Generation of abnormal distributions of inter- and intramolecular δ13C compositions in hydrocarbons from gold tube pyrolysis of an Australian torbanite

IF 2.6 3区 地球科学 Q2 GEOCHEMISTRY & GEOPHYSICS
Zhirong Zhang , Caiming Zhang , Yan’e Chen , John K. Volkman , Yongge Sun
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Abstract

Abnormal stable carbon isotopic (δ13C) compositions, deviating from the conventional order of δ13C1 < δ13C2 < δ13C3, are frequently observed in natural gas reservoirs. For thermogenic gas, these anomalies, such as δ13C1 < δ13C3 < δ13C2 or δ13C1 > δ13C2 > δ13C3, have multiple formation mechanisms including gas mixing in conventional systems and desorption processes of gaseous hydrocarbons in unconventional shale gas systems due to their inconsistency with Rayleigh fractionation processes. Considering distinct reaction pathways (e.g., C1 polymerized to C2), these aberrant δ13C signatures are often construed as intrinsic hallmarks of extensively evolved natural gas. However, on the basis of gas generation simulation, not all findings exhibit abnormal δ13C values, hinting at multifaceted and intricate mechanisms governing the isotopic fractionation of alkane gas components. This study conducted gold tube pyrolysis of an Australian torbanite, revealing four distinct types of δ13C anomalies in hydrocarbon classes. Polycyclic aromatic hydrocarbons (PAHs) exhibited δ13C values more negative than co-occurring n-alkanes. δ13C3 displayed a negative trend shift from EasyRo = 3.5 %, resulting in a partially δ13C-reversed gas (δ13C1 < δ13C3 < δ13C2) formed at EasyRo ≈ 4.1 %. Moreover, intramolecular δ13C3 (both terminal and central carbons, termed δ13Ca and δ13Cb, respectively) reversed alongside the overall δ13C3 trend. Additionally, the evolution of site preference in δ13C3 (termed ‰SP = δ13Ca – δ13Cb) transitioned from progressively negative to positive. The results of this study demonstrate that the potential conversion between saturated hydrocarbons, aromatic hydrocarbons, and alkane gases is at least partially responsible for δ13C anomalies, but also that gaseous hydrocarbons formed from other fractions at high maturity cannot be ruled out, such as kerogen and pyrobitumen.

澳大利亚托班石金管热解产生的碳氢化合物分子间和分子内 δ13C 成分的异常分布
在天然气储层中经常可以观察到异常的稳定碳同位素(δ13C)组成,它们偏离了常规的 δ13C1 < δ13C2 < δ13C3 的顺序。对于热成因气体,这些异常(如 δ13C1 < δ13C3 < δ13C2 或 δ13C1 > δ13C2 > δ13C3)有多种形成机制,包括常规系统中的气体混合和非常规页岩气系统中的气态碳氢化合物解吸过程,因为它们与瑞利分馏过程不一致。考虑到不同的反应途径(如 C1 聚合为 C2),这些反常的 δ13C 特征通常被认为是广泛演化的天然气的固有特征。然而,根据气体生成模拟,并非所有研究结果都显示出异常的 δ13C 值,这表明烷烃气体成分的同位素分馏具有多方面的复杂机制。本研究对澳大利亚的一种托班石进行了金管热解,揭示了碳氢化合物类别中四种不同类型的 δ13C 异常。多环芳烃 (PAH) 的 δ13C 值比共存的正构烷烃更负。从 EasyRo = 3.5 % 开始,δ13C3 呈负趋势变化,导致在 EasyRo ≈ 4.1 % 时形成部分δ13C 反转气体(δ13C1 < δ13C3 < δ13C2)。此外,分子内 δ13C3(末端碳和中心碳,分别称为 δ13Ca 和 δ13Cb)与总体 δ13C3趋势同时发生逆转。此外,δ13C3(术语为 ‰SP = δ13Ca - δ13Cb)的位点偏好演化也逐渐由负转正。这项研究结果表明,饱和碳氢化合物、芳香烃和烷烃气体之间的潜在转化至少是造成δ13C异常的部分原因,但也不能排除其他馏分在高成熟度时形成的气态碳氢化合物,如角质和焦沥青。
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来源期刊
Organic Geochemistry
Organic Geochemistry 地学-地球化学与地球物理
CiteScore
5.50
自引率
6.70%
发文量
100
审稿时长
61 days
期刊介绍: Organic Geochemistry serves as the only dedicated medium for the publication of peer-reviewed research on all phases of geochemistry in which organic compounds play a major role. The Editors welcome contributions covering a wide spectrum of subjects in the geosciences broadly based on organic chemistry (including molecular and isotopic geochemistry), and involving geology, biogeochemistry, environmental geochemistry, chemical oceanography and hydrology. The scope of the journal includes research involving petroleum (including natural gas), coal, organic matter in the aqueous environment and recent sediments, organic-rich rocks and soils and the role of organics in the geochemical cycling of the elements. Sedimentological, paleontological and organic petrographic studies will also be considered for publication, provided that they are geochemically oriented. Papers cover the full range of research activities in organic geochemistry, and include comprehensive review articles, technical communications, discussion/reply correspondence and short technical notes. Peer-reviews organised through three Chief Editors and a staff of Associate Editors, are conducted by well known, respected scientists from academia, government and industry. The journal also publishes reviews of books, announcements of important conferences and meetings and other matters of direct interest to the organic geochemical community.
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