Enhanced in-situ oxygen evolution and hydrogen peroxide production by a floatable ZnO-incorporated polyurethane photocatalyst for sulfamethoxazole degradation.

[Display omitted] • Floatable P-ZsZc was prepared by pre-seeding ZnO followed by hydrothermal treatment. • P-ZsZc shows an uplifted valence band and new covalent Zn-O-C bonds. • Combining ZnO with PU improves photo-corrosion by boosting the h+ mobility. • Scavenger experiments and ESR spin trap analysis revealed H 2 O 2 as the main ROS. • The P-ZsZc achieved up to ∼ 90% SMX removal in continuous flow experiments. A highly efficient rigid floatable photocatalyst was prepared by seeding ZnO in polyurethane (PU) and subsequent hydrothermal ZnO coating (P-ZsZc). Compared to pristine ZnO, granular P-ZsZc had an uplifted valence band (VB) and generated new covalent Zn-O-C bond between PU and ZnO, resulting in a significantly enhanced photocorrosion resistance by boosting the mobility of photoexcited holes. In addition, the VB of P-ZsZc was favorable for the in-situ oxygen evolution reaction (OER) and H 2 O 2 production. As a result, the P-ZsZc achieved ∼ 98% removal of sulfamethoxazole (SMX) within 2 h for 5 consecutive cycles. Moreover, the SMX removal rate and Zn(II) leaching remained at ∼ 0.036 min−1 and 0.17 mg L−1, respectively, even during the fifth cycle for 10 h. Furthermore, scavenger experiments and electron spin resonance (ESR) spin trap analysis revealed that the main photogenerated reactive oxygen species (ROS) was H 2 O 2. Floatable P-ZsZc showed constant SMX removal of ∼ 90% in continuous flow experiments (CFEs) for up to 10 h of operation. This study offers a new approach to prepare floatable rigid photocatalysts capable of in-situ oxygen and H 2 O 2 production to degrade organic pollutants. [ABSTRACT FROM AUTHOR]