IP Library Granted Patent US 11,918,977
Granted Patent B2
US 11,918,977 · App. 17/892,186 · Granted Mar 5, 2024

Contaminate sequestering coatings and methods of using the same

Inventors: Christopher M. Hoffman, Jr. (Odenton, MD); Zhiyong Xia (Rockville, MD); James K. Johnson (Silver Spring, MD)
Assignee: The Johns Hopkins University
B01J20/22B01D39/086B01J20/28038B01J20/3208B01J20/3221B01J20/3246C02F1/288B01D2239/0478B01D2239/0618C02F1/285C02F2101/20C02F2101/36
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Quick Facts
Patent No.
US 11,918,977
App. No.
17/892,186
Granted
Mar 5, 2024
Kind
B2
Abstract

Contaminate-sequestering coatings including a network of hydrolyzed silane compounds including a plurality of thiol functional groups, a plurality of fluorinated functionalities, or both are provided. The contaminate-sequestering coatings may sequester one or more per- and polyfluoroalkyl substances (PFAS), heavy metals, biological species or any combination thereof. Methods of functionalizing a substrate surface with contaminate-sequestering functionalities that sequester one or more PFAS, heavy metals, or both are also provided. Methods of removing contaminants from contaminate-containing liquids, and devices including the contaminate-sequestering coatings are also provided.

Claims (15)

1. A method of removing contaminants from a contaminant-containing liquid, comprising:

contacting the contaminant-containing liquid with a contaminant-sequestering coating, wherein the contaminant-sequestering coating comprises a network of hydrolyzed silane compounds including a plurality of fluorinated functionalities,

wherein the network of hydrolyzed silane compounds includes a fluorinated silane comprising (i) a hydrophilic polar head region, wherein a polar region comprises one or multiple units of ethylene glycol (EG) functionality; (ii) a fluorine-containing region; and (iii) an anchor region including silicon atom(s).

2. The method of claim 1 , wherein the contaminant-containing liquid comprises water that comprises one or more poly, perfluoroalkyl substances (PFAS) compounds.

3. The method of claim 2 , wherein the contaminant-sequestering coating sequesters from about 50% to about 100% by weight of an initial quantity of the one or more PFAS compounds.

4. The method of claim 2 , wherein the contaminant-sequestering coating sequesters from about 80% to about 100% by weight of an initial quantity of the one or more PFAS compounds.

5. The method of claim 2 , wherein the contaminant-sequestering coating reduces an initial quantity of the one or more PFAS compounds present in the contaminant-containing liquid to less than about 80 parts-per-trillion (ppt).

6. The method of claim 2 , wherein the contaminant-sequestering coating reduces an initial quantity of the one or more PFAS compounds present in the contaminant-containing liquid to less than about 70 parts-per-trillion (ppt).

7. The method of claim 2 , wherein the contaminant-sequestering coating is bonded to at least a portion of a substrate, and the contaminant-containing liquid is passed across and/or through the substrate having the contaminant-sequestering coating bonded thereon.

8. The method of claim 7 , wherein the contaminant-containing liquid is recirculating across and/or through the substrate until a desired reduction of the one or more PFAS compounds is realized.

9. The method of claim 7 , wherein the substrate comprises a filter or an ion-exchange bed.

10. The method of claim 1 , wherein the network of hydrolyzed silane compounds includes a fluorinated silane comprising a cyclic hydrocarbon including from 3 to 60 carbon atoms.

11. The method of claim 1 , wherein the network of hydrolyzed silane compounds includes a fluorinated silane including from 4 to about 200 fluorine atoms.

12. The method of claim 1 , wherein the network of hydrolyzed silane compounds includes a fluorinated silane comprising a substituted hydrocarbon including at least one heteroatom selected from oxygen, nitrogen, sulfur, phosphorus, or combinations thereof.

13. The method of claim 1 , wherein the network of hydrolyzed silane compounds includes a first group of fluorinated silane compounds and a second group of fluorinated compounds, and wherein the first group of fluorinated silane compounds includes from about 1.5 to about 5 times more fluorine atoms than the second group of fluorinated compounds.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 27, 2022
From: THE JOHNS HOPKINS UNIVERSITY APPLIED PHYSICS LABORATORY LLC
To: THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY
Reel/Frame 061552/0037 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2022
From: HOFFMAN, CHRISTOPHER M., JR.; XIA, ZHIYONG; JOHNSON, JAMES K.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 060854/0326 →
Continuity (2)
Continuation 16445310 · Jun 19, 2019
Related Publication 20230001378A1 · Jan 5, 2023