Patent Application
20130338278
The invention relates to a polymer composition containing a polymer, which polymer contains residues of a dimerised fatty acid and/or a derivative thereof.
The use in polymers, of residues that may be obtained from renewable sources is increasingly important. The use of the monomer units obtainable from renewable resources that need not be produced from fossil carbon is a desirable way of reducing the greenhouse gasses released by the production of polymers. A good example is the use of a dimerised fatty acid residue in polymers. Dimerised fatty acid residues are used to impart flexibility to a polymer.
From US 2006/0235190 a semi crystalline, melt processable, partially aromatic copolyamide is known containing a residue of a dimerised fatty acid.
The dimerised fatty acid contains two carboxylic groups that may be used for copolymerizing the fatty acid. In order to copolymerize the dimerised fatty acid into the polyamide aliphatic diamines, for example hexamethylene diamine, are used. The same principle is for example known for thermoplastic elastomers containing polyester hard segments. In that case the dimerised fatty acid may be used without the modification of the two carboxylic acid groups. Parts produced of the polymer composition according to the invention have to be able to withstand high temperatures for a certain period of time, for example parts that get exposed to the sun or car parts during the painting process of the car or because the car parts are used under the hood. For that reason it is important that the polymer composition shows a sufficient thermal stability.
It is well known to improve the thermal stability of polymer compositions by the addition of thermal stabilizers. So called primary anti-oxidants of which phenolic type anti-oxidants are a good example, have proven to be most effective for this purpose. See for example Plastics Additives Handbook, Hansers Publishers, Munich, ISBN 978-3-446-40801-2 (2009), p. 54, FIG. 1.27 and Handbook of Polymer Degradation, Marcel Dekker, New York, ISBN 0-8247-0324-3 (2000), p.86, FIG. 1.
Object of the invention is to provide a polymer composition containing a polymer, which polymer contains residues of a dimerised fatty acid and/or a derivative thereof, which polymer composition has an increased thermal stability.
Surprisingly this object is obtained by providing a polymer composition that contains a secondary anti-oxidant.
The polymer composition according to the inventions shows a very good thermal stability, which is considerably higher the composition containing an other heat stabilizer, for example a primary anti-oxidant. This is contrary to what has been known about the stabilization of polymer compositions until now.
It is especially surprisingly that the thermal stability of the polymer composition is in an absolute sense ate a very high level. The thermal stability of the composition according to the invention is considerably higher than the thermal stability of a composition containing a similar polymer, however without the residues of a dimerised fatty acid and/or a derivative thereof, the composition nonetheless containing optimal types and amounts of thermal stabilizers. This is especially true if the polymer is a thermoplastic elastomer.
The dimerised fatty acids may be obtained from monomeric unsaturated fatty acids by an oligomerisation reaction. The oligomer mixture is further processed, for example by distillation, to yield a mixture having a high content of the dimerised fatty acid. The double bonds in the dimerised fatty acid may be saturated by catalytic hydrogenation. The term dimerised fatty acid as it is used here relates to both types of these dimerised fatty acids, the saturated and the unsaturated. It is preferred that the dimerised fatty acid is saturated.
It is also possible to produce derivatives of the dimerised fatty acid. For example a dimerised fatty diol may be obtained as a derivative of the dimerised fatty acid by hydrogenation of the carboxylic acid groups of the dimerised fatty acid, or of an ester group made thereof. Further derivatives may be obtained by converting the carboxylic acid groups, or the ester groups made thereof, into an amide group, a nitril group, an amine group or an isocyanate group.
The dimerised fatty acids may contain from 32 up to 44 carbon atoms. Preferably the dimerised fatty acid contains 36 carbon atoms.
Further details relating to the structure and the properties of the dimerised fatty acids may be found in the corresponding leaflet “Pripol C36-Dimer acid” of the company UNICHEMA (Emmerich, Germany) or in the brochure of the Company COGNIS (Düsseldorf, Germany) “Empol Dimer and Poly-basic Acids; Technical Bulletin 114C (1997)”.
In the production of the polymer containing the residue of the dimerised fatty acid and/or a derivative thereof the dimerised fatty acid and its derivative may be used as a monomer or as a pre-cursor oligomer or polymer. In one example the pre-cursor oligomer or polymer is a polyester, formed of dimerised fatty acid and/or dimerised fatty diol with any combination of diols or dicarboxylic acids. In another example the pre-cursor oligomer or polymer is a polyamide, formed of dimerised fatty acid and/or dimerised fatty diamines with any combination of diamines or dicarboxylic acids forming polyamides.
In a preferred embodiment the pre-cursor is a precursor oligomer or polymer of a dimerised fatty acid and a dimerised fatty amine. Depending on the ratio of dimerised fatty acids and dimerised fatty amines as well as the degree of polymerization of the fatty acid and the fatty amine the endgoups of the precursor are tuned to be acid groups or amine groups. Depending on the further monomers and/or pre-polymers that are used to produce the final polymer, it might be desirable to have acid endgroups or amine endgroups.
The precursor oligomer or polymer preferably has a number average molecular weight (Mn) of at least 600 kg/kmol, more preferably at least 1000 kg/kmol, even more preferably at least 2000 kg/kmol. The Mn is preferably at most 5000 kg/kmol, more preferably at most 2500 kg.kmol.
Examples of polymers containing the residue of the dimerised fatty acid and/or derivatives thereof are thermoplastic elastomers having hard segments of polyester, nylon and polycarbonate, the soft segments containing the residue of the dimerised fatty acid and/or a derivative.
The polymer may contain between 1 and 70 wt. % of the residue of the dimerised fatty acid and/or a derivative thereof. Preferably the polymer contains between 5 and 50, more preferably between 10 and 30 wt. % of the residue of the dimerised fatty acid and/or a derivative thereof.
Preferably the thermoplastic elastomer is a polymer containing hard segments of polyester and the soft segments containing the residue of a dimerised fatty acid and/or a derivative thereof.
Such a thermoplastic elastomer suitably contains hard segments that are built up from repeating units derived from at least one alkylene diol and at least one aromatic dicarboxylic acid or an ester thereof. The linear or cycloaliphatic alkylene diol contains generally 2-8 C-atoms, preferably 2-4 C-atoms. Examples thereof include ethylene glycol, propylene diol and butylene diol. Preferably propylene diol or butylene diol are used, more preferably 1,4-butylene diol. Examples of suitable aromatic dicarboxylic acids include terephthalic acid, 2,6-naphthalenedicarboxylic acid, 4,4′-biphenyldicarboxylic acid or combinations of these. The advantage thereof is that the resulting polyester is generally semi-crystalline with a melting point of above 150, preferably above 175, and more preferably of above 190° C. The hard segments may optionally further contain a minor amount of units derived from other dicarboxylic acids, for example isophthalic acid, which generally lowers the melting point of the polyester. The amount of other dicarboxylic acids is preferably limited to not more than 10, more preferably not more than 5 mol %, based on the total amount of dicarboxylic acids, so as to ensure that, among other things, the crystallization behaviour of the copolyether ester is not adversely affected. The hard segment is preferably built up from ethylene terephthalate, propylene terephthalate, and in particular from butylene terephthalate as repeating units. Advantages of these readily available units include favourable crystallisation behaviour and a high melting point, resulting in a thermoplastic elastomer according to the invention with good processing properties, excellent thermal and chemical resistance and good puncture resistance.
Secondary anti-oxidants may act by reducing hydro peroxides. The most important secondary anti-oxidants are trivalent phosphorous containing anti-oxidants and thio-ether containing anti-oxidants. Some stabilizers both act as secondary and primary stabilizers. For the purpose of this invention they will be regarded as secondary anti-oxidants.
Examples of trivalent phosphorous containing compounds are: Trisnonylphenyl phosphite Trilauryl phosphite Tris (2,4-di-t-butylphenyl) phosphite Di-Isooctylphosphite Triisodecyl phosphite Diisodecylphenylphosphite Diphenyl isodecyl phosphite Triphenyl phosphite tris(tridecyl)phosphite Diphenyl isooctyl phosphite 12H-Dibenzo[d,g][1,3,2]dioxaphosphocin, 2,4,8,10-tetrakis(1,1-dimethylethyl)-6-(octyloxy)-2,2′-Ethylidenebis (4,6-di-t-butylphenyl) fluorophosphonite Di-sodium-hydrogen-phosphite Phosphorous acid, bis[2,4-bis(1,1-dimethylethyl)-6-methylphenyl]ethyl ester 2,4,6 Tri-t-butylphenyl-2-butyl-2-ethyl-1,3-propane-diol-phosphite Triisooctyl phosphite Tris (dipropyleneglycol) phosphite Diisooctyl octylphenyl phosphite Tris-(2,4-di-tert.butyl-5-methylphenyl)-phosphite (phenylethyl)phenylphosphites Diphenylphosphite Phenylneopentyleneglycolphosphite Phosphorous acid, trioctadecyl ester Phosphorous acid, dinonylphenyl bis(nonylphenyl) ester Phosphorous acid, 2-ethylhexyl diphenyl ester 9,10-Dihydro-9-oxa-10-phosphaphenanthren-10-oxide Diphenyl Tridecyl Phosphite Phosphonic acid, dioctyl ester Phosphorous acid, 2-ethylhexyl diphenyl ester Bis(octadecyloxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Tetrakis-(2,4-di-tert-butyl-phenyl)-4,4′-bi-phenylene-di-phosphonite Bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite Bis-(2,6-di-tbutyl-4-methyl-phenyl)-pentaerythritol-di-phosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis[2,4,6-tris(1,1-dimethylethyl)phenoxy]-Poly 4,4′ isopropylidenediphenol C12-15 Alcohol phosphite Tetrakis isodecyl 4,4″-isopropylidene diphosphite Bis-(2,4-dicumylphenyl)-pentaerytritol-diphosphite Phosphorous acid, (1-methylethylidene)di-4,1-phenylene-tetraoctadecyl ester Phosphorous acid, oxybis (methyl-2,1 ethane diyl) tetraphenyl ester Diisodecyl pentaerythritol diphosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-bis[2-(1,1-dimethylethyl)-4-(1-methyl-1-phenylethyl)phenoxy]-Tetra(tridecyl)-4,4′-butylidene-bis(6-t-butyl-2-methyldiphenol)diphosphite Phosphonous acid, [1,1′-biphenyl]-3,3′-diylbis-, tetrakis[2,4-bis(1,1-dimethylethyl)-5-methylphenyl] ester Poly(dipropyleneglycol)phenylphosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-bis(nonylphenoxy)-2-[[2,4,8,10-Tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy]-N,N-bis[2[[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy-ethyl]ethanamine 3,6,8,11,14,16,19,22,24,27-Decaoxa-7,15,23-triphosphanonacosane-1,29-diol Phosphorous acid, P,P′,P″-[(1-methyl-1-propanyl-3-ylidene)tris[2-(1,1-dimethylethyl)-5-methyl-4, 1-phenylene]] P,P,P′,P′,P″,P″-hexatridecyl ester Trilauryl trithiophosphite
Prefered are: Trisnonylphenyl phosphite Trilauryl phosphite Triisodecyl phosphite Diisodecylphenylphosphite Diphenyl isodecyl phosphite tris(tridecyl)phosphite Diphenyl isooctyl phosphite Phosphorous acid, bis[2,4-bis(1,1-dimethylethyl)-6-methylphenyl]ethyl ester Triisooctyl phosphite Bis(octadecyloxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite Bis-(2,6-di-tbutyl-4-methyl-phenyl)-pentaerythritol-di-phosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis[2,4,6-tris(1,1-dimethylethyl)phenoxy]-Poly 4,4′isopropylidenediphenol C12-15 Alcohol phosphite Tetrakis isodecyl 4,4″-isopropylidene diphosphite Bis-(2,4-dicumylphenyl)-pentaerytritol-diphosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-bis[2-(1,1-dimethylethyl)-4-(1-methyl -1-phenylethyl)phenoxy]-Tetra(tridecyl)-4,4′-butylidene-bis(6-t-butyl-2-methyldiphenol)diphosphite Poly(dipropyleneglycol)phenylphosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-bis(nonylphenoxy)-2-[[2,4,8,10-Tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy]-N,N-bis[2[[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy-ethyl]ethanamine
Most prefered are: Bis(octadecyloxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite Bis-(2,6-di-tbutyl-4-methyl-phenyl)-pentaerythritol-di-phosphite Bis-(2,4-dicumylphenyl)-pentaerytritol-diphosphite 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-bis(nonylphenoxy)-2-[[2,4,8,10-Tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy]-N,N-bis[2[[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]oxy-ethyl]ethanamine
Examples of thio-ether containing compounds for use as thermal stabilizers are: Dilauryl thiodipropionate Dimyristyl thiodipropionate Distearyl thiodipropionate Ditridecyl thiodipropionate 3,3-Thiodipropionic acid used as monomer in the polymerization Lauryl-stearylthiodiprionate Disulfide, dioctadecyl Cyclohexane, 1-(octadecylthio)-3-[2-(octadecylthio)ethyl]-Propanoic acid, 3-(dodecylthio)-, 1,1′-[oxybis(2,1-ethanediyloxy-2,1-ethanediyl)] ester Pentaerythrityl tetrakis (β-laurylthiopropionate) Bis[2-methyl-4-{3-n-alkyl(C12 or 014) thiopropionyloxy}-5-t-butylphenyl]sulphide Propanoic acid, 3,3′-thiobis-, 1,1′-dimethyl ester, polymer with 1,4cyclohexanedimethanol, octadecyl ester
Prefered are: Dilauryl thiodipropionate Distearyl thiodipropionate Ditridecyl thiodipropionate Disulfide, dioctadecyl Pentaerythrityl tetrakis (β-laurylthiopropionate) Propanoic acid, 3,3′-thiobis-, 1,1′-dimethyl ester, polymer with 1,4cyclohexanedimethanol, octadecyl ester
Most prefered are: Dilauryl thiodipropionate Distearyl thiodipropionate Pentaerythrityl tetrakis (β-laurylthiopropionate) Propanoic acid, 3,3′-thiobis-, 1,1′-dimethyl ester, polymer with 1,4cyclohexanedimethanol, octadecyl ester
The amount of secondary anti-oxidant in the composition according to the invention may be between 0.01 and 5 wt. %. The amount of secondary heat stabilizer in the composition according to the invention is preferably between 0.1 and 2.0 wt. %, more preferably between 0.2 and 1.5 wt. %, more preferably between 0.3 and 1.0 wt. %.
It is also possible that the composition according to the invention contains, next to the secondary anti-oxidant, a primary anti-oxidant. The amount of primary anti-oxidant may be between 0.01 and 2 wt. % of the composition according to the invention. The amount of primary anti-oxidnat in the composition according to the invention is preferably between 0.1 and 1.5 wt. %.
Primary anti-oxidants are radical scavangers such as for example phenolic anti-oxidants or aromatic amines.
Examples of phenolic anti-oxidants are: Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-octadecyl ester 2-Propyleneacid, 2-isopentane 6[(3-isopentane-2-hydroxy-5-isopentane-phenyl)-ethyl]-4-isopentanephenylester 2-Propenoic acid, 2-(1,1-dimethylethyl)-6-[[3-1,1-dimethylethyl)-2-hydroxy-5-methylphenyl]methyl]-4-methylphenylester Di-ethyl-ester of 3,5-di-t-butyl-4-hydroxy-benzyl-phosphoric acid 2,5,7,8-Tetra-methyl-2-(4′,8′,12′-tri-methyl-tri-decyl)-chroman-6-ol Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, isooctyl ester Benzenepropionic acid, 3,5-bis (1,1-dimethylethyl)-4-hydroxy, isotridecyl ester Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-C13-15 branched and linear alkyl esters 2,2″-Methylenebis (6-t-butyl-4-methylphenol) 2,2″-Methylenebis (4-ethyl-6-t-butylphenol) 2,2″-Methylenebis 6-(1-methylcyclohexyl)-p-cresol 4,4″-Butylidenebis (6-t-butyl-3-methyl-phenol) 2,2″-Ethylidenebis (4,6-di-t-butylphenol) Phenol, 4,4′-methylenebis[2,6-bis(1,1-dimethylethyl)-2,2″-Isobutylidenebis (4,6-dimethylphenol) N,N″-Hexamethylene bis (3,5-di-t-butyl-4-hydroxyhydrocinnamamide) 3,9-Bis(1,1-dimethyl-2-β-(3-t-butyl-4-hydroxy-5-methyl-phenyl)-propyonyl-oxy)-ethyl)-2,4,8,10-tetraoxospiro Ethylenebis (oxyethylene) bis (3-t-butyl-4-hydroxy-5-methylhydrocinnamate) Hexamethylenebis (3,5-di-t-butyl-4-hydroxycinnamate) Benzenepropanamide, N,N′-1,3-propanediylbis[3,5-bis(1,1-dimethylethyl)-4-hydroxy-] Calcium bis[monoethyl(3,5-di-t-butyl-4-hydroxybenzyl)phosphonate] Phenol, 2,2′-methylenebis[4-methyl-6-nonyl-] 1,1,3-Tris(2-methyl-4-hydroxy-5-t-butyl phenyl)butane Phenol, 4,4′4′″-[(2,4,6-trimethyl-1,3,5-benzenetriyl)-tris-(methylene)Hris-2,6-bis(1,1-dimethylethyl) -Bis-[3,3-bis-(4′-hydroxy-3′-t-butylphenyl butanoic acid]-glycol ester Tris(3,5-di-t-butyl-4-hydroxy benzyl) isocyanurate 1,3,5-Tris (4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione 3-(3,5-Di-t-butyl-4-hydroxy-phenyl) propion acid ester with 1,3,5-tris (2-hydroxy-ethyl)-iso-cyanurate Tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] methane p-Cresol/dicyclopentadiene butylated reaction product 1,1,3-tris[2-methyl-4-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyloxy]-5-tert-butylphenyl]butane
Prefered are: Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-octadecyl ester 2,5,7,8-Tetra-methyl-2-(4′,8′,12′-tri-methyl-tri-decyl)-chroman-6-ol Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, isooctyl ester Benzenepropionic acid, 3,5-bis (1,1-dimethylethyl)-4-hydroxy, isotridecyl ester Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-C13-15 branched and linear alkyl esters 2,2′-Methylenebis (6-t-butyl-4-methylphenol) N,N′-Hexamethylene bis (3,5-di-t-butyl-4-hydroxyhydrocinnamamide) Ethylenebis (oxyethylene) bis (3-t-butyl-4-hydroxy-5-methylhydrocinnamate) Hexamethylenebis (3,5-di-t-butyl-4-hydroxycinnamate) 1,1,3-Tris(2-methyl-4-hydroxy-5-t-butyl phenyl)butane Phenol, 4,4′4′″-[(2,4,6-trimethyl-1,3,5-benzenetriyl)-tris-(methylene)]tris-2,6-bis(1,1-dimethylethyl) -Bis-[3,3-bis-(4′-hydroxy-3′-t-butylphenyl butanoic acid]-glycol ester Tris(3,5-di-t-butyl-4-hydroxy benzyl) isocyanurate 1,3,5-Tris (4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione 3-(3,5-Di-t-butyl-4-hydroxy-phenyl) propion acid ester with 1,3,5-tris (2-hydroxy-ethyl)-iso-cyanurate Tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] methane
Most prefered are: Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-octadecyl ester 2,5,7,8-Tetra-methyl-2-(4′,8′,12′-tri-methyl-tri-decyl)-chroman-6-ol N,N′-Hexamethylene bis (3,5-di-t-butyl-4-hydroxyhydrocinnamamide) Ethylenebis (oxyethylene) bis (3-t-butyl-4-hydroxy-5-methylhydrocinnamate) Hexamethylenebis (3,5-di-t-butyl-4-hydroxycinnamate) Phenol, 4,4′4′″-(2,4,6-trimethyl-1,3,5-benzenetriyl)-tris-(methylene)tris-2,6-bis(1,1-dimethylethyl)-Bis-[3,3-bis-(4′-hydroxy-3′-t-butylphenyl butanoic acid]-glycol ester Tris(3,5-di-t-butyl-4-hydroxy benzyl) isocyanurate 1,3,5-Tris (4-t-butyl-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione Tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] methane 3-(3,5-Di-t-butyl-4-hydroxy-phenyl) propion acid ester with 1,3,5-tris (2-hydroxy-ethyl)-iso-cyanurate
Examples of Aromatic Amines are: 4,4′-Di-cumyl-di-phenyl-amine N, N′-Diphenyl-p-phenylenediamine 2,2,4-Trimethyl-1,2-dihydroquinoline polymer 4,4′-Dioctyl-diphenyl-amine 1,4-Benzenediamine, N, N′-bis(1-methylpropyl) N-Isopropyl-N′-phenyl-paraphenylenediamine N-1,3-dimethyl-butyl-N′-phenyl-paraphenylene-diamine N,N″-Bis (1,4-dimethylpentyl)-p-phenylenediamine 2-Naphthalenamine, N-phenyl-1,4-Benzenediamine, N-(1-methylethyl)-N′-phenyl-Benzenamine, N-phenyl-,reaction product with 2,4,4 trimethyl pentane 1,4-Benzenediamine, N,N′-bis[4-(1-phenylethyl)phenyl]-p-(p-Toluene-sulfonylamido)-diphenylamine Benzeneamine, N-{4-[(1,3-dimethylbutyl)imino]-2,5-cyclohexadien-1-ylidine N-phenyl-N′-1-phenylethyl-1,4-phenylenediamine reaction product of diphenyl amine and acetone Mixture of styrenated diphenylamines Phenyl-α-naphtylamine Nonylated diphenylamine A blend of reaction products of: N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine and N-(4-[α,α′dimethylbenzyl]phenyl) -N′-(1,3-dimethylbutyl) p-phenylendiamine Blend of alkyl-aryl-p-phenylenediamines Blend of alkyl-aryl- and dialkyl-p-phenylenediamines 1,2-Dihydro-2,2,4-trimethylquinolene 1,4-benzenediamine-N-(α-methylbenzyl)-N′-phenyl
Prefered are: 4,4′-Di-cumyl-di-phenyl-amine N,N′-Diphenyl-p-phenylenediamine 2,2,4-Trimethyl-1,2-dihydroquinoline polymer 4,4′-Dioctyl-diphenyl-amine 1,4-Benzenediamine, N,N′-bis(1-methylpropyl) N-Isopropyl-N′-phenyl-paraphenylenediamine N-1,3-dimethyl-butyl-N′-phenyl-paraphenylene-diamine
N,N′-Bis (1,4-dimethylpentyl)-p-phenylenediamine Benzenamine, N-phenyl-,reaction product with 2,4,4 trimethyl pentane
Most prefered is: 4,4′-Di-cumyl-di-phenyl-amine
Examples of stabilizers acting both as primary and as secondary stabilizers are 4,4′-Thio-bis-(2-t-butyl-5-methyl-phenol) 2,4-Bis-octyl-mercapto-6-(4-hydroxy-3,5-di-t-butyl-anilo)-1,3,5-triazine 2,2′-Thio-ethanol-bis-3-(3,5-di-t-butyl-4-hydroxy-phenyl)-propionate Phenol, 2,2′-Thiobis[6-(1,1-dimethylethyl)-4-methyl-] Phenol, 4,4′-thiobis[2-(1,1-dimethylethyl)-6-methyl]-Phenol,2-methyl-4,6-bis[(octylthio)methyl]-4,6-bis-(dodecylthiomethyl)-O-cresol
6-[3-(3-t-Butyl-4-hydroxy-5-methyl)propoxy]-2,4,8,10-tetra-t-butyldibenz[d,f][1,3,2]-dioxaphosphepin Phenol, 4,4′-thiobis 2-(1,1-dimethylethyl) phosphite Tris-(2-t-butyl-4-thio-(2′-methyl-4′-hydroxy-5′-t-butyl)phenyl-5-methyl]phenyl phosphite
Prefered are: 4,4′-Thio-bis-(2-t-butyl-5-methyl-phenol) 2,4-Bis-octyl-mercapto-6-(4-hydroxy-3,5-di-t-butyl-anilo)-1,3,5-triazine 2,2′-Thio-ethanol-bis-3-(3,5-di-t-butyl-4-hydroxy-phenyl)-propionate Phenol, 2-methyl-4,6-bis[(octylthio)methyl]-4,6-bis-(dodecylthiomethyl)-O-cresol 6-[3-(3-t-Butyl-4-hydroxy-5-methyl)propoxy]-2,4,8,10-tetra-t-butyldibenz[d,f][1,3,2]-dioxaphosphepin Phenol, 4,4′-thiobis 2-(1,1-dimethylethyl) phosphite Tris-(2-t-butyl-4-thio-(2′-methyl-4′-hydroxy-5′-t-butyl)phenyl-5-methyl]phenyl phosphite
Most prefered are: 2,4-Bis-octyl-mercapto-6-(4-hydroxy-3,5-di-t-butyl-anilo)-1,3,5-triazine 2,2′-Thio-ethanol-bis-3-(3,5-di-t-butyl-4-hydroxy-phenyl)-propionate Phenol,2-methyl-4,6-bis[(octylthio)methyl]-Tris-(2-t-butyl-4-thio-(2′-methyl-4′-hydroxy-5′-t-butyl)phenyl-5-methyl]phenyl phosphite
The invention will further be explained by the examples.
Preparation of test samples.
Materials
Irganox 1330 from BASF, phenol, 4,4′4′″-(2,4,6-trimethyl-1,3,5-benzenetriyl)-tris -(methylene)Hris-2,6-bis(1,1- dimethylethyl)-, a primary anti-oxidant. Irganox PS 802 from BASF, distearyl thiopropionate, a secondary anti-oxidant. Irgafos 126 from BASF, Bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite, a secondary anti-oxidant.
Polymer 1: polymer containing 30 wt. % of residues of a dimerised fatty acid having 36 C-atoms, the balance being hard segments of 1,4-butylene diol and terphthalic acid.
Polymer 2: polymer containing 15wt. % of residues of a dimerised fatty acid having 36 C-atoms, the balance being hard segments of 1,4-butylene diol and terphthalic acid.
Polymer 3: a copolymer containing 30 wt. % of soft blocks of polyTHF, the balance being hard segments of 1,4-butylene diol and terphthalic acid.
Compounding
Compounds were produced by feeding a dry blend consisting of one of the polymers and one or more of the thermal stabilizers to a 25 mm Werner and Pfleiderer™ twin screw extruder. The strand of the mixture leaving the extruder was cooled and cut into granulate having a diameter of about 6 mm.
Thermal Stability Test
Granules were placed in a reactor, the reactor was filled with a 100% oxygen atmosphere of 1 bar after which the reactor was closed. After that the temperature of the reactor was kept at 170° C. for 25 hours. The pressure drop due to the reaction of the oxygen with the polymer granules was monitored. From the pressure drop the amount of oxygen that has reacted with the film was calculated. The amount of oxygen that has reacted with the granules is taken as a measure for the thermal stability of the polymer composition. The results are shown in table I.
Is granulate of a composition consisting of polymer 1. The polymer was processed via the twin screw extruder as for the blends of the polymer and the stabilizers. The result of the thermal stability test are given in table 1.
Is granulate of a composition consisting of 99.5 wt. % of polymer 1 and 0.5 wt. % of Irganox 1330, a primary anti-oxidant. The result of the thermal stability test are given in table 1.
Is a granulate of a composition consisting of 99 wt. % of polymer 3, 0.5 wt % Irganox PS 802 and 0.5% Irganox 1330.
In examples 1 a composition is tested existing of 99.5 wt. % of polymer 1 and 0.5 wt. % of Irgafos 126, a secondary anti-oxidant. The result of the thermal stability test are given in table 1.
In examples 2 a composition is tested existing of 99.5 wt. % of polymer 1 and 0.5 wt. % of Irganox PS 802, a secondary anti-oxidant. The result of the thermal stability test are given in table 1.
In example 3 a composition is tested existing of 99 wt. % of polymer 1 and 0.5 wt. % Irgafos 126, a secondary anti-oxidant, and 0.5% Irganox 1330, a primary anti-oxidant. The result of the thermal stability test are given in table 1.
In example 3 a composition is tested existing of 99 wt. % of polymer 1 and 0.5 wt. % Irgafos 126, a secondary anti-oxidant, and 0.5% Irganox 1330, a primary anti-oxidant. The result of the thermal stability test are given in table 1.
As example IV, however polymer 2 is used, comprising 15 wt. % of residues of a dimerised fatty acid, instead of 30 wt. %.
From the results in table 1 it is clear that the secondary anti-oxidants have a pronounced effect on the thermal stability of the polymer composition, also in combination with further stabilizers.
From the comparison of comparative experiment C and the examples it is clear that the composition according to the invention containing the polymer comprising the residue of a dimerised fatty acid and/or a derivative thereof shows a good thermal stability compared to a similar polymer containing a different soft block.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10195293.5 | Dec 2010 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP11/72444 | 12/12/2011 | WO | 00 | 9/3/2013 |
