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利用基于深共晶氯化胆碱-氯化钙的新途径原位捕获和转化大气 CO 为纳米 CaCO。

In-situ capture and conversion of atmospheric CO into nano-CaCO using a novel pathway based on deep eutectic choline chloride-calcium chloride.

机构信息

Maham Tajhizat Parla Co., Chemistry & Chemical Engineering Research Center, Tehran, Iran.

Maham Tajhizat Parla Co., Chemistry & Chemical Engineering Research Center, Tehran, Iran.

出版信息

J Environ Manage. 2018 Jan 15;206:516-522. doi: 10.1016/j.jenvman.2017.11.005. Epub 2017 Nov 8.

Abstract

This study presents a newfangled method and provides a new approach toward capturing-entrapping the toxic and harmful greenhouse gas CO and subsequently employing it as a useful precursor for the production of value-added calcite (CaCO) nanoparticles. All the processes are done in a single system (one-pot and in-situ processing) based on deep eutectic choline chloride-calcium chloride (Calcoline) at mild temperature of 50 °C in direct contact with air. The Calcoline eutectic mixture shows the calcite production yield of 6.2 mg/ml that is reduced up to 22.6% upon recycling. The eutectic mixture provides an interesting all-in-one system acting as carbon dioxide trapper/adsorbent, solvent to solubilize CO, and reagent to convert solubilized CO into pure calcite nanoparticles with average particle size of 30 nm. The featured properties of the developed method including simplicity, recyclability, mobility, affordability, and sustainability make it feasible for large scale applications by which the simultaneous elimination of CO from the environment and conversion of it into value added nano-products will be practicable.

摘要

本研究提出了一种新颖的方法,为捕获和困住有毒有害温室气体 CO 提供了一种新的途径,随后将其用作生产增值碳酸钙 (CaCO) 纳米粒子的有用前体。所有过程都在基于深共晶氯化胆碱-氯化钙 (Calcoline) 的单一体系(一锅法和原位处理)中,在 50°C 的温和温度下直接与空气接触完成。Calcoline 共晶混合物显示出 6.2mg/ml 的方解石产量,回收后降至 22.6%。该共晶混合物提供了一个有趣的一体化系统,可用作二氧化碳捕集/吸附剂、溶解 CO 的溶剂以及将溶解的 CO 转化为平均粒径为 30nm 的纯方解石纳米粒子的试剂。所开发方法的特点包括简单性、可回收性、移动性、可负担性和可持续性,使其适用于大规模应用,从而可以从环境中同时消除 CO 并将其转化为增值纳米产品。

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