Profiling Alkyl Phosphates in Industrial Petroleum Samples by Comprehensive Two-Dimensional Gas Chromatography with Nitrogen Phosphorus Detection (GC 脳 GC鈥揘PD), Post-column Deans Switching, and Concur

详细信息    查看全文

• 作者：Katie D. Nizio ; James J. Harynuk
• 刊名：Energy & Fuels
• 出版年：2014
• 出版时间：March 20, 2014
• 年：2014
• 卷：28
• 期：3
• 页码：1709-1716
• 全文大小：272K
• 年卷期：v.28,no.3(March 20, 2014)
• ISSN：1520-5029

文摘

Several refinery fouling incidents in North America have been due to the presence of alkyl phosphates in the crude oil feed. These phosphates originate in some cases from their use as gellants (viscosity builders) for fracturing fluids used in the process of hydraulic fracturing in water-sensitive geologies. Industry responded with an inductively coupled plasma鈥搊ptical emission spectroscopy (ICP鈥揙ES) method for the analysis of total volatile phosphorus. Applied to distillate fractions of crude oil, this method is plagued with limited precision and a high limit of detection (0.5 卤 1 渭g of phosphorus mL^鈥?). This approach provides only total P with no speciation information; thus, it cannot be used to develop an understanding of alkyl phosphate fouling at a molecular level. Our group previously presented an approach using comprehensive two-dimensional gas chromatography with nitrogen phosphorus detection (GC 脳 GC鈥揘PD) and post-column Deans switching that provided qualitative and quantitative profiles of alkyl phosphates in industrial petroleum samples with increased precision and at levels comparable to or below those achievable by ICP鈥揙ES. Here, we present a refinement to this method that incorporates splitless injection and concurrent backflushing. Using this technique, it is possible to quantify alkyl phosphates to levels 2 orders of magnitude lower than those achieved with our previous approach and 2鈥? orders of magnitude lower than what is possible by ICP鈥揙ES while still maintaining an increased precision over ICP鈥揙ES. The addition of concurrent backflushing provided column protection, reducing instrument maintenance and improving the reproducibility of retention times when analyzing heavier industrial petroleum fractions. A recovery study performed in two different industrial petroleum samples demonstrated the reliability of calibrations performed in solvent when used for quantification of alkyl phosphates in real samples. Finally, a profiling study of alkyl phosphates in 14 different industrial petroleum samples (crude oil and mixtures of crude oil and fracture fluid) is also presented.