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This work has been selected by scholars as being culturally important and is part of the knowledge base of civilization as we know it. This work is in the public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. To ensure a quality reading experience, this work has been proofread and republished using a format that seamlessly blends the original graphical elements with text in an easy-to-read typeface. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.
Analysis of Petroleum for Trace Elements details the methods for detecting the elements that are natural in various forms in petroleum. The book covers research and control applications, along with various types of petroleum stocks and products. The selection first covers the occurrence and importance of traces of non-hydrocarbon constituents, and then proceeds to tackling the principles and practices. The subsequent chapters cover the analytical and recommended method for analysis of a specific element, such as copper, iron, lead, and sulfur. The book will be of great use to scientists, engineers, and technicians involved in the oil industry.
This work has been selected by scholars as being culturally important and is part of the knowledge base of civilization as we know it. This work is in the public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. To ensure a quality reading experience, this work has been proofread and republished using a format that seamlessly blends the original graphical elements with text in an easy-to-read typeface. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.
The advent of inductively coupled plasma quadrupole mass spectrometry (ICP MS) largely contributed to reliable and fast multielement trace analysis of petroleum samples but the inherent problems related to plasma instability, carbon deposition on the sampler and skimmer cones and carbon-related polyatomic interferences are omnipresent. The goal of this work was to address several analytical tasks impossible to be successfully handled by ICP quadrupole ICP MS. They include the determination of non-metals, such as sulphur and silicon, simultaneous multielement trace analysis at the low ng g-1 levels, and insight into the molecular binding of the trace elements present. The method developed for the sulphur determination in gasoline was based on the formation of microemulsion introduced directly into the ICP. Quantification was carried out by ICP AES using external calibration which allowed high throughput analysis. The developed method was applied for total sulphur analysis in diesel samples from various gas stations in Thailand. Problems related to spectral interferences were alleviated by the use of a double-focusing sector field ICP MS optimized for the direct simultaneous determination of Ag, Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Pb, Sn, Ti, and V. Polyatomic interferences originating from the carbon-rich matrix were completely eliminated at a resolution of 4000 allowing the detection limits at the low pg g-1 level to be obtained (typically one order of magnitude lower than using a quadrupole ICP MS). A method for the routine comprehensive trace element analysis of xylene solutions of oil samples using external calibration was developed, validated by the analysis of CRMs and applied to the analysis of gas condensate and oil samples. Another method based on the micro-flow injection total consumption sample introduction was developed for the silicon determination allowing the detection limits down to 1 ng g-1. The effects of the sample matrix and of the chemical form of silicon on the sensitivity were investigated and alleviated when necessary by heating the spray chamber and sample dilution. Laser ablation-ICP-SF MS was developed for direct multielement analysis in crude oils and asphaltenes. A silica gel plate was impregnated for 30 min with a sample solution and analyzed by laser ablation-ICP MS. Carbon-related polyatomic interferences and matrix suppression effects were absent enabling quantitation by external calibration. The detection limits were in the low ng g-1 range. The method was validated by the analysis of NIST 1084a and 1085b certified reference materials (wear metals in lubricating oils) and applied to the analysis of crude oil and asphaltene samples. An insight into the chemical forms of Co, Cr, Fe, Ni, S, Si, V and Zn present in crude oil and oil vacuum distillation residue was gained by the coupling of microchromatography using permeation through gels with the increasing exclusion limit (5000, 400 000 and 20 000 000 Da) with high resolution (R = 4000) ICP MS. The method allowed the acquisition of chromatograms with high sensitivity competitive to the existing methods, showing element- and sample origin-dependent morphology. Normal phase HPLC-ICP MS and size-exclusion ICP MS were proposed to evaluate the purity of the silicon standard compounds, their reactivity with different petroleum-related matrices and speciation of silicon.