Direct Hydraulic Parameter and Function Estimation for Diverse Soil Types Under Infiltration and Evaporation

A new computationally efficient direct method is applied to estimating unsaturated hydraulic properties during steady-state infiltration and evaporation at soil surface. For different soil types with homogeneous and layered heterogeneity, soil hydraulic parameters and unsaturated conductivities are estimated. Unlike the traditional indirect inversion method, the direct method does not require forward simulations to assess the measurement-to-model fit; thus, the knowledge of model boundary conditions (BC) is not required. Instead, the method employs a set of local approximate solutions to impose continuity of pressure head and soil water fluxes throughout the inversion domain, while measurements act to condition these solutions. Given sufficient measurements, it yields a well-posed system of nonlinear equations that can be solved with optimization in a single step and is thus computationally efficient. For both Gardner’s and van Genuchten’s soil water models, unsaturated hydraulic conductivities and pressure heads (including the unknown BC) can be accurately recovered. When increasing measurement errors are imposed, inversion becomes less accurate, but the solution is stable, i.e., estimation errors remain bounded. Moreover, when the unsaturated conductivity model is known, inversion can recover its parameters; if it is unknown, inversion can recover a nonparametric, piecewise continuous function to which soil parameters can be obtained via fitting. Overall, inversion accuracy of the direct method is influenced by (1) measurement density and errors; (2) rate of infiltration or evaporation; (3) variation of the unsaturated conductivity; (4) flow direction; (5) the number of soil layers.     

An efficient synthesis of 2-(guaiazulen-1-yl)furan derivatives via intramolecular Wittig reactions

An efficient and mild synthesis of 2-(guaiazulen-1-yl)furans,starting from easily accessible 1-(3-aryl-2-cyanopropenoyl) guaiazulenes,tributylphosphine and acyl chlorides,is described.The strategy employs the intramolecular Wittig protocol as a key step to append the crticial furan ring,leading to the highly functional furans in good yields.     

Magnetic separation of heavy metal ions and evaluation based on surface‐enhanced Raman spectroscopy: Copper(II) ions as a case study

A new approach was developed for the magnetic separation of copper(II) ions with easy operation and high efficiency. p‐Mercaptobenzoic acid served as the modified tag of Fe₂O₃@Au nanoparticles both for the chelation ligand and Raman reporter. Through the chelation between the copper(II) ions and carboxyl groups on the gold shell, the Fe₂O₃@Au nanoparticles aggregated to form networks that were enriched and separated from the solution by a magnet. A significant decrease in the concentration of copper(II) ions in the supernatant solution was observed. An extremely sensitive method based on surface‐enhanced Raman spectroscopy was employed to detect free copper(II) ions that remained after the magnetic separation, and thus to evaluate the separation efficiency. The results indicated the intensities of the surface‐enhanced Raman spectroscopy bands from p‐mercaptobenzoic acid were dependent on the concentration of copper(II) ions, and the concentration was decreased by several orders of magnitude after the magnetic separation. The present protocol effectively decreased the total amount of heavy metal ions in the solution. This approach opens a potential application in the magnetic separation and highly sensitive detection of heavy metal ions.     

Dispersive liquid–liquid microextraction combined with online preconcentration MEKC for the determination of some phenoxyacetic acids in drinking water

A fast and simple technique composed of dispersive liquid–liquid microextraction (DLLME) and online preconcentration MEKC with diode array detection was developed for the determination of four phenoxyacetic acids, 2,4,5‐trichlorophenoxyacetic acid, 2,4‐dichlorophenoxyacetic acid, 2,6‐dichlorophenoxyacetic acid, and 4‐chlorophenoxyacetic acid, in drinking water. The four phenoxyacetic acids were separated in reversed‐migration MEKC to the baseline. About 145‐fold increases in detection sensitivity were observed with online concentration strategy, compared with standard hydrodynamic injection (5 s at 25 mbar pressure). LODs ranged from 0.002 to 0.005 mg/L using only the online preconcentration procedures without any offline concentration of the extract. A DLLME procedure was used in combination with the proposed online preconcentration strategies, which achieved the determination of analytes at limits of quantification ranging from 0.2 to 0.5 μg/kg, which is far lower than the maximum residue limits established by China. The satisfactory recoveries obtained by DLMME spiked at two levels ranged from 67.2 to 99.4% with RSD <15%, making this proposed method suitable for the determination of phenoxyacetic acids in water samples.