Very-high-resolution tandem Fabry-Perot etalon cylindrical beam volume hologram spectrometer for diffuse source spectroscopy

We demonstrate a compact and slitless spectrometer with high resolution formed by cascading a Fabry-Perot etalon (FPE) and a cylindrical beam volume hologram (CBVH). The most significant advantage of this combined spectrometer is that we can independently encode spectral information of a diffuse beam in a 2D plane. Also, we show that in this slitless configuration we can simultaneously benefit from the advantages of both elements: the high resolution of the FPE and the large spectral range of the CBVH. Here, we report on the experimental demonstration of a spectrometer with better than 0.2 nm resolution.     

Manufacture and Characterization of Poly (butylene terephthalate) Nanofibers by Electrospinning

Poly (butylene terephthalate) (PBT) nanofiber mats were prepared by electrospinning, being directly deposited in the form of a random fibers web. The effect of changing processing parameters such as solution concentration and electrospinning voltage on the morphology of the electrospun PBT nanofibers was investigated with scanning electron microscopy (SEM). The electrospun fibers diameter increased with rising concentration and decreased by increasing the electrospinning voltage, thermal and mechanical properties of electrospun fibers were characterized by DSC and tensile testing, respectively.     

An electrochemical sensor based on octahedral composite modified glassy carbon electrode for voltammetric detection of cocaine

The current work aimed to fabricate a new cocaine sensor of octahedral palladium-doped cobaltite composite (Oh-Pd²⁺ : Co₃O₄-C) using a simple hydrothermal protocol. As-fabricated cocaine sensing approach was validated by various methods. Energy dispersive X-ray analysis, X-ray diffraction and scanning electron microscopy were recruited to characterize our charged modified composite. The electrode could sensitively detect cocaine, with a lengthy linear range (0.01 μM–900.0 μM) and a limit of detection (1.3 nM). The quantitative cocaine determination was achieved in the biological specimens using our modified electrode, the results of which displayed admirable outcomes.     

Correction to: Comparing the performance of a CI engine after replacing the mechanical injector with a common rail solenoid injector

Journal of Thermal Analysis and Calorimetry - Unfortunately, in the original publication of the article the second author’s first name was inadvertently misspelled     

Correction to: An experimental investigation of the injection timing effect on the combustion phasing and emissions in reactivity-controlled compression ignition (RCCI) engine

Journal of Thermal Analysis and Calorimetry - Unfortunately, in the original publication of the article the second author’s first name was inadvertently misspelled. The corrected author name...     

Synthesis and characterizations of ultra-small ZnS and Zn(1-x)Fe(x)S quantum dots in aqueous media and spectroscopic study of their interactions with bovine serum albumin

This work reports a new experimental methodology for the synthesis of ultra small zinc sulfide and iron doped zinc sulfide quantum dots in aqueous media. The nanoparticles were obtained using a simple procedure based on the precipitation of ZnS in aqueous solution in the presence of 2-mercaptoethanol as a capping agent, at room temperature. The effect of Fe(3+) ion concentration as dopant on the optical properties of ZnS was studied. The size of quantum dots was determined to be about 1nm, using scanning tunneling microscopy. The synthesized nanoparticles were characterized by X-ray diffraction, UV-Vis absorption and photoluminescence emission spectroscopies. The presence and amount of iron impurity in the structure of Zn((1-x))Fe(x)S nanocrystals were confirmed by atomic absorption spectrometry. A blue shift in band-gap of ZnS was observed upon increasing incorporation of Fe(3+) ion in the iron doped zinc sulfide quantum dots. The photoluminescence investigations showed that, in the case of iron doped ZnS nanoparticles, the emission band of pure ZnS nanoparticles at 427nm shifts to 442nm with appearance of a new sharp emission band around 532nm. The X-ray diffraction analysis indicated that the iron doped nanoparticles are crystalline, with cubic zinc blend structure, having particle diameters of 1.7±022nm. Finally, the interaction of the synthesized nanoparticles with bovine serum albumin was investigated at pH 7.2. The UV-Vis absorption and fluorescence spectroscopic methods were applied to compare the optical properties of pure and iron doped ZnS quantum dots upon interaction with BSA. It was proved that, in both cases, the fluorescence quenching of BSA by the quantum dots is mainly a result of the formation of QDs-BSA complex in solution. In the steady-state fluorescence studies, the interaction parameters including binding constants (K(a)), number of binding sites (n), quenching constants ( [Formula: see text] ), and bimolecular quenching rate constants (k(q)) were determined at three different temperatures and the results were then used to evaluate the corresponding thermodynamic parameters ΔH, ΔS and ΔG.     

Reprint of: Extraction of fluoxetine from aquatic and urine samples using sodium dodecyl sulfate-coated iron oxide magnetic nanoparticles followed by spectrofluorimetric determination

A new method based on the combination of magnetic solid phase extraction (MSPE) and spectrofluorimetric determination was developed for isolation and preconcentration of fluoxetine form aquatic and biological samples using sodium dodecyl sulfate (SDS) coated Fe₃O₄ nanoparticles (NPs) as a sorbent. The unique properties of Fe₃O₄ NPs including high surface area and strong magnetism were utilized effectively in the MSPE process. Effect of different parameters influencing the extraction efficiency of fluoxetine including the amount of Fe₃O₄ and SDS, pH value, sample volume, extraction time, desorption solvent and time were optimized. Under optimized condition, the method was successfully applied to the extraction of fluoxetine from water and urine samples and absolute recovery amount of 85%, detection limit of 20 μg L⁻¹ and a relative standard deviation (RSD) of 1.4% were obtained. The method linear response was over a range of 50–1000 μg L⁻¹ with R² = 0.9968. The relative recovery in different aquatic and urine matrices were investigated and values of 80% to 104% were obtained. The whole procedure showed to be conveniently fast, efficient and economical for extraction of fluoxetine from environmental and biological samples.     

Evaluating flood extent mapping of two hydraulic models, 1D HEC‐RAS and 2D LISFLOOD‐FP in comparison with aerial imagery observations in Gorgan flood plain,Iran

We compared flood mapping techniques using a one‐dimensional (1D) hydraulic model HEC‐RAS and two‐dimensional (2D) LISFLOOD‐FP for a 10‐km reach of Gorgan River in Iran. Both models were run using the same hydrologic input data. The input into the models was a steady discharge of 90 cm, corresponds to a flood peak occurred on March 25, 2012. Flood maps generated using these two models were compared with an observed flood inundation map, using F‐statistic. The roughness coefficients of the models were calibrated by maximizing the value of the F‐statistic. Based on the F‐statistic, LISFLOOD‐FP gives a slightly better result (F = 0.69) than HEC‐RAS (F = 0.67). Visual comparison of the flood extents generated by the two models showed reasonably good agreement. Validation was done using a flood event occurred on May 31, 2014. The LISFLOOD‐FP model gave a better result for validation as well. The 2D model showed more consistency in comparison with the 1D model.     

A numerical scheme for a class of nonlinear Fredholm integral equations of the second kind

In this paper an iterative approach for obtaining approximate solutions for a class of nonlinear Fredholm integral equations of the second kind is proposed. The approach contains two steps: at the first one, we define a discretized form of the integral equation and prove that by considering some conditions on the kernel of the integral equation, solution of the discretized form converges to the exact solution of the problem. Following that, in the next step, solution of the discretized form is approximated by an iterative approach. We finally on some examples show the efficiency of the proposed approach.