FI65188C - Tryckkaensligt kopieringssystem - Google Patents
Tryckkaensligt kopieringssystem Download PDFInfo
- Publication number
- FI65188C FI65188C FI782771A FI782771A FI65188C FI 65188 C FI65188 C FI 65188C FI 782771 A FI782771 A FI 782771A FI 782771 A FI782771 A FI 782771A FI 65188 C FI65188 C FI 65188C
- Authority
- FI
- Finland
- Prior art keywords
- solvent
- weight
- color
- copying system
- xylene
- Prior art date
Links
- 239000002904 solvent Substances 0.000 claims description 59
- 239000000203 mixture Substances 0.000 claims description 37
- 239000000126 substance Substances 0.000 claims description 23
- -1 phthalide compound Chemical class 0.000 claims description 16
- 239000003085 diluting agent Substances 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 12
- 239000004615 ingredient Substances 0.000 claims description 10
- WNZQDUSMALZDQF-UHFFFAOYSA-N isobenzofuranone Natural products C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- 239000000758 substrate Substances 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000011877 solvent mixture Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 4
- 229920000620 organic polymer Polymers 0.000 claims description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000006069 physical mixture Substances 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 25
- 235000019645 odor Nutrition 0.000 description 25
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 24
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 20
- 239000000376 reactant Substances 0.000 description 17
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 16
- 230000002378 acidificating effect Effects 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- 239000008096 xylene Substances 0.000 description 14
- 239000003094 microcapsule Substances 0.000 description 13
- 238000011161 development Methods 0.000 description 9
- 230000018109 developmental process Effects 0.000 description 9
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 5
- 229940073608 benzyl chloride Drugs 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 229920001568 phenolic resin Polymers 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 150000003738 xylenes Chemical class 0.000 description 5
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 4
- HKTCLPBBJDIBGF-UHFFFAOYSA-N 1-phenyl-2-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC=C1C1=CC=CC=C1 HKTCLPBBJDIBGF-UHFFFAOYSA-N 0.000 description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical class C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 3
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 125000005506 phthalide group Chemical group 0.000 description 3
- 239000003549 soybean oil Substances 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- MRAKLTZPBIBWFH-ARJAWSKDSA-N (z)-2-ethenylbut-2-enedioic acid Chemical compound OC(=O)\C=C(\C=C)C(O)=O MRAKLTZPBIBWFH-ARJAWSKDSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical group C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000005574 benzylation reaction Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000001911 terphenyls Chemical class 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 1
- AGPLQTQFIZBOLI-UHFFFAOYSA-N 1-benzyl-4-phenylbenzene Chemical group C=1C=C(C=2C=CC=CC=2)C=CC=1CC1=CC=CC=C1 AGPLQTQFIZBOLI-UHFFFAOYSA-N 0.000 description 1
- KTHUKEZOIFYPEH-UHFFFAOYSA-N 1-benzylnaphthalene Chemical class C=1C=CC2=CC=CC=C2C=1CC1=CC=CC=C1 KTHUKEZOIFYPEH-UHFFFAOYSA-N 0.000 description 1
- VXVRAGONKSWKEZ-UHFFFAOYSA-N 3,3-bis(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C3=C(N(C4=CC=CC=C43)C)C)=C(C)N(C)C2=C1 VXVRAGONKSWKEZ-UHFFFAOYSA-N 0.000 description 1
- FNVUVCSZVQWREE-UHFFFAOYSA-N 3,3-bis(2-phenyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C12=CC=CC=C2C(=O)OC1(C=1C2=CC=CC=C2NC=1C=1C=CC=CC=1)C(C1=CC=CC=C1N1)=C1C1=CC=CC=C1 FNVUVCSZVQWREE-UHFFFAOYSA-N 0.000 description 1
- MLJCAUJSTUJCIN-UHFFFAOYSA-N 3-(1,2-dimethylindol-3-yl)-3-(2-methyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C=3C4=CC=CC=C4NC=3C)=C(C)N(C)C2=C1 MLJCAUJSTUJCIN-UHFFFAOYSA-N 0.000 description 1
- CJSOSUBVRGWJCL-UHFFFAOYSA-N 3-(ethylamino)-3h-2-benzofuran-1-one Chemical group C1=CC=C2C(NCC)OC(=O)C2=C1 CJSOSUBVRGWJCL-UHFFFAOYSA-N 0.000 description 1
- MQJTWPAGXWPEKU-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-3-(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C3=CC=CC=C3N(C)C=2C)C2=CC=CC=C2C(=O)O1 MQJTWPAGXWPEKU-UHFFFAOYSA-N 0.000 description 1
- VJBVGLAFSLVHOY-UHFFFAOYSA-N 3-[4-(methylamino)phenyl]-3h-2-benzofuran-1-one Chemical compound C1=CC(NC)=CC=C1C1C2=CC=CC=C2C(=O)O1 VJBVGLAFSLVHOY-UHFFFAOYSA-N 0.000 description 1
- OPLBFHRSNKSMKD-UHFFFAOYSA-N 3H-2-benzofuran-1-one 1H-indole Chemical class C1=CC=C2NC=CC2=C1.C1=CC=C2C(=O)OCC2=C1 OPLBFHRSNKSMKD-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- RNRINRUTVAFUCG-UHFFFAOYSA-N 5-(dimethylamino)-3,3-bis(1,2-dimethylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C=4C5=CC=CC=C5N(C)C=4C)OC(=O)C4=CC=C(C=C43)N(C)C)=C(C)N(C)C2=C1 RNRINRUTVAFUCG-UHFFFAOYSA-N 0.000 description 1
- QTTJEVLAPAZDQK-UHFFFAOYSA-N 5-(dimethylamino)-3,3-bis(9-ethylcarbazol-2-yl)-2-benzofuran-1-one Chemical compound C(C)N1C2=CC=CC=C2C=2C=CC(=CC1=2)C1(OC(=O)C2=CC=C(C=C12)N(C)C)C1=CC=2N(C3=CC=CC=C3C=2C=C1)CC QTTJEVLAPAZDQK-UHFFFAOYSA-N 0.000 description 1
- UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Chemical group C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 1
- IPAJDLMMTVZVPP-UHFFFAOYSA-N Crystal violet lactone Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C=CC(=CC=2)N(C)C)C2=CC=C(N(C)C)C=C2C(=O)O1 IPAJDLMMTVZVPP-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 206010024769 Local reaction Diseases 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- ZKURGBYDCVNWKH-UHFFFAOYSA-N [3,7-bis(dimethylamino)phenothiazin-10-yl]-phenylmethanone Chemical group C12=CC=C(N(C)C)C=C2SC2=CC(N(C)C)=CC=C2N1C(=O)C1=CC=CC=C1 ZKURGBYDCVNWKH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 150000004074 biphenyls Chemical class 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000004432 carbon atom Chemical group C* 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
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000000003 hoof Anatomy 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Chemical group CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Chemical group C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229940107698 malachite green Drugs 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- YRMHIELITJAHGD-UHFFFAOYSA-K nitromethane;trichloroalumane Chemical compound [Al+3].[Cl-].[Cl-].[Cl-].C[N+]([O-])=O YRMHIELITJAHGD-UHFFFAOYSA-K 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000000424 optical density measurement Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000013042 solid detergent Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 150000003751 zinc Chemical class 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
- B41M5/165—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 characterised by the use of microcapsules; Special solvents for incorporating the ingredients
- B41M5/1655—Solvents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/914—Transfer or decalcomania
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
Landscapes
- Color Printing (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83269877 | 1977-09-12 | ||
| US05/832,698 US4130299A (en) | 1977-09-12 | 1977-09-12 | Low-odor dye solvents for pressure-sensitive copying systems |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI782771A7 FI782771A7 (fi) | 1979-03-13 |
| FI65188B FI65188B (fi) | 1983-12-30 |
| FI65188C true FI65188C (fi) | 1984-04-10 |
Family
ID=25262383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI782771A FI65188C (fi) | 1977-09-12 | 1978-09-11 | Tryckkaensligt kopieringssystem |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4130299A (en, 2012) |
| JP (1) | JPS5451612A (en, 2012) |
| BE (1) | BE870371A (en, 2012) |
| BR (1) | BR7805916A (en, 2012) |
| CA (1) | CA1107501A (en, 2012) |
| DE (1) | DE2839512A1 (en, 2012) |
| ES (1) | ES473236A1 (en, 2012) |
| FI (1) | FI65188C (en, 2012) |
| FR (1) | FR2402535A1 (en, 2012) |
| GB (1) | GB2004310B (en, 2012) |
| IT (1) | IT1099039B (en, 2012) |
| MX (1) | MX149597A (en, 2012) |
| NL (1) | NL184728C (en, 2012) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4275906A (en) * | 1979-07-18 | 1981-06-30 | Diamond Shamrock Corporation | Pressure sensitive recording sheets |
| US4547222A (en) * | 1984-05-21 | 1985-10-15 | Ncr Corporation | High print intensity marking fluid |
| JPS6141593A (ja) * | 1984-08-06 | 1986-02-27 | Nippon Petrochem Co Ltd | 感圧紙染料用溶剤 |
| US4636818A (en) * | 1985-06-05 | 1987-01-13 | Moore Business Forms, Inc. | Carbonless system including solvent-only microcapsules |
| US4737189A (en) * | 1985-06-13 | 1988-04-12 | Kawaguti & Partners | Solvent of a chromogenic dye-precursor material for pressure-sensitive recording paper, the pressure-sensitive recording paper and process for producing the solvent |
| US4795493A (en) * | 1986-01-07 | 1989-01-03 | Kureha Kagaku Kogyo Kabushiki Kaisha | Solvent for chromogenic dye-precursor material for pressure-sensitive recording paper sheet and pressure-sensitive recording paper sheet prepared by using the solvent |
| FR2618142B1 (fr) * | 1987-07-16 | 1989-10-06 | Atochem | Compositions d'oligomeres de polyarylalcanes contenant des motifs xylene et leur procede de fabrication |
| GB0112180D0 (en) | 2001-05-18 | 2001-07-11 | Eastman Kodak Co | A method and system for processing of photographic materials |
| US6939826B2 (en) | 2002-06-25 | 2005-09-06 | Appleton Papers, Inc. | Product authentication |
| US6790899B2 (en) * | 2002-10-29 | 2004-09-14 | General Electric Company | Method for making fire-retarded polycarbonate and related compositions |
| US7108190B2 (en) * | 2003-02-28 | 2006-09-19 | Appleton Papers Inc. | Token array and method employing authentication tokens bearing scent formulation information |
| US20060063125A1 (en) * | 2003-04-22 | 2006-03-23 | Hamilton Timothy F | Method and device for enhanced dental articulation |
| US6932602B2 (en) * | 2003-04-22 | 2005-08-23 | Appleton Papers Inc. | Dental articulation kit and method |
| US20040251309A1 (en) * | 2003-06-10 | 2004-12-16 | Appleton Papers Inc. | Token bearing magnetc image information in registration with visible image information |
| US7915215B2 (en) | 2008-10-17 | 2011-03-29 | Appleton Papers Inc. | Fragrance-delivery composition comprising boron and persulfate ion-crosslinked polyvinyl alcohol microcapsules and method of use thereof |
| CN103833508A (zh) * | 2012-11-23 | 2014-06-04 | 中国石油天然气股份有限公司 | 一种固体酸催化剂催化合成二苄基甲苯的方法 |
| CN103833509A (zh) * | 2012-11-23 | 2014-06-04 | 中国石油天然气股份有限公司 | 一种固体酸催化剂催化合成苄基甲苯的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1053935A (en, 2012) * | 1964-08-27 | 1900-01-01 | ||
| US4003589A (en) * | 1970-07-11 | 1977-01-18 | Kureha Kagaku Kogyo Kabushiki Kaisha | Carbonless copying paper |
| JPS492126B1 (en, 2012) * | 1970-10-27 | 1974-01-18 | ||
| CA986714A (en) * | 1971-03-02 | 1976-04-06 | Yoshiaki Aida | Pressure-sensitive record material employing diaryl alkane solvents |
| GB1361638A (en) * | 1971-09-23 | 1974-07-30 | Wiggins Teape Res Dev | Pressure-sensitive copying systems |
| BE790321A (fr) * | 1971-10-20 | 1973-04-19 | Monsanto Co | Solvants pour colorants de materiaux d'enregistrement sensiblesa la pression |
| US3996405A (en) * | 1973-01-24 | 1976-12-07 | Ncr Corporation | Pressure-sensitive record material |
| US3901986A (en) * | 1974-01-28 | 1975-08-26 | Ncr Co | Ink supply transfer medium |
-
1977
- 1977-09-12 US US05/832,698 patent/US4130299A/en not_active Expired - Lifetime
-
1978
- 1978-09-11 DE DE19782839512 patent/DE2839512A1/de active Granted
- 1978-09-11 FI FI782771A patent/FI65188C/fi not_active IP Right Cessation
- 1978-09-11 FR FR7826054A patent/FR2402535A1/fr active Granted
- 1978-09-11 CA CA311,068A patent/CA1107501A/en not_active Expired
- 1978-09-11 BE BE190396A patent/BE870371A/xx not_active IP Right Cessation
- 1978-09-11 GB GB7836380A patent/GB2004310B/en not_active Expired
- 1978-09-11 NL NLAANVRAGE7809239,A patent/NL184728C/xx not_active IP Right Cessation
- 1978-09-11 BR BR7805916A patent/BR7805916A/pt unknown
- 1978-09-11 ES ES473236A patent/ES473236A1/es not_active Expired
- 1978-09-11 JP JP11082778A patent/JPS5451612A/ja active Pending
- 1978-09-11 IT IT27520/78A patent/IT1099039B/it active
- 1978-09-11 MX MX174836A patent/MX149597A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB2004310A (en) | 1979-03-28 |
| GB2004310B (en) | 1982-01-20 |
| IT7827520A0 (it) | 1978-09-11 |
| ES473236A1 (es) | 1979-10-16 |
| FI782771A7 (fi) | 1979-03-13 |
| JPS5451612A (en) | 1979-04-23 |
| MX149597A (es) | 1983-11-30 |
| FI65188B (fi) | 1983-12-30 |
| BR7805916A (pt) | 1979-05-02 |
| DE2839512A1 (de) | 1979-03-22 |
| FR2402535A1 (fr) | 1979-04-06 |
| FR2402535B1 (en, 2012) | 1984-09-21 |
| US4130299A (en) | 1978-12-19 |
| BE870371A (fr) | 1979-03-12 |
| NL184728C (nl) | 1989-10-16 |
| IT1099039B (it) | 1985-09-18 |
| NL7809239A (nl) | 1979-03-14 |
| NL184728B (nl) | 1989-05-16 |
| DE2839512C2 (en, 2012) | 1988-07-21 |
| CA1107501A (en) | 1981-08-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: MONSANTO COMPANY |