GB937494A - Acylation of pulp and manufacture of paper therefrom useful in photography - Google Patents

Acylation of pulp and manufacture of paper therefrom useful in photography

Info

Publication number
GB937494A
GB937494A GB1091/60A GB109160A GB937494A GB 937494 A GB937494 A GB 937494A GB 1091/60 A GB1091/60 A GB 1091/60A GB 109160 A GB109160 A GB 109160A GB 937494 A GB937494 A GB 937494A
Authority
GB
United Kingdom
Prior art keywords
pulp
acid
weight
water
bath
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
GB1091/60A
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.)
Kodak Ltd
Original Assignee
Kodak 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 Kodak Ltd filed Critical Kodak Ltd
Publication of GB937494A publication Critical patent/GB937494A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • C08B3/08Preparation of cellulose esters of organic acids of monobasic organic acids with three or more carbon atoms, e.g. propionate or butyrate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • C08B3/06Cellulose acetate, e.g. mono-acetate, di-acetate or tri-acetate
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H11/00Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D21H11/16Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
    • D21H11/20Chemically or biochemically modified fibres
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/71Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
    • D21H17/72Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic material
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/775Photosensitive materials characterised by the base or auxiliary layers the base being of paper
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/17Ketenes, e.g. ketene dimers
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • D21H17/28Starch
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45Nitrogen-containing groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Paper (AREA)

Abstract

Wood pulp is acylated by impregnation with an aliphatic acid having from 2-4 carbon atoms containing water in a proportion of not more than 15% by weight based on the total weight of the acid and water, the impregnated wood pulp is then immersed in at least 20 parts by weight, based on the dry weight of the pulp, of a bath comprising at least 25% by weight of the anhydride of an aliphatic acid having from 2-4 carbon atoms, an aliphatic acid and a catalyst which will not combine with the pulp and the bath is maintained at a temperature or temperatures below 35 DEG C. until the pulp has an acetyl content of from 15 to 25% by weight, based on the weight of the acylated pulp, or the equivalent content of another acyl group having from 2 to 4 carbon atoms, the proportion of catalyst in the bath being such that said temperature or temperatures can be maintained. The pulp may be kraft wood pulp, preferably bleached, having a tear value above 5 and an initial cuprammonium intrinsic viscosity of at least 5, determined at 25 DEG C. in a cuprammonium liquid containing 3\sB0,05 gms. Cu, 16,05\sB0,1 gms. NH3 and approximately 1 gm. sugar, all per 100 ml. solution. Acylation of such a pulp may be effected to an acetyl content of 20% by weight. The impregnated pulp, after removal of excess of the aqueous aliphatic acid, may contain 0,6-1 parts by weight of the acid per part by weight of dry pulp. Each aliphatic acid is preferably acetic acid, but acylation with other fatty acyl radicals containing 3 or 4 carbon atoms, e.g. propionyl or butyryl, may be effected in the same way. Desirably, the bath contains 30-84% by weight, especially 50-53%, of acetic anhydride, and from 20-50 parts by weight of the bath, based on the dry weight of the pulp, are employed, the bath also containing 0,45-1,6% by weight of sulphoacetic acid as catalyst. Other specified catalysts include phosphoric acid, perchloric acid, methane sulphonic acid, methane trisulphonic acid, phenol sulphonic acid and phenol trisulphonic acid. The pulp may be impregnated by soaking the pulp sheet directly in the aqueous aliphatic acid, suitably containing 5% by weight of water, based on the total weight of acid and water, and then removing excess acid. Alternatively, the pulp may be impregnated with the aliphatic acid containing water by first slushing in water and then soaking with the aliphatic acid in anhydrous form until sufficient water is displaced from the pulp to reduce the weight of water in the total weight of acid and water in the pulp to 15% or less. The temperature of the bath before immersion of the pulp may be 13 DEG -16 DEG C., and during the acylation may be held at 17 DEG -25 DEG C. After acylation, sodium acetate may be added to the bath to neutralize acid catalyst before separating the acylated pulp therefrom. The acylated pulp may be separated from the acylation bath and then either washed with water, or sprayed with acetic acid and washed with water containing a weak alkali. The acylated pulp, containing if desired up to 25% of its dry weight of unacylated wood pulp, may be used in the manufacture of paper (see Group VIII), especially for use as a photographic support. Specifications 724,827, 858,060, U.S.A. Specifications 2,992,156 and 3,057,755 are referred to.
GB1091/60A 1959-01-12 1960-01-12 Acylation of pulp and manufacture of paper therefrom useful in photography Expired GB937494A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US78604159A 1959-01-12 1959-01-12
US78604259A 1959-01-12 1959-01-12
US78604559A 1959-01-12 1959-01-12
US81702559A 1959-06-01 1959-06-01

Publications (1)

Publication Number Publication Date
GB937494A true GB937494A (en) 1963-09-25

Family

ID=27505765

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1091/60A Expired GB937494A (en) 1959-01-12 1960-01-12 Acylation of pulp and manufacture of paper therefrom useful in photography

Country Status (3)

Country Link
BE (1) BE586431A (en)
FR (1) FR1244859A (en)
GB (1) GB937494A (en)

Also Published As

Publication number Publication date
BE586431A (en)
FR1244859A (en) 1960-10-28

Similar Documents

Publication Publication Date Title
KR870005588A (en) Manufacturing method of dried rice
KR900015642A (en) Improved Alkaline Peroxide Treatment of Non-Wood Lignocellulosic Substrates
GB937494A (en) Acylation of pulp and manufacture of paper therefrom useful in photography
US2539451A (en) Method of preparing sulfuric acid esters of cellulose
US2622080A (en) Method for the manufacture of high butyryl cellulose esters
GB863792A (en) Acyl derivatives of esters of citric acid
GB581046A (en) Improvements in bleaching organic acid esters of cellulose
Dieckert et al. A simplified technique for the preparation of glass paper impregnated with silicic acid
GB885677A (en) Improved poultry feed
US2152071A (en) Preparation of stable cellulose esters
ES456679A1 (en) Process for the preparation of alkali cellulose
SU405991A1 (en)
US2903369A (en) Edible oils
SU116158A1 (en) The method of obtaining cellulose acetate and acetobutyratecellulose
GB785890A (en) Improvements in manufacture of alkali cellulose by cellulose slurry-steeping
GB340555A (en) Improvements relating to the manufacture of cellulose esters or ethers
Hilditch et al. CCV.—A quantitative study of the oxidation of methyl oleate and elaidate by hydrogen peroxide in presence of acetic acid
US2043946A (en) Method of dehydrating cellulose derivatives and products therefrom
SU108299A1 (en) Method for racemization of L- (+) -p-nitro-a-acetylamino-p-oxypropiophenone
GB1108282A (en) Alkali metal salts of carboxymethyl cellulose
GB707120A (en) Production of organic acid esters of cellulose
GB325254A (en) Improvements in and relating to the treatment of nitrocellulose
GB676232A (en) Improvements in and relating to the production of cellulose esters
GB792007A (en) Process for reducing the ash content of cellulose
Iwakura et al. THE FIBROUS ACETYLATION OF VISCOSE RAYON WITH KETENE (1) THE EFFECT OF CATALYSTS IN ACETYLATION