Electrochemical Degradation Mechanism of Desert Sand Concrete Under the Combined Action of Electric Field and Sulfate

To promote the sustainable utilization of desert sand as a regional resource in the infrastructure construction of saline-alkali areas, this paper proposes an accelerated test method based on the coupling of an external electric field (60 V) and a 2% Na2SO4 solution for rapid evaluation of its sulfate erosion resistance. The optimal mix proportion (FA 10%, water-to-binder ratio 0.33, cement-to-sand ratio 1:1.5, SF 10%) was determined through orthogonal experiments. By employing multi-scale analytical techniques including electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), X-ray diffraction (XRD) and thermal analysis (TG-DTG), the differentiated deterioration mechanisms driven by the electric field were systematically revealed. The results show that the charge-transfer resistance (Rct) decreased by about 95% within 28 d, demonstrating the characteristic of “micro-scale deterioration preceding macro-scale strength loss.” The anode region was dominated by dissolution of hydration products (porosity 5.1%), while the cathode region, due to enrichment of sulfate ions (S content 3.37 wt.%), generated a large amount of expansive products, leading to more pronounced structural damage (porosity 8.3%) and greater mass loss (cathode 12.56% > anode 9.85%). This study not only elucidates the deterioration mechanisms of desert sand concrete under coupled environmental action, but also provides a mechanism-explicit, rapid and efficient laboratory evaluation method for its sulfate resistance, offering practical guidance for durability design and prevention in engineering structures exposed to saline-alkali conditions.