Oil industry waste based non-magnetic and magnetic hydrochar to sequester potentially toxic post-transition metal ions from water.

Solid waste conversion to value-added products is a stepping stone towards sustainable environment. Herein, sesame oil cake (SOC), an oil industry waste was utilized as a precursor to develop hydrochar (HC) samples by varying reaction temperature (150-250 °C) and time span (2-8 h), chemically treated with 10% H2O2 to optimize a sample with maximum yield and Pb(II) adsorption. Highest yield (29.2 %) and Pb(II) (24.57 mg/g at Co: 15 mg/L) adsorption was observed on SOCHC@200 °C/6 h, magnetized (mSOCHC@200 °C/6 h) for comparative study. XRD displayed highly crystalline SOCHC@200 °C/6 h and amorphous mSOCHC@200 °C/6 h, both having a characteristic cellulose peak at 14.9°. mSOCHC@200 °C/6 h displayed superparamagnetic behavior with 11.2 emu/g saturation magnetization. IR spectra confirmed the development of samples rich in oxygen containing functionalities; an additional peak for iron oxides appeared at 586 cm-1 in mSOCHC@200°C/6 h spectrum. Four major peaks at 531.9, 399.9, 348.2 and 284.7 eV, assigned to O 1s, N 1s, Ca 2p and C 1s, respectively were observed during XPS analyses. An additional peak at 710.3 eV, ascribed to Fe 2p was observed in mSOCHC@200C/6 h XPS spectrum, while a peak at 143.2 eV for Pb 4f appeared in spectra of both Pb(II) saturated samples. pH dependent (maximum at ∼6.7), exothermic Pb(II) adsorption was found. About 50-70% (at Co: 25 mg/L) adsorption on both SOCHC@200 °C/6 h and mSOCHC@200 °C/6 h was accomplished in a minute, attaining equilibrium in 180 and 240 min, respectively. Error functions and superimposed qe, exp. and qe, cal. values supported Langmuir isotherm model applicability, with respective qm values of 304.9 and 361.7 mg/g at 25 °C for SOCHC@200 °C/6 h and mSOCHC@200 °C/6 h. Kinetic data was fitted to PSO model. Highest (between 92.2 and 88.9 %) amount of Pb(II) from SOCHC@200 °C/6 h and mSOCHC@200 °C/6 h was eluted by 0.01 M HCl.

Heteroatom-doped magnetic hydrochar to remove post-transition and transition metals from water: Synthesis, characterization, and adsorption studies.

Efforts to improve water quality have led to the development of green and sustainable water treatment approaches. Herein, nitrogen-doped magnetized hydrochar (mSBHC-N) was synthesized, characterized, and used for the removal of post-transition and transition heavy metals, viz. Pb2+ and Cd2+ from aqueous environment. mSBHC-N was found to be mesoporous (BET surface area - 62.5 m2/g) and paramagnetic (saturation magnetization - 44 emu/g). Both, FT-IR (with peaks at 577, 1065, 1609 and 3440 cm-1 corresponding to Fe - O stretching vibrations, C - N stretching, N - H in-plane deformation and stretching) and XPS analyses (with peaks at 284.4, 400, 530, 710 eV due to C 1s, N 1s, O 1s, and Fe 2p) confirmed the presence of oxygen and nitrogen containing functional groups on mSBHC-N. The adsorption of Pb2+ and Cd2+ was governed by oxygen and nitrogen functionalities through electrostatic and co-ordination forces. 75-80% of Pb2+ and Cd2+ adsorption at Co: 25 mg/L, either from deionized water or humic acid solution was accomplished within 15 min. The data was fitted to pseudo-second-order kinetic and Langmuir isotherm models, with maximum monolayer adsorption capacities being 323 and 357 mg/g for Cd2+and Pb2+ at 318 K, respectively. Maximum Cd2+ (82.6%) and Pb2+ (78.7%) were eluted with 0.01 M HCl, simultaneously allowing minimum iron leaching (2.73%) from mSBHC-N. In conclusion, the study may provide a novel, economical, and clean route to utilize agro-waste, such as sugarcane bagasse (SB), for aquatic environment remediation.