# Effects of w/b Ratio on Sodium Sulfate Crystallization Damage and Degradation Mechanisms in Semi-Immersed Alkali-Activated Slag Mortar

**Authors:** Zhenwei Zhou, Yuetao Qiu, Peng Liu, Jianxiong Ye, Kunpeng Yin, Linwen Yu, Changhui Yang

PMC · DOI: 10.3390/ma18132988 · Materials · 2025-06-24

## TL;DR

This study examines how water-to-binder ratios affect sodium sulfate crystallization damage in alkali-activated slag mortars under semi-immersion conditions.

## Contribution

The study reveals how varying w/b ratios influence crystallization-induced degradation mechanisms in alkali-activated slag mortars.

## Key findings

- Higher w/b ratios worsen surface crystallization and spalling due to accelerated ion transport and pore coarsening.
- Early strength gains occur from pore refinement via sulfate deposition and hydration, but prolonged exposure causes microstructural degradation.
- Open porosity increases by 58.9% and strength declines by 30.6% at 360 days for a w/b of 0.5 compared to 0.4.

## Abstract

This study investigates the long-term durability and crystallization-induced degradation mechanisms of alkali-activated slag (AAS) mortars with varying water-to-binder ratios (w/b, 0.4, 0.45, 0.5) under semi-immersion in 5 wt.% sodium sulfate solution. Through 360 d of exposure, the evolution of physical–mechanical properties (mass change, open porosity, compressive/flexural strength) and ion migration patterns (SO42−, Na+, Ca2+) were analyzed to unravel the interplay between pore structure, ion transport, and crystallization-induced deterioration. Results demonstrated that higher w/b ratios exacerbated surface crystallization and spalling due to accelerated ion transport and pore coarsening. Early-stage strength gains (up to 25.15% at 120–180 d) stemmed from pore refinement via sulfate deposition and continued slag hydration. However, prolonged exposure triggered microstructural degradation, with open porosity increasing by 58.9% and strength declining by 30.6% at 360 d for a w/b of 0.5 compared to a w/b of 0.4. This was driven by crystallization pressure and the decalcification of hydration products. Ion migration analysis revealed SO42− enrichment in evaporation area and outward Na+ diffusion, establishing supersaturation gradients that aligned with crystallization damage progression. These findings provide critical insights for optimizing AAS mortar formulations to mitigate sulfate crystallization risks in semi-immersed environments.

## Linked entities

- **Chemicals:** sodium sulfate (PubChem CID 24436), SO42− (PubChem CID 1117), Na+ (PubChem CID 923), Ca2+ (PubChem CID 271)

## Full-text entities

- **Chemicals:** Na+ (MESH:D012964), Ca2+ (-), water (MESH:D014867), Alkali (MESH:D000468), Sodium Sulfate (MESH:C012036), sulfate (MESH:D013431)

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12251537/full.md

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Source: https://tomesphere.com/paper/PMC12251537