Blood purification column
US-2015374898-A1 · Dec 31, 2015 · US
US9327267B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9327267-B2 |
| Application number | US-201514697711-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 28, 2015 |
| Priority date | Jul 22, 2011 |
| Publication date | May 3, 2016 |
| Grant date | May 3, 2016 |
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A powder-based adsorbent and a related method of manufacture are provided. The powder-based adsorbent includes polymer powder with grafted side chains and an increased surface area per unit weight to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. A method for forming the powder-based adsorbent includes irradiating polymer powder, grafting with polymerizable reactive monomers, reacting with hydroxylamine, and conditioning with an alkaline solution. Powder-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.
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The invention claimed is: 1. A method for forming a powder-based adsorbent for the recovery of metal ions from an aqueous solution, the method comprising: exposing a polymer fiber to ionizing radiation, the polymer fiber defining a mean diameter of less than 15 microns; co-grafting polymerizable monomers containing nitrile and hydrophilic groups onto the irradiated polymer fiber to form grafted side chains; reacting the nitrile groups in the grafted side chains with a reagent to convert the nitrile groups into amidoxime groups; conditioning the polymer fiber with an alkaline solution; and grinding the co-grafted polymer fiber into polymer granules to form a powder-based adsorbent having grafted side chains with amidoxime groups. 2. The method according to claim 1 wherein the polymer granules have a mean diameter of less than approximately 5 microns. 3. The method according to claim 1 wherein the polymer fibers are polyethylene, polypropylene, or polyacrylonitrile. 4. The method according to claim 1 wherein the reagent is selected from the group consisting of hydroxylamine, hydroxylamine derivatives, hydrazine, hydrazine derivatives, N-methylhydroxylamine, acetohydroxamic acid, N-benzylhydroxylamine hydrochloride, hydroxyurea, tert-butyl n-hydroxycarbamate, sym-diphenylhydrazine, methylhydrazine sulfate, and phenylhydrazine hydrochloride. 5. The method according to claim 1 wherein the polymer fiber includes a non-circular morphology for increasing the fiber surface area. 6. The method according to claim 5 wherein the non-circular morphology includes a trilobial-shaped, gear-shaped, or flower-shaped cross-section.
Fibres or filaments (fibres or filaments in the form of membranes B01J20/28038; B01J20/28007 takes precedence) · CPC title
After-treatment (C08J9/22 takes precedence) · CPC title
of unsaturated nitriles · CPC title
Homopolymers or copolymers of nitriles · CPC title
Polyalkenes, polymers or copolymers of compounds with alkenyl groups bonded to aromatic groups · CPC title
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