Quantification of C10–C14 Adamantanes in High-Viscosity Naphthenic Oils

IF 1.3 4区 工程技术 Q3 CHEMISTRY, ORGANIC
M. G. Kulkov, G. T. Salakhidinova, E. A. Vtorushina, R. I. Butyrin, A. E. Aliev
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Abstract

The paraffin–naphthenic fractions (with boiling points below 310°C) prepared from three high-viscosity naphthenic crude oils, classified as types B1 and B2 (according to Petrov’s classification), were subjected to thiocarbamide complexation. The molecular composition of polycyclic hydrocarbon biomarkers and C11–C13 adamantanes in the oil samples suggested a predominantly marine genotype of the precursor organic matter (OM). The molecular composition also suggested source rocks of a clayey type. Nonetheless, the biomarkers detected in one sample indicated some contribution of terrigenous components to the precursor OM. All the oils were generated under the conditions of the main oil generation zone and, presumably, underwent microbial transformations in the deposits. The compositions of C10–C14 adamantanes in the initial paraffin–naphthenic fraction, in the thiocarbamide adduct, and in the filtrate that remained after the adduction were comparatively characterized for each oil sample. The test conditions allowed us to have adamantane more than 100-fold concentrated (in the adduct), to quantify it in the oils, and to evaluate the concentrations of C11–C14 alkyladamantanes in the oils using adamantane as an internal standard. C10–C14 adamantanes exhibited selective adduction ability, with the extraction ratios of individual components being different. Taking into account these extraction ratios, the component concentrations were evaluated on crude oil basis: 2.7 to 7.6×10–3 wt % for adamantane and 87 to 267×10–3 wt % for total C10–C14 adamantanes. The identification of adamantanes in the initial paraffin–naphthenic fractions, adducts, and filtrates revealed the presence of some other tricyclanes (probable precursors of alkyladamantanes) as well as decaline homologues. Like adamantanes, these compounds exhibited selective ability to complex with thiocarbamide.

Abstract Image

高粘度环烷油中 C10-C14 金刚烷的定量分析
摘要 对从三种高粘度环烷原油中制备的石蜡-环烷馏分(沸点低于 310°C)进行了硫代甲酰胺络合,这些原油被划分为 B1 和 B2 类型(根据 Petrov 的分类)。油样中多环烃类生物标记物和 C11-C13 金刚烷的分子组成表明,前体有机物 (OM) 主要是海洋基因型。分子组成也表明源岩属于粘土类型。不过,在一个样本中检测到的生物标记表明,前体有机物中含有一些陆生成分。所有油类都是在主要石油生成区的条件下产生的,可能在沉积物中经历了微生物转化。我们对每个油样的初始石蜡-环烷馏分、硫代甲酰胺加成物和加成后残留滤液中的 C10-C14 金刚烷组成进行了比较分析。测试条件允许我们将金刚烷的浓度(在加合物中)提高 100 倍以上,对油品中的金刚烷进行定量,并使用金刚烷作为内标来评估油品中 C11-C14 烷基金刚烷的浓度。C10-C14 金刚烷具有选择性吸附能力,各组分的萃取比各不相同。考虑到这些萃取率,以原油为基础对各组分的浓度进行了评估:金刚烷的浓度为 2.7 至 7.6×10-3 wt %,C10-C14 金刚烷总量的浓度为 87 至 267×10-3 wt %。通过对最初石蜡-环烷馏分、加成物和滤液中金刚烷的鉴定,发现了一些其他三环类化合物(可能是烷基金刚烷的前体)和癸碱同系物。与金刚烷类化合物一样,这些化合物也表现出与硫代甲酰胺络合的选择性能力。
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来源期刊
Petroleum Chemistry
Petroleum Chemistry 工程技术-工程:化工
CiteScore
2.50
自引率
21.40%
发文量
102
审稿时长
6-12 weeks
期刊介绍: Petroleum Chemistry (Neftekhimiya), founded in 1961, offers original papers on and reviews of theoretical and experimental studies concerned with current problems of petroleum chemistry and processing such as chemical composition of crude oils and natural gas liquids; petroleum refining (cracking, hydrocracking, and catalytic reforming); catalysts for petrochemical processes (hydrogenation, isomerization, oxidation, hydroformylation, etc.); activation and catalytic transformation of hydrocarbons and other components of petroleum, natural gas, and other complex organic mixtures; new petrochemicals including lubricants and additives; environmental problems; and information on scientific meetings relevant to these areas. Petroleum Chemistry publishes articles on these topics from members of the scientific community of the former Soviet Union.
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