CA2197643A1 - Catalysts and processes for the polymerization of olefins - Google Patents
Catalysts and processes for the polymerization of olefinsInfo
- Publication number
- CA2197643A1 CA2197643A1 CA002197643A CA2197643A CA2197643A1 CA 2197643 A1 CA2197643 A1 CA 2197643A1 CA 002197643 A CA002197643 A CA 002197643A CA 2197643 A CA2197643 A CA 2197643A CA 2197643 A1 CA2197643 A1 CA 2197643A1
- Authority
- CA
- Canada
- Prior art keywords
- carbon atoms
- substituents
- formula
- alkyl
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- 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
-
- 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
- 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
-
- 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
- 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
-
- 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
- Y10S526/943—Polymerization with metallocene catalysts
Abstract
Catalysts for the polymerization of olefins comprise the product of the reaction between: (A) a titanium, zirconium or hafnium product with substituted cyclopentadiene ligands, (B) a mixture of two organometallic aluminium compounds, with at least one of the groups bound to the aluminium being other than a linear alkyl, and (C) water. When used in the polymerization of olefins, these catalysts show higher activities, at short residence times, than corresponding catalysts obtained from the individual components of the above-mentioned mixtures of aluminium compounds.
Description
~ t ~
WO97/~B97 I~I/L~ l5 TI~LE:
CATALYSTS AND PROCESSES FOR THE POLYMERIZATION OF OLEFINS
The present invention relates to catalysts for the polymerization of olefins, obtained from cyclopentadienyl com-pounds, organometallic aluminium compounds and water.
Homogeneous catalyst systems for the polymerization of olefins are known which comprise a metallocene and the product of the reaction between water and an aluminium alkyl, where the alkyl is other than methyl.
In European Patent Application EP 384 171, catalysts are described which are suitable for the polymerization of olefins and comprise the product of the reaction between:
(A~ a metallocene compound of the general formula:
~csR~ Rl~)(csRl~l)Mx~-m where (C5R'") is a cyclopentadienyl group in which R' is hydrogen, an alkyl, alkenyl, aryl, alkylaryl or arylalkyl rad-ical having from 1 to 20 C atoms or a group CR2SiR3 or a group SiR3 with R being defined as for R', or two ~or four) substituents R' of one and the same cyclopentadienyl group form one (or two) rings having from 4 to 6 C atoms, R" is a divalent radical selected from an optionally substituted alkylene group having from 1 to 8 C atoms, an SiR2, PR or NR group with R being defined as for R', which forms a bridge link between two cyclo-pentadienyl groups, X is hydrogen, halogen, -OMX(C5R'")2, -OH or -OR with R being defined as for R', or a hydrocar~on radical having the meaning of R', M is a transition metal of valency 3 or 4, selected from Ti, ~r or Hf, p is 0 or 1, m is 0, 1 or 2, and, if m = 0, p = 0 and, if p = 0, at least one radical R' is other than hydrogen, n = 4, if p = 1, and n = 5, if p = 0; and ~ ~7~43 W097~00897 PCT~P9~02~515 (P) an alumoxan~ of the formula:
\ Al - O - Al R~ / \ R4 in which R~, R~, R3 and R4 can generically be alkyl, alkenyl or alkylaryl radicals having 2-~0 carbon atoms.
The alumoxanes (B~ can be prepared by reacting the cor-responding trialkylaluminium with water in a 2:l molar ratio. In the embodiment exa~,ples, alumoxanes are used in which R1, R~, R3 and R4 are ethyl, isobutyl or 2-methylpentyl groups.
European Patent Application ~P 575 87s describes homogene-ous catalyst systems for the polymerization of olefins, obtained by contacting the following components:
~) a cyclopentadienyl compound of the general formula:
(C5Rx~ Hs-x)R~l~(csRly-lrlH5-y),lM~3ll in which M is I~i, Zr or ~f, C5R1x,nHsx and C5R1y~H5y are cyclopentadiene rings substituted in the same way or dif-ferent ways, the substituents R1 which can be identical or different are alky', alkenyl, aryl, alkylaryl or arylalkyl radicals which have from l to 20 carbon atoms and can also contain si or Ge atoms, or are Si(CH3~3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R- is a group forming a bri~ge link between the two cyclopentadiene rings and is selected from CR3~, C,R34, SiRl~, si,R34, GeR3~, Ge~R3~, R375iCR32, NR1 or PR1, with the substituents R3 which can be identical or dif-ferent being R1 or hydrogen, or also two or four sub-stituents R3 can form one or two rings having from 3 to 6 2 l 9 7~43 W097/00897 PCT~P96/02615 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, OH, SH, R1, OR1, SR1, NR12 or PR12, m can be O or l, n can be 0 or l, being l if m = l, x is an integer between (m+l) and 5, and y is an integer between m and 5;
(B) an organometallic aluminium compound of the general formula AlR33zHz, in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from l to lO carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one the substituents R3 is other than a linear alkyl group, and z is 0 or l; and (C) water.
The molar ratio between the organometallic aluminium com-pound and the water is between l:l and l00:l. In the embodiment examples, the organometallic aluminium compounds used are only triisobutylaluminium and triisohexylaluminium.
In Italian Patent Application No. MI/54A/l5l6, homogeneous catalyst systems for the polymerization of olefins are described which possess an activity improved over those exemplified in the abovementioned patent application ~P 575 8~5, which systems com-prise the product obtained by contacting the following components:
(A) a cyclopentadienyl compound o~ the formula:
(CsR~ Hs-x~R~ csR~ s-y)l~MQ3ll in which ~ is rL'i, Zr or Hf, C5R1~,nH5~ and C5Rly1nH5y are cyclopentadiene rings substituted in the same way or dif-ferent ways, the substituents p~1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl ~ 2 ~ q76~3 W047/00897 pCT~P9~U2615 radicals which have from 1 to 20 carbon ator~s and can also contain si or Ge atoms, or are si(CH3J3 groups, or also two or four substituents Rl of one and the same cyclopentadienyl group car, form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR32, C~R34r SiR32, ~i,R34, ~eR32, Ge2R34, R3~SiCR32, NRI or PRI, with the substituents R3 which can be identical or di~-ferent being Rl or hydroqen, or also two or four sub-stituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q whicn can be identical or different are halogen, hydrogen, Rl, ORI, SRI, NR12 or PRI2, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between (m+1~ and 5 and y is an Lnteger between m and 5;
(BJ an organometallic aluminium compound of the formula:
Al-(CH,-CR4R5R6)3z~z in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to lO carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to lO
carbon atoms, or R4 and R5 are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to lO car-bon atoms and z is O or 1; and (C) water.
The molar ratio between the organometallic aluinium com-pound and the water is between 1:1 and lOO:l.
The polymerization yields of the catalysts described in the abovementioned patent applications are, albeit relatively high, ~ WO 97~00897 ~ 1 q ~t ~ 4 3 ~ 7~15 not altogether satisfactory if the residence times of the reac-tion mixture in the reactor are short. This is particularly important in industrial polymerization processes, especially in those which operate continuously, where it is very advantageous to operate with short residence times.
It would therefore be desirable to improve the productivity of the abovementioned catalysts at short residence times.
It has now been found, unexpectedly, that catalysts for the polymerization of olefins, of the type of those described in the abovementioned patent applications, obtained from particular mixtures of organometallic aluminium compounds, show superior activities at short residence times than the corresponding cata-lysts obtained from the individual components of the abovementioned mixtures of aluminium compounds.
The catalysts which are the subject of the present invention comprise the product obtained by contacting the fol-lowing components:
(A) a cyclopentadienyl compound of the formula (I):
(CsRl~lDH~)R~ (csRy-mHs-~DMQ3-~
in which M is Ti, Zr or Hf, C5RI~,~H5~ and C~RIymH5y are cyclopentadiene rings substituted in the same way or differ-ent ways, the substituents Ri which can be identical or dif-ferent are alkyl, alkenyl, aryl, alkylaryl or arylalkyl rad-icals which have from 1 to 20 carbon atoms and can also con-tain Si or Ge atomf" or Si(CH;)3 groups, or also two or four substituents Rl of one and the same cyclopentadienyl group can form one or two rings having from ~ to ~ carbon atoms, R2 is a group forming a bridge linh between the two cyclo-pentadiene rings and is selected from CR3~, C2R34, SiR32, 2 1 q7643 097~0897 p~t/~ C
Si2R34, GeR3~, Ge,R3~, R325iCR32, NRI or PRI, with the substituents R3 which can be identical or different being Rl or hydrogen, or also two or four substituents R3 can form one or two ring~ having from 3 to 6 carbon atoms~ the sub-stituents Q which can be identical or different are haloqen, hydrogen, Rl, OR~, SRI, NRI~ or PRI~, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between (m+lJ
and 5, and y is an integer between m and 5;
~B) a mixture composed of:
(B1) 1-99 mol-% of an organometallic aluminium compound of the formula ~
Al-(CH-,-CR4RSR6~3zH, (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and RS zre fused together to form a ring having from 4 to Ç carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is O or l;
~B2) 1-99 mol-% of an organometallic aluminium compound of the formula (III):
AlR33~H,~ (III~
in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also con-tain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl 21 ~ ~47) group, and w is 0 or l, the compounds o~ the formula (II) defined above being excluded; and (C) water.
The molar ratio between the total of the organometallic alu-minium compounds and the water is between 1:1 and lO0:1, prefer-ably between l:l and 50:1 and more preferably between l:l and 10:1.
The molar ratio between the aluminium and the metal of the cyclopentadienyl compound is between about 50 and 10,000, pre-ferably between about 500 and 5000 and more preferably between lO00 and 2000.
The molar ratio ~Bl)J(B2) between the two components of the mixture (B) of organometallic aluminium compounds is preferably between about 10:90 and about 90:lO, and more preferably is between about 25:75 and about 75:25. Those mixtures (B) are par-ticularly preferred in which the components (Bl) and (B2) are present in approximately equimolar quantities.
In the case of m=o, particularly suitable cyclopentadienyl compounds are those in which M i5 Zr and the groups CSRIx,nH5~ and C5~1y~H5y are pentamethyl-cyclopentadienyl, indenyl or 4,5,6,7-tetrahydroindenyl, while the substituents Q are chlorine atoms or hydrocarbon groups containing from l to 7 carbon atoms.
Non-limiting examples of cyclopentadienyl compounds (A) with m = 0 are:
(Me3cp)2Mcl2 ~Me4Cp),MCl, (MesCp)2Mcl2 (Mescp)2MMe2 (MesCp)~(ol~e)2 (MesCp)2M(C6Hs)2 (Me5Cp)2M(CH3) Cl (Etr~e4cp) ,~rlcl2 [ (CbHS)Me4CP]2MCl2 (E:tSCP)2MC12 (Me5Cp).M(CbH5)cl (Ind)2l~cl2 (Ind)2MMe2 (~.Ind),r~Cl2 (}14Ind)2MMe2 W097/~0897 ,~~ n?~-[si(c1~3)3cp]2Mclz {[Sl(cM3)3]2cP}2Mcl2 (Me4cp~(Mescp1Mcl2 ~Me5CpJMCl3 (~lesCp)MRenz3 (Ind)MBenz3 (H4Ind)MBenz3 where Me = methyl, Et = ethyl, Cp = cyclopentadienyl, Ind =
indenyl, H4Ind = 4,5,6,7-tetrahydroindenyl, Benz = benzyl, M is Ti, Zr or Mf and preferably is Zr.
In the case of m = l, particularly suitable cyclopentadienyl compounds are those in which M is Zr and the groups C5R~H5~ and C5RIy~mH5y are tetramethyl-cyclopentadienyl, indenyl or tetrahydroindenyl and R- is a group ~CH3)~Si or C2~4~ while the substituents Q are chlorine atoms or hydrocarbon groups having from l to 7 carbon atoms.
Non-limiting examples of cyclopentadienyl compounds (R) with m = l are:
Ne2Si(Me4CP)21'qCl2 Me25i(Me4CP)2MMe2 Me2C(Me4CP)~MeCpJMC12 Me2Si(Ind)2MCl2 Me2CSi(lnd~2MMe2 Me25i(~5e4Cp)2MCl(OEtJ
c2H4~Ind~2~C12 C2~14(Ind~2MMe2 C2H4(Ind)2M(NMe2)2 C2H4(H4Lnd)2~5Cl2 C2H4(H4Ind)~MMe2 C2M4(114Ind)2M(NMe2)~Me Ph(Me)Si(Ind)2MC12 Ph,Si(Ind)2MC12 Me2C(FlU)lCP)~ICl2 C2H4(Me4CP)2MCl2 C2Me,l(Ind)~MCl2 Me2SiCH2(Ind)2MCl2 C2H4(2-MeInd)2MC12 C,M4(3-MeInd)~MC12 C2H4(4,7-Me2Ind),MC12 C2H4 ( S, 6-Me2Ind ) 2~5C12 where Me = methyl, Cp = cyc1Opentadienyl, Ind = indenyl, Flu =
fluorenyl, Ph = phenyl, M~Ind = 4,5,6,7-tetrahydroindenyl, M is Ti, Zr or Hf and preferab~y is Zr.
In the organometallic aluminium compound of the formula (IIJ
which can be used a~ component (Bl), R4 is preferably a methyl or ethyl group, while R~ is preferably a hydrogen atom.
~ W097/00897 2 1 9 7 h 4 3 r~ c rarticularly preferred as components (Bl) are the organometallic aluminium compounds in which R4 is a methyl group, RS is an alkyl group with a branched chain having a num-ber of carbon atoms greater than 4 and R6 is a hydrogen atom.
Non-limiting examples of organometallic aluminium : a~ln~c which can be used as components (B1~ are:
tris-(2,4,4-trimethyl-pentyl)-aluminium and di-(2,4,4-trimethyl-pentyl)-aluminium hydride.
The particularly preferred compound is tris-(2,4,4-trimethyl-pentyl)-aluminium ~TIOA).
In the organometallic aluminium compound of the formula (II) which can be used as component (Bl), preferably all the substituents R7 are non-linear alkyl, alkenyl or alkylaryl rad-icals. More preferably, all the substituents R7 of the organometallic aluminium compound are isoalkyl radicals.
Non-limiting examples of organometallic aluminium compounds which can be used as components (B2) are:
triethylaluminium, di-methylisobutylaluminium, methyl-di-isobutylaluminium, tri-isobutylaluminium, di-isobutylaluminium monohydride and tris-(2,2-dimethylpropyl)aluminium.
The particularly preferred compound is triisobutylaluminium (TIBA).
The components constituting the catalysts of the present invention can be brought into contact in various ways.
In an embodiment example, the mixture of aluminium compounds is contacted with watel-, and then the reaction product thus w~ g7,00897 2 I q 7 6~ 3 obtained is brought into contact with the cyclopentadienyl com-pound.
A further subject of the present invention is therefore a catalyst for the polymerization of olefins, comprising the prod-uct obtained by contacting the following components:
(A) a cyclopentadienyl compound of the formula (I):
( C5R I 1~ ~nH5 X ) R?~l ( CsR 1~ Hs ~. )"MQ3~
in which M is Ti, Zr or Hf, C5R~ ,H5~ and C5RIymH5y are cyclopentadi.ene rings substituted in the same way or differ-ent ways, the substituents Rl which can be identical or dif-ferent are alkyl, al~enyl, aryl, alkylaryl or arylalkyl rad-icals which have from 1 to 2U carbon atoms and can also con-tain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents Rl of orte and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, RZ is a group forming a bridge link between the two cyclo-pentadiene rings and is selected from CR32, C,R34, SiR3~, sizR34l GeR3~, Ge.R34, R3~SiCR3~, NRI or PRI, with the substituents R3 WtliC~ can be identical or different being Rl or hydrogen, or also two or ~our substituents R3 can fornt one or two rings having from 3 to 6 c~rbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, Rl, ORI, SRI, NR~2 or PR12, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between ~m~1) and 5, and y is an integer between m and 5;
and (B) the product of the reaction between water and a mixtu.re consisting of:
21 97~43 097/00897 I~l~t~
(sl) 10-90 mol-'8 of an orqanometallic aluminium com-pound of the formula (II):
Al-(CH7-CR4~5R~)3zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from l to lO carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and RS are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1; and (S~) 10-90 mol-~ of an organometallic aluminium com-pound of the formula (III~:
AlR3;;~.H" (III~
in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also con-tain si or ~e atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or l, the compounds of the formula (II~ defined above being excluded.
The molar ratio between the organometallic aluminium compounds and the water is between 1:1 and 100:1, preferably between 1:1 and 50:1, more preferably between 1:1 and 10:1.
The component.s of the catal~sts of the present invention can be brought into contact by various methods.
For example, it is possible gradually to add water to the mixture of aluminium compounds in solution in an inert aliphatic or aromatic hydrocarbon solvent such as, for example, heptane or w0.~7~00897 ~ 1 ~ 7 6 4 3 P .,~. C"~' l!i ~
toluene. The solution thus obtained is contacted with a solution of a cyclopentadienyl compound in a suitable solvent as, for example, toluene.
According to another way of proceeding, the water can be introduced in the n~onomer, or in one of the monomers, to be polymerized; in this case, the mixture of aluminium compounds and the cyclopentadienyl compound are first brought into contact before they are used in the polymerization. Moreover, the water can be made to react in a combined form as a hydrated salt, or it can be adsorbed or absorbed on an inert support such as sil-ica. Another preparation method is the reaction of the aluminium compounds with boric anhydride or boric acid.
The catalysts of the present invention can also be used on inert supports. This is effected by depositing the cyclopentadienyl cor,pound, or the product of the reaction there-of with the aluminium compounds pre-reacted with water, or the aluminium compounds pre-reacted with water and then the cyclopentadienyl com~ound, on inert supports such as, for example, silica, alumina, styrene/ divinylbenzene copolymers, polyethylene or polypropylene.
A particularly suitable class of inert supports which can be used is that constituted by porous organic supports functionalized with qroups having active hydrogen atoms. Those are particularly preierred in which the organic support i5 a partially crosslinked styrene polymer. Supports of this type are described in European Application EP-633 272, the content of which is understood to be incorporated in the present descrip-tion.
2 i 97643 WO97/008s7 PCT/EP96/02615 The solid compound thus obtained, in combination with the further addition of aluminium alkyl compounds, whether pre-reacted with water or not, can be used in the gas-phase polymerization.
The catalysts of the present invention can be used in the polymerization reactions of olefins.
A further subject of the present invention is therefore a process for the polymerization of at least one olefin of the formula CH,=CHR, in which R is hydroqen or an alkyl radical hav-ing from 1 to 20 carbon atoms, comprising the polymerization reaction of the said olefins in the presence of a catalyst as described above.
The catalysts according to the present invention can advan-tageously be used in the homopolymerization of ethylene and, in particular, for the preparation of HDPE, and for the copolymerization of ethylene and, in particular, for the prep-aration of LLDPE.
The LLDPE copolymer~, which are obtained have a content of ethylene units of between ~0 and 99 mol-%. Their density is between 0.~7 and O.g5 g/cml3 and they are characterized by a uni-form distribution of the comonomer units within the polyme~
chain.
The olefins which can be used as comonomers comprise c~-olefins of the formula CH,=CH~, where R is a linear or branched or cyclic alkyl radical havinq from 1 to 20 carbon atoms, or cycloolefins. ~xamples of such olefins are propylene, l-butene, l-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, allylcyclohexane, cyclopentene, cyclohexene, norbornene and 4,6-dimethyl-1-heptene. The units derived from the olefins of the 2 l ~ 3 WO ~7/00897 . ~
formula CH~=CH~ or from the cycloole~ins are present in the copolymers in quantities from 1 to 20 mol-%.
The copolymers can also contain units derived from polyenes, in particular conjugated or non-conjugated, linear or cyclic dienes such as, for example, 1,4-hexadiene, isoprene, 1,3-butadiene, 1,5-hexadiene and 1,6-heptadiene.
A further use of interest is the preparation of elastomeric copolymers of ethylene with ~-olefins of the formula CH~=CHR, where R is an al~.yl radical having from l to lO carbon atoms, the said copolymers optimally containing minor proportions of units derived from a polyene.
The saturated elastomeric polymers obtainable by means of the catalysts of the present invention contain from 15 to 85 mol-% o~ ethylene units, the complement up to lOO consisting of units of one or more ~-olefins and/or of one non-conjugated diolefin capable ol' cyclopolymerizing. The unsaturated elastomeric copolymers contain, besides the units derived from the polymerization of ethylene and ~-olefins, also minor propor-tions of unsaturated units derived from the copolymerization of one or ~ore polyenes. The content of unsaturated units can vary from 0.1 to 5Yo by weight and is preferably between 0.2 and 2% by weight.
The copolymers obtainable are characterized by valuable properties, such as a lO~! dSh content and a uniform distribution of the comonomers in the copolymer chain.
The ~-olefins ~/hich can be used comprise, for ex.ample, propylener 1-butene and 4-methyl-1-pentene. The preferred ~-olefin is propylene.
~ =
~ W097l00~97 2 1 9 7 6 4 ~ I i '7'1~
The non-conjugated diole~ins capable of cyclopolymerizing, which can be used, are 1,5-hexadiene, 1,6-heptadiene and 2-methyl-1,5-hexadiene.
The polyenes capable of giving unsaturated units, which can be used, are:
- conjugated dienes such as, for example, butadiene and isoprene;
- non-conjugated linear dienes such as, for example, trans-1,4-hexadiene, cis-1,4-hexadiene, 6-methyl-1,5-heptadiene, 3,7-dimethyl-1,6-octadiene and ll-methyl-1,10-dodecadiene;
- monocyclic diolefins such as, for example, cis-1,5-cyclooctadiene and 5-methyl-1,5-cyclooctadiene;
- bicyclic diolefins such as, for example, 4,5,8,9-tetrahydroindene and 6- and/or 7-methyl-4,5,8,9-tetrahydroindene;
- alkenyl- or alkylid~ne-norbornenes such as, for example, 5-ethylidene-2-norbornene, 5-isopropylidene-2-norbornene, exo-5-isopropenyl-2-norbornene and 5-vinyl-2-norbornene;
- polycyclic diolefins such as, for example, dicyclo-pentadiene, tricyclo[~.Z.1.0-7]4,9-undecadiene and its 4-methyl derivative.
Preferred polyenes are 5-ethylidene-2-norbornene, trans-1,4-hexadiene and cis-1,-~-hexadiene. 5-Ethylidene-2-norbornene (ENB~
is particularly preferred.
The polymerization processes, which use the catalysts of the invention, can be carried out in the liquid phase, in the pres-ence or absence of an inert hydrocarbon solvent, or in the gas phase. The hydrocarbon solvent can be aromatic such as toluene, W097~0897 ~ ~97643 r~
or aliphatic such as propane, hexane, heptane, isobutane and cyclohexane.
l'he polymerization temperature is generally between -100~C
and 250~C. In particular, in the processes for the preparation of HDPE or LLDPE, it is qenerally between 20CC and 150~C and especially between 40~C and gooe. In the processes for the prep-aration of elastomeric copolymers, it is generally between 20~C
and 100~C and especially between 30~C and 80~C.
The molecular weight o~ the polymers can be ~aried simply by altering the polymerization tempeaature, the type or the concen-tration of the catalyst components or using molecular weight regulators such as, for example, hydrogen.
The molecular weight distribution can be varied by using mixtures of different cyclopentadienyl compounds or by carrying out the polymerization in several stages which differ in the polymerization temperatures andJor in the concentrations of the molecular weight regulator.
The catalyst components can be brought into mutual contact before the polymerization. The contact time is generally between 1 and 60 minutes, preferably between 5 and 20 minutes. The pre-contact concentrations for the cyclopentadienyl compound are ~etween lO-' and 10-3 n~olfl, ~hile, for the product of the reac-tion between alumini~m al~.yl and water, they are between 10 and 103 mol/l. The precontact is in general effected in the presence of a hydrocarbon solvent and, if appropriate, small quantities of monomer.
Figure 1 show~ a graph of the productivity, to give ethylene/propylene copo~ymers~ of catalysts according to the invention and accordirtg to tt-e known technology as a function of ~ WO97l00897 ~ G4~ l 17~1~
the polymerization time. This graph clearly shows the higher productivity of the catalysts according to the invention as com-pared with known catalysts at short polymerization times.
The following examples are given for illustrative purposes and do not limit the invention.
CHARACTERIZATIONS
The intrinsic viscosity [~] was measured in tetralin at ~35~C.
The comonomer content in the elastomeric ethylene/propylene copolymers was determined by IR.
The catalyst components were prepared as follows:
CYCLOPENTADIENYL COMPOUNDS
rac-ETHYLENE-BIS(4,5,6,7-TETRAHYDROINDENYL)ZIRCONIUM DIr~Tl~Tn~
(r-EBTHIZrCl,) This was prepared according to the procedure described in EP
575,875.
~R~ MT!~ALLIC ALUMINIUM COMPOUNDS
TRI-ISOBUTYLALUNINIUM [TI3A]
The commercial product ~rom WITCO was used.
TRIS-l2,4,4-TRIMETHYL-PENTYLj-ALUMINIUM [TIOA]
This was prepared according to the method described in Liebigs Ann. Chem. vol. 62C~, Ziegler et al. "Aluminumtrialkyle und Dialkyl-aluminumhydride aus Aluminumisobutyl-Verbindungen [Aluminium trialk~1s and dialkyl-a~uminium hydrides from alumin-ium isobutyl compounds]", pdges 14-19Ø
Preparation of elastomeric C~/C~-copolymers 1324 g (2 litres) of n-hexane, 44.7 g of ethylene, 388 g of propylene and 0.94 mmol of water were introduced at ambient tem-W097~08g7 2l q76~43 r~ 5 perature into a 4.2s litre autoclave fitted with stirrer, mano-meter, temperature indicator, catalyst-charging system, monomer feed lines and thermostat jacket, and purified by purging with ethylene at 80~C.
The catalyst solution was prepared by adding the quantities of aluminium alkyls given ir- Table 1 to a suspension of 0.8 mg o~ r-F.BT}IT2ZrC12 in a hydrocarbon solvent consisting of about 2 ml of solvent per mg of metallocene. Stirring of the mixture was continued for ~ minutes at a temperature of 2CCC, and the 501-ution was then injected into the autoclave under ethylene pres-sure at a temperature about 2~C lower than the polymerization temperature. The temperature was then raised within about 2 min-utes to 50~C and ~:ept constant for the whole duration of the polymerization.
The pressure was k.ept constant at a value of 9.6 bar by feeding an ethylene/propylene mixture in a 60:40 ratio. The con-sumption o~ monomers fed was monitored at regular time intervals ~2 minutes) throughout the whole duration o~ the polymerization.
When the total quantity of monomers fed reached a value of 60 g, the reaction wa~ stopped by degassing the mcnomers. The polymer obtained was dried in an oven at 60~C in vacuo.
The data relating to the polymerization and to the characterization of the copolymer obtained are given in Table 1.
The data relatincJ tO the consumption of monomers as a func-tion of the polymerization time are given in '~'able 2.
E~hPLES 4-5 ~comParison) Preparation of elastomeric C,/C~-copolymers 4 3 ~ ~7 wo g71008g7 r r,~ S
The procedure described in Examples 1-3 was followed, but with the difference that only one of the components of the mix-ture (B~ of aluminium compounds was used.
The data relating to the polymerization and to the characterization of the polymer obtained are given in Table 1.
The data relating to the monomer consumption as a function of the polymerization time are given in Table 2.
W097/00897 ~ ~ 7 6 4 3 r~ . . C~..LI~ ~
T~3LE 1 EXAMPLE TILA TIOA Al/~,O time C2 units [~]
~m mol~ ~mmolj (moi) ~min) 1~ by (dl/
weight) g) 1 0.94 0.94 2 31 57.3 3.75 2 0.4~ 1.41 2 33 55.6 3.70 3 1.41 0.47 2 39 62.3 4.20 4 l~8a 0 2 59 ~3.1 4.56 ~comp.) 0 1.88 2 42 5~.9 3.93 (comp.) ~ wo 97,008g7 ~ ! ~ 7 ~ 4 3 F~ ~ s polymeri7ationtotal monomers ed (q) (m~nl EX.l E.Y.2 EX.3 EX.4 EX.5 (comP) (com 2 0 0.2 1.3 3.9 0.1 4 5.8 5 12.1 6.8 4.1 6 13.9 12.4 17 8.3 8.2 8 20.8 19.4 2G 10.5 11.6 26.2 24.6 23.6 12.3 14.8 12 30.7 29.1 27.5 14.1 17.9 14 34.5 33.1 31 16 20.9 16 38 36.7 34 18 24.8 18 41.2 39.9 36.8 19.9 28.4 44.2 43.1 39.3 21.8 31.9 22 47.5 46.s 41.8 23.6 35.4 24 50.7 49.7 44.3 25.6 38.6 Z6 53.7 52.3 47 27.8 42.1 28 56.3 54.9 49.4 30 45.5 58.7 56.9 51.7 32.1 48.4 32 60~ 58.9 53.8 34.3 51.1 34 60- 55.7 36.3 53.3 36 57.4 38.3 55.2 38 58.9 40.1 56.9 42 58.3 42 43.8 60 44 45.7 46 47.5 48 49.3 51.3 s2 53.2 54 55.2 S8 58.6 * 31 minutes ~ 33 minutes
WO97/~B97 I~I/L~ l5 TI~LE:
CATALYSTS AND PROCESSES FOR THE POLYMERIZATION OF OLEFINS
The present invention relates to catalysts for the polymerization of olefins, obtained from cyclopentadienyl com-pounds, organometallic aluminium compounds and water.
Homogeneous catalyst systems for the polymerization of olefins are known which comprise a metallocene and the product of the reaction between water and an aluminium alkyl, where the alkyl is other than methyl.
In European Patent Application EP 384 171, catalysts are described which are suitable for the polymerization of olefins and comprise the product of the reaction between:
(A~ a metallocene compound of the general formula:
~csR~ Rl~)(csRl~l)Mx~-m where (C5R'") is a cyclopentadienyl group in which R' is hydrogen, an alkyl, alkenyl, aryl, alkylaryl or arylalkyl rad-ical having from 1 to 20 C atoms or a group CR2SiR3 or a group SiR3 with R being defined as for R', or two ~or four) substituents R' of one and the same cyclopentadienyl group form one (or two) rings having from 4 to 6 C atoms, R" is a divalent radical selected from an optionally substituted alkylene group having from 1 to 8 C atoms, an SiR2, PR or NR group with R being defined as for R', which forms a bridge link between two cyclo-pentadienyl groups, X is hydrogen, halogen, -OMX(C5R'")2, -OH or -OR with R being defined as for R', or a hydrocar~on radical having the meaning of R', M is a transition metal of valency 3 or 4, selected from Ti, ~r or Hf, p is 0 or 1, m is 0, 1 or 2, and, if m = 0, p = 0 and, if p = 0, at least one radical R' is other than hydrogen, n = 4, if p = 1, and n = 5, if p = 0; and ~ ~7~43 W097~00897 PCT~P9~02~515 (P) an alumoxan~ of the formula:
\ Al - O - Al R~ / \ R4 in which R~, R~, R3 and R4 can generically be alkyl, alkenyl or alkylaryl radicals having 2-~0 carbon atoms.
The alumoxanes (B~ can be prepared by reacting the cor-responding trialkylaluminium with water in a 2:l molar ratio. In the embodiment exa~,ples, alumoxanes are used in which R1, R~, R3 and R4 are ethyl, isobutyl or 2-methylpentyl groups.
European Patent Application ~P 575 87s describes homogene-ous catalyst systems for the polymerization of olefins, obtained by contacting the following components:
~) a cyclopentadienyl compound of the general formula:
(C5Rx~ Hs-x)R~l~(csRly-lrlH5-y),lM~3ll in which M is I~i, Zr or ~f, C5R1x,nHsx and C5R1y~H5y are cyclopentadiene rings substituted in the same way or dif-ferent ways, the substituents R1 which can be identical or different are alky', alkenyl, aryl, alkylaryl or arylalkyl radicals which have from l to 20 carbon atoms and can also contain si or Ge atoms, or are Si(CH3~3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R- is a group forming a bri~ge link between the two cyclopentadiene rings and is selected from CR3~, C,R34, SiRl~, si,R34, GeR3~, Ge~R3~, R375iCR32, NR1 or PR1, with the substituents R3 which can be identical or dif-ferent being R1 or hydrogen, or also two or four sub-stituents R3 can form one or two rings having from 3 to 6 2 l 9 7~43 W097/00897 PCT~P96/02615 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, OH, SH, R1, OR1, SR1, NR12 or PR12, m can be O or l, n can be 0 or l, being l if m = l, x is an integer between (m+l) and 5, and y is an integer between m and 5;
(B) an organometallic aluminium compound of the general formula AlR33zHz, in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from l to lO carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one the substituents R3 is other than a linear alkyl group, and z is 0 or l; and (C) water.
The molar ratio between the organometallic aluminium com-pound and the water is between l:l and l00:l. In the embodiment examples, the organometallic aluminium compounds used are only triisobutylaluminium and triisohexylaluminium.
In Italian Patent Application No. MI/54A/l5l6, homogeneous catalyst systems for the polymerization of olefins are described which possess an activity improved over those exemplified in the abovementioned patent application ~P 575 8~5, which systems com-prise the product obtained by contacting the following components:
(A) a cyclopentadienyl compound o~ the formula:
(CsR~ Hs-x~R~ csR~ s-y)l~MQ3ll in which ~ is rL'i, Zr or Hf, C5R1~,nH5~ and C5Rly1nH5y are cyclopentadiene rings substituted in the same way or dif-ferent ways, the substituents p~1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl ~ 2 ~ q76~3 W047/00897 pCT~P9~U2615 radicals which have from 1 to 20 carbon ator~s and can also contain si or Ge atoms, or are si(CH3J3 groups, or also two or four substituents Rl of one and the same cyclopentadienyl group car, form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR32, C~R34r SiR32, ~i,R34, ~eR32, Ge2R34, R3~SiCR32, NRI or PRI, with the substituents R3 which can be identical or di~-ferent being Rl or hydroqen, or also two or four sub-stituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q whicn can be identical or different are halogen, hydrogen, Rl, ORI, SRI, NR12 or PRI2, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between (m+1~ and 5 and y is an Lnteger between m and 5;
(BJ an organometallic aluminium compound of the formula:
Al-(CH,-CR4R5R6)3z~z in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to lO carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to lO
carbon atoms, or R4 and R5 are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to lO car-bon atoms and z is O or 1; and (C) water.
The molar ratio between the organometallic aluinium com-pound and the water is between 1:1 and lOO:l.
The polymerization yields of the catalysts described in the abovementioned patent applications are, albeit relatively high, ~ WO 97~00897 ~ 1 q ~t ~ 4 3 ~ 7~15 not altogether satisfactory if the residence times of the reac-tion mixture in the reactor are short. This is particularly important in industrial polymerization processes, especially in those which operate continuously, where it is very advantageous to operate with short residence times.
It would therefore be desirable to improve the productivity of the abovementioned catalysts at short residence times.
It has now been found, unexpectedly, that catalysts for the polymerization of olefins, of the type of those described in the abovementioned patent applications, obtained from particular mixtures of organometallic aluminium compounds, show superior activities at short residence times than the corresponding cata-lysts obtained from the individual components of the abovementioned mixtures of aluminium compounds.
The catalysts which are the subject of the present invention comprise the product obtained by contacting the fol-lowing components:
(A) a cyclopentadienyl compound of the formula (I):
(CsRl~lDH~)R~ (csRy-mHs-~DMQ3-~
in which M is Ti, Zr or Hf, C5RI~,~H5~ and C~RIymH5y are cyclopentadiene rings substituted in the same way or differ-ent ways, the substituents Ri which can be identical or dif-ferent are alkyl, alkenyl, aryl, alkylaryl or arylalkyl rad-icals which have from 1 to 20 carbon atoms and can also con-tain Si or Ge atomf" or Si(CH;)3 groups, or also two or four substituents Rl of one and the same cyclopentadienyl group can form one or two rings having from ~ to ~ carbon atoms, R2 is a group forming a bridge linh between the two cyclo-pentadiene rings and is selected from CR3~, C2R34, SiR32, 2 1 q7643 097~0897 p~t/~ C
Si2R34, GeR3~, Ge,R3~, R325iCR32, NRI or PRI, with the substituents R3 which can be identical or different being Rl or hydrogen, or also two or four substituents R3 can form one or two ring~ having from 3 to 6 carbon atoms~ the sub-stituents Q which can be identical or different are haloqen, hydrogen, Rl, OR~, SRI, NRI~ or PRI~, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between (m+lJ
and 5, and y is an integer between m and 5;
~B) a mixture composed of:
(B1) 1-99 mol-% of an organometallic aluminium compound of the formula ~
Al-(CH-,-CR4RSR6~3zH, (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and RS zre fused together to form a ring having from 4 to Ç carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is O or l;
~B2) 1-99 mol-% of an organometallic aluminium compound of the formula (III):
AlR33~H,~ (III~
in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also con-tain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl 21 ~ ~47) group, and w is 0 or l, the compounds o~ the formula (II) defined above being excluded; and (C) water.
The molar ratio between the total of the organometallic alu-minium compounds and the water is between 1:1 and lO0:1, prefer-ably between l:l and 50:1 and more preferably between l:l and 10:1.
The molar ratio between the aluminium and the metal of the cyclopentadienyl compound is between about 50 and 10,000, pre-ferably between about 500 and 5000 and more preferably between lO00 and 2000.
The molar ratio ~Bl)J(B2) between the two components of the mixture (B) of organometallic aluminium compounds is preferably between about 10:90 and about 90:lO, and more preferably is between about 25:75 and about 75:25. Those mixtures (B) are par-ticularly preferred in which the components (Bl) and (B2) are present in approximately equimolar quantities.
In the case of m=o, particularly suitable cyclopentadienyl compounds are those in which M i5 Zr and the groups CSRIx,nH5~ and C5~1y~H5y are pentamethyl-cyclopentadienyl, indenyl or 4,5,6,7-tetrahydroindenyl, while the substituents Q are chlorine atoms or hydrocarbon groups containing from l to 7 carbon atoms.
Non-limiting examples of cyclopentadienyl compounds (A) with m = 0 are:
(Me3cp)2Mcl2 ~Me4Cp),MCl, (MesCp)2Mcl2 (Mescp)2MMe2 (MesCp)~(ol~e)2 (MesCp)2M(C6Hs)2 (Me5Cp)2M(CH3) Cl (Etr~e4cp) ,~rlcl2 [ (CbHS)Me4CP]2MCl2 (E:tSCP)2MC12 (Me5Cp).M(CbH5)cl (Ind)2l~cl2 (Ind)2MMe2 (~.Ind),r~Cl2 (}14Ind)2MMe2 W097/~0897 ,~~ n?~-[si(c1~3)3cp]2Mclz {[Sl(cM3)3]2cP}2Mcl2 (Me4cp~(Mescp1Mcl2 ~Me5CpJMCl3 (~lesCp)MRenz3 (Ind)MBenz3 (H4Ind)MBenz3 where Me = methyl, Et = ethyl, Cp = cyclopentadienyl, Ind =
indenyl, H4Ind = 4,5,6,7-tetrahydroindenyl, Benz = benzyl, M is Ti, Zr or Mf and preferably is Zr.
In the case of m = l, particularly suitable cyclopentadienyl compounds are those in which M is Zr and the groups C5R~H5~ and C5RIy~mH5y are tetramethyl-cyclopentadienyl, indenyl or tetrahydroindenyl and R- is a group ~CH3)~Si or C2~4~ while the substituents Q are chlorine atoms or hydrocarbon groups having from l to 7 carbon atoms.
Non-limiting examples of cyclopentadienyl compounds (R) with m = l are:
Ne2Si(Me4CP)21'qCl2 Me25i(Me4CP)2MMe2 Me2C(Me4CP)~MeCpJMC12 Me2Si(Ind)2MCl2 Me2CSi(lnd~2MMe2 Me25i(~5e4Cp)2MCl(OEtJ
c2H4~Ind~2~C12 C2~14(Ind~2MMe2 C2H4(Ind)2M(NMe2)2 C2H4(H4Lnd)2~5Cl2 C2H4(H4Ind)~MMe2 C2M4(114Ind)2M(NMe2)~Me Ph(Me)Si(Ind)2MC12 Ph,Si(Ind)2MC12 Me2C(FlU)lCP)~ICl2 C2H4(Me4CP)2MCl2 C2Me,l(Ind)~MCl2 Me2SiCH2(Ind)2MCl2 C2H4(2-MeInd)2MC12 C,M4(3-MeInd)~MC12 C2H4(4,7-Me2Ind),MC12 C2H4 ( S, 6-Me2Ind ) 2~5C12 where Me = methyl, Cp = cyc1Opentadienyl, Ind = indenyl, Flu =
fluorenyl, Ph = phenyl, M~Ind = 4,5,6,7-tetrahydroindenyl, M is Ti, Zr or Hf and preferab~y is Zr.
In the organometallic aluminium compound of the formula (IIJ
which can be used a~ component (Bl), R4 is preferably a methyl or ethyl group, while R~ is preferably a hydrogen atom.
~ W097/00897 2 1 9 7 h 4 3 r~ c rarticularly preferred as components (Bl) are the organometallic aluminium compounds in which R4 is a methyl group, RS is an alkyl group with a branched chain having a num-ber of carbon atoms greater than 4 and R6 is a hydrogen atom.
Non-limiting examples of organometallic aluminium : a~ln~c which can be used as components (B1~ are:
tris-(2,4,4-trimethyl-pentyl)-aluminium and di-(2,4,4-trimethyl-pentyl)-aluminium hydride.
The particularly preferred compound is tris-(2,4,4-trimethyl-pentyl)-aluminium ~TIOA).
In the organometallic aluminium compound of the formula (II) which can be used as component (Bl), preferably all the substituents R7 are non-linear alkyl, alkenyl or alkylaryl rad-icals. More preferably, all the substituents R7 of the organometallic aluminium compound are isoalkyl radicals.
Non-limiting examples of organometallic aluminium compounds which can be used as components (B2) are:
triethylaluminium, di-methylisobutylaluminium, methyl-di-isobutylaluminium, tri-isobutylaluminium, di-isobutylaluminium monohydride and tris-(2,2-dimethylpropyl)aluminium.
The particularly preferred compound is triisobutylaluminium (TIBA).
The components constituting the catalysts of the present invention can be brought into contact in various ways.
In an embodiment example, the mixture of aluminium compounds is contacted with watel-, and then the reaction product thus w~ g7,00897 2 I q 7 6~ 3 obtained is brought into contact with the cyclopentadienyl com-pound.
A further subject of the present invention is therefore a catalyst for the polymerization of olefins, comprising the prod-uct obtained by contacting the following components:
(A) a cyclopentadienyl compound of the formula (I):
( C5R I 1~ ~nH5 X ) R?~l ( CsR 1~ Hs ~. )"MQ3~
in which M is Ti, Zr or Hf, C5R~ ,H5~ and C5RIymH5y are cyclopentadi.ene rings substituted in the same way or differ-ent ways, the substituents Rl which can be identical or dif-ferent are alkyl, al~enyl, aryl, alkylaryl or arylalkyl rad-icals which have from 1 to 2U carbon atoms and can also con-tain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents Rl of orte and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, RZ is a group forming a bridge link between the two cyclo-pentadiene rings and is selected from CR32, C,R34, SiR3~, sizR34l GeR3~, Ge.R34, R3~SiCR3~, NRI or PRI, with the substituents R3 WtliC~ can be identical or different being Rl or hydrogen, or also two or ~our substituents R3 can fornt one or two rings having from 3 to 6 c~rbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, Rl, ORI, SRI, NR~2 or PR12, m can be O or 1, n can be O or 1, being 1, if m = 1, x is an integer between ~m~1) and 5, and y is an integer between m and 5;
and (B) the product of the reaction between water and a mixtu.re consisting of:
21 97~43 097/00897 I~l~t~
(sl) 10-90 mol-'8 of an orqanometallic aluminium com-pound of the formula (II):
Al-(CH7-CR4~5R~)3zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from l to lO carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and RS are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1; and (S~) 10-90 mol-~ of an organometallic aluminium com-pound of the formula (III~:
AlR3;;~.H" (III~
in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also con-tain si or ~e atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or l, the compounds of the formula (II~ defined above being excluded.
The molar ratio between the organometallic aluminium compounds and the water is between 1:1 and 100:1, preferably between 1:1 and 50:1, more preferably between 1:1 and 10:1.
The component.s of the catal~sts of the present invention can be brought into contact by various methods.
For example, it is possible gradually to add water to the mixture of aluminium compounds in solution in an inert aliphatic or aromatic hydrocarbon solvent such as, for example, heptane or w0.~7~00897 ~ 1 ~ 7 6 4 3 P .,~. C"~' l!i ~
toluene. The solution thus obtained is contacted with a solution of a cyclopentadienyl compound in a suitable solvent as, for example, toluene.
According to another way of proceeding, the water can be introduced in the n~onomer, or in one of the monomers, to be polymerized; in this case, the mixture of aluminium compounds and the cyclopentadienyl compound are first brought into contact before they are used in the polymerization. Moreover, the water can be made to react in a combined form as a hydrated salt, or it can be adsorbed or absorbed on an inert support such as sil-ica. Another preparation method is the reaction of the aluminium compounds with boric anhydride or boric acid.
The catalysts of the present invention can also be used on inert supports. This is effected by depositing the cyclopentadienyl cor,pound, or the product of the reaction there-of with the aluminium compounds pre-reacted with water, or the aluminium compounds pre-reacted with water and then the cyclopentadienyl com~ound, on inert supports such as, for example, silica, alumina, styrene/ divinylbenzene copolymers, polyethylene or polypropylene.
A particularly suitable class of inert supports which can be used is that constituted by porous organic supports functionalized with qroups having active hydrogen atoms. Those are particularly preierred in which the organic support i5 a partially crosslinked styrene polymer. Supports of this type are described in European Application EP-633 272, the content of which is understood to be incorporated in the present descrip-tion.
2 i 97643 WO97/008s7 PCT/EP96/02615 The solid compound thus obtained, in combination with the further addition of aluminium alkyl compounds, whether pre-reacted with water or not, can be used in the gas-phase polymerization.
The catalysts of the present invention can be used in the polymerization reactions of olefins.
A further subject of the present invention is therefore a process for the polymerization of at least one olefin of the formula CH,=CHR, in which R is hydroqen or an alkyl radical hav-ing from 1 to 20 carbon atoms, comprising the polymerization reaction of the said olefins in the presence of a catalyst as described above.
The catalysts according to the present invention can advan-tageously be used in the homopolymerization of ethylene and, in particular, for the preparation of HDPE, and for the copolymerization of ethylene and, in particular, for the prep-aration of LLDPE.
The LLDPE copolymer~, which are obtained have a content of ethylene units of between ~0 and 99 mol-%. Their density is between 0.~7 and O.g5 g/cml3 and they are characterized by a uni-form distribution of the comonomer units within the polyme~
chain.
The olefins which can be used as comonomers comprise c~-olefins of the formula CH,=CH~, where R is a linear or branched or cyclic alkyl radical havinq from 1 to 20 carbon atoms, or cycloolefins. ~xamples of such olefins are propylene, l-butene, l-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, allylcyclohexane, cyclopentene, cyclohexene, norbornene and 4,6-dimethyl-1-heptene. The units derived from the olefins of the 2 l ~ 3 WO ~7/00897 . ~
formula CH~=CH~ or from the cycloole~ins are present in the copolymers in quantities from 1 to 20 mol-%.
The copolymers can also contain units derived from polyenes, in particular conjugated or non-conjugated, linear or cyclic dienes such as, for example, 1,4-hexadiene, isoprene, 1,3-butadiene, 1,5-hexadiene and 1,6-heptadiene.
A further use of interest is the preparation of elastomeric copolymers of ethylene with ~-olefins of the formula CH~=CHR, where R is an al~.yl radical having from l to lO carbon atoms, the said copolymers optimally containing minor proportions of units derived from a polyene.
The saturated elastomeric polymers obtainable by means of the catalysts of the present invention contain from 15 to 85 mol-% o~ ethylene units, the complement up to lOO consisting of units of one or more ~-olefins and/or of one non-conjugated diolefin capable ol' cyclopolymerizing. The unsaturated elastomeric copolymers contain, besides the units derived from the polymerization of ethylene and ~-olefins, also minor propor-tions of unsaturated units derived from the copolymerization of one or ~ore polyenes. The content of unsaturated units can vary from 0.1 to 5Yo by weight and is preferably between 0.2 and 2% by weight.
The copolymers obtainable are characterized by valuable properties, such as a lO~! dSh content and a uniform distribution of the comonomers in the copolymer chain.
The ~-olefins ~/hich can be used comprise, for ex.ample, propylener 1-butene and 4-methyl-1-pentene. The preferred ~-olefin is propylene.
~ =
~ W097l00~97 2 1 9 7 6 4 ~ I i '7'1~
The non-conjugated diole~ins capable of cyclopolymerizing, which can be used, are 1,5-hexadiene, 1,6-heptadiene and 2-methyl-1,5-hexadiene.
The polyenes capable of giving unsaturated units, which can be used, are:
- conjugated dienes such as, for example, butadiene and isoprene;
- non-conjugated linear dienes such as, for example, trans-1,4-hexadiene, cis-1,4-hexadiene, 6-methyl-1,5-heptadiene, 3,7-dimethyl-1,6-octadiene and ll-methyl-1,10-dodecadiene;
- monocyclic diolefins such as, for example, cis-1,5-cyclooctadiene and 5-methyl-1,5-cyclooctadiene;
- bicyclic diolefins such as, for example, 4,5,8,9-tetrahydroindene and 6- and/or 7-methyl-4,5,8,9-tetrahydroindene;
- alkenyl- or alkylid~ne-norbornenes such as, for example, 5-ethylidene-2-norbornene, 5-isopropylidene-2-norbornene, exo-5-isopropenyl-2-norbornene and 5-vinyl-2-norbornene;
- polycyclic diolefins such as, for example, dicyclo-pentadiene, tricyclo[~.Z.1.0-7]4,9-undecadiene and its 4-methyl derivative.
Preferred polyenes are 5-ethylidene-2-norbornene, trans-1,4-hexadiene and cis-1,-~-hexadiene. 5-Ethylidene-2-norbornene (ENB~
is particularly preferred.
The polymerization processes, which use the catalysts of the invention, can be carried out in the liquid phase, in the pres-ence or absence of an inert hydrocarbon solvent, or in the gas phase. The hydrocarbon solvent can be aromatic such as toluene, W097~0897 ~ ~97643 r~
or aliphatic such as propane, hexane, heptane, isobutane and cyclohexane.
l'he polymerization temperature is generally between -100~C
and 250~C. In particular, in the processes for the preparation of HDPE or LLDPE, it is qenerally between 20CC and 150~C and especially between 40~C and gooe. In the processes for the prep-aration of elastomeric copolymers, it is generally between 20~C
and 100~C and especially between 30~C and 80~C.
The molecular weight o~ the polymers can be ~aried simply by altering the polymerization tempeaature, the type or the concen-tration of the catalyst components or using molecular weight regulators such as, for example, hydrogen.
The molecular weight distribution can be varied by using mixtures of different cyclopentadienyl compounds or by carrying out the polymerization in several stages which differ in the polymerization temperatures andJor in the concentrations of the molecular weight regulator.
The catalyst components can be brought into mutual contact before the polymerization. The contact time is generally between 1 and 60 minutes, preferably between 5 and 20 minutes. The pre-contact concentrations for the cyclopentadienyl compound are ~etween lO-' and 10-3 n~olfl, ~hile, for the product of the reac-tion between alumini~m al~.yl and water, they are between 10 and 103 mol/l. The precontact is in general effected in the presence of a hydrocarbon solvent and, if appropriate, small quantities of monomer.
Figure 1 show~ a graph of the productivity, to give ethylene/propylene copo~ymers~ of catalysts according to the invention and accordirtg to tt-e known technology as a function of ~ WO97l00897 ~ G4~ l 17~1~
the polymerization time. This graph clearly shows the higher productivity of the catalysts according to the invention as com-pared with known catalysts at short polymerization times.
The following examples are given for illustrative purposes and do not limit the invention.
CHARACTERIZATIONS
The intrinsic viscosity [~] was measured in tetralin at ~35~C.
The comonomer content in the elastomeric ethylene/propylene copolymers was determined by IR.
The catalyst components were prepared as follows:
CYCLOPENTADIENYL COMPOUNDS
rac-ETHYLENE-BIS(4,5,6,7-TETRAHYDROINDENYL)ZIRCONIUM DIr~Tl~Tn~
(r-EBTHIZrCl,) This was prepared according to the procedure described in EP
575,875.
~R~ MT!~ALLIC ALUMINIUM COMPOUNDS
TRI-ISOBUTYLALUNINIUM [TI3A]
The commercial product ~rom WITCO was used.
TRIS-l2,4,4-TRIMETHYL-PENTYLj-ALUMINIUM [TIOA]
This was prepared according to the method described in Liebigs Ann. Chem. vol. 62C~, Ziegler et al. "Aluminumtrialkyle und Dialkyl-aluminumhydride aus Aluminumisobutyl-Verbindungen [Aluminium trialk~1s and dialkyl-a~uminium hydrides from alumin-ium isobutyl compounds]", pdges 14-19Ø
Preparation of elastomeric C~/C~-copolymers 1324 g (2 litres) of n-hexane, 44.7 g of ethylene, 388 g of propylene and 0.94 mmol of water were introduced at ambient tem-W097~08g7 2l q76~43 r~ 5 perature into a 4.2s litre autoclave fitted with stirrer, mano-meter, temperature indicator, catalyst-charging system, monomer feed lines and thermostat jacket, and purified by purging with ethylene at 80~C.
The catalyst solution was prepared by adding the quantities of aluminium alkyls given ir- Table 1 to a suspension of 0.8 mg o~ r-F.BT}IT2ZrC12 in a hydrocarbon solvent consisting of about 2 ml of solvent per mg of metallocene. Stirring of the mixture was continued for ~ minutes at a temperature of 2CCC, and the 501-ution was then injected into the autoclave under ethylene pres-sure at a temperature about 2~C lower than the polymerization temperature. The temperature was then raised within about 2 min-utes to 50~C and ~:ept constant for the whole duration of the polymerization.
The pressure was k.ept constant at a value of 9.6 bar by feeding an ethylene/propylene mixture in a 60:40 ratio. The con-sumption o~ monomers fed was monitored at regular time intervals ~2 minutes) throughout the whole duration o~ the polymerization.
When the total quantity of monomers fed reached a value of 60 g, the reaction wa~ stopped by degassing the mcnomers. The polymer obtained was dried in an oven at 60~C in vacuo.
The data relating to the polymerization and to the characterization of the copolymer obtained are given in Table 1.
The data relatincJ tO the consumption of monomers as a func-tion of the polymerization time are given in '~'able 2.
E~hPLES 4-5 ~comParison) Preparation of elastomeric C,/C~-copolymers 4 3 ~ ~7 wo g71008g7 r r,~ S
The procedure described in Examples 1-3 was followed, but with the difference that only one of the components of the mix-ture (B~ of aluminium compounds was used.
The data relating to the polymerization and to the characterization of the polymer obtained are given in Table 1.
The data relating to the monomer consumption as a function of the polymerization time are given in Table 2.
W097/00897 ~ ~ 7 6 4 3 r~ . . C~..LI~ ~
T~3LE 1 EXAMPLE TILA TIOA Al/~,O time C2 units [~]
~m mol~ ~mmolj (moi) ~min) 1~ by (dl/
weight) g) 1 0.94 0.94 2 31 57.3 3.75 2 0.4~ 1.41 2 33 55.6 3.70 3 1.41 0.47 2 39 62.3 4.20 4 l~8a 0 2 59 ~3.1 4.56 ~comp.) 0 1.88 2 42 5~.9 3.93 (comp.) ~ wo 97,008g7 ~ ! ~ 7 ~ 4 3 F~ ~ s polymeri7ationtotal monomers ed (q) (m~nl EX.l E.Y.2 EX.3 EX.4 EX.5 (comP) (com 2 0 0.2 1.3 3.9 0.1 4 5.8 5 12.1 6.8 4.1 6 13.9 12.4 17 8.3 8.2 8 20.8 19.4 2G 10.5 11.6 26.2 24.6 23.6 12.3 14.8 12 30.7 29.1 27.5 14.1 17.9 14 34.5 33.1 31 16 20.9 16 38 36.7 34 18 24.8 18 41.2 39.9 36.8 19.9 28.4 44.2 43.1 39.3 21.8 31.9 22 47.5 46.s 41.8 23.6 35.4 24 50.7 49.7 44.3 25.6 38.6 Z6 53.7 52.3 47 27.8 42.1 28 56.3 54.9 49.4 30 45.5 58.7 56.9 51.7 32.1 48.4 32 60~ 58.9 53.8 34.3 51.1 34 60- 55.7 36.3 53.3 36 57.4 38.3 55.2 38 58.9 40.1 56.9 42 58.3 42 43.8 60 44 45.7 46 47.5 48 49.3 51.3 s2 53.2 54 55.2 S8 58.6 * 31 minutes ~ 33 minutes
Claims (16)
1. Catalyst for the polymerization of olefins, comprising the product of the reaction between the following components:
(A) a cyclopentadienyl compound of the formula (I):
(C5R1x-mH5-x)R2m(C5R1y-mH5-y)nMQ3-n in which M is Ti, Zr or Hf, C5R1x-mH5-x and C5R1y-mH5-y cyclopentadiene rings substituted in the same way or different ways, the substituents R1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl radicals which have from 1 to 20 carbon atoms and can also contain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR3 2, C2R3 4, SiR3 2, Si2R3 4, GeR3 2, Ge2R3 4, R31SiCR3 2, NR1 or PR2, with the substituents R3 which can be identical or different being R1 or hydrogen, or also two or four substituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, R1, OR1, SR1, NR1 2 or PR1 2, m can be 0 or 1, n can be 0 or 1, being 1, if m = 1, x is an integer between (m+1) and 5, and y is an integer between m and 5;
(B) a mixture composed of:
(B1) 1-99 mol-% of an organometallic aluminium compound of the formula (II):
Al-(CH2-CR4R5R6)3-zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and R5 are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1;
(B2) 1-99 mol-% of an organometallic aluminium compound of the formula (III):
AlR3 3-wHw (III) in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or 1, the compounds of the formula (II) defined above being excluded; and (C) water, the molar ratio between the organometallic aluminium compounds and the water being between 1:1 and 100:1.
(A) a cyclopentadienyl compound of the formula (I):
(C5R1x-mH5-x)R2m(C5R1y-mH5-y)nMQ3-n in which M is Ti, Zr or Hf, C5R1x-mH5-x and C5R1y-mH5-y cyclopentadiene rings substituted in the same way or different ways, the substituents R1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl radicals which have from 1 to 20 carbon atoms and can also contain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR3 2, C2R3 4, SiR3 2, Si2R3 4, GeR3 2, Ge2R3 4, R31SiCR3 2, NR1 or PR2, with the substituents R3 which can be identical or different being R1 or hydrogen, or also two or four substituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, R1, OR1, SR1, NR1 2 or PR1 2, m can be 0 or 1, n can be 0 or 1, being 1, if m = 1, x is an integer between (m+1) and 5, and y is an integer between m and 5;
(B) a mixture composed of:
(B1) 1-99 mol-% of an organometallic aluminium compound of the formula (II):
Al-(CH2-CR4R5R6)3-zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and R5 are fused together to form a ring having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1;
(B2) 1-99 mol-% of an organometallic aluminium compound of the formula (III):
AlR3 3-wHw (III) in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or 1, the compounds of the formula (II) defined above being excluded; and (C) water, the molar ratio between the organometallic aluminium compounds and the water being between 1:1 and 100:1.
2. Catalyst according to Claim 1, wherein the molar ratio between the organometallic aluminium compound and the water is between 1:1 and 10:1.
3. Catalyst according to Claim 1, wherein the molar ratio between the aluminium of the organometallic aluminium compound and the metal M of the cyclopentadienyl compound is between 50 and 10,000.
4. Catalyst according to Claim 1, wherein in the cyclopentadienyl compound (A), m = , the groups C5R1x-mH5-x and C5R1y-mH5-y are pentamethyl-cyclopentadienyl, indenyl or 4,5,6,7-tetrahydroindenyl, M is Zr and the substituents Q are chlorine atoms or hydrocarbon groups containing from 1 to 7 carbon atoms.
5. Catalyst according to Claim 1, wherein in the cyclopentadienyl compound (A), m = 1, n = 1, R2 is a divalent group (CH3)2Si or C2H4 and the groups C5R1x-mH5-x and C5R1y-mH5-y are selected from tetramethyl-cyclo-pentadienyl, indenyl or 4,5,6,7-tetrahydroindenyl, 2-methyl-4,5,6,7-tetrahydroindenyl, 4,7-dimethyl-4,5,6,7-tetrahydroindenyl, 2,4,7-trimethyl-4,5,6,7-tetra-hydroindenyl and fluorenyl.
6. Catalyst according to Claim 1, wherein in the cyclopentadienyl compound of the formula (I) the substituents Q are chlorine atoms or methyl groups.
7. Catalyst according to Claim 1, wherein in the organometallic aluminium compound of the formula (II) R4 is a methyl or ethyl group.
8. Catalyst according to one of Claims 1 to 7, wherein in the organometallic aluminium compound of the formula (II) R6 is hydrogen.
9. Catalyst according to Claim 8, wherein in the organometallic aluminium compound of the formula (II) R4 is a methyl group and R5 is an alkyl group with a branched chain having a number of carbon atoms greater than 4.
10. Catalyst according to Claim 1, wherein the organometallic aluminium compound of the formula (II) is tri-(2,4,4-trimethyl-pentyl)-aluminium.
11. Catalyst for the polymerization of olefins, comprising the product obtained from contacting the following components:
(A) a cyclopentadienyl compound of the formula (I) (C5R1x-mH5-x)R2m(C5R1y-mH5-y)nMQ3-n (I) in which M is Ti, Zr or Hf, C5R1x-mH5-x and C5R1y-mH5-y are cyclopentadiene rings substituted in the same way or different ways, the substituents R1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl radicals which have from 1 to 20 carbon atoms and can also contain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR3 2, C2R3 4, SiR3 2, Si2R3 4, GeR3 2, Ge2R3 4, R32SiCR3 2, NR1 or PR1, with the substituents R3 which can be identical or different being R1 or hydrogen, or also two or four substituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, R1, OR1, SR1, NR1 2 or PR1 2, m can be 0 or 1, n can be 0 or 1, being 1, if m = 1, x is an integer between (m+1) and 5, and y is an integer between m and 5;
and (B) the product of the reaction between water and a mixture composed of:
(B1) 10-90 mol-% of an organometallic aluminium compound of the formula (II):
Al-(CH2-CR4R5R6)3zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and R5 are fused together to form a cycle having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1;
(B2) 10-90 mol-% of an organometallic aluminium compound of the formula (III):
AlR3 3-wHw (III) in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or 1, the compounds of the formula (II) defined above being excluded;
the molar ratio between the organometallic aluminium compounds and the water being between 1:1 and 100:1.
(A) a cyclopentadienyl compound of the formula (I) (C5R1x-mH5-x)R2m(C5R1y-mH5-y)nMQ3-n (I) in which M is Ti, Zr or Hf, C5R1x-mH5-x and C5R1y-mH5-y are cyclopentadiene rings substituted in the same way or different ways, the substituents R1 which can be identical or different are alkyl, alkenyl, aryl, alkylaryl or arylalkyl radicals which have from 1 to 20 carbon atoms and can also contain Si or Ge atoms, or Si(CH3)3 groups, or also two or four substituents R1 of one and the same cyclopentadienyl group can form one or two rings having from 4 to 6 carbon atoms, R2 is a group forming a bridge link between the two cyclopentadiene rings and is selected from CR3 2, C2R3 4, SiR3 2, Si2R3 4, GeR3 2, Ge2R3 4, R32SiCR3 2, NR1 or PR1, with the substituents R3 which can be identical or different being R1 or hydrogen, or also two or four substituents R3 can form one or two rings having from 3 to 6 carbon atoms, the substituents Q which can be identical or different are halogen, hydrogen, R1, OR1, SR1, NR1 2 or PR1 2, m can be 0 or 1, n can be 0 or 1, being 1, if m = 1, x is an integer between (m+1) and 5, and y is an integer between m and 5;
and (B) the product of the reaction between water and a mixture composed of:
(B1) 10-90 mol-% of an organometallic aluminium compound of the formula (II):
Al-(CH2-CR4R5R6)3zHz (II) in which R4 is an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, R5 is an alkyl, alkenyl or alkylaryl group with a branched chain having from 3 to 10 carbon atoms, or R4 and R5 are fused together to form a cycle having from 4 to 6 carbon atoms, R6 is hydrogen or an alkyl, alkenyl or arylalkyl group having from 1 to 10 carbon atoms, and z is 0 or 1;
(B2) 10-90 mol-% of an organometallic aluminium compound of the formula (III):
AlR3 3-wHw (III) in which the substituents R3 which can be identical or different are alkyl, alkenyl or alkylaryl radicals which have from 1 to 10 carbon atoms and can also contain Si or Ge atoms, with the proviso that at least one of the substituents R3 is other than a linear alkyl group, and w is 0 or 1, the compounds of the formula (II) defined above being excluded;
the molar ratio between the organometallic aluminium compounds and the water being between 1:1 and 100:1.
12. Process for the polymerization of at least one olefin of the formula CH2=CHR, in which R is hydrogen or an alkyl, cycloalkyl or aryl radical having from 1 to 20 carbon atoms, comprising the polymerization reaction of said olefins in the presence of a catalyst according to one of Claims 1 to 11.
13. Process for the preparation of ethylene homopolymers, comprising the polymerization reaction of ethylene in the presence of a catalyst according to one of Claims 1 to 11.
14. Process for the preparation of ethylene copolymers with one or more .alpha.-olefins of the formula CH2=CHR, where R
is a linear, branched or cyclic alkyl radical having from 1 to 20 carbon atoms or a cycloolefin, the said copolymers containing from 80 to 99 mol-% of units derived from ethylene and from 1 to 20 mol-% of units derived from alpha-olefins or cycloolefins and optionally minor proportions of units derived from a polyene, comprising the polymerization reaction of the ethylene as a mixture with the .alpha.-olefin(s) or cycloolefin(s) and optionally with the polyene in the presence of a catalyst according to one of Claims 1 to 11.
is a linear, branched or cyclic alkyl radical having from 1 to 20 carbon atoms or a cycloolefin, the said copolymers containing from 80 to 99 mol-% of units derived from ethylene and from 1 to 20 mol-% of units derived from alpha-olefins or cycloolefins and optionally minor proportions of units derived from a polyene, comprising the polymerization reaction of the ethylene as a mixture with the .alpha.-olefin(s) or cycloolefin(s) and optionally with the polyene in the presence of a catalyst according to one of Claims 1 to 11.
15. Process for the preparation of elastomeric ethylene copolymers with one or more alpha-olefins of the formula CH2=CHR, where R is an alkyl radical having from 1 to 10 carbon atoms, the said copolymers optionally containing minor proportions of units derived from a polyene, comprising the polymerization reaction of the ethylene as a mixture with one or more alpha-olefins and optionally with minor proportions of a polyene in the presence of a catalyst according to one of Claims 1 to 11.
16. Process according to Claim 15, wherein the copolymers contain from 15 to 85 mol-% of ethylene and from 85 to 15 mol-% of an alpha-olefin selected from propylene, 1-butene and 4-methyl-1-pentene.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI95A001316 | 1995-06-20 | ||
| IT95MI001316A IT1276752B1 (en) | 1995-06-20 | 1995-06-20 | CATALYSTS AND PROCEDURES FOR THE POLYMERIZATION OF OLEFINE |
| PCT/EP1996/002615 WO1997000897A1 (en) | 1995-06-20 | 1996-06-18 | Catalysts and processes for the polymerization of olefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2197643A1 true CA2197643A1 (en) | 1997-01-09 |
Family
ID=11371837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002197643A Abandoned CA2197643A1 (en) | 1995-06-20 | 1996-06-18 | Catalysts and processes for the polymerization of olefins |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US6191240B1 (en) |
| EP (1) | EP0776340B1 (en) |
| JP (1) | JP3781431B2 (en) |
| KR (1) | KR970705580A (en) |
| AT (1) | ATE172990T1 (en) |
| CA (1) | CA2197643A1 (en) |
| DE (1) | DE69600913T2 (en) |
| ES (1) | ES2125109T3 (en) |
| IT (1) | IT1276752B1 (en) |
| WO (1) | WO1997000897A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6294625B1 (en) * | 1990-03-20 | 2001-09-25 | Exxonmobil Chemical Patents Inc. | Catalyst system of enhanced productivity and its use in polymerization process |
| IT1276752B1 (en) * | 1995-06-20 | 1997-11-03 | Spherilene S P A Ora Montell I | CATALYSTS AND PROCEDURES FOR THE POLYMERIZATION OF OLEFINE |
| US5990114A (en) * | 1996-02-28 | 1999-11-23 | Recordati, S.A., Chemical And Pharmaceutical Company | Use of 5-HT1A receptor antagonists for the treatment of urinary incontinence |
| AU4564699A (en) * | 1998-08-17 | 2000-03-06 | Dow Chemical Company, The | Activator composition comprising aluminum compound mixture |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0780933B2 (en) * | 1986-11-20 | 1995-08-30 | 三井石油化学工業株式会社 | Olefin Polymerization Method |
| US5006500A (en) * | 1988-10-27 | 1991-04-09 | Exxon Chemical Patents Inc. | Olefin polymerization catalyst from trialkylaluminum mixture, silica gel and a metallocene |
| IT1237398B (en) | 1989-01-31 | 1993-06-01 | Ausimont Srl | CATALYSTS FOR THE POLYMERIZATION OF OLEFINE. |
| ATE195326T1 (en) | 1992-06-18 | 2000-08-15 | Montell Technology Company Bv | CATALYST FOR OLEFIN POLYMERIZATION |
| IT1264680B1 (en) | 1993-07-07 | 1996-10-04 | Spherilene Srl | SUPPORTED CATALYSTS FOR THE POLYMERIZATION OF OLEFINS |
| IT1273661B (en) | 1994-07-20 | 1997-07-09 | Spherilene Srl | CATALYSTS FOR THE POLYMERIZATION OF OLEFINS |
| IT1276752B1 (en) * | 1995-06-20 | 1997-11-03 | Spherilene S P A Ora Montell I | CATALYSTS AND PROCEDURES FOR THE POLYMERIZATION OF OLEFINE |
-
1995
- 1995-06-20 IT IT95MI001316A patent/IT1276752B1/en active IP Right Grant
-
1996
- 1996-06-18 AT AT96920823T patent/ATE172990T1/en active
- 1996-06-18 CA CA002197643A patent/CA2197643A1/en not_active Abandoned
- 1996-06-18 ES ES96920823T patent/ES2125109T3/en not_active Expired - Lifetime
- 1996-06-18 DE DE69600913T patent/DE69600913T2/en not_active Expired - Fee Related
- 1996-06-18 EP EP96920823A patent/EP0776340B1/en not_active Expired - Lifetime
- 1996-06-18 JP JP50234197A patent/JP3781431B2/en not_active Expired - Fee Related
- 1996-06-18 WO PCT/EP1996/002615 patent/WO1997000897A1/en not_active Application Discontinuation
- 1996-06-18 KR KR1019970701106A patent/KR970705580A/en not_active Application Discontinuation
- 1996-06-18 US US08/793,863 patent/US6191240B1/en not_active Expired - Fee Related
-
2000
- 2000-01-14 US US09/484,361 patent/US6534607B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ATE172990T1 (en) | 1998-11-15 |
| EP0776340A1 (en) | 1997-06-04 |
| KR970705580A (en) | 1997-10-09 |
| IT1276752B1 (en) | 1997-11-03 |
| DE69600913D1 (en) | 1998-12-10 |
| ES2125109T3 (en) | 1999-02-16 |
| JPH10505385A (en) | 1998-05-26 |
| JP3781431B2 (en) | 2006-05-31 |
| WO1997000897A1 (en) | 1997-01-09 |
| ITMI951316A0 (en) | 1995-06-20 |
| EP0776340B1 (en) | 1998-11-04 |
| US6534607B1 (en) | 2003-03-18 |
| US6191240B1 (en) | 2001-02-20 |
| DE69600913T2 (en) | 1999-04-15 |
| ITMI951316A1 (en) | 1996-12-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0643078B1 (en) | Process for the preparation of ethylene polymers and products obtained therefrom | |
| AU660808B2 (en) | Catalysts for the polymerization of olefins | |
| US6559252B1 (en) | Catalysts and processes for the polymerization of olefins | |
| EP0720627B1 (en) | Catalysts and processes for the polymerization of olefins | |
| AU688349B2 (en) | Process for the preparation of elastomeric copolymers of ethylene and products obtained therefrom | |
| CA2197643A1 (en) | Catalysts and processes for the polymerization of olefins | |
| US5910464A (en) | Catalysts for the polymerization of olefins | |
| US6476163B2 (en) | Catalysts for the polymerization of olefins and process for the preparation thereof | |
| EP0816399A1 (en) | Slurry process for the preparation of elastomeric ethylene copolymers | |
| RU2172746C2 (en) | Catalysis for polymerization of alpha-olefins, method of homo-and copolymerization of alpha-olefins and method of preparing elastomeric ethylene copolymers |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |
Effective date: 20030618 |
|
| FZDE | Discontinued |
Effective date: 20030618 |