WO2001025286A1 - Gasphasenpolymerisationsverfahren - Google Patents
Gasphasenpolymerisationsverfahren Download PDFInfo
- Publication number
- WO2001025286A1 WO2001025286A1 PCT/EP2000/009474 EP0009474W WO0125286A1 WO 2001025286 A1 WO2001025286 A1 WO 2001025286A1 EP 0009474 W EP0009474 W EP 0009474W WO 0125286 A1 WO0125286 A1 WO 0125286A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polymerization
- zone
- settling
- mixture
- gas phase
- Prior art date
Links
Classifications
-
- 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
- C08F6/00—Post-polymerisation treatments
- C08F6/001—Removal of residual monomers by physical means
- C08F6/005—Removal of residual monomers by physical means from solid polymers
-
- 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
- B01J8/005—Separating solid material from the gas/liquid stream
- B01J8/007—Separating solid material from the gas/liquid stream by sedimentation
-
- 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
- B01J8/08—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
- B01J8/10—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by stirrers or by rotary drums or rotary receptacles or endless belts
-
- 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
- B01J8/1872—Details of the fluidised bed reactor
-
- 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
-
- 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
Definitions
- the invention relates to a process for the polymerization of gaseous, unsaturated monomers, in particular ethylene and at least one ⁇ -olefin in the gas phase, and a device for carrying out such a process.
- Gas phase polymerization processes have been practiced on an industrial scale for many years, but they still have one or two disadvantages.
- One such field of work is the transition between the actual polymerization zone and the generally subsequent relaxation zone for the mixture of solid (co) polymer, unreacted monomer or unreacted monomers and inerts leaving the polymerization zone.
- EP-B 0 341 540 describes a process for the continuous production of copolymers from ethylene and ⁇ -olefins, in which the monomers are reacted by catalytic dry-phase copolymerization in a stirred or swirled polymerization zone (for example a fluidized bed reactor). The resulting mixture of solid copolymer and unreacted gaseous monomers is transferred to a de-steaming zone. After this pressure reduction, the mixture is separated into a solid and a gaseous phase.
- the procedure is such that the solid phase is rinsed with gaseous ethylene and then rinsed with an N 2 / H 2 O vapor mixture (in each case in a shaft apparatus).
- the gaseous phases can be returned to the process, and the copolymer is largely free of residual monomers, odors and flavors.
- this preparation can lead to the formation of specks, which severely impair the usability of the (co) polymer.
- this contains, for example, a pointed roof or umbrella-shaped installation which divides the boiler into a first zone of treatment with the first dry / flushing gas and a second zone of treatment with the second dry / flushing gas, and which also serves collect this second dry / purge gas after use in the second zone and remove it from the boiler.
- the cylindrical kettle is curved upwards at the upper end and tapers at the lower end, so that the outlet for the dry polymer lies at the lowest point of the kettle.
- the presence of catalyst and supplied polymerizable monomer results in postpolymerization, which - as already mentioned - can lead to speck formation.
- the process according to the invention found as a solution to this problem is based on the known process for the polymerization of gaseous olefins, in particular ethylene and at least one ⁇ -olefin, in the gas phase in a stirred or swirled polymerization zone containing catalyst and at least one polymerization zone subsequent relaxation zone.
- the process according to the invention is then characterized in that the mixture of solid (co) polymer and unreacted monomers leaving the polymerization zone passes through a settling zone before the relaxation zone.
- the settling area is preferably realized by so-called settling legs, the opening of which protrudes into the polymerization zone; in the settling leg the gas and heat exchange with the reactor are largely interrupted.
- the polymerization preferably relates to the production of copolymers, but it can also be used to produce homopolymers, e.g. made of ethylene or propylene.
- the mixture passes through a settling leg
- the co-component is only an ⁇ -olefin, in particular 1-hexene
- the mixture in the settling leg heats up by at least 1 K, preferably by at least 2 K, measured between its temperature when it enters the Leg and when it exits.
- Another solution is a device for performing a gas phase Polymerization containing
- reaction kettle in a) and a treatment kettle for relaxation, and the device has a plurality of settling legs, wherein devices with only one settling leg are also possible on the reaction kettle.
- Figure 1 is a schematic representation of the structure of a conventional plant for gas phase polymerization and in
- FIG. 2 shows the part of a reaction container which has the installation of a settling leg according to the invention.
- the gaseous reaction mixture from the reaction vessel 1, in which it flows upwards through a stirred or swirled polymerization zone 2, which contains the catalyst and the solid mono- or copolymer formed, is returned to the boiler 1 in the circuit 3.
- the catalyst is introduced into the boiler 1 in partial steps or continuously via the inlet 4.
- the crude product of the polymerization - essentially comprising solid (co) polymer, catalyst components and unreacted monomers - is removed in partial steps or continuously, expanded in a first treatment vessel 6 and rinsed with, for example, N 2 , which flows over the Line 7 is introduced. Residual monomers removed from the solid polymer can thus be returned to reaction vessel 1 via outlet 8.
- the pre-rinsed polymer is brought via line 9 from the first treatment vessel 6 into a second treatment vessel 10, in which it can additionally be deodorized, for example with the aid of an N 2 / H 2 O vapor mixture introduced via line 11 to be removed from the system via the outlet 12. Residual monomers that are still present are fed via outlet 13, for example to catalytic exhaust gas combustion.
- FIG. 2 shows the part of a reaction vessel, for example a reaction vessel 1, which contains the installation of a so-called settling leg 14 according to the invention.
- a reaction vessel for example a reaction vessel 1, which contains the installation of a so-called settling leg 14 according to the invention.
- This is understood to mean a generally tubular plant part with a different cross section, for example is arranged between the actual reaction part of a reaction container and the outlet for the reaction product, and in which a solid reaction product formed can settle.
- a strut contains an outlet 15, which can be a valve, for example.
- the inlet opening 16 of the settling leg is arranged in the reaction vessel 1 in such a way that it is located in the lower part of the polymerization zone 2, the outer tube wall half, as viewed from the center of the vessel, being integrated into the inner wall of the vessel near the opening.
- the inner half of the raw wall is then inside the boiler.
- Most of the settling leg 14, which means at least 60% of its total length, is located outside the reaction vessel 1.
- the polymer which can be removed from the settling leg can then be fed to a conventional expansion tank, for example a first treatment vessel 6 or a second treatment vessel 10 as shown in FIG ,
- ethylene and 1-hexene were placed over a conventional chromium-containing catalyst supported on SiO 2, which was treated over a period of 2 hours at a temperature of 700 ° C. copolymerized.
- the crude product (150 kg) had a density of 0.942 g / cm 3 , the average particle size was 800 ⁇ m, measured according to Rosin, Rammler, Sperling, Bennett, DIN 66145, and the density of the fluidized bed was 290 kg / m 3 .
- the part outside the reactor was thermally insulated.
- the set residence time of the reaction mixture was 1 min in the weaning leg. During this time, the temperature of the product to be discharged rose by 3 K.
- a copolymer was produced in the gas phase reactor under the same conditions as in Example 1, but the product was immediately transferred to the expansion tank without an additional dwell time in the settling leg. The results are shown in the table below:
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU10200/01A AU1020001A (en) | 1999-10-06 | 2000-09-28 | Gas phase polymerization method |
US10/089,749 US6596822B1 (en) | 1999-10-06 | 2000-09-28 | Gas phase polymerization method |
DE50006763T DE50006763D1 (de) | 1999-10-06 | 2000-09-28 | Gasphasenpolymerisationsverfahren |
EP00971293A EP1226182B1 (de) | 1999-10-06 | 2000-09-28 | Gasphasenpolymerisationsverfahren |
JP2001528452A JP3834235B2 (ja) | 1999-10-06 | 2000-09-28 | 気相重合法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19948280.2 | 1999-10-06 | ||
DE19948280A DE19948280A1 (de) | 1999-10-06 | 1999-10-06 | Gasphasenpolymerisationsverfahren |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001025286A1 true WO2001025286A1 (de) | 2001-04-12 |
Family
ID=7924794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2000/009474 WO2001025286A1 (de) | 1999-10-06 | 2000-09-28 | Gasphasenpolymerisationsverfahren |
Country Status (7)
Country | Link |
---|---|
US (1) | US6596822B1 (de) |
EP (1) | EP1226182B1 (de) |
JP (1) | JP3834235B2 (de) |
CN (1) | CN1159347C (de) |
AU (1) | AU1020001A (de) |
DE (2) | DE19948280A1 (de) |
WO (1) | WO2001025286A1 (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1332746C (zh) * | 2003-07-31 | 2007-08-22 | 中国石油化工股份有限公司 | 一种气固反应设备 |
CN101884897B (zh) * | 2004-03-31 | 2012-05-30 | 中国石油化工股份有限公司 | 一种气体与固体颗粒反应的方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4665143A (en) * | 1982-07-12 | 1987-05-12 | Cities Service Oil & Gas Corp. | Co-catalyst dispersion method |
EP0341540A2 (de) * | 1988-05-06 | 1989-11-15 | BASF Aktiengesellschaft | Verfahren zur Niederdruckcopolymerisation von Ethylen mit alpha-Olefinen und Ethylencopolymerisate mit niederem Restmonomerengehalt |
EP0415427A2 (de) * | 1989-08-30 | 1991-03-06 | Phillips Petroleum Company | Verfahren zur Rückgewinnung von Polymer |
EP0728772A1 (de) * | 1995-02-24 | 1996-08-28 | BP Chemicals Limited | Verfahren zur Olefinpolymerisation in der Gasphase |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5799412A (en) | 1996-04-11 | 1998-09-01 | Mitsui Petrochemical Industries, Ltd. | Drying solid polymer apparatus |
-
1999
- 1999-10-06 DE DE19948280A patent/DE19948280A1/de not_active Withdrawn
-
2000
- 2000-09-28 US US10/089,749 patent/US6596822B1/en not_active Expired - Fee Related
- 2000-09-28 AU AU10200/01A patent/AU1020001A/en not_active Abandoned
- 2000-09-28 EP EP00971293A patent/EP1226182B1/de not_active Revoked
- 2000-09-28 WO PCT/EP2000/009474 patent/WO2001025286A1/de active IP Right Grant
- 2000-09-28 CN CNB008139164A patent/CN1159347C/zh not_active Expired - Fee Related
- 2000-09-28 DE DE50006763T patent/DE50006763D1/de not_active Revoked
- 2000-09-28 JP JP2001528452A patent/JP3834235B2/ja not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4665143A (en) * | 1982-07-12 | 1987-05-12 | Cities Service Oil & Gas Corp. | Co-catalyst dispersion method |
EP0341540A2 (de) * | 1988-05-06 | 1989-11-15 | BASF Aktiengesellschaft | Verfahren zur Niederdruckcopolymerisation von Ethylen mit alpha-Olefinen und Ethylencopolymerisate mit niederem Restmonomerengehalt |
EP0415427A2 (de) * | 1989-08-30 | 1991-03-06 | Phillips Petroleum Company | Verfahren zur Rückgewinnung von Polymer |
EP0728772A1 (de) * | 1995-02-24 | 1996-08-28 | BP Chemicals Limited | Verfahren zur Olefinpolymerisation in der Gasphase |
Also Published As
Publication number | Publication date |
---|---|
CN1159347C (zh) | 2004-07-28 |
US6596822B1 (en) | 2003-07-22 |
DE50006763D1 (de) | 2004-07-15 |
AU1020001A (en) | 2001-05-10 |
EP1226182B1 (de) | 2004-06-09 |
JP3834235B2 (ja) | 2006-10-18 |
EP1226182A1 (de) | 2002-07-31 |
DE19948280A1 (de) | 2001-04-12 |
JP2003511487A (ja) | 2003-03-25 |
CN1378562A (zh) | 2002-11-06 |
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