Stability of electronic nose (e-nose) as determined by considering date-pits heated at different temperatures

Variability and sensitivity of a portable electronic nose (32 sensors) was assessed by considering different variables for measurement (i.e., reference, standard, first and second purges, sample draw time, waiting time for the volatiles released in the headspace, and mass of sample or headspace volume of the jar containing sample). In this study, dried date-pits were used a model sample. The highest stability was achieved when both reference and standard (i.e., dried date-pits, no heating treatment) were used before test sample measurement. Higher sample draw time more than 10 s significantly decreased the stability, whereas optimum second purge was observed at 50 s. Optimum time to generate volatile was observed as 24 h. A sample of 100 g increased the signal intensity compared to the 50 g sample for the 60°C and 100°C treated samples, while an opposite trend was observed for the 150°C treated sample. Finally, the responses of volatile components in date-pits heated at different temperatures (60°C, 100°C, and 150°C) were measured using the optimum operating conditions. Principal component analysis explored the relationships between the volatile features and classified date-pits heated at different temperatures. The results showed that an electronic nose was able to classify date-pits based on their volatile components generated by different degrees of heating (93.3% accuracy).     

Corrosion Inhibition of Mild Steel in Acidic Medium using 2-amino Thiophenoland 2-Cyanomethyl Benzothiazole

The corrosion inhibition characteristics of 2-amino thiophenol (ATP) and 2-cyanomethyl benzothiazole (CNMBT) on two types of steel in 1m HCl medium were investigated at different temperatures (25, 30, 35, 40 and 50°C). The pitting corrosion behaviour for the same system was studied using a potentiodynamic technique. The pitting corrosion resistance of steel samples increased with increase in concentration of the ATP and CNMBT. Some samples were examined by scanning electron microscopy. The effects of the inhibitors on the general corrosion of the two samples were investigated by using gravimetric and galvanostatic polarization techniques. The inhibition efficiencies increased with increase their concentration but decreased with increase in temperature. Free energies of activation, enthalpies and entropies for the inhibition processes were determined from rate constant data measured and different temperatures at different concentrations of ATP and CNMBT. Results were compared with fits obtained from the application of the Langmuir isotherm. Results were correlated to the chemical structure of the inhibitors. The inhibition efficiency of CNMBT is higher than that of ATP.     

Monitoring of Changes in Composition of Soybean Oil During Deep-Fat Frying with Different Food Types

Changes in the composition of soybean oil during deep‐fat frying with wheat dough (WD) and chicken breast meat (CBM) were comparatively investigated using gas chromatography–mass spectrometry and Fourier transform infrared spectroscopy (FTIR). The amounts of saturated fatty acids (FAs) and short‐chain FAs were increased. The amount of unsaturated FAs was decreased as the processing time increased. An increase in the amount of tetradecanoic acid and 9‐cis‐hexadecanoic acid was observed during the CBM frying only. The FTIR spectrum of frying oil was analyzed by extracting the entire information as the area ratios based on vibration absorptions of the specific functional groups. Changes in content of functional groups, namely cis C=C, trans C=C, C=O, C–O, O–H, and C–H, were studied by the FTIR‐based method. Based on the changes in the content of FAs and functional groups, soybean oil fried with CBM degraded more quickly than that fried with WD. Moreover, good linear correlations between the change in contents of functional groups and the mass percentages of FAs were also observed. The FTIR‐based method could be used in real time to monitor the quality of frying oil during the deep‐fat frying.     

Detection of Fat Concentration in Milk Using Ternary Photonic Crystal

Silicon - Rapid and sensitive detection of fat concentration in milk is a necessary part for citizens in each country. Bio-photonic sensing techniques are an accurate best way to detect biosensing...     

TLM modelling of diffusion,drift and recombination of charge carriers in semiconductors

The paper provides an extension to the one-dimensional TLM diffusion model. The extended diffusion node presented here models the exact transport equation with diffusion drift and recombination of charge carriers in semiconductors. A general algorithm for providing a numerical solution to the transport phenomena is also presented here. The analytical solution for infinitely long semiconductors is compared with the TLM numerical results.     

化学合成制药综合废水的处理

本文介绍了化学合成制药废水的处理工艺、原理和运行效果,该工艺处理后的污水完全达到国家规定的污水排放标准。     

精炼工艺对椰子油品质的影响

研究了精炼工艺对椰子油品质的影响。分析了毛椰油、碱炼油、脱色油、脱臭油的理化指标、脂肪酸、甘油酯组成和脂肪伴随物(甾醇、生育酚、多酚)的变化情况。结果表明:精炼工艺使椰子油的酸值、过氧化值显著降低,脂肪酸和甘油酯组成无显著变化;总甾醇、总生育酚和多酚含量显著降低,损失率分别为63.77%、68.03%、71.20%。综上表明,精炼能够显著影响油脂品质,需注重油脂适度加工技术的应用。     

Synthesis of trideuteratedO-alkyl platelet activating factor and lyso derivatives

Racemic heavy isotope analogs of 1-O-alkyl-sn-glycero-3-phosphocholine (lysoPAF) and 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine (PAF) were prepared for use as internal standards to facilitate quantitative studies based on mass spectrometry. Starting from pentadencane-1,15-diol andrac-glycerol-1,2-acetonide, a convergent synthesis of 1-O-[16′-²H₃]hexadecyl and 1-O-[18′-²H₃]octadecylrac-glycero-3-phosphocholine and their acetyl derivatives is described. Three deuterium atoms were introduced at the terminal position of the 1-O-alkyl group by displacement of thep-toluensulfonyl group from 1-O-alkyl-15′-p-toluensulfonate and 1-O-alkyl-17′-p-toluensulfonate with [²H₃]-methylmagnesium iodide. The 1-O-alkyl-17′-p-toluensulfonate was obtained by reaction of the 1-O-alkyl-15′-p-toluensulfonate with allylmagnesium bromide, followed by reductive ozonolysis and treatment withp-toluenesulfonyl chloride. The hydroxyl group at C-2 was protected by a benzyl group and removed at a late stage in the synthesis. This provided the corresponding lysoderivatives or allowed preparation of racemic PAF by subsequent acetylation of the free hydroxy group. The phosphocholine moiety was introduced at glycerol C-3 by reaction with bromoethyldichlorophosphate and trimethylamine. The synthetic compounds were analyzed by FAB/MS and GC/NICIMS. They were shown to contain less than 0.6% protium impurity.     

Graft polymerization of methyl methacrylate onto wool initiated by a hydrogen peroxide-sodium thiosulphate redox system. Part II kinetics and mechanism of the grafting reaction

Methyl methacrylate was grafted onto wool in the presence of an aqueous dioxane solution with a hydrogen peroxide-sodium thiosulphate initiator system, using the optimum conditions found in our previous paper¹⁹. It was stated that up to 90% conversion for the rate of reaction the following equation holds: \documentclass{article}\pagestyle{empty}\begin{document}${\rm R}_{\rm p} = - \frac{{{\rm d}\left[ {\rm M} \right]}} {{{\rm dt}}} = {\rm K} \cdot \left[ {\rm M} \right]^{1.5}$\end{document} where R_p is the overall rate of the graft polymerization, and [M] is the monomer concentration at the time t. The degree of polymerization of the isolated poly(methyl methacrylate) was found to be linearly proportional with the monomer concentration [M]. Investigations of the effect of the ratio of solvent to monomer concentration [S]/[M] on the reciprocal of the degree of polymerization showed that there was no chain transfer caused by the solvent dioxane. The number average molecular weight M?_n of the polymer separated from the grafted wool was found to be within the range of 3–15.9 × 10⁶ as determined by viscosimetry. The molecular weight distribution of the isolated poly(methyl methacrylate) samples was determined by turbidimetric titration. The following relationship was established between the volume fraction of the non-solvent, γ and the number average molecular weight M?ⁿ. of poly(methyl methacrylate): \documentclass{article}\pagestyle{empty}\begin{document}$\gamma = - 0.0285 + \frac{{50.54}}{{\sqrt[3]{{\overline M _n }}}}. $\end{document} The molecular weight distribution curves were found to be rather homogeneous indicating approximately the same chain length of the grafted poly(methy1 methacrylate) on the wool backbone. It was stated before³³ that the number average molecular weight could be determined from the inflection point of the turbidimetric curves. This method can be used for determining the molecular weight of all kinds of poly(methy1 methacrylate) occurring in practice.