CA1263048A - Systeme d'imagerie a transfert par diffusion - Google Patents

Systeme d'imagerie a transfert par diffusion

Info

Publication number: CA1263048A
Authority: CA; Canada
Prior art keywords: dye; receptor; image; layer; dyes
Prior art date: 1984-08-23
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

CA000488900A

Other languages

English (en)

Inventor

Ranjana C. Patel

John H. A. Stibbard

Michael G. Fisher

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.)

3M Co

Original Assignee

Minnesota Mining and Manufacturing 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.)

1984-08-23

Filing date

1985-08-16

Publication date

1989-11-21

1985-08-16 Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co

1989-11-21 Application granted granted Critical

1989-11-21 Publication of CA1263048A publication Critical patent/CA1263048A/fr

Status Expired legal-status Critical Current

Links

238000009792 diffusion process Methods 0.000 title claims abstract description 52
238000003384 imaging method Methods 0.000 title claims abstract description 19
238000000034 method Methods 0.000 claims abstract description 42
MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 claims abstract description 38
230000008569 process Effects 0.000 claims abstract description 38
230000005855 radiation Effects 0.000 claims abstract description 22
239000007788 liquid Substances 0.000 claims abstract description 16
238000004061 bleaching Methods 0.000 claims abstract description 8
239000000975 dye Substances 0.000 claims description 212
-1 iodonium compound Chemical class 0.000 claims description 45
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 38
239000011230 binding agent Substances 0.000 claims description 21
125000000217 alkyl group Chemical group 0.000 claims description 19
239000000758 substrate Substances 0.000 claims description 19
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125000003118 aryl group Chemical group 0.000 claims description 15
125000004429 atom Chemical group 0.000 claims description 15
150000001450 anions Chemical class 0.000 claims description 14
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 12
125000000623 heterocyclic group Chemical group 0.000 claims description 10
229910052760 oxygen Inorganic materials 0.000 claims description 10
125000001424 substituent group Chemical group 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 7
229910052740 iodine Inorganic materials 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 7
229910052717 sulfur Inorganic materials 0.000 claims description 7
150000001768 cations Chemical class 0.000 claims description 6
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 5
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239000004408 titanium dioxide Substances 0.000 claims description 5
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
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150000003839 salts Chemical class 0.000 description 5
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ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
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LWVVNNZRDBXOQL-AATRIKPKSA-O [(e)-3-(dimethylamino)prop-2-enyl]-dimethylazanium Chemical compound CN(C)\C=C\C[NH+](C)C LWVVNNZRDBXOQL-AATRIKPKSA-O 0.000 description 3
238000002835 absorbance Methods 0.000 description 3
150000001299 aldehydes Chemical class 0.000 description 3
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239000003963 antioxidant agent Substances 0.000 description 3
235000006708 antioxidants Nutrition 0.000 description 3
235000010323 ascorbic acid Nutrition 0.000 description 3
239000011668 ascorbic acid Substances 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
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OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 3
239000002131 composite material Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 3
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
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239000011734 sodium Substances 0.000 description 3
241000894007 species Species 0.000 description 3
238000005406 washing Methods 0.000 description 3
DUSDTBJACCAARX-UHFFFAOYSA-M (4-butoxyphenyl)-phenyliodanium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.C1=CC(OCCCC)=CC=C1[I+]C1=CC=CC=C1 DUSDTBJACCAARX-UHFFFAOYSA-M 0.000 description 2
KFDVPJUYSDEJTH-UHFFFAOYSA-O 4-ethenylpyridine;hydron Chemical compound C=CC1=CC=[NH+]C=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-O 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 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
241001082241 Lythrum hyssopifolia Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
239000012190 activator Substances 0.000 description 2
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125000003710 aryl alkyl group Chemical group 0.000 description 2
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QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
230000006378 damage 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
239000012530 fluid Substances 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
239000011630 iodine Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 2
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239000001632 sodium acetate Substances 0.000 description 2
235000017281 sodium acetate Nutrition 0.000 description 2
PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 2
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JZDQKBZKFIWSNW-UHFFFAOYSA-N (4-methoxyphenyl)-phenyliodanium Chemical compound C1=CC(OC)=CC=C1[I+]C1=CC=CC=C1 JZDQKBZKFIWSNW-UHFFFAOYSA-N 0.000 description 1
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101100087530 Caenorhabditis elegans rom-1 gene Proteins 0.000 description 1
ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 1
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AEEAZFQPYUMBPY-UHFFFAOYSA-N [I].[W] Chemical compound [I].[W] AEEAZFQPYUMBPY-UHFFFAOYSA-N 0.000 description 1
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TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 description 1
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PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
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229920000136 polysorbate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920002717 polyvinylpyridine Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000007639 printing Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
230000001235 sensitizing effect Effects 0.000 description 1
239000002356 single layer Substances 0.000 description 1
238000002791 soaking Methods 0.000 description 1
235000010378 sodium ascorbate Nutrition 0.000 description 1
229960005055 sodium ascorbate Drugs 0.000 description 1
235000010352 sodium erythorbate Nutrition 0.000 description 1
PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
238000002834 transmittance Methods 0.000 description 1
238000011282 treatment Methods 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000012463 white pigment Substances 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

Landscapes

Ink Jet Recording Methods And Recording Media Thereof (AREA)

CA000488900A 1984-08-23 1985-08-16 Systeme d'imagerie a transfert par diffusion Expired CA1263048A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB848421400A GB8421400D0 (en)	1984-08-23	1984-08-23	Diffusion transfer imaging system
GB84.21400		1984-08-23

Publications (1)

Publication Number	Publication Date
CA1263048A true CA1263048A (fr)	1989-11-21

Family

ID=10565713

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000488900A Expired CA1263048A (fr)	1984-08-23	1985-08-16	Systeme d'imagerie a transfert par diffusion

Country Status (2)

Country	Link
CA (1)	CA1263048A (fr)
GB (1)	GB8421400D0 (fr)

1984
- 1984-08-23 GB GB848421400A patent/GB8421400D0/en active Pending
1985
- 1985-08-16 CA CA000488900A patent/CA1263048A/fr not_active Expired

Also Published As

Publication number	Publication date
GB8421400D0 (en)	1984-09-26

Legal Events

Date	Code	Title	Description
1998-11-23	MKLA	Lapsed

Publication	Publication Date	Title
EP0175504B1 (fr)	1989-04-05	Système de formation d'images par diffusion ou sublimation
US4701402A (en)	1987-10-20	Oxidative imaging
US5948600A (en)	1999-09-07	Method and material for the formation of a heat mode image
US5055373A (en)	1991-10-08	Multicolor recording material
CA1198925A (fr)	1986-01-07	Fixage de systemes revelateurs d'image a base de tetra(hydrocarbyl)borate
US4962009A (en)	1990-10-09	Microcapsule containing photo-oxidizing agent and leuco dye
JPS60235134A (ja)	1985-11-21	写真要素
US4196002A (en)	1980-04-01	Photothermographic element containing heat sensitive dye materials
JPH08292517A (ja)	1996-11-05	赤外線照射により退色し得る紫外線吸収媒体
US5595854A (en)	1997-01-21	Method for the formation of heat mode image
JPH0554648B2 (fr)	1993-08-13
EP0719217A1 (fr)	1996-07-03	Procede et materiau de formation d'image en mode thermique
US3615481A (en)	1971-10-26	Leuco dye/hexaarylbiimidazole thermally activated imaging process
JPH0536779B2 (fr)	1993-05-31
US5306686A (en)	1994-04-26	Negative-acting thermographic materials
CA1264594A (fr)	1990-01-23	Systeme d'imagerie a transfert par sublimation
US3753395A (en)	1973-08-21	Photo-thermographic recording process with 5-pyrazolane
EP0120601B1 (fr)	1988-10-19	Formation d'images par oxydation
CA1263048A (fr)	1989-11-21	Systeme d'imagerie a transfert par diffusion
US4769459A (en)	1988-09-06	Oxidative imaging
JP3842633B2 (ja)	2006-11-08	フォトサーモグラフィ要素
US5840469A (en)	1998-11-24	Gallic acid as a laser direct thermal developer
JPS6332177B2 (fr)	1988-06-28
JPH0360420B2 (fr)	1991-09-13
US3704127A (en)	1972-11-28	Co-irradiation method for producing positive images utilizing phototropic spiropyran or indenone oxide or dual response photosensitive composition