US1775074A - Process of dyeing pelts, hairs, feathers, and the like - Google Patents

Process of dyeing pelts, hairs, feathers, and the like Download PDF

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Publication number
US1775074A
US1775074A US238222A US23822227A US1775074A US 1775074 A US1775074 A US 1775074A US 238222 A US238222 A US 238222A US 23822227 A US23822227 A US 23822227A US 1775074 A US1775074 A US 1775074A
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United States
Prior art keywords
feathers
hairs
dyeing
naphthalene
aminophenylamino
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Expired - Lifetime
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US238222A
Inventor
Virck Paul
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General Aniline Works Inc
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General Aniline Works Inc
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Publication date
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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/02Material containing basic nitrogen
    • D06P3/04Material containing basic nitrogen containing amide groups
    • D06P3/30Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts
    • D06P3/305Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts with oxidation dyes

Definitions

  • Y means H, 'OH, -'-NH --NH- aryl-NH or halogen.
  • mordanted or not mordanted goods are treated with an aqueous solution of a salt of such a 4-amino-aryl-amino-derivative of the naphthalene and then with a suitable oxidizing agent; there are thus produced fast red-violet to black-blue and greenish grey tints.
  • Example 1 a bath containing er liter 2 grams of 2-(4'-aminophenylamino -naphthalene hydrochloride, some alcoholand a quite small proportion of hydrochloric acid, a thoroughly killed and, if necessary, mordanted skin is handled at the ordinary temperature for some hours. The skin'is then washed and treated for one hour in a sepagrams of potassium bichromatc and 20 grams of acetic acid of 30 per cent strength. There isobtained a blue-green dyeing.
  • a skin which has been thus mordantcd with potassium bichromate is dyed bluer when it is subjected to the first treatment rescribed in Example 1 and then to a su sequent treatment with hydrogen peroxide in ammoniacal solution; when the preliminary lnordant is a copper compound a blackblue dyeing is produced.
  • Red-violet to currant tints are obtainable when 1- (4'-aminophenylamino) -naphthalene is used under-the conditions named in Exam- With 2 (4' aminophenylamino) 6- (4 aminophenylamino) -naphthalene there is obtamed asnmlar rather more greenish-grey tint 1- (4'-aminophenylamino) -5- (4'-amino-' phenylamino) -naphthalene yields violet grey dyeings when the subsequent treatment is with a solution of alkali bichromate and acetic acid.
  • Y means H or an univalent substituent of the group consisting of --OH, NH NHaryl-NH and halogen) and with an oxidizing agent.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Description

- rate bath containing per liter 20 Patented Sept. 2, 1930 UNITED STATES PATENT OFFICE PAUL VIRCK, OF DESSU IN ANHEIM, GERMAN-Y, ASSIGN OR TO GENEBAL ANILINE WORKS, INC., OF'NEW YORK, N. Y., AICOBPOBATION OI DELAWARE rnocnss or prams rams, nuns, marinas, m) run man;
No Drawing. Application filed December 6, 1927, Serial No. 238,222, and in Germany September '14, 1926.
I have filed an application in Germany I, 29,039 IV/8m, filed bept. 14, 1926; Austria:
November 4th, 1927, Poland: filed November x X CNYHQHNQNBE x x wherein X means hydrogen or a univalent substituent such as alkyl or halogen and,
wherein Y means H, 'OH, -'-NH --NH- aryl-NH or halogen. j
The mordanted or not mordanted goods are treated with an aqueous solution of a salt of such a 4-amino-aryl-amino-derivative of the naphthalene and then with a suitable oxidizing agent; there are thus produced fast red-violet to black-blue and greenish grey tints.
The following examples illustrate the in,- vention:
Example 1.-Ii1 a bath containing er liter 2 grams of 2-(4'-aminophenylamino -naphthalene hydrochloride, some alcoholand a quite small proportion of hydrochloric acid, a thoroughly killed and, if necessary, mordanted skin is handled at the ordinary temperature for some hours. The skin'is then washed and treated for one hour in a sepagrams of potassium bichromatc and 20 grams of acetic acid of 30 per cent strength. There isobtained a blue-green dyeing. A skin which has been thus mordantcd with potassium bichromate is dyed bluer when it is subjected to the first treatment rescribed in Example 1 and then to a su sequent treatment with hydrogen peroxide in ammoniacal solution; when the preliminary lnordant is a copper compound a blackblue dyeing is produced.
Red-violet to currant tints are obtainable when 1- (4'-aminophenylamino) -naphthalene is used under-the conditions named in Exam- With 2 (4' aminophenylamino) 6- (4 aminophenylamino) -naphthalene there is obtamed asnmlar rather more greenish-grey tint 1- (4'-aminophenylamino) -5- (4'-amino-' phenylamino) -naphthalene yields violet grey dyeings when the subsequent treatment is with a solution of alkali bichromate and acetic acid. 1'- (4'-aminophenylamino) 5-hydroxynapht-halene yields under like conditions a blue-violet, 2- (4-aminophenylamino) 47-hydroxynaphthalene a bluish violet, 2- (4'-aminophenylamino) -7- (4'-aminophenylamino)-naphthalene a violet grey tint which by prolonged treatment with bichromate and acetic acid becomes violet or bluish.
When the phenyl group contains a substituent such as alkyl or halogen, the applicability of the naphthalene derivative is not affected. 7
What I claim is v L-A process of dyeing pelts, hairs and feathers, by successively treating the goods with an aqueous solution of a salt of a naphthalenederivative of the general formula:
(wherein X means H or an univalent substituent ofthe group consisting of alkyl and.
halogen and wherein Y means H or an univalent substituent of the group consisting of --OH, NH NHaryl-NH and halogen) and with an oxidizing agent.
7. A process of dyeing pelts, hairs and feathers, by successively treating the goods with an aqueous solution of 2-(4-aminophenylamino)-naphthalene hydrochloride and an oxidizing agents.
8. A process of dyeing pelts, h irs and feathers, by successively treating t e mo'rdanted goods with an aqueous solution of .2- (V-aminophenylamino) -naphthalene hydrochloride and an oxidizing agent.
' In testimony whereof, I aifix my signature.
PAUL VIRCK.
2. A process of dyeing pelts, hairs and V feathers, by successively treating the Inordanted goods with'anaqueous solution of a salt of,a.'naphthalene derivative of the gen eral formula:
(wherein X means or an univalent substituent of the group consisting of alkyl and halogen and wherein Y means H or an univalent substituent of the groups consisting of -OH, -'-NH --NHaryl-NH and halogen) and with an oxidizing agent.
3. A process of, dyeing pelts, hairs and feathers, by successively 'treatingthe goods with an aqueous solution of a. salt of a naphthalene derivative of the general formula:
, agent. 40"
danted goods with an aqueous solution of 'a salt of a naphthalene derivative of the gen:
eral formula:
cmHa smNONm)...
(m being a whole number not less than 1 and not greater than 2) and an oxidizing agent.
5. A process of. dyeing pelt s, hairs and feathers, by successively treating the goods with an aqueous solution of a salt of a naphthalene derivative of the general formula:
CnHzHNONH:
and an oxidizing agent.
6. A process of dyeing pelts, hairs and feathers, by successively treating the mor-' T danted goods with an aqueous solution ,of a salt of a naphthalene derivative of the general formula:
and an oxidizing agent.
iss-
US238222A 1926-09-14 1927-12-06 Process of dyeing pelts, hairs, feathers, and the like Expired - Lifetime US1775074A (en)

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DE1775074X 1926-09-14

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4329504A (en) * 1976-08-20 1982-05-11 Andree Bugaut Metaphenylenediamines

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4329504A (en) * 1976-08-20 1982-05-11 Andree Bugaut Metaphenylenediamines

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