1
Cynthia Hoover
Scott Houston Meiere, Cynthia A Hoover: Method for producing organometallic compounds. Praxair Technology, Gerald L Coon, October 26, 2004: US06809212 (7 worldwide citation)

This invention relates to liquid cyclopentadienyltrimethylplatinum compounds selected from (isopropylcyclopentadienyl)trimethylplatinum and (tert-butylcyclopentadienyl)trimethylplatinum. This invention also relates to a process for producing a film, coating or powder by decomposing a cyclopentadieny ...


2
Cynthia Hoover
David M Thompson, Cynthia A Hoover: Methods for making metallocene compounds. Praxair Technology, Gerald L Coon, April 26, 2005: US06884901 (6 worldwide citation)

A method for producing Group 8 (VIII) metallocene or metallocene-like compounds employs a compound that includes a Cp′ anion, such as found, together with a counterion, in a cyclopentadienide or cyclopentadienide-like salt. In one embodiment, the method includes reacting a metal salt, a (Cp) compoun ...


3
Cynthia Hoover
David M Thompson, Cynthia A Hoover: Asymmetric group 8 (VIII) metallocene compounds. Praxair Technology, Gerald L Coon, July 19, 2005: US06919468 (3 worldwide citation)

Asymmetric, disubstituted metallocene compounds have the general formula CpMCp′ where M is a metal selected from the group consisting of Ru, Os and Fe; Cp is a first substituted cyclopentadienyl or indenyl moiety that includes at least one substituent group D1; Cp′ is a second substituted cyclopenta ...


4
Moinuddin Ahmed, James R Nelson, Charles A Gibson: Process for preparing alkanolamines. Union Carbide Corporation, Gerald L Coon, July 4, 1989: US04845296 (69 worldwide citation)

A process is provided for preparing alkanolamines having a high yield of monoalkanolamine which comprises reacting in a reaction mixture an alkylene oxide having from two to four carbon atoms with ammonia in a molar ratio of ammonia to alkylene oxide within the range from about 15.1 to about 50.1 at ...


5
James C Hatfield: Encapsulation of phase change materials. Union Carbide Corporation, Gerald L Coon, November 24, 1987: US04708812 (69 worldwide citation)

Solid phase change materials, such as CARBOWAX.RTM. polyethylene glycol 8000, are encapsulated in a condensation polymeric shell to provide heat storage material for use in such things as solar heating devices. The phase change material is put into particulate form and then is coated with a reactive ...


6
George E Totten, Gordon C Johnson: Random polyether foam control agents. Union Carbide Corporation, Gerald L Coon, June 6, 1989: US04836951 (52 worldwide citation)

Improved mechanical dishwasher formulations are provided which are characterized by the use of a random copolyether foam control agent, and wherein the foam control agent imparts the desirable properties of cleaning and defoaming without the concurrent buildup of spots and films on the dishes. The f ...


7
Willis W Weber, Joseph A Herbst: Process of preparing high purity alumina bodies. Union Carbide Corporation, Gerald L Coon, April 5, 1983: US04379134 (48 worldwide citation)

High purity alpha-alumina bodies useful as catalyst supports are made by peptizing boehmite alumina in an acidic mixture containing fluoride anions, extruding the peptized alumina into shaped bodies and drying and calcining the bodies. The alpha-alumina bodies are characterized by a narrow pore-size ...


8
Steven W Kaiser: Production of light olefins. Union Carbide Corporation, Gerald L Coon, June 21, 1988: US04752651 (46 worldwide citation)

The process for the production of light olefins from a feedstock comprising at least an aliphatic hetero compound comprising contacting said feedstock in the presence of an aromatic diluent with a non-zeolitic molecular sieve at effective process conditions to produce light olefins.


9
Thomas N Wheeler: Biocidal 2-aryl-1,3-cyclohexanedione enol ester compounds. Union Carbide Corporation, Gerald L Coon, April 21, 1987: US04659372 (45 worldwide citation)

2-Aryl-1,3-cyclohexanedione enol ester compounds exhibit outstanding miticidal, mite ovicidal and herbicidal activity.


10
Thomas N Wheeler, Mathias H J Weiden: Biocidal enol esters of non-ortho substituted 2-aryl-1-3-cycloalkanedione compounds. Union Carbide Corporation, Gerald L Coon, July 2, 1985: US04526723 (43 worldwide citation)

Non-ortho substituted 2-aryl-1,3-cycloalkanedione enol ester compounds exhibit outstanding acaricidal and herbicidal activity.



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