Catalyst composition for polymerization of olefins
US-9688790-B2 · Jun 27, 2017 · US
US9868799B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9868799-B2 |
| Application number | US-201415104808-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 19, 2014 |
| Priority date | Dec 20, 2013 |
| Publication date | Jan 16, 2018 |
| Grant date | Jan 16, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to a procatalyst for polymerization of olefins. The invention also relates to a process for preparing said procatalyst. Furthermore, the invention is directed to a catalyst system for polymerization of olefins comprising the said procatalyst, a co-catalyst and optionally an external electron donor; a process of preparing polyolefins by contacting an olefin with said catalyst system and to polyolefins obtained or obtainable by said process. The invention also relates to the use of said procatalyst in the polymerization of olefins.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing a procatalyst for preparing a catalyst composition for olefin polymerization, said process comprising: i) contacting a compound R 4 z MgX 4 2-z with an alkoxy- or aryloxy-containing silane compound to give a first intermediate reaction product, being a solid Mg(OR 1 ) x X 1 2-x , wherein: R 4 is the same as R 1 being a linear, branched or cyclic hydrocarbyl group independently selected from alkyl, alkenyl, aryl, aralkyl, or alkylaryl groups, and one or more combinations thereof; wherein said hydrocarbyl group may be substituted or unsubstituted, may contain one or more heteroatoms; X 4 and X 1 are each independently selected from the group consisting of fluoride (F − ), chloride (Cl − ), bromide (Br − ) or iodide (I − ); z is in a range of larger than 0 and smaller than 2, being 0<z<2; x is in a range of larger than 0 and smaller than 2, being 0<x<2; ii) optionally contacting the solid Mg(OR 1 ) x X 1 2-x obtained in step i) with at least one activating compound selected from the group formed by activating electron donors and metal alkoxide compounds of formula M 1 (OR 2 ) v-w (OR 3 ) w or M 2 (OR 2 ) v-w (R 3 ) w , to obtain a second intermediate reaction product; wherein: M 1 is a metal selected from the group consisting of Ti, Zr, Hf, Al or Si; M 2 is a metal being Si; v is the valency of M 1 or M 2 ; w is smaller than v; R 2 and R 3 are each a linear, branched or cyclic hydrocarbyl group independently selected from alkyl, alkenyl, aryl, aralkyl, alkoxycarbonyl or alkylaryl groups, and one or more combinations thereof; wherein said hydrocarbyl group may be substituted or unsubstituted, may contain one or more heteroatoms; iii) contacting the first or second intermediate reaction product obtained in step i) or ii) respectively, with a halogen-containing titanium compound and either an activator or an internal electron donor to obtain a third intermediate reaction product; iv) modifying the third intermediate reaction product obtained in step iii) with a modifier having the formula M(p)X p , wherein M is selected from the group consisting of aluminum, boron, gallium, zinc, copper, thallium, indium, vanadium, chromium and iron, p is the oxidation state of M, and wherein X is a halide, to yield a modified intermediate reaction product; and v) contacting said modified intermediate reaction product obtained in step iv) with a halogen-containing titanium compound and, in the case that in step iii) an activator was used, an internal donor to obtain the procatalyst. 2. The process according to claim 1 , wherein the activator added during step iii) is selected from the group consisting of alkylbenzoate, benzamide, and monoester. 3. The process according to claim 1 , wherein the activator added during step iii) is ethylbenzoate and the internal donor used during step v) is 4-[benzoyl(methyl)amino]pentan-2-yl benzoate. 4. The process according to claim 1 , wherein during step iv) aluminum halide is used as the modifier. 5. The process according to claim 1 , wherein the compound of formula R 4 MgX 4 2-z used in step i), the halogen-containing titanium compound used in step iii) and step v) and the modifier used in step iv) are used in such amounts that the resulting procatalyst comprises in wt. % based on the total weight of the procatalyst: magnesium: from 15 to 24; titanium: from 1 to 4; modifier: from 0.05 to 2.0. 6. The process according to claim 1 , wherein step ii) is carried out using a combination of an alcohol and an tetra alkoxy titanium compound, as the activating compounds. 7. The process according to claim 1 , wherein steps iii), iv) and v) are carried out in the same reactor. 8. The process according to claim 1 , wherein the internal donor used during step iii) or step v) is selected from the group consisting of dicarboxylic acid esters according to Formula VI and aminobenzoates according to formula XI: wherein R 40 and R 41 are each independently a linear, branched or cyclic, and substituted or unsubstituted hydrocarbyl group selected from alkyl, alkenyl, aryl, aralkyl, alkoxycarbonyl or alkylaryl groups, and one or more combinations thereof; and wherein R 42 , R 43 , R 44 , R 45 are each independently selected from hydrogen, a halide or a linear, branched or cyclic, and a substituted or unsubstituted hydrocarbyl group and one or more combinations thereof; wherein R 80 is a substituted or unsubstituted aromatic group, selected from aryl or alkylaryl groups, having from 6 to 20 carbon atoms; R 81 , R 82 , R 83 , R 84 , R 85 , and R 86 are each independently selected from hydrogen or a linear, branched or cyclic, and substituted or unsubstituted hydrocarbyl group and one or more combinations thereof. 9. The process according to claim 5 , wherein the resulting procatalyst comprises in wt. % based on the total weight of the procatalyst: magnesium: from 19.0 to 19.5; titanium: from 1.5 to 3.5; Group 13 or transition metal: from 0.1 to 0.4.
Propene · CPC title
and aluminium or compounds thereof · CPC title
Broad molecular weight distribution, i.e. Mw/Mn > 6 · CPC title
with magnesium or compounds thereof · CPC title
and metals of C08F4/64 or compounds thereof · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.