储层气体中的二氧化碳:来自盆地和油气系统建模的新见解

N. Koronful, K. Peters, M. F. Ali, J. Skulsangjuntr, Longcong Jiang, A. Kleine, Depnath Basu, J. Bencomo, Jonathan Hernandez, G. Brink
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引用次数: 1

摘要

在许多含油气盆地,特别是在东南亚,储层中的高二氧化碳限制了成功的勘探。近海Malay盆地的高储层二氧化碳是一个重大的勘探挑战。一些油田的二氧化碳含量超过80%,这使得它们不适合开发。关于二氧化碳起源的各种假设已经提出,但仍有争议。本文表明,地球化学和先进的石油系统建模有助于解决储层二氧化碳的来源,并允许在钻探前对潜在储层目标的二氧化碳进行定量估计。一种新的工作流程基于对CO2起源的化学机制的了解和地质埋藏史的数值模拟来估算储层中的CO2含量。热流、覆盖岩沉积和特定反应机制的动力学控制了CO2生成的时间和不同来源CO2的相对贡献。利用稳定碳同位素比值(δ13CCO2和δ13CCH4,‰)确定马来盆地天然气样品中CO2的来源。例如,图3显示了附近油田不同深度样品的δ13CCO2和δ13CCH4。同位素数据表明,样品中含有来自两个不同来源的不同机制的混合CO2。以%CO2为因变量,对61个样品的δ13CCO2和δ13CCH4与深度进行偏最小二乘回归分析,结果表明预测值与实测值之间存在系统相关性。交替最小二乘法(ALS)证实了两个端元气体的混合作用:(1)较浅样品中CO2含量较低,同位素富集于δ13CCH4和δ13CCO2;(2)较深样品中CO2含量较高,同位素富集于δ13CCH4和δ13CCO2。可以计算出每种气体在混合物中各端元的相对比例。附近气田近端气体的例子(图3)有:(1)干酪根裂解产生的浅层热成因CO2,如1681 m, 5% CO2, δ13CCH4 = -60‰,δ13CCO2 = -13‰,(100:0混合);(2)碳酸盐分解产生的深层CO2,如2918 m, 74% CO2, δ13CCH4 = -32‰,δ13CCO2 = -3‰(15:85混合)。这些结果与马来盆地中新世圈闭的一般观测结果一致,表明靠近碳酸盐基底的深层圈闭中CO2浓度较高。在盆地的其他地区,生物源CO2可能是第三个端元。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbon Dioxide in Reservoir Gases: New Insights from Basin and Petroleum System Modeling
High carbon dioxide in reservoirs limits successful exploration in many petroliferous basins, particularly in Southeast Asia. High reservoir CO2 in the offshore Malay Basin represents a significant exploration challenge. Some fields contain >80% CO2, which makes them unattractive targets for development. Various hypotheses on the origin of CO2 have been proposed but remain controversial. This paper shows that geochemistry and advanced petroleum system modeling help to resolve the origins of reservoir CO2 and allow quantitative estimates of CO2 in prospective reservoir targets prior to drilling. A novel workflow estimates the CO2 content in reservoirs based on knowledge of the chemical mechanisms for the origin of the CO2 and numerical simulation of geologic burial history. Heat flow, deposition of overburden rock, and the kinetics of specific reaction mechanisms control the timing of CO2 generation and the relative contributions of CO2 from different sources. In this study, stable carbon isotope ratios of CO2 and methane (δ13CCO2 and δ13CCH4, ‰) were used to identify the source of the CO2 in Malay Basin gas samples. For example, Figure 3 shows δ13CCO2 and δ13CCH4 for samples from various depths in the nearby field. The isotope data indicate that the samples contain mixed CO2 derived by different mechanisms from two sources. Partial least squares (PLS) regression of δ13CCO2 and δ13CCH4 and depth for 61 samples from the nearby field, where %CO2 was set as the dependent variable, resulted in a systematic correlation between predicted and measured %CO2. Alternate least squares (ALS) confirms that the data can be explained by mixing of gases from two endmembers: (1) shallower samples show lower %CO2 that is isotopically depleted in δ13CCH4 and δ13CCO2, and (2) deeper samples show higher %CO2 that is isotopically enriched in δ13CCH4 and δ13CCO2. The relative proportion of each endmember in the mixture can be calculated for each gas. Examples of near endmember gases in the nearby field (Figure 3) are: (1) shallow thermogenic CO2 derived by cracking of kerogen, e.g., 1681 m, 5% CO2, δ13CCH4 = -60‰, δ13CCO2 = -13‰, (100:0 mix); and (2) deep CO2 from carbonate decomposition, e.g., 2918 m, 74% CO2, δ13CCH4 = -32‰, δ13CCO2 = -3‰ (15:85 mix). These results are consistent with the general observation that tested Miocene traps in the Malay Basin and show a general trend of higher concentrations of CO2 in the deeper traps that are nearer carbonate basement. Biogenic CO2 may represent a third endmember in other parts of the basin.
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