WO2012067818A1 - Additives for reducing drag - Google Patents
Additives for reducing drag Download PDFInfo
- Publication number
- WO2012067818A1 WO2012067818A1 PCT/US2011/058904 US2011058904W WO2012067818A1 WO 2012067818 A1 WO2012067818 A1 WO 2012067818A1 US 2011058904 W US2011058904 W US 2011058904W WO 2012067818 A1 WO2012067818 A1 WO 2012067818A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- additive
- phthalate
- drag reducing
- latex formulation
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
Definitions
- a stable DRA (drag reducing agent) suspension is generally comprised of (1)
- DRA polymer particles (2) liquid carrier, and (3) suspension aids.
- the DRA polymer may be obtained from solution polymerization of a water-insoluble monomer or a mixture of monomers which are subsequently precipitated to form the solid polymer particles, or from bulk polymerization (i.e., polymerization with no solvent) of said monomer(s) to form polymer which is subsequently ground into particles (which grinding may tend to degrade the polymer and its drag reduction efficiency), or produced by emulsion polymerization whereby the monomer(s) are dispersed with a large quantity of surfactant in a continuous liquid carrier prior to polymerization.
- the subsequent emulsion polymerization produces extremely small particles of polymer from the dispersed monomer.
- the liquid carrier is preferentially a non-solvent for the DRA polymer and can vary widely, including aqueous and non-aqueous liquids, e.g., water or aqueous solutions of various pH and ionic strengths, alcohols and fatty alcohols, glycols and diols, glycol ethers, glycol esters, or mixtures of these.
- aqueous and non-aqueous liquids e.g., water or aqueous solutions of various pH and ionic strengths, alcohols and fatty alcohols, glycols and diols, glycol ethers, glycol esters, or mixtures of these.
- Suspension aids are a necessity for DRA polymer suspensions made from solution or bulk polymerization, since such polymer particles are soft and tacky and will form films, when their unaltered surfaces come in mutual contact.
- Many suspension aids may be employed, e.g., stearic acid and stearate salts (magnesium stearate, calcium stearate), stearamides, polyolefm homopolymers and copolymers of various densities; oxidized polyethylene (PE); polystyrene and copolymers; carbon black and graphites; micronized polyphenyl sulfide (PPS), polypropylene oxide (PPO), polyamides, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyvinyl chloride (PVC); precipitated and fumed silicas; natural or synthetic clays, and organo-clays; aluminum oxides; boric acid; magnesium, calcium and barium phosphates, s,
- a composition comprising a drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive.
- the use of the composition results in a decrease of film formation while injected through a pump head when compared to the drag reducing latex formulation injected through the pump head.
- the composition comprises an acrylate drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive.
- the additive is added in the range between 1% to 20% by weight, and the composition results in a decrease of film formation of at least 50% when compared to the acrylate drag reducing latex formulation injected through the pump head through a four hour time frame.
- a method is also taught wherein a composition is injected through a pump head wherein the composition produces at least 50% less film formation through a four hour time frame than injection of a drag reducing latex formulation through the pump head.
- the composition comprises the drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive.
- a method is taught where a composition is injected through a pump head wherein the composition produces at least 50% less film formation through a four hour time frame than injection of a drag reducing latex formulation through the pump head.
- the composition comprises the acrylate drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive added in the range between 1% to 20%> by weight.
- a composition comprises a drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive.
- the use of the composition results in a decrease of film formation while injected through a pump head when compared to the drag reducing latex formulation injected through the pump head.
- the drag reducing latex formulation is any known drag reducing latex formulation that would create a film formation when injected through a pump head.
- the film formation on the pump head causes clogging of the pump head and an inability for the drag reducing latex formulation to be injected.
- the problem of film formation is particularly evident when utilizing latex drag reducing formulations for hydrocarbons.
- the problem is even more evident when using acrylate based drag reducing latex formulation. It is important to note that the drag reducing latex formulations decrease the drag of the hydrocarbon fluid they are injected into without significantly altering the viscosity of the hydrocarbon fluid.
- the additive that is added to the drag reducing latex formulation is any additive that would cause the composition to result in a decrease of film formation of at least 10% when compared to the drag reducing latex formulation injected through the pump head through a four hour time frame.
- the decrease of film formation of the composition can range from 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% even 90% or higher over the drag reducing latex formulation injected through a similar pump head through a four hour time frame.
- the pump head can be any pump head currently known in the art capable of injecting a drag reducing latex formulation.
- Commonly known pumps currently in use include packed reciprocating plunger pumps, high-pressure hydraulically actuated diaphragm pumps or even pneumatically driven plunger pumps.
- the additive can be a single chemical additive or mixture of more than one chemical additive.
- the additive can be an ester derivative, which is capable of reducing film formation when injected through a pump head.
- the additive is an ester derivative of a polyol or an ester derivative of a poly(carboxylic acids) or combinations of these ester deriviatives such that there is one or more ester functionality on the individual molecules.
- the additive is a 2,2,4-trimethyl-l,3-pentanediol diisobutyrate, bis(2ethylhexyl) adipate, glyceryl tributyrate, trimethyl pentanediol monoisobutyrate, dibutyl phthalate, dioctyl phthalate, glyceryl triacetate, dioctyl azelate, epoxidized tallate, triisooctyl trimellitate, triisononyl trimellite epoxidized soybean oil, , dibutyl phthalate, butyl benzyl phthalate, dihexyl phthalate, C 6 -Cn phthalate, diisononyl phthalate, diisodecyl phthalate, ditridecyl phthalate or combinations of these additives.
- the additive can be added to the drag reducing latex formulation in the range between 1% to 8% or 1% to 10% or even 1% to 20%> by weight.
- the upper limit of adding the additive to the drag reducing latex formulation is limited by the economics and the lowered efficiency of the drag reducing latex formulation as a whole due to the dilution of the active drag reducing latex formulation.
- the addition of the additive to the drag reducing latex formulation is not dependent upon the method of manufacturing the drag reducing latex formulation.
- the additive can be incorporated prior to the reaction into the reagent mixture or it can be added and mixed into the drag reducing latex formulation as a post-additive.
- the composition comprises an acrylate drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive comprising 2,2,4-trimethyl-l,3-pentanediol diisobutyrate.
- the additive is added in the range between 1% to 8% by weight, and the composition results in a decrease of film formation of at least 50% when compared to the drag reducing latex formulation injected through the pump head through a four hour time frame.
- a method is also taught wherein a composition is injected through a pump head wherein the composition produces at least 30% less film formation through a four hour time frame than injection of a drag reducing latex formulation through the pump head.
- the composition comprises the drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive.
- a method is taught where a composition is injected through a pump head wherein the composition produces at least 30% less film formation through a four hour time frame than injection of a drag reducing latex formulation through the pump head.
- the composition comprises the acrylate drag reducing latex formulation produced by emulsion polymerization to create solid particles dispersed in an aqueous medium and an additive of 2,2,4-trimethyl-l,3-pentanediol diisobutyrate added in the range between 1% to 8%) by weight.
- a peristaltic pump is used to simulate the injection of drag reducing latex formulation through a pump head.
- a latex meth(acrylate) drag reducer was utilized.
- the rate of flow through the peristaltic pump was 40 cc/min over a time frame of four hours.
- the flex tubing of the peristaltic pump was weighed prior to the pumping and post pumping to determine the build up of film formation inside the flex tubing.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymerisation Methods In General (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EA201390718A EA030209B1 (en) | 2010-11-16 | 2011-11-02 | Formulation for reducing drag of hydrocarbons (embodiments) and method of injecting latex agent (embodiments) |
ES11842067T ES2769633T3 (en) | 2010-11-16 | 2011-11-02 | Additives to reduce resistance |
CN201180055135.2A CN103210053B (en) | 2010-11-16 | 2011-11-02 | For the additive of drag reduction |
MX2013005541A MX357217B (en) | 2010-11-16 | 2011-11-02 | Additives for reducing drag. |
CA2817325A CA2817325C (en) | 2010-11-16 | 2011-11-02 | Additives for a drag reducing composition |
BR112013012093-2A BR112013012093B1 (en) | 2010-11-16 | 2011-11-02 | ADDITIVES TO REDUCE DRAG |
EP11842067.8A EP2640799B1 (en) | 2010-11-16 | 2011-11-02 | Additives for reducing drag |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41429810P | 2010-11-16 | 2010-11-16 | |
US61/414,298 | 2010-11-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012067818A1 true WO2012067818A1 (en) | 2012-05-24 |
Family
ID=46048365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2011/058904 WO2012067818A1 (en) | 2010-11-16 | 2011-11-02 | Additives for reducing drag |
Country Status (13)
Country | Link |
---|---|
US (2) | US10053595B2 (en) |
EP (1) | EP2640799B1 (en) |
CN (1) | CN103210053B (en) |
AR (2) | AR083899A1 (en) |
BR (1) | BR112013012093B1 (en) |
CA (1) | CA2817325C (en) |
CO (1) | CO6720972A2 (en) |
EA (1) | EA030209B1 (en) |
EC (1) | ECSP13012623A (en) |
ES (1) | ES2769633T3 (en) |
MX (1) | MX357217B (en) |
PE (1) | PE20140620A1 (en) |
WO (1) | WO2012067818A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112013012093B1 (en) * | 2010-11-16 | 2020-10-06 | Liquidpower Specialty Products Inc | ADDITIVES TO REDUCE DRAG |
US9267094B2 (en) | 2013-01-22 | 2016-02-23 | Flowchem, Ltd. | Drag reducing compositions and methods of manufacture and use |
US8933149B2 (en) | 2013-01-22 | 2015-01-13 | Flowchem, Ltd. | Drag reducing compositions and methods of manufacture and use |
CN107166173B (en) * | 2015-09-30 | 2018-11-20 | 江苏博拓电气设备有限公司 | Additive is used in pipeline drag reduction conveying |
CN108150834A (en) * | 2016-10-21 | 2018-06-12 | 李奕萱 | Double active principle oil product drag reducer product suspensions |
CN106545750B (en) * | 2016-10-27 | 2018-07-13 | 段恒宇 | The preparation method of low-temperature stabilization type poly alpha olefin oil product drag reducer suspension system |
GB201712813D0 (en) | 2017-08-10 | 2017-09-27 | Mexichem Fluor Sa De Cv | Compositions |
US11767487B2 (en) | 2020-07-13 | 2023-09-26 | Baker Hughes Oilfield Operations Llc | Inverting aids for latex-based drag reducing agents |
CN112961555A (en) * | 2021-02-08 | 2021-06-15 | 山东深海农湾科技有限公司 | Special anticorrosive and anti-parasitic material and method for deep-sea net cage |
WO2024077217A1 (en) | 2022-10-06 | 2024-04-11 | Championx Llc | Apparatus for pumping suspended polymer liquid |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050049327A1 (en) * | 2003-09-02 | 2005-03-03 | Vladimir Jovancicevic | Drag reducing agents for multiphase flow |
US20050209368A1 (en) * | 2004-03-17 | 2005-09-22 | Baker Hughes Incorporated | Polymeric nanoemulsion as drag reducer for multiphase flow |
US20060148928A1 (en) | 2004-12-30 | 2006-07-06 | Harris William F | Modified latex drag reducer and processes therefor and therewith |
US20080149530A1 (en) | 2006-12-22 | 2008-06-26 | Conocophillips Company | Drag reduction of asphaltenic crude oils |
US20090209679A1 (en) * | 2008-02-14 | 2009-08-20 | Conocophillips Company | Core-shell flow improver |
US20090326121A1 (en) * | 2006-10-19 | 2009-12-31 | Eastman Chemical Company | Low voc additives for extending the wet edge and open time of aqueous coatings |
US20100130681A1 (en) * | 2006-07-28 | 2010-05-27 | Conocophillips Company | Hydrate inhibited latex flow improver |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3857402A (en) | 1972-08-31 | 1974-12-31 | Nalco Chemical Co | Transmission of oil |
US6242388B1 (en) | 1998-11-23 | 2001-06-05 | Eastman Chemical Company | Mutual solvents comprising 2,2,4-trimethyl-1,3-pentanediol mono-or di-isobutyrate and stable emulsions thereof |
US7361628B2 (en) * | 2004-12-30 | 2008-04-22 | Conocophillips Company | Remote delivery of latex drag-reducing agent without introduction of immiscible low-viscosity flow facilitator |
US7256224B2 (en) | 2005-09-21 | 2007-08-14 | Baker Hughes Incorporated | Stabilized polymer drag reducing agent slurries |
AU2007285548B2 (en) * | 2006-08-16 | 2012-01-12 | Halliburton Energy Services, Inc. | Subterranean treatment fluids, friction reducing copolymers, and associated methods |
BR112013012093B1 (en) * | 2010-11-16 | 2020-10-06 | Liquidpower Specialty Products Inc | ADDITIVES TO REDUCE DRAG |
US8933149B2 (en) * | 2013-01-22 | 2015-01-13 | Flowchem, Ltd. | Drag reducing compositions and methods of manufacture and use |
-
2011
- 2011-11-02 BR BR112013012093-2A patent/BR112013012093B1/en active IP Right Grant
- 2011-11-02 US US13/287,340 patent/US10053595B2/en active Active
- 2011-11-02 CN CN201180055135.2A patent/CN103210053B/en active Active
- 2011-11-02 CA CA2817325A patent/CA2817325C/en active Active
- 2011-11-02 EA EA201390718A patent/EA030209B1/en not_active IP Right Cessation
- 2011-11-02 MX MX2013005541A patent/MX357217B/en active IP Right Grant
- 2011-11-02 WO PCT/US2011/058904 patent/WO2012067818A1/en active Application Filing
- 2011-11-02 PE PE2013001085A patent/PE20140620A1/en active IP Right Grant
- 2011-11-02 ES ES11842067T patent/ES2769633T3/en active Active
- 2011-11-02 EP EP11842067.8A patent/EP2640799B1/en active Active
- 2011-11-16 AR ARP110104283A patent/AR083899A1/en active IP Right Grant
-
2013
- 2013-05-15 CO CO13119338A patent/CO6720972A2/en unknown
- 2013-05-15 EC ECSP13012623 patent/ECSP13012623A/en unknown
-
2018
- 2018-08-20 US US16/105,041 patent/US11098221B2/en active Active
- 2018-08-28 AR ARP180102437A patent/AR112880A2/en active IP Right Grant
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050049327A1 (en) * | 2003-09-02 | 2005-03-03 | Vladimir Jovancicevic | Drag reducing agents for multiphase flow |
US20050209368A1 (en) * | 2004-03-17 | 2005-09-22 | Baker Hughes Incorporated | Polymeric nanoemulsion as drag reducer for multiphase flow |
US20060148928A1 (en) | 2004-12-30 | 2006-07-06 | Harris William F | Modified latex drag reducer and processes therefor and therewith |
US7763671B2 (en) | 2004-12-30 | 2010-07-27 | Conocophillips Company | Modified latex drag reducer and processes therefor and therewith |
US20100130681A1 (en) * | 2006-07-28 | 2010-05-27 | Conocophillips Company | Hydrate inhibited latex flow improver |
US20090326121A1 (en) * | 2006-10-19 | 2009-12-31 | Eastman Chemical Company | Low voc additives for extending the wet edge and open time of aqueous coatings |
US20080149530A1 (en) | 2006-12-22 | 2008-06-26 | Conocophillips Company | Drag reduction of asphaltenic crude oils |
US20090209679A1 (en) * | 2008-02-14 | 2009-08-20 | Conocophillips Company | Core-shell flow improver |
Also Published As
Publication number | Publication date |
---|---|
EA030209B1 (en) | 2018-07-31 |
PE20140620A1 (en) | 2014-06-08 |
BR112013012093B1 (en) | 2020-10-06 |
AR083899A1 (en) | 2013-04-10 |
CN103210053A (en) | 2013-07-17 |
MX2013005541A (en) | 2013-08-01 |
EP2640799A1 (en) | 2013-09-25 |
AR112880A2 (en) | 2019-12-26 |
MX357217B (en) | 2018-06-29 |
EP2640799A4 (en) | 2018-01-03 |
ES2769633T3 (en) | 2020-06-26 |
BR112013012093A2 (en) | 2016-08-16 |
US10053595B2 (en) | 2018-08-21 |
EP2640799B1 (en) | 2019-11-13 |
CN103210053B (en) | 2016-05-11 |
CO6720972A2 (en) | 2013-07-31 |
EA201390718A1 (en) | 2013-10-30 |
US20120123019A1 (en) | 2012-05-17 |
US11098221B2 (en) | 2021-08-24 |
CA2817325A1 (en) | 2012-05-24 |
US20180355209A1 (en) | 2018-12-13 |
CA2817325C (en) | 2020-06-09 |
ECSP13012623A (en) | 2013-07-31 |
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