可回收化学品在可持续二氧化碳原地矿化方面的进展

Song Zhou , Liang Li , Long Ji , Baiqian Dai , Ziliang Wang , Emad Benhelal , Nanthi S. Bolan , Paul Feron , Hai Yu
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引用次数: 0

摘要

21 世纪面临着大气中二氧化碳含量上升和人为固体废物的问题。通过与固体废弃物反应将二氧化碳转化为稳定的碳酸盐的原地二氧化碳矿化技术前景广阔。然而,对化学品大量消耗的担忧促使人们寻求可持续和可回收的替代品。本文对用于与各种工业固体废物进行二氧化碳矿化的可回收化学品进行了严格审查,并对其功效和反应机制进行了系统研究。主要研究结果概述如下:首先,我们强调了捕集和回收利用 NH3 气体对于利用铵盐实现高效二氧化碳矿化的关键作用。其次,用矿化装置取代传统的汽提塔,扩大基于胺的矿化是可行的。这一转变取决于技术挑战的解决,例如胺的低浸出能力和对含有水溶性含钙/镁物质的固体原料的有限适用性。第三,利用其独特的齐聚物结构,氨基酸可以满足不同的工业需求,并在低温条件下实现令人满意的二氧化碳矿化效率和良好的可回收性。第四,一种名为 "氧-吡咯水解 "的新型盐酸再生技术可在一个步骤中同时实现二氧化碳矿化和盐酸再生。不过,基于氨基酸的矿化和富氧-吡罗水解都是新兴技术,需要进一步研究以确定其适用性并推动其发展。第五,尽管采用了可回收化学品,但在使用高温的情况下,矿化的运营成本可能仍然很高。因此,应探索能源优化策略,如探索低能耗化学品和整合废物能量收集装置。本综述论文旨在阐述利用可回收化学品进行具有成本效益的二氧化碳矿化的潜在途径,从而减轻与化学品残留物相关的后处理成本和环境问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Progress in recyclable chemicals for sustainable ex-situ CO2 mineralisation

The 21st century grapples with rising atmospheric CO2 and anthropogenic solid waste. Ex-situ CO2 mineralisation, converting CO2 into stable carbonates via reacting with solid waste, shows great promise. However, concerns over the extensive consumption of chemicals urge sustainable and recyclable alternatives. This paper critically reviews recyclable chemicals for CO2 mineralisation with various industrial solid wastes, and systematically examines their efficacy and reaction mechanisms. This study offers a comprehensive comparison of these chemicals and outlines clear future research directions.

The main findings are briefed below: first, we emphasize the pivotal role of trapping and recycling NH3 gas for achieving effective and efficient CO2 mineralisation using ammonium salts. Second, scaling up amines-based mineralisation could be feasible by replacing conventional strippers with mineralisation units. This transition is contingent upon resolving technical challenges such as amines' low leaching capacity and limited applicability to solid feedstocks that contain water-soluble Ca/Mg-bearing species. Third, leveraging their unique zwitterionic structures, amino acids may cater to diverse industrial needs and achieve a satisfactory CO2 mineralisation efficiency with good recyclability at low temperatures. Fourth, a novel HCl regeneration technology known as ‘oxy-pyrohydrolysis,’ can achieve simultaneous CO2 mineralisation and HCl regeneration in a single step. However, both amino acids-based mineralisation and oxy-pyrohydrolysis are nascent technologies requiring further research to ascertain their applicability and advance their development. Fifth, despite employing recyclable chemicals, operational costs of mineralisation could remain significant when high temperatures are used. Thus, energy optimization strategies should be explored, such as exploring low-energy consumption chemicals and integrating waste energy harvesting units. This review paper aims to delineate potential avenues for cost-effective CO2 mineralisation facilitated by recyclable chemicals, thereby alleviating post-processing costs and environmental concerns associated with chemical residues.

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