FIELD OF THE INVENTION

[0001] The present disclosure relates to a soft and thermoplastic polyolefin composition having low values of shore hardness in combination with good tensile and elastic properties.

BACKGROUND OF THE INVENTION

[0002] Polyolefin compositions having high softness while maintaining a good thermoplastic behavior are disclosed in the art. They have been used in many application fields, due to the valued properties which are typical of polyolefins (such as chemical inertia, mechanical properties and nontoxicity).

[0003] The compositions generally comprise crystalline and amorphous portions, in various relative amounts.

[0004] Such crystalline and amorphous portions can be present in the same polymer chain, and/or in distinct phases.

[0005] Depending upon the chemical composition of such portions, their relative amounts and the way in which they are combined in the polyolefin composition, different sets of properties are obtained.

[0006] However, it is always difficult to achieve a good balance of softness, flexibility and thermoplastic behavior.

[0007] An example of soft, flexible and thermoplastic composition is provided in PCT Publication No. WO2009080485, wherein low values of flexural modulus and Shore hardness are obtained by combining a crystalline copolymer of propylene and hexene-1 with a highly soluble, thus highly amorphous ethylene copolymer. Examples of compositions suited for preparing extruded or molded profiles, comprising blends of butene-1 copolymers and propylene copolymers, are provided in EP 2631 271 Al.

[0008] It has now been found that by combining specific butene-1 polymers with reduced amounts of ethylene polymers, it is possible to obtain a soft polyolefin composition having an excellent and unusual set of properties.

[0009] Such properties make it possible to use the compositions for preparing gaskets for closures, capable of providing a tight and durable seal.

[0010] Gaskets are used as sealing elements in a very wide range of closure types.

[0011] In particular they are widely used in twist closures for containers like jars and bottles, generally made of glass or plastic materials. [0012] Depending upon the use of the container, the closures are subject to different and often demanding requirements, in the fulfillment of which a critical role is played by the gasket.

[0013] In particular the gasket should be soft and elastic enough to ensure a tight seal even after long use.

[0014] For instance, in U.S. Patent No. 5849418 it is explained that the gaskets should be hard enough to withstand compression, but soft enough such that a good seal can be formed. A Shore A hardness range from about 70 to about 100 is recommended.

[0015] On the other hand, the material from which the gasket is obtained should be easy to apply and shape on the inner surface of the closure.

[0016] For gaskets of plastic materials, a thermoplastic behavior is thus desirable.

[0017] However it is always difficult to achieve a good balance of softness, flexibility and thermoplastic behavior.

[0018] It has now been found that by using the present polyolefin composition, it is possible to obtain gaskets for closures with an unusual profile of properties in response to the said requirements.

[0019]

SUMMARY OF THE INVENTION

[0020] The present disclosure provides for a polyolefin composition comprising:

A) from 60 to 89% by weight, preferably from 65 to 85% by weight, more preferably from 65 to 82% by weight, of a copolymer of butene-1 with ethylene having a copolymerized ethylene content of up to 18% by mole and no melting peak detectable at the DSC at the second heating scan;

B) from 11 to 40% by weight, preferably from 15 to 35% by weight, more preferably from 18 to 35% by weight, of an ethylene polymer having a density of from 0.900 to 0.970 g/cm ³ , preferably 0.900 to 0.965 g/cm ³ , measured according to ISO 1183 at 23°C;

wherein the amounts of A) and B) refer to the total weight of A) + B) and the DSC second heating scan is carried out with a heating rate of 10°C per minute.

[0021] The composition provided herein has high softness (a Shore A value of lower than 90), good tensile properties (an elongation at break of 900 -1000%) and elastic properties (a compression set at 23 °C of lower than 60) while still maintaining a thermoplastic behavior due to the presence of a crystalline fraction, as revealed by the melting enthalpy values. DETAILED DESCRIPTION OF THE INVENTION

[0022] The polyolefin composition as provided herein has a melting temperature T _m which is generally equal or close to the melting temperature T _m of the component B), namely from 105°C to 135°C, preferably from 105°C to 125°C, more preferably from 110°C to 115°C.

[0023] Generally a single melting peak is detected in the second DSC scan of the polyolefin composition in the said temperature range.

[0024] Should more than one peak be detected, the temperature of the most intense melting peak in the said temperature range is to be taken as the T _m value for both component B) and the polyolefin composition comprising A) and B).

[0025] Thus the Δ¾ _δ value for the polyolefin composition as provided herein is preferably given by the area of the melting peak or the total area of melting peaks (if more than one) in the DSC temperature range from 105°C to 135°C.

[0026] In particular, the present polyolefin composition has a Δ¾ _δ , measured by DSC at the second heating scan, of from 7 to 35 J/g, preferably from 8 to 28 J/g.

[0027] Preferred values of MIE for the said composition are from 0.5 to 8 g/10 min., where MIE is the melt flow index at 190°C with a load of 2.16 kg, determined according to ISO 1133.

[0028] Preferred Shore A values for the said composition are of lower than 90, particularly equal to or lower than 88, the lower limit being of 60.

[0029] Correspondingly, the Shore D values are equal to or or lower than 20, in particular from 20 to 5, more preferably lower than 20, in particular from lower than 20 to 5.

[0030] The butene-1 copolymer component A) just after it has been melted and cooled does not show a melting peak at the second heating scan. However it is crystallizable, i.e. after about 10 days that it has been melted the polymer shows a measurable melting point and a melting enthalpy measured by DSC. In other words the butene-1 copolymer shows no melting temperature attributable to polybutene-1 crystallinity (Tmll) DSC, measured after cancelling the thermal history of the sample, according to the DSC method described in the experimental section of the present application.

[0031] Moreover, the butene-1 copolymer component A) can have at least one of the following additional features:

- a MIE of from 0.5 to 3 g/10 min.;

- a lower limit of the copolymerized ethylene content of 12% by mole;

- a Shore A value equal to or lower than 80, more preferably equal to or lower than 70, in particular from 80 to 40 or from 70 to 40; - a Shore D value equal to or lower than 20, in particular from 20 to 5, more preferably lower than 20, in particular from lower than 20 to 5;

- a Mw/Mn value, where Mw is the weight average molar mass and Mn is the number average molar mass, both measured by GPC, equal to or lower than 3, in particular from 3 to 1.5.

- a tension set of less than 30% at 100% of deformation at 23°C (ISO 2285), more preferably equal to or less than 20%, wherein the lower limit is of 5;

- a percentage of butene-1 units in the form of isotactic pentads (mmmm%) greater than 80%, preferably equal to or greater than 85%, even more preferably equal to or greater than 90%, wherein the upper limit is 99%;

- a tensile stress at break, measured according to ISO 527, of from 3 MPa to 20 MPa, more preferably from 4 MPa to 13 MPa;

- a tensile elongation at break, measured according to ISO 527, of from 550% to 1000%; more preferably from 700% to 1000%;

- an intrinsic viscosity (I.V.) equal to or higher than ldl/g; more preferably equal to or higher than 1.5 dl/g, wherein the upper limit is of 3 dl/g;

- a crystallinity of less than 30% measured via X-ray, more preferably of less than 20%;

- a density of 0.895 g/cm ³ or less, more preferably of 0.875 g/cm ³ or less; wherein the lower limit is of 0.86 g/cm ³ ; and

- a content of xylene insoluble fraction at 0°C of less than 15% by weight, wherein the lower limit is of 0%.

[0032] The butene-1 copolymer component A) can be obtained by polymerizing the monomer(s) in the presence of a metallocene catalyst system obtainable by contacting:

- a stereorigid metallocene compound;

- an alumoxane or a compound capable of forming an alkyl metallocene cation; and, optionally,

- an organo aluminum compound.

[0033] Preferably the stereorigid metallocene compound belongs to the following formula

(I):

wherein:

M is an atom of a transition metal selected from those belonging to Group 4 of the Periodic Table of Elements; preferably M is zirconium;

X, equal to or different from each other, is a hydrogen atom, a halogen atom, a R, OR, OR'O, OSO2CF ₃ , OCOR, SR, NR ₂ or PR ₂ group wherein R is a linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl, C3-C ₂ o-cycloalkyl, C6-C ₂ o-aryl, C7-C ₂ o-alkylaryl or C7-C ₂ o-arylalkyl radical, optionally containing heteroatoms belonging to Groups 13-17 of the Periodic Table of the Elements; and R' is a Ci-C ₂ o-alkylidene, C6-C ₂ o-arylidene, C7-C ₂ o-alkylarylidene, or C7-C ₂ o-arylalkylidene radical; preferably X is a hydrogen atom, a halogen atom, a OR'O or R group; more preferably X is chlorine or a methyl radical;

R ¹ , R ² , R ⁵ , R ⁶ , R ⁷ , R ⁸ and R ⁹ , equal to or different from each other, are hydrogen atoms, or linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl, C3-C ₂ o-cycloalkyl, C6-C ₂ o-aryl, C7-C ₂ o-alkylaryl or C7-C ₂ o-arylalkyl radicals, optionally containing heteroatoms belonging to Groups 13-17 of the Periodic Table of the Elements; or R ⁵ and R ⁶ , and/or R ⁸ and R ⁹ can optionally form a saturated or unsaturated, 5 or 6 membered rings, said ring can bear Ci-C ₂ o alkyl radicals as substituents; with the proviso that at least one of R ⁶ or R ⁷ is a linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl radical, optionally containing heteroatoms belonging to Groups 13-17 of the Periodic Table of the Elements; preferably a Ci-Cio-alkyl radical;

R ³ and R ⁴ , equal to or different from each other, are linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl radicals, optionally containing heteroatoms belonging to Groups 13-17 of the Periodic Table of the Elements; preferably R ³ and R ⁴ equal to or different from each other are Ci-Cio-alkyl radicals; more preferably R ³ is a methyl, or ethyl radical; and R ⁴ is a methyl, ethyl or isopropyl radical.

[0034] Preferably the compounds of formula (I) have the general formula (la):

(la)

Wherein:

M, X, R ¹ , R ² , R ⁵ , R ⁶ , R ⁸ and R ⁹ have been described above; R ³ is a linear or branched, saturated or unsaturated Ci-C2o-alkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R ³ is a Ci-Cio-alkyl radical; more preferably R ³ is a methyl, or ethyl radical.

[0035] Specific examples of metallocene compounds are dimethylsilanediyl{(l-(2,4,7- trimethylindenyl)-7-(2,5-dimethyl-cyclopenta[l,2-b:4,3-b']-d ithiophene)}Zirconium dichloride and dimethylsilanediyl{(l-(2,4,7-trimethylindenyl)-7-(2,5-dimeth yl-cyclopenta[l,2-b:4,3-b']- dithiophene) } Zirconium dimethyl.

[0036] Examples of alumoxanes are methylalumoxane (MAO), tetra-(isobutyl)alumoxane (TIBAO), tetra-(2,4,4-trimethyl-pentyl)alumoxane (TIOAO), tetra-(2,3- dimethylbutyl)alumoxane (TDMBAO) and tetra-(2,3,3-trimethylbutyl)alumoxane (TTMBAO).

[0037] Examples of compounds able to form an alkylmetallocene cation are compounds of formula D ⁺ E ^" , wherein D ⁺ is a Br0nsted acid, able to donate a proton and to react irreversibly with a substituent X of the metallocene of formula (I) and E ^" is a compatible anion, which is able to stabilize the active catalytic species originating from the reaction of the two compounds, and which is sufficiently labile to be able to be removed by an olefinic monomer. Preferably, the anion E ^" comprises of one or more boron atoms.

[0038] Examples of organo- aluminum compounds are trimethylaluminum (TMA), triisobutylaluminium (TIBAL), tris(2,4,4-trimethyl-pentyl)aluminum (TIOA), tris(2,3- dimethylbutyl)aluminium (TDMBA) and tris(2,3,3-trimethylbutyl)aluminum (TTMBA).

[0039] Examples of the said catalyst system and of polymerization processes employing such catalyst system can be found in WO2004099269 and WO2009000637.

[0040] In general, the polymerization process for the preparation of the butene-1 copolymer component A) can be carried out according to known techniques, for example slurry polymerization using as diluent a liquid inert hydrocarbon, or solution polymerization using for example the liquid butene-1 as a reaction medium. Moreover, it may also be possible to carry out the polymerization process in the gas-phase, operating in one or more fluidized bed or mechanically agitated reactors. The polymerization carried out in the liquid butene-1 as a reaction medium is preferred.

[0041] As a general rule, the polymerization temperature is generally of from -100°C to 200°C, preferably from 20°C to 120°C, more preferably from 40°C to 90°C, most preferably from 50°C to 80°C.

[0042] The polymerization pressure is generally comprised between 0.5 bar and 100 bar. The polymerization can be carried out in one or more reactors that can work under same or different reaction conditions such as concentration of molecular weight regulator, comonomer concentration, temperature, pressure etc. [0043] The ethylene polymer B) can be selected in the group consisting of HDPE (High Density Polyethylene, typically having a density from 0.935 to 0.970 g/cm ³ , in particular from 0.935 to 0.965 g/cm ³ ), MDPE and LLDPE (Medium Density and Linear Low Density Polyethylene, typically having a density from 0.915 to 0.934 g/cm ³ ), VLDPE (Very Low Density Polyethylene, typically having a density 0.900 to 0.914 g/cm ³ ), and LDPE (Low Density Polyethylene). LDPE is preferred.

[0044] Mixtures of the above said ethylene polymers are also comprised in the definition of the ethylene polymer B).

[0045] In particular, the LDPE that can be used for component B) is an ethylene homopolymer or an ethylene copolymer containing minor amounts of other comonomers, like butyl acrylate, prepared by high pressure polymerization using free radical initiators.

[0046] LDPE homopolymers are particularly preferred.

[0047] The density of said LDPE typically ranges from 0.914 to 0.935 g/cm ³ .

[0048] The MIE of the ethylene polymer B), in particular of said LDPE, is preferably from

0.5 to 50 g/10 min., more preferably from 1 to 40 g/10 min., in particular from 1 to 10 g/10 min.

[0049] The melting point of said LDPE is generally from 110 to 115° C.

[0050] Such kinds of LDPE are well known in the art and available on the market. Specific examples are the polymers available under the tradenames Escorene and Lupolen.

[0051] The said HDPE, MDPE LLDPE and VLDPE polymers described herein are well known in the art as well and can be prepared with low pressure polymerization in the presence of a Ziegler-Natta or a single site polymerization catalyst.

[0052] Typically a Ziegler-Natta catalyst comprises the product of the reaction of an organometallic compound of Group 1, 2 or 13 of the Periodic Table of Elements with a transition metal compound of Groups 4 to 10 of the Periodic Table of Elements (new notation). In particular, the transition metal compound can be selected among compounds of Ti, V, Zr, Cr and Hf and is preferably supported on MgCl ₂ .

[0053] Particularly preferred catalysts comprise the product of the reaction of said organometallic compound of group 1, 2 or 13 of the Periodic Table of elements, with a solid catalyst component comprising a Ti compound and an optionally electron donor compound supported on MgCl ₂ .

[0054] Preferred organometallic compounds are the aluminum alkyl compounds.

[0055] While the HDPE can be either a homopolymer or a copolymer of ethylene, MDPE and LLDPE are copolymers. [0056] In all the said copolymers, the comonomers are generally selected from C4-C1 ₀ alpha- olefins having the general formula CH ₂ =CHR wherein R is an alkyl radical, linear or branched, or an aryl radical, having from 2 to 8 carbon atoms.

[0057] Specific examples of C4-C1 ₀ alpha-olefins are butene-1, pentene-1, 4-methylpentene- 1, hexene-1 and octene-1.

[0058] The amount of comonomers in the ethylene copolymers may be from 1 to 40% by weight, in particular from 2 to 35% by weight, referred to the weight of the concerned copolymer.

[0059] The polyolefin composition can also contain additives commonly employed in the art, such as antioxidants, light stabilizers, heat stabilizers, colorants and fillers.

[0060] The polyolefin composition can also contain additional polyolefins, in particular selected from crystalline propylene homopolymers and copolymers of propylene with ethylene and/or a C4-C1 ₀ alpha-olefin (specific examples being as provided above), and elastomeric copolymers, like copolymers of ethylene with propylene and/or higher alpha-olefins, like in particular butene-1, hexene-1 or octene-1. Such ethylene copolymers are commonly known as EPR or EPDM copolymers.

[0061] The amount of comonomers in the propylene copolymers may be from 1 to 15% by weight, in particular from 2 to 12% by weight, referred to the weight of the concerned copolymer.

[0062] Preferred amounts of said additional polyolefins are from 1 to 20% by weight, more preferably from 3 to 15% by weight with respect to the total weight of the polyolefin composition.

[0063] In a particular embodiment, the present polyolefin composition does not contain more than 20%, in particular not more than 15% by weight of propylene polymers, based on the total weight of the polyolefin composition.

[0064] Such amounts represent the total of the propylene polymers present in the composition, where "propylene polymers" mean propylene homopolymers or polymers containing prevailing amounts of propylene, in particular 85% by weight or more of propylene.

[0065] The polyolefin composition may be manufactured by mixing the components together, extruding the mixture, and pelletizing the resulting composition using known techniques and apparatus.

[0066] The present disclosure also provides manufactured articles made of or comprising the said polyolefin composition.

[0067] Such articles are soft and flexible. [0068] In general, the present polyolefin compositions are suited for preparing articles by extrusion, with equipment and processes well known in the art.

[0069] Specific examples of such articles are gaskets, in particular gaskets for closures, preferably plastic and/or metal closures.

[0070] As previously said, the gaskets for closures are widely used in twist closures for containers like jars and bottles, generally made of glass or plastic materials.

[0071] The twist closures are commonly in the form of caps of a circular shape, generally made of metal or plastics, hosting the gasket on the inner surface facing the opening in the threaded circular neck of the container.

[0072] The gasket is used to achieve a tight seal on the rim of the opening.

[0073] By twisting (rotating) the closure it is thus possible to close and open the container.

[0074] However, caps such as the Press-on/Twist-off® caps are first pressed on the container to close it by elastic deformation of the gasket against the threading elements of the neck of the container, and then twisted to open.

[0075] So, depending upon the type of closure, the gasket can have various kinds of shapes and functions.

[0076] In particular, while it generally has a sealing function, in the Press-on/Twist-off® caps it has both a sealing and a holding function.

[0077] In other kinds of closures, the holding function is performed by threads or lugs in the body of the closure itself.

[0078] The said closures are particularly for use in food and pharmaceutical packaging.

[0079] By using the present polyolefin composition, air and liquid tight gaskets are obtained.

[0080] In general, gaskets are prepared from the present polyolefin composition by a process comprising the following steps:

a) laying down the polyolefin composition in the molten state on the inner surface of the closure;

b) forming the laid polyolefin composition.

[0081] The above defined step a) is generally carried out by using extruders and metering devices well known in the art, so to achieve a controlled laying down of the polyolefin composition. For "controlled" it is meant that amount and shape of the laid material are controlled.

[0082] Extrusion temperatures generally applied in step a) are from 160°C to 220°C.

[0083] Before carrying out the step a), the inner surface of the closure can be coated with a protective film of a varnish or a lacquer. [0084] The above defined step b) is carried out by compression molding the molten polyolefin composition against the inner surface of the closure.

[0085] The above described processes and equipment are well known in the art, as disclosed, for example, in US5451360.

[0086] The resulting gaskets can have different shapes, like in particular "o-ring" or flat film of variable thickness depending upon the final use of the closure.

[0087] From the previously described properties of the present polyolefin composition, from which the gaskets are obtained, it is immediately evident that such gaskets are soft and elastic, hence they provide a tight and durable seal even after prolonged use.

[0088] Another important advantage is that the properties of the present polyolefin composition are obtained without adding softening agents. Such softening agents are in general made of low molecular weight materials, like mineral oils, and are easily extractable by contact with free fat/oil components of foods, for instance.

EXAMPLES

[0089] The practice and advantages of the various embodiments, compositions and methods as provided herein are disclosed below in the following examples. These Examples are illustrative only, and are not intended to limit the scope of the invention in any manner whatsoever.

[0090] The following analytical methods are used to characterize the polymer compositions.

[0091] Thermal properties (melting temperatures and enthalpies)

[0092] Determined by Differential Scanning Calorimetry (DSC) on a Perkin Elmer DSC-7 instrument.

The melting temperatures of the butene-1 copolymer A) were determined according to the following method:

- Tmll (measured in second heating scan): a weighted sample (5-10 mg) obtained from the polymerization was sealed into aluminum pans and heated at 200°C with a scanning speed corresponding to 10°C/minute. The sample was kept at 200°C for 5 minutes to allow a complete melting of all the crystallites thus cancelling the thermal history of the sample. Successively, after cooling to -20°C with a scanning speed corresponding to 10°C/minute, the peak temperature was taken as crystallization temperature (T _c ). After standing 5 minutes at -20°C, the sample was heated for the second time at 200°C with a scanning speed corresponding to 10°C/min. In this second heating run, the peak temperature, when present is taken as the melting temperature of the polybutene-1 (PB) crystalline form II (Tmll) and the area as the global melting enthalpy (ΔΗίΊΙ). The butene-1 copolymer component A) of the present polyolefin composition does not have a Tmll peak.

- In order to determine the Tml, the sample was melted, kept at 200°C for 5 minutes and then cooled down to 20°C with a cooling rate of 10°C/min.

The sample was then stored for 10 days at room temperature. After 10 days the sample was subjected to DSC, it was cooled to -20°C, and then it was heated at 200°C with a scanning speed corresponding to 10°C/min. In this heating run, the first peak temperature coming from the lower temperature side in the thermogram was taken as the melting temperature (Tml).

The melting temperatures of the component B) and of the overall composition comprising the polymer components A) and B) were measured at the second heating scan under the same conditions as above reported for the determination of Tmll of the butene-1 copolymer component A).

Both component B) and the overall composition of the examples show a single melting peak between 110 and 115°C, corresponding to the melting temperature T _m .

The area of such melting peak of the overall composition is taken as the melting enthalpy Δ¾ _δ of the polyolefin composition.

[0093] Flexural elastic modulus

[0094] According to norm ISO 178, measured 10 days after molding.

[0095] Shore A and D

[0096] According to norm ISO 868, measured 10 days after molding.

[0097] Tensile stress and elongation at break

[0098] According to norm ISO 527 on compression molded plaques, measured 10 days after molding.

[0099] Tension set

[0100] According to norm ISO 2285, measured 10 days after molding.

[0101] Compression set

[0102] According to norm ISO 815, measured 10 days after molding;

[0103] MIE

[0104] Determined according to norm ISO 1133 with a load of 2.16 kg at 190 °C.

[0105] MIL

[0106] Determined according to norm ISO 1133 with a load of 2.16 kg at 230 °C.

[0107] Intrinsic viscosity

[0108] Determined according to norm ASTM D 2857 in tetrahydronaphthalene at 135 °C.

[0109] Density

[0110] Determined according to norm ISO 1183 at 23°C. [0111] Comonomer contents

[0112] Determined by IR spectroscopy or by NMR.

[0113] Particularly for the butene-1 copolymers the amount of comonomer is calculated from the ¹³ C-NMR spectra of the copolymers. Measurements were performed on a polymer solution (8-12 wt ) in dideuterated 1,1,2,2-tetrachloro-ethane at 120 °C. The ¹³ C NMR spectra were acquired on a Bruker AV-600 spectrometer operating at 150.91 MHz in the Fourier transform mode at 120 °C using a 90° pulse, 15 seconds of delay between pulses and CPD (WALTZ16) to remove ^] H- ¹³ C coupling. About 1500 transients were stored in 32K data points using a spectral window of 60 ppm (0-60 ppm).

[0114] Copolymer Composition

[0115] Diad distribution is calculated from ¹³ C NMR spectra using the following relations:

PP = 100 Ii /∑

PB = 100 I ₂ /∑

BB = 100 (I ₃ - Ii ₉ )/∑

PE = 100 (I ₅ + I ₆ )/∑

BE =100 (I ₉ + Iio)/∑

EE = 100 (0.5(Ii5 + I ₆ + Iio) + 0.25 (Ii ₄ ))/∑

Where∑ = I ₁₊ + h - ₉ + + h + + ho + 0.5(I ₁₅ + I ₆ + Iio) + 0.25 (I ₁₄ )

The molar content is obtained from the diads using the following relations:

P (m%)= PP + 0.5 (PE+PB)

B (m%)= BB + 0.5 (BE+PB)

E (m%)= EE + 0.5 (PE+BE)

Ii, I ₂ , I3, I5, I ₆ , I9, I ₆ , Iio, Ii ₄ , lis, I19 are integrals of the peaks in the ¹³ C NMR spectrum (peak of EEE sequence at 29.9 ppm as reference). The assignments of these peaks are made according to J.C. Randal, Macromol. Chem Phys., C29, 201 (1989), M. Kakugo, Y. Naito, K. Mizunuma and T. Miyatake, Macromolecules, 15, 1150, (1982), and H.N. Cheng, Journal of Polymer Science, Polymer Physics Edition, 21, 57 (1983). They are collected in Table A (nomenclature according to C.J. Carman, R.A. Harrington and C.E. Wilkes, Macromolecules, 10, 536 (1977)). Table A.

[0116] For the propylene copolymers the comonomer content is 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 .

[0117] Sample Preparation

[0118] Using a hydraulic press, a thick sheet is obtained by pressing about g 1 of sample between two aluminum foils. If homogeneity is in question, a minimum of two pressing operations are recommended. A small portion is cut from this sheet to mold a film. Recommended film thickness ranges between 0.02-:0.05 cm (8 - 20 mils).

[0119] Pressing temperature is 180+10°C (356°F) and about 10 kg/cm ² (142.2 PSI) pressure for about one minute. Then the pressure is released and the sample is removed from the press and cooled the room temperature. [0120] The spectrum of a pressed film of the polymer is recorded in absorbance vs. wavenumbers (cm ¹ ). The following measurements are used to calculate ethylene and butene-1 content:

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

If ethylene is present, Area (AC2) of the absorption band between 750-700 cm ^"1 after two proper consecutive spectroscopic subtractions of an isotactic non additivated polypropylene spectrum and then, if butene-1 is present, of a reference spectrum of a butene-1 -propylene random copolymer in the range 800-690 cm ^"1 .

If butene-1 is present, the height (DC4) of the absorption band at 769 cm ^"1 (maximum value), after two proper consecutive spectroscopic subtractions of an isotactic non additivated polypropylene spectrum and then, if ethylene is present, of a reference spectrum of an ethylene-propylene random copolymer in the range 800-690 cm ^"1 .

In order to calculate the ethylene and butene-lcontent, calibration straight lines for ethylene and butene-1 obtained by using samples of known amount of ethylene and butene-1 are needed.

[0121] Mw/Mn determination by GPC

[0122] The determination of the means Mn and Mw, and Mw/Mn derived therefrom was carried out using a Waters GPCV 2000 apparatus, which was equipped with a column set of four PLgel Olexis mixed-gel (Polymer Laboratories) and an IR4 infrared detector (PolymerChar). The dimensions of the columns were 300 x 7.5 mm and their particle size 13 μιη. The mobile phase used was 1-2-4-trichlorobenzene (TCB) and its flow rate was kept at 1.0 ml/min. All the measurements were carried out at 150°C. Solution concentrations were 0.1 g/dl in TCB and 0.1 g/1 of 2,6-diterbuthyl-/?-chresole were added to prevent degradation. For GPC calculation, a universal calibration curve was obtained using 10 polystyrene (PS) standard samples supplied by Polymer Laboratories (peak molecular weights ranging from 580 to 8500000). A third order polynomial fit was used for interpolating the experimental data and obtaining the relevant calibration curve. Data acquisition and processing was done using Empower (Waters). The Mark-Houwink relationship was used to determine the molecular weight distribution and the relevant average molecular weights: the K values were KPS = 1.21 x 10 ^"4 dL/g and K _PB = 1.78 x 10 ^"4 dL/g for PS and PB respectively, while the Mark-Houwink exponents a= 0.706 for PS and a= 0.725 for PB were used.

[0123] For butene-1 /ethylene copolymers, as far as the data evaluation is concerned, it is assumed that the composition is constant in the whole range of molecular weight and the K value of the Mark-Houwink relationship is calculated using a linear combination as reported below: ^Ά ΕΒ ^λ Ε ^Ά ΡΕ ^" · ^{" λ} Ρ ^Ά ΡΒ

where Κ _Ε Β is the constant of the copolymer, K _PE (4.06 x 10 ^"4 , dL/g) and K _PB (1.78 x 10 ^"4 dl/g) are the constants of polyethylene and polybutene and XE and XB are the ethylene and the butene- 1 weight content. The Mark-Houwink exponents a= 0.725 is used for all the butene- 1/ethylene copolymers independently of their composition.

[0124] Fractions soluble and insoluble in xylene at 0°C (XS-0°C)

[0125] 2.5 g of the polymer sample are dissolved in 250 ml of xylene at 135°C under agitation. After 30 minutes the solution is allowed to cool to 100°C, still under agitation, and then placed in a water and ice bath to cool down to 0°C. Then, the solution is allowed to settle for 1 hour in the water and ice bath. The precipitate is filtered with filter paper. During the filtering, the flask is left in the water and ice bath so as to keep the flask inner temperature as near to 0°C as possible. Once the filtering is finished, the filtrate temperature is balanced at 25 °C, dipping the volumetric flask in a water-flowing bath for about 30 minutes and then, divided in two 50 ml aliquots. The solution aliquots are evaporated in nitrogen flow, and the residue dried under vacuum at 80° C until constant weight is reached. The weight difference in between the two residues must be lower than 3%; otherwise the test has to be repeated. Thus, one calculates the percent by weight of polymer soluble (Xylene Solubles at 0°C = XS 0°C) from the average weight of the residues. The insoluble fraction in o-xylene at 0°C (xylene Insolubles at 0°C = XI 0°C) is:

XI 0°C=100-XS 0°C.

[0126] Fractions soluble and insoluble in xylene at 25 °C (XS-25°C)

[0127] 2.5 g of polymer are dissolved in 250 ml of xylene at 135° C under agitation. After 20 minutes the solution is allowed to cool to 25° C, still under agitation, and then allowed to settle for 30 minutes. The precipitate is filtered with filter paper, the solution evaporated in nitrogen flow, and the residue dried under vacuum at 80° C until constant weight is reached. Thus, one calculates the percent by weight of polymer soluble (Xylene Solubles - XS) and insoluble at room temperature (25° C).

[0128] The percent by weight of polymer insoluble in xylene at room temperature (25 °C) is considered the isotactic index of the polymer. This value corresponds substantially to the isotactic index determined by extraction with boiling n-heptane, which by definition constitutes the isotactic index of polypropylene polymers.

[0129] Determination of isotactic pentads content

[0130] 50 mg of each sample were dissolved in 0.5 ml of C2D2CI4. [0131] The ^1J C NMR spectra were acquired on a Bruker DPX-400 (100.61 Mhz, 90° pulse, 12s delay between pulses). About 3000 transients were stored for each spectrum; the mmmm pentad peak (27.73 ppm) was used as the reference.

[0132] The microstructure analysis was carried out as described in the literature (Macromolecules 1991, 24, 2334-2340, by Asakura T. et al. and Polymer, 1994, 35, 339, by Chujo R. et al.).

[0133] The percentage value of pentad tacticity (mmmm ) for butene- 1 copolymers is the percentage of stereoregular pentads (isotactic pentad) as calculated from the relevant pentad signals (peak areas) in the NMR region of branched methylene carbons (around 27.73 ppm assigned to the BBBBB isotactic sequence), with due consideration of the superposition between stereoirregular pentads and of those signals, falling in the same region, due to the comonomer.

[0134] Determination of X-ray crystallinity

[0135] The X-ray crystallinity was measured with an X-ray Diffraction Powder Diffractometer using the Cu-Kal radiation with fixed slits and collecting spectra between diffraction angle 2Θ = 5° and 2Θ = 35° with step of 0.1° every 6 seconds.

[0136] Measurements were performed on compression molded specimens in the form of disks of about 1.5-2.5 mm of thickness and 2.5-4.0 cm of diameter. These specimens are obtained in a compression molding press at a temperature of 200°C + 5°C without any appreciable applied pressure for 10 minutes, then applying a pressure of about 10 kg/cm ² for about few second and repeating this last operation 3 times.

[0137] The diffraction pattern was used to derive all the components necessary for the degree of crystallinity by defining a suitable linear baseline for the whole spectrum and calculating the total area (Ta), expressed in counts/sec'20, between the spectrum profile and the baseline. Then a suitable amorphous profile was defined, along the whole spectrum, that separate, according to the two phase model, the amorphous regions from the crystalline ones. Thus it is possible to calculate the amorphous area (Aa), expressed in counts/sec20, as the area between the amorphous profile and the baseline; and the crystalline area (Ca), expressed in counts/sec20, as Ca = Ta- Aa

The degree of crystallinity of the sample was then calculated according to the formula:

Cr = lOO x Ca / Ta

[0138] Example 1 and Comparative Example 1

[0139] Materials used in the examples

PB-1: butene- 1/ethylene copolymer containing 16% by moles of copolymerized ethylene, produced according to the process described in WO2009000637 and inline blended with a propylene copolymer composition (I) added in amount of 7% by weight with respect to the total weight of the butene-l/ethylene copolymer and the propylene copolymer composition (I).

Such propylene copolymer composition (I) has MFRL of 5.5 g/10 min., total copolymerized ethylene content of 3% by weight, total copolymerized butene-1 content of 6% by weight; XS-25°C of 19% by weight and T _m of 133°C, and is made of the following two components:

Γ) 35% by weight of a copolymer of propylene with ethylene (3.2% by weight in the copolymer), and

I") 65% by weight of a copolymer of propylene with ethylene (3.2% by weight in the copolymer) and butene-1 (6% by weight in the copolymer);

wherein the amounts of Γ) and Γ ') are referred to the total weight of Γ) + 1");

LDPE: low density polyethylene homopolymer Lupolen 3020, having a density of 0.928 g/cm ³ and MIE of 4 g/10 min., sold by LyondellBasell;

Stabilizers: blend of 0.05% by weight of pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4- hydroxyphenyl)propionate (Irganox ^® 1010, sold by BASF) and 0.05% by weight of tris (2.4-di-tert-butylphenyl) phosphite (Irgafos ^® 168, sold by BASF), said percent amounts being referred to the total weight of the poly olefin composition;

Lubricants: blend of 1% by weight of erucamide (Crodamide ^® ER, sold by Croda), 1% by weight of Oleamide (Crodamide ^® OR, sold by Croda) and 1% by weight of Glyceryl Stearate (Atmer ^® 129, sold by Croda), said percent amounts being referred to the total weight of the polyolefin composition;

Pigment: titanium dioxide Ti-Pure ^® R-104, sold by DuPont.

[0140] Due to the reduced content of propylene polymers, no melting peak is detected in the DSC analysis (second scan) of the above described PB-1.

[0141] The said materials are melt-blended in a co-rotating twin screw extruder Coperion ZSK40SC, with screw diameter of 40 mm and screw length/diameter ratio of 43:1, under the following conditions:

- extrusion temperature of 180-200°C;

- screw rotation speed of 220 rpm;

- production rate of 60 kg/hour.

[0142] The properties of the so obtained final compositions are reported in Table 1.

[0143] In Table 1 are also reported the properties of the above described PB-1 for comparison purpose (Comparison Example 1). Table I

Note: * weight % with respect to the total weight of A) + B).