GB1049100A - Plasticized acrylic ester resins - Google Patents

Plasticized acrylic ester resins

Info

Publication number
GB1049100A
GB1049100A GB3275563A GB3275563A GB1049100A GB 1049100 A GB1049100 A GB 1049100A GB 3275563 A GB3275563 A GB 3275563A GB 3275563 A GB3275563 A GB 3275563A GB 1049100 A GB1049100 A GB 1049100A
Authority
GB
United Kingdom
Prior art keywords
esters
acid
acrylic
plasticized
ester
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
GB3275563A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB1049100A publication Critical patent/GB1049100A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/38Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D303/40Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
    • C07D303/42Acyclic compounds having a chain of seven or more carbon atoms, e.g. epoxidised fats
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/10Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/15Heterocyclic compounds having oxygen in the ring
    • C08K5/151Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
    • C08K5/1515Three-membered rings
    • 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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08Homopolymers or copolymers of acrylic acid esters

Abstract

Epoxy fatty acid esters are prepared by treating with a 40% solution of peracetic acid in acetic acid the esters obtained by:- (a) Heating benzyl alcohol with the methyl ester of safflower oil or soybean oil fatty acids in xylene containing sodium methoxide and removing the methanol evolved by distillation; (b) Adding the chloride of tall oil, soybean oil or linseed oil fatty acids to phenol in chloroform and pyridine; (c) Heating oleic acid, linseed oil fatty acids or tall oil fatty acids with benzyl chloride and potassium carbonate in xylene; (d) Heating tetrahydrofurfuryl alcohol with tall oil, soybean oil or linseed oil fatty acids in xylene in the presence of zinc dust and removing the water of reaction by distillation; (e) Heating under similar conditions as in (d) above cyclohexanol with tall oil, safflower oil or linseed oil fatty acids; (f) Heating tall oil fatty acids with the monobutyl ether of ethylene glycol or diethylene glycol in xylene in the presence of zinc oxide and removing the water of reaction by distillation.ALSO:Resins comprising or consisting of units of at least one ester of acrylic or methacrylic acid and having a solubility parameter d (as defined in the Specification) from 8:4 to 9.7 are plasticized with one or more epoxy esters of the formula RCOOA where R represents the residue of an epoxidized fatty acid and A represents the residue, after removal of a hydroxyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) an ether group of the formula R1(OCH2CH2)nOCH2CH2\t where R1 is a C1-C4 alkyl group and n is 0 or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. Apart from the specified groups (a) and (b), A generally represents a hydrocarbon group, such as aryl, alkaryl, aralkyl and cycloalkyl, or derivatives thereof containing, for example, halo or hydroxy substituents; A may also represent a heterocyclic group, e.g. furfuryl and derivatives thereof. The residue R of the epoxy ester may contain from 11 to 22 carbon atoms and is typically derived from vegetable or animal oils; for example, R may be derived from oleic acid or safflower oil, soybean oil, linseed oil or tall oil fatty acids. The ester resin is preferably derived from monomeric material containing at least 50% by weight of one or more alkyl or cycloalkyl esters of acrylic or methacrylic acid in which the alkyl or cycloalkyl group contains up to 18 carbon atoms; the resin may also comprise units of vinyl-pyridines, acrylonitrile, methacrylonitrile, acrylic or methacrylic acid and amides and salts thereof, itaconic or citraconic acid and their derivatives, e.e. esters, maleic anhydride, maleic, chloromaleic or fumaric acid and esters of these acids, vinyl ethers, vinyl esters, e.g. vinyl acetate, vinylidene chloride, vinyl sulphides, styrene and its derivatives and analogues thereof, vinylcarbazole, ethylenically unsaturated urea derivatives, allyl esters of monocarboxylic acids, aminoalkyl esters of acrylic and methacrylic acids, hydroxy alkyl esters or amides of acrylic and methacrylic acids, and acrylyl and methacrylyl dicyandiamides. The plasticized compositions may contain other polymers in addition to the acrylic ester resin and may also contain additional plasticizers, e.g. phthalate and phosphate esters, mixed benzoic acid and fatty oil acid esters of pentaerythritol, poly-(propyleneadipate) dibenzoate, diethylene glycol dibenzoate, tetrabutyl thiodisuccinate, butyl phthalyl butyl glycolate, acetyl tributyl citrate, dibenzyl sebacate, toluene ethyl sulphonamide, the di-2-ethylhexyl ester of hexamethylene diphthalate and di(methylcyclohexyl) phthalate. The plasticized composition may be incorporated in a solvent for coating or impregnating purposes and a pigment may also be included, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, and also a filler or extender, e.g. talc, barytes, china clay and diatomaceous earth. The plasticized esters may also be used in aqueous dispersion containing conventional emulsifiers (many specified) and, if desired, an aminoplast resin, particularly reaction products of aldehydes, e.g. formaldehyde, with compounds such as urea, thiourea, biuret and derivatives thereof, and triazines including melamine and derivatives thereof.ALSO:Substrates such as wood, metal, ceramics, linoleum, vinyl resin tiles and textile fabrics are coated with solutions or aqueous dispersions of plasticized resin compositions comprising an acrylic ester resin comprising or consisting of units of at least one ester of acrylic or methacrylic acid and having a solubility parameter d (as defined in the Specification) from 8.4 to 9.7 and, as plasticizer therefor, one or more epoxy esters of the formula R C O O A where R represents the residue of an epoxidised fatty acid and generally contains from 11 to 22 carbon atoms, and A represents the residue, after removal of a hydronyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) on ether group of the formula R1 (O CH2 CH2)n O CH2 CH2 where R1 is a C1-C4 alkyl group and n is O or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. The coating compositions may also include other polymers in addition to the aerylic ester resin, additional plasticizers (many specified), pigments, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, fillers or extenders, e.g. talc, barytes, china clay and diatomaceous earth, and aminoplast resins, particularly condensation products of various amino or amido compounds with aldehydes, e.g. formaldehyde. The aqueous dispersions may also include an emulsifier. Coating may be effected by air-spraying (with or without heating), steam spraying, electrostatic spraying, spraying a preheated coating composition, dipping, brushing or roller-coating. The coatings may be dried at room or elevated temperature, e.g. from 140 DEG to 300 DEG F. In an Example (No. 3), "Dacron" (Registered Trade Mark) taffeta fabric is coated with an aqueous dispersion of a copolymer of methyl methacrylate, methacrylic acid and N-[b -(a -methacryloxyacetamido) ethyl]-N, N1-ethylene urea (96 : 2 : 2) plasticized with the tetrahydrofurfuryl ester of epoxy linseed oil fatty acids; a solution of the same copolymer-plasticiser combination is used to cast a film on a metal (unspecified) sheet.ALSO:The fibres of a non-woven fibrous mass are bound together by impregnating the fibrous mass of, for example, wool, silk, mohair, fur, cotton, linen, rayon, nylon, or acrylonitrile polymers, with a solution or aqueous dispersion of a plasticized acrylic ester resin and drying the impregnated mass. The acrylic ester resin comprises or consists of units of at least one ester of acrylic or methacrylic acid, has a solubility parameter d (as defined in the Specification) from 8.4 to 9.7, and preferably contains groups which form cross-links or can be cross-linked by reaction with aminoplast resins; such groups include amide and N-methylol groups. The resin is plasticized with one or more epoxy esters of the formula RCOOA where R represents the residue of an epoxidized fatty acid and generally contains from 11 to 22 carbon atoms, and A represents the residue, after removal of a hydroxyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) an ether group of the formula R1 (O CH2 CH2)n O CH2 CH2 where R1 is a C1 - C4 alkyl group and n is O or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. The binder compositions may also include other polymers in addition to the acrylic ester resin, additional plasticizers (many specified), pigments, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, fillers or extenders, e.g. talc, barytes, china clay and diatomaceous earth, and aminoplast resins, particularly condensation products of various amino or amido compounds with aldehydes, e.g. formaldehyde. The aqueous dispersions may also include an emulsifier. In an Example (No. 6), a non-woven carded web of 75/25 viscose (3 denier, 1 inch staple)-bleached cotton (middling 15/16 inch) is impregnated with an aqueous dispersion of an ethyl acrylate-methyl methacrylate (45:55) copolymer plasticized with the benzyl ester of epoxyoleic acids.
GB3275563A 1962-08-28 1963-08-19 Plasticized acrylic ester resins Expired GB1049100A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US22008462A 1962-08-28 1962-08-28

Publications (1)

Publication Number Publication Date
GB1049100A true GB1049100A (en) 1966-11-23

Family

ID=22821984

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3275563A Expired GB1049100A (en) 1962-08-28 1963-08-19 Plasticized acrylic ester resins

Country Status (4)

Country Link
BE (1) BE636698A (en)
ES (1) ES290609A1 (en)
GB (1) GB1049100A (en)
NL (1) NL296556A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991000895A1 (en) * 1989-07-07 1991-01-24 Basf Lacke + Farben Aktiengesellschaft Process for making a multi-layer paint and basic paint for making the basic layer of a multi-layer paint
WO1998015685A1 (en) * 1996-10-09 1998-04-16 Hercules Incorporated Ester lubricants as hydrophobic fiber finishes
WO1998028356A1 (en) * 1996-12-24 1998-07-02 Dlw Aktiengesellschaft Material containing polyreactions products and method for the production thereof
WO2000015708A1 (en) * 1998-09-11 2000-03-23 Ciba Specialty Chemicals Holding Inc. Polymer compound with improved gloss properties
WO2006014483A2 (en) * 2004-07-08 2006-02-09 Archer-Daniels-Midland Company Epoxidized esters of vegetable oil fatty acids as reactive diluents
WO2011090812A2 (en) 2010-01-22 2011-07-28 Archer Daniels Midland Company Processes for making high purity renewable source-based plasticizers and products made therefrom
EP3002301A1 (en) * 2014-09-30 2016-04-06 Rohm and Haas Company Aqueous dispersion of composite particles
JP2016530384A (en) * 2013-09-06 2016-09-29 スリーエム イノベイティブ プロパティズ カンパニー Acid-modified epoxidized vegetable oil and (meth) acrylic copolymer curable composition or cured composition

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991000895A1 (en) * 1989-07-07 1991-01-24 Basf Lacke + Farben Aktiengesellschaft Process for making a multi-layer paint and basic paint for making the basic layer of a multi-layer paint
WO1998015685A1 (en) * 1996-10-09 1998-04-16 Hercules Incorporated Ester lubricants as hydrophobic fiber finishes
US5972497A (en) * 1996-10-09 1999-10-26 Fiberco, Inc. Ester lubricants as hydrophobic fiber finishes
WO1998028356A1 (en) * 1996-12-24 1998-07-02 Dlw Aktiengesellschaft Material containing polyreactions products and method for the production thereof
US6150436A (en) * 1996-12-24 2000-11-21 Dlw Aktiengesellschaft Material containing polyreactions products and method for the production thereof
WO2000015708A1 (en) * 1998-09-11 2000-03-23 Ciba Specialty Chemicals Holding Inc. Polymer compound with improved gloss properties
US6569926B1 (en) 1998-09-11 2003-05-27 Ciba Specialty Chemicals Corporation Polymer compound with improved gloss properties
WO2006014483A3 (en) * 2004-07-08 2006-10-05 Archer Daniels Midland Co Epoxidized esters of vegetable oil fatty acids as reactive diluents
WO2006014483A2 (en) * 2004-07-08 2006-02-09 Archer-Daniels-Midland Company Epoxidized esters of vegetable oil fatty acids as reactive diluents
GB2431160A (en) * 2004-07-08 2007-04-18 Archer Daniels Midland Co Epoxidized esters of vegetable oil fatty acids as reactive diluents
WO2011090812A2 (en) 2010-01-22 2011-07-28 Archer Daniels Midland Company Processes for making high purity renewable source-based plasticizers and products made therefrom
US20120277357A1 (en) * 2010-01-22 2012-11-01 Archer Daniels Midland Company Processes for making high purity renewable source-based plasticizers and products made therefrom
WO2011090812A3 (en) * 2010-01-22 2013-03-14 Archer Daniels Midland Company Processes for making high purity renewable source-based plasticizers and products made therefrom
US8703849B2 (en) * 2010-01-22 2014-04-22 Archer Daniels Midland Company Processes for making high purity renewable source-based plasticizers and products made therefrom
JP2016530384A (en) * 2013-09-06 2016-09-29 スリーエム イノベイティブ プロパティズ カンパニー Acid-modified epoxidized vegetable oil and (meth) acrylic copolymer curable composition or cured composition
EP3002301A1 (en) * 2014-09-30 2016-04-06 Rohm and Haas Company Aqueous dispersion of composite particles
US9587135B2 (en) 2014-09-30 2017-03-07 Dow Global Technologies Llc Aqueous dispersion of composite particles
AU2015227422B2 (en) * 2014-09-30 2019-08-01 Dow Global Technologies Llc Aqueous dispersion of composite particles

Also Published As

Publication number Publication date
ES290609A1 (en) 1963-12-16
NL296556A (en)
BE636698A (en)

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