CA1148356A - Feuille d'enregistrement sensible a un agent acide - Google Patents

Feuille d'enregistrement sensible a un agent acide

Info

Publication number: CA1148356A
Authority: CA; Canada
Prior art keywords: record sheet; sensitized record; sensitized; fraction; biphenyl
Prior art date: 1978-12-11
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

Application number

CA000337270A

Other languages

English (en)

Inventor

Theodore Maierson

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Standard Register Co

Original Assignee

Standard Register Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1978-12-11

Filing date

1979-10-10

Publication date

1983-06-21

1979-10-10 Application filed by Standard Register Co filed Critical Standard Register Co

1983-06-21 Application granted granted Critical

1983-06-21 Publication of CA1148356A publication Critical patent/CA1148356A/fr

Status Expired legal-status Critical Current

Links

239000002904 solvent Substances 0.000 claims abstract description 35
229920005989 resin Polymers 0.000 claims abstract description 20
239000011347 resin Substances 0.000 claims abstract description 20
239000002243 precursor Substances 0.000 claims abstract description 19
230000002378 acidificating effect Effects 0.000 claims abstract description 12
239000000463 material Substances 0.000 claims abstract description 9
239000003054 catalyst Substances 0.000 claims abstract description 5
150000003751 zinc Chemical class 0.000 claims abstract description 4
239000000376 reactant Substances 0.000 claims abstract description 3
LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 claims abstract 2
239000002253 acid Substances 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 13
239000003795 chemical substances by application Substances 0.000 claims description 10
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 10
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 8
150000002191 fatty alcohols Chemical class 0.000 claims description 7
239000013032 Hydrocarbon resin Substances 0.000 claims description 6
229920006270 hydrocarbon resin Polymers 0.000 claims description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 6
239000003960 organic solvent Substances 0.000 claims description 6
AMBHHSBRXZAGDZ-UHFFFAOYSA-N 1-phenyl-2,3-di(propan-2-yl)benzene Chemical group CC(C)C1=CC=CC(C=2C=CC=CC=2)=C1C(C)C AMBHHSBRXZAGDZ-UHFFFAOYSA-N 0.000 claims description 5
235000010290 biphenyl Nutrition 0.000 claims description 5
239000004305 biphenyl Substances 0.000 claims description 5
238000009835 boiling Methods 0.000 claims description 5
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 4
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 4
239000012965 benzophenone Substances 0.000 claims description 4
229960000541 cetyl alcohol Drugs 0.000 claims description 4
QTKIQLNGOKOPOE-UHFFFAOYSA-N 1,1'-biphenyl;propane Chemical group CCC.C1=CC=CC=C1C1=CC=CC=C1 QTKIQLNGOKOPOE-UHFFFAOYSA-N 0.000 claims description 3
LXTFIEUQJZSWSQ-UHFFFAOYSA-N 1-phenyl-2,3,4,5-tetra(propan-2-yl)benzene Chemical group CC(C)C1=C(C(C)C)C(C(C)C)=CC(C=2C=CC=CC=2)=C1C(C)C LXTFIEUQJZSWSQ-UHFFFAOYSA-N 0.000 claims description 3
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims description 3
VNTDZUDTQCZFKN-UHFFFAOYSA-L zinc 2,2-dimethyloctanoate Chemical compound [Zn++].CCCCCCC(C)(C)C([O-])=O.CCCCCCC(C)(C)C([O-])=O VNTDZUDTQCZFKN-UHFFFAOYSA-L 0.000 claims description 3
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 claims description 3
YYKBFGMYHQMXIL-UHFFFAOYSA-N 1-phenyl-2,3,4-tri(propan-2-yl)benzene Chemical group CC(C)C1=C(C(C)C)C(C(C)C)=CC=C1C1=CC=CC=C1 YYKBFGMYHQMXIL-UHFFFAOYSA-N 0.000 claims description 2
VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 claims description 2
239000012190 activator Substances 0.000 claims description 2
YLZSIUVOIFJGQZ-UHFFFAOYSA-N bis[4-(dimethylamino)phenyl]methanol Chemical compound C1=CC(N(C)C)=CC=C1C(O)C1=CC=C(N(C)C)C=C1 YLZSIUVOIFJGQZ-UHFFFAOYSA-N 0.000 claims description 2
MXODCLTZTIFYDV-UHFFFAOYSA-L zinc;1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Zn+2].C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O.C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O MXODCLTZTIFYDV-UHFFFAOYSA-L 0.000 claims description 2
FXJVNINSOKCNJP-UHFFFAOYSA-N 4-methylbenzenesulfinic acid Chemical class CC1=CC=C(S(O)=O)C=C1 FXJVNINSOKCNJP-UHFFFAOYSA-N 0.000 claims 1
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
230000008018 melting Effects 0.000 claims 1
238000002844 melting Methods 0.000 claims 1
239000000976 ink Substances 0.000 description 34
239000010408 film Substances 0.000 description 8
229910052725 zinc Inorganic materials 0.000 description 7
239000011701 zinc Substances 0.000 description 7
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
150000007513 acids Chemical class 0.000 description 4
238000000576 coating method Methods 0.000 description 4
-1 dimethylphthala~e Chemical compound 0.000 description 4
238000007639 printing Methods 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
239000011248 coating agent Substances 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
239000000975 dye Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
239000004927 clay Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
238000009472 formulation Methods 0.000 description 2
125000001041 indolyl group Chemical group 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
239000003094 microcapsule Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
230000002028 premature Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000758 substrate Substances 0.000 description 2
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
BHNHHSOHWZKFOX-UHFFFAOYSA-N 2-methyl-1H-indole Chemical compound C1=CC=C2NC(C)=CC2=C1 BHNHHSOHWZKFOX-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
FBEHFRAORPEGFH-UHFFFAOYSA-N Allyxycarb Chemical compound CNC(=O)OC1=CC(C)=C(N(CC=C)CC=C)C(C)=C1 FBEHFRAORPEGFH-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
239000003929 acidic solution Substances 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
229960002903 benzyl benzoate 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
150000001734 carboxylic acid salts Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000000368 destabilizing effect Effects 0.000 description 1
229960002380 dibutyl phthalate Drugs 0.000 description 1
QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 description 1
238000010410 dusting Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
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
239000003350 kerosene Substances 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
238000007644 letterpress printing Methods 0.000 description 1
QTWZICCBKBYHDM-UHFFFAOYSA-N leucomethylene blue Chemical compound C1=C(N(C)C)C=C2SC3=CC(N(C)C)=CC=C3NC2=C1 QTWZICCBKBYHDM-UHFFFAOYSA-N 0.000 description 1
239000003550 marker Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000004950 naphthalene Chemical class 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
229920003986 novolac Polymers 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
HJHVQCXHVMGZNC-JCJNLNMISA-M sodium;(2z)-2-[(3r,4s,5s,8s,9s,10s,11r,13r,14s,16s)-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12,13,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoate Chemical compound [Na+].O[C@@H]([C@@H]12)C[C@H]3\C(=C(/CCC=C(C)C)C([O-])=O)[C@@H](OC(C)=O)C[C@]3(C)[C@@]2(C)CC[C@@H]2[C@]1(C)CC[C@@H](O)[C@H]2C HJHVQCXHVMGZNC-JCJNLNMISA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 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

Landscapes

Color Printing (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)

CA000337270A 1978-12-11 1979-10-10 Feuille d'enregistrement sensible a un agent acide Expired CA1148356A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US96813078A	1978-12-11	1978-12-11
US968,130		1978-12-11

Publications (1)

Publication Number	Publication Date
CA1148356A true CA1148356A (fr)	1983-06-21

Family

ID=25513782

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000337270A Expired CA1148356A (fr)	1978-12-11	1979-10-10	Feuille d'enregistrement sensible a un agent acide

Country Status (1)

Country	Link
CA (1)	CA1148356A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0601690A1 (fr) *	1992-12-02	1994-06-15	Koch Industries, Inc.	Solvant contenant du diisopropylbiphényl et du triisopropylbiphényl pour l'utilisation dans un papier sans carbone et produits l'utilisant

1979
- 1979-10-10 CA CA000337270A patent/CA1148356A/fr not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0601690A1 (fr) *	1992-12-02	1994-06-15	Koch Industries, Inc.	Solvant contenant du diisopropylbiphényl et du triisopropylbiphényl pour l'utilisation dans un papier sans carbone et produits l'utilisant

Legal Events

Date	Code	Title	Description
2000-06-21	MKEX	Expiry

Publication	Publication Date	Title
US3732120A (en)	1973-05-08	Pressure-sensitive recording sheet
KR100209030B1 (ko)	1999-07-15	마이크로캅셀함유 유성도액 및 잉크와 그 제조방법, 이 잉크를 도포하여 이루어진 쉬트와 그 제조방법
US4112138A (en)	1978-09-05	Manifold carbonless form and process for the production thereof
US3079351A (en)	1963-02-26	Copying materials and emulsions
US4097619A (en)	1978-06-27	Manifold carbonless form and process for the continuous production thereof
US4352855A (en)	1982-10-05	Transfer-onto-plain paper type pressure-sensitive copying paper
GB1591361A (en)	1981-06-17	Pressure-sensitive carbonless sheet sets and processes for producing them
GB1581758A (en)	1980-12-17	Coating compositions substrates coated thereby and microcapsules for use therein
US4929710A (en)	1990-05-29	Hydroxycarboxylic acid/Unsaturated aromatic hydrocarbon resin useful as recording material
US4744685A (en)	1988-05-17	Thermal transfer ribbon and method of making same
US4138508A (en)	1979-02-06	Process for producing pressure-sensitive transfer sheets using novel radiation curable coatings
CA1107955A (fr)	1981-09-01	Formules sans carbone pliees en accordeon, et methode de production continue connexe
US4296947A (en)	1981-10-27	Pressure-sensitive transfer sheets using novel radiation curable coatings
US4337968A (en)	1982-07-06	Sensitized record sheet
US3940275A (en)	1976-02-24	Record material and marking liquid
CA1224922A (fr)	1987-08-04	Support d'enregistrement
US4205865A (en)	1980-06-03	Latent sensitizing ink
US3793075A (en)	1974-02-19	Dialkyl tartrate-heteropolyacid developing system for dye precursor compounds
US4060262A (en)	1977-11-29	Record material
CA1221535A (fr)	1987-05-12	Support d'enregistrement
US4186115A (en)	1980-01-29	Novel radiation curable coating compositions for pressure-sensitive transfer sheets
US4833117A (en)	1989-05-23	Novel correction compositions and process for using same
JPS58136483A (ja)	1983-08-13	感圧記録用複写シ−ト
CA1109609A (fr)	1981-09-29	Encre a sensibilisation latente
US4372581A (en)	1983-02-08	Pressure sensitive copying material

CA1148356A - Feuille d'enregistrement sensible a un agent acide - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=25513782

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

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Legal Events