Surgery Associates North TexasSurgery Associates Of North Texas 3322 Colorado Blvd STE 101, Denton, TX 76210 9403877588 (phone), 9405660881 (fax)
Education:
Medical School University of Texas Medical Branch at Galveston Graduated: 2003
Procedures:
Bariatric Surgery Endoscopic Retrograde Cholangiopancreatography (ERCP) Gallbladder Removal Hallux Valgus Repair Laparoscopic Gallbladder Removal Proctosigmoidoscopy Sigmoidoscopy Small Bowel Resection Thyroid Gland Removal Tracheostomy Hernia Repair Mastectomy Upper Gastrointestinal Endoscopy
Conditions:
Abdominal Hernia Appendicitis Breast Disorders Cholelethiasis or Cholecystitis Inguinal Hernia
Languages:
English Spanish
Description:
Dr. Lester graduated from the University of Texas Medical Branch at Galveston in 2003. He works in Denton, TX and specializes in General Surgery. Dr. Lester is affiliated with Denton Regional Medical Center.
Clark Graybill - Lake Charles LA, US Stephen Lester - Pittsburgh PA, US
International Classification:
C07C017/358
US Classification:
570256000
Abstract:
Describes a method for recovering trans-1,2-dichloroethene from a liquid feed composition comprising both the cis- and trans-isomers of 1,2-dichloroethene and contaminating amounts of other chlorinated hydrocarbons, e.g., lower alkyl chlorinated hydrocarbons, such as CCchlorinated hydrocarbons. In one of the described methods, the liquid feed composition is introduced into a first distillation column wherein the stereoisomers and chlorinated hydrocarbons more volatile than the stereoisomers are removed as overhead and charged to a second distillation column . In column , the stereoisomers are separated from the more volatile chlorinated hydrocarbons, and a bottoms fraction comprising the stereoisomers are charged to a reaction distillation column wherein the cis-isomer, is isomerized to the trans-isomer in the liquid phase and in the presence of an organic free-radical initiator, e.g., an azonitrile initiator. Substantially pure trans-1;2-dichloroethene is recovered as overhead from reaction distillation column
Process For Producing Chlorinated Hydrocarbons In The Presence Of A Polyvalent Molybdenum Compound
- Atlanta GA, US Stephen Robert Lester - Pittsburgh PA, US
International Classification:
C07C 17/10 B01J 27/132
Abstract:
The preparation of chlorinated hydrocarbons by reacting a chlorinated alkane substrate, such as 1,1,1,3-tetrachloropropane, with a source of chlorine, such as chlorine (Cl), in the presence of a polyvalent molybdenum compound, such as molybdenum pentachloride, is described. With the method of the present invention, the chlorinated alkane product has covalently bonded thereto at least one more chlorine group than the chlorinated alkane substrate, and the chlorinated alkane substrate and the chlorinated alkane product each have a carbon backbone structure that is in each case the same.
Processes For Producing Chlorinated Hydrocarbons And Methods For Recovering Polyvalent Antimony Catalysts Therefrom
- Atlanta GA, US Stephen Robert Lester - Pittsburgh PA, US
International Classification:
C07C 17/25 B01J 31/12 B01J 35/00 B01J 27/10
Abstract:
The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of polyvalent antimony compound that includes a pentavalent antimony compound, as well as methods for recovering polyvalent antimony compounds from such processes.
Processes For Producing Chlorinated Hydrocarbons And Methods For Recovering Polyvalent Antimony Catalysts Therefrom
- Atlanta GA, US Stephen Robert Lester - Pittsburgh PA, US
International Classification:
C07C 17/23 B01J 31/12 C07C 17/06 B01J 27/10
Abstract:
The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of polyvalent antimony compound that includes a pentavalent antimony compound, as well as methods for recovering polyvalent antimony compounds from such processes.
Processes For Producing Chlorinated Hydrocarbons And Methods For Recovering Polyvalent Antimony Catalysts Therefrom
The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of polyvalent antimony compound that includes a pentavalent antimony compound, as well as methods for recovering polyvalent antimony compounds from such processes.
- Atlanta GA, US Stephen Robert Lester - Pittsburgh PA, US
International Classification:
C07C 17/35
US Classification:
570216
Abstract:
The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of ferric chloride and a polyvalent antimony compound that includes a pentavalent antimony compound.
- Atlanta GA, US Stephen Robert Lester - Pittsburgh PA, US
Assignee:
Axiall Ohio, Inc. - Atlanta GA
International Classification:
C07C 17/23 C07C 17/06
US Classification:
570230, 570247
Abstract:
The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of ferric chloride and a polyvalent antimony compound that includes a pentavalent antimony compound.
I am the youngest of 4 brothers - Jeff, Joey, & Michael.I graduated in 2003 from Fairview High School where I was president of the Beta Club and a big part in the marching band and TV production c...
With the arrival of the Q60 were going to see that escalate quite dramatically, said Stephen Lester, managing director, Infiniti Canada, during the global press conference in San Diego. Were already on pace to set another record in Canada for Infiniti sales.
Date: Oct 03, 2016
Source: Google
Walk-Out By Chicago Symphony Orchestra Players Adds To Nation-Wide Trend Of ...
"I think we were all surprised," said CSO bass player Stephen Lester to The Chicago Tribune. "The negotiating committee had gone more than we wanted to go to try to get a deal, and their last actions sent a very clear and distinct message that they were not interested in an agreement. They tried to