doctoralThesis
Desenvolvimento de método para determinação de cloro em petróleo via molécula MgCl por HR-CS MAS
Fecha
2017-07-28Registro en:
OLIVEIRA, Izabel Kaline da Silva. Desenvolvimento de método para determinação de cloro em petróleo via molécula MgCl por HR-CS MAS. 2017. 74f. Tese (Doutorado em Ciência e Engenharia de Petróleo) - Centro de Ciências Exatas e da Terra, Universidade Federal do Rio Grande do Norte, Natal, 2017.
Autor
Oliveira, Izabel Kaline da Silva
Resumen
Chloride is considered an important contaminant of petroleum as it interferes with the process of transportation and refining and can be transferred to the final product derivatives. During refining, the presence of chloride may lead to the formation of HCl, causing serious corrosion problems. A methodology for the determination of chlorine in petroleum samples prepared by emulsions was developed by high resolution molecular absorption spectrometry with continuum source through the diatomic molecule MgCl, in the wavelength 377.01 nm. The preparation of the emulsion was optimized through centroid-simplex design. The conditions of preparation of the emulsions were: 0.5 mL of 5% (v / v) HNO3, 0.5 mL of xylene and 2 mL of a mixture of n-Propanol / Triton X-100 solvents in the ratio 5:1. The crude oil mass used was about 0.20 g. Magnesium was used as the precursor of the molecule, the optimized concentration was 10 g L-1. The proportional studies between Mg and Cl for the formation of molecules show that to ensure the formation of a MgCl molecule is required for a mass ratio of at least 500 Mg: 1 Cl. A mass of 5 μg of Pd was introduced at each cycle that chemical modifier for increase the thermal stability of the molecular species. The optimized pyrolysis and vaporization temperatures were 800 ° C and 2300 ° C, respectively. For chlorine analysis, eight crude oil samples from the Potiguar Basin and two certified reference materials, lubricated oil (NIST 1848) and fuel oil (NIST 1634c) were used, to verify the accuracy of the method. The calibration strategy against aqueous standards was possible, obtaining the LOD of 5 mg kg-1. Addition / recovery tests were performed and the values obtained were between 92 and 117%, values acceptable analytically. The proposed methodology is simple, fast with simplified sample preparation.