Use of oligo-quaternary compositions to increase scale inhibitor lifetime in a subterranean formation
View Patent ↗A method of inhibiting scale in a subterranean formation comprises pretreating the subterranean formation with a polyquaternary amine that serves as a squeeze life extension (SLE) agent, and then introducing a scale inhibitor pill into the subterranean formation, wherein the scale inhibitor pill includes one or more scale inhibitor compositions. For example, the polyquaternary amine may be a polymer having up to 5 quaternary amine centers, but is preferably a nonpolymeric diquaternary amine having a molecular weight of from 250 to 500. One such example is 1,3-propandiaminium, 2-hydroxy-N,N,N,N′,N′,N′-hexamethyl-, dichloride. The SLE agent is preferably introduced into the formation in a brine solution having a concentration from 0.1 to 20 weight percent. The SLE agents may be used with a variety of known scale inhibitors and scale inhibitor chemistries.
1. A method of inhibiting scale in a subterranean formation, comprising:
pretreating the subterranean formation with a squeeze life extension agent comprising a nonpolymeric diquaternary amine salt; and then
introducing a scale inhibitor pill into the subterranean formation, wherein the scale inhibitor pill includes one or more scale inhibitors, and wherein squeeze lifetime of the scale inhibitor pill is extended as compared to the same method without the pretreating step.
2. The method of claim 1 , wherein the nonpolymeric diquaternary amine salt has a cation with a molecular weight of from about 170 to 1500.
3. The method of claim 1 , wherein the nonpolymeric diquaternary amine salt is introduced into the formation in a brine solution having a nonpolymeric diquaternary amine salt concentration of from 0.1 to 20 weight percent.
4. The method of claim 3 , wherein the one or more scale inhibitors comprises BHMT phosphonate, DETA phosphonate, a phosphorus-containing polycarboxylate, a phosphorus-containing polymer, or a sulfonated polyacrylate.
5. The method of claim 1 , wherein the nonpolymeric diquaternary amine salt is thermally stable to 180° C.
6. The method of claim 1 , wherein the nonpolymeric diquaternary amine is symmetrical.
7. The method of claim 1 , wherein the nonpolymeric diquaternary amine is non-symmetrical.
8. The method of claim 1 , wherein the nonpolymeric diquaternary amine salt is:
(a) 1,3-propandiaminium, 2-hydroxy-N,N,N,N′,N′,N′-hexamethyl-, dichloride;
(b) 1,3-propandiaminium, 2-hydroxy-N-(2-hydroxyethyl),N,N,N′,N′,N′-pentamethyl-, dichloride; or
(c) 1,3-propandiaminium, 2-hydroxy-N,N-(2-hydroxyethyl),N,N′,N′N′-tetramethyl-, dichloride.
9. The method of claim 8 , wherein the nonpolymeric diquaternary amine salt is introduced into the subterranean formation in a brine solution having a nonpolymeric diquaternary amine salt concentration of from 0.1 to 20 weight percent.
10. The method of claim 1 , wherein the one or more scale inhibitors is a phosphonate.
11. The method of claim 10 , wherein the nonpolymeric diquaternary amine salt is introduced into the formation in a brine solution having a nonpolymeric diquaternary amine salt concentration of from 0.1 to 20 weight percent.
12. The method of claim 10 , wherein the nonpolymeric diquaternary amine is thermally stable to 180° C.
13. The method of claim 10 , wherein a cation of the nonpolymeric diquaternary amine is:
(a) 1,3-propandiaminium, 2-hydroxy-N,N,N,N′,N′,N′-hexamethyl-;
(b) 1,3-propandiaminium, 2-hydroxy-N-(2-hydroxyethyl),N,N,N′,N′,N′-pentamethyl-; or
(c) 1,3-propandiaminium, 2-hydroxy-N,N-(2-hydroxyethyl),N,N′,N′N′-tetramethyl-.
14. The method of claim 13 , wherein the nonpolymeric diquaternary amine is introduced into the formation in a brine solution having a nonpolymeric diquaternary amine concentration of from 0.1 to 20 weight percent.
15. The method of claim 1 , wherein the one or more scale inhibitors is a polymeric scale inhibitor.
16. The method of claim 1 , wherein the step of pretreating the subterranean formation with a nonpolymeric diquaternary amine salt includes introducing the nonpolymeric diquaternary amine salt into the subterranean formation in a brine.
17. The method of claim 16 , wherein the brine comprises water and one or more salts comprising a sodium halide, a calcium halide, or a magnesium halide, and wherein the brine has an electrical conductivity of greater than 0.1 mS/cm.
18. The method of claim 1 , wherein a cation of the nonpolymeric diquaternary amine salt is:
(a) 1,3-propandiaminium, 2-hydroxy-N,N,N,N′,N′,N′-hexamethyl-;
(b) 1,3-propandiaminium, 2-hydroxy-N-(2-hydroxyethyl),N,N,N′,N′,N′-pentamethyl-; or
(c) 1,3-propandiaminium, 2-hydroxy-N,N-(2-hydroxyethyl),N,N′,N′N′-tetramethyl-.
19. The method of claim 18 , wherein the nonpolymeric diquaternary amine salt is introduced into the formation in a brine solution having a nonpolymeric diquaternary amine salt concentration of from 0.1 to 20 weight percent.
20. The method of claim 1 , wherein the one or more scale inhibitors comprises a scale inhibitor including at least one anionic group, a scale inhibitor including at least one phosphonate or phosphate ester group, or a polymeric scale inhibitor including at least one carboxylate, phosphonate, or phosphonate ester group.
21. The method of claim 20 , wherein the step of pretreating the subterranean formation with a nonpolymeric diquaternary amine salt includes introducing the nonpolymeric diquaternary amine salt into the subterranean formation in a brine.
22. The method of claim 21 , wherein the brine comprises water and one or more salts comprising a sodium halide, a calcium halide, or a magnesium halide, and wherein the brine has an electrical conductivity of greater than 0.1 mS/cm.
23. The method of claim 20 , wherein the one or more scale inhibitors is a phosphonate.
24. The method of claim 20 , wherein the one or more scale inhibitors is a polymeric scale inhibitor.
25. The method of claim 1 , wherein the one or more scale inhibitors comprises a polymeric scale inhibitor derived from monomers of formulae (I) or (II):
wherein:
R 3 is CO 2 Z, SO 3 Z, PO 3 Z 2 , or an alkyl or aryl group substituted with at least one CO 2 Z, SO 3 Z or PO 3 Z 2 group in which Z is a hydrogen atom or a univalent metal atom; and
R 4 , R 5 and R 6 are each independently hydrogen, a substituted or unsubstituted alkyl or aryl group having from 1 to 8 carbon atoms, or an R 3 group.
26. The method of claim 25 , wherein the nonpolymeric diquaternary amine salt is:
(a) 1,3-propandiaminium, 2-hydroxy-N,N,N,N′,N′,N′-hexamethyl-, dichloride;
(b) 1,3-propandiaminium, 2-hydroxy-N-(2-hydroxyethyl),N,N,N′,N′,N′-pentamethyl-, dichloride; or
(c) 1,3-propandiaminium, 2-hydroxy-N,N-(2-hydroxyethyl),N,N′,N′N′-tetramethyl-, dichloride.
27. The method of claim 1 , wherein the one or more scale inhibitors comprises BHMT phosphonate, DETA phosphonate, a phosphorus-containing polycarboxylate, a phosphorus-containing polymer, or a sulfonated polyacrylate.