Irreversible covalent organic framework for efficient and selective gold recovery and preparation method thereof
The disclosure discloses an irreversible covalent organic framework for efficient and selective gold recovery and a preparation method thereof, and belongs to the technical field of precious metal recovery from an aqueous solution. In the disclosure, metal trifluoromethanesulfonate is used as a catalyst, and a solvothermal method is used to prepare a mother covalent organic framework, and then the corresponding structural unit is used to perform an exchange reaction to prepare an irreversible amide-linked covalent organic framework material. The disclosure solves the problem of preparation of high-stability irreversible covalent organic framework, the introduced amide bond gives the covalent organic framework the ability to quickly and selectively recover precious metal gold from an aqueous solution, and the covalent organic framework can be used repeatedly. The application of the covalent organic framework as an efficient adsorbent in the field of adsorption and separation is expanded, and a new material is provided for efficient recovery or removal of metal salts.
1. A method for preparing an irreversible covalent organic framework material, comprising the following steps:
(1) under action of a catalyst, first performing a condensation reaction on a triamino compound represented by formula I-1 and a p-dicarboxaldehyde compound represented by formula II-1; and
(2) then adding and mixing a p-diformyl chloride compound represented by formula III-1 for performing an exchange reaction;
or,
(1) under action of the catalyst, first performing a condensation reaction on a p-diamino compound represented by formula I-2 and a tricarboxaldehyde compound represented by formula II-2; and
(2) then adding and mixing a triformyl chloride compound represented by formula III-2 for performing an exchange reaction;
wherein A is selected from nitrogen, benzene ring and s-triazine ring; and B is selected from phenyl, biphenyl and triphenyl.
2. The method of claim 1 , wherein the catalyst in step (1) is a metal trifluoromethanesulfonate.
3. The method of claim 1 , wherein the condensation reaction in step (1) is carried out in an organic solvent, and the organic solvent comprises one or more of dioxane, mesitylene, tetrahydrofuran and N,N-dimethylacetamide.
4. The method of claim 1 , wherein the amount of the catalyst used is 5-10% of a total mass of the two reactants as structural units.
5. The method of claim 1 , wherein the p-diformyl chloride compound equivalent of the p-dicarboxaldehyde compound, or the triformyl chloride compound equivalent of the tricarboxaldehyde compound is added for the exchange reaction.
6. The method of claim 1 , wherein a temperature of the exchange reaction is 4-25° C.
7. An irreversible covalent organic framework material prepared by the method of claim 1 .