More stringent environmental regulations as well as higher demands presently being imposed on the sulfur content of natural gas feed‐stocks for chemical processes necessitate the development of new analytical procedures for sulfur determination in natural gas. Only analytical procedures based on gas chromatography can meet the sensitivity and accuracy requirements dictated by environmental regulation institutions and modern chemical industry. The complexity of the natural gas matrix as well as the extremely low concentration levels at which the sulfur species occur make the development of these analytical methods a true challenge. In this review the three steps common for analytical methods for trace analysis in complex matrices, i.e. pretreatment, chromatographic separation, and detection, are discussed in detail. Possible methods for calibration of the system are discussed in the final section.
Various techniques to determine sulfur in natural gas are described. Depending on the application, the most suitable system has to be selected. For example, for on‐line application in a hazardous area a simple and rugged system is required, i.e. a simple gas chromatograph with a flame photometric detector, while for laboratory application a more complex instrument including preconcentration, column switching, and more exotic detection systems could be more suitable. Therefore it is crucial to define the requirements of the instrument at an early stage and use the information in this review article to develop/select a dedicated instrument/procedure for the problem at hand.
The [OH]- chemical ionization spectra of methadone and three metabolites and of l-alpha-methadol and six metabolites are presented. The spectra are simple, but the methadol compounds exhibit much fragmentation. The ionization sensitivity is somewhat greater than that in CH4 positive chemical ionization.
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