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LW
Verified CAS / Academic Author3 Decoded Studies

Prof. LI Wentao

Nanjing University, State Key Laboratory of Water Pollution Control and Green Resources Recycling

Co-Affiliations:Beijing University of Chemical TechnologyNational Engineering Research Center of New Energy Power Generation, North China Electric Power University, Beijing 102206, China

Research Publications & English Decoded Briefs

Showing 3 publications
Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2025102002

Influence of UV Intensity on Escherichia coli Inactivation Efficiency in the UV/Cl2 Process

The ultraviolet/chlorine (UV/Cl2) advanced oxidation process generates multiple radical species, enabling synergistic disinfection. However, the systematic influence of UV intensity on process performance remains inadequately characterized. This study investigated UV intensities from 0.25 to 2.0 mW·cm−2, assessing chlorine photolysis kinetics, bacterial inactivation, and disinfection by-product (DBP) formation. Results demonstrate that inactivation efficiency is not solely governed by total UV energy but is co-regulated by reaction kinetics and mass transfer. Increasing UV intensity accelerated chlorine photolysis by 33.7%–277.8%, elevating steady-state concentrations of hydroxyl radicals and chlorine radicals by factors of 1.6–3.8 and 1.3–3.2, respectively, thereby enhancing initial inactivation rates. However, higher intensities reduced cumulative chlorine exposure (CT value) to 14.3%–55.7% of baseline, causing overall inactivation to first increase then decrease. At a fixed UV dose of 150 mJ·cm−2, an intensity of 1.0 mW·cm−2 achieved optimal 6.5-log inactivation of Escherichia coli and the lowest bacterial reactivation rate (0.07%). Common water constituents (HCO3−, Cl−, natural organic matter) inhibited disinfection, with natural organic matter exerting the strongest suppression (2.7-log reduction). Notably, 1.0 mW·cm−2 exhibited the greatest resistance to interference. Elevated intensity reduced total organic halogen formation from 33.7 μg·L−1 to 19.0 μg·L−1. Balancing disinfection efficacy and DBP risk, 1.0 mW·cm−2 is identified as the optimal UV intensity for the UV/Cl2 process in sand-filtered water treatment.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4081-y

Multifunctional mitochondria-targeting energy disruptor for enhancing imaging-guided low-temperature photothermal therapy of melanoma

The evolution of precision medicine has propelled multimodal imaging-guided phototheranostics to the forefront for precise tumor diagnosis and therapy. Low-temperature photothermal therapy (PTT) offers a promising approach for the treatment of melanoma due to its non-invasiveness and minimal damage to normal tissues. However, its efficacy is limited by cancer cell thermal tolerance. To address this, a new type of multifunctional energy disruptor (CAMeO-Q NPs) is developed featuring homologous targeting and mitochondria targeting, and synergistically enhancing low-temperature PTT in melanoma by reversing heat shock protein 90 (Hsp90)-mediated thermal tolerance and blocking mitochondrial adenosine triphosphate (ATP) biosynthesis. The multifunctional energy disruptor enables precise trimodal imaging (fluorescence imaging/FLI, photoacoustic imaging/PAI, and photothermal imaging/PTI) guidance for low-temperature PTT. Comprising a mitochondria-targeting photothermal agent and an Hsp90 inhibitor, CAMeO-Q NPs induce selective mitochondrial damage under 660 nm laser irradiation and downregulate cellular HSP expression by ATP inhibition and Hsp90 inhibitor. This multifunctional energy disruptor provides a novel strategy for enhancing multimodal imaging-guided low-temperature photothermal therapy through combined homologous targeting, mitochondria-targeting, and Hsp90 inhibition.

Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(26)60662-7

Mechanistic Insights into Low-Temperature CO2 Methanation over LaNiO3/CeO2 Perovskite Catalyst

Perovskite-type catalysts show promise for CO2 methanation, yet their low-temperature performance and mechanisms remain unclear. Here, a LaNiO3/CeO2 catalyst was synthesized via sol-gel and impregnation. In situ reduction decomposed the perovskite into highly dispersed Ni0 particles (average 12.6 nm) on CeO2, which provided abundant oxygen vacancies (Ce3+/(Ce3++Ce4+) = 9.2%) and weak/moderate basic sites. This synergy enhanced CO2 adsorption and activation. At 200–300 °C, the catalyst achieved ~100% CH4 selectivity and CO2 conversion up to 23.6% at 300 °C. Comparative studies with LaNiO3, LaCeNiO4, Ni/CeO2, and La-Ni/CeO2 revealed that the perovskite pre-structuration and in situ reduction optimize Ni dispersion and metal-support interactions, stabilizing Ni0 and tuning surface basicity and oxygen vacancies. This work provides a design strategy for efficient low-temperature CO2 methanation catalysts.