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首页> 外文期刊>Organic Geochemistry: A Publication of the International Association of Geochemistry and Cosmochemistry >Bound hydrocarbons and structure of pyrobitumen rapidly formed by asphaltene cracking: Implications for oil-source correlation
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Bound hydrocarbons and structure of pyrobitumen rapidly formed by asphaltene cracking: Implications for oil-source correlation

机译:沥青质裂缝快速形成的烧焦烧结霉菌和结构:对油源相关的影响

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The pyrobitumen in conventional petroleum reservoirs is a thermally altered product of ancient oil pools, which may provide valuable source information using its molecular and isotopic signatures. Pyrobitumen formation is often associated with thermal alteration of asphaltene or polar-rich components rather than that of oil as a whole. Although asphaltenes are useful in source correlation of altered oils, the geochemical characteristics of asphaltene-derived pyrobitumen are poorly understood. In this study, artificial pyrobitumen formation through oil asphaltene cracking was performed at different thermal simulation (i.e., pyrolysis) temperatures. Systematic variations in the amounts and distributions of extractable and bound hydrocarbons, released by catalytic hydropyrolysis of the artificially produced pyrobitumen were studied. Pyrobitumen production yield was high at pyrolysis temperatures corresponding to post oil peak maturities, with a maximum yield of similar to 70 wt% of asphaltene being reached in the early condensate-wetgas stage. The molecular structure of pyrobitumen varied only slightly over the high maturity range (EasyRo 1.64-2.51%). Compared with the parent asphaltene, the pyrobitumen had a low biomarker (e.g., regular steranes and terpanes) content, and even the carbon isotopic values of the more stable bound n-alkanes were strongly altered. Thermal cracking of asphaltene alone, rather than whole oil, accelerates cross-linking of aromatic units, and cleavage or condensation of molecules bound in the pyrobitumen. These molecular changes suggest that care is needed when using the geochemical characteristics of bound hydrocarbons in natural pyrobitumen for source determinations. Nevertheless, the carbon isotopic ratios of bulk pyrobitumen hydropyrolysate were similar to those of bulk oil or pyrobitumen, even at very high maturities, suggesting these may be reliable indices for source tracing. A comparison of carbon isotopic compositions between pyrobitumen-bound and solvent-extractable n-alkanes could be useful in determining whether they have the same origin. Furthermore, the compositional and isotopic characteristics of bound hydrocarbons in pyrobitumen may provide information on the stage of maturity under geological conditions. The investigation of free and bound molecules may thus elucidate pyrobitumen genesis as related to its source, thermal maturity, and possible later hydrocarbon charging. (C) 2020 Elsevier Ltd. All rights reserved.
机译:传统的石油储层中的哒来自古代油池的热改变产物,可以使用其分子和同位素签名提供有价值的源信息。吡虫蛋白形成通常与沥青质或极性富含组分的热改变而不是整体油的热改变。虽然沥青质可用于改变油的源相关性,但是沥青质衍生的吡虫松的地球化学特征是较差的理解。在该研究中,在不同的热模拟(即热解)温度下进行通过油沥青质裂纹形成人造芘。研究了通过人工制作的芘中催化水解物释放的可萃取和结合烃的量和分布的系统变化。在对应于油峰峰期达到后的热解温度下的热解温度下吡虫脲产率高,在早期的冷凝物 - 湿度阶段达到最大屈服于70wt%的沥青质。芘的分子结构仅在高分状态范围内略微不同(EasyRO 1.64-2.51%)。与父母沥青烯相比,吡脲具有低生物标志物(例如,正常的Steanes和萜状物)含量,甚至甚至都强烈地改变了更稳定的N-烷烃的碳同位素值。单独的沥青质的热裂解,而不是全油,加速芳族单元的交联,并在吡虫皮中结合的分子切割或缩合。这些分子变化表明,当使用天然芘中的结合烃的地球化学特性进行源测定时,需要小心。尽管如此,即使在非常高的情况下,本体吡虫吡脲氢吡硼酸氢吡吡硼酸盐液的碳同位素比例也与散装油或哒杆菌的碳同位素比例相似,这表明这些可能是用于源追踪的可靠指标。拟合溶剂 - 溶剂可萃取的N-烷烃之间的碳同位素组合物的比较可用于确定它们是否具有相同的起源。此外,芘中结合烃的组成和同位素特征可以在地质条件下提供有关成熟阶段的信息。因此,对自由和结合分子的研究可以阐明与其来源,热成熟度和可能的以后的烃充电有关的哒虫蛋白成因。 (c)2020 elestvier有限公司保留所有权利。

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