WO1998058977A1 - Process for preparing polypropylene alloys - Google Patents
Process for preparing polypropylene alloys Download PDFInfo
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- WO1998058977A1 WO1998058977A1 PCT/FI1998/000555 FI9800555W WO9858977A1 WO 1998058977 A1 WO1998058977 A1 WO 1998058977A1 FI 9800555 W FI9800555 W FI 9800555W WO 9858977 A1 WO9858977 A1 WO 9858977A1
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- 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2415—Tubular reactors
- B01J19/2435—Loop-type reactors
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
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- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
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- 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
- C08L23/10—Homopolymers or copolymers of propene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00121—Controlling the temperature by direct heating or cooling
- B01J2219/00128—Controlling the temperature by direct heating or cooling by evaporation of reactants
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00162—Controlling or regulating processes controlling the pressure
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00164—Controlling or regulating processes controlling the flow
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00184—Controlling or regulating processes controlling the weight of reactants in the reactor vessel
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- 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
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
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- 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
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- 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
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/905—Polymerization in presence of transition metal containing catalyst in presence of hydrogen
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/92—Apparatus for use in addition polymerization processes
Definitions
- the present invention relates to propylene polymerization.
- the present invention concerns a process for preparing alloys of homopolymers and copolymers of propylene in a reactor system comprising a combination of at least one slurry reactor and at least one gas phase reactor.
- a large number of processes for preparing propylene homo- and copolymers are known in the art.
- MgCl 2 *TiCl 4 a conventional, supported high-yield catalyst
- numerous different kinds of bulk and gas phase processes can be employed.
- the bulk process is a slurry process, wherein the reaction takes place in pure monomer or in a reaction medium containing more than 60 wt-% of the monomer.
- the method is very useful because of high productivity, and no inert hydrocarbon intermediate is needed.
- the gas phase processes have lower activity, but instead their investment costs are lower in particular because no special recovery is needed for monomer recycling.
- the operation of gas phase processes is safer due to low monomer inventory and low pressure.
- a further advantage is the possibility to produce high comonomer content products.
- the monomers are separated from the polymer of the polymerization product in a flash system.
- the polymerization product from the reactor outlet is heated and expanded in a flash pipe and/or flash tank in order to evaporate the reaction medium.
- the evaporated reaction medium is separated for recovery e.g. by condensing.
- the flash pipe can be jacketed and heated preferably by steam Hydr.Carb.Proc, Nov 1984 p.1 3-117,
- any non-evaporated liquid in the separation tank is a risk for blocking the device.
- the flash system is highly sensitive to high soluble polymer fractions, e.g. with high comonomer content or low molar mass, but also to fines in the polymer product. This is particularly true for cyclone type of devices operated at high pressures.
- the recovery of the monomer can be simplified by condensing the off gas with cooling water Hydro carb. Proc. , Nov 1984 p.113-117, DiDrusco&Rinaldi.
- the off gas has to be pressurised with a compressor, or even more advantageously, by using high enough off gas separation pressure.
- the hydrogen concentration is not limited in gas phase reactors.
- the gas phase reactor also provides flexible production rate control because the bed level and monomer pressure can be controlled.
- the heat transfer is better than in a mechanically fluidized reactor but inferior to the heat transfer in a bulk loop reactor.
- the cooling of the fluid bed reactor is effective due to high circulation flow of reactor gas through the heat transfer, and it can be further improved by cooling the circulation gas below the dew point of the gas, cf. EP 0 089 691, US 4,543,399, US 4,588,790, WO 96/04321.
- Conventionally up to 20 wt-% of the circulation stream can be condensed, and with a special control arrangements up to 50 wt-% is possible, cf. US 93/03946, WO 94/25495.
- a gas phase process for polyolefins where a special catalyst with spherical form is employed, has been proposed in EP-A 0 560 312 and EP-A 0 517 183.
- the catalyst is prepolymerized in a loop reactor using more than 5 parts polymer and 1 part catalyst up to 10 % (w/w) of total production.
- the process according to the present invention is based on the use of a combination of at least one slurry reactor and at least one gas phase reactor connected in series, in that order, to form a cascade.
- Propylene homo- and copolymers are prepared in the presence of a catalyst at elevated temperature and pressure.
- the reaction product of at least one slurry reactor is subjected to product separation by reducing the pressure thereof to evaporate volatile components.
- the solid substances of the product separation operation are conducted to a first gas phase reactor.
- the evaporated reaction medium including the unreacted monomers are separated from the other volatile components and also fed to a gas phase reactor, whereas hydrogen and inert hydrocarbons (e.g. lower alkanes), if any, are removed.
- the invention achieves a number of considerable advantages. With the present arrangement it has been found that the monomer fed into the first reactor can, to a large extent or fully, be consumed in the gas phase reactor(s) after the slurry reactor. This is possible due to gas phase operation with high gas hold-up and a minimum of off-gases.
- the loop reactor dynamics in the cascade provides fast transitions. Fast start-ups are also possible because the gas phase bed material is available directly from the loop reactor.
- the at least one gas phase reactor provides high flexibility in the reaction rate ratio between the first and second part of the product because of adjustable bed level and reaction rate. Further, the gas phase reactor having no solubility limitations makes it possible to produce polymers of high and very high comonomer content or, alternatively, very high melt flow rate.
- the separation of light components before feeding of the recovered monomer to the gas phase makes it possible independently to control polymerization conditions and provides maximum flexibility for polymer alloy preparation.
- Figure 1 depicts in a schematic fashion the process configuration of a preferred embodiment of the invention.
- polymer alloy or “alloy” denotes a combination of (propylene) polymers of essentially different composition having a synergetic influence on the strength properties of the combination.
- Slurry reactor designates any reactor, such as a continuous or simple stirred tank reactor or loop reactor, operating in bulk or slurry and in which the polymer forms in particulate form.
- Bulk means a polymerization in reaction medium that comprises at least 60 wt-% monomer.
- the slurry reactor comprises a bulk loop reactor.
- gas phase reactor any mechanically mixed or fluid bed reactor.
- gas phase reactor comprises a mechanically agitated fluid bed reactor with gas velocities of at least 0.2 m/sec.
- High temperature polymerization stands for polymerization temperatures above a limiting temperature of 80 °C known to be harmful for high yield catalysts of related prior art. At high temperatures the stereospecificity of the catalyst and the morphology of the polymer powder can be lost. This does not take place with the particularly preferred type of catalysts used in the invention which is described below. The high temperature polymerization takes place above the limiting temperature and below the corresponding critical temperature of the reaction medium.
- Super critical polymerization designates polymerization that takes place above a corresponding critical temperature and pressure of the reaction medium.
- indirect feed is meant a process wherein the content of the slurry reactor is fed into the gas phase reactor fluidized bed, the polymerization product via a reaction medium separation unit and the reaction medium as an off gas from the separation unit.
- some component e.g. hydrogen
- the reaction medium can be fully or partially removed therefrom with various technical means, such as membranes or by condensing.
- reaction zone stands for one or several reactors of similar type producing the same type or characteristics of polymer connected in the series.
- the present invention concerns a multistage process consisting of a bulk reaction zone including at least one slurry reactor, and a gas phase reaction zone including at least one gas phase reactor in cascade after at least one slurry reactor with a minimum or no recycling of monomer back to the first reactor and with indirect feed to the gas phase for homo- or copolymerizing propylene.
- the product outlet from the slurry reactor can be discontinuous, or preferably continuous, as described in FI Patent Applications Nos. 971367 and 971368.
- the slurry is led as such without separation of any particle streams based on different particle size. No particles are returned to the slurry reactor.
- the conduit between the slurry reactor and the reaction medium separation unit can be heated.
- the content of the slurry reactor is first conducted into a reaction medium separation unit.
- the polymer is separated from the reaction medium and fed into the gas phase reactor fluidized bed from said separation unit.
- the gas from the separation unit is conducted into the gas phase reactor in gaseous form.
- the gas from the separation unit is fully or partially freed from, e.g. hydrogen, using various technical gas separation means e.g. membranes, distillation or stripping.
- the gas can be condensed, and optionally hydrogen or other light components can be removed before the liquid monomer is fed into the gas phase reactor.
- Gaseous monomer can be fed to any suitable place in the gas phase reactor, e.g. into the recycle stream before the compressor of such a stream or directly into the reactor.
- the liquid monomer can be fed optionally into the polymer bed, above the gas distribution plate, e.g. into the powder feed line or, even more preferably, into the recycle stream before or after the gas phase circulation heat exchanger (circulation cooler).
- reaction is continued in the gas phase reactor(s). All monomer entering the gas phase from the slurry reactor is part of the reactor gas inventory until it is converted into the polymer.
- the polymer leaving the gas phase reactor with the outlet system enters a solid/gas separation unit.
- the polymer from the bottom is fed to further processing steps and the gas is compressed and circulated back to the gas phase reactor after purification steps.
- light inerts such as methane and ethane, and heavier inerts such as propane and oligomers are removed in these purification steps.
- the purification can be performed with distillation or membrane separation. In case of distillation the monomers are circulated back to the gas phase reactor mainly as liquid.
- the polymer leaving the 1 st gas phase reactor with the outlet system enters a solid/gas separation unit.
- the polymer from the bottom is fed further to 2nd gas phase reactor and the gas is compressed and circulated back to the 1 st gas phase reactor after purification steps.
- light inerts such as methane and ethane, and heavier inerts such as propane and oligomers are removed in these purification steps.
- the purification can be performed with distillation or membrane separation. In case of distillation the monomers are circulated back to the gas phase reactor mainly as liquid.
- the polymer leaving the 1 st gas phase reactor with the outlet system enters the 2nd gas phase reactor directly with the accompanying gas.
- the polymer leaving the 2nd gas phase reactor with the outlet system enters a solid/gas separation unit.
- the polymer from the bottom is fed to further processing steps and the gas is compressed and partly circulated back to the 2nd gas phase reactor directly, partly after purification steps.
- light inerts such as methane and ethane, and heavier inerts such as propane and oligomers are removed in these purification steps.
- the purification can be performed with distillation or membrane separation. In case of distillation an ethylene rich stream is circulated back to the 2nd gas phase reactor and a propylene-propane stream is fed to propane and oligomers removal steps.
- the polymerization products are obtained by using a catalyst.
- the catalyst can be any catalyst providing adequate activity at elevated temperature.
- the preferred catalyst system used comprises a high yield Ziegler-Natta catalyst having catalyst component, a co-catalyst component, an external donor and, optionally, an internal donor.
- Another preferred catalyst system is a metallocene-based catalyst having a bridged ligand structure giving high stereoselectivity, and which is impregnated on a carrier or support in the form of an activated complex.
- the polymerization temperature for homopolymers is at least 80 °C and for copolymers at least 60 °C.
- the slurry reactor is operated at elevated pressure at least 35 bar up to 100 bar, and the gas phase reactor(s) at least 10 bar up to dew point pressure.
- any reactor of the reactors in the series can be operated above the critical temperature and pressure, but lower than the melting/fusing point of the corresponding polymer produced.
- Propylene and optionally one or more other C 2 to C 16 olefins e.g. ethylene, 1-butene, 4- methyl- 1-pentene, 1-hexene, dienes, or cyclic olefins
- ethylene, 1-butene, 4- methyl- 1-pentene, 1-hexene, dienes, or cyclic olefins is subjected to polymerization and copolymerization, respectively, in a plurality of polymerization reactors connected in series.
- the optional olefin(s) can be used in any of the reactors. Different amounts of hydrogen can be used as a molar mass modifier or regulator in any or every reactor.
- the desired homo- or copolymers of propylene can be recovered from the product separation means of the gas phase reaction zone.
- any stereospecific catalyst for propylene can be used, which has high yield and useful polymer properties e.g. isotacticity and morphology at the high temperature and possible supercritical polymerization.
- the polymerization products are obtained by using a catalyst.
- the preferred catalyst system used comprises a high yield Ziegler-Natta catalyst having catalyst component, a cocatalyst component, optionally, an external donor and an internal donor.
- Another preferred catalyst system is a metallocene catalyst having a bridged ligand structure giving high stereoselectivity, and which has an active complex impregnated on a carrier.
- the catalyst is preferable any other catalyst providing adequate activity at elevated temperature.
- the catalyst can be prepolymerized prior to feeding into the first polymerization reactor of the series. During prepolymerization the catalyst components are contacted with a monomer, such as an olefin monomer, before feeding into the reactor. Examples of suitable systems are described in, for example, FI Patent Application No. FI 961152.
- a viscous substance such as an olefinic wax
- the catalyst prepolymerized in wax will allow for easy dosing of the catalyst into the polymerization reactors. Examples of suitable systems are described in, for example, FI Patent No. 95387. 32. Typically about 1 part of catalyst is used for a maximum of 4 parts of polymer.
- the monomer used for prepolymerization can be selected from the group consisting of propylene, 1-butene, 4-methyl-l-pentene, 3-methyl-l-butene, vinylcyclohexane, cyclopentene, 1-hexene, 1-octene, and 1-decene.
- the prepolymerization can be performed batchwise in wax or in a continuous pre- polymerization reactor or in a continuous plug flow type prepolymerization reactor.
- the invention is based on the combination of at least one slurry reactor and at least one gas phase reactor connected in series, called a cascade.
- the equipment of the polymerization step can comprise polymerization reactors of any suitable type.
- the slurry reactor can be any continuous or batch stirred tank reactor or loop reactor operating in bulk or slurry and the polymer forms in particular form in the reactor.
- Bulk means a polymerization in reaction medium that comprises of at least 60 % (w/w) monomer.
- the gas phase reactor can be any mechanically mixed or fluid bed reactor. According to the present invention the slurry reactor is preferably a bulk loop reactor and the gas phase reactor is a fluidized bed type reactor with a mechanical stirrer.
- Any reactor in the process can be a super critical polymerization reactor.
- the production split between the slurry reactor and the 1st gas phase reactor(s) is 67:33 - 50:50 when monomer recycling back to the slurry reactor is allowed.
- the production split between the slurry reactor and the gas phase reactor(s) is less than or equal to 50:50 when no recycling back to the slurry reactor is required.
- the production in the slurry reactor is more than 10 wt-% (split is greater than 10:90).
- 10 to 50 % of the polymer is prepared in the slurry reaction zone and no monomer is recycled.
- a small monomer amount of the monomer has to be recycled to the slurry reactor from the gas phase reaction zone.
- the polymerization process comprises at least the following steps of
- process can comprise also the following additional steps of • recovering the polymerization product from the second reaction zone,
- propylene with the optional comonomer(s) together with the activated catalyst complex and optional cocatalyst and other aid components are fed into the first polymerization reactor.
- hydrogen as a molar mass regulator can be fed into the reactor in the amount required for achieving the desired molar mass of the polymer.
- no circulation back to the slurry reactor only fresh monomer is fed into the first reactor.
- the feed of the reactor can consist of the recycled monomer from the following reactor(s), passed through recovery system, if any, together with added fresh monomer, hydrogen, optional comonomer(s) and catalyst components.
- the activated catalyst complex will polymerize and form a product in particulate form in the slurry reactor, i.e. polymer particles, which are suspended in the fluid circulated in the reactor.
- the polymerization medium typically comprises the monomer and/or a hydrocarbon, and the fluid is either liquid or gaseous.
- the fluid is liquid and the suspension of polymer is circulated continuously through the slurry reactor, whereby more suspension of polymer in particle form in hydrocarbon medium or monomer will be produced.
- the first polymerization or copolymerization reaction is carried out in a reaction medium mainly consisting propylene. Preferably at least 60 weight percent of the medium is propylene.
- the conditions of the slurry reactor are selected so that at least 10 wt-%, preferably at least 12 wt-% of the whole production is polymerised in the first slurry reactor.
- the temperature is in the range of 40 to 110 °C, preferably in the range of 50 to 100 °C, and even more preferably for homopolymers 80 to 100 °C and for copolymers 60 to 80 °C.
- the reaction pressure is in the range of 30 to 100 bar, preferably 35 to 80 bar.
- slurry polymerization zone more than one reactor can be used in series.
- the polymer suspension in an inert hydrocarbon or in monomer produced in the 1 st slurry reactor is fed without separation of inert components and monomers periodically or continuously to the following slurry reactor, which acts at lower pressure than the previous slurry reactor.
- the polymerization heat is removed by cooling the reactor with a cooling jacket.
- the residence time in the slurry reactor must be at lest 10 minutes, preferably 20-100 min for obtaining a sufficient degree of polymerization. This is necessary to achieve polymer yields of at least 40 kg PP/g cat. It is also advantageous to operate the slurry reactor with high solid concentrations, e.g. 50 % for homopolymers and 35 or 40 % for some copolymers when the particles are swelling. If the solid concentration in the loop reactor is too low, the amount of reaction medium conducted to the second reaction zone or gas phase reactor is increasing.
- the first polymerization reaction is carried out in the presence of hydrogen, then the pressure of the first polymerization product including the reaction medium is optionally reduced after the reaction zone in order to evaporate volatile components of the products, e.g. in a flash tank.
- the polymer is led into the gas phase reactor fluidized bed.
- the off gas from the separation unit is lead to the gas phase reactor in gaseous form (indirect feed).
- some components e.g. hydrogen can be fully or partially removed from the off gas of the separation unit with various technical solutions, e.g. with membranes, condensing and stripping or distilling.
- the separation unit product can be led into the gas phase reactor in liquid form.
- the second reactor is preferably a gas phase reactor, wherein propylene and optionally comonomer(s) are polymerized in reaction medium which consists of gas or vapour.
- the gas phase reactor can be an ordinary fluidized bed reactor, although other types of gas phase reactors can be used.
- a fluidized bed reactor the bed consists of the formed and growing polymer particles as well as still active catalyst come along with the polymer fraction.
- the bed is kept in a fluidized state by introducing gaseous components, e.g. monomer on such flow rate (at least 0.2 m/s) which make the particles act as a fluid.
- the fluidizing gas can contain also inert gases, like nitrogen and also hydrogen as a modifier. In the invention it is not recommendable to use unnecessary inert gases which may cause problems in the recovery section.
- the gas phase reactor used can be operated in the temperature range of 50 to 115 °C, preferably between 60 and 110 °C and reaction pressure between 10 and 40 bar and the partial pressure of the monomer is preferably between 2 and 30 bar or more, but always below the dew point pressure.
- no fresh propylene is fed to the first gas phase reactor other than what is required for various flushings.
- the pressure of the second polymerization product including the gaseous reaction medium is then reduced after the first gas phase reactor in order to separate part of the gaseous and possible volatile components (e.g. heavy comonomers and compounds used for catalyst feeds) of the product e.g. in a flash tank. Some of the monomers, typically the heavier comonomers, can be recycled to the bulk reaction zone.
- the overhead gas stream is recirculated through the recovery system back to the first gas phase reactor or partly to the first gas phase reactor and partly to the slurry reactor.
- the polymerization product can be fed into a second gas phase reactor and subjected to a third polymerization reaction to produce a modified polymerization product from which the polypropylene is separated and recovered.
- the third polymerization reaction is carried out in a gas phase reactor in the presence of comonomers which give the third polymerization product properties e.g. improved impact strength, ductility or softness.
- copolymers are produced by means of the present invention they contain at least 0.5 wt-% of comonomer(s), in particular at least about 2 wt-% and preferably up to 20 wt-% of at least one comonomer.
- a typical comonomer content of a copolymer fed to the first gas phase reactor is about 2 to 16 wt-% and that comonomer content can be raised in the gas phase reactor to up to about 20 wt-%.
- - propylene and optionally comonomers are polymerised in a loop reactor at a pressure of 40 to 80 bar, at a temperature of 60 to 100 °C and hydrogen is used to control the molar mass of the polymerization product,
- the polymerization product from the loop reactor is recovered and conducted to a flash separator, from where the hydrocarbon medium is removed from the top as the overhead and the polymer from the bottom,
- the overhead is treated in e.g. membrane unit to remove hydrogen and/or other components,
- the polymerization product from the first gas phase reactor is recovered and conducted to a flash tank, wherein the pressure of the product is reduced to produce an overhead product containing essentially non-reacted monomer(s) and hydrogen and a bottom product primarily containing polymerised solids,
- the polymerization product from the second polymerization can be conducted directly or via a flash tank to a third (fourth etc.) gas phase polymerization reactor, wherein polymerization is carried out in the presence of comonomers.
- the preferred process configuration for preparing propylene homo- or copolymers comprises - at least one slurry reactor and at least one gas phase reactor, arranged in series to form a cascade,
- a flash tank for separating polymer from reaction medium containing unreacted monomers and volatile compounds, said tank having an inlet for a polymerization product and an outlet for the polymer and an outlet for the reaction medium, - a separation means, such as membranes, condensing means, stripping means or distilling means, for separating volatile compounds from the reaction medium, said separation means having an inlet for the reaction medium and an outlet for the reaction medium and an outlet for the volatile compounds,
- catalyst from reservoir 30 is fed to the feeding device 31 together with optional diluent or monomer from line 32.
- the feeding device 31 feeds the catalyst/diluent mixture into the prepolymerization chamber 1 via line 33.
- Monomer is fed through 34 and cocatalyst and possible donors can be fed into the reactor 1 through conduits or preferably contacted with catalyst and donor already in line 33.
- the prepolymerized catalyst is removed preferably directly through line 36 and transferred to a loop reactor 40.
- the polymerization is continued by adding optional diluent from the line 42, monomer from line 43, hydrogen from line 44 and an optional comonomer from line 45 through the line 46.
- An optional cocatalyst can also be introduced into the loop reactor 40.
- the polymer-hydrocarbon mixture is fed through one or several exhaust valves 47.
- the product of the slurry reactor 40 is conducted to a flash separator 50.
- the hydrocarbon medium is removed from the polymer particles, the remaining monomer and hydrogen are removed from the flash separator 50 either through the line 51 to the recovery unit (not presented) or preferably to gas phase reactor 60 through the line 69 after possible separation of light components e.g. hydrogen.
- the numeral 70 signifies separation means, such as a membrane unit or a stripping column which is capable of freeing the overhead of the flash separator 50 from hydrogen or light inert hydrocarbons.
- the reactor 60 In the lower part of the gas phase reactor 60 there is a fluid bed consisting of polymer particles, which will be kept in a fluidized state in an ordinary way by circulating the gases removed from the top of the reactor 60 though line 61, compressor 62 and a heat exchanger (not presented) to the lower part of the reactor 60 or preferably recycle stream in an ordinary way.
- the reactor 60 is advantageously, but not necessarily, equipped with a mixer (not presented).
- the product will be removed from the reactor 60 continually or periodically through the transfer line 66 to the flash tank 68.
- the overhead product of the recovery system is circulated to the gas phase reactor via a monomer recovery system.
- the recovered product can be led to an additional gas removal tank thereafter to a rubber gas phase (reactor).
- the numeral 71 signifies separation means, such as a membrane unit or a stripping column, which is capable of freeing the recycle monomer of the gas phase reactor 60 or of the separator 50 from hydrogen and/or light inert hydrocarbons typically having a lower boiling point than the monomer(s).
- separation means such as a membrane unit or a stripping column, which is capable of freeing the recycle monomer of the gas phase reactor 60 or of the separator 50 from hydrogen and/or light inert hydrocarbons typically having a lower boiling point than the monomer(s).
- the process according to the invention is useful for preparing propylene copolymers with good impact and creep properties.
- the process can be employed to produce alloys of homo/random and random/homo propylene polymers.
- a production scale plant was simulated to produce continuously PP-copolymer with good impact and creep properties.
- the plant comprises a catalyst, alkyl, donor, ethylene and propylene feed systems, a prepolymerization reactor, a loop reactor, a flash tank and 2 fluidized bed gas phase reactors.
- Catalyst, alkyl, donor and propylene were fed to prepolymerization reactor.
- the polymer slurry from the prepolymerization reactor was fed to a loop reactor in which also hydrogen and more propylene was fed.
- the polymer slurry from the loop reactor was fed to a flash tank where propylene and polymer were separated.
- the polymer from flash tank was fed to the first GPR.
- Propylene from flash tank was fed to the first GPR after removal of hydrogen.
- Ethylene and additional propylene was fed to the first GPR.
- the polymer from the first GPR was fed to the second GPR.
- Ethylene, some hydrogen and additional propylene were fed to the second GPR.
- the production in the reactors comprised 300 kg/h in prepolymerization, 10 t/h in loop and 10 t/h in the first GPR and 6 t/h in the second GPR.
- the prepolymerization reactor was operated at a pressure of 56 bar and a temperature of 20 °C.
- the loop reactor was operated at a pressure of 55 bar and a temperature of 85 °C.
- the MFR (2.16 kg, 230 °C) of the PP-homopolymer produced in the loop was adjusted to 100 by regulating the hydrogen feed.
- the GPR was operated at a pressure of 35 bar and a temperature of 80 °C.
- the MFR (2.16 kg, 230 °C) of the PP taken out of the GPR was set at 0.4 by controlling the production split between the reactors and the efficiency of hydrogen removal of flashed propene.
- Ethylene content was adjusted to 2 % w/w by regulating the partial pressure of ethylene and controlling the production split between the reactors.
- the second GPR was operated at a pressure of 20 bar and a temperature of 70 °C.
- the MFR (2.16 kg, 230 °C) of the PP-copolymer in taken out of the second GPR was set at 0.3 by adjusting the partial hydrogen pressure and by controlling the production split between the reactors. Minor amounts of propylene were circulated from the second GPR back to the loop reactor.
- a production scale plant was simulated to produce continuously PP-copolymer with good creep properties.
- the plant comprises a catalyst, alkyl, donor, ethylene and propylene feed systems, a prepolymerization reactor, a loop reactor, a flash tank and a fluidized bed gas phase reactor.
- the polymer slurry from the prepolymerization reactor was fed to a loop reactor in which also hydrogen and more propylene was fed.
- the polymer slurry from the loop reactor and additional hydrogen and propylene was fed to GPR.
- the catalyst, alkyl, donor and propylene were fed to the prepolymerization reactor.
- the polymer slurry from the prepolymerization reactor was fed to a loop reactor into which also ethylene and more propylene was fed.
- the polymer slurry from the loop reactor was fed to a flash tank where monomers and polymer were separated.
- the polymer from the flash tank was fed to the GPR.
- Propylene from the flash tank was fed to the GPR after removal of ethylene. Hydrogen and additional propylene was fed to the GPR.
- the production in the reactors comprised 300 kg/h in prepolymerization, 10 t h in loop and 10 t/h in the first GPR
- the prepolymerization reactor was operated at a pressure of 56 bar and a temperature of 20 °C.
- the loop reactor was operated at a pressure of 55 bar and a temperature of 75 °C.
- the MFR (2.16 kg, 230 °C) of the random-PP produced in the loop was below 0.1 and the ethylene content was adjusted to 3.5 % w/w by regulating the ethylene feed.
- the GPR reactor was operated at a pressure of 35 bar and a temperature of 80 °C.
- the MFR (2.16 kg, 230 °C) of the PP-copolymer taken out of the GPR was set at 0.3 by adjusting the partial pressure of hydrogen.
- the ethylene content was controlled to be 1.8 % w/w via the production split between the reactors.
- Ethylene in the loop outlet was recovered from flash gases and circulated back to the loop reactor.
- Propylene in GPR outlet was recovered and fed to the loop reactor after removal of hydrogen.
- the once-through conversion of the propylene and ethylene were 83 % and 84 %, respectively.
- a pilot plant operated continuously is used to produce PP-copolymer with good impact and creep properties.
- the plant comprises a catalyst, alkyl, donor, propylene and ethylene feed systems, a prepolymerization reactor, a loop reactor and two fluidized bed gas phase reactors (GPR).
- the catalyst, alkyl, donor and propylene are fed to the prepolymerization reactor.
- the polymer slurry from the prepolymerization reactor is fed to a loop reactor in which also hydrogen, ethylene and additional propylene are fed.
- the polymer slurry from the loop reactor and additional hydrogen and propylene are fed to the 1st GPR.
- the polymer from 1st GPR is fed to 2nd GPR.
- Ethylene, some hydrogen and additional propylene was fed to the second GPR.
- the formed polymer and unreacted propylene are separated after removal from 2nd GPR.
- the catalyst used is a highly active and stereospecific ZN-catalyst made according to U.S. Patent 5,234,879.
- the catalyst is contacted with triethylaluminium (TEA) and dicyclo- pentyldimethoxysilane (DCPDMS) (Al/Ti ratio is 150 and Al/Do 10 (mole)) before feeding to the prepolymerization reactor.
- TEA triethylaluminium
- DCPDMS dicyclo- pentyldimethoxysilane
- the catalyst is fed according to U.S. Patent US-5.385.992 and is flushed with propylene to the loop reactor.
- the prepolymerization reactor is operated at a pressure of 51 bar, a temperature of 20 °C and a mean residence time of the catalyst of 7 min.
- the loop reactor is operated at 50 bar pressure, 75 °C temperature and mean residence time of the catalyst at 1 h.
- the MFR (2.16 kg, 230 °C) of the PP-randompolymer produced in the loop is controlled to be 7 via hydrogen feed.
- the ethylene content is controlled to be 3.5 % w/w via ethylene feed.
- the polymer slurry from the loop reactor is transferred to the 1st GPR.
- the 1st GPR reactor is operated at 29 bar total pressure and 21 bar partial pressure of propylene, 80 °C temperature and mean residence time of the catalyst at 1.5 h.
- the MFR (2.16 kg, 230 °C) of the PP- randompolymer taken out of the GPR is controlled to be 10 via partial pressure of hydrogen.
- the ethylene content is controlled to be 2 % w/w via production split between the reactors.
- the polymer from the 1st GPR is transferred to the 2nd GPR.
- the 2nd GPR reactor is operated at 10 bar total pressure and 7 bar partial pressure of monomers, 80 °C temperature and mean residence time of the catalyst at 1.5 h.
- the MFR (2.16 kg, 230 °C) of the PP-copolymer taken out of the GPR is controlled to be 7 via partial pressure of hydrogen.
- the ethylene content is controlled to be 10 % w/w via partial pressure of ethylene and controlling the production split between the reactors.
- Desired properties are achieved with production split 1 % in prepolymerization, 40 % in loop and 40 % in the first GPR and 19 % in the second GPR.
- a pilot plant operated continuously was used to produce PP-copolymer with good creep properties.
- the plant comprises a catalyst, alkyl, donor, propylene and ethylene feed systems, prepolymerization reactor, loop reactor and a fluidized bed gas phase reactor (GPR).
- GPR fluidized bed gas phase reactor
- Catalyst, alkyl, donor and propylene was fed to the prepolymerization reactor.
- the polymer slurry from the prepolymerization reactor was fed to a loop reactor in which also hydrogen, additional propylene was fed.
- the polymer slurry from the loop reactor was fed to a flash tank where monomers and polymer were separated.
- the polymer from flash tank was fed to the GPR.
- Propylene from flash tank was fed to the GPR after removal of hydrogen. Ethylene, additional hydrogen and additional propylene was fed to the GPR.
- the catalyst used was a highly active and stereospecific ZN-catalyst made according to U.S. Patent 5.234.879.
- the catalyst was contacted with triemylaluminium (TEA) and dicyclopentyldimethoxysilane (DCPDMS) (Al Ti ratio was 140 and Al/Do 10 (mole)) before feeding to the prepolymerization reactor.
- TEA triemylaluminium
- DCPDMS dicyclopentyldimethoxysilane
- the catalyst was fed according to U.S. Patent No. 5,385,992 and was flushed with propylene to the loop reactor.
- the prepolymerization reactor was operated at a pressure of 51 bar, a temperature of 20 °C and a mean residence time of the catalyst of 7 min.
- the loop reactor was operated at a pressure of 50 bar, a temperature of 75 °C and a mean residence time of the catalyst of 1 h.
- the MFR (2.16 kg, 230 °C) of the PP-randompolymer produced in the loop was adjusted to 10 by regulating the hydrogen feed.
- the GPR reactor was operated at a total pressure of 29 bar and a partial propylene pressure of
- the MFR (2.16 kg, 230 °C) of the PP-copolymer taken out of the GPR was adjusted to 5 by regulating the partial hydrogen pressure and by adjusting the production split between the reactors.
- the ethylene content was set at 3.5 % w/w by adjusting the production split between the reactors and the partial pressure of ethylene.
- the desired properties are achieved with a production split of 1 % in prepolymerization, 40 % in loop and 59 % in the GPR.
- the polymer from the GPR could have been transferred to another GPR to produce
Abstract
Description
Claims
Priority Applications (5)
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DE69833324T DE69833324T2 (en) | 1997-06-24 | 1998-06-24 | METHOD FOR PRODUCING POLYPROPYLENE ALLOYS |
EP98929462A EP0991684B1 (en) | 1997-06-24 | 1998-06-24 | Process for preparing polypropylene alloys |
JP50385599A JP3825478B2 (en) | 1997-06-24 | 1998-06-24 | Method for producing polypropylene alloy |
AU79212/98A AU7921298A (en) | 1997-06-24 | 1998-06-24 | Process for preparing polypropylene alloys |
US09/446,333 US6469110B1 (en) | 1997-06-24 | 1998-06-24 | Process for preparing polypropylene alloys |
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FI972729A FI111846B (en) | 1997-06-24 | 1997-06-24 | Process and apparatus for preparing mixtures of polypropylene |
FI972729 | 1997-06-24 |
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US (1) | US6469110B1 (en) |
EP (1) | EP0991684B1 (en) |
JP (1) | JP3825478B2 (en) |
CN (1) | CN1140555C (en) |
AT (1) | ATE316539T1 (en) |
AU (1) | AU7921298A (en) |
DE (1) | DE69833324T2 (en) |
ES (1) | ES2256942T3 (en) |
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CN114555656B (en) | 2019-09-05 | 2024-02-20 | 埃克森美孚化学专利公司 | Process for preparing polyolefin and impact copolymers having broad molecular weight distribution and high stiffness |
WO2021053154A1 (en) | 2019-09-20 | 2021-03-25 | Borealis Ag | Heterophasic propylene polymer composition with improved property profile |
EP3835327A1 (en) | 2019-12-09 | 2021-06-16 | Borealis AG | System for producing polyolefin and process for recovering polymerization product from gas phase reactor |
EP3838971B1 (en) | 2019-12-16 | 2023-02-08 | Abu Dhabi Polymers Co. Ltd (Borouge) Llc. | Foamed polypropylene composition suitable for sheets and articles |
EP4093780A1 (en) | 2020-01-24 | 2022-11-30 | ExxonMobil Chemical Patents Inc. | Methods for producing bimodal polyolefins and impact copolymers |
WO2021167850A1 (en) | 2020-02-17 | 2021-08-26 | Exxonmobil Chemical Patents Inc. | Propylene-based polymer compositions having a high molecular weight tail |
WO2021191018A1 (en) | 2020-03-24 | 2021-09-30 | Borealis Ag | Polyethylene composition for a film layer |
US20230193002A1 (en) | 2020-03-24 | 2023-06-22 | Borealis Ag | Polyethylene composition for a film layer |
US20230227637A1 (en) | 2020-07-23 | 2023-07-20 | Borealis Ag | Multimodal ethylene copolymer |
CN114058112B (en) * | 2020-08-06 | 2023-08-22 | 中国石油天然气股份有限公司 | Low-melt-index random copolymer polypropylene resin and preparation method thereof |
WO2022106710A1 (en) | 2020-11-23 | 2022-05-27 | Borealis Ag | In-situ reactor blend of ziegler-natta catalysed, nucleated polypropylene and a metallocene catalysed polypropylene |
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KR20240040100A (en) | 2021-08-04 | 2024-03-27 | 보레알리스 아게 | Multi-layer non-woven structure |
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WO2024025741A1 (en) | 2022-07-27 | 2024-02-01 | Exxonmobil Chemical Patents Inc. | Polypropylene compositions with enhanced strain hardening and methods of producing same |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4740550A (en) * | 1986-06-18 | 1988-04-26 | Shell Oil Company | Multistage copolymerization process |
US4740551A (en) * | 1986-06-18 | 1988-04-26 | Shell Oil Company | Multistage copolymerization process |
WO1997013790A1 (en) * | 1995-10-10 | 1997-04-17 | Borealis A/S | Process for making propylene homo or copolymers |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3622553A (en) | 1967-12-18 | 1971-11-23 | Phillips Petroleum Co | Agitated reactor and gas fluidized bed reactor in series for polymerization of vinyl chloride |
GB1532231A (en) | 1975-04-18 | 1978-11-15 | Ici Ltd | Polymerisation process |
DE2803281C2 (en) | 1978-01-26 | 1982-12-02 | Chemische Werke Hüls AG, 4370 Marl | Process for the multistage polymerization of ethylene, alone or together with other olefins |
US4492787A (en) * | 1981-09-18 | 1985-01-08 | Mitsubishi Chemical Industries Limited | Process for continuously producing propylene-ethylene block copolymer |
US4424341A (en) | 1981-09-21 | 1984-01-03 | Phillips Petroleum Company | Separation of solid polymers and liquid diluent |
US4543399A (en) | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
US4588790A (en) | 1982-03-24 | 1986-05-13 | Union Carbide Corporation | Method for fluidized bed polymerization |
DZ520A1 (en) | 1982-03-24 | 2004-09-13 | Union Carbide Corp | Improved process for increasing the space-time yield of an exothermic polymerization reaction in a fluidized bed. |
EP0254234B1 (en) * | 1986-07-22 | 1996-03-13 | Mitsubishi Chemical Corporation | Method for producing an alpha-olefin block copolymer |
CA1284549C (en) * | 1986-09-26 | 1991-05-28 | Fathi David Hussein | Process for the polymerization of propylene |
EP0282929B2 (en) * | 1987-03-14 | 1997-10-22 | Mitsubishi Kasei Corporation | Method for producing a propylene-alpha-olefin block copolymer |
US5234879A (en) | 1990-12-19 | 1993-08-10 | Neste Oy | Method for the modification of catalysts intended for the polymerization of olefins |
FI89929C (en) | 1990-12-28 | 1993-12-10 | Neste Oy | Process for homo- or copolymerization of ethylene |
FI86867C (en) | 1990-12-28 | 1992-10-26 | Neste Oy | FLERSTEGSPROCESS FOR FRAMSTAELLNING AV POLYETEN |
FI94164C (en) | 1991-03-21 | 1995-07-25 | Borealis Polymers Oy | Process for dosing a polymerization catalyst made liquid to a polymerization reactor |
FI88048C (en) | 1991-05-09 | 1993-03-25 | Neste Oy | Coarse-grained polyolefin, its method of preparation and a catalyst used in the method |
FI88047C (en) | 1991-05-09 | 1993-03-25 | Neste Oy | Catalyst-based catalyst for polymerization of olivines |
FI88049C (en) | 1991-05-09 | 1993-03-25 | Neste Oy | Large pore polyolefin, process for its preparation and a catalyst used in the process |
IT1246614B (en) | 1991-06-03 | 1994-11-24 | Himont Inc | PROCEDURE FOR THE GAS PHASE POLYMERIZATION OF OLEFINS |
IT1254279B (en) | 1992-03-13 | 1995-09-14 | Montecatini Tecnologie Srl | PROCEDURE FOR THE GAS PHASE POLYMERIZATION OF OLEFINS |
FI95387C (en) | 1992-12-29 | 1996-01-25 | Borealis As | Process for polymerizing olefins and prepolymerized catalyst composition and process for its preparation |
CA2161419C (en) | 1993-04-26 | 1999-05-04 | Marc Louis Dechellis | Process for polymerizing monomers in fluidized beds |
ZA943399B (en) | 1993-05-20 | 1995-11-17 | Bp Chem Int Ltd | Polymerisation process |
FI96615C (en) | 1993-06-04 | 1996-07-25 | Neste Oy | Process for Polymerization of C4-C40 Olefins or Copolymerization with Other Olefins |
US5453471B1 (en) | 1994-08-02 | 1999-02-09 | Carbide Chemicals & Plastics T | Gas phase polymerization process |
FI96216C (en) * | 1994-12-16 | 1996-05-27 | Borealis Polymers Oy | Process for the production of polyethylene |
JP3355864B2 (en) * | 1995-04-24 | 2002-12-09 | チッソ株式会社 | Continuous production of high-rigidity propylene / ethylene block copolymer |
FI105820B (en) * | 1995-10-10 | 2000-10-13 | Borealis Tech Oy | Process for the preparation of homopolymers or copolymers of propylene |
FI105818B (en) | 1996-03-13 | 2000-10-13 | Borealis Tech Oy | Process for the polymerization of olefin monomers |
FI963707A0 (en) | 1996-09-19 | 1996-09-19 | Borealis Polymers Oy | Free polymerization of an alpha-olefin, by polymerization with an optional catalyst and further preparation of a polymer |
-
1997
- 1997-06-24 FI FI972729A patent/FI111846B/en active
-
1998
- 1998-06-24 DE DE69833324T patent/DE69833324T2/en not_active Expired - Lifetime
- 1998-06-24 JP JP50385599A patent/JP3825478B2/en not_active Expired - Fee Related
- 1998-06-24 CN CNB988085011A patent/CN1140555C/en not_active Expired - Fee Related
- 1998-06-24 ES ES98929462T patent/ES2256942T3/en not_active Expired - Lifetime
- 1998-06-24 WO PCT/FI1998/000555 patent/WO1998058977A1/en active IP Right Grant
- 1998-06-24 AU AU79212/98A patent/AU7921298A/en not_active Abandoned
- 1998-06-24 EP EP98929462A patent/EP0991684B1/en not_active Expired - Lifetime
- 1998-06-24 US US09/446,333 patent/US6469110B1/en not_active Expired - Lifetime
- 1998-06-24 AT AT98929462T patent/ATE316539T1/en not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4740550A (en) * | 1986-06-18 | 1988-04-26 | Shell Oil Company | Multistage copolymerization process |
US4740551A (en) * | 1986-06-18 | 1988-04-26 | Shell Oil Company | Multistage copolymerization process |
WO1997013790A1 (en) * | 1995-10-10 | 1997-04-17 | Borealis A/S | Process for making propylene homo or copolymers |
Non-Patent Citations (2)
Title |
---|
FILE WPI, Derwent Accession No. 83-803582, "Polyolefin mfr. - by Polymerising Olefin in Liq. Propylene, Passing Slurry to Vaporising Tank, Collecting Sepd. Powdery Polyolefin"; & JP,A,58 065 710 (MITSUBISHI CHEM. IND. LTD.) 19-04-83, DW8344. * |
FILE WPI, Derwent Accession No. 91-146186, "Prepn. of Propylene-Ethylene Block Copolymer in Continuous Process - Using Classification Method to Separate Fine and Coarse Polypropylene Particles in Slurry etc."; & JP,A,03 084 014 (MITSUBISHI KASEI CORP.) 09-04-91, DW9120. * |
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US7115687B2 (en) | 2002-10-30 | 2006-10-03 | Borealis Technology Oy | Process and apparatus for producing olefin polymers |
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WO2012000956A1 (en) | 2010-06-29 | 2012-01-05 | Borealis Ag | Process for producing a prepolymerised catalyst, such prepolymerised catalyst and its use for producing a polymer |
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Also Published As
Publication number | Publication date |
---|---|
AU7921298A (en) | 1999-01-04 |
ES2256942T3 (en) | 2006-07-16 |
EP0991684A1 (en) | 2000-04-12 |
ATE316539T1 (en) | 2006-02-15 |
FI111846B (en) | 2003-09-30 |
JP3825478B2 (en) | 2006-09-27 |
JP2002504955A (en) | 2002-02-12 |
FI972729A (en) | 1998-12-25 |
EP0991684B1 (en) | 2006-01-25 |
DE69833324D1 (en) | 2006-04-13 |
FI972729A0 (en) | 1997-06-24 |
US6469110B1 (en) | 2002-10-22 |
CN1268146A (en) | 2000-09-27 |
DE69833324T2 (en) | 2006-09-21 |
CN1140555C (en) | 2004-03-03 |
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