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K-g-C3N4
NEW JOURNAL OF CHEMISTRY · 2025 · IF 2.5

K-g-C3N4@PDA nanozyme for the colorimetric detection of ferric ammonium citrate in edible salt

Limei Yang,Ye Liu,Rongxue Wang,Linqian Hou,Yaling Yang

A K-doped carboxylated polydopamine (PDA) modification of the g-C3N4 (K-g-C3N4@PDA) nanozyme was effectively performed by one-step potassium salt-assisted thermal copolymerization and hydrothermal strategies. K-g-C3N4@PDA showed excellent peroxidase (POD)-like activity, and ferric ammonium citrate (FAC) efficiently promoted the generation of hydroxyl radicals (˙OH). Furthermore, K-g-C3N4@PDA oxidized 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) in the presence of H2O2 to produce a blue-green product, and FAC boosted the POD-like activity with an exceptional linear relationship and low detection limit (0.018 μg mL−1). Importantly, a recovery rate of 94.09–105.17% was attained when the developed method was effectively used to assess FAC in culinary salt samples using a spiking procedure.

研究领域: 纳米技术 · 分析化学 · 酶模拟物 · 食品安全 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 29 ·期 26 ·39027-39040 · IF 5.19

Photocatalytic concrete for degrading organic dyes in water

Zhou Yiming,Elchalakani Mohamed,Liu Houfeng,Briseghella Bruno,Sun Chuanzhi

Since the advent of photocatalytic degradation technology, it has brought new vitality to the environmental governance and the response to the energy crisis. Photocatalysts harvest optical energy to drive chemical reactions, which means people can use solar energy to complete some resource-consuming activities by photocatalysts, such as environmental governance. In recent years, researchers have tried to combine photocatalyst TiO 2 with building materials to purify urban air and obtained good results. One of the important functions of photocatalysts is to degrade organic pollutants in water through light energy, but this technology has not been reported in the practical application areas. To extend this technology to practical application areas, photocatalytic concrete for degrading pollutants in waters was proposed and demonstrated for the first time in this paper. The photocatalytic concrete proposed based on the K-g-C 3 N 4 shows a strong ability to degrade the organic dyes. According to the experiment results, the angle of light source plays an important role in the process of photocatalytic degradation, while waters with pH value of 6.5–8.5 hardly influenced the degradation of organic dyes. When the angle of light source is advantageous for photocatalytic concrete to absorb more visible light, more organic dyes will be degraded by photocatalytic concrete. The degradation rate of methylene blue could reach about 80% in ½ hour under desirable conditions and is satisfied compared with that of reported works. This study implicates that photocatalytic concrete can effectively degrade organic dyes in water. The influences of changes in the water environment hardly affect the degradation of organic pollutants, which means photocatalytic concrete can be widely used in green infrastructures to achieve urban sewage treatment.

CAS / MDL: 7778-80-5
研究领域: 环境科学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Interface engineering of AgI/(P, K)-g-C3N4 novel S-scheme heterostructures as a highly efficient photocatalyst for RhB degradation

Zhangwei Sun,Yuhao Qi,Kaile Wang,Jiaming Li,Xiaoyu Qiu,Yunhe Zhao,Li Guo

In this study, we developed an in-situ deposition method to load small-sized AgI nanoparticles as an oxidative photocatalyst (OP) onto phosphorus (P) and potassium (K) co-doped two-dimensional porous g-C 3 N 4 (PK-CN-N) as a reductive photocatalyst (RP), forming an S-scheme heterojunction photocatalyst AgI/PK-CN-N. PK-CN-N achieved morphology control and element doping, leading to surface functionalization and heterostructure formation for the AgI/PK-CN-N photocatalyst. Notably, the 50AgI/PK-CN-N composite demonstrated an approximately 95 % removal efficiency for RhB within 30 minutes, 17.6 times higher than pure g-C 3 N 4 , surpassing most reported g-C 3 N 4 -based photocatalysts. The enhanced photocatalytic efficiency is attributed to the surface modification strategy and heterostructure formation of g-C 3 N 4 , which broadens the visible light response range, increases the number of active sites, improves the separation of photogenerated electron-hole pairs, and enhances REDOX capabilities. The band structure of the composite was elucidated through Mott-Schottky analysis and UV–vis DRS. The formation of the AgI/PK-CN-N S-scheme heterojunction and its charge transfer mechanism was confirmed through XPS, band structure analysis, KPFM, and EPR spectroscopy. Experimental data confirmed the presence of a strong and effective interface electric field between the two semiconductors, leading to band bending and accelerated charge separation. Additionally, the introduction of small-sized AgI semiconductors enhanced the exposure of the coupling interface, further improving catalytic performance. The reusability and lifespan of the catalyst were also analyzed, showing that after four cycles, the photocatalytic activity remained above 92 %.

CAS / MDL: 64-17-5
研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Efficient degradation of antibiotics in different water matrices through the photocatalysis of inverse opal K-g-C3N4: Insights into mechanism and assessment of antibacterial activity

Juying Lei,Bin Chen,Liang Zhou,Ningkai Ding,Zhengqing Cai,Lingzhi Wang,Su-Il In,Changzheng Cui,Yanbo Zhou,Yongdi Liu,Jinlong Zhang

The efficient degradation of fluoroquinolone antibiotics and the reduction of their antimicrobial activity were achieved in different water matrices through the photocatalysis of inverse opal potassium-doped carbon nitride (IO K-CN). The IO K-CN photocatalyst with optimum doping ratio of potassium performed much better than bulk carbon nitride and pure inverse opal carbon nitride for removing fluoroquinolone antibiotics, such as levofloxacin (LVX) and norfloxacin (NOR). The remarkably narrowed band gap resulting from potassium doping and the unique properties of the inverse opal construction jointly contributed to enhancing the activity of the photocatalyst. A possible mechanism and degradation pathway for LVX was proposed on the basis of a series of characterizations including electron spin resonance (ESR) experiments, and liquid chromatography-mass spectrometry (LC-MS) analysis. Meanwhile, the byproducts during the LVX photocatalytic degradation were shown to have much lower sterilization effect, implying that the toxicity and the potential risk of LVX were excellently reduced. The potential application for the treatment of antibiotic-containing wastewater was indicated by the excellent treatment efficiency and favorable durability of this photocatalyst.

研究领域: 环境科学 · 材料科学 · 微生物学
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