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硼酸催化碳酸酐酶机制的二氧化碳水合反应。

Borate-catalyzed carbon dioxide hydration via the carbonic anhydrase mechanism.

机构信息

State Key Laboratory of Chemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.

出版信息

Environ Sci Technol. 2011 Jun 1;45(11):4802-7. doi: 10.1021/es200590m. Epub 2011 May 2.

Abstract

The hydration of CO(2) plays a critical role in carbon capture and geoengineering technologies currently under development to mitigate anthropogenic global warming and in environmental processes such as ocean acidification. Here we reveal that borate catalyzes the conversion of CO(2) to HCO(3)(-) via the same fundamental mechanism as the enzyme carbonic anhydrase, which is responsible for CO(2) hydration in the human body. In this mechanism the tetrahydroxyborate ion, B(OH)(4)(-), is the active form of boron that undergoes direct reaction with CO(2). In addition to being able to accelerate CO(2) hydration in alkaline solvents used for carbon capture, we hypothesize that this mechanism controls CO(2) uptake by certain saline bodies of water, such as Mono Lake (California), where previously inexplicable influx rates of inorganic carbon have created unique chemistry. The new understanding of CO(2) hydration provided here should lead to improved models for the carbon cycle in highly saline bodies of water and to advances in carbon capture and geoengineering technology.

摘要

CO(2) 的水合作用在当前开发的碳捕集和地球工程技术中起着关键作用,这些技术旨在缓解人为全球变暖,并在海洋酸化等环境过程中发挥作用。在这里,我们揭示了硼酸盐通过与负责人体中 CO(2) 水合作用的碳酸酐酶相同的基本机制,催化 CO(2) 转化为 HCO(3)(-)。在这个机制中,四羟基硼酸盐离子,B(OH)(4)(-),是硼的活性形式,它与 CO(2)直接反应。除了能够加速用于碳捕集的碱性溶剂中的 CO(2)水合作用之外,我们假设这种机制控制着某些盐水体(如加利福尼亚州的莫诺湖)中 CO(2)的吸收,在这些盐水体中,以前无法解释的无机碳流入率创造了独特的化学性质。这里提供的对 CO(2)水合作用的新理解,应该会导致对高盐水体中碳循环的改进模型,并推动碳捕集和地球工程技术的发展。

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