Texas Tech Physicians Of Lubbock Family Medicine 3601 4 St, Lubbock, TX 79430 (806)7432757 (phone), (806)7432563 (fax)
Education:
Medical School University of North Texas College of Osteopathic Medicine Graduated: 1993
Procedures:
Destruction of Benign/Premalignant Skin Lesions Electrocardiogram (EKG or ECG) Osteopathic Manipulative Treatment Vaccine Administration
Conditions:
Atrial Fibrillation and Atrial Flutter Bronchial Asthma Diabetes Mellitus (DM) Disorders of Lipoid Metabolism Gastroesophageal Reflux Disease (GERD)
Languages:
English Spanish
Description:
Dr. Cook graduated from the University of North Texas College of Osteopathic Medicine in 1993. He works in Lubbock, TX and specializes in Family Medicine. Dr. Cook is affiliated with Covenant Medical Center and University Medical Center.
8655 E Via De Ventura #G200, Scottsdale, AZ 85258 9960 Coporate Campus Dr #200, Louisville, KY 40223 8655 E Via De Vensure #G200, Scottsdale, AZ 85258 1209 Orange St, Wilmington, DE 19801
Ronald L. Cook Assistant Vice-Presi
Energy Performance Services, Inc
Ronald L. Cook VICE-PRESIDENT, TAXATION
TransCanada Energy Ltd HOLDING COMPANY
Ronald L. Cook Vice-President, Taxation
TransCanada Energy Marketing Ltd Wholesale Energy Marketing.
Isbn (Books And Publications)
Wills Practice: Materials Prepared for a Continuing Legal Education Seminar Held in Vancouver, B.C. on November 18, 1986
Ronald L. Cook - Aurora IL Anthony F. Sammells - Naperville IL
Assignee:
Gas Research Institute - Chicago IL
International Classification:
C25B 304
US Classification:
204 59R
Abstract:
A process and apparatus for gas phase electrochemical reduction of CO. sub. 2 and/or CO to hydrocarbons at ambient temperatures. The process is carried out by passing an electrical current between a cathode in contact with one side of a hydrogen ion conducting solid polymer electrolyte and an anode in ionic communication with the opposite side of the solid polymer electrolyte. In one embodiment, the anode material may be in contact with the opposite side of the hydrogen ion conducting solid polymer electrolyte, and in another embodiment, an anode may be separated from the opposite side of the solid polymer electrolyte by an aqueous inorganic salt solution. At least one of CO. sub. 2 and CO are passed in contact with the cathode and hydrogen ions passing through the solid polymer electrolyte reduce at least a portion of the CO. sub. 2 and CO to gaseous hydrocarbon products such as CH. sub. 4 and C. sub. 2 H. sub. 4 at the solid polymer electrolyte/cathode interface.
Electrochemical Reduction Of Co.sub.2 To Ch.sub.4 And C.sub.2 H.sub.4
Ronald L. Cook - Aurora IL Robert C. MacDuff - Naperville IL Anthony F. Sammells - Naperville IL
Assignee:
Gas Research Institute - Chicago IL
International Classification:
C25C 112 C25B 304
US Classification:
204 521
Abstract:
A process for electrochemical reduction of CO. sub. 2 to CH. sub. 4 and C. sub. 2 H. sub. 4 providing both high current densities and high Faradaic efficiencies. The process is carried out in an electrochemical cell wherein copper is electrodeposited in situ on the cathode surface making freshly deposited copper available for the electrochemical reduction. Faradaic efficiencies of about 75 to about 98 percent for production of CH. sub. 4 and C. sub. 2 H. sub. 4 are obtained.
Method For Deriving Phenyl Isocyanate From Benzene And Potassium Isocyanate
A method deriving phenyl isocyanate includes providing an electrolyte. The electrolyte is separated by an ion transferrable member so as to form a catholyte and an anolyte from the electrolyte. A cathode is placed in the catholyte and an anode is placed in the anolyte. Benzene and potassium isocyanate are provided to the anolyte. An electric voltage is applied across the cathode and the anode causing a reaction of the benzene and potassium isocyanate to yield phenyl isocyanate.
Electrolytic Method For Reducing Oxalic Acid To A Product
Apparatus for reducing oxalic acid to a product includes a cell. A separator which separates the cell into two chambers; a catholyte chamber and an anolyte chamber. Each chamber has an inlet and an outlet. A porous cathode having a catalyst is arranged within the catholyte chamber so that an aqueous catholyte, having ammonium chloride, entering the inlet of the catholyte chamber will pass through the cathode. A porous anode is arranged within the anolyte section so that an aqueous electrolyte, having ammonium chloride, entering the inlet of the anolyte section will pass through the anode and exit through the outlet of anolyte section. A source provides the catholyte which is a mixture of oxalic acid and an aqueous electrolyte, having ammonium chloride, to the inlet of the catholyte chamber while another source provides the electrolyte to the inlet of the anolyte chamber. A d. c. voltage is provided between the cathode and the anode so as to cooperate in the reduction of oxalic acid within the porous cathode to a product which exits the catholyte chamber by way of its outlet.
Means And Method For The Electrochemical Reduction Of A Nitroaromatic To Provide A Dye
Apparatus and method for the electrochemical reduction of a nitroaromatic to a dye includes a housing divided into two sections by membrane. An electrolyte solution including a non-aqueous electrolyte dimethylformamide and a supporting electrolyte is provided to the two sections of the housing. A cathode is located in one section of the housing while an anode is located in the other section. A nitroaromatic is provided to the section having the cathode. A direct voltage is provided to the cathode and to the anode so that a current can pass and cooperate in a reaction between the nitroaromatic and the electrolyte solution to provide a dye.
Ronald L. Cook - Aurora IL Anthony F. Sammells - Naperville IL
Assignee:
Gas Research Institute - Chicago IL
International Classification:
C25B 304
US Classification:
204 72
Abstract:
A process for photoelectrochemical reduction of CO. sub. 2 and/or CO to gaseous hydrocarbons, predominately methane, in a liquid aqueous containing electrolyte dispersion of semiconductors in the presence of copper which may be deposited on the semiconductor surface or dispersed in the electrolyte and transiently in contact with the semiconductor surface.
Method For Forming Ethylene Glycol From Sodium Methoxide
Method and apparatus for forming ethylene glycol from sodium methoxide includes combining the sodium methoxide with an anhydrous methanol to provide a mixture. The mixture is then flowed past an anode and then past a cathode. A DC voltage is provided across the anode and the cathode so that the mixture forms ethylene glycol as a product.
Electrocatalytic Oxidative Dimerization Of Methane
Nirupama U. Pujare - Naperville IL Ronald L. Cook - Aurora IL Anthony F. Sammells - Naperville IL
Assignee:
Gas Research Institute - Chicago IL
International Classification:
H01M 810
US Classification:
429 17
Abstract:
A solid oxide fuel cell and process for direct conversion of natural gas into DC electricity concurrently with the electrocatalytic partial oxidation of methane to C. sub. 2 hydrocarbon species C. sub. 2 H. sub. 4, C. sub. 2 H. sub. 6, and minor amounts of C. sub. 2 H. sub. 2.
dose can be given as early as 6 months old. If a child has already received the first dose at 12 months, doctors can give the second dose about a month later, saidDr. Ronald Cook, chief health officer at the Texas Tech University Health Sciences Center in Lubbock and health authority for the city.