The effect of biochar mild air oxidation on the optimization of lead(II) adsorption from wastewater

Abstract

In the present study, the effects of mild air oxidation of a biochar produced by the Pyrovac Inc. pyrolysis process, on the adsorption of lead(II) from synthetic wastewater under batch experimental conditions have been investigated. The adsorption experiments were performed under several conditions suggested by the response surface methodology, which allowed finding the optimal conditions, in order to maximize the adsorption capacity (Q(mgg^-1)), as well as the extraction efficiency (E (%)). The optimal conditions of lead ions adsorption were as follows: pH = 5, agitation time = 300 min, adsorbent mass = 0.5 g (per 50 cm³ of solution), and lead initial concentration = 100gm^-3, resulted in an adsorption capacity of 7.9 mg g^-1. Equilibrium adsorption was then obtained by keeping pH and adsorbent mass at the optimal values and changing the lead initial concentration for a sufficient agitation time. Results showed that mild air oxidation increased the equilibrium adsorption capacity of biochar from 2.5 to 44 mg g^-1. Oxidized biochar after equilibrium adsorption was submitted to SEM/EDX and XPS analysis. From SEM it was found that lead particles were distributed heterogeneously after adsorption. From XPS analysis, it was revealed that the external surface of oxidized biochar particles becomes saturated for the initial point of equilibrium diagram, obtained at lead initial concentration of 100gm^-3, suggesting that for a higher concentration, the internal surfaces of particles participate in the cations adsorption. The participation of surface functional groups in the adsorption process showed that carbonyl, carboxylic, and aromatic rings of oxidized biochar were involved in the adsorption. This work suggests that the very simple process of mild air oxidation can be used instead of the usual costly chemical activation, in order to improve biochar cation exchange capacity.

Keywords: Adsorption mechanisms; Lead adsorption; Mild air oxidation; Pyrolysis biochar; Response surface methodology; Wastewater.