Hydrochar a carbon-rich material resulting from hydrothermal carbonization of biomass, has received substantial attention because of its potential application in various areas such as carbon sequestration, bioenergy production and environmental amelioration. A series of hydrochars were prepared by metal chloride-assisted hydrothermal carbonization of rice husk and characterized by elemental analysis, zeta potential, X-ray diffraction, Brunauer–Emmett–Teller measurements, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy and scanning electron microscopy. The results reveal that the prepared hydrochars have carbon contents ranging from 45.01 to 58.71%, BET specific areas between 13.23 and 45.97 m2/g, and rich O-containing functional groups on the surfaces. The metal chlorides added in the feedwater could improve the degree of carbonization and show significant effects on the physical, chemical and adsorption properties of the hydrochars. The adsorption of the selected organics on the hydrochars is a spontaneous and physisorption-dominated process. The hydrochars possess larger adsorption capacities for 2-naphthol than for berberine hydrochloride and Congo red, and the modeling maximum adsorption capacities of 2-naphthol are in the range of 170.1–2680 mg/g. The adsorption equilibrium could be accomplished in 10, 40 and 30 min for 2-naphthol, berberine hydrochloride and Congo red, respectively. These results suggest metal chloride-assisted hydrothermal carbonization a promising method for converting biomass waste into effective adsorbents for wastewater treatment.

Hydrochars produced via hydrothermal carbonization of rice husk were post-treated using three different acids and two bases. The post-treated hydrochars were characterized using different methods and evaluated for adsorption of dyes and antibiotics from aqueous solutions. The post-treated hydrochars had carbon and oxygen contents in the range of 37.4% to 44.7% and 29.9% to 38.6%, respectively, and their surfaces were rich in oxygen-containing functional groups and negative surface charges. Post-treatment remarkably influenced the physico-chemical properties of the hydrochars’ surfaces. All post-treated hydrochars could adsorb the model organics from aqueous solutions with the highest adsorption amount of 327, 353, 336, and 309 mg/g for Congo red, berberine hydrochloride, tetracycline, and acridine orange, respectively, at 0.3 mg/mL and 25 °C. The combined effects of functional groups, surface area, and negative surface charge of the hydrochars could assist in the adsorption of organics. The Langmuir-isotherm model provided a good fit for the adsorption of acridine orange, tetracycline, and berberine hydrochloride on the selected hydrochars, while the adsorption of Congo red generated linear isotherms indicating a partition-involved mechanism. The adsorption of the organics onto the hydrochars is a spontaneous and mainly physical adsorption process with a quite fast adsorption rate.