This report describes a rapid, onsite method to analyze the dichlorvos pesticide in water. Dichlorvos is a broad-spectrum pesticide that has been used worldwide. As an organophosphorus pesticide, dichlorvos disrupts the nervous system by inhibiting the activity of acetyl cholinesterase. Traditional analysis of dichlorvos by chromatography is time-consuming and environmentally unfriendly. Therefore, rapid, on-site methods to analyze dichlorvos are needed. Here, we used for the first time Fourier transform near infrared spectroscopy combined with partial least square-discriminant analysis to determine the dichlorvos directly in water samples. Results were compared with traditional high-performance liquid chromatography data as reference. We found that over 9,000–8,333?cm?1, the new method had a good performance with a classification accuracy of 100?% and a correlation coefficient of 0.92 between measured and reference data. The new method can also be used as a “concentration sieve” by setting up different levels of boundary, a parameter of partial least square-discriminant analysis, thus allowing rapid on-site screening. 相似文献
Urea synthesis, currently the largest use of carbon dioxide in organic synthesis, is conventionally operated at high pressure and high temperature. Here, we report for the first time that urea forms at atmosphere and ambient temperatures by negative corona discharge in gas phase. The conversion of CO2 and yields of a solid mixture of urea and ammonium carbamate, which was identified by the 13C NMR spectrum, rise with reducing temperatures and increasing molar ratios of NH3/CO2 and discharge frequencies. The conversion of carbon dioxide was found to be 82.16?% at 20?°C and 1?atm with a molar flow ratio of n(NH3)/n(CO2) of 2.5. High pressure and high temperature as energy inputs are not necessary. 相似文献
We designed photoelectrochemical cells to achieve efficient oxidation of rhodamine B (RhB) without the need for photocatalyst or supporting electrolyte. RhB, the metal anode/cathode, and O2 formed an energy-relay structure, enabling the efficient formation of O2– species under ultraviolet illumination. In a single-compartment cell (S cell) containing a titanium (Ti) anode, Ti cathode, and 10 mg·mL–1 RhB in water, the zero-order rate constant of the photoelectrochemical oxidation (kPEC) of RhB was 0.049 mg·L–1·min–1, while those of the photochemical and electrochemical oxidations of RhB were nearly zero. kPEC remained almost the same when 0.5 mol·L–1 Na2SO4 was included in the reactive solution, regardless of the increase in the photocurrent of the S cell. The kPEC of the illuminated anode compartment in the two-compartment cell, including a Ti anode, Ti cathode, and 10 mg·mL–1 RhB in water, was higher than that of the S cell. These results support a simple, eco-friendly, and energysaving method to realize the efficient degradation of RhB.