It has been discovered that borate crosslinked fracturing fluid breaker mechanisms are improved by the inclusion of a polyol together with an enzyme. In fact, synergistic results may be achieved when both are used together as contrasted to the cases where each are used separately. Removing the borate ion from the crosslinked polymer reduces the pH of the fluid and in turn increases the activity of the enzyme. That is, once the pH is lowered, viscosity reduction (breaking) occurs by uncrosslinking of the polymer within the fracturing fluid, and by initiating or increasing activity of an enzyme breaker, if present. In one embodiment, the polyol has at least two cis-hydroxyl groups. In another embodiment, the polyols are monosaccharides such as glycerols and sugar alcohols, and may include mannitol, sorbitol, glucose, fructose, galactose, mannose, allose, etc. and mixtures thereof. Oligosaccharides and derivatives of monosaccharides and oligosaccharides are also useful.
Borate Crosslinked Fracturing Fluid Viscosity Reduction Breaker Mechanism And Products
It has been discovered that borate crosslinked fracturing fluid breaker mechanisms are improved by the inclusion of a cation-releasing material. When cations are released or liberated within the fracturing fluid, they complex with the hydroxide or carbonate pH buffers used within the borate crosslinked fracturing fluid, which in turn reduces the pH of the fracturing fluid. Once the pH is lowered, viscosity reduction (breaking) occurs by uncrosslinking of the polymer within the fracturing fluid, and by initiating or increasing activity of an enzyme breaker, if present. In one embodiment, the cations are divalent cations. The divalent cations are preferably slowly released over a period of time. Two specific, preferred materials for releasing divalent cations are calcium lignosulfonate and calcium chloride, the latter preferably in encapsulated form.
Aminocarboxylic Acid Breaker Compositions For Fracturing Fluids
It has been discovered that aminocarboxylic acids are effective breakers for polymer-gelled aqueous fracturing fluids, particularly in the temperature range between about 120Â F. (49Â C. ) and about 280Â F. (138Â C. ). The aminocarboxylic acids are believed to act directly on the polymer and not to any great extent or not to as an effective extent on a crosslinking agent, if present. The polymer may be a polysaccharide, and the aminocarboxylic acid may be selected from the group including, but not necessarily limited to, tetrasodium ethylenediaminetetraacetic acid (Na EDTA), tetrasodium propylenediaminetetraacetic acid (Na PDTA), trisodium hydroxyethylenediaminetetraacetic acid (Na HEDTA), trisodium nitrilotriacetic acid (Na NTA), salts of these acids, and mixtures thereof.
Bacteria-Based And Enzyme-Based Mechanisms And Products For Viscosity Reduction Breaking Of Viscoelastic Fluids
It has been discovered that fluids viscosified with viscoelastic surfactants (VESs) may have their viscosities reduced (gels broken) by the direct or indirect action of a biochemical agent, such as bacteria, fungi, and/or enzymes. The biochemical agent may directly attack the VES itself, or some other component in the fluid that produces a by-product that then causes viscosity reduction. The biochemical agent may disaggregate or otherwise attack the micellar structure of the VES-gelled fluid. The biochemical agent may produce an enzyme that reduces viscosity by one of these mechanisms. A single biochemical agent may operate simultaneously by two different mechanisms, such as by degrading the VES directly, as well as another component, such as a glycol, the latter mechanism in turn producing a by-product (e. g. an alcohol) that causes viscosity reduction. Alternatively, two or more different biochemical agents may be used simultaneously.
Biodegradable Chelant Compositions For Fracturing Fluid
It has been discovered that biodegradable and non-toxic chelant compositions can perform multiple beneficial functions in an aqueous fracturing fluid through the chelation of ions. Some of the multiple functions include various combinations of the following: demulsifier, demulsifier enhancer, scale inhibitor, crosslink delay agent, crosslinked gel stabilizer, enzyme breaker stabilizer, and the like. Some of the chelants used in the compositions include, but are not necessarily limited to, sodium polyaspartate; sodium iminodisuccinate; disodium hydroxyethyleneiminodiacetate (NaHEIDA); sodium gluconate; sodium glucoheptonate; sugar alcohols; monosaccharides; disaccharides; and mixtures thereof.
It has been discovered that fracturing fluid breaker mechanisms are improved by the inclusion of a catalyzed polyol alone that directly degrades the polysaccharide backbone, and optionally additionally by removing the crosslinking ion, if present. That is, viscosity reduction (breaking) occurs by breaking down the chemical bonds within the backbone directly. The gel does not have to be crosslinked for the method of the invention to be successful, although it may be crosslinked. In one non-limiting embodiment, the polyol has at least two hydroxyl groups on adjacent carbon atoms. In another embodiment, the polyols are simple sugars and sugar alcohols, and may include mannitol, sorbitol, glucose, fructose, galactose, mannose, lactose, maltose, allose, etc. and mixtures thereof. The catalyzing metal ion may employ a metal selected from Groups VIB, VIIB, VIII, IB, and IIB of the Periodic Table (previous IUPAC American Group notation).
It has been discovered that fracturing fluid breaker mechanisms are improved by the inclusion of a polyol alone that directly degrades the polysaccharide backbone, and optionally additionally by removing the crosslinking ion, if present. That is, viscosity reduction (breaking) occurs by breaking down the chemical bonds within the backbone directly, rather than by merely removing the crosslinking ion, if present. The gel does not have to be crosslinked for the method of the invention to be successful, although it may be crosslinked. In one non-limiting embodiment, the polyol has at least two hydroxyl groups on adjacent carbon atoms. In another embodiment, the polyols are monosaccharides such as glycerols and sugar alcohols, and may include mannitol, sorbitol, glucose, fructose, galactose, mannose, lactose, maltose, allose, etc. and mixtures thereof.
Aminocarboxylic Acid Breaker Compositions For Fracturing Fluids
It has been discovered that aminocarboxylic acids are effective breakers for polymer-gelled aqueous fracturing fluids, particularly in the temperature range between about 120 F. (49 C. ) and about 280 F. (138 C. ). The aminocarboxylic acids are believed to act directly on the polymer and not to any great extent or not to as an effective extent on a crosslinking agent, if present. The polymer may be a polysaccharide, and the aminocarboxylic acid may be selected from the group including, but not necessarily limited to, tetrasodium ethylenediaminetetraacetic acid (NaEDTA), tetrasodium propylenediaminetetraacetic acid (NaPDTA), trisodium hydroxyethylenediaminetetraacetic acid (NaHEDTA), trisodium nitrilotriacetic acid (NaNTA), salts of these acids, and mixtures thereof.
Director of Infrastructure Services at Yusen Logistics (Americas), Inc.
Location:
Cordova, Tennessee
Industry:
Logistics and Supply Chain
Work:
Yusen Logistics (Americas), Inc. - 1900 Charles Bryan Road Suite 250| Cordova, TN 38016 since Sep 2011
Director of Infrastructure Services
The West Clinic/Memphis Heart Clinic Oct 2010 - Mar 2011
Director of Architecture and Infrastructure
The West Clinic/Memphis Heart Clinic May 2008 - Oct 2010
IT Manager
Crewsen.com LLC Jan 1999 - May 2008
CTO/President
Education:
The University of Memphis 1993 - 1994
Skills:
Networking Security Data Center System Administration Management VMware Disaster Recovery Telecommunications VPN Active Directory Microsoft Technologies Strategic Planning Software Documentation SAN
Interests:
Racquetball, camping, Family
Honor & Awards:
MCSE, MCP+I
Certifications:
Microsoft Certified Systems Engineer, Microsoft
Name / Title
Company / Classification
Phones & Addresses
James Crews Principal
Cecilia Crews Artist Services-Misc
5206 Sunshine Pt, Conroe, TX 77318
James J. Crews Chairman, COO
Bishop & Associates, Inc
James T. Crews Secretary
CREWS ENTERPRISES, INCORPORATED Business Services
262 Chestnut Oak Dr, Mandeville, LA 70448 C/O Wanda Braud Crews, Mandeville, LA 70448
James Crews Director
The House of The Risen Son, Inc
James T Crews MM
THE CREWS RANCH LLC
242 Rosenwall Rd, Huntsville, TX 77320 262 Chestnut Oak Dr, Mandeville, LA 70448
Dr. Crews graduated from the University of Tennessee College of Medicine at Memphis in 1998. He works in Jackson, MS and 1 other location and specializes in Obstetrics & Gynecology. Dr. Crews is affiliated with Baptist Health System.
Rockbridge Internists 204 E Washington St, Lexington, VA 24450 5404635055 (phone), 5404631079 (fax)
Education:
Medical School University of Virginia School of Medicine Graduated: 1978
Languages:
English
Description:
Dr. Crews graduated from the University of Virginia School of Medicine in 1978. He works in Lexington, VA and specializes in Internal Medicine. Dr. Crews is affiliated with Carilion Stonewall Jackson Hospital.
ic, said Antoinette Robinson, president of the American Postal Workers Union Local 67 in Kansas City. These are post offices that the inner-city people rely on. The post office said you can go to James Crews station on Truman Road, but one lady said she would have to take two bus transfers.