Effect of Pressure and Surface Wettability on Thermal Resistance across Solid-Liquid Interface in Supercritical Regime

被引:2
|
作者
Dong, Ming [1 ]
Xu, Jinliang [1 ,3 ]
Wang, Yan [2 ]
Liu, Guanglin [1 ]
机构
[1] North China Elect Power Univ, Beijing Key Lab Multiphase Flow & Heat Transfer Lo, Beijing 102206, Peoples R China
[2] Beijing Huairou Lab, Beijing 101400, Peoples R China
[3] North China Elect Power Univ, Key Lab Power Stn Energy Transfer Convers & Syst, Minist Educ, Beijing 102206, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 09期
基金
中国国家自然科学基金;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; HEAT-TRANSFER; TEMPERATURE-DEPENDENCE; KAPITZA RESISTANCE; TRANSPORT; WATER; GRAPHENE; CHALLENGES; GRAPHITE; GAS;
D O I
10.1021/acs.jpcc.3c07909
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Micro- and nanoscale effects such as temperature jumps have a significant impact on heat transfer processes at the fluid-solid interface. Pressure is an important parameter for describing subcritical and supercritical fluids (SFs). However, with the wide application of the SFs heat transfer process in shale and deep geothermal systems, the effect of pressure on thermal resistance at the supercritical fluid-solid interface is unknown. In this study, the heat conduction process at the supercritical water-graphene interface is performed by molecular dynamics simulations. The effect of pressure on the interfacial thermal resistance under different surface wettabilities is investigated. The results show that the interfacial thermal resistance decreases with increasing pressure under all surface wettability. The effect of pressure becomes weaker as the surface wettability or pressure increases. The interfacial thermal resistance is determined by the peak density and structure factor of the first fluid layer and linearly related to the inverse of the product of the peak density and structure factor. The vibrational coupling of in-plane and out-of-plane phonon density of states is characterized by the structure factor and peak density, which represent the horizontal ordering mechanism and vertical layering mechanism of interfacial heat transfer, respectively. Moreover, the vertical layering mechanism is the main determinant of the interfacial thermal resistance. The mechanism of interfacial thermal resistance proposed in this study is verified for application to a wide range of wettability and supercritical water-copper interfaces. The lower interfacial thermal resistance of the supercritical water-copper interface results from the enhanced ordering of interfacial fluid represented by the horizontal mechanism. This study deepens the understanding of the mechanism of interfacial thermal resistance and is helpful for supercritical heat transfer at the micro- and nanoscale.
引用
收藏
页码:4024 / 4037
页数:14
相关论文
共 50 条
  • [41] The structure of the solid-liquid interface: Atomic size effect
    Geysermans, P
    Pontikis, V
    JOURNAL DE PHYSIQUE IV, 2002, 12 (PR8): : 239 - 248
  • [42] Effect of cosolvents on the adsorption of peptides at the solid-liquid interface
    Mungikar, A
    Forciniti, D
    BIOMACROMOLECULES, 2006, 7 (01) : 239 - 251
  • [43] HEAT TRANSFER ACROSS A SOLID-LIQUID INTERFACE IN PRESENCE OF ACOUSTIC STREAMING
    GOULD, RK
    JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1966, 40 (01): : 219 - &
  • [44] Phase and solute fields across the solid-liquid interface of a binary alloy
    Conti, M
    PHYSICAL REVIEW E, 1999, 60 (02): : 1913 - 1920
  • [45] Solid-Liquid Triboelectrification Control and Antistatic Materials Design Based on Interface Wettability Control
    Li, Xiaojuan
    Zhang, Liqiang
    Feng, Yange
    Zhang, Xiaolong
    Wang, Daoai
    Zhou, Feng
    ADVANCED FUNCTIONAL MATERIALS, 2019, 29 (35)
  • [46] Pitch deposition at the solid-liquid interface: Effect of surface hydrophobicity/hydrophilicity and cation specificity
    Lee, Roland
    Garnier, Gil
    Lewis, Trevor
    Richardson, Desmond
    Van De Ven, Theo G. M.
    Stack, Karen
    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2011, 388 (1-3) : 84 - 90
  • [47] Measuring the Au(111) surface state at the solid-liquid interface
    Hulsken, B
    Gerritsen, JW
    Speller, S
    SURFACE SCIENCE, 2005, 580 (1-3) : 95 - 100
  • [48] The effects of surface curvature on the adsorption of surfactants at the solid-liquid interface
    Farrow, Matthew R.
    Camp, Philip J.
    Dowding, Peter J.
    Lewtas, Ken
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (28) : 11653 - 11660
  • [49] The effective surface pH during reactions at the solid-liquid interface
    Katsounaros, Ioannis
    Meier, Josef C.
    Klemm, Sebastian O.
    Topalov, Angel A.
    Biedermann, P. Ulrich
    Auinger, Michael
    Mayrhofer, Karl J. J.
    ELECTROCHEMISTRY COMMUNICATIONS, 2011, 13 (06) : 634 - 637
  • [50] Surface modification of polymers by ion irradiation at the solid-liquid interface
    Kobayashi, Tomohiro
    Miyamoto, So
    Ikeda, Tokihiro
    Kojima, Takao M.
    Ogiwara, Kiyoshi
    Yamazaki, Yasunori
    NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 2012, 272 : 405 - 408