GB497335A - Improvements in or relating to the preparation of coated materials - Google Patents

Improvements in or relating to the preparation of coated materials

Info

Publication number
GB497335A
GB497335A GB1665337A GB1665337A GB497335A GB 497335 A GB497335 A GB 497335A GB 1665337 A GB1665337 A GB 1665337A GB 1665337 A GB1665337 A GB 1665337A GB 497335 A GB497335 A GB 497335A
Authority
GB
United Kingdom
Prior art keywords
cellulose
phenol
formaldehyde
prepared
coating
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
GB1665337A
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.)
British Cellophane Ltd
Original Assignee
British Cellophane 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 British Cellophane Ltd filed Critical British Cellophane Ltd
Publication of GB497335A publication Critical patent/GB497335A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/042Coating with two or more layers, where at least one layer of a composition contains a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/043Improving the adhesiveness of the coatings per se, e.g. forming primers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/048Forming gas barrier coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2301/00Characterised by the use of cellulose, modified cellulose or cellulose derivatives
    • C08J2301/06Cellulose hydrate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2477/00Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31801Of wax or waxy material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31844Of natural gum, rosin, natural oil or lac
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31942Of aldehyde or ketone condensation product
    • Y10T428/31949Next to cellulosic
    • Y10T428/31953Modified or regenerated cellulose

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)

Abstract

Resins prepared by condensing a non-aromatic amine, a phenol and an aldehyde, in any order, are used as an anchoring layer between a water-sensitive cellulosic base material and a coating material. The resins must be substantially insoluble in water and 5 per cent aqueous ammonia but must be soluble in 2 per cent acetic acid. The resins may be used in the form of aqueous solutions of their salts with acids such as acetic, formic citric, glycollic, malic, maleic, succinic, adipic, phthalic, tartaric, benzoic or hydrochloric acids. Glycerine may be added as a plasticizer. On drying the coating it becomes hard and insoluble. The cellulosic base materials include sheets of regenerated cellulose (which may be derived from viscose or cuprammonium cellulose), cellulose ethers (ethylcellulose, methylcellulose, glycolcellulose or cellulose glycollic acid) or cellulose esters (cellulose phthalate) tubes, sausage casings, bottle caps, bands or moulded articles or various cellulosic materials, rayon fabrics, paper or cotton cloth. The coating material to be anchored may be discontinuous such as printing on regenerated cellulose sheets, tubes, caps and sausage casings. The surface coating may be any coating composition containing a cellulose derivative base such as cellulose nitrate, cellulose acetate, ethyl cellulose, or benzyl cellulose or, preferably, a moisture proofing coating comprising a cellulose derivative, a wax or wax-like material, a blending agent and a plasticizer. In an example, regenerated cellulose sheet in the gel state prepared from viscose is coated with a composition prepared by dissolving a resin prepared from phenol or m-cresol, formaldehyde, dimethylamine and ammonia in a mixture of aqueous acetic acid and glycerine with or without the addition of de-acetylated chitin, the sheet is then dried and coated with a moisture-proofing composition comprising pyroxylin, gum dammar, dibutyl phthalate, paraffin wax, zinc stearate, ethyl stearate, toluene, alcohol and acetone. Specifications 282,435, [Class 2 (iii)], 283,109, [Class 95], 317,452, [Class 2 (ii)], and 458,814, are referred to.ALSO:Resins prepared by condensing a non-aromatic amine, a phenol and an aldehyde, in any order, are used as an anchoring layer between a water - sensitive cellulosic base material and a coating material. The resins must be substantially insoluble in water and 5 per cent aqueous ammonia but must be soluble in 2 per cent acetic acid. The resins may be used in the form of aqueous solutions of their salts with acids such as acetic, formic, citric, glycollic, malic, maleic, succinic, adipic, phthalic, tartaric, benzoic or hydrochloric acids. Glycerine may be added as a plasticizer. On drying the coating it becomes hard and insoluble. Preferably the phenolic body has at least two free reactive positions and only organic groups as ring constituents and the amine contains not more than six carbon atoms and at least one amino-nitrogen atom joined to a carbon atom which is not part of an aromatic ring and also to at least one hydrogen atom. The cellulosic base materials include sheets of regenerated cellulose (which may be derived from viscose or cuprammonium cellulose), cellulose ethers (ethylcellulose, methylcellulose, glycolcellulose or cellulose glycollic acid) or cellulose esters (cellulose phthalate) tubes, sausage casings, bottle caps, bands or moulded articles of various cellulosic materials, rayon fabrics, paper or cotton cloth. The coating material to be anchored may be discontinuous such as printing on regenerated cellulose sheets, tubes, caps and sausage casings. The surface coating may be any coating-composition containing a cellulose derivative base such as cellulose nitrate, cellulose acetate, ethyl cellulose, or benzyl cellulose or, preferably, a moistureproofing coating comprising a cellulose derivative, a wax or wax-like material, a blending agent and a plasticizer. In examples suitable resins are prepared from (a) phenol formaldehyde, dimethylamine and ammonia, (b) phenol, lignin, formaldehyde and dimethylamine, (c) phenol, formaldehyde and dimethylamine, (d) phenol, formaldehyde and dimethylaminoethanol, and (e) phenol, formaldehyde and cyclohexylamine. Other resins include those prepared from phenol, formaldehyde, and (2) lignin and methylamine, (3) cyclohexanolamine, (4) p-toluene sulphonamide and methylamine, (6) dimethylamine, and (9) ammonia and diethanolamine, from (1) xylenol, formaldehyde and methylamine, from (7) m-cresol, formaldehyde and dimethylamine, and from (8) xylenol, or (5) diphenylolcyclohexanone, formaldehyde and dimethylaminomethanol. In examples: (1) regenerated cellulose sheet in the gel state prepared from viscose is coated with a composition prepared by dissolving the resin from example (a) or a corresponding resin prepared from m-cresol instead of phenol in a mixture of aqueous acetic acid and glycerine, with or without the addition of de-acetylated chitin, the sheet is then dried and coated with a moistureproofing composition comprising pyroxylin, gum dammar, dibutyl phthalate, paraffin wax, zinc stearate, ethyl stearate, toluene, alcohol and acetone. Specifications 282,435, [Class 2 (iii)], 283,109, [Class 95], 317,452, [Class 2 (ii)], and 458,814 are referred to. A phenol-lignin condensate is prepared by heating phenol and spruce wood flour in the presence of hydrochloric acid.
GB1665337A 1936-06-17 1937-06-15 Improvements in or relating to the preparation of coated materials Expired GB497335A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US8576936 US2122433A (en) 1936-06-17 1936-06-17 Coated films and method of making the same

Publications (1)

Publication Number Publication Date
GB497335A true GB497335A (en) 1938-12-15

Family

ID=22193815

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1665337A Expired GB497335A (en) 1936-06-17 1937-06-15 Improvements in or relating to the preparation of coated materials

Country Status (2)

Country Link
US (1) US2122433A (en)
GB (1) GB497335A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2650172A (en) * 1949-01-21 1953-08-25 American Viscose Corp Moistureproofing of nonfibrous cellulosic material

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2432542A (en) * 1944-07-13 1947-12-16 Du Pont Method of producing coated cellulosic sheets
US2462185A (en) * 1946-02-19 1949-02-22 Du Pont Moistureproof, heat-sealable wrapping material and process
US2556885A (en) * 1946-06-27 1951-06-12 Du Pont Coated products
US3012912A (en) * 1958-07-16 1961-12-12 American Cyanamid Co Non-fibrous regenerated cellulose film containing bis-amide polymer as anchor agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2650172A (en) * 1949-01-21 1953-08-25 American Viscose Corp Moistureproofing of nonfibrous cellulosic material

Also Published As

Publication number Publication date
US2122433A (en) 1938-07-05

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