Classifications

• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
  • B01J37/0027—Powdering
• • 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
  • C08F10/02—Ethene
• • 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
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
  • B01J23/24—Chromium, molybdenum or tungsten
  • B01J23/26—Chromium
• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/08—Heat treatment
• • 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
  • C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
  • C08F110/02—Ethene

Definitions

• the present invention relates to a method for producing Phillips catalysts, in which an oxidic support material in a suspension is treated with a chromium salt solution and then, after removal of the solvent, is calcined in an oxygen-containing atmosphere at temperatures above 300 ° C.
• a method of this kind is known and is e.g. in the
• the catalysts produced thereafter are also comminuted and have particle sizes in the range from 20 to 2000 ⁇ m, in particular from 40 to 300 ⁇ m.
• This object is achieved by a method of the type mentioned at the outset, the characteristic features of which can be seen in the fact that the oxidic support material before the calcination and / or the catalyst after the calcination are comminuted until an average grain size of ⁇ 100 ⁇ m is reached is, the particle proportion with a grain size of ⁇ 50 microns is at least 30%.
• a silica gel is used as the oxidic carrier material, which has a solids content, calculated as silicon dioxide, in the range from 10 to 30% by weight, preferably from 11 to 25% by weight, and which is largely spherical.
• a silica gel is obtained by introducing a solution containing sodium or potassium water glass into a swirling stream of a mineral acid along and tangential to the direction of flow of the stream and spraying the resulting silicic acid hydrosol into a gaseous medium in drops. The sprayed hydrosol then solidifies in the gaseous medium and is freed of adhering salts by washing with water.
• the spherical hydrosol is then treated with an organic liquid from the series of alcohols with 1 to 4 carbon atoms until at least 60% of the water contained in the hydrosol is extracted. Then the dewatered hydrogel treated with the alcoholic liquid is dried until the residual alcohol content is below 10% by weight at temperatures of> 160 ° C. using an inert entraining gas.
• the xerogel obtained in this way is then made from a 0.05 to 5% by weight solution of chromium trioxide in a ketone with 3 to 5 C atoms or from a 0.05 to 15% by weight solution of one under the conditions
• the chromium compound which is calcined in chromium trioxide is loaded with chromium in an alcohol having 1 to 4 carbon atoms and then the solvent is evaporated off in vacuo.
• the oxidic carrier material loaded with chromium is kept in a water-free gas stream containing oxygen for a period of 10 to 1000 minutes at a temperature in the range of 300 to 1100 ° C.
• the inventive reduction of the oxidic carrier material or the catalyst material obtained as described above is carried out by dry grinding with a ball mill or in a fan-type beater mill, as described for example in DE-A 36 40 802. By taking samples at certain times Intervals determines the length of time for grinding, which is necessary to achieve the desired grain size.
• the polymerization itself is carried out at temperatures in the range from 30 to 150 ° C. under a pressure in the range from 0.2 to 10 15 MPa.
• 25 polyethylene can achieve results comparable to those obtained with conventional catalysts with grain sizes of> 100 ⁇ m.
• the method according to the invention provides particularly optimal results if the particle proportion with a grain size of ⁇ 50 ⁇ m is in the range from 40 to 80%.
• the catalyst support was produced as in the
• the catalyst carrier was produced as in Example 1, with the exception that the particle fraction with a grain size of ⁇ 50 ⁇ m was only 30%.
• the catalyst carrier was produced as in Example 1, with the exception that the particle fraction with a grain size of ⁇ 50 ⁇ m was only 15%.
• the catalyst was prepared as in Example 1 according to DE-A 36 40 802 (page 7, line 15).
• the carrier particles had an average grain size in the range from 50 to 100 ⁇ m (page 8, line 26).
• the catalyst was produced as in comparative experiment 1 according to DE-A 36 40 802 (page 9, line 16).
• the carrier particles had an average grain size in the range from 1 to 300 ⁇ m.
• Catalyst 1 was prepared in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), with the exception that 15 kg of the oxidic support material from Example 1 were used.
• Catalyst 2 was prepared in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), with the exception that 15 kg of the oxidic support material from Example 1 were used.
• Catalyst 2 was prepared in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), with the exception that 15 kg of the oxidic support material from Example 1 were used.
• Catalyst 2 was prepared in accordance with Example 1 of
• Comparative catalyst 3 was produced in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), with the exception that 15 kg of the oxidic support material from Example 3 were used.
• Comparative catalyst 4 was produced in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), 15 kg of the oxidic support material from Example 4 as described in DE-A 36 40 802 being used.
• Comparative catalyst 5 was produced in accordance with Example 1 of DE-A 36 40 802 (page 8, line 31), 15 kg of the oxidic support material from Example 5 as described in DE-A 36 40 802 being used.
• a conventional and known loop reactor was used for the polymerization of ethylene, the reaction chamber of which consisted of a tube circle of 6 m3 content.
• the reaction space contained a suspension of liquid i-butane, polyethylene solid, 6% by weight of dissolved ethene and 0.4% by weight of dissolved hexene-1 at a pressure of 4.0 MPa.
• the polymerization temperature was 103.5 to 103.8 ° C.
• the suspension was pumped through a propeller pump at 3000 rpm. With a constant reactor output of 900 kg PE / h, attempts were made to set the polyethylene solids content in the suspension as high as possible. The realizable PE solids content was limited by reactor fouling (build-up on the reactor walls or faults in the power consumption of the propeller pump).
• the following table shows the results obtained with catalysts 1 to 5:
• the polyethylene bulk density and the fine or coarse grain fraction ( ⁇ 125 ⁇ m,> 2000 ⁇ m) are practically unchanged in the examples according to the invention and at the same level as in the comparative examples.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Medicinal Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Polymers & Plastics (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Polymerization Catalysts (AREA)
• Catalysts (AREA)

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• 1999
  • 1999-09-09 DE DE19943206A patent/DE19943206A1/de not_active Withdrawn
• 2000
  • 2000-08-31 KR KR1020027003073A patent/KR100685331B1/ko not_active Expired - Fee Related
  • 2000-08-31 JP JP2001521458A patent/JP2003517506A/ja active Pending
  • 2000-08-31 EP EP00960568A patent/EP1218102B1/de not_active Revoked
  • 2000-08-31 US US10/070,805 patent/US6699947B1/en not_active Expired - Fee Related
  • 2000-08-31 AU AU72821/00A patent/AU7282100A/en not_active Abandoned
  • 2000-08-31 AT AT00960568T patent/ATE268219T1/de not_active IP Right Cessation
  • 2000-08-31 WO PCT/EP2000/008508 patent/WO2001017676A1/de not_active Ceased
  • 2000-08-31 CN CNB008127433A patent/CN1134298C/zh not_active Expired - Fee Related
  • 2000-08-31 ES ES00960568T patent/ES2220534T3/es not_active Expired - Lifetime
  • 2000-08-31 DE DE50006697T patent/DE50006697D1/de not_active Expired - Lifetime

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