US2009202655A1PendingUtilityA1
Titanosilicate molecular sieve supported metallic nanodots and methods of use to adsorb noble gases
Est. expiryNov 15, 2027(~1.3 yrs left)· nominal 20-yr term from priority
Inventors:Steven M. Kuznicki
C01B 2210/0082B01D 2253/112B01D 2257/11B01D 2255/20761A61K 33/38B01J 20/28007C01B 2210/0085B01D 2255/102B01D 2253/304C01B 2210/0081C01B 2210/0046B01D 2255/20707B01D 2256/10B01D 2255/20753C01B 2210/0087B82Y 30/00C01B 2210/0084B01D 53/02B01D 2256/12A61K 33/34B01D 2255/104B01J 20/186C01B 13/027A61P 31/00C01B 2210/0079B01D 2259/40088B01D 2255/106B01D 2253/108A61K 33/243A61K 33/242A61K 33/24
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Claims
Abstract
A metal nanodot material is formed by ion-exchange with an ETS zeolite, followed by activation to form metallic nanodots. The nanodot may be formed from silver, nickel, copper, gold or a platinum group metal.
Claims
exact text as granted — not AI-modified1 . A method of forming surface accessible metal nanodots, comprising the steps of:
(a) performing ion-exchange with a solution of the metal ions and an ETS zeolite; and (b) activating the ion-exchanged ETS zeolite.
2 . The method of claim 1 wherein the ETS zeolite comprises ETS-4 or ETS-10.
3 . The method of claim 1 wherein the metal comprises silver, copper, nickel, gold or a member of the platinum group.
4 . The method of claim 3 wherein the metal comprises silver.
5 . The method of claim 1 wherein the activation step comprises drying or annealing the material.
6 . The method of claim 5 wherein the activation step is performed under reducing conditions.
7 . The method of claim 5 wherein the activation step is performed under oxidizing conditions.
8 . The method of claim 5 wherein the activation step is performed at a temperature greater than about 75° C. and less than about 500° C.
9 . The method of claim 8 wherein the activating step is performed at a temperature between about 75° C. and 400° C.
10 . The method of claim 1 wherein the ion-exchange occurs with an excess of metallic ions.
11 . An ETS supported metal nanoparticulate material, comprising surface-accessible metal nanodots having a particle size less than about 100 nm.
12 . The material of claim 11 wherein the nanodots have a particle size less than about 50 nm.
13 . The material of claim 12 wherein the nanodots have a particle size less than about 15 nm and greater than about 5 nm.
14 . The material of claim 11 wherein the metal comprises silver, copper, nickel, gold or a member of the platinum group, or mixtures thereof
15 . The material of claim 14 wherein the metal comprises silver.
16 . The material of claim 11 wherein the ETS material comprises ETS-10.
17 . A method of selectively adsorbing a noble gas from a gas stream containing the noble gas, using an adsorbent comprising metal nanodots formed from the process of claim 1 , or comprising the material comprising metal nanodots of claim 11 , the method comprising the step of passing the gas stream over the surface accessible metal nanodot ETS.
18 . The method of claim 17 wherein the noble gas comprises xenon.
19 . The method of claim 18 which occurs at a temperature between 20° C. and 150° C.
20 . The method of claim 18 further comprising the step of releasing the xenon from the adsorbent by heating the adsorbent under a reduced pressure.
21 . The method of claim 20 wherein the xenon is released from the adsorbent by heating to about 150° C. under a full or partial vacuum.
22 . The method of claim 17 wherein the noble gas comprises argon.
23 . The method of claim 22 wherein the method comprises a method of producing substantially pure oxygen from a gas stream comprising oxygen and argon.
24 . A method of preventing or treating an infection in a body part by contacting the body part with metal nanodots formed from the process of claim 1 , or the material comprising metal nanodots of claim 11 .Join the waitlist — get patent alerts
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