Polyolefin resin composition

Abstract

Polyolefin resins are thermally stabilized and are also stabilized against yellowing from nitrogen oxide gases by incorporating 3,9-bis[2- 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy -1,1-dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane.

Description

The present invention relates to a method for improving the thermal stability of polyolefin resins and also preventing the resins from yellowing by nitrogen oxide gases (hereinafter referred to as NO.sub.x).

Polyolefin resins have excellent physical, chemical and electrical properties, so that they are formed into molded products, pipes, sheets, films, etc. by various methods such as blow molding, extrusion molding, injection molding, celendering, etc. and used in many fields. It is well known that, when polyolefin resins such as polyethylene, polypropylene, etc. are used alone, they deteriorate in quality due to the action of heat, oxygen and light on processing or use, thereby showing a remarkable reduction in the physical properties accompanied by phenomena such as softening, embrittlement, etc. For the purpose of preventing such phenomena, methods are so far known in which various kinds of antioxidants and light stabilizers are added alone or in combination to the production or processing process for polyolefin resins. Such antioxidants include phenolic type, sulfur-containing and phosphite type antioxidants, etc., and such light stabilizers include benzophenone type, benzotriazole type, cyanoacrylate type, nickel type and hindered piperidine type light stabilizers, etc. On the other hand, recently, such problems have come to be suddenly revealed that the appearance of polyolefin resins is markedly damaged by yellowing caused by NO.sub.x in waste gases represented by combustion gases from automobiles outdoors, combustion gases from oilstoves indoors, etc. But, for preventing such yellowing by NO.sub.x, the foregoing method is not sufficiently effective, although it is effective to prevent deterioration by heat, etc. The appearance of methods to improve the thermal stability of polyolefin resins and also to prevent the yellowing of the resins by NO.sub.x, has therefore been demanded.

In view of this situation the present inventors extensively studied a method for improving the thermal stability of polyolefin resins and also preventing the resins from yellowing by NO.sub.x, and as a result, found that such objects can be attained by incorporating a particular phenolic type compound in polyolefin resins.

Further, the present inventors found that, even if the particular phenolic type compound is used together with thioether type and phosphite type antioxidants or light stabilizers generally added as assistants, in order to prevent deterioration by heat, light, etc. and discoloration by heat, there is no reduction at all in the effect of said compound to prevent NO.sub.x yellowing, and therefore, that said compound can be used together with these antioxidants and light stabilizers. The present inventors thus completed the present invention.

The present invention provides a method for improving the thermal stability of polyolefin resins and also preventing the resins from yellowing by NO.sub.x characterized by blending polyolefin resins with 0.001 to 5 parts by weight of 3,9-bis[2-{3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy}-1,1-dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane (hereinafter referred to as present phenolic type compound) based on 100 parts by weight of said resins.

The phenolic type compound used in the present invention is well known and described in Japanese Patent Kokai (Laid-open) No. 25,826/1984. This Patent Kokai Publication relates to stabilized synthetic resin compositions comprising an ester compound having a group represented by the general formula, ##STR1## in the molecule obtained by adding the material to synthetic resins, and gives a wide range of phenolic type compounds. But, it gives no description at all on the NO.sub.x yellowing preventing effect of the compounds on polyolefin resins.

The present inventors studied a wide range of phenolic type compounds described in said Patent Kokai Publication, and as a result, found an unexpected fact that, in the phenolic type compounds represented by the general formula (I), ##STR2## including the present phenolic type compound, when a substituent R is a hydrogen atom or an ethyl, propyl, butyl group, etc., the compound (I) exhibits little effect to prevent NO.sub.x yellowing, and that only when R is a methyl does the compound (I) exhibit a specifically excellent effect in preventing NO.sub.x yellowing.

In the present invention, when the amount of the present phenolic type compound added to polyolefins is too small, sufficient thermal stability is not obtained, while when said amount is too large, the effect corresponding to such amounts is difficult to obtain, being also disadvantageous economically. In order to attain improvement in the thermal stability and prevention of NO.sub.x yellowing at the same time, said amount is generally 0.001 to 5 parts by weight, preferably 0.01 to 1 part by weight based on 100 parts by weight of polyolefin resins.

A method to blend the present phenolic type compound with polyolefin resins is not particularly limited, and the well-known apparatus and procedures generally employed to incorporate stabilizers, pigments, fillers, etc. in polyolefin resins can be used almost as such.

Polyolefin resins used in the present invention include poly .alpha.-olefins such as low-density polyethylene, medium- to high-density polyethylene, linear low-density polyethylene, polypropylene, polybutene-1, etc., poly .alpha.-olefin copolymers such as propylene/ethylene random or block copolymers, ethylene/butane-1 random copolymers, etc., copolymers of poly .alpha.olefin with vinyl monomer such as maleic acid anhydride-modified polypropylene, etc., and mixtures thereof. Further, blends of the polyolefins with rubbers such as isoprene rubber (IR), butyl rubber (IIR), nitrile rubber (NBR), styrene/butadiene copolymeric rubber (SBR), ethylene/propylene rubber (EPM, EPDM), etc. are also included in the scope of the polyolefin resins used in the present invention. Particularly, the present phenolic type compound is effective for polypropylene.

Thus, according to the method of the present invention, polyolefin resins can be improved in thermal stability and besides prevented from yellowing by NO.sub.x, so that they can be used more advantageously in practical use.

The present invention will be illustrated in detail with reference to the following examples, but it is not limited to these examples.

EXAMPLE 1

100 Parts by weight of unstabilized polypropylene resin, 0.1 part by weight of calcium stearate and a pre-determined amount, as described in Table 2, of various test compounds were mixed for 5 minutes on a mixer, and melt-kneaded on a mixing roll at 180.degree. C. to obtain a composition. Every compound was formed into a sheet 1 mm thick on a hot press kept at 210.degree. C., and test pieces of 100.times.40.times.1 mm (thick) and 40.times.40.times.1 mm (thick) in size were prepared from each sheet.

According to "Testing Method for Color Fastness to Nitrogen Oxides" (JIS L 0855), the test piece 100.times.40.times.1 mm (thick) was exposed to an atmosphere having an NO.sub.x concentration of 2%, and the NO.sub.x yellowing resistance of the test piece was evaluated based on the degree of coloration after 24 hours' exposure graded in nine steps as follows:

1: yellowish brown 1.5: yellowish brown to yellow 2: yellow 2.5: yellow to pale yellow 3: pale yellow 3.5: pale yellow to very pale yellow 4: very pale yellow 4.5: very pale yellow to colorless 5: colorless

The test piece 40.times.40.times.1 mm (thick) was placed in a Geer oven kept at 160.degree. C., and measured for a period of time required for 30% of its area to become brittle. This period of time was taken as thermal embrittlement induction period and used for evaluation of the thermal and oxidation stability. The results are shown in Table 2.

Of the test compounds described in Table 2, compounds I-1 and A0-1 to A0-4 are ones shown in Table 1, and compounds A0-5 to A0-9 and LS-1 are ones shown below.

TABLE 1______________________________________ ##STR3##Compound R______________________________________I-1 CH.sub.3AO-1 HAO-2 CH.sub.2 CH.sub.3AO-3 ##STR4##AO-4 C(CH.sub.3).sub.3AO-5 Pentaerythritol tetrakis{3-(3,5-di-tert-butyl-4- hydroxyphenyl)propionate}AO-6 n-Octadecyl 3-(3,5-di-tert-butyl-4-hydroxy- phenyl)propionateAO-7 1,3,5-Tris(4-tert-butyl-3-hydroxy-2,6-dimethyl- benzyl)isocyanuric acidAO-8 Distearyl thiodipropionateAO-9 Tris(2,4-di-tert-butylphenyl)phosphiteLS-1 Bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate______________________________________ TABLE 2__________________________________________________________________________ Phenolic type Sulfur-contain- Phosphite type Light compound ing compound compound stabilizer Amount Amount Amount Amount NO.sub.x Thermal (part by (part by (part by (part by yellowing embrittlementExample No. No. Kind weight) Kind weight) Kind weight) Kind weight) resistance induction period__________________________________________________________________________ (hr)Present 1 I-1 0.1 4 400example 2 " 0.3 4 630 3 " 0.5 4 890 4 " 0.1 AO-8 0.15 4 760 5 " 0.1 AO-9 0.15 4 410 6 " 0.1 LS-1 0.15 4 370Compa- 7 AO-1 0.1 2.5 350rative 8 " 0.3 2 530example 9 AO-2 0.1 2.5 360 10 " 0.3 2 540 11 AO-3 0.1 2 360 12 " 0.3 1.5 540 13 AO-4 0.1 2.5 350 14 " 0.3 2 530 15 " 0.1 AO-8 0.15 2 600 16 " 0.1 AO-9 0.15 2 360 17 " 0.1 LS-1 0.15 2 340 18 AO-5 0.1 2 370 19 " 0.3 1.5 570 20 AO-6 0.1 1.5 270 21 " 0.3 1.5 380 22 AO-7 0.1 2.5 280 23 " 0.3 2 400__________________________________________________________________________

Claims

1. A method for improving the thermal stability of polyolefin resin and preventing said resin from yellowing by nitrogen oxide gases which comprises blending a polyolefin resin with 0.001 to 5 parts by weight of 3,9-bis[2-{3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy}-1,1-dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane based on 100 parts by weight of said resin.

2. A method as described in claim 1, wherein the polyolefin resin in polypropylene.

3. A composition which comprises a polyolefin resin having incorporated therein 0.001 to 5 parts by weight of 3,9-bis[2-{3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy}-1,1-dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane based on 100 parts by weight of said resin.

4. A composition according to claim 3, wherein the polyolefin resin is polypropylene.