Analysis of PCBs in Biotic Matrices by Two-Dimensional GC-ECD

Abstract

The suitability of three GC-ECD systems for the separation of a model mixture containing various congeners of PCBs together with persistent chlorinated aromatics (pesticides and their metabolites, industrial chemicals) was tested. Analyses were performed on two parallel capillaries, the stationary phase of one of them was always in routine practice very common 5% phenyl-methylpolysiloxane, the second one was either 50% phenylmethylpolysiloxane or 7% phenyl-7% cyanopropyl-methylpolysiloxane. The number of unresolved (coeluted) analytes was significantly reduced in these systems and thus unbiased quantitation of PCBs and other components used for regulation was possible. The utilization of this type of multidimensional chromatography for rapid and reliable analysis of real samples (fish oil, human fat) was documented.     

试论《洪水》杂志与时代的互动

《洪水》作为创造社出版部的一份重要刊物,一方面,紧跟时代发展潮流,凸显刊物的价值追求,要破坏旧世界,创造新世界,另一方面,积极营造公共空间,努力争取读者支持,摈弃大量商业性广告,凸显文学本色,从而扩大杂志的影响力与号召力,发挥杂志媒介的社会功能和政治功能。     

A numerical investigation of the influence of the aspect ratio in three‐dimensional separated flows

The influence of aspect ratio in three‐dimensional, numerical experiments of separated flows is studied in the case of the backward‐facing step at Reynolds numbers 600, 800, and 950. The computational domain is designed as an actual laboratory experiment. The governing equations are the steady state, isothermal, and incompressible Navier–Stokes equations. The expansion ratio of the computational domain is 1:2. The aspect ratio varies from 1:10 to 1:40. The results of the computations focus on the spanwise variations of the length and the strength of the two eddies along the lower and upper wall. It is concluded that both numerical and laboratory experiments should be designed with an aspect ratio of at least 1:20, if only the accuracy of the position of the detachment and the re‐attachment points matters. If the accuracy of the shear‐stress distributions is also taken into account, then an aspect ratio of at least 1:30 should be chosen. Finally, if the magnitudes of the vortex centers are also considered, then only the aspect ratio of 1:40 qualifies for a realization of two‐dimensional flow conditions in the plane of symmetry. This is contrary to the common practice in the field, at least from the side of laboratory experiments, where an aspect ratio of 1:10 is still considered adequate for this purpose. Copyright © 2011 John Wiley & Sons, Ltd.     

Pressure drop effects on selectivity and resolution in packed column supercritical fluid chromatography

The influence of pressure drop on retention, selectivity, plate height and resolution was investigated systematically in packed supercritical fluid chromatography (SFC) using pure carbon dioxide as the mobile phase. Numerical methods developed previously which enabled the prediction of pressure gradients, diffusivities, capacity factors, plate heights and resolutions along the length of the column were used for the model calculations. The effects of inlet pressure and supercritical fluid flow rate on selectivity and resolution are studied. In packed column SFC with pure carbon dioxide as the mobile phase, the pressure drop can have a significant effect on resolution. The flow rate is shown to have a larger effect than generally realized. The calculated data are shown to be in good agreement with the experimental results. Finally, the variation of the chromatographic parameters along a 5.5 meter long model SFC column is illustrated. The possibilities and limitations of using long packed columns in SFC are discussed. It is demonstrated that long columns with large plate numbers do not necessarily yield better separations.     

Simulation of Organic Liquid Product Deoxygenation through Multistage Countercurrent Absorber/Stripping Using CO2 as Solvent with Aspen-HYSYS: Process Modeling and Simulation

In this work, the deoxygenation of organic liquid products (OLP) obtained through the thermal catalytic cracking of palm oil at 450 °C, 1.0 atmosphere, with 10% (wt.) Na₂CO₃ as a catalyst, in multistage countercurrent absorber columns using supercritical carbon dioxide (SC-CO₂) as a solvent, with an Aspen-HYSYS process simulator, was systematically investigated. In a previous study, the thermodynamic data basis and EOS modeling necessary to simulate the deoxygenation of OLP was presented. This work addresses a new flowsheet, consisting of 03 absorber columns, 10 expansions valves, 10 flash drums, 08 heat exchanges, 01 pressure pump, and 02 make-ups of CO₂, aiming to improve the deacidification of OLP. The simulation was performed at 333 K, 140 bar, and (S/F) = 17; 350 K, 140 bar, and (S/F) = 38; 333 K, 140 bar, and (S/F) = 25. The simulation shows that 81.49% of OLP could be recovered and that the concentrations of hydrocarbons in the extracts of absorber-01 and absorber-02 were 96.95 and 92.78% (wt.) on a solvent-free basis, while the bottom stream of absorber-03 was enriched in oxygenated compounds with concentrations of up to 32.66% (wt.) on a solvent-free basis, showing that the organic liquid products (OLP) were deacidified and SC-CO₂ was able to deacidify the OLP and obtain fractions with lower olefin contents. The best deacidifying condition was obtained at 333 K, 140 bar, and (S/F) = 17.     

环形压气机叶棚内部分离流结构分析 第二部分:流道内分离流

1前言认识压气机叶栅内部分离流动的结构和特性,对于揭示压气机内复杂的流动机制、改善叶栅气动性能、减少流动损失和提高压气机喘振裕度具有重要意义山。本文采用激光片光层加示踪粒子流场显示技术,观察和摄取了环形压气机叶栅在约十14”大攻角下的内部流动图像;采用七孔气     

Results from solvophobic theory applied to methylene selectivity in reversed-phase HPLC

A significant amount of work has been previously dedicated to the understanding of methylene selectivity parameter. The conventional theory applied for this understanding was mostly based on the assumption that the difference in the Gibbs free energy of transfer from the mobile phase to the stationary phase is a constant for any two compounds in a homologous series that differ by a CH₂ group. In the present study, it is shown based on solvophobic theory that this assumption is indeed correct, but it provides a theoretical justification for it. Exemplification of the results of theory was obtained using the values for methylene selectivity (α(CH₂)) measured experimentally for seven different C18 chromatographic columns including two core–shell columns and using water and either methanol or acetonitrile as an organic component. Four different homologous series of compounds were used for evaluation. The study proved the theoretical prediction that the values for α(CH₂) obtained using different homologous series of compounds are only slightly different from those obtained using the toluene–butylbenzene series. Even using different homologous series, the same type of information regarding the columns comparison, and the changes in log α(CH₂) with the solvent composition was obtained.     

HPLC separations of meropenem and selected pharmaceuticals using a polar endcapped octadecylsilane narrow bore column

Summary Stability indicating high performance liquid chromatography methods have been developed for the assay of meropenem in combination with either dopamine (A), aminophylline (B), metoclopramide (C) or ranitidine (D) in intravenous fluid mixtures. Separations B, C and D were performed on a polar endcapped ODS column (150×2 mm) with aqueous, pH 3.0—acetonitrile (89∶11, 88∶12, and 92∶8) eluent and detection at 270, 290, 317 nm respectively. Meropenem was linear over the concentration ranges 126.88–507.50, 131.25–525, and 131.25–525 gmg mL⁻¹. Aminophylline, metoclopramide and ranitidine were linear over the concentration ranges 13–52, 37.5–150, and 25–100 μg mL⁻¹. Separation A was performed on a conventional ODS column (150×2.1 mm) with aqueous, pH 3.0—acetonitrile (85∶15) eluent and detection at 280 nm. Meropenem and dopamine were linear in the 61.25–245 and 10–40 μg mL⁻¹ ranges, respectively. Accuracy and precision for all methods were 0.20–3.30% and 0.10–1.58%, respectively. Accelerated stability studies have been carried out on each drug by exposure to acid, base, H₂O₂, and heat for different time periods.     

Calculation of amino acid hydrophilicity indices for retention of peptides on amide, diol and silica columns in normal-phase liquid chromatography

Summary A set of hydrophilicity parameters in a normal-phase liquid chromatography of peptides is presented in order to clarify the contribution of individual amino acid residues to peptide retention and to predict retention times. The retention of 100 peptides was studied using normal-phase liquid chromatography on amide, diol and silica columns. An acetonitrile-water mixed solution containing 0.2% trifluoroacetic acid +0.2% triethylamine was used as the mobile phase in a linear gradient elution system. The contribution of each residue upon retention was calculated by linear multiple regression analysis. This paper described the contribution values as “hydrophilicity retention coefficients”. Using these hydrophilicity retention coefficients, retention times could be predicted for peptides of known amino acid content and sequence. A set of hydrophilicity retention coefficients on each column was successfully explained by contributions to the degree of retention.     

斜拉桥悬臂施工阶段分离式钢箱梁的剪力滞效应分析

以荆岳长江公路大桥为研究背景,采用ANSYS软件建立了该斜拉桥主梁最大单悬臂、主梁最大双悬臂和悬臂施工2号梁段三个工况的分离式钢箱主梁的区段仿真模型.利用空间有限元法,针对悬臂施工状态下分离式钢箱的空间受力状态进行剪力滞效应的计算分析.研究结果表明,分离式钢箱梁在不同施工工况下,其顶、底板剪力滞系数分布规律不同;钢箱梁顶板在外腹板处剪力滞效应较大,并随着离开外腹板处,其剪力滞效应减小较快.在施工过程中,分离式钢箱主梁的同一截面会同时出现正、负剪力滞效应.