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The used signal precision models were built from previously observed repeatability variation throughout the calibration interval adjusted to daily precision condition from a residual standard deviation adjustment factor. This approach was implemented in a user-friendly MS-Excel file and was successfully applied to the analysis of As, Cd, Ni and Pb in marine sediment extracts by Absorption Spectroscopy. Evaluations were tested by the metrological compatibility of estimated and reference values of control standards for confidence levels of 95% and 99%. The success rates of the compatibility tests were statistically equivalent to the confidence level (p-value>0.01).Herein, MgO cathode and graphene Mn-Ce bimetallic oxide were utilized to jointly enhance the removal of toluene in pulsed discharge plasma (PDP). Compared to the common cathode, the MgO cathode enhanced the density of high energy electrons, and then induced to higher removal of toluene. However, the removal of toluene by PDP/MgO system was still insufficient, and there was a large amount of underutilized O3 in the products. Based on this, Mn-Ce/graphene catalysts were introduced into PDP/MgO system. The Mn-Ce (81)/graphene catalyst had the highest catalytic activity. Under the discharge power of 2.1 W, toluene degradation rate and CO2 selectivity increased by 27.5% and 22.0%, respectively. This was ascribed to the synergistic effect of the solid solution formed between MnOx and CeOx, increasing the proportion of Oads on the surface of the catalyst. The higher Oads/Olatt ratio lead to the better catalytic activity, which was conducive to the complete transformation of the intermediate products to CO2 and H2O. According to the detected products, the degradation pathway and the mechanism of toluene degradation were proposed finally. The PDP itself, field emission effect of MgO cathode and catalytic effect of Mn-Ce/graphene for jointly improve the toluene removal and CO2 selectivity.Due to the neutral charge of As(III) oxy-ions that make approaching the traditional adsorbent very improbable compared to the As(V) case, making it harder to be separated. To enhance the adsorption of As(Ш), the FeOOH coated cellulose acetate (CA) membrane doped with MnO2 nanoparticles (FeOOH@MnO2@CAM) was fabricated and then to removes As(Ш) in water through the synergistic effect of oxidation and adsorption, and the maximum adsorption capacity can reach 50.34 mg/g. Temsirolimus FeOOH@MnO2@CAM was fabricated with CA as a substrate by dipping-precipitation phase inversion and hydrothermal method. Langmuir and pseudo-second-order model showed that As(Ш) was adsorbed by chemical interactions through the monolayer and thermodynamic showed that As(Ш) adsorption was an exothermic and spontaneous process. The results of the pH study showed that as the pH increases from 3 to 11, the adsorption capacity of As(Ш) decreases from 50.34 to 14.32 mg/g, which was attributed to the acidic environment promoting the protonation of the surface of FeOOH@MnO2@CAM, which increases the electrostatic attraction, and the alkaline environment increases electrostatic repulsion due to deprotonation. The competitive ions exhibited the PO43- significantly reduce the adsorption capacity of As(Ш)，and as the PO43- content increases, the adsorption capacity of As(Ш) decreases from 29.76 to 18.57 mg/g, which was attributed to the similar chemical properties of PO43- and arsenate. Importantly, FeOOH@MnO2@CAM still maintains an adsorption capacity of 20.19 mg/g after seven cycles, demonstrating that it is a kind of environmentally friendly material to remove As(Ш) in the water environment.Ferrate (Fe(VI)) is usually effective for oxidizing a variety of organic pollutants within a few seconds, but some recalcitrant asorganophosphorus pesticides such as dimethoate require higher dose of Fe(VI) and inorganic phosphorus produced by mineralization is difficult to remove. In this study, acid-activated ferrate (Fe(VI)) was firstly used to degrade organophosphorus pesticides dimethoate and simultaneously remove total phosphorus (TP) from solution under simulated sunlight. At a Fe(VI)dimethoate molar radio of 151, dimethoate was almost completely removed within 20 min and 47% of TP in the solution was removed by the reduction product of Fe(VI) within 240 min. Electron paramagnetic resonance (EPR) and terephthalic acid (TA) fluorescence experiments showed that •OH radicals were continuously generated in the system, and •OH formation pathway was proposed. Importantly, the involvement of •OH in acid-activated Fe(VI) process was confirmed for the first time by EPR. In the acid-activated Fe(VI)/simulated sunlight system, the removal of dimethoate and TP gradually increased with the decrement of activation pH, whereas the increase of molar ratio of Fe(VI)dimethoate enhanced the removal of dimethoate and TP. The addition of inorganic anions (HCO3- and NO2-) had obvious inhibitory effects on dimethoate and TP removal. Eight degradation products including O,O,S-trimethylphosphorothiate, omethoate and 2-S-methyl-(N-methyl) acetamide were determined by gas chromatography mass spectrometry (GC-MS) analysis, and two possible degradation pathways were proposed. The insights gained from this study open a new avenue to simultaneously degrade and remove organic contaminants.The threat of antibiotics in the environment causing antibiotics resistance is a global health concern. Enzymes catalyze pollutant transformations, and how commercially available enzymes like horseradish peroxidase (HRP), with or without a redox mediator, may be used to degrade antibiotics in water treatment is of great interest. This work demonstrates tetracycline transformation by HRP, and how it is significantly enhanced by free radicals created from the mediator 2,2-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Water temperature and pH strongly influence the tetracycline removal rate due to their correlation with the enzyme activity, abundance and stability of ABTS•+. Four transformation products were identified in the pure HRP system using a liquid chromatography tandem mass spectrometry hybrid quadrupole-orbitrap mass spectrometer system. Addition of 25 μmol L-1 ABTS not only accelerated the degradation of tetracycline, but also expanded the range of degradation pathways. Potential tetracycline transformation pathways are proposed based on these observations, which include a range of mechanisms such as hydroxylation, demethylation, dehydration, decarbonylation and secondary alcohol oxidation.
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