The aim of this study was to optimize the adsorption performance of activated carbon (AC), derived from the shell of Penaeus vannamei prawns, on heavy metal ions. Inexpensive, non-toxic, and renewable prawn shells were subjected to carbonization and, subsequently, KOH-activation to produce nanoporous K-Ac. Carbonized prawn shells (CPS) and nanoporous KOH-activated carbon (K-Ac) from prawn shells were prepared and characterized by FTIR, XRD, BET, SEM, and TEM. The results showed that as-produced K-Ac samples were a porous material with microporous and mesoporous structures and had a high specific surface area of 3160 m²/g, average pore size of about 10 nm, and large pore volume of 2.38 m³/g. Furthermore, batches of K-Ac samples were employed for testing the adsorption behavior of Cd²⁺ in solution. The effects of pH value, initial concentration, and adsorption time on Cd²⁺ were systematically investigated. Kinetics and isotherm model analysis of the adsorption of Cd²⁺ on K-Ac showed that experimental data were not only consistent with the Langmuir adsorption isotherm, but also well-described by the quasi-first-order model. Finally, the adsorption behaviors of as-prepared K-Ac were also tested in a ternary mixture of heavy metal ions Cu²⁺, Cr⁶⁺, and Cd²⁺, and the total adsorption amount of 560 mg/g was obtained.

This study, for the first time, rendered crab shell activated biochar modified by potassium hydroxide (KOH) impregnation (CSAB), revealing a new potential application in the removal of diesel oil from oily wastewater. The structural characteristics of crab shell biochar (CSB) and CSAB were investigated by SEM, and the crystal structure and optical properties of as-prepared samples were analyzed using XRD and FTIR. Results showed that CSAB had stratified surface structure morphology, abundant functional groups, and that its high specific surface area could reach up to 2441 m²/g, which was about eight times larger than that of untreated CSB (307 m²/g). An adsorption isotherm study indicated that the actual adsorption process both of CSAB and CSB were found to fit better with the Freundlich equation. Moreover, chemical interaction controlled the adsorption kinetics efficiency while the adsorption equilibrium capacity was 93.9 mg/g. Due to its highly developed pore structure, unique surface characteristics, and effective adsorption performance, this low-cost activated carbon had the potential to serve as an efficient adsorbent for water pollution purification.

Spartina alterniflora is an invasive plant from coastal wetlands, and its use in applications has garnered much interest. In this study, a composite photocatalyst (ZnO@BC) was synthesized by preparing zinc oxide (ZnO) nanoparticles with S. alterniflora extracts, S. alterniflora, and one-step carbonization, which was characterized using scanning electron microscope (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), Raman, X-ray photoelectron spectroscopy, ultraviolet–visible spectroscopy (UV–vis DRS), photoluminescence (PL) and N₂ adsorption–desorption isotherm. The degradation capacity and mechanism of malachite green (MG) using ZnO@BC were analyzed under visible irradiation, and the degradation products of malachite green were detected by LC–MS. The results show that ZnO@BC has a larger surface area (83.2 m²/g) and various reactive groups, which enhance its photocatalytic efficiency, with the presence of oxygen vacancy further improving the photocatalytic activity. The total removal rate of malachite green (400 mg/L) using ZnO@BC is up to 98.38%. From the LC–MS analysis, it could be concluded that malachite green is degraded by demethylation, deamination, conjugate structure and benzene ring structure destruction. This study provides a novel idea for the high-value utilization of S. alterniflora.

In this study, the synchronous magnetized carbonization method was utilized for preparing photocatalysis ZnO-Fe@SC heterostructure, which exhibited degradation efficiency 99.14% (60 min) for malachite green (200 mg/L) and could still maintain good performance after 5 cycles. The prepared ZnO-Fe@SC was analyzed using UV–Vis DRS, PL, SEM, TEM, BET, FTIR, XPS and VSM, and LC–MS for degradation products. The results indicate that photocatalyst has favorable magnetic properties, chemical stability and low charge carriers (e⁻/h⁺) recombination rate. The modification of bimetals enables the composite photocatalyst to enhance the intensity of photogenerated electron transition. Moreover, quenching experiment revealed that the photo-generated holes (h⁺) and superoxide radicals (·O²⁻) were the dominant active species during the photocatalytic process, which degraded malachite green into small molecules by demethylation, deamination, ring-opening reactions as deducted from LC–MS analysis. ZnO-Fe@SC was prepared using a green, safe, low cost and operable synthetic method, which has a broad market potential in the field of environmental remediation. Graphical Abstract

In this work, a new nano-Bi₂MoO₆/diatomite composite photocatalyst was successfully synthesized by a facile solvothermal method. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and UV-vis diffuse reflection spectroscopy (DRS) were employed to investigate the morphology, crystal structure, and optical properties. It was shown that nanometer-scaled Bi₂MoO₆ crystals were well-deposited on the surface of Bi₂MoO₆/diatomite. The photocatalytic activity of the obtained samples was evaluated by the degradation of rhodamine B (RhB) under the visible light (λ > 420 nm) irradiation. Moreover, trapping experiments were performed to investigate the possible photocatalytic reaction mechanism. The results showed that the nano-Bi₂MoO₆/diatomite composite with the mass ratio of Bi₂MoO₆ to diatomaceous earth of 70% exhibited the highest activity, and the RhB degradation efficiency reached 97.6% within 60 min. The main active species were revealed to be h⁺ and•O²⁻. As a photocatalytic reactor, its recycling performance showed a good stability and reusability. This new composite photocatalyst material holds great promise in the engineering field for the environmental remediation.