首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Electropolymerized Carbonic Anhydrase Immobilization for Carbon Dioxide Capture
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Electropolymerized Carbonic Anhydrase Immobilization for Carbon Dioxide Capture

机译:电聚合固定化碳酸酐酶用于二氧化碳捕集

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摘要

Biomimetic carbonation carried out with carbonic anhydrase (CA) in CO_2-absorbing solutions, such as methyldiethanolamine (MDEA), is one approach that has been developed to accelerate the capture of CO_2. However, there are several practical issues, such as high cost and limited enzyme stability, that need to be overcome. In this study, the capacity of CA immobilization on a porous solid support was studied to improve the instability in the tertiary amine solvent. We have shown that a 63% porosity macroporous carbon foam support makes separation and reuse facile and allows for an efficient supply and presentation of CO_2 to an aqueous solvent and the enzyme catalytic center. These enzymatic supports conserved 40% of their initial activity after 42 days at 70 °C in an amine solvent, whereas the free enzyme shows no activity after 1 h in the same conditions. In this work, we have overcome the technical barrier associated with the recovery of the biocatalyst after operation, and most of all, these electropolymerized enzymatic supports have shown a remarkable increase of thermal stability in an aminebased CO_2 sequestration solvent.
机译:用碳酸酐酶(CA)在吸收CO_2的溶液(如甲基二乙醇胺(MDEA))中进行仿生碳酸化是已开发的一种加快捕获CO_2的方法。但是,有一些实际问题需要克服,例如高成本和有限的酶稳定性。在这项研究中,研究了将CA固定在多孔固体支持物上的能力,以改善叔胺溶剂的不稳定性。我们已经表明,孔隙率为63%的大孔碳泡沫载体使分离和再利用变得容易,并允许将CO_2有效地供应和呈递到水性溶剂和酶催化中心。这些酶载体在胺溶剂中于70°C下放置42天后,其原始活性保持40%,而在相同条件下1小时后,游离酶则没有活性。在这项工作中,我们克服了与操作后生物催化剂回收相关的技术障碍,最重要的是,这些电聚合酶载体在胺基CO_2螯合溶剂中显示出显着的热稳定性。

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