Cross-link polyamino acid type metal adsorbent, method for preparing same and method for adsorbing metal
A polyamino acid, amino acid type technology, applied in chemical instruments and methods, adsorption water/sewage treatment, water/sludge/sewage treatment, etc., to achieve good environmental protection effects
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[0052] The present invention also provides a method for preparing a cross-linked polyamino acid metal adsorbent, comprising the following steps:
[0053] Perform polycondensation reaction of one or more amino acids with a cross-linking agent with a functionality ≥ 2 to obtain a cross-linked polyamino acid;
[0054] Or carry out a cross-linking reaction between a straight-chain polyamino acid and a cross-linking agent with a functionality ≥ 2 to obtain a cross-linked polyamino acid;
[0055] Or carry out a crosslinking reaction between branched polyamino acid and a crosslinking agent with a functionality ≥ 2 to obtain crosslinked polyamino acid;
[0056] Or carry out a crosslinking reaction with a mixture of linear polyamino acid and branched polyamino acid and a crosslinking agent with a functionality ≥ 2 to obtain a crosslinked polyamino acid.
[0057] In the present invention, the content of the cross-linking agent with functionality ≥ 2 is X, where 0%
Embodiment 1
[0081] To prepare hyperbranched polylysine, add 100 grams of lysine to a 500-milliliter round-bottomed flask equipped with a Dean-Stock trap, heat to 180° C. and stir for 12 hours, then vacuumize for 10 hours. The reaction system was cooled to room temperature to obtain 89 grams of hyperbranched polylysine.
Embodiment 2
[0083] For the preparation of polyglutamic acid, add 59g of ground L-glutamic acid and 52mL of benzyl alcohol into a 500mL three-necked bottle, after mechanically stirring evenly, slowly add 48mL of 60% concentrated sulfuric acid dropwise with a constant pressure dropping funnel, The temperature of the oil bath was controlled at 70°C until the reaction solution became clear. Heating was stopped, and after the reaction solution dropped to normal temperature, it was added to 65 g of sodium bicarbonate in ice water. After filtration, the crude product was recrystallized with distilled water at 70°C to obtain flaky crystals, washed with ethanol and ether in sequence, and dried in vacuum to obtain the white product γ-benzyl-L-glutamic acid.
[0084] Add 10g of γ-benzyl-L-glutamic acid into 100mL of anhydrous tetrahydrofuran, add 5g of triphosgene while stirring, and react in an oil bath at 50-60°C for 3 hours. Hydrogen chloride gas. After the solution was clarified, the heating w...
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