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Dynamic vapor sorption and thermoporometry to probe water in celluloses

机译:动态蒸气吸附和热孔法可探测纤维素中的水

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Dynamic vapor sorption and thermoporometry probe complementary dimensions of water interaction with cellulose. While sorption is primarily sensitive to the first hydration layers, thermoporometry is primarily sensitive to the nanometric water-filled pores. In this article, these analytical techniques are detailed and applied tomodelmesoporousmaterials and to a wide spectrum of celluloses. Correlations between techniques are explored. In dynamic vapor sorption, celluloses present a general characteristic time of desorption. On the other hand, they present highly variable characteristic times of sorption, indicating that material-specific properties may be inferred from sorption kinetics. Regarding thermoporometry, the thermodynamics of ice melting in irregular pore shapes is introduced.Moreover, in our thermoporometry analysis with differential scanning calorimeter, freezing temperature is extended to -70 ℃, allowing pores smaller than a few nanometers to be measured. Nevertheless, several data corrections are required for accurate thermoporometry at this condition. Comparisons between techniques show that sorption hysteresis is positively correlated with wet porosity. The presented developments and results will guide future application of these techniques to probe water in celluloses.
机译:动态蒸气吸附和热孔法探测水与纤维素相互作用的互补尺寸。虽然吸附主要对​​第一水合层敏感,但热孔法主要对纳米水填充孔敏感。在本文中,将详细介绍这些分析技术,并将其应用于模型中微孔的材料和各种纤维素。探索了技术之间的相关性。在动态蒸气吸附中,纤维素具有解吸的一般特征时间。另一方面,它们呈现出高度可变的吸附特征时间,表明可以从吸附动力学推断出特定于材料的特性。关于热孔法,介绍了冰在不规则形状的孔中融化的热力学。此外,在我们用差示扫描量热仪进行的热孔法分析中,冷冻温度扩展到-70℃,可以测量小于几纳米的孔。但是,在这种情况下,需要进行一些数据校正才能获得准确的热孔法。两种技术之间的比较表明,吸附滞后与湿孔隙率正相关。提出的进展和结果将指导这些技术在纤维素中探测水的未来应用。

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