Abstract
Polyurethane (PU) grouting materials are widely used in underground engineering rehabilitation, particularly in reinforcement and waterproofing engineering in deep-water environments. The long-term effect of complex underground environments can lead to nanochannel formation within PU, weakening its repair remediation effect. However, the permeation behavior and microscopic mechanisms of water molecules within PU nanochannels remain unclear. In this paper, a model combining PU nanochannels and water molecules was constructed, and the molecular dynamics simulations method was used to study the effects of water pressure and channel width on permeation behavior and microstructural changes. The results reveal a multi-stage, layered permeation process, with significant acceleration observed at water pressures above 3.08 MPa. Initially, water molecules accelerate but are then blocked by the energy barrier of PU nanochannels. After about 20 ps, water molecules overcome the potential barrier and enter the nanochannel, displaying a secondary acceleration effect, with the maximum permeation depth rises from 1.8 nm to 11.8 nm. As the channel width increases, the maximum permeation depth increases from 7.5 nm to 11.6 nm, with the rate of increase diminishing at larger widths. Moreover, higher water pressure and wider channels enhance the stratification effect. After permeation, a hydrophobic layer of approximately 0.5 nm thickness forms near the channel wall, with a density lower than that of the external water. The middle layer shows a density slightly higher than the external water, and the formation of hydrogen bonds between water molecules increases toward the channel center.