Abstract

In the present investigation, physico-chemical characterization of composite material revealed the presence of fluffy surface structure with crystalline look and negatively charged surface functional groups. The study of adsorption flux by using dimensionless numbers φ (2.62), Nk (62.68) and λ (1.17 × 10−5) proved that adsorption of nickel ions on the surface of composite material was mostly film diffusion-limited with maximum surface area coverage coupled with weakened surface tension. The results of intraparticle diffusivity and Boyd plot model showed that at the onset of process, film diffusion was the primary mechanism involved and at the later stage intraparticle diffusion played a critical role as rate governing step. The values of film (0.65 × 10−8 cm2 sec−1) and pore diffusivity (1.8 × 10−12 cm2 sec−1) coefficients showed that the adsorption process is dependent upon two different types of diffusion namely film and pore diffusion. Overall, transport and reshuffling mechanism had no substantial role in adsorption dynamics of nickel ions on the surface of composite material. Sorption isotherm and kinetics modeling showed higher values of regression coefficients for Langmuir isotherm (R2 = 0.99) and pseudo-second-order kinetic model (R2 = 0.99) compared to other models. This showed that sorption of nickel followed monolayer coverage with chemisorption at optimized process parameters like pH 6, biosorbent dose 0.1 g/L, temperature 50 °C, agitation rate180 rpm, adsorbate concentration100 mg/L and contact time 60 minutes. The positive value of enthalpy of adsorption (ΔH = + 10.41 kJ/mole) and entropy (ΔS = +58.19 J/mol K) showed that binding of nickel ions on the surface of the composite material was endothermic with improved randomness at solid-liquid interface. The negative value of (ΔG = −6.4 to -8.67 kJ/mol) showed spontaneous nature of nickel adsorption on composite material in the liquid phase.

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