GB741521A - Nitrocellulose lacquers - Google Patents

Nitrocellulose lacquers

Info

Publication number
GB741521A
GB741521A GB26154/53A GB2615453A GB741521A GB 741521 A GB741521 A GB 741521A GB 26154/53 A GB26154/53 A GB 26154/53A GB 2615453 A GB2615453 A GB 2615453A GB 741521 A GB741521 A GB 741521A
Authority
GB
United Kingdom
Prior art keywords
mixture
per cent
silico
oil acids
weight
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
GB26154/53A
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.)
Midland Silicones Ltd
Original Assignee
Midland Silicones 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 Midland Silicones Ltd filed Critical Midland Silicones Ltd
Publication of GB741521A publication Critical patent/GB741521A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D101/00Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
    • C09D101/08Cellulose derivatives
    • C09D101/16Esters of inorganic acids
    • C09D101/18Cellulose nitrate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Silicon Polymers (AREA)

Abstract

A lacquer composition consists essentially of (1) 25-90 per cent by weight of cellulose nitrate, and (2) 10-75 per cent of a silicoalkyd resin which is a reaction product of (a) 25-90 per cent by weight of one or more organo-silicon compounds of an average general formula RnSiX4-n or a partial condensate thereof, R being a monovalent hydrocarbon radical, n having a value of 1 to 2 inclusive, and X being a hydrolysable radical or hydroxyl radical, (b) 2.5-49 per cent by weight of glycerol, (c) 5.2-62 per cent of a dicarboxylic acid or anhydride, alkyl ester or acid chloride derivative thereof, and optionally (d) up to 60 per cent of a fatty acid containing 8-20 carbon atoms in the molecule; there being in the final product from 2 to 30 per cent by weight, calculated on the total weight of (1) and (2), of the reaction residue of the organosilicon component (a), the weight of this residue being calculated on the basis of the formula RnSiO (4-n)/2 . The lacquer compositions have high stability on exposure to atmospheric conditions, this being shown by high gloss retention and freedom from crazing and cracking. The lacquers may be applied as coatings to metal surfaces such as motor bodies. Silanes in which R is cyclohexyl, methyl, allyl, stearyl, phenyl or xylyl, and in which X is an alkoxy, acyloxy, halogen (e.g. chlorine or bromine), amino or hydroxyl group, may be used for preparing the silico-alkyd resin. A partially condensed alkoxy silane may also be used for making the silico-alkyd resin. An alkoxy silane may be hydrolysed with less than the theoretical amount of water required for complete hydrolysis. The dicarboxylic acid may be phthalic, terephthalic, isophthalic, malonic or maleic acid. The fatty acid containing 8-20 carbon atoms may be stearic acid or 2-ethyl hexoic acid or it may be a mixture of tung oil acids, castor oil acids, linseed oil acids or oiticica oil acids. The reactants for forming the silico-alkyd resins may be brought together in any desired order. Solvent mixtures of toluene, xylene, alcohols and ketones may be used to produce lacquer solutions of the cellulose nitrate and the resin. Driers such as cobalt naphthenate and pigments may be incorporated in the lacquers. In an example, a mixture of phenyl methyl dimethoxy silane and phenyl trimethoxy silane is partially hydrolysed and condensed. The condensate is heated and stirred with a liquid linseed oil acid mixture at 200 DEG C. Methanol is distilled off and the mixture is then cooled to 150 DEG C. Glycerol is added and the mixture is again heated to 200 DEG C. and methanol is distilled off. The mixture is cooled to 150 DEG C., phthalic anhydride is added and the mixture is heated to 200 DEG C. to remove volatile constituents, xylene being added during the distillation so as to remove residual water as an azeotrope. The mixture is then diluted with a mixture of xylene and a high boiling aromatic petroleum solvent. In other examples, silico-alkyd resins are produced in a similar manner except that coconut oil acids or dehydrated castor oil acids are used instead of linseed oil acids. Other examples describe the production of lacquers containing cellulose nitrate, a silico-alkyd resin and a solvent mixture. The silico-alkyd resin may be prepared by condensing 7.2 gm. mols. of phenyl methyl diethoxy silane and 0.8 gm. mols. of phenyl triethoxy silane with 8.35 gm. mols. of glycerol and 4.57 gm. mols. of phthalic anhydride. Specifications 583,754, 650,247 and 722,484 are referred to.
GB26154/53A 1952-11-17 1953-09-22 Nitrocellulose lacquers Expired GB741521A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US741521XA 1952-11-17 1952-11-17

Publications (1)

Publication Number Publication Date
GB741521A true GB741521A (en) 1955-12-07

Family

ID=22118023

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26154/53A Expired GB741521A (en) 1952-11-17 1953-09-22 Nitrocellulose lacquers

Country Status (1)

Country Link
GB (1) GB741521A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106883687A (en) * 2017-03-23 2017-06-23 陕西省文物保护研究院 The benefit gold repair materials and method repaired for ancient times painted clay sculpture layer gold

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106883687A (en) * 2017-03-23 2017-06-23 陕西省文物保护研究院 The benefit gold repair materials and method repaired for ancient times painted clay sculpture layer gold

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