A series of activated biochar (KBBC-700, KBBC-800 and KBBC-900) which were modified by KOH and pyrolysis at various temperatures from ball-milling bamboo powder were obtained. The physicochemical properties and pore structures of activated biochar were investigated by scanning electron microscopy (SEM), fourier transform infrared spectoscopy (FT-IR), X-ray diffraction (XRD) and N₂ adsorption/desorption. The adsorption performance for the removal of methylene blue (MB) was deeply studied. The results showed that KBBC-900 obtained at activation temperature of 900 °C exhibited a great surface area which reached 562 m²/g with 0.460 cm³/g of total pore volume. The enhancement of adsorption capacity could be ascribed to the increase of surface oxygen-containing functional groups, aromatization and mesoporous channels. The adsorption capacity was up to 67.46 mg/g under the optimum adsorption parameters with 2 g/L of adsorbent dose, 11 of initial solution pH and 298 K of the reactive temperature. The adsorption capacity was 70.63% of the first time after the material was recycled for three cycles. The kinetics indicated that the adsorption equilibrium time for MB on KBBC-900 was of about 20 min with the data fitted better to the pseudo-second-order kinetics model. The adsorption process was mainly dominated by chemical adsorption. Meanwhile, the adsorption isotherm showed that the Langmuir model fitted the best, and thermodynamic parameters revealed that the adsorption reaction was the endothermic nature and the spontaneous process. Adsorption of MB mainly attributed to electrostatic interactions, cation-π electron interaction and redox reaction. This study suggested that the activated biochar obtained by KOH activation from bamboo biochar has great potentials in the practical application to remove MB from wastewater. Graphical Abstract

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.

Recycling of residual biomass in the form of carbonaceous materials is a sustainable and economically viable management option with zero net carbon dioxide emissions. Mesoporous bamboo biochars were produced via microwave-assisted hydrothermal/soft template treatment. Then they were characterized and evaluated for their adsorption capabilities for three organics. The biochars were found to have mesoporous structures with BET surface areas of 13.0 to 288 m2/g, total pore volumes in the range of 0.017 to 0.313 cm3/g, and average pore diameters between 4.0 and 6.7 nm in size. The surface areas and pore volumes were highly related to the hydrothermal treatment conditions. The mesoporous bamboo biochars showed adsorption amounts for 2-naphthol, berberine hydrocholoride, and Congo red in the range of 35.0 to 155.7, 76.1 to 129.6, 57.9 to 114.4 mg/g, respectively, at the adsorbate concentration of 0.5 mg/mL, and their adsorption capabilities depended on both the porosity and the surface groups. The adsorption of the three organics on the selected sample was a spontaneous and exothermic process with physical adsorption as the dominant mechanism. The adsorption could achieve equilibrium within 20, 40, and 60 min for 2-naphthol, berberine hydrochloride, and Congo red, respectively. This study provides a prospective method to produce biomass-derived mesoporous carbon adsorbents for adsorptive separation of organics from water.