Amperometric detection for liquid chromatographic separation of polynuclear hydrocarbons

Oxidative electrochemical detection is used for liquid chromatographic separation of polynuclear aromatic hydrocarbons (PAH's). The amperometric response is shown to be dependent on the working potential, ionic strength, flow rate, pH, temperature and pretreatment of the glassy carbon electrode surface. These experimental factors were optimized by choosing the maximum signal-to-noise ratio for anthracene and benz(a)-anthracene. The figures of merit (sensitivity, limit of detection and linear dynamic range) of six PAH's are reported and compared with ultraviolet absorption detection. Varying the applied potential gives the capability for selective detection.     

Tungstate sulfuric acid (TSA)/KMnO4 as a novel heterogeneous system for rapid deoximation

Neat chlorosulfonic acid reacts with anhydrous sodium tungstate to give tungstate sulfuric acid (TSA), a new dibasic inorganic solid acid in which two sulfuric acid molecules connect to a tungstate moiety via a covalent bond. A variety of oximes were oxidized to their parent carbonyl compounds under mild conditions with excellent yields in short times by a heterogeneous wet TSA/KMnO4 in dichloromethane system.     

Provably recursive functions of constructive and relatively constructive theories

In this paper we prove conservation theorems for theories of classical first-order arithmetic over their intuitionistic version. We also prove generalized conservation results for intuitionistic theories when certain weak forms of the principle of excluded middle are added to them. Members of two families of subsystems of Heyting arithmetic and Buss-Harnik’s theories of intuitionistic bounded arithmetic are the intuitionistic theories we consider. For the first group, we use a method described by Leivant based on the negative translation combined with a variant of Friedman’s translation. For the second group, we use Avigad’s forcing method.     

Dual-Mode Sorption of Inorganic Acids in Polybenzimidazole (PBI) Membrane

The sorption behaviors of sulfuric, perchloric, and phosphoric acids in polybenzimidazole membranes have been investigated. The results of sorption isotherms are consistent with the general form of a dual-mode sorption isotherm. The dual-mode sorption parameters were found using a least-squares program by fitting experimental data to a dual-mode equation. Results indicate a correlation between permeant properties like acidity, size, and the affinity constant in Langmuir-mode sorption species. Moreover, the results show that the size of the permeants has the dominant effect on Henry's constant. The obtained results for , site saturation constant, in Langmuir-mode sorption in the case of perchloric and phosphoric acids, reveals that the two acid molecules interact with two N?H basic groups in the polybenzimidazole repeat units. But in the case of sulfuric acid, it is shown that sulfuric acid neutralizes some of the basic groups in the polymer by its strong second hydrogen and the obtained value for was 1.25.     

An efficient and facile synthesis of 3-amino-5-chromenyl-butenolides from 3-formyl chromone, dialkyl acetylenedicarboxylate, and primary amines

A three-component reaction of 3-formyl chromones, dialkyl acetylenedicarboxylate, and isocyanides in the presence of $\text{ POCl}_{3}$ was used as a highly efficient and practical approach for the synthesis of 3-amino-5-chromenyl-butenolides. High yields and high bond forming efficiency, and simple operations are the advantages of this method. Graphical abstract      

Image-based gating of intravascular ultrasound pullback sequences

Intravascularultrasound (IVUS) sequences recorded in vivo are subject to a wide array of motion artifacts as the majority of these studies are performed within the coronary arteries of a beating heart. To eliminate these artifacts, an electrocardiogram (ECG) signal is typically used to gate (collect) those frames recorded at the points in time associated with a particular fraction of the cardiac cycle. However, this technique may be suboptimal for a number of reasons, among which is the difficulty of determining the optimal fraction at which to gate. This value is generally nonobvious. To circumvent this problem, we introduce a frame-gating method for IVUS pullbacks that mimics ECG (i.e., in the sense that it selects only one frame per cardiac cycle), but will automatically choose the fraction of the cycle that renders the most stable gated frame set. Stability here is gauged by measuring interframe similarity. Our method operates exclusively on the imagery data and does not require ECG or any form of image segmentation or other high-level image analysis. To validate our algorithm, we compare its behavior versus true ECG gating.     

Lagrangian Description of World-Line Deviations

We introduce a Lagrangian which can be varied to give both the equation of motion and world-line deviations of spinning particles simultaneously.     

Role of sodium decoration on the methane storage properties of BC3 nanosheet

First-principles calculations including dispersion correction are carried out to investigate pristine and Na-decorated graphene-like BC₃ (h-BC₃) for their application as methane storage materials. Structural optimization shows that the methane is physisorbed on the pristine sheet via van der Waals forces with adsorption energy of ?2.7 kcal/mol. It was found that unlike the pristine graphene, sodium decorated sheet can effectively interact with the CH₄ molecule, so that each metal atom bound on sheet may adsorb up to four CH₄. Furthermore, no bond dissociation was observed for the adsorption of CH₄ on Na-decorated h-BC₃, which means that decorated sheet can act as a storage device for methane safety storage. The results indicate that decoration of the Na atom on surface of sheet induces significant changes in electronic properties of the sheet and its E _g is unchanged after adsorption of CH₄ molecules. Theoretical methane storage capacity of Na-decorated BC₃ nanosheet could approach 18.1 wt%.     

Optimization of profenofos organophosphorus pesticide degradation by zero-valent bimetallic nanoparticles using response surface methodology

This study synthesized bimetallic Fe/Ni nanoparticles and used them for catalytic degradation of profenofos, an organophosphorus pesticide. This novel bimetallic catalyst (Fe/Ni) was characterized by scanning electron microscopy (SEM), energy-dispersive X-ray analysis spectroscopy (EDAX) and X-ray diffraction (XRD). The bimetallic nano-catalyst was prepared at diameters of 20–50 nm and was shown to effectively degrade profenofos. A three-factor central composite design combined with response surface methodology was used to maximize profenofos removal using the bimetallic system. A quadratic model was built to predict degradation efficiency. ANOVA was used to determine the significance of the variables and interactions between them. Good correlation between the experimental and predicted values was confirmed by the high F-value (16.38), very low P-value (<0.0001), non-significant lack of fit, an appropriate coefficient of determination (R² = 0.936) and adequate precision (14.75). The highest removal rate attained was 94.51%.