EP1453905A2 - Composition stabilisante, production et utilisation de ladite composition - Google Patents

Composition stabilisante, production et utilisation de ladite composition

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Publication number
EP1453905A2
EP1453905A2 EP02795118A EP02795118A EP1453905A2 EP 1453905 A2 EP1453905 A2 EP 1453905A2 EP 02795118 A EP02795118 A EP 02795118A EP 02795118 A EP02795118 A EP 02795118A EP 1453905 A2 EP1453905 A2 EP 1453905A2
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EP
European Patent Office
Prior art keywords
perchlorate
organic
onium
stabilizer composition
composition according
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.)
Ceased
Application number
EP02795118A
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German (de)
English (en)
Inventor
Stefan Fokken
Juergen Hauk
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Baerlocher GmbH
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Baerlocher GmbH
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Filing date
Publication date
Application filed by Baerlocher GmbH filed Critical Baerlocher GmbH
Publication of EP1453905A2 publication Critical patent/EP1453905A2/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41—Compounds containing sulfur bound to oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C08K5/19—Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/50—Phosphorus bound to carbon only

Definitions

  • Stabilizer composition its manufacture and use
  • the present invention relates to a stabilizer composition for halogen-containing polymers, their production and their use.
  • halogen-containing plastics tend to undergo undesirable decomposition and degradation reactions when subjected to thermal stress during processing or in long-term use.
  • the degradation of halogenated polymers, especially PVC produces hydrochloric acid, which is eliminated from the polymer strand, which results in a discolored, unsaturated plastic with coloring polyene sequences.
  • halogen-containing polymers only have the rheological framework necessary for processing at a relatively high processing temperature. At such temperatures, however, a noticeable decomposition of the polymer already begins in the case of unstabilized polymers, which leads both to the undesired color change described above and to a change in the material properties.
  • the hydrochloric acid released from unstabilized, halogen-containing polymers at such a processing temperature can lead to noticeable corrosion of the processing plants.
  • This process plays a role in particular when, during the processing of such halogenated polymers to give shaped articles, for example by extrusion, production is interrupted and the polymer mass remains in the extruder for a longer period of time. During this time, the above-mentioned decomposition reactions can occur, rendering the batch in the extruder unusable and possibly damaging the extruder.
  • halogen-containing polymers for processing are usually added as so-called stabilizers, which are intended to prevent the above-mentioned decomposition reactions as far as possible.
  • stabilizers are solids which are added to the polymer to be processed before it is processed.
  • Perchlorates are suitable as stabilizers, for example, the perchlorates according to the prior art generally being used as inorganic perchlorates, for example as sodium perchlorate.
  • the problem with these connections is that they do not always meet the requirements placed on them.
  • solid stabilizers often have the disadvantage that they can lead to undesirable cloudiness in the end product, particularly in the case of transparent processing forms.
  • opacities restrict the acceptance of such end products by users who process them further and prevent the end products from being used in applications in which the greatest possible transparency is important.
  • liquid stabilizers containing sodium perchlorate for example, have been proposed.
  • a disadvantage of these stabilizers is that the stabilizer properties leave something to be desired in terms of improving the initial color.
  • the object of the present invention was therefore to provide a stabilizer composition which can be used in the production of halogen-containing polymers and which leads to an improvement in the initial color. Furthermore, it was an object of the present invention to provide a liquid stabilizer composition which can be used in the production of halogen-containing polymers and which reduces the haze in transparent end products, for example made of hard or soft PVC. The invention was also based on the object of providing a stabilizer composition which shows an improvement in the initial color when processing halogen-containing polymers in comparison with stabilizers known from the prior art.
  • solid and liquid stabilizer compositions which contain at least one organic onium perchlorate achieve the above-mentioned objects.
  • a first object of the present invention is therefore a stabilizer composition comprising an organic onium salt of perchloric acid or a mixture of two or contains more organic onium salts of perchloric acid and at least one organic solvent.
  • a “stabilizer composition” is understood to mean a composition which can be used to stabilize halogen-containing polymers.
  • a stabilizer composition according to the invention is generally mixed with a halogen-containing polymer provided for stabilization and then processed.
  • liquid means the physical state of a stabilizer composition according to the invention at least within a temperature range from approximately 45 to approximately 100 ° C., preferably within a temperature range from approximately 30 to approximately 120 ° C., for example within a temperature range from about 15 to about 150 ° C. and in particular within a temperature range of about 0 to about 200 ° C.
  • solvent is understood to mean a compound which can dissolve an organic onium salt of perchloric acid or a mixture of two or more organic onium salts of perchloric acid in an amount of at least 0.1% by weight.
  • an "onium salt” is a compound which is an ammonium, sulfonium or phosphonium salt.
  • An “onium salt” according to the present invention is an organic onium salt. This means that the ammonium, sulfonium or phosphonium group of the onium salt carries at least one organic radical.
  • An onium salt according to the present invention can, depending on the type of onium group, carry 1, 2, 3 or 4 organic radicals.
  • the organic radicals can be connected to the onium radical, for example via a CX linkage, where X stands for S, N or P. However, it is also possible that the organic residues are connected to the onium residue via a further heteroatom, for example an O atom.
  • An onium perchlorate which can be used in the context of the present invention has at least one positively charged N, P or S atom or two or more such positively charged N, P or S atoms or mixtures of two or more of the positively charged atom types mentioned on.
  • compounds are used as onium perchlorates which carry at least one organic radical on the N, S or P atom and at most the maximum possible number of organic radicals. If an onium perchlorate which can be used according to the invention carries fewer organic residues than are necessary for the formation of a positively charged onium ion, the positive charge is generated in a conventional manner known to the person skilled in the art by protonation using a suitable acid, so that the corresponding onium perchlorate in this case in addition to an organic residue carries at least one proton.
  • a peralkylated onium perchlorate which can be used according to the invention has an aryl, alkaryl, cycloalkyl, alkenyl, alkynyl or cycloalkenyl radical.
  • an onium salt which can be used in the context of a stabilizer composition according to the invention has two or optionally more different types of substituents, for example an alkyl and a cycloalkyl radical or an alkyl and an aryl radical. It is also possible and envisaged in the context of the present invention that an onium salt which can be used in the context of a stabilizer composition according to the invention has substituents which in turn are substituted by one or more functional groups are.
  • “functional groups” are groups which improve the effects of the stabilizer composition or at least not or only slightly deteriorate them. Corresponding functional groups can be, for example, NH groups, NH 2 groups, OH groups, SH groups, ester groups, ether groups, thioether groups, isocyanurate groups or keto groups or mixtures of two or more thereof.
  • Phosphonium perchlorates which can be used according to the invention can be obtained, for example, by appropriate reaction of tetraalkyl, tetracycloalkyl or tetraaryl phosphorus halides.
  • Suitable phosphonium perchlorates are therefore derived, for example, from tetraalkylphosphorus salts such as tetra-n-ethylphosphonium bromide, tetra-n-propylphosphonium bromide, tetra-n-butylphosphonium bromide, tetra-n-isobutylphosphonium bromide, tetra-n-pentylphylbromidium, and the like Tetraalkyl phosphorus salts.
  • tetraalkylphosphorus salts such as tetra-n-ethylphosphonium bromide, tetra-n-propylphosphonium bromide, tetra-n-butylphosphonium bromide, tetra-n-isobutylphosphonium bromide, tetra-n-pentylphylbromidium, and the like Tetraalkyl phosphorus salts.
  • phosphonium perchlorates which are derived, for example, from tetracycloalkyl phosphorus salts or tetraaryl phosphorus salts are suitable in principle for use in the stabilizer compositions according to the invention. Suitable phosphonium perchlorates are therefore based, for example, on tetracycloalkyl or tetraaryl phosphorus salts such as tetracyclohexylphosphonium bromide or tetraphenylphosphonium bromide and the like tetracycloalkyl or tetraaryl phosphorus salts.
  • the abovementioned compounds can be unsubstituted in the context of the present invention, but they can also have one or more of the abovementioned substituents, provided that these substituents have no adverse effects in the context of the stabilizer composition and do not adversely affect the intended use of the stabilizer composition.
  • Organic phosphonium perchlorates which carry different types of organic substituents on a phosphorus atom, which can optionally be substituted differently, can also be used in the context of the present invention.
  • tetra-n-butylphosphonium perchlorate or triphenylbenzylphosphonium perchlorate are used as phosphonium perchlorates.
  • Sulfonium perchlorates which can be used according to the invention can be obtained, for example, by appropriate reaction of sulfides such as alkyl monosulfides, alkyl disulfides, dialkyl sulfides or polyalkyl sulfides.
  • Suitable sulfonium perchlorates are therefore derived, for example, from dialkyl sulfides such as ethylbenzyl sulfide, allylbenzyl sulfide or alkyl disulfides such as hexane disulfide, heptane disulfide, octane disulfide and the like alkyl disulfides.
  • dialkyl sulfides such as ethylbenzyl sulfide, allylbenzyl sulfide or alkyl disulfides such as hexane disulfide, heptane disulfide, octane disulfide and the like alkyl disulfides.
  • sulfonium perchlorates which are derived, for example, from tricycloalkylsulfonium salts or triarylsulfonium salts are suitable in principle for use in the stabilizer compositions according to
  • Suitable sulfonium perchlorates are therefore based, for example, on tricycloalkyl or triarylsulfonium salts such as tricyclohexylsulfonium bromide or triphenylsulfonium bromide and the like tricycloalkyl or triarylsulfonium salts.
  • Tricycloalkyl or triarylsulfonium salts such as tricyclohexylsulfonium bromide or triphenylsulfonium bromide and the like tricycloalkyl or triarylsulfonium salts.
  • Trialkyl, triaryl or tricycloalkylsulfoxonium salts such as trimethylsulfoxonium perchlorate are also suitable.
  • the abovementioned compounds can be unsubstituted in the context of the present invention, but they can also have one or more of the abovementioned substituents, provided that these substituents have no adverse effects in the context of the stabilizer composition and do not adversely affect the intended use of the stabilizer composition.
  • Organic sulfonium perchlorates which carry different types of organic substituents on a sulfur atom, which can optionally be substituted differently, can also be used in the context of the present invention.
  • trimethyl sulfoxonium perchlorate is used as the sulfonium perchlorate.
  • ammonium perchlorates which can be used according to the invention can be obtained, for example, by appropriate reaction of amines or amides such as alkylmonoamines, alkylenediamines, alkylpolyamines, secondary or tertiary amines or dialkylamines.
  • Suitable ammonium perchlorates are therefore derived, for example, from primary mono- or polyamino compounds having 2 to about 40, for example 6 to about 20, carbon atoms.
  • these are ethylamine, n-propylamine, i-propylamine, n-butylamine, sec-butylamine, tert-butylamine, substituted amines with 2 to about 20 C atoms, such as 2- (N, N-dimethylamino) -l- aminoethane.
  • Suitable diamines have, for example, two primary, two secondary two tertiary or one primary and one secondary or one primary and one tertiary or one secondary and one tertiary amino group.
  • Examples include diaminoethane, the isomeric diaminopropanes, the isomeric diamino-butanes, the isomeric diaminohexanes, piperazine, 2,5-dimethylpiperazine, amino-3-aminomethyl-3,5,5-trimethylcyclohexane (isophorone diamine, IPDA), 4,4 ' -Diamino- dicyclohexylmethane, 1, 4-diaminocyclohexane, aminoethylethanolamine, hydrazine, hydrazine hydrate or triamines such as the diethylenetriamine or l, 8-diamino-4-aminomethyloctane or tertiary amines such as triethylamine, tributylamine, dimethylbenzylamine, N- Methyl, N-cyclohexylmorpholine, dimethylcyclohexylamine, dimorpholinodiethyl ether,
  • aliphatic amino alcohols with 2 to about 40, preferably 6 to about 20, carbon atoms, for example triethanolamine, tripropanolamine, tributanolamine, tripentanolamine, l-amino-3,3-dimethyl-pentan-5-ol, 2-aminohexane -2 ', 2 "-diethanolamine, 1-amino-2,5-dimethylcyclohexan-4-ol-2-aminopropanol, 2-aminobutanol, 3-aminopropanol, 1-amino-2-propanol, 2-amino-2-methyl -l-propanol, 5-aminopentanol, 3-aminomethyl-3,5,5-trimethylcyclohexanol, 1-amino-1-cyclopentane-methanol, 2-amino-2-ethyl-l, 3-propanediol, 2- (dimethylaminoethoxy) -ethanol,
  • the perchlorates of heterocyclic compounds which have a cyclic ring system having amino groups are used as ammonium perchlorates.
  • the perchlorates of heterocyclic amino alcohols are used which have at least 2, preferably at least 3 amino groups in the ring.
  • the trimerization products of isocyanates are particularly suitable as the central ring component of the ammonium perchlorates which can be used according to the invention.
  • hydroxyl-containing isocyanurates of the general formula I are suitable
  • grapples Y and the indices m are each the same or different and m represents an integer from 0 to 20 and Y represents a hydrogen atom or a linear or branched, saturated or unsaturated alkyl grappe having 1 to about 10 C atoms.
  • TEEIC tris (hydroxymethyl) isocyanurate
  • ammonium perchlorates are, for example, compounds in which the amino group is bound to a substituted aromatic or heteroaromatic system. which is present, for example aminobenzoic acid, aminosalicylic acid or aminopyridinecarboxylic acid and their suitable derivatives.
  • the ammonium perchlorates used are 2-ethylcarboxypyridinium perchlorate, formamidinium perchlorate, tetra-n-butylphosphonium perchlorate, trimethylsulfoxonium perchlorate, the perchlorate salt of trishydroxyethyl isocyanurate, the perchlorate salt of 2- (diethylamino) n- droxyethyl) morpholinium perchlorate or trioctylammonium perchlorate or mixtures of two or more thereof.
  • a stabilizer composition according to the invention can contain, for example, only one of the above-mentioned onium perchlorates.
  • a stabilizer composition according to the invention contains a mixture of two or more of the above-mentioned onium perchlorates. It can be a mixture of two or more different types of onium perchlorates, i.
  • a stabilizer composition according to the invention is a mixture of two or more onium perchlorates of one type, i.e. H. contains a mixture of two or more ammonium perchlorates and a mixture of two or more sulfonium perchlorates and a mixture of two or more phosphonium perchlorates.
  • a stabilizer composition according to the invention contains a mixture of two or more onium perchlorates, these two or more onium perchlorates can in principle be present in any ratio in the stabilizer composition according to the invention.
  • a stabilizer composition according to the invention contains, based on the total composition, from 0.01 to about 30% by weight, for example about 0.1 to about 20% by weight of an organic onium salt of a perchlorate or a mixture of two or more organic onium salts of perchlorates.
  • a stabilizer composition according to the invention preferably contains an ammonium or a sulfonium salt or a mixture of two or more thereof, in particular an ammonium salt, as the organic onium salt.
  • a stabilizer composition according to the invention can have, in addition to an onium perchlorate, for example one or more of the solvents listed below or one or more of the following additives.
  • a stabilizer composition according to the invention also contains at least one organic solvent.
  • a “solvent” is understood to mean a compound or a mixture of two or more compounds which is liquid within a certain temperature range and is capable of an onium perchlorate present in a composition according to the invention or a mixture of two or more to dissolve such onium perchlorates.
  • a solvent which is suitable in the context of the present invention is at least within a temperature range from approximately 45 to approximately 100 ° C., preferably within a temperature range from approximately 30 to approximately 120 ° C., for example within a temperature range from approximately 15 to approximately 150 ° C. and in particular within a temperature range of about 0 to about 200 ° C liquid.
  • compounds or mixtures of two or more compounds which are suitable as plasticizers for halogen-containing polymers are used as solvents.
  • Suitable solvents in the sense of the present text are therefore, for example, compounds from the group of phthalic acid esters such as dimethyl, diethyl, dibutyl, dihexyl, di- 2-ethylhexyl, di-n-octyl, di-iso-octyl , Di-iso-nonyl, di-iso-decyl, dicyclohexyl, di methylcyclohexyl, dimethylglycol, dibutylglycol, benzylbutyl or diphenyl phthalate and mixtures of phthalates, for example mixtures of alkyl phthalates with 7 to 9 or 9 to 11 carbon atoms in the ester alcohol or mixtures of alkyl phthalates with 6 to 10 and 8 to 10 carbon atoms in ester alcohol.
  • phthalic acid esters such as dimethyl, diethyl, dibutyl, dihexyl, di- 2-ethylhexyl,
  • Particularly suitable for the purposes of the present invention are dibutyl, dihexyl, di-2-ethylhexyl, di-n-octyl, di-iso-octyl, di-iso-nonyl, di-iso-decyl, Di-iso-tridecyl and benzyl butyl phthalate and the mixtures of alkyl phthalates mentioned.
  • esters of aliphatic dicarboxylic acids in particular the esters of adipic, azelaic or sebacic acid or mixtures of two or more thereof.
  • examples of such solvents are di-2-ethylhexyl adipate, di-isooctyl adipate, di-isononyl adipate, di-iso-decyl adipate, benzyl butyl adipate, benzyl octyl adipate, di-2-ethyl hexyl azelate, di-2-ethyl hexyl sebacate and di-iso-decylseb.
  • preference is given to di-2-ethylhexyl acetate and di-iso-octyl adipate.
  • trimellitic acid esters such as tri-2-ethylhexyl trimellithate, tri-iso-tridecyl trimellithate, tri-iso-octyl trimellithate and trimellitic acid esters with 6 to 8, 6 to 10, 7 to 9 or 9 to 11 carbon atoms in the ester group or mixtures of two or more of the compounds mentioned.
  • Suitable solvents are, for example, polymer plasticizers, as described in "Kunststoffadditive”, R. Gumbleter / H. Müller, Carl Hanser Verlag, 3rd edition, 1989, chapter 5.9.6, pages 342-489, or "PVC Technology", WV Titow, 4th edition, Elsevier Publishers, 1984, pages 165-170.
  • polyester plasticizers are considered to be part of the disclosure of the present text.
  • dicarboxylic acids such as adipic, phthalic, azelaic or sebacic acid and diols such as 1,2-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol and neopentyl glycol or diethylene glycol or mixtures of two or more thereof.
  • phosphoric acid esters are also suitable as plasticizers.
  • suitable phosphoric acid esters are tributyl phosphate, tri-2-ethylbutyl phosphate, tri-2-ethylhexyl phosphate, trichloroethyl phosphate, 2-ethyl-hexyl-di-phenyl phosphate, triphenyl phosphate, tricresyl phosphate or trixylenyl phosphate, or mixtures of two or more thereof.
  • a stabilizer composition according to the invention the abovementioned solvents can each be present alone or as a mixture of two or more thereof. If a stabilizer composition according to the invention is a liquid stabilizer composition which contains two or more of the abovementioned compounds as solvents, one or more of the compounds can lie outside the above definition of the term "liquid", provided that the entire solvent mixture is within this definition lies.
  • a stabilizer composition according to the invention contains solvents or solvent mixtures in an amount of about 99.99 to about 2 percent by weight, for example about 98 to about 3 or about 95 to about 5 percent by weight.
  • the solvent content can vary within wide limits, depending on whether the stabilizer composition according to the invention is used as the sole stabilizer or together with one or more additives or is to be in a solid or liquid state.
  • a liquid stabilizer composition according to the present invention can contain about 20 to about 99.99% by weight or about 99 to about 30% by weight or about 95 to about 35% by weight or about 90 to about 40% by weight of solvent .-% or about 85 to about 50 wt .-%.
  • a stabilizer composition according to the invention can contain one or more further additives in an amount of up to up to about 95% by weight, for example up to about 93% by weight or about 91% by weight or about 0 to about 90% by weight or about 1 to about 85% by weight.
  • additives which are distributed in a polymer to be stabilized, preferably dissolved in such a way that a stabilized polymer does not become opaque due to the additives.
  • Solid stabilizer compositions according to the present invention can in principle be produced using any method known to those skilled in the art for mixing different solid or solid and liquid substances, for example by simply mixing an onium perchlorate with other additives.
  • the liquid stabilizer composition according to the invention can be produced in different ways.
  • to produce a stabilizer composition according to the invention it is possible, for example, to dissolve an onium perchlorate in a suitable organic solvent.
  • the present invention therefore relates to a method for producing a stabilizer composition according to the invention, in which an onium perchlorate is dissolved in an organic solvent.
  • an onium perchlorate from an organic compound capable of forming an onium salt or a salt of such a compound by reaction with perchloric acid or a suitable inorganic salt of perchloric acid.
  • This onium perchlorate can then be separated off and dissolved in an appropriate organic solvent.
  • the reaction is preferably carried out in aqueous solution, the perchloric acid or the corresponding suitable salt of perchloric acid usually being added dropwise as an aqueous solution with a concentration of about 50 to about 70% by weight. If it is insoluble in water, the onium perchlorate formed can be separated off as a precipitate by means of customary separation methods, for example filtration or centrifugation.
  • the present invention therefore furthermore relates to a process for the preparation of a stabilizer composition according to the invention, in which an organic compound capable of forming an onium salt or a salt of such a compound is mixed with perchloric acid or an inorganic salt of perchloric acid, the onium salt formed in the process separated organic compound and dissolved in an organic solvent.
  • an alkali perchlorate for example sodium perchlorate or potassium perchlorate
  • an onium chloride in aqueous solution as the inorganic salt of perchloric acid.
  • the water-insoluble organic onium perchlorate can be separated off in the usual way and then dissolved in an organic solvent. If necessary, water can also be removed from the organic onium perchlorate in an intermediate step.
  • the organic compound used to form an onium salt forms a water-soluble organic perchlorate
  • a compound which forms a water-soluble chloride is used as the inorganic salt of perchloric acid.
  • the water-soluble chloride can be separated off in the usual way.
  • the soluble onium perchlorate can then be freed of water in the usual way.
  • a water-soluble organic onium chloride is used as the organic compound capable of forming an onium salt
  • silver perchlorate is preferably used as the inorganic salt of perchloric acid.
  • silver perchlorate is added to the water-soluble organic onium chloride in aqueous solution
  • an insoluble silver chloride forms a precipitate and an aqueous solution of an organic onium perchlorate is formed.
  • the precipitate is then filtered off and the organic onium perchlorate in aqueous solution is isolated by customary separation methods, for example by distilling off the water.
  • the present invention therefore also relates to a process for the preparation of a stabilizer combination according to the invention, in which an organic onium chloride is used as the organic compound capable of forming an onium salt and an alkali perchlorate is used as the inorganic salt of perchloric acid, the organic onium chloride being mixed with an aqueous solution of the alkali perchlorate is, whereby a water-soluble organic onium perchlorate and alkali chloride is formed and the water-soluble organic onium perchlorate is separated.
  • an onium perchlorate and a stabilizer composition according to the invention is not only possible from an aqueous solution. It is also possible to produce an appropriate onium perchlorate in organic solution.
  • an aqueous solution of an organic compound capable of forming an onium salt or a salt of such a compound is mixed with aqueous perchloric acid or an aqueous solution of an inorganic salt of perchloric acid.
  • An organic onium perchlorate is formed, which remains in the organic solution. It is possible to work both in organic solvents that are not miscible with water and in organic solvents that are miscible with water. The water is then removed from the mixture.
  • the present invention therefore also relates to a process for producing a stabilizer composition according to the invention, in which an organic solution of an organic compound capable of forming an onium salt or a salt of such a compound is admixed with aqueous perchloric acid or an aqueous solution of an inorganic salt of perchloric acid, where a solution of an organic onium perchlorate is formed.
  • a stabilizer composition according to the invention can, as is evident from the processes described by way of example, in principle contain any suitable compound as a solvent.
  • a stabilizer composition according to the invention can contain a compound as a solvent or as a component of the solvent, which compound serves as the basis for the production of an onium chlorate, in particular can serve as the basis for the production of an onium perchlorate contained in a stabilizer composition according to the invention.
  • a stabilizer composition according to the invention can contain, in addition to the obligatory compounds already described above (onium perchlorate or onium perchlorate and at least one organic solvent), one or more further additives in an amount mentioned above.
  • additives are listed below which are suitable in principle for use in a stabilizer composition according to the invention alone or as a mixture of two or more thereof.
  • aminouracil compounds of the general formula II are suitable as additives in the context of the present invention
  • radicals R and R are each independently of one another hydrogen, an optionally substituted linear or branched, saturated or unsaturated aliphatic alkyl radical having 1 to 44 C atoms, an optionally substituted saturated or unsaturated cycloalkyl radical having 6 to 44 C atoms or an optionally substituted aryl radical having 6 to 44 carbon atoms or an optionally substituted aralkyl radical having 7 to 44 carbon atoms or the radical R 1 is an optionally substituted acyl radical having 2 to 44 carbon atoms and the radical R 3 is hydrogen , an optionally substituted linear or branched, saturated or unsaturated aliphatic hydrocarbon radical with 1 to 44 C atoms, an optionally substituted saturated or unsaturated cycloa- lipatic hydrocarbon radical having 6 to 44 carbon atoms or an optionally substituted aromatic hydrocarbon radical having 6 to 44 carbon atoms.
  • radicals R a , R b , R 4 and R 5 each independently of one another for hydrogen, an optionally substituted linear or branched, saturated or unsaturated aliphatic alkyl radical having 1 to 44 C atoms, one optionally substituted saturated or unsaturated cycloalkyl radical having 6 to 44 carbon atoms or an optionally substituted aryl radical having 6 to 44 carbon atoms or an optionally substituted aralkyl radical having 7 to 44 carbon atoms or the radical R 4 is an optionally substituted acyl radical with 2 up to 44 carbon atoms or the radicals R 4 and R 5 are linked to form an aromatic or heterocyclic system and in which the radical R 6 is hydrogen, an optionally substituted, linear or branched, saturated or unsaturated aliphatic alkyl or alkylene radical or oxyalkyl radical or oxyalkylene or mercaptoalkyl or mercaptoalkylene or aminoalkyl or amine
  • a compound based on an ⁇ , ⁇ -unsaturated ⁇ -aminocarboxylic acid in particular a compound based on ⁇ -aminocrotonic acid, is used as the compound of the general formula I.
  • the esters or thioesters of the corresponding aminocarboxylic acids with monohydric or polyhydric alcohols or mercaptans are particularly suitable here, where X in the cases mentioned is in each case O or S.
  • radical R 6 together with X represents an alcohol or mercaptan radical
  • a radical can be composed, for example, of methanol, ethanol, propanol, isopropanol, butanol, 2-ethylhexanol, isooctanol, isononanol, decanol, lauryl alcohol, myristyl alcohol, palmityl alcohol , Stearyl alcohol, ethylene glycol, propylene glycol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, 1,10-decanediol, diethylene glycol, thio-diethanol, trimethylolpropane, glycerin, tris (2-hydroxymethyl) isocyanurate , Triethanolamine, pentaerythritol, di-trimethylolpropane, diglycerol, sorbitol, mannitol, xylitol
  • a compound of the general formula III is used in which R is a linear alkyl radical having 1 to 4 carbon atoms, R 5 is hydrogen and R 6 is a linear or branched, saturated, mono- to hexavalent alkyl or alkylene radical having 2 to 12 carbon atoms or a linear, branched or cyclic 2- to 6-valent ether alcohol radical or thioether alcohol radical.
  • Suitable compounds of the general formula III include, for example,
  • Aminocrotonic acid stearyl ester 1,4-butanediol-di (ß-aminocrotonic acid) ester, thio-diethanol-ß-aminocrotonic acid ester, trimethylolpropane-tri-ß-aminocrotonic acid ester, pentaerythritol-tetra-ß-aminocrotonic acid ester, dipentaerythritol-aminocrotonate and the like-aminocrotonic acid.
  • the Compounds mentioned can be contained in a stabilizer composition according to the invention either alone or as a mixture of two or more of them.
  • compounds of the general formula III are, for example, compounds in which the radicals R 4 and R 5 are linked to form an aromatic or heteroaromatic system, for example aminobenzoic acid, aminosalicylic acid or aminopyridinecarboxylic acid and their suitable derivatives.
  • Suitable additives are compounds which have a mercapto-functional sp 2 -hybridized carbon atom, carbazoles, carbazole derivatives or 2,4-pyrrolidinedione or 2,4-pyrrolidinedione derivatives.
  • the sp - hybridized carbon atom can be part of an optionally substituted aliphatic compound or part of an aromatic system.
  • Suitable types of compounds are, for example, thiocarbamic acid derivatives, thiocarbamates, thiocarboxylic acids, thiobenzoic acid derivatives, thioacetone derivatives or thiourea or thiourea derivatives.
  • thiourea or a thiourea derivative is used as an additive with at least one mercapto-functional, sp 2 -hybridized carbon atom.
  • Epoxy compounds are also suitable as additives.
  • examples of such epoxy compounds are epoxidized soybean oil, epoxidized olive oil, epoxidized linseed oil, epoxidized castor oil, epoxidized peanut oil, epoxidized corn oil, epoxidized cottonseed oil and glycidyl compounds.
  • 1,3-dicarbonyl compounds in particular the ⁇ -diketones and ⁇ -keto esters.
  • dicarbonyl compounds of the general formula R ' C (O) CHR “ -C (O) R " as described, for example, on page 5 of EP-1 046 668, to which, in particular, with regard to the Radicals R ', R "and R'" is expressly referred to and the disclosure of which is considered to be part of the disclosure of the present text.
  • Hydroxycapronylbenzoylmethane tribenzoylmethane, bis (4-methylbenzoyl) methane, benzoyl-p-chlorobenzoylmethane, bis (2-hydroxybenzoyl) methane, 4-methoxybenzoylbenzoylmethane, bis (4-methoxybenzoyl) methane, benzoyllacetylmethyl, phenyl 1 Stearoyl-4-methoxybenzoylmethane, bis (4-tert-butylbenzoyl) methane, benzoylphenylacetylmethane, bis (cyclohexanoyl) methane, dipivaloylmethane, 2-
  • 1,3-diketo compounds can be contained in an inventive stabilizer composition in an amount of up to about 20% by weight, for example up to about 10% by weight.
  • polyols are, for example, pentaerythritol, dipentaerythritol, tripentaerythritol, bistrimethylolpropane, inositol, polyvinyl alcohol, Bistrimetylolethan, trimethylolpropane, sorbitol, maltitol, isomaltitol, lactitol, lycasin, mannitol, lactose, leucrose, tris (hydroxymethyl) isocyanurate, palatinite, tetramethylolcyclohexanol, Tetramethylolcyclopenta - nol, tetramethylolcycloheptanol, glycerol, diglycerol, polyols.
  • the polyols suitable as additives can be contained in a stabilizer composition according to the invention in an amount of up to about 30% by weight, for example up to about 10% by weight.
  • Suitable as additives are, for example, sterically hindered amines as mentioned on pages 7 to 27 of EP-A 1 046 668. Reference is expressly made to the sterically hindered amines disclosed therein, the compounds mentioned there are considered to be part of the disclosure of the present text.
  • the sterically hindered amines suitable as additives can be present in an inventive stabilizer composition in an amount of up to about 30% by weight, for example up to about 10% by weight.
  • a stabilizer composition according to the invention can furthermore contain, as an additive, an organotin compound or a mixture of two or more organotin compounds.
  • organotin compounds are, for example, methyltin tris (isooctyl thioglycolate), methyltin tris (isooctyl 3-mercaptopropionate), methyltin tris (isodecyl thioglycolate), dimethyltin bis (isooctyl thioglycolate), dibutyltin (isooctyl thioglycolate), monobutyltin tris (isooctyl thioglycolate), dioctyltin bis (isooctyl thioglycolate), monooctyltin tris (isooctyl thioglycolate) or dimethyltin bis- (2-ethylhexaptopylate).
  • organotin compounds mentioned in EP-A 0 742 259 on pages 18 to 29 and described in their preparation can be used in the context of the stabilizer compositions according to the invention. Reference is expressly made to the above-mentioned disclosure, the compounds mentioned there and their preparation being understood as part of the disclosure of the present text.
  • a stabilizer composition according to the invention can contain the organotin compounds described in an amount of up to about 40% by weight, in particular up to about 20% by weight.
  • a stabilizer composition according to the invention can contain organic phosphite esters with 1 to 3 identical, pairwise identical or different organic radicals.
  • Suitable organic radicals are, for example, linear or branched, saturated or unsaturated alkyl radicals having 1 to 24 carbon atoms, optionally substituted alkyl radicals having 6 to 20 carbon atoms or optionally substituted aralkyl radicals having 7 to 20 carbon atoms.
  • organic phosphite esters are tris (nonylphenyl), trilauryl, tributyl, trioctyl, tridecyl, tridodecyl, triphenyl, octyldiphenyl, dioctylphenyl, tri (octylphenyl), tribenzyl, butyl dikresyl -, octyl-di (octylphenyl) -, tris- (2-ethylhexyl) -, tritolyl-, tris- (2-cyclohexyl-phenyl) -, tri- ⁇ -naphthyl-, tris- (phenylphenyl) -, tris- ( 2-phenylethyl), tris (dimethylphenyl), tricresyl or tris (p-nonylphenyl) phosphite or tristearyl sorbi
  • a stabilizer composition according to the invention can contain the phosphite compounds described in an amount of up to about 30% by weight, in particular up to about 10% by weight.
  • a stabilizer composition according to the invention can also contain blocked mercaptans as additives, as are mentioned on pages 4 to 18 of EP-A 0 742 259.
  • the disclosure in the cited document is expressly referred to and is understood to be part of the disclosure of the present.
  • a stabilizer composition according to the invention can contain the blocked mercaptans described in an amount of up to about 30% by weight, in particular up to about 10% by weight.
  • a stabilizer composition according to the invention can furthermore contain lubricants such as montan wax, fatty acid esters, purified or hydrogenated natural or synthetic triglycerides or partial esters, polyethylene waxes, amide waxes, chlorinated paraffins, glycerol esters or alkaline earth soaps, provided that these lubricants do not fall under the term “solvent” in the sense of the present text Lubricants that can be used as additives are also described in "Kunststoffadditive", R. Gumbleter / H. Müller, Carl Hanser Verlag, 3rd edition, 1989, pp. 478 - 488.
  • lubricants such as montan wax, fatty acid esters, purified or hydrogenated natural or synthetic triglycerides or partial esters, polyethylene waxes, amide waxes, chlorinated paraffins, glycerol esters or alkaline earth soaps, provided that these lubricants do not fall under the term “solvent” in the sense
  • Fat ketones such as these are also suitable as additives are described in DE 4,204,887, and silicone-based lubricants, as they are called, for example, EP-A 0 259 783, or combinations thereof, as they are mentioned in EP-A 0 259 783.
  • the documents mentioned are hereby expressly referred to, their disclosure regarding lubricants is part of the disclosure the present text.
  • a stabilizer composition according to the invention can contain the described lubricants in an amount of up to about 70% by weight, in particular up to about 40% by weight.
  • additives for stabilizer compositions according to the present invention are organic plasticizers, provided that these plasticizers do not already fall under the term “solvent” in the sense of the present text.
  • Suitable plasticizers are, for example, the compounds mentioned above in the description of the solvents from the group of phthalic acid esters, such as dimethyl, diethyl, dibutyl, dihexyl, di-2-ethylhexyl, di-n-octyl, di- iso-octyl, di-isononyl, di-iso-decyl, dicyclohexyl, dimethylcyclohexyl, dimethylglycol, dibutylglycol, benzylbutyl or diphenylphthalate as well as mixtures of phthalates, for example mixtures of alkyl phthalates with 7 up to 9 or 9 to 11 carbon atoms in the ester alcohol or mixtures of alkyl phthalates with 6 to 10 and 8 to 10 carbon atoms in the ester alcohol.
  • Particularly suitable for the purposes of the present invention are dibutyl, dihexyl, di-2-ethylhexyl, di-n- octyl, di-iso-octyl, di-iso-nonyl, di-iso-decyl, di-iso-tridecyl and benzyl butyl phthalate and the mixtures of alkyl phthalates mentioned.
  • plasticizers are the esters of aliphatic dicarboxylic acids, in particular the esters of adipic, azelaic or sebacic acid or mixtures of two or more thereof.
  • plasticizers are di-2-ethylhexyl adipate, di-isooctyl adipate, di-iso-nonyl adipate, di-iso-decyl adipate, benzyl butyl adipate, benzyl octyl adipate, di-2-ethylhexyl azelate, di-2-ethylhexyl sebacate and di-iso-decylseb.
  • preference is given to di-2-ethylhexyl acetate and di-iso-octyl adipate.
  • Trimellitic acid esters such as tri-2-ethylhexyl trimellithate, tri-iso-tridecyl trimellithate, tri-iso-octyl trimellithate and trimellitic acid esters with 6 to 8, 6 to 10, 7 to 9 or 9 to 11 carbon atoms in the ester group are also suitable as plasticizers or mixtures of two or more of the compounds mentioned.
  • plasticizers are, for example, polymer plasticizers, as described in "Kunststoffadditive”, R. Gumbleter / H. Müller, Carl Hanser Verlag, 3rd edition, 1989, chapter 5.9.6, pages 412-415, or "PVC Technology”, W.V. Titow, 4th edition, Elsevier Publishers, 1984, pages 165-170.
  • polyester plasticizers are, for example, dicarboxylic acids such as adipic, phthalic, azelaic or sebacic acid and diols such as 1,2-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol or diethylene glycol or mixtures of two or more thereof.
  • dicarboxylic acids such as adipic, phthalic, azelaic or sebacic acid
  • diols such as 1,2-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol or diethylene glycol or mixtures of two or more thereof.
  • phosphoric acid esters are also suitable as plasticizers.
  • suitable phosphoric acid esters are tributyl phosphate, tri-2-ethylbutyl phosphate, tri-2-ethylhexyl phosphate, trichloroethyl phosphate, 2-ethyl-hexyl-diphenyl phosphate, triphenyl phosphate, tricresyl phosphate or trixylenyl phosphate, or mixtures of two or more thereof.
  • plasticizers are chlorinated hydrocarbons (paraffins) or hydrocarbons as described in "Kunststoffadditive", R. Gumbleter / H. Müller, Carl Hanser Verlag, 3rd edition, 1989, chapter 5.9.14.2, pp. 422-425 and chapter 5.9.14.1, p. 422.
  • a stabilizer composition according to the invention can contain the plasticizers described in an amount of up to about 99.5% by weight, in particular up to about 30% by weight, up to about 20% by weight or up to about 10% by weight ,
  • the lower limit for the plasticizers described as part of the stabilizer compositions according to the invention is about 0.1% by weight or more, for example about 0.5% by weight, 1% by weight, 2 % By weight or 5% by weight.
  • the stabilizer compositions according to the invention can contain antioxidants, UV absorbers or light stabilizers. Suitable antioxidants are described, for example, on pages 33 to 35 of EP-A 1 046 668. Suitable UV absorbers and light stabilizers are listed on pages 35 and 36. Both disclosures are expressly referred to here, the disclosures being considered part of the present text.
  • a stabilizer composition according to the invention can contain, in addition to a polymer and a stabilizer composition according to the invention, further additives which are not soluble in the stabilizer compositions according to the invention.
  • all additives are suitable, for example those which do not or not significantly affect the transparency of a polymer composition produced with the aid of such a stabilizer composition.
  • hydrotalcites hydrocalumites, zeolites and alkali alumocarbonates.
  • Suitable hydrotalcites, hydrocalumites, zeolites and alkali alumocarbonates are described, for example, in EP-A 1 046 668 on pages 27 to 29, EP-A 256 872 on pages 3, 5 and 7, and DE-C 41 06 411 on page 2 and 3 or DE-C 41 06 404 on page 2 and 3 or DE-C 198 60 798.
  • EP-A 1 046 668 on pages 27 to 29, EP-A 256 872 on pages 3, 5 and 7, and DE-C 41 06 411 on page 2 and 3 or DE-C 41 06 404 on page 2 and 3 or DE-C 198 60 798.
  • hydrotalcites, hydrocalumites, zeolites and alkali alumocarbonates suitable as additives can be present in an inventive stabilizer composition in an amount of up to about 50% by weight, for example from 0 to about 30% by weight.
  • the metal oxides, metal hydroxides or metal soaps suitable as additives preferably have a divalent cation; the cations of calcium or zinc or mixtures thereof are particularly suitable.
  • carboxylic acid anions include anions of monovalent carboxylic acids such as acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid, oenanthic acid, octanoic acid, neodecanoic acid, 2-ethylhexanoic acid, pelargonic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, myristic acid, lauric acid, palmitic acid, palmitic acid, palmitic acid 12-hydroxystearic acid, 9,10-dihydroxystearic acid, oleic acid, 3,6-dioxaheptanoic acid, 3,6,9-trioxadecanoic acid, behenic acid, benzoic acid, p-tert-butylbenzoic acid, dimethylhydroxybenzoic acid, 3,5-di-tert- butyl-4-hydroxybenzoic acid, tolylic acid, dimethyl
  • metal soaps are preferably used, the anions of which are derived from saturated or unsaturated carboxylic acids or hydroxycarboxylic acids having about 8 to about 20 C atoms. Stearates, oleates, laurates, palmitates, behenates, versatates, hydroxystearates, dihydroxystearates, p-tert-butylbenzoates or (iso) octanoates of calcium or zinc or mixtures of two or more thereof are particularly preferred.
  • a polymer composition according to the invention has calcium stearate or zinc stearate or a mixture thereof.
  • a stabilizer composition according to the invention can contain the metal oxides, metal hydroxides or metal soaps mentioned or a mixture of two or more thereof in an amount of up to about 50% by weight, for example in an amount of up to about 30% by weight.
  • a stabilizer composition according to the invention can also contain fillers as described in the "Handbook of PVC Formulating", EJ Wickson, John Wiley & Sons, Inc., 1993, pages 393-449 or reinforcing agents as described in the "Taschenbuch der Kunststoffadditive”, R. Gumbleter / H. Müller, Carl Hanser Verlag, 1990, pages 549-615, or contain pigments.
  • a stabilizer composition according to the invention may also contain impact modifiers and processing aids, gelling agents, antistatic agents, biocides, metal deactivators, optical brighteners, flame retardants and antifogging compounds.
  • impact modifiers and processing aids gelling agents, antistatic agents, biocides, metal deactivators, optical brighteners, flame retardants and antifogging compounds.
  • Suitable compounds of these classes of compounds are described, for example, in "Kunststoff Additive”, R. Kessler / H. Müller, Carl Hanser Verlag, 3rd edition, 1989 and in the "Handbook of PVC Formulating", E.J. Wilson, J. Wiley & Sons, 1993.
  • the onium salts of perchlorates are suitable for stabilizing halogen-containing organic polymers.
  • the present invention therefore relates to a polymer composition containing at least one halogenated organic polymer and an onium salt of a perchlorate.
  • the amounts of onium salts to be used correspond to the amounts described in the context of the further text for the stabilizer compositions according to the invention.
  • halogen-containing organic polymers are polymers of vinyl chloride, vinyl resins which contain vinyl chloride units in the polymer backbone, copolymers of vinyl chloride and vinyl esters of aliphatic acids, in particular vinyl acetate, copolymers of vinyl chloride with esters of acrylic and methacrylic acid or acrylonitrile or mixtures of two or more thereof, copolymers of vinyl chloride with diene compounds or unsaturated dicarboxylic acids or their anhydrides, for example copolymers of vinyl chloride with diethyl maleate, diethyl fumarate or maleic anhydride, post-chlorinated polymers and copolymers of vinyl chloride, copolymers of vinyl chloride and vinylidene chloride with unsaturated aldehydes, ketones and other compounds such as acrolein, cronones - nylmethyl ketone, vinyl methyl ether, vinyl isobutyl ether and the like, polymers and copolymers of vinyli
  • the graft polymers of PVC with EVA, ABS or MBS are also suitable for stabilization with the stabilizer compositions according to the invention.
  • Preferred substrates for such graft copolymers are also the homo- and copolymers mentioned above, in particular mixtures of vinyl chloride homopolymers with other thermoplastic or elastomeric polymers, in particular blends with ABS, MBS, NBR, SAN, EVA, CPE; MBAS, PAA (polyalkyl acrylate), PAMA (polyalkyl methacrylate), EPDM, polyamides or polylactones.
  • halogenated and non-halogenated polymers for example mixtures of the above-mentioned non-halogenated polymers with PVC, in particular mixtures of polyurethanes and PVC, are also suitable for stabilization with the stabilizer compositions according to the invention.
  • recyclates of chlorine-containing polymers can also be stabilized with the stabilizer compositions according to the invention, with basically all recyclates of the above-mentioned halogenated polymers being suitable for this.
  • PVC recyclate for example, is suitable in the context of the present invention.
  • Another object of the present invention therefore relates to a polymer composition containing at least one halogenated polymer and a stabilizer composition according to the invention.
  • a polymer composition according to the invention contains the stabilizer composition according to the invention in an amount of 0.1 to 20 phr, in particular approximately 0.5 to approximately 15 phr or approximately 1 to approximately 12 phr.
  • the unit phr stands for "per hundred resin” and thus relates to parts by weight per 100 parts by weight of polymer.
  • a polymer composition according to the invention preferably contains PVC as a halogenated polymer, the PVC content being in particular at least about 20, preferably at least about 50% by weight, for example at least about 80 or at least about 90% by weight.
  • the present invention also relates to a method for stabilizing halogen-containing polymers, in which a halogen-containing polymer or a mixture of two or more halogen-containing polymers or a mixture of one or more halogen-containing polymers and one or more halogen-free polymers is mixed with a stabilizer composition according to the invention.
  • the mixing of polymers or polymers and the stabilizer composition according to the invention can, in principle, take place at any time before or during the processing of the polymer.
  • the stabilizer composition can be mixed with the polymer in powder or granule form before processing.
  • a polymer composition according to the invention can be brought into a desired shape in a known manner. Suitable processes are, for example, calendering, extruding, injection molding, sintering, extrusion blowing or the plastisol process. A polymer composition according to the invention can also be used, for example, for the production of foams. In principle, the polymer compositions according to the invention are suitable for the production of rigid or, in particular, soft PVC. A polymer composition according to the invention can be processed into moldings. The present invention therefore also relates to moldings containing at least one stabilizer composition according to the invention or a polymer composition according to the invention.
  • the term “molded body” basically encompasses all three-dimensional structures that can be produced from a polymer composition according to the invention.
  • the term “molded body” encompasses, for example, wire jackets, automotive components, for example automotive components such as are used in the interior of the automobile, in the engine compartment or on the outer surfaces, cable insulating rods, decorative foils, agricultural foils, hoses, sealing profiles, office foils, hollow bodies ( Bottles), packaging films (thermoformed films), blown films, pipes, foams, heavy profiles (window frames), light wall profiles, building profiles, sidings, fittings, plates, foam plates., Coextradates with recycled core or housing for electrical equipment or machines, for example computers or household appliances.
  • moldings which can be produced from a polymer composition according to the invention are synthetic leather, floor coverings, textile coatings, wallpapers, coil coatings or underbody protection for motor vehicles.
  • the present invention also relates to the use of a stabilizer composition according to one of claims 1 to 4 or a stabilizer composition produced according to one of claims 5 to 8 or a polymer composition according to one of claims 9 or 10 in the production of polymeric moldings or surface coating compositions.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne une composition stabilisante, contenant au moins un perchlorate d'onium et au moins un solvant organique, destinée à des polymères de préférence halogénés.
EP02795118A 2001-12-11 2002-12-06 Composition stabilisante, production et utilisation de ladite composition Ceased EP1453905A2 (fr)

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DE10160662A DE10160662A1 (de) 2001-12-11 2001-12-11 Stabilisatorzusammensetzung, deren Herstellung und Verwendung
PCT/EP2002/013881 WO2003054072A2 (fr) 2001-12-11 2002-12-06 Composition stabilisante, production et utilisation de ladite composition

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CN1289584C (zh) 2006-12-13
US20050040367A1 (en) 2005-02-24
WO2003054072A3 (fr) 2004-06-17
DE10160662A1 (de) 2003-06-18
AU2002361023A1 (en) 2003-07-09
CN1602337A (zh) 2005-03-30
WO2003054072A2 (fr) 2003-07-03

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