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

机译:基于酯和酰胺连接基的多孔有机聚合物在宽温度和压力下用于二氧化碳捕集和分离的研究

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摘要

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 cm2/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.
机译:人们正在研究有机化合物,例如共价有机骨架,金属有机骨架和共价有机聚合物,以取代众所周知的基于CO2的胺基溶剂吸附技术,并引入最有效,最经济的CO2捕获和储存材料。具有低官能团的各种有机聚合物已经被研究用于低压和高压CO 2捕集。然而,寻找有前途的材料以克服选择性低,捕获能力低,传质系数低以及在高压和各种温度下材料性能不稳定的问题仍在进行中。在这里,我们报告了六种共价有机聚合物(COP)的合成及其在高达200 bar的低压和高压下的CO2,N2和CH4吸附性能。使用元素分析方法,傅立叶变换红外光谱(FTIR)和固态核磁共振(NMR)光谱技术对所有提出的COPs材料进行了表征。通过BET分析在77 K下确定了材料的物理性质,例如表面积,孔体积和孔径。使用最先进的设备,磁悬浮天平(MSB)对所有材料的CO2,CH4和N2吸附进行了测试。 。结果表明,基于酰胺的材料,即COP-33,具有最大的孔体积为0.2cm 2 / g,在室温和10巴的压力下可以捕获最多1.44mmol / g的CO 2。但是,在200 bar和308 K酯基化合物的较高压力下,COP-35吸附量高达144 mmol / g,这是迄今为止获得的所有COPs材料中最大的气体捕获能力。重要的是,在所有条件下,基于单一气体测量的COP-33选择性都比所有其他COPs材料更好。然而,COP-35吸附速率和吸附热的整体性能表明,该材料可以考虑作为有效的和廉价的可用于CO2捕集和分离的固体吸附剂材料进行进一步的研究。

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