masterThesis
Avaliação de metodologia de preparo de amostra de petróleo por digestão ácida auxiliada por microondas para determinação de metais por ICP-OES
Avaliação de metodologia de preparo de amostra de petróleo por digestão ácida auxiliada por microondas para determinação de metais por ICP-OES
Fecha
2012-12-14Registro en:
SILVA, Izabel Kaline Vicente da. Avaliação de metodologia de preparo de amostra de petróleo por digestão ácida auxiliada por microondas para determinação de metais por ICP-OES. 2012. 62 f. Dissertação (Mestrado em Pesquisa e Desenvolvimento em Ciência e Engenharia de Petróleo) - Universidade Federal do Rio Grande do Norte, Natal, 2012.
Autor
Silva, Izabel Kaline Vicente da
Resumen
This project describes a methodology optimization that would allow for a more
efficient microwave assisted digestion process for petroleum samples. With the
possible chance to vary various factors at once to see if any one factor was significant
enough in the answers, experimental planning was used. Microwave assisted digestion
allows, through the application of potency, an increasing number of collisions between
the HNO3 and H2O2 molecules, favoring sample opening for complex matrixes. For
this, a 24 factorial experimental planning was used, varying potency, time and the
volumes for HNO3 65% and H2O2 30%. To achieve the desired answers, several
elements were monitored (C, Cu, Cr, Fe, Ni, Zn and V) through Inductively coupled
plasma atomic emission spectroscopy (ICP-OES). With this initial study it was noticed
that the HNO3 was not a significant factor for any of the statistical studies for any of
the analytes and the other 3 factors and their interactions showed statistical
significance. A Box Behnken experimental planning was used taking in consideration
3 factors: H2O2 volume, time (min) and Potency (W), Nitric Acid kept at 4mL for a
mass of 0,1g of petroleum. The results were extremely satisfying showing higher
efficiency in the digestion process and taking in a responsibility between the answers
for each analyte and the carbon monitoring was achieved in the following conditions:
7mL of H2O2, 700 Watts of potency and a reaction time of 7 minutes with 4mL de
HNO3 for a mass of 0,1g of petroleum. The optimized digestion process was applied to
four different petroleum samples and the analytes determined by ICP-OES