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Insights into oil cracking based on laboratory experiments

机译:根据实验室实验洞悉石油裂化

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The objectives of this pyrolysis investigation were to determine changes in (1) oil composition, (2) gas composition and (3) gas carbon isotope ratios and to compare these results with hydrocarbons in reservoirs. Laboratory cracking of a saturate-rich Devonian oil by confined, dry pyrolysis was performed at T=350-450 degreesC, P=650 bars and times ranging from 24 h to 33 days. Increasing thermal stress results in the C15+ hydrocarbon fraction cracking to form C6-14 and C1-5 hydrocarbons and pyrobitumen. The C6-14 fraction continues to crack to C1-5 gases plus pyrobitumen at higher temperatures and prolonged heating time and the delta C-13(ethane)-delta C-13(propane) difference becomes greater as oil cracking progresses. There is considerable overlap in product generation and product cracking. Oil cracking products accumulate either because the rate of generation of any product is greater than the rate of removal by cracking of that product or because the product is a stable end member under the experimental conditions. Oil cracking products decrease when the amount of product generated from a reactant is less than the amount of product cracked. If pyrolysis gas compositions are representative of gases generated from oil cracking in nature, then understanding the processes that alter natural gas composition is critical. (C) 2003 Elsevier Ltd. All rights reserved. [References: 70]
机译:热解研究的目的是确定(1)石油成分,(2)气体成分和(3)气体碳同位素比的变化,并将这些结果与储层中的碳氢化合物进行比较。在T = 350-450摄氏度,P = 650巴,时间为24小时至33天的条件下,通过密闭的干法热解法对饱和饱和泥盆纪油进行实验室裂解。热应力的增加导致C15 +烃馏分裂解形成C6-14和C1-5烃和焦土。在更高的温度和延长的加热时间下,C6-14馏分继续裂化为C1-5气体和焦碳酸盐,随着油裂的进行,δC-13(乙烷)-δC-13(丙烷)的差值变得更大。在产品生成和产品开裂方面存在大量重叠。油裂化产物的积聚是因为任何产物的生成速率大于该产物裂化的去除速率,或者因为该产物在实验条件下是稳定的末端成员。当从反应物产生的产物的量小于裂化的产物的量时,油裂化的产物减少。如果热解气体的成分代表自然界中石油裂解产生的气体,那么了解改变天然气成分的过程就至关重要。 (C)2003 Elsevier Ltd.保留所有权利。 [参考:70]

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