Plastics stabilized against ultraviolet radiation

Information

  • Patent Grant
  • 3931104
  • Patent Number
    3,931,104
  • Date Filed
    Monday, June 10, 1974
    50 years ago
  • Date Issued
    Tuesday, January 6, 1976
    49 years ago
Abstract
Thermoplastic polymers are stabilized against ultra-violet radiation by incorporating therein as a stabilizer a stabilizing amount, e.g., 0.1 to 5% by weight of a tertiary phosphine oxide or sulfide of the general formula: ##EQU1## in which X is oxygen or sulfur and R.sub.1, R.sub.2 and R.sub.3 are each selected from hydroxyalkyl, haloalkyl, carbalkoxyalkyl, acyloxyalkyl, phenylhydroxyalkyl wherein the phenyl radical may be substituted by one or more halogens, and cyanoalkyl wherein the alkyl radical has 1 to 6 carbon atoms.
Description

It is already known that plastics, for example polyolefines, are attacked and gradually destroyed by the action of ultraviolet radiation, for example ultraviolet radiation of the sunlight. In order to reduce this destruction, so-called inhibitors or stabilizers are added to the plastics.
The present invention therefore provides plastics stabilized against ultraviolet radiation and containing as stabilizer a compound of the formula ##EQU2## wherein X represents an oxygen or sulfur atom, R.sub.1 and R.sub.2 are either .beta.-cyanoethyl radicals or have the same definition as R.sub.3, R.sub.3 represents a hydroxyalkyl or a hydroxyalkylphenyl group, the phenyl radical of the latter being optionally substituted by one or more halogen atoms, or a halogenoalkyl carbalkoxyalkyl, acyloxyalkyl or cyanoalkyl group the alkyl radical of which has from 1 to 6 carbon atoms.
The tertiary phosphine oxides to be used according to the invention can be prepared by various known methods, for example by hydrolysis of phosphine dihalides or quaternary phosphonium compounds, by Michael's-Arbusov's-reaction from phosphinous acid esters, or most simply by direct oxidation of the corresponding tertiary phosphines.
The tertiary phosphine sulfides to be used according to the invention can be easily prepared by the addition of elementary sulfur on the corresponding tertiary phosphines according to known methods. Suitable tertiary phosphine oxides are for example bis-(2-cyanoethyl)-hydroxymethyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxyethyl-phosphine oxide, bis-(2-cyanoethyl)-2-chloro-1-hydroxyethyl-phosphine oxide, bis-(2-cyanoethyl)-2,2,2-trichloro-1hydroxyethyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxycyclohexyl-phosphine oxide, bis-(2-cyanoethyl)-2-carboxymethylethyl-phosphine oxide, bis-(2-cyanoethyl)-1,2-dicarboxymethylethyl-phosphine oxide, bis-(2-cyanoethyl)-2,2-dichloro-1-hydroxy-ethyl-phosphine oxide, bis-(2-cyanoethyl)-bis-chloromethyl-hydroxy-methyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxy-2-phenyl-ethyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxyl-1-phenyl-2-chloro-ethyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxy-1-phenyl-ethyl-phosphine oxide, bis-(2-cyanoethyl)-1-hydroxy-1-(4-bromophenyl)-ethyl-phosphine oxide, bis-(2-cyanoethyl)-hydroxy-(2,4-dichlorophenyl)-methyl-phosphine oxide.
Tris-chloromethyl-phosphine oxide, oxethylated tris-hydroxymethyl-phosphine oxide, tris-hydroxymethyl-phosphine oxide, oxpropylated tris-hydroxymethyl-phosphine oxide, tris-(2-cyanoethyl)-phosphine oxide, tris-acetoxymethyl-phosphine oxide, tris-stearoyloxymethyl-phosphine oxide, tris-benzoyloxymethyl-phosphine oxide, tris-(2-carbethoxy)-ethyl-phosphine oxide, tris-(1-hydroxy-2-chloro-ethyl)-phosphine oxide, tris-(1-hydroxy-1-phenyl-ethyl)-phosphine oxide.
Suitable tertiary phosphine sulfides are, for example, tris-hydroxymethyl-phosphine sulfide, tris-(2-cyanoethyl)-phosphine sulfide, tris-stearoyloxy-methyl-phosphine sulfide, tris-(2-carbomethoxy)-ethyl-phosphine sulfide, bis-(2-cyanoethyl)-hydroxymethyl-phosphine sulfide. The compounds to be used according to the invention are especially suitable as stabilizers against ultraviolet radiation for polyethylene, polypropylene, polybutene, poly-(4-methyl-1-pentene), copolymers of these substances as well as for polystyrene.
They are added to the polymers in an amount of 0.1 to 5 % by weight, preferably of 0.5 to 2 % by weight.
They may be incorporated into the polymer in the usual manner, for example by mixing, kneading or grinding. In this process it may also be advantageous to use mixtures of the additives.
Moreover, further components, such as pigments, lubricants, fillers or antistatic agents may be added to the plastics. In most applications, it can also be desirable to use antioxidants, for example of thiodipropionic acid or distearyl sulfide type and/or antioxidants corresponding to the general formulae ##SPC1##
wherein
n=O-6
R.sub.1 = alkyl having from 1 to 20 C-atoms
R.sub.2 = alkyl having from 1 to 6 C-atoms
The compounds of the invention differ from known UV-absorbers containing hydroxyl groups in not being colored, even after exposure to ultraviolet light, as well as in their partly better stabilizer properties.





The invention is illustrated by the following examples.
EXAMPLES 1- 13
100 Parts of polypropylene stabilized with 0.1 % of 2,2-isopropylidene-bis-(4-isononylphenol) and 0.25 % of thiodipropionic acid lauryl ester are mixed with one part of the additives mentioned below in a kneader-mixer provided with heating means at a temperature of 200.degree.C.
In order to determine the stabilizing effect under the action of ultraviolet light, the brittle time of sheets mounted on an aluminium foil and having a thickness of 100 .mu. is measured by means of the Xenon test apparatus 450 of the Cassella system, manufactured by Messrs. Heraeus at Hanau (W. Germany); it is the time after which the test sheet exhibits a clod-like rupture by pulling a cotton thread imbedded therein.
The results are summarized in the following table.
__________________________________________________________________________Example stabilizer brittle time color after exposure toNo. (hours) ultra-violet radiation__________________________________________________________________________1 bis-(2-cyanoethyl)-hydroxymethyl- 910 colorless phosphine oxide2 bis-(2-cyanoethyl)-1-hydroxy- 850 colorless ethyl-phosphine oxide3 bis-(2-cyanoethyl)-2-chloro-1- 860 faintly yellow hydroxyethyl-phosphine oxide4 bis-(2-cyanoethyl)-2,2,2-tri- 780 faintly yellow chloro-1-hydroxyethyl-phosphine oxide5 bis-(2-cyanoethyl)-1,2-dicarboxy- 910 colorless methylethyl-phosphine oxide6 tris-hydroxymethyl-phosphine oxide 1025 colorless7 oxethylated tris-hydroxymethyl-phos- 1280 colorless phine oxide8 oxpropylated tris-hydroxymethyl- 830 colorless phosphine oxide9 tris-2-(cyanoethyl)-phosphine sulfide 1125 colorless10 tris-stearoyloxymethyl-phosphine sul- 880 colorless fide11 tris-(2-carbmethoxy)-ethyl-phos- 810 colorless phine sulfide12 comparative experiment without an additive 16213 2-(2'-hydroxy-3', 5'-di-tert.- 920 yellow butylphenyl)-5-chloro-benzotriazole__________________________________________________________________________
Claims
  • 1. A plastic material consisting essentially of a polymer selected from homopolymers and copolymers of ethylene, propylene, butene and 4-methyl-1-pentene and polystyrene and from 0.5 to 2% by weight of an ultra-violet radiation stabilizer which is a tertiary phosphine oxide or sulfide of the formula ##EQU3## in which X is oxygen or sulfur and either (a) R.sub.1 and R.sub.2 are .beta.-cyano-ethyl and R.sub.3 is a radical other than .beta.-cyanoethyl selected from the group of radicals consisting of hydroxyalkyl, haloalkyl, hydroxy haloalkyl carbalkoxyalkyl, acyloxyalkyl, phenylhydroxyalkyl wherein the phenyl radical may be substituted by one or more halogens, and cyanoethyl wherein the alkyl radical has 1 to 6 carbon atoms or (b) R.sub.1, R.sub.2 and R.sub.3 are the same and each is selected from said group of radicals.
  • 2. A plastic material according to claim 1 wherein said polymer is polypropylene.
  • 3. A plastic material according to claim 1 wherein at least one of R.sub.1, R.sub.2 and R.sub.3 is hydroxyhaloalkyl.
  • 4. A plastic material according to claim 1 wherein said stabilizer is bis-(2-cyanoethyl)-hydroxymethyl-phosphine oxide.
  • 5. A plastic material according to claim 1 wherein said stabilizer is bis-(2-cyanoethyl)-1-hydroxyethyl-phosphine oxide.
  • 6. A plastic material according to claim 1 wherein said stabilizer is bis-(2-cyanoethyl)-2-chloro-1-hydroxyethyl-phosphine oxide.
  • 7. A plastic material according to claim 1 wherein said stabilizer is bis-(2-cyanoethyl)-2,2,2-tri-chloro-1-hydroxyethyl-phosphine oxide.
  • 8. A plastic material according to claim 1 wherein said stabilizer is bis-(2-cyanoethyl)-1,2-dicarboxymethylethyl-phosphine oxide.
  • 9. A plastic material according to claim 1 wherein said stabilizer is tris-hydroxymethyl-phosphine oxide.
  • 10. A plastic material according to claim 1 wherein said stabilizer is oxethylated tris-hydroxymethyl-phosphine oxide.
  • 11. A plastic material according to claim 1 wherein said stabilizer is oxpropylated tris-hydroxymethyl-phosphine oxide.
  • 12. A plastic material according to claim 1 wherein said stabilizer is tris-(2-cyanoethyl)-phosphine sulfide.
  • 13. A plastic material according to claim 1 wherein said stabilizer is tris-stearolyoxymethyl-phosphine sulfide.
  • 14. A plastic material according to claim 1 wherein said stabilizer is tris-(2-carbmethoxy)-ethyl-phosphine oxide.
  • 15. A thermoplastic polymer containing a stabilizing amount of an ultra-violet radiation stabilizer which is a tertiary phosphine oxide or sulfide of the formula ##EQU4## in which X is oxygen or sulfur and R.sub.1, R.sub.2 and R.sub.3 are each selected from hydroxyalkyl, haloalkyl, hydroxy haloalkyl carbalkoxyalkyl, acyloxyalkyl, phenylhydroxyalkyl wherein the phenyl radical may be substituted by one or more halogens, and cyanoalkyl wherein the alkyl radical has 1 to 6 carbon atoms, provided that said stabilizer does not contain more than two cyanoalkyl groups.
  • 16. A thermoplastic polymer according to claim 15 containing from 0.5 to 2% by weight of said stabilizer.
Priority Claims (1)
Number Date Country Kind
2329782 Jun 1973 DT
US Referenced Citations (6)
Number Name Date Kind
3269963 Ilgemann et al. Aug 1966
3341625 Gillham et al. Sep 1967
3532668 Savides Oct 1970
3594346 Hermann et al. Jul 1971
3629365 Gardner Dec 1971
3676393 Piirma Jul 1972