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Kestutis A Keblys

from Southfield, MI

Kestutis Keblys Phones & Addresses

  • Southfield, MI

Us Patents

  • Preparation Of Cobalt Complex

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  • US Patent:
    39352285, Jan 27, 1976
  • Filed:
    Oct 23, 1973
  • Appl. No.:
    5/408635
  • Inventors:
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C07D21316
    C07D21506
  • US Classification:
    260270J
  • Abstract:
    A process for preparing cobalt complexes and their use as hydroesterification catalysts are disclosed.
  • Preparation Of Metal Bromides

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  • US Patent:
    42488508, Feb 3, 1981
  • Filed:
    Feb 26, 1979
  • Appl. No.:
    6/015067
  • Inventors:
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C01F 1134
    C01G 904
  • US Classification:
    423491
  • Abstract:
    Metal bromides, and particularly alkali and alkaline earth metal bromides, are prepared from a basic metal compound and bromine in the presence of added formaldehyde as a reducing agent.
  • Halogen-Containing Diphosphonates

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  • US Patent:
    40368092, Jul 19, 1977
  • Filed:
    Oct 2, 1975
  • Appl. No.:
    5/618890
  • Inventors:
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C08K 553
  • US Classification:
    260 457P
  • Abstract:
    Compounds such as tetramethyl [(2,3,5-tetrabromo-p-phenylene)-dimethylene] diphosphonate are useful as flame retardants in polymers and resins such as unsaturated polyesters and polyester fibers, polystyrene, and the like.
  • Chemical Process For Preparing 3-Phenoxybenzyl Chloride

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  • US Patent:
    43777139, Mar 22, 1983
  • Filed:
    Jan 18, 1982
  • Appl. No.:
    6/340321
  • Inventors:
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C07C 4122
  • US Classification:
    568639
  • Abstract:
    Reaction of 3-phenoxytoluene with bromine at elevated temperature yields 3-phenoxybenzyl bromide, 3-phenoxybenzal bromide, or a mixture thereof. In contrast to teachings of the prior art, phosphorus halide catalysis or u. v. activation is not required to achieve a desirable amount of side-chain bromination with a minimum of nuclear halogenation. For example, it was observed that at 265. +-. 5. degree. C. , good yields of the desired benzyl and benzal bromide were obtained, but no nuclear halogenated by-product was detected by gas chromatography. The comparable chlorination is also effective.
  • Iodine Recovery Process

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  • US Patent:
    41316452, Dec 26, 1978
  • Filed:
    Nov 21, 1974
  • Appl. No.:
    5/525870
  • Inventors:
    Kestutis A. Keblys - Southfield MI
    John M. McEven - Lake Orion MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C01B 714
  • US Classification:
    423501
  • Abstract:
    Iodine is recovered from an aqueous solution containing iodide such as underground brine by repeated cycles of (1) passing the brine through a basic anion exchange resin to adsorb iodide, and (2) oxidizing adsorbed iodide to iodine by passing an acidified aqueous iodate solution (e. g. , NaIO. sub. 3) through the resin. The cycle is repeated many times until the resin is iodine-loaded. Iodine is then eluted from the resin, for example, with aqueous NaOH and recovered from the eluate by conventional means.
  • Preparation Of Bromine

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  • US Patent:
    39610330, Jun 1, 1976
  • Filed:
    Mar 6, 1975
  • Appl. No.:
    5/555801
  • Inventors:
    Joseph P. Kleiman - Birmingham MI
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C01B 700
  • US Classification:
    423502
  • Abstract:
    Bromine is produced by reacting chlorine and ethylene dibromide in the presence of an aluminum halide catalyst, e. g. aluminum chloride. A small amount of bromine present prior to chlorine addition shortens the induction period. Some decomposition of the organic product occurs if it is distilled in the presence of aluminum-containing residues. These residues can be removed by water wash which can be followed by drying with H. sub. 2 SO. sub. 4. After such treatment, ethylene dichloride can be recovered by distillation without substantial decomposition.
  • Method Of Winning Copper, Nickel, And Other Metals

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  • US Patent:
    39679586, Jul 6, 1976
  • Filed:
    Aug 27, 1973
  • Appl. No.:
    5/391619
  • Inventors:
    Thomas H. Coffield - Waterloo, BE
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C22B 1510
    C22B 2304
  • US Classification:
    75103
  • Abstract:
    The invention is a process for winning nickel by treating an aqueous ammonium salt solution of nickel salts with a carbon monoxide-containing gas under reducing conditions to produce nickel carbonyl and subsequently recovering nickel therefrom. Optionally, the production of nickel carbonyl can be catalyzed, for example, by cyanide. Also, an essentially water-immiscible solvent for nickel carbonyl can optionally be employed. The aqueous ammoniacal solution is typically an aqueous ammoniacal ammonium chloride, carbonate, sulfate, hydroxide, or mixture thereof. The valuable metals associated with nickel, e. g. , copper, cobalt, iron, and precious metals, are also separated and recovered by this process. The general nature of the process allows a wide variety of primary and secondary sources of nickel to be utilized by combining this process with a number of known ore-treatment steps.
  • Thermal Process For Preparing 3-Phenoxybenzyl Bromide

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  • US Patent:
    43260896, Apr 20, 1982
  • Filed:
    Sep 26, 1977
  • Appl. No.:
    5/836428
  • Inventors:
    Kestutis A. Keblys - Southfield MI
  • Assignee:
    Ethyl Corporation - Richmond VA
  • International Classification:
    C07C 4122
  • US Classification:
    568639
  • Abstract:
    Reaction of 3-phenoxytoluene with bromine at elevated temperature yields 3-phenoxybenzyl bromide, 3-phenoxybenzal bromide, or a mixture thereof. In contrast to teachings of the prior art, phosphorus halide catalysis or u. v. activation is not required to achieve a desirable amount of side-chain bromination with a minimum of nuclear halogenation. For example, it was observed that at 265. +-. 5. degree. C. , good yields of the desired benzyl and benzal bromide were obtained, but no nuclear halogenated by-product was detected by gas chromatography.

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