Thermo-responsive solution, and method of use therefor
The present invention relates to a thermo-responsive solution and in particular, a solution for use in an osmosis process that is suitable for separating or purifying solutes and or water from an aqueous solution on a large scale and under energy efficient conditions.
1. A thermo-responsive osmotic solution having a lower critical solution temperature in a solvent, the thermo-responsive osmotic solution comprising:
a) at least one tertiary amine containing compound; and
b) at least one enolisable carbonyl compound of Formula I,
wherein
i) R 1 and R 2 are independently selected from a —C 1 -C 7 alkyl, a —C 3 -C 7 monocyclic or a -phenyl; or
ii) one of R 1 or R 2 is selected from a —O—(C 1 -C 7 alkyl) and the other is selected from a —C 1 -C 7 alkyl; or
iii) the carbonyl of Formula I forms
a. a 3-15 membered monocyclic ketone; or
b. a 3-15 membered monocyclic heterocyclic ketone; or
c. acetophenone;
wherein the at least one tertiary amine containing compound or the at least one enolisable carbonyl compound is immiscible with the solvent at or above 20 degrees Celsius and at 1 atmosphere; and wherein the solvent is water.
2. The solution as claimed in claim 1 , wherein the solution comprises a combination of more than one enolisable carbonyl compound of Formula I.
3. The solution as claimed in claim 2 , wherein the one or more enolisable carbonyl compounds of Formula I are selected from acetone, acetophenone, methylethylketone (2-butanone), cyclohexanone, cyclopentanone, 2-propanone, 2-pentanone, 3-pentanone, 4-methyl-2-pentanone, 2-octanone and 3-methyl-2-butanone, or a combination thereof.
4. The solution as claimed in claim 1 , wherein the solution comprises a combination of more than one tertiary amine containing compound.
5. The solution as claimed in claim 1 , wherein at least one tertiary amine containing compound in the solution is a Lewis base.
6. The solution as claimed in claim 5 , wherein the Lewis base forms a Lewis adduct with at least one enolisable carbonyl compound of Formula I.
7. The solution as claimed in claim 5 , wherein the solution comprises a molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I of about 1:99 or 99:1.
8. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:50 or 50:1.
9. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:10 or 10:1.
10. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:5 or 5:1.
11. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:3 or 3:1.
12. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:2 or 2:1.
13. The solution as claimed in claim 7 , wherein the molar ratio of the Lewis base to the at least one enolisable carbonyl compound of Formula I is about 1:1.
14. The solution as claimed in claim 1 , wherein at least one tertiary amine containing compound in the solution is immiscible with the solvent at or above 20 degrees Celsius and at 1 atmosphere.
15. The solution as claimed in claim 1 , wherein at least one tertiary amine containing compound in the solution is selected from a conjugated, aliphatic, asymmetric or cyclic tertiary amine.
16. The solution as claimed in claim 15 , wherein at least one tertiary amine containing compound in the solution is selected from:
17. The solution as claimed in claim 15 , wherein at least one tertiary amine containing compound in the solution is a N(C 1 -C 7 alkyl) 3 .
18. The solution as claimed in claim 17 , wherein at least one tertiary amine containing compound in the solution is a N(C 1 -C 4 alkyl) 3 .
19. The solution as claimed in claim 18 , wherein at least one tertiary amine containing compound in the solution is N(C 2 alkyl) 3 (triethylamine).
20. The solution as claimed in claim 1 , wherein R 1 and R 2 of Formula I are independently selected from a —C 1 -C 7 alkyl.
21. The solution as claimed in claim 20 , wherein R 1 and R 2 are independently selected from methyl and ethyl.
22. The solution as claimed in claim 1 , wherein the at least one carbonyl compound of Formula I, forms a cyclic system selected from a 4-8 membered monocyclic ketone or a monocyclic ester.
23. The solution as claimed in claim 1 , wherein each R 1 and R 2 of the at least one carbonyl compound of Formula I are further substituted with one or more substituents selected from -halo, —OH, —CN, —NO 2 , —C≡CH, —SH, —C 1 -C 7 alkyl, —(C 1 -C 7 alkyl)-OH, —NH 2 , —NH(C 1 -C 7 alkyl), —N(C 1 -C 7 alkyl) 2 , —O(C 1 -C 7 alkyl), —C(O)—O(—C 1 -C 7 alkyl), —C(O)OH; —C(O)—H, or —C(O)—(C 1 -C 7 alkyl).
24. A method for separating one or more solvents from a first solution using a thermo-responsive osmotic solution as defined in claim 1 , the method comprising:
1) bringing a first solution comprising one or more solvents into contact with a semi-permeable membrane;
2) allowing the one or more solvents in the first solution to flow through the semi-permeable membrane from the first solution into the thermo-responsive osmotic solution by osmosis to form a second solution comprising the thermo-responsive solution and the one or more solvents, wherein the thermo-responsive osmotic solution is at a higher osmotic concentration than the first solution;
3) raising the temperature of the second solution to or above the lower critical solution temperature of the thermo-responsive osmotic solution to cause the thermo-responsive osmotic solution in the second solution to become immiscible with the one or more solvents; and
4) separating the one or more solvents in the second solution from the immiscible thermo-responsive osmotic solution.
25. The method as claimed in claim 24 , wherein the first solution further includes one or more dissolved solutes.
26. The method as claimed in claim 24 , wherein the first solution includes water as a solvent.
27. The method as claimed in claim 24 , wherein the first solution is selected from seawater, brackish water, industrial water waste streams, compromised water sources, sewage, wastewater liquors, digestates, food & beverage processing effluents, grey water, fruit juices, vegetable juices, milk, produced waters, leachates, or flue gas scrubber discharge.
28. A method for separating one or more solvents from a first solution using a thermo-responsive osmotic solution as defined in claim 1 , the method comprising:
1) bringing the first solution comprising the one or more solvents into contact with a semi-permeable membrane;
2) allowing the one or more solvents in the first solution to flow through the semi-permeable membrane from the first solution into the thermo-responsive osmotic solution by osmosis to form a second solution comprising the thermo-responsive osmotic solution and the one or more solvents, wherein the thermo-responsive osmotic solution is at a higher osmotic concentration than the first solution;
3) adjusting the lower critical solution temperature of the second solution to cause the thermo-responsive osmotic solution in the second solution to become immiscible with the one or more solvents; and
4) separating the one or more solvents in the second solution from the immiscible thermo-responsive osmotic solution.
29. The method as claimed in claim 28 , wherein the lower critical solution temperature of the thermo-responsive osmotic solution is adjusted by adding one or more tertiary amine containing compounds as defined in claim 1 .
30. The method as claimed in claim 28 , wherein the lower critical solution temperature of the thermo-responsive osmotic solution is adjusted by adding one or more enolisable carbonyl compounds as defined in claim 1 .
31. The method as claimed in claim 28 , wherein the lower critical solution temperature of the thermo-responsive osmotic solution is adjusted by adding one or more tertiary amine containing compounds and one or more enolisable carbonyl compounds as defined in claim 1 .
32. The method as claimed in claim 28 , wherein the first solution further includes one or more dissolved solutes.
33. The method as claimed in claim 28 , wherein the first solution includes water as a solvent.
34. The method as claimed in claim 28 , wherein the first solution is selected from seawater, brackish water, industrial water waste streams, compromised water sources, sewage, wastewater liquors, digestates, food & beverage processing effluents, grey water, fruit juices, vegetable juices, milk, produced waters, leachates, or flue gas scrubber discharge.