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WO2020136164A1 - Procédé de production d'une composition de film de polyoléfine et films ainsi préparés - Google Patents

Procédé de production d'une composition de film de polyoléfine et films ainsi préparés Download PDF

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Publication number
WO2020136164A1
WO2020136164A1 PCT/EP2019/086916 EP2019086916W WO2020136164A1 WO 2020136164 A1 WO2020136164 A1 WO 2020136164A1 EP 2019086916 W EP2019086916 W EP 2019086916W WO 2020136164 A1 WO2020136164 A1 WO 2020136164A1
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WO
WIPO (PCT)
Prior art keywords
ethylene
copolymer
polymer mixture
polymerisation
ethylene polymer
Prior art date
Application number
PCT/EP2019/086916
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English (en)
Inventor
Tuan Anh TRAN
Anna Hartl
Jarmo Kela
Original Assignee
Borealis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Borealis Ag filed Critical Borealis Ag
Priority to EP19828782.3A priority Critical patent/EP3902850A1/fr
Publication of WO2020136164A1 publication Critical patent/WO2020136164A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/08—Copolymers of ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04—Homopolymers or copolymers of ethene
    • C08J2323/08—Copolymers of ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/16—Applications used for films
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend

Definitions

  • the present invention is directed to a method for producing multimodal ethylene polymer film compositions and films prepared thereof. Especially, the present invention is directed to a method for making multimodal ethylene copolymer film composition by a process comprising polymerizing ethylene in at least three polymerization stages. Further, the present invention is directed to films comprising the multimodal ethylene copolymer composition produced by the method comprising at least three polymerization stages. Further, the invention is directed to the use of such multimodal ethylene copolymer compositions for making films with improved processability and throughput.
  • WO-A-2004000902 discloses bimodal low density PE resins. The document does not disclose multimodal ethylene polymer composition produced in three polymerisation stage.
  • EP-A-2067799 discloses multimodal LLDPE resins which have been produced in two polymerization stages in a loop and a gas phase reactor in the presence of a ligand-modified catalyst. The document does not disclose a third polymerization stage.
  • EP-A-2246369 discloses LLDPE produced in the presence of a Ziegler-Natta catalyst with specific halogenated aluminium alkyl compounds as a cocatalyst. While the document briefly refers to two-stage polymerization its examples are one-stage polymerization runs. The document does not disclose any three-stage polymerization.
  • EP-A-2246372 discloses LLDPE produced in the presence of a Ziegler-Natta catalyst with a halogenated aluminium alkyl compounds as a cocatalyst.
  • the document discloses ethylene copolymerisation in two-stage polymerization configuration. It’s only generally mentioned that optionally additional reactors may be used. It does not, however, disclose the nature of the polymers produced in such stages and it exemplifies only two-stage polymerization.
  • EP-A-2228394 discloses LLDPE polymers produced in two polymerization stages using amulticomponent catalyst comprising titanium and vanadium compounds.
  • the document discloses that it is possible to include further polymerization stages, such as a third and a fourth polymerization stage which are preferably conducted in gas phase. It does not, however, disclose the nature of the polymers produced in such stages and it exemplifies only two-stage polymerization.
  • EP-A-2186833 discloses a three-stage polymerization in a cascaded reactor sequence of two loop reactors followed by a gas phase reactor.
  • a polymer having an M FR 2 of preferably 200 to 1000 g/10 min and a density of preferably 945 to 978 kg/m 3 is produced in the first stage.
  • the polymer produced in the second stage is disclosed to have an MFR 2 of preferably 200 to 1000 g/10 min and a density of preferably 945 to 978 kg/m 3 .
  • the final polymer had an MFR 21 of preferably 5 to 30 g/10 min and a density of preferably 940 to 970 kg/m 3 .
  • the polymers produced in the first and second stages had the same MFR 2 .
  • the polymers produced in the first two stages were homopolymers and the final resins had MFR 5 of from 0.2 to 0.4 g/10 min and density of about 955 kg/m 3 .
  • EP2415598 discloses a multilayer film comprising at least one layer of a multimodal terpolymer, e.g. a bimodal linear low density ethylene/1 -butene/C6-Ci2-alpha-olefin terpolymer.
  • the multimodal polymer comprises a low molecular weight component corresponding ethylene homopolymer or a low molecular weight ethylene copolymer and a high molecular weight component corresponding to ethylene terpolymer with higher alpha-olefin comonomers.
  • the low molecular weight component is an ethylene homoplymer and the high molecular weight component is ethylene/1 -butene/1 -hexene terpolymer.
  • the multimodal terpolymer is produced in a two stage polymerisation process. Final densities are disclosed to be in the range of 910 - 950 kg/m 3 or 935 - 970 kg/m 3 or 900 - 935 kg/m 3 ; and MFR21 (190 °C, 21 ,6 kg load, IS01133) 7 to 60 g/10min or 2 to 35 g/10min or 15 to 80 g/10min, respectively.
  • WO 2015/086812 (EP2883887) describes a process for making multimodal ethylene copolymers where the method comprises polymerising ethylene and comonomers in three polymerisation stages, and further use of said copolymers for making films.
  • the ethylene copolymer produced according to the process has the density of 906 to 925 kg/m 3 and MFR 5 (190 °C, 5,0 kg load, IS01133) of 0,5 to 5,0 g/10 min.
  • the copolymer produced in the first polymerisation stage and the first copolymer mixture being a mixture of the first polymer and polymer produced in the second stage have claimed densities in the range of 945 to 955 kg/m 3 and melt flow rates MFR 2 in the range of 150 to 1000 kg/m 3 .
  • EP2883885 describes similar type of polymers as described in WO 2015/086812.
  • bimodal ethylene polymers have desired properties for different application needs. Suitable densities and melt flow rates are normal decisive features of polyethylene film materials.
  • Such bimodal terpolymers are known in the state of the art and are described e.g. in WO 03/066698 or WO 2008/034630 or are commercially available, such as BorShapeTM FX1001 and BorShapeTM FX1002 (both from Borealis AG, Vienna, Austria).
  • the present invention therefore provides especially for example good mechanical properties, such as for example DDI and/or tear, of polymer film composition and/or good processability and/or high throughput in a film making process.
  • the present invention concerns a process for producing multimodal ethylene polymer film compositions comprising the steps of
  • PE1 ethylene homo- or copolymer having a melt flow rate MFR2 of from 15 to 300 g/10 min and optionally a density of from 940 to 980 kg/m 3 ;
  • first ethylene polymer mixture comprising the first ethylene homo- or copolymer and a second ethylene copolymer, said first ethylene polymer mixture having a density of from 940 to 980 kg/m 3 and a melt flow rate MFR2 of from 100 to 600 g/10 min, and wherein the MFR2 0f the first ethylene homo- or copolymer (PE1) is lower than first ethylene polymer mixture (PEM1) and the second ethylene homo- or copolymer (PE2) has a melt flow rate MFR2 of from 400 to 2000 g/10min and optionally a density of from 940 to 980 kg/m 3 ; and
  • the present process for producing polyethylene film composition comprises polymerisation of ethylene and at least one a-olefin in multiple polymerisation steps in the presence of a polymerisation catalyst.
  • multiple polymerisation steps mean a process comprising at least three polymerisation steps.
  • the at least one a-olefin one alpha-olefin comonomer may be selected from a-olefins having from 4 to 10 carbon atoms and their mixtures. Especially suitable a-olefins are those having from 4 to 8 carbon atoms, including their mixtures. In particular 1-butene, 1-hexene and 1- octene and their mixtures are the preferred a-olefins.
  • the a-olefin used in the different polymerisation steps may be the same or different.
  • the polymerisation steps may be connected in any order, i.e. the first polymerisation step may precede the second polymerisation step, or the second polymerisation step may precede the first polymerisation step or, alternatively, polymerisation steps may be connected in parallel. However, it is preferred to operate the polymerisation steps in cascaded mode.
  • the polymerisation is conducted in the presence of an olefin polymerisation catalyst.
  • the catalyst may be any catalyst which is capable of producing all components of the multimodal ethylene copolymer. Suitable catalysts are, among others, Ziegler - Natta catalysts based on a transition metal, such as titanium, zirconium and/or vanadium or metallocene catalysts or late transition metal catalysts, as well as their mixtures. Especially Ziegler - Natta catalysts are useful as they can produce polymers within a wide range of molecular weight and other desired properties with a high productivity. Ziegler - Natta catalysts used in the present invention are supported on an external support.
  • Suitable Ziegler - Natta catalysts preferably contain a magnesium compound, an aluminium compound and a titanium compound supported on a particulate support.
  • the particulate support typically used in Ziegler-Natta catalysts comprises an inorganic oxide support, such as silica, alumina, titania, silica-alumina and silica-titania or a MgCh based support.
  • the catalyst used in the present invention is supported on an inorganic oxide support. Most preferably the Ziegler-Natta catalyst used in the present invention is supported on silica.
  • the average particle size of the silica support can be typically from 10 to 100 mhi. However, it has turned out that special advantages can be obtained if the support has an average particle size from 15 to 30 mhi, preferably from 18 to 25 mhi. Alternatively, the support may have an average particle size of from 30 a 80 mhi, preferably from 30 to 50 mhi. Examples of suitable support materials are, for instance, ES747JR produced and marketed by Ineos Silicas (former Crossfield), and SP9-491 , produced and marketed by Grace.
  • the magnesium compound is a reaction product of a magnesium dialkyl and an alcohol.
  • the alcohol is a linear or branched aliphatic monoalcohol. Preferably, the alcohol has from 6 to 16 carbon atoms. Branched alcohols are especially preferred, and 2-ethyl-1-hexanol is one example of the preferred alcohols.
  • the magnesium dialkyl may be any compound of magnesium bonding to two alkyl groups, which may be the same or different. Butyl-octyl magnesium is one example of the preferred magnesium dialkyls.
  • aluminium compound is chlorine containing aluminium alkyl.
  • Especially preferred compounds are aluminium alkyl dichlorides, aluminium dialkyl chlorides and aluminium alkyl sesquichlorides.
  • the transition metal is preferably titanium.
  • the titanium compound is a halogen containing titanium compound, preferably chlorine containing titanium compound.
  • Especially preferred titanium compound is titanium tetrachloride.
  • the catalyst can be prepared by sequentially contacting the carrier with the above mentioned compounds, as described in EP-A-688794 or WO-A-99/51646. Alternatively, it can be prepared by first preparing a solution from the components and then contacting the solution with a carrier, as described in WO-A-01/55230.
  • the Ziegler - Natta catalyst is used together with an activator, which is also called as cocatalyst.
  • Suitable activators are metal alkyl compounds, typically Group 13 metal alkyl compounds, and especially aluminium alkyl compounds. They include trialkylaluminium compounds, such as trimethylaluminium, triethylaluminium, tri-isobutylaluminium,
  • Aluminium alkyl compounds may also include alkyl aluminium halides, such as ethylaluminium dichloride, diethylaluminium chloride,
  • ethylaluminium sesquichloride dimethylaluminium chloride and the like and alkylaluminium oxy- compounds, such as methylaluminiumoxane, hexaisobutylaluminiumoxane and
  • isoprenylaluminium isoprenylaluminium.
  • cocatalysts are trialkylaluminiums, of which
  • triethylaluminium, trimethylaluminium and tri-isobutylaluminium are particularly preferred.
  • the amount in which the activator is used depends on the specific catalyst and activator.
  • triethylaluminium is used in such amount that the molar ratio of aluminium to the transition metal, like Al/Ti, is for example from 1 to 1000, preferably from 3 to 100 and in particular from about 5 to about 30 mol/mol.
  • the process may comprise a prepolymerisation step preceding the actual polymerisation steps.
  • the purpose of the prepolymerisation is to polymerise a small amount of polymer onto the catalyst at a low temperature and/or a low monomer concentration. By prepolymerisation it is possible to improve the performance of the catalyst in slurry and/or modify the properties of the final polymer.
  • the prepolymerisation step is conducted in slurry.
  • the prepolymerisation step may be conducted in a loop reactor.
  • the prepolymerisation is then preferably conducted in an inert diluent, typically a hydrocarbon diluent such as methane, ethane, propane, n-butane, isobutane, pentanes, hexanes, heptanes, octanes etc., or their mixtures.
  • diluent is a low-boiling hydrocarbon having from 1 to 4 carbon atoms or a mixture of such hydrocarbons.
  • the temperature in the prepolymerisation step is typically from 0 to 90 °C, preferably from 20 to 80 °C and more preferably from 55 to 75 °C.
  • the pressure is not critical and is typically from 1 to 150 bar, preferably from 40 to 80 bar.
  • the amount of monomer is typically such that from about 0.1 to 1000 grams of monomer per one gram of solid catalyst component is polymerised in the prepolymerisation step.
  • prepolymerisation reactor do not all contain the same amount of prepolymer. Instead, each particle has its own characteristic amount which depends on the residence time of that particle in the prepolymerisation reactor. As some particles remain in the reactor for a relatively long time and some for a relatively short time, then also the amount of prepolymer on different particles is different and some individual particles may contain an amount of prepolymer which is outside the above limits. However, the average amount of prepolymer on the catalyst typically is within the limits specified above.
  • the molecular weight of the prepolymer may be controlled by hydrogen as it is known in the art. Further, antistatic additive may be used to prevent the particles from adhering to each other or the walls of the reactor, as disclosed in WO-A-96/19503 and WO-A-96/32420.
  • the catalyst components are preferably all (separately or together) introduced to the
  • the amounts of hydrogen and comonomer are adjusted so that the presence of the prepolymer has no effect on the properties of the final multimodal polymer.
  • melt flow rate of the prepolymer is greater than the melt flow rate of the final polymer but smaller than the melt flow rate of the polymer produced in the first polymerisation stage.
  • density of the prepolymer is greater than the density of the final polymer.
  • the density is approximately the same as or greater than the density of the polymer produced in the first polymerisation stage.
  • the amount of the prepolymer is not more than about 5 % by weight of the multimodal polymer comprising the prepolymer.
  • the first polymerisation step typically operates at a temperature of from 20 to 150 °C, preferably from 50 to 110 °C and more preferably from 60 to 100 °C.
  • the polymerisation may be conducted in slurry, gas phase or solution.
  • the first homo- or copolymer of ethylene is produced.
  • the first ethylene homo-or copolymer has a melt flow rate MFR2 of from 15 to 300 g/10 min and optionally a density of from 940 to 980 kg/m 3 .
  • the catalyst may be transferred into the first polymerisation step by any means known in the art. It is thus possible to suspend the catalyst in a diluent and maintain it as homogeneous slurry. Especially preferred it is to use oil having a viscosity form 20 to 1500 mPa-s as diluent, as disclosed in WO-A-2006/063771. It is also possible to mix the catalyst with a viscous mixture of grease and oil and feed the resultant paste into the first polymerisation step. Further still, it is possible to let the catalyst settle and introduce portions of thus obtained catalyst mud into the first polymerisation step in a manner disclosed, for instance, in EP-A-428054.
  • the first polymerisation step may also be preceded by a prepolymerisation step, in which case the mixture withdrawn from the prepolymerisation step is directed into the first polymerisation step.
  • the a-olefin Into the first polymerisation step ethylene, the a-olefin, optionally an inert diluent, and optionally hydrogen are introduced. Hydrogen and the a-olefin are introduced in such amounts that the melt flow rate MFR2 and the density of the first ethylene homo-or copolymer are in the desired values.
  • a-olefin or the alpha-olefin comonomer (these terms may be used interchangeably herein) is as defined above having from 4 to 10 carbon atoms and their mixtures, and especially suitable a-olefins are those having from 4 to 8 carbon atoms, including their mixtures. In particular 1 -butene, 1 -hexene and 1-octene and their mixtures are the preferred a-olefins.
  • the polymerisation of the first polymerisation step may be conducted in slurry. Then the polymer particles formed in the polymerisation, together with the catalyst fragmented and dispersed within the particles, are suspended in the fluid hydrocarbon. The slurry is agitated to enable the transfer of reactants from the fluid into the particles.
  • the polymerisation usually takes place in an inert diluent, typically a hydrocarbon diluent such as methane, ethane, propane, n-butane, isobutane, pentanes, hexanes, heptanes, octanes etc., or their mixtures.
  • a hydrocarbon diluent such as methane, ethane, propane, n-butane, isobutane, pentanes, hexanes, heptanes, octanes etc., or their mixtures.
  • the diluent is a low-boiling hydrocarbon having from 1 to 4 carbon atoms or a mixture of such hydrocarbons.
  • An especially preferred diluent is propane, possibly containing minor amount of methane, ethane and/or butane.
  • the ethylene content in the fluid phase of the slurry may be from 1 to about 50 % by mole, preferably from about 1.5 to about 20 % by mole and in particular from about 2 to about 15 % by mole.
  • the benefit of having a high ethylene concentration is that the productivity of the catalyst is increased but the drawback is that more ethylene then needs to be recycled than if the concentration was lower.
  • the slurry polymerisation may be conducted in any known reactor used for slurry
  • Such reactors include a continuous stirred tank reactor and a loop reactor. It is especially preferred to conduct the polymerisation in loop reactor. In such reactors the slurry is circulated with a high velocity along a closed pipe by using a circulation pump. Loop reactors are generally known in the art and examples are given, for instance, in US-A-4582816, US-A- 3405109, US-A-3324093, EP-A-479186 and US-A-5391654.
  • the first ethylene homo-or copolymer is produced in conditions where the ratio of the a-olefin to ethylene is not more than about 400 mol/kmol, such as not more than 300 mol/kmol, then it is usually advantageous to conduct the slurry polymerisation above the critical temperature and pressure of the fluid mixture. Such operation is described in US-A-5391654.
  • the polymerisation in the first polymerisation step is conducted as slurry polymerisation the polymerisation in the first polymerisation step is conducted at a temperature within the range of from 50 to 115 °C, preferably from 70 to 110 °C and in particular from 80 to 105 °C.
  • the pressure in the first polymerisation step is then from 1 to 300 bar, preferably from 40 to 100 bar.
  • the amount of hydrogen is adjusted based on the desired melt flow rate of the first ethylene homo-or copolymer and it depends on the specific catalyst used.
  • the molar ratio of hydrogen to ethylene is for example from 10 to 2000 mol/kmol, preferably from 20 to 1000 mol/kmol and in particular from 40 to 800 mol/kmol.
  • the amount of the a-olefin is adjusted based on the desired density of the first ethylene homo- or copolymer and it, too, depends on the specific catalyst used.
  • the molar ratio of the a-olefin to ethylene is for example from 100 to 1000 mol/kmol, preferably from 150 to 600 mol/kmol.
  • the polymerisation of the first polymerisation step may also be conducted in gas phase.
  • a preferable embodiment of gas phase polymerisation reactor is a fluidised bed reactor. There the polymer particles formed in the polymerisation are suspended in upwards moving gas. The gas is introduced into the bottom part of the reactor. The upwards moving gas passes the fluidised bed wherein a part of the gas reacts in the presence of the catalyst and the unreacted gas is withdrawn from the top of the reactor. The gas is then compressed and cooled to remove the heat of polymerisation. To increase the cooling capacity it is sometimes desired to cool the recycle gas to a temperature where a part of the gas condenses. After cooling the recycle gas is reintroduced into the bottom of the reactor.
  • Fluidised bed polymerisation reactors are disclosed, among others, in US-A-4994534, US-A-4588790, EP-A-699213, EP-A-628343, FI-A-921632, FI-A-935856, US-A-4877587, FI-A-933073 and EP-A-75049.
  • the polymerisation of the first polymerisation step is conducted in slurry.
  • the polymerisation is conducted at a temperature exceeding the critical temperature of the fluid mixture and pressure exceeding the critical pressure of the fluid mixture.
  • At least one a-olefin may be present in the first polymerisation step, where the polymer produced in the first step is the first ethylene homo- or copolymer.
  • the density of the first ethylene homo-or copolymer is for example from 940 to 980 kg/m 3 .
  • the polymerisation is preferably conducted as a slurry polymerisation in liquid diluent at a
  • the molar ratio of the a-olefin to ethylene may be for example from 100 to 1000 mol/kmol, and preferably from 150 to 600 mol/kmol.
  • the polymerisation rate in the first polymerisation step is suitably controlled to achieve the desired amount of the first ethylene homo-or copolymer in the second ethylene polymer mixture.
  • the second ethylene polymer mixture contains from 10 to 35 % by weight, preferably 13 to 26 % by weight, further preferred > 15 to ⁇ 25 % by weight of the first ethylene homo- or copolymer.
  • the polymerisation rate is suitably controlled by adjusting the ethylene
  • the concentration in the first polymerisation step is suitably for example from 0.5 to 10 % by mole and preferably from 1 to 8 % by mole.
  • the molar ratio of hydrogen to ethylene is suitably from 50 to 350 mol/kmol, preferably from 75 to 325 mol/kmol and in particular from 100 to 300 mol/kmol in the first polymerisation step.
  • the second homo- or copolymer of ethylene is produced in the second polymerisation step in the presence of the first homo- or copolymer of ethylene.
  • the second polymerisation step typically operates at a temperature of from 20 to 150 °C, preferably from 50 to 110 °C and more preferably from 60 to 100 °C.
  • the polymerisation may be conducted in slurry, gas phase or solution.
  • the second homo- or copolymer of ethylene is produced in the presence of the first homo- or copolymer of ethylene.
  • the first homo- or copolymer of ethylene (PE1) and the second homo- or copolymer of ethylene (PE2) together form the first ethylene polymer mixture (PEM1).
  • the first ethylene polymer mixture has a density of from 940 to 980 kg/m 3 and a melt flow rate MFR2 of from 100 to 600 g/10 min.
  • the first homo- or copolymer of ethylene (PE1) is transferred from the first polymerisation step to the second polymerisation step by using any method known to the person skilled in the art. If the first polymerisation step is conducted as slurry polymerisation in a loop reactor, it is advantageous to transfer the slurry from the first polymerisation step to the second
  • ethylene optionally an inert diluent, and optionally hydrogen and/or the a-olefin are introduced. Hydrogen and the a-olefin, are introduced in such amounts that the melt flow rate MFR2 and the density of the first ethylene polymer mixture are within the desired values.
  • the polymerisation of the second polymerisation step may be conducted in slurry in the same way as it was discussed above for the first polymerisation step.
  • the amount of hydrogen in the second polymerisation step is adjusted based on the desired melt flow rate of the first ethylene polymer mixture and it depends on the specific catalyst used.
  • the molar ratio of hydrogen to ethylene is for example from 100 to 2000 mol/kmol, preferably from 200 to 1000 mol/kmol and in particular from 250 to 800 mol/kmol.
  • the amount of the a-olefin is adjusted based on the desired density of the first ethylene polymer mixture and it, too, depends on the specific catalyst used.
  • the molar ratio of the a-olefin to ethylene is for example from 0 to 1000 mol/kmol, preferably from 0 to 800 mol/kmol and in particular from 0 to 700 mol/kmol.
  • the polymerisation of the second polymerisation step may also be conducted in gas phase in the same way as was discussed above for the first polymerisation step.
  • the second polymerisation step is conducted in slurry phase as described above.
  • the molar ratio of hydrogen to ethylene is suitably from 350 to 600 mol/kmol, preferably from 375 to 550 mol/kmol and in particular from 400 to 500 mol/kmol in the second polymerisation step.
  • the polymerisation is conducted at a temperature exceeding the critical temperature of the fluid mixture and pressure exceeding the critical pressure of the fluid mixture.
  • the a-olefin is present in the first polymerisation step and in the second polymerisation step.
  • the density of the first ethylene homo-or copolymer is controlled by the molar ratio of the a-olefin to ethylene in the first polymerisation step and the density of the first ethylene polymer mixture is controlled by the molar ratio of the a-olefin to ethylene in the second polymerisation step.
  • the molar ratio of the a-olefin to ethylene may then be for example from 50 to 1000 mol/kmol, and preferably from 100 to 600 mol/kmol in the second polymerisation step.
  • the a-olefin used in the second polymerisation step may be the same or different as used in the first polymerisation step.
  • the polymerisation rate in the second polymerisation step is suitably controlled to achieve the desired amount of the second ethylene homo- or copolymer in the second ethylene polymer mixture.
  • the second ethylene polymer mixture contains from 10 to 35 % by weight, preferably 13 to 26 % by weight, further preferred > 15 to ⁇ 25 % by weight of the second ethylene copolymer.
  • the polymerisation rate is suitably controlled by adjusting the ethylene concentration in the second polymerisation step.
  • the mole fraction of ethylene in the reaction mixture is suitably from 2 to 10 % by mole and preferably from 3 to 8 % by mole.
  • the mole fraction of ethylene in % by mole in the reaction mixture in the second polymerisation step may thereby be lower than the mole fraction of ethylene in % by mole in the reaction mixture in the first polymerisation step.
  • the melt flow rate MFR2 0f the first ethylene homo-or copolymer (PE1) is in the range 15 to 300 g/10 min and the melt flow rate MFR2 of the first ethylene homo-or copolymer mixture (PEM1) is in the range 100 to 600 g/10 min and MFR 2 (PE1) ⁇
  • MFR 2 (PEM1). I.e. the MFR2 0f the polymer produced in the first reactor is lower than the polymer mixture produced in the second polymerisation reactor.
  • the ratio of MFR 2 (PEM1)/MFR 2 (PE1) may be for example between 1 and 60, preferably between > 1 and 5 or 2 and 30, further preferred between 1.5 and 4 or 15 and 25.
  • the second ethylene polymer mixture (PEM2) comprising the first ethylene polymer mixture (PEM1) and the third ethylene copolymer (PE3) is formed.
  • ethylene Into the third polymerisation step are introduced ethylene, at least one a-olefin having 4 to 10 carbon atoms, hydrogen and optionally an inert diluent.
  • polymerisation step is conducted at a temperature within the range of from 50 to 100 °C, preferably from 60 to 100 °C and in particular from 70 to 95 °C.
  • the pressure in the third polymerisation step is for example from 1 to 300 bar, preferably from 5 to 100 bar.
  • the polymerisation in the third polymerisation step may be conducted in slurry.
  • polymerisation may then be conducted along the lines as was discussed above for the first and second polymerisation steps.
  • the amount of hydrogen in the third polymerisation step is adjusted for achieving the desired melt flow rate of the second ethylene polymer mixture.
  • the molar ratio of hydrogen to ethylene depends on the specific catalyst used. For many generally used Ziegler - Natta catalysts the molar ratio of hydrogen to ethylene is for example from 0 to 50 mol/kmol, preferably from 3 to 35 mol/kmol.
  • the ratio of the a-olefin (sum of a-olefins) to ethylene depends on the type of the catalyst and the type of the a-olefin. The ratio is typically for example from 100 to 1000 mol/kmol, preferably from 150 to 800 mol/kmol. If more than one a-olefin is used the ratio of the a-olefin to ethylene is the ratio of the sum of all the a-olefins to ethylene.
  • the a-olefin used in the third polymerisation step may be the same or different as used in the previous polymerisation steps.
  • the a-olefin is preferably an a-olefin of 4 to 8 carbon atoms or mixtures thereof.
  • 1-butene, 1-hexene and 1-octene and their mixtures are the preferred a-olefins, especially preferred 1 -butene and 1 -hexene.
  • the polymerisation in the third polymerisation step may be, and preferably is, conducted in gas phase.
  • hydrogen is typically added in such amount that the ratio of hydrogen to ethylene is for example from 3 to 100 mol/kmol, preferably from 4 to 50 mol/kmol for obtaining the desired melt index of the second ethylene polymer mixture.
  • the amount of a-olefin having from 4 to 10 carbon atoms is adjusted to reach the targeted density of the second ethylene polymer mixture.
  • the ratio of the a-olefin to ethylene is typically from 100 to 1000 mol/kmol, preferably from 150 to 800 mol/kmol, further preferred ⁇ 150 to 300 mol/kmol. If more than one a-olefin is used the ratio of the a-olefin to ethylene is the ratio of the sum of all the a-olefins to ethylene.
  • the gas phase reactor preferably is a vertical fluidised bed reactor. There the polymer particles formed in the polymerisation are suspended in upwards moving gas. The gas is introduced into the bottom part of the reactor. The upwards moving gas passes the fluidised bed wherein a part of the gas reacts in the presence of the catalyst and the unreacted gas is withdrawn from the top of the reactor. The gas is then compressed and cooled to remove the heat of
  • Fluidised bed polymerisation reactors are disclosed, among others, in US-A-4994534, US-A-4588790, EP-A-699213, EP-A-628343, FI-A-921632, FI-A-935856, US-A-4877587, FI-A-933073 and EP-A-75049.
  • the polymer is suitably transferred from the second polymerisation step into the third polymerisation step as described in EP-A-1415999.
  • the procedure described in paragraphs [0037] to [0048] of EP-A-1415999 provides an economical and effective method for product transfer.
  • the conditions in the third polymerisation step are adjusted so that the resulting second ethylene polymer mixture (PEM2) has MFRs of from 0.1 to 5 g/10 min, preferably > 0.1 to 2 g/10 min, preferably 0.2 to 1 g/10min, further preferred 0.3 to ⁇ 0.8 g/10 min.
  • the second ethylene polymer mixture has a density in the range of 920 to 940 kg/m 3 , 925 to 936 kg/m 3 , preferably 926 to 935 kg/m 3 .
  • the polymerisation rate in the third polymerisation step is suitably controlled to achieve the desired amount of the third ethylene copolymer in the second ethylene polymer mixture.
  • the second ethylene polymer mixture contains from 45 to 65 % by weight, preferably 50 to 62 % by weight, further preferred > 50 to 60 % by weight by weight of the third ethylene copolymer.
  • the polymerisation rate is suitably controlled by adjusting the ethylene
  • the mole fraction of ethylene in the reactor gas is suitably from 3 to 50 % by mole and preferably from 5 to 15 % by mole.
  • the gas also comprises an inert gas.
  • the inert gas can be any gas which is inert in the reaction conditions, such as a saturated hydrocarbon having from 1 to 5 carbon atoms, nitrogen or a mixture of the above-mentioned compounds. Suitable hydrocarbons having from 1 to 5 carbon atoms are methane, ethane, propane, n-butane, isobutane, n-pentane, isopentane and mixtures thereof.
  • process steps for removing residual hydrocarbons from the polymer are well known in the art and can include pressure reduction steps, purging steps, stripping steps, extraction steps and so on. Also combinations of different steps are possible.
  • a part of the hydrocarbons is removed from the polymer powder by reducing the pressure.
  • the powder is then contacted with steam at a temperature of from 90 to 110 °C for a period of from 10 minutes to 3 hours. Thereafter the powder is purged with inert gas, such as nitrogen, over a period of from 1 to 60 minutes at a temperature of from 20 to 80 °C.
  • the polymer powder is subjected to a pressure reduction as described above. Thereafter it is purged with an inert gas, such as nitrogen, over a period of from 20 minutes to 5 hours at a temperature of from 50 to 90 °C.
  • the inert gas may contain from 0.0001 to 5 %, preferably from 0.001 to 1 %, by weight of components for deactivating the catalyst contained in the polymer, such as steam.
  • the purging steps are preferably conducted continuously in a settled moving bed.
  • the polymer moves downwards as a plug flow and the purge gas, which is introduced to the bottom of the bed, flows upwards.
  • Suitable processes for removing hydrocarbons from polymer are disclosed in WO-A-02/088194, EP-A-683176, EP-A-372239, EP-A-47077 and GB-A-1272778.
  • the polymer is preferably mixed with additives as it is well known in the art.
  • additives include antioxidants, process stabilisers, neutralisers, lubricating agents, nucleating agents, pigments and so on.
  • the polymer particles are mixed with additives and extruded to pellets as it is known in the art.
  • a counter-rotating twin screw extruder is used for the extrusion step.
  • Such extruders are manufactured, for instance, by Kobe and Japan Steel Works.
  • a suitable example of such extruders is disclosed in EP-A-1600276.
  • SEI specific energy input
  • the melt temperature is typically from 220 to 290 °C.
  • the a-olefin comonomer may be selected from the group consisting of a-olefins having from 4 to 10 carbon atoms and their mixtures, preferably from the group consisting of a-olefins having from 4 to 8 carbon atoms and their mixtures, further preferred from the group consisting of 1 -butene, 1 -hexene and 1-octene, further preferred wherein only ethylene is polymerized in the first and second polymerization steps and two comonomers are used in the third polymerization step, whereby the a-olefin comonomers in the third polymerization step are 1 -butene and 1 -hexene.
  • the third polymerisation step is conducted in gas phase, preferably in a gas phase fluidized bed reactor, further preferred connected in series.
  • At least one of the first and the second polymerisation step(s) is/are conducted as a slurry polymerisation in a loop reactor, preferably both the first and the second polymerisation steps are conducted as a slurry polymerisation in two loop reactors, preferably connected in series.
  • the diluent in the slurry in an embodiment of the process according to the invention, the diluent in the slurry
  • polymerisation may comprises at least 90 % of hydrocarbons having from 3 to 5 carbon atoms.
  • the second ethylene polymer mixture may comprise from 10 to 35 % by weight, preferably 13 to 26 % by weight, further preferred > 15 to ⁇ 25 % by weight of the first ethylene homo- or copolymer, from 10 to 35 % by weight, preferably 13 to 26 % by weight, further preferred > 15 to ⁇ 25 % by weight of the second ethylene homo- or copolymer and from 45 to 65 % by weight, preferably 50 to 62 % by weight, further preferred > 50 to 60 % by weight of the third ethylene copolymer.
  • the second ethylene polymer mixture may have a density of from 925 to 936 kg/m 3 , preferably 926 to 935 kg/m 3 , and/or a melt flow rate MFRs of from > 0.1 to 2 g/10 min, preferably 0.2 to 1 g/10min, further preferred 0.3 to ⁇ 0.8 g/10 min.
  • the second ethylene polymer mixture may have a density of from 927 to 936 kg/m 3 , preferably 926 to 935 kg/m 3
  • the first ethylene homo- or copolymer (PE1) may have a density of from 940 to 980 kg/m 3 and/or a melt flow rate MFR2 of from 20 to 280 g/10 min
  • the first ethylene polymer mixture (PEM1) may have a density of from 940 to 980 kg/m 3 and a melt flow rate MFR2 of from 150 to 550 g/10 min.
  • the ratio MFR 2 (PEM1) / MFR 2 (PE1) may be between 1 and 60, preferably between > 1 and 5 or 2 and 30, further preferred between 1.5 and 4 or 15 and 25.
  • the present invention also concerns a multimodal ethylene polymer film composition having density of from 920 to 940 kg/m 3 and/or a melt flow rate MFR5 of from 0.1 to 5 g/10 min and produced according to any of claim 1 to 1 0.
  • a multimodal ethylene- alpha-olefin copolymer film composition according to the invention may have density of from 920 to 940 kg/m 3 and a melt flow rate MFR5 of from 0.1 to 5 g/10 min and comprising a first ethylene homo- or copolymer (PE1), a second ethylene homo- or copolymer (PE2) and a third ethylene copolymer (PE3), wherein the first ethylene homo- or copolymer (PE1) and the second ethylene homo- or copolymer (PE2) form a first ethylene polymer mixture (PEM1) and the first ethylene polymer mixture (PEM1) and the third ethylene copolymer (PE3) form the second ethylene polymer mixture (PEM2), and wherein
  • the first ethylene homo- or copolymer (PE1) has a melt flow rate MFR2 of from 15 to 300 g/10 min and optionally a density of from 940 to 980 kg/m 3 ;
  • the first ethylene polymer mixture (PEM1) has a melt flow rate MFR2 of from 100 to
  • the second ethylene polymer mixture has a density of from 920 to 940 kg/m 3 and a melt flow rate MFRs of from 0.1 to 5 g/10 min.
  • MFR 2 (PEM1) / MFR 2 (PE1) may be between 1 and 60, preferably between > 1 and 5 or 2 and 30, further preferred between 1.5 and 4 or 15 and 25.
  • the multimodal film composition of the present invention is produced in at least three polymerisation steps, and may be a trimodal polyethylene composition.
  • the film according to the present invention comprises the multimodal ethylene copolymer film composition, preferably a trimodal polyethylene film composition.
  • the film composition may also contain antioxidants, process stabilizers, slip agents, pigments, UV-stabilizers and other additives known in the art.
  • stabilizers are hindered phenols, hindered amines, phosphates, phosphites and phosphonites.
  • pigments are carbon black, ultramarine blue and titanium dioxide.
  • other additives are e. g. clay, talc, calcium carbonate, calcium stearate, zinc stearate and antistatic additives like.
  • the additives can be added as single components or as part of a masterbatch as is known in the art.
  • Suitable antioxidants and stabilizers are, for instance, 2,6-di-tert-butyl-p-cresol, tetrakis- [methylene-3-(3’,5-di-tert-butyl-4’hydroxyphenyl)propionate]methane, octadecyl-3-3(3’5’-di-tert- butyl-4’-hydroxyphenyl)propionate, dilaurylthiodipropionate, distearylthiodipropionate, tris- (nonylphenyl)phosphate, distearyl-pentaerythritol-diphosphite and tetrakis(2,4-di-tert- butylphenyl)-4,4’-biphenylene-diphosphonite.
  • Some hindered phenols are sold under the trade names of Irganox 1076 and Irganox 1010 or commercially available blends thereof, like Irganox B561.
  • Commercially available blends of antioxidants and process stabilizers are also available, such as Irganox B225 marketed by Ciba-Geigy.
  • Suitable acid scavengers are, for instance, metal stearates, such as calcium stearate and zinc stearate. They are used in amounts generally known in the art, typically from 300 ppm to 10000 ppm and preferably from 400 to 5000 ppm.
  • the polymer of the invention can be provided in the form of powder or pellets, preferably pellets. Pellets are obtained by conventional extrusion, granulation or grinding techniques and are an ideal form of the polymer of the invention because they can be added directly to converting machinery. Pellets are distinguished from polymer powders where particle sizes are less than 1 mm. The use of pellets ensures that the composition of the invention is capable of being converted in a film, e.g. monolayer film, by the simple in line addition of the pellets to the converting machinery.
  • the multimodal ethylene polymer film compositions of the invention allow the formation of films having good mechanical properties.
  • the composition can be extruded to films according to any method known in the art.
  • the film preparation process steps of the invention are known and may be carried out in a film line in a manner known in the art, such as flat film extrusion or blown film extrusion.
  • Well known film lines are commercially available, for example from
  • the ethylene polymer compositions of the invention have extraordinary processing properties. Multimodality, especially trimodality, of the polyethylene film composition of the invention makes it very beneficial for making films. Benefits can be seen in excellent
  • the maximum output of the film composition of the invention with 40 pm film is at least 15 % higher, preferably at least 20 % higher, more preferably at least 25 % higher, even more than 30 % higher than with commercial film composition having corresponding MFR and density as composition of the invention.
  • the multimodal film composition of the invention is very attractive in film making point of view.
  • the films of the invention are preferably monolayer films or the polymer composition of the invention is used to form a layer within a multilayer film.
  • Any film of the invention may have a thickness of 3 to 1000 pm, preferably 5 to 500 pm, more preferably 10 to 250 pm, still more preferably 10 to 150 pm, such as e.g. 10 to 100 pm, or even 10 to 60 pm. Selected thickness is dependent on the needs of the desired end application.
  • compositions produced according to the process of the present invention are suitable for making blown films.
  • the films of the invention can be manufactured using simple in line addition of the polymer pellets to an extruder.
  • it is especially preferred to thoroughly blend the components for example using a twin screw extruder, preferably a counter- rotating extruder prior to extrusion and film blowing.
  • the film of the invention is a blown film. Blown films are typically produced by extrusion through an annular die, blowing into a tubular film by forming a bubble which is collapsed between nip rollers after solidification. This film can then be slit, cut or converted (e.g. gusseted) as desired. Conventional film production techniques may be used in this regard.
  • the composition will be extruded at a temperature in the range 160°C to 240°C, and cooled by blowing gas (generally air) at a temperature of 10 to 50°C to provide a frost line height of 1 or 2 to 8 times the diameter of the die.
  • blowing gas generally air
  • the blow up ratio (BUR) should generally be in the range 1.5 to 4, e.g. 2 to 4, preferably 2.5 to 3.
  • the films of the invention exhibit high dart impact strengths and tear strengths, especially in the machine direction.
  • certain parameters are given based on a specific film thickness. This is because variations in thickness of the film cause a change to the size of the parameter in question so to obtain a quantitative value, a specific film thickness is quoted. This does not mean that the invention does not cover other film thicknesses rather it means that when formulated at a given thickness, the film should have the given parameter value.
  • Impact resistance on film (ASTM D1709, method“A”) may be between 280 g and 500 g, further preferred between 300 g and 400 g and/or have a tensile modulus between 300 and 490 MPa, preferably 400 and 480 MPa in MD (ISO 527-3).
  • the present invention further concerns a process for producing a film, comprising the steps of
  • the a-olefin comonomer may be selected from the group consisting of a-olefins having from 4 to 10 carbon atoms and their mixtures, preferably from the group consisting of a-olefins having from 4 to 8 carbon atoms and their mixtures, further preferred from the group consisting of 1 -butene, 1- hexene and 1-octene, further preferred wherein the a-olefin comonomer in the first and second polymerization steps is 1- butene and the a-olefin comonomer in the third polymerization step is 1 -butene and 1 -hexene.
  • the invention also concerns a film comprising the multimodal film composition according to the invention.
  • the melt flow rate is determined according to ISO 1133 and is indicated in g/10 min.
  • the MFR is an indication of the melt viscosity of the polymer.
  • the MFR is determined at 190°C for PE.
  • the load under which the melt flow rate is determined is usually indicated as a subscript, for instance MFR 2 is measured under 2.16 kg load, MFR 5 is measured under 5 kg load and MFR 21 is measured under 21.6 kg load.
  • MFR values can be determined on samples as explained above or calculated, for example in a way well known in the art, from MFR values determined on samples as explained above, especially for example an MFR value for the second ethylene homo- or copolymer can be calculated based on a measured MFR value for the first ethylene homo- or copolymer, a measured MFR value for the first ethylene polymer mixture and the respective amounts of the first and second ethylene homo- or copolymers, since the MFR of the first ethylene polymer mixture results from the first and second ethylene homo- or copolymers.
  • Density of the polymer was measured according to ISO 1183-2 / 1872-2B.
  • Co-monomer content can be determined according to any suitable method well known in the art to do so, such as for example NMR.
  • Film thickness can be determined according to any suitable method well known in the art to do so, such as for example any suitable measuring device.
  • the tear strength or tear resistance is measured using the ISO 6383/2 method.
  • the force required to propagate tearing across a film specimen is measured using a pendulum device.
  • the pendulum swings under gravity through an arc, tearing the specimen from a pre-cut slit.
  • the specimen is fixed on one side by the pendulum and on the other side by a stationary clamp.
  • the tear strength or tear resistance is the force required to tear the specimen.
  • the relative tear resistance (N/mm) can be calculated by dividing the tear resistance by the thickness of the film.
  • the films were produced as described below in the film preparation example.
  • the tear strength or tear resistance is measured in machine direction (MD) and/or transverse direction (TD).
  • E-Mod Tensile modulus
  • Rheological parameters such as Shear Thinning Index SHI and Viscosity were determined by using a Anton Paar Phisica MCR 300 Rheometer on compression moulded samples under nitrogen atmosphere at 190 °C using 25 mm diameter plates and plate and plate geometry with a 1.2 mm gap.
  • the oscillatory shear experiments were done within the linear viscosity range of strain at frequencies from 0.05 to 300 rad/s (ISO 6721-1). Five measurement points per decade were made.
  • Shear thinning index (SHI) which correlates with MWD and is independent of Mw, was calculated according to Heino (“Rheological characterization of polyethylene fractions” Heino, E.L., Lehtinen, A., Tanner J., Seppala, J., Neste Oy, Porvoo, Finland, Theor. Appl. Rheol., Proc. Int. Congr. Rheol, 11th (1992), 1 , 360-362, and“The influence of molecular structure on some rheological properties of polyethylene”, Heino, E.L., Borealis Polymers Oy, Porvoo, Finland, Annual Transactions of the Nordic Rheology Society, 1995).
  • SHI value is obtained by calculating the complex viscosities at given values of complex modulus and calculating the ratio of the two viscosities. For example, using the values of complex modulus of 5 kPa and 300 kPa, then h*(5 kPa) and h*(300 kPa) are obtained at a constant value of complex modulus of 5 kPa and 300 kPa, respectively.
  • the shear thinning index SHI5/300 is then defined as the ratio of the two viscosities h*(5 kPa) and h*(300 kPa), i.e. h(5)/h(300).
  • the films were prepared as described below in the film preparation method A.
  • a loop reactor having a volume of 50 dm 3 was operated at a temperature of 70 °C and a pressure of 57 bar.
  • ethylene, 1-butene, propane diluent and hydrogen so that the feed rate of ethylene was 2.0 kg/h, of 1-butene 99 g/h, of hydrogen was 5 g/h and of propane was 50 kg/h.
  • a solid polymerization catalyst component produced as described above and in Example 1 of EP 1378528 was introduced into the reactor together with triethylaluminium cocatalyst so that the molar ratio of Al/Ti was about 15.
  • the estimated production rate was for example about 1.3 kg/h.
  • a stream of slurry was continuously withdrawn and directed to a loop reactor having a volume of 150 dm 3 and which was operated at a temperature of 95 °C and a pressure of 55 bar.
  • Into the reactor were further fed additional ethylene, propane diluent and hydrogen so that the ethylene concentration in the fluid mixture was 3.7% for IE1 , 4.4% for IE2 and 3.6% for IE3 % by mole, the hydrogen to ethylene ratio was 134 mol/kmol for IE1 , 157.9 mol/kmol for IE2 and 267.2 mol/kmol for IE3 and the fresh propane feed was 78-79 kg/h for all three lEs.
  • the production rate was for example about 14 kg/h.
  • the resulting copolymer had MFR2 of 26 g/10min for IE1 , 57 g/10min for IE2 and 195 g/10min for IE3 and density of for example about 968 kg/m 3 for all three lEs.
  • a stream of slurry from the reactor was withdrawn intermittently and directed into a loop reactor having a volume of 350 dm 3 and which was operated at 95 °C temperature and 52-53 bar pressure.
  • Into the reactor was further added a fresh propane, ethylene, and hydrogen so that the ethylene content in the reaction mixture was 3.1-3.3 mol-% and the molar ratio of hydrogen to ethylene was 465.9 mol/kmol for IE1 , 436.5 mol/kmol for IE2 and 487.2 mol/kmol for IE3 and the molar ratio of 1-butene to ethylene was 21-22 mol/kmol for all three lEs.
  • the ethylene copolymer withdrawn from the reactor had MFR2 of 200 g/10min for IE1 , 197 g/10min for IE2 and 468 g/10min for IE3 and density of for example about 968 kg/m 3 for all three lEs
  • the production rate was for example about 24 kg/h.
  • the slurry was withdrawn from the loop reactor intermittently and directed to a flash vessel operated at a temperature of 50 °C and a pressure of 3 bar. From there the polymer was directed to a fluidized bed gas phase reactor operated at a pressure of 20 bar and a
  • the polymer had a melt flow rate MFRs of 0.69 g/10 min for IE1 , 0.78 g/10min for IE2 and 0,79 g/10min for IE3 and a density of 931.0 kg/m 3 for IE1 , 931.4 kg/m 3 for both IE2 and IE3
  • the production split (weight-% prepolymer/weight-% 1st step component/weight-% 2nd step component/weight-% 3rd step component) was about 1/19 /22 /58 .
  • the polymer powder was mixed under nitrogen atmosphere with 1200 ppm of Irganox B561 and 400 ppm Ca-stearate. Then it was compounded and extruded under nitrogen atmosphere to pellets by using a JSW CIMP90 twin screw extruder so that the SEI was 155 kWh/ton for IE1 , 163-164 kWh/ton for IE2 and IE3 and the melt temperature of 250 °C.
  • the pelletised resin had a melt flow rate MFRs of 0.64 g/10 min for IE1 , 0.78 g/10min for IE2 and 0.71 g/10min for IE3, a density of 930 kg/for IE1 and 932 kg/m 3 for both IE2 and IE3. They have the SHI (5/300) of 93.1 for IE1 , 74.6 for IE2 and 99.2 for IE3.
  • Blown films were made in 7-layer Alpine line under the following conditions: Extruder temperature settings were for all extruders: 220-230-230-230-230-235-235 in all test points. Further the following parameters were used: Blow Up Ratio (BUR) of 3.0; frost line height of 850 0mm, which is about 3 times of die diameter (300mm); and die gap of 1 ,5mm. Layered structure of the monolayer film produced from 7-layer Alpine line of 14/14/14/14/14/15/15.
  • BUR Blow Up Ratio
  • BUR Blow Up Ratio
  • BUR indicates the increase in the bubble diameter over the die diameter.
  • a blow-up ratio greater than 1 indicates that the bubble has been blown to a diameter greater than that of the die orifice.
  • Maximum output rate (kg/h) was tested for materials at 40 micron film thickness.
  • the blown film is wound to form reels which are followed by film cutting into respective dimension for further mechanical testing.

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Abstract

La présente invention concerne un procédé de production d'une composition de polymère d'éthylène multimodal convenant à la production de films par moulage par soufflage. La présente invention concerne un procédé qui comprend les étapes qui consistent à (i) (co)polymériser de l'éthylène et éventuellement un comonomère d'alpha-oléfine dans une première étape de polymérisation, en présence d'un catalyseur de polymérisation Ziegler-Natta sur silice, pour produire un premier homopolymère ou copolymère d'éthylène (PE1) présentant un indice de fluidité MFR2 compris entre 15 et 300 g/10 mn ; (ii) à (co)polymériser l'éthylène et éventuellement un comonomère d'alpha-oléfine dans une deuxième étape de polymérisation, en présence du premier homopolymère ou copolymère d'éthylène, afin de produire un premier mélange de polymères d'éthylène (PEM1) comprenant le premier homopolymère ou copolymère d'éthylène et un deuxième copolymère d'éthylène, ledit premier mélange de polymères d'éthylène présentant une densité comprise entre 940 et 980 kg/m3 et un indice de fluidité MFR2 compris entre 100 et 600 g/10 mn, le MFR2 du premier homopolymère ou copolymère d'éthylène (PE1) étant inférieur à celui du premier mélange de polymères d'éthylène (PEM1) et le deuxième homopolymère ou copolymère d'éthylène (PE2) présentant un indice de fluidité MFR2 compris entre 400 et 2000 g/10 mn ; et (iii) à copolymériser l'éthylène et au moins un un comonomère d'alpha-oléfine dans une troisième étape de polymérisation, en présence du premier mélange de polymères d'éthylène, afin de produire un deuxième mélange de polymères d'éthylène (PEM2) comprenant le premier mélange de polymères d'éthylène et un troisième copolymère d'éthylène (PE3), ledit deuxième mélange de polymères d'éthylène présentant une densité comprise entre 920 et 940 kg/m3 et un indice de fluidité MFR5 compris entre 0,1 et 5 g/10 mn.
PCT/EP2019/086916 2018-12-28 2019-12-23 Procédé de production d'une composition de film de polyoléfine et films ainsi préparés WO2020136164A1 (fr)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022258804A1 (fr) 2021-06-11 2022-12-15 Borealis Ag Procédé de production d'un polymère d'éthylène multimodal et films préparés à partir de ce dernier
EP4344869A1 (fr) 2022-09-30 2024-04-03 Borealis AG Composition de copolymère d'éthylène multimodal et films la comprenant

Citations (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3324093A (en) 1963-10-21 1967-06-06 Phillips Petroleum Co Loop reactor
US3405109A (en) 1960-10-03 1968-10-08 Phillips Petroleum Co Polymerization process
GB1272778A (en) 1968-09-26 1972-05-03 Basf Ag Removing volatile constituents from particulate olefin polymers produced by gas-phase polymerization
EP0047077A1 (fr) 1980-09-02 1982-03-10 Union Carbide Corporation Procédé de dégazage pour éliminer les monomères non polymérisés à partir de polymères d'oléfines
EP0075049A1 (fr) 1981-09-21 1983-03-30 Mitsui Petrochemical Industries, Ltd. Agitateur ayant la forme d'une ancre destiné au récipient de polymérisation en phase gazeuse
US4582816A (en) 1985-02-21 1986-04-15 Phillips Petroleum Company Catalysts, method of preparation and polymerization processes therewith
US4588790A (en) 1982-03-24 1986-05-13 Union Carbide Corporation Method for fluidized bed polymerization
US4877587A (en) 1984-08-24 1989-10-31 Union Carbide Chemicals And Plastics Company Inc. Fluidized bed polymerization reactors
EP0372239A2 (fr) 1988-11-12 1990-06-13 BASF Aktiengesellschaft Procédé de préparation de polymères d'éthylène à l'aide d'un système catalytique Ziegler à base de Vanadium avec destruction des restes catalytiques.
US4994534A (en) 1989-09-28 1991-02-19 Union Carbide Chemicals And Plastics Company Inc. Process for producing sticky polymers
EP0428054A1 (fr) 1989-11-14 1991-05-22 Neste Oy Dispositif pour introduire un mélange de catalyseurs en forme de boue dans un réacteur de polymérisation
EP0479186A2 (fr) 1990-10-01 1992-04-08 Phillips Petroleum Company Appareil et méthode de préparation de polymères d'éthylène
FI921632A (fi) 1992-04-10 1993-10-11 Neste Oy Leijupetireaktori
EP0628343A1 (fr) 1993-05-19 1994-12-14 BP Chemicals Limited Procédé et dispositif d'introduction d'une matière solide dans un réacteur
FI933073A (fi) 1993-07-05 1995-01-06 Borealis Polymers Oy Menetelmä olefiinien polymeroimiseksi leijupetipolymerointireaktorissa
US5391654A (en) 1990-12-28 1995-02-21 Neste Oy Method for homo- or copolymerizing ethene
FI935856A (fi) 1993-12-27 1995-06-28 Borealis Polymers Oy Leijupetireaktori
EP0683176A1 (fr) 1994-05-16 1995-11-22 BP Chemicals Limited Procédé de polymérisation d'oléfine en phase gazeuse
EP0688794A1 (fr) 1994-06-20 1995-12-27 Borealis Polymers Oy Procatalyseur pour la production de polymère d'éthylène, méthode pour sa préparation et utilisation
EP0691367A1 (fr) 1994-07-08 1996-01-10 Union Carbide Chemicals & Plastics Technology Corporation Feuille extrudé d'un mélange de copolymères d'éthylène
EP0699213A1 (fr) 1993-05-20 1996-03-06 BP Chemicals Limited Procede de polymerisation
WO1996019503A1 (fr) 1994-12-22 1996-06-27 Borealis Polymers Oy Procede empechant l'encrassement des reacteurs de polymerisation
WO1996032420A1 (fr) 1995-04-12 1996-10-17 Borealis Polymers Oy Procede pour prevenir l'encrassement et le depot de strates dans des reacteurs en phase gazeuse
WO1999051646A1 (fr) 1998-04-06 1999-10-14 Borealis Technology Oy Composant catalyseur de polymerisation d'olefines, sa preparation et son utilisation
WO2001055230A1 (fr) 2000-01-27 2001-08-02 Borealis Technology Oy Catalyseur
WO2002088194A1 (fr) 2001-04-25 2002-11-07 Bp Chemicals Limited Traitement aux polymeres permettant de separer des matieres volatiles
WO2003066698A1 (fr) 2002-02-04 2003-08-14 Borealis Technology Oy Film a forte resistance aux chocs
WO2004000902A1 (fr) 2002-06-24 2003-12-31 Borealis Technology Oy Procede de production d'une composition de polyethylene lineaire a faible densite
EP1415999A1 (fr) 2002-10-30 2004-05-06 Borealis Technology Oy Procédé et dispositif pour la production de polymères d' oléfines
EP1600276A1 (fr) 2004-05-24 2005-11-30 Borealis Technology Oy Extrudeuse à deux vis contra-rotatives
WO2006063771A1 (fr) 2004-12-17 2006-06-22 Borealis Technology Oy Procede de polymerisation d'olefines en presence d'un catalyseur de polymerisation d'olefines
WO2008034630A1 (fr) 2006-09-22 2008-03-27 Borealis Technology Oy Film multicouche
EP2067799A1 (fr) 2007-12-05 2009-06-10 Borealis Technology OY Polymère
EP2186833A1 (fr) 2008-11-17 2010-05-19 Borealis AG Procédé multi-niveaux pour produire du polyéthylène avec une formation de gel diminuée
EP2228394A1 (fr) 2009-02-24 2010-09-15 Borealis AG Procédé en plusieurs étapes pour la production d'un polymère de polyéthylène de faible densité
EP2246372A1 (fr) 2009-04-30 2010-11-03 Borealis AG Procédé multi-étapes amélioré pour la production de polyéthylène multimodal linéaire de faible densité
EP2246369A1 (fr) 2009-04-30 2010-11-03 Borealis AG Polyéthylène linéaire à faible densité avec une distribution de composition de comonomère uniforme ou inversée
EP2415598A1 (fr) 2010-08-06 2012-02-08 Borealis AG Film multicouche
EP2883887A1 (fr) 2013-12-13 2015-06-17 Borealis AG Procédé en plusieurs étapes de production de compositions de polyéthylène
EP2883885A1 (fr) 2013-12-13 2015-06-17 Borealis AG Procédé en plusieurs étapes de production de compositions de polyéthylène
WO2018060029A1 (fr) * 2016-09-28 2018-04-05 Borealis Ag Procédé de production d'un tuyau revêtu
WO2018095790A1 (fr) * 2016-11-25 2018-05-31 Borealis Ag Procédé de production d'une composition de film de polyoléfine, et films préparés correspondants

Patent Citations (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3405109A (en) 1960-10-03 1968-10-08 Phillips Petroleum Co Polymerization process
US3324093A (en) 1963-10-21 1967-06-06 Phillips Petroleum Co Loop reactor
GB1272778A (en) 1968-09-26 1972-05-03 Basf Ag Removing volatile constituents from particulate olefin polymers produced by gas-phase polymerization
EP0047077A1 (fr) 1980-09-02 1982-03-10 Union Carbide Corporation Procédé de dégazage pour éliminer les monomères non polymérisés à partir de polymères d'oléfines
EP0075049A1 (fr) 1981-09-21 1983-03-30 Mitsui Petrochemical Industries, Ltd. Agitateur ayant la forme d'une ancre destiné au récipient de polymérisation en phase gazeuse
US4588790A (en) 1982-03-24 1986-05-13 Union Carbide Corporation Method for fluidized bed polymerization
US4877587A (en) 1984-08-24 1989-10-31 Union Carbide Chemicals And Plastics Company Inc. Fluidized bed polymerization reactors
US4582816A (en) 1985-02-21 1986-04-15 Phillips Petroleum Company Catalysts, method of preparation and polymerization processes therewith
EP0372239A2 (fr) 1988-11-12 1990-06-13 BASF Aktiengesellschaft Procédé de préparation de polymères d'éthylène à l'aide d'un système catalytique Ziegler à base de Vanadium avec destruction des restes catalytiques.
US4994534A (en) 1989-09-28 1991-02-19 Union Carbide Chemicals And Plastics Company Inc. Process for producing sticky polymers
EP0428054A1 (fr) 1989-11-14 1991-05-22 Neste Oy Dispositif pour introduire un mélange de catalyseurs en forme de boue dans un réacteur de polymérisation
EP0479186A2 (fr) 1990-10-01 1992-04-08 Phillips Petroleum Company Appareil et méthode de préparation de polymères d'éthylène
US5391654A (en) 1990-12-28 1995-02-21 Neste Oy Method for homo- or copolymerizing ethene
FI921632A (fi) 1992-04-10 1993-10-11 Neste Oy Leijupetireaktori
EP0628343A1 (fr) 1993-05-19 1994-12-14 BP Chemicals Limited Procédé et dispositif d'introduction d'une matière solide dans un réacteur
EP0699213A1 (fr) 1993-05-20 1996-03-06 BP Chemicals Limited Procede de polymerisation
FI933073A (fi) 1993-07-05 1995-01-06 Borealis Polymers Oy Menetelmä olefiinien polymeroimiseksi leijupetipolymerointireaktorissa
FI935856A (fi) 1993-12-27 1995-06-28 Borealis Polymers Oy Leijupetireaktori
EP0683176A1 (fr) 1994-05-16 1995-11-22 BP Chemicals Limited Procédé de polymérisation d'oléfine en phase gazeuse
EP0688794A1 (fr) 1994-06-20 1995-12-27 Borealis Polymers Oy Procatalyseur pour la production de polymère d'éthylène, méthode pour sa préparation et utilisation
EP0691367A1 (fr) 1994-07-08 1996-01-10 Union Carbide Chemicals & Plastics Technology Corporation Feuille extrudé d'un mélange de copolymères d'éthylène
WO1996019503A1 (fr) 1994-12-22 1996-06-27 Borealis Polymers Oy Procede empechant l'encrassement des reacteurs de polymerisation
WO1996032420A1 (fr) 1995-04-12 1996-10-17 Borealis Polymers Oy Procede pour prevenir l'encrassement et le depot de strates dans des reacteurs en phase gazeuse
WO1999051646A1 (fr) 1998-04-06 1999-10-14 Borealis Technology Oy Composant catalyseur de polymerisation d'olefines, sa preparation et son utilisation
WO2001055230A1 (fr) 2000-01-27 2001-08-02 Borealis Technology Oy Catalyseur
WO2002088194A1 (fr) 2001-04-25 2002-11-07 Bp Chemicals Limited Traitement aux polymeres permettant de separer des matieres volatiles
WO2003066698A1 (fr) 2002-02-04 2003-08-14 Borealis Technology Oy Film a forte resistance aux chocs
WO2004000902A1 (fr) 2002-06-24 2003-12-31 Borealis Technology Oy Procede de production d'une composition de polyethylene lineaire a faible densite
EP1378528A1 (fr) 2002-06-24 2004-01-07 Borealis Technology Oy Procede pour la production d'une composition lldpe
EP1415999A1 (fr) 2002-10-30 2004-05-06 Borealis Technology Oy Procédé et dispositif pour la production de polymères d' oléfines
EP1600276A1 (fr) 2004-05-24 2005-11-30 Borealis Technology Oy Extrudeuse à deux vis contra-rotatives
WO2006063771A1 (fr) 2004-12-17 2006-06-22 Borealis Technology Oy Procede de polymerisation d'olefines en presence d'un catalyseur de polymerisation d'olefines
WO2008034630A1 (fr) 2006-09-22 2008-03-27 Borealis Technology Oy Film multicouche
EP2067799A1 (fr) 2007-12-05 2009-06-10 Borealis Technology OY Polymère
EP2186833A1 (fr) 2008-11-17 2010-05-19 Borealis AG Procédé multi-niveaux pour produire du polyéthylène avec une formation de gel diminuée
EP2228394A1 (fr) 2009-02-24 2010-09-15 Borealis AG Procédé en plusieurs étapes pour la production d'un polymère de polyéthylène de faible densité
EP2246372A1 (fr) 2009-04-30 2010-11-03 Borealis AG Procédé multi-étapes amélioré pour la production de polyéthylène multimodal linéaire de faible densité
EP2246369A1 (fr) 2009-04-30 2010-11-03 Borealis AG Polyéthylène linéaire à faible densité avec une distribution de composition de comonomère uniforme ou inversée
EP2415598A1 (fr) 2010-08-06 2012-02-08 Borealis AG Film multicouche
EP2883887A1 (fr) 2013-12-13 2015-06-17 Borealis AG Procédé en plusieurs étapes de production de compositions de polyéthylène
EP2883885A1 (fr) 2013-12-13 2015-06-17 Borealis AG Procédé en plusieurs étapes de production de compositions de polyéthylène
WO2015086812A1 (fr) 2013-12-13 2015-06-18 Borealis Ag Procédé en plusieurs étapes pour la production de compositions de polyéthylène
WO2018060029A1 (fr) * 2016-09-28 2018-04-05 Borealis Ag Procédé de production d'un tuyau revêtu
WO2018095790A1 (fr) * 2016-11-25 2018-05-31 Borealis Ag Procédé de production d'une composition de film de polyoléfine, et films préparés correspondants
WO2018095788A1 (fr) * 2016-11-25 2018-05-31 Borealis Ag Procédé de production d'une composition de film de polyoléfine et films ainsi préparés

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
HEINO, E.L.: "Annual Transactions of the Nordic Rheology Society", 1995, BOREALIS POLYMERS OY, article "The influence of molecular structure on some rheological properties of polyethylene"
HEINO, E.L.LEHTINEN, A.TANNER J.SEPPALA, J.: "Theor. Appl. Rheol., Proc. Int. Congr. Rheol", vol. 1, 1992, NESTE OY, article "Rheological characterization of polyethylene fractions", pages: 360 - 362

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022258804A1 (fr) 2021-06-11 2022-12-15 Borealis Ag Procédé de production d'un polymère d'éthylène multimodal et films préparés à partir de ce dernier
EP4344869A1 (fr) 2022-09-30 2024-04-03 Borealis AG Composition de copolymère d'éthylène multimodal et films la comprenant
WO2024068977A1 (fr) 2022-09-30 2024-04-04 Borealis Ag Composition de copolymère d'éthylène multimodal et films la comprenant

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