Authors :
Ndukwu D. E.; Ogukwe C. E.; Enenebeaku C. K.; Akalezi C. O.; Didacus D. E.; Chukwueke K. A.; Igbomezie M. C.
Volume/Issue :
Volume 11 - 2026, Issue 7 - July
Google Scholar :
https://tinyurl.com/mrt2any7
Scribd :
https://tinyurl.com/yfkphxz8
DOI :
https://doi.org/10.38124/ijisrt/26jul1844
Note : A published paper may take 4-5
working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and
ResearchGate.
Abstract :
Chromium showed
peak adsorption at pH 2 (67%), consistent with electrostatic attraction of chromate anions to protonated surface sites, while
the four cationic metals performed best at pH 6. Unlike many lignocellulosic biosorbents, equilibrium data for all five metals
including Cr(VI) conformed to the Langmuir isotherm model (R² = 0.957–0.998), indicating predominantly monolayer
adsorption on a comparatively homogeneous set of binding sites across the tubular, lignocellulosic COS matrix. The PseudoSecond-Order kinetic model provided an excellent fit for all metals (R² = 0.997–0.999), with calculated equilibrium capacities
closely matching experimental values, implicating chemisorption as the dominant rate-controlling mechanism.
Thermodynamic analysis yielded negative ΔG° (−0.414 to −0.731 kJ/mol), negative ΔH°, and positive ΔS° values for all five
metals, confirming that adsorption is spontaneous, mildly exothermic, and entropically driven. Scanning electron
micrographs showed the characteristic rough tubular pre-adsorption texture becoming densely aggregated after metal
loading, while FTIR spectroscopy identified hydroxyl, carboxylic, thiol, and aliphatic C–H groups as primary binding sites,
with post-adsorption shifts in the O–H stretching region confirming metal–ligand complexation. These findings establish
COS as a high-performing, and readily available biosorbent for metal water remediation.
Keywords :
Biosorption; Corn Stalk; Zea Mays; Heavy Metals; Langmuir Isotherm; Pseudo-Second-Order Kinetics; Thermodynamics; Agricultural Waste; Wastewater Treatment.
References :
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Chromium showed
peak adsorption at pH 2 (67%), consistent with electrostatic attraction of chromate anions to protonated surface sites, while
the four cationic metals performed best at pH 6. Unlike many lignocellulosic biosorbents, equilibrium data for all five metals
including Cr(VI) conformed to the Langmuir isotherm model (R² = 0.957–0.998), indicating predominantly monolayer
adsorption on a comparatively homogeneous set of binding sites across the tubular, lignocellulosic COS matrix. The PseudoSecond-Order kinetic model provided an excellent fit for all metals (R² = 0.997–0.999), with calculated equilibrium capacities
closely matching experimental values, implicating chemisorption as the dominant rate-controlling mechanism.
Thermodynamic analysis yielded negative ΔG° (−0.414 to −0.731 kJ/mol), negative ΔH°, and positive ΔS° values for all five
metals, confirming that adsorption is spontaneous, mildly exothermic, and entropically driven. Scanning electron
micrographs showed the characteristic rough tubular pre-adsorption texture becoming densely aggregated after metal
loading, while FTIR spectroscopy identified hydroxyl, carboxylic, thiol, and aliphatic C–H groups as primary binding sites,
with post-adsorption shifts in the O–H stretching region confirming metal–ligand complexation. These findings establish
COS as a high-performing, and readily available biosorbent for metal water remediation.
Keywords :
Biosorption; Corn Stalk; Zea Mays; Heavy Metals; Langmuir Isotherm; Pseudo-Second-Order Kinetics; Thermodynamics; Agricultural Waste; Wastewater Treatment.