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Patent · US8530017B2 · B2 · US

Method for preparing styrene-butadiene copolymer using reactive emulsifier and styrene-butadiene copolymer prepared by the same

(11) Publication number
US8530017B2
(21) Application number
13/167,073
(22) Filing date
2011-06-23
(30) Priority date
2010-12-27
(43) Publication date
2013-09-10
(45) Date of grant
2013-09-10
(51) IPC
B32B 1/08; C08F 236/14
(52) CPC
  • C08K Use of inorganic or non-macromolecular organic substances as compounding ingredients: 3/36
  • B60C Vehicle tyres; tyre inflation; tyre changing; connecting valves to inflatable elastic bodies in general; devices or arrangements related to tyres: 1/00
  • B65G Transport or storage devices, e.g. conveyors for loading or tipping, shop conveyor systems or pneumatic tube conveyors: 15/32
  • C08F Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds: 212/08, 236/06, 236/10
  • F16G Belts, cables, or ropes, predominantly used for driving purposes; chains; fittings predominantly used therefor: 1/06, 5/04
  • F16L Pipes; joints or fittings for pipes; supports for pipes, cables or protective tubing; means for thermal insulation in general: 11/04
  • Y10T Technical subjects covered by former us classification: 428/139
(73) Assignee
Korea Kumho Petrochemical Co Ltd
(72) Inventors
Gwanghoon Kwag; Dong Hyuk Na; Jun Keol CHOI
(54) Title
Method for preparing styrene-butadiene copolymer using reactive emulsifier and styrene-butadiene copolymer prepared by the same
(57) Abstract

Provided is a method for preparing a styrene-butadiene copolymer having improved silica affinity through introduction of a novel reactive emulsifier. The styrene-butadiene copolymer prepared according to the disclosed method has superior affinity for thereby and thus has superior processability and tensile properties and remarkably improved dynamic properties. Therefore, when the styrene-butadiene copolymer according to the present invention is used as a tire tread material, it can greatly improve its physical properties.

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Claims (15)

  1. A method for preparing a styrene-butadiene copolymer by radical emulsion polymerizing a styrene monomer with a butadiene monomer using a reactive emulsifier represented by Chemical Formula 1, 2, or 3; wherein each of R 1, R 2 and R 3 is independently hydrogen or a C 1 -C 6 alkyl group, l is an integer from 1 to 20, m is an integer from 1 to 20, n is an integer from 1 to 20, and X is an ammo group, an ammonium group, a hydroxyl group, a sulfonate group, a carboxylate group or a phosphate group.
  2. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the styrene monomer is one or more selected from styrene, α-methylstyrene, dimethylstyrene and halogenated styrene.
  3. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the styrene monomer is used in an amount of 10-50 wt % based on the weight of the total reactants.
  4. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the butadiene monomer is one or more selected from 1,3-butadiene, isoprene and halogenated butadiene.
  5. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the butadiene monomer is used in an amount of 45-85 wt % based on the weight of the total reactants.
  6. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the reactive emulsifier is polyoxyethylene phosphate methacrylate, polyoxyethylene carboxylate methacrylate polyoxyethylene sultanate methacrylate, polyoxyethylene hydroxymethacrylate, polyoxyethylene glycol methacrylate, polyoxypropylene phosphate methacrylate, polyoxypropylene carboxylate methacrylate, polyoxypropylene sultanate methacrylate, polyoxypropylene llydroxymethacrylate, polyoxypropylene glycol methacrylate, polyoxypropylene glycol phosphate acrylate, polyoxyethylene phosphate acrylate, polyoxyethylene carboxylate acrylate, polyoxyethylene sulfonate acrylate, polyoxyethylene hydroxyacrylate, polyoxyethylene glycol acrylate, polyoxypropylene phosphate acrylate, polyoxypropylene carboxylate acrylate, polyoxypropylerie sulfonate acrylate, polyoxyptopylene hydroxyacrylate, polyoxypropylene glycol acrylate, allyl alcohol ethoxylate, allyl alcohol polyethylene oxide phosphate, alkylcarboxylate acrylate, alkylcarboxylate methacrylate, alkyl phosphate acrylate, alkyl phosphate methacrylate, alkylsulfonate acrylate, alkylsulfonate methacrylate, alkylhydroxy acrylate, or alkylhydroxy methacrylate (wherein each alkyl is C 1 -C 6 alkyl).
  7. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the reactive emulsifier is used in an amount of 0.1-10 wt % based on the weight of the total reactants.
  8. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein, in the radical emulsion polymerization, one or more initiator(s) selected from potassium persulfate, ammoniam persulfate, acetylacetone peroxide, benzyl peroxide, dicumyl peroxide, methane hydroperoxide, 2,4-dichlorobenzyl peroxide., t-butyl peracetate 2,2′-azobis(isobutyramidine) dihydrochloride, azobisisobutyronitrile, hydrogen peroxide, redox system and ferrous sulfate is used.
  9. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the initiator is used in an amount of 0.05-3 parts by weight based on 100 parts of the total reactants by weight.
  10. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein, in the radical emulsion polymerization, one or more of an anionic surfactant, a cationic surfactant and a non-ionic surfactant is used in addition to the reactive emulsifier represented by Chemical Formula 1, 2 or 3.
  11. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the radical emulsion polymerization is performed at 0-80° C. for 1-48 hours.
  12. A styrene-butadiene copolymer prepared by the method according to claim 1, which is represented by Chemical Formula 4, 5 or 6: wherein each of R 1, R 2 and R 3 is independently hydrogen or a C 1 -C 6 alkyl group, l is an integer from 1 to 20, m is an integer from 1 to 20, n is an integer from 1 to 20, X is an amino group, an ammonium group, a hydroxyl group, a sulfonate group, a carboxylate group or a phosphate group, o is from 0.1 to 0.5, p is from 0.40 to 0.85, q is from 0.01 to 0.10, and o+p+q=1.
  13. A silica composite which is a mixture of the styrene-butadiene copolymer of claim 12 with silica.
  14. The silica composite according to claim 13, wherein the styrene-butadiene copolymer and the silica are mixed at a ratio of 100:30-100 based on weight.
  15. The silica composite according to claim 13, which is used as an industrial material for a tire, a hose or a belt.

Description

(a) Technical Field

The present invention relates to a method for preparing a styrene-butadiene copolymer that can be used as an industrial material for tires, belts, hoses, etc., and a styrene-butadiene copolymer prepared by the same.

(b) Background Art

Styrene-butadiene copolymers or styrene-butadiene-polar monomer copolymers are mainly prepared by emulsion polymerization. These copolymers are used for tires, coating materials, toners, or the like. Several patents are disclosed about the techniques of preparing the styrene-butadiene copolymer or the styrene-butadiene-polar monomer copolymer by emulsion polymerization.

For example, U.S. Pat. Nos. 3,575,913 and 3,563,946 disclose preparation of a styrene-butadiene or styrene-butadiene-acrylate copolymer in emulsion state using potassium persulfate or azobisisobutyronitrile. U.S. Pat. No. 4,064,081 discloses emulsion polymerization of a butadiene-styrene copolymer using potassium persulfate as a polymerization initiator. U.S. Pat. Nos. 5,274,027 and 5,302,655 describe preparation of a styrene-butadiene-acrylate copolymer by emulsion polymerization from acrylate monomers such as itaconic acid, methyl methacrylate, etc., by using, for example, an ammonium persulfate initiator.

U.S. Pat. Nos. 6,512,053 and 6,716,925 describe preparation of a styrene-butadiene-acrylate copolymer by emulsion polymerization from hydroxyalkyl acrylate monomers such as 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate and hydroxymethylmethacrylamide, by using, for example, an ammonium persulfate initiator.

Citations (13)

  • US3563946A
  • US3575913A
  • US4064081A
  • US5274027A
  • US5302655A
  • JPH08333489A
  • US6512053B1
  • JP2003119202A
  • US6716925B2
  • US7585927B2
  • US20080245989A1
  • US20090286933A1
  • US20110034622A1
Record as JSON
{
  "publication_number": "US8530017B2",
  "country": "US",
  "kind": "B2",
  "title": "Method for preparing styrene-butadiene copolymer using reactive emulsifier and styrene-butadiene copolymer prepared by the same",
  "abstract": "Provided is a method for preparing a styrene-butadiene copolymer having improved silica affinity through introduction of a novel reactive emulsifier. The styrene-butadiene copolymer prepared according to the disclosed method has superior affinity for thereby and thus has superior processability and tensile properties and remarkably improved dynamic properties. Therefore, when the styrene-butadiene copolymer according to the present invention is used as a tire tread material, it can greatly improve its physical properties.",
  "claims": [
    "1. A method for preparing a styrene-butadiene copolymer by radical emulsion polymerizing a styrene monomer with a butadiene monomer using a reactive emulsifier represented by Chemical Formula 1, 2, or 3; wherein each of R 1, R 2 and R 3 is independently hydrogen or a C 1 -C 6 alkyl group, l is an integer from 1 to 20, m is an integer from 1 to 20, n is an integer from 1 to 20, and X is an ammo group, an ammonium group, a hydroxyl group, a sulfonate group, a carboxylate group or a phosphate group.",
    "2. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the styrene monomer is one or more selected from styrene, α-methylstyrene, dimethylstyrene and halogenated styrene.",
    "3. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the styrene monomer is used in an amount of 10-50 wt % based on the weight of the total reactants.",
    "4. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the butadiene monomer is one or more selected from 1,3-butadiene, isoprene and halogenated butadiene.",
    "5. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the butadiene monomer is used in an amount of 45-85 wt % based on the weight of the total reactants.",
    "6. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the reactive emulsifier is polyoxyethylene phosphate methacrylate, polyoxyethylene carboxylate methacrylate polyoxyethylene sultanate methacrylate, polyoxyethylene hydroxymethacrylate, polyoxyethylene glycol methacrylate, polyoxypropylene phosphate methacrylate, polyoxypropylene carboxylate methacrylate, polyoxypropylene sultanate methacrylate, polyoxypropylene llydroxymethacrylate, polyoxypropylene glycol methacrylate, polyoxypropylene glycol phosphate acrylate, polyoxyethylene phosphate acrylate, polyoxyethylene carboxylate acrylate, polyoxyethylene sulfonate acrylate, polyoxyethylene hydroxyacrylate, polyoxyethylene glycol acrylate, polyoxypropylene phosphate acrylate, polyoxypropylene carboxylate acrylate, polyoxypropylerie sulfonate acrylate, polyoxyptopylene hydroxyacrylate, polyoxypropylene glycol acrylate, allyl alcohol ethoxylate, allyl alcohol polyethylene oxide phosphate, alkylcarboxylate acrylate, alkylcarboxylate methacrylate, alkyl phosphate acrylate, alkyl phosphate methacrylate, alkylsulfonate acrylate, alkylsulfonate methacrylate, alkylhydroxy acrylate, or alkylhydroxy methacrylate (wherein each alkyl is C 1 -C 6 alkyl).",
    "7. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the reactive emulsifier is used in an amount of 0.1-10 wt % based on the weight of the total reactants.",
    "8. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein, in the radical emulsion polymerization, one or more initiator(s) selected from potassium persulfate, ammoniam persulfate, acetylacetone peroxide, benzyl peroxide, dicumyl peroxide, methane hydroperoxide, 2,4-dichlorobenzyl peroxide., t-butyl peracetate 2,2′-azobis(isobutyramidine) dihydrochloride, azobisisobutyronitrile, hydrogen peroxide, redox system and ferrous sulfate is used.",
    "9. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the initiator is used in an amount of 0.05-3 parts by weight based on 100 parts of the total reactants by weight.",
    "10. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein, in the radical emulsion polymerization, one or more of an anionic surfactant, a cationic surfactant and a non-ionic surfactant is used in addition to the reactive emulsifier represented by Chemical Formula 1, 2 or 3.",
    "11. The method for preparing a styrene-butadiene copolymer according to claim 1, wherein the radical emulsion polymerization is performed at 0-80° C. for 1-48 hours.",
    "12. A styrene-butadiene copolymer prepared by the method according to claim 1, which is represented by Chemical Formula 4, 5 or 6: wherein each of R 1, R 2 and R 3 is independently hydrogen or a C 1 -C 6 alkyl group, l is an integer from 1 to 20, m is an integer from 1 to 20, n is an integer from 1 to 20, X is an amino group, an ammonium group, a hydroxyl group, a sulfonate group, a carboxylate group or a phosphate group, o is from 0.1 to 0.5, p is from 0.40 to 0.85, q is from 0.01 to 0.10, and o+p+q=1.",
    "13. A silica composite which is a mixture of the styrene-butadiene copolymer of claim 12 with silica.",
    "14. The silica composite according to claim 13, wherein the styrene-butadiene copolymer and the silica are mixed at a ratio of 100:30-100 based on weight.",
    "15. The silica composite according to claim 13, which is used as an industrial material for a tire, a hose or a belt."
  ],
  "description_excerpt": "(a) Technical Field\n\nThe present invention relates to a method for preparing a styrene-butadiene copolymer that can be used as an industrial material for tires, belts, hoses, etc., and a styrene-butadiene copolymer prepared by the same.\n\n(b) Background Art\n\nStyrene-butadiene copolymers or styrene-butadiene-polar monomer copolymers are mainly prepared by emulsion polymerization. These copolymers are used for tires, coating materials, toners, or the like. Several patents are disclosed about the techniques of preparing the styrene-butadiene copolymer or the styrene-butadiene-polar monomer copolymer by emulsion polymerization.\n\nFor example, U.S. Pat. Nos. 3,575,913 and 3,563,946 disclose preparation of a styrene-butadiene or styrene-butadiene-acrylate copolymer in emulsion state using potassium persulfate or azobisisobutyronitrile. U.S. Pat. No. 4,064,081 discloses emulsion polymerization of a butadiene-styrene copolymer using potassium persulfate as a polymerization initiator. U.S. Pat. Nos. 5,274,027 and 5,302,655 describe preparation of a styrene-butadiene-acrylate copolymer by emulsion polymerization from acrylate monomers such as itaconic acid, methyl methacrylate, etc., by using, for example, an ammonium persulfate initiator.\n\nU.S. Pat. Nos. 6,512,053 and 6,716,925 describe preparation of a styrene-butadiene-acrylate copolymer by emulsion polymerization from hydroxyalkyl acrylate monomers such as 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate and hydroxymethylmethacrylamide, by using, for example, an ammonium persulfate initiator.",
  "cpc": [
    "C08K 3/36",
    "B60C 1/00",
    "B65G 15/32",
    "C08F 212/08",
    "C08F 236/06",
    "C08F 236/10",
    "F16G 1/06",
    "F16G 5/04",
    "F16L 11/04",
    "Y10T 428/139"
  ],
  "ipc": [
    "B32B 1/08",
    "C08F 236/14"
  ],
  "assignees": [
    "Korea Kumho Petrochemical Co Ltd"
  ],
  "inventors": [
    "Gwanghoon Kwag",
    "Dong Hyuk Na",
    "Jun Keol CHOI"
  ],
  "filing_date": "2011-06-23",
  "publication_date": "2013-09-10",
  "grant_date": "2013-09-10",
  "priority_date": "2010-12-27",
  "application_number": "US-201113167073-A",
  "family_id": "46317491",
  "cited_by_count": 0,
  "citations": [
    "US3563946A",
    "US3575913A",
    "US4064081A",
    "US5274027A",
    "US5302655A",
    "JPH08333489A",
    "US6512053B1",
    "JP2003119202A",
    "US6716925B2",
    "US7585927B2",
    "US20080245989A1",
    "US20090286933A1",
    "US20110034622A1"
  ]
}

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