US2117699A - Dyeing of leather - Google Patents

Dyeing of leather Download PDF

Info

Publication number
US2117699A
US2117699A US123545A US12354537A US2117699A US 2117699 A US2117699 A US 2117699A US 123545 A US123545 A US 123545A US 12354537 A US12354537 A US 12354537A US 2117699 A US2117699 A US 2117699A
Authority
US
United States
Prior art keywords
leather
dyeing
minutes
water
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US123545A
Inventor
Burchill John
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Application granted granted Critical
Publication of US2117699A publication Critical patent/US2117699A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • D06P3/32Material containing basic nitrogen containing amide groups leather skins
    • D06P3/3246Material containing basic nitrogen containing amide groups leather skins using vat, sulfur or indigo dyes

Definitions

  • This invention relates to new colored leathers
  • toleathers which are dyed with a class of leuco vat dyestufis and to processes of dyeing leathers.
  • dyestufi sulphuric esters may be conveniently applied according to the invention and particularly illustrated in the invention is more the following examples which are illustrative and not, limitative of the invention.
  • Example 11 50 lbs. of chamois leather were stripped and wetted back with warm water in which was dissolved lb. soda ash, rinsed and immersed in 30 gallons of water at 35 C. in the drum. 5 lbs. of the leuco sulphuric ester of the dyestufi known as 5:5'-dichloro-6:6'-dimethyl-2:2'-bisthionaphthene indigo (Color Index 1212) dissolved in 10 gallons of water were added and after i ,20 minutes agitation, 3 lbs. of glacial acetic acid diluted with 2 quarts of water were added slowly, dyeing being completed in a further 30 minutes. The exhausted dye liquor was then run of!
  • Example III Leukanol stained chrome tanned cabretta glove leather was wet out with-a dilute ammonia solution, the treatment bei carried on for 30 minutes at 102 F. After ashing and striking out excess water a 5% solution of 'a mixture of equal parts of formic and'sulphuric. acid was brushed on the grain side to prevent undue penetration of the dyestuif and the excess water was struck out.
  • the dyeing was of a full bright-shade having much better fastness to washing than dyeings obtainable with water solutions of acid, direct, chrome or basic dyestuifs.
  • the leather was col ored only on one side and there was no undue penetration of the dyestufi', such as that which is undesirable on leather for women's gloves.
  • Example IV The dyes used in accordance with Example III were used to dye Leukanol stained chrome tanned cabretta glove leather in the drum.
  • the leather was wet out for 30 minutes at 102 F. with 2% ammonia solution, then 5% by weight of the dyestuif was added and the leather was run in the drum for 30 minutes.
  • 2 of formic acid and 2 of sulphuric acid were then added, and after 5 minutes sodium nitrite to make the solution up to 2% was added, and run for 20 minutes.
  • the dveings had good fastness to washing and compared favorably with the results obtained by brush treatment as illustrated in Example III.
  • Still other types of leather e. g. paddles, may be used.
  • the process which comprises dyeing at least an outer layer of a wet-out leather with an aqueous solution of the sulphuric ester of a leuco vat dyestuif, gradually acidifying with a dilute acid and there developing the color by applying a dilute acidified solution of an oxidizing agent, the temperature of said saturating, acidifying and development not exceeding 50 C.

Description

' veloped on the leather to Patented May 17, 1938 John Bur-chill,
assignor to Imperi Blackley, Manchester, England,
al Chemical industries Limited, a corporation of Great Britain No Drawing. Application February 1, 1937, Se- I rial No. 123,545. In Great Britain January 30,
1 Claim.
This invention relates to new colored leathers,
and especially toleathers which are dyed with a class of leuco vat dyestufis and to processes of dyeing leathers.
Dyeings on leather which are-fast improved to wash ing, moreespecially the dyeings on glove leather, have been obtainable generally only in pale or dull shades, such as dyeings produced by sulphur Bright shades on leather which have dyestuffs.
been produced were not entirely satisfactory from the'standpoint of fastness to washing, such as' leathers dyed with the acid or direct colors. For'example, it has hitherto been found impossible to obtain bright reds, oranges, blues and greens, especially on glove leather which had good light fastness and would withstand reasonable washing treatment.
It is among the objects of provide dyed leathers the invention to in bright shades which have good fastness to washing and light. Another object is to provide improved processes for dyeing leathers. Other objects of the will be apparent from the following tailed description of the invention.
invention more de- The objects of the-invention are attained by applying to leather, such as aldehyde-tanned chamois and other washable leathers to which leathers the invention lends particular value, compounds which are sulphuric, esters of leuco vat dyestuffs and these compounds are thendethe vast dyestuifs themselves, whereupon the dyed leathers may be finished by fat liquoring preceded, if desired, by soaping treatment. By means of my invention shades may be produced on-leather of a fastness to washing and light hitherto unattainable. The
' leuco vat. dyestufi sulphuric esters may be conveniently applied according to the invention and particularly illustrated in the invention is more the following examples which are illustrative and not, limitative of the invention.
- Example I lbs. of aldehyde dressed sheepskin splits were washedby drummingior 5 minutes in warm 1 water, rinsed and then immersed in 30 gallons of water at 35 C. i'n the drum. After rotating for a few minutes, 5'lbs. of the leuco sulphuric ester of thedyestufi v zanthrone (Color Index 1101), solved in 3 gallons of water at 50 and after a further'20 minutes-1V known as dimethoxydibenpreviously dis- -C.' were added lbs.
of glacial acetic acid diluted with twice the volume of water was introduced I of the next 15 minutes and drumming gradually during the course continued were further treated as in Example 1.
Example 11 50 lbs. of chamois leather were stripped and wetted back with warm water in which was dissolved lb. soda ash, rinsed and immersed in 30 gallons of water at 35 C. in the drum. 5 lbs. of the leuco sulphuric ester of the dyestufi known as 5:5'-dichloro-6:6'-dimethyl-2:2'-bisthionaphthene indigo (Color Index 1212) dissolved in 10 gallons of water were added and after i ,20 minutes agitation, 3 lbs. of glacial acetic acid diluted with 2 quarts of water were added slowly, dyeing being completed in a further 30 minutes. The exhausted dye liquor was then run of! and the skins refioated in a 1% aqueous sulphuric acid solution at 20 C. to which 1 lbs. sodium nitrite were added. After 5 minutes the skins Example III Leukanol stained chrome tanned cabretta glove leather was wet out with-a dilute ammonia solution, the treatment bei carried on for 30 minutes at 102 F. After ashing and striking out excess water a 5% solution of 'a mixture of equal parts of formic and'sulphuric. acid was brushed on the grain side to prevent undue penetration of the dyestuif and the excess water was struck out. 'A 2% aqueous solution of -Ponsol jade green soluble was brushed on, and followed immediately by a 1% aqueous solution of sodium nitrite. The surface was then washed with a liberal flow of fresh water at F. followed 45 by-tumbling for 5 minutes. Finally it wasfat liquored with s'ulphonated neats-foot oil.
The dyeing was of a full bright-shade having much better fastness to washing than dyeings obtainable with water solutions of acid, direct, chrome or basic dyestuifs. The leather was col ored only on one side and there was no undue penetration of the dyestufi', such as that which is undesirable on leather for women's gloves.
' leather which was prepared for dyeing in the same manner.
Example IV The dyes used in accordance with Example III were used to dye Leukanol stained chrome tanned cabretta glove leather in the drum. The leather was wet out for 30 minutes at 102 F. with 2% ammonia solution, then 5% by weight of the dyestuif was added and the leather was run in the drum for 30 minutes. 2 of formic acid and 2 of sulphuric acid were then added, and after 5 minutes sodium nitrite to make the solution up to 2% was added, and run for 20 minutes. After washing the stock was fat liquored with sulphonated neats-foot oil and was found to be dyed medium shades of green and blue accordingly as the green or blue dye was used. The dveings had good fastness to washing and compared favorably with the results obtained by brush treatment as illustrated in Example III.
Similar results were obtained when similar treatment was applied to sumac stained chrome tanned cabretta glove leather.
As illustrative of other suitable coloring matters of the kind which can be used according to the invention as illustrated are the leuco sulphuric esters of the dyestuffs known as fiavanthrone (Color Index 1118) dichloroisodibenzanthrone (Color Index 1104) 5:7:5':7'-tetrabromindigotin (Color Index ,1184), trichloro-N-dihydro- 1:2:1:2'-anthraquinoneazine. The most of the leucoesters of vat dyestuffs which are used 'in ac- 2,117,699 treatment when "Ponsol Blue BF Soluble was cordance with the invention are of excellent fastness to light and all are of very good fastness to Washing.
In certain cases, as exemplified, for instance. in
-Example I, itis advisable to add the acid gradually to the dye bath to promote greater levelness of shade. The degree of penetration into the leather may be regulated by increasing or diminishing the time of dyeing previous to adding the acid. Development may be carried out in the exhausted dye liquor or in a fresh solution and other developingagents, for instance, ammonium persulphate in dilute mineral acid, may be employed in place of acidified nitrite.
Incorporation of soap up to 2 parts per 1000 in the fat liquor or separate soaping in a similar strength solution at C. may be employed, if desired, to give brighter shades and better fastness to rubbing.
As still other modifications of the invention will be suggested to those skilled in the art without departing from the spirit and scope of the invention, it is .to be understood that no limitations are intended other than those which are specifically expressed in the appended claims or are imposed by the prior art.
Still other types of leather e. g. paddles, may be used.
I claim:
The process which comprises dyeing at least an outer layer of a wet-out leather with an aqueous solution of the sulphuric ester of a leuco vat dyestuif, gradually acidifying with a dilute acid and there developing the color by applying a dilute acidified solution of an oxidizing agent, the temperature of said saturating, acidifying and development not exceeding 50 C.
JOHN BURCHILL.
dyeing machinery,
US123545A 1936-01-30 1937-02-01 Dyeing of leather Expired - Lifetime US2117699A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2117699X 1936-01-30

Publications (1)

Publication Number Publication Date
US2117699A true US2117699A (en) 1938-05-17

Family

ID=10898945

Family Applications (1)

Application Number Title Priority Date Filing Date
US123545A Expired - Lifetime US2117699A (en) 1936-01-30 1937-02-01 Dyeing of leather

Country Status (1)

Country Link
US (1) US2117699A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2872277A (en) * 1955-12-29 1959-02-03 Gen Aniline & Film Corp Dyeing of leather
US5964899A (en) * 1995-03-10 1999-10-12 Clariant Finance (Bvi) Limited Azo dyes, their production and use

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2872277A (en) * 1955-12-29 1959-02-03 Gen Aniline & Film Corp Dyeing of leather
US5964899A (en) * 1995-03-10 1999-10-12 Clariant Finance (Bvi) Limited Azo dyes, their production and use

Similar Documents

Publication Publication Date Title
US2164930A (en) Process for reducing vat dyestuffs
US2117699A (en) Dyeing of leather
CN109385916A (en) A kind of low liquor ratio colouring method of sheep shearing
US2368690A (en) Process for the improvement of the properties of artificial masses and fibers manufactured from proteinlike substances
US2298147A (en) Textile printing process
US2872277A (en) Dyeing of leather
US2420729A (en) Dyeing with indigoid vat dyestuffs
US2077546A (en) Process for dyeing leather
US2044099A (en) Treatment of leather
US2585610A (en) Process for dyeing furs using an aqueous alcohol solution of a complex metal compound of an azo dyestuff free from acid groups
US2937067A (en) New process for the coloration of synthetic materials and the industrial products resulting therefrom
US2189807A (en) Washing of discharge prints
US2150389A (en) Coloring of leather
US2553375A (en) Process of dyeing fur skins with insoluble azo dyestuffs
US2524093A (en) Union dyeing of mixed fabrics of cellulose ester and animal fibers with alkaline reduced vat dye solutions containing swelling agents
US3409384A (en) Method of dyeing leather with azoic dyestuffs and products so produced
US2183752A (en) Dyeing of furs
US1816766A (en) Process of dyeing and printing cellulose esters
US1841007A (en) Dyeing of chamois-leather
GB769174A (en) Improvements in or relating to the dying of suede leather
US2405165A (en) Process for dyeing of suede
US2138602A (en) Dyeing of hardened casein
US2074031A (en) Continuous dyeing process
DE2126814C3 (en)
US2109372A (en) Dye