Evaluating MTBSTFAderivatization reagents for measuring naphthenic acids by gas chromatography-mass spectrometry

Abstract

Naphthenic acids (general formula C_nH_2n+ZO₂) are found in petroleum and oil sands deposits. Release of these acids to aquatic environments is a concern because of their potential toxicity. Naphthenic acids consist of a complex mixture of carboxylic acids, and estimating their concentrations in environmental samples is a challenge. Two recent reports have described gas chromatography-mass spectrometry (GC-MS) methods to selectively detect these acids in fish flesh and water samples. The methods use N-methyl-N-(t-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA) with 1% t-butyldimethylchlorosilane (t-BDMCS) to derivatize naphthenic acids to their t-butyldimethylsilyl derivatives. Single ion monitoring (SIM) was used to detect the fragment m/z 267, which corresponds to the derivatives of one isomer class (n = 13 and Z = −4) of naphthenic acids. The SIM chromatograms give a characteristic naphthenic acids hump between retention times 15 and 20 min and a sharp peak for the t-butyldimethylsilyl derivatized surrogate standard, 9-fluorenecarboxylic acid. Integration of this hump and the peak from the surrogate standard allows quantification of the naphthenic acids. Using newly purchased MTBSTFA containing 1% t-BDMCS (from three different suppliers) yielded SIM chromatograms with one or two large contaminating peaks (eluting at 16.7 and 18.8 min) that interfered with integration of the hump, rendering the method unreliable. The contaminants were traced to the presence of t-BDMCS. Each of the three suppliers sells MTBSTFA devoid of t-BDMCS, and using MTBSTFA without 1% t-BDMCS was found to be suitable for the GC-MS method.