Environmentally friendly hydrofracturing friction reducer for harsh conditions

Patent metadata

Field	Value
Publication number	US-11268015-B2
Application number	US-202117248606-A
Country	US
Kind code	B2
Filing date	Jan 29, 2021
Priority date	Feb 4, 2019
Publication date	Mar 8, 2022
Grant date	Mar 8, 2022

Abstract

A composition for an environmentally friendly hydrofracturing friction reducer product can be synthesized. A method for synthesis of a friction reducer emulsion can include using gas-to-liquid synthesized oil as a continuous phase in invert emulsion polymerization. The composition can be optimized by using a suitable amount of salt tolerant monomer for the best performance with salt tolerant features. Various inverting agents can be utilized for the self-inverting in brine with good product stability. The optimized friction reducer can be used in weighted brine hydrofracturing.

First claim

What is claimed is:

1. A method of preparing a friction reducer for a wellbore comprising
preparing an oil phase by mixing about 10-70 parts gas-to-liquid synthesized base oil with about 1-20 parts emulsifier comprising sorbitan monostearate and sorbitan fatty acid ester ethoxylate surfactant;
mixing the resulting oil phase until it is clear;
preparing an aqueous phase comprising about 5-35 parts of monomers comprising mixing an AM, an AMPS, an AA, and a water and adjusting the pH to 6-8;
mixing the oil phase with the aqueous phase to form a mixture;
emulsifying the resulting mixture to form an emulsion with a viscosity of greater than 200 cP;
purging the emulsion with nitrogen for 30 minutes;
adding about 0.001-1 parts an initiator selected from the group comprising ammonium peroxodisulfate, tert-butyl hydroperoxide, dimethane sulfonyl peroxide, potassium persulfate, benzoyl peroxide, lauroyl peroxide, sodium persulfate, 2,2′-Azobis(isobutyronitrile), 2,2′-Azobis(4-methoxy-2,4-dimethylvaleronitrile), 2,2′-Azobis(2,4-dimethylvaleronitrile), Dimethyl 2,2′-azobis(2-methylpropionate), 2,2′-Azobis(2-methylbutyronitrile), 1, 1′-Azobis(cyclohexane-1-carbonitrile), 2,2′-Azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride, 2,2′-Azobis(2-methylpropionamidine)dihydrochloride, 2,2′-Azobis[N-(2-carboxyethyl)-2-methylpropionamidine]tetrahydrate, diethyl 2,2′-azobisisobutyrate, dimethyl 2,2′-azobisisobutyrate, 2-methyl 2′-ethyl azobisisobutyrate, dimethyl 2,2′-azobis(isobutyrate), 2,2′-Azobis[2-(2-imidazolin-2-yl)propane], 2,2′-Azobis[2-methyl-N-(2-hydroxyethyl)propionamide], 4,4′-Azobis(4-cyanovaleric acid), or combinations thereof to the emulsion;
increasing a temperature of the emulsion from room temperature to 40° C. over a period of about 30 minutes;
incubating the emulsion for about 3 hours at 40° C.;
incubating the emulsion for about 1 hour at 50° C.; and
incubating the emulsion for about 1 hour at 70° C.

2. The method of preparing of claim 1 further comprising charging the emulsion into a glass-jacketed kettle equipped with a paddle stirrer and thermometer.

3. The method of preparing of claim 1 wherein the amount of the gas-to-liquid synthesized base oil is about 20 parts.

4. The method of preparing of claim 1 wherein the emulsifier is sorbitan monostearate and a sorbitan fatty acid ester ethoxylate surfactant and the amount of the emulsifier is about 2 parts.

5. The method of preparing of claim 1 wherein the amount of the AM is about 20 parts, the amount of the AMPS is about 2 parts, and the amount of the AA is about 8 parts.

6. The method of preparing of claim 1 wherein the amount of the water is about 40 parts.

7. The method of preparing of claim 1 wherein the initiator is 2,2′-Azobis(isobutyronitrile) and the amount of the 2,2′-Azobis(isobutyronitrile) is about 0.01 parts.

8. The method of preparing of claim 1 further comprising adding a surfactant with an HLB of at least about 10 at about 2 wt. %.

Assignees

• Cnpc Usa Corp

Inventors

• Bai Litao
• Lin Lijun

Classifications

• C09K8/64

  Oil-based compositions · CPC title

• C09K8/28

  containing organic additives · CPC title

• C09K8/03 Primary

  Specific additives for general use in well-drilling compositions · CPC title

• C09K2208/28

  Friction or drag reducing additives · CPC title

• C08F220/56

  Acrylamide; Methacrylamide · CPC title