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酯基和酰胺基连接的多孔有机聚合物在宽温度和压力范围内用于二氧化碳捕集和分离的研究。

Investigation of Ester- and Amide-Linker-Based Porous Organic Polymers for Carbon Dioxide Capture and Separation at Wide Temperatures and Pressures.

机构信息

Department of Chemical Engineering, Qatar University , PO Box 2713, Doha, Qatar.

Department of Chemistry, University of Burgos , 09001 Burgos, Spain.

出版信息

ACS Appl Mater Interfaces. 2016 Aug 17;8(32):20772-85. doi: 10.1021/acsami.6b05927. Epub 2016 Aug 5.

Abstract

Organic compounds, such as covalent organic framework, metal-organic frameworks, and covalent organic polymers have been under investigation to replace the well-known amine-based solvent sorption technology of CO2 and introduce the most efficient and economical material for CO2 capture and storage. Various organic polymers having different function groups have been under investigation both for low and high pressure CO2 capture. However, search for a promising material to overcome the issues of lower selectivity, less capturing capacity, lower mass transfer coefficient and instability in materials performance at high pressure and various temperatures is still ongoing process. Herein, we report synthesis of six covalent organic polymers (COPs) and their CO2, N2, and CH4 adsorption performances at low and high pressures up to 200 bar. All the presented COPs materials were characterized by using elemental analysis method, Fourier transform infrared spectroscopy (FTIR) and solid state nuclear magnetic resonance (NMR) spectroscopy techniques. Physical properties of the materials such as surface areas, pore volume and pore size were determined through BET analysis at 77 K. All the materials were tested for CO2, CH4, and N2 adsorption using state of the art equipment, magnetic suspension balance (MSB). Results indicated that, amide based material i.e. COP-33 has the largest pore volume of 0.2 cm(2)/g which can capture up to the maximum of 1.44 mmol/g CO2 at room temperature and at pressure of 10 bar. However, at higher pressure of 200 bar and 308 K ester-based compound, that is, COP-35 adsorb as large as 144 mmol/g, which is the largest gas capturing capacity of any COPs material obtained so far. Importantly, single gas measurement based selectivity of COP-33 was comparatively better than all other COPs materials at all condition. Nevertheless, overall performance of COP-35 rate of adsorption and heat of adsorption has indicated that this material can be considered for further exploration as efficient and cheaply available solid sorbent material for CO2 capture and separation.

摘要

有机化合物,如共价有机骨架、金属有机骨架和共价有机聚合物,一直被用于替代众所周知的基于胺的溶剂吸附 CO2 技术,并引入最有效和最经济的 CO2 捕获和储存材料。各种具有不同官能团的有机聚合物都被用于低压和高压 CO2 捕获。然而,寻找一种有前途的材料来克服选择性较低、捕获能力较低、在高压和各种温度下材料性能的传质系数较低以及不稳定性等问题,仍然是一个正在进行的过程。在此,我们报告了六种共价有机聚合物(COPs)的合成及其在低压和高压下(高达 200 巴)对 CO2、N2 和 CH4 的吸附性能。所有呈现的 COP 材料均通过元素分析方法、傅里叶变换红外光谱(FTIR)和固态核磁共振(NMR)光谱技术进行了表征。通过在 77 K 下使用 BET 分析测定了材料的物理性质,如比表面积、孔体积和孔径。使用最先进的设备,即磁悬浮天平(MSB),对所有材料进行了 CO2、CH4 和 N2 吸附测试。结果表明,酰胺基材料即 COP-33 具有最大的孔体积 0.2 cm2/g,可在室温下和 10 巴的压力下最大捕获 1.44 mmol/g CO2。然而,在更高的 200 巴和 308 K 压力下,基于酯的化合物,即 COP-35,吸附量高达 144 mmol/g,这是迄今为止获得的任何 COPs 材料的最大气体捕获能力。重要的是,在所有条件下,基于单气体测量的 COP-33 的选择性均优于所有其他 COPs 材料。然而,COP-35 的吸附速率和吸附热的综合性能表明,该材料可以作为一种有效的、廉价的 CO2 捕获和分离用固体吸附剂材料进行进一步探索。

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