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首页> 外文期刊>Oil & gas science and technology >Natural Geochemical Analogues for Carbon Dioxide Storage in Deep Geological Porous Reservoirs, a United Kingdom Perspective
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Natural Geochemical Analogues for Carbon Dioxide Storage in Deep Geological Porous Reservoirs, a United Kingdom Perspective

机译:英国深层地质多孔储层中二氧化碳储存的天然地球化学类似物

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Elevated concentrations of atmospheric CO2 are implicated in global warming. Mitigation of this requires capture of CO2 from fossil fuel power sources and storage in subsurface aquifers or depleted hydrocarbon fields. Demonstration projects and financial analysis suggest that this is technologically feasible. CO2 must retained below ground for 104 y into the future to enable the surface carbon cycle to reduce atmospheric CO2 levels. To provide robust predictions of the performance of disposal sites at the required timescale, one approach is to study natural CO2 accumulations, which give insight into rock-CO2-brine interactions over timescales of 103 - 5.106 y. In contrast to geochemical modelling predictions, natural CO2 fields in the North Sea (Brae, Miller, Magnus, Sleipner), at 4.0 km and deeper, do not show the mineral products which are predicted to form. Calcite and feldspar still comprise 5-20% of the rock, and dawsonite is absent. SE Australian and Arizona reservoir sandstones also do not fit to geochemical predictions. A state of disequilibrium possibly exists, so that existing geochemical modelling is not capable of accurately predicting kinetic-controlled and surface-chemistry controlled mineral dissolution or precipitation in natural subsurface sandstones on the required timescales. Improved calibration of models is required. Geochemical evidence from laboratory experiments (months to years duration), or from enhanced oil recovery (30 y duration) are again too short in timescale. To help to bridge the 104 y gap, it may be useful to examine natural analogues (103-106 y), which span the timescale required for durable disposal. The Colorado Plateau is a natural CO2 system, analogous to an hydrocarbon system, where 100 Gm3 CO2 fields occur, sourced from 0-5 Ma volcanics. Deep erosion has exposed the sediments which formed CO2 source, CO2 carrier, CO2 reservoir, CO2 trap, CO2 seal. Some very large CO2 traps are now exhumed, and some are currently leaking to form cool travertine springs at the surface. Natural examples at Salt Wash Green River, and at Moab Fault are briefly described. These show extensive bleaching of haematite which may be locally redeposited, carbonate cementation ?13C -70 around point sources, and silica precipitation, which may seal leak-off on buried anticline crests. Accurate geochemical modelling of the long-term performance of CO2 storage sites, requires improved understanding of CO2 reaction paths and reaction rates with aquifer reservoirs and with overlying seals. Robust prediction of disposal site performance is not possible without this.
机译:大气中二氧化碳浓度升高与全球变暖有关。要减轻这种状况,需要从化石燃料动力源中捕获CO2,并将其存储在地下含水层或枯竭的油气田中。示范项目和财务分析表明,这在技术上是可行的。未来必须将CO2保留在地下104 y,以使地表碳循环降低大气中的CO2水平。为了对所需时间范围内的处置场的性能提供可靠的预测,一种方法是研究自然的CO2积累,从而深入了解103-5.106 y时间范围内岩石与CO2盐水的相互作用。与地球化学模拟预测相反,北海(Brae,Miller,Magnus,Sleipner)的自然CO2场(4.0公里或更深)没有显示出预计会形成的矿物产品。方解石和长石仍占岩石的5-20%,而片钠铝石则不存在。东南澳大利亚和亚利桑那州的储层砂岩也不符合地球化学预测。可能存在不平衡状态,因此现有的地球化学模型无法在所需的时间尺度上准确预测天然地下砂岩中动力学控制和表面化学控制的矿物溶解或降水。需要改进模型的校准。实验室实验(持续数月至数年)或提高采油率(持续30年)的地球化学证据在时间尺度上也太短了。为了帮助弥合104 y的差距,研究天然的类似物(103-106 y)可能有用,它跨越了持久处置所需的时间范围。科罗拉多高原是天然的CO2系统,类似于碳氢化合物系统,其中100 Gm3的CO2气田来自0-5 Ma的火山岩。深层侵蚀暴露了形成CO2源,CO2载体,CO2储集层,CO2捕集器,CO2封口的沉积物。现在挖掘出一些非常大的二氧化碳捕集阱,一些目前正在泄漏,从而在地表形成冷石灰华弹簧。简要描述了盐洗绿河和摩押断层的自然实例。这些表明赤铁矿的广泛漂白可能在局部重新沉积,点源周围的碳酸盐胶结物δ13C-70以及二氧化硅沉淀,这可能密封了埋在背斜顶的泄漏。要对CO2储存地点的长期性能进行准确的地球化学建模,就需要对CO2反应路径和含水层储层以及上覆海豹的反应速率有更好的了解。没有这个,就不可能对处置场的性能进行可靠的预测。

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