| PATENT NUMBER | This data is not available for free |
| PATENT GRANT DATE | August 31, 1999 |
| PATENT TITLE |
Atactic polypropylene |
| PATENT ABSTRACT |
Amorphous propylene polymers are disclosed having the following characteristics: (a) intrinsic viscosity ›.eta.!>1 dl/g; (b) % (r)-% (m)>0, wherein % (r) is the % of syndiotactic diads and % (m) is the % of isotactic diads; (c) less than 2% of the CH.sub.2 groups contained in sequences (CH.sub.2).sub.n, with n.gtoreq.2; (d) Bernoullianity index (B)=1.+-.0.2; (e) melting enthalpy value lower than 10 J/g; and (f) Mw/Mn being less than 5. |
| PATENT INVENTORS | This data is not available for free |
| PATENT ASSIGNEE | This data is not available for free |
| PATENT FILE DATE | June 18, 1997 |
| PATENT FOREIGN APPLICATION PRIORITY DATA | This data is not available for free |
| PATENT PARENT CASE TEXT | This data is not available for free |
| PATENT CLAIMS |
What is claimed is: 1. An amorphous propylene polymer, directly obtained from a propylene polymerization reaction, having the following characteristics: (a) intrinsic viscosity ›.eta.! greater than 1 dl/g; (b) the percentage of syndiotactic diads (r) minus the percentage of isotactic diads (m) being greater than 0; (c) less than 2% of the CH.sub.2 groups contained in sequences (CH.sub.2).sub.n, with n being greater than or equal to 2; (d) Bemouillianity index (B)=1.+-.0.2; (e) melting enthalpy value lower than 10 J/g; and (f) Mw/Mn being less than 5. 2. The amorphous propylene polymer according to claim 1, having intrinsic viscosity ›.eta.! greater than 1.5 dl/g. 3. The amorphous propylene polymer according to claim 1, having a melting enthalpy value of 0 J/g. 4. An amorphous propylene polymer having the following characteristics: (a) intrinsic viscosity ›.eta.! greater than 1 dl/g; (b) the percentage of syndiotactic diads (r) minus the percentage of isotactic diads (m) being greater than 0; (c) less than 2% of the CH.sub.2 groups contained in sequences (CH.sub.2).sub.n, with n being greater than or equal to 2; (d) Bernoullianity index (B)=1.+-.0.2; (e) M.sub.w /M.sub.n being less than 5; and (f) melting enthalpy value lower than 10 J/g. 5. The amorphous propylene polymer according to claim 4, having intrinsic viscosity ›.eta.! greater than 1.5 dl/g. 6. The amorphous propylene polymer according to claim 4, having a melting enthalpy value of 0 J/g. -------------------------------------------------------------------------------- |
| PATENT DESCRIPTION |
The present invention relates to an amorphous polymer of propylene having substantially atactic structure and high molecular weight, and to the process for its preparation. BACKGROUND OF THE INVENTION As well known, products of the propylene homopolymerization can be either crystalline or amorphous. Whereas the polypropylene having isotactic or syndiotactic structure is crystalline, the polypropylene having essentially atactic structure appears to be amorphous. The atactic polypropylene, in the representation by the Fischer formula as described in "M. Farina, Topics Stereochem., 17, (1987), 1-111", shows methyl groups casually arranged from one or from the other side of the polymeric chain. As described in the above mentioned publication, useful information on the structure can be obtained from the NMR analysis. The amorphous polypropylene available on the market is mainly used in adhesive compositions and as additive in bitumens. Generally, it is a by-product of the isotactic polypropylene obtained in the presence of catalysts of the Ziegler-Natta type. However, the separation of the small fractions of amorphous polypropylene from the remainder product involves inconvenient separation processes with solvents. By operating with catalysts of the metallocene type, polypropylenes having high crystallinity degrees are generally obtained. However, some metallocene catalytic systems are able to polymerize the propylene to amorphous polypropylene. A drawback of these polymers is that they are endowed with low molecular weights. U.S. Pat. No. 4,542,199 describes a catalytic system for the polymerization of olefins comprising a bis(cyclopentadienyl)zirconium compound and an alumoxane. From the polymerization reaction of propylene carried out in the presence of this catalyst, low molecular weight atactic polypropylene is obtained. European patent application No. 283,739 describes a catalytic system for the polymerization of olefins comprising a partially substituted bis(cyclopentadienyl)zirconium compound and an alumoxane. From the polymerization reaction of propylene carried out in the presence of this catalyst, low molecular weight atactic polypropylene is obtained. U.S. Pat. No. 4,931,417 describes catalysts for the polymerization of olefins comprising a metallocene compound wherein two cyclopentadienyl rings are joined through a radical containing a silicon or germanium atom. The polymerization reaction of propylene carried out in the presence of these compounds partially substituted on the cyclopentadienyl rings gives raise to isotactic polypropylene, whereas with dimethylsilanediylbis(cyclopentadienyl)zirconium dichloride low molecular weight atactic polypropylene is obtained. Finally, in European patent application No. 399,347 it is described a process for the polymerization of propylene in the presence of a catalyst comprising a bridged metallocene having a cyclopentadienyl ring and a fluorenyl ring, such as isopropyliden(9-fluorenyl)(3-methylcyclopentadienyl)zirconium dichloride. An amorphous polypropylene is obtained, the structure of which is however not atactic, but is defined as syndioisoblocks. Namely, it is a structure wherein syndiotactic and isotactic sequences alternate. SUMMARY OF THE INVENTION Hence, it would be very useful to obtain an amorphous polypropylene having high molecular weight, which can be directly obtained by the polymerization reaction of propylene as the only product, thus avoiding expensive separation processes from other polypropylene components present in the product of the polymerization reaction. It is therefore an object of the present invention to provide an amorphous propylene polymer, which can be obtained directly from the polymerization reaction of propylene, having the following characteristics: (a) intrinsic viscosity ›.eta.!>1 dl/g; (b) % (r)-% (m)>0, wherein % (r) is the % of syndiotactic diads and % (m) is the % of isotactic diads; (c) less than 2% of the CH.sub.2 groups contained in sequences (CH.sub.2).sub.n, with n.gtoreq.2; (d) Bernoullianity index (B)=1.+-.0.2. Another object of the present invention is a propylene amorphous polymer, having the following characteristics: (a) ›.eta.!>1 dl/g; (b) % (r)-% (m)>0; (c) less than 2% of the CH.sub.2 groups contained in sequences (CH.sub.2).sub.n, with n.gtoreq.2; (d) B=1.+-.0.2; (e) M.sub.w /M.sub.n <5. Still another object of the present invention is a process for the preparation of the above said polymers of propylene. DETAILED DESCRIPTION OF THE INVENTION Propylene polymers according to the present invention are essentially free of crystallinity. The melting enthalpy values are generally lower than 20 J/g and, preferably, lower than 10 J/g. In most cases, the polymers of the invention have melting enthalpy values of 0 J/g. Preferably, the polymers of the invention have intrinsic viscosity values higher than 1.5 dl/g and, more preferably, higher than 2 dl/g. Analysis .sup.13 C-NMR carried out on the polypropylene of the invention give information on the tacticity of the polymeric chains, that is on the distribution of the configurations of the tertiary carbon atoms. The structure of the polymers of the invention is substantially atactic. Nevertheless, it is observed that the syndiotactic diads (r) appear to be more numerous than the isotactic diads (m). Namely, % (r)-% (m)>0 and, preferably, % (r)-% (m)>5. The Bernoullianity index (B), defined as: B=4›mm!›rr!/›mr!.sup.2 has values near to the unit, generally comprised in the range 0.8-1.2, preferably comprised in the range 0.9-1.1. The structure of the polypropylene according to the invention appears to be very regioregular. In fact, from the .sup.13 C-NMR, signals relating to sequences (CH.sub.2).sub.n wherein n.gtoreq.2 are not detectable. Generally, less than 2% and, preferably, less than 1% of the CH.sub.2 groups are contained in sequences (CH.sub.2).sub.n wherein n.gtoreq.2. The polypropylene of the invention is soluble in commonly used solvents, such as chloroform, heptane, diethylether, toluene. Propylene polymers according to the present invention are endowed with interesting elastomeric properties. Molecular weights of the polymers of the invention, besides to be high, are distributed within enough restricted ranges. An index of the molecular weight distribution is represented by the ratio M.sub.w /M.sub.n. Preferably, the polymers of the invention have values of M.sub.w /M.sub.n <4; more preferably, M.sub.w /M.sub.n <3. Propylene polymers according to the present invention can be prepared by a process, which is a further object of the present invention, and which comprises the polymerization reaction of propylene in the presence of a catalyst comprising the product of the reaction between: (A) a compound of formula (I) ##STR1## wherein substituents R.sup.1, the same or different from each other, are hydrogen atoms, C.sub.1 -C.sub.20 alkyl radicals, C.sub.3 -C.sub.20 cycloalkyl radicals, C.sub.2 -C.sub.20 alkenyl radicals, C.sub.6 -C.sub.20 aryl radicals, C.sub.7 -C.sub.20 alkylaryl radicals, or C.sub.7 -C.sub.20 arylalkyl radicals, optionally two adjacent substituents R.sup.1 can form a cycle comprising from 5 to 8 carbon atoms and, furthermore, substituents R.sup.1 can contain Si or Ge atoms; M is Ti, Zr or Hf; substituents R.sup.2, the same or different from each other, are halogen atoms, --OH, --SH, R.sup.1, --OR.sup.1, --SR.sup.1, --NR.sup.1.sub.2 or PR.sup.1.sub.2, wherein R.sup.1 is defined as above; the group R.sup.3 is selected from >CR.sup.1.sub.2, >SiR.sup.1.sub.2, >GeR.sup.1.sub.2, >NR.sup.1 or >PR.sup.1, wherein R.sup.1 is defined as above and optionally, when R.sup.3 is >CR.sup.1.sub.2, >SiR.sup.1.sub.2 or >GeR.sup.1.sub.2, both substituents R.sup.1 can form a cycle comprising from 3 to 8 atoms; optionally as reaction product with an aluminum organometallic compound of formula AlR.sup.4.sub.3 or Al.sub.2 R.sup.4.sub.6, wherein substituents R.sup.4, the same of different from each other, are R.sup.1 or halogen, and (B) an alumoxane, optionally mixed with an aluminum organometallic compound of formula AlR.sup.3 or AlR.sup.4.sub.31 , wherein substituents R.sup.4, the same or different from each other, are defined as above, or one or more compounds able to give a metallocene alkyl cation. The alumoxane used as component (B) can be obtained by reaction between water and an aluminum organometellic compound of formula AlR.sup.4.sub.3 or Al.sub.2 R.sup.4.sub.6, wherein substituents R.sup.4, the same or different from each other, are defined as above, with the proviso that at least one R.sup.4 is different from halogen. In that case, these are reacted in molar rations Al/water comprised between about 1:1 and 100:1. The molar ratio between the aluminum and the metal of the metallocene compound is comprised between about 10:1 and about 5000:1, and preferably between about 100:1 and 4000:1. Particularly suitable metallocene compounds of formula (I) are those wherein M=Zr, substituents R.sup.1 are hydrogen atoms, substituents R.sup.2 are chlorine or methyl groups, and the group R.sup.3 is a radical >Si(CH.sub.3).sub.2, such as, for example, dimethylsilandiylbis(fluorenyl)zirconium dichloride. The alumoxane used in the catalyst according to the invention is a linear, branched or cyclic compound, containing at least one group of the type: ##STR2## wherein substituents R.sup.5, the same or different from each other, are R.sup.1 or a group --O--Al(R.sup.5).sub.2, and optionally some R.sup.5 can be halogen or hydrogen atoms. In particular, it is possible to use alumoxanes of formula: ##STR3## in the case of linear compounds, wherein n is 0 or an integer comprised between 1 and 40, or alumoxanes of formula: ##STR4## in the case of cyclic compounds, with n which is an integer comprised between 2 and 40. Radicals R.sup.1 are preferably methyl, ethyl or isobutyl. Examples of alumoxanes suitable for the use according to the present invention are methylalumoxane (MAO) and isobutylalumoxane (TIBAO). Non limitative examples of aluminum compounds of formula AlR.sub.3 or Al.sub.2 R.sup.4.sub.6 are: ______________________________________ Al(Me).sub.3, Al(Et).sub.3, AlH(Et).sub.2, Al(iBu).sub.3, AlH(iBu).sub.2, Al(iHex).sub.3, Al(C.sub.6 H.sub.5).sub.3, Al(CH.sub.2 C.sub.6 H.sub.5).sub.3, Al(CH.sub.2 CMe.sub.3).sub.3, Al(CH.sub.2 SiMe.sub.3).sub.3, Al(Me).sub.2 iBu, Al(Me).sub.2 Et, AlMe(Et).sub.2, AlMe(iBu).sub.2, Al(Me).sub.2 iBu, Al(Me).sub.2 Cl, Al(Et).sub.2 Cl, AlEtCl.sub.2, Al.sub.2 (Et).sub.3 Cl.sub.3, ______________________________________ wherein Me=methyl, Et=ethyl, iBu=isobutyl, iHex=isohexyl. Among the above mentioned aluminum compounds, trimethyl aluminum and triisobuthyl aluminum are preferred. Non limitative examples of compounds able to form a metallocene alkyl cation are compounds of formula Y.sup.+ Z.sup.-, wherein Y.sup.+ is a Bronsted acid, able to give a proton and to react irreversibly with a substituent R.sup.2 of the metallocene of formula (I), and Z.sup.- is a compatible anion, which does not coordinate, which is able to stabilize the active catalytic species which originates from the reaction of the two compounds and which is sufficiently labile to be able to be removed from an olefinic substrate. Preferably, the anion Z.sup.- comprises one or more boron atoms. More preferably, the anion Z.sup.- is an anion of the formula BAr.sup.(-).sub.4, wherein substituents Ar, the same or different from each other, are aryl radicals such as phenyl, pentafluorophenyl, bis(trifluoromethyl)phenyl. Particularly preferred is the tetrakis-pentafluorophenyl borate. Furthermore, compounds of formula BAr.sub.3 can be suitably used. The catalysts used in the process of the present invention can be also used on inert supports. This is obtained by depositing the metallocene (A), or the product of the reaction of the same with the component (B), or the component (B) and thereafter the metallocene (A), on inert supports such as for example silica, alumina, styrene-divinylbenzene copolymers or polyethylene. The solid compound thus obtained, combined with a further addition of alkylaluminium compound either as such or prereacted with water, if necessary, is usefully used in the gas phase polymerization. The propylene polymerization process in the presence of the catalysts above described can be carried out either in liquid phase, in the presence or not of an inert aliphatic or aromatic hydrocarbon solvent, such as hexane or toluene, or in gas phase. The polymerization temperature is generally comprised between 0.degree. C. and 250.degree. C., in particular between 20.degree. C. and 150.degree. C., and more particularly between 40.degree. C. and 90.degree. C. The molecular weight of polymers can be varied merely by changing the polymerization temperature, the type or the concentration of the catalytic components or by using molecular weight regulators such as, for example, hydrogen. The molecular weight distribution can be varied by using mixtures of different metallocene compounds, or by carrying out the polymerization in several steps which differ as to the polymerization temperature and/or the concentrations of the molecular weight regulator. Polymerization yields depend on the purity of the metallocene component of the catalyst. Therefore, the metallocene compounds can be used as such or subjected to purification treatments. The components of the catalyst can be contacted among them before the polymerization. The contact time is generally comprised between 1 and 60 minutes, preferably between 5 and 20 minutes |
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