GB427248A - Improvements in or relating to the production of cellulosic pigments - Google Patents

Improvements in or relating to the production of cellulosic pigments

Info

Publication number
GB427248A
GB427248A GB24446/34A GB2444634A GB427248A GB 427248 A GB427248 A GB 427248A GB 24446/34 A GB24446/34 A GB 24446/34A GB 2444634 A GB2444634 A GB 2444634A GB 427248 A GB427248 A GB 427248A
Authority
GB
United Kingdom
Prior art keywords
cellulose
solution
sodium
parts
dye
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
GB24446/34A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB427248A publication Critical patent/GB427248A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B63/00Lakes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Coloring (AREA)

Abstract

A process for the production of cellulose pigments suitable for paints, printing inks, printing of wall paper or colouring of plastics, includes the step of regenerating the cellulose in a finely divided form from a solution of a soluble cellulose derivative in the presence of or with the subsequent addition of a solution of a dye which is stable to hydrolysis and which has an affinity for cellulose, but which is other than an ester salt of a body, yielding by oxidation a coloured compound. In a preferred form, the cellulose is regenerated by heating an alkaline aqueous solution of an alkali soluble salt of a cellulose mono-ester of a dicarboxylic acid, for example sodium cellulose phthalate, in the presence of excess alkali to a temperature high enough to hydrolyze the ester, for example above 50 DEG C. The regenerated cellulose may be filtered. The dye solution may be present during the regeneration, or may be added subsequently to the regenerated cellulose suspension, or the cellulose may be separated and separately treated with the dye. The term "solution of a dye" covers solutions not only of dyes as such, e.g. direct azo dyes but also of the leuco vat dyes. Specific examples are: (1) To a solution of 5 parts of Ponsol Blue GD, 6,4 parts sodium hydroxide and 5 parts sodium hydrosulphite in 1000 parts of water at 50 DEG C. is added a solution of 21 parts of sodium cellulose phthalate in 1000 parts of water, and the whole is heated to 90 DEG C. with the addition of a further 10 parts of sodium hydroxide. When hydrolysis is complete, the product is cooled, filtered, and washed. To ensure complete oxidation of the dye the product may be suspended in water through which air is passed or oxidizing agents such as mixtures of acetic acid and sodium or potassium bichromate, sodium perborate or hydrogen peroxide may be employed. Other similar examples are given employing alkaline solutions of ethyl cellulose hydrogen quinolate or cellulose benzoate hydrogen phthalate with a variety of other vat dyes, and of sodium cellulose phthalate with azo and sulphur dyes. Especially advantageous results are obtained with cellulose mono-ester of dicarboxylic acids which form inner anhydrides, e.g. the mono-esters obtained by reacting cellulose with phthalic succinic, quinolic, maleic or adipic anhydride in presence of a tertiary amine. Suitable alkali-soluble salts of these mono-esters are sodium, potassium, lithium and ammonium salts. The desired alkalinity of the solution may be maintained with any of the common alkalies.
GB24446/34A 1933-08-24 1934-08-24 Improvements in or relating to the production of cellulosic pigments Expired GB427248A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US427248XA 1933-08-24 1933-08-24

Publications (1)

Publication Number Publication Date
GB427248A true GB427248A (en) 1935-04-17

Family

ID=21923422

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24446/34A Expired GB427248A (en) 1933-08-24 1934-08-24 Improvements in or relating to the production of cellulosic pigments

Country Status (1)

Country Link
GB (1) GB427248A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2175946A1 (en) * 1972-03-15 1973-10-26 Becker & Co Naturinwerk

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2175946A1 (en) * 1972-03-15 1973-10-26 Becker & Co Naturinwerk

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