It is promising for internet-of-things (IOT) sensing networks or even wearables for personal exposure assessment.Xuan-paper waste residue (XPWR) is an unfamiliar and unique solid waste in China, which caused serious environmental pollution and waste of resources. Therefore, it is extremely important to explore the characteristics of XPWR and its application. In this paper, XPWR was analyzed and used as a reinforcing filler to prepare red mud/waste polyethylene/Xuan-paper waste residue (RM/WPE/XPWR) composites by molding method at 160 °C with a pressure of 10 MPa for 5-10 min. There were about 27 wt% of mineral particles and 63 wt% of organic fibers in XPWR, indicating that XPWR can be used as a reinforcing filler. When 60 wt% of XPWR was added in RM/WPE, the bending strength reached 71.81 MPa, which surpassed 43.08 % than that of RM/WPE. Besides, the addition of XPWR increased the water absorption of the composites and helped to promote the crystallization of the composites. This work presented the characteristics of XPWR and provided a new way to use XPWR.To recover the spent vanadium compound, Rhodamine-B-based Schiff's base ligand (L1) was synthesized via ultrasonication process and was evaluated with vanadyl sulfate (VOSO4), which has shown considerable selectivity towards V(IV). The change of the solution color from colorless to pink is attributed to L1 after the reaction with vanadium ion owing to the successful formation of the vanadium complex and the opening of the spirolactam ring in the L1 structure. In FT-IR spectra, the vanadyl peaks are co-existed with the L1 structure, which confirmed the complex formation of the L1 with vanadium. Similarly, the binding energy of V(IV) was identified at 516.2 eV for V2p3/2 in XPS spectra. https://www.selleckchem.com/mTOR.html The new strategy for VOSO4 recovery was established through solvent extraction and acid leaching. After recovery process, the absence of vanadium peak in the XPS confirmed the complete removal of V(IV) from the complex. The recovered VOSO4 solution used as an electrolyte in vanadium redox flow battery (VRFB) systems, where the unit cell performance is comparable with the conventional electrolyte solution. The advantage of study is reuse of VOSO4 as a resource for energy storage applications.In this study, magnetic material based reduced graphene oxide (M-rGO) was prepared through co-precipitation and displayed high catalytic efficiency together with persulfate (PS) for simultaneous p-arsanilic acid (p-ASA) decomposition and arsenic removal. Linear sweep voltammetry and chronoamperometric measurements with M-rGO revealed that PS was effectively bound to M-rGO surface and probably formed charge transfer complex, in which M-rGO was pivotal in mediating facile electron transfer. The effects of pH, temperatures, anions, p-ASA concentration, PS, and M-rGO dosages on p-ASA decomposition were studied in the system. Excellent degradation of p-ASA was carried out at a wide range of pH values, which was unattainable by other Fenton-like processes. Under optimal conditions, M-rGO exhibited prominent removal of both p-ASA (98.8 %) and inorganic arsenic (89.8 %). M-rGO had reasonably excellent repeatability and stability, and 77.7 % p-ASA degraded in the third recovered catalyst. The advantages of environmental friendliness, short reaction time, and straightforward synthesis of M-rGO will facilitate the development of heterogeneous Fenton-like catalysts under neutral conditions.Trace element contamination from abandoned mine sites is a major threat to the environment. The distribution of trace elements in various particle size fractions of soils from abandoned mine sites plays a critical role in designing remediation approaches. This study investigated the geochemical distribution of trace element enrichment and mineralogical composition in various particle size fractions from contrasting abandoned mine sites (Webbs Consols, Halls Peak and Mole River, Australia). Results revealed that arsenic and other element concentrations increased with decreasing particle size for samples from Webbs Consols and Halls Peak. The highest arsenic (3.05%), lead (3.23%) and zinc (1110 mg/kg) were found in the finest fraction ( less then 0.053 mm). In Mole River, the highest concentration of arsenic (10.8%), lead (209 mg/kg) and zinc (351 mg/kg) were observed in coarse fractions. Arsenic fractionation by sequential extraction showed that arsenic was strongly associated with the amorphous and crystalline iron phases. X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies revealed that tooeleite (a ferric arsenite mineral, also confirmed by Transmission electron microscopy (TEM)), arsenopyrite, scorodite and arsenolite were the dominant arsenic minerals. The study showed elevated levels of arsenic bearing minerals across particle sizes which has significant implications for remediation approaches at abandoned mine sites.Graphene oxide (GO) as the most studied hydrophilic graphene derivative can be deployed in a broad spectrum of environmental technologies opening the issue of its ecotoxicity. Nevertheless, the information about its behavior in complex aquatic environment is still not sufficient. Here, we studied the interaction of three differently oxidized GO systems with planktonic and benthic crustaceans. By standard toxicity tests, we observed the importance of feeding strategy as well as the surface oxidation of GO with respect to GO's ecotoxicity. However, to gain a clearer insight into GO's environmental fate, we introduced a pre-treatment with algae as the most common source of food for crustaceans. Such an adjustment mimicking the conditions in real aquatic ecosystems resulted in complete mitigation of acute toxicity of GOs to all organisms and, more importantly, to the eradication of oxidative stress caused by GOs. We argue, that the pre-exposition of food is a crucial factor in GO's overall environmental fate, even though this fact has been completely neglected in recent studies. These experiments proved that GO is not a hazardous material in complex aquatic environments because its acute toxicity can be successfully mitigated through the interaction with algae even at very high concentrations (25 mg/L).