阅读说明：本技术 循环聚乙烯-聚丙烯共混物的增容 (Compatibilization of recycled polyethylene-polypropylene blends ) 是由 苏珊娜·卡伦 赫尔曼·布劳恩 刘毅 马库斯·加莱特纳 格哈德·哈布纳 于 2020-03-26 设计创作，主要内容包括：本发明涉及一种包含共混物(A)和增容剂(B)的聚乙烯-聚丙烯组合物,共混物(A)为循环材料,所述共混物包含聚丙烯和聚乙烯,增容剂(B)为C-(2)C-(3)C-(4)三元共聚物。此外,本发明涉及包含所述聚乙烯-聚丙烯组合物的制品和用于制备所述聚乙烯-聚丙烯组合物的方法。本发明还涉及作为C-(2)C-(3)C-(4)三元共聚物的增容剂(B)用于改善共混物(A)的抗冲性-刚度平衡和形态的用途。(The invention relates to a polyethylene-polypropylene composition comprising a blend (A) which is a recycled material and a compatibilizer (B) which is C 2 C 3 C 4 A terpolymer. Furthermore, the present invention relates to an article comprising said polyethylene-polypropylene composition and to a process for preparing said polyethylene-polypropylene composition. The invention also relates to the compounds as C 2 C 3 C 4 Use of a compatibilizer (B) of a terpolymer for improving the impact-stiffness balance and morphology of the blend (a).)

1. A polyethylene-polypropylene composition obtainable by blending a)85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition, of a blend (A) comprising

i) Polypropylene, and

ii) a Polyethylene (PE),

wherein the weight ratio of polypropylene to polyethylene is 3: 7 to 7: 3, and

wherein blend (a) is recycled material recovered from waste plastic material derived from post-consumer waste and/or industrial waste;

and

b)1.0 to 15.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition, of a compatibilizer (B) of C₂C₃C₄Terpolymer, the density of the compatibilizer (B) being equal to or lower than 880kg/m determined according to ISO 1183³Preferably between 850 and 875kg/m³More preferably from 855 to 872kg/m³Still more preferably 860 to 870kg/m³Within the range of (1).

2. According to the rightThe polyethylene-polypropylene composition of claim 1, wherein said C₂C₃C₄Melt flow Rate MFR, determined according to ISO 1133, of the terpolymer₂(230 ℃, 2.16kg) is in the range of 2.0 to 40.0g/10min, preferably in the range of 3.0 to 38.0g/10min, more preferably in the range of 3.5 to 35.0g/10min, still more preferably in the range of 4.0 to 30.0g/10 min.

3. The polyethylene-polypropylene composition according to claim 1 or 2, wherein the weight ratio between the blend (a) and the compatibilizer (B) is in the range of 99: 1 to 5:1, preferably in the range of 49: 1 to 7: 1, more preferably in the range of 32: 1 to 8: 1, still more preferably in the range of 19: 1 to 9: 1, in the above range.

4. The polyethylene-polypropylene composition according to any of the preceding claims, wherein based on the C₂C₃C₄Total weight of terpolymer, said C₂C₃C₄The terpolymer has

i) An ethylene content in the range of 2.0 to 15.0 wt.%, and/or

ii) a 1-butene content in the range of 5.0 to 30.0 wt.%.

5. The polyethylene-polypropylene composition according to any one of the preceding claims, wherein said C₂C₃C₄The terpolymer has a melting temperature Tm determined according to ISO 11357 of less than 180 ℃, preferably in the range of from 120 to less than 180 ℃, more preferably in the range of from 140 to 170 ℃, still more preferably in the range of from 150 to 165 ℃.

6. The polyethylene-polypropylene composition according to any one of the preceding claims, wherein said C₂C₃C₄The glass transition temperature Tg of the terpolymer is less than-5 deg.C, preferably in the range of from-30 deg.C to less than-5 deg.C, more preferably in the range of from-27 deg.C to-10 deg.C, still more preferably in the range of from-25 deg.C to-12 deg.C.

7. The polyethylene-polypropylene composition according to any one of the preceding claims, wherein the limonene content of blend (a) determined by using solid phase microextraction (HS-SPME-GC-MS) is

(i) From 1ppm to 100ppm, preferably from 1ppm to 50ppm, more preferably from 2ppm to 50ppm, most preferably from 3ppm to 35 ppm; or

(ii) From 0.10ppm to less than 1ppm, preferably from 0.10 to less than 0.85ppm, most preferably from 0.10 to less than 0.60 ppm.

8. Polyethylene-polypropylene composition according to any one of the preceding claims, wherein the relative amount of units derived from ethylene in blend (A) is more than 20 wt. -%, based on the total weight of blend (A).

9. Polyethylene-polypropylene composition according to any one of the preceding claims, wherein blend (A) contains based on the total weight of blend (A)

i) Up to 6.0% by weight, preferably from 0.1 to 6.0% by weight, of polystyrene, and/or

ii) up to 3% by weight, preferably from 0.1 to 3% by weight, of talc, and/or

iii) up to 5.0% by weight, preferably from 0.2 to 5.0% by weight, of a polyamide, and/or

iv) chalk in an amount of up to 3% by weight, preferably 0.1 to 3% by weight.

10. Polyethylene-polypropylene composition according to any one of the preceding claims, having a melt flow rate MFR determined according to ISO 1133 in the range of from 0.1 to 50.0g/10min₂(230℃，2.16kg)。

11. The polyethylene-polypropylene composition according to any one of the preceding claims, having at least 6.0kJ/m²Preferably from 6.0 to 15.0kJ/m²More preferably in the range of 7.0 to 10.0kJ/m²Still more preferably in the range of 8.0 to 9.0kJ/m²Within a range ofSimple beam notched impact strength determined according to ISO 179/1eA at 23 ℃.

12. Polyethylene-polypropylene composition according to any one of the preceding claims, having a tensile modulus determined according to ISO 527-2 of at least 600MPa, preferably in the range of 600 to 830MPa, more preferably in the range of 620 to 800MPa, still more preferably in the range of 640 to 760 MPa.

13. An article comprising the polyethylene-polypropylene composition according to any one of claims 1 to 12.

14. A process for preparing a polyethylene-polypropylene composition according to any one of claims 1 to 12, comprising the steps of

a) The blend (A) is provided in an amount of 85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition,

b) the compatibilizer (B) is provided in an amount of 1.0 to 15.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition,

c) melting and mixing the blend of blend (A) and compatibilizer (B), optionally in the presence of 0 to 1.0 weight percent of a stabilizer or stabilizer mixture, and

d) optionally granulating.

15. Use of a compatibilizer (B) C for improving the impact-stiffness balance of a blend (A)₂C₃C₄A terpolymer, the compatibilizer (B) having

i) Equal to or lower than 880kg/m³Preferably between 850 and 875kg/m³More preferably from 855 to 872kg/m³Still more preferably 860 to 870kg/m³A density determined according to ISO 1183, and/or

ii) in the range of 2.0 to 40.0g/10min, preferably in the range of 3.0 to 38.0g/10min, more preferably in the range of 3.5 to 35.0g/10min, still more preferably in the range of 4.0 to 30.0g/10minmelt flow Rate MFR determined according to ISO 1133 in the min range₂(230℃，2.16kg)，

The blend (A) comprises

a) Polypropylene, and

b) the Polyethylene (PE) is added to the polyethylene,

wherein the weight ratio of polypropylene to polyethylene is 3: 7 to 7: 3, and

wherein blend (a) is recycled material recovered from waste plastic material derived from post-consumer waste and/or industrial waste.

Technical Field

The invention relates to a polyethylene-polypropylene composition comprising a blend (A) which is a recycled material and a compatibilizer (B) which is C₂C₃C₄A terpolymer. Furthermore, the present invention relates to an article comprising said polyethylene-polypropylene composition and to a process for preparing said polyethylene-polypropylene composition. The invention also relates to the use of a compatibilizer (B) C for improving the impact-stiffness balance and morphology of the blend (A)₂C₃C₄A terpolymer.

Background

Mechanical recycling of polymer waste from various collection systems is a major goal of current developments in this field. Mixing cycles of chemically similar polymers (e.g. styrene homopolymers and copolymers or polyamides) are often seen as a way to get rid of the classification dilemma that limits the process. Polypropylene and polyethylene are certainly candidate materials for such blends, but their inherent limited compatibility and miscibility often forces the application of some compatibilization in order to obtain compositions with good mechanical properties.

It is well known in the art that higher impact strength can be achieved by adding an elastomer (e.g., ethylene propylene rubber) as a compatibilizer, but this limits the stiffness of the resulting composition. Furthermore, many such elastomers are only provided in higher molecular weight forms or non-particulate forms, the latter requiring specific mixing equipment. WO 2015/169690 provides an alternative method by using a heterophasic ethylene-propylene copolymer as compatibilizer. The heterophasic copolymer comprises a crystalline matrix and an elastomeric component, which limits the stiffness loss but at the same time requires the addition of considerable amounts.

Disclosure of Invention

It is therefore an object of the present invention to provide a composition comprising recycled polypropylene and polyethylene, which composition is characterized by a high impact strength while the stiffness is also kept at a high level.

The present invention therefore relates to a polyethylene-polypropylene composition obtainable by blending

a)85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition, of a blend (A) comprising

i) Polypropylene, and

ii) a Polyethylene (PE),

wherein the weight ratio of polypropylene to polyethylene is 3: 7 to 7: 3, and

wherein blend (a) is a recycled material, which is recycled from waste plastic material derived from post-consumer waste and/or industrial waste;

and

b)1.0 to 15.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition, of a compatibilizer (B) which is C₂C₃C₄The density of the terpolymer, compatibilizer (B) is equal to or lower than 880kg/m determined according to ISO 1183³Preferably between 850 and 875kg/m³More preferably from 855 to 872kg/m³Still more preferably 860 to 870kg/m³Within the range of (1).

According to one embodiment of the invention, C₂C₃C₄Melt flow Rate MFR, determined according to ISO 1133, of the terpolymer₂(230 ℃, 2.16kg) is in the range of 2.0 to 40.0g/10min, preferably in the range of 3.0 to 38.0g/10min, more preferably in the range of 3.5 to 35.0g/10min, still more preferably in the range of 4.0 to 30.0g/10 min.

According to another embodiment of the invention, the weight ratio between blend (a) and compatibilizer (B) is between 99: 1 to 5:1, preferably in the range of 49: 1 to 7: 1, more preferably in the range of 32: 1 to 8: 1, still more preferably in the range of 19: 1 to 9: 1, in the above range.

According to a further embodiment of the invention, based on C₂C₃C₄Total weight of terpolymer, C₂C₃C₄The terpolymer has

i) An ethylene content in the range of 2.0 to 15.0 wt.%, and/or

ii) a 1-butene content in the range of 5.0 to 30.0 wt.%.

According to one embodiment of the invention, C₂C₃C₄The terpolymer has a melting temperature Tm determined according to ISO 11357 of less than 180 ℃, preferably in the range of from 120 to less than 180 ℃, more preferably in the range of from 140 to 170 ℃, still more preferably in the range of from 150 to 165 ℃.

According to a further embodiment of the invention, C₂C₃C₄The glass transition temperature Tg of the terpolymer is less than-5 deg.C, preferably in the range of from-30 deg.C to less than-5 deg.C, more preferably in the range of from-27 deg.C to-10 deg.C, still more preferably in the range of from-25 deg.C to-12 deg.C.

According to a first embodiment of the invention, the limonene (or limonene) content of the blend (A) determined by using solid phase microextraction (HS-SPME-GC-MS) is from 1ppm to 100ppm, preferably from 1ppm to 50ppm, more preferably from 2ppm to 50ppm, most preferably from 3ppm to 35 ppm. In a second embodiment, the limonene content of the blend (A), as determined by using solid phase microextraction (HS-SPME-GC-MS), is from 0.10ppm to less than 1ppm, preferably from 0.10 to less than 0.85ppm, most preferably from 0.10 to less than 0.60 ppm.

According to a further embodiment of the present invention, the relative amount of units derived from ethylene in blend (a) is greater than 20% by weight, based on the total weight of blend (a).

Particularly preferred is a blend wherein the blend (A) contains based on the total weight of the blend (A)

i) Up to 6.0% by weight, preferably from 0.1 to 6.0% by weight, of polystyrene, and/or

ii) up to 3% by weight, preferably from 0.1 to 3% by weight, of talc, and/or

iii) up to 5.0% by weight, preferably from 0.2 to 5.0% by weight, of a polyamide, and/or

iv) chalk in an amount of up to 3% by weight, preferably 0.1 to 3% by weight.

According to one embodiment of the invention, the polyethylene-polypropylene composition has a melt flow rate MFR determined according to ISO 1133 in the range of 0.1 to 50.0g/10min₂(230℃，2.16kg)。

According to one embodiment of the invention, the polyethylene-polypropylene composition has at least 6.0kJ/m²Preferably from 6.0 to 15.0kJ/m²More preferably in the range of 7.0 to 10.0kJ/m²Still more preferably in the range of 8.0 to 9.0kJ/m²A Charpy notched impact strength (impact strength) of the simple beam determined according to ISO 179/1eA at 23 ℃.

According to another embodiment of the present invention, the polyethylene-polypropylene composition has a tensile modulus determined according to ISO 527-2 of at least 600MPa, preferably in the range of 600 to 830MPa, more preferably in the range of 620 to 800MPa, still more preferably in the range of 640 to 760 MPa.

The invention further relates to an article comprising the above polyethylene-polypropylene composition.

The invention also relates to a process for preparing the above polyethylene-polypropylene composition comprising the following steps

a) Blend (A) is provided in an amount of 85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition,

b) the compatibilizer (B) is provided in an amount of 1.0 to 15.0 weight percent based on the total weight of the polyethylene-polypropylene composition,

c) melting and mixing the blend of blend (A) and compatibilizer (B), optionally in the presence of 0 to 1.0 weight percent of a stabilizer or stabilizer mixture, and

d) optionally granulating.

It is particularly preferred that the process comprises a granulation step d).

The invention also relates to the use of a compatibilizer (B) C for improving the impact-stiffness balance of the blend (A)₂C₃C₄A terpolymer and having

i) Equal to or lower than 880kg/m³Preferably between 850 and 875kg/m³More preferably from 855 to 872kg/m³Still more preferably 860 to 870kg/m³A density determined according to ISO 1183, and/or

ii) a melt flow rate MFR determined according to ISO 1133 in the range from 2.0 to 40.0g/10min, preferably in the range from 3.0 to 38.0g/10min, more preferably in the range from 3.5 to 35.0g/10min, still more preferably in the range from 4.0 to 30.0g/10min₂(230℃，2.16kg)，

The blend (A) comprises

a) Polypropylene, and

b) the Polyethylene (PE) is added to the polyethylene,

wherein the weight ratio of polypropylene to polyethylene is 3: 7 to 7: 3, and

wherein blend (a) is a recycled material, which is recycled from waste plastic material derived from post-consumer waste and/or industrial waste.

Detailed Description

The present invention will be described in more detail below.

Polyethylene-polypropylene composition

As outlined above, the present invention relates to a polyethylene-polypropylene composition comprising a blend of polypropylene and polyethylene (A) and a compatibilizer (B) being C₂C₃C₄A terpolymer.

In particular, the polyethylene-polypropylene composition of the invention is obtainable by blending,

based on the total weight of the polyethylene-polypropylene composition,

a)85.0 to 99.0 wt.%, preferably 86.0 to 98.0 wt.%, more preferably 87.0 to 98.0 wt.%, still more preferably 88.0 to 95.0 wt.%, still more preferably 88.0 to 93.0 wt.%, such as 88.0 to 90.0 wt.% of blend (A), and

b)1.0 to 15.0 wt. -%, preferably 2.0 to 14.0 wt. -%, more preferably 3.0 to 13.0 wt. -%, yet more preferably 5.0 to 12.0 wt. -%, still more preferably 7.0 to 12.0 wt. -%, like 10.0 to 12.0 wt. -% of a compatibilizer (B).

The polyethylene-polypropylene composition according to the present invention may further comprise an Additive (AD).

It is therefore preferred that the polyethylene-polypropylene composition of the invention is obtainable by blending,

based on the total weight of the polyethylene-polypropylene composition,

a)85.0 to 99.0 wt. -%, preferably 86.0 to 98.0 wt. -%, more preferably 87.0 to 98.0 wt. -%, still more preferably 88.0 to 95.0 wt. -%, yet more preferably 88.0 to 93.0 wt. -%, like 88.0 to 90.0 wt. -% of blend (A),

b)1.0 to 15.0 wt. -%, preferably 2.0 to 14.0 wt. -%, more preferably 3.0 to 13.0 wt. -%, still more preferably 5.0 to 12.0 wt. -%, still more preferably 7.0 to 12.0 wt. -%, like 10.0 to 12.0 wt. -% of a compatibilizer (B), and

c) optionally 0.001 to 3.0 wt%, more preferably 0.01 to 2.0 wt%, such as 0.1 to 1.0 wt% of an Additive (AD).

The Additive (AD) will be described in more detail below.

Furthermore, it is preferred that the weight ratio between blend (a) and compatibilizer (B) is in the range of 99: 1 to 5:1, more preferably in the range of 49: 1 to 7: 1, still more preferably in the range of 32: 1 to 8: 1, still more preferably in the range of 19: 1 to 9: 1, for example 9: 1.

the polyethylene-polypropylene composition according to the present invention preferably has a melt flow rate MFR determined according to ISO 1133 in the range of from 0.1 to 50.0g/10min, more preferably in the range of from 1.0 to 20.0g/10min, still more preferably in the range of from 2.0 to 15.0g/10min, such as in the range of from 4.0 to 10.0g/10min₂(230℃，2.16kg)。

As outlined above, it is understood that the polyethylene-polypropylene composition according to the present invention is characterized by good impact strength without compromising stiffness properties.

Thus, it is preferred that the polyethylene-polypropylene composition of the invention has at least 6.0kJ/m²More preferably from 6.0 to 15.0kJ/m²Still more preferably in the range of 7.0 to 10.0kJ/m²In the range of, e.g., 8.0 to 9.0kJ/m²Simple beam notched impact strength measured at 23 ℃ according to ISO 179/1 eA.

Furthermore, it is preferred that the polyethylene-polypropylene composition of the invention has a tensile modulus as determined according to ISO 527-2 of at least 600MPa, more preferably in the range of 600 to 830MPa, still more preferably in the range of 620 to 800MPa, such as in the range of 640 to 760 MPa.

The blend (A) of polypropylene and polyethylene and as C will be described in more detail below₂C₃C₄A compatibilizer (B) for the terpolymer.

Blend (A)

The polyethylene-polypropylene composition according to the invention comprises from 85.0 to 99.0 wt.% of the blend (a). The essence of the present invention is that the blend (a) is obtained from a recycled waste stream. The blend (a) may be recycled post-consumer waste or industrial waste (such as for example waste from the automotive industry), or alternatively a combination of both.

It is particularly preferred that the blend (a) consists of recycled post-consumer waste and/or industrial waste.

For the purposes of this specification and the appended claims, the term "recycled waste" is used to denote material recovered from post-consumer waste and industrial waste, rather than virgin polymer. Post-consumer waste means that the article has at least completed its first use cycle (or life cycle), i.e. has been used for its first purpose; whereas industrial waste refers to manufacturing waste that does not typically reach the consumer.

On the other hand, the term "virgin" refers to materials and/or articles that were newly produced prior to their first use, which have not been recycled.

Many different types of polyethylene or polypropylene may be present in "recycled waste".

In particular, the polypropylene fraction may comprise: isotactic propylene homopolymer, propylene with ethylene and/or C₄-C₈Random copolymers of alpha-olefins, heterophasic copolymers comprising a propylene homopolymer and/or at least one copolymer of C2 or C4-C8 alpha-olefins, and elastomeric fractions comprising copolymers of ethylene with propylene and/or C4-C8 alpha-olefins, optionally containing small amounts of dienes.

Likewise, the polyethylene fraction may comprise ethylene homopolymers or random co-copolymers of ethylene with propylene and/or C4-C8 alpha-olefinsAnd (3) a polymer. The polyethylene fraction in the recycled material may comprise recycled high density polyethylene (rhpe), recycled medium density polyethylene (rMDPE), recycled low density polyethylene (rhldpe), recycled linear low density polyethylene (rLLDPE) and mixtures thereof. In a certain embodiment, the recycled material is high density polyethylene having an average density greater than 0.7g/cm³Preferably greater than 0.75g/cm³Most preferably greater than 0.8g/cm³。

The term "recycled material" as used herein means material that is reprocessed from "recycled waste".

A polymer blend is a mixture of two or more polymer components. Typically, the blend may be prepared by mixing two or more polymer components. A suitable mixing procedure known in the art is a post-polymerization blending procedure. Post-polymerization blending can be dry blending of the polymer components (e.g., polymer powder and/or composite polymer pellets), or melt blending by melt mixing the polymer components.

The polypropylene/polyethylene weight ratio in blend (a) was in the range of 7: 3 to 3: 7, in the above range.

Preferably, blend (a) is obtained from recycled waste by plastic recycling processes known in the art. Such recyclates are commercially available from, for example, Corepla (Italian treasures, responsible for the collection, recovery and Recycling of packaging plastic waste), Resource Plastics Corp (Brampton, ON), Kruschitz GmbH, Plastics and Recycling (AT), Vogt Plastics GmbH (DE), Mtm Plastics GmbH (DE), and the like. Non-exhaustive examples of polyethylene rich recycled materials include DIPOLEN S (Mtm Plastics GmbH), food grade rhhdpe (bifapaplc) and a range of polyethylene rich materials such as HD-LM02041 by PLASgran ltd.

In a certain preferred embodiment, the recycled polyethylene rich material is DIPOLEN (mtm Plastics gmbh), such as DIPOLEN S or DIPOLEN H, DIPOLEN PP or DIPOLEN SP, preferably DIPOLEN S. DIPOLEN is derived from a domestic waste stream (i.e. it is a product of the life cycle), such as the "yellow bag" circulation system operated in some germany.

The relative amount of units derived from ethylene in the combined polypropylene and polyethylene fraction of blend (a) may be more than 20 wt%, preferably more than 27 wt%, more preferably more than 30 wt%, still more preferably more than 35 wt%, most preferably more than 40 wt%, relative to the total weight of blend (a).

Furthermore, the relative amount of propylene-derived units in the combined polypropylene and polyethylene fraction of blend (a) may be greater than 30 wt% but less than 70 wt%, relative to the total weight of blend (a).

According to a first embodiment of the present invention, it is preferred that blend (A) has a limonene content as determined using solid phase microextraction (HS-SPME-GC-MS) of from 1ppm to 100ppm, preferably from 1ppm to 50ppm, more preferably from 2ppm to 50ppm, most preferably from 3ppm to 35 ppm. Limonene is commonly found in recycled polyolefin materials and originates from packaging applications in the field of cosmetics, detergents, shampoos and similar products. Thus, when blend (A) contains materials derived from such domestic waste streams, blend (A) contains limonene. In a second embodiment of the present invention, the blend (A) has a limonene content as determined by using solid phase microextraction (HS-SPME-GC-MS) of from 0.10ppm to less than 1ppm, preferably from 0.10 to less than 0.85ppm, most preferably from 0.10 to less than 0.60 ppm. The blend (a) according to the second embodiment may be prepared by subjecting the blend (a) according to the first embodiment to washing and/or aeration. Washing may be achieved by an industrial scrubber (e.g. supplied by Herbold mecksheim GmbH). Depending on the source of the waste stream, multiple wash cycles may be required. Various aeration methods as described in US 5,767,230 are also known in the art. US 5,767,230 is incorporated herein by reference. The process described in US 5,767,230 is preferably combined with a washing stage as described above.

The fatty acid content is another indication of the source of recycling of blend (a).

Due to the recycling source, the blend (A) may also contain

i) An organic filler, and/or

ii) an inorganic filler, and/or

iii) additives

The content thereof is at most 4% by weight relative to the weight of blend (A).

The blend (A) preferably contains

(i) Up to 6.0 wt% polystyrene; and/or

(ii) Up to 3 wt% talc; and/or

(iii) Up to 5.0 wt.% of a polyamide; and/or

(iv) Chalk in an amount of up to 3% by weight.

The blend (A) typically contains

(i)0.1 to 6.0 wt% polystyrene; and/or

(ii)0.1 to 3 weight percent talc; and/or

(iii)0.2 to 5.0 wt.% of a polyamide; and/or

(iv)0.1 to 3% by weight of chalk.

The blend (a) may further contain polyethylene terephthalate (PET) and polyvinyl chloride (PVC). Preferably, the blend (A) further contains, based on the total weight of the blend (A)

(vi) (vii) up to 5.0 wt.%, more preferably 0.2 to 5.0 wt.% of polyethylene terephthalate (PET), and/or (vii) up to 5.0 wt.%, more preferably 0.2 to 5.0 wt.% of polyvinyl chloride (PVC).

Compatibilizer (B)

The polyethylene-polypropylene composition of the present invention further comprises a compatibilizer (B).

A "compatibilizer" is a substance in polymer chemistry that is added to an immiscible polymer blend to increase its stability.

The compatibilizer (B) according to the invention is C₂C₃C₄Terpolymers, i.e. copolymers of propylene, ethylene and 1-butene.

Preferably based on C₂C₃C₄Total weight of terpolymer, said C₂C₃C₄The ethylene content of the terpolymer is in the range of 2.0 to 15.0 wt%, more preferably in the range of 3.0 to 12.0 wt%, still more preferably in the range of 4.0 to 10.0 wt%, such as in the range of 4.5 to 9.0 wt%。

Additionally or alternatively, it is preferred that C is based on₂C₃C₄Total weight of terpolymer, C₂C₃C₄The terpolymer has a 1-butene content in the range of 5.0 to 30.0 wt.%, more preferably in the range of 5.5 to 27.0 wt.%, still more preferably in the range of 6.0 to 23.0 wt.%, such as in the range of 7.0 to 20.0 wt.%.

Further, it is preferable that C₂C₃C₄Melt flow Rate MFR, determined according to ISO 1133, of the terpolymer₂(230 ℃, 2.16kg) is in the range of 2.0 to 40.0g/10min, more preferably in the range of 3.0 to 38.0g/10min, still more preferably in the range of 3.5 to 35.0g/10min, such as in the range of 4.0 to 30.0g/10 min.

Preferably C₂C₃C₄The melting temperature Tm of the terpolymer, determined according to ISO 11357, is below 180 ℃, more preferably in the range of 120 to below 180 ℃, still more preferably in the range of 140 to 170 ℃, such as in the range of 150 to 165 ℃.

Further, it is preferable that C₂C₃C₄The glass transition temperature of the terpolymer is less than-5 ℃, more preferably in the range of from-30 ℃ to less than-5 ℃, still more preferably in the range of from-27 ℃ to-10 ℃, such as in the range of from-25 ℃ to-12 ℃.

The density of the compatibilizer (B) is equal to or lower than 880kg/m determined according to ISO 1183³More preferably 850 to 875kg/m³Still more preferably from 855 to 872kg/m³In the range of 860 to 870kg/m, for example³Within the range of (1).

Preferably, the compatibilizer (B) is C, which is known in the art₂C₃C₄Terpolymers, e.g. C of the TAFMER series commercially available from Mitsui₂C₃C₄A terpolymer.

Additive (AD)

As indicated above, the polyethylene-polypropylene composition according to the invention may contain additives.

In particular, the polyethylene-polypropylene composition of the invention may contain up to 1.0% by weight of a stabilizer or stabilizer mixture. The content of the stabilizer is preferably 0.1 to 1.0% by weight, based on the total weight of the polyethylene-polypropylene composition.

Stabilizers are well known in the art and may be, for example, antioxidants, antacids, anti-blocking agents, anti-uv agents, nucleating agents or antistatic agents.

Examples of antioxidants commonly used in the art are sterically hindered phenols (e.g. CAS No. 6683-19-8, also available from BASF as Irganox1010FF^TMOr Irganox 225 by BASF^TMSold), phosphorus based antioxidants (e.g., CAS number 31570-04-4, also by Clariant as Hostanox PAR 24(FF)^TMSold or otherwise available from BASF as Irgafos 168(FF)^TMSold), sulfur based antioxidants (e.g., CAS number 693-36-7, Irganox PS-802FL available from BASF^TMSold), nitrogen-based antioxidants (such as 4,4 '-bis (1, 1' -dimethyl-benzyl) diphenylamine), or antioxidant blends.

Antacids are also well known in the art. Examples are calcium stearate, sodium stearate, zinc stearate, oxides of magnesium and zinc, synthetic hydrotalcite (e.g. SHT, CAS No. 11097-59-9), lactate (or lactate) and lactate (lactylate), and calcium stearate (CAS No. 1592-23-0) and zinc stearate (CAS No. 557-05-1).

A common anti-caking agent is a natural silica, such as diatomaceous earth (e.g., CAS No. 60676-86-0 (SuperfFloss)^TM) CAS number 60676-86-0(SuperFloss E)^TM) Or CAS number 60676-86-0(Celite 499)^TM) Synthetic silica (e.g., CAS No. 7631-86-9, CAS No. 112926-00-8, CAS No. 7631-86-9, or CAS No. 7631-86-9), silicates (e.g., aluminum silicate (kaolin) CAS No. 1318-74-7, sodium aluminum silicate CAS No. 1344-00-9, calcined kaolin CAS No. 92704-41-1, aluminum silicate CAS No. 1327-36-2, or calcium silicate CAS No. 1344-95-2), synthetic zeolites (e.g., hydrated calcium aluminum silicate CAS No. 1344-01-0, or calcium aluminum silicate hydrate CAS No. 1344-01-0).

Examples of the ultraviolet screening agent include bis- (2,2,6, 6-tetramethyl-4-piperidyl) -sebacate (CAS No. 52829-07-9, Tinuvin 770); 2-hydroxy-4-n-octyloxy-benzophenone (CAS No. 1843-05-6, Chimassorb 81).

Nucleating agents are, for example, sodium benzoate (CAS No. 532-32-1); 1,3:2, 4-bis (3, 4-dimethylbenzylidene) sorbitol (CAS 135861-56-2, Millad 3988).

Suitable antistatics are, for example, glycerol esters (CAS No. 97593-29-8) or ethoxylated amines (CAS No. 71786-60-2 or 61791-31-9) or ethoxylated amides (CAS No. 204-393-1).

These stabilizers are generally added in amounts of 100 to 2000ppm for each individual component of the polymer.

The polyethylene-polypropylene composition preferably contains between 1.0 and 2.0 wt% of PO ash.

Method

The process according to the present invention for providing a polyethylene-polypropylene composition comprises the steps of:

a) blend (A) is provided in an amount of 85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition,

b) the compatibilizer (B) is provided in an amount of 1.0 to 15.0 weight percent based on the total weight of the polyethylene-polypropylene composition,

c) melting and mixing the blend of blend (A) and compatibilizer (B), optionally in the presence of 0 to 1.0 weight percent of a stabilizer or stabilizer mixture, and

d) optionally granulating.

It is particularly preferred that the process comprises a granulation step d).

Thus, it is preferred that the process for providing a polyethylene-polypropylene composition comprises the following steps

a) Blend (A) is provided in an amount of 85.0 to 99.0 wt. -%, based on the total weight of the polyethylene-polypropylene composition,

b) the compatibilizer (B) is provided in an amount of 1.0 to 15.0 weight percent based on the total weight of the polyethylene-polypropylene composition,

c) melting and mixing the blend of blend (A) and compatibilizer (B), optionally in the presence of 0 to 1.0 weight percent of a stabilizer or stabilizer mixture, and

d) and (6) granulating.

All preferred aspects, definitions and embodiments as described above shall also apply to the method.

Use of

The invention further relates to the use of a compatibilizer (B) to improve the impact-stiffness balance of the blend (A), the compatibilizer (B) being C₂C₃C₄A terpolymer of, and having

i) Equal to or lower than 880kg/m³According to ISO 1183, and/or

ii) a melt flow rate MFR determined according to ISO 1133 in the range of 2.0 to 40.0g/10min₂(230℃，2.16kg)

The blend (A) comprises

a) Polypropylene, and

b) the Polyethylene (PE) is added to the polyethylene,

wherein the weight ratio of polypropylene to polyethylene is 3: 7 to 7: 3, and

wherein blend (a) is a recycled material, which is recycled from waste plastic material derived from post-consumer waste and/or industrial waste.

All preferred aspects, definitions and embodiments as described above shall also apply for this use.

Experimental part

The following examples are included to demonstrate certain aspects and embodiments of the invention as set forth in the claims. However, those skilled in the art will appreciate that the following description is illustrative only and should not be construed as limiting the invention in any way.

Test method

Tensile Modulus (TM) was measured according to ISO 527-2 (crosshead speed 1mm/min for modulus determination, then switched to 50mm/min until fracture at 23 ℃) using injection moulded specimens (dog bone shape, 4mm thickness) as described in EN ISO 5247-2. The measurement was carried out after a conditioning time of 96 hours for the sample.

Impact strength was determined according to ISO 179-1eA at +23 ℃ as simple beam Notched Impact Strength (NIS) on 80X 10X 4mm injection-molded specimens prepared according to EN ISO 1873-2. According to this standard, the samples were tested after 96 hours.

Comonomer content of poly (propylene-co-ethylene-co-butylene)

Use to¹H and¹³c Bruker Avance III 500NMR spectrometers operating at 500.13 and 125.76MHz respectively record quantitation in the molten state¹³C{¹H } NMR spectrum. All pneumatic units were purged with nitrogen at 180 deg.C¹³A C-optimized 7mm Magic Angle Spinning (MAS) probe recorded all spectra. Approximately 200mg of material was loaded into a 7mm outer diameter zirconia MAS rotor and rotated at 4.5 kHz. This setting was chosen primarily for the high sensitivity {1, 2, 6} required for fast identification and accurate quantification. NOE {3, 1} and RS-HEPT decoupling schemes {4, 5} are utilized with short cycle delays using standard single pulse excitation. A total of 1024(1k) transient signals per spectrum were acquired.

Will quantify¹³C{¹H NMR spectra were processed, integrated and the relevant quantitative properties were determined from the integration. All chemical shifts are internally referenced to methyl isotactic pentads (mmmm) at 21.85 ppm.

No signature 11 corresponding to the area defect was observed. The amount of propylene was quantified based on the major S α methylene sites at 44.1 ppm:

p is total ═ I_Sαα

A characteristic signal corresponding to the incorporation of 1-butene was observed and the comonomer content was quantified in the following manner. The amount of isolated 1-butene incorporated into the PPBPP sequence was quantified using the integral of the α B2 site at 44.1ppm and taking into account the number of reporter sites per comonomer:

B＝I_αB2/2

the amount of 1-butene continuously incorporated in the PPBBPP sequence was quantified using the integral of α α B2 sites at 40.5ppm and taking into account the number of reporter sites per comonomer:

BB＝2*I_ααB2

the total 1-butene content was calculated based on the sum of the isolated incorporation and the continuously incorporated 1-butene:

total of B is B + BB

The total mole fraction of 1-butene in the polymer was then calculated as: fB ═ B total/(E total + P total + B total)

A characteristic signal corresponding to the incorporation of ethylene was observed and the comonomer content was quantified in the following manner. The amount of isolated ethylene incorporated in the PPEPP sequence was quantified using the integral of S α γ sites at 37.9ppm and taking into account the number of reporter sites per comonomer:

E＝I_Sαγ/2

in case no sites indicating continuous incorporation were observed, the total ethylene comonomer content was calculated based on this amount only:

e Total ═ E

The total mole fraction of ethylene in the polymer was then calculated as:

fE ═ E total/(E total + P total + B total)

The mole percent comonomer incorporation is calculated from the mole fraction:

b [ mol% ] -100 fB

E [ mol% ] -100 fE

The weight percent comonomer incorporation is calculated from the mole fraction:

b [ wt% ] ═ 100 (fB × 56.11)/((fE × 28.05) + (fB × 56.11) + ((1- (fE + fB)) × 42.08))

E [ wt% ] ═ 100 (fE × 28.05)/((fE × 28.05) + (fB × 56.11) + ((1- (fE + fB)) × 42.08))

Reference documents:

1)Klimke,K.,Parkinson,M.,Piel,C.,Kaminsky,W.,Spiess,H.W.,Wilhelm,M.,Macromol.Chem.Phys.2006；207:382.

2)Parkinson,M.,Klimke,K.,Spiess,H.W.,Wilhelm,M.,Macromol.Chem.Phys.2007；208:2128.

3)Pollard,M.,Klimke,K.,Graf,R.,Spiess,H.W.,Wilhelm,M.,Sperber,O.,Piel,C.,Kaminsky,W.,Macromolecules 2004；37:813.

4)Filip,X.,Tripon,C.,Filip,C.,J.Mag.Resn.2005,176,239.

5)Griffin,J.M.,Tripon,C.,Samoson,A.,Filip,C.,and Brown,S.P.,Mag.Res.in Chem.200745,S1,S198.

6)Castignolles,P.,Graf,R.,Parkinson,M.,Wilhelm,M.,Gaborieau,M.,Polymer 50(2009)2373.

7)Busico,V.,Cipullo,R.,Prog.Polym.Sci.26(2001)443.

8)Busico,V.,Cipullo,R.,Monaco,G.,Vacatello,M.,Segre,A.L.,Macromolecules 30(1997)6251.

9)Zhou,Z.,Kuemmerle,R.,Qiu,X.,Redwine,D.,Cong,R.,Taha,A.,Baugh,D.Winniford,B.,J.Mag.Reson.187(2007)225.

10)Busico,V.,Carbonniere,P.,Cipullo,R.,Pellecchia,R.,Severn,J.,Talarico,G.,Macromol.Rapid Commun.2007,28,1128.

11)Resconi,L.,Cavallo,L.,Fait,A.,Piemontesi,F.,Chem.Rev.2000,100,1253.

ratio of units derived from C2 and C3: the ethylene content of the blend (A) was determined by quantitative Fourier transform Infrared Spectroscopy (FTIR) and compared with the quantitative¹³The results obtained by C NMR spectroscopy were phase-calibrated.

The film was pressed at 190 ℃ to a thickness between 300 and 500 μm and the spectrum was recorded in transmission mode. The associated instrument settings include 5000 to 400 wave numbers (cm)^-1) Spectral window of 2.0cm^-1And 8 scans.

Use pair¹H and¹³c Bruker Advance III 400NMR spectrometers operating at 400.15 and 100.62MHz respectively record quantitative measurements in solution¹³C{¹H } NMR spectrum. All spectral uses¹³C optimized 10mm extended temperature probe was recorded at 125 ℃, using nitrogen for all pneumatic devices. About 200mg of material was mixed with chromium (III) acetylacetonate (Cr (acac)₃) Dissolved together in 3ml of 1, 2-tetrachloroethane-d 2(TCE-d2) to give a 65mM solution of relaxant in solvent (Singh, G., Kothari, A., Gupta, V., Polymer Testing 285 (2009), 475). To ensure homogeneity of the solution, after preparation of the initial sample in the heating block, the NMR tube was further heated in a rotary oven for at least 1 hour. After insertion into the magnet, the tube was rotated at 10 Hz. SelectingThis setting is chosen primarily for high resolution and is quantitatively needed due to the quantification of accurate ethylene content. Using standard single pulse excitation without NOE, an optimized tip angle (tip angle), 1s cycle delay and a dual-stage WALTZ16 decoupling scheme (Zhou, z., Kuemmerle, r., Qiu, x., Redwine, d., conv, r., Taha, a., Baugh, d.winnford, b., j.mag.reson.187(2007) 225; Busico, v., Carbonniere, p., Cipullo, r., pellechia, r., Severn, j., Talarico, g., macro.rapid commu.2007, 28,1128) was used. A total of 6144(6k) transient signals were acquired per spectrum. For quantitative determination¹³C{¹H NMR spectra were processed, integrated and the relevant quantitative properties were determined from the integration. Using the chemical shifts of the solvent, all chemical shifts are indirectly referenced to the central methylene group of the ethylene block (EEE) at 30.00 ppm. This approach allows comparable referencing even if the structural unit is not present. A characteristic signal corresponding to the incorporation of ethylene was observed (Cheng, h.n., Macromolecules 17(1984),1950), and the ethylene fraction was calculated as the fraction of ethylene in the blend relative to all monomers in the polymer: by applying the method of Wang et al (Wang, W-j., Zhu, s., Macromolecules 33(2000),1157) to (E/(P + E))¹³C{¹H spectrum the ethylene fraction is quantified by integrating multiple signals over the entire spectral region. This method was chosen for its robustness and ability to account for the presence of regional defects when needed. The integration region is adjusted slightly to improve applicability over the entire range of comonomer contents encountered. Mole percent ethylene was calculated from mole fraction: e [ mol%]100 × fE. The weight percentage of comonomer incorporation was calculated from the mole fraction: e [ wt.%]＝100*(fE*28.06)/((fE*28.06)+((1-fE)*42.08))

iPP, PE, PS, PA and PE content:

calibration standards were prepared by blending iPP and HDPE to establish a calibration curve. The film thickness of the calibration standard was 300. mu.m. To quantify the iPP, PS and PA6 content in the samples, quantitative infrared spectra were recorded in the solid state using a Bruker Vertex 70FTIR spectrometer. The spectra were recorded on 25X 25mm square films 50 to 100 μm thick, prepared by compression moulding at 190 ℃ and 4 to 6 mPa. MiningUsing standard transmission FTIR spectroscopy, using a spectral range of 4000 to 400cm^-1Aperture of 6mm and spectral resolution of 2cm^-116 background scans, 16 spectral scans, a zero fill factor of 32 for the interferogram, Norton Beer strong apodization.

Measuring iPP at 1167cm^-1The absorption of the band and the iPP content was quantified according to a calibration curve (absorption/thickness (cm) versus iPP content (% by weight)).

Measurement 1601cm^-1(PS) and 3300cm^-1(PA6) and quantification of PS and PA6 contents according to calibration curves (absorption/thickness (cm) versus PS and PA contents (% by weight)). The PE content was obtained by subtracting iPP, PS and PA6 from 100. The analysis was performed as a double assay.

Talc and chalk content: measured by thermogravimetric analysis (TGA); experiments were performed using a Perkin Elmer TGA 8000. Approximately 10 to 20mg of material was placed in a platinum pan. The temperature was equilibrated at 50 ℃ for 10 minutes and then raised to 950 ℃ under nitrogen at a ramp rate of 20 ℃/min. Will lose Weight (WCO) between about 550 ℃ and 700 DEG C₂) Ascribed to CaCO₃CO liberated₂The chalk content was therefore evaluated as:

chalk content 100/44 × WCO₂

The temperature was then reduced to 300 ℃ at a cooling rate of 20 ℃/min. The gas was then switched to oxygen and the temperature was again raised to 900 ℃. The weight loss in this step is attributed to carbon black (Wcb). With known carbon black and chalk content, the ash content excluding chalk and carbon black is calculated as:

ash content (ash) -56/44 x WCO₂–Wcb

Wherein the ash is the weight% measured at 900 ℃ in the first step carried out under nitrogen. The ash content was estimated to be the same as the talc content of the recyclates studied.

MFR: as indicated, the melt flow rate was 2.16kg load (MFR) at 230 ℃ or 190 ℃₂) Measured as follows. The melt flow rate is determined according to the ISO 1133 standard on a test apparatus at a temperature of 230 ℃ (or 190 ℃) under a load of 2.16kg in 10 minutesThe amount of polymer extruded is in grams.

Melting temperature was determined by DSC according to ISO 11357.

The glass transition temperature Tg is determined by dynamic mechanical analysis according to ISO 6721-7. Compression moulding of a sample (40X 10X 1 mm) at a heating rate of 2 ℃/min and a frequency of 1Hz between-100 ℃ and +150 DEG C³) The measurement was performed in the torsional mode.

The density is determined according to ISO 1183.

Limonene content in DIPELEN

Measuring

The quantification of limonene was performed by standard addition using solid phase microextraction (HS-SPME-GC-MS).

50mg of the ground sample was weighed into a 20mL headspace vial, and after the addition of different concentrations of limonene and a glass-coated magnetic stir bar, the vial was capped with a silicone/PTFE lined magnetic cap. A known concentration of diluted limonene standard was added to the sample using a microcapillary tube (10 pL). The addition of 0, 2, 20 and 100ng amounts corresponded to 0mg/kg, 0.1mg/kg, 1mg/kg and 5mg/kg of limonene, furthermore standard amounts of 6.6mg/kg, 11mg/kg and 16.5mg/kg of limonene were used in combination with some of the samples tested in this application. Ions 93 collected in SIM mode are used for quantification. The volatile components were enriched by headspace solid phase microextraction using a 2cm stationary flex 50/30pm DVB/Carboxen/PDMS fiber, enriched for 20 minutes at 60 ℃. The desorption was carried out directly at the heated inlet of the GCMS system at 270 ℃.

GCMS parameters:

column: 30m HP 5MS 0.25X 0.25

Sample injector: no split, with 0.75mm SPME liner, 270 deg.C

Temperature program: -10 ℃ (1min)

Carrier gas: helium 5.0, 31cm/s linear velocity, constant flow

MS: a single quadrupole rod, a direct interface, the interface temperature of 280 DEG C

Collecting: SIM scanning mode

Scanning parameters are as follows: 20 to 300amu

SIM parameters: m/Z93, 100ms residence time

Table 1: limonene content in DIPOLENE (blend (A))

Sample (I)	Limonene [ mg/kg]HS-SPME-GC-MS[1]
		Dipolen S	31.5±2.6

^[1]And (4) headspace solid phase microextraction. The material is available from mtm plastics GmbH, according to 2018 specification.

Total free fatty acid content

Quantification of fatty acids was performed by standard addition using headspace solid phase microextraction (HS-SPME-GC-MS).

50mg of the ground sample was weighed into a 20mL headspace vial, and after the addition of different concentrations of limonene and a glass-coated magnetic stir bar, the vial was capped with a silicone/PTFE lined magnetic cap. Diluted free fatty acid mixture (acetic, propionic, butyric, valeric, caproic and caprylic) standards of known concentration were added to the samples at three different levels using 10 μ L microcapillaries. The addition of 0, 50, 100 and 500ng corresponded to 0mg/kg, 1mg/kg, 2mg/kg and 10mg/kg of each individual acid. All acids except propionic acid (here ion 74) were quantified using ion 60 collected in SIM mode.

GCMS parameters:

column: 20m ZB Wax plus 0.25 × 0.25

Sample injector: split ratio (split)5:1, split gasket with glass liner, 250 deg.C

Temperature program: 40 deg.C (1min) @6 deg.C/min to 120 deg.C and @15 deg.C to 245 deg.C (5min)

Carrier gas: helium 5.0, 40cm/s linear velocity, constant flow

MS: a single quadrupole rod is directly connected with the interface, and the temperature of the interface is 220 DEG C

Collecting: SIM scanning mode

Scanning parameters are as follows: 46 to 250amu 6.6 scans/sec

SIM parameters: m/z 60.74, 6.6 scans/sec

Table 2: total fatty acid content in Dipolen (blend (A))

Sample (I)	Total fatty acid concentration [ mg/kg][1]
		Dipolen S	70.6

^[1]The concentrations of acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, pelargonic acid and capric acid in each sample were added together to give the total fatty acid concentration value.

Experiment of

Many blends were produced using DIPOLEN S as blend (a), a polyethylene-polypropylene blend from Mtm Plastics GmbH, a material meeting 2018 month 8 specification.

5 to 10% by weight of a compatibilizer (B) derived from the reactor is added to each blend. The following commercially available terpolymers were used as compatibilizer (B):

table 3: properties of the compatibilizer (B)

Compatibilizer		B1	B2
						Tafmer PN 0040	Tafmer PN 20300
MFR	[g/10min]	4.0	30.0
				Tm	[℃]	160	160
Tg	[℃]	-16	-26
				Density of	[kg/m3]	868	868
C2	[ weight% ]]	4.7	19.9
				C4	[ weight% ]]	8.9	7.1

The compositions were prepared by melt blending on a co-rotating twin screw extruder with 0.3 wt% of Irganox B225F (AO) as a stabilizer. The polymer melt mixture is discharged and pelletized. To test mechanical properties, test specimens were produced and tested according to ISO179 using a 1eA notched specimen to measure simple beam Notched Impact Strength (NIS) and according to ISO 527-1/2 using a 1A specimen to measure tensile properties at room temperature. The results are summarized in table 4.

Table 4: compositions and Properties of examples and comparative examples of the present invention

		CE1	IE1	IE2	IE3	IE4
							A	[ weight% ]]	99.7	94.7	89.7	94.7	89.7
B1	[ weight% ]]	-	5	10	-	-
							B2	[ weight% ]]	-	-	-	5	10
AO	[ weight% ]]	0.3	0.3	0.3	0.3	0.3
							NIS	[kJ/m2]	5.7	6.8	8.9	6.4	8.2
TM	[MPa]	850	736	640	755	641

As can be seen from table 4, the compositions according to the examples of the present invention have higher impact strength than the reference without compatibilizer while the tensile modulus is maintained at a high level.