Method for separation of 90Y from 90Sr
Abstract
Inorganic ion exchange materials for the separation of 90 Y from 90 Sr include chabazite, clinoptilolite, potassium pharmacosiderite, sodium titanosilicate and sodium nonatitanate. These materials are suitable for making a 90 Y generator that contains 90 Sr immobilized on an ion exchange column of the materials. The materials have a very high selectivity for 90 Sr, a very low selectivity for 90 Y, good radiation and thermal stability, low toxicity, fast reaction kinetics, and can be readily and reproducibly synthesized. A method is thus provided for eluting 90 Y from the ion exchange material with an eluant solution. The eluant solution is preferably aqueous, preferably has a pH greater than about 5, and preferably includes a chelating agent. Preferred chelating agents include gluconic acid, oxalic acid, iminodiacetic acid, nitrilotriacetic acid, citric acid, and combinations thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A process, comprising:
adsorbing strontium-90 onto an inorganic ion exchange material from an aqueous solution comprising a source of strontium-90; and eluting yttrium-90 from the inorganic ion exchange material with a solution having a pH greater than about 5 and including a chelating agent.
2 . The process of claim 1 , wherein the solution is aqueous.
3 . The process of claim 1 , wherein the chelating agent is selected from gluconic acid, oxalic acid, iminodiacetic acid, nitrilotriacetic acid, citric acid, and combinations thereof.
4 . The process of claim 1 , where the solution is neutral.
5 . The process of claim 1 where the solution is alkaline.
6 . The process of claim 1 , wherein the inorganic ion exchange material is selected from clinoptilolite, chabazite, potassium titanosilicate pharmacosiderite, sodium titanosilicate, sodium nonatitanate, and combinations thereof.
7 . The process of claim 6 , wherein the aqueous solution includes a chelating agent selected from gluconic acid, oxalic acid, iminodiacetic acid, nitrilotriacetic acid, citric acid, and combinations thereof.
8 . The process of claim 1 , wherein the inorganic ion exchange material is sodium nonatitanate prepared by reacting titanium isopropoxide and aqueous sodium hydroxide at a temperature between 100° C. and 250° C. for a period between 12 hours and 2 weeks.
9 . The process of claim 1 , wherein the inorganic ion exchange material is sodium titanosilicate prepared by hydrothermally heating a titanium silicate gel in NaOH.
10 . The process of claim 9 , wherein the titanium silicate gel is hydrothermally heated in 6M NaOH at 170° C. for 2 days.
11 . The process of claim 1 , wherein the inorganic ion exchange material is a titanosilicate having the general formula:
M 3 H(AO) 4 (BO 4 ) 3 .x H 2 O where: M is a cation selected from H, K, Na, Rb, Cs and mixtures thereof;
A is selected from Ti and Ge; and
B is selected from Si and Ge; and
x is a value between 4 and 6.
12 . The process of claim 1 , further comprising forming the inorganic ion exchange material into pellets.
13 . The process of claim 12 , wherein the pellets are formed with an average diameter between 0.1 and 1.0 mm.
14 . The process of claim 12 , wherein the pellets are formed with an average diameter between 0.2 and 0.5 mm.
15 . The process of claim 12 , wherein the pellets comprise a polymeric binder.
16 . The process of claim 15 , wherein the polymeric binder comprises polyacrylonitrile as a binder.
17 . The process of claim 12 , wherein the pellets comprise an inorganic binder.
18 . The process of claim 17 , wherein the inorganic binder is amorphous.
19 . The process of claim 17 , wherein the pellets comprise an inorganic binder selected from amorphous titanium dioxide, amorphous silica, amorphous zirconium oxide, and combinations thereof.
20 . A process, comprising:
(a) preparing a first solution including strontium-90; (b) adsorbing strontium-90 from the first solution onto an inorganic ion exchange material; and (c) allowing yttrium-90 to grow into the inorganic ion exchange material; and (d) eluting yttrium-90 from the inorganic ion exchange material with a second solution including a chelating agent.
21 . The process of claim 20 , further comprising:
repeating steps (c) and (d).
23 . The process of claim 20 , wherein the inorganic ion exchange material is selected from clinoptilolite, chabazite, potassium titanosilicate pharmacosiderite, sodium titanosilicate, sodium nonatitanate, and combinations thereof.
24 . The process of claim 20 , wherein the first solution has a pH greater than about 5.
25 . The process of claim 20 , wherein the second solution has a pH greater than about 5.
26 . The process of claim 20 , where the second solution is neutral.
27 . The process of claim 20 , where the second solution is alkaline.
28 . The process of claim 20 , wherein the second solution includes a chelating agent.
29 . The process of claim 28 , wherein the chelating agent is selected from gluconic acid, oxalic acid, iminodiacetic acid, nitrilotriacetic acid, citric acid, and combinations thereof.
30 . The process of claim 20 , further comprising:
(e) washing the inorganic ion exchange material to remove poorly bound strontium-90 prior to eluting.Join the waitlist — get patent alerts
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