Effects of processing parameters on the mechanical properties of polypropylene random copolymer

The mechanical properties of polypropylene random copolymer (PP-R) with different processing parameters were studied. Special attention is devoted to the investigation of the influence of masterbatch addition on the variation in the mechanical properties of injection moulded PP-R. Tensile, instrumented Charpy impact, Shore D hardness, differential scanning calorimeter (DSC) and Vicat softening temperature (VST) tests were conducted on the test samples containing different colour masterbatches varying from 0.5 to 10 wt%. The observed changes in the mechanical behaviour are explained by the type and level of masterbatch content. The natural UV weathering performance of the PP-R material was studied from the masterbatch type point of view. The effect of processing parameters on material performance was studied on samples which were directly obtained from extruded pipes and on injection moulded samples.

Finally, the effects of storage time on the polymer properties were investigated.     

Analytical and approximate solutions of(2+1)-dimensional time-fractional Burgers-Kadomtsev-Petviashvili equation

In this paper, we applied the sub-equation method to obtain a new exact solution set for the extended version of the time-fractional Kadomtsev-Petviashvili equation, namely BurgersKadomtsev-Petviashvili equation(Burgers-K-P) that arises in shallow water waves.Furthermore, using the residual power series method(RPSM), approximate solutions of the equation were obtained with the help of the Mathematica symbolic computation package. We also presented a few graphical illustrations for some surfaces. The fractional derivatives were considered in the conformable sense. All of the obtained solutions were replaced back in the governing equation to check and ensure the reliability of the method. The numerical outcomes confirmed that both methods are simple, robust and effective to achieve exact and approximate solutions of nonlinear fractional differential equations.     

Search for top quark FCNC couplings in Z′ models at the LHC and CLIC

The top quark is the heaviest particle to date discovered, with a mass close to the electroweak symmetry breaking scale. It is expected that the top quark would be sensitive to the new physics at the TeV scale. One of the most important aspects of the top quark physics can be the investigation of the possible anomalous couplings. Here, we study the top quark flavor changing neutral current (FCNC) couplings via the extra gauge boson Z′ at the Large Hadron Collider (LHC) and the Compact Linear Collider (CLIC) energies. We calculate the total cross sections for the signal and the corresponding Standard Model (SM) background processes. For an FCNC mixing parameter x=0.2 and the sequential Z′ mass of 1 TeV, we find the single top quark FCNC production cross sections 0.38(1.76) fb at the LHC with $\sqrt{s_{pp}}=7(14)$ TeV, respectively. For the resonance production of sequential Z′ boson and decays to single top quark at the Compact Linear Collider (CLIC) energies, including the initial state radiation and beamstrahlung effects, we find the cross section to be 27.96(0.91) fb at $\sqrt{s_{e^{+}e^{-}}}=1(3)$ TeV, respectively. We make the analysis to investigate the parameter space (mixing-mass) through various Z′ models. It is shown that the results benefit from the flavor tagging.     

Determination of some trace metals in waters by flame atomic absorption spectrometry after preconcentration on Amberlite XAD-16 resin with sodium tetraborate

A method was described for the determination of the elements Cr, Mn, Fe, Co, Ni, Cu, Cd, Pb, and Bi in waters by flame atomic absorption spectrometry (FAAS) after separation and preconcentration on Amberlite XAD-16 resin with sodium tetraborate using a chromatographic column. Parameters influencing the analytical performance, including pH and the volume of sample, amount of analyte and interfering effect of co-existing ions, were studied in detail. The recovery values were quantitative (> or = 95%), and the relative standard deviation (RSD) and detection limit (DL) varied in the range of 1.1-2.4% (n=10) and 0.002-0.177 microg m(-1) (3s, n=20), respectively. After being optimized, the proposed method was applied to the drinking water, waste water and artificial sea water samples. Recovery values of the elements investigated, were quantitative for tap water and synthetic sea water, except for Mn, Co and Ni (including also Cd for synthetic sea water). Recovery values of Cd, Pb, Cu and Co were found to be 95, 102, < or = 87, and < or = 83%, respectively, for the waste water samples.     

A sensitive determination of dopamine in the presence of ascorbic acid using a nafion-coated clinoptilolite-modified carbon paste electrode

A selective dopamine determination using a nafion-coated clinoptilolite-modified carbon paste electrode in the presence of ascorbic acid was studied. Both cyclic voltammetry (CV) and differential pulse anodic stripping voltammetry (DPASV) were used for measurements of dopamine. To improve the selectivity of the clinoptilolite-modified carbon paste electrode in presence of a high concentration of ascorbic acid, the electrode surface was coated with nafion membrane. Experimental parameters affecting the determination of dopamine, including the clinoptilolite ratio, nafion membrane thickness, preconcentration time, preconcentration solution pH, stripping solution pH and interferences are discussed. The developed sensor has a wide linear range, a low detection limit, and good stability and reproducibility. The sensor offers a good alternative to existing analytical methods for dopamine, permits a relatively short analysis time, and is simple, selective and inexpensive.     

Determination of Naphthazarin Derivatives in 16 Alkanna Species by RP-LC Using UV and MS for Detection

As part of our ongoing studies, a new and validated method for analysis of isohexenyl-naphthazarines in Turkish Alkanna species was developed. By using reversed phase material (Synergi MAX RP) it was possible to determine four known isohexenylnaphthazarin-derivatives, namely alkannin, acetylalkannin, deoxyalkannin, and β,β-dimethylacrylalkannin within 25 min in n-hexane extracts of the roots. The quantification of these compounds in 16 Anatolian Alkanna species is described for the first time. In order to assure peak identity LC-MS experiments were performed. Quantitative results revealed that the most dominant compound in the extracts was β,β-dimethylacrylalkannin.     

The Synthesis,Characterization, and Electrochemical Investigation of Novel Thio- and Alkoxy-Substituted Benzoquinone Derivatives

Abstract

Novel thio- and alkoxy-substituted benzoquinone derivatives were synthesized from the reactions of p-chloranil (1) and related nucleophiles in a sodium carbonate (Na₂CO₃) solution of acetonitrile or in chloroform with Et₃N. The structures of novel compounds were characterized by using microanalysis, FTIR, ¹H NMR, ¹³C NMR, MS, CV, and fluorescence spectroscopy.

[Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.]     

Influences of Co-60 gamma-ray irradiation on electrical characteristics of Al2O3 MOS capacitors

Effects of gamma-ray irradiation on the electrical characteristics of Al₂O₃ MOS capacitors such as barrier height, acceptor concentration, series resistance and interface state parameters have been studied by analyzing capacitance–voltage (C–V) and conductance–voltage (G/ω–V) measurements. The fabricated MOS capacitors were irradiated with gamma-rays at doses up to five grays. C–V and G/ω–V measurements were recorded prior to and after irradiation at high frequency. The results show that the measured capacitance and conductance values decreased with increasing in irradiation dose and C–V and G/ω curves has been shifted toward the negative voltages. Moreover, the series resistance (R _s) and density of interface states increased with increasing in irradiation dose and density of interface states (D _it) were calculated as order of 10¹² eV^?1cm^?2 prior to and after irradiation. Due to presence and variations in the R _s values, the corrected and the measured C–V and G/ω–V exhibited different behaviors. Therefore other electrical characteristics were assessed from corrected C _c characteristics. It was observed that acceptor concentration decreased with increasing in barrier height of device due to changes in interface states and diffusion potential.     

Estimating the manipulation errors in finite element analysis, Part I

In Part I of this two-part work, the relative errors in representing and processing real numbers in digital computers are reviewed, and the computation of the digits lost from the relative errors is shown. The upper bound estimate of the relative error in the solution of Kξ = p for the displacements ξ is given as a function of the condition number of the stiffness matrix K, and the relative errors in K and the load vector p. The computation of relative errors for p and K by equilibrium checks is outlined, and various estimates for the condition number of the stiffness matrix are given.     

Site‐Selective C−S Bond Formation at C−Br over C−OTf and C−Cl Enabled by an Air‐Stable,Easily Recoverable,and Recyclable Palladium(I) Catalyst

This report widens the repertoire of emerging Pd^I catalysis to carbon–heteroatom, that is, C?S bond formation. While Pd⁰‐catalyzed protocols may suffer from the formation of poisonous sulfide‐bound off‐cycle intermediates and lack of selectivity, the mechanistically diverse Pd^I catalysis concept circumvents these challenges and allows for C?S bond formation (S–aryl and S–alkyl) of a wide range of aryl halides. Site‐selective thiolations of C?Br sites in the presence of C?Cl and C?OTf were achieved in a general and a priori predictable fashion. Computational, spectroscopic, X‐ray, and reactivity data support dinuclear Pd^I catalysis to be operative. Contrary to air‐sensitive Pd⁰, the active Pd^I species was easily recovered in the open atmosphere and subjected to multiple rounds of recycling.