GB399191A - Improvements in cellulose derivative products - Google Patents
Improvements in cellulose derivative productsInfo
- Publication number
- GB399191A GB399191A GB5065/32A GB506532A GB399191A GB 399191 A GB399191 A GB 399191A GB 5065/32 A GB5065/32 A GB 5065/32A GB 506532 A GB506532 A GB 506532A GB 399191 A GB399191 A GB 399191A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- mixture
- parts
- higher fatty
- acetone
- 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
Links
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Liquid and solid compositions, filaments, threads, films, and the like of improved waterproof properties, comprise cellulose ethers, ether-esters, or esters, in which the organic ester groups are derived from lower fatty acids, and relatively small proportions of cellulose derivatives containing radicles of higher fatty acids as sole substituent groups. The proportion of cellulose derivative containing radicles of higher fatty acids as sole substituent groups is preferably between 5 and 15 per cent by weight of the total cellulose derivatives. In a modification, films or sheets having a basis of regenerated cellulose, cellulose ethers, etheresters, or esters, in which the organic ester groups are derived from lower fatty acids, are coated with compositions comprising cellulose derivatives containing radicles of higher fatty acids as sole substituent groups. Suitable higher fatty acid esters are cellulose oleate, laurate, stearate, and palmitate. In the production of films from mixtures of cellulose derivatives and cellulose higher fatty acid esters, a common solvent or mixture of solvents should be employed, for example, a mixture of acetone and benzene is used to dissolve a mixture of cellulose acetate and cellulose laurate, stearate, or palmitate. High boiling solvents, plasticizers, resins, fire retardants, fillers, colouring matters, and the like may also be added. The following examples are given: (1) A mixture of cellulose acetate (85-90 parts), cellulose stearate (10-15 parts), tricresyl phosphate, and diethyl phthalate, is dissolved in a mixture of acetone and benzene, and the solution cast on to a film wheel, band, or the like. (2) A mixture of cellulose acetate (90-95 parts), cellulose palmitate (5-10 parts), diacetone alcohol, and diethyl phthalate, is dissolved in acetone-benzene mixture and cast on a suitable surface. (3) 90 parts of cellulose acetate-propionate dissolved in acetone are mixed with 10 parts of cellulose stearate-laurate dissolved in benzene, incorporated with triphenyl phosphate and diethyl phthalate, and the solution employed in the production of films. (4) A cellulose acetate foil is passed through a 5-10 per cent solution of cellulose stearate in acetone-benzene mixture, which solution may also contain dibutyl phthalate. The Provisional Specification refers generally to processes for the production of filaments or films (1) from a mixture of a cellulose ester of a lower fatty acid and a cellulose ester of a higher fatty acid, (2) from a mixed cellulose ester containing both lower and higher fatty acid radicals, and (3) by coating a film of a cellulose ester of a lower fatty acid with a cellulose ester of a higher fatty acid. Specification 319,073, [Class 2 (ii), Cellulose &c.], is referred to.ALSO:Liquid and solid compositions of improved waterproof properties, comprise cellulose ethers, ether-esters, or esters, in which the organic ester groups are derived from lower fatty acids, and relatively small proportions of cellulose derivatives containing radicles of higher fatty acids as sole substituent groups. The proportion of cellulose derivative containing radicles of higher fatty acids as sole substituent groups is preferably between 5 and 15 per cent by weight of the total cellulose derivatives. Suitable higher fatty acid esters are cellulose oleate, laurate, stearate, and palmitate. In the production of films from mixtures of cellulose derivatives and cellulose higher fatty acid esters, a common solvent or mixture of solvents should be employed, for example, a mixture of acetone and benzene is used to dissolve a mixture of cellulose acetate and cellulose laurate, stearate, or palmitate. High-boiling solvents, plasticizers, resins, fire retardants, fillers, colouring matters, and the like may also be added. The following examples are given:-(1) A mixture of cellulose acetate (85-90 parts), cellulose stearate (10-15 parts), tricresyl phosphate, and diethyl phthalate, is dissolved in a mixture of acetone and benzene, and the solution cast on to a film wheel, band, or the like. (2) A mixture of cellulose acetate (90-95 parts), cellulose palmitate (5-10 parts), diacetone alcohol, and diethyl phthalate, is dissolved in acetone-benzene mixture and cast on a suitable surface (3) 90 parts of cellulose acetate-propionate dissolved in acetone are mixed with 10 parts of cellulose stearate-laurate dissolved in benzene, incorporated with triphenyl phosphate and diethyl phthalate, and the solution employed in the production of films. Specification 319,073, [Class 70, Indiarubber &c.], is referred to.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5065/32A GB399191A (en) | 1932-02-19 | 1932-02-19 | Improvements in cellulose derivative products |
US655777A US2073687A (en) | 1932-02-19 | 1933-02-08 | Cellulose derivative products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5065/32A GB399191A (en) | 1932-02-19 | 1932-02-19 | Improvements in cellulose derivative products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB399191A true GB399191A (en) | 1933-09-19 |
Family
ID=9789084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5065/32A Expired GB399191A (en) | 1932-02-19 | 1932-02-19 | Improvements in cellulose derivative products |
Country Status (2)
Country | Link |
---|---|
US (1) | US2073687A (en) |
GB (1) | GB399191A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443918A (en) * | 1944-06-19 | 1948-06-22 | Rhone Poulenc Sa | Light-diffusing cellulose acetate compositions |
KR101009968B1 (en) * | 2006-01-06 | 2011-01-20 | 애버리 데니슨 코포레이션 | High gloss laminates for decorative automotive parts |
-
1932
- 1932-02-19 GB GB5065/32A patent/GB399191A/en not_active Expired
-
1933
- 1933-02-08 US US655777A patent/US2073687A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US2073687A (en) | 1937-03-16 |
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