Ozone degradation of tetracycline hydrochloride enhanced by magnetic nanofluid composed of Fe3O4 nanoparticles.

Magnetic Fe3O4 nanoparticles were added into the aqueous phase to form nanofluid systems, in which ozone was used for the oxidation of tetracycline hydrochloride (TC) in the solution. The nanomaterials were characterized using SEM, XRD, EDS, and FT-IR. The effects of nanoparticles size, addition ratio, and number of cycles on the process of ozone oxidation of TC were investigated. The results indicated that the addition ratio of nanoparticles have a certain impact on the performance of ozone oxidation. When the addition ratio increased from 0.02% to 0.4%, the removal rate of TC in the solution was improved significantly. Besides, the particle size of nanoparticles showed a greater impact on ozone oxidation. At the nanoscale, Fe3O4 nanoparticles exhibited significant strengthening properties, which is attributed to the construction of nanofluid systems. The removal rate of TC in solution decreased obviously with the increase of nanoparticles size. The Fe3O4 nanoparticles with particle size of 20 nm showed the most significant effect on TC degradation. The recycling experiment showed that magnetic Fe3O4 nanoparticles had stable regeneration performance. For three times of recycling treatment, with a Fe3O4 addition ratio of 0.4%, the removal rate of TC reached 98.7%, 97.21%, and 96%, respectively. Based on the characterization results, the strengthening mechanism was analyzed. The experimental results indicated that construction of nanofluids systems could improve the utilization rate of ozone, and Fe3O4 nanoparticles were reusable and easily recyclable.

Insight into the enhancement effect of amino functionalized carbon nanotubes on the H2S removal performance of nanofluid system.

By constructing nanofluid system, trace functionalized nanoparticles can significantly enhance the absorption performance of basic liquid. In this work, amino functionalized carbon nanotubes (ACNTs) and carbon nanotubes (CNTs) were introduced into alkaline deep eutectic solvents to build nanofluid systems and used for the dynamic absorption of H2S. The experiment results showed that the introduction of nanoparticles can significantly enhance the H2S removal performance of original liquid. When performing H2S removal experiments, the optimal mass concentrations of ACNTs versus CNTs were 0.05 % and 0.01 %, respectively. The characterization showed that the surface morphology and structure of the nanoparticles unchanged significantly during the absorption-regeneration process. A double mixed gradientless gas-liquid reactor was used to explore the gas-liquid absorption kinetics characteristics of the nanofluid system. It was found that the gas-liquid mass transfer rate increased significantly after the addition of nanoparticles. The highest total mass transfer coefficient of the nanofluid system of ACNTs was increased to more than 400 % of the value before the addition of nanoparticles. The analysis showed that the shuttle effect and hydrodynamic effect of nanoparticles play important role in the process of enhancing gas-liquid absorption, and the amino functionalization enhanced the shuttle effect of nanoparticles significantly.

Effects of forest age on soil erosion and nutrient loss in Dianchi watershed, China.

Soil erosion and nutrient loss are important environmental and ecological problems in the Dianchi watershed in southwestern China. Woodlands-the primary land type in the Dianchi watershed-play an important ecological role in controlling soil and water loss. In this study, we compared soil erosion and loss of total organic carbon (TOC), total nitrogen (TN), and total phosphorus (TP) in woodlands of different ages, i.e., young forest, medium forest, and near-mature forest, at the Dongda River catchment in south-western Dianchi watershed. Furthermore, changes in stoichiometries in soil were analyzed. The average degree of erosion of each forest age stage was below moderate. Based on the non-arable soil erosion modulus models of 137Cs and 210Pbex, the soil erosion rates decreased gradually with the increasing forest age. The forest age affected soil nutrient distribution and loss. The losses of TOC and TP gradually decreased, while the losses of TN first increased and then decreased with the growth of forest age. TOC, TN, and TP were enriched in the topsoil. Forest age affected soil stoichiometry and soil nutrient supply level. In general, the forest can effectively reduce soil erosion and nutrient loss in the red soil area with the forest age increasing.

Historical evolution of polycyclic aromatic hydrocarbon pollution in Chaihe Reservoir from 1863 to 2018.

Pollution from polycyclic aromatic hydrocarbons (PAHs) spreads and changes worldwide. The pollution evolution in the regional water environment evolves in response to multiple factors, requiring considerable attention. PAH heterogeneity in the sediment core from Chaihe Reservoir was investigated to indicate dynamic changes in PAH pollution levels and sources and propose recommendations for controlling PAHs. Dynamic PAH patterns showed that the overall decline in PAH pollution was in association with local anthropogenic activities, temperature, and precipitation over the period 1863-2018. Nevertheless, coal, oil, and natural gas consumptions still played significant roles in transferring PAHs to the reservoir. Meanwhile, there were dominant local origins, including grass, wood, and coal combustion. The results highlight that the joint action of natural and anthropogenic interventions mitigated PAH pollution in the reservoir. Promoting improved fuels, new energy vehicles, and cleaner energy may further lower PAH pollution.

Biochar improves soil quality and wheat yield in saline-alkali soils beyond organic fertilizer in a 3-year field trial.

The objective of this study was to examine the effects of biochar compared to organic fertilizer on soil quality and wheat yield in the saline-alkaline lands. A 3-year field trial was conducted on moderately saline-alkaline land in the Yellow River Delta region (YRD) with six treatments: biochar (B1: 5 t, B2: 10 t, B3: 20 t ha-1 year-1) and organic fertilizer (OF1: 5 t, OF2: 7.5 t ha-1 year-1) as well as control (CK). The results showed that both biochar and organic fertilizer increased total organic carbon (TOC), total nitrogen (TN), NH4+-N, and NO3--N, and reduced pH, thereby increasing soil microbial biomass carbon (MBC) and nitrogen (MBN), MBC/TOC ratio, and MBN/TN ratio, but organic fertilizer increased soil nutrients and microbial biomass better than biochar. Correlation analysis revealed that soil water content (SWC), soil salt content (SSC), and Na+ were the most important factors influencing wheat yield. When compared to CK, the SSC and Na+ decreased by 5.55-7.52% and 3.86-9.39%, respectively, and SWC increased by 5.14-5.62% in the biochar treatment, while they increased by 1.07-10.19%, 1.08-7.58%, and 2.96-3.84% in the organic fertilizer treatment, respectively. Accordingly, wheat yield of biochar treatment was 0.90-14.71% higher than that of organic fertilizer treatment (4.49-4.80 t ha-1) and CK (4.47 t ha-1). Collectively, B2 had the lowest SSC and Na+ and the highest yield and was significantly better than the organic fertilizer treatment, as well as efficiently increasing soil nutrients and microbial biomass, suggesting that it may be a better agricultural practice for improving soil quality and increasing wheat yield in the YRD.

Coffee ground derived biochar embedded Ov-NiCoO2 nanoparticles for efficiently catalyzing a boron­hydrogen bond break.

The catalytic boron­hydrogen bond break is usually regarded as an important reaction both in the area of environment treatment and hydrogen energy, attracting increasing attention in the past decades. Due to the limitation of conventional noble metal-based catalyst, cost-effective transition metal-based catalysts with high activity have been recently developed to become the promising candidates. Herein, the coffee ground waste was utilized as the biochar substrate loaded with ultrafine NiCoO2 nanoparticles. The abundant function groups on the biochar substrate efficiently adsorbed the metal ions and confined the crystal growth spatially, making the NiCoO2 nanoparticles highly dispersed on the surface. Moreover, the oxygen vacancies were further created in the catalysts by a vacuum-calcination strategy to boost their catalytic activity towards boron­hydrogen bond break both in the systems of 4-nitrophenol reduction by NaBH4 and hydrogen release from NH3BH3. The results indicated that the moderate presence of oxygen vacancies could effectively accelerate the boron­hydrogen bond break and the catalytic activity performed a satisfied stability during several recycles. The theoretical calculation method was adopted to analysis and discuss the mechanism within this process. This design strategy on active catalysts not only offered a novel solution of biowaste resource reuse but also demonstrated the significant role of oxygen vacancies in energy and environmental catalysis.

Removal of sulfadiazine from aqueous solution by in-situ activated biochar derived from cotton shell.

Phosphoric acid is used to in-situ activate biochar pyrolyzed by cotton shells to enhance the adsorption ability of sulfadiazine (SDZ). To confirm the optimum condition, different impregnation ratios and impregnation times were investigated. It was found that the biochar (BC) pyrolyzed under the condition of an impregnation ratio of 2.5 and an impregnation time of 6 h showed the highest performance for the removal of SDZ. The maximum adsorption ability was 86.89 mg/g at a temperature of 298 K. The pseudo-second-order model was used to disclose the adsorption process of SDZ by BCs. The experimental data were described by the Langmuir and Temkin isotherms at different temperatures. It was found that the sorption of SDZ was an exothermic process according to the thermomechanical analysis. The activated BC could be recycled for at least five times with a high removal rate of SDZ. Thus, activated BCs are regarded as promising adsorbents for SDZ removal.

Plasma-catalytic degradation of ciprofloxacin in aqueous solution over different MnO2 nanocrystals in a dielectric barrier discharge system.

The α-MnO2, ß-MnO2 and γ-MnO2 samples were prepared by the hydrothermal method and were used for the degradation of ciprofloxacin (CIP) wastewater in a combined DBD-catalytic process. The physical and chemical properties of the samples were systematically studied by several analytical techniques including BET, XRD, SEM, HRTEM, XPS, and H2-TPR. The combination of DBD with α-MnO2 showed the highest CIP degradation efficiency, and the efficiency could reach 93.1% after 50 min, which was 10.8% and 18.1% higher, respectively, than those of ß-MnO2 and γ-MnO2 catalysts in the plasma-catalytic system. According to the model of response surface methodology, the contribution of key experimental parameters on the CIP degradation decreased in the order: peak voltage > air flow rate > initial concentration > initial pH. The optimum operating parameters were peak voltage 17 kV, air flow rate 2.5 L min-1, an initial concentration 5 mg L-1 and an initial pH 6.9. The quenching experiments of active species showed that OH and O2- were critical to the CIP degradation. The generated O3 might be adsorbed by the α-MnO2 catalyst and resulted in more OH generation. The intermediate products of CIP degradation in DBD+α-MnO2 system were analyzed by LC-MS, and three possible degradation pathways were proposed. This research provides an insight into the use of the crystallographic structures in discharge plasma system for antibiotics in water.

[Effects of Biochar and Organic Fertilizer on Saline-alkali Soil N2 O Emission in the North China Plain].

Based on the winter wheat-summer maize rotation field experiment, the effects of biochar and organic fertilizer on saline-alkali soil N2O emissions in the summer maize season were studied in Binzhou in the Shandong Province to provide a theoretical basis for reducing N2O emissions from saline-alkali soil. The experiment includes six treatments with three replications:CK[N:0.2 t·(hm2·a)-1, P2O5:0.12 t·(hm2·a)-1, K2O:0.2 t·(hm2·a)-1], C1[5 t·(hm2·a)-1biochar], C2[10 t·(hm2·a)-1 biochar], C3[20 t·(hm2·a)-1 biochar], M1[7.5 t·(hm2·a)-1 organic fertilizer], and M2[10 t·(hm2·a)-1 organic fertilizer]. The same nitrogen, phosphorus, and potassium fertilizer was applied for each treatment. The results showed that the dynamic trend of the soil N2O fluxes among different treatments were similar. The peak N2O emissions occurred after fertilization (base fertilizer and topdressing). The N2O cumulative emission fluxes accounted for nearly half of the emissions during the whole growth period, and the N2O emissions of the C1, C2, and C3 treatments were lower than that of CK after fertilization. Compared with CK, the N2O cumulative emissions from C1 and C2 were reduced by 45.3% and 31.6%, respectively, but C3, M1, and M2 increased by 17.3%, 37.4%, and 27.6%, respectively. Biochar and organic fertilizer both affected N2O emission fluxes. Applying biochar can reduce N2O emissions, while organic fertilizer can increase N2O emissions. In summary, biochar has a great advantage in reducing N2O emissions in the farmland.