JPH11152309A - Molded article of modified polyethylene - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a molded article obtained by using a modified polyethylene having a high melt strength and excellent moldability. SOLUTION: 1-10 mmol of a di-2-ethylhexyl peroxy bicarbonate per 100 g of polyethylene is reacted in an inert gas atmosphere at a temperature of 50-130 deg.C for 10 min to 3 hr and thereafter kneaded by melting to obtain the molded article of a modified polyethylene which has (1) a relation of log (MS)>4.66×log[η]-0.340 between a melt strength(MS) at 190 deg.C and an inherent viscosity [η] determined at 135 deg.C in tetralin and (2) the extracted residue of a boiled xylene of not more than 1 wt.%. In the case where a polyethylene having the same inherent viscosity is used, the melt strength of the modified polyethylene is increased about three times or more than that of an unmodified polyethylene and is increased about 40% or more than that of a polyethylene modified by other organic peroxides.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

[0001] The present invention relates to a method for producing a modified polyethylene. More specifically, the melt tension is high,
The present invention relates to a method for producing a modified polyethylene having a high melt tension, which is excellent in moldability and can be re-melted after being used as a molded article and recycled.

[0002]

2. Description of the Related Art Polyethylene produced using a Ziegler-based catalyst has excellent mechanical properties, chemical resistance, etc., and is extremely useful in terms of economical balance. ing. However, it has a low melt tension and is inferior in moldability such as hollow molding, foam molding and extrusion molding.

As a method for increasing the melt tension of polyethylene, a method of reacting an organic peroxide with polyethylene in a molten state (JP-A-57-38837,
JP-A-58-71904, JP-A-59-8934
No. 1) and a method of further reacting an organic peroxide with a crosslinking aid (JP-A-59-89341). The improvement in tension was insufficient. Furthermore, the method using a crosslinking aid has a problem that an odor remains in the modified polyethylene obtained due to the residual crosslinking aid. In addition, the improvement in melt tension is only a certain degree. If the amount of organic peroxide and crosslinking aid is increased to further increase the melt tension, gel will be generated and moldability will deteriorate, and it will be re-melted and recycled. It was impossible to do that.

[0004]

As described above, the polyethylene obtained by the method of the prior art is not sufficient in improving the melt tension, and also has an odor and contains a gel, so that the molded article is not formed. After reusing it, it is impossible to recycle it.

[0005] The present inventors have intensively studied to solve the problems of the prior art and to invent a method for producing a modified polyethylene suitable for hollow molding, foam molding, extrusion molding and the like. As a result, a specific organic peroxide is reacted with polyethylene under specific conditions and further melt-kneaded to obtain a modified polyethylene having a high melt tension, and the modified polyethylene having a high melt tension is used as a molded article. For example, they have found that the problems of the prior art can be solved, and have reached the present invention.

As is apparent from the above description, an object of the present invention is to use a modified polyethylene which has a high melt tension and is excellent in moldability, and which can be recycled after being used as a molded article and then re-melted. To provide molded articles made of

[0007]

The present invention has the following arrangement. (1) Polyethylene 10 in an inert gas atmosphere
1 to 10 mmol of di-2-ethylhexyl peroxydicarbonate was added to and mixed with 0 g per 50 g.
After reacting at a temperature of 130 ° C. for 10 minutes to 3 hours, the melt tension (MS) at 190 ° C. obtained by melt-kneading and the intrinsic viscosity [η] measured at 135 ° C. in tetralin are obtained. , Log (M
S) A molded article using a modified polyethylene having a relationship represented by> 4.66 × log [η] −0.340 and a boiling xylene extraction residual ratio of 1% by weight or less.

(2) The molded article according to (1), wherein the polyethylene is an ethylene homopolymer.

(3) Ethylene containing not more than 30% by weight of olefin polymerized units other than ethylene.
The molded article according to the above (1), which is an olefin random copolymer.

The configuration and effects of the present invention will be described in detail below. The polyethylene used in the present invention includes not only an ethylene homopolymer but also an ethylene-olefin random copolymer containing 30% by weight or less of an olefin polymerized unit other than ethylene. Used in this sense.

The polyethylene used for producing the modified polyethylene of the present invention is a linear polyethylene obtained using a Ziegler catalyst, and preferably has an intrinsic viscosity [η] of 0.2 in tetralin measured at 135 ° C. ~ 6dl /
g, particularly preferably 0.4 to 5 dl / g, is desirably used from the viewpoint of moldability. Further, not only homopolymers of ethylene but also olefins other than ethylene, for example, linear monoolefins such as propylene, butene-1, pentene-1, hexene-1, heptene-1, and octene-1,
Branched chain monoolefins such as 4-methylpentene-1 and 2-methylpentene-1, and random copolymers of styrene and ethylene with ethylene can also be used. When using a copolymer, the olefin other than ethylene is not limited to one kind,
Even if more than one kind is included, it can be accepted. In particular,
Propylene-ethylene copolymer, ethylene-butene-1
Copolymer, ethylene-hexene-1 copolymer, ethylene-octene-1 copolymer, propylene-4-methylpentene-1 copolymer, propylene-ethylene-butene-1
And a propylene-ethylene-4-methylpentene-1 copolymer. At this time, it is necessary that the olefin polymerization unit other than ethylene is 30% by weight or less. If it exceeds 30% by weight, a gel is formed in the obtained polyethylene, which is outside the scope of the present invention. It not specifically defined for the density of these polyethylenes, but those usually 0.900 g / cm ³ of 0.980 g / cm ³ can be used.

Such polyethylene is composed of, for example, a combination of a titanium catalyst component (a solid composition in which a titanium halide is supported on a support such as a magnesium chloride compound) and an organoaluminum compound.
Slurry polymerization in which ethylene is polymerized in an inert solvent using a so-called Ziegler-based catalyst in which an electron donor component having any one of nitrogen, phosphorus and sulfur atoms is further combined as a third component of the catalyst, It can be obtained by a known method by gas phase polymerization performed in a gas phase mainly containing gas.

The polyethylene used in the present invention may be in the form of powder, pellets, film, sheet, or the like. However, for reasons of reaction efficiency and commercial production, the polyethylene is obtained by the above-mentioned various methods. The powder in a state immediately after the completion of the polymerization step and before pelletization is a preferred embodiment. The average particle size of the powder is about 50 μm to 5 mm. It is preferable that the particle size is small in terms of reaction efficiency, but it is preferable that the particle size is large from the viewpoint of powder fluidity. Therefore, it is preferable to use one having a particle size suitable for the purpose.

In the present invention, di-2-ethylhexyl peroxydicarbonate reacted with polyethylene is:
When the half-life is 1 minute, the decomposition temperature is 92 ° C, and the half-life is 1
It is an organic peroxide having a decomposition temperature of 60 ° C. over time. The use of similar percarbonates having similar decomposition temperatures does not achieve the objects of the present invention, as will be apparent from the examples below.

When adding and mixing with polyethylene, toluene, xylene,
It is convenient to use those diluted with an inert solvent typified by a hydrocarbon solvent such as isoparaffin, octane and decane. The concentration of di-2-ethylhexyl peroxydicarbonate in the solvent is about 10 to 90% by weight.

The reaction between polyethylene and di-2-ethylhexylperoxydicarbonate in the method according to the present invention is as follows. First, polyethylene is reacted with di-2-ethylhexylperoxydicarbonate in an inert gas atmosphere such as nitrogen or argon in a reaction vessel. Add and mix the dicarbonate. The temperature at this time is desirably 40 ° C. or less and 0 ° C. or more. In addition, it is desirable to stir so as to sufficiently mix. The addition amount is preferably 1 to 10 mmol, particularly preferably 2 to 10 mmol, per 100 g of polyethylene. If the amount used is small, the effect of the reforming is insufficient, and if it is too large, not only the effect cannot be expected to be improved, but also the odor remains,
This results in unstable modified polyethylene with large deterioration over time.

The mixed polyethylene and di-2-ethylhexyl peroxydicarbonate are subsequently added in an inert gas atmosphere in a reaction vessel, optionally with stirring, at 50 to 130 ° C., preferably 55 to 130 ° C. 130
5 minutes to 5 hours, preferably 10 minutes to 3
Let react for hours.

After the reaction, the reaction product is taken out of the reaction vessel and further melt-kneaded to obtain the polypropylene of the present invention. For the melt kneading, a known melt kneading method is used. For example, using a single-screw extruder, a twin-screw extruder, an extruder combining these and a gear pump, a Brabender, a Banbury mixer, etc.
Melt and kneaded at a temperature equal to or higher than the melting point of polyethylene for about 10 seconds to 1 hour, preferably for about 20 seconds to 10 minutes.

After the melt-kneading, it is usually cut into granules to form pellets, which are used for various molded products. However, they can be processed immediately after the melt-kneading to obtain molded products. In addition,
After washing with an inert solvent if necessary in a powder state before melt-kneading, it is also possible to dry and then melt-knead.

In melt kneading, if necessary, an antioxidant, an ultraviolet absorber, an antistatic agent, a nucleating agent, a lubricant, a flame retardant, an antiblocking agent, a coloring agent,
Various additives such as inorganic or organic fillers can be blended.

Although the modified polyethylene used in the product of the present invention can be obtained by the above-mentioned method, the reaction product is successively added under an inert gas atmosphere and optionally under a stirring condition after the completion of the reaction and before the melt-kneading. In the above, a preferred embodiment of the present invention is to perform a post-heating treatment at 60 to 130 ° C. The processing time is 10 minutes to 2 hours, preferably 15 minutes to 1 hour. By the post-heating treatment, the reaction efficiency is increased, the odor of the modified polyethylene obtained is further reduced, and a stabilized polyethylene with little change over time is obtained.

According to the above-mentioned method, the desired modified polyethylene used in the product of the present invention can be obtained, and the modified polyethylene must have the following characteristics. Unless these characteristics are satisfied, the object of the present invention cannot be achieved.

The modified polyethylene obtained by the production method according to the present invention has the following two essential requirements. That is, the melt tension (MS) at 190 ° C. and the intrinsic viscosity [η] measured at 135 ° C. in tetralin are logarithmic.
(MS)> 4.66 log [η] −0.340, and the boiling xylene extraction residual ratio must satisfy 1% by weight or less.

Here, the melt tension at 190 ° C. (M
S) was measured by using a melt tension tester type 2 manufactured by Toyo Seiki Seisaku-Sho, Ltd. at a temperature of 190.degree.
The molten polyethylene is extruded from a 2.095 mm diameter nozzle at a speed of 20 mm / min into the atmosphere at 23 ° C. to form a strand, and the tension of the filamentous polyethylene when the strand is taken off at a speed of 3.14 m / min. It measured and set it as melt tension (MS).

Further, the modified polyethylene obtained by the method according to the present invention has a boiling xylene extraction residual ratio of 1 as described above.
% By weight, more preferably 0.6% by weight or less. If the extraction residual ratio is large, the moldability deteriorates, and it becomes extremely difficult to re-melt and recycle after use as a molded article.

The boiling xylene extraction residue ratio was determined by placing 1 g of polyethylene in a 2-mesh wire net using a Soxhlet extractor, extracting with 200 ml of p-xylene with boiling xylene for 6 hours, and then drying and weighing the extraction residue. It was calculated as (weight of extraction residue / weight before extraction) × 100%.

The modified polyethylene thus obtained by the method according to the present invention has a high melt tension and excellent moldability, and can be recycled after being used as a molded article and then re-melted. Suitable for molding, foam molding, extrusion molding, but not limited to the molding field, various types of containers such as hollow containers, films, sheets, pipes, fibers, etc., by injection molding, T-die molding, thermoforming, etc. It can be used for molded articles.

[0028]

The reaction mechanism for obtaining the modified polyethylene in the method according to the present invention is not known at present, but the radical generated from di-2-ethylhexyl peroxydicarbonate has any interaction with the polyethylene. It is presumed that this causes the melting behavior characteristic of the modified polyethylene according to the method of the present invention, which is not seen in the known linear polyethylene, to occur.

[0029]

Next, the present invention will be described in detail with reference to Examples and Examples. Definitions of terms used in Examples and Comparative Examples and measurement methods are as follows. (1) Intrinsic viscosity: [η], measured at 135 ° C. in tetralin. (Unit: dl / g) (2) Melt tension: (MS), measured by the method described above. (Unit: gf)

Reference Example 1 After replacing the reactor with a stirrer equipped with inclined blades with nitrogen gas, Example 1 in JP-A-61-40306 was used.
An intrinsic viscosity [η] of 1.20 dl / g, obtained by slurry polymerization of ethylene in n-hexane using a catalyst obtained by combining the supported titanium catalyst component obtained in the above-described method and triethylaluminum, 10 kg of an ethylene homopolymer powder having an average particle size of 180 μm was added. Then, the operation of evacuating the reactor and supplying nitrogen gas to atmospheric pressure was repeated 10 times, and then di-2-ethylhexyl having a concentration of 70% by weight in toluene solution at 25 ° C. under a nitrogen gas atmosphere with stirring. Peroxydicarbonate 0.3
5 mol was added and mixed. Subsequently, the temperature in the reactor was reduced to 1
The temperature was raised to 00 ° C., and the reaction was performed at the same temperature for 30 minutes. After the elapse of the reaction time, the temperature in the reactor was further increased to 110 ° C,
Post-treatment was performed at the same temperature for 30 minutes. After the post-treatment, the reactor was cooled to room temperature and then opened to obtain a modified polyethylene. Subsequently, the resulting modified polyethylene 1
00 parts by weight, tetrakis [methylene-3-
(3'-5'-di-t-butyl-4'-hydroxyphenyl) propionate] 0.1 part by weight of methane and 0.1 part by weight of calcium stearate are mixed, and the mixture is extruded and granulated with a screw diameter of 40 mm. 210 ° C using a machine
And pelletized. The intrinsic viscosity [η] and the melt tension of the pellet were measured.
It was 21 dl / g and 2.6 gf.

Reference Examples 2 and 3 Modified polyethylene was prepared in the same manner as in Reference Example 1 except that the intrinsic viscosity of the polyethylene used in the reaction and the reaction conditions and post-treatment conditions were changed as shown in the table. A pellet was obtained.

Comparative Reference Examples 1 to 3 In Reference Examples 1 to 3, granulation was carried out in the same manner as in Reference Example 1 without reacting di-2-ethylhexyl peroxydicarbonate with the ethylene homopolymer used as a raw material. To obtain pellets.

Reference Examples 1 to 3 and Comparative Reference Example 1
Table 1 shows the conditions and results of Nos. 1 to 3.

[0034]

[Table 1]

Comparative Reference Example 4 In Reference Example 1, the decomposition temperature was 85 ° C. when the half-life was 1 minute and the decomposition was 1 hour when the half-life was 1 hour, instead of di-2-ethylhexyl peroxydicarbonate. Temperature 57
The reaction was carried out in the same manner as in Reference Example 1 except that di-3-methoxybutyl peroxydicarbonate was used.
Post-processing was performed.

Comparative Reference Example 5 In Comparative Reference Example 3, tetrakis [methylene-3- (3′-5′-di-) was added to polyethylene powder before granulation.
t-butyl-4'-hydroxyphenyl) propionate] In addition to 0.1 part by weight of methane and 0.1 part by weight of calcium stearate, the decomposition temperature at a half-life of 1 minute is 181 ° C., and the half-life is 1 part. Decomposition temperature at time 1
Pellets were obtained in the same manner as in Comparative Reference Example 3 except that 0.03 parts by weight of 2,5-dimethyl-2,5-di- (t-butylperoxy) -hexane at 38 ° C was added.

Reference Example 4 In Reference Example 1, the polyethylene used in the reaction was
Butene-1 unit content is 1.0% by weight, intrinsic viscosity [η]
The modified polyethylene pellets were obtained in the same manner as in Reference Example 1 except that 10 kg of an ethylene-butene-1 random copolymer powder having an average particle size of 1.70 dl / g and an average particle size of 150 μm was used.

Comparative Reference Example 6 In Reference Example 4, granulation was carried out in the same manner as in Reference Example 4 without reacting di-2-ethylhexyl peroxydicarbonate with the ethylene-butene-1 random copolymer used as a raw material. Then, a pellet was obtained.

The above Reference Example 4, Comparative Reference Example 4,
Table 2 shows the conditions and results of 5 and 6.

[0040]

[Table 2]

Example 1 Using a direct blow molding machine having a screw diameter of 65 mm, the modified polyethylene obtained by the same method as in Reference Example 4 was molded at a molding temperature of 200 ° C. and a mold temperature of 20 ° C. to have an inner volume of 5 l.
When the water tank was blow-molded, a homogeneous blow-molded product without unevenness in thickness was obtained without drawdown of the parison.

Comparative Example 1 When hollow molding was performed in the same manner as in Example 1 except that polyethylene pellets obtained by the same method as in Comparative Reference Example 6 were used, the parison was greatly drawn down, so that hollow molding was not possible. Was.

[0043]

As is clear from the above-mentioned reference example,
The modified polyethylene obtained by the method according to the present invention has a high melt tension and is excellent in moldability, so that it is possible to expand the field of use which was limited with the conventional polyethylene.

Claims (3)

[Claims] In an inert gas atmosphere, 1 to 10 mmol of di-2-ethylhexyl peroxydicarbonate is added to and mixed with 100 g of polyethylene, and mixed at a temperature of 50 to 130 ° C. for 10 minutes to 3 minutes. After reacting for hours, melt kneading, the melt tension at 190 ° C. (MS) and the intrinsic viscosity [η] measured in tetralin at 135 ° C. are log (M
S) A molded article using a modified polyethylene having a relationship represented by> 4.66 × log [η] −0.340, and having a boiling xylene extraction residual ratio of 1% by weight or less. 2. The molded article according to claim 1, wherein the polyethylene is an ethylene homopolymer. 3. The molded article according to claim 1, wherein the polyethylene is an ethylene-olefin random copolymer containing 30% by weight or less of olefin polymerized units other than ethylene.