Colorimetric detection of uranium in water
View Patent ↗Disclosed are methods, materials and systems that can be used to determine qualitatively or quantitatively the level of uranium contamination in water samples. Beneficially, disclosed systems are relatively simple and cost-effective. For example, disclosed systems can be utilized by consumers having little or no training in chemical analysis techniques. Methods generally include a concentration step and a complexation step. Uranium concentration can be carried out according to an extraction chromatographic process and complexation can chemically bind uranium with a detectable substance such that the formed substance is visually detectable. Methods can detect uranium contamination down to levels even below the MCL as established by the EPA.
1. A method for determining the presence or quantity of uranium in an aqueous test sample, the method comprising:
concentrating the uranium in the aqueous test sample, wherein the step of concentrating the uranium is comprised of:
a) binding the uranium to an extractant to form a uranium/extractant complex,
b) separating the uranium from the extractant by use of a separation agent, interaction between the uranium/extractant complex and the separation agent forming a first complex comprising the uranium, the first complex being more favorable chemically than the uranium/extractant complex; and
c) interacting the first complex with a compound to form a second complex comprising the uranium;
following the step of concentrating the uranium, interacting the second complex with a detectable substance to form a uranium/detectable substance complex, the uranium/detectable substance complex being more favorable chemically than the second complex; and
detecting the complex of the uranium and the detectable substance to obtain information with regard to the presence or quantity of the uranium in the aqueous test sample.
2. The method according to claim 1 , further comprising removal of metals other than uranium from the aqueous test sample.
3. The method according to claim 1 , wherein the concentrating step comprises a solvent-based extraction chromatography process.
4. The method according to claim 1 , wherein the concentrating step comprises a solid-phase extraction chromatography process.
5. The method according to claim 1 , wherein the concentrating step comprises a liquid-liquid extraction process.
6. The method according to claim 1 , further comprising comparing the visibly detected complex with calibration data.
7. The method according to claim 1 , further comprising pretreating the aqueous test sample.
8. The method according to claim 1 , the method further comprising separating one or more metals other than uranium from the extractant prior to separating the uranium from the extractant.
9. The method according to claim 1 , wherein the first complex is a uranyl carbonate complex.
10. The method according to claim 1 , wherein the complex of the uranium and the detectable substance is visibly detected.
11. The method according to claim 1 , wherein the aqueous test sample is natural water.
12. The method according to claim 11 , wherein the aqueous test sample is drinking water.
13. The method according to claim 1 , wherein the second complex is a uranyl nitrate complex.
14. The system according to claim 13 , wherein the separation agent is sodium carbonate or sodium bicarbonate.
15. The method according to claim 1 , wherein the second complex comprising the uranium is formed according to a process that includes boiling a solution comprising the first complex and nitric acid.
16. The system according to claim 15 , wherein the compound is nitric acid.
17. A system for detecting the presence or quantity of uranium in an aqueous test sample, the system comprising:
an extraction chromatography column comprising an extractant for binding uranium;
a separation agent that interacts with uranium on the extraction chromatography column to remove uranium from the extractant and form a first complex comprising the uranium;
a compound that interacts with the first complex to form a second complex comprising the uranium; and
a detectable substance that interacts with the second complex to form a detectable complex with uranium; wherein
the system is a portable test system.
18. The system of claim 17 , the extraction chromatography column comprising the extractant directly bound to a support phase.
19. The system of claim 17 , the extraction chromatography column comprising the extractant dissolved in a liquid extraction medium, the liquid extraction medium comprising an organic solvent.
20. The system of claim 17 , wherein the detectable substance is Br-PADAP.
21. The system of claim 17 , wherein the extractant is selected from the group consisting of a diamyl amylphosphonate extractant, a dyglycolamide extractant, a phosphonic acid extractant, a tricarboxylic calix[6]arene, and a trishydroxamic calix[6] arene.
22. The system according to claim 17 , wherein the first complex is a uranyl carbonate complex.
23. The system according to claim 17 , wherein the second complex is a uranyl nitrate complex.
24. The system according to claim 17 , wherein the detectable complex is visibly detectable.
25. The system of claim 17 , the extraction chromatography column comprising a stationary phase held on a support phase, the stationary phase comprising the extractant that binds uranium.
26. The system of claim 25 , wherein the stationary phase is impregnated within pores of the support phase.
27. The system of claim 17 , further comprising a treatment reagent.
28. The system of claim 27 , wherein the treatment reagent is a pH modifier.
29. The system of claim 27 , wherein the treatment reagent reacts with a metal of the aqueous test sample, the metal being a metal other than uranium.