Univation Technologies, LLC

Dow Global Technolgoies LLC

Exxonmobil Chemical Patents Inc.

Wesley R Mariott

Kevin Joseph Cann

Phuong Anh Cao

Mark Gregory Goode

John H Moorhouse

F David Hussein

Michael D Awe

Thomas Oswald

C Dale Lester

Timothy R Lynn

Richard B Pannell

C Jeff Harlan

Daniel Paul Zilker, Jr

Ping P Cai

Yuanqiao Rao

Bruce Jon Savatsky

Chi-I Kuo

David Michael Glowczwski

Nitin Borse

Roger L Kuhlman

John Francis Szul

Ching-Tai Lue

James McLeod Farley

Fathi David Hussein

Haiqing Peng

Abarajith S Hari

Robert J Jorgensen

Pradeep Jain

Daniel D VanderLende

Lixin Sun

John Henry Oskam

Swapnil B Chandak

Cliff Robert Mure

Ian M Munro

Brandon C Locklear

Daniel D Vanderlende

Ann M Schoeb-Wolters

Daniel P Zilker

Chuan C He

John Joseph Bielak

Mark K Davis

F Gregory Stakem

Jesse C Beilhart

John J Bielak

Jeff C Harlan

Marke G Goode

David F Hussein

Gregory F Stakem

Embodiments of the present disclosure are directed towards catalyst formulations including a metallocene and a stearic compound selected from bis 2-hydroxyethyl stearyl amine, aluminum distearate, and combinations thereof, where the metallocene is represented by the following formula: (Formula (I)) wherein each n-PR is n-propyl, and each X is independently CH, Cl, or F. 

Catalyst formulations

A spray-dried zirconocene catalyst system comprising a zirconocene catalyst and a hydrophobic fumed silica, which supports the zirconocene catalyst. A spray-drying method of making same. Polyolefins; methods of making and using same; and articles containing same.

Spray-dried zirconocene catalyst system

Polymerization process control methods for making polyethylene are provided. The process control methods include performing a polymerization reaction in a polymerization reactor to produce the polyethylene, where ethylene, and optionally one or more comonomers, in the polymerization reaction is catalyzed by an electron donor-free Ziegler-Natta catalyst and an alkyl aluminum co-catalyst. A melt flow ratio (I/I) of the polyethylene removed from the polymerization reactor is measured and an amount of long chain branching (LCB) of the polyethylene from the polymerization reactor is controlled by adjusting a weight concentration of the alkyl aluminum co-catalyst present in the polymerization reactor. In addition, an electron donor-free Ziegler-Natta catalyst productivity of the polyethylene being produced in the polymerization reactor is measured from which the amount of LCB of the polyethylene from the polymerization reactor is determined using the measured electron donor-free Ziegler-Natta catalyst productivity and a predetermined relationship between the electron donor-free Ziegler-Natta catalyst productivity and the LCB.

Process control for long chain branching control in polyethylene production

An activated, titanium-based, spray-dried Ziegler-Natta catalyst system containing a titanium-based Ziegler-Natta catalyst, a carrier material, and an activator mixture comprising an effective amount of an activator mixture comprising triethylaluminum and diethylaluminum chloride for producing a substantially uniform comonomer composition distribution. Also, polyolefins; methods of making and using same; and articles containing same.

Activated spray-dried Ziegler-Natta catalyst system

A modified spray-dried Ziegler-Natta (pro)catalyst system comprising a Ziegler-Natta (pro)catalyst, a carrier material, and a tetrahydrofuran/ethanol modifier; polyolefins; methods of making and using same; and articles containing same.

Modified spray-dried Ziegler-Natta (pro)catalyst systems

Methods of making spray-dried Ziegler-Natta (pro)catalyst systems containing titanium Ziegler-Natta (pro)catalysts, a hydrophobic silica carrier material, and tetrahydrofuran. The spray-dried Ziegler-Natta (pro)catalyst systems made by the method. Methods of polymerizing olefin (co)monomer(s) with the spray-dried Ziegler-Natta catalyst system to make polyolefin polymers, and the polyolefin polymers made thereby.

Spray-dried Ziegler-Natta (pro)catalyst systems

A method for increasing the melt strength of a polyolefin polymer composition is provided. The method includes mixing a first polyolefin composition derived from at least one olefin polymerization catalyst (a) and at least one olefin polymerization catalyst (b) with a second polyolefin composition derived from the at least one olefin polymerization catalyst (b) or from at least one olefin polymerization catalyst (c), and obtaining the polyolefin polymer composition.

Methods for making polyolefin polymer compositions

The present disclosure provides a method for improving the activity of Ziegler-Natta (ZN) catalysts. The method includes forming a modified precursor composition of a ZN catalyst by providing a precursor composition of the ZN catalyst for treatment with an aluminum alkyl compound in a liquid organic solvent. The precursor composition of the ZN catalyst includes at least one titanium compound. The at least one titanium compound in the precursor composition is treated with the aluminum alkyl compound in the liquid organic solvent, where the aluminum alkyl compound converts the at least one titanium compound in the precursor composition into a modified state of the ZN catalyst. At least a portion of the aluminum alkyl compound not consumed in converting the at least one titanium compound in the precursor composition into the modified state of the ZN catalyst and reaction by-product compounds in the liquid organic solvent are removed to form the modified precursor composition of the ZN catalyst.

Method for improving Ziegler-Natta catalyst activity

Catalyst systems and methods for making and using the same are provided. The catalyst system can include a catalyst support, wherein the catalyst support has an average particle size of about 2 microns to about 200 microns. Nanoparticles are adhered to the catalyst support, wherein the nanoparticles have an average particle size of about 2 to about 200 nanometers. A catalyst is supported on the catalyst support.

Supported catalyst with improved flowability

Polymerization process control methods for making polyethylene are provided. The process control methods include performing a polymerization reaction in a polymerization reactor to produce the polyethylene, where ethylene, and optionally one or more comonomers, in the polymerization reaction is catalyzed by an electron donor-free Ziegler-Natta catalyst and an alkyl aluminum co-catalyst. A melt flow ratio (I/I) of the polyethylene removed from the polymerization reactor is measured and an amount of long chain branching (LCB) of the polyethylene from the polymerization reactor is controlled by adjusting a weight concentration of the alkyl aluminum co-catalyst present in the polymerization reactor. In addition, an electron donor-free Ziegler-Natta catalyst productivity of the polyethylene being produced in the polymerization reactor is measured from which the amount of LCB of the polyethylene from the polymerization reactor is determined using the measured electron donor-free Ziegler-Natta catalyst productivity and a predetermined relationship between the electron donor-free Ziegler-Nana catalyst productivity and the LCB.

Polymerization catalyst compositions are provided as are methods of their preparation. The compositions comprise fatty amines and find advantageous use in olefin polymerization processes. The catalyst composition comprises at least one supported polymerization catalyst wherein the catalyst composition is modified with at least one fatty amine wherein the fatty amine is substantially free of particulate inorganic material.

Catalyst composition, methods of preparation and use in a polymerization process

Catalyst systems and methods for making and using the same. A method for making a catalyst support includes forming a mixture of a support material and a fluoride donor. The mixture is added to a fluidized bed reactor. The mixture is fluidized to form a fluidized bed while maintaining a flow rate of a fluidizing gas of about 0.1 ft./sec at less than about 370&#xb0; C. and greater than about 0.35 ft./sec at temperatures greater than about 370&#xb0; C. The mixture is calcined to decompose the fluoride donor, forming a fluorinated support.

Fluorinated catalyst supports and catalyst systems

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Freeport, TX, United States of America

Wesley R Mariott