Naphthalene sulfonic acid is widely used in the industry. In this study, H acid (1-amino-8-naphthol-3,6-disulfonic acid) was selected as the characteristic pollutant, and the alkali-activated, thermally-activated, and alkali-heat-complex activated persulfate (PS) degradation of H acid was analyzed. The effects of other factors on complex activation were discussed. The experimental results showed that with the addition of calcium oxide from 0 to 1250 mg ·L-1, the H acid removal rate increased from 42.5% to 82.8% after 100 min of reaction. The removal rate of H acid in thermal activation is positively correlated with temperature. The removal rate of H acid at 65℃ is 77.5%, and the apparent activation energy is 37.85 kJ ·mol-1. Although composite activation speeds up the reaction rate, rapid degradation of PS at high temperatures caused the degradation of H acid to be worse than single thermal activation. The change in PS concentration did not significantly improve the removal rate of H acid, and the inorganic anion CO32- was not conducive to the removal of H acid. Compound activation is not ideal for the mineralization of H acid, and the removal rate of TOC is only 16%. GC-MS identified the degradation product of H acid as terephthalic acid, indicating that phthalic anhydride may be formed after the naphthalene ring is opened.
Keywords: H acid; alkali activation; oxidation; persulfate; thermal activation.