ABSTRACT
A visible light-catalyzed radical coupling reaction of polysulfide reagents with aryldiazonium was developed, which gave thiosulfonates under mild conditions. In this reaction, the thiosulfonates were isolated in good yields with a broad tolerance to functional groups. And the synthesis of diaryl monosulfides were achieved through a step-by-step reaction of two molecular aryldiazonium with DBSPS, where the sulfur source was provided by DBSPS. It was worth noting that the reaction of this monosulfides could also be achieved by a one pot two-step process. The described polysulfide reagents were able to produce three new radicals: sulfonyl radicals, sulfur-sulfonyl radicals and sulfur-sulfur-sulfonyl radicals.
ABSTRACT
A comprehensive monitoring and risk assessment of arsenic (As) pollution concerning surface water and sediment is performed in the Jie River basin, where gold smelting enterprises are concentrated. The study area is divide into six regions, labeled as A, B, C, D, E, and F, from sewage outlets to downstream. Results shows that with far away from the sewage outlets, the total As concentrations in water and sediment gradually decrease from regions A to F. However, in region F, the concentration of bioavailable As significantly increases in the sediment due to the higher pH, leading to the transformation of As(V) into more mobile As(III). In sediment, Paracladius sp. exhibits strong resistance to As pollution in sediment, which can potentially elevate the risk of disease transmission. In water bodies, diatoms and euglena are the main phytoplankton in the Jie River while toxic cyanobacteria exhibits lower resistance to As pollution. Overall, measures should be taken to ecologically remediate the sediment in downstream while implementing appropriate isolation methods to prevent the spread of highly contaminated sediments from regions near sewage outlets.
Subject(s)
Arsenic , Environmental Monitoring , Geologic Sediments , Gold , Rivers , Water Pollutants, Chemical , Geologic Sediments/chemistry , Geologic Sediments/analysis , Arsenic/analysis , Rivers/chemistry , Water Pollutants, Chemical/analysis , China , Metallurgy , Pilot ProjectsABSTRACT
Sulfone compounds and thioether compounds are two highly valuable classes of compounds, but it is challenging to prepare sulfone and thioether compounds simultaneously and efficiently. Here we report that sulfides/selenides and sulfones can be obtained simultaneously using allyl bromide/benzyl bromide-activated alkyl bromides and thiosulfonates/selenosulfonates using a nickel-catalyzed reductive coupling and SN2 synergistic strategy, which is characterized by excellent atom and step economy, mild reaction conditions, broad functional group compatibility, and excellent yields.
ABSTRACT
Herein, we report a novel method for the synthesis of thioesters and acyl disulfides via nickel-catalyzed reductive cross-electrophile coupling of acid chlorides with tetrasulfides. This approach for the synthesis of thioesters and acyl disulfides is convenient and practical under mild reaction conditions, relying on easy availability. In addition, a wide range of thioesters and acyl disulfides were obtained in medium to good yields with good functional group tolerance. Moreover, thioesters and acyl disulfides can also be prepared at the gram scale, indicating that they have certain potential for industrial application.
ABSTRACT
Vivianite recovery from wastewater driven by Geobacter is one of the promising approaches to address the challenges of phosphorus (P) resource shortage and eutrophication. However, the interfere of heavy metals which are prevalent in many actual wastewater with this process is rarely reported. In this study, we investigated the impact of heavy metals (i.e., Cu and Zn ions) on microbial activity, Fe reduction, P recovery efficiency, and their fate during Geobacter-induced vivianite recovery process. The experimental results showed that low and medium concentrations of Cu and Zn prolonged the Fe reduction and P recovery time but had little effect on the final P recovery efficiency. However, high concentrations of Cu and Zn ultimately inhibit vivianite formation. In addition, the different concentrations of Cu and Zn showed different effects on the morphology of the recovered vivianite. The migration of Cu and Zn was analysed by stepwise extraction of heavy metals in the vivianite. Medium concentrations of Cu and Zn were more likely to co-precipitate with vivianite, while adsorption was the primary mechanism at low concentrations. Furthermore, there were differences in the fate of Cu and Zn, and a competition mechanism was observed. Finally, we found that increasing the Fe/P ratio can significantly reduce the residues of heavy metals in vivianite. It also increased the adsorbed Cu and Zn proportion and reduced co-precipitation. These results provide insights into improving the efficiency of vivianite recovery and managing the environmental risks of heavy metal in the recovered product.
ABSTRACT
The microalgae-based system attracts more attention in wastewater treatment for high quality effluent, low carbon emission, and resource utilization. Light is the key factor for algae growth, but the light masking in sewage will cause low efficiency of the system. This study designed laboratory scale experiments with Chlorella to investigate the influence of cerium on the nutrient removal by algae wastewater treatment system under different light intensities. The best removal rates of NH4-N, TP, and COD were 72.43%, 88.87%, and 68.08% under 50 µmol/(m 2·s) light intensity and 1 mg/L Ce. Low concentration of Ce could activate protein synthesis, electron transfer, and antioxidase, while excessive Ce might cause toxicity which could be relieved by strong light for energy supply and further activating superoxide dismutase (SOD) and catalase (CAT). Comparing to other similar experiences, this system reached an equal or greater performance on nutrients removal with better efficiency in light utilization. It might provide a new idea for microalgae-based system development.
Subject(s)
Cerium , Chlorella , Microalgae , Water Purification , Wastewater , Biomass , NitrogenABSTRACT
Herein, we provide a novel method for the synthesis of 1,3-dibenzenesulfonylpolysulfane (DBSPS), which further reacts with boronic acids to afford thiosulfonates. Commercially available boron compounds greatly expanded the range of thiosulfonates. Experimental and theoretical mechanistic investigations suggested that DBSPS could provide both thiosulfone fragments and dithiosulfone fragments, but the generated aryl dithiosulfonates were unstable and decomposed into thiosulfonates.
ABSTRACT
Discovery of remarkable porous materials for CO2 capture from wet flue gas is of great significance to reduce the CO2 emissions, but elucidating the most critical structure features for boosting CO2 capture capabilities remains a great challenge. Here, machine-learning-assisted Monte Carlo computational screening on 516 experimental covalent organic frameworks (COFs) identifies the superior secondary building units (SBUs) for wet flue gas separation using COFs, which are tetraphenylporphyrin units for boosting CO2 adsorption uptake and functional groups for boosting CO2/N2 selectivity. Accordingly, 1233 COFs are assembled using the identified superior SBUs. Density functional theory calculation analysis on frontier orbitals, electrostatic potential, and binding energy reveals the influencing mechanism of the SBUs on the wet flue gas separation performance. The "electron-donating-induced vdW interaction" effect is discovered to construct the better-performing COFs, which can achieve high CO2 uptake of 4.4 mmol·g-1 with CO2/N2 selectivity of 104.8. Meanwhile, the "electron-withdrawing-induced vdW + electrostatic coupling interaction" effect is unearthed to construct the better-performing COFs with superior CO2/N2 selectivity, which can reach 277.6 with CO2 uptake of 2.2 mmol·g-1; in this case, H2O plays a positive contribution in improving CO2/N2 selectivity. This work provides useful guidelines for designing optimized two-dimensional-COF adsorbents for wet flue gas separation.
ABSTRACT
The complexity of secondary building units (SBUs), an indicator that can not only be calculated but also visually estimated, is proposed as a highly indicative predictor of hydrogen storage performance. With optimal pore sizes and void fractions, selecting COFs consisting of simple SBUs greatly improves the probability of top-performing COFs towards the ultimate DOE hydrogen storage target, as an easy principle for experimentalists to select hydrogen adsorbents.