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US3642483A Expired / Lapsed US ⏱️ 0.0 years remaining

Thermally developable diazotype copying materials

Assignee: Ricoh Co Ltd
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Filing: 1967-10-26
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Granted: 1972-02-15
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Expires: 1987-10-26
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Abstract

Abstract A thermally developable diazotype copying material is manufactured which comprises a supporting sheet and a lightsensitive copying layer coated on said supporting sheet, said layer consisting of a water soluble light-sensitive diazo compound, a water soluble heat fugitive acidic salt (base generating agent) and a water insoluble coupler. Another thermally developable diazotype copying material is also obtained, which is of a similar structure but said copying layer further contains an additional component consisting of an agent for lowering the melting point of said coupler besides said diazo compound, said salt and said coupler.

Inventors

  • 👤 Keishi Kubo
  • 👤 Sadao Matsumura

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 11:49
CPC Classifications
G; G03; G03C; G03C1/00; G03C1/52; G03C1/61

Claims Analysis

Total Claims: 1
Claim 1
Independent Claim 284 words
A thermally developable diazotype copying material having on one surface of a supporting sheet a two-layer light-sensitive coating comprising a diazonium compound, an azo coupling compound, a base generating agent, an acidic stabilizer and a compound for lowering the melting point of said azo coupling compound, in which a. the first layer consists of a binder resin containing a water-insoluble azo coupling compound uniformly dispersed in said binder resin in the form of fine particles and a compound for lowering the melting point of said azo coupling compound, said azo coupling compound being selected from the group consisting of 2,3-dihydroxy-naphthalene, 2,3-dihydroxy-naphthalene-6-sulfonamide-naphthalene, 2,3-dihydroxy-6-dihydroxyethyl-sulfonamide-naphthalene, 1-carboxy-2,3-dihydroxy-naphthalene, 1,4-dichloro-2,3-dihydroxy-naphthalene and 3,3-dihydroxy-2-naphthanilide; and said compound for lowering the melting point of said azo coupling compound being selected from the group consisting of guanidine-tartaric acid salt, amino-guanidine-hydrochloric acid salt, cyanoguanidine, ethylbiguanide-hydrochloric acid salt, dimethyl-biguanide-hydrochloric acid salt, 3-methoxy benzoguanidine, 1-butyl-3-nitroguanidine, 2-guanyl phthalic acid amide, acetamide, acrylamide, propionamide, butylamide and malonamide, the amount of said compound for lowering the melting point being in the range of 0.14 to 0.25 part by weight per one part by weight of said azo coupling compound and forming a eutectic with the azo coupling compound; b. a second layer containing a water-soluble, light-sensitive diazonium compound, a water-soluble, heat-fugitive, acidic salt as the base generating agent and an acidic stabilizer, said second layer overlying said first layer, said diazonium compound being selected from the group consisting of zinc chloride and cadmium chloride double salts of p-dimethyl-aminobEnzene diazonium chloride, p-diethyl-aminobenzene diazonium chloride, p-methyl-hydroxyethyl-aminobenzene diazonium chloride and p-ethylhydroxyethyl-aminobenzene diazonium chloride, and said heat-fugitive acidic salt being selected from the group consisting of alkali metal salts, ammonium salts, ethanolamine salts and isopropylamine salts of halogenoacetic acids, cyanoacetic acid and halogenomalonic acids.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1975-02-14 1975-08-16 1976-02-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1979-02-14 1979-08-16 1980-02-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1983-02-14 1983-08-16 1984-02-15 $7700.00 Window Closed / Lapsed

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