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Breakage mechanics for granular materials in surface-reactive environments

机译:表面反应性环境中粒状材料的断裂机理

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摘要

It is known that the crushing behaviour of granular materials is sensitive to the state of the fluids occupying the pore space. Here, a thermomechanical theory is developed to link such macroscopic observations with the physico-chemical processes operating at the microcracks of individual grains. The theory relies on the hypothesis that subcritical fracture propagation at intra-particle scale is the controlling mechanism for the rate-dependent, water-sensitive compression of granular specimens. First, the fracture of uniaxially compressed particles in surface-reactive environments is studied in light of irreversible thermodynamics. Such analysis recovers the Gibbs adsorption isotherm as a central component linking the reduction of the fracture toughness of a solid to the increase of vapour concentration. The same methodology is then extended to assemblies immersed in wet air, for which solid-fluid interfaces have been treated as a separate phase. It is shown that this choice brings the solid surface energy into the dissipation equations of the granular matrix, thus providing a pathway to (i) integrate the Gibbs isotherm with the continuum description of particle assemblies and (ii) reproduce the reduction of their yield strength in presence of high relative humidity. The rate-effects involved in the propagation of cracks and the evolution of breakage have been recovered by considering non-homogenous dissipation potentials associated with the creation of surface area at both scales. It is shown that the proposed model captures satisfactorily the compression response of different types of granular materials subjected to varying relative humidity. This result was achieved simply by using parameters based on the actual adsorption characteristics of the constituting minerals. The theory therefore provides a physically sound and thermodynamically consistent framework to study the behaviour of granular solids in surface-reactive environments.
机译:已知粒状材料的破碎行为对占据孔空间的流体的状态敏感。在这里,发展了一种热力学理论,以将这种宏观观察与在单个晶粒的微裂纹处进行的物理化学过程联系起来。该理论基于以下假设:颗粒内尺度下的亚临界裂缝扩展是颗粒状样品速率相关,水敏压缩的控制机制。首先,根据不可逆的热力学研究了表面反应环境中单轴压缩颗粒的断裂。这样的分析回收了吉布斯吸附等温线,并将其作为将固体的断裂韧性降低与蒸气浓度增加联系起来的主要成分。然后,将相同的方法扩展到浸入湿空气中的组件,对于该组件,已将固体-流体界面视为单独的相。结果表明,这种选择将固体表面能带入了颗粒基质的耗散方程,从而提供了一种途径(i)将吉布斯等温线与颗粒组件的连续描述相结合,以及(ii)重现其屈服强度的降低在较高的相对湿度下。通过考虑与在两个尺度上产生表面积相关的非均质耗散势,已经恢复了裂纹扩展和断裂发展所涉及的速率效应。结果表明,所提出的模型可以令人满意地捕获经受相对湿度变化的不同类型颗粒材料的压缩响应。仅通过使用基于构成矿物的实际吸附特性的参数即可获得此结果。因此,该理论提供了一个物理上合理且热力学上一致的框架,以研究颗粒状固体在表面反应环境中的行为。

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  • 作者单位

    University of Colorado Boulder, Department of Civil, Environmental and Architectural Engineering;

    Northwestern University, Department of Civil and Environmental Engineering;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 02:59:42

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