WO2012036848A1 - Supported metallocene catalysts - Google Patents
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- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
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- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
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- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/10—Polymerisation reactions involving at least dual use catalysts, e.g. for both oligomerisation and polymerisation
- B01J2231/12—Olefin polymerisation or copolymerisation
- B01J2231/122—Cationic (co)polymerisation, e.g. single-site or Ziegler-Natta type
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- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
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- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
- C08F4/65927—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually bridged
Definitions
- This invention relates to catalysts and processes for the production of isotactic ethylene-propylene copolymers and more particularly to supported bridged cyclopentadienyl- fluorenyl metallocenes which are supported on alumoxane-treated silica supports and their use in polymerizing isospecific ethylene-propylene copolymers.
- Cyclopentadienyl-fmorenyl based metallocene catalysts are effective catalysts in the polymerization, including homopolymerization or copolymerization of olefin monomers such as ethylene, propylene and higher olefins or other ethylenically unsaturated monomers.
- olefin monomers such as ethylene, propylene and higher olefins or other ethylenically unsaturated monomers.
- Such metallocenes typically have metallocene ligand structures characterized by bridged cyclopentadienyl and fhiorenyl groups.
- An example is isopropylidene
- cyclopentadienyl (fluorenyl) zirconium dichloride.
- the cyclopentadienyl group or the fluorenyl group or both can be modified by the inclusion of substituent groups in the cyclopentadienyl ring or the fluorenyl group which modifies the structure of the catalyst and ultimately the characteristics of the polymers produced.
- olefin polymers such as polyethylene, polypropylene, which may be atactic or stereospecific such as isotactic or syndiotactic, and ethylene-higher alpha olefn copolymers such as ethylene propylene copolymers, can be produced under various polymerization conditions and employing various polymerization catalysts.
- the metallocene catalysts based upon a bridged cyclpentadienylf!uorenyl ligand structure can be produced by the reaction of 6,6-dimethyl fulvene, which may be substituted or unsubstituted with fluorene, which in turn may be substituted or unsubstituted, to produce the bridged isopropylidene cyclopentadienylfluorenyl ligand structure.
- This ligand is, in turn, reacted with a transition metal halide such as zirconium tetrachloride to produce the bridged zirconium dichloride compound.
- Fluorenyl ligand may be characterized by a numbering scheme for the fluorenyl ligand in which the number 9 indicates the bridgehead carbon atom. The remaining carbon atoms available to accept substiuents are indicated by numbers 1-4 for one C6 ring of the fluorenyl ligand, and by numbers 5-8 for the other C6 ring of the fluorenyl ligand.
- the cyclopentadienyl group produced by the 6,6 dimethy fulvene may be characterized by a numbering scheme in which 1 designates the bridge head carbon atom, with numbers 2 and 5 designating the proximal carbon atoms and 3 and 4 the distal atoms.
- Alpha olefin homopolymers or copolymers may be produced using metallocene catalysts under various conditions in polymerization reactors which may be batch type reactors or continuous reactors.
- Continuous polymerization reactors typically take the form of loop-type reactors in which the monomer stream is continuously introduced into the reactor and a polymer product is continuously withdrawn.
- polymers such as polypropylene, polyethylene or ethylene-propylene copolymers involve the introduction of a monomer stream into the continuous loop-type reactor along with an appropriate catalyst system to produce the desired olefin homopolymer or copolymer.
- the resulting polymer is withdrawn from the loop-type reactor in the form of a "fluff which is then processed to produce the polymer as a raw material in particulate form as pellets or granules.
- a "fluff which is then processed to produce the polymer as a raw material in particulate form as pellets or granules.
- C 3+ alpha olefins such as propylene, 1- butene, 4-methyl-l pentene, 1-hexene, 1-octene, or substituted ethylenically unsaturated monomers such as styrene or vinyl chloride
- the resulting polymer product may be characterized in terms of stereoregularity, for example, isotactic polypropylene or syndiotactic polypropylene.
- isotactic polypropylene can be described as one having the methyl groups attached to the tertiary carbon atoms of successive monomelic units falling on the same side of a hypothetical plane through the main chain of the polymer, e.g., the methyl groups are all above or below the plane.
- the stereochemical sequence of isotactic polypropylene is described as follows:
- each vertical segment indicates a methyl group on the same side of the polymer backbone.
- Another way of describing the structure is through the use of NMR. Bovey's NMR nomenclature for an isotactic pentad as shown above is ...mmmm...with each "m” representing a "meso" dyad, or successive pairs of methyl groups on the same side of the plane of the polymer chain. As is known in the art, any deviation or inversion in the structure of the chain lowers the degree of isotacticity and ciystallinity of the polymer.
- the supported catalyst composition of the present invention comprises a metallocene catalyst component supported on a particulate silica support having an average particle size within the range of 10-40 microns, a pore volume within the range of 1.3- 1.6 ml/g, and a surface area within the range of 200-400 m2/g.
- An alkylalumoxane cocatalyst component is incorporated onto said silica support in an amount to provide a weight ratio of alumoxane to silica within the range of 0.6-0.8.
- the isospecific metallocene catalyst component is supported on said particulate silica support in an amount of at least 0.5 weight percent of the silica and alkylalumoxane and is characterized by the formula:
- Cp is a substituted cyclopentadienyl group
- Fl is a fiuorenyl group substituted at the 2 and 7 positions
- Ra is a substituent on the cyclopentadienyl group which is in a distal position to the bridge and comprises a bulky group of the formula XR* 3 in which X is carbon or silicon and R* is the same or different and is chosen from hydrogen or a hydrocarbyl group having from 1-20 carbon atoms, provided that at least one R* is not hydrogen
- Rb is a substituent on the cyclopentadienyl ring which is proximal to the bridge and positioned non- vicinal to the distal substituent and is of the formula YR# 3 in which Y is silicon or carbon and each R# is the same or different and chosen from hydrogen or a hydrocarbyl group, an alkoxy group, a thioalky group, or an amino, alkyl group containing from 1 to 7 carbon atoms and is less bulky than the substituent Ra, each R' is the same or different and is a hydrocarbyl group, an alkoxy group, a thioalky group,
- M is a transition metal selected from the group consisting of titanium, zirconium, hafnium and vanadium;
- Q is a halogen or a C1-C4 alkyl group
- n is an integer of from 0-4,
- Cp' is a substituted cyclopentadienyl group
- Fl' is a fluorenyl group
- R'a is a substituent on the cyclopentadienyl group which is in a distal position to the bridge and comprises a bulky group of the formula XR*3 in which X is carbon or silicon and R* is the same or different and is chosen from hydrogen or a hydrocarbyl group having from 1-20 carbon atoms, provided that at least one R* is not hydrogen
- R'b is a substituent on the cyclopentadienyl ring which is proximal to the bridge and positioned non- vicinal to the distal substituent and is of the formula YR# 3 in which Y is silicon or carbon and each R# is the same or different and chosen from hydrogen or a hydrocarbyl group, an alkoxy group, a thioalky group or an aminoalkyl, or an alkyl group containing from 1 to 7 carbon atoms and is less bulky than the substituent R'a
- M' is a transition metal selected from the group consisting of titanium, zirconium, hafnium and vanadium;
- Q' is a halogen or a C[.C4 alkyl group
- n' is an integer of from 0-4.
- the alkylalumoxane component and said metallocene component are present in relative amounts ⁇ provide an Al/M mole ratio within the range of 1-1000.
- a supported metallocene catalyst component comprising an isospecific metallocene catalyst component characterized by Formula (1) or Formula (2) as described above.
- the metallocene catalyst component further comprises an alkyl alumoxane catalyst component and a particulate silica support characterized by a particle size of 10-40 microns, a surface area of 200-400 m 2 /gram, and a pore volume within the range of 1.3-1.6 ml./gram.
- the catalyst is contacted in a polymerization reaction zone with a mixture of propylene and ethylene in an amount within the range of 0.01-20 mole % of ethylene in the ethylene-propylene mixture.
- the reaction zone is operated under temperature and pressure conditions effective to provide for the isospecific polymerization of the propylene in the presence of the ethylene and at a production of at least 1000 grams of polymer per gram of catalyst.
- An isotactic ethylene propylene copolymer having a melting temperature of no more than 150 ° C is recovered from the reaction zone.
- the alkylalumoxane co- catalyst is methyl alumoxane which is incorporated into the silica support initially followed by the incorporation of the isospecific metallocene component in an amount within the range of 0.6-0.8 grams of methylalumoxane per gram of silica.
- the silica support has an average particle size of 33 microns.
- the foregoing method for the production of isotactic ethylene propylene copolymer is carried out employing an isospecific metallocene catalyst component characterized by Formula (2) as described above.
- This metallocene catalyst component and an aklyalumoxane co-catalyst component are supported on a particulate silica support characterized by the particle size, surface area, pore volume, and pore diameter characteristics as described above.
- the substituent R'a of the metallocene component is a phenyl group or a substituted phenyl group or is selected from the group consisting of C(CH 3 ) 3 , C(CH3) 2 Ph, CPh.3, and Si(CH 3 ) 3 . More specifically, the substituent R'a is a tert butyl group or a substituted or unsubstituted phenyl group and the substituent R'b is a methyl group or an ethyl group.
- the bridge B of the isospecific metallocene catalyst component is selected from the group consisting of an alkylidene group having 1 to 20 carbon atoms, a dialkyl germanium or silicon or siloxane, alkyl phosphine or amine. More specifically, the bridge B is an isopropylene group and M is zirconium or titanium.
- a process for the production of an isotactic ethylene-propylene co-polymer carried out with a supported metallocene catalyst comprising an isospecific metallocene catalyst component characterized by Formula (1) as described above.
- the supported metallocene catalyst further comprises an alklylalumoxane cocatalyst component and a particulate silica support.
- the catalyst incorporating the metallocene catalyst component, the alkyialumoxane co-cataiyst component and the particulate silica support is contacted in a polymerization reaction zone with a mixture of propylene and ethylene in an amount within the range of 0.01-20 mole percent of ethylene in the ethylene-propylene mixture.
- the polymerization reaction zone is operated under temperature and pressure conditions effective to provide for the isospecific polymerization of said propylene in the presence of said ethylene at a production of at least 1000 grams of polymer per gram of catalyst to produce an isotactic ethylene propylene copolymer having a melting temperature of no more than 150° C.
- the copolymer has a melt flow rate of no more than 20 grams per 10 minutes.
- the polymerization process can include a prepolymerization phase.
- the isotactic ethylene propylene copolymer has a melting temperature of no more than 120 ° C and a melt flow rate of no more than 10 grams per 10 minutes.
- the ethylene is supplied to the reaction zone in an amount to provide an isotactic ethylene-propylene copolymer having an ethylene content of no more than 10 wt. % ethylene.
- the ethylene-propylene copolymer exhibits a melt flow rate which has an incremental variance with ethylene content when the ethylene content is between 2-7 wt.% of no more than 10 grams per ten minutes and, more specifically, an incremental variance of no more than 5 grams per 10 minutes.
- the melt flow index (Ml 2 ) does not vary by an incremental amount of more than 10 grams per 10 minutes, and more specifically, it does not vaiy by an increment of more than 5 grams per 10 minutes.
- the ethylene-propylene copolymer recovered from the reaction zone has a melt flow rate for an ethylene content within the range of 3.0-7.0 wt. % which is less than the melt flow rate for a corresponding ethylene-propylene copolymer having an ethylene content within the range of 2.0-2.9 wt. %.
- R a is a bulky liydrocarbyl group containing from 4 to 20 carbon atoms
- Rb is a methyl group or ethyl group
- R is a bulky liydrocarbyl group containing from 4 to 20 carbon atoms
- M is a transition metal selected from the group consisting of titanium, zirconium, hafnium, and vanadium
- Q is a halogen or a C ⁇ - C 4 hydrocarbyl group.
- B is a structural bridge extending between the cyclopentadienyl and fluorenyl groups, and is an ethylene group or is characterized by the formula:
- the catalyst further comprises an alkylalumoxane cocatalyst component, and a particulate silica support.
- the catalyst is contacted in a polymerization reaction zone with a mixture of propylene and ethylene in an amount within the range of 0,01-20 mole percent of ethylene in the ethylene propylene mixture.
- the reaction zone is operated under temperature and pressure conditions effective to provide for the isospecific polymerization of the propylene in the presence of the ethylene at an activity of at least 1000 grams of polymer per gram of metallocene catalyst to produce an isotactic ethylene propylene copolymer having a melt flow rate of no more than 20 grams per 10 minutes and a melting temperature of no more than 120° C.
- the isospecific metallocene catalyst component characterized by Formula (3) is further characterized by a substituent Rb which is a methyl group and a substituent Ra which is a tertiary butyl group.
- the substituent R' may also be a tertiary butyl group.
- the bridge substituent b is a phenyl group, and more particular, the bridge B is a diphenyl methylene group.
- Figure 1 is a graphical representation showing the relationship between the hydrogen concentration on the abscissa and the catalyst activity and polymer fluff melt flow on the ordinate for copolymerization with catalysts identified as catalysts CI or C2.
- Figure 2 is a corresponding graphical representation showing catalyst activity and polymer fluff melt flow on the ordinate as a function of ethylene delivery rate on the abscissa.
- Figure 3 is a corresponding graphical representation showing catalyst activity (kg/PP/g/h) and polymer fluff melt flow rate on the ordinate as a function of polymerization time on the abscissa.
- bridged metallocene denotes a transition metal coordination compound in which a cyclopentadiendyl group and a fluorenyl group are bridged together with a structural bridge to provide a stereorigid structure and which are coordinated to a central metal ion which may be provided by a Group 3, 4, or 5 transition metal or metal halide, alkyl, alkoxy, aryloxy, or alkoxy halide aryl or the like.
- the cyclopentadienyl and the fluorenyl groups of the ligand structure are oriented above and below the plane of the central coordinated metal atom.
- the structural bridge interconnecting the cyclopentadienyl-fluorenyl ligand structure imparts stereorigidity to the metallocene complex to prevent rotation of the cyclopentadienyl and fluorenyl groups about their coordination axes with the transition metal atom.
- Cyclopentadienyl-fluorenyl Hgands may be characterized by the following structural formula in which the upper and lower cyclopentadienyl and fluorenyl groups are interconnected by a chemical bridge B as described previously.
- Formula (5) indicates the numbering scheme used herein in which the bridge head carbon atom of the cyclopentadienyl group is numbered 1 and the bridge head carbon atom of the fluorenyl group is 9.
- the conjugated carbon atoms of the fluorenyl group are numbered in a sequence in which the directly proximal carbon atoms are numbered 1 and 8 and the distal carbon atoms are numbered 3, 4, 5, and 6.
- This numbering sequence is shown in the above Formula (5). It is a conventional practice to refer to the symmetry of such ligand structures in terms of a line of symmetry which extends through the two bridge head carbon atoms and the structural bridge as shown by the vertical broken line of Formula (5).
- the present invention employs cyclop entadienyl-fluorenyl metallocene structures which are substituted in a manner to provide an asymmetrical conformation to the cyclopentadienyl group and a symmetrical conformation to the fluorenyl group.
- the cyclopentadienyl group is substituted on one side of the broken line at the distal position with a relatively bulky group and on the other side of the broken line at the non-vicinal proximal position with a less bulky group.
- the fluorenyl group is unsubstituted or substituted at the 2 and 7 positions in combination with the asymmetrical cyclopentadienyl group to provide a symmetrical structure.
- Substituents on the fluorenyl group at the 2,7 positions or on the cyclopentadienyl group at the 3 position which are relatively bulky, include tertiary-butyl groups and phenyl groups which can be substituted or unsubstituted.
- Substituted phenyl groups attached to the fluorenyl ligand at the 2,7 positions or on the cyclopentadienyl group at the 3 position include 2,6 dimethylphenyl and 2,6 tnfluoromethylphenyi groups.
- Other 2,6 substituents on the phenyl groups include ethyl and isopropyl groups.
- Substituents on the cyclopentadienyl group at the 5 position (proximal to the bridge) can include hydrocarbyl, alkoxy, thiolkoxy, or amino alkyl groups as described previously which are less bulky than the substituents on the cyclopentadienyl group at the 3 position.
- substituents can include cyclic structures such as cyclopropane, cyclobutane, cyclopentane, furan and thiophene.
- the metallocenes of the present invention can be employed in conjunction with a suitable scavenging or polymerization cocatalyst which can be generally characterized by organo-metallic compounds of metals of Groups IA, IIA, and ⁇ of the Periodic Table of Elements, As a practical matter, organoaluminum compounds are normally used as cocatalysts in polymerization reactions. Some specific examples include triethyl aluminum (TEAL), tri- isobutyl aluminum, diethyl aluminum chloride, diethyl aluminum hydride and the like. In addition to scavenging agents such as TEAL, other additives such as anti-fouling agents may be employed in carrying out the present invention.
- TEAL triethyl aluminum
- other additives such as anti-fouling agents may be employed in carrying out the present invention.
- an anti-fouling agent such as pluronic L121, available from BASF Corporation, may be added to the catalyst system.
- the use of such scavenging agents and anti-fouling agents is disclosed in European Patent Application EP1 316 566A3 to Tharappel et al.
- the supported cocatalyst component incorporated onto the silica support is an alkyalumoxane.
- Such compounds include oligomeric or polymeric compounds having repeating units of the formula:
- R is an alkyl group generally having 1 to 5 carbon atoms.
- Alumoxanes are well known in the art and are generally prepared by reacting an organo aluminum compound with water, although other synthetic routes are known to those skilled in the art. Alumoxanes may be either linear polymers or they may be cyclic, as disclosed for example in U.S. Patent No. 4,404,344. Thus, alumoxane is an oligomeric or polymeric aluminum oxy compound containing chains of alternating aluminum and oxygen atoms, whereby the aluminum carries a substituent, such as an alkyl group.
- linear and cyclic alumoxanes are not known but is generally believed to be represented by the general formulae --(Al(R)-0-)-m for a cyclic alumoxane, and R 2 Al-0-(Al(R)- 0)m-AlR 2 for a linear compound wherein R is independently at each occurrence a Ci-Cio hydrocarbyl, specifically an alkyl, or halide and m is an integer ranging from 1 to about 50, usually at least about 4.
- Alumoxanes also exist in the configuration of cage or cluster compounds. Alumoxanes are typically the reaction products of water and an aluminum alkyl, which in addition to an alkyl group may contain halide or alkoxide groups.
- alumoxanes Reacting several different aluminum alkyl compounds, such as, for example, trimethylaluminum and tri-isobutyl aluminum, with water yields so-called modified or mixed alumoxanes.
- Specific alumoxanes are methylalumoxane including methylalumoxane modified with minor amounts of other higher alkyl groups such as isobutyl, Alumoxanes may contain minor to substantial amounts of starting aluminum alkyl compounds, Non-hydrolytic means to produce alumoxanes are also known in the art.
- the silica supports employed in carrying out the present invention may vary depending upon the nature of the metallocene component.
- the metallocene component incorporates an unsubstituted fluorenyl group in combination with a 3,5 substituted cyclopentadienyl group in accordance with Formula 2
- the silica support has an intermediate particle size of 20-35 microns in combination with a surface area of 200-400 m /gram.
- the silica support is further characterized by pore volume within the range of 1.3-1.6 ml/gram.
- a specific support designated herein as Support SI has the following parameters, a particle size of 30-35 microns, a surface area of 250-350 m 2 /g, and a pore volume of 1.4 ml/g.
- a silica support as thus characterized may also be employed in carrying out the invention with a metallocene component incoiporating a fluorenyl group substituted at the 2 and 7 positions as depicted by the metallocene component of Formula 1.
- other silica supports may also be employed in carrying out the invention.
- Such silica supports include, in addition to the previously described silica supports, silica supports as the type described in U.S. Patent Nos. 6,777,366 to Gauthier, et al, 6,777,367 to Gauthier, and 6,855,783 to Gauthier, et al.
- Such silica supports are characterized generally as having a particle size within the range of 10- 100 microns, a surface area within the range of 200-900 m 2 /gram, and a pore volume within the range of 0.5-3.5 ml/gram.
- Such silica supports include support materials having an average particle size within the range of 20-60 microns and an average effective pore diameter within the range of 100-400A which accommodate a substantial amount of alumoxane cocatalyst within the internal pore volume of the silica particles as described in U.S. Patent No. 6,777,366.
- silica supports suitable for use for this aspect of the invention, include silica supports having an average particle size of 10-60 microns and more specifically 10-15 microns incorporating the alumoxane catalyst predominately on the external surface thereof as described in U.S. Patent No. 6,777,367.
- Additional silicate supports which may be employed in carrying out this aspect of the present invention are characterized by having an average particle size of 10-50 microns and a surface area within the range of 200-900 m 2 /g with a pore volume within the range of 0.9-2.1 ml/gram as described in U.S. Patent No. 6,855,783.
- Exemplary silica supports which may be employed in this aspect of the invention are disclosed in U.S. Patent No. 6,855,783 as set forth in the following table where they are designated as Supports A, B, C, D, E, and F, together with the characteristic properties of particle size, surface area, and pore volume.
- silica Supports A and C can be obtained from the Asahi Glass Company under the designations H-121 and H- 122, respectively.
- Silica B is available from Fuji Silysia Chemical, Ltd., under the designation P-10.
- the MAO (methylalumoxane) and metallocene would be preferentially supported inside the support for Silicas B and C, whereas the MAO and metallocene would be primarily surface- supported in the case of Support A.
- Supports A, B, and C are of a roughly spheroidal configuration.
- Supports D and E can be formulated from commercially available silicas available from PQ Coiporation under the designations M.S.-3030 and M.S.-3060, respectively.
- Silica Support F is of a spheroidal configuration and is available from the Asahi Glass Company under the designation H-202.
- the supported metallocene of the present invention is formed by initially incorporating the alkylalumoxane component onto the silica support followed by the incorporation of the isospecific metallocene catalyst component.
- the alkylalumoxane, specifically methylalumoxane is incorporated onto the silica support in an amount to provide 0.4- 1 grams per gram silica, and more specifically, 0.6-0.8 grams of methylalumoxane per gram of silica support.
- ethylene-propylene copolymerization studies were carried out employing two catalyst systems having metallocene components exemplary of the metallocene components characterized by Formulas (1) and (2).
- the metallocene was supported on the silica support identified previously as Support S-1 which had been pretreated with methylalumoxane to provide about 0.7 grams of methylalumoxane per gram of silica support.
- the metallocene component was diphenylmethylene (2-methyl-4-tertiary-butyl- cyclopentadienyl-2, 7-di-tertiary-butyl-1-fluorenyl) zirconium dichloride.
- a metallocene catalyst component exemplary of the component depicted by Formula 2 was employed on the same silica support S-1 pretreated with methylalumoxane similarly as for Catalyst C-l .
- the metallocene catalyst was diphenylmethylene (2-methyl-4- tertiary-butyl- cyclopentadienyl-fluorenyl) zirconium dichloride.
- the metallocene components were loaded onto the methlylalumoxane treated silica support to provide a mole ratio of aluminum to zirconium of about 175.
- the copolymerization activity increased for both of catalysts CI and C2 along with the hydrogen concentration.
- the hydrogen attendance changes the activity of catalyst CI about ten fold within the range of 0 ⁇ 60 ppm.
- the increase is about three times.
- catalyst C2 is at least more than twice as active than CI under the same copolymerization conditions (55 °C and bulk) with ethylene delivery rate of 167 mg/min (integrated to 10 g over one hour).
- the activity difference varies over the whole range of initial hydrogen concentration of 0 to 60 ppm.
- Catalyst CI offered lower copolymer melt flow than catalyst C2 when the hydrogen concentration is lower than 25 ppm, which corresponds to melt flow of 35 g/lOmin. Since CI shows stronger hydrogen response on melt flow, higher melt flow random copolymer is then obtained by CI when hydrogen concentration is over 25 ppm as reported in Table 2 and shown in Figure 1.
- the melt flow rates reported herein are for the melt flow index (MI 2 ) measured in accordance with the ASTM D1238 at 230° C and 2.16 kilograms.
- Catalyst Cl offers lower copolymer melt flow than C2, as shown in Figure 2.
- the copolymer melt flow decreases at first with the ethylene concentration; and it starts to increase, as the concentration is over 15 g.
- the copolymer melt flows are less than 7 g/lOmin, which are much smaller than 19 g/10 min of homopolymer (Entry 1).
- the melt flows for all copolymers for catalyst C2 are higher than the value of 4.7 g/10 min for the homopolymer.
- the copolymer melt flow increases from 4,7 to 41 g/10 min as the comonomer concentration increases.
- C2 shows much more stronger ethylene response on copolymer melt flow than CI as shown in Figure 2.
- Table 4 sets forth the kinetics of propylene copolymerization with ethylene for both catalysts CI and C2.
- the study condition is 55 °C and bulk with an ethylene delivery rate of 333 mg/min (integrated to 20 g over one hour) under hydrogen concentration of 10 ppm.
- Bench observation shows that the copolymerization activity increases for both C2 and CI catalysts along with the reaction time.
- the activity of both catalysts is about two times higher than the initial periods ( ⁇ 30 min).
- catalyst C2 is about two to three times more active than CI .
- the activity disparity remains almost the same for the whole time of investigation.
- Catalyst CI offers lower copolymer melt flow than C2 as shown in Figure 3.
- the copolymer melt flow decreases first with the polymerization time; and it starts to increase as time goes on.
- C2 starts much earlier at about 20 min, and CI at a later time of polymerization (45 min).
- all the copolymer melt flows for CI are less than 10 g/10 min, and the melt flows for C2 are higher than 16 g/10 min.
- C2 shows stronger time response on copolymer melt flow than CI.
- catalyst C2 homopolymerizations offers lower resin melt flow and higher catalyst activity under the same laboratory conditions as compared to homopolymerization with catalyst Cl.
- ethylene acts as an activity booster for both catalyst Cl and catalyst C2 systems.
- Copolymerization activity with catalyst C2 can be enhanced as high as 8 times of homopolymerization activity while for catalyst Cl enhancement is about three times.
- Ethylene acts as a chain transfer agent in C2 type systems but not in Cl systems. Copolymer produced with catalyst C2 gives a higher melt flow than the corresponding homopolymer produced under the same hydrogen conditions.
- Catalyst Cl therefore offers a lower melt flow copolymer. Hydrogen appears to act as "slower" chain transfer agent in the copolymerization of propylene with ethylene and the homopolymerization process employing the catalyst Cl system. Lower melt flow component is obtained for the corresponding homopolymer. Under the same copolymerization conditions catalyst Cl offers lower melt flow resins (less than 30g/10 min) than C2 even though catalyst C2 activity is about 2 to 4 times higher. [0036]
- the polymers produced in the present invention can be employed in the production of a broad range of products. Thus, the copolymer may be employed to produce films, tapes and fibers. Further, they may be employed to produce molded products by injection molding or blow molding applications.
- the resins produced exhibit desirably low xylene soluble levels compared to traditional Z-N catalyst systems which is advantageous for organoleptic qualities for instance.
- the resins may exhibit a xylene soluble level of less than about 0.3 wt.%.
- the ability to produce a very broad range of MF values from low to high is another considerable advantage of these catalysts and the resins thus produced.
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Abstract
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JP2013529164A JP2013537256A (en) | 2010-09-15 | 2011-08-22 | Supported metallocene catalyst |
KR1020137007793A KR20130106382A (en) | 2010-09-15 | 2011-08-22 | Supported metallocene catalysts |
CN2011800445989A CN103108889A (en) | 2010-09-15 | 2011-08-22 | Supported metallocene catalysts |
EP11825629.6A EP2616491A4 (en) | 2010-09-15 | 2011-08-22 | Supported metallocene catalysts |
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US12/882,268 US8299188B2 (en) | 2007-05-18 | 2010-09-15 | Supported metallocene catalysts |
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EP (1) | EP2616491A4 (en) |
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CN105658686A (en) * | 2013-06-24 | 2016-06-08 | 沙特基础工业公司 | Titanated chromium-based catalysts to produce high density polyethylene |
US10100135B2 (en) * | 2014-06-12 | 2018-10-16 | Total Research & Technology Feluy | Process for preparing a polyethylene in at least one continuously stirred tank reactor |
US11043679B2 (en) * | 2014-12-30 | 2021-06-22 | Ess Tech, Inc. | Alternative low cost electrodes for hybrid flow batteries |
US10280233B2 (en) | 2015-06-05 | 2019-05-07 | Exxonmobil Chemical Patents Inc. | Catalyst systems and methods of making and using the same |
US9725569B2 (en) | 2015-06-05 | 2017-08-08 | Exxonmobil Chemical Patents Inc. | Porous propylene polymers |
US10077325B2 (en) | 2015-06-05 | 2018-09-18 | Exxonmobil Chemical Patents Inc. | Silica supports with high aluminoxane loading capability |
US9738779B2 (en) | 2015-06-05 | 2017-08-22 | Exxonmobil Chemical Patents Inc. | Heterophasic copolymers and sequential polymerization |
US10723821B2 (en) | 2015-06-05 | 2020-07-28 | Exxonmobil Chemical Patents Inc. | Supported metallocene catalyst systems for polymerization |
US9920176B2 (en) | 2015-06-05 | 2018-03-20 | Exxonmobil Chemical Patents Inc. | Single site catalyst supportation |
US10570219B2 (en) | 2015-06-05 | 2020-02-25 | Exxonmobil Chemical Patents Inc. | Production of heterophasic polymers in gas or slurry phase |
US9725537B2 (en) | 2015-06-05 | 2017-08-08 | Exxonmobil Chemical Patents Inc. | High activity catalyst supportation |
EP3303423A1 (en) | 2015-06-05 | 2018-04-11 | ExxonMobil Chemical Patents Inc. | Single reactor production of polymers in gas or slurry phase |
EP3303417A4 (en) * | 2015-06-05 | 2018-08-22 | ExxonMobil Chemical Patents Inc. | Porous propylene polymers |
US10280235B2 (en) | 2015-06-05 | 2019-05-07 | Exxonmobil Chemical Patents Inc. | Catalyst system containing high surface area supports and sequential polymerization to produce heterophasic polymers |
US10329360B2 (en) | 2015-06-05 | 2019-06-25 | Exxonmobil Chemical Patents Inc. | Catalyst system comprising supported alumoxane and unsupported alumoxane particles |
US9809664B2 (en) | 2015-06-05 | 2017-11-07 | Exxonmobil Chemical Patents Inc. | Bimodal propylene polymers and sequential polymerization |
US10294316B2 (en) | 2015-06-05 | 2019-05-21 | Exxonmobil Chemical Patents Inc. | Silica supports with high aluminoxane loading capability |
CN109312013A (en) | 2016-05-27 | 2019-02-05 | 埃克森美孚化学专利公司 | Metallocene catalyst compositions and the polymerization for using it |
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US5869417A (en) * | 1995-09-01 | 1999-02-09 | Korea Advanced Institute Of Science And Technology | Process for preparing metallocene catalyst for polyolefin polymerization |
US6630547B1 (en) * | 2002-06-11 | 2003-10-07 | Equistar Chemicals, Lp | Use of silanes to control molecular weight in olefin polymerizations |
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JP4554133B2 (en) | 1999-10-08 | 2010-09-29 | 三井化学株式会社 | Metallocene compound, method for producing metallocene compound, olefin polymerization catalyst, method for producing polyolefin, and polyolefin |
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US20030236365A1 (en) * | 2002-06-24 | 2003-12-25 | Fina Technology, Inc. | Polyolefin production with a high performance support for a metallocene catalyst system |
DE602005021980D1 (en) | 2004-08-30 | 2010-08-05 | Mitsui Chemicals Inc | PROCESS FOR PREPARING PROPYLENE POLYMER |
US7220806B2 (en) * | 2005-04-29 | 2007-05-22 | Fina Technology, Inc. | Process for increasing ethylene incorporation into random copolymers |
US7514510B2 (en) * | 2006-07-25 | 2009-04-07 | Fina Technology, Inc. | Fluorenyl catalyst compositions and olefin polymerization process |
AU2007292139B2 (en) | 2006-09-05 | 2010-06-17 | Prime Polymer Co., Ltd. | Multilayered stretched hollow material |
CN101511930B (en) | 2006-09-12 | 2012-07-04 | 三井化学株式会社 | Polypropylene resin and blown container |
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2010
- 2010-09-15 US US12/882,268 patent/US8299188B2/en active Active
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2011
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- 2011-08-22 JP JP2013529164A patent/JP2013537256A/en not_active Withdrawn
- 2011-08-22 EP EP11825629.6A patent/EP2616491A4/en not_active Ceased
- 2011-08-22 KR KR1020137007793A patent/KR20130106382A/en not_active Application Discontinuation
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US6630547B1 (en) * | 2002-06-11 | 2003-10-07 | Equistar Chemicals, Lp | Use of silanes to control molecular weight in olefin polymerizations |
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JP2013537256A (en) | 2013-09-30 |
US20140005035A1 (en) | 2014-01-02 |
US8563671B2 (en) | 2013-10-22 |
EP2616491A1 (en) | 2013-07-24 |
KR20130106382A (en) | 2013-09-27 |
US9127105B2 (en) | 2015-09-08 |
CN103108889A (en) | 2013-05-15 |
US8299188B2 (en) | 2012-10-30 |
US20110112262A1 (en) | 2011-05-12 |
US20130018157A1 (en) | 2013-01-17 |
EP2616491A4 (en) | 2014-05-14 |
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