首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of volatile and non-volatile nickel and vanadium compounds in crude oil using electrothermal atomic absorption spectrometry after oil fractionation into saturates, aromatics, resins and asphaltenes
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Determination of volatile and non-volatile nickel and vanadium compounds in crude oil using electrothermal atomic absorption spectrometry after oil fractionation into saturates, aromatics, resins and asphaltenes

机译:将油分馏成饱和物,芳烃,树脂和沥青质后,使用电热原子吸收光谱法测定原油中的挥发性和非挥发性镍和钒化合物

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In recent work, it has been shown that electrothermal atomic absorption spectrometry (ET AAS) can be used to differentiate between volatile and non-volatile nickel and vanadium compounds in crude oil. In the present work, the distribution of these two groups of compounds over different fractions of crude oil was investigated. For this purpose two crude oil samples were separated in two steps: firstly, the asphaltenes were precipitated with n-heptane, and secondly, the maltenes were loaded on a silica column and eluted with solvents of increasing polarity. The four fractions of maltenes eluted from silica column were: F1, saturated and light aromatics; F2, polyaromatics; F3, resins; and F4, polar compounds. Fractions F1 and F2 were further investigated using gas chromatography, and all fractions were characterized by CHN analysis, confirming the increase of aromatics in the fractions 2, 3, 4 and asphaltenes. For the determination of Ni and V by ET AAS, oil-in-water emulsions were prepared. The speciation analysis was carried out measuring without chemical modifier (stable compounds) and with 20 mu g palladium (total Ni and V) and the volatile fraction was calculated by difference. The limits of detection were 0.02 mu g g(-1) and 0.06 mu g g(-1), for Ni and V, respectively, based on an emulsion of 2 g of oil in 10 mL. The volatile species of Ni and V were associated with fractions F3 and F4, while only thermally stable Ni and V was precipitated in part together with the asphaltenes. (c) 2007 Elsevier B.V. All rights reserved.
机译:在最近的工作中,已经表明,电热原子吸收光谱法(ET AAS)可用于区分原油中的挥发性和非挥发性镍和钒化合物。在本工作中,研究了这两组化合物在不同馏分原油中的分布。为此,在两个步骤中分离了两个原油样品:首先,用正庚烷沉淀沥青质,其次,将麦芽糖装入硅胶柱上,并用极性增加的溶剂洗脱。从硅胶柱上洗脱的麦芽汁的四个部分为:F1,饱和芳烃和轻质芳烃; F2,聚芳烃; F3,树脂;和F4,极性化合物。使用气相色谱进一步研究馏分F1和F2,并通过CHN分析对所有馏分进行表征,确认馏分2、3、4和沥青质中芳烃的增加。为了通过ET AAS测定Ni和V,制备了水包油乳液。在没有化学改性剂(稳定化合物)和有20μg钯(总Ni和V)的情况下进行了形态分析,并通过差值计算了挥发性分数。基于2 g油在10 mL中的乳液,Ni和V的检出限分别为0.02μg g(-1)和0.06μgg(-1)。 Ni和V的挥发性物质与馏分F3和F4有关,而只有热稳定的Ni和V与沥青质一起部分沉淀。 (c)2007 Elsevier B.V.保留所有权利。

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