No abstract

A novel nanocomposite ] was constructed by combining ferrocene (Fc) with the porous structural metal−organic framework ]. The proposed composite material could simultaneously and efficiently remove hexavalent chromium [Cr(VI)] and imidacloprid and reduced strongly noxious Cr(VI) to weakly noxious trivalent chromium [Cr(III)]. The removal efficiencies of the composite material for Cr(VI) and imidacloprid could reach 95% after 15 h. The adsorption process was determined by kinetics, isotherms, and thermodynamics. The results demonstrated that the adsorption kinetics of Cr(VI) followed the pseudosecond-order model mainly by chemisorption; meanwhile, the adsorption of imidacloprid by the material conformed to the pseudo-first-order kinetics, which indicated that physical adsorption was the main process. Additionally, the intraparticle diffusion model revealed that the uptake of imidacloprid and Cr(VI) occurred via intraparticle diffusion at the composite material. The adsorption procedure for Cr(VI) was fitted to the Langmuir model (R 2 = 0.995) via monolayer adsorption, and that for imidacloprid was fitted to the Freundlich model (R 2 = 0.995) due to multilayer or heterogeneous adsorption. The thermodynamic research confirmed that the adsorption procedure was exothermic and spontaneous. Infrared spectroscopy, X-ray photoelectron spectra, and the pH effect implied that intermolecular hydrogen bonding and electrostatic interaction played a crucial role during the removal process. Fc-MIL-100(Fe) also exhibited long-term stability and satisfactory regeneration and reusability. Therefore, this method may enhance an environmentally friendly and prospective approach for concurrently removing imidacloprid and Cr(VI) from wastewater.

Herein, a novel magnetic iron-based carbon microsphere was prepared by cohydrothermal treatment of tobacco waste liquid (TWL) and waste iron residue (WIR) to form WIR@TWL. After that, WIR@TWL was coated with sodium polyacrylate (S.P.) to fabricate WIR@TWL@SP, whose removal efficiency for bivalent cadmium (Cd(II)) was studied in water and soil. As a result, WIR@ TWL@SP possessed a high Cd(II) removal efficiency, which could reach 98.5% within 2 h. The adsorption process was consistent with the pseudo-second-order kinetic model because of the higher value of adjusted R 2 (0.99). The thermodynamic data showed that the adsorption process was spontaneous (ΔG°< 0) and exothermic (ΔH°= 32.42 KJ•mol −1 > 0). Cd(II) removal mechanisms also include cation exchange, electrostatic attraction, hydrogen-bond interaction, and cation−π interaction. Notably, pot experiments demonstrated that WIR@TWL@SP could effectively reduce Cd absorption by plants in water and soil. Thus, this study offers an effective method for remediating Cd(II)-contaminated water and soil and may have a practical application value.

The modification of biochar is essential for the development of multifunctional biochar materials with enhanced remediation effects on contaminated water. In this work, a biochar-based microcatalyst with sunlight sensitivity was synthesized by a creative modification method that involved the rapid fabrication of MnO2 microspheres by high-energy electron beam (HEEB) irradiation, and loading them into corn straw-derived honeycomb-like KOH-modified biochar (MBC) to obtain a sunlight-sensitive microcatalyst (SSM). The honeycomb-like structure of MBC facilitated the improvement in MnO2 dispersion and photocatalytic property through confinement effect. The effects of photocatalyst dosage, initial chlortetracycline (CTC) concentration, solution pH, temperature and coexisting ions on the photocatalytic performance of SSM were systemically investigated. The results indicated that SSM could efficiently degrade CTC in water and swine urine under sunlight, and exhibited high stability against coexistence of urea, Cl− and SO42−. Moreover, SSM showed good reusability in regeneration studies. This work provides a novel method for degrading CTC with potential application prospect.

Every year, a large amount of tobacco waste liquid (TWL) is discharged into the environment, resulting in serious pollution for the environment. In this work, a TWL-based particle (OACT) was fabricated by CaO, attapulgite (ATP), and TWL, and, then, OACT was coated by amino silicon oil (ASO) to form OACT@ASO. Therein, OACT@ASO had high controlled-release ability for fulvic acid (FA), because of the nanonetworks structure for ATP and the high content of FA in TWL. The release ratio (RR) of FA from OACT@ASO reached 94% at 75 h in deionized water, and 23% at 32 d in silica sand. Furthermore, the release mechanism of FA from OACT@ASO was consistent with the First-order law. Additionally, OACT@ASO also possessed high immobilization capacity for Cu(II), Cd(II), and Pb(II) (CCP) in soil. Notably, a pot experiment indicated that OACT@ASO could facilitate the growth of pakchoi seedlings and decrease the absorption of CCP by pakchoi seedlings. Thus, this study provides a new kind of organic fertilizer which could not only release FA, but also immobilize CCP in soil.

A fuel cell, an energy transducer, can convert chemical energy into electrical energy. In this work, graphite felt (GF) loaded with polypyrrole (PPy) and carboxylic carbon nanotubes (CNTs–COOH) was used as a cathode (GF/PPy/CNTs–COOH) in a double-chamber nonbiofuel cell (D-nBFC) to remove Cr­(VI) efficiently. Therein, Na2S2O3 in an alkaline solution and Cr­(VI) in a strongly acidic solution were employed as anode and cathode solutions, respectively. An agar salt bridge, consisting of saturated KCl solution, was used to transport ions between the anode and cathode. This system suggested that the removal efficiency of Cr­(VI) could reach 99.6%. The maximum current, power, and power density could achieve 136.8 μA, 18.7 μW, and 20.8 mW/m2 at 90 min, respectively. Additionally, GF/PPy/CNTs–COOH also had good electrocatalytic stability and reusability after four cycles, which played an important role in the development of the D-nBFC system. Therefore, this study provides an environmentally friendly and efficient method to remove Cr­(VI) and generate electricity simultaneously.

Fertilizer application can increase yields, but nutrient runoff may cause environmental pollution and affect soil quality. A network-structured nanocomposite used as a soil conditioner is beneficial to crops and soil. However, the relationship between the soil conditioner and soil microbes is unclear. We evaluated the soil conditioner’s impact on nutrient loss, pepper growth, soil improvement, and, especially, microbial community structure. High-throughput sequencing was applied to study the microbial communities. The microbial community structures of the soil conditioner treatment and the CK were significantly different, including in diversity and richness. The predominant bacterial phyla were Pseudomonadota, Actinomycetota, and Bacteroidota. Acidobacteriota and Chloroflexi were found in significantly higher numbers in the soil conditioner treatment. Ascomycota was the dominant fungal phylum. The Mortierellomycota phylum was found in significantly lower numbers in the CK. The bacteria and fungi at the genus level were positively correlated with the available K, available N, and pH, but were negatively correlated with the available P. Our results showed that the loss of nutrients controlled by the soil conditioner increased available N, which improved soil properties. Therefore, the microorganisms in the improved soil were changed. This study provides a correlation between improvements in microorganisms and the network-structured soil conditioner, which can promote plant growth and soil improvement.

In this work, the performance of medium-pressure UV/peracetic acid (MPUV/PAA/H2O2) was explored on removing reactive black 5 (RB5), aniline (ANL), and polyvinyl alcohol (PVA), three typical refractory contaminants in printing and dyeing wastewater, compared with MPUV/H2O2. MPUV/PAA/H2O2 showed 75.0, 44.9, and 57.7% removals of RB5, ANL, and PVA, respectively, within 5 min. The removal of RB5 increased from 68.98 to 91.2%, with pH increasing from 6 to 9, while the removals of ANL and PVA were much less pH-dependent. Quenching experiment results indicated that UV photolysis and radical (i.e., •OH and R-C•) oxidation contributed to RB5 removal, while PAA showed high activity in the oxidation of ANL. For PVA, •OH oxidation and UV photolysis were likely the main mechanisms. The coexisting natural organic matter had a negative effect on the degradation of RB5 and PVA. In addition, MPUV/PAA/H2O2 could effectively degrade those pollutants without increasing the toxicity. This work provides a theoretical reference for the utilization of MPUV/PAA/H2O2 in removing structurally diverse refractory contaminants from printing and dyeing wastewater.