GB675244A - Improvements in the production of coloured artificial thread-forming substances and of threads, foils, and the like therefrom - Google Patents

Improvements in the production of coloured artificial thread-forming substances and of threads, foils, and the like therefrom

Info

Publication number
GB675244A
GB675244A GB13565/50A GB1356550A GB675244A GB 675244 A GB675244 A GB 675244A GB 13565/50 A GB13565/50 A GB 13565/50A GB 1356550 A GB1356550 A GB 1356550A GB 675244 A GB675244 A GB 675244A
Authority
GB
United Kingdom
Prior art keywords
leuco
vat
viscose
coloured
threads
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
Application number
GB13565/50A
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB675244A publication Critical patent/GB675244A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0041Optical brightening agents, organic pigments

Abstract

Artificial thread-forming substances such as cellulose esters and ethers, viscose, superpolyamides, superpolyurethanes, polyesters, polyacrylonitrile, and polyvinyl chloride, are coloured by incorporating in them a pigment consisting of a water-insoluble ester of a leuco vat dyestuff of the anthraquinone series and a monocarboxylic acid having up to 7 carbon atoms. Leuco vat dyestuffs of dibenzanthrone, isodibenzanthrone, dibenzpyrenequinone, indanthrone, flavanthrone, or pyranthrone may be esterified with carboxylic acid anhydrides or halides which do not contain hydrophilic groups, e.g. acetyl anhydride or chloride, or benzoyl chloride. The esterification may be carried out with the dry leuco compounds in inert solvents or diluents, if desired in presence of acid binding agents, such as alkali acetates, pyridine, or quinoline, but the aqueous solution of an alkali leuco compound may be directly treated with the esterifying agent. The vat dyestuffs themselves may be reacted with the esterifying agents in the presence of metals having a reducing action such as zinc or aluminium. By carrying out the latter process in the presence of pyridine or quinoline, the reducing metal may be dispensed with in some cases, e.g. in the case of indanthrone. The carboxylic acid esters of leuco vat dyestuffs of the anthraquinone series may be added to spinning solutions or masses. The threads or fibres obtained are coloured in a manner fast to washing and light and stable to aqueous alkalies and acids. The colourings are vat stable so that when a mixed fabric of undyed cotton and viscose rayon or viscose staple fibre, which has been obtained from a spinning solution coloured in the described manner, is subsequently vat dyed, the viscose rayon retains its original colour. In an example, 2.5 parts by weight of the acetic acid ester of leucodibenzanthrone in a fine powdered form are added to 1,000 parts by weight of viscose containing 75 parts of cellulose. The viscose is then spun to form threads of a permanent deep red - brown shade. In another example, the acetic acid ester of the leuco compound of the vat dyestuff resulting from alcoholic potash fusion of bz-1-benzanthronyl-1-amino-anthraquinone is dispersed in a small proportion of a solution of cellulose acetate in presence of a reaction product of ethylene oxide and octyl alcohol. The pigment preparation is dried and rolled. It is then stirred into a cellulose acetate spinning solution. In a similar manner, a pigment preparation of the acetic acid ester of leuco-N,N1-dihydro-1,2,21,11-anthraquinoneazine (leucoindanthrone) may be obtained and may be incorporated in a spinning solution of polyacrylonitrile. Specifications 24604/08, [Class 2], 337,741, [Class 2 (iii)], and 506,803, are referred to.
GB13565/50A 1949-06-18 1950-05-31 Improvements in the production of coloured artificial thread-forming substances and of threads, foils, and the like therefrom Expired GB675244A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE675244X 1949-06-18

Publications (1)

Publication Number Publication Date
GB675244A true GB675244A (en) 1952-07-09

Family

ID=6592717

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13565/50A Expired GB675244A (en) 1949-06-18 1950-05-31 Improvements in the production of coloured artificial thread-forming substances and of threads, foils, and the like therefrom

Country Status (1)

Country Link
GB (1) GB675244A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2980755A (en) * 1958-01-20 1961-04-18 British Insulated Callenders Electric cables

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2980755A (en) * 1958-01-20 1961-04-18 British Insulated Callenders Electric cables

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