GB782455A - Manufacture of moisture-resistant coated films of regenerated cellulose - Google Patents
Manufacture of moisture-resistant coated films of regenerated celluloseInfo
- Publication number
- GB782455A GB782455A GB9335/55A GB933555A GB782455A GB 782455 A GB782455 A GB 782455A GB 9335/55 A GB9335/55 A GB 9335/55A GB 933555 A GB933555 A GB 933555A GB 782455 A GB782455 A GB 782455A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- phosphorus
- imine
- amine
- reaction product
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/052—Forming heat-sealable coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/06—Cellulose hydrate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Abstract
A regenerated cellulose film is impregnated with a water-soluble reaction product of phosphorus oxychloride, or phosphorus thiotrichloride, with an alkylene imine, or with a mixture of an alkylene imine and a subordinate amount of a secondary aliphatic amine, and subsequently coated with a moisture-resistant, preferably heat-sealing coating. For impregnation, the reaction product may be added to an aqueous bath, preferably the softening bath used in the treatment of the film during manufacture, or the dried film may be treated with a solution of the reaction product in, e.g. ethyl or methyl alcohol. The reaction products may be monomers or low-degree polymers. The monomer is prepared by reacting the phosphorus compound with, e.g. ethylene imine, with or without dimethyl- or diethyl-amine, in the ratio 1 mol. amine to 2 mol. imine per atom of phosphorus present, in the presence of an acid-binding agent, e.g. ammonia, or trimethyl- or triethyl-amine, in, e.g. chloroform, benzene, toluene or chlorobenzene as solvent. Polymerization is effected by heating at up to 100 DEG C., or by catalysts, e.g. sulphuric, sulphurous, or carbonic acid, dimethyl-, diethyl-, dipropyl-, or dibutyl-sulphate, the methyl or ethyl ester of p-toluene sulphonic acid, or water, and solvents, e.g. benzene, toluene or xylene, may or may not be present. The polymer is precipitated by dilution with, e.g. benzene, toluene or acetone. Mixtures of reaction products may be used. An acid or acid-reacting salt may be added to the impregnation bath or the film may be treated before or after impregnation with an acid or acid-reacting salt, e.g. boric, lactic, glycollic, citric, gallic, succinic or maleic acid or monosodium or monopotassium phosphates. In examples: (1) film is passed through an aqueous softening bath containing glycerol and a polymerized product of phosphorus oxychloride and ethylene imine, dried, and coated with a composition containing nitrocellulose, dibutyl- and dicyclohexyl-phthalates, modified phthalate resin, urethane-formaldehyde resin, and paraffin wax dissolved in 1/1 ethyl acetate-benzene; (4) dried film before coating with the composition of (1) is passed through an ethyl alcohol solution of equal parts of the polymerized reaction product of phosphorus oxychloride and ethylene imine and the monomer reaction product of phosphorus thiotrichloride and ethylene imine; (5) film before coating as in (1) is passed through an aqueous softening bath containing ethylene glycol, the reaction product of (1) and gallic acid.ALSO:The monomer reaction products of phosphorus oxychloride or phosphorus thiotrichloride with an alkylene imine or with a mixture of an alkylene imine with a subordinate amount of a secondary aliphatic amine may be used to impregnate regenerated cellulose film before coating with a moisture-proofing coating. The monomer is prepared by reacting the phosphorus compound with e.g. ethylene imine with or without dimethyl- or diethyl-amine, in the ratio 1 mol. amine to 2 mols. imine per atom of phosphorus present, in the presence of an acid-binding agent, e.g. ammonia, or trimethyl-, or triethyl-amine, in e.g. chloroform, benzene, toluene, or chlorobenzene as solvent.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEK21679A DE1045866B (en) | 1954-03-31 | 1954-03-31 | Process for painting films made from regenerated cellulose |
Publications (1)
Publication Number | Publication Date |
---|---|
GB782455A true GB782455A (en) | 1957-09-04 |
Family
ID=7216252
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9335/55A Expired GB782455A (en) | 1954-03-31 | 1955-03-30 | Manufacture of moisture-resistant coated films of regenerated cellulose |
Country Status (4)
Country | Link |
---|---|
US (1) | US2784116A (en) |
DE (1) | DE1045866B (en) |
FR (1) | FR1121423A (en) |
GB (1) | GB782455A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3513055A (en) * | 1964-11-12 | 1970-05-19 | Fmc Corp | Method of preparing heat-sealable composite sheets |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE575304A (en) * | 1958-02-10 | 1900-01-01 | ||
NL257294A (en) * | 1959-11-03 | |||
US3884972A (en) * | 1970-06-24 | 1975-05-20 | Us Agriculture | Tris (2-chloroethyl)phosphoramide{13 {0 a crosslinking agent for cellulosic compositions |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1857163A (en) * | 1929-05-14 | 1932-05-10 | Celanese Corp | Method of treating fabrics and product thereof |
DE753191C (en) * | 1943-05-25 | 1953-05-11 | Kalle & Co Ag | Process for increasing the adhesive strength of hydrophobic layers on cellulose hydrate films |
US2606900A (en) * | 1951-07-25 | 1952-08-12 | American Cyanamid Co | Phosphoric acid derivatives and methods of preparing the same |
US2698793A (en) * | 1952-04-11 | 1955-01-04 | American Cyanamid Co | Sized paper comprising a polymerized alkylenimine |
US2654738A (en) * | 1952-08-02 | 1953-10-06 | American Cyanamid Co | Organic derivatives of phosphonic acids and method of preparing the same |
-
1954
- 1954-03-31 DE DEK21679A patent/DE1045866B/en active Pending
-
1955
- 1955-03-29 FR FR1121423D patent/FR1121423A/en not_active Expired
- 1955-03-30 US US498108A patent/US2784116A/en not_active Expired - Lifetime
- 1955-03-30 GB GB9335/55A patent/GB782455A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3513055A (en) * | 1964-11-12 | 1970-05-19 | Fmc Corp | Method of preparing heat-sealable composite sheets |
Also Published As
Publication number | Publication date |
---|---|
DE1045866B (en) | 1958-12-04 |
US2784116A (en) | 1957-03-05 |
FR1121423A (en) | 1956-08-14 |
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