JPH0337974Y2 - - Google Patents

Info

Publication number: JPH0337974Y2
Authority: JP; Japan
Prior art keywords: acid; colored; heated; support; recording
Prior art date: 1985-04-16
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

JP5662885U

Other languages

English (en)

Japanese (ja)

Other versions

JPS61173376U (de

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.)

1985-04-16

Filing date

1985-04-16

Publication date

1991-08-12

1985-04-16 Application filed filed Critical

1985-04-16 Priority to JP5662885U priority Critical patent/JPH0337974Y2/ja

1986-10-28 Publication of JPS61173376U publication Critical patent/JPS61173376U/ja

1991-08-12 Application granted granted Critical

1991-08-12 Publication of JPH0337974Y2 publication Critical patent/JPH0337974Y2/ja

Status Expired legal-status Critical Current

Links

238000010669 acid-base reaction Methods 0.000 claims description 12
239000000463 material Substances 0.000 claims description 12
239000000126 substance Substances 0.000 claims description 9
230000002401 inhibitory effect Effects 0.000 claims description 5
239000000155 melt Substances 0.000 claims description 3
239000010410 layer Substances 0.000 description 13
238000010438 heat treatment Methods 0.000 description 11
150000001875 compounds Chemical class 0.000 description 9
238000004040 coloring Methods 0.000 description 6
-1 amino, substituted amino Chemical group 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
239000002253 acid Substances 0.000 description 3
150000007530 organic bases Chemical class 0.000 description 3
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003086 colorant Substances 0.000 description 2
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
150000007529 inorganic bases Chemical class 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
239000007793 ph indicator Substances 0.000 description 2
KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
SEULWJSKCVACTH-UHFFFAOYSA-N 1-phenylimidazole Chemical compound C1=NC=CN1C1=CC=CC=C1 SEULWJSKCVACTH-UHFFFAOYSA-N 0.000 description 1
VVFVRTNNLLZXAL-UHFFFAOYSA-N 2-(2-methylphenyl)guanidine Chemical compound CC1=CC=CC=C1N=C(N)N VVFVRTNNLLZXAL-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
ZDYGICOMCMZARA-UHFFFAOYSA-N 2-benzyl-1-(2-benzylnaphthalen-1-yl)oxynaphthalene Chemical compound C=1C=C2C=CC=CC2=C(OC=2C3=CC=CC=C3C=CC=2CC=2C=CC=CC=2)C=1CC1=CC=CC=C1 ZDYGICOMCMZARA-UHFFFAOYSA-N 0.000 description 1
SGBQUMZTGSQNAO-UHFFFAOYSA-N 2-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(O)=CC=C21 SGBQUMZTGSQNAO-UHFFFAOYSA-N 0.000 description 1
XCSGHNKDXGYELG-UHFFFAOYSA-N 2-phenoxyethoxybenzene Chemical compound C=1C=CC=CC=1OCCOC1=CC=CC=C1 XCSGHNKDXGYELG-UHFFFAOYSA-N 0.000 description 1
POTXZUQLERIXIW-UHFFFAOYSA-N 2-phenoxyethyl 2,4-dihydroxybenzoate Chemical compound OC1=CC(O)=CC=C1C(=O)OCCOC1=CC=CC=C1 POTXZUQLERIXIW-UHFFFAOYSA-N 0.000 description 1
ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 1
UHPALUGVFOSLRU-UHFFFAOYSA-N 2-phenylethyl 3,4,5-trihydroxybenzoate Chemical compound OC1=C(O)C(O)=CC(C(=O)OCCC=2C=CC=CC=2)=C1 UHPALUGVFOSLRU-UHFFFAOYSA-N 0.000 description 1
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
WEMYXYMZQRSPIA-UHFFFAOYSA-N 4-(2,4-dihydroxyphenyl)sulfanylbenzene-1,3-diol Chemical compound OC1=CC(O)=CC=C1SC1=CC=C(O)C=C1O WEMYXYMZQRSPIA-UHFFFAOYSA-N 0.000 description 1
RWXZXCZBMQPOBF-UHFFFAOYSA-N 5-methyl-1H-benzimidazole Chemical compound CC1=CC=C2N=CNC2=C1 RWXZXCZBMQPOBF-UHFFFAOYSA-N 0.000 description 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
OAZWDJGLIYNYMU-UHFFFAOYSA-N Leucocrystal Violet Chemical compound C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 OAZWDJGLIYNYMU-UHFFFAOYSA-N 0.000 description 1
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
IHRIVUSMZMVANI-UHFFFAOYSA-N azane;2-methylbenzenesulfonic acid Chemical compound [NH4+].CC1=CC=CC=C1S([O-])(=O)=O IHRIVUSMZMVANI-UHFFFAOYSA-N 0.000 description 1
RDMHHMURPNVWQK-UHFFFAOYSA-N benzyl 2,4,6-trihydroxybenzoate Chemical compound OC1=CC(O)=CC(O)=C1C(=O)OCC1=CC=CC=C1 RDMHHMURPNVWQK-UHFFFAOYSA-N 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
235000004515 gallic acid Nutrition 0.000 description 1
229940074391 gallic acid Drugs 0.000 description 1
CZLCEPVHPYKDPJ-UHFFFAOYSA-N guanidine;2,2,2-trichloroacetic acid Chemical compound NC(N)=N.OC(=O)C(Cl)(Cl)Cl CZLCEPVHPYKDPJ-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
238000000034 method Methods 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
QKRLLHNFWIVXIH-UHFFFAOYSA-N n-fluoro-3-methylbutan-1-amine Chemical compound CC(C)CCNF QKRLLHNFWIVXIH-UHFFFAOYSA-N 0.000 description 1
WMIWKXQBBHIBDO-UHFFFAOYSA-N phenyl 1-hydroxy-2h-naphthalene-1-carboxylate Chemical compound C1C=CC2=CC=CC=C2C1(O)C(=O)OC1=CC=CC=C1 WMIWKXQBBHIBDO-UHFFFAOYSA-N 0.000 description 1
LYKRPDCJKSXAHS-UHFFFAOYSA-N phenyl-(2,3,4,5-tetrahydroxyphenyl)methanone Chemical compound OC1=C(O)C(O)=CC(C(=O)C=2C=CC=CC=2)=C1O LYKRPDCJKSXAHS-UHFFFAOYSA-N 0.000 description 1
SYACZRCLOYMVKR-UHFFFAOYSA-N phenylmethanesulfonate;triethylazanium Chemical compound CC[NH+](CC)CC.[O-]S(=O)(=O)CC1=CC=CC=C1 SYACZRCLOYMVKR-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920006267 polyester film Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
239000002356 single layer Substances 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Landscapes

Heat Sensitive Colour Forming Recording (AREA)

JP5662885U 1985-04-16 1985-04-16 Expired JPH0337974Y2 (de)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP5662885U JPH0337974Y2 (de)	1985-04-16	1985-04-16

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP5662885U JPH0337974Y2 (de)	1985-04-16	1985-04-16

Publications (2)

Publication Number	Publication Date
JPS61173376U JPS61173376U (de)	1986-10-28
JPH0337974Y2 true JPH0337974Y2 (de)	1991-08-12

Family

ID=30580407

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5662885U Expired JPH0337974Y2 (de)	1985-04-16	1985-04-16

Country Status (1)

Country	Link
JP (1)	JPH0337974Y2 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0741741B2 (ja) *	1987-03-16	1995-05-10	富士写真フイルム株式会社	感熱記録材料
JP4235466B2 (ja) *	2003-02-24	2009-03-11	Ａｚエレクトロニックマテリアルズ株式会社	水溶性樹脂組成物、パターン形成方法及びレジストパターンの検査方法
JP4012480B2 (ja)	2003-03-28	2007-11-21	Ａｚエレクトロニックマテリアルズ株式会社	微細パターン形成補助剤及びその製造法

1985
- 1985-04-16 JP JP5662885U patent/JPH0337974Y2/ja not_active Expired

Also Published As

Publication number	Publication date
JPS61173376U (de)	1986-10-28

Publication	Publication Date	Title
US5085607A (en)	1992-02-04	Toy that stably exhibits different colors with indicator for proper temperature application
EA008721B1 (ru)	2007-06-29	Система для термического формирования изображений
JPH0430355B2 (de)	1992-05-21
US3953659A (en)	1976-04-27	Thermal paper coating
JPS58191190A (ja)	1983-11-08	感熱透明記録材料
JPH0337974Y2 (de)	1991-08-12
JPS63173684A (ja)	1988-07-18	可逆性記録材料
JPS6290282A (ja)	1987-04-24	感圧感熱多重複写紙
JPH07100769B2 (ja)	1995-11-01	色彩記憶性塗料
JPS57129785A (en)	1982-08-11	Heat sensitive recording paper
JPH0211437B2 (de)	1990-03-14
JPS62244693A (ja)	1987-10-26	感熱記録材料
JP3606666B2 (ja)	2005-01-05	可逆性熱変色記録材料および可逆性熱変色記録媒体
JPH0280285A (ja)	1990-03-20	感熱記録材料
JPH0533151B2 (de)	1993-05-18
JPS60257289A (ja)	1985-12-19	可逆的画像形成材料
JPS60112484A (ja)	1985-06-18	像受容体
JPH11105425A (ja)	1999-04-20	感温変色性熱転写記録媒体およびその製造方法
JPH025199B2 (de)	1990-01-31
JPS6176387A (ja)	1986-04-18	感熱記録紙
JPS63236683A (ja)	1988-10-03	感熱記録材料
JPH06155891A (ja)	1994-06-03	透光性記録媒体及びそれを用いたインクジェット記録方法
JPS60145884A (ja)	1985-08-01	感熱記録体
JPS63134281A (ja)	1988-06-06	感熱記録材料
JPH1178267A (ja)	1999-03-23	感温変色性熱転写記録媒体