Polyazacrown-based materials for mercury capture and synthesis of those materials
View Patent ↗Polyazacrown polymers based on the azacrown monomer 1,4,7,10,13,16,21,24-octaazabicyclo[8.8.8]hexacosane (“H 6 Aza222”) are disclosed. Azacrown monomer units are preferably linked with a suitable linking agent, and the resulting polymers are can absorb mercury from a water stream and form a stable complex therewith. Methods of making and using the polyazacrown polymers are also disclosed. The polymers have a high absorption capacity for and selectivity towards mercury, which properties are useful for the remediation of mercury-contaminated water. The polymers can be regenerated by the efficient removal of the absorbed mercury. Further, the absorbed mercury that is liberated from the polyazacrown polymers can be effectively concentrated and captured to prevent its re-release into the environment.
1. A polyazacrown polymer comprising:
linked azacrown moieties of the formula C 18 H 36 N 8 L x R 6-x ,
wherein:
L is one or more linking units derived from one or more linking agents having two or more leaving groups;
R is one or more of hydrogen (H), a functionalizing moiety, and combinations thereof; and,
x ranges from 2 to 6.
2. The polyazacrown polymer of claim 1 , wherein R consists of hydrogen (H).
3. The polyazacrown polymer of claim 1 , wherein:
the linking agents comprise hydrocarbon-based chains being 2 or more atoms in length; and,
the leaving groups are selected from the group consisting of vinyl groups, epoxides, halogens, tosyl groups, tetrahydrothiophenes, sulfonic acids, nitriles, and combinations thereof.
4. The polyazacrown polymer of claim 3 , wherein the linking agents are selected from the group consisting of 1,4-di-chloromethyl benzene, 4,4′-bis(chloromethyl)-1,1′-biphenyl, and combinations thereof.
5. The polyazacrown polymer of claim 1 , wherein x is more than 2 and the polyazacrown polymer is a network polymer.
6. The polyazacrown polymer of claim 5 , wherein x is about 3 or more.
7. The polyazacrown polymer of claim 1 , wherein the polyazacrown polymer has a microporous structure.
8. The polyazacrown polymer of claim 7 , wherein the microporous structure has a porosity ranging from about 0.5 to about 0.9.
9. The polyazacrown polymer of claim 1 , wherein the polyazacrown polymer has a fractal structure.
10. The polyazacrown polymer of claim 1 , further comprising:
one or more cations retained by the azacrown moieties.
11. The polyazacrown polymer of claim 10 , wherein the cations are selected from the group consisting of Cd 2+ , Hg 2+ , Pb 2+ , Tl 3+ , and combinations thereof.
12. The polyazacrown polymer of claim 10 , wherein the cations comprise Hg 2+ .
13. The polyazacrown polymer of claim 1 , further comprising:
one or more mercury derivatives retained by the azacrown moieties.
14. The polyazacrown polymer of claim 13 , wherein the mercury derivatives are selected from the group consisting of Hg, Hg 2 2+ , Hg 2+ , MeHg + , Me 2 Hg, PhHg + , and combinations thereof.
15. An azacrown derivative comprising:
an azacrown moiety of the formula C 18 H 36 N 8 L x R 6-x ,
wherein:
L is one or more linking units derived from one or more linking agents having two or more leaving groups;
R is one or more of hydrogen (H), a functionalizing moiety, and combinations thereof; and,
x ranges from 2 to 6.
16. The azacrown derivative of claim 15 , wherein R consists of hydrogen (H).
17. The azacrown derivative of claim 15 , wherein the linking agents comprise one or more of 1,4-bis(chloromethyl)benzene and 4,4′-bis(chloromethyl)-1,1′-biphenyl.
18. The azacrown derivative of claim 15 , wherein x is 3 or more.
19. A polyazacrown compound comprising: two or more azacrown moieties of the azacrown derivative of claim 15 , wherein adjacent azacrown moieties are linked by at least one linking unit.
20. A method of forming a polyazacrown polymer, the method comprising:
providing an azacrown monomer of the formula C 18 H 36 N 8 R 6 , wherein (1) R is one or more of hydrogen (H), a functionalizing moiety, and combinations thereof and (2) at least 2 of the R groups are hydrogen; and,
reacting the azacrown monomer with a sufficient amount of one or more linking agents having two or more leaving groups to form a polyazacrown polymer comprising linked azacrown moieties of the formula C 18 H 36 N 8 L x R 6-x , wherein x ranges from 2 to 6.
21. The method of claim 20 , further comprising reacting the azacrown monomer with the linking agents in the presence of a base.
22. The method of claim 21 , wherein consists of hydrogen (H).
23. The method of claim 21 , wherein the base comprises a poorly nucleophilic base.
24. The method of claim 21 , wherein the base is selected from the group consisting of N,N-diisopropyl-N-ethyl amine, N,N-diisopropyl-N-ethanol amine, N,N-dicyclohexyl-N-methyl amine, and combinations thereof.
25. The method of claim 20 , further comprising:
reacting the azacrown monomer with the linking agents in the presence of a structure-directing agent; and,
removing the structure-directing agent after the polyazacrown polymer is formed, such that the resulting polyazacrown polymer has a microporous structure.
26. The method of claim 25 , wherein the structure-directing agent comprises polyethylene oxide.
27. The method of claim 25 , further comprising:
reacting the azacrown monomer with the linking agents in the presence of polyethylene oxide and a glass frit; and,
removing the polyethylene oxide and the glass frit after the polyazacrown polymer is formed, such that the resulting polyazacrown polymer has a fractal structure.
28. The method of claim 20 , further comprising reacting the azacrown monomer with the linking agents in the presence of a solvent.
29. The method of claim 28 , wherein the solvent is selected from the group consisting of water, ethylene glycol, dimethylformamide, dimethylacetamide, benzyl cyanide, decalin, mineral oil, and combinations thereof.
30. The method of claim 20 , wherein reacting the azacrown with the linking agents further is performed at a temperature ranging from about 0° C. to about 220° C.
31. The method of claim 30 , wherein reacting the azacrown monomer with the linking agents further is performed at a temperature ranging from about 100° C. to about 220° C.
32. The method of claim 20 , wherein the linking agents comprise one or more of 1,4-bis(chloromethyl)benzene and 4,4′-bis(chloromethyl)-1,1′-biphenyl.
33. The method of claim 20 , wherein x is more than 2 and the polyazacrown polymer is a network polymer.