Nitrogen (N)-containing compounds are naturally present in petroleum, and they are responsible for several deleterious effects that reduce the quality of products and negatively affect the processes involved in the upgrading of feedstock. The speciation of such compounds in petroleum heavy fractions is still a challenge. In the present work, N-containing compounds were characterized in heavy gas oil (HGO) fractions using a solid−liquid fractionation scheme and comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry. Classification and identification of compounds were carried out based on seven different categories of analytical information viz. retention times in first and second dimensions, analytical standards co-injection, the structured pattern of the separation space, the structured pattern of the separation space with the selection of specific m/z values, the library mass spectra match factor, and the characteristic deconvoluted mass spectra. All of these interpretations were available from a single analytical run followed by a standard injection. Compounds were extracted from the sample using an ion-exchange resin method to separate neutral and basic N-containing compounds, after a pre-fractionation step, using neutral aluminum oxide. This methodology allowed for the identification of 120 N-containing compounds and tentative identification of a further 108 compounds using their deconvoluted characteristic mass spectra as a basis for identification. Identified components included alkyl-indols, alkyl-carbazols, alkyl-benzocarbazols, alkyl-quinolines, alkyl-indene-pyridines, alkyl-benzoquinolines, and alkyl-dibenzoquinolines.

No abstract

Qualitative and quantitative study of nitrogencontaining compounds in heavy gas oil using comprehensive two-dimensional gas chromatography with nitrogen phosphorus detectionIn this work, a GC6GC -nitrogen -phosphorus detection (NPD) methodology was developed to separate and quantitate nitrogen-containing compounds in Brazilian heavy gas oil. First, the NPD performance was improved in order to achieve best GC6GC performance. The geometry of this detector was also evaluated. The use of an extended jet improved significantly the peak shape. The GC6GC separation was studied using both first and second dimension columns with different internal diameters. The use of a thicker film in both dimensions provided better performance. LODs of 0.16 -8.49 pg of individual compounds were achieved. Two different extraction techniques of the neutral and basic nitrogen-containing compounds were also evaluated. The method using ion-exchange resins to separate neutral and basic nitrogen-containing compounds was more efficient than the method using modified silica. As an example, the amounts (lg/g) of each class reported were: indole (2.77), alkyl carbazoles ranging from C 0 to C 6+ (1.467), alkyl benzocarbazoles from C 0 to C 4+ (793), alkyl quinolines (31.2) and alkyl benzoquinolines (21.6) were quantitated.

The identification of compounds by using gas chromatography (GC) in samples with significant complexity comprising a range of isomeric species, where characterization is based on peak retention times and mass spectra, generates uncertainty for the analyst. This leads to identification errors. The most reliable way to confirm the identification of each compound is based on authentic standard co-injection, which in several cases is economically prohibitive, and often unachievable in the time available for analysis. Retention index procedures are important tools to minimize misidentification of compounds in conventional chromatography. The introduction of comprehensive two-dimensional GC (GC × GC) for analysis of complex samples was a decisive step to increase the analytical capacity of chromatographic techniques. For many samples, the chromatographic resolution increase leads to quantitative expansion in the number of peaks identified, compared with conventional GC analysis. Notwithstanding this improved resolution, limitations still persist in correct peak identification, which suggests the use of retention indices may assist in supporting component identification in this important technique. In this work, approaches to use of the retention index in GC × GC are discussed, based on an evaluation of the literature in this area. Interpretation of effective chain length data for fatty acid methyl esters in the first and second dimensions is presented.

The detector is an integral and important part of any chromatographic system. The chromatographic peak profiles (i.e. peak separation) should, ideally, be unaffected by the detector--it should only provide the sensing capacity required at the end of a column separation process. The relatively new technique of comprehensive 2-D GC (GC x GC) extends the performance of GC manyfold, but comes at a price--existing GC systems may not be adequately designed with the requirements of GC x GC in mind. This is primarily the need for precise measurement of very fast peaks entering the detector (e.g. as fast as 50 ms basewidth in some instances). The capacity of the detector to closely track a rapidly changing chromatographic peak profile depends on a number of factors, such as design of flow paths and make-up gas introduction, type of detector response mechanism, and the chemistry of the response. These factors are discussed here as a means to appreciate the technical demands of detection in GC x GC. The MS detector will not be included in this review.