GB584217A - Improvements in or relating to the manufacture of non-fibrous films of water-sensitive, organic film-forming material - Google Patents
Improvements in or relating to the manufacture of non-fibrous films of water-sensitive, organic film-forming materialInfo
- Publication number
- GB584217A GB584217A GB25203/44A GB2520344A GB584217A GB 584217 A GB584217 A GB 584217A GB 25203/44 A GB25203/44 A GB 25203/44A GB 2520344 A GB2520344 A GB 2520344A GB 584217 A GB584217 A GB 584217A
- Authority
- GB
- United Kingdom
- Prior art keywords
- film
- resins
- per cent
- urea
- formaldehyde
- 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
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- 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
- C08J7/052—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
- 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
- C08J7/048—Forming gas barrier 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
- C08J2301/02—Cellulose; Modified cellulose
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Water-sensitive organic films, e.g. films of regenerated cellulose, cellulose ethers and polyvinyl alcohol, are impregnated with 30 to 60 per cent of a softener, and an insoluble artificial resin of one of the classes specified below which is capable of being formed in situ by heating to 60-90 DEG C. The classes of resins which may be used are phenol-formaldehyde resins, dimethylol urea resins, dimethylol urea ether resins, melamine-formaldehyde resins, aminotriazine-aldehyde resins, aldehyde condensation products (such as casein-formaldehyde, guanidine-formaldehyde, aliphatic and aryl ketones with formaldehyde, urethane-aldehyde and cyanamide-aldehyde), furfuramide resins and furfural reaction products with amines, phenols and ketones, thiocyanate resins, thio-urea resins, acrolein-urea resins and urea-aldehyde modified phthalic acid glycerine resins. The amount of artificial resin in the finished film is preferably from 1-10 per cent. Suitable softeners for use in the process are glycerine, glycols, amines or amino-alcohols and salts thereof, hydroxy-amides, ether-alcohols, sulphones, sulphoxides and urea. The film may be impregnated by passing it through an aqueous bath containing the softener and the incompletely condensed or polymerized water-soluble product and thereafter drying the film at 60 DEG to 90 DEG C.; or by first passing it through the aqueous bath containing the softener and then spraying it with a solution of the incompletely condensed or polymerized product and finally drying at 60 DEG to 90 DEG C.; or by incorporating the incompletely condensed or polymerized product into the solution from which the film is cast and thereafter passing the film through an aqueous bath containing the softener and finally drying by heating as before. Condensing agents such as maleic acid and paratoluene sulphonic acid may be used in conjunction with the incompletely condensed products. The products of the invention may be moisture-proofed by coating in known manner. Examples are given of the preparation of films comprising (1) 43.3 per cent glycerine and 5.3 per cent dimethylol urea resin; (2) 45 per cent glycerine and 2 per cent of phenol-formaldehyde resin; (3) 45 per cent glycerine and 7 per cent monomethyl ether of dimethylol urea; (4) 43.7 per cent glycerine and 5 per cent melamine-formaldehyde resin; (5) as in (1), but the film is coated with a composition containing urea-formaldehyde resin and nitrocellulose; (6) as in (1), but the film is coated with a composition containing nitrocellulose, paraffin wax, dammar and ethylene glycol "Heet-Rex" (3-isopropyl-6-methyl-3,6-endoethylene-delta-4-tetrahydrophthalic anhydride); (7) as in (1), but the film is then coated firstly with the composition of (5) and secondly with the composition of (6); (8) as in (1), but the film is coated with a composition containing nitrocellulose, urea-formaldehyde monomeric alcohol resin, "Beckacite" (R.T.M.) (ester gum-rosin and maleic acid glyceride complex) and paraffin wax; (9) as in (4), but the film is coated with the composition of (6); (10) urea-formaldehyde resin and glycerine, and the film is then coated as in (6). Specification 211,446, [Class 2 (ii)], is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US584217XA | 1943-12-18 | 1943-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB584217A true GB584217A (en) | 1947-01-09 |
Family
ID=22016712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB25203/44A Expired GB584217A (en) | 1943-12-18 | 1944-12-15 | Improvements in or relating to the manufacture of non-fibrous films of water-sensitive, organic film-forming material |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB584217A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2597624A (en) * | 1949-04-05 | 1952-05-20 | Textile & Chem Res Co Ltd | Process for treating cellulosic materials |
US3472804A (en) * | 1966-01-29 | 1969-10-14 | Ledoga Spa | Insoluble films based on polyvinyl alcohol and process for the preparation thereof |
-
1944
- 1944-12-15 GB GB25203/44A patent/GB584217A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2597624A (en) * | 1949-04-05 | 1952-05-20 | Textile & Chem Res Co Ltd | Process for treating cellulosic materials |
US3472804A (en) * | 1966-01-29 | 1969-10-14 | Ledoga Spa | Insoluble films based on polyvinyl alcohol and process for the preparation thereof |
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