JPS6140190A

JPS6140190A - 感熱記録材料

感熱記録材料

Info

Publication number: JPS6140190A
Authority: JP; Japan
Prior art keywords: compound; transition point; heat; recording material; glass transition
Prior art date: 1984-04-11
Legal status : Granted

Application number

JP7238284A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0437795B2 (enrdf_load_stackoverflow

Inventor

Shohei Yoshida

昌平吉田

Toshiharu Tanaka

俊春田中

Tomomasa Usami

宇佐美　智正

Current Assignee

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date

1984-04-11

Filing date

1984-04-11

Publication date

1986-02-26

1984-04-11 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1984-04-11 Priority to JP7238284A priority Critical patent/JPS6140190A/ja

1985-04-11 Priority to GB08509299A priority patent/GB2160327B/en

1986-02-26 Publication of JPS6140190A publication Critical patent/JPS6140190A/ja

1992-06-22 Publication of JPH0437795B2 publication Critical patent/JPH0437795B2/ja

Status Granted legal-status Critical Current

Links

239000000463 material Substances 0.000 title claims abstract description 61
239000000126 substance Substances 0.000 claims abstract description 45
239000003094 microcapsule Substances 0.000 claims abstract description 37
150000008049 diazo compounds Chemical class 0.000 claims abstract description 32
238000005859 coupling reaction Methods 0.000 claims abstract description 26
230000008878 coupling Effects 0.000 claims abstract description 25
238000010168 coupling process Methods 0.000 claims abstract description 25
230000009477 glass transition Effects 0.000 claims abstract description 17
150000001875 compounds Chemical class 0.000 claims abstract description 13
-1 carbamic acid ester compound Chemical class 0.000 abstract description 15
230000007704 transition Effects 0.000 abstract description 15
238000002844 melting Methods 0.000 abstract description 12
239000003795 chemical substances by application Substances 0.000 abstract description 11
230000008018 melting Effects 0.000 abstract description 10
150000002440 hydroxy compounds Chemical class 0.000 abstract description 4
150000007514 bases Chemical class 0.000 abstract 1
238000000576 coating method Methods 0.000 description 17
239000002775 capsule Substances 0.000 description 16
239000011248 coating agent Substances 0.000 description 15
239000011162 core material Substances 0.000 description 15
238000003860 storage Methods 0.000 description 13
238000011161 development Methods 0.000 description 12
238000000034 method Methods 0.000 description 11
239000010410 layer Substances 0.000 description 10
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239000000243 solution Substances 0.000 description 8
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FUPAJKKAHDLPAZ-UHFFFAOYSA-N 1,2,3-triphenylguanidine Chemical compound C=1C=CC=CC=1NC(=NC=1C=CC=CC=1)NC1=CC=CC=C1 FUPAJKKAHDLPAZ-UHFFFAOYSA-N 0.000 description 6
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125000003118 aryl group Chemical group 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
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GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
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238000001035 drying Methods 0.000 description 3
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OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 2
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CYYZDBDROVLTJU-UHFFFAOYSA-N 4-n-Butylphenol Chemical compound CCCCC1=CC=C(O)C=C1 CYYZDBDROVLTJU-UHFFFAOYSA-N 0.000 description 2
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239000004640 Melamine resin Substances 0.000 description 2
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NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
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PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
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 2
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125000003545 alkoxy group Chemical group 0.000 description 2
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125000001769 aryl amino group Chemical group 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
239000002585 base Substances 0.000 description 2
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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
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VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
239000001923 methylcellulose Substances 0.000 description 2
235000010981 methylcellulose Nutrition 0.000 description 2
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VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
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125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
238000001454 recorded image Methods 0.000 description 2
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IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 1
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VYOWNYLBHHBVDR-UHFFFAOYSA-N 1-(3-methylbutyl)-2-phenylbenzene Chemical group CC(C)CCC1=CC=CC=C1C1=CC=CC=C1 VYOWNYLBHHBVDR-UHFFFAOYSA-N 0.000 description 1
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KUFFULVDNCHOFZ-UHFFFAOYSA-N 2,4-xylenol Chemical compound CC1=CC=C(O)C(C)=C1 KUFFULVDNCHOFZ-UHFFFAOYSA-N 0.000 description 1
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QXOYFCJDRWUAMR-UHFFFAOYSA-N 4-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound C=1C2=CC=CC=C2C(O)=CC=1C(=O)NC1=CC=CC=C1 QXOYFCJDRWUAMR-UHFFFAOYSA-N 0.000 description 1
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MOZDKDIOPSPTBH-UHFFFAOYSA-N Benzyl parahydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCC1=CC=CC=C1 MOZDKDIOPSPTBH-UHFFFAOYSA-N 0.000 description 1
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
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