Materials
·
2024
·Vol. 17
·期 6
·1440
·
IF 3.1
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.
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高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2021
·
IF 6.953
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.
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高影响因子
Advanced Optical Materials
·
2019
·Vol. 7
·期 10
·1900006
·
IF 7.125
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.
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高影响因子
Catalysis Science & Technology
·
2021
·Vol. 12
·期 3
·737-749
·
IF 6.119
Zhicheng Xu,Yuran Li,Yuting Lin,Bin Wang,Panting Gao,Tingyu Zhu
The reduction of NO by CO was proposed to be applied for regeneration gas to remove NOx from industrial flue gas with activated carbon purification technology. To improve the activity and sulfur resistance for the reduction of NO by CO in regeneration gas, Cu and Fe modifications on activated carbon were investigated. And various samples were characterized by XRD, XPS, TPD, H2-TPR, in situ DRIFTS and DFT calculations to explain the reaction mechanism and poisoning mechanism. The synergistic effects of oxygen-containing functional groups and metal sites show that –COOH acts as an anchor site for metals and that C–O–C acts as a protective site for Fe3+ under a SO2 atmosphere. Cu2+ sites have a high activity at low temperatures due to the large amount of adsorbed NO and the intermediate NOx− participating in the reaction with the NOx− pathway. Fe3+ sites have a high activity at high temperatures due to the high N–O dissociation activity with the *N pathway and –NCO pathway. DFT calculations proved that the binding Cu2+ and Fe3+ sites have higher activity than free Cu2+ and Fe3+ sites. A high content of SO2 exhibits various poisoning effects, mainly including the sulfation of metal sites, deposition of S, and consumption of CO. AC-Fe-H exhibits excellent resistance and stability against SO2 and H2O due to less S deposition caused by consumption through the S–CO reaction, slight sulfation caused by the protective effect of Fe2+ and C–O–C on Fe3+ sites and better hydrophobicity.
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高影响因子
ACS Catalysis
·
2021
·
IF 13.084
Fei Rao,Gangqiang Zhu,Weibin Zhang,Yunhua Xu,Baowei Cao,Xianjin Shi,Jianzhi Gao,Yuhong Huang,Yu Huang,Mirabbos Hojamberdiev
Constructing oxygen vacancies (OVs) in metal-oxide semiconductors is an effective and simple way to enhance the photocatalytic performance via promoting the utilization of solar light and boosting the formation of surface reactive oxygen species (ROS). The presence of different oxygen atoms in the same crystal structure can possibly lead to the formation of different types of OVs with distinct physicochemical and optoelectronic properties. Particularly, the two different crystallographic positions of oxygen atoms in the [BiO]22+ layer of (BiO)2CO3 (BOC) allow the construction of two types of OVs (OVs1 and OVs2). In this work, OVs1-BOC and OVs2-BOC are synthesized via introducing the OVs1 and OVs2 on the surface of the BOC. The influence of OVs1 and OVs2 on the generation of ROS in the BOC is demonstrated based on theoretical and experimental studies by analyzing the separation and redox potentials of photogenerated charge carriers, absorption surface adsorbates (H2O and O2), and reaction active energy. The photocatalytic performance is evaluated by photo-oxidative nitric oxide (NO) removal efficiency under visible light irradiation. The OVs1-BOC and OVs2-BOC exhibit 50.0 and 41.6% photo-oxidative NO removal efficiencies, while generating 15.6 and 16.54 ppb NO2, respectively. The in situ Fourier transform infrared spectroscopy and estimated NO conversion pathway reveal the photo-oxidative NO removal mechanism and suppression of NO2 formation on the surfaces of OVs1-BOC and OVs2-BOC. This work demonstrates a straightforward approach for enhancing the photo-oxidative NO removal via manipulating the OV defect position in semiconductors.
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高影响因子
Horticulturae
·
2026
·Vol. 12
·期 4
·430
·
IF 3.4
Hongli Li,Dandan Huang,Chengkun Li
The storage quality of fresh-cut peach fruit is compromised by weight loss and chromatic aberration. In this experiment, taurine at 30 mg L−1was applied to fresh-cut peaches to evaluate its effect on storage quality. Changes in weight loss, chromatic aberration, antioxidant system, endogenous nitric oxide (NO) metabolism, endogenous hydrogen sulfide (H2S) metabolism, and phenylpropanoid metabolism were studied. The results indicated that 30 mg L−1taurine effectively improved the ability to scavenge ROS, including •OH, O2•−, MDA, and H2O2, by inhibiting the decrease in the activities of SOD and CAT, enhancing POD activity, reducing PPO activity, and maintaining the AsA-GSH cycle. Moreover, taurine treatment increased the activities of 4CL and PAL and retarded the decrease in the activities of SKDH and C4H, thereby improving the accumulation of total phenols, flavonoids, and lignin. These findings showed that taurine mitigated oxidative damage in fresh-cut peaches by enhancing the antioxidant defense system. Exogenous taurine consistently enhanced NOS-like activity while decreasing NR activity in the early storage phase, and elevated the contents of L-Arginine, nitrite, and endogenous NO. Taurine treatment up-regulated the activities of SAT, L-CD, and OAS-TL, thus promoting endogenous H2S content in fresh-cut peaches. Taurine alleviated weight loss and chromatic aberration in fresh-cut peaches during storage by enhancing the antioxidant system and modulating NO, H2S and phenylpropanoid metabolism.
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高影响因子
JOURNAL OF CONTROLLED RELEASE
·
2026
·
IF 11.5
Ying-Tong Ye,Xi Xiao,Hong-Ying Xia,Jie Li,Zhen-Zhen Gong,Ai-Zheng Chen,Shi-Bin Wang,Ranjith Kumar Kankala
Despite the success of various intelligent materials in meeting the multiple needs of diabetic ulcer wounds (DUW) healing, it is often challenging to consider the entire healing process, from early antibacterial and anti-inflammatory effects to late matrix remodeling and angiogenesis characteristics, by releasing multiple active ingredients in stages and on demand. Herein, we designed a versatile bilayer (GCM/Clean-GDA/Cure) hydrogel dressing with light-controlled, spatiotemporal sequential release of MXene nanosheets (MX NSs)/nitric oxide (NO) gas for the healing of methicillin-resistant Staphylococcus aureus (MRSA) biofilm-infected DUWs. Initially, the lower GCM layer comprised carboxymethyl chitosan-gelatin and cerium oxide (CeO 2 )-decorated MX NSs (CO-MX), and the upper GDA layer consisted of dopamine-modified methacrylated gelatin (GelMA-DA) with L-arginine (L-Arg) as a precursor. Under NIR irradiation, the GCM hydrogel releases photothermal-induced CO-MX NSs as self-regenerating antioxidants, exhibiting 98.25 % inhibition against MRSA and 96.37 % inhibition against Pneumonia aeruginosa. The abundant oxygen vacancies and reversible Ce(III)/Ce(IV) redox pairs of the released Ce species from CO-MX NSs could attenuate inflammation and promote early macrophage polarization. The light-assisted gel–sol thermal transition of the lower GCM layer further exposes the upper GDA layer, providing a conducive microenvironment for angiogenesis and tissue remodeling. L-Arg in the GDA layer could enable light-controlled in situ release of NO gas activated by elevated reactive oxygen species (ROS), reaching 7.71 μM within 10 min of exposure to NIR light. Thus, the NIR-assisted bilayer treatment group achieved a 97.74 % wound closure rate. Finally, the transcriptomic analysis validated the activation of regenerative pathways and suppression of excessive inflammatory and metabolic stress signals. Together, the photo-controlled sequential release of MX NSs and NO gas from the bilayer could expand the application of light-responsive nanomaterials, providing an innovative therapeutic modality for in situ treatment of diabetic wounds infected by highly drug-resistant MRSA biofilms.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Youzhou He,Shuang Luo,Xueli Hu,Yaling Cheng,Yumin Huang,Shengming Chen,Min Fu,Yiming Jia,Xingyan Liu
The bifunctional photocatalyst CDs@NH 2 -MIL-125(Ti), carbon nanodots (CDs) encapsulated in NH 2 -MIL-125(Ti), was constructed in situ by a simple and convenient low-temperature calcination approach, which exhibited great capacity in NO removal (at air level) and H 2 evolution simultaneously under visible-light irradiation. The NO removal rate of CDs@NH 2 -MIL-125(Ti) (10 mM) reached 53%, which was 28.4% higher than pristine NH 2 -MIL-125(Ti). Moreover, the H 2 production rate was 5820.95 μmol g −1 , which was 5.34 times higher than that of original NH 2 -MIL-125(Ti). The corresponding optical and electrical performances of CDs@NH 2 -MIL-125(Ti) characterized by UV–Vis, UCPL, ESR, and in situ DRIFTS , etc. indicated that the encapsulated CDs uniformly dispersed in the pores of NH 2 -MIL-125(Ti) could improve the visible light utilization via the up-conversion effect and photosensitization, and serve as an electron-receiver to significantly prolong the lifetime of the photogenerated charge carriers, thus enhancing the photocatalytic performance. The results revealed that fabricating CDs with metal-organic frameworks (MOFs) could be an available strategy for us to boost the photocatalytic NO elimination and H 2 evolution activity simultaneously.
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Molecular Catalysis
·
2023
·
IF 4.6
Jing Li,Suxia Ma,Ke Ren,Nuo Xu
SSZ-13 zeolite was synthesized from fly ash using a combined alkali fusion hydrothermal method. The optimal synthesis parameters are as follows: NaOH/FA=1.4, SiO 2 /Al 2 O 3 =50, H 2 O/SiO 2 =1800, TMAda-OH/Al 2 O 3 =7, the amount of SSZ-13-seed=10%, and crystallization time and temperature were 160 °C and 40 h. Based on this, a series of fly ash-based Fe-SSZ-13 catalysts were prepared using three different methods and tested in catalytic oxidation with H 2 O 2 for NO removal. The experiment results showed that the NO removal efficiency catalyzed by Fe-SSZ-13-SSIE, Fe-SSZ-13-LIE and Fe-SSZ-13-IM were 78%, 87% and 84%, respectively. ESR was used to detect hydroxyl radicals, UV-vis, XPS and H 2 -TPR were applied to test the composition, state and distribution of iron species, while NH 3 -TPD and Py-FTIR were performed to analyze the intensity and type of acidic sites, and finally to determine the relationship between catalyst structure, active species and catalytic performance in combination with NO removal experiments. The catalytic oxidation mechanism analysis revealed that the excellent catalytic performance can be attributed to the dual function of strong Brønsted acidity on the surface and isolated Fe 3+ with high dispersion, which can rapidly decompose H 2 O 2 into ·OH and efficiently achieve NO oxidation. In conclusion, the preparation of fly ash catalysts has great potential for achieving the dual function of waste utilization and pollutant removal.
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高影响因子
Food Science & Nutrition
·
2019
·Vol. 7
·期 3
·949-958
·
IF 1.747
Yaqiong Zhang,Ming Li,Hang Gao,Bo Wang,Xu Tongcheng,Boyan Gao,Liangli (Lucy) Yu
In this study, a new red sorghum variety (Ji Liang No. 1) was investigated for its triacylglycerol (TAG) and fatty acid profiles, carotenoid and tocopherol compositions, total phenolic, total flavonoid and phenolic acid contents, and antioxidant and anti-inflammatory properties. A total of 17 TAGs were identified in the red sorghum oil. Linoleic and oleic acids were the primary fatty acids, contributing more than 80% of the total fatty acids. β-Carotene was the primary carotenoid at a level of 26.14 μg/g. α-, γ-, and δ-tocopherols were at levels of 0.19, 4.08, and 0.10 μg/g, respectively. Moreover, acetone–water (60:40, v/v) extract of the red sorghum exhibited the greatest total phenolic content of 2.77 mg GAE/g and total flavonoid content of 5.44 mg RE/g. The extract had scavenging capacities against DPPH, ABTS + , and peroxyl radicals and suppressed LPS stimulated IL-1β, IL-6, and COX-2 mRNA expressions in a dose-dependent manner. Ferulic, p -coumaric, isoferulic, and p -hydroxybenzoic acids were found in the red sorghum, with ferulic acid as the predominant phenolic acid and mostly in an insoluble bound form. These data indicated a potential utilization of the red sorghum in health-promoting functional food or supplemental products.
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高影响因子
APPLIED CATALYSIS A-GENERAL
·
2018
·
IF 4.521
Xiaoqiang Wang,Yue Liu,Qingji Ying,Weiyuan Yao,Zhongbiao Wu
In this paper, a series of Nb modified Cu-Ce-Ti mixed oxides (Nb y CCT) were synthesized using wetness impregnation method for the selective catalytic reduction of NO with ammonia (NH 3 -SCR). The activity tests indicated that Nb y CCT catalysts had shown superior SCR performances. Among which, Nb 0.05 CCT catalyst exhibited a NO conversion of more than 90% within a broad operation temperature window (180–360 °C) under the GHSV of 40,000 h −1 . After that, corresponding characterizations were performed to correlate the physical structures and surface properties to catalytic performances. These results revealed that the strong interactions among the active phases induced by Nb addition could not only enhance the redox property of the catalysts but also inhibit the over-oxidation of NH 3 , which would be beneficial to SCR performance within a wide temperature range and good reaction selectivity. Furthermore, DRIFTS results suggested that the doping of Nb could promote the formation of NO 2 , thereby enhancing the “fast” SCR reaction process (Langmuir-Hinshelwood reaction pathway). Moreover, the Nb 0.05 CCT catalyst showed a better sulfur tolerance compared to Nb free catalyst that over 85% NO conversion could be retained after 12 h SCR reaction in the presence of SO 2 and H 2 O.
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Molecular Catalysis
·
2018
·
IF 0
Sher Ali,Yushi Li,Tianrui Zhang,Syed ul Hasnain Bakhtiar,Xuesong Leng,Zhibin Li,Fulong Yuan,Xiaoyu Niu,Yujun Zhu
Citric acid method was employed to prepare a series of Nb-promoted Fe x -Nb 0 . 5- x -Ce 0.5 ( x = 0.45, 0.4, 0.35) oxides for selective catalytic reduction with NH 3 (NH 3 -SCR) of NO process. The structure, redox ability and reactivity of NH 3 and absorbed NO species on the catalysts were explored by using various characterization techniques such as X-ray diffraction (XRD), temperature program reduction with H 2 (H 2 -TPR), temperature program desorption of NH 3 (NH 3 -TPD), temperature program desorption of NO (NO-TPD), X-ray photoelectron spectroscopy (XPS) and in situ diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS). It was found that the Nb promoted Fe x -Nb 0 . 5- x -Ce 0.5 ( x = 0.45, 0.4, 0.35) oxides catalysts showed outstanding NH 3 -SCR of NO activity, excellent N 2 selectivity and remarkable SO 2 /H 2 O resistance, meanwhile, Fe 0.4 -Nb 0.1 -Ce 0.5 exhibited above 90% NO conversion in the range of 180–400 °C, together with near 100% N 2 selectivity. The characterization results point out that the excellent catalytic performance of Fe 0.4 -Nb 0.1 -Ce 0.5 can be ascribed to the strong interaction among Nb, Fe and Ce oxides. The strong interaction not only increases the BET surface area and redox ability of the catalyst, but also significantly improves the acid amount leading to the enhancement of the adsorption and activation of NH 3 , which is advantage of the reactivity of adsorbed nitrate together with the adsorbed NH 3 species.
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