Abstract: The present invention relates to a multi-stage process for producing a C2 to C8 olefin polymer composition in a process comprising at least two reactors, wherein a pre-polymerized solid Ziegler-Natta catalyst is prepared by carrying out an off-line pre-polymerization of a solid Ziegler-Natta catalyst component with a C2 to C4 olefin monomer before feeding to the polymerization process.

Abstract: A multimodal polyethylene composition having a lower molecular weight (LMW) ethylene homo or copolymer component (A) and a higher molecular weight ethylene copolymer component (B); wherein the LMW component comprises two fractions (ai) and (aii); wherein the polymer composition has a density of 930 kg/m3 or more (ISO1183), such as 938 to 955 kg/m3, an MFR2 (ISO1133 at 190° C. and 2.16 kg load) in the range of 0.05 to 10 g/10 min, a flex modulus of up to 800 MPa (ISO 178:2010), such as 300 to 800 MPa (ISO 178:2010) and a taber abrasion resistance of 8.0 to 13.0 mg/1000 cycle (ASTM D 4060: 2014).

Abstract: The present invention relates to a multimodal polymer of ethylene, to the use of the multimodal polymer of ethylene in film applications and to a film comprising the multimodal polymer of ethylene of the invention.

Abstract: The present invention relates to a multimodal ethylene copolymer composition having a density of 920 to 949 kg/m3 and a flexural modulus, wherein said flexural modulus is following the equation: Flexural modulus [MPa]<21.35·density [kg/m3]?19585 [1]. The multimodal ethylene copolymer composition according to the invention can be used in a highly flexible cable jacket, preferably a power cable jacket.

Abstract: The present invention is directed to a multimodal polyethylene copolymer comprising a first and a second copolymer of ethylene and at least two alpha-olefin comonomers. Such multimodal copolymers are highly suitable for conversion processes that require a high Draw Down Ratio, like the production of thin films. Such multimodal polyethylene copolymers provide a good impact strength in the sense of a high Dart drop impact strength (DDI) and good isotropy of the films produces thereof. The invention further presents final articles such as films made therefrom.

Abstract: A process for polymerizing olefin monomer(s) in a gas-solids olefin polymerization reactor comprising a top zone; a middle zone, which comprises a top end in direct contact with said top zone and which is located below said top zone, the middle zone having a generally cylindrical shape; and a bottom zone, which is in direct contact with a bottom end of the middle zone and which is located below the middle zone; comprising the following steps: introducing a fluidization gas stream into the bottom zone; polymerizing olefin monomer(s) in the presence of a polymerization catalyst in a dense phase formed by particles of a polymer of the olefin monomer(s) suspended in an upwards flowing stream of the fluidization gas in the middle zone; introducing a jet gas stream through one or more jet gas feeding ports in a jet gas feeding area of the middle zone at the dense phase in the middle zone of the gas-solids olefin polymerization reactor; wherein the kinetic energy (EJG) input in the reactor by the jet stream is betwe

Abstract: The present invention relates to a multi-stage process for producing a C2 to C8 olefin polymer composition in a process comprising at least two reactors, wherein a pre-polymerized solid Ziegler-Natta catalyst is prepared by carrying out an off-line pre-polymerization of a solid Ziegler-Natta catalyst component with a C2 to C4 olefin monomer before feeding to the polymerization process.

Abstract: The present invention relates to a multimodal ethylene copolymer composition having a density of 920 to 949 kg/m3 and a flexural modulus, wherein said flexural modulus is following the equation: Flexural modulus [MPa]<21.35·density [kg/m3]?19585 [1]. The multimodal ethylene copolymer composition according to the invention can be used in a highly flexible cable jacket, preferably a power cable jacket.

Abstract: The present invention relates to a multimodal ethylene copolymer composition having a density of 920 to 949 kg/m3 and a flexural modulus, wherein said flexural modulus is following the equation: Flexural modulus [MPa]<21.35·density [kg/m3]?19585 [1]. The multimodal ethylene copolymer composition according to the invention can be used in a highly flexible cable jacket, preferably a power cable jacket.

Abstract: The invention provides a process for the preparation of a multimodal high density polyethylene (HDPE) having a melt flow rate (MFR2) of 0.1 to 4.0 g/10 min, said process comprising: (i) polymerising ethylene in a first polymerisation stage in the presence of a Ziegler-Natta catalyst to prepare a first ethylene homopolymer having a MFR2 from 10 to 500 g/10 min; (ii) polymerising ethylene in a second polymerisation stage in the presence of said catalyst and said first ethylene homopolymer to prepare an ethylene homopolymer mixture comprising said first ethylene homopolymer and a second ethylene homopolymer, said mixture having a MFR2 from 50 to 1000 g/10 min; and (iii) polymerising ethylene and at least one alpha-olefin comonomer in a third polymerisation stage in the presence of said catalyst and said ethylene homopolymer mixture to prepare said multimodal HDPE.

Abstract: An adhesive polymer composition comprising a non-elastomeric copolymer of ethylene and one or more comonomers having 3 to 10 carbon atoms, and an elastomer is disclosed herein. The non-elastomeric copolymer is present in an amount of 60 to 95% by weight, based on the adhesive polymer composition, has a weight average molecular weight Mw of from 50 000 to 80 000 g/mol, molecular weight distribution Mw/Mn of 2.0 to 5.5, density of from 0.925 to 0.945 g/cm3, and at most 0.1 vinyl groups/1000 carbon atoms. The non-elastomeric copolymer or the non-elastomeric copolymer and the elastomer have been grafted with an acid grafting agent.

Abstract: A polyethylene composition comprising a base resin is disclosed herein. The base resin includes an ethylene homo- or copolymer fraction (A1), and an ethylene homo- or copolymer fraction (A2). Fraction (A1) has a lower weight average molecular weight than fraction (A2). The base resin has a melt flow rate MFR21 of equal to or less than 8.0 g/10 min and a density of 930 to 950 kg/m3. The polyethylene composition has a melt flow rate MFR5 of 0.01 to 0.3 g/10 min, a flow rate ratio FRR21/5 of equal to or more than 20 and a ratio of the weight average molecular weight and the number average molecular weight (Mw/Mn) of equal to or less than 30. Also the polyethylene composition has a tensile modulus of less than 1000 MPa. Also a process for the production of a polyethylene composition comprising polyethylene base resin is disclosed herein.

Abstract: The present invention relates to a process for producing ethylene copolymers in a multistage process comprising at least one slurry phase polymerization stage and at least one gas phase polymerization stage in the presence of Ziegler Natta catalyst comprising a solid catalyst component, a cocatalyst of a compound of group 13 metal and an external additive selected from alkoxysilanes of formula (I) R1nSi(OR2)4-n, (I) where n is an integer 0 to 3, each R1 are equal or different and are selected among H, halogen, alkyl groups of 1 to 6 carbon atoms optionally substituted with one or more halogen atoms, alkenyl groups of 2 to 6 carbon atoms optionally substituted with one or more halogen atoms, and aryl groups of 6 to 12 carbon atoms optionally substituted with one or more halogen atoms, or the R?groups can form with the Si atom they are linked to a ring of 3 to 8 ring atoms, provided that all R1 are not hydrogen, R2 are equal or different and are selected among alkyl groups of 1 to 6 carbon atoms optionally subs

Abstract: The present invention is directed to a multimodal polyethylene copolymer comprising a first and a second copolymer of ethylene and at least two alpha-olefin comonomers. The multimodal polyethylene copolymer is highly suitable for the production of films providing high impact strength in the sense of high Dart drop impact strength (DDI) and low extractables. The invention further presents final articles such as films made therefrom.

Abstract: A process for producing copolymers of ethylene and at least one alpha-olefin having from 4 to 10 carbon atoms in the presence of a solid Ziegler-Natta catalyst comprising of magnesium, titanium, halogen and an internal organic compound, the copolymer having a density of from 906 to 937 kg/m3 and a melt flow rate MFR21 measured at 190° C. under 21.6 kg load of from 3 to 150 g/10 min. The process includes the steps of (A) homopolymerising ethylene or copolymerising ethylene and a first alpha-olefin having from 4 to 10 carbon atoms in a first polymerisation stage in the presence of the polymerisation catalyst, hydrogen and optionally the first alpha-olefin; (B) copolymerising ethylene and a second alpha-olefin having from 4 to 10 carbon atoms in a second polymerisation stage in the presence of the first homo- or copolymer of ethylene and the Ziegler-Natta catalyst; and (C) recovering the polymer mixture.

Abstract: An adhesive polymer composition comprising a non-elastomeric copolymer of ethylene and one or more comonomers having 3 to 10 carbon atoms, and an elastomer is disclosed herein. The non-elastomeric copolymer is present in an amount of 60 to 95% by weight, based on the adhesive polymer composition, has a weight average molecular weight Mw of from 50 000 to 80 000 g/mol, molecular weight distribution Mw/Mn of 2.0 to 5.5, density of from 0.925 to 0.945 g/cm3, and at most 0.1 vinyl groups/1000 carbon atoms. The non-elastomeric copolymer or the non-elastomeric copolymer and the elastomer have been grafted with an acid rafting agent.

Abstract: A polyethylene composition comprising a base resin is disclosed herein. The base resin includes an ethylene homo- or copolymer fraction (A1), and an ethylene homo- or copolymer fraction (A2). Fraction (A1) has a lower weight average molecular weight than fraction (A2). The base resin has a melt flow rate MFR21 of equal to or less than 8.0 g/10 min and a density of 930 to 950 kg/m3. The polyethylene composition has a melt flow rate MFR5 of 0.01 to 0.3 g/10 min, a flow rate ratio FRR21/5 of equal to or more than 20 and a ratio of the weight average molecular weight and the number average molecular weight (Mw/Mn) of equal to or less than 30. Also the polyethylene composition has a tensile modulus of less than 1000 MPa. Also a process for the production of a polyethylene composition comprising polyethylene base resin is disclosed herein.

Abstract: The present invention relates to a process for producing ethylene copolymers in a multistage process comprising at least one slurry phase polymerization stage and at least one gas phase polymerization stage in the presence of Ziegler Natta catalyst comprising a solid catalyst component, a cocatalyst of a compound of group 13 metal and an external additive selected from alkoxysilanes of formula (1) R1nSi(OR2)4-n, (I) where n is an integer 0 to 3, each R1 are equal or different and are selected among H, halogen, alkyl groups of 1 to 6 10 carbon atoms optionally substituted with one or more halogen atoms, alkenyl groups of 2 to 6 carbon atoms optionally substituted with one or more halogen atoms, and aryl groups of 6 to 12 carbon atoms optionally substituted with one or more halogen atoms, or the R1 groups can form with the Si atom they are linked to a ring of 3 to 8 ring atoms, provided that all R1 are not hydrogen, R2 are equal or different and are selected among alkyl groups of 1 to 6 carbon atoms optionally

Abstract: The present invention relates to a process for producing ethylene copolymers in a multistage process comprising at least one slurry phase polymerization stage and at least one gas phase polymerization stage in the presence of Ziegler Natta catalyst comprising a solid catalyst component, a cocatalyst of a compound of group 13 metal and an external additive selected from alkoxysilanes of formula (I) R1nSi(OR2)4-n, (I) where n is an integer 0 to 3, each R1 are equal or different and are selected among H, halogen, alkyl groups of 1 to 6 10 carbon atoms optionally substituted with one or more halogen atoms, alkenyl groups of 2 to 6 carbon atoms optionally substituted with one or more halogen atoms, and aryl groups of 6 to 12 carbon atoms optionally substituted with one or more halogen atoms, or the R1 groups can form with the Si atom they are linked to a ring of 3 to 8 ring atoms, provided that all R1 are not hydrogen, R2 are equal or different and are selected among alkyl groups of 1 to 6 carbon atoms optionally

Abstract: The present invention deals with a process for polymerizing ethylene in the presence of an olefin polymerization catalyst comprising titanium, magnesium and halogen in at least one polymerization stage where ethylene is polymerized in slurry, the process comprising treating the polymerization catalyst in a pre-treatment step by polymerizing an olefin on the polymerization catalyst so that the ratio of the weight of the olefin polymer to the weight of the original solid catalyst component is from 0.1 to 10 g/g and using the pre-treated catalyst in the production of ultra-high molecular weight polyethylene.