Functionalized porous organic polymers as uranium nano-traps for efficient uranium extraction

Patent metadata

Field	Value
Publication number	US-11628419-B2
Application number	US-201916961158-A
Country	US
Kind code	B2
Filing date	Jan 12, 2019
Priority date	Jan 12, 2018
Publication date	Apr 18, 2023
Grant date	Apr 18, 2023

Abstract

Compositions are provided for efficient uranium extraction, for example from wastewater, seawater, or other water sources. The compositions can include a functionalized porous organic polymer functionalized with one or more uranium binding moieties, e.g. having a plurality of amidoxime or amidrazone groups covalently attached thereto. The compositions can include covalent organic frameworks, porous aromatic frameworks, and various porous organic polymers, especially those having a hierarchical pore size distribution over a range of pore sizes. The compositions can have functional groups such as amidoxime or an amidrazone covalently attached thereto. The hierarchical pore size distribution can be determined based upon at least 60% of the pore sizes in the range of pore sizes having a pore volume of at least 0.01 cm3 g−1 in the pore size distribution at 77 K. Methods of making the compositions and methods of using the compositions are also provided.

First claim

We claim:

1. A composition for uranium capture, the composition comprising a porous organic polymer comprising a plurality of amidoxime or amidrazone groups covalently attached thereto;
wherein the composition comprises a covalent organic framework (COF) comprising a plurality of two-dimensional polymers (2d-polymers), each comprising repeat units according to the following formula:

where each occurrence of R 1 is independently a hydrogen, a halide, an alkyl or heteroalkyl having 1 to 3 carbon atoms, a hydrogen-bond donor, an amidoxime, or an amidrazone so long as at least one occurrence of R 1 is an amidoxime or an amidrazone, and where n is an integer from 2 to 12;
wherein each of the 2d-polymers in the plurality of 2d-polymers stacks via non-covalent interactions to form a plurality of pores.

2. The composition according to claim 1 , wherein n is 4 to 6.

3. A method of making the composition of claim 1 , the method comprising:
(i) condensing a plurality of 2,5-diamino-substituted phenyl monomers with a plurality of triformylphloroglucinol monomers to form a plurality of nitrile functionalized two-dimensional polymers (2d-polymers);
wherein the 2,5-diamino-substituted phenyl monomers have a structure according to the following formula:

where each occurrence of R 1 in the 2,5-diamino-substituted phenyl monomer is independently a hydrogen, a halide, an alkyl or heteroalkyl having 1 to 3 carbon atoms, a hydrogen-bond donor, or a nitrile so long as at least one occurrence of R 1 is a nitrile; and
(ii) converting the at least one nitrile into an amidoxime or an amidrazone to form a plurality of two-dimensional polymers (2d-polymers), each comprising repeat units according to the following formula

where each occurrence of R 1 in the 2d-polymer is independently a hydrogen, a halide, an alkyl or heteroalkyl having 1 to 3 carbon atoms, a hydrogen-bond donor, an amidoxime, or an amidrazone so long as at least one occurrence of R 1 is an amidoxime or an amidrazone, and where n is an integer from 2 to 12;
wherein each of the 2d-polymers in the plurality of 2d-polymers self assembles via non-covalent interactions to form a three-dimension structure comprising a plurality of pores.

4. The method according to claim 3 , wherein n is 4 to 6.

5. The method according to claim 3 , wherein each occurrence of R 1 in the 2d-polymer is independently a hydrogen, a hydrogen-bond donor, or an amidoxime;
wherein as at least one occurrence of R 1 is an amidoxime; and
wherein at least one occurrence of R 1 is a hydrogen-bond donor.

6. A method of making the composition of claim 1 , the method comprising:
forming a mixture comprising a precursor monomer and a free radical initiator in an aprotic solvent, wherein the precursor monomer has a structure according to the formula CH 2 ═CHA 1 CH═CH 2 where A 1 is a conjugated core having one or more nitrile moieties covalently attached thereto;
heating the mixture to a first elevated temperature for a first period of time to form the porous organic polymer having nitrile moieties covalently attached thereto;
converting the nitrile moieties into an amidoxime or an amidrazone to form the porous organic polymer having one or more amidoxime or amidrazone moieties covalently attached thereto.

Assignees

• Univ South Florida

Inventors

• Ma Shengqian
• Sun Qi
• Aguila Briana

Classifications

• Y02P10/20

  Recycling · CPC title

• B01J20/28083

  being in the range 2-50 nm, i.e. mesopores · CPC title

• B01J20/28071

  being less than 0.5 ml/g · CPC title

• C02F2303/16

  Regeneration of sorbents, filters · CPC title

• B01J20/3085

  Chemical treatments not covered by groups B01J20/3007 - B01J20/3078 · CPC title