EXAMPLES 1 to 6
One hundred parts by weight of polypropylene(homopolymer) powders (intrinsic viscosity [.xi.],2.20), 0.05 part by weight of calcium stearate, the phenolic compound, metal deactivator and sulfur-containing compound were mixed. The mixture was mixed on a Henschel mixer and extruded into pellets at a temperature of 230.degree. C. on a 65 mm .phi. extruder in a nitrogen gas atmosphere. The pellets thus obtained were measured for melt index (MI) according to JIS K 7210.
These pellets were pre-heated for 10 minutes at a temperature of 230.degree. C. and formed into a press sheet of 1 mm in thickness. The press sheet obtained was brought into contact with a copper plate and placed in a Geer oven kept at a temperature of 150.degree. C. to measure the thermal stability.
Separately, the yellowness index (YI) of this press sheet was measured according to ASTM D 1925. The results are shown in Table 4.
Comparative examples 1 to 3
Test was carried out in the same manner as in Example 1 under conditions shown in Table 4 using the conventional pentaerythrito tetrakis [3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate](A-3) as the phenolic compound. The results are shown in Table 4.
Examples 7 to 10
Procedure was carried out in the same manner as in Example 1 except that a propylene/ethylene block copolymer (ethylene content, 7.3 wt. %; [.xi.]=2.45) was used as the polyolefin, and that 100 parts by weight of this block copolymer, 0.05 part by weight of calcium stearate the phenolic compound, metal deactivator, sulfur-containing compound and phosphite type compound, bis(2,4-di-tert-butylphenyl) pentaerythitol diphosphite, were blended together. The results are shown in Table 4.
Abbreviations in Table 4 represent the following compounds. Phenolic compound: ##STR24## A-3 Pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] ##STR25##
Sulfur-containing compound:
C-1 Dimyristyl thiodipropionate ##STR26##
Phosphite type compound:
D-1 Bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite
Examples 11 to 15
One hundred parts by weight of a resin composition comprising propylene/ethylene block copolymer powders (intrinsic viscosity [.xi.], 2.45; ethylene content, 7.3 wt. %) and talc (Micron White 5000S; a product of Hayashi Kasei K.K.) which was an inorganic filler was mixed with 0.05 part by weight of calcium stearate, the phenolic compound, metal deactivators sulfur-containing compound and 0.05 part by weight of bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite. The mixture obtained was mixed on a Henschel mixer, kneaded and pelletized on a 65 mm.phi. extruder. The pellets obtained were preheated at a temperature of 230.degree. C. for 10 minutes and formed into a press sheet of 1 mm in thickness. The sheet obtained was brought into contact with a copper plate and placed in a Geer oven kept at a temperature of 150.degree. C. to measure the thermal stability.
The melt index (MI) of the pellets was measured according to JIS K 7210. the yellowness index (YI) of the press sheet was measured according to ASTM D 1925. The results obtained and the proportions of the materials are shown together in Table 5.
Comparative examples 4 and 5
Test was carried out in the same manner as in Example 11 under conditions shown in Table 5 using pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate](A-3) as the phenolic compound. The results are shown in Table 5.
Abbreviations A-1, A-2, A-3, B-1, B-2, C-1 and C-2 in Table 5 are the same as described above. Abbreviations, F-1, F-2 and F-3, of inorganic filler represent the following substances:
F-1 talc
F-2 calcium carbonate
F-3 calcium silicate.
Examples 16 to 18
Test was carried out in the same manner as in Example 11 under conditions shown in Table 5 using varying kinds of inorganic filler. The results are shown in Table 5 together with the results of other examples.
Comparative example 6
Test was-carried out-in the same manner as in Example 16 under a condition shown in Table 5 using A-3 as the phenolic compound The result is shown in Table 5.
According to the present invention, there is provided a composition stabilized against heavy metals which comprises blending a polyolefin such as polypropylene containing or not containing an inorganic filler with the particular phenolic compound, metal deactivator and sulfur-containing compound. This composition exhibits a greatly improved thermal stability as compared with the conventional compositions particularly when brought into contact with copper plates at high temperatures. This composition has also an improved coloration property.