Abstract

Carbonation and leaching are likely to be the primary concrete degradation mechanisms for concrete utilized in geological repositories when the concrete is fully saturated and in contact with host rock pore water containing increased CO2 content. This work describes the changes in the microstructure and transport properties of cement pastes caused by coupled chemical degradation processes that occur at the cement paste-clay interface. In the laboratory, an experimental program was designed to accelerate the interface interaction under carbonation and leaching by bringing highly porous cement pastes (to mimic backfill materials used in geological disposal) and Boom Clay into contact in either accelerated percolation or batch-type experiments. Mercury intrusion porosimetry (MIP) was used to investigate the microstructural alteration. Inductively coupled plasma optical emission spectrometer (ICP-OES) and permeability, diffusion measurements were used to determine the evolution of chemical and transport properties, respectively. The results of the porosity change at the interface demonstrate an increase in porosity of the cement paste interface due to Ca leaching, which overwhelms the carbonation. As a result, the transport properties increase. This suggests that clogging of the cementitious material side is unlikely.

Abstract

The application of organic coatings is one of the most effective and economic methods to protect concrete structures from deterioration. However, organic coatings are prone to degradation under aggressive environmental actions, so the protective function may loss. While ultraviolet (UV) aging is often blamed for the degradation of organic coatings, water may play a more important role on the interfacial adhesion between the coatings and the substrate. To uncover the effect of water on the degradation performance of coating-substrate system, mortar samples coated with water-borne epoxy resin (WER) were exposed to three assigned environments, i.e., UV radiation, UV/water immersion, and UV/dry-wet cycle, up to 60 days. The surface appearance, chemical structure, wettability, and surface micro-morphology of the aged WER coatings were characterized via image process analysis, attenuated total reflectance flourier transform infrared spectroscopy (ATR–FTIR), static water contact angle, and scanning electronic microscopy (SEM). Results show that the UV/water immersion resulted in severest blistering on the WER-mortar interface, while the UV/wet-dry cycle caused the formation of micro-pinholes on the WER surface. In contrast, the UV radiation did not induce such severe aging. The data implied that water can accelerate the aging of WER-mortar system.