US2008058487A1PendingUtilityA1

Polymerization reactor operability using static charge modifier agents

Assignee: UNIVATION TECH LLCPriority: Dec 1, 2000Filed: Oct 26, 2007Published: Mar 6, 2008
Est. expiryDec 1, 2020(expired)· nominal 20-yr term from priority
C08F 10/00B01J 31/146B01J 31/1616B01J 31/2295B01J 2531/48C08F 4/65912C08F 4/65916C08F 4/65927C08F 210/16Y10S526/943C08F 2410/02
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Claims

Abstract

The present invention relates to a catalyst composition and a method for making the catalyst composition of a polymerization catalyst and a static charge modifier. The invention is also directed to the use of the catalyst composition in the polymerization of olefin(s). In particular, the polymerization catalyst system is supported on a carrier. More particularly, the polymerization catalyst comprises a bulky ligand metallocene-type catalyst system.

Claims

exact text as granted — not AI-modified
1 . A continuous process for polymerizing olefin monomers in a reactor under polymerization conditions, the process comprising the steps of: 
 a. introducing one or more olefin monomers into the reactor;    b. introducing a polymerization catalyst comprising (i) a bulky ligand metallocene-type catalyst compound, and (ii) a static charge modifier having the formula [C]+[A]− wherein C is a cation that does not possess an active hydrogen or other reactive group and [A]− is a weakly coordinating metal or metalloid containing anion; and    c. withdrawing a polymer from the reactor.    
     
     
         2 . The process of  claim 1  wherein the process is a slurry process.  
     
     
         3 . The process of  claim 1  wherein said process is a gas phase process.  
     
     
         4 . The process of  claim 1  wherein said olefins comprise ethylene ∀-olefin having from 3 to 20 carbon atoms, diolefins having from 6 to 20 carbon atoms and mixtures of 2 or more of olefins or diolefins.  
     
     
         5 . The process of  claim 1  wherein the anion [C]+ satisfies the formula [XR1 . . . Rn]+ wherein X is an atom having a permanent charge, selected from Group 15 of the Periodic Table and each R is independently an aliphatic or aromatic hydrocarbyl and n is the number of substitutions required to exhaust the ability of X to form additional chemical bonds.  
     
     
         6 . The process of  claim 1  wherein [A]− has the chemical formula [YR′1 . . . Rn]− wherein Y is a metal or metalloid and each R′ is, independently, hydride radicals, bridged or unbridged dialkylamido radicals, alkoxide and aryloxide radicals, hydrocarbyl and substituted hydrocarbyl radicals, and hydrocarbyl and halohydrocarbyl substituted organometalloid radicals where m is an integer equal to the valence state of Y′.  
     
     
         7 . The process of  claim 6  wherein said metalloid is boron 5.  
     
     
         8 . The process of  claim 1  wherein said polymerization catalyst further comprises a carrier.  
     
     
         9 . The process of  claim 8  wherein said carrier is an inorganic oxide carrier.  
     
     
         10 . The process of  claim 1  further comprising a carrier and an activator.  
     
     
         11 . The process of  claim 10  wherein said activator is alumoxane.  
     
     
         12 . The process of  claim 1  wherein said static charge modifier is present in an amount ranging from 0.5 to 500 weight percent.  
     
     
         13 . A method for controlling static charges in a polymerization reactor comprising the step of introducing a static charge modifier into said reactor said static charge modifier comprising a compound having the general formula [C]+[A]− wherein [C]+ is a cation that does not possess an active hydrogen or other reactive group and [A]− is a weakly coordinating metal or metalloid containing cation.  
     
     
         14 . The method of  claim 13  further comprising the steps of dissolving said static charge modifier in a hydrocarbon diluent and introducing the solution into said reactor.  
     
     
         15 . The method of  claim 13  wherein said static charge modifier is further liquefied in that the anion [C]+ satisfies the formula [XR1 . . . Rn]+ wherein X is an atom having a permanent charge, selected from Group 15 of the Periodic Table and each R is independently an aliphatic or aromatic hydrocarbyl and n is the number of substitutions required to exhaust the ability of X to form additional chemical bonds.  
     
     
         16 . The method of  claim 13  wherein [A]− has the chemical formula [YR′1 . . . Rn]− wherein Y is a metal or metalloid and each R′ is, independently, hydride radicals, bridged or unbridged dialkylamido radicals, alkoxide and aryloxide radicals, hydrocarbyl and substituted hydrocarbyl radicals, and hydrocarbyl and halohydrocarbyl substituted organometalloid radicals and where m is an integer equal to the valence of Y+1.  
     
     
         17 . The method of  claim 16  wherein said metalloid is boron 5.

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