TY - JOUR
T1 - Charge transfer-driven enhanced lithium extraction using poly(acrylic) acid-modified layered double hydroxide
AU - Pan, Yanan
AU - Ji, Bin
AU - Zhang, Wencai
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/8/15
Y1 - 2024/8/15
N2 - This study presents an advanced strategy for developing a novel poly(acrylic) acid-modified layered double hydroxide (PAA@LDH) for enhanced lithium adsorption. The optimal modification conditions include the use of a 2.5 % PAA solution in deionized water, an LDH powder dosage of 90 mL/g, and direct mixing at 333 K. Under these conditions, additional negatively charged functional groups were introduced into the material structure, thereby improving charge transfer, increasing electron cloud density, and lowering equipotential charge, as determined by DFT calculations. Consequently, the modified adsorbent exhibited a substantial rise in lithium adsorption capacity, increasing from 2.08 mg/g to 3.41 mg/g in produced water with low lithium concentration. Adsorption kinetics were rapid, reaching equilibrium within 40 min, and the adsorption behavior conformed to the Langmuir isotherm model. Besides, the adsorbent exhibited excellent selectivity for Li+ ions and maintained its performance at approximately 3.40 mg/g over seven cycles when regenerated under neutral conditions. The findings establish a robust framework for designing innovative adsorbent systems for lithium recovery from aqueous sources like produced water.
AB - This study presents an advanced strategy for developing a novel poly(acrylic) acid-modified layered double hydroxide (PAA@LDH) for enhanced lithium adsorption. The optimal modification conditions include the use of a 2.5 % PAA solution in deionized water, an LDH powder dosage of 90 mL/g, and direct mixing at 333 K. Under these conditions, additional negatively charged functional groups were introduced into the material structure, thereby improving charge transfer, increasing electron cloud density, and lowering equipotential charge, as determined by DFT calculations. Consequently, the modified adsorbent exhibited a substantial rise in lithium adsorption capacity, increasing from 2.08 mg/g to 3.41 mg/g in produced water with low lithium concentration. Adsorption kinetics were rapid, reaching equilibrium within 40 min, and the adsorption behavior conformed to the Langmuir isotherm model. Besides, the adsorbent exhibited excellent selectivity for Li+ ions and maintained its performance at approximately 3.40 mg/g over seven cycles when regenerated under neutral conditions. The findings establish a robust framework for designing innovative adsorbent systems for lithium recovery from aqueous sources like produced water.
KW - Electronic density
KW - Layered double hydroxide
KW - Lithium adsorption
KW - Polymer modification
KW - Produced water
UR - https://www.scopus.com/pages/publications/85196140793
UR - https://www.scopus.com/pages/publications/85196140793#tab=citedBy
U2 - 10.1016/j.cej.2024.152939
DO - 10.1016/j.cej.2024.152939
M3 - Article
AN - SCOPUS:85196140793
SN - 1385-8947
VL - 494
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 152939
ER -