Green Synthesis of Carbon Nitride‐Based Conjugated Copolymer for Efficient Photocatalytic Degradation of Tetracycline

Upcycling waste plastics into advanced semiconductor photocatalysts provides a new strategy to reasonably and economically solve the huge amount of waste plastics, which remains challenging. Herein, a carbon nitride-based donor-acceptor (D-A) conjugated copolymer by copolymerization of dicyandiamide and terephthalic acid from discarded polyethylene terephthalate (PET) using Zn(OH)2 as catalyst and template at 360-440 °C is synthesized. The morphology and structure of the conjugated copolymer are well regulated by the calcination temperature. The resultant conjugated copolymer exhibits merits of high light absorption and low electron-hole recombination probability. Consequently, it works excellently in the persulfate-based advanced oxidation process for visible light-driven photocatalytic degradation of tetracycline. The kinetic constant (3.4 × 10-2 min-1 ) is 40.5 and 2.3 times that of the conjugated copolymer system and persulfate system, respectively. Furthermore, the reactive species (including •OH, SO4•- , •O2- , 1 O2 , and h+ ) and degradation intermediates of tetracycline are analyzed to expound its degradation process. This work not only pioneers design guidelines on upcycling of waste plastics in a sustainable manner, but also provides a facile strategy to synthesize carbon nitride-based D-A conjugated copolymers for the efficient activation of persulfate-based advanced oxidation process in wastewater treatment.