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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Fast charge separation from synergistic effect of plasma Bi metal and BiOCl/SrTiO3 S-scheme heterojunction promotes NO deep removal

Jiaoping Si,Hongjing Liu,Wendong Zhang,Dengyu Jiao,Wangxing Ai,Yuerui Ma,Lihuan Feng,Xing’an Dong,Wenjie He,Peng Chen

The catalytic conversion of nitrogen oxides (NO x ) to non-toxic products has emerged as a critical strategy for air pollution control under stringent emission regulations. Photocatalytic NO x removal performance highly depends on the transmission of photogenerated electrons and the amount of reactive oxygen species (ROS) generated. Herein, the Bi/BiOCl/SrTiO 3 heterostructure photocatalyst was prepared by a simple in situ synthesis method to address the limitations of conventional NOx removal systems. Due to the synergistic effect of bismuth (Bi) surface plasmon resonance (SPR) and the built-in electric field in BiOCl/SrTiO 3 S-scheme heterojunction, Bi/BiOCl/SrTiO 3 showed strong light absorption ability and high charge separation efficiency, with the highest NO removal efficiency reaching 70 %. The enhanced electronic interaction between Bi and BiOCl/SrTiO 3 induced Bi-O covalent bonds with the BiOCl layer to facilitate fast charge separation, promoting the rapid transfer of interfacial photogenerated carriers, this process induces the activation of O 2 and H 2 O to form reactive oxygen species (ROS) to promote the oxidative removal of NO. This study provides new insights into the development of effective photocatalysts with fast charge separation by synergistic metal active sites and built-in electric field of heterojunction for air pollutant purification.

CAS / MDL: 16940-66-2
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JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS · 2021 · IF 3.995

Promotional effect of phosphorus addition on improving the SO2 resistance of V2O5-MoO3/TiO2 catalyst for NH3-SCR of NO

Li Huang,Yiqing Zeng,Yibo Gao,Hu Wang,Yuhao Zong,Zhengfeng Chang,Shule Zhang,Pei Han,Yang Yu

The oxidation of SO 2 into SO 3 promote the formation of NH 4 HSO 4 (ABS), which can cover surface active sites catalyst, and then leading to the decrease of NH 3 -SCR De-NO x activity. In this work, phosphorus species were loaded on the V 2 O 5 -MoO 3 /TiO 2 De-NO x catalyst to enhance its SO 2 resistance via inhibiting the SO 2 /SO 3 conversion. XRD and N 2 -adsorption results showed that phosphorus has little impact on the structure and pore property of the catalyst. The results of XPS , H 2 -TPR, and NH 3 -TPD analyses illustrated that suitable amount of phosphorus (1%) increases the content of polymeric vanadate and chemisorbed oxygen (O α ) of the catalyst, which is benefit to the SCR process. Phosphorus species decreases the SO 2 absorbability and SO 2 oxidation activity of V-Mo-P/Ti catalysts, thus it exhibits higher NH 3 -SCR activity than that of the P-free catalyst at presence of SO 2 due to the lower SO 2 /SO 3 conversion and fewer amount of NH 4 HSO 4 deposition.

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Reaction Kinetics Mechanisms and Catalysis · 2019 ·Vol. 128 ·期 2 ·681-693 · IF 1.428

Constructing hollow silkworm structure in MnOx–TiO2 catalysts for improving the performance in selective catalytic reduction of NO by NH3

Xie Chong,Yang Shenghui,Shi Jian-Wen,Niu Chunming

A novel MnO x –TiO 2 catalyst with hollow silkworm structure was synthesized successfully via an ethanol-thermal strategy by using activated carbon fiber felt as template for the first time. The silkworm-like MnO x –TiO 2 catalyst (MnTi) exhibited higher NO x conversion in the whole experimental temperature region (90–330 °C) under a high space velocity of 36,000 h −1 in comparison with the common MnO x –TiO 2 catalyst without hollow silkworm structure (MnTi-B). The excellent catalytic performance of MnTi can be attributed to its high specific surface area, large content of active surface oxygen species (O S ), and more surface acid sites. In addition, the MnTi catalyst also exhibited excellent resistance to water or SO 2 poisoning.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

The key role of surface hydroxyls on the activity and selectivity in photocatalytic degradation of organic pollutants and NO removal

Tianxing Cui,Yumei Su,Xionghui Fu,Yi Zhu,Yuanming Zhang

Herein, we fabricated hydroxyl groups decorated Bi 4 O 5 I 2 nanosheets, and the contents of hydroxyl groups on the surface could be controlled by changing the reducibility of organic solvents. The stronger reducibility of organic solvents, the more hydroxyl groups on the surface. The hydroxyl groups on the surface of Bi 4 O 5 I 2 nanosheets have significant effects on photocatalytic activity. For degradation of organic pollutants, the surface hydroxyls form hydrogen bonds with organic pollutants, which is conducive to the adsorption of the substrates. For NO removal, the NO adsorbed on the hydroxyl groups is more oxidized into a toxic by-product NO 2 instead of NO 3 - , so less hydroxyl groups are important for photocatalysts towards NO removal. These new discoveries provide new insights to improve photocatalytic activities by modulating surface functional groups of photocatalysts.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Innovative MRSA-infected wound repair strategy: NIR-triggered controllable NO releasing from plant extracts quercetin composite chitosan/hyaluronic acid hydrogel

Yifu Wang,Jinjin Li,Linlin Ding,Xiaolan Gao,Zhilan Chi,Shanshan Ma,Leiliang He,Yamin Xiong

Bacterial infection reduces quality of wound healing and even cause severe complications, but most current dressings adopt single antibacterial mode showed limited effectiveness. Herein, a plant extract quercetin (Que) composite chitosan/hyaluronic acid hydrogel (named CBCQ) with near-infrared (NIR) triggered controllable NO releasing was developed for efficient photothermal therapy/nitric oxide (PTT/NO) synergistic antibacterial and wound healing. Specifically, CBCQ hydrogel with chemical/physical crosslinked network was fabricated via host-guest interaction, metal coordination and Schiff base reaction. It exhibited porous structure, excellent injectability, self-healing, adhesion, antioxidant, and biocompatible properties suitable for wound dressings. Notably, superior PTT effect generated from Que-Fe 3+ has been demonstrated, which served as a photothermal switch for the controllable NO release, thereby enable to utilize the physiological functions of NO at different concentrations, improving antibacterial efficiency by integrating PTT and NO benefits, and further allowing sustained antibacterial through Que when NIR was off. Importantly, CBCQ hydrogel achieved better healing of skin incision than commercial 3M medical glue and Film, and significantly improved the healing rate and quality of Methicillin-resistant Staphylococcus aureus (MRSA) infected wound by efficient and sustained antibacterial activity, inhibiting inflammation, and promoting collagen deposition and angiogenesis, highlighting its promising application in skin incisions and infected full-thickness skin wounds.

CAS / MDL: 7790-28-5
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Food Chemistry-X · 2026 · IF 9.2

Homologous divergence: Processing reshapes metabolite variations and relative odor activity values in black and green teas derived from Gougunao no. 2

Yongfa Guo,Jie Zhou,Zhuangzi Zhong,Shuang Li,Junjie Lu,Dingkun Liu,Li He,Shuaiwen Yin,Yang Wu,Huimin Sun

Using leaves from a single origin and the same harvest batch, processing was the sole variable: homologous Gougunao No. 2 green and black teas were produced. An integrated workflow (UHPLC–HRMS and HS-SPME–GC–MS) was combined with flavonoid contents and multiple antioxidant assays to probe how processing reshapes the composition–function–aroma nexus. Multivariate analysis clearly separated the two teas, with green tea showing higher flavonoids and stronger antioxidant readouts. In non-volatile fraction, 1988 features were detected, of which 713 changed significantly, implicating remodelling of flavonoid- and catechin-centred pathways and purine metabolism. In volatile fraction, 1066 compounds were annotated, with 76 differing significantly; relative odor activity value based analysis indicated that unsaturated aldehydes and sulphur-containing compounds drive a roasted, full-bodied profile in black tea, whereas alcohols, esters and selected terpenoids confer fresher, fruity notes in green tea. Overall, these results support a processing-associated bitterness–aroma rebalancing pattern and nominate candidate chemical indicators for quality evaluation.

CAS / MDL: 7632-00-0 7784-27-2
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AQUACULTURE NUTRITION · 2026 ·Vol. 2026 ·期 1 ·4395252 · IF 4.6

Dietary Arginine Regulates Glycometabolism in Hybrid Grouper (Epinephelus fuscoguttatus ♀ × Epinephelus lanceolatus ♂) via the IGF-1 and NO-cGMP Pathways

Haoran Yin,Lixing Wang,Zexin Lin,Ruilin Li,Qinxiao Cai,Zhiyu Zhou,Xiaoyi Wu

The hybrid grouper ( Epinephelus fuscoguttatus ♀ × Epinephelus lanceolatus ♂), a typical carnivorous fish, has a limited ability to utilize dietary carbohydrates (CHOs). This study investigated the effects of different dietary arginine (Arg) levels (2.55 and 3.65%) and CHO-to-lipid ratios (C/L: 3.57, 2.39, 1.61) on the glycometabolism of hybrid grouper. Juvenile hybrid grouper (mean initial body length and weight: 7.8 cm and 13.04 g) were manually fed to fullness two times per day throughout a 7-week growth trial. The results showed that the C/L3.67 diets significantly elevated 2-h postprandial blood glucose concentration, as well as reduced hepatic glycogen level, intraperitoneal fat ratio (IPF), and the whole-body and hepatic lipid contents relative to the C/L2.39 and C/L1.61 diets. Dietary Arg supplementation significantly improved this metabolic disorder. These improvements were associated with enhanced plasma insulin-like growth factor 1 (IGF-1) concentration, hepatic phosphofructokinase (PFK) activity, nitric oxide (NO), and cyclic guanosine monophosphate (cGMP) levels. They were also linked to the upregulated expression of key molecules in related pathways, including IGF-1 receptor (igf1r), phosphatidylinositol 3-kinase (pi3k), protein kinase AMP-activated catalytic subunit α (ampk-α), and protein kinase B (Akt) genes, as well as glucose transporter 4 (GLUT4) and mechanistic target of rapamycin (mTOR) proteins. Generally, suitable dietary Arg supplementation can reduce postprandial blood glucose and hepatic glycogen concentrations in hybrid grouper fed high C/L diets by regulating key genes and proteins within the IGF-1 and NO-cGMP pathways. This finding provided a nutritional intervention to enhance CHO utilization in hybrid grouper aquaculture.

CAS / MDL: 8032-32-4 60-24-2
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Journal of the American Chemical Society · 2026 · IF 16.6

Water-Enabled Conversion of NO and CO to NH3 over CuO x Clusters via Hydrolysis of Surface –NCO Intermediates

Wei Tan,Xueqing Liu,Jiawei Yang,Xiaoyu Ji,Kailong Ye,Shaohua Xie,Ge Yao,Chuanzhi Sun,Fudong Liu,Lin Dong

Abstract The catalytic conversion of gaseous NO to NH3 offers a promising dual-benefit strategy for environmental remediation and sustainable chemical synthesis. Herein, CuO/Al2O3 catalysts with varied CuO loadings (x wt %, xCu/Al) were developed for the possible NH3 production from NO reduction by CO with the assistance of H2O. While increasing CuO loading (1–12 wt %) monotonically improved NO conversion to N2 under dry conditions, the introduction of H2O dramatically boosted NO conversion on 5Cu/Al with highly dispersed CuOx clusters, raising its NO conversion comparable to that of 12Cu/Al. Further analysis revealed that NH3 was generated on xCu/Al catalysts under wet conditions, with NH3 generation on 5Cu/Al initiating at the lowest temperature (275 °C) and being the most vigorous. Combined experimental and theoretical analysis suggested that, on CuOx clusters, H2O facilitated the conversion of the NCO* intermediate to NH3 with a much lower activation barrier compared to its CO-mediated pathway to N2, well explaining the boosted NO conversion and NH3 yield on the 5Cu/Al catalyst upon H2O addition to NO + CO flow. This work highlights that a simple, earth-abundant Cu catalyst enabled the efficient and cost-effective synthesis of NH3 from air pollutants of NO and CO under mild conditions, underscoring a sustainable strategy that simultaneously addresses pollution abatement and resource recovery.

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ACS Applied Materials & Interfaces · 2025 · IF 8.2

Coaxial Fibrous Dressing Enabling Sequential NO/H2 Release for Temporally Programmed Antibacterial and Healing-Promoting Functions in Infected Diabetic Wound Treatment

Zishuo Hou,Wuyang Zhang,Gangfeng Li,Hannan Cui,Hongli Chen,Tengjiao Wang,Yafei Feng,Peng Li

Infected diabetic wounds have become a major global health threat due to their complex conditions, making them difficult to heal. Herein, a coaxial fibrous dressing capable of sequential release of nitric oxide (NO) and molecular hydrogen (H2) was designed for the treatment of infected diabetic wounds. The outer layer of the coaxial fibers was physically loaded with the NO donor, enabling the first stage of rapid and high-level NO release (over 170 μM). The released NO contributed to the antibacterial function of the dressing (in vitro antibacterial assays demonstrated eradication rates of 99.99% and 99.04% against S. aureus and E. coli, respectively), thus facilitating accelerated transition of the wound through the inflammatory phase. The inner layer of coaxial fibers becomes progressively exposed following structural disintegration, enabling the hydrolysis of encapsulated H2 donor to achieve on-demand release of H2 under near-infrared (NIR) irradiation. The released H2 could promote wound healing through reactive oxygen species (ROS) scavenging and macrophage M2 polarization, as validated by in vitro cell assessments. In vivo infected full-thickness skin defect model in diabetic mice demonstrated that the NO/H2 sequential release coaxial fibrous dressing significantly accelerated healing of infected wounds through rapid bactericidal action via substantial NO release, followed by further sequential H2 release promoting repairing and regeneration. This temporally sequential delivery of antibacterial and healing-promoting functions significantly accelerated the healing of infected diabetic wounds.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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CHEMOSPHERE · 2022 · IF 8.943

Engineering multiscale polypyrrole/carbon nanotubes interface to boost electron utilization in a bioelectrochemical system coupled with chemical absorption for NO removal

Wei Li,Huanyu Yue,Chunyan Zhang,Junyu Hu,Qiaoli Wang,Yuanming Li,Shihan Zhang,Jianmeng Chen,Jingkai Zhao

The chemical absorption-bioelectrochemical reduction (CABER) integrated system provides an alternative of good potential for NO removal. The efficient utilization of cathode electrons directly determines the system performance and operating cost. Herein, we synthesize a polypyrrole/carbon nanotubes (PPy/CNTs) composite to engineer a micro-and nanoscale interface with low resistance and high biocompatibility between the cathode and biofilms in the CABER system. The resulting PPy/CNTs biocathodes exhibit 36.4% increase in biomass density, 40.7%–302.6% increase in Faraday efficiency along Fe(III)EDTA reduction, and 204% increase in Fe(II)EDTA-NO reduction rate. The enrichment of functional microorganisms is validated to be a key strengthening factor, as the proportion of which increased from 57.9% to 84.6%. Moreover, for efficient electron transfer and utilization, a low-resistance electron transfer route, “electrode substrate → PPy (→ CNTs) → microbial cells → Fe(III)EDTA or Fe(II)EDTA-NO”, is realized in the multiscale conductive networks constructed of PPy/CNTs composite and microbial nanowires .

CAS / MDL: 109-97-7 657-84-1
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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

In situ synthesis of an advanced Z-scheme Bi/BiOI/black TiO2 heterojunction photocatalysts for efficient visible-light-driven NO purification

Qian Li,Jing Hu,Haiqiang Wang,Zhongbiao Wu

Limited light absorption and severe charge recombination have been widely acknowledged as the two main obstacles restricting the application of P25 in NO photocatalytic conversion. In this work, an advanced heterojunction photocatalyst of Bi/BiOI/black TiO 2 was synthesized via an in-situ solid-state chemical reduction method. The black TiO 2 extended the light absorption to the full spectral region. It constructed a direct Z-scheme heterojunction with BiOI nanosheets, not only promoting the charge separation, but also preserving the strong oxidation ability of photogenerated holes in black TiO 2 and strong reducing ability of photogenerated electrons in BiOI. Thus, more •O 2 − and •OH radical could form when Bi/BiOI/black TiO 2 was subjected to visible light irradiation. Besides, the introduced Bi metal nanoparticles could also enhance the light utilization and served as a cocatalyst to accept the electrons. Therefore, enhanced NO photocatalytic oxidation activity was obtained, with the optimal sample Bi/BiOI/black TiO 2 exhibiting a high NO conversion efficiency of ~70% and NO x removal of ~45%. This work may provide a refreshing perspective for the design of heterojunction photocatalysts for efficient NO photocatalytic purification and other photocatalytic applications.

CAS / MDL: 10035-06-0 7681-11-0
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ENERGY & FUELS · 2020 · IF 3.421

FeII(EDTA)–NO Reduction by Mn Powder in Wet Flue Gas Denitrification Technology Coupled with Mn2+ Recycling: Performance, Kinetics, and Mechanism

Jun Chen,Yi Chen,Dzmitry Hrynsphan,Yu Mei,Hua Pan,Jiali Wu,Jianmeng Chen,Jiachao Yao

FeII(EDTA) solution has been considered an efficient option in wet flue gas denitrification, whereas the generated FeII(EDTA)–NO restricts its wide application, suggesting that FeII(EDTA)–NO reduction is the key to this process. This work investigated the performance, kinetics, and mechanism of FeII(EDTA)–NO reduction by Mn powder coupled with manganese ion (Mn2+) recovery. We initially studied the performance of FeII(EDTA)–NO reduction with respect to the major influencing factors (i.e., the particle size of Mn powder, initial FeII(EDTA)–NO concentration, Mn powder concentration, stirring speed, and temperature). Shrinking core model and Arrhenius law were applied to illustrate the kinetics and mechanism between FeII(EDTA)–NO solution and Mn powder, suggesting that the solid–liquid reaction was fitted on chemical reaction control, and the activation energy was calculated as 43.0 kJ mol–1. The effects of main operating parameters, such as precipitant concentration, pH value, and temperature, were studied on Mn2+ recovery. Results indicated that the pseudo-second-order model could precisely describe the kinetics of Mn2+ recovery. Finally, according to Arrhenius and Eyring–Polanyi equations, the reaction activation energy, enthalpy of activation, and entropy of activation for Mn2+ recovery were calculated as 17.25 kJ mol–1, 14.55 kJ mol–1, and 252.07 J (k mol)−1, respectively.

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