US20070296120A1

US20070296120A1 - Novel Propylene Polymer Compositions

Info

Publication number: US20070296120A1
Application number: US11/667,883
Authority: US
Inventors: Johannes Wolfschwenger; Christelle Grein; Klaus Bernreitner; Markus Gahleitner; Thor Kamfjord
Original assignee: Borealis Technology Oy
Current assignee: Borealis Technology Oy
Priority date: 2004-11-18
Filing date: 2005-11-09
Publication date: 2007-12-27
Also published as: EP1833909A1; US8912263B2; ES2318562T3; CN101061173A; WO2006053661A8; DE602005012153D1; US20110218293A1; EP1659151A1; EP1833909B1; ATE419304T1; CN101061173B; WO2006053661A1

Abstract

The invention relates to propylene polymer compositions comprising 50-70 wt % of a propylene homo- or copolymer, 5-20 wt % of a first elastomeric ethylene-propylene copolymer, 5-25 wt % of a second elastomeric ethylene-propylene copolymer and 5-30 wt % of an ethylene polymer. The propylene polymer compositions are suitable for moulding and they have low haze and a good impact strength/stiffness balance with good impact strengths at low temperatures.

Description

FIELD OF INVENTION

The present invention relates to propylene polymer compositions which are suitable for moulding, especially injection moulding. More particularly the propylene polymer compositions can be used for packaging applications, especially for deep freeze packaging applications because they have excellent impact strength/stiffness balance at low temperatures, sufficient flowability and good optical properties.

DESCRIPTION OF PRIOR ART

Transparent polypropylene compositions with superior toughness at low temperatures have become an important market trend in recent years. One type of targeted products is rather stiff with flexural moduli well above 800 MPa. Materials with good stiffness are required because structural integrity is necessary for the intended products in the moulding segment, e.g. for boxes, crates, thin wall packaging, etc.
Types of propylene polymers having the required transparency are for example propylene random copolymers with ethylene as comonomer. However, their impact resistance below 0° C. is insufficient and stiffness is below the required level.
There are also propylene polymers known, which have the required impact resistance at low temperatures. These polymers are heterophasic propylene copolymers, having a rubber phase (usually about 20-30 wt % rubber phase with 40-60 wt % propylene) dispersed in a continuous matrix phase. For a good low temperature impact resistance, the molecular weight of the rubber phase is higher than the molecular weight of the matrix phase. These heterophasic propylene copolymers are however very opaque. If the molecular weight of the polymer in the dispersed phase is lower than that of the matrix phase, transparency is increased and impact resistance is decreased. A lower total MFR of the composition results in an increased impact strength, however, the processability of the polymer composition which is required for the intended application (injection moulding) decreases.

OBJECT OF THE INVENTION

It is therefore the object of the invention, to provide a polypropylene composition for moulding, which has low haze and which simultaneously shows a good impact strength/stiffness balance with good impact strengths at low temperatures.
The above object was achieved with a polypropylene composition having an MFR (230° C./2.16 kg)≧8 g/10 min comprising
A) 50-70 wt % of a propylene polymer comprising a propylene homopolymer and/or a propylene copolymer with up to 5 wt % ethylene and/or one or more C₄-C₈α-olefins and having an intrinsic viscosity IV_A1.00-2.20 dl/g
B) 5-20 wt % of a first elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_B1.65-2.50 dl/g and an ethylene content of 20-40 wt %, preferably of 20-30 wt %, with IV_B>IV_A,
C) 5-25 wt % of a second elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_Cof 0.90-1.60 dl/g and an ethylene content of 45-85 wt %, preferably of 50-75 wt %,
D) 5-30 wt % of an ethylene polymer having an ethylene content of at least 80 mol % and having a melt index MI (190° C., 2.16 kg) of at least 5 g/10 min and a density of 905-925 kg/m³.
The propylene polymer A used for the propylene polymer composition according to the invention is either a propylene homopolymer or a propylene copolymer or mixtures thereof. When the propylene polymer comprises a propylene copolymer, the copolymer contains up to 5 wt % of ethylene and/or one or more C₄-C₈α-olefins, preferably up to 2 mol % of comonomers. Among possible comonomers, ethylene and 1-butene are preferred.
It is further important, that the propylene polymer A has an intrinsic viscosity IV_A1.00-2.20 dl/g in order to guarantee a high flowability of the end-product.
It is also essential for the present invention, that a first elastomeric ethylene-propylene copolymer B having a low ethylene content of 20-40 wt % and a high intrinsic viscosity IV_Bof 1.65-2.50 dl/g and a second elastomeric ethylene-propylene copolymer C having a high ethylene content of 45-85 wt % and a low intrinsic viscosity of 0.90-1.60 dl/g are present.
It was found, that it is beneficial for the impact strength, when the molecular weight of the elastomeric ethylene-propylene copolymer B with the low ethylene content is higher than the molecular weight of the propylene polymer A. Therefore, it is required that IV_B>IV_A.
A further essential component of the present invention is an ethylene polymer having an ethylene content of at least 80 mol %. For achieving good optical properties it is important for the ethylene polymer to have a melt index MI (190° C., 2.16 kg) of at least 5 g/10 min. Lower melt indices do not result in a composition having low haze. When the melt index of the ethylene polymer is too high, especially when it is >100 g/10 min the mechanical properties of the compositions, in particular toughness, are not sufficient.
Preferred ethylene polymers are LDPE and LLDPE.
The compositions of the present invention preferably have an MFR (230° C., 2.16 kg) of from 8 to 60 g/10 min.
According to an advantageous embodiment, the first elastomeric ethylene-propylene copolymer has an intrinsic viscosity IV_Bof 1.80-2.25 dl/g.
It is further preferred, that the second elastomeric ethylene-propylene copolymer has an intrinsic viscosity IV_Cof 0.90-1.50 dl/g.
For the polypropylene compositions according to the invention it is preferred, that the difference between the intrinsic viscosities of the first and second elastomeric ethylene-propylene copolymers IV_B−IV_Cis ≧0.2 dl/g. It is still more preferred, that IV_B−IV_Cis ≧0.4 dl/g.
For the polypropylene compositions of the present invention it is preferred that they contain, based on the total weight of components A to D, from 0.01-2 wt % of (X-nucleating agents.
The addition of α-nucleating agents (of which some may also act as clarifiers) to propylene polymers increases their stiffness (and transparency). α-nucleating agents and clarifiers are therefore added for a high absolute level of stiffness and transparency.
Suitable α-nucleating agents include talc having a particle size of 0.01-1.0 μm, sodium benzoate, sodium-2,2′-methylene-bis(4,6-di-t-butylphenyl)phosphate, sodium-bis(4-t-butylphenyl)phosphate, 1,3,2,4-di(3′,4′-dimethylbenzylidene)sorbitol and “ADK STAB NA21 E” available from Asahi Denka Kogyo (Japan). If talc is used as nucleating agent, it is usually present in an amount of 0.01-1.0 wt %, which is an effective amount for α-nucleating, but which is not a sufficient amount where talc would already act as filler. A preferred nucleating agent is 1,3,2,4-di(3′,4′-dimethylbenzylidene)sorbitol, which is available as “MILLAD 3988” from Milliken.
According to an advantageous embodiment the ratio (B+C)/D of the amounts of elastomeric copolymers (B+C) to the amount of ethylene polymer D is from 0.3 to 2.5.
It has been found, that outside of this ratio haze and impact strength are unsatisfactory.
The polypropylene compositions of the present invention are preferably produced by mixing
A) 50-70 wt % of a propylene polymer comprising a propylene homopolymer and/or a propylene copolymer with up to 5 wt % ethylene and/or one or more C₄-C₈α-olefins and having an intrinsic viscosity IV_A1.00-2.20 dl/g,
B) 5-20 wt % of a first elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_B1.65-2.50 dl/g and an ethylene content of 20-40 wt %, with IV_B>IV_A,
C) 5-25 wt % of a second elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_Cof 0.90-1.60 dl/g and an ethylene content of 45-85 wt %,
D) 5-30 wt % of an ethylene polymer having an ethylene content of at least 80 mol % and having a melt index MI (190° C., 2.16 kg) of at least 10 g/10 min and a density of 905-925 kg/m³, melting and homogenising and cooling and pelletising the mixture.
The propylene polymer compositions of the present invention are preferably produced by combining the propylene polymer A in the form of powder or granules, the elastomeric copolymers B and C and the ethylene polymer D and any additives and/or nucleating agents in a melt mixing device.
Melt mixing devices suited for this process are discontinuous and continuous kneaders, twin screw extruders and single screw extruders with special mixing sections and co-kneaders. The residence time must be chosen such that a sufficiently high degree of homogenisation is achieved.
Due to their advantageous property profile, the polymer compositions of the present invention are especially suited for injection moulding applications. The polymer compositions of the present invention are particularly suited for packaging applications, including thin wall packaging, for low temperatures.
Production of Propylene Polymer A
The propylene polymer A may be produced by single- or multistage process polymerisation of propylene or propylene and ethylene such as bulk polymerisation, gas phase polymerisation, slurry polymerisation, solution polymerisation or combinations thereof using conventional catalysts. A homo- or copolymer can be made either in loop reactors or in a combination of loop and gas phase reactor. Those processes are well known to one skilled in the art.
A suitable catalyst for the polymerisation of the propylene polymer is any stereospecific catalyst for propylene polymerisation which is capable of polymerising and copolymerising propylene and comonomers at a temperature of 40 to 110° C. and at a pressure from 10 to 100 bar. Ziegler Natta catalysts as well as metallocene catalysts are suitable catalysts.
One skilled in the art is aware of the various possibilities to produce propylene homo- and copolymers and will simply find out a suitable procedure to produce suitable polymers which are used in the present invention.
Production of Elastomeric Copolymers B and C
An ethylene propylene elastomeric copolymer may be produced by known polymerisation processes such as solution, suspension and gas-phase polymerisation using conventional catalysts. Ziegler Natta catalysts as well as metallocene catalysts are suitable catalysts.
A widely used process is the solution polymerisation. Ethylene, propylene and catalyst systems are polymerised in an excess of hydrocarbon solvent. Stabilisers and oils, if used, are added directly after polymerisation. The solvent and unreacted monomers are then flashed off with hot water or steam, or with mechanical devolatilisation. The polymer, which is in crumb form, is dried with dewatering in screens, mechanical presses or drying ovens. The crumb is formed into wrapped bales or extruded into pellets.
The suspension polymerisation process is a modification of bulk polymerisation. The monomers and catalyst system are injected into the reactor filled with propylene. The polymerisation takes place immediately, forming crumbs of polymer that are not soluble in the propylene. Flashing off the propylene and comonomer completes the polymerisation process.
The gas-phase polymerisation technology consists of one or more vertical fluidised beds. Monomers and nitrogen in gas form along with catalyst are fed to the reactor and solid product is removed periodically. Heat of reaction is removed through the use of the circulating gas that also serves to fluidise the polymer bed. Solvents are not used, thereby eliminating the need for solvent stripping, washing and drying.
The production of ethylene propylene elastomeric copolymers is also described in detail in e.g. U.S. Pat. No. 3,300,459, U.S. Pat. No. 5,919,877, EP 0 060 090 A1 and in a company publication by EniChem “DUTRAL, Ethylene-Propylene Elastomers”, pages 1-4 (1991).
Alternatively, elastomeric ethylene-propylene copolymers, which are commercially available and which fulfil the indicated requirements, can be used.
Alternatively, polymers A, B and C may be produced in a series of reactors, e.g. starting with the production of polymer A in a loop reactor, transferring the product into a first gas phase reactor, where copolymer B is polymerised and finally transferring the product of the first two reactors into a second gas phase reactor, where copolymer C is polymerised.
Production of Ethylene Polymers D
It is preferred to use ethylene polymers which are commercially available, e.g. MA9230, CA9150, MA8200 from Borealis A/S. Alternatively, suitable ethylene polymers may be produced according to the following descriptions.
Low density polyethylene may be produced by free-radical-initiated polymerization using free radical initiators such as peroxide or oxygen in high pressure processes. The polymerization is carried out in tubular or stirred autoclave reactors at a temperature of about 130 to 330° C. and at a pressure around 700 to 3000 bars.
Linear low density polyethylene is made by the copolymerisation of ethylene and α-olefins. It may be produced in low pressure processes such as gas-phase process (for which the Unipol technology is a typical example), a solution-phase polymerisation process, a slurry process, or combinations thereof like staged gas phase (Union Carbide), staged slurry/gas phase (Borealis) or staged solution phase (Nova). A suitable catalyst for the polymerisation of LLDPE is any stereospecific catalyst which is capable of polymerising and copolymerising ethylene and comononers. Ziegler-Natta as well as metallocene catalysts are suitable catalysts. In the gas-phase process, reactor temperatures are usually below 100° C. with pressures of about 20 bars. In the solution process, reactor temperatures are usually 170-250° C. with pressures of 40-140 bars. In the solution-phase polymerisation process, reactor temperatures are usually 70-110° C. with pressures of 30-50 bars.
Measurement Methods
MFR
The melt flow rates were measured with a load of 2.16 kg at 230° C. for polypropylene and at 190° C. for polyethylene. The melt flow rate is that quantity of polymer in grams which the test apparatus standardised to ISO 1133 extrudes within 10 minutes at a temperature of 230° C. or 190° C. respectively, under a load of 2.16 kg.
The expressions “melt flow rate”, “MFR” and “melt index MI” are in this document used synonymously for the respective property of propylene polymers and ethylene polymers.
Comonomer contents were measured with Fourier transform infrared spectroscopy (FTIR) calibrated with ¹³C-NMR.
Intrinsic Viscosity
Intrinsic Viscosity was measured according to DIN ISO 1628-1 (October 1999) in Decalin at 135° C.
Puncture Test
Impact strength was determined under biaxial loading. Puncture tests according to IS06603/2 at −20° C. were performed using 60*60*2 mm injection moulded samples. Two parameters were determined: F_max, the maximum of the load-deflection curve, and W_tot, the total energy absorbed by the sample (i.e. the area under the load-deflection curve).
Bending Test
Bending tests were performed according to ISO 178 using 80*10*4 mm injection moulded specimens as described in EN ISO 1873-2. Bending modulus, E-modulus, was determined according to ISO 178 at 2 mm/min in between strains of 0.05% to 0.25%.
Haze
Haze was determined according to ASTM D 1003-92 on injection moulded test plaques (60×60×2 mm).

EXAMPLES

Preparation of Polymers A

The propylene polymers A used for the present invention were prepared according to the following procedure:
Homopolymers:
Raw Materials:
Hexane dried over molecular sieve (3/10A)
TEAL: 93% from Sigma-Aldrich
Donor: Dicyclopentyldimethoxysilane: ex Wacker Chemie (99%).
N₂: supplier AGA, quality 5.0; purification with catalyst BASF R0311, catalyst G132 (CuO/ZNO/C), molecular sieves (3/10A) and P₂O₅.
Propylene: polymerisation grade
Hydrogen: supplier AGA, quality 6.0
The catalyst ZN104 is commercially available from Basell.
Sandostab P-EPQ is commercially available from Clariant.
A 20 l autoclave reactor has been purified by mechanical cleaning, washing with hexane and heating under vacuum/N₂cycles at 160° C. After testing for leaks with 30 bar N₂over night reactor has been vacuumed and filled with 5250 g propylene by weighing and 51.4 nl H₂by pressure monitoring from a 50 l steel cylinder.
80 mg of ZN104-catalyst are activated for 5 minutes with a mixture of Triethylaluminium (TEAl; solution in hexane 1 mol/l) and Dicyclopentyldimethoxysilane as donor (0.3 mol/l in hexane)—in a molar ratio of 4 after a contact time of 5 min—and 10 ml hexane in a catalyst feeder. The molar ratio of TEAl and Ti of catalyst is 250. After activation the catalyst is spilled with 250 g propylene into the stirred reactor with a temperature of 23° C. Stirring speed is hold at 250 rpm. After 6 min prepolymerisation at 23° C. temperature is increased to 70° C. in about 14 min. After holding that temperature for 1 hour polymerisation is stopped by flashing propylene and cooling to room temperature.
After spilling the reactor with N₂the homopolymer powder is transferred to a steel container and stabilized with 0.1 wt % of Sandostab P-EPQ and 0.2 wt % of Ionol in acetone and dried over night in a hood and additionally for 2 hours at 50° C. under vacuum.
The amount of polymer powder (A2) was 1864 g and the MFR (230° C., 2.16 kg) was 44 g/10 min.
Random Copolymers
Raw Materials:
Hexane dried over molecular sieve (3/10A)
TEAL: 93% from Sigma-Aldrich
Donor: Dicyclopentyldimethoxysilane: ex Wacker Chemie (99%).
N₂: supplier AGA, quality 5.0; purification with catalyst BASF R0311, catalyst G132 (CuO/ZNO/C), molecular sieves (3/10A) and P₂O₅.
Ethylene, Propylene: polymerisation grade
Hydrogen: supplier AGA, quality 6.0
The catalyst ZN101 is commercially available from Basell.
Sandostab P-EPQ is commercially available from Clariant.
A 20 l autoclave reactor has been purified by mechanical cleaning, washing with hexane and heating under vacuum/N₂cycles at 160° C. After testing for leaks with 30 bar N₂over night reactor has been vacuumed and filled with 4250 g propylene by weighing.
23.9 mg of ZN101-catalyst are activated for 5 minutes with a mixture of Triethylaluminium (TEAl; solution in hexane 1 mol/l) and Dicyclopentyldimethoxysilane as donor (0.3 mol/l in hexane)—in a molar ratio of 20 after a contact time of 5 min—and 10 ml hexane in a catalyst feeder. The molar ratio of TEAl and Ti of catalyst is 100. After activation the catalyst is spilled with 250 g propylene into the stirred reactor. Stirring speed is hold at 215 rpm. After 15 min prepolymerisation at 13° C. 30 nl H₂have been dosed into the reactor and constant ethylene dosing has been started to achieve the target ethylene content in the product. Stirring speed is increase to 250 rpm and temperature to 70° C. (achieved after 16 min). After holding these conditions for 124 min (starting from dosing of H₂), polymerisation is stopped by flashing and cooling to room temperature.
After spilling the reactor with N₂the random copolymer is transferred to a steel container and stabilized with 0.1 wt % of Sandostab P-EPQ and 0.2 wt % of Ionol in acetone and dried over night in a hood and additionally for 2 hours at 50° C. under vacuum.
The amount of polymer powder (A1) was 1520 g, ethylene content 1.2 wt % and the MFR (230° C., 2.16 kg) was 16 g/10 min.
The following polymers A were prepared: according to the above procedures:

polymer MFR C2 IV

No. [g/10 min] [wt %] [dl/g]

A1 16 1.2 1.48

A2 44 0 1.19

Preparation of Elastomeric Copolymers B and C

The elastomeric copolymers of the present invention were prepared according to the following procedure:
A 5 l-reactor (autoclave) filled with about 0.2 barg propylene (polymerisation grade) is pressured up with 3.0 barg H₂. Then 300 g of propylene are added.
5 mg of a ZN104 catalyst is contacted with 0.3 ml white oil for about 16 hours and then activated for 5 minutes with a mixture of Triethylaluminium (TEAl; solution in hexane 1 mol/l) and Dicyclopentyldimethoxysilane as donor (0.3 mol/l in hexane)—in a molar ratio of 76 using a contact time of 5 min. The molar ratio of TEAl and Ti of catalyst was 380 and TEAl concentration in TEAl/donor mixture 12.6 mg/ml hexane. After activation the catalyst is transferred to the reactor by spilling in with 500 g propylene. After 12 min pre-polymerisation at 30° C. 90 g of ethylene is added to the reactor and the temperature is increased to 55° C. During heating up additional ethylene dosing is started to achieve the pressure of 34.2 barg at 55° C. Total pressure is hold constantly via continuously dosing of ethylene during polymerisation. 30 min after end of prepolymerisation the reaction is stopped by flashing of monomers and cooling.
The amount of polymer powder was 102 g.
The polymer is stabilized with 0.1 wt % of Sandostab P-EPQ and 0.2 wt % of Ionol in acetone and dried over night in a hood and additionally for 2 hours at 50° C. under vacuum.
The resulting rubber copolymer (B3) has an intrinsic viscosity of 2.11 dl/g and an ethylene content of 49.8 wt %.
The following elastomeric ethylene-propylene copolymers were prepared according to the above procedure, except that H₂and ethylene amounts were varied to achieve different intrinsic viscosities and comonomer concentrations.

polymer i.V. C2

No. [dl/g] [wt %]

B1 2.00 22.8

B2 2.01 25.9

B3 2.11 49.8

B4 2.17 29.5

B5 1.51 25.2

C1 1.05 67.4

C2 1.58 54.6

C3 1.03 70.5

C4 1.19 51.9

Ethylene Polymers D

The ethylene polymers D which are used for the present invention are selected among commercially available homo- and copolymers.
The following ethylene homo- and copolymers were used in the examples:

Melt Index

poly- commercial comonomer (190° C.,

mer grade content 2.16 kg) density

No. designation comonomer [wt %] [g/10 min] [g/cm³]

D1 MA9230 — — 22.0 0.923

D2 CA9150 — — 15.0 0.915

D3 MA8200 — — 7.0 0.920

D4 FB4230 1-butene 6.5 0.4 0.923
The ethylene polymers MA9230, CA9150, MA8200 and FB4230 are commercially available from Borealis A/S.
For the examples (E1 to E8, CE1 to CE13), the appropriate amounts of propylene polymers A1 and A2, elastomeric ethylene-propylene copolymers B1 to B5 and C1 to C4, ethylene polymers D1 to D4, conventional additives (0.05 wt % Hydrotalcite (DHT-4A), 0.1 wt % Irgafos 168, 0.1 wt % Irganox 1010, 0.05 wt % Ca-stearate, in each case based on the sum of the weights of components A to D) and nucleant (0.2 wt % Millad 3988, based on the sum of the weights of components A to D) were mixed in an intensive mixer (Henschel mixer) for 25 seconds. The compositions were then compounded in a twin screw extruder at a temperature of 250° C. The strands were quenched in cold water and pelletised.
The compositions (E2, CE4) were subjected to peroxidic degradation (visbreaking) with Altrix 3021. The MFR was increased up to about 30 g/10 min.

The amounts of each component and the results of the measurements are shown in Tables 1 and 2.

TABLE 1


component	component	component	component
A	B	C	D

	amount		amount		amount		amount	MFR
type	[pbw]	type	[pbw]	type	[pbw]	type	[pbw]	[g/10 min]	visbroken

CE1	A1	76.5	B1	10.0	C1	13.5	—	—	12.1	no	Influence of presence of
E1	A1	68.8	B1	9.0	C1	12.2	D2	10.0	12.7	no	component D and of
E2	A1	68.8	B1	9.0	C1	12.2	D2	10.0	33.8	yes	visbreaking
CE2	A1	75.5	—	—	C2	24.5	—	—	12.3	no	Influence of presence of
CE3	A1	68.0	—	—	C2	22.0	D2	10.0	12.0	no	component B and of
CE4	A1	68.0	—	—	C2	22.0	D2	10.0	30.7	yes	visbreaking
CE5	A2	77.2	B2	8.5	C3	14.3	—	—	26.6	no	Influence of presence of
E3	A2	65.7	B2	7.2	C3	12.1	D2	15.0	24.0	no	component D with different
CE6	A2	79.0	B5	21.0	—	—	—	—	35.3	no	components B and C
CE7	A2	67.1	B5	17.9	—	—	D2	15.0	34.5	no
CE8	A2	78.5	B3	7.9	C4	13.6	—	—	31.5	no
CE9	A2	66.7	B3	6.7	C4	11.6	D2	15.0	29.4	no
CE10	A2	75.6	B4	4.7	C4	4.7	D2	15.0	31.9	no	Influence of total amount of
CE11	A2	71.4	B4	6.8	C4	6.8	D2	15.0	29.1	no	components B and C
E4	A2	67.2	B4	8.9	C4	8.9	D2	15.0	26.7	no
CE11	A2	71.4	B4	6.8	C4	6.8	D2	15.0	29.1	no	Influence of amount of
CE12	A2	67.4	B4	6.3	C4	6.3	D2	20.0	28.9	no	component D
E5	A2	63.4	B4	5.8	C4	5.8	D2	25.0	30.4	no
E6	A2	59.9	B2	9.4	C3	15.7	D1	15.0	21.8	no	Influence of type of
E7	A2	59.9	B2	9.4	C3	15.7	D2	15.0	20.6	no	component D
E8	A2	59.9	B2	9.4	C3	15.7	D3	15.0	19.1	no
CE13	A2	59.9	B2	9.4	C3	15.7	D4	15.0	15.9	no
E3	A2	65.7	B2	7.2	C3	12.1	D2	15.0	24.0	no	Influence of ratio (B + C)/D
CE14	A2	73.3	B2	8.1	C3	13.6	D2	5.0	25.0	no

TABLE 2


MFR	Haze	Fmax	Wtot	E-Modulus
[g/10 min]	[%]	[N]	[J]	[MPa]

CE1	12.1	88.2	1856	6.8	1128	Influence of presence of
E1	12.7	59.4	2125	24.4	955	component D and of visbreaking
E2	33.8	75.7	2100	22.9	922
CE2	12.3	95.5	2591	15.9	1112	Influence of presence of
CE3	12.0	84.8	2710	27.6	983	component B and of visbreaking
CE4	30.7	95.6	2643	25.6	880
CE5	26.6	95.0	1820	7.1	1495	Influence of presence of
E3	24.0	71.6	2631	21.3	1238	component D with different
CE6	35.3	91.9	254	0.2	1390	components B and C
CE7	34.5	61.8	388	0.4	1120
CE8	31.5	98.6	2297	10.2	1502
CE9	29.4	84.3	2656	20.7	1250
CE10	31.9	52.7	276	0.2	1269	Influence of total amount of
CE11	29.1	61.4	524	0.6	1179	components B and C
E4	26.7	68.7	2695	20.6	1096
CE11	29.1	61.4	524	0.6	1179	Influence of amount of
CE12	28.9	60.5	541	0.7	1242	component D
E5	30.4	53.3	2710	19.1	1066
E6	21.8	74.3	2527	28.9	1029	Influence of type of
E7	20.6	76.3	2510	28.1	1027	component D
E8	19.1	78.7	2524	28.1	1033
CE13	15.9	93.1	2527	27.1	1018
E3	24.0	71.6	2631	21.3	1238	Influence of ratio (B + C)/D
CE14	25.0	91.0	1850	7.5	1435

Claims

1. A polypropylene composition for moulding having an MFR (230° C./2.16 kg)≧8 g/10 min comprising

A) 50-70 wt % of a propylene polymer comprising a propylene homopolymer and/or a propylene copolymer with up to 5 wt % ethylene and/or one or more C₄-C₈α-olefins and having an intrinsic viscosity IV_A1.00-2.20 dl/g,

B) 5-20 wt % of a first elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_B1.65-2.50 dl/g and an ethylene content of 20-40 wt %, with IV_B>IV_A,

C) 5-25 wt % of a second elastomeric ethylene-propylene copolymer having an intrinsic viscosity IV_Cof 0.90-1.60 dl/g and an ethylene content of 45-85 wt %,

D) 5-30 wt % of an ethylene polymer having an ethylene content of at least 80 mol % and having a melt index MI (190° C., 2.16 kg) of at least 5 g/10 min and a density of 905-925 kg/m³.

2. Polypropylene composition according to claim 1, wherein the first elastomeric ethylene-propylene copolymer has an intrinsic viscosity IV_Bof 1.80-2.25 dl/g.

3. Polypropylene composition according to claim 1 or 2, wherein the second elastomeric ethylene-propylene copolymer has an intrinsic viscosity IV_Cof 0.90-1.50 dl/g.

4. Polypropylene composition, according to claim 1 or 2, wherein IV_B−IV_C≧0.2 dl/g.

5. Polypropylene composition according to claim 1 or 2, it contains further comprising, based on the total weight of A to D, 0.01-2 wt % of α-nucleating agents.

6. Polypropylene composition according to claim 1 or 2, wherein the ratio (B+C)/D of the amounts of elastomeric copolymers (B+C) to the amount of ethylene polymer D is from 0.3:1 to 2.5:1.

7. Process for producing a polypropylene composition of claim 1 or 2, comprising mixing

melting and homogenising and

cooling and pelletising the mixture.

8. (canceled)

9. Polypropylene composition, according to claim 1 or 2, wherein IV_B−IV_C≧0.4 dl/g.

10. A method of producing a shaped article, comprising injection molding a composition of claim 1 or 2.

11. A method of producing packaging, comprising injection molding a composition of claim 1 or 2.

12. A method of producing this wall packaging, comprising injection molding a composition of claim 1 or 2.

13. A shape article produced by the method of claim 9.

14. A shape article produced by the method of claim 10.

15. A shape article produced by the method of claim 11.