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

机译:量化不同长度尺度上纳米多孔材料的吸附诱导变形

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摘要

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 two-dimensional hexagonally ordered cylindrical mesopores. The use of an H2O/D2O 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 H2O at large scattering vectors.
机译:结合小角度中子散射(SANS)和膨胀法的新的原位设置用于测量具有分层孔隙率的整体式二氧化硅样品的水吸附诱导形变。该样品显示出由大孔和含有二维六边形有序圆柱中孔的支柱组成的无序骨架。使用具有零散射长度密度的H2O / D2O水混合物作为吸附剂,可以根据相应衍射峰的移动来定量确定孔晶格应变。将该径向支撑杆变形与同时使用膨胀法测量的样品宏观长度变化进行了比较,并基于在不同长度尺度下有效的变形机理,讨论了两个量之间的差异。结果表明,SANS数据还提供了一种简便的方法,可以通过评估H2O在大散射矢量处的非相干散射贡献来定量确定材料的吸附等温线。

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