AI Article Synopsis

  • Concrete structures in agriculture and food industries are vulnerable to organic acid attacks, prompting this study to verify thermodynamic models for cement pastes under acetic acid conditions.
  • The research employs IPHREEQC modeling through Matlab and compares results to measured pH levels, ion concentrations, and solid compositions from dissolution experiments.
  • An 11% replacement of cement with silica fume significantly reduced Portlandite content in cement paste, improving cement stability but the model showed some discrepancies at very high acid concentrations due to limitations in modeling gel phases.

Article Abstract

Concrete structures are increasingly becoming exposed to organic acid attack conditions, such as those found in agriculture and food-related industries. This paper aims to experimentally verify the thermodynamic modeling of cement pastes under acetic acid attack. For this, a modeling approach implemented in IPHREEQC via Matlab is described, and results are compared with measured pH and compositions of equilibrated solutions (MP-AES) as well as unreacted/precipitated solids (XRF, XRD and STA) for a wide range of acid concentrations. The 11% replacement of cement by silica fume (SF) led to a 60 or 70% reduction (measured or modeled, respectively) of Portlandite content in the hardened cement paste due to the pozzolanic reaction resulting in higher content of CSH phases, which has effects on the progression of dissolution processes and a resulting pH with increased acid concentrations. Considering that no fitting parameter was used, the model predictions showed good agreement with measured values of pH, dissolved ion concentrations and composition of the remaining (degraded) solids overall. The discrepancies here were more pronounced at very high acid concentrations (equilibrium pH < ~4), i.e., after the full dissolution of hydrate phases due to limitations in the model used to describe Al-, Si- and Fe-gel phases and/or identified experimental challenges in precipitation of calcium and aluminum acetate hydrates.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738739PMC
http://dx.doi.org/10.3390/ma15238355DOI Listing

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