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The present study aimed at utilizing technically hydrolyzed lignin (THL), industrial biomass residue, derived in high-temperature diluted sulfuric acid hydrolysis of softwood and hardwood chips to sugars. The THL was carbonized in a horizontal tube furnace at atmospheric pressure, in inert atmosphere and at three different temperatures (500, 600, and 700 °C). Biochar chemical composition was investigated along with its HHV, thermal stability (thermogravimetric analysis), and textural properties. Surface area and pore volume were measured with nitrogen physisorption analysis often named upon Brunauer-Emmett-Teller (BET). Increasing the carbonization temperature reduced volatile organic compounds (40 ÷ 96 wt. %), increased fixed carbon (2.11 to 3.68 times the wt. % of fixed carbon in THL), ash, and C-content. Moreover, H and O were reduced, while N- and S-content were below the detection limit. This suggested biochar application as solid biofuel. The biochar Fourier-transform infrared (FTIR) spectra revealed that the functional groups were gradually lost, thus forming materials having merely polycyclic aromatic structures and high condensation rate. The biochar obtained at 600 and 700 °C proved having properties typical for microporous adsorbents, suitable for selective adsorption purposes. Based on the latest observations, another biochar application was proposed-as a catalyst.

Kitchen-waste-derived biochar (KBC) was produced by thermal treatment at 400 °C, and a series of KBC/BiOX (X = Br, Cl) photocatalysts were developed using ultrasonication and solvothermal treatment. The as-prepared photocatalysts were characterized by several tests and investigated by photocatalytic reactions towards methyl orange (MO) and tetracycline (TC). The best photocatalysts, 0.15KBC/BiOBr and 0.15KBC/BiOCl separately achieved complete MO photodegradation in 20 min and 35 min. Further study confirmed that 0.15KBC/BiOBr and 0.15KBC/BiOCl possessed excellent photocatalytic efficiency that was 17.9 and 14.8 times higher than BiOBr and BiOCl, respectively. In addition, 0.15KBC/BiOX showed higher activity removal of TC than pure BiOX in 60 min. Notably, 0.15KBC/BiOX maintained a reproducible high photocatalytic efficiency after five recycles. Estimated band gap energy for 0.15KBC/BiOBr (2.40 eV) and 0.15KBC/BiOCl (3.00 eV) was considerably lower than that of BiOBr (2.73 eV) and BiOCl (3.30 eV), indicating a delocalized state was created when forming electronic pathways on the interface. Besides, visible-light harvesting of photocatalysts got promoted by the modification of KBC. Active species trapping experiments and electron paramagnetic resonance (EPR) tests illustrated that photogenerated holes were the principal active species, while ∙OH was involved in the reaction. The successful synthesis of 0.15KBC/BiOX catalyst provided a new approach on simultaneously degrading organic contaminants in water and disposing of excessive kitchen waste., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

The study focuses on degradation efficiency of non-radical activation and radical activation systems of persulfate (PS) to degrade imidacloprid (IMI) by using sodium persulfate (SPS) as PS source. Copper oxide (CuO)-SPS and CuO/biochar (BC)-SPS were selected as PS non-radical activation systems, and pyrite (PyR)-SPS was selected as PS radical activation system. The degradation by CuO-SPS, CuO/BC-SPS and PyR-SPS systems was investigated from acidic to basic conditions (pH 3.0-11.0). Highest degradation by CuO-SPS and CuO/BC-SPS systems was achieved over pH 11.0. In contrast, highest degradation by PyR-SPS system was achieved over pH 3.0, however, PyR-SPS system was also found effective up to pH 9.0. It was found that degradation was more efficient in PS radical activation system, indicating that IMI could be oxidized by radicals rather than by activated PS. Electron paramagnetic resonance (EPR) analysis was carried out to investigate the generation of sulfate (SO 4 - ) and hydroxyl (OH) radicals, which indicated the presence of SO 4 - and OH in CuO-SPS, CuO/BC and PyR-SPS systems. However, free radical quenching analysis indicated that radicals were main reactive oxygen species for degradation. The lower degradation in PS non-radical activation systems was probably resulted from radicals existed as minor reactive oxygen species. The findings indicated that non-radical oxidation systems showed low reality for degradation and good degradation could be achieved by radical oxidation system. The degradation was also carried out in real waters to investigate the potential applicability of applied systems, which supported PyR-SPS system for effective degradation., (Copyright © 2019 Elsevier Inc. All rights reserved.)