The present invention is directed to a moulded article comprising a polypropylene composition (C) comprising a base polymer being a first isotactic propylene homopolymer (H-PP) and a second polypropylene (PP2). The present invention is further directed to a sterilized packaging comprising the moulded article, a process for gamma-ray sterilization of the moulded article and the use of the second polypropylene (PP2) in the polypropylene composition (C) for reducing the level of overall migration or reducing discoloration in the polymer composition (C), as well as for improving resistance to gamma-ray sterilization of said polypropylene composition (C).

Polypropylene (PP) is one of the most frequently used plastics in packaging applications ln a continuously increasing part of this market, especially in the pharmaceutical area, but also in food packaging and especially in medical applications (syringes, pouches, tubes etc.), the material is sterilized in either heat (steam), radiation (b / electrons or g) or chemicals (mostly ethylene oxide). However, sterilization processes will inevitably affect the mechanical and optical properties. For instance, due to strong influence of the radiation, sometimes the discoloration becomes visible in the goods. The application of radiation, especially gamma radiation, can induce chain scission and similar degradation effects, resulting in a reduced melt viscosity and severe embrittlement ft has also been found out that these degradation events continue for extended periods of time after the actual sterilization process, making long-term studies necessary for studying the effects. Several strategies have been published in the prior art for the reduction of these effects including the use of“mobilizing agents” (paraffinic oils) and special stabilizer formulations. Mobilizing agents have multiple functions in this area. However, only sufficient amounts of mobilizing agents will be able to give a noticeable‘gamma absorbing’ activity, while insufficient amounts fail to show a protection effect. Another drawback of using mobilizing agents is migration ft is evident that this fraction can migrate to the surface and the medium which is in contact with the surface. Thus, there is a need in the art for moulded articles formed from a polypropylene material featuring an improved mechanical resistance to gamma-ray sterilization.

The present invention is directed to a moulded article comprising a polypropylene composition (C), the polypropylene composition comprising, based on the total weight of the polypropylene composition (C),

i) 70.0 to 95.0 wt.-%, based on the overall weight of the polypropylene composition (C), of a first isotactic propylene homopolymer (H-PP), which has

(i-a) a melt flow rate MFR2 determined according to 1S01133 at 230 °C and 2.16 kg in the range from 4.0 to 22.0 g/ 10 min; and

(i-b) a melting temperature in the range of 145 to 162 °C as determined by differential scanning calorimetry (DSC); and

(i-c) a content of 2, 1 erythro regio-defects in the range from 0.1 to 1.3 mol % as

determined by ¹³ C-NMR spectroscopy

and

ii) 5.0 to 30.0 wt.-%, based on the overall weight of the polypropylene composition (C), of a second polypropylene (PP2) being different from the first isotactic propylene homopolymer (H-PP) and having a melting temperature Tm as measured by differential scanning calorimetry (DSC) according to 1SO 11357 in the range of 50 to 125 °C.

According to still another embodiment, the present invention is directed to sterilized packaging comprising the moulded article according to the present invention.

The present invention is further directed to a process for gamma-ray sterilization of the moulded article according to the present invention, comprising the steps of providing the moulded article according to the present invention and subjecting said moulded article to gamma-ray sterilization.

According to another embodiment, the present invention is directed to uses of the second polypropylene (PP2) as contained in the polymer composition (C) or in a random copolymer for (a) reducing the level of overall migration in the polymer composition (C) as determined according to EN ISO 1186-14:2002 on injection moulded plaques,

60 x 60 x 1 mm ³ to less than 10.0 mg/dm ² , preferably of less than 8.0 mg/dm ² , more preferably less than 6.0 mg/dm ² and even more preferably less than 5.0 mg/dm ² ;

(b) improving the resistance to gamma resistance of said polymer composition (C); and/or

(c) reducing discoloration of the polymer composition (C) after gamma-ray

sterilization at 50kGy and 60 days of aging at 80°C as defined by yellowness index (YI) of not higher than 20, more preferably not higher than 16 as determined on injection moulded plaques 60 x 60 x 1 mm ³ according to standard method ASTM E313.

In the following, the present invention is described in more detail.

The polypropylene composition (C)

The inventive moulded article comprises a polypropylene composition (C) as the main component. Said polypropylene composition (C) comprises a first isotactic propylene homopolymer (H-PP) and a second polypropylene (PP2) as the two main components. The second polypropylene (PP2) preferably functions as a processing aid.

Accordingly, the polypropylene composition (C) preferably comprises

70.0 to 95.0 wt.-%, preferably 75.0 to 93.0 wt.-%, more preferably 80.0 to 92.0 wt.-%, still more preferably 85.0 to 91.0 wt.-%, of the first isotactic propylene homopolymer (H-PP) and

5.0 to 30.0 wt.-%, preferably 7.0 to 25.0 wt.-%, more preferably 9.0 to 20.0 wt.-%, still more preferably 8.0 to 15.0 wt.-% of the second polypropylene (PP2), based on the total weight of the polypropylene composition (C).

The polypropylene composition (C) may include additives (AD). Accordingly, it is preferred that the polypropylene composition (C) comprises, more preferably consists of, 70.0 to 95.0 wt.-%, preferably 75.0 to 93.0 wt.-%, more preferably 80.0 to 92.0 wt.-%, still more preferably 86.0 to 91.0 wt.-%, of the first isotactic propylene homopolymer (H-PP) and 5.0 to 30.0 wt.-%, preferably 7.0 to 25.0 wt.-%, more preferably 8.0 to 20.0 wt.-%, still more preferably 9.0 to 15.0 wt.-% of the second polypropylene (PP2), and 0.0 to 5.0 wt.-%, more preferably 0.05 to 4.0 wt.-%, still more preferably 0.1 to 3.0 wt.-% of additives (AD), based on the total weight of the polypropylene composition (C). The additives (AD) are described in more detail below. The amounts of the components total up to 100 wt.-% of the polypropylene composition (C). Preferably, the polypropylene composition (C) does not comprise (a) further polymeric material different to the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2) in an amount exceeding 5.0 wt.-%, preferably in an amount exceeding 3.0 wt.-%, more preferably in an amount exceeding 2.5 wt.-%, based on the overall weight of the polypropylene composition (C).

Accordingly, it is preferred that the polymeric material of the polypropylene composition (C) consists of the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2). In one embodiment the polypropylene composition (C) comprises the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2) in a weight ratio from 75:25 to 95:5 more preferably in a weight ratio from 98:20 to 93:7, still more preferably in a weight ratio from 85:15 to 92:8. The MFR of the polypropylene composition (C) depends on the desired final end application and can be adjusted with MFR values of the components (PP1) and (PP2) over a broader range, as it will be known for a skilled person. Preferably the polypropylene composition (C) has a melt flow rate MFR2 (230 °C, 2.16 kg) determined according to ISO 1133 in the range of 0.1 to 100.0 g/lO min, more preferably in the range of 1.0 to 70.0 g/lO min, even more preferably in the range of 3.0 to 40.0 g/lOmin, still more preferably in the range of 5.0 to 25.0 g/lO min, and most preferably in the range of 6.0 to 23.0 g/lOmin. Another especially preferred range is a melt flow rate MFR2 determined according to ISOl 133 at 230 °C and 2.16 kg from 7.0 to 20.0 g/lO min.

Further, the polypropylene composition (C) preferably has a melting temperature of at least 145 °C, more preferably in the range of 145 to 162 °C, still more preferably in the range of

148 to 161 °C, like in the range of 150 to 160 °C.

The polypropylene composition (C) preferably has a xylene soluble content (XCS) below 10.0 wt.-%, preferably from 1.0 to 8.0 wt.-%, more preferably from 1.5 to 6.5 wt.-%, and most preferably from 1.8 to 6.0 wt.-%.

The polypropylene composition (C) preferably has flexural modulus in the range from 1250 to 1800 MPa, more preferably from 1350 to 1600 MPa, and even more preferably from 1400 to 1550 MPa. ln another preferred embodiment, the polypropylene composition (C) is further characterized by a Charpy notched impact strength in the range of 2.5 to 15.0 kJ/m ² , preferably in the range of 2.8 to 12.0 kJ/m ² as determined according to 1SO 179 leA, and a retention of said impact strength after gamma sterilization at 50kGy and 60 days of aging of more than 85%, preferably of more than 88%, and most preferably of more than 90%.

Preferably, the polypropylene composition (C) is obtained by melt blending the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2) together with optional additives in a ratio as outlined above. The blending is typically carried out as meltmixing in a mixer at elevated temperature above the softening temperature of the polymer componcnt(s) using conventional, e.g. commercially available, mixing equipment, like extruder. The meltmixing and the mixing equipment are well known and documented in the literature. Moreover, the polypropylene composition (C) can be produced e.g. before supplying it to the article convertor or during the production of an article. The mixing conditions and equipment can be chosen by a skilled person. In the following, the first polypropylene composition (H-PP) and the second polypropylene (PP2) are separately described in more detail.

The first isotactic propylene homopolymer (H-PP)

The first isotactic propylene homopolymer (H-PP) is the major component of the polypropylene composition (C), which is included as a main component in the moulded article of the present invention. The first isotactic propylene homopolymer (H-PP) can be a propylene copolymer or a propylene homopolymer. Preferably the first isotactic propylene homopolymer (H-PP) is a propylene homopolymer.

However, in case the first polypropylene (PP1) is the less preferred propylene copolymer, the first isotactic propylene homopolymer (H-PP) comprises propylene and comonomers copolymerised with propylene, for example comonomers such as ethylene and/or C ₄ to Cio a-olefins, in particular ethylene and/or C ₄ to C a-olefins, in particular ethylene and/or C ₄ to Ce a-olefins, e.g. 1 -butene and/or 1 -hexene. In case the first isotactic propylene

homopolymer is a propylene copolymer, then preferably the first isotactic propylene homopolymer (H-PP) according to the invention comprises, especially consists of, propylene and comonomers copolymerised with propylene from the group consisting of ethylene, 1 - butene and 1 -hexene, preferably of ethylene.

Further, in case the first isotactic propylene homopolymer (H-PP) is a propylene copolymer, the first isotactic propylene homopolymer (H-PP) is most preferably a random propylene copolymer (R-PP). The term“random” indicates that the comonomer of the random propylene copolymer (R-PP) is randomly distributed within the copolymer of propylene. The term random is understood according to IUPAC (Glossary of basic terms in polymer science; IUPAC recommendations 1996). Thereby, a random copolymer of propylene includes a fraction, which is insoluble in xylene, i.e. xylene cold insoluble (XCU) fraction, preferably when measured as defined below under“1. Measuring methods”, in an amount of at least 80 wt.-%, still more preferably of at least 85 wt.-% and most preferably of at least 90 wt.-%, based on the total amount of the random copolymer of propylene.

As known for a skilled person, a random copolymer is different from heterophasic polypropylene. Generally, a heterophasic polypropylene is a propylene copolymer comprising a propylene homo- or random copolymer matrix component (1) and an elastomeric copolymer component (2) of propylene with one or more of ethylene and C _t- Cs- olefin comonomers, wherein the elastomeric (amorphous) copolymer component (2) is dispersed in said propylene homo- or random copolymer matrix polymer (1). The presence of an elastomeric phase or of the so-called inclusions is for instance visible by high resolution microscopy, like electron microscopy or atomic force microscopy, or by dynamic mechanical thermal analysis (DMTA). A random copolymer does not contain an elastomeric polymer phase dispersed therein.

Thereby, the term“random copolymer of propylene” according to the present invention excludes heterophasic systems. In other words, the first isotactic propylene homopolymer (H-PP) , like the random propylene copolymer (R-PP), does not comprise an elastomeric phase, i.e. is monophasic.

According to one embodiment of the present invention, the first isotactic propylene homopolymer (PP-H) has preferably a comonomer content equal or below 10.0 mol-%. The comonomer content of the first propylene homopolymer (PP-H) is preferably in the range of 0.0 to 5.0 mol-%, yet more preferably in the range of 0.0 to 3.0 mol-%, still more preferably in the range of 0.0 to 1.0 mol-%. ln case of the random propylene copolymer (R-PP), the comonomer content, like the ethylene content, is preferably in the range of 0.6 to 5.0 mol-%, yet more preferably in the range of 0.8 to 3.0 mol-%, still more preferably in the range of 0.8 to 1.5 mol-%.

However, it is especially preferred that the first isotactic propylene homopolymer (H-PP) is a propylene homopolymer in the strict sense. According to the present invention, the expression“propylene homopolymer”, as used for the first isotactic propylene homopolymer, relates to a polypropylene that consists substantially, i.e. of at least 99.4 mol-%, more preferably of at least 99.6 mol-%, still more preferably of at least 99.7 mol-%, like of at least 99.9 mol-%, of propylene units. In another embodiment only propylene units are detectable, i.e. only propylene has been polymerized. The definition“propylene homopolymer” has a well-known meaning in the art.

The first isotactic propylene homopolymer (H-PP) is preferably obtained by polymerization with a metallocene catalyst. This is important because polypropylenes prepared by using an isospecific, C2-symmetric metallocene provide a different microstructure compared to polypropylenes prepared by using Ziegler-Natta (ZN) catalysts. The most significant difference is the presence of regio-defects in metallocene-made polypropylenes. These regio- defects can be of three different types, namely 2,l-erythro (2,le), 2,l-threo (2,lt) and 3,1 defects. A detailed description of the structure and mechanism of formation of regio-defects in polypropylene can be found in Chemical Reviews 2000, 100(4), pages 1316-1327.

Accordingly, the term“regio defects” herein defines the sum of 2,1 erythro regio-defects, 2,1 threo regio-defects and 3,1 regio-defects. Consequently, the amount of defects, i.e. regio defects, like 2,1 regio defects, i.e. 2,1 erythro regio-defects and 2,1 threo regio-defects, and 3,1 regio-defects, is indicated by“mol %” of the average percentage of propylene units in the polymer chain.

In another preferred embodiment, the first isotactic propylene homopolymer (H-PP) has a sum of 2,1 erythro regio-defects, 2,1 threo regio-defects and 3,1 regio-defects from 0.1 to 1.3 mol%, preferably from 0.2 to 1.1 mol%, even more preferably from 0.2 to 1.0 mol%, and most preferably from 0.3 to 0.8 mol%, as determined by ¹³ C-NMR spectroscopy.

The presence of such amount of regio-defects is a sufficient (although not a mandatory) feature to unambiguously identify a polypropylene as produced with a metallocene catalyst instead of a Ziegler-Natta-type catalyst. In another preferred embodiment, the first isotactic propylene homopolymer (H-PP) is characterized by a high isotacticity, defined as pentad regularity [mmmm] of more than 96.0 mol%, preferably of more than 96.5 mol%, most preferably of 97.0 mol%, as determined by ¹³ C-NMR spectroscopy.

It is preferred that the first isotactic propylene homopolymer (H-PP) has a melt flow rate MFR2 (230 °C, 2.16 kg) determined according to ISO 1133 in the range of 4.0 to

22.0 g/lO min, preferably in the range of 5.0 to 20.0 g/lO min, still more preferably in the range of 6.0 to 18.0 g/lO min.

It is preferred that the first isotactic propylene homopolymer (H-PP) is featured by rather low cold xylene solubles (XCS) content, i.e. by a xylene cold solubles (XCS) below 6.0 wt.-%. Accordingly, the first isotactic propylene homopolymer (H-PP) , has preferably a xylene cold solubles (XCS) content in the range of 0.5 to 7.0 wt.-%, more preferably in the range of 1.5 to 6.0 wt.-%, still more preferably in the range of 2.5 to 5.0 wt.-%.

The amount of xylene cold solubles (XCS) additionally indicates that the first isotactic propylene homopolymer (H-PP) is preferably free of any elastomeric polymer component, like an ethylene propylene rubber. In other words, the first isotactic propylene homopolymer (H-PP) is preferably not a heterophasic polypropylene, i.e. a system consisting of a polypropylene matrix in which an elastomeric phase is dispersed. Such systems are featured by a rather high xylene cold soluble content. In other words, the first isotactic propylene homopolymer (H-PP) is a monophasic polypropylene. Further, the first isotactic propylene homopolymer (H-PP) is preferably a crystalline propylene homopolymer. The term“crystalline” indicates that the first isotactic propylene homopolymer (H-PP) has a relatively high melting temperature. In particular it is preferred that the first isotactic propylene homopolymer (H-PP) has a melting temperature Tm in the range from 145 to l62°C, preferably in the range from 148 to l6l°C, more preferably in the range from 150 to l60°C, as measured by differential scanning calorimetry (DSC) according to ISO 11357. In another preferred embodiment, the first isotactic propylene homopolymer (H-PP) has a polydispersity (Mw/Mn) in the range from 2.0 to 4.5, more preferably from 2.5 to 4.2, and even more preferably from 2.8 to 4.0, as determined by GPC according to ISO 16014. The first isotactic propylene homopolymer (H-PP) may contain suitable additives as known in the art. According to this invention, the additives of the first isotactic propylene homopolymer (H-PP) are regarded being part of the“additives (AD)” as described in more detail in the below section“The Additives”. The second polypropylene (PP2)

The second polypropylene (PP2) is another essential component of the polypropylene composition (C). The second polypropylene (PP2) is different from the first isotactic propylene homopolymer (H-PP).

It is preferred that the second polypropylene (PP2) has a low melting temperature. Therefore, the second polypropylene (PP2) has a melting temperature Tm measured by differential scanning calorimetry (DSC) of 130 °C or less, preferably in the range of 50 to 125 °C, more preferably in the range of 55 to 120 °C, still more preferably in the range of 60 to 1 l5°C, still more preferably in the range of 75 to 110 °C, still more preferably in the range of 70 to 100 °C, still more preferably in the range of 70 to 90 °C.

In another preferred embodiment, the second polypropylene (PP2) has either no

crystallization or, preferably, only low crystallinity, which is controlled by rather low isotacticity, defined by a triad regularity [mm] in the range from 50.0 to 70.0 mol%, preferably in the range from 55.0 to 65.0 mol%.

Preferably the second polypropylene (PP2) has a molecular weight distribution M _w /M _n in the range of 1.0 to 5.0, preferably 1.0 to 4.0, preferably 1.8 to 3.0, still more preferably in the range of 1.8 to 2.5. Further, it is preferred that the second polypropylene (PP2) is featured by a rather high molecular weight. Accordingly, it is preferred that the second polypropylene (PP2) has a weight molecular weight M _w in the range of 20 to 300 kg/mol, more preferably in the range of 38 to 200 kg/mol, still more preferably in the range of 40 to 140 kg/mol.

The second polypropylene (PP2) has preferably a tensile modulus determined according to ISO 527 on injection-molded specimens in the range of 50 to 500 MPa, more preferably of 60 to 400 MPa, still more preferably of 70 to 300 MPa, yet more preferably of 70 to 200 MPa, like 80 to 150 MPa.

Preferably, the second polypropylene (PP2) has a melt flow rate MFR2 (230 °C, 2.16 kg) determined according to ISO 1133 in the range of 30 to 3000 g/lO min, more preferably in the range of 35 to 2500 g/lO min, still more preferably in the range of 40 to 2200 g/lO min, like in the range of 45 to 2100 g/lO min, wherein MFR2 values of 1000 g/lO min or above are converted from the B-viscosity (190 °C) determined according to ASTM D 3236. In one embodiment MFR2 of from 45 to 2000 g/lO min, preferably of 45 to 1000 g/lO min, preferably of 45 to 900 g/lO min, preferably of 45 to 700 g/lO min, preferably of 45 to 500 g/lO min, preferably of 45 to 400 g/lO min is desired. Preferably, the second polypropylene (PP2) has a B-Viscosity (190 °C, ASTM D 3236) in the range of 5000 to 500 000 mPa-s, more preferably of 7000 to 450 000 mPa-s, still more preferably of 8000 to 450 000 mPa-s. In one embodiment the B-Viscosity is preferably in a range of 10 000 to 450 000 mPa-s, more preferably of 20 000 to 450 000 mPa-s, still more preferably of 30 000 to 450 000 mPa-s. An especially preferred range is 40 000 to 400 000 mPa-s.

Further, it is preferred that the second polypropylene (PP2) has a density below 900 kg/m ³ , preferably in a range of 850 to 900 kg/m ³ , still more preferably in a range of 855 to 890 kg/m ³ , like in a range of 857 to 880 kg/m ³ . The second polypropylene (PP2) is preferably not heterophasic, but is monophasic according to the definition provided above.

Accordingly, the second polypropylene (PP2) can be a propylene copolymer or a propylene homopolymer.

In case the second polypropylene (PP2) is a propylene copolymer, then comonomers copolymerizable with propylene are preferably selected from ethylene and/or G to G a- olefins, in particular ethylene and/or G to G a-olefins, preferably from the group consisting of ethylene, 1 -butene and 1 -hexene.

In case the second polypropylene (PP2) is a propylene copolymer, then it is preferably a random propylene copolymer (R-PP2). Regarding the terms“random” and“random copolymer”, reference is made to the definition provided above with regard to the first polypropylene (PP 1 ) .

The second polypropylene (PP2) is preferably a homopolymer of polypropylene, i.e. a propylene homopolymer (H-PP2). Regarding the expression“propylene homopolymer”, reference is made to the definition provided above.

The second polypropylene (PP2) may contain suitable additives as known in the art.

According to this invention, the additives of the second polypropylene (PP2) are regarded being part of the“additives (AD)” as described in more detail in the below section“The Additives”.

The second polypropylene (PP2), is preferably obtained by polymerizing propylene in the presence of a metallocene catalyst. In particular, the second polypropylene (PP2) is preferably obtained by using IDEMITSU metallocene catalyst for producing commercial L- MODU™ polypropylene polymer. Suitable metallocene catalysts are described by Y.

Minami et al, Polymer Journal 2015, 45, pages 227-234. Alternatively, and preferably, the second polypropylene (PP2) is a polypropylene known in the art and commercially available or can be produced in manner as given in the literature as well known for a skilled person in the art. A suitable second polypropylene (PP2) is inter alia commercially available, e.g. one of the commercial propylene homopolymers L-MODU S400, L-MODU S600 or L-MODU S901 supplied by Idemitsu.

The additives (AD)

The polypropylene composition (C) may include additives (AD). The additives (AD) may be added separately to the polypropylene composition and/or are introduced as part of the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2).

The amount of additives (AD in the polypropylene composition (C) is 0.0 to 5.0 wt.-%, more preferably 0.05 to 4.0 wt.-%, still more preferably 0.1 to 3.0 wt.-% of additives (AD), based on the total weight of the polypropylene composition (C).

Typical additives are acid scavengers, antioxidants, colorants, light stabilisers, plasticizers, slip agents, anti-scratch agents, dispersing agents, processing aids, nucleating agents, lubricants, pigments, fillers, and the like. Especially preferred is the addition of at least one antioxidant and/or at least one light stabilizer and/or at least one nucleating agent lf an antioxidant is present, it is preferably not a hindered amine antioxidant.

The term“antioxidant (AO)” as used herein includes primary and secondary antioxidants. Primary antioxidants act as radical scavengers in the oxidation cycle. Primary antioxidants stabilize polypropylene material by scavenging radicals formed in a polypropylene thereby interrupting the oxidation cycle that slows leads to the degradation of the polypropylene over time. The auto-oxidation cycle in polypropylenes is basically a free-radical initiated chain reaction, which can be inhibited by the presence of radical scavengers. Primary antioxidants includes the class of hindered phenols and hindered amines.

Hindered phenols are sterically hindered phenols, which act as H-donors by forming a phenoxyl radical that is stabilized by steric hindrance of bulky substitutents in the 2,6- position. However, as indicated above, it is preferred that the polypropylene composition (C) of the present invention includes at least one antioxidant (AO) with the proviso that the antioxidant is not a hindered phenol compound or, alternatively, the antioxidant is not a hindered phenol compound and not a hindered amine. The presence of a hindered phenol compound in a polypropylene subjected to gamma-ray sterilization can lead to the degradation of the hindered phenol and the built-up of colored degradation products which negatively affect the optical properties of the polypropylene composition. In other words, the antioxidant when optionally used in the present invention is preferably a hindered amine compound. This class of compounds is also sometimes referred to as hindered amine light stabilizers (HALS). Hindered amine compounds are preferably secondary aromatic amines, which scavenge radicals through a nitroxyl radical formed from the hindered amine.

Secondary antioxidants, which also belong to the antioxidants (AO) of the present invention, do not primarily act by scavenging radicals but show a synergistic effect when combined with primary antioxidants. Preferred secondary antioxidants (AO) are phosphites and thio compounds, like thioesters.

Such additives are commercially available and for example described in“Plastic Additives Handbook”, 6 ^th edition 2009 of Hans Zweifel (pages 1141 to 1190). Furthermore, the term“additives (AD)” according to the present invention may also include any carrier materials, for instance polymeric carrier materials, like polymeric carrier material(s) present in optional masterbatch (MB) of an additive (AD). Accordingly the carrier material, like the polymeric carrier material, is part of the additives (AD) and not considered as a“polymeric material” as defined above.

Therefore any polymer being a carrier material for additives (AD) is calculated neither to the amount of first isotactic propylene homopolymer (H-PP) nor the second polypropylene (PP2) as indicated in the present invention, but to the amount of the respective additive (AD). The moulded article The present invention is directed to a moulded article comprising the polypropylene composition (C) comprising the first isotactic propylene homopolymer (H-PP) and the second polypropylene (PP2) as described above. The moulded article of the present invention preferably comprises at least 90 wt.-%, more preferably at least 95 wt.-%, yet more preferably at least 98 wt.-% of the polymer composition (C), based on the total weight of the moulded article. Even more preferably, the moulded article consists of the polypropylene composition (C) as defined above. Preferably, the moulded article has been gamma-ray sterilized at a dose of at least 5 kGy, like at least 15 kGy, or more preferably with a dose of gamma radiation from 15 to 150 kGy, even more preferably from 25 to 100 kGy, or most preferably from 30 to 60 kGy.

The moulded article is preferably characterized by a Charpy notched impact strength in the range of 2.5 to 15.0 kJ/m ² , as determined according to 1SO 179 leA, and a retention of said impact strength after gamma sterilization at 50kGy and 60 days of aging of more than 75%, preferably of more than 80%, and most preferably of more than 85%.

The moulded article according to the present invention is preferably an injection moulded article. With respect to the field of application of the moulded article and its preferred use, the moulded article preferably is a medical, pharmaceutical or diagnostic article.

With respect to its use in the medical or pharmaceutical field or its use for diagnostic applications, the moulded article according to the present invention is preferably selected from the list of articles consisting of catheters, intravenous sets, laparoscopic instrument components, surgery instrument components, surgical trays, caddies, drug delivery devices, surgical tools, in-vitro diagnostics, tube connectors, tube closures, valves, vials, syringes, plungers, laboratory dishes, and droppers. ln another aspect, the present invention is directed to a sterilized packaging comprising the moulded article of the present invention comprising the polypropylene composition (C). In another aspect, the present invention is also directed to a process for gamma-ray sterilization of the moulded article as herein defined, comprising the steps of:

providing the moulded article, and

subjecting said moulded article to gamma-ray sterilization.

Preferably, in said process, the gamma-ray sterilization operation is carried out at a dose in the range of 15 to 150 kGy.

In another aspect, the present invention is directed to the use of the second polypropylene (PP2) as herein defined in the polymer composition (C) as defined above or in a random copolymer for

(a) reducing the level of overall migration in said polymer composition (C) as determined according to EN ISO 1186-14:2002 on injection moulded plaques,

60 x 60 x 1 mm ³ to less than 80.0 mg/dm ² , preferably of less than 10.0 mg/dm ² , more preferably less than 8.0 mg/dm ² and even more preferably less than 6.0 mg/dm ² ;

and/or

(b) improving the resistance to gamma resistance of said polymer composition (C); and/or

(c) reducing discoloration of said polymer composition (C) after gamma-ray

sterilization at 50kGy and 60 days of aging at 80°C as defined by yellowness index (YI) of not higher than 20, more preferably not higher than 16 as determined on injection moulded plaques 60 x 60 x 1 mm ³ according to standard method ASTM E313.

The present invention will be described in further detail by the examples provided below.

E X A M P L E S

A. Measuring methods

The following definitions of terms and determination methods apply for the above general description of the invention as well as to the below examples unless otherwise defined. MFR2 (230 °C) is measured according to ISO 1133 (230 °C, 2.16 kg load). Quantification of microstructure by NMR spectroscopy

Quantitative nuclear-magnetic resonance (NMR) spectroscopy was used to quantify the comonomer content and comonomer sequence distribution of the polymers. Quantitative ¹³ C{ ¹ H} NMR spectra were recorded in the solution-state using a Bruker Advance III 400 NMR spectrometer operating at 400.15 and 100.62 MHz for H and ¹³ C respectively. All spectra were recorded using a ¹³ C optimised 10 mm extended temperature probehead at l25°C using nitrogen gas for all pneumatics. Approximately 200 mg of material was dissolved in 3 ml of 7,2-tetrachloroethane-i/ ₂ (TCE-cT) along with chromium-(III)- acetylacetonate (Cr(acac)3) resulting in a 65 mM solution of relaxation agent in solvent (Singh, G., Kothari, A., Gupta, V., Polymer Testing 28 5 (2009), 475). To ensure a homogenous solution, after initial sample preparation in a heat block, the NMR tube was further heated in a rotatary oven for at least 1 hour. Upon insertion into the magnet the tube was spun at 10 Hz. This setup was chosen primarily for the high resolution and

quantitatively needed for accurate ethylene content quantification. Standard single-pulse excitation was employed without NOE, using an optimised tip angle, 1 s recycle delay and a bi-level WALTZ16 decoupling scheme (Zhou, Z., Kuemmerle, R., Qiu, X., Redwine, D., Cong, R., Taha, A., Baugh, D. Winniford, B., J. Mag. Reson. 187 (2007) 225; Busico, V., Carbonniere, P., Cipullo, R., Pellecchia, R., Severn, J., Talarico, G., Macromol. Rapid Commun. 2007, 28, 1128). A total of 6144 (6k) transients were acquired per spectra.

Quantitative ¹³ C {¾} NMR spectra were processed, integrated and relevant quantitative properties determined from the integrals using proprietary computer programs. All chemical shifts were indirectly referenced to the central methylene group of the ethylene block (EEE) at 30.00 ppm using the chemical shift of the solvent. This approach allowed comparable referencing even when this structural unit was not present. Characteristic signals corresponding to the incorporation of ethylene were observed Cheng, H. N., Macromolecules 17 (1984), 1950).

For polypropylene homopolymers all chemical shifts are internally referenced to the methyl isotactic pentad (mmmm) at 21.85 ppm.

Characteristic signals corresponding to regio defects (Resconi, L., Cavallo, L., Fait, A., Piemontesi, F., Chem. Rev. 2000, 100, 1253; Wang, W-J., Zhu, S., Macromolecules 33 (2000), 1157; Cheng, H. N., Macromolecules 17 (1984), 1950) or comonomer were observed. The tacticity distribution was quantified through integration of the methyl region between 23.6-19.7 ppm correcting for any sites not related to the stereo sequences of interest (Busico, V., Cipullo, R., Prog. Polym. Sci. 26 (2001) 443; Busico, V., Cipullo, R., Monaco, G., Vacatello, M., Segre, A.L., Macromoleucles 30 (1997) 6251).

Specifically the influence of regio defects and comonomer on the quantification of the tacticity distribution was corrected for by subtraction of representative regio defect and comonomer integrals from the specific integral regions of the stereo sequences.

The isotacticity was determined at the pentad level and reported as the percentage of isotactic pentad (mmmm) sequences with respect to all pentad sequences:

[mmmm] % = 100 * ( mmmm / sum of all pentads )

In an analogous way, the content of isotactic triads [mm] was determined.

The presence of 2,1 erythro regio defects was indicated by the presence of the two methyl sites at 17.7 and 17.2 ppm and confirmed by other characteristic sites.

Characteristic signals corresponding to other types of regio defects were not observed (Resconi, L., Cavallo, L., Fait, A., Piemontesi, F., Chem. Rev. 2000, 100, 1253).

The amount of 2, 1 erythro regio defects was quantified using the average integral of the two characteristic methyl sites at 17.7 and 17.2 ppm:

P _21e = ( I _e6 + I _e8 ) / 2

The amount of 1 ,2 primary inserted propene was quantified based on the methyl region with correction undertaken for sites included in this region not related to primary insertion and for primary insertion sites excluded from this region:

Pl2 = I _CH3 + P 12 _e

The total amount of propene was quantified as the sum of primary inserted propene and all other present regio defects:

P tota _l = P _l2 + P21 _e

The mole percent of 2,1 erythro regio defects was quantified with respect to all propene:

[2le] mol% = 100 * ( P _2ie / Ptotai )

For copolymers characteristic signals corresponding to the incorporation of ethylene were observed (Cheng, H. N., Macromolecules 17 (1984), 1950).

With regio defects also observed (Resconi, L., Cavallo, L., Fait, A., Piemontesi, F., Chem.

Rev. 2000, 100, 1253; Wang, W-J., Zhu, S., Macromolecules 33 (2000), 1157; Cheng, H. N., Macromolecules 17 (1984), 1950) correction for the influence of such defects on the comonomer content was required.

The comonomer fraction was quantified using the method of Wang et. al. (Wang, W-J., Zhu, S., Macromolecules 33 (2000), 1157) through integration of multiple signals across the whole spectral region in the ¹³ C {¾} spectra. This method was chosen for its robust nature and ability to account for the presence of regio-defects when needed. Integral regions were slightly adjusted to increase applicability across the whole range of encountered comonomer contents.

For systems where only isolated ethylene in PPEPP sequences was observed the method of Wang et. al. was modified to reduce the influence of non- zero integrals of sites that are known to not be present. This approach reduced the overestimation of ethylene content for such systems and was achieved by reduction of the number of sites used to determine the absolute ethylene content to:

E = 0.5(S O + S y + S d + 0.5(Sa + Say))

Through the use of this set of sites the corresponding integral equation becomes:

E = 0.5(I _H +I _G + 0.5(Ic + ID))

using the same notation used in the article of Wang et. al. (Wang, W-J., Zhu, S.,

Macromolecules 33 (2000), 1157). Equations used for absolute propylene content were not modified.

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

E [mol%] = 100 * fE

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

E [wt%] = 100 * (fE * 28.06) / ((fE * 28.06) + ((1-fE) * 42.08))

The comonomer sequence distribution at the triad level was determined using the analysis method of Kakugo et al. (Kakugo, M., Naito, Y., Mizunuma, K., Miyatake, T.

Macromolecules 15 (1982) 1150). This method was chosen for its robust nature and integration regions slightly adjusted to increase applicability to a wider range of comonomer contents.

Number average molecular weight (M„), weight average molecular weight (M _w ) and molecular weight distribution (MWD) Molecular weight averages (Mw, Mn), and the molecular weight distribution (MWD) or polydispersity, i.e. the ratio Mw/Mn (wherein Mn is the number average molecular weight and Mw is the weight average molecular weight), were determined by Gel Permeation Chromatography (GPC) according to ISO 16014-4:2003 and ASTM D 6474-99. A

PolymerChar GPC instrument, equipped with infrared (IR) detector was used with 3 x Olexis and lx Olexis Guard columns from Polymer Laboratories and 1,2, 4-trichlorobenzene (TCB, stabilized with 250 mg/L 2,6-Di tert butyl-4-methyl-phenol) as solvent at 160 °C and at a constant flow rate of 1 mL/min. 200 pL of sample solution were injected per analysis. The column set was calibrated using universal calibration (according to ISO 16014-2:2003) with at least 15 narrow MWD polystyrene (PS) standards in the range of 0,5 kg/mol to 11 500 kg/mol. Mark Houwink constants for PS, PE and PP used are as described per ASTM D 6474-99. All samples were prepared by dissolving 5.0 - 9.0 mg of polymer in 8 mL (at 160 °C) of stabilized TCB (same as mobile phase) for 2.5 hours for PP or 3 hours for PE at max. 160°C under continuous gentle shaking in the autosampler of the GPC instrument. DSC analysis, melting temperature (T _m ) and melting enthalpy (H _m ), crystallization temperature (T _c ) and crystallization enthalpy (H _c ): measured with a TA Instrument Q200 differential scanning calorimetry (DSC) on 5 to 7 mg samples. DSC is run according to ISO 3146 / part 3 /method C2 in a heat / cool / heat cycle with a scan rate of 10 °C/min in the temperature range of -30 to +225°C. Crystallization temperature (T _c ) and crystallization enthalpy (H _c ) are determined from the cooling step, while melting temperature (T _m ) and melting enthalpy (H _m ) are determined from the second heating step.

Density of the polymer is measured according to ISO 1183-187. Sample preparation is done by compression moulding in accordance with ISO 1872-2:2007.

The xylene solubles (XCS, wt.-%): Content of xylene cold solubles (XCS) is determined at 25 °C according ISO 16152; first edition; 2005-07-01. The part which remains insoluble is the xylene cold insoluble (XCI) fraction.

Flexural Modulus: The flexural modulus was determined in 3 -point-bending according to ISO 178 on injection molded specimens of 80 x 10 x 4 mm prepared in accordance with ISO 294-1 :1996.

Impact: Charpy notched impact strength is determined according to ISO 179 / leA at 23 °C by using injection moulded test specimens as described in EN ISO 1873-2 (80 x 10 x 4 mm). Haze was determined according to ASTM D1003-00 on 60x60x1 mm ³ plaques injection molded in line with EN ISO 1873-2 using a melt temperature of 200°C and on cast films of 50 pm thickness produced on a monolayer cast film line with a melt temperature of 220°C and a chill roll temperature of 20°C.

B-Viscosity was determined according to ASTM D 3236 at 190 °C.

Overall migration

Overall Migration is determined according to EN 1SO 1186-14:2002 on injection moulded plaques, 60 x 60 x 1 mm ³ .

Irradiation

Injection moulded test specimen of 80x10x4 mm ³ for Charpy or 60x60x1 mm ³ for

Yellowness Index, both prepared in accordance with EN ISO 1873-2, were exposed to gamma-ray irradiation at 50 kGy using a 60Co g-ray source. Consecutively the samples were aged at 80°C in a circulating air oven up to 60 days as indicated below. Once the desired time was reached, the samples were taken out from the oven and aged at 23 °C for 24 hours before the impact test according to Charpy ISO l79/leA+23°C was performed.

Parallel to the irradiated samples, according non-irradiated samples were aged at 80 °C in a circulating air oven up to 60 days.

B. Examples

1. The first propylene homopolymer (H-PP1):

The first propylene homopolymer (H-PP1) was prepared by polymerization using a metallocene catalyst as described in detail in WO 2015/011135 Al (metallocene complex MC1 with methylaluminoxane (MAO) and borate resulting in Catalyst 3 described in WO 2015/011135 Al) with the proviso that the surfactant is 2,3,3,3-tetrafluoro-2- (l,l,2,2,3,3,3-heptafluoropropoxy)-l-propanol. The metallocene complex (MC1 in WO 2015/011135 Al) is prepared as described in WO 2013/007650 Al (metallocene E2 in

WO 2013/007650 Al).

Off-line prepolymerization procedure

The catalyst MC-l was pre-polymerized according to the following procedure: Off-line pre polymerization experiment was done in a 125 mL pressure reactor equipped with gas- feeding lines and an overhead stirrer. Dry and degassed perfluoro-l.3-dimethylcyclohexane (15 cm ³ ) and the desired amount of the catalyst to be pre-polymerized were loaded into the reactor inside a glove box and the reactor was sealed. The reactor was then taken out from the glove box and placed inside a water cooled bath kept at 20°C. The overhead stirrer and the feeding lines were connected and stirring speed set to 450 rpm. The experiment was started by opening the propylene feed into the reactor. The total pressure in the reactor was raised to about 5 barg and held constant by propylene feed via mass flow controller until the target degree of polymerization was reached (10 min). The reaction was stopped by flashing the volatile components. Inside glove box, the reactor was opened and the content poured into a glass vessel. The perfluoro-l,3-dimethylcyclohexane was evaporated until a constant weight was obtained to yield the pre-polymerized catalyst.

Table 1: Off-line prepolymerization

Table 2: Preparation of propylene homopolymer (H-PP1) and final properties

2. The second polypropylene (PP2)

As the second polypropylene (PP2), the commercial polypropylene material L-MODU S400 by Idemitsu was used. The properties of this second polypropylene (PP2) material are summarized in Table 3. Table 3 Properties of the second polypropylene (PP2) L-MODU S400 (Idemitsu)

Comparative Example CE2 was the commercial polypropy ene HD810MO (Bormed™ of

Borealis AG) having a melt flow rate MFR2 of 10.0 g/lO min, a melting temperature Tm of 164 °C, and a density of 907 kg/m ³ .

3. Preparation of the polypropylene composition (C)

The polypropylene compositions (C) were prepared by compounding of the polymer components (H-PP) and (PP2) and additivation with the list of additives as described below. The properties of the comparative and inventive compositions are found in Tables 4 and 5.

Table 4 Composition and properties of the comparative and inventive examples

Arenox DL dodecyl 3- {[3-(dodecyloxy)-3-oxopropyl]sulfanyl}propanoate (CAS-no.

123-28-4);

Tinuvin 622 Dimethyl succinate polymer with 4-hydroxy-2,2,6,6-tetramethyl- 1 - piperidine ethanol commercially available from BASF SE;

Hostavin NOW 2,2,6,6-tetramethylpiperidin-4-yl-hexadecanoate and 2, 2,6,6- tetramethylpiperidin-4-yl-octadecanoate, reaction product with an oxidized polyethylene wax from Clariant;

lrgafos 168 Tris(2,4-tert-butylphenyl) Phosphite commercially available from BASF SE; FS042 N,N-di(alkyl)hydroxylamine produced by the direct oxidation of N,N- difhydrogenated tallow)amine (Irgastab® FS-042, CAS-no. 143925-92-2, BASF SE);

Primol 352 While oil; a purified mixture of liquid saturated hydrocarbons; Kinematic viscosity (40°C; ASTM D 445) = 65.0-75.0 mm ² /s; Kinematic viscosity (l00°C; ASTM D 445) = 8.5 mm ² /s; Average molecular weight (ASTM D 2502) = 480, commercially available from ExxonMobil;

Millad 3988 is 1,3:2, 4 bis(3,4-dimethylbenzylidene)sorbitol (CAS-no. 135861-56-2), commercially available from Milliken;

As derivable from the values shown in Table 4, the inventive compositions have much lower overall migration than the comparative compositions although the mechanical and optical properties of the compositions were comparable. The mechanical profile with respect to toughness have been analysed based on retention of Charpy notched impact strength (% N1S retention) of samples after gamma-ray sterilization and aging after 60 days. Comparative and inventive samples were prepared from injection moulded specimen having size of

60x60xlmm ³ . Samples were sterilized at 50kGy and aged at 80°C for 2 months (60 days) before measurement of Charpy notched impact strength (Table 5).

Table 5 Toughness after gamma- ray sterilization and up to 60 days of aging

Retention of Charpy notched impact strength (NIS %) was determined by comparing the values measured for NIS after 60 days without/with gamma-ray sterilization of the corresponding samples (Table 6).

Table 6 Retention of toughness after gamma-ray sterilization and 60 days of aging

Charpy notched impact strength as well as % NIS retention were essentially improved in the inventive materials relative to the comparative samples.

Analysis of discoloration after gamma-ray sterilization has been determined by measurement of yellowness index (YI). Samples were sterilized at 50kGy and aged at 80°C for 2 months (60 days). Yellowness index of the aged samples was successively determined during/after ageing at 1, 7, 14, 30 and 60 days (Table 7).

*): samples not gamma sterilized;

It was found that the degree of discoloration of the materials as indicated by yellowness index after gamma-ray sterilization and ageing is substantially lower in the inventive materials compared to the comparative materials.