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US4083680A Expired / Lapsed US ⏱️ 0.0 years remaining

Printing inks for transfer printing

Assignee: Bayer AG
•
Filing: 1976-02-17
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Granted: 1978-04-11
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Expires: 1996-02-17
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Abstract

Abstract Printing inks for the preparation of temporary supports for transfer printing on acid-modified textile fibre materials, containing (a) as a dyestuff intermediate a dyestuff base which can be sublimed at 160°-240° C, of the formula ##STR1## wherein R 1 and R 2 are alkyl, R 3 is hydrogen, alkyl, cycloalkyl or aralkyl, R 4 is hydrogen or a non-ionic substituent, R 5 is hydrogen, an alkyl, alkoxycarbonyl or nitrile group, R 6 and R 7 are hydrogen or non-ionic substituents, B represents --CH--, --N═ or ##STR2## (B) A ORGANIC SOLVENT AND (C) A NEUTRAL RESIN.

Inventors

  • 👤 Hubertus Psaar

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 05:47
CPC Classifications
C; C09; C09B; C09B23/00; C09B23/16; C09B23/162; C09B23/164; D; D06; D06P; D06P5/00; D06P5/003; D06P5/004; D06P5/006

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 193 words
In a process for transfer printing of acid-modified textile fiber materials wherein a dyestuff is applied to a temporary carrier web and subsequently transferred to the textile material by being pressed against the textile and heated to cause the dyestuff to sublime and be adsorbed by the textile material, the improvement which comprises employing a printing ink consisting essentially of (a) as a dyestuff intermediate a dyestuff base which can be sublimed at 160°-240° C, of the formula ##STR18## wherein R 1 and R 2 represent an alkyl or conjointly with the C atom by which they are linked form a carbocyclic ring; R 3 denotes hydrogen alkyl, cycloalkyl or aralkyl; R 4 denotes hydrogen, alkyl, cycloalkyl, aryl, aryl, aralkyl, alkoxy, aryloxy, aralkoxy, alkylamino, dialkylamino, arylamino, aralkylamino, acylamino, sulphonamido, carbonamido, alkoxycarbonyl, acyl, nitrile or halogen; R 5 denotes hydrogen, alkyl, alkoxycarbonyl, or nitrile; R 6 and R 7 denote hydrogen, alkyl, alkoxy, aralkoxy, acylamino, dialkylamino or alkylmercapto; or R 6 and R 7 conjointly form a heterocyclic structure; and B represents CH, N, or C-alkyl; (b) a practically anhydrous neutral organic solvent; and (c) a neutral resin which is soluble in this solvent.
Claim 2
Dependent Claim 193 words
In a process for transfer printing of acid-modified textile fiber materials wherein a dyestuff is applied to a temporary carrier web and subsequently transferred to the textile material by being pressed against the textile and heated to cause the dyestuff to sublime and be adsorbed by the textile material, the improvement which comprises employing a printing ink consisting essentially of (a) as a dyestuff intermediate a dyestuff base which can be sublimed at 160°-240° C, of the formula ##STR18## wherein R 1 and R 2 represent an alkyl or conjointly with the C atom by which they are linked form a carbocyclic ring; R 3 denotes hydrogen alkyl, cycloalkyl or aralkyl; R 4 denotes hydrogen, alkyl, cycloalkyl, aryl, aryl, aralkyl, alkoxy, aryloxy, aralkoxy, alkylamino, dialkylamino, arylamino, aralkylamino, acylamino, sulphonamido, carbonamido, alkoxycarbonyl, acyl, nitrile or halogen; R 5 denotes hydrogen, alkyl, alkoxycarbonyl, or nitrile; R 6 and R 7 denote hydrogen, alkyl, alkoxy, aralkoxy, acylamino, dialkylamino or alkylmercapto; or R 6 and R 7 conjointly form a heterocyclic structure; and B represents CH, N, or C-alkyl; (b) a practically anhydrous neutral organic solvent; and (c) a neutral resin which is soluble in this solvent.
Claim 3
Dependent Claim 53 words
Process of claim 1 wherein R 1 , r 2 and R 3 denote methyl, R 4 denotes H, methyl, methoxy or chlorine, R 5 denotes H or methyl and R 6 and R 7 denote H, methyl, methoxy, ethoxy, methylmercapto, dimethylamino, diethylamino or acetyl or conjointly form a thiazole or dioxane radical.

References Cited (Backward Citations)

GB769163A Cited
GB951987A Cited
US3995992A Cited
US4040779A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-04-10 1981-10-10 1982-04-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-04-10 1985-10-10 1986-04-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-04-10 1989-10-10 1990-04-11 $7700.00 Window Closed / Lapsed

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