Herein, biochars derived from corn stalks, rice husks, and bamboo powder were modified by nitric acid oxidation and sodium hydroxide alkali activation to identify efficient and cost-effective polycyclic aromatic hydrocarbon-adsorbent and microbial-immobilized carriers. The surface characterization and adsorption investigation results suggested that acid/alkali modification promoted the phenanthrene removal ability in an aqueous solution of biochars via facilitating π–π/n–π electron donor–acceptor interactions, electrostatic interactions, hydrogen bonds, and hydrophobic interactions. Subsequently, the degrading bacteria Rhodococcus sp. DG1 was successfully immobilized on the rice husk-derived biochar with nitric acid oxidation (RBO), which exhibited the maximum phenanthrene adsorption efficiency (3818.99 µg·g⁻¹), abundant surface functional groups, and a larger specific surface area (182.6 m²·g⁻¹) and pore volume (0.141 m³·g⁻¹). Degradation studies revealed that the microorganisms immobilized on RBO by the adsorption method yielded a significant phenanthrene removal rate of 80.15% after 30 days, which was 38.78% higher than that of the control. Conversely, the polymer gel network-based microenvironment in the microorganism-immobilized RBO by the combined adsorption–embedding method restricted the migration and diffusion of nutrients and pollutants in the reaction system. This study thus introduces an innovative modified biochar-based microbial immobilization technology characterized by a simple design, convenient operation, and high adsorption efficiency, offering valuable insights into material selection for PAH contamination bioremediation.

In this paper, carbon-matrix-supported copper (Cu) and cobaltous oxide (CoO) nanoparticles were obtained by using coordination polymers (CPs) as a precursor. The aqueous solutions of copper methacrylate (CuMA) and cobalt methacrylate (CoMA) were preferentially prepared, which were then mixed with anhydrous ethanol to fabricate dual metal ion coordination polymers (CuMA/CoMA). After calcination under an argon atmosphere, the Cu-CoO/C nanocomposite was obtained. Scanning electron microscope (SEM) and transmission electron microscope (TEM) showed that the material has banded morphology, and the dual functional nanoparticles were highly dispersed in the carbon matrix. The prepared material was used in a heterogeneous Fenton-like reaction, with the aim of replacing traditional ferric catalysts to solve pH constraints and the mass production of ferric slime. The obtained nanocomposite showed excellent catalytic performance on the degradation of methylene blue (MB) at near-neutral conditions; the discoloration efficiency is about 98.5% within 50 min in the presence of 0.15 mmol/mL H₂O₂ and 0.5 mg/mL catalyst. And good reusability was verified via eight cycles. The plausible pathway for MB discoloration and the possible catalytic mechanism was also proposed.