Olefin polymerisation catalyst
Abstract
The present invention relates to particulate olefin polymerisation catalyst components comprising an alkaline earth metal, a compound of a transition metal and an electron donor, characterized in that the catalyst particle size distribution of the catalyst component is essentially monomodal and has a SPAN value below 1.2, where SPAN is defined as: (Particle diameter at 90% cumulative size)-(Particle diameter at 10% cumulative size)/(Particle diameter at 50% cumulative size). The particulate olefin polymerisation catalyst components of the present invention are provided by a process which comprises preparing a solution of a complex of an alkaline earth metal and an electron donor by reacting a compound of said metal with said electron donor or a precursor thereof in an organic liquid reaction medium, reacting said complex in the solution form with a compound of a transition metal to produce a dispersion, wherein the dispersed phase predominantly contains the alkaline earth metal in said complex, and solidifying said dispersed phase to obtain said catalyst component, and is characterized in that a second organic liquid medium is added to the reactor after mixing the alkaline earth metal complex with the transition metal compound.
Claims
exact text as granted — not AI-modified1 . A process for producing an olefin polymerisation catalyst component in the form of particles, which comprises
preparing a solution of a complex of an alkaline earth metal and an electron donor by reacting a compound of said metal with said electron donor or a precursor thereof in an organic liquid medium, reacting said complex in solution form with a compound of a transition metal wherein a dispersion is formed, wherein the dispersed phase predominantly contains the alkaline earth metal in said complex, and solidifying said dispersed phase to obtain said catalyst component, and wherein
a second organic liquid medium is added to the reactor after mixing the alkaline earth metal complex with the transition metal compound.
2 . The process according to claim 1 , wherein the organic liquid medium comprises C 6 -C 10 aromatic hydrocarbons.
3 . The process according to claim 1 , wherein the organic liquid medium comprises toluene.
4 . The process according to claim 1 , wherein the second organic liquid medium is an aliphatic hydrocarbon selected from straight, branched or cyclic hydrocarbons having 5, 6, 7 or 8 C-atoms.
5 . The process according to claim 1 , wherein the second organic liquid medium is selected from pentane, hexane, heptane, octane or cyclohexane or mixtures or isomers thereof.
6 . The process according to claim 1 , wherein the second organic liquid medium is heptane.
7 . The process according to claim 1 , wherein said transition metal is a Group 4 metal.
8 . The process according to claim 1 , wherein said alkaline earth metal is magnesium.
9 . The process according to claim 1 , wherein said dispersion is composed of a dispersed phase which is TiCl 4 /toluene-insoluble and has a molar ratio of Group 4 metal/alkaline earth metal of greater than 0.1 and less than 10 and a continuous phase which is less dense than the dispersed phase and has a molar ratio of Group 4 metal/alkaline earth metal of 10 to 100.
10 . The process according to claim 9 , wherein the molar ratio of Group 4 metal/alkaline earth metal in said continuous phase is 20 to 80.
11 . The process according to claim 9 , wherein the molar ratio of Group 4 metal/alkaline earth metal in said continuous phase is 45 to 75.
12 . The process according to claim 1 , wherein said complex and said transition metal compound are reacted at a temperature of 10 to 60° C.
13 . The process according to claim 1 , wherein the solidification of said dispersed phase is effected by heating.
14 . The process according to claim 1 , wherein said electron donor is an aromatic carboxylic acid ester.
15 . The process according to claim 14 , wherein said electron donor is di(ethyl-hexyl) phthalate.
16 . The process according to claim 1 , wherein said electron donor is formed in situ by reaction of an aromatic carboxylic acid chloride precursor with a C 2 -C 16 alkanol and/or diol.
17 . The process according to claim 1 , wherein the dispersion is maintained by agitation.
18 . The process according to claim 1 , wherein the dispersion is maintained by the addition of a dispersion stabilizer.
19 . The process according to claim 18 , wherein said dispersion stabilizer comprises a surfactant.
20 . The process according to claim 19 , wherein said surfactant comprises an acrylic or methacrylic polymer.
21 . The process according to claim 9 , wherein the molar ratio of Group 4 metal/alkaline earth metal in said dispersed phase is 2 to 4 and that of the continuous phase is 55 to 65.
22 . The process according to claim 21 , wherein the ratio of the molar ratio of Group 4 metal/alkaline earth metal in the continuous phase to that of the dispersed phase is at least 10.
23 . The process according to claim 1 , wherein the dispersion is heated to a temperature of 70 to 150° C. to solidify said dispersed phase.
24 . The process according to claim 23 , wherein the temperature to which the dispersion is heated is to 90 to 110° C.
25 . The process according to claim 1 , wherein the preparation of the alkaline earth metal complex is carried out at a temperature of 20 to 80° C.
26 . The process according to claim 25 , wherein the alkaline earth metal is magnesium and the preparation of the magnesium complex is carried out at a temperature of 50 to 70° C.
27 . The process according to claim 7 , wherein said Group 4 metal is titanium.
28 . The process according to claim 7 , wherein said compound of a Group 4 metal is a halide.
29 . The process according to claim 1 , wherein said transition metal is a Group 5 metal and/or a Group 6 metal.
30 . The process according to claim 1 , wherein said transition metal is Cu, Fe, Co, Ni and/or Pd.Join the waitlist — get patent alerts
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