US1708635A - Process of treating animal fibers - Google Patents

Process of treating animal fibers Download PDF

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Publication number
US1708635A
US1708635A US238224A US23822427A US1708635A US 1708635 A US1708635 A US 1708635A US 238224 A US238224 A US 238224A US 23822427 A US23822427 A US 23822427A US 1708635 A US1708635 A US 1708635A
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parts
bath
hour
animal fibers
treating animal
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US238224A
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Schoner Bernhard
Virck Paul
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Grasselli Dyestuff Corp
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Grasselli Dyestuff Corp
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    • 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
    • D06P1/32General 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 oxidation dyes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/916Natural fiber dyeing
    • Y10S8/917Wool or silk

Definitions

  • This invention relates to a process of treating animal fibers in an acid bath with a sulphonated derivative of naphthylamines of the general formula wherein Y means H or univalent substituents such as OH, NH or halogen and wherein R and R mean H, alkyl, aryl or substituted aryl residues and w stands for a whole number not greater than 2, these naphthylamine derivatives containing at least one ,SO H
  • Example 2.100 parts of wool are entered at ordinary temperatureinto a bath consisting of 4000 parts of water, 6 parts of 1.4-di-(6- In similar manner a black dyeing is obsulpho-Q-naphthylam'in) -benzene of the for mula 10 parts of crystallized sodium sulphate and 5 parts of. sulphuric acid.
  • the temperature is raised to theboiling, boiling continued for one hour, 3 parts of potassium bichromate added and boiling continued for a further half hour; the goods are then washed and dried, there is thus obtained afast deep black.
  • E wample 3.100' parts of wool are entered into a bath consisting of-6 parts of the sodium salt -of 4-a-naphthylamino-4-aminodiphe- HOaS 'nylamine-2-sulphonicacid of the formula 10 parts of crystallized sodium sulphate and 15 parts of acetic acid in 4000 parts of water.
  • the bath is maintained boiling for an hour, where upon the wool iswashed and handled for about half an hour in a boiling hot bath of 3 parts of potassium bichromate and 3 parts of sulphuric acid in 4000 parts of water,
  • E wample 4.100 parts of wool are treatedas above described in a bath consisting of 6 parts of the sodium salt of 4-B-naphthylamino-4'-oxydiphenylamine-Q-sulphonic acid of the formula v v @NHQNH-O-OH,
  • Example 6.100 parts of wool are boiled for one hour in a bath consisting of 6 parts of H
  • Example 7.-100 parts of wool are handled for 1 hour at the boiling point in a bath consisting of 3 parts of 2.6'-di(4-amino-2-sulphophenylamin'o) -naphthalene of the formula NHAC +NH2 Elm-GEN sour 10 parts of crystallized sodium sulphate, 4 parts of sulphuric acid and 4000 parts of water and then for a further'half an hour in thesame bath after addition of 15 parts of potassium bichromate. There is produced a dark green dyeing. v

Description

Patented Apr. 9, 1929.
UNITED STATES PATENT OFFICE.
IBERNHARD SCHONER, OF WOLFEN, KR. BITTERFELD, ANI) PAUL VIRCK, OF DESSAU IN -ANHALT, GERMANY, ASSIGNORS TO GRASSELLI DYESTUFF CORPORATION, OF NEW YORK, N. Y., A CORPORATION OF DELAWARE.
PROCESS OF TREATING ANIMAL FIBERS.
N Drawing. Application filed December 6, 1927, Serial No. 238,224, and in Germany June 16, 1926.
This invention relates to a process of treating animal fibers in an acid bath with a sulphonated derivative of naphthylamines of the general formula wherein Y means H or univalent substituents such as OH, NH or halogen and wherein R and R mean H, alkyl, aryl or substituted aryl residues and w stands for a whole number not greater than 2, these naphthylamine derivatives containing at least one ,SO H
group, and then treating the fibers with a formula NHQNHz, O 311 10 parts of crystallized sodiumsulphate and 5 parts of acetic acid. The temperature is raised to boiling, 3 parts of sulphuric acid are added and the whole is boiled for 1 hour. After the goods have been washed they are handled for abouthalf an hour in an boiling bath of-3 parts of potassium bichromate and 3 parts of sulphuric acid in 4000 parts of water, whereby a black having a full bloom is produced on the fiber;
@NEONQ, HOaS is used.
Example 2.100 parts of wool are entered at ordinary temperatureinto a bath consisting of 4000 parts of water, 6 parts of 1.4-di-(6- In similar manner a black dyeing is obsulpho-Q-naphthylam'in) -benzene of the for mula 10 parts of crystallized sodium sulphate and 5 parts of. sulphuric acid. The temperature is raised to theboiling, boiling continued for one hour, 3 parts of potassium bichromate added and boiling continued for a further half hour; the goods are then washed and dried, there is thus obtained afast deep black.
E wample 3.100' parts of wool are entered into a bath consisting of-6 parts of the sodium salt -of 4-a-naphthylamino-4-aminodiphe- HOaS 'nylamine-2-sulphonicacid of the formula 10 parts of crystallized sodium sulphate and 15 parts of acetic acid in 4000 parts of water. The bath is maintained boiling for an hour, where upon the wool iswashed and handled for about half an hour in a boiling hot bath of 3 parts of potassium bichromate and 3 parts of sulphuric acid in 4000 parts of water,
whereby a fast black is produced.
The like result is obtained when 4-,8-naphthylamino 4 aminodipheuylamine 2 sulphonic acid of the formula is used.
E wample 4.100 parts of wool are treatedas above described in a bath consisting of 6 parts of the sodium salt of 4-B-naphthylamino-4'-oxydiphenylamine-Q-sulphonic acid of the formula v v @NHQNH-O-OH,
10 parts of crystallized sodium sulphate, 10 parts of sulphuric acid and 4000 parts of water. The washed wool is then subsequentin a bath consisting of 6 parts of the sodium 1y treated as described in Example 3. There salt of 1.4-di (4-,8-naphthylamino-Q-sulphois produced a fast full black.
- I Example 5.100 parts of wool are handled phenylamino) -benzene of the formula @buP-ONHfONEkQ- m;
10parts of crystallized sodium sulphate, 4
I parts of sulphuricacid and 4000 parts of water for 1 hour while the. bath is boiling hot; the treatment is then continued in the same bath for half an hour after addition of 3 parts of potassium bichromate. There is produced a fast black dye.
A like result is obtained when the correspolnding a-naphthyl derivative of the formu a Y is used.
Example 6.100 parts of wool are boiled for one hour in a bath consisting of 6 parts of H|O NH H 7 311 10 parts of crystallized sodium sulphate, 4
parts of sulphuric acid and 4000 parts of water; after washing the goods they are further threated in a boiling bath of 3 parts of duced a full blue black.
potassium bichromate and 3 parts of sul phuric acid in 4000 parts'of water for half an hour. There is produced a deep black.
Example 7.-100 parts of wool are handled for 1 hour at the boiling point in a bath consisting of 3 parts of 2.6'-di(4-amino-2-sulphophenylamin'o) -naphthalene of the formula NHAC +NH2 Elm-GEN sour 10 parts of crystallized sodium sulphate, 4 parts of sulphuric acid and 4000 parts of water and then for a further'half an hour in thesame bath after addition of 15 parts of potassium bichromate. There is produced a dark green dyeing. v
E xample 8-100 parts'of weighted silk are handled in a bath of 16 parts of 4 aminosulphophenyl-2-naphthylamine (see Example '1) 15 parts of acetic acid, 10 parts of crystallized sodium sulphate and 1000 parts of water which is kept boiling hot {the goods are then washed and after-chromed. There is pro- 3. A process of 1.5 di (4 -paramethylphenylamino-3-sulphophenylamino) naphthalene of the formula NHQNH-O-OH:
OzH
What we claim is:
1. A process of treating animal fibers in an acid bath with a sulphonated derivative of naphthylamines of the general formula NQ Q wherein Y means H or univalcnt substituents such as OH, NH or halogen and wherewherein R and R mean H, alkyl, aryl or substitu'ted aryl residues and x stands for a whole number not greater than 2, these naphthylamine derivatives containing at least one -SO I-I group, and then treating the fibers with an oxidizing agent. L
treating animal fibers in an acid bath with a sulphonated derivative of aminoaryl residue, these derivatives contain naphthylamines of the general formula ing at least one SO H group, and then treating the fibers with an oxidizing agent.
4. A process of treating animal fibers in 10 CmH7HN-O-NH-O-X U i an and bath wlth a sulphonated derivative X meaning H, alkyl, -OH, NH or an of n'aphthylamines of the general formula ommnNQNmO-NHpNHmm sO=H 0:11
5. A process of treating animal fibers in WNHOHM NHQNHKI) an acid bath with a sulphonated derivative of 2-naphthylamine of the general formula BERNHARD SGHONERQ and then treating the fibers with an ox idiz- PAUL VIRCK.
ing agent. I
In testimony whereof, we' aflix our signatures.
US238224A 1926-06-16 1927-12-06 Process of treating animal fibers Expired - Lifetime US1708635A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2539334A (en) * 1949-05-21 1951-01-23 Us Rubber Co Gaseous depinking method
US3185696A (en) * 1959-03-12 1965-05-25 Jack M Tien 3', 6'-diaminofluoran derivatives of gamma-lactam

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2539334A (en) * 1949-05-21 1951-01-23 Us Rubber Co Gaseous depinking method
US3185696A (en) * 1959-03-12 1965-05-25 Jack M Tien 3', 6'-diaminofluoran derivatives of gamma-lactam

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