TY - JOUR
T1 - High-performance functionalized keratin for efficient lithium recovery
T2 - Experimental and statistical physics insights
AU - Abujayyab, Mohammed
AU - Hasan, Shadi W.
AU - Lemaoui, Tarek
AU - AlNashef, Inas M.
AU - Arafat, Hassan A.
AU - Banat, Fawzi
N1 - Publisher Copyright:
© 2025
PY - 2025/7/1
Y1 - 2025/7/1
N2 - This study investigates the potential of functionalized biosorbents for efficient lithium recovery from aqueous solution. Six biosorbents (keratin, calcium alginate, cellulose, chitosan, pectin, and date seeds) were functionalized with acetic, sulfuric, or phosphoric acid. Phosphoric acid-functionalized keratin (keratin@PA) exhibited the highest lithium adsorption capacity. Characterization techniques, including FTIR, XRD, TGA, SEM, SEM-EDX, and BET analyses, confirmed successful functionalization and revealed structural modifications, enhanced thermal stability, and increased surface porosity. Adsorption kinetics followed a pseudo-second-order model, while equilibrium data best fit the Langmuir isotherm, indicating monolayer adsorption on a homogeneous surface with a maximum adsorption capacity of 189.8 mg/g at an initial lithium concentration of 100 mg/L. Advanced statistical physics modeling, particularly the monolayer model with one energy level (M1), provided insights into the adsorption mechanism, revealing that keratin@PA facilitates multi-molecular adsorption with lithium ions adopting non-parallel orientations. The increase in saturation adsorption capacity with temperature suggests an endothermic process and enhanced adsorption efficiency at elevated temperatures. Regeneration tests validated the reusability of keratin@PA, demonstrating high initial desorption efficiency and stable performance over multiple cycles. Keratin@PA also exhibited exceptional selectivity for Li-ions, demonstrated by high separation factors ranging from 11.3 to 22.0 relative to common competing ions (Mg, K, Na, Ca). This work presents keratin@PA as a potential biosorbent for sustainable lithium recovery applications.
AB - This study investigates the potential of functionalized biosorbents for efficient lithium recovery from aqueous solution. Six biosorbents (keratin, calcium alginate, cellulose, chitosan, pectin, and date seeds) were functionalized with acetic, sulfuric, or phosphoric acid. Phosphoric acid-functionalized keratin (keratin@PA) exhibited the highest lithium adsorption capacity. Characterization techniques, including FTIR, XRD, TGA, SEM, SEM-EDX, and BET analyses, confirmed successful functionalization and revealed structural modifications, enhanced thermal stability, and increased surface porosity. Adsorption kinetics followed a pseudo-second-order model, while equilibrium data best fit the Langmuir isotherm, indicating monolayer adsorption on a homogeneous surface with a maximum adsorption capacity of 189.8 mg/g at an initial lithium concentration of 100 mg/L. Advanced statistical physics modeling, particularly the monolayer model with one energy level (M1), provided insights into the adsorption mechanism, revealing that keratin@PA facilitates multi-molecular adsorption with lithium ions adopting non-parallel orientations. The increase in saturation adsorption capacity with temperature suggests an endothermic process and enhanced adsorption efficiency at elevated temperatures. Regeneration tests validated the reusability of keratin@PA, demonstrating high initial desorption efficiency and stable performance over multiple cycles. Keratin@PA also exhibited exceptional selectivity for Li-ions, demonstrated by high separation factors ranging from 11.3 to 22.0 relative to common competing ions (Mg, K, Na, Ca). This work presents keratin@PA as a potential biosorbent for sustainable lithium recovery applications.
KW - Advanced statistical physics
KW - Aqueous solution
KW - Biosorbents
KW - Keratin
KW - Lithium-ion
KW - Regeneration
UR - http://www.scopus.com/inward/record.url?scp=86000165166&partnerID=8YFLogxK
U2 - 10.1016/j.desal.2025.118782
DO - 10.1016/j.desal.2025.118782
M3 - Article
AN - SCOPUS:86000165166
SN - 0011-9164
VL - 606
JO - Desalination
JF - Desalination
M1 - 118782
ER -