Effect of Satureja khuzestanica essential oil on oxidative stability of sunflower oil during accelerated storage

In this study, the application of various concentrations (0.02%, 0.04%, 0.06% and 0.08%) of Satureja khuzestanica essential oil (EO) was examined on the oxidative stability of sunflower oil and compared to butylated hydroxyanisole (BHA) during storage at 60°C. Gas chromatography (GC) and GC-mass spectrometry analyses of the oils revealed that carvacrol (87.7%) was the major component of EO. Peroxide value and anisidine value measurements in sunflower oil showed that all concentrations of EO had antioxidant effects in comparison to BHA. Oil samples supplemented with EO concentration of 0.08% were the most stable during storage (p?相似文献   

Magnetic nondestructive technology for detection of tempered martensite embrittlement

A nondestructive eddy current technique is used to evaluate tempered martensite embrittlement in 4340 AISI steels after quench and tempering in the range 240–550 °C. A relation between the responses of the magnetic induction (normalized impedance of the coil) and destructive Charpy impact test results has been established. The study shows that the eddy current method could be used to separate brittle parts due to the microstructure changes.     

Two new XP(O)[NHC(CH3)3]2 phosphoramidates,with X = (CH3)2N and [(CH3)3CNH]2P(O)(O)

In N,N′‐di‐tert‐butyl‐N′′,N′′‐dimethylphosphoric triamide, C₁₀H₂₆N₃OP, (I), and N,N′,N′′,N′′′‐tetra‐tert‐butoxybis(phosphonic diamide), C₁₆H₄₀N₄O₃P₂, (II), the extended structures are mediated by P(O)...(H—N)₂ interactions. The asymmetric unit of (I) consists of six independent molecules which aggregate through P(O)...(H—N)₂ hydrogen bonds, giving R₂¹(6) loops and forming two independent chains parallel to the a axis. Of the 12 independent tert‐butyl groups, five are disordered over two different positions with occupancies ranging from to . In the structure of (II), the asymmetric unit contains one molecule. P(O)...(H—N)₂ hydrogen bonds give S(6) and R₂²(8) rings, and the molecules form extended chains parallel to the c axis. The structures of (I) and (II), along with similar structures having (N)P(O)(NH)₂ and (NH)₂P(O)(O)P(O)(NH)₂ skeletons extracted from the Cambridge Structural Database, are used to compare hydrogen‐bond patterns in these families of phosphoramidates. The strengths of P(O)[...H—N]_x (x = 1, 2 or 3) hydrogen bonds are also analysed, using these compounds and previously reported structures with (N)₂P(O)(NH) and P(O)(NH)₃ fragments.     

Comment on "Structure and thermodynamics of hard-core Yukawa fluids: thermodynamic perturbation approaches" [J. Chem. Phys, 135, 034505 (2011)

We would like to show that what has been presented in the paper by Kim, Kim, and Seong [J. Chem. Phys, 135, 034505 (2011)] is nothing but an unnecessarily complicated version of (optimized) random phase approximation.     

Modelling of Power-law Fluid Flow Through Porous Media Using Smoothed Particle Hydrodynamics

The flow of non-Newtonian fluids through two-dimensional porous media is analyzed at the pore scale using the smoothed particle hydrodynamics (SPH) method. A fully explicit projection method is used to simulate incompressible flow. This study focuses on a shear-thinning power-law model (n < 1), though the method is sufficiently general to include other stress-shear rate relationships. The capabilities of the proposed method are demonstrated by analyzing a Poiseuille problem at low Reynolds numbers. Two test cases are also solved to evaluate validity of Darcy’s law for power-law fluids and to investigate the effect of anisotropy at the pore scale. Results show that the proposed algorithm can accurately simulate non-Newtonian fluid flows in porous media.     

Temperature Dependence of the Back-Stress in Shear for Glassy Polycarbonate

Summary: Back-stress is the equilibrium stress and represents conditions under which relaxation events in the material stop and the material can carry an applied load indefinitely without a change in strain. In most models for glassy polymers, back-stress plays a central role since relaxation in materials is closely related to the distance of the current conditions from equilibrium. A number of these models that are commonly used for modeling glassy polymers use a modeling structure similar to large deformation plasticity. The flow rule for the plastic strain in these models are directly connected to the “over-stress,” a properly invariant difference between the stress and the back-stress. The importance of correctly evaluating the back-stress to use in these models is clear. For this class of models, the authors have recently developed a method for directly calculating the back-stress under shear deformations. This method is based on evaluating the slope of the stress-strain response under conditions of similar elastic and plastic strain, but different strain rates. Since plastic flow goes to zero at equilibrium, the back-stress can be found by locating points of zero plastic strain rate. Using the proposed method, the back-stress in glassy polycarbonate has been evaluated under shear in isothermal tests going from room temperature to 120 °C, just below the glass transition temperature for polycarbonate. The proposed method provided a full map of the back-stress for polycarbonate over a large range of shear strain and temperature.     

The effect of process and structural parameters on the stability,thermo-mechanical and thermal degradation of polymers with hydrocarbon skeleton containing PE,PP, PS,PVC, NR,PBR and SBR

Journal of Thermal Analysis and Calorimetry - Many studies have been done on the stability, thermo-mechanical degradation and pyrolysis of polymers with hydrocarbon skeleton. According to the main...     

Theory of a Two-Dimensional Rotating Wigner Cluster

JETP Letters - A two-dimensional Wigner cluster (2DWC) with the number of electrons up to 200 in a parabolic potential well has been studied numerically and analytically. It has been shown that the...     

The use of cubic B‐spline scaling functions for solving the one‐dimensional hyperbolic equation with a nonlocal conservation condition

Problems for parabolic partial differential equations with nonlocal boundary conditions have been studied in many articles, but boundary value problems for hyperbolic partial differential equations have so far remained nearly uninvestigated. In this article a numerical technique is presented for the solution of a nonclassical problem for the one‐dimensional wave equation. This method uses the cubic B‐spline scaling functions. Some numerical results are reported to support our study. © 2007 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq, 2007     

Dissociation Behavior of <Emphasis Type="SmallCaps">l</Emphasis>(+)-Lactic Acid in Aqueous Solutions of (1-Alkyl-4-methylpyridinium bromide + Poly (ethyleneglycol)) at <Emphasis Type="Italic">T</Emphasis> = (288.15–318.15) K

The effect of 1-alkyl-4-methylpyridinium based ionic liquids on the conductivity behavior of l(+)-lactic acid (LaH) was studied in Poly(ethylene glycol) (PEG) aqueous solutions. The molar conductivities of LaH in the aqueous solutions of PEG, (PEG + 1-hexyl-4-methylpyridinium bromide) and (PEG + 1-octyl-4-methylpyridinium bromide) were measured over the temperature ranges of 288.15–318.15 K. The molar conductivity data were analyzed by applying the Quint–Viallard (QV) conductivity equation to determine the limiting molar conductivities (Λ ⁰) and dissociation constants (\( K_{\text{D}} \)). The results show that the values of limiting molar conductivity increased as the temperature increased, which indicates that the dissociation process is endothermic. The \( K_{\text{D}} \) values were also used to calculate the dissociation standard thermodynamic functions (\( \Delta G_{\text{D}}^{0} \), \( \Delta S_{\text{D}}^{0} \) and \( \Delta H_{\text{D}}^{0} \)). The results revealed that the dissociation process of LaH is controlled by entropy at all temperatures.