in an aging tank.
8. The method according to claim 1, wherein the temperature of the aging reaction in the step (2) is 25 to 75 ℃.
9. The method according to claim 1, wherein the hydrogenation reaction in step (3) is carried out in a hydrogenation reactor.
10. The method of any one of claims 1 to 9, comprising the steps of:
(1) preparing a base adhesive with 8-15wt% of solid glue solution and molecular weight of 30000-200000 in a polymerization kettle by utilizing three-stage polymerization with initiation temperature of 55-65 ℃, transferring the obtained base adhesive into a hydrogenation kettle, and introducing hydrogen to terminate the polymerization reaction; the three-stage polymerization reaction specifically comprises the following steps: adding styrene and an initiator into a system of a nonpolar hydrocarbon solvent to carry out a first-stage polymerization reaction; after the first-stage polymerization reaction is finished, adding butadiene into the system to perform a second-stage polymerization reaction; after the second-stage polymerization reaction is finished, adding styrene into the system to carry out a third-stage polymerization reaction; the initiator comprises n-butyllithium and/or sec-butyllithium, and the non-polar hydrocarbon solvent comprises cyclohexane and/or n-hexane;
(2) mixing titanocene dichloride and n-butyllithium in an aging kettle according to the Li/Ti molar ratio of 10-15, and carrying out an aging reaction at the temperature of 25-75 ℃ to obtain a hydrogenation catalyst; the dosage of the titanocene dichloride is 0.2-0.3mmol/100g of base glue;
(3) mixing the basic adhesive obtained in the step (1) and the hydrogenation catalyst obtained in the step (2) in a hydrogenation kettle, and introducing hydrogen to carry out hydrogenation reaction at the hydrogenation temperature of 70-80 ℃, the hydrogenation pressure of 1-2.5MPa and the hydrogenation time of 90-180min to prepare a hydrogenated styrene-butadiene block copolymer with the hydrogenation degree of more than or equal to 98%;
wherein, the step (1) and the step (2) are not in sequence; and (4) adopting recycle hydrogen after the hydrogenation temperature reaches a peak value in the hydrogenation reaction in the step (3).
CN202110772697.4A 2021-07-08 2021-07-08 Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof Active CN113278119B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110772697.4A CN113278119B (en) 2021-07-08 2021-07-08 Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110772697.4A CN113278119B (en) 2021-07-08 2021-07-08 Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof

Publications (2)

Publication Number Publication Date
CN113278119A CN113278119A (en) 2021-08-20
CN113278119B true CN113278119B (en) 2022-09-30

Family

ID=77286532

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110772697.4A Active CN113278119B (en) 2021-07-08 2021-07-08 Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof

Country Status (1)

Country Link
CN (1) CN113278119B (en)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4501857A (en) * 1983-01-20 1985-02-26 Asahi Kasei Kogyo Kabushiki Kaisha Method for hydrogenation of polymer
CN102453125B (en) * 2010-10-15 2013-06-05 中国石油化工股份有限公司 Hydrogenation method for olefin unsaturated bond-containing polymer
CN105175659B (en) * 2015-07-23 2017-11-03 湖南博瑞康新材料有限公司 A kind of transparent type hydrogenated polystyrene b random copolymerizations conjugated diene/styrene resin and preparation method thereof
CN105085724B (en) * 2015-09-14 2017-11-21 山东聚圣科技有限公司 A kind of hydrogenation plant and method of hydrotreating for polymer continuously hydrogen adding
CN109206568B (en) * 2017-06-29 2021-09-03 中国石油化工股份有限公司 SBS containing 1,2 structure uniformly distributed butadiene block and hydride thereof, preparation and application method
CN111087495B (en) * 2018-10-24 2023-03-14 中国石油化工股份有限公司 Hydrogenation catalyst for producing hydrogenated styrene-conjugated diene copolymer, method for producing hydrogenation catalyst, hydrogenation method, and hydrogenated copolymer
CN109810209A (en) * 2018-12-25 2019-05-28 山东玉皇化工有限公司 A kind of preparation method of hydrogenated styrene-butadiene-styrene block copolymers
CN111875720A (en) * 2020-07-13 2020-11-03 沈阳化工研究院有限公司 Functionalized SEBS and preparation method thereof

Also Published As

Publication number Publication date
CN113278119A (en) 2021-08-20

Similar Documents

Publication Publication Date Title
JP3460005B2 (en) Hydrogenated polymer
CN109206568B (en) SBS containing 1,2 structure uniformly distributed butadiene block and hydride thereof, preparation and application method
US4152370A (en) Preparation, composition, and use of block polymers
KR101928079B1 (en) Method for preparing of dicyclopentadiene based resin, and dicyclopentadiene based resin
CN109880109B (en) Aromatic modified petroleum resin and preparation method thereof
TW201120127A (en) Elastomeric thermoplastic composition
CN113278119B (en) Hydrogenated styrene-butadiene block copolymer and preparation method and application thereof
EP0430014A2 (en) Tapered block copolymers
CN107674137B (en) Hydrogenated styrene thermoplastic elastomer and synthesis method and application thereof
US20040082727A1 (en) Process for hydrogenation of conjugated diene polymer
CN108840980B (en) SEBS elastomer and preparation method thereof
CN107674166B (en) Hydrogenated styrene thermoplastic elastomer and synthesis method and application thereof
CN109134788B (en) Carboxyl-terminated SBS, preparation and application thereof in asphalt modification
CN109836547A (en) Five block styrene analog thermoplastic elastomers of a kind of hydrogenation and preparation method thereof
JPH0578563B2 (en)
CN105330773A (en) Composition for rare earth catalyst, rare earth catalyst, and preparation method and application thereof
JP2013237806A (en) Purification method of polymer solution
KR20050024375A (en) High-softening-point copolymer, process for producing the same, and product of hydrogenation thereof
CN116174037A (en) Catalyst for selectively partially hydrogenating conjugated diene polymer and preparation method thereof
KR20140087203A (en) Petroleum Resin and Process of Preparing for the Same
CN102453168B (en) Titanium system catalyst composition as well as preparation method and application thereof, and application of alkyl tetrahydrofurfuryl ether compound in titanium system catalyst
CN113929843A (en) Styrene-piperylene-styrene block copolymer and synthetic method and application thereof
CN111793150B (en) Preparation method of low molecular weight polymer
CN112409540B (en) Method for synthesizing random solution polymerized styrene butadiene rubber
CN113930042A (en) SEBS/TPU alloy material and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20211102

Address after: 525000 No.1, South ethylene Road, Qijing Town, high tech Zone, Maoming City, Guangdong Province

Applicant after: Guangdong Zhonggao Technology Co.,Ltd.

Address before: 525000 No.1, South ethylene Road, Qijing Town, high tech Zone, Maoming City, Guangdong Province

Applicant before: Guangdong Zhonggao Technology Co.,Ltd.

Applicant before: GUANGDONG ZHONGHE ZHONGDE FINE CHEMICAL RESEARCH DEVELOPMENT Co.,Ltd.

GR01 Patent grant
GR01 Patent grant
CP01 Change in the name or title of a patent holder
CP01 Change in the name or title of a patent holder

Address after: 525000 No.1, South ethylene Road, Qijing Town, high tech Zone, Maoming City, Guangdong Province

Patentee after: Guangdong Zhonghe High Tech Co.,Ltd.

Address before: 525000 No.1, South ethylene Road, Qijing Town, high tech Zone, Maoming City, Guangdong Province

Patentee before: Guangdong Zhonggao Technology Co.,Ltd.