GB1108063A - Coating articles - Google Patents

Coating articles

Info

Publication number
GB1108063A
GB1108063A GB3098365A GB3098365A GB1108063A GB 1108063 A GB1108063 A GB 1108063A GB 3098365 A GB3098365 A GB 3098365A GB 3098365 A GB3098365 A GB 3098365A GB 1108063 A GB1108063 A GB 1108063A
Authority
GB
United Kingdom
Prior art keywords
tri
polymer
xylene
coated
acid
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
GB3098365A
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.)
Celanese Corp
Original Assignee
Celanese Corp
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 Celanese Corp filed Critical Celanese Corp
Publication of GB1108063A publication Critical patent/GB1108063A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/10Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by other chemical means
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • B01J2/30Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic using agents to prevent the granules sticking together; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/18Processes for applying liquids or other fluent materials performed by dipping
    • B05D1/22Processes for applying liquids or other fluent materials performed by dipping using fluidised-bed technique
    • B05D1/24Applying particulate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

A surface is coated with a layer of a substance which on thermal decomposition yields on acid product and leaves a solid residue, thermal decomposition of the layer then being effected, and thereafter an oxymethylene polymer coating is formed on the treated surface by fusion of particles of the polymer in contact with the surface. Suitable materials for forming the thermally decomposable layer are nitrocellulose, cellulose acetate, polyvinyl acetate and polyvinyl chloride, and may be applied in a suitable vehicle say by spraying, painting, or dipping, along with pigments, e.g. titanium dioxide, carbon, iron oxide and mixtures thereof, and metal powders; a catalyst which reduces the temperature at which the decomposition takes place e.g. tris-beta-chloroethyl phosphate; substances which facilitate the decomposition of the said catalyst e.g. a mineral acid such as nitric acid, an organic acid e.g. acetic acid or mixtures thereof; fire retardants such as organo-borates of formula: (RO)3B wherein R is an alkyl group having up to 10 carbon atoms e.g. tri-n-butyl, tri-ethyl and tri-propyl borate. The oxymethylene polymers may be homopolymers end capped by esterification or etherification, or preferably copolymers consisting predominantly of chains of oxymethylene groups containing dispersed along their groups having adjacent carbon atoms forming links in the polymer chains e.g. oxyethylene groups. Such copolymers e.g. those obtained by copolymerising trioxane and ethylene oxide or dioxolane are preferably subjected to treatment before use to eliminate terminal oxymethylene groups such that all or most of the terminal groups of the polymer molecules have adjacent carbon atoms. The polymers may be blended with chemical stabilizers such as an anti-oxidant and an agent to repress chain scission e.g. a bisphenol and a trivalent nitrogen containing compound such as cyanoguanidine, benzoguanidine, melamine, N, N', N"-tri-n-propyl-melamine. Articles coated may be of metal e.g. aluminium, aluminium alloys such as aluminium alloyed with 5 to 12% silicon, nickel, magnesium, tin chromium or titanium, iron and low and high carbon steels and other iron alloys e.g. those containing chromium, molybdenum, silica, manganese or titanium, brass, bronze, copper, zinc or magnesium; or of glass, ceramic and plastics e.g. thermosetting resins of the phenolic, urea and melamine type. The article may be heated while the polymer particles are brought into contact with it, by say interior circulation of a heating fluid or induction heating or the article may be preheated to a temperature above the melting point of the polymer. To improve the glass and reduce porosity, the coated article may be reheated. The coated article may then be coated again with polymer particles to build up the thickness of the coating and the coated articles then cooled or quenched in water. The polymer particles may be applied by spraying or in a fluidised bed process. In the Examples liquid compositions for applying the thermally decomposible substance to the surface comprise a blend of 1 to 4 parts of a composition comprising Ethanol, isopropanol, ethyl acetate, methyl ethyl ketone, n-propanol, n-butanol, methyl isobutyl ketone, toluene, xylene, titanium dioxide, carbon, nitrocellulose, and trisbeta-chloroethyl phosphate, with 1 part of: (a) a composition comprising ethanol, isopropanol, methyl ethyl ketone, n-propanol, n-butanol, methyl isobutyl ketone, toluene, m-xylene, 2-methyl-pentanol-4, tri-n-butyl borate, nitric acid, acetic acid; or (b) a composition comprising isopropanol, ethyl acetate, isopropyl acetate, benzene, n-propanol, n-butanol, methyl isobutyl ketone, toluene, n-butylacetate, p-xylene, m-xylene, xylene, tri-n-butyl borate, nitric acid, acetic acid. The articles treated in the Examples comprise a cold rolled steel strap, steel sheet, and an aluminium rectangle.
GB3098365A 1964-07-30 1965-07-21 Coating articles Expired GB1108063A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US38639864A 1964-07-30 1964-07-30

Publications (1)

Publication Number Publication Date
GB1108063A true GB1108063A (en) 1968-04-03

Family

ID=23525412

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3098365A Expired GB1108063A (en) 1964-07-30 1965-07-21 Coating articles

Country Status (4)

Country Link
BE (1) BE667683A (en)
DE (1) DE1546871A1 (en)
GB (1) GB1108063A (en)
NL (1) NL6509862A (en)

Also Published As

Publication number Publication date
DE1546871A1 (en) 1970-10-08
NL6509862A (en) 1966-01-31
BE667683A (en) 1966-01-31

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