Phosphorus adsorption from aqueous solutions using different types of cement: kinetics, isotherms, and mechanisms.

Abstract

Exploring low-cost and high-performance phosphorus (P) adsorbents is key to controlling P contamination in water. This study evaluated the P adsorption performance of three types of cement: Ordinary Portland cement (OPC), Portland slag cement (PSC), and Portland pozzolana cement (PPC). Furthermore, SEM-EDS, XRD, XPS, and FTIR were employed to reveal the adsorption mechanism. The results showed that the pseudo-second-order model exhibited higher regression coefficients than the pseudo-first-order model, indicating that chemisorption dominated the adsorption process. The Langmuir equation fitted the P adsorption data well, with maximum P adsorption capacities of 245.8, 226.1, and 210.0 mg g-1 for OPC, PSC, and PPC at 25 °C, respectively. P adsorption capacities decreased gradually with increasing initial pH and reached their maximum values at pH 3. The anions of F-, CO32-, and SO42- negatively affected P adsorption due to the competitive adsorption with Ca2+. The results of XPS, XRD, and FTIR confirmed that Ca-P precipitates (i.e., hydroxyapatite) were the main removal mechanism. A real domestic sewage experiment showed that 0.6 g L-1 OPC effectively reduced the P concentration from 2.4 to below 0.2 mg L-1, with a dosage cost of 0.034 $ per ton. This study indicated that cement, as a low-cost and efficient P adsorbent, has great potential for application in removing P from acidic and neutral wastewater.