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Donald W Pickens

age ~72

from Columbus, MS

Also known as:
  • Donald C Pickens
Phone and address:
109 Countryside Ln, Columbus, MS 39702
(662)3280059

Donald Pickens Phones & Addresses

  • 109 Countryside Ln, Columbus, MS 39702 • (662)3280059
  • 93 Nash Rd, Columbus, MS 39705
  • Waco, TX
  • Millport, AL
  • Newark, NJ
  • 109 Countryside Ln, Columbus, MS 39702

Resumes

Donald Pickens Photo 1

Selfemployeed

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Location:
Waco, TX
Industry:
Automotive
Work:
Small Engine Repair By Fifty
Selfemployeed
Donald Pickens Photo 2

Donald Pickens

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Donald Pickens Photo 3

Donald Pickens

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Name / Title
Company / Classification
Phones & Addresses
Donald W. Pickens
D.W. PICKENS INDUSTRIES, INC
Donald Pickens
Director
The Rector, Wardens and Vestry of St. David of Wales Episcopal Church, Denton, Texas, Inc

Us Patents

  • Fluorinated Surfactant Monomers For Polymer Surface Modification

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  • US Patent:
    50047906, Apr 2, 1991
  • Filed:
    Feb 15, 1989
  • Appl. No.:
    7/311316
  • Inventors:
    Daniel F. Harnish - Morristown NJ
    Donald Pickens - Mendham NJ
    Andrew M. Zweig - West Orange NJ
  • Assignee:
    Allied-Signal Inc. - Morris Township, Morris County NJ
  • International Classification:
    C08F 1220
  • US Classification:
    526242
  • Abstract:
    A novel class of fluorinated surfactant monomers which when blended and cured with conventional non-fluorinated monomers produces resins with dramatically modified surfaces. Resins which may be thus modified include urethanes, epoxides, acrylates, polyesters and other thermosetting materials.
  • Producing Silane From Silicon Tetrafluoride

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  • US Patent:
    44077831, Oct 4, 1983
  • Filed:
    Aug 16, 1982
  • Appl. No.:
    6/408408
  • Inventors:
    Harry E. Ulmer - Morristown NJ
    Donald Pickens - Mendham NJ
    Forrest J. Rahl - Hackettstown NJ
    Philip A. Lefrancois - Cranford NJ
  • Assignee:
    Allied Corporation - Morris Township, Morris County NJ
  • International Classification:
    C01B 3304
  • US Classification:
    423347
  • Abstract:
    Silicon tetrafluoride is reacted with sodium hydride in a cyclic ether reaction medium such as tetrahydrofuran or 1,4-dioxane or in dimethoxyethane. Sodium aluminum hydride is dissolved in the solvent and catalyzes the reaction in amounts of 4-25%, by weight of combined sodium hydride and sodium aluminum hydride.
  • Magnetic Coating Compositions Containing Fluoropolyols

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  • US Patent:
    50615777, Oct 29, 1991
  • Filed:
    Nov 28, 1988
  • Appl. No.:
    7/277089
  • Inventors:
    Daniel F. Harnish - Morristown NJ
    Donald Pickens - Mendham NJ
    Richard J. Brautigam - Westfield NJ
  • Assignee:
    Allied-Signal Inc. - Morristown NJ
  • International Classification:
    G11B 2300
  • US Classification:
    428694
  • Abstract:
    A class of fluorinated polyols which when added to formulated dispersions used to make a magnetic particle based coating not only improves the dispersion of the particles in the formulation during manufacture but also improves the wear characteristics of the cured coating during use. The fluorinated polyol may be prepared either by the reaction of a diglycidyl ether with a diol or by the reaction of two diols with epichlorohydrin.
  • Production Of Acetaldehyde Oxime

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  • US Patent:
    43237061, Apr 6, 1982
  • Filed:
    Dec 18, 1980
  • Appl. No.:
    6/217938
  • Inventors:
    John H. Bonfield - Basking Ridge NJ
    Stephen E. Belsky - Parsippany NJ
    Donald Pickens - Mendham NJ
  • Assignee:
    Allied Corporation - Morris Township, Morris County NJ
  • International Classification:
    C07C13100
  • US Classification:
    564253
  • Abstract:
    Acetaldehyde oxime, a commercially useful intermediate in the production of pesticides, is prepared by oximating acetaldehyde with an aqueous hydroxylamine-containing solution to form an aqueous oximation reaction mixture and recovering acetaldehyde oxime from the aqueous oximation reaction mixture by distilling a mixture of acetaldehyde oxime and water directly from the aqueous oximation reaction mixture.
  • Removing Aqueous Ammonium Sulfate From Oxime Product

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  • US Patent:
    42566681, Mar 17, 1981
  • Filed:
    Jun 20, 1979
  • Appl. No.:
    6/050356
  • Inventors:
    Chempolil T. Mathew - Randolph NJ
    Donald Pickens - Mendham NJ
  • Assignee:
    Allied Chemical Corporation - Morris Township, Morris County NJ
  • International Classification:
    C07C13100
    C07C13104
  • US Classification:
    564255
  • Abstract:
    An organic, substantially water-insoluble oxime product is recovered from the liquid reaction mixture of water, ammonium sulfate and the oxime product. First the reaction mixture is separated into a first liquid layer containing an aqueous ammonium sulfate solution and a second liquid layer containing an emulsion of the oxime product as the continuous phase and aqueous ammonium sulfate as the discontinuous phase. These layers are separated and the second liquid layer is contacted with solid ammonium sulfate for a time sufficient to agglomerate the discontinuous phase. The agglomerated discontinuous phase is then removed from the continuous phase. Thereafter, either a lites fraction can be distilled from the continuous phase or the oxime product can be distilled from the continuous phase, or both. The process is particularly applicable to the production of oximes such as Aldicarb oxime, cyclohexanone oxime and methylethylketoxime from aqueous reaction mixtures in which by-product ammonium sulfate is formed.
  • Process For Halogenation Of Aldehydes And Production Of Oximes Therefrom

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  • US Patent:
    40961877, Jun 20, 1978
  • Filed:
    Aug 4, 1977
  • Appl. No.:
    5/821898
  • Inventors:
    John Henry Bonfield - Basking Ridge NJ
    Andiappan Kumaresa Murthy - Lake Hiawatha NJ
    Donald Pickens - Mendham NJ
  • Assignee:
    Allied Chemical Corporation - Morris Township NJ
  • International Classification:
    C07C 4714
    C07C13100
  • US Classification:
    260601H
  • Abstract:
    In the halogenation under reflux conditions of an aldehyde of the formula ##STR1## with Cl. sub. 2, Br. sub. 2 or I. sub. 2, the aldehyde and halogen are continuously fed into a reactor at a molar ratio of halogen to aldehyde between about 0. 8:1 and about 1. 1:1 and water is continuously fed into the reactor at a rate of between about 1 and about 20% by weight of aldehyde. The product. alpha. -haloaldehyde is thioalkylated and then oximated to form a 2-hydrocarbylthioaldoxime of the formula ##STR2## with improved yield and quality because of the improved yield and quality of. alpha. -haloaldehyde. An exemplary process includes the chlorination of isobutyraldehyde (IBA) to form. alpha. -chloroisobutyraldehyde (CIBA), the thiomethylation of CIBA to form 2-methyl-2 methylthio-propionaldehyde (MTIBA) and the oximation of MTIBA to form 2-methylthio-propionaldehyde oxime (aldicarb oxime or ADO).
  • Process For Preparing .Alpha.- And .Beta.-Hydroxy Oximes

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  • US Patent:
    41338340, Jan 9, 1979
  • Filed:
    Jan 3, 1978
  • Appl. No.:
    5/866421
  • Inventors:
    Donald Pickens - Mendham NJ
  • Assignee:
    Allied Chemical Corporation - Morris Township, Morris County NJ
  • International Classification:
    C07C13100
  • US Classification:
    260566A
  • Abstract:
    An improved process is disclosed for preparing. alpha. -and. beta. -hydroxy oximes wherein said oximes are prepared in the presence of a water soluble compound capable of contributing ferric or ferrous ions to the reaction medium. Such oximes are useful as metal complexing agents. Such complexing agents are used in processes of extracting metals from an ore solution.
  • Process For Halogenation Of Aldehydes And Production Of Oximes Therefrom

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  • US Patent:
    41559339, May 22, 1979
  • Filed:
    Apr 10, 1978
  • Appl. No.:
    5/894870
  • Inventors:
    John H. Bonfield - Basking Ridge NJ
    Andiappan K. Murthy - Lake Hiawatha NJ
    Donald Pickens - Mendham NJ
  • Assignee:
    Allied Chemical Corporation - Morris Township, Morris County NJ
  • International Classification:
    C07C13100
  • US Classification:
    260566A
  • Abstract:
    In the halogenation under reflux conditions of an unhalogenated aldehyde of the formula ##STR1## with Cl. sub. 2, Br. sub. 2 or I. sub. 2, the aldehyde and halogen are continuously fed into a reactor at a molar ratio of halogen to unhalogenated aldehyde between about 0. 8:1 and about 1. 1:1 and water is continuously fed into the unhalogenated reactor at a rate of between about 1% and about 20% by weight of aldehyde. The product. alpha. -haloaldehyde is thiohydrocarbylated and then oximated to form a 2-hydrocarbylthioaldoxime of the formula ##STR2## with improved yield and quality because of the improved yield and quality of unhalogenated. alpha. -haloaldehyde. An exemplary process includes the chlorination of isobutyraldehyde (IBA) to form. alpha. -chloroisobutyraldehyde (CIBA), the thiomethylation of CIBA to form 2-methyl-2 methylthio-propionaldehyde (MTIBA) and the oximation of MTIBA to form 2-methylthio-propionaldehyde oxime (aldicarb oxime or ADO).

Youtube

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Classmates

Donald Pickens Photo 4

Donald Pickens

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Schools:
Pennsboro High School Pennsboro WV 1971-1975
Community:
Lyndon Collins, Kimberly Moneypenny, Cathy Cole

Googleplus

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