A supported polymerisation catalyst system comprises: (a) a polymerisation catalyst, (b) a cocatalyst, and (c) a porous support, and is characterised in that the porous support has been pretreated with (i) a chemical dehydration agent and (ii) a hydroxy compound wherein the hydroxy compound is not a cocatalyst or component thereof. The preferred polymerisation catalyst is a transition metal compound for example a metallocene and by use of the supported catalyst systems improved activity may be achieved.
C08F 4/64 - Titanium, zirconium, hafnium, or compounds thereof
C08F 4/76 - MetalsMetal hydridesMetallo-organic compoundsUse thereof as catalyst precursors selected from metals not provided for in group selected from refractory metals selected from titanium, zirconium, hafnium, vanadium, niobium, or tantalum
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
C08F 10/00 - Homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
C08F 4/659 - Component covered by group containing a transition metal-carbon bond
C08F 4/6592 - Component covered by group containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
The present invention relates to a process for polymerization of olefins, in particular gas phase polymerization of olefins, with the aid of a supported chromium oxide based catalyst.
Process for the gas-phase polymerization of olefins in a fluidized bed reactor, by a) passing a fluidizing gas containing an olefin monomer through a fluidized bed of polymer particles in the presence of a polymerization catalyst, b) withdrawing a first gaseous stream containing solid particles from the reactor, c) passing the first gaseous stream to a gas/solids separator, separating solid particles, and forming a second gaseous stream containing residual solid particles, d) passing a portion of the second gaseous stream to a heat exchanger(s) to remove heat and e) recycling a portion of the cooled stream from (d) as the fluidizing gas in (a). The fouling rate of the heat exchanger (s) is such that i) the increase in pressure drop across the heat exchanger is equivalent to less than 5%/year, and/or ii) the decrease in heat transfer of the heat exchanger is equivalent to less than 5%/year.
B01J 8/24 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles according to "fluidised-bed" technique
Process for the transition between an ethylene co-polymerization process in a polymerization reactor in the presence of a catalyst and of ethylene E and an olefin co-monomer A to produce an ethylene copolymer PEA into an ethylene co-polymerization process carried out in the same polymerization reactor in the presence of a catalyst and of ethylene E and an olefin co-monomer B to produce an ethylene copolymer PEB. Co-monomers A and B are different and are both present in the reactor during at least part of the transition from PEA to PEB. The transition is performed continuously by (i) starting the transition by stopping steady state production of ethylene copolymer PEA and (ii) ending the transition when steady state production of ethylene copolymer PEB is achieved.
C08F 210/00 - Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
B01J 8/18 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
7.
Apparatus and process for the polymerisation of olefins
Apparatus and process for gas phase polymerisation of olefins. The apparatus includes (a) a reaction zone having a grid at its base, (b) an inlet located in the lower half of the reaction zone for introducing a reaction gas to the reaction zone, (c) an outlet located in the upper half of the reaction zone for removing the reaction gas from the reaction zone, and (d) a solids separation unit having an inlet fluidly connected to the outlet for removing the reaction gas from the reaction zone. The inlet of the solids separation unit is located at a vertical height lower than the outlet for removal of reaction gas from the reaction zone and such that the angle to the horizontal of a straight line drawn between the inlet of the solids separation unit and the outlet for removal of reaction gas from the reaction zone is greater than 20°.
B01J 19/24 - Stationary reactors without moving elements inside
B01J 8/38 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation
C08F 10/00 - Homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
B01J 8/00 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
B01J 8/24 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles according to "fluidised-bed" technique
Process for maintaining a continuous gas-phase (co-) polymerization of olefins in a large fluidized bed reactor in a homogeneous mode while operating at high space time yield and condensation rate in the presence of a polymerization catalyst.
Process for the activation of a supported chromium oxide based catalyst in a fluidized bed activation reactor which has a catalyst bed being fluidized by a fluidization gas. The activation includes treatment at temperatures above 500° C., in which in an initial stage, where there is an initial temperature increase, the fluidization velocity (Vf1) of the fluidization gas is maintained below 6.5 centimeters per second (cm/sec) until the temperature inside the activation reactor reaches at least 200° C., and the fluidization gas is then brought to a value (Vf2) which is at least 1 cm/sec higher than Vf1.
Interlock for use in a process for degassing of a polymer powder in a degassing vessel. The interlock includes the steps of 1. measuring the temperature of the polymer powder within or exiting the degassing vessel, 2. comparing the measurement value to a threshold value in order to ascertain whether it is lower than the threshold value or not, and 3. if the measured temperature is lower than the threshold value taking one or more actions to reduce the concentration of hydrocarbons in the polymer powder exiting the degassing vessel and/or to stop the polymer powder withdrawal from that degassing vessel.
F16B 39/28 - Locking of screws, bolts, or nuts in which the locking takes place during screwing down or tightening by special members on, or shape of, the nut or bolt
Interlock for use in a process for degassing of a polymer powder in a degassing vessel. The interlock includes (a) measuring the temperature of the vapor phase resulting from a liquid-vapor separation, which vapor phase is used as a purge gas in a degassing vessel, (b) comparing the measured temperature to a threshold value, and (c) in the event that the measured temperature is above the threshold value then use of the vapor as purge gas is stopped or reduced.
The present invention relates to production of polymer, and in particular provides an interlock for use in a process for production of a polymer in a reactor, which process comprises: a. polymerising a monomer and optionally a comonomer in the reactor to produce polymer, optionally in the presence of an inert hydrocarbon, and b. withdrawing produced polymer from the reactor, said interlock being based on the temperature in the reactor, and comprising: 1. measuring the temperature in the reactor or a temperature representative of the temperature in the reactor, and 2. comparing said measured temperature to a threshold temperature, said interlock being characterized in that withdrawal is allowed if the measured temperature is greater than the threshold temperature but is prevented if the measured temperature is lower than the threshold temperature.
F16B 39/28 - Locking of screws, bolts, or nuts in which the locking takes place during screwing down or tightening by special members on, or shape of, the nut or bolt
Process for the continuous transition between two ethylene copolymers containing a different comonomer. In particular, the process is for the continuous transition between two ethylene copolymers containing a different comonomer.
C08F 210/00 - Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
B01J 8/18 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles
C08F 2/38 - Polymerisation using regulators, e.g. chain terminating agents
B01J 8/24 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles according to "fluidised-bed" technique
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
Polymer powder vessel having a silo including a main vertical cylinder and a hopper at the bottom of the cylinder, a polymer powder which occupies the full volume of the hopper and at least a part of the volume of the cylinder, a polymer powder silo inlet pipe connected to the silo at a height located above the polymer powder, and a polymer hopper withdrawal pipe is also connected to the hopper. The polymer powder hopper withdrawal pipe is also connected to the silo at a location above the polymer powder for recirculating a part of the polymer powder within the silo.
2 and an outer tube forming an annulus around the inner tube with a cross-sectional area of 1-10 times the internal cross-sectional area of the inner tube. The polymerization catalyst and a carrier gas are passed through the inner tube into the gas-phase fluidized bed at a carrier gas linear velocity of 4-14 m/s and a carrier gas mass flow rate of 10-35 kg/h. A shielding gas is passed through the outer tube and into the gas-phase fluidized bed at a shielding gas linear velocity of 1-10 times the linear velocity of the carrier gas through the inner tube and at a shielding gas mass flow rate of 100-500 kg/h. No cooled recycle process gas is provided to the injection device.
Process for producing a degassed polymer powder, by a) feeding i) a principal monomer, and ii) one or more comonomers in an amount of at least 5000 ppmw relative to the principal monomer feed rate, and iii) optionally an added alkane having 2 to 10 carbon atoms, fed in an amount of at least 1000 ppmw relative to the principal monomer feed rate; into a polymerization reactor. The monomer and comonomers react to form a polymer including residual hydrocarbons having one or more hydrocarbons with 3 to 10 carbon atoms, and b) passing the polymer to a degassing step where it is contacted with a purge gas to remove some of the residual hydrocarbons.
Method for transitioning from a first process for producing a first polymer to a second process for producing a second polymer. The first and second processes each include contacting a principal olefin and a comonomer with a catalyst under gas phase polymerization conditions to form the first or second polymer. The first and second processes utilize the same olefin but differ in at least one of the comonomer used and the reaction temperature at which the polymer is produced. The respective first or second polymer is then contacted with a purge gas to remove unreacted monomers. The method includes changing the flow rate of purge gas from a first rate to a second rate defined relative to a flow rate and temperature used for an earlier polymer produced using the same comonomer as the second process.
2 and an outer tube forming an annulus around the inner tube with a cross-sectional area of 1 to 10 times the internal cross-sectional area of the inner tube. The polymerization catalyst and a carrier gas are passed through the inner tube and into the gas-phase fluidized bed at a carrier gas linear velocity of 4 to 14 m/s and a carrier gas mass flow rate of 10-35 kg/h. A shielding gas is passed through the outer tube and into the gas-phase fluidized bed at a linear velocity of 1 to 10 times the carrier gas linear velocity through the inner tube and at a mass flow rate of 100-500 kg/h. No cooled recycle process gas is provided to the injection device.
C08F 2/01 - Processes of polymerisation characterised by special features of the polymerisation apparatus used
B01J 8/24 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with fluidised particles according to "fluidised-bed" technique
23.
Apparatus and process for gas phase fluidised bed polymerisation reaction
B29C 47/00 - Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor (extrusion blow-moulding B29C 49/04)
A method for the preparation of copolymers of ethylene and α-olefins having a fraction (%) of the molecular weight component of >1,000,000 of less than 6% comprises polymerising ethylene and an α-olefin in the presence of a supported polymerisation catalyst system comprising (a) a transition metal compound (b) a porous support material, and (c) an activator characterized in that the support material has been (i) dried at a temperature in the range 0° C. to 195° C. in an inert atmosphere, and (ii) treated with an organometallic compound. The resultant supported catalyst systems show improved productivity and allow for control of the resultant polymer properties. Particularly preferred supported catalyst systems are those comprising metallocene complexes.
C08F 4/64 - Titanium, zirconium, hafnium, or compounds thereof
C08F 4/6592 - Component covered by group containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
C08F 4/6592 - Component covered by group containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
Process for producing homopolymers or copolymers of conjugated dienes by contacting monomeric material having at least one conjugated diene with a catalyst system including two or more different transition metal compounds and optionally one or more activators. Preferred transition metal compounds are based on cobalt and chromium, especially complexes thereof having benzimidazole ligands.
C08F 4/06 - Metallic compounds other than hydrides and other than metallo-organic compoundsBoron halide or aluminium halide complexes with organic compounds containing oxygen
C08F 4/26 - Metallic compounds other than hydrides and other than metallo-organic compoundsBoron halide or aluminium halide complexes with organic compounds containing oxygen of manganese, iron group metals, or platinum group metals
C08F 4/70 - Iron group metals, platinum group metals, or compounds thereof
C08F 4/80 - MetalsMetal hydridesMetallo-organic compoundsUse thereof as catalyst precursors selected from metals not provided for in group selected from iron group metals or platinum group metals
C08F 136/00 - Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
B01J 23/00 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group
2 are donor atoms or groups; X is an anionic group, L is a neutral donor group; n=m=zero or 1; y and z are independently zero or integers such that the number of X and L groups satisfy the valency and oxidation state of the metal M.
C08F 4/602 - Component covered by group with an organo-aluminium compound
C08F 236/20 - Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds unconjugated
A complex compound comprising the skeletal unit of Formula A,
2 are each selected from chlorine, bromine or iodine; x is zero or 1, O is oxygen, E is nitrogen, phosphorus or arsenic, Q represents a divalent bridging group comprising one or more Group 14 atoms; M is a metal selected from Groups 3 to 7; X represents a monovalent atom or group covalently or ionically bonded to M; L is a mono- or bidentate molecule datively bound to M, y satisfies the valency of M and z is from 0 to 5. The complex can be used to polymerise olefins optionally with organo-A1 or -B compounds as activator.
The present invention provides a process for preparing a catalyst useful in gas phase polymerization of olefins wherein the hydrogen response of the catalyst can be improved by using a ketone as the electron donor in the catalyst. The catalyst consists of compounds of Ti, Mg, Al and a ketone preferably supported on an amorphous support.
The present invention provides a process for preparing a catalyst useful in gas phase polymerization of olefins wherein the hydrogen response of the catalyst can be improved by using a ketone as the electron donor in the catalyst. The catalyst consists of compounds of Ti, Mg, Al and a ketone preferably supported on an amorphous support.
Process for producing homopolymers or copolymers of conjugated dienes by contacting monomeric material including at least one conjugated diene with a catalyst system comprising (A) a first transition metal compound selected from Cr, Mo and W compounds, and a second transition metal compound selected from Fe, Co and Ni compounds, (B) a catalyst modifier and, optionally, (C) one or more catalyst activators.
C08F 4/69 - Chromium, molybdenum, tungsten or compounds thereof
C08F 4/70 - Iron group metals, platinum group metals, or compounds thereof
C08F 36/04 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
3, (b) a molecular weight distribution (Mw/Mn) in the range 3.5 to 4.5, (c) a melt elastic modulus G′ (G″=500 Pa) in the range 40 to 150 Pa, (d) an activation energy of flow (Ea) in the range 28-45 kJ/mol, and (e) a melt index (g/10 ml) in the range 1.0-3.5. The copolymers are suitably prepared in the gas phase by use of a supported metallocene catalyst system. The copolymers show improved processability and are particular suitable for use in blown film applications.
C08F 210/16 - Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
C08F 4/6592 - Component covered by group containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Chemicals; polyolefins and mixtures and chemically modified derivatives thereof, all being chemical substances; chemical compositions prepared from the aforesaid goods; unprocessed artificial resins; unprocessed plastics. Plastics in the form of sheets, blocks, rods and tubes; semiprocessed plastics; plastics film other than for wrapping; plastics in extruded form for manufacture; components and assemblies in moulded form for use in manufacture; packing and insulating materials; polyolefin fibres not for textile use.
A supported catalyst for olefin polymerization comprises a selected ionic activator, a selected organometallic catalyst and a support material. The selected activator must contain an active hydrogen moeity. The organometallic catalyst is characterized by having a phosphinimine ligand and a substituted cyclopentadienyl ligand (which contains from 7 to 30 carbon atoms). The supported catalyst exhibits excellent activity in gas phase olefin polymerizations and may be used under substantially “non-fouling” polymerization conditions.
C08F 4/6592 - Component covered by group containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
B01J 31/14 - Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
The use of high activity “Single Site” polymerization catalysts often causes the fouling of polymerization reactors. The problem is particularly acute with gas phase polymerizations. While not wishing to be bound by theory it is believed that the fouling is initiated by the buildup of static charges in the reactor. The use of anti-static agents mitigates this problem, but typical antistatic agents contain polar species, which can deactivate the polymerization catalyst. We have now discovered that the use of a porous metal oxide support allows large levels of a selected antistatic agent to be used in a manner that reduces static/fouling problems in highly active polymerization catalysts.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Chemical products for use in industry and manufacture; artificial and synthetic resins; plasticizers; ethylene, propylene, butadiene, styrene; polyethylene, polypropylene, polybutenes, polystyrene; polyalphaolefins; linear alpha olefins; polyolefins and derivatives thereof all being chemical substances; chemical compositions prepared from the aforesaid goods all for use in the manufacture of plastics and articles made from plastics. Plastics and synthetic resins in semi-processed form; plastics in extruded form for use in manufacture or packing; plastics in sheet, rod, film or tube form; plastics in fibre form (not for textile use); compounds of plastics (semi-processed); compounds of synthetic resins (semi-processed) components and assemblies in moulded form for use in manufacture; packing, stopping and insulating materials.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Chemical products for use in industry and manufacture;
artificial and synthetic resins; plasticizers; ethylene,
propylene, butadiene, styrene; polyethylene, polypropylene,
polybutenes, polystyrene; nitriles, acetonitrile, hydrogen
cyanide, acetone cyanhydrin, oxazole, butanediols;
oxygenated solvents, ethanol, glycol ethers and esters;
polyalphaolefins; linear alpha olefins; detergents and
degreasing agents; polyolefins and derivatives thereof all
being chemical substances; chemical compositions prepared
from polyolefins and derivatives thereof all for use in the
manufacture of plastics and articles made from plastics. Plastics and synthetic resins in semi-processed form;
plastics in extruded form for use in manufacture or packing;
plastics in sheets, rod, film or tube form; plastics in
fibre form (not for textile use); compounds of plastics
(semi-processed); compounds of synthetic resins
(semi-processed) components and assemblies in moulded form
for use in manufacture; packing, stopping and insulating
materials.
39.
POLYMER BLENDS COMPRISING ETHYLENE/.ALPHA.OLEFIN COPOLYMERS AND LOW DENSITY POLYETHYLENE
Novel polymer blends comprise (a) 1 - 99% by weight of a copolymer of ethylene and an alpha olefin having from 3 to 10 carbon atoms, said copolymer having (iv) a density in the range 0.905 to 0.940 g cm-3, (v) a melt elastic modulus G' (G"= 500 Pa) in the range 10 to 150 Pa, and (vi) a melt index in the range 5 to 50, and (b) from 1 - 99% by weight of a low density polyethylene (LDPE) polymer having a density from 0.914 to 0.928 g cm-3 wherein the sum of (a) and (b) is 100 %. The copolymers of component (a) are typically prepared by use of metallocene catalysts. The blends exhibit advantageous melt elastic modulus in the range 30 to 200 Pa. The blends are particularly suitable for extrusion coating applications.
01 - Chemical and biological materials for industrial, scientific and agricultural use
04 - Industrial oils and greases; lubricants; fuels
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Chemical products for use in industry and manufacture; artificial and synthetic resins; plasticizers; ethylene, propylene, butadiene, styrene; polyethylene, polypropylene, polybutenes, polystyrene; nitriles, acetonitrile, hydrogen cyanide, acetone cyanhydrin, oxazole, butanediols; oxygenated solvents, ethanol, glycol ethers and esters; polyalphaolefins; linear alpha olefins; detergents and degreasing agents, polyolefins and derivatives thereof all being chemical substances; chemical compositions prepared from polyolefins and derivates thereof all for use in the manufacture of plastics and articles made from plastics; synthetic fluids for industrial use namely chemical petroleum additives, hydraulic fluids, heat transfer fluids, refrigerant fluids, and chemicals for use in oil drilling processes. Industrial oils and greases (other than edible oils and fats and essential oils); lubricants. Plastics and synthetic resins in semi-processed form; plastics in extruded form for use in manufacture or packing; plastic in sheet, rod, film or tube form; plastics in fibre form (not for textile use); compounds of plastics (semi-processed); compounds of synthetic resins (semi-processed) components and assemblies in moulded form for use in manufacture; packing, stopping and insulating materials.