Polymer moulding compositions stabilised with phosphorous acid esters

Abstract

Thermoplastic moulding compositions containingA) polymers selected from the group comprising polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers, and thermoplastic polyurethanes, andB) esters of phosphorous acid which contain at least one oxetane group and at least one radical of a dihydric or polyhydric phenol per molecule, andoptionallyC) fillers and reinforcing materials,D) flame retardant additives,E) elastomeric modifiers.

Description

This invention relates to moulding compositions comprising polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers and/or thermoplastic polyurethanes, which contain phosphorous acid esters.

Phosphorous acid esters are added to polycarbonate and polyester, particularly to polyalkylene terephthalate moulding compositions, for stabilisation during thermal loading, particularly for preventing discoloration phenomena during the production of these products, during compounding and subsequent granulation of the products and during the processing of the products to form thermoplastic moulded bodies (e.g. DE-OS 2 140 207, DE-OS 2 255 639 and DE-OS 2 615 341).

Furthermore, it is known that discoloration during production and processing can be reduced by the addition of tertiary phosphorous acid esters to polycarbonate (DE-AS 1 128 653 and U.S. Pat. No. 3 305 520).

It is also known that phosphorous acid esters can be used in combination with Ba, Sr or Ca carbonate for the stabilisation of mixtures containing brominated polycarbonate (DE-OS 2 064 599).

It has now been found that a significant reduction in discoloration behaviour is observed, particularly in ageing tests, with moulding compositions comprising polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers and/or thermoplastic polyurethanes, and which contain phosphorous acid esters. The moulding compositions according to the invention possess a good resistance to hydrolysis and good thermal stability.

The present invention relates to thermoplastic moulding compositions containing

A) polymers selected from the group comprising polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers, and thermoplastic polyurethanes, and

B) esters of phosphorous acid which contain at least one oxetane group and at least one radical of a dihydric or polyhydric phenol per molecule, and

optionally

C) fillers and reinforcing materials,

D) flame retardant additives,

E) elastomeric modifiers.

The content of polymers as defined by component A) is generally 20 to 99.99, preferably 40 to 99.97, particularly 60 to 99.95 parts by weight.

The content of phosphorous acid esters as defined by component B) in the moulding composition is generally 0.01 to 2.5, preferably 0.03 to 1.0, particularly 0.05 to 0.4 parts by weight (with respect to the total mixture).

If fillers and reinforcing materials are added to the mixture, preferably up to 45, most preferably 10 to 40 parts by weight of fillers and reinforcing materials are used.

Mineral flame retardant additives are preferably added in amounts of 30 to 55 parts by weight.

The moulding compositions according to the invention may contain up to 20, preferably 3 to 18, particularly 6 to 15 parts by weight of halogenated compounds, and up to 8, preferably 2 to 6, parts by weight of antimony compounds, particularly antimony trioxide or antimony pentoxide.

EIastomeric modifiers as defined by component E) are preferably added in amounts of up to 30 parts by weight, most preferably 5 to 25 parts by weight. The quantitative data are quoted with respect to the total mixture in each case.

Component A

Polyolefines according to the invention are polymers of aliphatic unsaturated hydrocarbons, such as ethylene, propylene, butylene or isobutylene for example, which are obtained by customary methods, e.g. radical-initiated polymerisation, and which have weight average molecular weights M.sub.W (measured by gel chromatography methods) between 5000 and 3,000,000. Both high pressure polyolefine and low pressure polyolefine can be used. The unsaturated hydrocarbons may also be copolymerised in the known manner with other vinyl monomers, such as vinyl acetate, acrylic acid or acrylic acid esters, for example, wherein the maximum content of vinyl monomers is 30% by weight, preferably up to 25% by weight.

Polyethylene and polypropylene are preferred.

Styrene polymers in the sense of the invention are homopolymers of styrene (polystyrene) or copolymers, preferably with acrylonitrile and/or maleic acid esters, which are produced from the monomers or from the mixture of monomers by suspension polymerisation in the presence of catalysts, for example. The styrene polymers generally have weight average molecular weights of 10,000 to 600,000 (measured in DMF at a concentration of 5 g/liter and at 20.degree. C.).

C.sub.1 -C.sub.4 alkyl methacrylate copolymers which are suitable according to the invention include known polymers of methyl, ethyl, propyl and butyl methacrylates, preferably methyl and ethyl methacrylates. It should be understood that these methacrylic acid esters include both homopolymers and copolymers. In addition, amounts up to a maximum of 9.5% by weight, with respect in each case to the total weight of these unsaturated monomers and methacrylic acid esters, of other ethylenically unsaturated, copolymerisable monomers can be copolymerised, so that the C.sub.1 -C.sub.4 -alkyl methacrylate copolymers which are suitable according to the invention are synthesised from 90.5% by weight to 100% by weight of alkyl methacrylate units and from 9.5% by weight to 0% by weight of other ethylenically unsaturated monomer units.

Examples of other ethylenically unsaturated monomers include (meth)acrylonitrile, (.alpha.-methyl)styrene, bromostyrene, vinyl acetate, acrylic acid C.sub.1 -C.sub.8 -alkyl esters, (meth)acrylic acid aryl esters, (meth)acrylic acid, ethylene, propylene, N-vinylpyrrolidone, vinyl sulphonic acid (salts) or styrenesulphonic acid (salts).

The C.sub.1 -C.sub.4 -alkyl methacrylate copolymers constitute substances which are soluble in defined organic solvents and which have a linear or branched structure. Polymers containing gels, i.e. those with crosslinked structures, are not polymers (b) in the sense of the invention.

The polyalkyl methacrylates can be produced by known polymerisation processes, but are preferably produced by radical-initiated or thermal polymerisation. Processes in emulsion, bulk, suspension or dispersion, particularly emulsion polymerisation, and preferably bulk or solution polymerisation, are suitable as polymerisation processes. The molecular weights may be varied within broad ranges by known measures determined by the process used, for example by the use of mercaptans as regulators. The polyalkyl methacrylates which can be used according to the invention usually have molecular weights (or limiting viscosity numbers or melt viscosities) which make it sensible to process them by thermoplastic injection moulding or extrusion.

Polyphenylene sulphides in the sense of the invention are described in EP-A 171 021, for example.

Thermoplastic polyurethanes in the sense of the invention are reaction products of diisocyanates with completely or predominantly aliphatic oligo- and/or polyesters and/or ethers and with one or more chain extenders. These thermoplastic polyurethanes are substantially linear and possess thermoplastic processing characteristics.

These thermoplastic polyurethanes are either known or can be produced by known methods (see U.S. Pat. No. 3,214,411, J. H. Saunders and K. C. Frisch, "Polyurethanes, Chemistry and Technology", Vol. II, pages 299 to 451, Interscience Publishers, New York, 1964, and Mobay Chemical Corporation, "A Processing Handbook for Texin Urethane Elastoplastic Materials", Pittsburgh, Pa., for example).

Examples of starting materials for the preparation of the oligoesters and polyesters include adipic acid, succinic acid, suberic acid, sebacic acid, oxalic acid, methyladipic acid, glutaric acid, pimelic acid, azelaic acid, phthalic acid, terephthalic acid and isophthalic acid.

Adipic acid is preferred in this respect.

Examples of glycols for preparing the oligoesters include ethylene glycol, 1,2- and 1,3-propylene glycol, 1,2-, 1,3-, 1,4-, 2,3-, and 2,4-butanediol, hexanediol, bis-hydroxymethyl cyclohexane, diethylene glycol and 2,2-dimethylpropylene glycol. In addition, small amounts of up to 1 mole % of trifunctional alcohols, or alcohols with a functionality greater than three, e.g. trimethylolpropane, glycerol, hexanetriol, etc., can be used in conjunction with the glycols.

The resulting hydroxyl-oligo- or polyesters have a molecular weight of at least 600, a hydroxyl number of about 25 to 190, preferably about 40 to 150, an acid number of about 0.5 to 2, and a water content of about 0.01 to 0.2%.

The oligo-esters or polyesters also include oligomeric or polymeric lactones, such as oligo-caprolactone or poly-caprolactone for example, and aliphatic polycarbonates, such as poly-1,4-butanediol carbonate or poly-1,6-hexanediol carbonate, for example.

A particularly suitable oligo radical, which can be used as a starting material for the thermoplastic polyurethanes, is prepared from adipic acid and a glycol which contains at least one primary hydroxyl group. Condensation is terminated when an acid number of 10, preferably about 0.5 to 2, is reached. The water formed during the reaction is separated simultaneously or subsequently, so that the final water content is within the range of about 0.01 to 0.05%, preferably 0.01 to 0.02%.

Examples of oligo- or polyethers for producing the thermoplastic polyurethanes include those based on tetramethylene glycol, propylene glycol and ethylene glycol.

Polyacetates are also to be understood as polyethers, and are usable.

The oligoethers or polyethers should have average molecular weights Mn (number average, determined via the OH number of the products) of 600 to 2000, preferably of 1000 to 2000.

4,4'-diphenylmethane diisocyanate is preferably used as the organic diisocyanate for producing the polyurethanes as defined by component A. It should contain less than 5% of 2,4'-diphenylmethane diisocyanate and less than 2% of the dimers of diphenylmethane diisocyanate. It is also desirable that its acidity, calculated as HCl, fails within the range of about 0.005 to 0.2%. The acidity, calculated as HCl, is determined by extracting the chloride from the isocyanate in hot, aqueous methanol solution or by releasing the chloride by hydrolysis with water and titrating the extract with standard silver nitrate solution, in order to ascertain the chloride ion concentration present therein.

Other diisocyanates may also be used for producing the thermoplastic polyurethanes, for example the diisocyanates of ethylene, ethylidene, propylene, butylene, 1,3-cyclopentylene, 1,4-cyclohexylene, 1,2-cyclohexylene, 2,4-tolylene, 2,6-tolylene, p-phenylene, n-phenylene, xylene, 1,4-naphthylene, 1,5-naphthylene, 4,4'-diphenylene, 2,2-diphenylpropane 4,4'-diisocyanate, azobenzene 4,4'-diisocyanate, diphenylsulphone 4,4'-diisocyanate, dichlorohexanemethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, 1-chlorobenzene-2,4-diisocyanate, furfuryl diisocyanate, dicyclohexylmethane diisocyanate, isophorone diisocyanate, diphenylethane diisocyanate and the bis(isocyanatophenyl) ethers of ethylene glycol, butanediol, etc.

Difunctional organic compounds which contain active hydrogen which is reactive with isocyanates can be used as chain extenders, e.g. diols, hydroxycarboxylic acids, dicarboxylic acids, aliamines, alkanolamines and water. Examples of these include ethylene glycol, propylene glycol, butylene glycol, 1,4-butanediol, butanediol, butinediol, xylylene glycol, amylene glycol, 1,4-phenylene-bis-.beta.-hydroxyethyl ether, 1,3-phenylene-bis-.beta.-hydroxylethyl ether, bis-(hydroxymethyl-cyclohexane), hexanediol, adipic acid, .omega.-hydroxycaproic acid, thiodiglycol, ethylenediamine-, propylene-, butylene-, hexamethylene-, cyclohexylene-, phenylene-, toluylene- and xylylene diamine, diaminodicyclohexylmethane, isophoronediamine, 3,3'-dichlorobenzidine, 3,3'-dinitrobenzidine, ethanolamine, aminopropyl alcohol, 2,2-dimethylpropanolamine, 3-aminocyclohexyl alcohol and p-aminobenzyl alcohol. The molar ratio of oligo- or polyester to difunctional chain extenders varies within the range of 1:1 to 1:50, preferably 1:2 to 1:30.

Apart from difunctional chain extenders, trifunctional chain extenders, or chain extenders having a functionality greater than three, can be used in secondary amounts up to about 5 mole % with respect to the moles of difunctional chain extenders used.

Examples of chain extenders of this type, which are trifunctional or which have a functionality greater than three, include glycerol, trimethylolpropane, hexanetriol, pentaerythritol and triethanolamine.

Monofunctional components, for example butanol, can also be use for producing the thermoplastic polyurethanes as defined by component A.

The diisocyanates, oligoesters, polyesters, polyethers, chain extenders and monofunctional components cited as synthesis components for the thermoplastic polyurethanes are either known from the literature or are obtainable by methods known from the literature.

The known production of the thermoplastic polyurethane component is described in DE-OS 4 309 981, for example.

ABS polymers in the sense of the invention are described in EP-A 345 522, for example.

Component B

Phosphorous acid esters in the sense of the invention are esters of phosphorous acid which contain at least one oxetane group and at least one radical of a dihydric or polyhydric phenol per molecule.

Phosphorous acid esters of formula (I) are preferred, ##STR1## where

n.sub.1 represents 1 or any integer >1, preferably 1 to 9,

n.sub.2 represents 0 or any integer >0, preferably 0 to 2,

n.sub.3 represents 1 or any integer >1, preferably 1 to 9,

R represents alkyl, aralkyl, cycloalkyl, aryl or heteroaryl, wherein at least one of the radicals R constitutes a monoalcohol containing at least one oxetane group, and

Ar represents aryl, which may optionally be substituted by alkyl and/or hydroxy, and where when n.sub.2 .noteq.0 Ar may be the same or different,

and compounds selected from tris-�(3-ethyloxetanyl-3)-methyl!-phosphite, tris-�(3-pentyloxetanyl-3)-methyl!-phosphite, phenyl-bis-�(3-ethyloxetanyl-3)-methyl!-phosphite, 2-phenoxy-spiro(1,3,2-dioxaphosphorinane-5,3'-oxetane), 3,3-bis-�spiro(oxetane-3',5"-(1",3",2"-dioxaphosphorinane-2"))-oxymethyl!-oxetane.

Examples of radicals R which are suitable in formula (I) include: C.sub.1 -C.sub.18 -alkyl, mono- or polynuclear C.sub.3 -C.sub.10 -cycloalkyl, phenyl-C.sub.1 -C.sub.2 -alkyl, mono- or polynuclear C.sub.6 -C.sub.18 -aryl such as phenyl, naphthyl, anthracyl, phenanthryl, biphenyl, phenoxyphenyl or fluorenyl, and also heteroaryls, such as tetrahydrofuryl, for example, wherein the aryl radicals may be substituted by alkyl and/or halogen, such as C.sub.1 -C.sub.18 -alkyl, chlorine and/or bromine, for example.

The radical R may also be a derivative of a C.sub.1 -C.sub.6 monoalcohol containing one or more oxetane groups P.

The heterocyclic radical ##STR2## is to be understood as the oxetane group P, where Z may be H, CH.sub.3, C.sub.2 H.sub.5, n-C.sub.5 H.sub.11, --CH.sub.2 --C.sub.5 H.sub.11, --CH.sub.2 --O--C.sub.6 H.sub.13 or CH.sub.2 --O--C.sub.2 H.sub.5.

The radical R in formula (I) above may also itself represent the oxetane group P, with Z.dbd.H for example.

The radical Ar is derived from phenols containing 2 phenolic hydroxyl groups. The radical Ar is preferably derived from the following compounds: hydroquinone, resorcinol, catechol, di-t-butyl catechol, 4,4'-dihydroxydiphenyl, bis-(hydroxyphenyl)-alkanes, such as C.sub.1 -C.sub.8 -alkylene- or C.sub.2 -C.sub.8 -alkylidene bisphenols for example, bis-(hydroxyphenyl)-cycloalkanes, such as C.sub.5 -C.sub.15 -cycloalkylene- or C.sub.5 -C.sub.15 -cycloalkylene bisphenols for example, .alpha.,.alpha.'-bis-(hydroxyphenyl)-diisopropylbenzene, and the corresponding compounds with alkylated or halogenated nuclei, for example bis-(4-hydroxy-phenyl)-propane-2,2 (bisphenol A), bis-(4-hydroxy-3,5-dichlorophenyl)-propane-2,2 (tetrachlorobisphenyl A), bis-(4-hydroxy-3,5-dibromophenyl)-propane-2,2 (tetrabromobisphenol A), bis-(4-hydroxy-3,5-dimethyl-phenyl)-propane-2,2 (tetramethylbisphenol A), bis-(4-hydroxy-3-methylphenyl)-propane-2,2-cyclohexane-1,1 (bisphenol Z), and also .alpha.,.alpha.'-bis-(4-hydroxyphenyl)-p-diisopropyl-benzene, dihydroxynaphthalenes and dihydroxyanthracenes.

Phloroglucinol and pyrogallol are suitable as phenols containing more than two phenolic hydroxy groups, for example.

Amongst the claimed compounds, compounds of formula (I) are preferred which are derived from 2,2-bis-(hydroxy-phenyl)-alkanes and from monoalcohols containing oxetane groups, i.e. compounds of formula (I) where Ar corresponds to a radical of formula (II) ##STR3## where

R.sup.1 and R.sup.2 are the same or different and represent H, C.sub.1 -C.sub.18 -alkyl, mono- or polynuclear C.sub.3 -C.sub.6 -cycloalkyl, or mono- or polynuclear C.sub.6 -C.sub.18 -aryl,

R.sup.3, R.sup.3', R.sup.4, R.sup.4', R.sup.5, R.sup.5', R.sup.6 and R.sup.6' are the same or different and represent H, C.sub.1 -C.sub.18 -alkyl, mono- or polynuclear C.sub.3 -C.sub.6 -cycloaklyl, mono- or polynuclear C.sub.6 -C.sub.18 -aryl, C.sub.1 -C.sub.18 -alkoxy, or halogen.

The alkyl substituents which are suitable as a substituent for compounds of formula (II) may be unbranched or branched, saturated or unsaturated. Suitable aryl substituents may comprise phenyl or biphenyl, for example. The preferred halogen substituents are Cl or Br.

The compounds of formula (I) in which Ar corresponds to a radical of formula (II) are by the reaction of the corresponding bisphenols of formula (III) ##STR4## where

R.sup.1 to R.sup.6 and R.sup.3' to R.sup.6' have the aforementioned meaning and are obtained in the manner described in DE-OS 2 255 639.

The compounds of the claimed type constitute high-boiling liquids, resins or solids. They are readily soluble in organic solvents, particularly in the solvents used in the production of polycarbonates, and are therefore particularly suitable for use as stabilisers in polycarbonates of high viscosity which are produced or processed at high temperatures.

These compounds, of which some examples are listed below, may be produced and used individually or in a mixture. The phosphites may have a linear or branched structure.

The following survey exemplifies a selection of them: ##STR5##

These phosphorous acid esters of formula (I) are known and can be prepared by the methods described in DE-OS 22 55 639 (=U.S. Pat. Nos. 4,073,769 and 4,323,501). The neutral esters of phosphorous acid which are also cited are likewise known (DE-OS 2 140 207, corresponding to U.S. Pat. No. 3,794,629).

The phosphites of formula (I) according to the invention, in which R is the radical of a monoalcohol containing an oxetane group, may be prepared, for example, by the reaction of a mixture consisting of a monoalcohol R-OH, which contains oxetane groups, and of an aryl compound which contains two or more phenolic hydroxyl groups, for example a bisphenol of formula (III), with triphenyl phosphite in the presence of an alkaline catalyst, wherein the desired product is formed with the splitting off of phenol. A suitable reaction temperature is 100.degree.-180.degree. C.; suitable catalysts include NaOH, NaOCH.sub.3, Na phenolate, Na.sub.2 CO.sub.3, KOH and tributylamine.

The reaction may be conducted in the absence of solvent or with the addition of solvents. The molar ratio of the reactants, namely the monoalcohol R--OH which contains oxetane groups, the aryl compound, and triphenyl phosphite, follows from the final product of formula (I) which is to be prepared.

The phosphites containing oxetane groups as defined by component B) may be added to the polymers either individually or in combination with each other in the said concentrations.

The stabilised polymers may be produced either by adding the phosphite in pure form to the molten polymer or optionally by adding the phosphite in solution in a low-boiling solvent to the polymer. The stabilised polymers can also be produced by saturating the powdered or granulated polymer and in each case optionally minerals, aerosils or other suitable supporting base with the phosphite (optionally with dissolution of the latter in a solvent, such as isopropanol for example) in a suitable mixing apparatus, optionally with subsequent compacting. The polymers according to the invention can also be produced by addition as a batch during the production/compounding process (production of the batch by incorporating the phosphite in the polymer, by extrusion for example), optionally as a batch based on polyalkylene terephthalate or optionally as a batch based on polycarbonate. The batch may be in the form of granules or in the form of a powder. Work-up/processing of the polymers according to the invention is effected by known techniques.

The same applies to the addition of the phosphite to the melt, or in a solvent, during the production of the polymer by known methods.

Component C

Glass fibres, glass spheres, mica, silicates, quartz, french chalk, titanium dioxide, wollastonite, etc., may be used as fillers and reinforcing materials, and may also be surface-treated. Commercially available glass fibres are the preferred reinforcing materials. The glass fibres, which generally have a fibre diameter between 8 and 18 .mu.m, may be used as continuous fibres or as chopped or milled fibres, wherein the fibres may or may not be provided with a suitable bonding agent or bonding agent system for the respective polymer which is used according to the invention.

Component D

Commercially available organic compounds or halogen compounds containing synergists, or commercially available organic nitrogen compounds, or organic/inorganic phosphorus compounds are suitable as flame retardant additives. Mineral flame retardant additives such as Mg hydroxide or Ca--Mg carbonate hydrate (e.g. DE-OS 4 236 122) may also be used.

The following are cited as examples of organic compounds containing halogens, particularly brominated and chlorinated compounds:

ethylene-1,2-bis-tetrabromophthalimide, epoxidised tetrabromobisphenol A resin, tetrabromobisphenol A oligocarbonate, tetrachlorobisphenol A oligocarbonate, pentabromopolyacrylate, brominated polystyrene.

Pentabromopolyacrylate generally has an average molecular weight M.sub.W (weight average) of 10,000 to 200,000; brominated polystyrene generally has an average molecular weight of 10,000 to 500,000.

Epoxidised tetrabromobisphenol A and tetrabromobisphenol A oligocarbonate are preferably used.

Epoxidised tetrabromobisphenol A is a known diepoxy resin with a molecular weight of about 350 to about 2100, preferably 360 to 1000, most preferably 370 to 400, and essentially consists of at least one condensation product of bisphenol A and epihalogenhydrin; it is characterised by formula (IV) ##STR6## where

X represents hydrogen or bromine, and

n is a mean numerical value between zero and less than 2.3 (see EP-A 180 471, for example).

Tetrabromobisphenol A oligocarbonate or tetrachlorobisphenol A oligocarbonate is characterised by formula (V), the oligomers being terminated either with phenol or with tribromophenol or trichlorophenol, respectively: ##STR7## in which ##STR8## where

X represents hydrogen, chlorine or bromine, and

n is a mean numerical value between 4 and 7.

Tetrabromo(chloro)bisphenol A oligocarbonate is known and can be prepared by known methods.

The phosphorus compounds according to EP-A 345 522 (U.S. Pat. No. 061,745) or DE-OS 43 28 656.9, in the amounts described therein, e.g. triphenyl phosphate, oligomeric phosphates, resorcinol diphosphate or a mixture thereof, are suitable as organic phosphorus compounds.

Component E

Suitable elastomeric modifiers include commercially available EP(D)M rubbers, graft rubbers based on butadiene, styrene, acrylonitrile, acrylate rubbers, thermoplastic polyurethanes (as described above) or EVA copolymers with or without functional coupling groups (e.g. EP-A 345 522). These elastomeric modifiers as suitable as blend coadjuvants for polyalkylene terephthalates, styrene polymers and polyphenylene sulphides.

The phosphorous acid esters according to the invention may be used to provide stabilisation from discoloration during the production, compounding and processing of the said thermoplastics.

The present invention therefore also relates to the use of the aforementioned phosphorous acid esters for the stabilisation of polyolefine and styrene polymer moulding compositions.

The moulding compositions according to the invention may contain customary additives, such as parting and demoulding agents, auxiliary processing agents, nucleating agents, antistatic agents and stabilisers.

The moulding compositions according to the invention, comprising the respective components and optionally other known additives such as stabilisers, colorants, pigments, parting and demoulding agents, reinforcing materials, nucleating agents and antistatic agents, can be produced by mixing the respective constituents in the known manner and compounding or extruding them as a melt at appropriate temperatures for polymers, in customary processing units such as internal kneaders, extruders or twin-shaft screw devices.

The moulding compositions according to the invention may be used for the production of moulded bodies and films which have been stabilised in relation to discoloration and degradation on thermal ageing and when subject to the long-term effects of hot water.

The present invention therefore also relates to the use of the aforementioned thermoplastic moulding compositions for the production of moulded bodies and films, and to the moulded bodies and films produced therefrom.

EXAMPLES

Phosphorous acid esters used:

phosphite A: ##STR9##

phosphite B: ##STR10##

Example 1

(comparison)

100% by weight polystyrene 476 L (BASF AG)

Example 2

(according to the invention)

99.90% by weight polystyrene 476 L (BASF AG)

0.10% by weight phosphite A

Example 3

(according to the invention)

99.4335% by weight polystyrene 476 L (BASF AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.1% by weight pure phosphite B,

0.4665% by weight isopropanol

Example 4

(comparison)

100% by weight Lucalen A 2910M (BASF AG)=polyethylene

Example 5

(according to the invention)

99.90% by weight Lucalen A 2910M (BASF AG)

0.10% by weight phosphite A

Example 6

(according to the invention)

99.4335% by weight Lucalen A 2910M (BASF AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.1% by weight pure phosphite B,

0.4665% by weight isopropanol

Example 7

(comparison)

100% by weight Novolen 1100 L (BASF AG)=polypropylene

Example 8

(according to the invention)

99.90% by weight Novolen 1100 L (BASF AG)

0.10% by weight phosphite A

Example 9

(according to the invention)

99.4335% by weight Novolen 1100 L

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.10% by weight pure phosphite B,

0.4665% by weight isopropanol.

Example 10

(comparison

100% by weight Lucryl G66 Q14 (BASF AG)=polymethylacrylate

Example 11

(according to the invention)

99.90% by weight Lucryl G66 Q14 (BASF AG)

0.10% by weight phosphite A

Example 12

(according to the invention)

99.4335% by weight Lucryl G66 Q14 (BASF AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.10% by weight pure phosphite B

0.4665% by weight isopropanol

Example 13

(comparison)

100% by weight Novodur P3T (BAYER AG)=acrylbutadienstyrene

Example 14

(comparison)

99.90% by weight Novodur P3T (BAYER AG)

0.10% by weight phosphite A

Example 15

(according to the invention)

99.4335% by weight Novodur P3T (BAYER AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.10% by weight pure phosphite B

0.4665% by weight isopropanol

Example 16

(comparison)

100% by weight Desmopan 385 S (BAYER AG)=thermoplastic polyurethane

Example 17

(according to the invention)

99.90% by weight Desmopan 385 S (BAYER AG)

0.10% by weight phosphite A

Example 18

(according to the invention)

99.4335% by weight Desmopan 385 S (BAYER AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.10% by weight pure phosphite B

0.4665% by weight isopropanol

Example 19

(comparison)

100% by weight Durethan B30S (BAYER AG)=polyamide

Example 20

(according to the invention)

99.90% by weight Durethan B30S (BAYER AG)

0.10% by weight phosphite A

Example 21

(according to the invention)

99.4335% by weight Durethan B30S (BAYER AG)

0.5665% by weight phosphite B as solution in isopropanol corresponding to

0.10% by weight pure phosphite B

0.4665% by weight isopropanol

Example 22

(comparison)

100% by weight Tedur KU 1-9510 (BAYER AG)=polyphenylenesulphide

Example 23

(according to the invention)

99.90% by weight Tedur KU 1-9510 (BAYER AG)

0.10% by weight phosphite A

Example 24

(according to the invention)

99.4335% by weight Tedur KU 1-9510 (BAYER AG)

0.5665% by weight phosphite B as a solution in isopropanol corresponding to

0.10% by weight pure phosphite B

0.4665% by weight isopropanol

The components were mixed and subsequently compounded by means of an extruder. The granular material obtained was injection moulded in a commercially available injection moulding machine to form moulded bodies.

TABLE 1______________________________________ Example 2 Example 3 Example 1 (according (according Specifi- (compari- to the to theTest Units cation Conditions son) invention) invention)______________________________________Izod kJ/m.sup.2 ISO Without 5.2 5.4 5.7notched 180/1A ageing, atimpact 23.degree. C., airstrengtha.sub.kIzod kJ/m.sup.2 ISO Without 8 .times. 95 9 .times. 100 8 .times. 106impact 180/1U ageing, atstrength 23.degree. C., aira.sub.na.sub.n kJ/m.sup.2 ISO 7 days/ 10 .times. 80 9 .times. 83 10 .times. 92 180/1U 90.degree. C. aira.sub.n kJ/m.sup.2 ISO 14 days/ 10 .times. 78 10 .times. 81 10 .times. 86 180/1U 90.degree. C. aira.sub.n kJ/m.sup.2 ISO 7 days/ 9 .times. 85 8 .times. 87 5 .times. 105 180/1U 90.degree. C. H.sub.2 Oa.sub.n kJ/m.sup.2 ISO 14 days/ 10 .times. 96 6 .times. 109 193 180/1U 90.degree. C. H.sub.2 OMVR cm.sup.3 / ISO 230.degree. C. 6.3 7.0 6.7 10 1133 2.16 kg minColour Visual Without light lighter as in Ex. 2 assess- ageing, at than Ex. 1 ment 23.degree. C., airColour Visual 7 days/ slight no dis- as in Ex. 2 assess- 90.degree. C. air yellowish coloration ment discolor- ationColour Visual 14 days/ consider- slightly as in Ex. 2 assess- 90.degree. C. air ably more yellow but ment yellowing much than after lighter 7 days than Ex. 1______________________________________ Ten test specimens were always tested for impact toughness. All the values which are not listed have therefore not been quoted because they were not broken during the test. TABLE 2______________________________________ Example 5 Example 6 Example 4 (according (according Specifi- (compari- to the to theTest Units cation Conditions son) invention) invention)______________________________________flexural N/ ISO 5 mm/min 3.1 3.3 3.3stress at mm.sup.2 178/3.5%strainflexural N/ ISO 5 mm/min 5.4 6.1 6.2strength mm.sup.2 178/flexural % ISO 5 mm/min 7.0 7.6 7.9strain at 178/flexuralstrengthIzod kJ/m.sup.2 ISO without not broken not broken not brokennotched 180/1A ageing, atimpact 23.degree. C., airstrengtha.sub.ka.sub.k kJ/m.sup.2 ISO 5 days/ not broken not broken not broken 180/1A 80.degree. C., aira.sub.k kJ/m.sup.2 ISO 10 days/ not broken not broken not broken 180/1A 80.degree. C., airMVR cm.sup.3 / ISO 230.degree. C./ 29.2 28.4 25.8 10 1130 2.16 kg minColour Visual Without grey- lighter lighter assess- ageing, at yellow, than than ment 23.degree. C., air trans- Ex. 4, Ex. 4, parent trans- trans- parent parentColour Visual 5 days/ more lighter as in Ex. 5 assess- 80.degree. C., air yellow, than ment not Ex. 4, complete- trans- ly trans- parent parentColour Visual 10 days/ consider- lighter as in Ex. 5 assess- 80.degree. C., air ably more than ment yellow, Ex. 4, almost trans- translucent parent______________________________________ TABLE 3______________________________________ Example 8 Example 9 Example 7 (according (according Specifi- (compari- to the to theTest Units cation Conditions son) invention) invention)______________________________________Izod kJ/m.sup.2 ISO At 23.degree. C. 7.1 7.7 7.9notched 180/1A in airimpactstrengtha.sub.kIzod kJ/m.sup.2 ISO Without 74 75 65impact 180/1U ageing, atstrength 23.degree. C., aira.sub.na.sub.n kJ/m.sup.2 ISO 5 days/ 67 75 66 180/1U 60.degree. C., aira.sub.n kJ/m.sup.2 ISO 10 day/ 71 72 63 180/1U 60.degree. C. airMVR cm.sup.3 / ISO 250.degree. C./ 12.7 12.3 12.2 10 1133 2.16 kg mincolour Visual Without milky lighter lighter assess- ageing, at light, than than ment 23.degree. C. translucent Ex. 7, Ex. 7, trans- trans- parent parentcolour Visual 5 day/ somewhat no change no change assess- 60.degree. C., air more ment yellos translucentcolour Visual 10 days/ more no change no change assess- 60.degree. C., air yellow, ment more translucent______________________________________ TABLE 4______________________________________ Example Example Example 11 12 10 (accord- (accord- Specifi- (compari- ing to the ing to theTest Units cation Conditions son) invention) invention)______________________________________Izod kJ/m.sup.2 ISO At 23.degree. C. 13 13 13impact 180/1U in airstrengtha.sub.na.sub.n kJ/m.sup.2 ISO 7 days/ 13 13 12 180/1U 60.degree. C., aira.sub.n kJ/m.sup.2 ISO 14 days/ 12 13 13 180/1U 60.degree. C., aira.sub.n kJ/m.sup.2 ISO 5 days/ 12 13 14 180/1U 60.degree. C. H.sub.2 Oa.sub.n kJ/m.sup.2 ISO 10 days/ 12 13 12 180/1U 60.degree. C. H.sub.2 OMVR cm.sup.3 / ISO 200.degree. C./ 0.55 0.58 0.59 10 1130 2.16 kg minColour Visual without trans- trans- trans- assess- ageing, at parent parent, parent, ment 23.degree. C. lighter lighter than than Ex. 10 Ex. 11Colour Visual 5 days/ trans- trans- trans- assess- 60.degree. C. air parent parent, parent, ment lighter lighter than than Ex. 10 Ex. 11Colour Visual 10 days/ trans- trans- trans- assess- 60.degree. C. air parent lucent, lucent, ment lighter lighter than than Ex. 10 Ex. 11Colour Visual 5 days/ trans- trans- trans- assess- 60.degree. C. parent lucent, lucent, ment H.sub.2 O lighter lighter than than Ex. 10 Ex. 11Colour Visual 10 days/ trans- trans- trans- assess- 60.degree. C. lucent lucent, lucent, ment H.sub.2 O lighter lighter than than Ex. 10 Ex. 11______________________________________ TABLE 5______________________________________ Example Example Example 14 15 13 (accord- (accord- Specifi- (compari- ing to the ing to theTest Units cation Conditions son) invention) invention)______________________________________Izod kJ/m.sup.2 ISO at 23.degree. C. 104 100 117impact 180/1U airstrengtha.sub.na.sub.n kJ/m.sup.2 ISO 7 days/ 83 70 95 180/1U 100.degree. C. aira.sub.n kJ/m.sup.2 ISO 7 days/ 107 112 129 180/1U 100.degree. C. H.sub.2 OMVR cm.sup.3/ ISO 220.degree. C./ 1.9 1.9 1.9 10 1133 10 kg minColour Visual without light light light assess- ageing at brown brown brown ment 23.degree. C. slightly colour darker as in than Ex. 13 Ex. 13Colour Visual 7 days/ brown brown brown assess- 100.degree. C. darker colour ment air than as in Ex. 13 Ex. 13Colour Visual 7 days/ white white light white assess- 100.degree. C. ment H.sub.2 O______________________________________ TABLE 6______________________________________ Example Example Example 17 18 16 (accord- (accord- Specifi- (compari- ing to the ing to theTest Units cation Conditions son) invention) invention)______________________________________tensile MPa ISO 50 mm/ 34 36 34stress at 527 minyieldbreak MPa ISO 50 mm/ 34 36 34stress 527 minelonga- % ISO 5 mm/ 380 394 388tion at 527 minbreaknotched kJ/m.sup.2 ISO at 23.degree. C. not broken not broken not brokenimpact 180/1A in airstrengtha.sub.ka.sub.k kJ/m.sup.2 ISO 7 days/ not broken not broken not broken 180/1A 130.degree. C. airMVR cm.sup.3 / ISO 200.degree. C./ 50 38 60 10 1133 10 kg minColour Visual without light light, light, assess- ageing at translucent almost lightest ment 23.degree. C. trans- colour, parent trans- parentColour Visual 7 days/ yellow, yellow, yellow, assess- 130.degree. C. almost trans- lightest ment air trans- parent colour, parent trans- parent______________________________________ TABLE 7______________________________________ Example Example Example 20 21 19 (accord- (accord- Specifi- (compari- ing to the ing to theTest Units cation Conditions son) invention) invention)______________________________________elonga- % ISO 5 mm/ 31 39 43tion at 527 minbreaknotched kJ/m.sup.2 ISO at 23.degree. C. 5.2 5.5 5.5impact 180/1A in airstrengtha.sub.k kJ/m.sup.2 ISO 7 days/ 8 10 8 180/1A 180.degree. C. aira.sub.k kJ/m.sup.2 ISO 14 days/ 11 9 12 180/1A 180.degree. C. airimpact kJ/m.sup.2 ISO at 23.degree. C. not broken not broken not brokenstrength 180/1U in aira.sub.na.sub.n kJ/m.sup.2 ISO 7 days/ not broken not broken not broken 180/1U 100.degree. C. H.sub.2 Oa.sub.n kJ/m.sup.2 ISO 14 days/ not broken not broken not broken 180/1U 100.degree. C. H.sub.2 OColour Visual without light- lighter lighter assess- ageing at yellow than than ment 23.degree. C. Ex. 19 Ex. 20Colour Visual 7 days/ yellow somewhat somewhat assess- 180.degree. C. lighter lighter ment air than than Ex. 19 Ex. 20Colour Visual 14 days/ a little bit lighter lighter assess- 180.degree. C. dark than than ment air yellow Ex. 19 Ex. 20Colour Visual 7 days/ light- somewhat somewhat assess- 100.degree. C. yellowish lighter lighter ment H.sub.2 O than than Ex. 19 Ex. 20Colour Visual 14 days/ light- somewhat somewhat assess- 100.degree. C. yellowish lighter lighter ment H.sub.2 O than than Ex. 19 Ex. 20______________________________________ TABLE 8______________________________________ Example Example Example 23 24 22 (accord- (accord- Specifi- (compari- ing to the ing to theTest Units cation Conditions son) invention) invention)______________________________________MVR cm.sup.3 / ISO 320.degree. C./ 57 61 59 10 1133 5 kg minColour Visual without dark grey lighter lighter assess- ageing than than ment Ex. 22 Ex. 23______________________________________

Claims

1. Thermoplastic moulding compositions containing

A) polymers selected from the group consisting essentially of polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers, and thermoplastic polyurethanes, and

B) esters of phosphorous acid which contain at least one oxetane group and at least one radical of a dihydric or polyhydric phenol per molecule, and

optionally, at least one of the following components,

C) fillers and reinforcing materials,

D) flame retardant additives, and

E) elastomeric modifiers.

2. Thermoplastic moulding compositions according to claim 1, wherein the moulding compositions contain 20 to 99.9 parts by weight of component A), 0.01 to 2.5 parts by weight of component B), up to 45 parts by weight of component C), up to 55 parts by weight of component D), and up to 30 parts by weight of component E).

3. Thermoplastic moulding compositions according to claim 1, wherein component B) is selected from phosphorous acid esters of formula (I) ##STR11## where n.sub.1 represents 1 or any integer >1,

n.sub.2 represents 0 or any integer >0,

n.sub.3 represents 1 or any integer >1,

R represents alkyl, aralkyl, cycloalkyl, aryl or heteroaryl, wherein at least one of the radicals R constitutes a monoalcohol containing at least one oxetane group, and

Ar represents aryl, which may optionally be substituted by alkyl and/or hydroxy, and where when n.sub.2 .noteq.0 Ar may be the same or different,

and compounds selected from the group consisting of

tris-�(3-ethyloxetanyl-3)-methyl!-phosphite,

tris-�(3-pentyloxetanyl-3)-methyl!-phosphite,

phenyl-bis-�(3-ethyloxetanyl-3)-methyl!-phosphite,

2-phenoxy-spiro(1,3,2-dioxaphosphorinane-5,3'-oxetane), and

3,3-bis-�spiro(oxetane-3',5"-(1",3",2"-dioxaphosphorinane-2"))-oxy-methyl!-oxetane.

4. Thermoplastic moulding compositions according to claim 3, wherein R in formula (I) represents C.sub.1 -C.sub.18 -alkyl, mono- or polynuclear C.sub.3 -C.sub.10 -cycloalkyl, phenyl-C.sub.1 -C.sub.2 -alkyl, mono- or polynuclear C.sub.6 -C.sub.18 -aryl, and heteroalkyl, wherein the aryl radicals may be substituted by alkyl and/or halogen, and R further represents an oxetane group ##STR12## where Z represents hydrogen, CH.sub.3, C.sub.2 H.sub.5, n-C.sub.5 H.sub.11, --CH.sub.2 --C.sub.5 H.sub.11, --CH.sub.2 --O--C.sub.6 H.sub.13 or CH.sub.2 --O--C.sub.2 H.sub.5.

5. Thermoplastic moulding compositions according to claim 3, wherein the radical Ar is derived from hydroquinone, resorcinol, catechol, di-t-butyl catechol, 4,4'-dihydroxydiphenyl, bis-(hydroxy-phenyl)-alkanes, bis-(hydroxyphenyl)-cycloalkanes, .alpha.,.alpha.'-bis-(hydroxyphenyl)-diisopropylbenzene and derivatives thereof which comprise alkylated or halogenated nuclei, phloroglucinol, or pyrogallol.

6. Thermoplastic moulding compositions according to claim 1, wherein component B) is ##STR13##

7. Thermoplastic moulding compositions according to claim 3, wherein component B) is ##STR14##

8. A method of using the moulding compositions according to claim 1, comprising the step of inserting one of the compositions into a mould.

9. Moulded bodies and films produced from moulding compositions according to claim 1.

10. A method of using the moulding compositions according to claim 1, comprising the step of forming one of said compositions into a film.

11. A thermoplastic moulding composition according to claim 1 wherein component A) is a polyolefine.

12. A thermoplastic moulding composition according to claim 1, wherein component A) is a styrene polymer.

13. A thermoplastic moulding composition according to claim 1, wherein component A) is a polyamide.

14. A thermoplastic moulding composition according to claim 1, wherein component A) is a polyalkyl methacrylate.

15. A thermoplastic moulding composition according to claim 1, wherein component A) is a polyphenylene sulphide.

16. A thermoplastic moulding composition according to claim 1, wherein component A) is a ABS graft polymer.

17. A thermoplastic moulding composition according to claim 1, wherein component A) is a thermoplastic polyurethane.

18. Thermoplastic moulding compositions consisting essentially of

A) polymers selected from the group consisting essentially of polyolefines, styrene polymers, polyamides, polyalkyl methacrylates, polyphenylene sulphides, ABS graft polymers, and thermoplastic polyurethanes, and

B) esters of phosphorous acid which contain at least one oxetane group and at least one radical of a dihydric or polyhydric phenol per molecule, and

optionally, at least one of the following components,

C) fillers and reinforcing materials,

D) flame retardant additives, and

E) elastomeric modifiers.

19. Thermoplastic moulding compositions according to claim 3, wherein the R groups in formula (I) may be the same or different and each R is C.sub.1 -C.sub.18 -alkyl, mononuclear C.sub.3 -C.sub.10 -cycloalkyl, polynuclear C.sub.3 -C.sub.10 -cycloalkyl, phenyl-C.sub.1 -C.sub.2 -alkyl, mononuclear C.sub.6 -C.sub.18 -aryl, polynuclear C.sub.6 -C.sub.18 -aryl, heteroalkyl or

an oxetane group having the formula ##STR15## where Z is hydrogen, CH.sub.3, C.sub.2 H.sub.5, n-C.sub.5 H.sub.11, --CH.sub.2 --C.sub.5 H.sub.11, --CH.sub.2 --O--C.sub.6 H.sub.13 or --CH.sub.2 --O--C.sub.2 H.sub.5,

further wherein when R is mononuclear C.sub.6 -C.sub.18 -aryl or polynuclear C.sub.6 -C.sub.18 -aryl, the aryl radicals may be substituted by alkyl and/or halogen.