Knapplehmann6907

The present study defines a novel green method for the synthesis of the nickel oxide nanocatalyst by using an aqueous latex extract of the Ficus elastic. The catalyst was examined for the conversion of novel Brachychiton populneus seed oil (BPSO) into biodiesel. The Brachychiton populneus seeds have a higher oil content (41 wt%) and free fatty acid value (3.8 mg KOH/g). The synthesised green nanocatalyst was examined by the Fourier transform infrared (FT-IR) spectroscopy, energy dispersive X-Ray (EDX) spectroscopy, X-Ray diffraction (XRD) spectroscopy and scanning electron microscopy (SEM). The obtained results show that the synthesised green nanocatalyst was 22-26 nm in diameter and spherical-cubic in shape with a higher rate of catalytic efficiency. It was utilised further for the conversion of BPSO into biofuel. Due to the high free fatty acid value, the biodiesel was synthesised by the two-step process, i.e., pretreatment of the BPSO by means of acid esterification and then followed by the transesterification reaction. MLi-2 mw The acidic catalyst (H2SO4) was used for the pretreatment of BPSO. The optimum condition for the transesterification of the pretreated BPSO was 19 of oil-methanol molar ratio, 2.5 wt % of prepared nanocatalyst concentration and 85 °C of reaction temperature corresponding to the highest biodiesel yield of 97.5 wt%. The synthesised biodiesel was analysed by the FT-IR and GC-MS technique to determine the chemical composition of fatty acid methyl esters. Fuel properties of Brachychiton populneus seed oil biodiesel (BPSOB) were also examined, compared, and it falls in the prescribed range of ASTM standards.Wastewater treatment plants (WWTPs) are important routes for releasing microplastics into the environment, with the produced sludge acting as a recipient of microplastics from wastewater. There is little information on the impact of sludge processes on the number of microplastics in sludge. In this study, the presence of microplastics in sludge produced by the Sari WWTP in northern Iran was investigated. Samples were taken in 3 replications and microplastics larger than 37 μm were extracted. The sludge from primary settling tank, clarifier, after sludge thickener and after aerobic digester, and after dewatering contained 214, 206, 200, 238, and 129 microplastics/g dry weight, respectively. According to the amount of sludge produced for each unit, this equals 280, 362, 599, 601, and 276 million microplastics/day, respectively, of which more than 85% were fibers. The numbers of microplastics in the sludge from the output of the sludge thickener and the aerobic digester did not significantly differ. However, their numbers decreased by more than 50% after dewatering, probably due to the destruction of flocs in the digestive process and the release of attached microplastics, which are returned into the wastewater treatment process with the rejected water. Polyester and polyethylene were the predominant types of fibers and particles, respectively. Given the annual amount of sludge produced, more than 100 billion microplastics enter the environment per year. Wastewater sludge, therefore, is an important source for the emission of microplastics, especially fibers, to the environment, warranting further evaluation of the associated environmental hazards.Photocatalytic systems comprising a hydrogenase-type catalyst and CdX (X = S, Se, Te) chalcogenide quantum dot (QD) photosensitizers show extraordinary hydrogen production rates under visible light excitation. What remains unknown is the mechanism of energy conversion in these systems. Here, we have explored this question by comparing the performance of two QD sensitizers, CdSe and CdTe, in photocatalytic systems featuring aqueous suspensions of a [Fe2 (μ-1,2-benzenedithiolate) CO6] catalyst and an ascorbic acid sacrificial agent. Overall, the hydrogen production yield for CdSe-sensitized reactions QDs was found to be 13 times greater than that of CdTe counterparts. According to emission quenching experiments, an enhanced performance of CdSe sensitizers reflected a greater rate of electron transfer from the ascorbic acid (kAsc). The observed difference in the QD-ascorbic acid charge transfer rates between the two QD materials was consistent with respective driving forces for these systems.The construction of a photoanode with several layers of titanium oxysulfate as a precursor to form titanium dioxide-TiO2 on boron doped diamond-BDD (TiO2/BDD), and its application for the photoelectro-degradation of glyphosate in aqueous medium are presented. The study was divided into three stages i) optimization of the number of layers of the TiO2 precursor to modify BDD using a novel method combining Sol-gel/Spin-Coating; ii) characterization of the TiO2/BDD electrodes, by scanning electron microscopy-SEM, dispersive energy spectroscopy-EDX, Ray diffraction-XRD, contact angle, and electrochemical response by cyclic voltammetry using [Fe(CN)6]3-/4- system; iii) degradation of glyphosate (50 mg L-1) by electrochemical oxidation on BDD and photoelectrocatalysis on TiO2/BDD in dark and UV-light conditions, at different current densities, for 5 h. The glyphosate degradation and mineralization were evaluated by High-Performance Liquid Chromatography, Total Organic Carbon, Chemical Oxygen Demand and inorganic-ions concentration (NO3-, PO43-, and NH4+). Also, the aminomethylphosphonic acid-AMPA was quantified by HPLC, as a degradation intermediate. Using five layers of the TiO2 precursor, in the construction of TiO2/BDD photoanode, and a lower contact angle, greater photoelectrocatalysis against the [Fe(CN)6]3-/4- redox system and better degradation of glyphosate compared to BDD without modification were achieved. The formation of TiO2 nanoparticles (14.79 ± 3.43 nm) in anatase phase on BDD was verified by SEM and XRD. Additionally, glyphosate degradation and mineralization were 2.3 times faster by photoelectrocatalysis on TiO2/BDD, relative to BDD, at 3 mA cm-2 and UV-light. Thus, the presence of TiO2 on BDD increases the rate and efficiency of glyphosate degradation with respect to electrochemical oxidation on BDD.