co2再升华的数值模拟

Michael Adebayo Oyinloye, S. Gubba, M. Cojocaru, D. Prabhudharwadkar, W. L. Roberts
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摘要

. 通过与低温液体直接接触从点源脱出二氧化碳是一种很有前途的捕获碳的方法。本文介绍了二氧化碳在固体表面上升华过程的三维数值模型的结果。由于其高三相压力(~5.2 bar),如果在大气压附近充分冷却,二氧化碳将直接从气相转化为固体(即再升华)。使用基于在CONVERGE中实现的扩散边界层模型的用户定义函数(UDF)对表面的去升华现象进行了建模。本文介绍了两种不同的测试用例在开发三维二氧化碳升华模型方面的初步工作:一种是单一的等温固体球形表面;另一种是多个固体等温球体垂直堆叠。结果表明:消升华速率与畴内球体数、点源浓度和球面温度有关。静态球体表面和区域内直接气相之间的CO 2局部摩尔浓度的降低表明该区域发生了再升华。这一点得到了区域内相同点的温差的支持。通过固体-蒸汽状态方程和能量、质量和物质平衡,对升华模型的数值公式进行了解析验证。开发的模型将用于未来评估基于升华的低温碳捕获系统,实验后验证
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NUMERICAL MODELING OF THE DESUBLIMATION OF CO2
. Desublimation of CO 2 from a point source through direct contact with a cryogenic liquid is a promising approach to capture carbon. This study presents the results of a 3D numerical model of the desublimation process of CO 2 onto a solid surface. Due to its high triple point pressure (~5.2 bar), CO 2 converts to solid directly from the gas phase (i.e., desublimates) if cooled sufficiently at around atmospheric pressure. Desublimation phenomena on the surface has been modeled using a user-defined function (UDF) based on the diffusion boundary layer model implemented in CONVERGE. Preliminary work on the development of a 3D CO 2 desublimation model is presented here with two different test cases: one with a single isothermal, solid, spherical surface; and the other with multiple solid isothermal spheres stacked vertically. The results show that the rate of desublimation is dependent on the number of spheres in the domain, the concentration of the point source, and the temperature of the spherical surface. The resulting decrease in the local molar concentration of CO 2 between the surface of the static sphere and the immediate gas phase in the domain suggests desublimation. This was supported by the temperature difference at the same points in the domain. The numerical formulation of the desublimation model is validated analytically through the solid-vapor equations of state and the energy, mass, and species balance. The developed model will be used in future assessment of the desublimation-based cryogenic carbon capture system, post-experimental validation
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