[0001] The present invention relates to polypropylene compositions comprising a heterophasic propylene polymer and a nucleating agent. The invention also relates to sheets obtained therefrom and to thermoformed articles obtained from such sheets.

[0002] It is long known that the impact resistance of polypropylene can be improved by the addition of an ethylene-based elastomeric copolymer, often an ethylene-propylene copolymer, either by mechanical mixing or by sequential polymerization. Heterophasic compositions comprising a crystalline polypropylene matrix and a rubbery phase formed by an ethylene-based elastomeric copolymer are described, for instance, in European patent applications 170255, 373660, 603723, 1 135440, 2084223 and 2247424.

[0003] Said compositions exhibit good impact resistance and, in certain cases, good optical properties. However, the overall balance of properties is still not totally satisfactory in the whole range of possible applications, in view of the high standards required by the market.

[0004] Therefore, there still remains a continuous demand for compositions of this kind with improved properties balanced for specific target applications. An excellent balance of properties, particularly for the production of sheets for thermoforming applications, has now been achieved by the polypropylene compositions according to the present invention.

[0005] Hence, according to a first object, the present invention provides a polypropylene composition comprising:

(a) 78 - 85 %, preferably 80 - 83 %, by weight of a propylene homopolymer or of a copolymer of propylene with ethylene having an ethylene content of up to 2.0 % by weight;

(b) 15 - 22 %, preferably 17 - 20 %, by weight of a copolymer of ethylene with propylene having an ethylene content of from 78 to 90 % by weight; and

(c) an effective amount of a clarifying agent;

wherein the composition has an intrinsic viscosity of the xylene soluble fraction (XSIV) at room temperature of from 0.5 to 1.5 dl/g and a melt flow rate (MFR), measured at 230°C and 2.16 kg, of from 0.5 to 10 g/10 min. [0006] The clarifying agent is generally present in the composition of the present invention in amount of from 0.05 to 1 % by weight, preferably from 0.1 to 0.5% by weight, more preferably from 0.2 to 0.4% by weight with respect to the total weight of the composition.

[0007] Clarifying agents for use in the composition according to the invention may include inorganic nucleating agents (such as pulverized clay, silicates, alkali salts, alkaline earth salts, aluminium salts, titanium salts, and metal oxides), organic nucleating agents (2-mercaptobenzimidazole, sorbitol derivatives, nonitol derivatives, and phosphate derivatives, for example), and 1 ,3,5- trisamide derivatives.

[0008] Preferred clarifying agents are sorbitol derivatives, particularly the 1 ,3:2,4- bis-(3,4-dimethylbenzylidene) sorbitol, nonitol derivatives, particularly the 1 ,2,3-trideoxy-4,6:5,7-bis-0-[(4-propylphenyl)methylene]-noni tol, phosphate derivatives, such as 2,2'-methylenebis(2,4-di-tert-butylphenyl)phosphate lithium salt, and 1 ,3,5-trisamide derivatives.

[0009] Typical examples of clarifying agents include, but are not limited to, Millad® 3988 and Millad® NX8000 (commercially available from Milliken Chemicals), ADK NA-21 and ADK NA-71 (commercially available from Amfine Chemicals), and CGX386 (commercially available from Ciba). These crystal nucleating agents may be used alone or in combination of two or more.

[0010] The compositions of the present invention are endowed with a valuable combination of properties, in particular of stiffness, impact resistance and transparency (in terms of haze and whiteness index).

[001 1] The compositions of the present invention can be prepared by a sequential polymerization, comprising at least two sequential steps, wherein components (a) and (b) are prepared in separate subsequent steps, operating in each step, except the first step, in the presence of the polymer formed and the catalyst used in the preceding step. The catalyst is added only in the first step, however its activity is such that it is still active for all the subsequent steps. Preferably component (a) is prepared before component (b).

[0012] Therefore, the present invention is further directed to a process for the preparation of the polyolefin compositions as reported above, said process comprising at least two sequential polymerization stages with each subsequent polymerization being conducted in the presence of the polymeric material formed in the immediately preceding polymerization reaction, wherein the polymerization stage of propylene to the polymer component (a) is carried out in at least one stage, then at least one copolymerization stage of mixtures of ethylene with propylene to the elastomeric polymer component (b) is carried out. The polymerisation stage is generally carried out in the presence of a stereospecific Ziegler-Natta catalyst.

[0013] The polymerisation stages may occur in liquid phase, in gas phase or liquid- gas phase. Preferably, the polymerisation of the polymer component (a) is carried out in liquid monomer (e.g. using liquid propylene as diluent), while the copolymerisation stages of the elastomeric copolymer component (b) is carried out in gas phase. Alternatively, all the sequential polymerisation stages can be carried out in gas phase.

[0014] The reaction temperature in the polymerisation stage for the preparation of the polymer component (a) and in the preparation of the elastomeric copolymer component (b) may be the same or different, and is preferably from 40 to 100° C; more preferably, the reaction temperature ranges from 50 to 90° C in the preparation of polymer component (a), and from 70 to 100° C for the preparation of copolymer component (b).

[0015] The pressure of the polymerisation stage to prepare polymer component (a), if carried out in liquid monomer, is the one which competes with the vapor pressure of the liquid propylene at the operating temperature used, and it may be modified by the vapor pressure of the small quantity of inert diluent used to feed the catalyst mixture, by the overpressure of optional monomers and by the hydrogen used as molecular weight regulator.

[0016] The polymerisation pressure preferably ranges from 33 to 43 bar, if done in liquid phase, and from 5 to 30 bar if done in gas phase. The residence times relative to the stages depend on the desired ratio between polymer components (a) and (b), and can usually range from 15 minutes to 8 hours. Conventional molecular weight regulators known in the art, such as chain transfer agents (e.g. hydrogen or ZnEt2), may be used. [0017] The compositions of the present invention can also be obtained by preparing separately the said components (a) and (b), by operating with the same catalysts and substantially under the same polymerization conditions as previously explained (except that a wholly sequential polymerization process will not be carried out, but the said components will be prepared in separate polymerization steps) and then mechanically blending said components in the molten or softened state. Conventional mixing apparatuses, like screw extruders, in particular twin screw extruders, can be used.

[0018] All the polymerisation stages are suitably carried out in the presence of a catalyst comprising a trialkylaluminium compound, optionally an electron donor, and a solid catalyst component comprising a halide or halogen- alcoholate of Ti and an electron-donor compound supported on anhydrous magnesium chloride. Catalysts having the above-mentioned characteristics are well known in the patent literature; particularly advantageous are the catalysts described in USP 4,399,054 and EP-A-45977. Other examples can be found in USP 4,472,524.

[0019] Preferably the polymerisation catalyst is a stereospecific Ziegler-Natta catalyst comprising a solid catalyst component comprising:

(i) Mg, Ti and halogen and an electron donor (internal donor);

(ii) an alkylaluminum compound and, optionally (but preferably); and

(iii) one or more electron-donor compounds (external donor).

[0020] The internal donor is suitably selected from the esters of mono or dicarboxylic organic acids such as benzoates, malonates, phthalates and certain succinates. They are described, for example, in US patent 4522930, European patent 45977 and International patent applications WO 00/63261 and WO 01/57099. Particularly suited are the phthalic acid esters and succinate acids esters. Among the phthalic acid esters, alkylphthalates such as diisobutyl, dioctyl and diphenyl phthalate and benzyl-butyl phthalate are generally used.

[0021] Preferred internal donors are those succinate-type compounds of formula (I) below:

wherein the radicals Ri and R2, equal to, or different from, each other, are a C1-C20 linear or branched alkyl, alkenyl, cycloalkyl, aryl, arylalkyl or alkylaryl group, optionally containing heteroatoms; the radicals R3 to R6, equal to, or different from, each other, are hydrogen or a C1-C20 linear or branched alkyl, alkenyl, cycloalkyl, aryl, arylalkyl or alkylaryl group, optionally containing heteroatoms, and any two of said R3 to R6 radicals can be linked together to form a cycle.

[0022] The Al-alkyl compounds used as co-catalysts comprise Al-trialkyls, such as Al-triethyl, Al-triisobutyl, Al-tri-n-butyl, and linear or cyclic Al-alkyl compounds containing two or more Al atoms bonded to each other by way of O or N atoms, or S04 or S03 groups. The Al-alkyl compound is generally used in such a quantity that the Al/Ti ratio be from 1 to 1000.

[0023] The external donor can be of the same type or it can be different from the succinates of formula (I). Suitable external electron-donor compounds include silicon compounds, ethers, esters such as phthalates, benzoates, succinates also having a different structure from those of formula (I), amines, heterocyclic compounds and particularly 2,2,6,6-tetramethylpiperidine, ketones and the 1 ,3-diethers of the general formula (II):

wherein Rl and Rl l are the same or different and are C1 -C18 alkyl, C3-C18 cycloalkyl or C7-C18 aryl radicals; Rill and RIV are the same or different and are C1 -C4 alkyl radicals; or the 1 ,3-diethers in which the carbon atom in position 2 belongs to a cyclic or polycyclic structure made up of 5, 6 or 7 carbon atoms and containing two or three unsaturations. [0025] Ethers of this type are described in published European patent applications 361493 and 728769.

[0026] Preferred electron-donor compounds that can be used as external donors include aromatic silicon compounds containing at least one Si-OR bond, where R is a hydrocarbon radical. A particularly preferred class of external donor compounds is that of silicon compounds of formula Ra7Rb8Si(OR9)c, where a and b are integer from 0 to 2, c is an integer from 1 to 3 and the sum (a+b+c) is 4; R7, R8, and R9, are C1 -C18 hydrocarbon groups optionally containing heteroatoms. Particularly preferred are the silicon compounds in which a is 1 , b is 1 , c is 2, at least one of R7 and R8 is selected from branched alkyl, alkenyl, alkylene, cycloalkyl or aryl groups with 3-10 carbon atoms optionally containing heteroatoms and R9 is a C1 -C10 alkyl group, in particular methyl. Examples of such preferred silicon compounds are cyclohexyltrimethoxysilane, t-butyltrimethoxysilane, t- hexyltrimethoxysilane, cyclohexylmethyldimethoxysilane, 3,3,3- trifluoropropyl-2-ethylpiperidyl-dimethoxysilane, diphenyldimethoxysilane, methyl-t-butyldimethoxysilane, dicyclopentyldimethoxysilane, 2- ethylpiperidinyl-2-t-butyldimethoxysilane, (1 ,1 ,1 -trifluoro-2-propyl)- methyldimethoxysilane and (1 , 1 , 1 -trifluoro-2-propyl)-2- ethylpiperidinyldimethoxysilane. Moreover, are also preferred the silicon compounds in which a is 0, c is 3, R8 is a branched alkyl or cycloalkyl group, optionally containing heteroatoms, and R9 is methyl. Particularly preferred specific examples of silicon compounds are (tert-butyl)2Si(OCH3)2, (cyclohexyl)(methyl) Si(OCH3)2, (phenyl)2Si(OCH3)2

(cyclopentyl)2Si(OCH3)2, and diiso-propyl dimethoxi silane.

[0027] Preferably the external electron donor compound is used in such an amount to give a molar ratio between the organoaluminum compound and said electron donor compound of from 0.1 to 500, more preferably from 1 to 300 and in particular from 3 to 30.

[0028] As explained above, the solid catalyst component comprises, in addition to the above electron donors, Ti, Mg and halogen. In particular, the catalyst component comprises a titanium compound, having at least a Ti-halogen bond and the above mentioned electron donor compounds supported on a Mg halide. The magnesium halide is preferably MgCI2 in active form, which is widely known from the patent literature as a support for Ziegler-Natta catalysts. Patents USP 4,298,718 and USP 4,495,338 were the first to describe the use of these compounds in Ziegler-Natta catalysis. It is known from these patents that the magnesium dihalides in active form used as support or co-support in components of catalysts for the polymerisation of olefins are characterized by X-ray spectra in which the most intense diffraction line that appears in the spectrum of the non-active halide is diminished in intensity and is replaced by a halo whose maximum intensity is displaced towards lower angles relative to that of the more intense line.

[0029] The preferred titanium compounds are TiCI4 and TiCI3; furthermore, also Ti- haloalcoholates of formula Ti(OR)n-yXy can be used, where n is the valence of titanium, y is a number between 1 and n, X is halogen and R is a hydrocarbon radical having from 1 to 10 carbon atoms.

[0030] The preparation of the solid catalyst component can be carried out according to several methods, well known and described in the art.

[0031] According to a preferred method, the solid catalyst component can be prepared by reacting a titanium compound of formula Ti(OR)n-yXy, where n is the valence of titanium and y is a number between 1 and n, preferably TiCI4, with a magnesium chloride deriving from an adduct of formula MgCI2 ^» pROH, where p is a number between 0.1 and 6, preferably from 2 to 3.5, and R is a hydrocarbon radical having 1-18 carbon atoms. The adduct can be suitably prepared in spherical form by mixing alcohol and magnesium chloride in the presence of an inert hydrocarbon immiscible with the adduct, operating under stirring conditions at the melting temperature of the adduct (100-130°C). Then, the emulsion is quickly quenched, thereby causing the solidification of the adduct in form of spherical particles.

[0032] Examples of spherical adducts prepared according to this procedure are described in USP 4,399,054 and USP 4,469,648. The so obtained adduct can be directly reacted with the Ti compound or it can be previously subjected to thermally controlled dealcoholation (80-130°C) so as to obtain an adduct in which the number of moles of alcohol is generally lower than 3, preferably between 0.1 and 2.5. The reaction with the Ti compound can be carried out by suspending the adduct (dealcoholated or as such) in cold TiCI4 (generally 0°C); the mixture is heated up to 80-130°C and kept at this temperature for 0.5-2 hours. The treatment with TiCI4 can be carried out one or more times. The electron donor compound(s) can be added during the treatment with TiCI4.

[0033] Regardless of the preparation method used, the final amount of the electron donor compound(s) is preferably such that the molar ratio with respect to the MgCI2 is from 0.01 to 1 , more preferably from 0.05 to 0.5.

[0034] The said catalyst components and catalysts are described in WO 00/63261 and WO 01/57099.

[0035] The catalysts may be precontacted with small quantities of olefin (prepolymerisation), maintaining the catalyst in suspension in a hydrocarbon solvent, and polymerising at temperatures from ambient to 60 ° C, thus producing a quantity of polymer from 0.5 to 3 times the weight of the catalyst. The operation can also take place in liquid monomer, producing, in this case, a quantity of polymer 1000 times the weight of the catalyst.

[0036] By using the above mentioned catalysts, the polyolefin compositions are obtained in spheroidal particle form, the particles having an average diameter from about 250 to 7,000 μιη, a flowability of less than 30 seconds and a bulk density (compacted) greater than 0.4 g/ml.

[0037] Besides the clarifying agent, the compositions of the present invention can contain other additives commonly employed in the art, such as antioxidants, light stabilizers, heat stabilizers, colorants and fillers.

[0038] The addition of inorganic fillers, such as talc, calcium carbonate and mineral fibers, brings about an improvement to some mechanical properties, such as flexural modulus and heat deflection temperature (HDT).

[0039] The compositions of the present invention can be used to prepare sheets endowed with a good balance of stiffness and impact resistance as well as a good transparency.

[0040] Thus, according to another object the present invention provides a sheet obtained from a propylene polymer composition comprising: (a) 78 - 85 %, preferably 80 - 83 %, by weight of a propylene homopolymer or of a copolymer of propylene with ethylene having an ethylene content of up to 2.0 % by weight;

(b) 15 - 22 %, preferably 17 - 20 %, by weight of a copolymer of ethylene with propylene having an ethylene content of from 78 to 90 % by weight; and

(c) an effective amount of a clarifying agent;

wherein the composition has an intrinsic viscosity of the xylene soluble fraction (XSIV) at room temperature of from 0.5 to 1.5 dl/g and a melt flow rate (MFR), measured at 230°C and 2.16 kg, of from 0.5 to 10 g/10 min.

[0041] The thus obtained sheets, due to their good balance of properties, are suitable for use in the production of thermoforming articles.

[0042] Hence, according to a further object the present invention provides a thermoformed article obtained from a propylene polymer composition comprising:

(a) 78 - 85 %, preferably 80 - 83 %, by weight of a propylene homopolymer or of a copolymer of propylene with ethylene having an ethylene content of up to 2.0 % by weight;

(b) 15 - 22 %, preferably 17 - 20 %, by weight of a copolymer of ethylene with propylene having an ethylene content of from 78 to 90 % by weight; and

(c) an effective amount of a clarifying agent;

wherein the composition has an intrinsic viscosity of the xylene soluble fraction (XSIV) at room temperature of from 0.5 to 1.5 dl/g and a melt flow rate (MFR), measured at 230°C and 2.16 kg, of from 0.5 to 10 g/10 min.

[0043] The following examples are given to illustrate the present invention without any limiting purpose.

Methods

Ethylene content

[0044] The content of ethylene comonomer was determined by infrared spectroscopy by collecting the IR spectrum of the sample vs. an air background with a Fourier Transform Infrared spectrometer (FTIR). The instrument data acquisition parameters are:

- purge time: 30 seconds minimum

- collect time: 3 minutes minimum - apodization: Happ-Genzel

- resolution: 2 cm- ¹ .

[0045] Sample Preparation - Using a hydraulic press, a thick sheet is obtained by pressing about 1 g of sample between two aluminum foils. A small portion is cut from this sheet to mold a film. Recommended film thickness ranges between 0.02 and 0.05 cm (8 - 20 mils). Pressing temperature is 180±10°C (356 ) and about 10 kg/cm2 (142.2 PSI) pressure for about one minute. After the pressure is released, the sample is removed from the press and cooled to room temperature.

[0046] The spectrum of pressed film sample is recorded in absorbance vs. wavenumbers (cm- ¹ ). The following measurements are used to calculate ethylene content:

- Area (At) of the combination absorption bands between 4482 and 3950 cm- ¹ which is used for spectrometric normalization of film thickness;

- Area (AC2) of the absorption band between 750 and 700 cm-1 after a spectroscopic subtraction of a reference spectrum of an isotactic non- additivated polypropylene in the range 800-690 cm-1 ;

[0047] In order to calculate the ethylene content, a calibration straight line for ethylene obtained by using samples of known amount of ethylene is needed and is obtained by plotting AC2/At versus ethylene molar percent (%C2m). The slope GC2 is calculated from a linear regression.

[0048] The spectra of the unknown samples are recorded and then (At) and (AC2) of the unknown sample are calculated. The ethylene content by weight is obtained being converted from the ethylene content (% molar fraction C2m) of the sample, which is calculated as follows:

[0049] The ethylene content of component (a) is determined on a propylene copolymer sample taken out from the first reactor.

[0050] The ethylene content of component (b) is determined on the precipitated "amorphous" fraction of the polymer. The precipitated "amorphous" fraction is obtained as follows: to one 100 ml aliquot of the filtered liquid obtained as described below in the paragraph headed "Intrinsic viscosity of the xylene- soluble fraction", 200 ml of acetone are added under vigorous stirring. Precipitation must be complete as evidenced by a clear solid-solution separation. The solid thus obtained is filtered on a metallic screen and dried in a vacuum oven at 70°C until a constant weight is reached. Since the portion of (b) with very high ethylene content crystallizes and is excluded from the Xylene-soluble fraction, a correction was made to the ethylene content of the "amorphous" fraction by using the following equation obtained from the data of copolymers of ethylene with propylene polymerized in an autoclave by using the same catalyst systems.

(ethylene content of component (b)) = 1.37 x (ethylene content of "amorphous" fraction) - 5.7

The above equation is valid when the ethylene content of "amorphous" is between 55% and 70% by weight (the ethylene content of (b) is between 70% and 90% by weight).

Intrinsic viscosity of the xylene-soluble fraction (XSIV)

[0051] 2.5 g of polymer and 250 ml of xylene were introduced in a glass flask equipped with a refrigerator and a magnetic stirrer. The temperature is raised in 30 minutes up to the boiling point of the solvent. The so obtained clear solution is then kept under reflux and stirring for further 30 minutes. The closed flask is then kept in thermostatic water bath at 25° C for 30 minutes. The so formed solid is filtered on quick filtering paper. A 100 ml aliquot of the filtered liquid was poured in an aluminium container, heated on a heating plate under nitrogen flow, to remove the solvent by evaporation. The sample for the measurement was removed from the container after cooling 30 minutes at room temperature. The intrinsic viscosity was determined in tetrahydronaphthalene at 135°C.

Melt flow rate (MFR)

[0052] Determined according to ISO 1 133 (230°C, 2.16 Kg).

Taber Stiffness

[0053] Determined according to ASTM D747.

Dart impact

[0054] Determined according to ISO 7765-1.

Haze [0055] Determined according to ISO 14782. Liquid Paraffin (KANTO CHEMICAL CO., INC., Catalog No. 32033-00) was painted with a brush on both sides of the sheet surface. Haze value was measured with a HM-150 (Murakami Color Research Laboratory) instrument.

Whiteness Index (Wl)

[0056] Determined according to ASTM E313. Liquid Paraffin (KANTO CHEMICAL CO., INC., Catalog No. 32033-00) was painted with a brush on both sides of the sheet surface. Whiteness Index was measured by reflection method with a SE-2000 (Nippon Denshoku Co., Ltd.) instrument after putting a slide glass on the front surface and a black glass (BK-7, Murakami Color Research Laboratory) on the back surface.

Draw-Down Time

[0057] A sheet attached to a metal frame of 100 x 150 mm was introduced into an oven kept at 210°C. Draw-Down Time is defined as T2 - T1 , wherein T1 is the time required for the sheet to stretch back and T2 the time required for 2cm sag of the center of the sheet due to its own weight after the stretch back.

Small Angle X-ray Scattering (SAXS)

[0058] PE crystals in component (b) were detected as streak scattering inclined 45° to machine direction (MD) in a Small Angle X-ray Scattering (SAXS) profile of the sheet. SAXS was measured at 0.1 nm of wave length, 2.3m of camera length, and 200msec of exposure time by using a detector system of image intensifier (II) and charge coupled device (CCD) in the BL03XU beamline of SPring-8, a synchrotron radiation facility located in Hyogo Prefecture, Japan and run by the Japan Synchrotron Radiation Research Institute.

Examples

[0059] A series of polymerization runs were carried out in a plant operating continuously in a series of a first liquid-phase reactor and a second fluidized bed gas-phase reactor, equipped with devices to transfer the product from the first to the second reactor.

Examples 1-7 and 10C-12C (comparative)

Preparation of the catalyst and pre-polymerization [0060] A Ziegler-Natta catalyst component was prepared according to Example 5, lines 48-55 of European Patent EP728769. The thus-prepared catalyst component was contacted at 12°C for 24 minutes with aluminium triethyl (TEAL) and dicyclopentyldimethoxysilane (DCPMS) as outside-electron- donor component. The weight ratio between TEAL and the solid catalyst component was 1 1 and the weight ratio between TEAL and DCPMS was 10. The thus-obtained catalyst system was subjected to pre-polymerization by maintaining it in suspension in liquid propylene at 20°C for about 5 minutes before introducing it into the first polymerization reactor.

Polymerization

[0061] A propylene homopolymer as component (a) was prepared in the first reactor, while an ethylene-propylene copolymer as component (b) was prepared in the second reactor. Temperature and pressure were maintained constant throughout the course of the reaction. Hydrogen was used as molecular weight regulator. The composition of the gas phase (propylene, ethylene and hydrogen) was continuously determined by gas- chromatography analysis. At the end of the run the powder is discharged and dried under a nitrogen flow. Data on the characterization of the obtained polymers are shown in Table 1. The polymer characterization data are obtained from measurements carried out on the so obtained polymers, stabilized when necessary.

Extrusion

[0062] The polymer particles were mixed with the quantities and type of clarifying agent indicated in Table 1 and with 0.1 phr of Irganox B225, a stabilizer commercialized by Ciba. "NX8000" stands for Millad® NX8000 (commercially available from Milliken Chemicals). "NA71" stands for ADK NA-71 (commercially available from Amfine Chemicals). The polymer particles were then introduced in an extruder and extruded under nitrogen atmosphere in a twin screw extruder, at a rotation speed of 220 rpm and a melt temperature of 200-250°C. The thus obtained pellets were used to prepare a sheet of 0.3 mm in thickness by operating at 220°C of extrusion temperature, 50°C of measured chilled roll temperature, and 1.1 m/min of take-up velocity by using a sheet extruder of 40φ for single layer (Tanabe). The thus prepared sheet specimen was used for all the tests for physical properties. Data relating to the physical-mechanical properties of the final polymer compositions, obtained from measurements carried out on the so- extruded polymers, are reported in Table 2. The SAXS profile for the sheet prepared in Example 3 is shown in Figure 1. The SAXS profile for the sheet prepared in Example 10C is shown in Figure 2.

Examples 8-9 and 13C-17C (comparative)

The procedure described for Examples 1 -7 and 10C-12C was repeated with the difference that the Ziegler-Natta catalyst was prepared according to Example 1 of International application WO 2009/050045 except that, for the first temperature increase, the temperature was raised to 1 10°C instead of 100°C. Data on the characterization of the obtained polymers are shown in Table 1. Data relating to the physical-mechanical properties of the final polymer compositions, obtained from measurements carried out on the so- extruded polymers, are reported in Table 2.

Table 1

Table 2

Y = existence of PE crystals in component (b) N = absence of PE crystals in component (b)