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US2282724A - Process of dyeing with substantive colors - Google Patents

Process of dyeing with substantive colors Download PDF

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Publication number
US2282724A
US2282724A US171644A US17164437A US2282724A US 2282724 A US2282724 A US 2282724A US 171644 A US171644 A US 171644A US 17164437 A US17164437 A US 17164437A US 2282724 A US2282724 A US 2282724A
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US
United States
Prior art keywords
dyeing
urea
substantive
wool
dyed
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Expired - Lifetime
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US171644A
Inventor
Haynn Richard
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GAF Chemicals Corp
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General Aniline and Film Corp
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Publication date
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Publication of US2282724A publication Critical patent/US2282724A/en
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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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/64General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
    • D06P1/642Compounds containing nitrogen
    • D06P1/649Compounds containing carbonamide, thiocarbonamide or guanyl groups
    • D06P1/6491(Thio)urea or (cyclic) derivatives
    • 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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/64General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
    • D06P1/642Compounds containing nitrogen
    • D06P1/6421Compounds containing nitrile groups

Definitions

  • the present invention relates to a process of dyeing with substantive colors and to composition of matter useful in such dyeing processes.
  • a urea or a derivative thereof such as urea itself, methyl urea, methylol urea, dimethylol urea or a salt of one of these compounds, for instance, a chloride, a nitrate, a sulfate or a like salt, or a substance capable of forming one of these substances, such as ammonium cyanate, cyanamide or a similar compound.
  • Such compounds have a protective action even in an alkaline dye bath and scarcely influence the pH-value of the dye bath during the dyeing operation
  • the said additions have a levelling and compensating eflect on the mixture of vegetable and animal fibers and thus facilitate the production of even tints on the mixed fibers. Even if the material is boiled for a long time, the wool is not too strongly dyed. The process, therefore, represents a considerable technical progress.
  • the prescribed additions may be mixed with substances hitherto used in dye ng xed thereto; the parts are by weight:
  • a textile fabric consisting of 70 parts of wool and parts of spun rayon (viscose artificial textile fiber) is dyed with 1 per cent. of the azo-dyestuff' 3-amino-6-hydroxy-l-benzoic acidalphanaphthyl-amine' gamma-acid with the addition of 30 per cent. of crystallized sodium sulfate and'5-10% of urea.
  • the dyeing which in the absence of the urea tends to be discolored shows the normal tint even if the material is boiled for several hours.
  • a textile fabric consisting of '10 parts of wool and 30 parts of spun rayon (viscose artificial textile fiber) is dyed with 1 per cent of the azo-dyestuff 3-amino-6-hydroxy-1-benzoic acid-+alphanaphthyl-aminegamma-acid while adding 30% of crystallized sodium sulfate and 0.5-2% of dimethylol urea.
  • the dyeing which in the absence of the dimethylol urea. tends to be discolored shows the normal tint even if the material is boiled for several hours.
  • a textile fabric is dyed in the manner indicated in Example 1, except that instead of urea, there is used 5% of ammonium cyanate, which, under the conditions of the dyeing process, is transformed into urea.
  • a textile fabric is dyed in the manner indicated in Example 1, 3% of urea chloride being used instead of urea.
  • ammonium sulfate may be used, with the same success.
  • Example '7 The material named in Example '7 is dyed in the manner described therein, 1% of urea ni- 5 trate being used instead of 5% of methyl urea.
  • ureanto the dyebath and 30 parts or viscose artificial textile fiber are 10 and t dyeing i t usualmannen dyed with 2% of the dyestui'i' No. 540 of Schultz's Farbstofltabellen, 1931, 5% of methyl urea (obtained by reaction of methyllamine sulfate with potassium cyanate) and 20 per cent. 01 crys- 2.
  • the process which comprises dyeing textile fibers with a. v substantive dyestufl in a boiling dyebath, in the presence of urea.

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

Description

Patented May 12, 1942 UNITED STATES PATENT OFFICE 2,282,724
rnocnss or nrmzo. wrrn suns'mnnvn mama Haynn. Frankiort-on-thc-Main, Germany, assignor to General Aniline a Film Corporation, a corporation of Delaware No Drawing.
Application October 29, 1937, Serial No. 171,644. In Germany November 3, 1936 2 Claims.
The present invention relates to a process of dyeing with substantive colors and to composition of matter useful in such dyeing processes.
In dyeing with substantive dyestuffs mixed textile fabrics consisting of wool, cotton and/or ar-.
tificial fibers, difiiculties frequently arise because in a prolonged, dyeing operation the shades are in part changed or discolored. The nature of this phenomenon has not yet been explained. It has, however, also been observed in. the dyeing of vegetable fiber alone where it is probably caused by a reducing action of the substances accompanying cotton. In the dyeing of mixed textile fabrics of wool and cotton as well as artificial textile fibers the defect is much more apparent and is even observed in the case of dyestuffs which behave normally on vegetable fiber. It
' invention, but they are not intended to limit it may be assumed that the detrimental action is due to degradation products of the wool formed by hydrolysis.
Attempts have been made to avoid this inconvenience by dyeing in an acid medium. This, however, involves the disadvantage that the substantive dyestufi dyes the wool much more intensely than the cotton andeven shades could be produced only with difllculty.
I have found that the said detrimental efiect is prevented by adding to the dye bath a urea or a derivative thereof, such as urea itself, methyl urea, methylol urea, dimethylol urea or a salt of one of these compounds, for instance, a chloride, a nitrate, a sulfate or a like salt, or a substance capable of forming one of these substances, such as ammonium cyanate, cyanamide or a similar compound. Such compounds have a protective action even in an alkaline dye bath and scarcely influence the pH-value of the dye bath during the dyeing operation According to this invention it is possible to prepare neutral baths and thus eliminate the disadvantages of the acid dye bath, namely a too strong absorption of the substantive dyestufi by the wool. Even if during the dyeing process the reaction of the bath should change to the alkaline side the said detrimental effect does not occur when the additions prescribed by this invention are made.
Moreover, the said additions have a levelling and compensating eflect on the mixture of vegetable and animal fibers and thus facilitate the production of even tints on the mixed fibers. Even if the material is boiled for a long time, the wool is not too strongly dyed. The process, therefore, represents a considerable technical progress. The prescribed additions may be mixed with substances hitherto used in dye ng xed thereto; the parts are by weight:
(1) A textile fabric consisting of 70 parts of wool and parts of spun rayon (viscose artificial textile fiber) is dyed with 1 per cent. of the azo-dyestuff' 3-amino-6-hydroxy-l-benzoic acidalphanaphthyl-amine' gamma-acid with the addition of 30 per cent. of crystallized sodium sulfate and'5-10% of urea. The dyeing which in the absence of the urea tends to be discolored shows the normal tint even if the material is boiled for several hours.
' preservative against discoloration.
(2) A textile fabric consisting of '10 parts of wool and 30 parts of spun rayon (viscose artificial textile fiber) is dyed with 1 per cent of the azo-dyestuff 3-amino-6-hydroxy-1-benzoic acid-+alphanaphthyl-aminegamma-acid while adding 30% of crystallized sodium sulfate and 0.5-2% of dimethylol urea. The dyeing which in the absence of the dimethylol urea. tends to be discolored shows the normal tint even if the material is boiled for several hours.
(3) A textile fabric is dyed in the manner indicated in Example 1, except that instead of urea, there is used 5% of ammonium cyanate, which, under the conditions of the dyeing process, is transformed into urea.
(4) A textile fabric is dyed in the manner indicated in Example 1, 3% of urea chloride being used instead of urea.
(5) 2 per cent. of the dyestuff No. 566 of Schultzis Farbstofitabellen," 1931, are used to dye the material named in Example 1 in the manner described therein, a mixture of 5% of urea and 1% of ammonium acetate being added as a Also this dyeing remains unobjectionable on prolonged boiling.
instead or ammonium acetate. ammonium sulfate may be used, with the same success.
(6) The material is dyed under the conditions taiiized sodium suliate. The normal tint remains even after boiling for two hours.
: m The material named in Example '7 is dyed in the manner described therein, 1% of urea ni- 5 trate being used instead of 5% of methyl urea.
I claim; 1. In the process of dye g textile fibers with substantive dyestufls in a boiling dyebath, the
step which comprises addin: ureanto the dyebath and 30 parts or viscose artificial textile fiber are 10 and t dyeing i t usualmannen dyed with 2% of the dyestui'i' No. 540 of Schultz's Farbstofltabellen, 1931, 5% of methyl urea (obtained by reaction of methyllamine sulfate with potassium cyanate) and 20 per cent. 01 crys- 2. The process which comprises dyeing textile fibers with a. v substantive dyestufl in a boiling dyebath, in the presence of urea.
\ RICHARD HAYNN.
US171644A 1936-11-03 1937-10-29 Process of dyeing with substantive colors Expired - Lifetime US2282724A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE206685X 1936-11-03

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US2282724A true US2282724A (en) 1942-05-12

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US (1) US2282724A (en)
CH (1) CH206685A (en)
FR (1) FR828616A (en)
GB (1) GB486010A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3096142A (en) * 1957-07-10 1963-07-02 Basf Ag Process for dye levelling with lactams
US4280814A (en) * 1979-03-19 1981-07-28 Eastman Kodak Company Dyeing process and compositions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2501184A (en) * 1944-04-06 1950-03-21 Lawrence Richard Bruce Inc Method of dyeing keratinous fibers
MX143090A (en) * 1975-06-20 1981-03-13 Burlington Industries Inc PROCEDURE FOR REAGENTLY HAVING TEXTILE SUBSTRATE WITH AN AROMATIC DYE SUBSTITUTED WITH CARBOXYLICON ACID GROUPS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3096142A (en) * 1957-07-10 1963-07-02 Basf Ag Process for dye levelling with lactams
US4280814A (en) * 1979-03-19 1981-07-28 Eastman Kodak Company Dyeing process and compositions

Also Published As

Publication number Publication date
FR828616A (en) 1938-05-24
GB486010A (en) 1938-05-20
CH206685A (en) 1939-08-31

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