Development of a stir bar sorptive extraction method coupled to solidification of floating droplets dispersive liquid–liquid microextraction based on deep eutectic solvents for the extraction of acidic pesticides from tomato samples

A stir bar sorptive extraction method coupled with deep eutectic solvent based solidification of floating organic droplets–dispersive liquid–liquid microextraction has been used for the simultaneous derivatization and extraction of some acidic pesticides in tomato samples. In this method, initially the analytes are adsorbed on a coated stir bar from tomato juice filled in a narrow tube. After extraction, the stir bar is removed and a water–miscible deep eutectic solvent is used to elute the analytes. Afterward, a derivatization agent and a water–immiscible deep eutectic solvent (as an extraction solvent) with melting point near to room temperature are added to the obtained eluant at µL–levels and the obtained mixture is rapidly injected into deionized water. Under the optimum conditions, the introduced method indicated high enhancement (1543–3353) and enrichment (2530–2999) factors, low limits of detection (7–14 ng/L) and quantification (23–47 ng/L), good linearity (r² ≥ 0.9982), and satisfactory repeatabilities (relative standard deviation ≤12% for intra– and inter–day precisions at a concentration of 100 ng/L of each analyte). Finally, the proposed method was applied in analysis of the analytes in tomato samples.     

Synthesis of Iridium Oxide Nanotubes by Electrodeposition into Polycarbonate Template: Fabrication of Chromium(III) and Arsenic(III) Electrochemical Sensor

For the first time iridium oxide (IrO₂) nanotubes are synthesized by electrodeposition in a polycarbonate (PC) template. Potential cycling (90 cycles) between 0.0 and 0.9 V is used for the preparation of IrO_x nanotubes onto the PC template with a pore diameter of 100 nm. Field‐emission scanning electron microscopy (FESEM) images show, that IrO₂ nanotubes with uniform diameters of 110±10 nm and an estimated length of 1–3 µm are formed. The electrochemical properties and the electrocatalytic activity of a glassy carbon‐IrO_x nanotube modified electrode toward Cr³⁺ and As³⁺ oxidation are investigated. Finally, the modified electrode is used for micromolar detection of the proposed analytes using differential pulse voltammetry.     

Polyol‐enhanced dispersive liquid–liquid microextraction coupled with gas chromatography and nitrogen phosphorous detection for the determination of organophosphorus pesticides from aqueous samples,fruit juices,and vegetables

Polyol‐enhanced dispersive liquid–liquid microextraction has been proposed for the extraction and preconcentration of some organophosphorus pesticides from different samples. In the present study, a high volume of an aqueous phase containing a polyol (sorbitol) is prepared and then a disperser solvent along with an extraction solvent is rapidly injected into it. Sorbitol showed the best results and it was more effective on the extraction recoveries of the analytes than inorganic salts such as sodium chloride, potassium chloride, and sodium sulfate. Under the optimum extraction conditions, the method showed low limits of detection and quantification within the ranges of 12–56 and 44–162 pg/mL, respectively. Enrichment factors and extraction recoveries were in the ranges of 2799–3033 and 84–92%, respectively. The method precision was evaluated at a concentration of 10 ng/mL of each analyte, and relative standard deviations were found to be less than 5.9% for intraday (n = 6) and less than 7.8% for interday (n = 4). Finally, some aqueous samples were successfully analyzed using the proposed method and four analytes (diazinon, dimethoate, chlorpyrifos, and phosalone) were determined, some of them at ng/mL level.     

An ultra-small heterostructure wavelength division multiplexer (WDM) with the ability to select two wavelengths from the s-band

In this article, a photonic crystal channel drop filter (CDF) based on \(2\times 3\) ring resonators is presented. At first, the effects of changing the radius of lattice rods and the lattice dielectric constant on the dropping efficiency of a 3-port CDF with one resonator are investigated. Then by developing this base structure, a new 4-port heterostructure CDF composed of two regions with rods made of silicone and germanium is presented, which can operate in the ‘S’ band of the communication window. The photonic crystal heterostructure CDF consists of a horizontal waveguide and two ring resonators that have been installed, in symmetry to the horizontal axis, in two regions with different refractive indices. These ring resonators act as energy couplers and capture at their resonant frequencies the electromagnetic energy which is propagated in the bus waveguide. For the analysis of transmission characteristics and the band structure of the filter, two methods have been employed: the two-dimensional Finite–difference time domain method and the Plane Wave Expansion method. In the final structure, dropping efficiencies of 97 and 89 % can be achieved at ports D and B, respectively, and also an acceptable quality factor can be obtained in the communication window. The overall size of this device is 174.14  \(\upmu \hbox {m}^{2}\) . Due to its small size, this structure can be used in Wavelength Division Multiplexer applications in the Optical Integrated Circuits.     

Renewable sol-gel carbon ceramic electrodes modified with a Ru-complex for the amperometric detection of l-cysteine and glutathione

A renewable three-dimensional chemically modified carbon ceramic electrode containing Ru [(tpy)(bpy)Cl] PF₆ was constructed by sol-gel technique. It exhibits an excellent electro-catalytic activity for oxidation of l-cysteine and glutathione at pH range 2-8. Cyclic voltammetry was employed to characterize the electrochemical behavior of the chemically modified electrode. The electrocatalytic behavior is further exploited as a sensitive detection scheme for l-cysteine and glutathione by hydrodynamic amperometry. Optimum pH value for detection is 2 for both l-cysteine and glutathione. The catalytic rate constants for l-cysteine and glutathione were determined, which were about 2.1×10³ and 2.5×10³ M⁻¹ s⁻¹, respectively. Under the optimized condition the calibration curves are linear in the concentration range 5-685 and 5-700 μM for l-cysteine and glutathione determination, respectively. The detection limit (S/N=3) and sensitivity is 1 μM, 5 nA/μM for l-cysteine and 1 μM, 7.8 nA/μM for glutathione. The relative standard deviation (RSD) for the amperogram's currents with five injections of l-cysteine or glutathione at concentration range of linear calibration is <1.5%. The advantages of this amperometric detector are: high sensitivity, good catalytic effect, short response time (t<3 s), remarkable long-term stability, simplicity of preparation and reproducibility of surface fouling (RSD for six successive polishing is 3.31%). This sensor can be used as a chromatographic detector for analysis of l-cysteine and glutathione.     

A Three‐Step Method for the Deposition of Large Cuboids of Organic–Inorganic Perovskite and Application in Solar Cells

A three‐step method for the deposition of CH₃NH₃PbI₃ perovskite films with a high crystalline structure and large cuboid overlayer morphology is reported. The method includes PbI₂ deposition, which is followed by dipping into a solution of C₄H₉NH₃I (BAI) and (BA)₂PbI₄ perovskite formation. In the final step, the poorly thermodynamically stable (BA)₂PbI₄ phase converts into the more stable CH₃NH₃PbI₃ perovskite by dipping into a solution of CH₃NH₃I. The final product is characterized by XRD, SEM, UV/Vis, and photoluminescence analysis methods. The experimental results indicate that the prepared perovskite has cuboids with high crystallinity and large sizes (up to 1 μm), as confirmed by XRD and SEM data. Photovoltaic investigations show that the three‐step method results in higher solar cell efficiency (15 % enhancement in efficiency) with a better reproducibility than the conventional two‐step deposition method.     

Highly sensitive carbon paste electrode with silver-filled carbon nanotubes as a sensing element for determination of free cyanide ion in aqueous solutions

We report on newly synthesized Ag(I)-filled multiwall carbon nanotubes as a potential sensing element in ion-selective carbon paste electrodes for the determination of free cyanide in aqueous solution. The electrode was obtained by entrapping the silver-filled nanotubes into a carbon paste and displays a Nernstian response with a slope of 59.8?±?0.3?mV decade^?1, a very wide linear range (from 21.0?nM to 0.1?M of cyanide), a lower detection limit of 13.0?nM, and a response time of <2?min. The operational lifetime is up to 3?months without significant deviation in normal function.

Radiation induced polymerization of vinyl monomers and their application for preparation of wood-polymer composites

Polymerizing effects of high energy radiation has been found suitable for preparation of wood-polymer composites. In the present work after evaluating polymer products that have been obtained by irradiation method, wood-polymer composites have been prepared by in situ polymerization of vinyl acetate, acrylic acid and acrylic acid/styrene mixture using two samples of Iranian hardwoods, Beech and Hornbeam. These woods and their composites have been tested for their physical and mechanical properties. The results have shown that chemical bonding between polymer and the cell wall component lead to better strength properties in the composites.     

On the range of influences in back-circulant Latin squares

In this note we obtain a large lower bound for the index of a certain critical set in the back-circulant Latin squares of odd order. This resolves in the negative a conjecture of Fitina, Seberry and Chaudhry [Back-circulant Latin square and the influence of a set, Austral. J. Combin. 20 (1999) 163-180].