Degradable perforation balls and associated methods of use in subterranean applications

• US 8,757,260 B2
• Filed: 02/11/2009
• Issued: 06/24/2014
• Est. Priority Date: 02/11/2009
• Status: Active Grant

• Current Assignee: Halliburton Energy Services Incorporated (Halliburton Company)
• Original Assignee: Halliburton Energy Services Incorporated (Halliburton Company)
• Inventors: Luo, Hongyu, Fulton, Dwight D.
• Primary Examiner(s): SAYRE, JAMES G
• Application Number:
  US12/378,083
• Publication Number:
  US 20100200235A1
• Time in Patent Office: 1,959 Days
• Field of Search: 507/265, 507/266, 507/267, 166/283, 166/191, 166/284
• US Class Current: 166/281
• CPC Class Codes: C09K 8/50 Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls compositions for consolidating loose sand or the like around wells C09K8/56
• CPC Class Codes: C09K 8/62 Compositions for forming crevices or fractures
• CPC Class Codes: C09K 8/76 for preventing or reducing fluid loss
• CPC Class Codes: E21B 33/138 Plastering the borehole wall; Injecting into the formation
• CPC Class Codes: Y10S 507/922 Fracture fluid

Abstract

Methods and compositions that include a method of treating a subterranean formation comprising the steps of providing a carrier fluid comprising degradable balls that comprise a carboxylic acid, a fatty alcohol, a fatty acid salt, a fatty ester, a fatty acid salt, or a combination thereof, and introducing the carrier fluid to the subterranean formation during a treatment.

Claims

1. A method comprising:

providing a carrier fluid comprising degradable balls that comprise at least one carboxylic acid selected from the group consisting of;

sebacic acid, stearic acid, pamoic acid, suberic acid, traumatic acid, thapsic acid, azelaic acid, camphoric acid, campholic acid, muconic acid, undecanedioic acid, brassylic acid, melissic acid, p-toluic acid, sorbic acid, dodecanedioc acid, tetradecanedioic acid, α

-Aleuritic acid, and combinations thereof; and

introducing the carrier fluid to a subterranean formation.

2. The method of claim 1 wherein the degradable balls have a diameter from about 0.2 inches (0.51 cm) to about 5 inches (12.7 cm).

3. The method of claim 1 wherein the subterranean formation has the temperature range of about 250°

F. to about 550°

F.

4. The method of claim 1 wherein the degradable balls are subjected to differential pressures from about 500 psi to about 3,000 psi.

5. The method of claim 1 wherein the degradable balls have a density from about 0.70 g/cc to about 1.5 g/cc.

6. The method of claim 1 wherein the degradable balls further comprise at least one fatty alcohol and/or one fatty ester selected from the group consisting of:

montanyl alcohol, tert-butylhydroquinone, cholesterol, cholesteryl nonanoate, benzoin, borneol, exo-norborneol, glyceraldehyde triphenylmethanol, dimethyl terephthalate, camphor, cholecalciferol, ricinoleyl alcohol, 1-Heptacosanol, 1-Tetratriacontanol, 1-Dotriacontanol, 1-Hentriacontanol, 1-Tricontanol, 1-Nonacosanol, 1-Octasanol, 1-Hexacosanol, 1,14-Tetradecanediol, 1,16-Hexadecanediol, 1,17-Heptadecanediol, 1,18-Octadecanediol, 1,19-Nonadecanediol, 1,20-Eicosanediol, 1,21-Heneicosanediol, 1,22-Docosanediol, prednisolone acetate, cellobiose tetraacetate, terephthalic acid dimethyl ester, ceryl palmitate, myricyl ceretate, myricyl alcohol, gliadin, hordein, secalin, zein, and avenin.

7. The method of claim 1 wherein the degradable balls further comprise at least one fatty acid salt from the group consisting of:

sucrose distearate, calcium stearate, glyceryl monostearate, zinc stearate, and magnesium stearate.

8. The method of claim 1 wherein the fatty acids, fatty alcohols, fatty acid salts, or esters present in the degradable balls comprise an amount greater than about 1% by weight.

9. The method of claim 1 wherein the carrier fluid comprises a water based liquid, an oil based liquid, a gas, and any combination thereof.

10. The method of claim 1 wherein the degradable balls further comprise filler materials.

11. The method of claim 10 wherein the filler materials comprise at least one material from the group consisting of:

sodium chloride, sugar, silica flour, calcium carbonate, fumed silica, finely ground nut shells, finely ground fruit pits, glass spheres, glass microspheres, glass beads, glass fibers, silica quartz sand, sintered Bauxite, silica flour, silica fibers, sand, silicate minerals, clays, Kaolinite clays, smectite clays, Illite clays, ceramic beads;

clay powders, finely crushed spent fluid-cracking catalysts, finely crushed ultra lightweight porous ceramics;

finely crushed economy lightweight ceramics;

finely crushed lightweight ceramics, finely crushed intermediate strength ceramics, transition metal powders, transition metal dust, plastic particles, nylon beads, nylon fibers, nylon pellets, nylon powder, SDVB (styrene divinyl benzene) beads, SDVB fibers, polytetrafluoroethylene fibers, carbon fibers, cured phenol-aldehyde novoloid “

S-type”

fillers, cured phenol-aldehyde novoloid “

S-type”

fibers, cured phenol-aldehyde novoloid “

S-type”

yarn, carbon powders, carbon dust, and any combination thereof.

12. A method of temporarily sealing off perforations comprising:

providing a carrier fluid comprising degradable balls that comprise at least one selected from the group consisting of;

a carboxylic acid, a fatty alcohol, a fatty acid salt, a fatty ester, and a combination thereof, wherein the carboxylic acid is selected from the group consisting of;

sebacic acid, stearic acid, phthalic acid, isophthalic acid, adipic acid, pamoic acid, suberic acid, succinic acid, traumatic acid, thapsic acid, azelaic acid, camphoric acid, campholic acid, muconic acid, undecanedioic acid, brassylic acid, melissic acid, p-toluic acid, sorbic acid, dodecanedioc acid, tetradecanedioic acid, α

-Aleuritic acid, and a combination thereof;

introducing the carrier fluid to a subterranean formation during a treatment wherein the subterranean formation has the temperature range of about 250°

F. to about 550°

F.;

introducing the carrier fluid to penetrate at least a portion of the perforation;

diverting at least a portion of the treatment fluid with the degradable balls; and

re-opening the perforation through degradation of the degradable balls in the subterranean formation.

13. The method of claim 12 wherein the degradable balls have a diameter from about ⅝

inches (1.58 cm) to about 1¼

inches (3.18 cm).

14. The method of claim 12 wherein the degradable balls are exposed to differential pressures from about 500 psi to about 3,000 psi.

15. The method of claim 12 wherein the degradable balls have a density from about 0.70 g/cc to about 1.5 g/cc.

16. The method of claim 12 wherein the fatty acids, fatty alcohols, fatty acid salts, or esters present in the degradable balls comprise an amount greater than about 1% by weight.

17. The method of claim 12 wherein the carrier fluid comprises a water-based liquid, an oil-based liquid, a gas, and combinations thereof.

18. The method of claim 12 wherein the portion of the fluid flow diverted is greater than about 90%.

19. The method of claim 12 wherein the degradable balls degrade in a time period ranging from about 1 hour to 72 hours.

20. The method of claim 12 wherein the degradable balls degrade by processes comprising melting, hydrolysis, solventolysis, complete dissolution, and combinations thereof.

21. A method comprising:

providing a carrier fluid comprising degradable balls that comprise at least one material selected from the group consisting of;

a carboxylic acid, a fatty alcohol, a fatty ester, or a combination thereof; and

,

introducing the carrier fluid to a subterranean formation wherein the subterranean formation has the temperature range of about 250°

F. to about 550°

F.

22. The method of claim 21 wherein the comprising degradable balls that comprise at least one carboxylic acid selected from the group consisting of:

sebacic acid, stearic acid, pamoic acid, suberic acid, traumatic acid, thapsic acid, azelaic acid, camphoric acid, campholic acid, muconic acid, undecanedioic acid, brassylic acid, melissic acid, p-toluic acid, sorbic acid, dodecanedioc acid, tetradecanedioic acid, α

-Aleuritic acid, and combinations thereof.