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Materials · 2024 ·Vol. 17 ·期 6 ·1440 · IF 3.1

Tailoring Iridium Valence States on ZSM-5 for Enhanced Catalytic Performance in CO Selective Catalytic Reduction of NO under Oxygen-Enriched Environments

Yarong Bai,Chuhan Miao,Weilong Ouyang,Lang Wang,Haiqiang Wang,Zhongbiao Wu

Barium and iridium supported on Zeolite Socony Mobil-5 (ZSM-5) are efficient catalysts for the selective catalytic reduction of nitric oxide by carbon monoxide (CO-SCR), with enhanced cyclic stability. The introduction of Ba hindered the oxidation of metallic Ir active species and enabled Ir to maintain an active metallic state, thereby preventing a decrease in catalytic activity in the CO-SCR reaction. Moreover, the Ba modification increased the NO adsorption of the catalyst, further improving the catalytic activity. Owing to the better anti-oxidation ability of Ir0in IrBa0.2/ZSM-5(27) than in Ir/ZSM-5(27), IrBa0.2/ZSM-5(27) showed better stability than Ir/ZSM-5(27). Considering that all samples in the present study were tested to simulate actual flue gases (such as sintering flue gas and coke oven flue gas), NH3was introduced into the reaction system to serve as an extra reductant for NOx. The NOxconversion to N2(77.1%) was substantially improved using the NH3-CO-SCR system. The proposed catalysts and reaction systems are promising alternatives for treating flue gas, which contains considerable amounts of NOxand CO in oxygen-enriched environments.

研究领域: 环境科学 · 催化化学
✓ 已验证 DOI PubMed 高影响因子
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Advanced Optical Materials · 2019 ·Vol. 7 ·期 10 ·1900006 · IF 7.125

No-Interference Reading for Optical Information Storage and Ultra-Multiple Anti-Counterfeiting Applications by Designing Targeted Recombination in Charge Carrier Trapping Phosphors

Zhangwen Long,Yugeng Wen,Junhe Zhou,Jianbei Qiu,Hao Wu,Xuhui Xu,Xue Yu,Dacheng Zhou,Jie Yu,Qi Wang

Charge carrier trapping phosphors are one of the most fascinating candidates for next-generation optical information storage technology and advanced anti-counterfeiting applications. However, there is a challenge in that shallow traps can result in interference with the real-time reading of optical information, and the anti-counterfeiting level also needs to be further enhanced. Here, a novel quasi-layer-structured Ca 3 Ga 4 O 9 :Bi 3+ phosphor is introduced to address this challenge, based on the targeted recombination phenomenon. This material shows turning electron-trapping ability and obvious differences in photoluminescence, long persistent luminescence, and photo-stimulated luminescence processes, which are beneficial in achieving information reading without interference and provide multiple anti-counterfeiting. As a proof of concept, information reading without interference is experimentally achieved by choosing an appropriate filter and excitation wavelength, and multiple anti-counterfeiting applications are demonstrated using a simple seal-photocopy method. The results indicate that the targeted recombination strategy is very effective for achieving multifunctional applications of charge carrier trapping phosphors.

研究领域: 材料科学 · 光学存储 · 光子学 · 防伪技术 · 发光材料
✓ 已验证 DOI 高影响因子
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MOLECULES · 2026 ·Vol. 31 ·期 16 ·2775 · IF 5.1

Comparative Effects of Ce, Co, or W Dopants on the Catalytic Performance of FeMnTiOx Catalysts for Low-Temperature NH3-SCR of NO

Binyu Wang,Cong Feng,Huan Liu

To clarify the role of metal dopants in low-temperature NH3-SCR of NO, FeMnTiOxcatalysts were synthesized by coprecipitation and separately modified with Ce, Co, or W. The catalysts were evaluated for NO conversion, separate O2/H2O switching response and dry-feed time-on-stream stability and characterized by XRD, SEM, N2adsorption–desorption, XPS, H2-TPR and NH3-TPD. Ce doping at Ce/Mn = 0.3 suppressed TiO2crystallization, increased the BET surface area from 136 to 231 m2g−1and the pore volume from 0.19 to 0.58 cm3g−1, raised the Mn4+/Mn3+ratio from 0.70 to 1.25, and increased the medium-strong-acid relative peak area from 555.4 to 1293.2 a.u. FeMnCe0.3TiOxmaintained at least 90% NO conversion from 140 to 360 °C, gave 75% conversion at 400 °C, and averaged 97.4% during a 40 h dry-feed test at 350 °C. The results show that the superior Ce-modified catalyst arises from the combined regulation of texture, surface redox balance and acidity.

CAS / MDL: 10026-22-9 12333-11-8
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LANGMUIR · 2025 · IF 3.9

A NIR-II Laser-Triggered Nb2C-Arg/Gel Composite Multifunctional Hydrogel with Photothermal, ROS Scavenging, and NO Release for Infected Wound Healing

Mi Liu,Weidan Zhao,Denghao Li,Dingyu Cui,Jiali Liu,Qingao Chen,Yan Zhou,Li Jiang,Huaibin Zhou

Infected wound healing remains a significant clinical challenge due to bacterial resistance and excessive inflammation. Herein, a multifunctional hydrogel dressing (Nb2C-Arg/Gel) is developed that integrates two-dimensional Nb2C nanosheets (photothermal agent) and arginine [nitric oxide (NO) donor] into a calcium ion cross-linked sodium alginate matrix. The hydrogel has a relatively high swelling capacity and good ability to scavenge reactive oxygen species (ROS), which are beneficial for absorbing wound exudate and reducing the inflammatory response of wounds. Under irradiation with a low-power NIR-II laser (1064 nm, 1 W cm–2), Nb2C-Arg/Gel achieves rapid photothermal heating (48.6 °C in 1 min), while thermally enhances arginine decomposition-triggered on-demand NO release. This synergistic mechanism provides superior antimicrobial efficacy against Staphylococcus aureus (97.65%) and methicillin-resistant S. aureus (90.05%). In vivo studies on MRSA-infected murine wounds demonstrate that the residual area on day 10 was 2.9%, which accelerated healing compared to that of the control group (17.8%), accompanied by reduced inflammation and enhanced angiogenesis. The excellent biocompatibility of hydrogel is validated by low hemolysis (<5%) and promoted fibroblast proliferation (125% cell viability). Combining with photothermal, NO-mediated antibacterial action, and ROS scavenging to alleviate oxidative stress, this antibiotic-free hydrogel dressing has great potential for clinical application for the treatment of refractory-infected wounds.

CAS / MDL: 10043-52-4
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2020 · IF 3.573

Gas–Solid Two-Phase Flow Synthesis Equipment: A New Method for Continuous, Large-Scale Preparation of Metal–Organic Frameworks with No Solvent

Jun Zhao,Rufang Peng

Here, we demonstrated the continuous synthesis of metal–organic frameworks (MOFs) (ZnBTeC/MnBTeC/Ni4[(phen)2(BeTC)]/Co4[(phen)2(BeTC)]) by using a brand new device—gas–solid two-phase flow synthesis equipment. Quantitative conversions occurred to give products at 60 kg h–1 rates. The single-crystal X-ray diffraction validated the precise structure of these MOFs. Also, it should be noted that the reactions were performed under completely solvent-free conditions. In addition, kinetic analysis was carried out to study the reaction mechanisms.

研究领域: 材料科学 · 化学工程
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2021 · IF 6.953

S-nitrosoglutathione functionalized polydopamine nanoparticles incorporated into chitosan/gelatin hydrogel films with NIR-controlled photothermal/NO-releasing therapy for enhanced wound healing

Wenyu Wang,Huan Sheng,Daihong Cao,Fenglian Zhang,Weifen Zhang,Fang Yan,Dejun Ding,Ni Cheng

Nitric oxide (NO) has aroused wide interest in the treating infected wounds due to its characteristic functionalities. However, its utilization is limited due to its volatile properties, high reactivity, direct potential toxicity, and byproducts of NO donors limited its application. Herein, endogenously NO donor S-nitrosoglutathione (GSNO) was connected covalently to polydopamine nanoparticles (PDA-GSNO NPs) to minimize the loss of NO in aqueous medium. Meanwhile, near-infrared (NIR)-controlled NO release and photothermal therapy (PTT) was obtained through the photothermal conversion by PDA. Then chitosan (CS)/gelatin (GE) biocomposite hydrogel films with preferable biocompatibility, surface hydrophilicity, hydroabsorptivity, and mechanical adhesive properties were constructed. By embedding PDA-GSNO NPs into the films, a multifunctional wound dressing was fabricated. Under NIR light irradiation, the combination of PTT, NO-releasing, and CS antibacterial agents can strengthen the in vitro antimicrobial efficacy and in vivo wound healing activities. Meanwhile, the obtained wound dressing presented good biocompatibility. This work outlines an approach for combating bacterial infections and demonstrating the possibility for synergistic NO-releasing wound healing.

研究领域: 生物医学工程 · 材料科学 · 药理学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Novel Co2+ passivated carbon nanodots with up-conversion effects combined with NH2-MIL-125 for improving photocatalytic NO purification and hydrogen evolution

Youzhou He,Shuang Luo,Yuwei Tan,Mingzuo Chen,Haibo Zhou,Jianning Yu,Linjiang Pu,Yumin Huang,Min Fu,Xingyan Liu

Novel ionic state Co passivated carbon nanodots (Co-CDs) combined with NH 2 -MIL-125 as efficient photocatalysts Co-CDs/NH 2 -MIL-125 were fabricated in a convenient process for the first time. These materials exhibited excellent photocatalytic activity in both NO purification and hydrogen production under visible light irradiation. The NO purification rate of Co-CDs/NH 2 -MIL-125 increased to 46.6%, which was 20.2% and 13.4% higher than that of NH 2 -MIL-125 and CDs/NH 2 -MIL-125, respectively. Moreover, the hydrogen production efficiency of Co-CDs/NH 2 -MIL-125 reached 2261 μmol g −1 , which was 6.86 times and 3.54 times of the values for NH 2 -MIL-125 and CDs/NH 2 -MIL-125, respectively. The corresponding properties characterized by Mott-Schottky, UCPL , and in situ DRIFTS , indicated that the introduction of Co 2+ could not only passivate the CDs to further improve physicochemical properties, but also enhance the photocatalytic activity via the photosensitization and up-conversion effect. This research provides a promising strategy that adding active metal ions passivated CDs in the catalyst platform to improve photocatalytic performance.

CAS / MDL: 50-99-7 546-68-9
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ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2021 · IF 9.028

Continuous Chemiluminescence Measurements of Dissolved Nitric Oxide (NO) and Nitrogen Dioxide (NO2) in the Ocean Surface Layer of the East China Sea

Ye Tian,Ke-Ke Wang,Gui-Peng Yang,Pei-Feng Li,Chun-Ying Liu,Riel Carlo O. Ingeniero,Hermann W. Bange

Nitric oxide (NO) is a short-lived intermediate of the oceanic nitrogen cycle, and it is produced by biological and photochemical processes in the ocean. Nitrogen dioxide (NO2) is a reactive atmospheric compound which has not been determined in the ocean so far. Here, we present the setup and validation of a novel continuous underway measurement system to measure dissolved NO and NO2 in the surface ocean. The system consists of a seawater/gas equilibration component coupled to a chemiluminescence detector. It was successfully deployed during a 12 day cruise to the East China Sea in May 2018. Dissolved NO and NO2 surface concentrations ranged from

✓ 已验证 DOI PubMed 高影响因子
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Time-resolved in situ/operando infrared spectroscopy of Cu-supported zeolite X catalyst during NH3–SCR of NO: A modulated excitation study

Jie Yang,Xinyu Li,Yujia Xu,Lin Chen,Shan Wang,Shan Ren,Junjiang Zhu

Zeolite X was used as support of copper catalyst (Cu/X) for selective catalytic reduction (SCR) of nitrogen oxide (NO) with ammonia (NH 3 ). Modulated excitation in situ/ operando infrared (IR) spectroscopy and phase-sensitive detection (PSD) were applied to study the reaction intermediates that formed on the Cu/X during transient experiments. Changing the gas concentration to periodically create unsteady conditions enabled the selective extraction of the dynamic species that were directly involved in the reaction. The IR results showed that only Lewis acid sites (L X ) existed on zeolite X,and Brønsted acid sites (B) and extra Lewis acid sites (L Cu ) were generated after Cu loading. The transient experiment results indicated that the SCR reactions on Cu/X obeys the Eley − Rideal (E − R) mechanism, in which NH 3 is first adsorbed on the L X and L Cu sites (L X –NH 3 , L Cu –NH 3 ) and then moved to the B sites (B–NH 3 ), where it reacted with gas-phase NO to form NH 2 NO intermediate, which finally decomposed into N 2 and H 2 O. Moreover, it is found that the NH 3 adsorbed on L Cu and B sites exhibits stronger reactivity than that on the L X sites.

CAS / MDL: 10031-43-3
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REACTIVE & FUNCTIONAL POLYMERS · 2023 · IF 5.1

Noninterventional target-embolization combined with NO gas therapy for solid tumors by pH-responsive poly(amino acid)s with S-nitrosothiols group

Zhengpeng Chen,Lei Wang,Yuanyuan Jin,Hongyun Guo,Yongdong Zhang,Mingzhong Ma,Xiaobo Wang,Xing Zhou,Ziqiang Lei,Dedai Lu

Gas therapy and embolization are important treatment methods for solid tumors. In order to improve the efficacy of NO therapy and simplify the operation of interventional embolization, we designed and prepared the microacidic-gelled poly[(L-Glutamic acid- ran -L-Tyrosine)- b -L-Threonine- b -L-S-nitrosocysteine]s (PGTTSNCs, obtained by the reaction of tert-butyl nitrite with thiol side groups of poly[(L-Glutamic acid- ran -L-Tyrosine)- b -L-Threonine- b -L-Cysteines]s, PGTTCs.) for noninterventional embolization combined with NO gas therapy for solid tumors. The results of in vivo experiments indicated that PGTTSNCs from PGTTCs-6.4 (the gelled-pH value is 6.4) has significant target-accumulation and therapy effects, and at 10 days post-injection only scars were found at the tumor site. After 20 days, the tumors of model mice were completely disappeared. The method is extremely simple and efficient for solid tumors, which is not only a great innovation of tumors theranostic, but also a qualitative development in nanomaterials .

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Green Energy & Environment · 2019 · IF 0

Novel synthesis of fly-ash-derived Cu-loaded SAPO-34 catalysts and their use in selective catalytic reduction of NO with NH3

Ge Li,Baodong Wang,Qi Sun,Wayne Qiang Xu,Ziran Ma,Hongyan Wang,Daojun Zhang,Jiali Zhou

A combined acid–alkali hydrothermal method was used to prepare fly ash –derived SAPO-34 molecular sieves from a thermal power plant in Inner Mongolia (China). The specific surface area of the prepared fly-ash-derived SAPO-34 molecular sieves was 579 m 2 g −1 , the total pore volume was about 0.27 cm 3 g −1 , and the pore size was 0.56 nm; the molar ratios of Al 2 O 3 :P 2 O 5 :SiO 2 were 1:0.86:0.45. Cu/SAPO-34 catalysts were prepared by impregnation of low-cost fly-ash-derived SAPO-34 molecular sieves as a support and tested in selective catalytic reduction with NH 3 (NH 3 -SCR). Powder X-ray diffraction (XRD), N 2 adsorption–desorption, X-ray photoelectron spectroscopy (XPS), H 2 temperature-programmed reduction (H 2 -TPR), NH 3 temperature-programmed desorption (NH 3 -TPD), electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), X-ray fluorescence analysis (XRF) and scanning electron microscopy (SEM) were used for catalyst characterization and investigation of the relationships between the catalyst structure and the catalytic activity. The actual silica:alumina ratio of the molecular sieves did not increase with increasing Cu loading, indicating that increasing the Cu loading does not change the original structure of the SAPO-34 molecular sieves. The XRF and NMR results showed that replacement by Cu results in more Si islands. The molecular sieve acidity decreased because of the increased number of Si islands. The NH 3 -TPD results showed that for the Cu/SAPO-34 catalysts there was a low correlation between the low-temperature activity and the amount of acidic sites. SCR activity is closely related to the location of Cu. The 4.47Cu/SAPO-34 catalyst has the highest isolated Cu 2+ showed the highest NH 3 -SCR activities (> 90%) at 250–350 °C. This work opens up new avenues for recycling fly ash formed in coal-fired power plants (reducing environmental pollution) and developing low-cost SCR catalysts for NO x pollution control.

CAS / MDL: 77-98-5
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DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY · 2018 · IF 1.883

Formulation optimization and pharmacokinetics evaluation of oral self-microemulsifying drug delivery system for poorly water soluble drug cinacalcet and no food effect

Mengyuan Cao,Xu Xue,Xixi Pei,Yiwen Qian,Lan Liu,Lili Ren,Guoguang Chen

The present research indicated that a new self-microemulsifying drug delivery systems (SMEDDS) were used to reduce the food effect of poorly water-soluble drug cinacalcet and enhance the bioavailability in beagle dogs by oral gavage. Ethyl oleate, OP-10, and PEG-200 was selected as the oil phase, surfactant and co-surfactant of cinacalcet-SMEDDS by the solubility and phase diagram studies. Central Composite Design-Response Surface Methodology was used to determine the ratio of surfactant and co-surfactant, the amount of oil for optimizing the SMEDDS formation. The prepared formulations were further characterized by the droplet size, self-microemulsifying time, zeta potential, polydispersity index (PDI), and robustness to dilution. The in vitro release profile of cinacalcet-SMEDDS was determined in four different release medium and in fasted state and fed state of simulated gastrointestinal fluid. Cinaclcet-SMEDDS were implemented under fed and fasted state in dogs and product REGPARA® was used as a comparison to the prepared formulation in the pharmacokinetics. The result showed the components of SMEDDS, the amount of oil, the ratio of surfactant, and co-surfactant was optimized using solubility, pseudo-ternary phase diagram studies, and response surface methodology. In vitro drug release studies indicated that the cinacalcet-SMEDDS eliminated the effect of pH variability in release medium and variational gastroenteric environments with improved drug release performance. Pharmacokinetic studies revealed that the profiles of cinacalcet-SMEDDS were similar both in the fasted and fed state compared with commercial product, indicating the formulation significantly promoted the absorption, enhanced bioavailability and had no food effect essentially. It is concluded that poorly water-soluble drug cinacalcet was improved in the solubility and bioavailability by using a successful oral dosage form the SMEDDS, and eliminated food effect as well.

CAS / MDL: 9041-29-6
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