Arsenic is a carcinogenic substance, with many cases of poisoning related to arsenic pollution in groundwater. In Taiwan arsenic in groundwater caused the notorious Blackfoot disease. Methods for arsenic removal from water include precipitation, membrane processes, ion exchange, and adsorption, but these processing technologies suffer from high investment costs and complex operations. The traditional adsorption method cannot be used for arsenic removal due to its high operating costs, difficulties in recovery, and low adsorption capacity. To address these issues, this study designed an adsorption material based on biochar for arsenic removal with higher adsorption properties and easy recovery. Biochar sources are readily available from waste wood as a cheap and environmentally friendly material. The efficiency of As (III) removal is also promoted by FeCl3 and KMnO4. The objectives of this research are to obtain optimum operation conditions by assessing the effects of different iron and manganese contents, different doses, different pH and different initial concentration. The adsorption mechanism between As (III) and biochar was studied by adsorption isotherms and the kinetic model. X-ray diffraction, energy-dispersive X-ray spectroscopy and elemental analyzer analysis results show that modified biochar has major elements of Fe and Mn. There is greater magnetism, 40 emu g− 1, in the modified biochar. The maximum adsorption efficiency of 81% and 0.72 mg g− 1 capacity occurs when the ratio of Mn, Fe and C is 4:1:1. The adsorption capacity is high under higher pH with pristine biochar and 1FeC under lower pH with 1Fe2MnC. The reaction mechanism is divided into four pathways. The first pathway is the attachment of As (III) ions into the pore of biochar via physical adsorption. In the second pathway, biochar can connect with As (III) through hydrogen bonding from the function group -OH in the biochar and the As (III) itself. In the third pathway, they can contact each other by electron force when the biochar surface is filled with a positive charge. In the fourth pathway, the compounds of manganese have strong oxidizability to oxidize As (III) to As(V). The iron ions then act as a bridge connecting the biochar and the As (III), resulting in the formation of new complex compounds.
While sustainable mobility and decarbonization of transportation sector are among the most comprehensive solutions to the problem of climate change, electric vehicles (EV) are becoming increasingly popular as the future mode of transport. In this study, the integration of a solar carport canopy to a potential EV charging station is analyzed using various operating conditions. A detailed analysis has been provided for the carport located in southern Taiwan, Kaohsiung city, where electricity generation, emission impacts, and financial analysis of the solar EV charging station are discussed. The results of a case study showed a potential of 140 MWh/year of solar energy yield, which could provide solar electricity of more than 3000 vehicles per month with 1-h parking time, generating 94% lower total carbon dioxide emission than the electricity produced from traditional grid methods. Taken into account the impact of carbon tax implementation on driver economics, the results demonstrated the viability of such photovoltaic (PV)-based charging stations, particularly for possible higher carbon tax scenarios in the future. The presented results can be implemented on a larger scale, offering guidelines and tools for constructing solar-powered EV charging station infrastructure.
Multilayer ZnO sheet-like flakes were synthesized by a simple method of precipitation and characterized by the techniques of X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The findings are proven that the SEM images show the overall morphology of a single sheet-like ZnO nanostructure made from uniformly thick nano-sheets. In an aqueous environment, the acoustic ability of the prepared material was assessed using ultrasound (US) radiation to degrade oxytetracycline (OTC) and norfloxacin (NF). To increase the degradation efficiency, a US/ZnO/peroxodisulfate system was developed by introducing ammonium persulfate ((NH4)2S2O8) and sodium persulfate (Na2S2O8), exhibiting excellent synergistic effects. Result show the decomposition efficiency for NF removal with Na2S2O8 (64%) appeared to be slightly better than with (NH4)2S2O8 (56%). By contrast, the ultrasonic catalytic efficiency of Na2S2O8 (98%) was slightly better than that of (NH4)2S2O8 (94%) for OTC removal. The addition of scavengers to the US/ZnO/peroxodisulfate system through the NF and OTC results in the largest effect of holes. The degradation is considered to be often caused by holes. In this system, the Na2S2O8 can have two roles to increase the rate of degradation: (1) The SO4− formed by Na2S2O8 under ultrasonic irradiation directly degraded to norfloxacin on ZnO surface; and (2) S2O82- behaved as an electron acceptor, inhibiting recombination of electron hole pairs, enabling the development of more ·OH. Therefore, the synergistic effect significantly increases US/ZnO/peroxodisulfate sonocatalytic activity (Hu, S.B., et al., 2017. Aqueous norfloxacin sonocatalytic degradation with multilayer flower-like ZnO in the presence of peroxydisulfate. Ultrasonics Sonochemistry, 38(1), pp.446–454).
1Graphene -titanium nanotube composites with different ratios of graphite oxide were prepared 2 via the hydrothermal method using ascorbic acid as a reducing agent. Properties of materials 3 were characterized by X-ray diffraction, fourier transform infrared spectroscopy, high resolution 4 transmission electron microscopy and UV-vis diffuse reflectance spectroscopy. The average 5 diameter of the titanium dioxide nanotubes was about 8nm. The photoresponse of 6 nanocomposites have been extended to visible-light regions. In addition, graphene-titanium 7 nanotube composites showed higher photocatalytic degradation efficiency for reactive black 5 8 (RBK5) than pure titanium dioxide and the 15%graphene -titanium nanotube composites 9 catalysts possessed the best photocatalytic activity. The degradation efficiency for RBK5 dyes 10 increased with increased dosage of graphite oxide from 3%-15% and decreased with increasing 11 initial RBK5 concentration. This paper not only reports the fabrication of highly active 12 photocatalysts but also provides insight into the photocatalytic mechanism of graphene-titanium 13 nanotube composites. 14 Keywords: TiO 2 nanotube, Graphene, Visible light, RBK5 15 16 Downloaded by [University of Montana] at 16:35 14 December 2014
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