4.8 Article

Elucidating the Mechanism of Condensation-Mediated Degradation of Organofunctional Silane Self-Assembled Monolayer Coatings

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 29, 页码 34923-34934

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c08496

关键词

self-assembled monolayer; low surface energy coatings; coating degradation; silane; enhanced condensation; dropwise condensation

资金

  1. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy [DE-EE0008605]
  2. American Chemical Society Petroleum Research Fund [61698-DNI9]
  3. J. Mike Walker '66 Department of Mechanical Engineering at Texas A&M University (TAMU)

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Research investigates the mechanism of organofunctional silane SAM coating degradation during water vapor condensation and finds that coatings prepared in a dry environment exhibit superior long-term robustness.
Dropwise condensation is favorable for numerous industrial and heat/mass transfer applications due to the enhanced heat transfer performance that results from efficient condensate removal. Organofunctional silane self-assembled monolayer (SAM) coatings are one of the most common ultrathin low surface energy materials used to promote dropwise condensation of water vapors because of their minimal thermal resistance and scalable synthesis process. These SAM coatings typically degrade (i.e., condensation transitions from the efficient dropwise mode to the inefficient filmwise mode) rapidly during water vapor condensation. More importantly, the condensation-mediated coating degradation/ failure mechanism(s) remain unknown and/or unproven. In this work, we develop a mechanistic understanding of water vapor condensation-mediated organofunctional silane SAM coating degradation and validate our hypothesis through controlled coating synthesis procedures on silicon/silicon dioxide substrates. We further demonstrate that a pristine organofunctional silane SAM coating resulting from a water/moisture-free coating environment exhibits superior long-term robustness during water vapor condensation. Our molecular/nanoscale surface characterizations, pre- and post-condensation heat transfer testing, indicate that the presence of moisture in the coating environment leads to uncoated regions of the substrate that act as nucleation sites for coating degradation. By elucidating the reasons for formation of these degradation nuclei and demonstrating a method to suppress such defects, this study provides new insight into why low surface energy silane SAM coatings degrade during water vapor condensation. The proposed approach addresses a key bottleneck (i.e., coating failure) preventing the adoption of efficient dropwise condensation methods in industry, and it will facilitate enhanced phase-change heat transfer technologies in industrial applications.

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