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• W4385716615 abstract "ABSTRACTIn this study, each cobalt tetra-aminophthalocyanine (CoTAPc) molecule was immobilised with four isonicotinic acid (INA) molecules by amide bonding, a novel and highly efficient catalyst pyridine-bridged cobalt tetra-aminophthalocyanine (CoTAPc-TINA) was synthesised. The introduction of INA molecules promoted CoTAPc to expose more active sites, and increased the electron cloud density of cobalt ions promoting O–O bond homolysis of PMS to generate more active species, which significantly enhanced catalytic activity. With the pharmaceutical of carbamazepine (CBZ) as model pollutant, 0.1 g/L CoTAPc-TINA in dark in the presence of 0.4 mM PMS, 98.8% CBZ was removed within 10 min. However, under the same conditions the removed of CBZ was only 58.9% by CoTAPc/PMS system. Radical capture experiments combined electron paramagnetic resonance technology demonstrate that hydroxyl radicals, sulphate radicals, superoxide radicals and singlet oxygen are the main active species in the CoTAPc-TINA/PMS system. As the reaction proceeded, all aromatic intermediates were transformed to small molecular acids by these active species. This investigation provided a new insight for application of metal phthalocyanine in wastewater treatment.KEYWORDS: Pyridine-bridgedcobalt tetra-aminophthalocyanineisonicotinic acidperoxymonosulphatedegradation pathway Disclosure statementNo potential conflict of interest was reported by the author(s).Data availability statementThe data that support the findings of this study are available from the corresponding author, Prof Lu, upon reasonable request.Additional informationFundingThis work was supported by the National Natural Science Foundation of China (No. 22006136)." @default.
• W4385716615 created "2023-08-11" @default.
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• W4385716615 date "2023-08-16" @default.
• W4385716615 modified "2023-10-02" @default.
• W4385716615 title "Pyridine-bridged cobalt tetra-aminophthalocyanine to active peroxymonosulphate for efficient degrading carbamazepine" @default.
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• W4385716615 doi "https://doi.org/10.1080/09593330.2023.2245541" @default.
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