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Experimental superheating of water and aqueous solutions

机译:水和水溶液的实验过热

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摘要

The metastable superheated solutions are liquids in transitory thermodynamic equilibrium inside the stability domain of their vapor (whatever the temperature is). Some natural contexts should allow the superheating of natural aqueous solutions, like the soil capillarity (low T superheating), certain continental and submarine geysers (high T superheating), or even the water state in very arid environments like the Mars subsurface (low T) or the deep crustal rocks (high T). The present paper reports experimental measurements on the superheating range of aqueous solutions contained in quartz as fluid inclusions (Synthetic Fluid Inclusion Technique, SFIT) and brought to superheating state by isochoric cooling. About 40 samples were synthetized at 0.75 GPa and 530-700 degrees C with internally-heated autoclaves. Nine hundred and sixty-seven inclusions were studied by micro-thermometry, including measuring the temperatures of homogenization (Th: L + V --> L) and vapor bubbles nucleation (Tn: L --> L + V). The Th-Tn difference corresponds to the intensity of superheating that the trapped liquid can undergo and can be translated into liquid pressure (existing just before nucleation occurs at Tn) by an equation of state. Pure water (840-935 kg m(-3)), dilute NaOH solutions (0.1 and 0.5 mol kg(-1)), NaCl, CaCl2 and CsCl solutions (1 and 5 mol kg(-1)) demonstrated a surprising ability to undergo tensile stress. The highest tension ever recorded to the best of our knowledge (-146 MPa, 100 degrees C) is attained in a 5 m CaCl2 inclusion trapped in quartz matrix, while CsCl solutions qualitatively show still better superheating efficiency. These observations are discussed with regards to the quality of the inner surface of inclusion surfaces (high P-T synthesis conditions) and to the intrinsic cohesion of liquids (thermodynamic and kinetic spinodal). This study demonstrates that natural solutions can reach high levels of superheating, that are accompanied by strong changes of their physico-chemical properties.
机译:亚稳态过热溶液是在其蒸气的稳定域内(无论温度如何)处于短暂热力学平衡的液体。一些自然环境应允许天然水溶液过热,例如土壤毛细作用(低T过热),某些大陆和海底间歇泉(高T过热),甚至是在非常干旱的环境(如火星地下)中的水状态(低T)。或深地壳岩石(高T)。本文报道了石英中作为流体包裹体(合成流体包裹体技术,SFIT)所含水溶液的过热度的实验测量结果,并通过等速冷却使其达到过热状态。用内部加热的高压釜在0.75 GPa和530-700摄氏度下合成了大约40个样品。通过微热法研究了967个夹杂物,包括测量均质化温度(Th:L + V-> L)和汽泡成核温度(Tn:L-> L + V)。 Th-Tn差对应于被捕集的液体可能经历的过热强度,并且可以通过状态方程将其转化为液体压力(在Tn刚好发生成核之前存在)。纯水(840-935 kg m(-3)),稀NaOH溶液(0.1和0.5 mol kg(-1)),NaCl,CaCl2和CsCl溶液(1和5 mol kg(-1))表现出令人惊讶的能力承受拉应力。据我们所知,最高张力是在捕获于石英基质中的5 m CaCl2夹杂物中获得的(-146 MPa,100摄氏度),而CsCl溶液定性显示出更高的过热效率。这些观察是关于内含物内表面的质量(高P-T合成条件)和液体的固有内聚力(热力学和动力学旋节线轴)进行讨论的。这项研究表明,天然溶液可以达到很高的过热度,并伴随着其理化性质的强烈变化。

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