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Title:

1-butene terpolymers

The present invention relates to a terpolymer of 1-butene, ethylene and higher linear alpha-olefins, such as 1-octene or 1-decene. The terpolymer has a very good elastic properties with respect to the copolymer containing only higher linear alpha-olefins. This class of copolymers is obtained by using a specific metallocene-based catalyst system. Butene-1 based polymers are well known in the art and+have found application in several highly demanding end uses, thanks to their high pressure resistance, creep resistance, impact strength, and flexibility. These properties can be modified by the use of comonomers. In particular Butene-1 copolymers with a higher content of comonomer can be used for example as components of blends with other polyolefin or polymeric products, in order to modulate particular properties such as sealing strength, flexibility and softness of the plastic materials.

EP 181 159 relates to random 1-butene copolymers comprising from 50% to 99% mol of 1-butene that can contains small amount of propylene or ethylene. The copolymers are described with very broad ranges of properties. In particular the melting point ranges from 30 to 120 ⁰ C depending on the type and the amount of the comonomer used. The applicant found that the terpolymers of the invention have lower melting point at the same comonomer content and thus a better randomization of the comonomers. This allows a better processability and it is the optimum for particular uses. EP 1 260 525 relates to 1-butene copolymers that can optionally contain ethylene having among other features a stereoregularity index (mmmm)/mmrr + rmmr at most 20. The polymers of the present invention are not endowed with this feature. The applicant found that terpolymers of 1-butene, 1-octene or higher alpha olefins and small amount of ethylene are endowed with improved elastic properties leaving the other properties substantially unchanged when compared with a copolymer of 1-butene, 1- octene or higher alpha olefins having the same amount of comonomer. An object of the present invention is a terpolymer of 1-butene, ethylene and a at least a C8-C12 alpha-olefin derived units, preferably at least 1-octene derived units, containing from 0.1% to 5 % by mole of ethylene derived units and from 1 from 20% by mol of Cs- C ₁₂ alpha-olefin derived units, endowed with the following properties :

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i) isotactic pentad mmmm higher than or equal to 90%; pentads (mmrr+mrrm) lower than 4 and pentad rmmr not detectable by ¹³ C NMR. ii) intrinsic viscosity (IV) measured in tetrahydronaphthalene at 135°C comprised between 0.8 and 5.0 dL/g; preferably comprised between 0.9 and 3.0 dL/g; iii) the melting point measured by DSC (TmI) and the Cs-Ci ₂ alpha-olefln content fulfil the following relationship:

Tml < 13OxC ^"03 wherein C is the molar content of Cs-Ci ₂ alpha-olefϊn derived units and TmI is the highest melting peak in the first melting transition measured by DSC on a compression moulded plaque aged for 10 minutes in an autoclave at 2000 bar at room temperature and then aged for at least 24 hours at 23°C; otherwise the melting point TmI is not detectable.

Preferably the terpolymer of the present invention contains from 0.2% to 3 % by mol of ethylene derived units and from 2% by mol to 10% by mol Of Cs-Ci ₂ alpha-olefϊn. More preferably the Cs-Ci ₂ alpha-olefin content ranges from 2% by mol to 8% by mol. The terpolymers of the present invention are substantially isotactic, with mmmm > 90 %, more preferably mmmm > 92 %, even more preferably mmmm > 95 %, thus enabling crystallization after aging and avoiding the intrinsic stickiness of atactic or poorly isotactic polymers.

The terpolymers of the present invention show an improved elasticity with respect to the copolymer having the same content Of Cs-Ci ₂ alpha-olefin derived units. Thus preferably the terpolymers of the present invention are further endowed with a tension set at 100% of deformation (%) that is lower than the tension set at 100% of deformation (%) of a copolymer containing the same amount Of Cs-Ci ₂ alpha-olefin derived units. Even more, if the terpolymer contains x% by mol of ethylene derived units and y% by mol of Cs-Ci ₂ alpha-olefin derived units its tension set at 100% of deformation (%) is lower than a 1- butene copolymer having a content of the same Cs-Ci ₂ alpha-olefin derived units equal to x+y% by mol.

Preferably the terpolymer of the present invention is endowed with a the tension set at 100% of deformation (%) is at least 10% lower, more preferably at least 20% lower, even

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more preferably at least 40% lower than the tension set at 100% of deformation (%) a copolymer containing the same amount of Cs-Ci ₂ alpha-olefin derived units.

Example of Cs-Ci ₂ alpha-olefin comonomers are 1-octene, 1-decene, 1-dodecene.

Preferably 1-octene and 1-decene are used, more preferably 1-octene is used.

The copolymers of the present invention are prepared by using metallocene -based catalyst system wherein the metallocene compound has a particular substitution pattern.

Thus the terpolymer of the present invention can be obtained by contacting under polymerization conditions 1-butene ethylene and at least one Cs-Ci ₂ alpha-olefin, in the presence of a catalyst system obtainable by contacting:

(A) a stereorigid metallocene compound;

(B) an alumoxane or a compound capable of forming an alkyl metallocene cation; and optionally

(C) an organo aluminum compound.

Preferably the stereorigid metallocene compound belongs to the following formula (I):

(I) wherein:

M is an atom of a transition metal selected from those belonging to group 4; preferably M is zirconium;

X, equal to or different from each other, is a hydrogen atom, a halogen atom, a R, OR, OR'O, OSO ₂ CF ₃ , OCOR, SR, NR ₂ or PR ₂ group wherein R is a linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl, C3-C ₂ o-cycloalkyl, C6-C ₂ o-aryl, C ₇ -C ₂ o-alkylaryl or C ₇ -C ₂ o-arylalkyl radical, optionally containing heteroatoms

belonging to groups 13-17 of the Periodic Table of the Elements; and R' is a

Ci-C2o-alkylidene, C6-C2o-arylidene, C7-C2o-alkylarylidene, or C7-C2o-arylalkylidene radical; preferably X is a hydrogen atom, a halogen atom, a OR'O or R group; more preferably X is chlorine or a methyl radical;

R ¹ , R ² , R ⁵ , R ⁶ , R ⁷ , R ⁸ and R ⁹ , equal to or different from each other, are hydrogen atoms, or linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl,

C ₃ -C ₂₀ -cycloalkyl, C ₆ -C ₂ o-aryl, C ₇ -C ₂ o-alkylaryl or C ₇ -C ₂ o-arylalkyl radicals, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; or R ⁵ and R , and/or R and R can optionally form a saturated or unsaturated, 5 or 6 membered rings, said ring can bear C ₁ -C ₂ 0 alkyl radicals as substituents; with the proviso that at least one of R or R is a linear or branched, saturated or unsaturated Ci-C2o-alkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably a

Ci-Cio-alkyl radical; preferably R , R , are the same and are C ₁ -C ₁₀ alkyl radicals optionally containing one or more silicon atoms; more preferably R and R are methyl radicals;

R and R , equal to or different from each other, are preferably C ₁ -C ₁₀ alkyl or

C6-C ₂ 0 aryl radicals; more preferably they are methyl radicals;

R ⁵ is preferably a hydrogen atom or a methyl radical; or can be joined with R ⁶ to form a saturated or unsaturated, 5 or 6 membered ring, said ring can bear C ₁ -C ₂ 0 alkyl radicals as substituents;

R is preferably a hydrogen atom or a methyl, ethyl or isopropyl radical; or it can be joined with R ⁵ to form a saturated or unsaturated, 5 or 6 membered rings as described above;

R is preferably a linear or branched, saturated or unsaturated Ci-C2o-alkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably a Ci-Cio-alkyl radical; more preferably R ⁷ is a methyl or ethyl radical; otherwise when R is different from a hydrogen atom, R is preferably a hydrogen atom

R ³ and R ⁴ , equal to or different from each other, are linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl radicals, optionally containing heteroatoms belonging to

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groups 13-17 of the Periodic Table of the Elements; preferably R ³ and R ⁴ equal to or different from each other are Ci-Cio-alkyl radicals; more preferably R is a methyl, or ethyl radical; and R is a methyl, ethyl or isopropyl radical;

(A) an alumoxane or a compound capable of forming an alkyl metallocene cation; and optionally (B) an organo aluminum compound.

In particular when the compound of formula (I) is used in the process according to the present invention the polymerization activity is much higher with respect to the polymerization activity obtained in the absence of ethylene.

Preferably the compounds of formula (I) have formula (Ia) or (Ib):

(Ia) (Ib)

Wherein

M, X, R ¹ , R ² , R ⁵ , R ⁶ , R ⁸ and R ⁹ have been described above;

R ³ is a linear or branched, saturated or unsaturated Ci-C ₂ o-alkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R ³ is a Ci-Cio-alkyl radical; more preferably R ³ is a methyl, or ethyl radical. Alumoxanes used as component B) can be obtained by reacting water with an organo- aluminium compound of formula H _j AlUs-, or H _j Al ₂ Ue- _J , where U substituents, same or different, are hydrogen atoms, halogen atoms, Ci-C ₂ o-alkyl, C3-C ₂ o-cyclalkyl, C6-C ₂ o-aryl, C ₇ -C ₂ o-alkylaryl or or C7-C20-arylalkyl radical, optionally containing silicon or germanium atoms with the proviso that at least one U is different from halogen, and j ranges from 0 to 1, being also a non-integer number. In this reaction the molar ratio of Al/water is preferably comprised between 1 :1 and 100:1. The molar ratio between aluminium and the metal of

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the metallocene generally is comprised between about 10: 1 and about 20000:1 , and more preferably between about 100:1 and about 5000:1. The alumoxanes used in the catalyst according to the invention are considered to be linear, branched or cyclic compounds containing at least one group of the type: wherein the substituents U, same or different, are described above. In particular, alumoxanes of the formula:

can be used in the case of linear compounds, wherein n ¹ is 0 or an integer from 1 to 40 and the substituents U are defined as above, or alumoxanes of the formula:

U (Al-O)n ² can be used in the case of cyclic compounds, wherein n is an integer from 2 to 40 and the U substituents are defined as above. Examples of alumoxanes suitable for use according to the present invention are methylalumoxane (MAO), tetra-(isobutyl)alumoxane (TIBAO), tetra-(2,4,4-trimethyl-pentyl)alumoxane (TIOAO), tetra-(2,3-dimethylbutyl)alumoxane (TDMBAO) and tetra-(2,3,3-trimethylbutyl)alumoxane (TTMBAO). Particularly interesting cocatalysts are those described in WO 99/21899 and in WO01/21674 in which the alkyl and aryl groups have specific branched patterns. Non-limiting examples of aluminium compounds according to WO 99/21899 and WOO 1/21674 are: tris(2,3,3-trimethyl-butyl)aluminium, tris(2,3-dimethyl-hexyl)aluminium, tris(2,3-dimethyl- butyl)aluminium, tris(2 ,3 -dimethyl-pentyl)aluminium, tris(2,3 -dimethyl-heptyl)aluminium, tris(2 -methyl-3 -ethyl-pentyl)aluminium, tris (2 -methyl-3 -ethyl-hexyl)aluminium, tris(2-methyl-3-ethyl-heptyl)aluminium, tris(2 -methyl-3 -propyl-hexyl)aluminium, tris(2 -ethyl-3 -methyl-butyl)aluminium, tris(2 -ethyl-3 -methyl-pentyl)aluminium, tris(2 ,3 -diethyl-pentyl)aluminium, tris(2-propyl-3 -methyl-butyl)aluminium, tris(2 -isopropyl- 3-methyl-butyl)aluminium, tris(2-isobutyl-3-methyl-pentyl)aluminium, tris(2,3,3-trimethyl-

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pentyl)aluminium, tris (2 ,3 ,3 -trimethyl-hexyl)aluminium, tris(2 -ethyl-3 ,3 -dimethyl- butyl)aluminium, tris(2-ethyl-3,3-dimethyl-pentyl)aluminium, tris (2 -isopropy 1-3,3 - dimethyl-butyl)aluminium, tris(2-trimethylsilyl-propyl)aluminium, tris(2-methyl-3-phenyl- butyl)aluminium, tris(2-ethyl-3-phenyl-butyl)aluminium, tris(2,3-dimethyl-3-phenyl- butyl)aluminium, tris(2 -phenyl-propyl)aluminium, tris [2-(4-fluoro-phenyl)- propyl]aluminium, tris[2-(4-chloro-phenyl)-propyl]aluminium, tris[2-(3-isopropyl-phenyl)- propyl]aluminium, tris(2-phenyl-butyl)aluminium, tris(3 -methyl-2-phenyl-butyl)aluminium, tris(2-phenyl-pentyl)aluminium, tris[2-(pentafluorophenyl)-propyl]aluminium, tris[2,2- diphenyl-ethyl] aluminium and tris [2 -phenyl-2-methyl-propyl] aluminium, as well as the corresponding compounds wherein one of the hydrocarbyl groups is replaced with a hydrogen atom, and those wherein one or two of the hydrocarbyl groups are replaced with an isobutyl group.

Amongst the above aluminium compounds, trimethylaluminium (TMA), triisobutylaluminium (TIBAL), tris(2,4,4-trimethyl-pentyl)aluminium (TIOA), tris(2,3- dimethylbutyl)aluminium (TDMBA) andtris(2,3,3-trimethylbutyl)aluminium (TTMBA) are preferred.

Non-limiting examples of compounds able to form an alkylmetallocene cation are compounds of formula D ⁺ E ^" , wherein D ⁺ is a Brønsted acid, able to donate a proton and to react irreversibly with a substituent X of the metallocene of formula (I) and E ^" is a compatible anion, which is able to stabilize the active catalytic species originating from the reaction of the two compounds, and which is sufficiently labile to be able to be removed by an olefinic monomer. Preferably, the anion E ^" comprises of one or more boron atoms. More preferably, the anion E ^" is an anion of the formula BAr ₄ ^, wherein the substituents Ar which can be identical or different are aryl radicals such as phenyl, pentafiuorophenyl or bis(trifluoromethyl)phenyl. Tetrakis -pentafiuorophenyl borate is particularly preferred examples of these compounds are described in WO 91/02012. Moreover, compounds of the formula BAr ₃ can conveniently be used. Compounds of this type are described, for example, in the published International patent application WO 92/00333. Other examples of compounds able to form an alkylmetallocene cation are compounds of formula BAr ₃ P wherein P is a substituted or unsubstituted pyrrol radicals. . These compounds are described in WO01/62764. Other examples of cocatalyst can be found in EP 775707 and DE

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19917985. Compounds containing boron atoms can be conveniently supported according to the description of DE-A- 19962814 and DE-A-19962910. All these compounds containing boron atoms can be used in a molar ratio between boron and the metal of the metallocene comprised between about 1 :1 and about 10:1; preferably 1 :1 and 2.1 ; more preferably about 1 : 1.

Non limiting examples of compounds of formula D ⁺ E ^" are:

Tributylammoniumtetrakispentafiuorophenylaluminate,

Tributylammoniumtetrakis(3,5-bis(trifiuoromethyl)phenyl)b orate,

Tributylammoniumtetrakis(4-fluorophenyl)borate,

N,N-Dimethylbenzylammonium-tetrakispentafluorophenylborat e,

N,N-Dimethylhexylammonium-tetrakispentafiuorophenylborate ,

N,N-Dimethylaniliniumtetrakis(pentafiuorophenyl)borate,

N,N-Dimethylaniliniumtetrakis(pentafiuorophenyl)aluminate ,

Di(propyl)ammoniumtetrakis(pentafluorophenyl)borate,

Di(cyclohexyl)ammoniumtetrakis(pentafiuorophenyl)borate,

Triphenylcarbeniumtetrakis(pentafiuorophenyl)borate,

Triphenylcarbeniumtetrakis(pentafiuorophenyl)aluminate,

Ferroceniumtetrakis(pentafluorophenyl)borate,

Ferroceniumtetrakis(pentafluorophenyl)aluminate.

Organic aluminum compounds used as compound C) are those of formula H _j AlU3_ _j or

H _j Al ₂ Ue- _J described above. The catalysts of the present invention can also be supported on an inert carrier. This is achieved by depositing the metallocene compound A) or the product of the reaction thereof with the component B), or the component B) and then the metallocene compound A) on an inert support such as, for example, silica, alumina, Al-Si,

Al-Mg mixed oxides, magnesium halides, styrene/divinylbenzene copolymers, polyethylene or polypropylene. The supportation process is carried out in an inert solvent such as hydrocarbon for example toluene, hexane, pentane or propane and at a temperature ranging from 0 ⁰ C to 100 ⁰ C, preferably the process is carried out at a temperature ranging from 25°C to 90 ⁰ C or the process is carried out at room temperature.

A suitable class of supports which can be used is that constituted by porous organic supports functionalized with groups having active hydrogen atoms. Particularly suitable are those in

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which the organic support is a partially crosslinked styrene polymer. Supports of this type are described in European application EP -633272. Another class of inert supports particularly suitable for use according to the invention is that of polyolefin porous prepolymers, particularly polyethylene.

A further suitable class of inert supports for use according to the invention is that of porous magnesium halides such as those described in International application WO 95/32995. the process for the polymerization of 1-butene and Cs-Ci ₂ alpha olefins according to the invention can be carried out in the liquid phase in the presence or absence of an inert hydrocarbon solvent. The hydrocarbon solvent can either be aromatic such as toluene, or aliphatic such as propane, hexane, heptane, isobutane or cyclohexane. Preferably the copolymers of the present invention are obtained by a solution process, i.e. a process carried out in liquid phase wherein the polymer is completely or partially soluble in the reaction medium.

As a general rule, the polymerization temperature is generally comprised between 0 ⁰ C and

+200 ⁰ C preferably comprised between 40° and 90 ⁰ C, more preferably between 50 ⁰ C and

80 ⁰ C. The polymerization pressure is generally comprised between 0,5 and 100 bar.

The lower the polymerization temperature, the higher are the resulting molecular weights of the polymers obtained.

The following examples are for illustrative purpose and do not intend to limit the scope of the invention.

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Examples

¹³ C NMR analysis

C-NMR spectra were acquired on a DPX-400 spectrometer operating at 100.61 MHz in the Fourier transform mode at 120 ⁰ C. The peak of the 2B2 carbon (nomenclature according to C. J. Carman, R. A. Harrington, C. E. Wilkes, Macromolecules 1977, 10, 535) of the mmmm BBBBB pentad was used as internal reference at 27.73. The samples were dissolved in I,l,2,2-tetrachloroethane-d2 at 120 ⁰ C with a 8% wt/v concentration. Each spectrum was acquired with a 90° pulse, 15 seconds of delay between pulses and CPD (WALTZ 16) to remove ¹ H- ¹³ C coupling. About 1500 transients were stored in 32K data points using a spectral window of 6000 Hz.

The assignments of the peaks for butene-ethylene were made according to Randall (Randall, J. C. MacromoL Chem Phys. 1989, C29. 201) and the triad distribution and copolymer compositions were determined according to the method proposed by Kakugo (Kakugo, M.;. Naito. Y; Mizunυraa. K.; Miyalakc, T. Macromolecules 1982, /5, 1 150). For C4C2 copolymers at low ethylene content (absence of EEE sequences in the 13C- NMR spectrum), the peak at 27.73 ppm of the methylene of the ethyl branch was used as internal reference. The composition of the 1 -butene based terpolymers was calculated as follows:

The assignments of the peaks for butene-ethylene were made according to Randall (Randall, J. C. MacromoL Chem Phys. 1989, C29. 2Oi ) and the triad distribution and compositions were determined according to the method proposed by Kakugo (Kakugo, M.;. Naito. Y; Mizunuma, K.: Miyaiake, T. Macromolecules 1982, 15. 1 150). For C4C2 copolymers at low ethylene content (absence of EEE sequences in the 13C-NMR spectrum), the peak at 27.73 ppm of the methylene of the ethyl branch was used as internal reference.

The assignments of the peaks for 1 -Butene/ 1-Octene was calculated as follows using the S _αα carbons:

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Where X is the 1 -octene comonomer

The total amount of 1-butene and 1 -octene as molar fraction is calculated from diads using the following relations:

[X] = XX+ 0.5BX

[B] = BB+ 0.5BX

Assignment of the ¹³ C NMR spectrum of 1-butene/l -octene copolymers is reported in table A, with carbon labeling as shown in formula (a)

(a) Table a

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Thermal analysis

The melting temperatures and relative enthalpy of fusion of the polymers (TmI, TmII, δHfl, δHfll) were measured by Differential Scanning Calorimetry (DSC) on a Perkin Elmer DSC- 1 calorimeter equipped with Pyris 1 software, performing scans in a flowing N ₂ atmosphere. DSC apparatus was previously calibrated at indium and zinc melting points with particular attention in determining the baseline with required accuracy. The preparation of the samples, for calorimetric investigations, was performed by cutting them into small pieces by using a cutter. The weight of the samples in every DSC crucible was kept at 6.0 ± 0.5 mg.

In order to obtain the melting temperatures of the copolymers, the weighted sample was sealed into aluminium pans and heated to 180 ⁰ C at 10°C/minute. The sample was kept at 180 ⁰ C for 5 minutes to allow a complete melting of all the crystallites, and then cooled down to -20 ⁰ C at 10°C/minute. After standing 2 minutes at -20 ⁰ C, the sample was heated for the second time to 180 ⁰ C at 10°C/min.

Melting temperature (TmI) and the relative enthalpy of fusion in the first heating DSC run were detected on compression-molded samples aged 10 minutes in the autoclave at high pressure (2000 bar) at room temperature and then aged at least 24 hours at 23°C. The glass transition temperature (T _g ) was also detected from DSC analysis in the second heating run from -90 ⁰ C up to 180 ⁰ C at 10°C/min. The weight of the samples in every DSC crucible was kept at 12.0 ± 1.0 mg. The value of the inflection point of the transition was taken as the T _g .

Stress-Strain

Mechanical tests were performed with a mechanical tester apparatus (INSTRON 4301), following the international standard ISO 527/1.

Compression-molded samples were prepared by heating the samples at temperatures higher than the melting temperatures (200 ⁰ C) under a press for 5 minutes and then cooling the melt to room temperature with a cooling rate of 30°C/min. Before Mechanical

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testing, these compression molded butene-octene copolymer samples were aged for 10 minutes in an autoclave (in water) at high pressure (2000 bar) at room temperature and then aged for additional 24 hours at 23 ⁰ C. Rectangular specimens 30 mm long, 5 mm wide, and 2 mm thick were uniaxially drawn up to the break at room temperature at 500 mm/min and stress-strain curves were collected. For each sample, 6 stress-strain curves were collected and averaged. In this way stress at yield, elongation at yield, stress at break and elongation at breack have been measured. Tension set calculation

Compression-molded samples were prepared by heating the samples at temperatures higher than the melting temperatures (200 ⁰ C) under a press for 5 minutes and then cooling the melt to room temperature with a cooling rate of 30°C/min. Before performing the tensile measurements, these compression molded butene copolymers were aged for 10 minutes in an autoclave (water) at high pressure (2000 bar) at room temperature and then aged for additional 24 hours at 23°C. The values of the tension set were measured according to the method ISO 2285. Rectangular specimens 50 mm long, 2 mm wide, and 2 mm thick were uniaxially drawn from their initial length Lo up to a length L _f =2Lo i.e., up to the elongation ε (deformation rate not constant but high), and held at this elongation for 10 minutes, then the tension was removed and the final length of the relaxed specimens L _r was measured after 10 minutes. The tension set was calculated by using the following formula: t _s (ε)=[(L _r -Lo)/Lo]*lOO.

The value of the tension set is the average of two measures. DMTA

Tensile modulus (at 23°C ) has been measured by using DMTA. Seiko DMS6100 equipped with liq. N ₂ cooling accessory instrument with heating rate of 2°C/min and frequency of IHz. The specimens were cut from compression molded plaque with dimensions of 50x6x1 mm. The investigated temperature range was from -80 ⁰ C to the softening point. Catalyst preparation

Dimethylsilanediyl{(l-(2,4,7-trimethylindenyl)-7-(2,5-dim ethyl-cyclopenta[l,2-b:4,3- b']-dithiophene)}Zirconium dichloride (Al) was prepared according to WO 01/47939. Methylalumoxane (MAO) was supplied by Albemarle as a 30% wt/wt toluene solution

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and used as such. Triisobutylaluminium (TIBA) was supplied by Crompton as pure chemical and diluted to about 100 g/L with anhydrous cyclohexane. All chemicals were handled using standard Schlenk techniques.

Preparation of the Catalytic solution (Al _tot /Zr = 400 molar, A1 _MAO /Zγ = 267 mol/mol in cyclohexane/ toluene)

22 mg of Al were charged at room temperature under nitrogen atmosphere into a 50 mL Schlenk flask, equipped with a magnetic stirrer. 16.2 mL of a mixture of MAO Albemarle 30% wt in toluene and TIBA in cyclohexane (25.3 g Al _tot /L; MAO/TIBA=2/1 molar) were added at room temperature under nitrogen atmosphere into the schlenk containing the Al (A1 _MAO /Zγ = 267; A1 _TIBA /Zγ = 133, Al _tot /Zr = 400). The resulting clear orange-red solution, having a concentration of Al of 1.36 mg/mL, was stirred for 1-2 hours at room temperature and used as such in polymerizations. Polymerization test

The polymerization tests were carried out in a 4.4 L jacketed stainless-steel autoclave equipped with a mechanical stirrer and a 35-mL stainless-steel vial, connected to a thermostat for temperature control, by using the following procedure. Prior to the polymerization experiment, the autoclave was purified by washing with a IM Al(Z-Bu) ₃ solution in hexane and dried at 70 ⁰ C in a stream of nitrogen. Subsequently, the scavenger (either an amount of a 25.3 g(Al _tot )/L solution in toluene/cyclohexane of MAO/TIB A=2/l molar corresponding to 4 mmol of Al) and then 1267 g of 1-butene, 117 g of 1 octene and 5 g of ethylene were charged at room temperature in the autoclave. The autoclave was then thermostated at the polymerization temperature of 70 ⁰ C. The solution containing the catalyst/cocatalyst mixture (containing 0.6 mg of metallocene) was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial. The polymerization was carried out at constant temperature for 1 h, by feeding 7.2 g of ethylene.

Then stirring was interrupted, the pressure into the autoclave was raised up to 20 bar- g with nitrogen, the bottom discharge valve was opened and the polymer/monomers mixture discharged into a heated steel tank containing water and treated for 10 min with a steam flow. The tank heating was switched off and a flow of nitrogen at 0.5 bar-g was fed

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to remove the water. The steel tank was finally opened, the wet polymer collected and dried overnight at 85°C in an oven under reduced pressure. The polymerization results are reported in table 1.

Table 1

For comparative purposes two polymerization tests have been carried out in order to obtain 1 -butene 1 -octene copolymers Polymerization tests

The polymerization tests were carried out in a 4.4 L jacketed stainless-steel autoclave equipped with a mechanical stirrer and a 35-mL stainless-steel vial, connected to a thermostat for temperature control, by using the following procedure. Prior to the polymerization experiment, the autoclave was purified by washing with a IM Al(Z-Bu) ₃ solution in hexane and dried at 70 ⁰ C in a stream of nitrogen. Subsequently, the scavenger (either an amount of a 25.3 g(Al _tot )/L solution in toluene/cyclohexane of MAO/TIB A=2/l molar corresponding to 4 mmol of Al, or 11.9 mL of a solution of TIBA 10%wt/V in iso- hexane, corresponding to 6 mmol of TIBA) and then the desired amounts (see Table 1) of butene and octene (or decene) were charged at room temperature in the autoclave. The autoclave was then thermostated at the polymerization temperature of 70 ⁰ C. The solution containing the catalyst/cocatalyst mixture was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial. The polymerization was carried out at constant temperature for 1 h, without feeding monomers.

Then stirring was interrupted, the pressure into the autoclave was raised up to 20 bar- g with nitrogen, the bottom discharge valve was opened and the polymer/monomers

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mixture discharged into a heated steel tank containing water and treated for 10 min with a steam flow. The tank heating was switched off and a flow of nitrogen at 0.5 bar-g was fed to remove the water. The steel tank was finally opened, the wet polymer collected and dried overnight at 85°C in an oven under reduced pressure. The polymerization results are reported in table 2.

Table 2

Table 2 continued

nd= not detectable; * comparative;

The copolymers obtained in the above examples have been analyzed:

Thermal analysis

Thermal analysis have been carried out according to the procedure described above, the results are reported in table 3

Table 3

nd = not detectable Mechanical analysis

Stress-strain, tension set and tensile moduli measurements have been carried out according to the procedure described above. The results of the mechanical analysis are shown in table 4. Table 4

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