Hold-up time in gas chromatography. V. Dependence of the retention of n-alkanes on the chromatographic variables in isothermal gas chromatography

The chromatographic behaviour of n-alkanes and other homologous series in isothermal gas chromatography has been shown to depart from the "linear" representation of the logarithms of the adjusted retention times vs. carbon number. One of the expressions proposed to describe this behaviour is tR(z)=A+exp(B+CzD). In this paper, a regression analysis shows that three of the parameters of the equation depend on different chromatographic variables such as hold-up time, average linear gas velocity, volume and polarity of the stationary phase and temperature of the column. The fourth parameter (D), responsible for the departure from the "linearity", does not depend on any chromatographic variable, and represents a gradual decrease of the contribution of the methylene groups to the general properties of n-alkanes, with no relation to the chromatographic phenomenon.     

A tool for evaluating the Kovats index from the retention time of a substance in gas chromatography

A computer program based on a mathematical simulation of gas chromatography was developed for the identification of components during the course of the chromatographic analysis of molecular mixtures. The source data for the program are natural parameters that characterize the stationary phase (certified characteristics) and easy-to-specify operational parameters of chromatograph units. An example of calculating the retention time of a component under specified conditions from a specified Kovats index or, vice versa, calculating the Kovats index from the elution time of a component peak is given.     

Hold-up time in gas chromatography I. New approach to its estimation

A new procedure to reach a good estimate of the hold-up time value (t_M) in gas chromatography is presented. The value of t_M obtained lies close to the experimental retention time of neon, the gas which has shown the shortest retention time in the columns studied. The new method, based on the retention of n-alkanes, is easily applied with any personal computer and may be used with detectors which do not respond to permanent gases. The procedure is reliable, produces very reproducible hold-up times and the value of t_M obtained may be safely used to calculate both chromatographic and thermodynamic parameters.     

A simple large volume injection system with a solid-phase sample loop for packed column supercritical fluid chromatography

Chromatographia - The design and use of an easy-to-build large-volume injection system for packed column supercritical fluid chromatography (SFC) are reported. Two 6-port injection valves are used....     

A simple atmospheric microwave-excited emissive detector for gas chromatography

An atmospheric pressure microwave-excited emissive argon plasma is evaluated for use as a detector in conventional gas-chromatographic analysis. A range of carbon-, oxygen-, nitrogen- and halogen-containing compounds was investigated in order to optimize the sensitivity, linear working range and plasma operating conditions. For the non-selective determination of carbon-containing compounds, the atomic carbon emission at 247.9 nm was found to be most useful. At this wavelength the sensitivities for all the compounds investigated were directly proportional to the amount of carbon in the compounds. The limit of detection for these compounds at 247.9 nm was 1.94·10^-l0 g of carbon per sec. The atomic lines at 206.2 nm (I) and 470.5 nm (Br) were the best for the selective determination of iodine- and bromine-containing compounds respectively, and a new band emission at 256 nm, characteristic of chlorinecontaining compounds, gave good sensitivity.     

Evaluation of retention time for temperature-programmed gas chromatography by use of a closed-form integral

A closed-form integral for the Arrhenius exponential was obtained by using an approximate relation instead of the usual one in a linear temperature program. The closed-form integral can be applied to predict the retention time very well both for a packed column and for a capillary column, in constant the velocity mode.     

A mass-balanced definition of corrected retention volume in gas chromatography

The mass balance equation of a chromatographic system using a compressible moving phase has been compiled for mass flow of the mobile phase instead of traditional volumetric flow allowing solution of the equation in an analytical form. The relation obtained correlates retention volume measured under ambient conditions with the partition coefficient of the solute. Compared to the relation in the ideal chromatographic system the equation derived contains an additional correction term accounting for the compressibility of the moving phase. When the retention volume is measured under the mean column pressure and column temperature the correction term is reduced to unit and the relation is simplified to those known for the ideal system. This volume according to International Union of Pure and Applied Chemistry (IUPAC) is called the corrected retention volume.     

Contribution of adsorption to retention data in glass capillary gas chromatography part. I. Polar stationary phases

Summary The influence of the film thickness of Carbowax 20M coated onto glass surfaces (series of columns with different mode of surface treatment) upon the retention indices of solutes which exhibit tendency to hydrogen bonding has been investigated. Limiting values of Kovats indices, I, are calculated for all the columns examined.Presented at the 14th International Symposium on Chromatography London, September, 1982     

A simple gas chromatography method for the analysis of monoethanolamine in air

A simple method determining airborne monoethanolamine has been developed. Monoethanolamine determination has traditionally been difficult due to analytical separation problems. Even in recent sophisticated methods, this difficulty remains as the major issue often resulting in time-consuming sample preparations. Impregnated glass fiber filters were used for sampling. Desorption of monoethanolamine was followed by capillary GC analysis and nitrogen phosphorous selective detection. Separation was achieved using a specific column for monoethanolamines (35% diphenyl and 65% dimethyl polysiloxane). The internal standard was quinoline. Derivatization steps were not needed. The calibration range was 0.5-80 μg/mL with a good correlation (R(2) = 0.996). Averaged overall precisions and accuracies were 4.8% and -7.8% for intraday (n = 30), and 10.5% and -5.9% for interday (n = 72). Mean recovery from spiked filters was 92.8% for the intraday variation, and 94.1% for the interday variation. Monoethanolamine on stored spiked filters was stable for at least 4 weeks at 5°C. This newly developed method was used among professional cleaners and air concentrations (n = 4) were 0.42 and 0.17 mg/m(3) for personal and 0.23 and 0.43 mg/m(3) for stationary measurements. The monoethanolamine air concentration method described here was simple, sensitive, and convenient both in terms of sampling and analytical analysis.