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J N Driscoll

Publications and source records attributed to J N Driscoll.

12 recordsLinked to original sources

Analysis of ppb levels of organics in water by means of purge-and-trap, capillary gas chromatography and selective detectors.

The Environmental Protection Agency (EPA) has issued a series of methods (500 and 600 series) for the analysis of organics in drinking water and industrial discharges. Methods 601 and 602 employ packed-column gas chromatography (GC) with electrolytic conductivity (E1CD) and photoionization detection (PID), respectively. A purge-and-trap system is used for concentration of volatiles. The EPA is in the process of converting methods 601 and 602 and certain 500-series methods to capillary column analysis. We have also initiated the conversion of a number of these methods, using E1CD and PID and have described them in detail in this paper. We have evaluated both 0.32- and 0.53-mm diameter capillary columns, using helium and nitrogen as carrier gases with each detector. We found that with nitrogen optimum results are obtained at a flow-rate of 15 ml/min, and with helium at 6-8 ml/min. As a result of system optimization, including operation of the two detectors in series, and converting from packed to capillary columns, we found that analysis time could be reduced from 80 min (for two methods separately) to ca. 30 min. In addition, the elution of more than five components in one peak, observed when the packed column specified in method 601 are used, was eliminated.

Chromatography, Gas↗

Trace analysis of organic compounds by high-performance liquid chromatography with photoionization detection.

Photoionization detection (PID) has now been successfully interfaced with modern high-performance liquid chromatography (HPLC) to provide a new "hyphenated" technique, HPLC-PID. This method is compatible with reversed-phase HPLC solvents and conditions, as well as with certain organic solvents used in normal-phase liquid chromatography. The HPLC-PID interface consists of a variable-ratio eluent splitter, operated inside a heated oven, which vaporizes both analytes and mobile phase prior to introduction into the detector. Depending on the energy (eV) of the photoionization detector lamp, most of the solvents commonly used in reversed-phase liquid chromatography are compatible with long-term, on-line, real-time, continuous photoionization detector operation. Virtually all organic classes now detectable by gas chromatography-PID can also be detected by HPLC-PID, but with somewhat poorer detection limits. In certain instances, minimum detection limits are in the 5-500 ng/injection range. The HPLC-PID system appears ideal for aromatic or aliphatic amines, substituted hydrocarbons, and certain other classes of organic compounds. Various applications of HPLC-PID, under reversed-phase conditions are illustrated and discussed.

Chromatography, Gas↗

Analysis of therapeutic and commonly abused drugs in serum and urine by gas-liquid chromatography using a photoionization detector.

A simple, rapid and sensitive gas chromatographic procedure using the photoionization detector (PID) was developed for the detection and quantitation of several drugs in serum and urine. In order to evaluate the performance of the PID, the results were compared with those of the flame-ionization detector (FID). The data indicate that the PID is 8-16 times more sensitive than the FID for the drugs studied in the barbiturate group. Excellent reproducibility was found for samples quantitated with the PID on a routine basis. The PID and FID produced statistically similar results on extracted serum samples. The correlation coefficient was 0.99. The PID also produced chromatograms with less background than those obtained with the FID for many extracted serum samples. The advantages of the PID for drug analysis in biological fluids include simplicity of operation, lack of solvent response, universal drug response, non-destructive character and stability.

Barbiturates↗