JP2846409B2 - Production method of new copolymer latex - Google Patents
Production method of new copolymer latexInfo
- Publication number
- JP2846409B2 JP2846409B2 JP14744990A JP14744990A JP2846409B2 JP 2846409 B2 JP2846409 B2 JP 2846409B2 JP 14744990 A JP14744990 A JP 14744990A JP 14744990 A JP14744990 A JP 14744990A JP 2846409 B2 JP2846409 B2 JP 2846409B2
- Authority
- JP
- Japan
- Prior art keywords
- copolymer latex
- weight
- latex
- meth
- coated paper
- 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.)
- Expired - Fee Related
Links
- 229920000126 latex Polymers 0.000 title claims description 36
- 239000004816 latex Substances 0.000 title claims description 35
- 229920001577 copolymer Polymers 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000178 monomer Substances 0.000 claims description 19
- 239000012986 chain transfer agent Substances 0.000 claims description 11
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 7
- 150000001993 dienes Chemical class 0.000 claims description 6
- 150000002790 naphthalenes Chemical class 0.000 claims description 4
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- -1 carpet packing Substances 0.000 description 19
- 230000001070 adhesive effect Effects 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- 239000000853 adhesive Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000007639 printing Methods 0.000 description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-methoxynaphthalene Chemical compound C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 238000007645 offset printing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000005385 peroxodisulfate group Chemical group 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- PBLNHHSDYFYZNC-UHFFFAOYSA-N (1-naphthyl)methanol Chemical compound C1=CC=C2C(CO)=CC=CC2=C1 PBLNHHSDYFYZNC-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- RXWNCMHRJCOWDK-UHFFFAOYSA-N 2-naphthalen-1-ylethanol Chemical compound C1=CC=C2C(CCO)=CC=CC2=C1 RXWNCMHRJCOWDK-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- 239000012935 ammoniumperoxodisulfate Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229950005228 bromoform Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
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- 150000001735 carboxylic acids Chemical class 0.000 description 1
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- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 1
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- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
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- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
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- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- KOODSCBKXPPKHE-UHFFFAOYSA-N propanethioic s-acid Chemical compound CCC(S)=O KOODSCBKXPPKHE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
- Polymerisation Methods In General (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、紙塗工用、カーペットパッキング用、繊維
結合用あるいは粘接着剤用に供される新規共重合体ラテ
ックスに関するものである。Description: TECHNICAL FIELD The present invention relates to a novel copolymer latex used for paper coating, carpet packing, fiber bonding, or adhesive.
従来、合成共重合体ラテックスは、例えば紙塗工用バ
インダー、カーペットバックサイジング用バインダー、
不織布や人工皮革などの繊維結合用バインダー、あるい
は各種材料の粘接着剤などとして広く用いられている。
そして、共重合体ラテックスがこのような用途に用いら
れる場合、該共重合体ラテックスは接着強度が高く、か
つ耐水性、乾燥加熱による耐ブリスター性などに優れて
いることが要求される。Conventionally, synthetic copolymer latex is, for example, a binder for paper coating, a binder for carpet backsizing,
It is widely used as a binder for bonding fibers such as nonwoven fabric and artificial leather, or as an adhesive for various materials.
When the copolymer latex is used for such a purpose, the copolymer latex is required to have high adhesive strength, and to be excellent in water resistance, blister resistance by drying and heating, and the like.
たとえば、塗工紙は、紙の印刷適性の向上および光沢
などの光学的特性の向上を目的として、妙造された原紙
表面に、カオリンクレー、炭酸カルシウム、サチンホワ
イト、タルク、酸化チタンなどの顔料、それらのバイン
ダーとしての共重合体ラテックスおび保水剤あるいは補
助バインダーとしてのスターチ、ポリビニルアルコー
ル、カルボキシメチルセルロースなどの水溶性高分子を
主構成成分とする塗料が塗工されたものであって、従来
からスチレンとブタジエンを主要単量体成分とし、これ
らを乳化重合して得られたスチレン−ブタジエン系共重
合体ラテックス、いわゆるSB系ラテックスがバインダー
として汎用的に用いられる。For example, coated paper has pigments such as kaolin clay, calcium carbonate, satin white, talc, and titanium oxide on the surface of a specially-made base paper to improve the printability of paper and optical properties such as gloss. Coated with a water-soluble polymer such as starch, polyvinyl alcohol, carboxymethyl cellulose as a main component, and a copolymer latex and a water retention agent as their binder or an auxiliary binder, Styrene and butadiene are used as main monomer components, and a styrene-butadiene copolymer latex obtained by emulsion polymerization of these, so-called SB latex, is generally used as a binder.
ところで、近年、カラー印刷された雑誌類やパンフレ
ット、広告類の需要の拡大に伴って塗工紙の生産が著し
く増大している。特に、オフセット印刷での高速印刷化
傾向に伴い、塗工紙および顔料バインダーの品質に対す
る要求水準もますます高度化しており、そのため、塗工
紙の品質の中でも特にインクピック抵抗性、いわゆるピ
ック強度の向上が強く求められている。しかも、このピ
ック強度性能は他の印刷物性、すなわち湿潤ピック強
度、耐ブリスター性、網点再現性などとは負の相関関係
にあるため、これらの諸物性を高水準にバランス化させ
る改良が一段と要求されている。塗工紙のこれらの性質
は、顔料バインダーとして用いられるSB系ラテックスの
設計に特に強く依存することから、これまで該SBラテッ
クスの性能について種々の検討が加えられてきた。By the way, in recent years, the production of coated paper has increased remarkably with the increase in demand for magazines, pamphlets and advertisements printed in color. In particular, with the trend toward high-speed printing in offset printing, the required level for the quality of coated paper and pigment binders is becoming increasingly sophisticated, and therefore, among the quality of coated paper, especially ink pick resistance, so-called pick strength There is a strong demand for improvement. Moreover, this pick strength performance is negatively correlated with other printing properties, such as wet pick strength, blister resistance, halftone dot reproducibility, etc., so further improvements to balance these various properties to a high level have been made. Has been requested. Since these properties of the coated paper greatly depend on the design of the SB latex used as the pigment binder, various studies have been made on the performance of the SB latex.
たとえば、共重合体ラテックス皮膜のベンゼン、トル
エン、テトラヒドロフランなどの溶剤に対する不溶解部
分の割合がピック強度と耐ブリスター性の支配因子であ
ることが確認されていることから、この面より種々の検
討がなされており、具体的にはラテックス中の共重合体
の組成およびゲル分率を特定の範囲に調製することによ
り、優れた性能を発揮させることが提案されている(特
公昭59−3598号公報、特公昭60−17879号公報、特開昭5
8−4894号公報)。このラテックスのゲル分率は単量体
組成、重合温度をはじめとした様々な重合因子によって
変化するが、これを所望の水準に調製する方法は連鎖移
動剤の添加が一般的かつ簡便である。連鎖移動剤とし
て、従来はおもに四塩化炭素に代表されるハロゲン化炭
化水素、t−あるいはn−ドデシルメルカプタンに代表
されるアルキルメルカプタン、スルフィドなどが使用さ
れていた。For example, it has been confirmed that the proportion of the insoluble portion of a copolymer latex film in a solvent such as benzene, toluene, and tetrahydrofuran is a controlling factor of pick strength and blister resistance. Specifically, it has been proposed to exhibit excellent performance by adjusting the composition and gel fraction of the copolymer in the latex to specific ranges (Japanese Patent Publication No. 59-3598). JP-B-60-17879, JP-A-5
No. 8-4894). Although the gel fraction of this latex varies depending on various polymerization factors such as the monomer composition and the polymerization temperature, a method for adjusting the gel fraction to a desired level generally and simply adds a chain transfer agent. Conventionally, as the chain transfer agent, halogenated hydrocarbons typified by carbon tetrachloride, alkyl mercaptans typified by t- or n-dodecyl mercaptan, sulfides and the like have been used.
しかしながら、一般的には塗工紙のピック強度はSB系
ラテックスにおいてそのゲル分率が75〜95重量%の範囲
で最も高くなるのに対して、耐ブリスター性はゲル分率
の低いものほど良好となることが認められており、ピッ
ク強度と耐ブリスター性の両方を同時に高い水準にまで
向上させるには、前記技術はいずれも十分に満足しうる
ものではない。However, in general, the pick strength of the coated paper is highest in SB-based latex when its gel fraction is in the range of 75 to 95% by weight, whereas the blister resistance is better as the gel fraction is lower. None of the above techniques are fully satisfactory for simultaneously increasing both pick strength and blister resistance to high levels.
また、オフセット印刷における湿潤ピック強度に最適
なブタジエン単位の分率は34重量%以下であり、ピック
強度の最適なブタジエン単位の分率とは相違するため、
その両物性を同時に高い水準にすることは困難であっ
た。In addition, the optimal butadiene unit fraction for wet pick strength in offset printing is 34% by weight or less, which is different from the optimal butadiene unit fraction for pick strength.
It was difficult to achieve both physical properties at the same time at a high level.
また、グラビア印刷紙においては、良好な網点再現性
と塗工紙製造時の耐スーパーカレンダー汚れ適性がとく
に重要であり、たとえば特開昭56−70071号公報などに
グラビア印刷紙用として良好なバインダーが開示されて
いるが、このものは高いブタジエン単位の分率に設計さ
れているため、耐スーパーカレンダー汚れ適性を損うこ
となく網点再現性を十分に満足しうる程度には改善され
るに至っていない。Further, in gravure printing paper, good halftone dot reproducibility and suitability for super calendar stain resistance during the production of coated paper are particularly important. For example, Japanese Patent Application Laid-Open No. 56-70071 discloses a good gravure printing paper. Although a binder is disclosed, since the binder is designed to have a high fraction of butadiene units, the reproducibility of the halftone dot can be sufficiently improved without deteriorating the supercalender stain resistance. Has not been reached.
また、カーペットバックサイジング用接着剤は、一般
に共重合体ラテックスに炭酸カルシウムまたは水酸化ア
ルミニウム等の充填剤および増粘剤などの他の添加剤を
配合した組成物である。この接着剤組成物は、タフテッ
ドカーペット、ニードルパンチカーペットなどの製造に
おいて、主にパイル(ふさ糸)の脱落防止ならびにジュ
ートなどの二次基布との接着のために用いられる。した
がって、この場合カーペットの最重要物性である接着強
度の向上が当業界での最大の技術課題の一つであり、そ
のため、共重合体ラテックスおよび組成内の配合面から
の改良検討がなされているが、これまで満足できる水準
のものが得られていないのが実状である。The adhesive for carpet backsizing is generally a composition in which a filler such as calcium carbonate or aluminum hydroxide and other additives such as a thickener are blended with a copolymer latex. The adhesive composition is used mainly for preventing piles (bushes) from falling off and for bonding to a secondary base fabric such as jute in the production of tufted carpets, needle punch carpets and the like. Therefore, in this case, improvement of the adhesive strength, which is the most important physical property of the carpet, is one of the biggest technical problems in the industry, and therefore, improvement studies from the copolymer latex and the composition in the composition are being studied. However, in reality, satisfactory levels have not yet been obtained.
さらに、粘着剤は、従来天然ゴムや合成ゴムなどを有
機溶剤に溶解し、基材に塗工して該有機溶剤を蒸発させ
ることにより、製造されていたが、近年、火災の危険性
や労働衛生上の問題から、水を分散媒とするポリマー水
分散液(ラテックス)を利用する機運が高まり、ゴム−
粘着付与樹脂の組合せの水分散液が開発されつつある
(特公昭57−28545号公報、特開昭55−48270号公報、特
開昭58−160378号公報、特開昭58−183771号公報)。こ
の合成ゴムラテックスと粘着付与樹脂とを含有する水分
散液は、ラテックスの固形分100重量部に対し、粘着付
与樹脂50〜100重量部を加えた組成物が一般的であっ
て、20〜23℃の測定温度においては良好な粘着物性を示
すが、0℃の温度における粘着力については満足できる
値が得られていない。また粘着付与樹脂が存在しなくと
もゴムラテックスのポリマーのみで粘着物性を得ること
ができるものも提案されている(特開昭56−145909号公
報、特開昭57−57707号公報)。しかしながら、このも
のはポリエチレンに対する接着力が極めて低いという欠
点を有している。Furthermore, adhesives have conventionally been produced by dissolving natural rubber, synthetic rubber, or the like in an organic solvent, applying the solution to a base material, and evaporating the organic solvent. Due to hygiene problems, the use of aqueous polymer dispersions (latex) using water as a dispersion medium has increased, and rubber-
Aqueous dispersions of combinations of tackifier resins are being developed (JP-B-57-28545, JP-A-55-48270, JP-A-58-160378, JP-A-58-183771). . The aqueous dispersion containing the synthetic rubber latex and the tackifier resin is generally a composition obtained by adding 50 to 100 parts by weight of the tackifier resin to 100 parts by weight of the solid content of the latex, and 20 to 23 parts by weight. Although good adhesive properties are exhibited at the measurement temperature of 0 ° C, no satisfactory value was obtained for the adhesive force at the temperature of 0 ° C. In addition, there has been proposed a resin capable of obtaining tackiness with only a polymer of rubber latex without the presence of a tackifier resin (JP-A-56-145909, JP-A-57-57707). However, this has the disadvantage that the adhesion to polyethylene is very low.
このように、将来技術では塗工紙の印刷のより一層の
高速化に対応することができず、高品質の塗工紙の製造
を可能にするバインダーとしての共重合体ラテックスの
出現が強く求められているのが現状である。また、カー
ペットならびに粘接着剤においても同様に高接着力を有
する共重合体ラテックスの出現が望まれている。As described above, future technologies cannot cope with higher speed printing of coated paper, and the emergence of copolymer latex as a binder that enables the production of high quality coated paper is strongly demanded. It is the present situation. Also, the appearance of a copolymer latex having a high adhesive force has been desired for carpets and adhesives.
本発明は、このような事情のもとで、印刷用塗工紙に
おけるピック強度と他の性能のバランスや、カーペット
バックサイジングおよび粘接着剤における接着力をより
向上させるための高性能の共重合体ラテックスを提供す
ることを目的として種々検討を行った結果、共役ジエ
ン、エチレン性不飽和カルボン酸およびこれらと共重合
可能なその他の単量体の乳化重合にあたって、連鎖移動
剤としてナフタレン誘導体を用いることにより得られた
共重合体ラテックスが、意外にも前記の目的を達成しう
ることを見いだし、本発明を完成するに至った。Under such circumstances, the present invention provides a high-performance common use for improving the balance between pick strength and other performances in coated paper for printing and further improving the adhesive strength in carpet backsizing and adhesives. As a result of conducting various studies with the aim of providing a polymer latex, a naphthalene derivative was used as a chain transfer agent in the emulsion polymerization of conjugated dienes, ethylenically unsaturated carboxylic acids and other monomers copolymerizable therewith. The present inventors have found that the copolymer latex obtained by using the same can surprisingly achieve the above object, and have completed the present invention.
すなわち、本発明は、共役ジエン、エチレン性不飽和
カルボン酸およびこれらと共重合可能なその他の単量体
の乳化共重合にあたって、連鎖移動剤として下記一般式
で示されるナフタレン誘導体 をもちいることを特徴とする共重合体ラテックスの製造
法である。That is, the present invention provides a naphthalene derivative represented by the following general formula as a chain transfer agent in the emulsion copolymerization of a conjugated diene, an ethylenically unsaturated carboxylic acid and other monomers copolymerizable therewith. This is a method for producing a copolymer latex, characterized by using:
以下、本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.
本発明の特徴は、乳化重合により共重合体ラテックス
を製造するにあたり、連鎖移動剤として下記一般式で表
されるナフタレン誘導体 を使用することにある。A feature of the present invention is that a naphthalene derivative represented by the following general formula is used as a chain transfer agent in producing a copolymer latex by emulsion polymerization. Is to use.
該連鎖移動剤としては、ナフタレン、1−ナフトー
ル、2−ナフトール、メトキシナフタレン、(ヒドロキ
シメチル)ナフタレン、(ヒドロキシエチル)ナフタレ
ンなどが挙げられる。Examples of the chain transfer agent include naphthalene, 1-naphthol, 2-naphthol, methoxynaphthalene, (hydroxymethyl) naphthalene, (hydroxyethyl) naphthalene and the like.
該連鎖移動剤の好ましい使用量は、単量体100重量部
に対し、0.2〜20重量部であり、さらに好ましくは、0.3
〜10重量部である。The preferred amount of the chain transfer agent is 0.2 to 20 parts by weight, more preferably 0.3 to 20 parts by weight, based on 100 parts by weight of the monomer.
~ 10 parts by weight.
また、該連鎖移動剤は他の周知の連鎖移動剤と併用し
て使うこともできる。他の周知の連鎖移動剤の例として
は、t−ドデシルメルカプタン、n−ドデシルメルカプ
タンなどのチオアルカン;メルカプトエタノール、メル
カプトロパノールなどのチオアルコール;チオグリコー
ル酸、チオプロピオン酸などのチオアルキルカルボン
酸;ジメチルスルフィド、ジエチルスルフィドなどのス
ルフィド;四塩化炭素、ブロモホルムなどのハロゲン化
炭化水素などを挙げることができる。Further, the chain transfer agent can be used in combination with other known chain transfer agents. Examples of other known chain transfer agents include thioalkanes such as t-dodecylmercaptan and n-dodecylmercaptan; thioalcohols such as mercaptoethanol and mercaptropanol; thioalkylcarboxylic acids such as thioglycolic acid and thiopropionic acid. Sulfides such as dimethyl sulfide and diethyl sulfide; and halogenated hydrocarbons such as carbon tetrachloride and bromoform.
また、連鎖移動剤の使用方法については周知のいずれ
の方法も用いることができる。すなわち、一括前添加方
法、連続追加添加方法、断続追加添加方法あるいは添加
速度を順次変化させた濃度勾配型添加方法などである。Further, as for the method of using the chain transfer agent, any known method can be used. That is, there are a batch addition method, a continuous addition method, an intermittent addition method, and a concentration gradient addition method in which the addition rate is sequentially changed.
共重合体ラテックスは、共役ジエン、エチレン性不飽
和カルボン酸およびこれらの共重合可能なその他の単量
体から構成される単量体を乳化共重合させて得られる。The copolymer latex is obtained by emulsion-copolymerizing a monomer composed of a conjugated diene, an ethylenically unsaturated carboxylic acid, and other copolymerizable monomers thereof.
本発明に用いる共役ジエンとしては、ブタジエン、イ
ソプレン、2−クロル−1,3−ブタジエンなどがある。
その使用量は全単量体基準で20〜90重量%の範囲である
ことが望ましい。さらに塗工紙用共重合体ラテックスの
場合、この共役ジエンの一層好ましい範囲は20〜70重量
%である。The conjugated diene used in the present invention includes butadiene, isoprene, 2-chloro-1,3-butadiene and the like.
The amount used is desirably in the range of 20 to 90% by weight based on the total monomers. Further, in the case of a copolymer latex for coated paper, the more preferable range of the conjugated diene is 20 to 70% by weight.
本発明に用いるエチレン性不飽和カルボン酸の例とし
ては、アクリル酸、メタクリル酸、クロトン酸などの一
塩基性カルボン酸、イタコン酸、マレイン酸、フマール
酸などの二塩基性カルボン酸およびそのモノエステルな
どを挙げることができる。Examples of the ethylenically unsaturated carboxylic acid used in the present invention include acrylic acid, methacrylic acid, monobasic carboxylic acid such as crotonic acid, itaconic acid, maleic acid, dibasic carboxylic acid such as fumaric acid and monoesters thereof And the like.
該エチレン性不飽和カルボン酸の使用量は全単量体基
準で0.5〜10重量%の範囲であることが好ましい。The amount of the ethylenically unsaturated carboxylic acid used is preferably in the range of 0.5 to 10% by weight based on the total monomers.
本発明に用いるその他の単量体のなかで、もっとも代
表的かつ有効にもちいられるとは、芳香族(ジ)ビニル
化合物であり、ついで(メタ)アクリル酸エステル、シ
アン化ビニル化合物、エチレン性アミドモノマーなどで
ある。芳香族(ジ)ビニル化合物としては、スチレン、
α−メチルスチレン、クロロスチレン、アルキルスチレ
ン、ジビニルベンゼンなどがあげられる。(メタ)アク
リル酸エステルとしては、メチル(メタ)アクリレー
ト、エチル(メタ)アクリレート、プロピル(メタ)ア
クリレート、ブチル(メタ)アクリレート、2−エチル
ヘキシル(メタ)アクリレート、ヒドロキシエチル(メ
タ)アクリレート、さらには、グリシジル(メタ)アク
リレート、エチレングリコールジ(メタ)アクリレート
などがあげられる。シアン化ビニル化合物としては、ア
クリロニトリル、メタクリロニトリルなどがあげられ
る。エチレン性アミノモノマーとしては(メタ)アクリ
ルアミド、N−メチロール(メタ)アクリルアミドなど
が挙げられる。そのほかに、酢酸ビニルのごときビニル
エステル、塩化ビニル、塩化ビニリデンのごときハロゲ
ン化ビニル、アミノエチル(メタ)アクリレート、ジメ
チルアミノエチル(メタ)アクリレート、ジエチルアミ
ノエチル(メタ)アクリレートなどのエチレン性アミン
モノマー、スチレンスルホン酸ソーダなどを例示するこ
とができる。Among the other monomers used in the present invention, the most typical and effective one is an aromatic (di) vinyl compound, followed by a (meth) acrylate, a vinyl cyanide compound, and an ethylenic amide. And monomers. As the aromatic (di) vinyl compound, styrene,
α-methylstyrene, chlorostyrene, alkylstyrene, divinylbenzene and the like. As the (meth) acrylate, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, hydroxyethyl (meth) acrylate, and furthermore Glycidyl (meth) acrylate, ethylene glycol di (meth) acrylate, and the like. Examples of the vinyl cyanide compound include acrylonitrile and methacrylonitrile. Examples of the ethylenic amino monomer include (meth) acrylamide and N-methylol (meth) acrylamide. In addition, ethylenic amine monomers such as vinyl esters such as vinyl acetate, vinyl halides such as vinyl chloride and vinylidene chloride, aminoethyl (meth) acrylate, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, and styrene Examples thereof include sodium sulfonate.
本発明の製造方法は、従来公知の通常の乳化重合法に
よって製造される。一般的に重合体濃度は40〜60重量%
の範囲である。共重合体ラテックスの粒子径は界面活性
剤および/またはシードラテックスの使用割合によって
調製することができ、慨ねその使用割合を高くするほど
生成共重合体ラテックスの粒子は小さくなる。The production method of the present invention is produced by a conventionally known ordinary emulsion polymerization method. Generally polymer concentration is 40-60% by weight
Range. The particle size of the copolymer latex can be adjusted by the usage ratio of the surfactant and / or the seed latex. Generally, the higher the usage ratio, the smaller the particles of the produced copolymer latex.
ここで、粒子径の好ましい範囲は0.05〜1μmであ
り、さらに好ましくは0.07〜0.5μmである。Here, the preferable range of the particle diameter is 0.05 to 1 μm, and more preferably 0.07 to 0.5 μm.
界面活性剤としては、脂肪酸せっけん、ロジン酸せっ
けん、アルキルスルホン酸塩、ジアルキルアリールスル
ホン酸塩、アルキルスルホコハク酸塩、ポリオキシエチ
レンアルキル硫酸塩、ポリオキシエチレンアルキルアリ
ール硫酸塩などアニオン性界面活性剤:ポリオキシエチ
レンアルキルエーテル、ポリオキシエチレンアルキルア
リールエーテル、ポリオキシエチレンソルビタン脂肪酸
エステル、オキシエチレンオキシプロピレンブロックコ
ポリマーなどのノニオン性界面活性剤、カチオン性界面
活性剤がある。界面活性剤は通常、アニオン性活性剤単
独またはアニオン性/ノニオンの混合系で用いられ、全
単量体に対する使用割合としては0.05〜2重量%の範囲
が一般的である。Examples of the surfactant include anionic surfactants such as fatty acid soap, rosin acid soap, alkyl sulfonate, dialkylaryl sulfonate, alkyl sulfosuccinate, polyoxyethylene alkyl sulfate, and polyoxyethylene alkylaryl sulfate. There are nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene sorbitan fatty acid ester, and oxyethylene oxypropylene block copolymer, and cationic surfactants. The surfactant is usually used in an anionic surfactant alone or in a mixed system of anionic and nonionic, and the use ratio of the surfactant to the entire monomer is generally in the range of 0.05 to 2% by weight.
重合の開始に必要な重合開始剤としては、熱または還
元性物質の存在下でラジカル分解して単量体の付加重合
を開始させるもので、水溶性又は油溶性のペルオキソ二
硫酸塩、過酸化物、アゾビス化合物などが一般的に用い
られる。その例としてはペルオキソ二硫酸カリウム、ペ
ルオキソ二硫酸ナトリウム、ペルオキソ二硫酸アンモニ
ウム、過酸化水素、t−ブチルハイドロパーオキサイ
ド、過酸化ベンゾイル、2,2−アゾビスイソブチロニト
リル、クメンハイドロパーオキサイドなどがあり、ペル
オキソ二硫酸塩が最も好ましくもちいられる。重合開始
剤の使用割合は全単量体に対して通常0.2〜1.5重量%で
ある。なお、重合温度は通常60〜90℃の範囲が一般的で
あるが、重合速度の促進あるいはより低温での重合を望
むときに重亜硫酸ナトリウム、アスコルビン酸あるいは
その塩、エリソルビン酸あるいはその塩、ロンガットな
どの還元剤を重合剤に組み合わせてもちいる、いわゆる
レドックス重合法を用いることができる。The polymerization initiator necessary for the initiation of polymerization is one that initiates addition polymerization of a monomer by radical decomposition in the presence of heat or a reducing substance, and is a water-soluble or oil-soluble peroxodisulfate, and a peroxide. Products, azobis compounds and the like are generally used. Examples thereof include potassium peroxodisulfate, sodium peroxodisulfate, ammonium peroxodisulfate, hydrogen peroxide, t-butyl hydroperoxide, benzoyl peroxide, 2,2-azobisisobutyronitrile, cumene hydroperoxide and the like. Yes, peroxodisulfate is most preferably used. The use ratio of the polymerization initiator is usually 0.2 to 1.5% by weight based on all monomers. The polymerization temperature is generally in the range of 60 to 90 ° C., but when it is desired to accelerate the polymerization rate or to carry out the polymerization at a lower temperature, sodium bisulfite, ascorbic acid or a salt thereof, erythorbic acid or a salt thereof, Rongat A so-called redox polymerization method in which a reducing agent such as the above is used in combination with a polymerization agent can be used.
また、所望によって種々の重合調製剤を添加すること
もしばしばおこなわれる。たとえば、水酸化ナトリウ
ム、水酸化カリウム、炭酸水素ナトリウム、炭酸ナトリ
ウム、リン酸水素二ナトリウムなどのpH調節剤やエチレ
ンジアミン四酢酸ナトリウムなどの各種キレート剤など
である。Also, various polymerization additives are often added as desired. For example, pH adjusters such as sodium hydroxide, potassium hydroxide, sodium hydrogen carbonate, sodium carbonate, disodium hydrogen phosphate, and various chelating agents such as sodium ethylenediaminetetraacetate.
本発明により製造された共重合ラテックスを紙塗工用
塗料のバインダーとして用いるには通常の実施態様でお
こなうことができる。すなわち、分散剤を溶解させた水
中に無機顔料および/または有機顔料、水溶性高分子、
各種添加剤とともに共重合体ラテックスを混合し、均一
分散液とする態様である。そして、この塗料は各種ブレ
ードコーター、ロールコーターなど通常の方法によって
原紙に塗工することができる。Use of the copolymer latex produced according to the present invention as a binder for a paper coating composition can be carried out in a usual embodiment. That is, an inorganic pigment and / or an organic pigment, water-soluble polymer,
In this embodiment, a copolymer latex is mixed together with various additives to form a uniform dispersion. The paint can be applied to the base paper by a usual method such as a blade coater or a roll coater.
以下、実施例により本発明をさらに詳細に説明する
が、本発明はこれらの例によってなんら限定されるもの
ではない。Hereinafter, the present invention will be described in more detail by way of examples, but the present invention is not limited to these examples.
なお、各特性は次のようにして求めた。 In addition, each characteristic was calculated | required as follows.
(イ)耐ブリスター性 RI印刷試験機(明製作所製)を用いて塗工紙の両面を
印刷インク(Webb Zett黄、大日本インク社製)0.3mlを
べた刷りする。この印刷された塗工紙を適当な大きさに
裁断し、その試験片を所定の温度に調製したシリコンオ
イル恒温槽に浸してブリスターが発生するか否かを観察
する。恒温槽の温度を変化させてこの試験をおこない、
ブリスターの発生程度を比較する。評価は10点満点方法
でおこない、耐ブリスター製に優れるものほど高得点と
した。(A) Blister resistance A printing ink (Webb Zett yellow, manufactured by Dainippon Ink) 0.3 ml is solid printed on both sides of the coated paper using an RI printing tester (manufactured by Meiji Seisakusho). The printed coated paper is cut into an appropriate size, and the test piece is immersed in a silicone oil thermostat adjusted to a predetermined temperature to observe whether blisters are generated. Perform this test by changing the temperature of the thermostat.
Compare the degree of blistering. The evaluation was performed according to a 10-point scale, and the higher the blister resistance, the higher the score.
(ロ)ドライピック強度 RI印刷試験機を用いて、印刷インク(SDスーパーデラ
ックス50紅B;タック値18、東華色素社製)0.4ml5回重ね
刷りをおこない、ゴムロールに現れたピッキング状態を
別の台紙に裏取りし、その程度を観察する。評価は10点
評価方法でおこない、ピッキング現象の少ないものほど
高得点とした。(B) Dry pick strength Using an RI printing tester, print ink (SD Super Deluxe 50 red B; tack value 18, manufactured by Toka Pigment Co., Ltd.) 0.4 ml five times, and repeat the picking condition that appeared on the rubber roll. Make a backing on the mount and observe the degree. The evaluation was performed by a 10-point evaluation method, and the smaller the picking phenomenon, the higher the score.
実施例及び比較例 直径0.04μmのシード粒子の水性分散体(シード固形
分濃度25重量%)4重量部を、かくはん装置と温度調節
用ジャケットを取り付けた耐圧反応容器に入れ、さらに
水70重量部、ラウリル硫酸ナトリウム0.2部、イタコン
酸2.5重量部を仕込み、内温を80℃に昇温し、ついで第
1表に示すモノマーおよび連鎖移動剤からなる油性混合
液と、水15重量部、ペルオキソ二硫酸ナトリウム1重量
部、水酸化ナトリウム0.2重量部、ラウリル硫酸ナトリ
ウム0.1重量部からなる水溶液とをそれぞれ4時間およ
び5時間をかけて一定の流速で添加した。そして80℃の
温度をそのまま一時間保ったのち冷却し、次いで生成し
た共重合体ラテックスを水酸化ナトリウムでpHを7に調
製してからスチームストリッピング法により未反応の単
量体などを除去し、網目75μmのろ布でろ過した。な
お、すべての共重合体ラテックスは最終的に固形分濃度
が50重量%になるように調製した。EXAMPLES AND COMPARATIVE EXAMPLES 4 parts by weight of an aqueous dispersion of seed particles having a diameter of 0.04 μm (solid content of seeds: 25% by weight) were placed in a pressure-resistant reaction vessel equipped with a stirring device and a jacket for temperature control, and 70 parts by weight of water were further added. , 0.2 parts by weight of sodium lauryl sulfate and 2.5 parts by weight of itaconic acid, the internal temperature was raised to 80 ° C., and an oily mixture comprising the monomers and the chain transfer agent shown in Table 1 was mixed with 15 parts by weight of water, An aqueous solution consisting of 1 part by weight of sodium sulfate, 0.2 part by weight of sodium hydroxide, and 0.1 part by weight of sodium lauryl sulfate was added at a constant flow rate over 4 hours and 5 hours, respectively. Then, the temperature was kept at 80 ° C. for 1 hour, followed by cooling. Then, the pH of the resulting copolymer latex was adjusted to 7 with sodium hydroxide, and then unreacted monomers were removed by steam stripping. And filtered with a filter cloth having a mesh of 75 μm. In addition, all copolymer latexes were prepared so that the solid content concentration was finally 50% by weight.
応用例 実施例および比較例で調製した共重合体ラテックスに
ついて、紙塗工用バインダーとしての性能評価をおこな
った。その結果を第4表に示す。Application Examples The performance of the copolymer latexes prepared in Examples and Comparative Examples as binders for paper coating was evaluated. Table 4 shows the results.
なお、塗工塗料は第2表に示す配合で、不揮発分濃度
が63重量%になる水量で高速かくはん機で調製した。塗
料のpHはアンモニア水で9.0に調製した。この塗料をも
ちいての塗工紙の調製条件を第3表にに示す。The coating composition was prepared by a high-speed stirrer with the composition shown in Table 2 and an amount of water at which the nonvolatile content was 63% by weight. The pH of the paint was adjusted to 9.0 with aqueous ammonia. Table 3 shows the conditions for preparing coated paper using this paint.
第4表から、本発明の共重合体ラテックスをバインダ
ーとして用いた塗工紙はピック強度と他の物性が高度に
バランスされたものであることが理解される。From Table 4, it is understood that the coated paper using the copolymer latex of the present invention as a binder has a highly balanced pick strength and other physical properties.
〔発明の効果〕 本発明によると、印刷用塗工紙におけるピック強度と
他の性能とのバランスや、カーペットバックサイジング
及び粘着剤における接着力をより向上させうる高性能の
共重合耐ラテックスを容易に得ることができる。 [Effects of the Invention] According to the present invention, a high-performance copolymerized latex that can improve the balance between pick strength and other properties in coated paper for printing and the adhesive strength in carpet backsizing and pressure-sensitive adhesives can be easily obtained. Can be obtained.
フロントページの続き (58)調査した分野(Int.Cl.6,DB名) C08F 2/00 - 2/60 C08F 36/00 - 36/22,136/00 - 136 /22,236/00 - 236/22 C08F 220/00 - 220/08,222/00 - 222 /28Continuation of the front page (58) Field surveyed (Int.Cl. 6 , DB name) C08F 2/00-2/60 C08F 36/00-36 / 22,136 / 00-136 / 22,236 / 00-236/22 C08F 220 / 00-220 / 08,222 / 00-222/28
Claims (1)
およびこれらと共重合可能なその他の単量体の乳化共重
合にあたって、連鎖移動剤として下記一般式で示される
ナフタレン誘導体 を用いることを特徴とする共重合体ラテックスの製造
法。1. A naphthalene derivative represented by the following general formula as a chain transfer agent in the emulsion copolymerization of a conjugated diene, an ethylenically unsaturated carboxylic acid and other monomers copolymerizable therewith. A method for producing a copolymer latex, comprising using:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14744990A JP2846409B2 (en) | 1990-06-07 | 1990-06-07 | Production method of new copolymer latex |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14744990A JP2846409B2 (en) | 1990-06-07 | 1990-06-07 | Production method of new copolymer latex |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0441504A JPH0441504A (en) | 1992-02-12 |
JP2846409B2 true JP2846409B2 (en) | 1999-01-13 |
Family
ID=15430605
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JP14744990A Expired - Fee Related JP2846409B2 (en) | 1990-06-07 | 1990-06-07 | Production method of new copolymer latex |
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Country | Link |
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JP (1) | JP2846409B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012236987A (en) * | 2011-04-28 | 2012-12-06 | Kawasaki Kasei Chem Ltd | Chain transfer agent having condensed polycyclic aromatic skeleton, polymer having the skeleton, and method for production of the polymer |
JP6137446B2 (en) * | 2012-11-06 | 2017-05-31 | 川崎化成工業株式会社 | Chain transfer agent having condensed polycyclic aromatic skeleton, polymer having condensed polycyclic aromatic skeleton, and method for producing polymer |
-
1990
- 1990-06-07 JP JP14744990A patent/JP2846409B2/en not_active Expired - Fee Related
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JPH0441504A (en) | 1992-02-12 |
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