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Quantifying adsorption-induced deformation of nanoporous materials on different length scales

机译:量化在不同长度尺度上的吸附诱导的纳米多孔材料变形

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A new in situ setup combining small-angle neutron scattering (SANS) and dilatometry was used to measure water-adsorption-induced deformation of a monolithic silica sample with hierarchical porosity. The sample exhibits a disordered framework consisting of macropores and struts containing twodimensional hexagonally ordered cylindrical mesopores. The use of an H_2O/ D_2O water mixture with zero scattering length density as an adsorptive allows a quantitative determination of the pore lattice strain from the shift of the corresponding diffraction peak. This radial strut deformation is compared with the simultaneously measured macroscopic length change of the sample with dilatometry, and differences between the two quantities are discussed on the basis of the deformation mechanisms effective at the different length scales. It is demonstrated that the SANS data also provide a facile way to quantitatively determine the adsorption isotherm of the material by evaluating the incoherent scattering contribution of H_2O at large scattering vectors.
机译:将小角度中子散射(SAN)和抗扩张物组合的新的原位设置用于测量具有分层孔隙率的水吸附诱导的单片二氧化硅样品的变形。该样品表现出一种由大孔和含有六方六角有序圆柱形中孔的巨大和支柱组成的无序框架。使用具有零散射长度密度作为吸附的H_2O / D_2O水混合物允许从相应的衍射峰的偏移来定量测定孔隙晶格应变。将该径向支柱变形与具有稀释物的样品的同时测量的宏观变形进行比较,并且基于在不同长度尺度的变形机制的基础上讨论两种数量之间的差异。证明SAN数据还提供了通过评估大散射载体的H_2O的不连贯散射贡献来定量地确定材料的吸附等温线。

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