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Predicting the suitability of aqueous solutions of deep eutectic solvents for preparation of co-continuous porous carbons via spinodal decomposition processes

机译:通过纺丝镜分解过程预测深阳晶溶剂水溶液的适用性,以通过旋光性分解方法制备共连碳碳

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Spinodal decomposition (SD) processes have proved effective for the synthesis of macro-and mesoporous materials. Despite the theoretical aspects of SD processes are well understood, finding the proper experimental conditions - both the components as well as the ratio in which they have to be combined - to attain co-continuous structures is a non-predictable and quite tedious process, typically based on trial and error. The challenge is finding a "tool" capable to predict the suitability of a particular starting solution to undergo SD processes. Here in, we used aqueous solutions of deep eutectic solvents (DESs) for the preparation via SD of co-continuous porous carbons, the morphologies of which ranged from spinodal to aggregates-of-particles-like just depending on dilution. Despite the starting DES/H2O binary mixture was macroscopically homogeneous, Brillouin spectroscopy revealed the occurrence of certain nanostructural rearrangements within a dilution range that coincided with that used for preparation of carbons with morphologies transitioning from spinodal to aggregates-of-particles-like. Moreover, carbons exhibited a noticeable degree of heteroatom co-doping - e.g. N and P - and proved particularly effective for CO2 capture with adsorptions of up to 4.7 mmol/g at 0 degrees C and 760 mbar. (C) 2017 Elsevier Ltd. All rights reserved.
机译:已经证明了SpinoDal分解(SD)方法对宏观和中孔材料的合成有效。尽管SD过程的理论方面得到了很好的理解,但寻找适当的实验条件 - 这些组件以及它们必须组合的比例 - 通常是一种不可预测和相当乏味的过程,通常是一种不可预测的和相当繁琐的结构。基于试验和错误。挑战在寻找能够预测特定启动解决方案以进行SD过程的适用性的“工具”。在此,我们使用深共晶溶剂(Dess)的水溶液通过共同连续多孔碳的SD制备,其形态学从旋光透视到颗粒状的含量,即就取决于稀释。尽管起始DES / H 2 O二元混合物宏观均匀的,布里渊光谱揭示了在稀释范围内的某些纳米结构重排的发生,其与用于制备碳的形态,其与从旋转晶片转换为聚集的颗粒状物质。此外,碳的杂原相具有明显的程度 - 例如,杂原子 - 例如。 N和P - 并证明在0摄氏度和760毫巴的可吸附中的吸附捕获特别有效。 (c)2017 Elsevier Ltd.保留所有权利。

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