Patent US4684703A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4684703A Expired / Lapsed US ⏱️ 0.0 years remaining

Polymerization catalyst for ethylene homopolymerization

Assignee: Union Carbide Corp
•
Filing: 1983-03-07
•
Granted: 1987-08-04
•
Expires: 2003-03-07
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A catalyst formed from selected organo aluminum compounds and a precursor composition of the formula Mg.sub.m Ti.sub.l (OR).sub.n X.sub.p [ED].sub.q wherein ED is a selected electron donor compound m is ≧0.5 to ≦56 n is 0 or 1 p is ≧6 to ≦116 q is ≧2 to ≦85 R is a C 1 to C 14 , aliphatic or aromatic hydrocarbon radical, or COR' wherein R' is a C 1 to C 14 aliphatic or aromatic hydrocarbon radical, and X is selected from the group consisting of Cl, Br, I, or mixtures thereof, which catalyst is in particulate form and diluted with an inert carrier material; a process for preparing such catalyst; a process for using said catalyst to readily prepare ethylene homopolymer having a density of about ≧0.958 to ≦0.972 and a melt flow ratio of ≧22 to ≦32 in a low pressure gas phase process at a productivity of ≧50,000 pounds of polymer per pound of Ti. Novel polymers and molded articles are prepared.

Inventors

  • 👤 Burkhard E. Wagner
  • 👤 Frederick J. Karol
  • 👤 George L. Goeke
  • 👤 Robert J. Jorgensen
  • 👤 Nils Friis

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 23:51
CPC Classifications
C; C08; C08F; C08F110/00; C08F110/02; C08F4/00; C08F4/42; C08F4/44; C08F4/60; C08F4/62; C08F4/64; C08F4/642; C08F4/6423; C08F4/6425; C08F4/65; C08F4/652; C08F4/654; C08F4/6543; C08F4/655; C08F4/6555; Y; Y10; Y10S; Y10S526/00; Y10S526/901; Y10S526/904

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 510 words
A catalytic process for producing ethylene homopolymer with a Ti containing catalyst at a productivity of ≧ 50,000 pounds of polymer per pound of Ti under a pressure of <1000 psi in a gas phase fluid bed reaction said polymer being produced in granular form and having a density of about ≧0.958 to ≦0.972 and a melt flow ratio of ≧22 to ≦32 which comprises homopolymerizing ethylene at a temperature of about 30° to 115° C. by contacting the monomer charge with, in the presence of about 0 to 2.0 mols of hydrogen per mol of ethylene in a gas phase reaction zone, particles of the catalyst formed by (A) forming a precursor composition of the formula Mg m Ti l (OR) n X p [ED] g wherein R is C 1 to C 14 aliphatic or aromatic hydrocarbon radical, or COR' wherein R' is a C 1 to C 14 aliphatic or aromatic hydrocarbon radical, X is selected from the group consisting of Cl, Br, I, or mixture thereof, ED is an electron donor compound, m is ≧0.5 to ≦56 n is 0 or 1 p is ≧6 to ≦116 and q is ≧2 to ≦85 by dissolving at least one magnesium compound and at least one titanium compound in at least one electron donor compound so as to thereby form a solution of said precursor composition in said electron donor compound, and recovering said precursor composition from said solution, said magnesium compound having the structure MgX 2 , said titanium compound having the structure Ti(OR) a X b wherein a is 0 or 1, b is 2 to 4 inclusive and a+b=3 or 4 said electron donor compound being a liquid organic compound in which said magnesium compound and said titanium compound are soluble and which is selected from the group consisting of alkyl esters of aliphatic and aromatic carboxylic acids, aliphatic esters, cyclic esters and aliphatic ketones, and said magnesium compound, said titanium compound and said electron donor compound being employed in such amounts as to satisfy the values of m, n, p and q, (B) diluting said precursor composition with about 1 to 10 parts by weight, per part by weight of said precursor composition, of at least one inert carrier material, (C) partially activating the precursor composition outside the polymerization zone in a hydrocarbon slurry with >0 to <10 mols of activator compound per mol of titanium in said precursor composition, said activator compound having the structure Al(R").sub.c X'.sub.d H.sub.e wherein X' is Cl or OR"', R" and R"' are the same or different and are C 1 to C 14 saturated hydrocarbon radicals, d is 0 to 1.5, e is 1 or 0 and c+d+e=3, and drying the mixture to remove the hydrocarbon solvent, and (D) completely activating the precursor composition in a fluid bed polymerization zone with ≧10 to about 400 mols of said activator compound in the absence of a solvent for said precursor composition so as to avoid the need for drying the fully active catalyst to remove the solvent therefrom.
Claim 2
Dependent Claim 510 words
A catalytic process for producing ethylene homopolymer with a Ti containing catalyst at a productivity of ≧ 50,000 pounds of polymer per pound of Ti under a pressure of <1000 psi in a gas phase fluid bed reaction said polymer being produced in granular form and having a density of about ≧0.958 to ≦0.972 and a melt flow ratio of ≧22 to ≦32 which comprises homopolymerizing ethylene at a temperature of about 30° to 115° C. by contacting the monomer charge with, in the presence of about 0 to 2.0 mols of hydrogen per mol of ethylene in a gas phase reaction zone, particles of the catalyst formed by (A) forming a precursor composition of the formula Mg m Ti l (OR) n X p [ED] g wherein R is C 1 to C 14 aliphatic or aromatic hydrocarbon radical, or COR' wherein R' is a C 1 to C 14 aliphatic or aromatic hydrocarbon radical, X is selected from the group consisting of Cl, Br, I, or mixture thereof, ED is an electron donor compound, m is ≧0.5 to ≦56 n is 0 or 1 p is ≧6 to ≦116 and q is ≧2 to ≦85 by dissolving at least one magnesium compound and at least one titanium compound in at least one electron donor compound so as to thereby form a solution of said precursor composition in said electron donor compound, and recovering said precursor composition from said solution, said magnesium compound having the structure MgX 2 , said titanium compound having the structure Ti(OR) a X b wherein a is 0 or 1, b is 2 to 4 inclusive and a+b=3 or 4 said electron donor compound being a liquid organic compound in which said magnesium compound and said titanium compound are soluble and which is selected from the group consisting of alkyl esters of aliphatic and aromatic carboxylic acids, aliphatic esters, cyclic esters and aliphatic ketones, and said magnesium compound, said titanium compound and said electron donor compound being employed in such amounts as to satisfy the values of m, n, p and q, (B) diluting said precursor composition with about 1 to 10 parts by weight, per part by weight of said precursor composition, of at least one inert carrier material, (C) partially activating the precursor composition outside the polymerization zone in a hydrocarbon slurry with >0 to <10 mols of activator compound per mol of titanium in said precursor composition, said activator compound having the structure Al(R").sub.c X'.sub.d H.sub.e wherein X' is Cl or OR"', R" and R"' are the same or different and are C 1 to C 14 saturated hydrocarbon radicals, d is 0 to 1.5, e is 1 or 0 and c+d+e=3, and drying the mixture to remove the hydrocarbon solvent, and (D) completely activating the precursor composition in a fluid bed polymerization zone with ≧10 to about 400 mols of said activator compound in the absence of a solvent for said precursor composition so as to avoid the need for drying the fully active catalyst to remove the solvent therefrom.
Claim 3
Dependent Claim 24 words
A process as in claim 1 which is conducted under a mass gas flow rate of about 1.5 to 10 times G mf .
Claim 4
Dependent Claim 14 words
A process as in claim 2 which is conducted at a productivity of ≧100,000.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-08-03 1991-02-02 1991-08-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-08-03 1995-02-02 1995-08-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-08-03 1999-02-02 1999-08-04 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag