Jaesang Lee 교수

Reports that promote persulfate-based advanced oxidation process (AOP) as a viable alternative to hydrogen peroxide-based processes have been rapidly accumulating in recent water treatment literature. Various strategies to activate peroxide bonds in persulfate precursors have been proposed and the capacity to degrade a wide range of organic pollutants has been demonstrated. Compared to traditional AOPs in which hydroxyl radical serves as the main oxidant, persulfate-based AOPs have been claimed

Select persulfate activation processes were demonstrated to initiate oxidation not reliant on sulfate radicals, although the underlying mechanism has yet to be identified. This study explored singlet oxygenation and mediated electron transfer as plausible nonradical mechanisms for organic degradation by carbon nanotube (CNT)-activated peroxymonosulfate (PMS). The degradation of furfuryl alcohol (FFA) as a singlet oxygen (¹O₂) indicator and the kinetic retardation of FFA oxi

The extraordinary chemical and physical properties of materials at the nanometer scale enable novel applications ranging from structural strength enhancement and energy conservation to antimicrobial properties and self-cleaning surfaces. Consequently, manufactured nanomaterials (MNMs) and nanocomposites are being considered for various uses in the construction and related infrastructure industries. To achieve environmentally responsible nanotechnology in construction, it is important to consider

The objective of this study was to investigate photochemical production of singlet oxygen (1O2) and superoxide radical anion (02*-) by C60 in water. It was demonstrated that photoexcited C60 in the aqueous phase efficiently mediated transfer of absorbed energy to oxygen and produced singlet oxygen when associated with surfactant (Triton X100 and Brij 78) or polymer (polyvinylpyrrolidone), which is consistent with previously observed behavior in organic solvents. However, when C60 was present as

Four novel hexakis C60 derivatives with varying functionalities were synthesized, and their photochemical properties and photodynamic disinfection efficiencies were quantitatively evaluated. All these C. derivatives generated O2 more efficiently than commercial multihydroxylated C60 (fullerol), as assessed by furfuryl alcohol consumption and electron paramagnetic resonance analysis. Despite significant agglomeration/aggregation in the aqueous phase to micrometer-sized particles, nanosecond laser

We recently reported that C-60 aminofullerenes Sunlight immobilized on silica support (aminoC(60)/silica) efficiently produce singlet oxygen (O-1(2)) and inactivate virus and bacteria under visible light irradiation.(1) We herein evaluate this new photocatalyst for oxidative degradation of 11 emerging organic contaminants, including pharmaceuticals such as acetaminophen, carbamazepine, cimetidine, propranolol, ranitidine, sulfisoxazole, and trimethoprim, and endocrine disruptors such as bispheno

The mechanism involved with (1) energy and electron transfer by C60 in the aqueous phase during UV irradiation and (2) subsequent production of reactive oxygen species (ROS) such as singlet oxygen and superoxide radical anion was investigated. Electron paramagnetic resonance (EPR) study showed that C60 embedded in micelles of nonionic surfactant (Triton X 100) or anionic surfactant (sodium dodecylbenzenesulfonate) produced ROS, but aggregated C60 did not, consistent with our earlier findings mad

This study reexamined the mechanisms for oxidative organic degradation by the binary mixture of periodate and H₂O₂ (PI/H₂O₂) that was recently identified as a new advanced oxidation process. Our findings conflicted with the previous claims that (i) hydroxyl radical (^•OH) and singlet oxygen (¹O₂) contributed as the primary oxidants, and (ii) ^•OH production resulted from H₂O₂ reduction by