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Long-term Renal Disease as well as Fibrosis: The Role of Uremic Maintenance Solutes.
% to 10 wt.% led to a dramatic decrease of purity by 10 wt.%.The efficient removal of ammonia is a difficult issue in wastewater treatment because ammonia is easily converted to nitrate instead of N2. The oxidation of ammonia by chlorine radical (Cl) is recognized as an effective method. However, the massive generation of toxic byproducts chlorate and nitrate pose great risk for its practical application due to the excessive oxidation capacity of hydroxyl radical. Herein, we propose a novel method to selectively generate Cl for efficient ammonia removal using BiVO4/WO3 photoanode in a self-driven photoelectrocatalytic (PEC) system. Cl was predominantly produced by regulating the valence band edge of WO3 though modifying BiVO4, which tuned the moderate oxidative force of hole to reduce OH generation and thereby inhibited the formation of chlorate and nitrate. The self-driven ammonia degradation was achieved by employing BiVO4/WO3 and Si photovoltaic cells as composite photoanodes to improve light-absorption and electron-hole separation, thus enhancing Cl production. These results showed that 10 mg L-1 of ammonia-N was completely removed (99.3 %) in 120 min with 80.1 % of total nitrogen removal. Toxic byproducts chlorate and nitrate were inhibited by 79.3 % and 31 %, respectively, compared to WO3. This work provides new insights to develop efficient, energy-saving and environment-friendly method for ammonia pollution treatment.The potential risks of sono-induced nitrosation and nitration side reactions and consequent toxic nitrogenous byproducts were first investigated via sono-degradation of diphenylamine (DPhA) in this study. The kinetic models for overall DPhA degradation and the formation of nitrosation byproduct (N-nitrosodiphenylamine, NDPhA) and nitration byproducts (2-nitro-DPhA and 4-nitro-DPhA) were well established and fitted (R2 > 0.98). Nitrosation contributed much more than nitration (namely, 43.3 - 47.3 times) to the sono-degradation of DPhA. The contribution of sono-induced nitrosation ranged from 0.4 to 56.6% at different conditions. The maximum NDPhA formation rate and the contribution of sono-induced nitrosation were obtained at 600 and 200 kHz, respectively, as ultrasonic frequencies at 200 to 800 kHz. Both NDPhA formation rate and the contribution of sono-induced nitrosation increased with increasing power density, while decreased with increasing initial pH and DPhA concentration. PO43-, HCO3-, NH4+ and Fe2+ presented negative impacts on sono-induced nitrosation in order of HCO3- > Fe2+ > PO43- > NH4+, while Br- exhibited a promoting effect. The mechanism of NDPhA formation via sono-induced nitrosation was first proposed.Microbial sulfidization of arsenic (As)-bearing jarosite involves complex processes and is yet to be fully elucidated. Here, we investigated the behavior of As during reductive dissolution of As(V)-bearing jarosite by a pure sulfate reducing bacterium with or without dissolved SO42- amendment. Changes of aqueous chemistry, mineralogical characteristics, and As speciation were examined in batch experiments. The results indicated that jarosite was mostly replaced by mackinawite in the system with added SO42-. In the medium without additional SO42-, mackinawite, vivianite, pyrite, and magnetite formed as secondary Fe minerals, though 24.55 % of total Fe was in form of an aqueous Fe2+ phase. The produced Fe2+ in turn catalyzed the transformation of jarosite. At the end of the incubation, 41.99 % and 48.10 % of As in the solid phase got released into the aqueous phase in the systems with and without added SO42-, respectively. The addition of dissolved SO42- mitigated the mobilization of As into the aqueous phase. In addition, all As5+ on the solid surface was reduced to As3+ during the microbial sulfidization of As-bearing jarosite. These findings are important for a better understanding of geochemical cycling of elements As, S, and Fe in acid mine drainage and acid sulfate soil environments.Most of the permanent hair dye products contain p-phenylenediamine (PPD), a well-known skin sensitizer. PPD may cause cutaneous reactions and leads to allergic contact dermatitis (ACD), a condition with major medical and financial repercussions. Hair dye-induced ACD represents a growing concern both for consumers and the cosmetics industry. In this study we introduced novel side chains on the PPD molecule with the goal of overcoming the hazard potential of PPD. Our strategy relies on the replacement of the colorless PPD with new, larger and intrinsically colorled PPD derivatives to reduce dermal penetration and thus the skin sensitization potential. We synthesized two oligomers with bulky side-chains, which displayed 7-8 times lower cytotoxicity than PPD, a significantly weaker sensitization potential (22.0 % and 23.8 % versus 55.5 % for PPD) in the Direct Peptide Reactivity Assay, minimal cumulative penetration through excised skin and an intrinsic ability to colour and preserve the nuance when applied on bleached hair. The lower skin permeation and sensitizing potential are absolutely crucial and give a clear advantage of our products over other standards. These novel PPD hair dyes show significantly less hazard potential than PPD and may, upon further risk assessment studies, replace PPD in consumer care products.A novel 2D/3D Z-scheme g-C3N4/SnS2 photocatalyst was successfully fabricated via self-assembly forming 3D flower-like SnS2 microspheres on the surface of the 2D g-C3N4 nanosheets. find more The photocatalytic performances of the samples were systematically explored through catalytic reduction of Cr6+ and oxidation of Bisphenol S (BPS) under the illumination of visible light, and the photocatalytic degradation pathway of BPS was also proposed based on the degradation products confirmed by GCMS. Among the as-prepared samples, 0.4-g-C3N4/SnS2 exhibited the most efficient photocatalytic performances, and the apparent quantum efficiency (QE) for the removal of Cr6+ could achieve 30.3 %, which is 2.8 times higher than that of the SnS2. The enhancing photocatalytic activities originated from the efficient interfacial charge migration and separation obtained in g-C3N4/SnS2, which was firstly verified via the photoluminescence spectra, time-resolved photoluminescence spectra and photoelectrochemical characterizations. Importantly, the DFT calculated shows that the band distribution of the g-C3N4/SnS2 sample is staggered near the forbidden, which can facilitate the efficient interfacial charge migration and separation as well as result in the improvement of the catalytic activity.
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