Recent progresses in PPCP removal technologies are summarized, especially on adsorption and advanced oxidation processes using various materials.

Efficient and low-cost catalysts for catalytic wet air oxidation (CWAO) under ambient conditions are of great significance for the degradation of hydrophobic organic contaminants. In this study, four LDH catalysts were prepared and their catalytic performance was studied by the degradation of nitrobenzene. The CuCoFe-LDH shows the best catalytic activity with an NB removal efficiency of 41.2%. The CuCoFe-LDH exhibited a typical layer structure, with a specific surface area of 167.32 m² g⁻¹, and Cu²⁺, Co²⁺ and Fe³⁺ were evenly dispersed on the crystal. The NB removal efficiency was increased by 12.5% through adding formic acid. After five recycling processes, the NB removal efficiency was 18.9% because 3.8 mg g⁻¹ of Co was leached out of the LDH. In the CWAO process, H₂O₂, ˙OH, ˙O₂ ⁻ and ¹O₂ were successfully formed through activated oxygen by the CuCoFe-LDH catalyst under ambient conditions. This work further broadens the application scope of layered double hydroxides (LDHs) in the degradation of organic pollutants by CWAO under ambient conditions.

Hydroxymetal-clay complexes, which contain reactive surface hydroxyl groups, have a strong affinity for both heavy-metal cations and oxyanions and hence can serve as efficient sorbents for ionic contaminants. The co-sorptive behavior of heavy-metal cations and oxyanions on the surface of hydroxymetal-clay complexes is not well understood, however. The objective of the present investigation was to help bridge that gap by determining the feasibility of co-sorbing Cd cations and phosphate from aqueous solution to a hydroxyiron-montmorillonite complex (HyFe-mont). A montmorillonite-rich clay from Inner Mongolia, China, was the starting material. The results showed that Cd and phosphate could be sorbed, simultaneously and synergistically, to HyFe-mont without a change in solution pH. Similarly, when phosphate was sorbed before Cd, the sorption capacities were comparable to those obtained in the simultaneous sorption experiment, and the solution pH did not change.When Cd was pre-sorbed, however, the subsequent sorption of both Cd and phosphate decreased as did solution pH. X-ray photoelectron spectroscopy (XPS) indicated that the binding energies of P_2p, Cd_3/2, and Cd_5/2 were of similar magnitude for both the simultaneous sorption system and the phosphate pre-sorbed system. In addition, the single Cd and Cd pre-sorbed systems had similar Cd_3/2 and Cd_5/2 binding energies. The combined sorption and XPS results suggested that sorbed phosphate and Cd formed P-bridged ternary complexes on the HyFe-mont surface, contributing to the synergistic uptake of the contaminants in the simultaneous sorption system.