JPS61273985A - Coating composition for pressure-sensitive copy paper - Google Patents
Coating composition for pressure-sensitive copy paperInfo
- Publication number
- JPS61273985A JPS61273985A JP60115465A JP11546585A JPS61273985A JP S61273985 A JPS61273985 A JP S61273985A JP 60115465 A JP60115465 A JP 60115465A JP 11546585 A JP11546585 A JP 11546585A JP S61273985 A JPS61273985 A JP S61273985A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- pressure
- copolymer latex
- weight
- coating composition
- 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.)
- Granted
Links
- 239000008199 coating composition Substances 0.000 title claims description 27
- 229920001577 copolymer Polymers 0.000 claims abstract description 52
- 239000004816 latex Substances 0.000 claims abstract description 47
- 229920000126 latex Polymers 0.000 claims abstract description 47
- 239000003094 microcapsule Substances 0.000 claims abstract description 27
- 239000011230 binding agent Substances 0.000 claims abstract description 20
- 239000000178 monomer Substances 0.000 claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 10
- 150000001993 dienes Chemical class 0.000 claims abstract description 10
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 9
- 230000009477 glass transition Effects 0.000 claims abstract description 7
- 239000003086 colorant Substances 0.000 claims description 11
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 1
- 239000011248 coating agent Substances 0.000 abstract description 14
- 238000000576 coating method Methods 0.000 abstract description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 12
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract description 8
- 239000000203 mixture Substances 0.000 abstract description 6
- 238000003860 storage Methods 0.000 abstract description 6
- 230000000379 polymerizing effect Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 15
- 239000002775 capsule Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 229920003169 water-soluble polymer Polymers 0.000 description 8
- 238000004040 coloring Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000003223 protective agent Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- -1 2-ethylhexyl Chemical group 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 238000005354 coacervation Methods 0.000 description 3
- 239000011162 core material Substances 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 2
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical group CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 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 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 239000004368 Modified starch Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- PCPYTNCQOSFKGG-UHFFFAOYSA-N 1-chlorobuta-1,3-diene Chemical compound ClC=CC=C PCPYTNCQOSFKGG-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- 101150007144 Intu gene Proteins 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 150000008360 acrylonitriles 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
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- QGVQVNIIRBPOAM-UHFFFAOYSA-N dodecyl naphthalene-1-sulfonate;sodium Chemical compound [Na].C1=CC=C2C(S(=O)(=O)OCCCCCCCCCCCC)=CC=CC2=C1 QGVQVNIIRBPOAM-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 108010025899 gelatin film Proteins 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000010406 interfacial reaction Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
- B41M5/155—Colour-developing components, e.g. acidic compounds; Additives or binders therefor; Layers containing such colour-developing components, additives or binders
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Color Printing (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、特に発色性ならびに発色カブリの点で改良さ
れた感圧複写紙用塗布組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a coating composition for pressure-sensitive copying paper that is improved particularly in terms of color development and color fog.
ノーカーボン複写紙と称される感圧複写紙としては、例
えば、発色剤を内包するマイクロカプセル(以下、「発
色剤マイクロカプセル」という。)を含む発色剤層と顕
色剤を含む顕色剤層とを、積重した2枚の支持体(通常
、紙)の裏面および表面にそれぞれ形成したタイプのも
の、あるいは下位の支持体の表面上に発色剤マイクロカ
プセルと顕色剤とを混合あるいは積層して記録層を形成
したタイプのものなどが知ら硅ている。かかる感圧パ
複写紙においては、上位の支持体の
表面において′□ 筆記具、タイプ
ライタ、その他各種の機械式ブリ、5′、・
・”□′ ンタなどによる機械的あ
るいは衝撃的な圧力が加□L
パ) えられると、これによって発
色剤を内包している′ マイクロカ
プセルが破壊され、カプセル内の発色゛(゛
剤が露出して顕色剤と接触することによっ
て発色・lli
室°シ、複写記・録が達成される。Pressure-sensitive copying paper called carbonless copying paper includes, for example, a color former layer containing microcapsules containing a color former (hereinafter referred to as "color former microcapsules") and a color developer containing a color developer. A type in which a layer is formed respectively on the back and front side of two stacked supports (usually paper), or a type in which a color former microcapsule and a color developer are mixed or mixed on the surface of a lower support. There are known types in which a recording layer is formed by laminating layers. The pressure sensitive
In the case of copy paper, mechanical or impact pressure is applied to the surface of the upper support by writing instruments, typewriters, other types of mechanical printers, printers, etc. This destroys the microcapsules that contain the coloring agent, and the coloring agent inside the capsules is destroyed.
When the agent is exposed and comes into contact with the color developer, color development, photocopying, and recording are achieved.
、\・
4λ
、、 −iに、上述の発色剤層
を構成するための塗布5;、:ユ &l*#4
!′Q@tf′I? 49 o”7′)b゛(11[j
PJ (Xパ ティルト)、バイン
ダーおよびその他の添加剤か゛、・′・)
\、4
・、ら ら構成されている。前記保
護剤は、発色剤マイク”t、’> oカy
+z、ailti:acヨa、:(7)?−1゜′、′
:゛ カプセルが複写記録を目的と
しないときに加えら、゛
れる不測の外力を直接的に受けて破壊されること□、\
丸゛1
:° を防止する機能を有し、通常
、発色剤マイクロ力・): プセル
よりやや大きい粒径を有する有機物質ある、゛
、 いは無機物質の微粒子によって
構成される。また、□ バインダー
は、発色剤マイクロカプセル、保護剤゛、
その他の添加剤を結着して支持体に固定する機能を有し
、従来、このようなバインダーとして、ポリビニルアル
コール、スターチ、変性スターチ、カルボキシメチルセ
ルロース、カゼイン等の水溶性高分子化合物が多く用い
られている。, \・4λ,, -i, coating 5 for forming the above-mentioned coloring agent layer;, :yu &l*#4
! 'Q@tf'I? 49 o”7′)b゛(11[j
It consists of PJ (X Patilt), a binder and other additives. The protective agent is a color former.
+z, ailti:ac yoa, :(7)? -1゜′,′ :゛ Has a function to prevent damage caused by direct exposure to unexpected external forces applied when the capsule is not intended for copying/recording. However, it is usually composed of microparticles of organic or inorganic substances with a particle size slightly larger than that of the color former. In addition, the binder has the function of binding and fixing the coloring agent microcapsules, the protective agent, and other additives to the support. Conventionally, such binders include polyvinyl alcohol, starch, modified starch, Water-soluble polymer compounds such as carboxymethyl cellulose and casein are often used.
しかし、バインダーとして上述のような水溶性高分子化
合物を用いた塗布組成物においては、次のような問題点
がある。However, coating compositions using water-soluble polymer compounds as described above as binders have the following problems.
■ 感圧複写紙においていわゆる発色カブリを生じやす
い。■ Pressure-sensitive copying paper tends to cause so-called color fog.
発色カブリとは、感圧複写紙の製造時あるいは貯蔵時な
どの、複写記録を目的とする使用時以外の取扱時におい
て加えられる機械的圧力、摩擦力あるいは熱などによっ
て発色剤マイクロカプセルが破壊され、不要に発色する
現象である。水溶性高分子化合物をバインダーに用いた
塗布組成物に □。Color fog occurs when the color former microcapsules are destroyed by mechanical pressure, frictional force, or heat applied during handling of pressure-sensitive copying paper other than when used for copying and recording purposes, such as during manufacturing or storage. , which is a phenomenon in which color develops unnecessarily. For coating compositions using water-soluble polymer compounds as binders □.
おいて、このような発色カブリが発生しやすい理由のひ
とつとしては、一般に、水溶性高分子物質によって形成
される乾燥塗膜は強固ではあるが弾力性に欠け、そのた
め塗膜に加えられた外力が吸収されずに発色剤マイクロ
カプセルに直接的に伝1、″ 達
されてこれに作用するためと考えられる。One of the reasons why such colored fog tends to occur is that the dried paint film formed from water-soluble polymeric substances is generally strong but lacks elasticity, and as a result, external forces applied to the paint film are It is thought that this is because the color former is not absorbed but is directly transmitted to the color former microcapsules and acts on them.
パ ■ 保存性が低い。■ Poor shelf life.
水溶性高分子化合物は腐敗しやすく、したかっ′:
□ゎ工、□ゆ間ッゎえ7□質。4い
よア1゜
゛ で保存することが困難である。Water-soluble polymer compounds are easily putrefied and are difficult to clean.
□ゎWork, □Yuma ゎE7□Quality. 4. It is difficult to preserve it at 1゜゛.
、、、 ■ 塗工性が低い。,,, ■ Poor coatability.
−水溶性高分子化合物を用いたバインダーは、粘〜
、 性が大きいので塗工作業を効率
よく円滑に行うこ□゛ とが難しく
、また優れた塗工性を得ようとすれば塗布組成物におけ
る固形分の含有割合を小さくし□゛
なければならない不都合を生ずる。- Binders using water-soluble polymer compounds have high viscosity and properties, making it difficult to perform coating operations efficiently and smoothly. Reduce the solid content percentage in □゛
This will cause inconvenience.
1ご棗
・\、・ 上記■における発色カブ
リの問題を解決するとメ;)。1 Natsume・\、・ This will solve the problem of color fogging in ① above;).
:、・ いう点よりすれば、保護剤の
含有割合を大きくす□゛ ることが有
効であるが、このようにすると、複写゛□
記録時において発色剤層に加えられる筆圧、印字
圧などの外力によっても発色剤カプセルが破壊されにく
くなり、その結果、感圧複写紙の発色濃度が低下する問
題を生ずる。:,・ From this point of view, it is effective to increase the content ratio of the protective agent, but if you do this, it will be difficult to copy.
The color former capsules are less likely to be destroyed by external forces such as writing pressure and printing pressure applied to the color former layer during recording, resulting in a problem in which the color density of the pressure-sensitive copying paper is reduced.
これらの問題点を解消することを目的とした感、
圧複写紙用の塗布組成物として、水溶性
高分子化金物にかえて、アクリル酸エステル重合体ラテ
ンクスを用いたもの(特開昭57−72891号公報)
およびラテックスを用いたもの(特開昭57−7758
9号公報)が提案されている。これらの塗布組成物にお
いては、バインダーとしてラテックスを用いているので
上記■の保存性および■の塗工性については十分な改善
がみられたが、上記■の発色カブリの点においてはいま
だ十分満足すべき結果は得られていない。The aim is to solve these problems,
A coating composition for pressure copying paper using an acrylic acid ester polymer Latinx instead of a water-soluble polymerized metal material (Japanese Patent Laid-Open No. 72891/1989)
and those using latex (Japanese Unexamined Patent Publication No. 57-7758
9) has been proposed. Since these coating compositions use latex as a binder, sufficient improvements were seen in the storage stability (2) and the coating properties (2) above, but they are still sufficiently satisfactory in terms of color fog (2) above. The desired results have not been obtained.
II!11”’N’r L −1−6t t 4 fo
t+5JIN、) (″本発明は、
発色カブリ、保存性ならびにや工性における従来技術の
問題点を総合的に解決し、特に、優れた発色性を保有し
ながら発色剤マイクロカプセルの不要の破壊による発色
カブリの発生“が十分に抑止された感圧複写紙を形成す
ることのできる感圧複写紙用塗布組成物を提供すること
を目的とする。II! 11"'N'r L -1-6t t 4 fo
t+5JIN,) (''The present invention is
Comprehensively solves the problems of conventional technology in terms of color fog, storage stability, and workability, and in particular, sufficiently prevents color fog from occurring due to unnecessary destruction of color former microcapsules while maintaining excellent color performance. It is an object of the present invention to provide a coating composition for pressure-sensitive copying paper that can form a pressure-sensitive copying paper with a high quality coating.
前記問題点は、
発色剤を内包するマイクロカプセルとバインダ−とを含
有する感圧複写紙用塗付組成物において、51、
前記バインダー成分として、以下の単
量体成分・′(8) 脂肪族共役ジエン 2
〜30重量%□ 山) エチレン性
不飽和カルボン酸エステル′
5〜70重量%(C1(b
l以外のエチレン性不飽和化合物10〜93重量%
を共重合させて得られる共重合体ラテックスを含有する
ことを特徴とする感圧複写紙用塗布組成物によって解決
される。The above-mentioned problem is solved in the coating composition for pressure-sensitive copying paper containing microcapsules encapsulating a coloring agent and a binder.
As the binder component, the following monomer component ・'(8) Aliphatic conjugated diene 2
~30% by weight □ Mountain) Ethylenically unsaturated carboxylic acid ester'
5-70% by weight (C1(b
The problem is solved by a coating composition for pressure-sensitive copying paper, which contains a copolymer latex obtained by copolymerizing 10 to 93% by weight of an ethylenically unsaturated compound other than 1.
すなわち、本発明の感圧複写紙用塗布組成物は、脂肪族
共役ジエンおよびエチレン性不飽和カルボン酸エステル
を主成分とし、これらを特定の割合い
で含む単量体組成物の重合によって得られる共重合体ラ
テックスを含むバインダー中に、発色剤マミ
イクロカプセル、保護剤その他必要に応じて加え□
られる添加剤を分散させて構成され
る。That is, the coating composition for pressure-sensitive copying paper of the present invention is a copolymer obtained by polymerizing a monomer composition containing an aliphatic conjugated diene and an ethylenically unsaturated carboxylic acid ester in a specific proportion. Add coloring agent Mami Microcapsules, protective agent, and other materials as necessary to the binder containing polymer latex.
It is composed of dispersed additives.
−ゝ
゛・ 以下、本発明の詳細な説明
する。−ゝ゛・ Hereinafter, the present invention will be explained in detail.
、)、−。, ), −.
パ 本発明における共重合体ラテ
ックスの製造に用・、□
し
。゛ いることのできる脂肪族共役
ジエンとしては、例えばブタジェン、イソプレン、2−
クロル−1,3ブタジエンなどを挙げることができ、特
にブタジェンが好ましい、脂肪族共役ジエンの使用量は
、単量体成分全体に対して2〜30重量%、好ましくは
5〜20重量%である。この使用量が2重量%未満であ
ると、感圧複写紙における発色性が不十分となり、−労
使用量が30重量%を越えると、感圧複写紙における摩
擦あるいは加熱に起因する発色カブリが生じやすくなり
、いずれも好ましくない。For use in the production of copolymer latex in the present invention. Examples of aliphatic conjugated dienes that can be present include butadiene, isoprene, 2-
Examples include chloro-1,3-butadiene, and butadiene is particularly preferred.The amount of aliphatic conjugated diene used is 2 to 30% by weight, preferably 5 to 20% by weight based on the entire monomer component. . If the amount used is less than 2% by weight, the color development in the pressure-sensitive copying paper will be insufficient, and if the amount used exceeds 30% by weight, coloring fog will occur due to friction or heating in the pressure-sensitive copying paper. Both are undesirable.
本発明における共重合体ラテックスの製造に用いること
のできるエチレン性不飽和カルボン酸エステルとしては
、例えばアクリル酸メチル、アクリル酸エチル、アクリ
ル酸ブチル、アクリル酸シクロヘキシル、アクリル酸−
2−エチルヘキシル、アクリル酸ヒドロキシエチル、メ
タクリル酸メチル、メタクリル酸エチル、メタクリル酸
ブチル、メタクリル酸シクロヘキシル、メタクリル酸−
2−エチルヘキシル、メタクリル酸ヒドロキシエチルな
どを挙げることができ、特にアクリル酸ブチル、アクリ
ル酸−2−エチルヘキシル、メタクリル酸ブチル、メタ
クリル酸−2−エチルヘキシルが好ましい。Examples of ethylenically unsaturated carboxylic acid esters that can be used in the production of the copolymer latex of the present invention include methyl acrylate, ethyl acrylate, butyl acrylate, cyclohexyl acrylate, and acrylic acid.
2-ethylhexyl, hydroxyethyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, methacrylic acid-
Examples include 2-ethylhexyl and hydroxyethyl methacrylate, with butyl acrylate, 2-ethylhexyl acrylate, butyl methacrylate, and 2-ethylhexyl methacrylate being particularly preferred.
エチレン性不飽和カルボン酸エステルの使用量は、単量
体成分全体に対し5〜70重量%、好ましくは10〜6
0重量%である。この使用量が5重量%未満であると、
加熱に起因する発色カブリが生じやすく、一方、使用量
が70重量%を越えると、圧力あるいは摩擦に起因する
発色カブリが生じやすくなり、いずれも好ましくない。The amount of ethylenically unsaturated carboxylic acid ester used is 5 to 70% by weight, preferably 10 to 6% by weight based on the total monomer components.
It is 0% by weight. If this usage amount is less than 5% by weight,
Color fogging due to heating tends to occur, while if the amount used exceeds 70% by weight, color fogging due to pressure or friction tends to occur, both of which are unfavorable.
本発明における共重合体ラテックスの合成に用いること
のできる、エチレン性不飽和カルボン酸エステル以外の
エチレン性不飽和化合物としては、アクリル酸、メタク
リル酸、クロトン酸、メタクロトン酸などのモノカルボ
ン酸、イタコン酸、マレイン酸、フマル酸等のジカルボ
ン酸およびこれらジカルボン酸の無水物などの不飽和カ
ルボン酸、スチレン、α−メチルスチレン、ビニルトル
エンなどの芳香族ビニル、アクリルアミド、メタクリル
アミド、N−メチロールアクリルアミド等の不飽和カル
ボン酸のアルキルアミド、アクリロニトリルなどのシア
ン化ビニル、酢酸ビニルなどを挙げることができ、これ
らは1種または2種以上を組合せて用いることができる
。Examples of ethylenically unsaturated compounds other than ethylenically unsaturated carboxylic acid esters that can be used in the synthesis of the copolymer latex of the present invention include monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, and methacrotonic acid; acids, unsaturated carboxylic acids such as dicarboxylic acids such as maleic acid and fumaric acid and anhydrides of these dicarboxylic acids, aromatic vinyls such as styrene, α-methylstyrene and vinyltoluene, acrylamide, methacrylamide, N-methylolacrylamide, etc. Examples include alkylamides of unsaturated carboxylic acids, vinyl cyanides such as acrylonitrile, and vinyl acetate, and these may be used alone or in combination of two or more.
本発明における共重合体ラテックスを構成する共重合体
のガラス転移温度は、好ましくは一50℃〜30℃、更
に好ましくは一40℃〜25℃である。このガラス転移
温度が一50℃より低くなるとバインダーの弾性が過大
となる傾向を有し、その結果感圧複写紙の発色性が低下
し、好ましくない。一方、ガラス転移温度が30℃を超
ると加熱に起因する発色カブリが発生しやすくなる傾向
を有し、好ましくない。The glass transition temperature of the copolymer constituting the copolymer latex in the present invention is preferably -50°C to 30°C, more preferably -40°C to 25°C. If the glass transition temperature is lower than 150° C., the elasticity of the binder tends to become excessive, resulting in a decrease in the color development of the pressure-sensitive copying paper, which is undesirable. On the other hand, if the glass transition temperature exceeds 30° C., color fogging due to heating tends to occur, which is not preferable.
本発明における共重合体ラテックスを構成する共重合体
のトルエン不溶分は、好ましくは30重量%以上、特に
好ましくは40〜100重量%である。The toluene insoluble content of the copolymer constituting the copolymer latex in the present invention is preferably 30% by weight or more, particularly preferably 40 to 100% by weight.
このトルエン不溶分が30重量%未満では感圧複写紙の
発色性が低下する傾向を有し、好ましくない。If the toluene-insoluble content is less than 30% by weight, the color development of the pressure-sensitive copying paper tends to decrease, which is not preferable.
ここにおけるトルエン不溶分とは、共重合体ラテックス
を水酸化ナトリウムによってpH6〜8に調整した後メ
タノールで凝固し、さらに洗浄乾燥□
して得られた凝固物を0.3g採取して試料とし、
□ この試料を1001のトルエン
に20時間浸漬したと゛ きに得
られた不溶分の試料全体に対する割合をいシ
バ・ う。The toluene-insoluble content here refers to copolymer latex that is adjusted to pH 6 to 8 with sodium hydroxide, coagulated with methanol, and then washed and dried.
0.3g of the coagulated material obtained was collected as a sample,
□ Calculate the ratio of insoluble matter to the total sample obtained when this sample was immersed in 1001 toluene for 20 hours.
゛。゛.
゛ 本発明における共重合体ラテ
ックスの使用量は、パ;・、
゛共重合体成分で換算してマイクロカプセル100重を
置部に対し好ましくは3〜50重量部、さらに好ま6
しくは5〜40重量部である。共重
合体ラテックスの使用量が3重量部未満では塗布組成物
の接着強゛、
度が不十分であり、一方、この使用量が50重量部−5
、
゛ を超えると塗布層中のマイクロ
カプセルが共重合体成分によって厚く覆われた状態とな
り、その結、 果、感圧複写紙にお
ける発色性が低下する。゛ The amount of copolymer latex used in the present invention is preferably 3 to 50 parts by weight, more preferably 6 parts by weight, based on 100 parts by weight of microcapsules in terms of copolymer components.
Preferably, it is 5 to 40 parts by weight. If the amount of copolymer latex used is less than 3 parts by weight, the adhesive strength of the coating composition will be insufficient;
, ゛, the microcapsules in the coating layer become thickly covered with the copolymer component, and as a result, the coloring properties of the pressure-sensitive copying paper deteriorate.
、1 本発明における共重合体ラ
テックスは、乳化型” 金時に単量
体を乳化分散するためにあるいは乳化重合後に生成した
共重合体粒子を安定に分散させと。, 1 The copolymer latex in the present invention is of an emulsion type, and is used to emulsify and disperse monomers or to stably disperse copolymer particles produced after emulsion polymerization.
1、IR,るために用いられる乳化剤を含んでいる。こ
のよ、1ユ、
(スうな乳化剤としては、陰イオン系界面活性剤、陽・
)ニア;
〉] イオン系界面活性剤、非イオ
ン系界面活性剤、両11.]
パ、゛ 生界面活性剤などが、単独
でまたは2種類以上組′:
合せて使用される。好ましい乳化剤は陰イオン系界面活
性剤であり、例えばラウリル硫酸ナトリウム、ドデシル
ベンゼンスルホン酸ナトリウム、ラウリルナフタレンス
ルホン酸ナトリウム、ジアルキルスルホコハク酸ナトリ
ウムなどを単独でまたは2種以上組合せて使用すること
ができる。1. Contains an emulsifier used for IR. This is 1 unit (such emulsifiers include anionic surfactants, positive and
) Near; 〉 ] Ionic surfactant, nonionic surfactant, both 11. ] Pa, ゛ Raw surfactants, etc. are used alone or in combination of two or more types. Preferred emulsifiers are anionic surfactants, such as sodium lauryl sulfate, sodium dodecylbenzenesulfonate, sodium laurylnaphthalenesulfonate, sodium dialkylsulfosuccinate, etc., which can be used alone or in combination of two or more.
共重合体ラテックスにおける乳化剤の含有量は、好まし
くは共重合体成分に対して1重量%以下、特に好ましく
は0.5重量%以下である。乳化剤の含有量が1重量%
を超えると感圧複写紙における発色性が低下する傾向を
有し、好ましくない。特に、発色剤マイクロカプセルと
してコアセルベーション法により合成されたゼラチンの
マイクロ力・プセルを用いるときには、ゼラチン膜の界
面活性剤に対する耐性が小さいため、カプセル内部の発
色剤が界面活性剤によって抽出されて発色カプリを生じ
やすくなるので、乳化剤の添加量を0.4重量%以下と
するのが好ましい。The content of the emulsifier in the copolymer latex is preferably at most 1% by weight, particularly preferably at most 0.5% by weight, based on the copolymer components. Emulsifier content is 1% by weight
If it exceeds 100%, the coloring properties of pressure-sensitive copying paper tend to decrease, which is not preferable. In particular, when gelatin microcapsules synthesized by the coacervation method are used as color former microcapsules, the color former inside the capsules may be extracted by the surfactant because the gelatin film has low resistance to surfactants. It is preferable that the amount of the emulsifier added is 0.4% by weight or less since coloring capri tends to occur.
本発明における共重合体ラテックスは、好ましくは上述
のガラス転移温度、トルエン不溶分およ、N
び乳化剤の含有量の条件をいずれか1つ含ん
だも、゛。The copolymer latex in the present invention preferably has the above-mentioned glass transition temperature, toluene-insoluble content, and N
and emulsifier content.
“ の、より好ましくは2つの条件
を含んだもの、さ5、 らに好まし
くは3つの条件を含んだものである。More preferably, it includes two conditions, and still more preferably, it includes three conditions.
本発明における発色剤マイクロカプセルは、例一
えば以下に具体的に述べるコアセルベーション法、t′
。The color former microcapsules in the present invention can be produced by, for example, the coacervation method specifically described below, t'
.
、□゛ 界面重合法、In 5itu
重合法などの各種方法によ”丁、”i、’
−y 7 ′i′′8 h !
6 (7) “JflkN4.:、& ”″。。, □゛ Interfacial polymerization method, In 5itu
"Ding,""i," by various methods such as polymerization method
-y 7 ′i′′8 h !
6 (7) “JflkN4.:, & “”.
■コアセルベーション法
、 この方法は、例えば米国特許
第2800457号明細゛1′ 書
、同2800458号明細書において開示されている、
□□
い・
、、 ように、発色剤を溶解した油
性液体を、ゼラチン、゛ アラビア
ゴム等の親水性高分子の水溶液に微小油滴状に乳化分散
させ、この微小油滴の表面に前記】
親水性高分子のコロイドを相分離(コアセルベート)さ
せ、これを硬化させて壁膜を形成し、マイ、
クロカプセルを得るものである。■Coacervation method: This method is disclosed in, for example, U.S. Patent Nos. 2,800,457 and 2,800,458.
□□ As shown above, an oily liquid in which a coloring agent has been dissolved is emulsified and dispersed in the form of minute oil droplets in an aqueous solution of a hydrophilic polymer such as gelatin or gum arabic, and the above is applied to the surface of these minute oil droplets. The hydrophilic polymer colloid undergoes phase separation (coacervate) and is cured to form a wall film.
This is to obtain black capsules.
: ■界面型合法
ミ
1、 この方法は、例えば特公昭
44−27257号公報、同42−771号公報、同4
6−18127号公報、同50−72507号公報に開
示されているように、親水性液体と疎水性液体の界面に
おいて互いに反応して不溶性の被膜を形成する二種類の
物質を、それぞれ親水性液体および疎水性液体に溶解し
て界面反応させることにより、例えばポリアミドのカプ
セル”、J、’++Id*“”? C17″ゞ/L41
1J(7) 、、である。: ■Interfacial method Mi1 This method is described, for example, in Japanese Patent Publication No. 44-27257, Japanese Patent Publication No. 42-771, Japanese Patent Publication No. 4
As disclosed in Publication No. 6-18127 and Publication No. 50-72507, two types of substances that react with each other to form an insoluble film at the interface of a hydrophilic liquid and a hydrophobic liquid are mixed into a hydrophilic liquid and a hydrophobic liquid, respectively. and by dissolving it in a hydrophobic liquid and causing an interfacial reaction, for example, a polyamide capsule",J,'++Id*""?C17"ゞ/L41
1J(7).
■In 5itu重合法
この方法は、例えば特公昭44−3495号公報に開示
されているように、芯材物質(発色剤を含む油滴)とリ
アクタントすなわちポリマーの形成に必 要なモノ
マー、プレポリマーあるいは触媒などの反応系成分とが
共存する分散系において重合を行なうことにより、芯材
物質の粒子と分散媒との界面でこれら両者に対して不溶
のボリマニを生成させ、これにより芯材物質の粒子表面
にポリマーの外殻を形成してマイクロカプセルを得るも
のである。この方法によればカプセル壁膜がメラミン−
ホルマリン樹脂、尿素−ホルマリン樹脂などより構成さ
れたマイクロカプセルを得ることができる。■In-5-itu polymerization method This method, as disclosed in Japanese Patent Publication No. 44-3495, uses a core material (oil droplets containing a coloring agent) and a reactant, that is, monomers and prepolymers necessary to form a polymer. Alternatively, polymerization may be carried out in a dispersion system in which reaction system components such as catalysts coexist, thereby forming a voluminous substance that is insoluble in the particles of the core material and the dispersion medium at the interface between the particles of the core material and the dispersion medium. Microcapsules are obtained by forming a polymer shell on the particle surface. According to this method, the capsule wall membrane is melamine-
Microcapsules made of formalin resin, urea-formalin resin, etc. can be obtained.
このようなIn 5itu法によるメラミンーホルマリ
ン樹脂、尿素−ホルマリン樹脂などの壁膜によ、
るマイクロカプセルは、耐熱性、耐溶剤性
、耐水。 性、耐薬品性において優
れ、しかも当該マイクロハ カプセル
は簡易なプロセスによって安定に製造す、−1、ること
ができる点で、本発明における発色剤マイ、
クロカプセルとして有利に用いることができ
る。By using wall membranes such as melamine-formalin resin and urea-formalin resin using the In 5 intu method,
The microcapsules are heat resistant, solvent resistant, and water resistant. The coloring agent of the present invention has excellent properties in terms of properties and chemical resistance, and the microcapsules can be stably produced by a simple process.
It can be advantageously used as a black capsule.
・ 上記発色剤マイクロカプセル
を構成する発色剤ゝ。- A color former that constitutes the color former microcapsule.
一、:’:’□、’(としては通常用いられているもの
でよく、例えば1、)□・S
八・ クリスタルバイオレットラ
クトン、ペンゾイルロ′4
0゛ イコメチレンブルー、フル
オラン類、スピαピラ、V、・
パフ。1, :':'□,' (for example, 1,) □・S 8. Crystal violet lactone, penzoyluro'4 0゛ Icomethylene blue, fluorans, Spiαpira, V ,・ Puff.
゛ン類などを使用することができる。You can use the following.
□ また、この発色剤と接触して
これを発色させるための顕色剤としては、例えば酸性白
土、活性臼、 土などの無機系顕色
剤、フェノール樹脂、サリチ−ル酸誘導体塩などの有機
系顕色剤を使用すること5. がで
きる。□ In addition, as a color developer that develops color by contacting this color former, for example, inorganic color developers such as acid clay, activated mortar, and earth, organic color developers such as phenolic resin, and salicylic acid derivative salts. 5. Use a color developer. I can do it.
本発明において用いられる保護剤としては、通常用いら
れているものでよく、例えばデンプン、セルロースなど
の有機物質あるいは無機物質の粉7
末が使用され、その使用量は一般に発色剤マイクロ
カプセル100重量部に対して20〜80重量部である
。The protective agent used in the present invention may be one that is commonly used, such as powders of organic substances such as starch and cellulose, or powders of inorganic substances.
The amount used is generally 20 to 80 parts by weight per 100 parts by weight of color former microcapsules.
采発明においては、さらに必要に応じて、消泡剤、耐水
化剤などの各種添加剤を含むことができる。また、バイ
ンダーとしては、本発明における共重合体ラテックスの
他に接着強度を補うために、必要に応じて水溶性高分子
、例えば水溶性の変性デンプン、ポリビニルアルコール
、ヒドロキシエチルセルロースなどを併用することがで
きる。In the kettle invention, various additives such as an antifoaming agent and a waterproofing agent can be further included as necessary. In addition to the copolymer latex used in the present invention, as a binder, water-soluble polymers such as water-soluble modified starch, polyvinyl alcohol, hydroxyethyl cellulose, etc. may be used in combination as necessary to supplement adhesive strength. can.
本発明の塗布組成物は、上述の各種材料を混合して調整
され、該塗布組成物中の固形分濃度は一般に15〜50
重量%とされる。この塗布組成物は、通常の塗被紙製造
に使用されているブレードコータ、エアナイフコータ、
バーコータ、ロールコータ、サイズプレスコータなどの
塗被装置を備えた )オンマシンコ
ータによって原紙に塗被されて感圧複写紙とされる0本
発明の塗布組成物の好ましい塗布量は、原紙の単位面積
あたり2〜5 g/nlであ する、原
紙としては、酸性あるいはアルカリ性の抄紙によって得
られる上質原紙、中質原紙などを使用することができる
。The coating composition of the present invention is prepared by mixing the above-mentioned various materials, and the solid content concentration in the coating composition is generally 15 to 50.
% by weight. This coating composition can be applied to blade coaters, air knife coaters, and
A preferred coating amount of the coating composition of the present invention is determined per unit of base paper by coating the base paper with an on-machine coater (equipped with a coating device such as a bar coater, roll coater, size press coater, etc.) to make pressure-sensitive copying paper. As the base paper, which has a density of 2 to 5 g/nl per area, high-quality base paper, medium-quality base paper, etc. obtained by acidic or alkaline paper making can be used.
以下、本発明の実施例について述べるが、本発明はこれ
らに限定されるものではない、なお、以下の記載におい
て「部」および「%」は、それぞれ重量部および重量%
を示す。Examples of the present invention will be described below, but the present invention is not limited thereto. In the following description, "parts" and "%" refer to parts by weight and % by weight, respectively.
shows.
、、 実施例1〜7.比較例1〜
4、(1)共重合体ラテックスA−Jの製造1,9
〈共重合体ラテックスA〉水160
部、アルキルベンゼンスルホン酸ナトリウム0.3部、
炭酸水素ナトリウム0.6部および過硫酸カリウム0.
5部を、容積1001のオートクレーブに仕込んだ。つ
いで、ブタジェン15部、スチレン62部、ブチルアク
リレート20部、アクリル酸1部およびフマル酸2部か
らなる単量体組成物を四塩化炭素2部とともに一括添加
し、攪拌しながら70℃まで加温した。この状態で重合
を20時間継続したところ、重合転化率100%に達し
た。このようにして得られた共重合体ラテックスは、重
合様態がよく、凝固物の発生も少なかった。この共重合
体ラテックスに水酸化ナトリウム溶液を添加し、pHを
9に調節した後、モノマーストリッピング、減圧蒸留に
よりラテックスを濃縮した。得られた共重合体ラテック
スを「ラテックスA」とする。,, Examples 1 to 7. Comparative example 1~
4. (1) Production of copolymer latex A-J 1,9
<Copolymer latex A> Water 160
parts, 0.3 parts of sodium alkylbenzenesulfonate,
0.6 parts of sodium bicarbonate and 0.6 parts of potassium persulfate.
5 parts were charged into a 1001 volume autoclave. Next, a monomer composition consisting of 15 parts of butadiene, 62 parts of styrene, 20 parts of butyl acrylate, 1 part of acrylic acid, and 2 parts of fumaric acid was added at once along with 2 parts of carbon tetrachloride, and the mixture was heated to 70°C while stirring. did. When polymerization was continued in this state for 20 hours, the polymerization conversion rate reached 100%. The copolymer latex obtained in this way had a good polymerization mode and little generation of coagulum. A sodium hydroxide solution was added to this copolymer latex to adjust the pH to 9, and then the latex was concentrated by monomer stripping and vacuum distillation. The obtained copolymer latex is referred to as "Latex A".
く共重合体ラテックスB−J>
共重合体ラテックスAと同様な手順により、第1表に示
す単量体成分を用いて9種の共重合体ラテックスを得た
。これらの共重合体ラテックスを「ラテックスB−JJ
とする。Copolymer Latex B-J> Nine types of copolymer latexes were obtained by the same procedure as Copolymer Latex A using the monomer components shown in Table 1. These copolymer latexes are called “Latex B-JJ”
shall be.
なお、ラテックスG−Jは比較用ラテックスであり、ラ
テックスGは、脂肪族共役ジエン((al ’)を含ま
ない場合、ラテックスHは脂肪族共役ジエン((al)
の割合が過大の場合、ラテックスIはエチレン性不飽和
カルボン酸エステル((bl)の割合が過小な場合、ラ
テックスJはエチレン性不飽和カルボン酸エステル((
bl )の割合が過大な場合の例である。Note that latex G-J is a latex for comparison; latex G does not contain an aliphatic conjugated diene ((al'), and latex H contains an aliphatic conjugated diene ((al)).
If the proportion of .
This is an example of a case where the ratio of bl ) is excessive.
以上のラテッスクA−Jのガラス転移温度(Tg)およ
びトルエン不溶分を第1表に併せて記載する。The glass transition temperature (Tg) and toluene insoluble content of the above latex A-J are also listed in Table 1.
(2)発色剤マイクロカプセルの合成
有機溶剤rsAs296J (目方側製) 100部
に対しクリスタルバイオレットラクトン3.5部を、、
溶解した発色剤溶液を、スチレン
−無水マレイン゛・ 酸共重合体4
部を含む水溶液に添加して乳化した。(2) Synthesis of color former microcapsules 3.5 parts of crystal violet lactone per 100 parts of organic solvent rsAs296J (manufactured by Megaga).
The dissolved color former solution was mixed with styrene-maleic anhydride/acid copolymer 4.
was added to an aqueous solution containing 100% of the total amount of 100% of the total amount of 100% of the product.
、\
ついで、固形分15%のメラミン−ホルマリン初期、
Ill r S R613J
(住友化学[[1製) O水tljH5′7
・・’ 60部を加えた後70’
Cまで加熱し、3時間にゎたっ、ゞ
ン\
、、・ て反応させた。つぎにこの
反応生成液にpH9,0に〈・、
一゛。,\ Next, the initial stage of melamine-formalin with a solid content of 15%,
Ill r S R613J
(Sumitomo Chemical [[manufactured by 1] O water tljH5'7...'70' after adding 60 parts)
The mixture was heated to C and allowed to react for 3 hours. Next, this reaction product solution was adjusted to pH 9.0.
ン(“6ま7水酸化ナトリ’7A(7)水溶液を添加し
・発・□;
111、 色剤マイクロカプセルの
分散体を作成した。この\は
9パ) マイクロカプセルの平均
粒径は4.5μmであった。111, A dispersion of colorant microcapsules was created. This \ is 9p) The average particle size of the microcapsules is 4. It was .5 μm.
、□・、
’::) (3>塗布組成物の調
整J
〕 以上のように得られた共重合
体ラテックスおよt〜
1 び発色剤マイクロカプセルを用
い、第2表に示す゛ 組伐の各材料を
混合し、固形分の割合が35%の塗□、
゛ 布組放物を、実施例につき7種
および比較例にっ□
゛、L
・、 き4種調整した。, □・, '::) (3> Preparation of coating composition J) Using the copolymer latex obtained as above, t~ 1 and color former microcapsules, the ゛ grouping shown in Table 2 was carried out. The following materials were mixed to prepare 7 types of coating materials with a solid content ratio of 35% and 4 types of □ ゛, L., and Comparative Examples.
1ゝ
(4)特性テスト
上記(3)で得られた各塗布組成物を、ロンドを用いて
塗布量が3.0g/rrlとなるようそれぞれ原紙に塗
布し、感圧複写紙用の上用紙を得た。これらの上用紙と
市販の下用紙1”ccpJ (十條製紙■製)とをそ
れぞれ重ね合せて感圧複写紙のサンプルを形成し、以下
の4項目についてテストを行った。1. (4) Characteristic test Each of the coating compositions obtained in (3) above was applied to base paper using a rondo so that the coating amount was 3.0 g/rrl, and the upper paper for pressure-sensitive copying paper was coated. I got it. These top paper and commercially available bottom paper 1''ccpJ (manufactured by Jujo Paper Industries, Ltd.) were overlapped to form samples of pressure-sensitive copying paper, and the following four items were tested.
■発色性
各サンプルをタイプライタ−によって印字し、30分後
における下用紙の発色濃度をハンター比色光度計によっ
て測定し、白色度(%)を求め、これにより発色性を評
価した。白色度の値が小さいほど発色性は良好である。(2) Color development Each sample was printed using a typewriter, and 30 minutes later, the color density of the lower paper was measured using a Hunter colorimeter to determine the degree of whiteness (%), and the color development was evaluated based on this. The smaller the whiteness value, the better the color development.
■耐圧性(加圧による発色カブリの発生状a)各サンプ
ルを圧力50−/−で5分間にねたつ、て加圧した後、
下用紙の白色度をハンター比色光度計によって測定した
。白色度の値が大きいほど発色カブリの発生が少なく、
耐圧性は良好である。■Pressure resistance (occurrence of color fog due to pressure a) After pressurizing each sample at a pressure of 50-/- for 5 minutes,
The whiteness of the bottom paper was measured using a Hunter colorimeter. The higher the whiteness value, the less color fog will occur;
Pressure resistance is good.
■耐摩擦性(摩擦による発色カブリの発生状B)各サン
プルの下用紙を上側にし、その上に重さ3kgのおもり
を載せてこれを一定の距離(30C1l)にわたって滑
らせた後、下用紙の白色度をハンター比色光度計によっ
て測定した。白色度の値が大きいほど発色カブリの発生
が少なく、耐摩擦性は良好である。■Abrasion resistance (state of color fogging caused by friction B) Place the bottom paper of each sample on top, place a weight of 3 kg on top of it, slide it over a certain distance (30C1l), and then place the bottom paper on top. The whiteness of the sample was measured using a Hunter colorimeter. The larger the whiteness value, the less color fog occurs and the better the abrasion resistance.
■耐熱性
各サンプルを120℃に設定したオープン中で3時間に
わたって加熱した後、下用紙の白色度をハ、3
ンター比色光度計によって測定した。白色
度の値が大きいほど発色カブリの発生が少なく、耐熱性
は良好である。■Heat resistance After heating each sample in an open oven set to 120℃ for 3 hours, the whiteness of the bottom paper was
It was measured by an internal colorimeter. The larger the whiteness value, the less color fog occurs and the better the heat resistance.
以上の特性テストの結果を第2表に示す。The results of the above characteristic tests are shown in Table 2.
、゛
、X′
♂
第2表に示す結果より明らかなように、本発明の実施例
においては、各特性テストにおいて実用上十分満足すべ
き結果が得られたが、比較例においては特性の全般にわ
たって良好な結果を得ることができなかった。すなわち
、比較例1においては、共重合体ラテックスの製造に用
いる単量体成分として脂肪族共役ジエンを含まず、発色
性が不十分である。比較例2においては、脂肪族共役ジ
エンが過大であり、摩擦あるいは加熱による発色カブリ
を生じやすい。比較例3においては、エチレン性不飽和
カルボン酸エステルが過小であり、加熱による発色カブ
リを生じやすい。比較例4においては、エチレン性不飽
和カルボン酸化エステルが過大であり、加圧あるいは摩
擦による発色カブリを生じやすい。, ゛, I couldn't get good results over time. That is, in Comparative Example 1, no aliphatic conjugated diene was included as a monomer component used in the production of the copolymer latex, and the color development was insufficient. In Comparative Example 2, the amount of aliphatic conjugated diene is excessive, and color fogging is likely to occur due to friction or heating. In Comparative Example 3, the amount of ethylenically unsaturated carboxylic acid ester is too small, and color fogging is likely to occur due to heating. In Comparative Example 4, the amount of ethylenically unsaturated carboxylic ester is excessive, and color fogging is likely to occur due to pressure or friction.
本発明の感圧複写紙用塗布組成物は、バインダーとして
、特定の単量体成分を特定の割合で含む単量体組成物の
重合によって得られる共重合体ラテックスを用いており
、以下の作用効果を有す、る。The coating composition for pressure-sensitive copying paper of the present invention uses a copolymer latex obtained by polymerizing a monomer composition containing specific monomer components in a specific ratio as a binder, and has the following effects. have an effect.
(1)塗工性が優れている。(1) Excellent coating properties.
本発明の塗布組成物は、バインダーとして共重合体ラテ
ックスを用い、粘度の大きい水溶性高分子化合物を用い
なくともよくあるいは用いたとしてもその使用量はわず
かでよいため、粘性が低く、したがって塗工作業を円滑
に行うことができる。The coating composition of the present invention uses a copolymer latex as a binder and does not require the use of a water-soluble polymer compound with high viscosity, or even if it is used, only a small amount thereof is used. Construction work can be carried out smoothly.
また、同様の理由により良好な塗工性を保持しながら塗
布組成物の固形分濃度を大きくすることができるので、
塗工生産性の点で有利である。In addition, for the same reason, the solid content concentration of the coating composition can be increased while maintaining good coating properties.
This is advantageous in terms of coating productivity.
(2)保存性が優れている。(2) Excellent storage stability.
本発明の塗布組成物は、バインダーとして共重合体ラテ
ックスを用い、腐敗しやすい水溶性高分子化合物を用い
なくともよくあるいは用いたとしてもその使用量はわず
かでよいため、保存性が良好で長期間にねたちで品質の
低下を招くことがない。The coating composition of the present invention uses a copolymer latex as a binder, and does not require the use of perishable water-soluble polymer compounds, or even if it is used, only a small amount is used, so it has good shelf life and long-lasting properties. There will be no deterioration in quality due to overtime.
(3)発色性ならびに発色カブリの点で優れた感圧複写
紙を得ることができる。(3) Pressure-sensitive copying paper excellent in color development and color fog can be obtained.
本発明の塗布組成物は、バインダーとして共重合体ラテ
ックスを用いているので塗膜(発色剤層)に適度な弾性
を付与することができ、その結果、感圧複写紙に使用時
以外に作用する外力、例えば製造時、貯蔵時などにおい
て必然的もしくは偶発的に作用する比較的小さな押圧力
、摩擦力、熱応力などに対しては、これを十分に吸収し
、発色剤カプセルに作用する力を弱めることができるの
で、使用時における発色機能を阻害することなく、発色
カブリの発生を効果的に防止することができる。Since the coating composition of the present invention uses a copolymer latex as a binder, it can impart appropriate elasticity to the coating film (color former layer), and as a result, it has an effect on pressure-sensitive copying paper even when not in use. It can sufficiently absorb external forces such as relatively small pressing force, frictional force, thermal stress, etc. that are inevitably or accidentally applied during manufacturing, storage, etc., and the force that acts on the color former capsule. Since the coloring function can be weakened, it is possible to effectively prevent coloring fog from occurring without impeding the coloring function during use.
Claims (1)
を含有する感圧複写紙用塗布組成物において、 前記バインダー成分として、以下の単量体成分(a)脂
肪族共役ジエン 2〜30重量% (b)エチレン性不飽和カルボン酸エステル 5〜70
重量% (c)(b)以外のエチレン性不飽和化合物 10〜9
3重量% を共重合させて得られる共重合体ラテックスを含有する
ことを特徴とする感圧複写紙用塗布組成物。 2)共重合体ラテックスにおける共重合体成分のガラス
転移温度が−50℃〜+30℃の範囲にある特許請求の
範囲第1項記載の感圧複写紙用塗布組成物。 3)共重合体ラテックスにおける共重合体成分のトルエ
ン不溶分が30重量%以上である特許請求の範囲第1項
記載の感圧複写紙用塗布組成物。 4)共重合体ラテックスにおける乳化剤の使用量が共重
合体成分に対して1重量%以下である特許請求の範囲第
1項記載の感圧複写紙用塗布組成物。[Scope of Claims] 1) A coating composition for pressure-sensitive copying paper containing microcapsules encapsulating a coloring agent and a binder, wherein the binder component includes the following monomer components (a) aliphatic conjugated diene 2 ~30% by weight (b) Ethylenically unsaturated carboxylic acid ester 5~70
Weight% (c) Ethylenically unsaturated compounds other than (b) 10-9
A coating composition for pressure-sensitive copying paper, characterized in that it contains a copolymer latex obtained by copolymerizing 3% by weight of a copolymer latex. 2) The coating composition for pressure-sensitive copying paper according to claim 1, wherein the copolymer component in the copolymer latex has a glass transition temperature in the range of -50°C to +30°C. 3) The coating composition for pressure-sensitive copying paper according to claim 1, wherein the toluene-insoluble content of the copolymer component in the copolymer latex is 30% by weight or more. 4) The coating composition for pressure-sensitive copying paper according to claim 1, wherein the amount of emulsifier used in the copolymer latex is 1% by weight or less based on the copolymer components.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60115465A JPS61273985A (en) | 1985-05-30 | 1985-05-30 | Coating composition for pressure-sensitive copy paper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60115465A JPS61273985A (en) | 1985-05-30 | 1985-05-30 | Coating composition for pressure-sensitive copy paper |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61273985A true JPS61273985A (en) | 1986-12-04 |
JPH0453190B2 JPH0453190B2 (en) | 1992-08-25 |
Family
ID=14663209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60115465A Granted JPS61273985A (en) | 1985-05-30 | 1985-05-30 | Coating composition for pressure-sensitive copy paper |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61273985A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61280985A (en) * | 1985-06-07 | 1986-12-11 | Nippon Zeon Co Ltd | Coating composition for pressure-sensitive recording paper |
DE3828084A1 (en) * | 1987-08-19 | 1989-03-02 | Mitsubishi Paper Mills Ltd | CARBON-FREE, PRESSURE-SENSITIVE RECORDING PAPER |
JPH02112982A (en) * | 1988-10-21 | 1990-04-25 | Mitsubishi Paper Mills Ltd | Carbonless pressure sensitive copy paper |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57185185A (en) * | 1981-04-30 | 1982-11-15 | Bayer Ag | Flexographic printing ink for manufacturing sensing copying paper |
JPS5955789A (en) * | 1982-09-24 | 1984-03-30 | Japan Synthetic Rubber Co Ltd | Coating composition for pressure sensitive copy paper |
JPS6097886A (en) * | 1983-11-02 | 1985-05-31 | Jujo Paper Co Ltd | Pressure-sensitive recording sheet |
-
1985
- 1985-05-30 JP JP60115465A patent/JPS61273985A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57185185A (en) * | 1981-04-30 | 1982-11-15 | Bayer Ag | Flexographic printing ink for manufacturing sensing copying paper |
JPS5955789A (en) * | 1982-09-24 | 1984-03-30 | Japan Synthetic Rubber Co Ltd | Coating composition for pressure sensitive copy paper |
JPS6097886A (en) * | 1983-11-02 | 1985-05-31 | Jujo Paper Co Ltd | Pressure-sensitive recording sheet |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61280985A (en) * | 1985-06-07 | 1986-12-11 | Nippon Zeon Co Ltd | Coating composition for pressure-sensitive recording paper |
JPH051149B2 (en) * | 1985-06-07 | 1993-01-07 | Nippon Zeon Co | |
DE3828084A1 (en) * | 1987-08-19 | 1989-03-02 | Mitsubishi Paper Mills Ltd | CARBON-FREE, PRESSURE-SENSITIVE RECORDING PAPER |
US4931422A (en) * | 1987-08-19 | 1990-06-05 | Mitsubishi Paper Mills Limited | No-carbon pressure-sensitive copying paper |
JPH02112982A (en) * | 1988-10-21 | 1990-04-25 | Mitsubishi Paper Mills Ltd | Carbonless pressure sensitive copy paper |
Also Published As
Publication number | Publication date |
---|---|
JPH0453190B2 (en) | 1992-08-25 |
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LAPS | Cancellation because of no payment of annual fees |