Advanced Healthcare Materials
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2022
·Vol. 11
·期 19
·2201323
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IF 11.092
Shuang Xie,Kun Huang,Jiawen Peng,Yuan Liu,Wenxiong Cao,Dandan Zhang,Xiaohong Li
Diabetic foot ulcer (DFU) treatment is challenged by persistent bacterial infection and hyperglycemia-caused vascular dysplasia. Herein, self-propelled nanomotors are designed to achieve biofilm microenvironment (BME)-activated multistage release of NO for effective sterilization and subsequent angiogenesis promotion. CaO 2 nanoparticles (NPs) are capped with PDA layers, followed by complexation with Fe 2+ and surface grafting of cysteine-NO to obtain Janus Ca@PDA Fe -CNO NPs. In response to low pH in BME, the decomposition of CaO 2 cores generates O 2 from one side of Janus NPs to propel biofilm penetration, and the released H 2 O 2 and Fe 2+ produce •OH through Fenton reaction. The concurrent glutathione-triggered release of NO can be converted into reactive nitrogen species, which exhibit significantly higher bactericidal efficacy than those with only generation of •OH or NO. The slow release of NO for an extended time period promotes endothelial cell proliferation and migration. On Staphylococcus aureus -infected skin wounds of diabetic mice, NP treatment eliminates bacterial infections and significantly elevates blood vessel densities, leading to full wound recovery and regeneration of arranged collagen fibers and skin accessories. Thus, the self-propelling and multistage release of NO provide a feasible strategy to combat biofilm infection without using any antibiotics and accelerate angiogenesis and wound healing for DFU treatment.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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2022
·
IF 6.76
Hongyu Zhang,Ling Chen,Baogang Xu,Ping Yang
The strong band-to-band visible light absorption obtained by changing the bandgap of photocatalysts is desirable but challenging for TiO 2 . In this paper, a mechanochemical pre-reaction and subsequent heat-treatment process were used to create TiO 2 /g-C 3 N 4 heterojunctions. Acid-treated H 2 Ti 3 O 7 nanobelts and superior thin g-C 3 N 4 nanosheets (CN) were ground evenly and further heat-treated to grow rhombic TiO 2 in situ on the nanosheets. The heterojunctions exhibited a band gap with the absorption in visible light region. Heterojunction formation effective tunes the surface and electronic structures of the composite, resulting in significant decrease of bandgap. g-C 3 N 4 -based heterojunctions (5TCN) exhibited excellent H 2 generation (4991 μmol/g/h) and NO removal. In contrast, a TiO 2 -based composite (95TCN) revealed efficient photo reduction of Cr(Ⅵ) which was 2 times of that of TiO 2 sample and 22 times of that of CN. The photochemical reaction mechanism of TiO 2 and g-C 3 N 4 -based composites was discussed with the ratio of TiO 2 and g-C 3 N 4 . The excellent performance is ascribed to single crystal rhombic TiO 2 nanoparticles grown in situ on g-C 3 N 4 to form well-developed heterojunctions which accelerate the carrier transfer. These results inspire the electronic structure engineering of photocatalysts to improve visible light absorption and provide a magic strategy for excellent photochemical activities.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Kean Chen,Binxian Chu,Qiuju Qin,Xuemei Ou,Runqi Zhao,Xiaoling Wei,Huan Wu,Bin Li,Lihui Dong
As an ideal substitute for the precious metals in the selective catalytic reduction of NO by CO, transition metal oxides perform very well. Thus, a series of CuO - Co 3 O 4 symbiotic oxide porous nanosheet catalysts are prepared with a CTAB-assisted hydrothermal method. Cu5 with the ratio of Cu and Co is 5 : 10, has the best activity on the premise of maintaining the nanosheet structure. Reduction pretreatment of Cu5 with H 2 is carried out, and the surface will be rapidly oxidized in air. In this period, Cu, CuO and Co 3 O 4 were produced and coexisted on surface. Cu5-re-163 exhibits greatly higher N 2 selectivity but a little inferior NO conversion. Further DFT calculation and characterizations proved that [N] free radicals exist during the reaction. The reaction on Cu5 and Cu-re-163 follow L-H and E-R mechanism respectively. [N] radicals on the latter are much easier to desorb, so that they are easy to combine with each other to form N 2 rather than with NO to generate N 2 O, as the reason why Cu5-re-163 has better selectivity.
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Green Energy & Environment
·
2022
·
IF 12.781
Yanqin Li,Junqi Tian,Zhisong Liu,Zhongqi Liu,Dong Dong,Fu Wang,Wei Wang,Minmin Liu,Jianming Dan,Yongsheng Li,Feng Yu,Bin Dai,Yunbo Yu
Photo-assisted SCR (PSCR) offers a potential solution for removal of NO at room temperature. MnTiO x as PSCR catalyst exhibits superior performance with NO removal of 100% at the room temperature. Electron paramagnetic resonance (EPR) analysis revealed the presence of numerous oxygen vacancies on MnTiO x . Optical carrier density functional theory (DFT) calculations showed that the three-dimensional orbital hybridization of Mn and Ti is significantly enhanced under light irradiation. The MnTiO x catalyst exhibited excellent electron–hole separation ability, which can adsorbe NH 3 and dissociate to form NH 2 fragments and H atoms. In-situ diffuse reflectance infrared fourier-transform spectroscopy (DRIFTS) indicated that the optical carrier enhanced NH 3 adsorption on MnTiO x , which makes it possess excellent PSCR activity. This work provided an additional strategy to NO removal with PSCR catalysts and showed potential for use in photocatalysis.
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JOURNAL OF HAZARDOUS MATERIALS
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2023
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IF 13.6
Yin Tang,Wen Cui,Songxia Wang,Fan Dong
Though photocatalytic purification of NO has been widely studied, how to avoid secondary pollution during gas-solid reaction is still a challenge, especially in inhibiting the formation of toxic intermediates (NO 2 ) and avoiding the blow away of powdery photocatalyst. Herein, we proposed a one-step solvothermal method to prepare melamine sponge (MS) supported and functionalized g-C 3 N 4 (CN), which simultaneously realizes the inhibition of NO 2 formation and catalyst loss. Sodium hydroxide , which plays a dual role, has been introduced during the preparation of supported photocatalyst. Specifically, sodium atom, as the modifier of performance, could facilitate the randomly distributed charge of pristine CN to be converged, which accelerates the adsorption/activation of reactants for efficient and deep NO oxidation . Hydroxyl group, as the binder between CN and MS, induces the interaction by forming hydrogen bonds , which contributes to the firm immobilization of powdery photocatalyst. The supported sample exhibits outstanding NO removal rate (58.90%) and extremely low NO 2 generation rate (1.41%), and the mass loss rate of photocatalyst before and after reaction is less than 1%. The promotion mechanism of performance also has been elaborated. This work takes environmental risks as a prerequisite to propose a feasible strategy for perfecting the practical application of photocatalytic technology .
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
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2021
·
IF 8.067
Wenyu Wang,Dejun Ding,Kunpeng Zhou,Man Zhang,Weifen Zhang,Fang Yan,Ni Cheng
Nitric oxide (NO) has emerged as a potential wound therapeutic agent due to its pivotal role in the wound healing processes. Nevertheless, NO-based therapy for clinical applications is still restricted due to its gaseous state and short half-life. Here we exploited a wound dressing by incorporating sodium nitroprusside doped prussian blue nanoparticals and Type I collagen into the chitosan/poly(vinyl alcohol) nanofibers through the electrospinning method. This hybrid nanofibrous scaffold possess the excellent abilities of NIR controlled NO release, photothermal therapy, and imitation of extra-cellular matrix-like architecture. These synergistic effects could enhance their anti-bactericidal effects in vitro and furthermore accelerate wound healing in vivo when compared to control groups. Histological analysis demonstrated the scaffold could promote fibroblast growth and accelerate epithelialization. Moreover, no apparent histological toxicology and negligible damage to major organs were observed, which provided sufficient biosafety for in vivo application. These data indicate the fabricated hybrid nanofibrous scaffold could be used as an ideal candidate for accelerating wound healing and treating chronic wounds.
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CHEMICAL ENGINEERING JOURNAL
·
2020
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IF 10.652
Benjun Huo,Jie Yang,Yao Bian,Daofu Wu,Julin Feng,Jiaer Zhou,Qiang Huang,Fan Dong,Xiaosheng Tang
The superior optical properties and adjustable bandgap allows for hybrid halide perovskite quantum dots to be promising photocatalytic materials, but the serious radiative recombination and instability inhibit the improvement of photocatalytic conversion efficiency. Herein, we successfully synthesized the FAPbBr 3 /A-SiO 2 nanocomposites photocatalyst by anchoring formamidinium (FA + , HC(NH 2 ) 2+ ) lead halide perovskite quantum dots on aminated silica spheres to construct the composite photocatalysts via N H chemical bonding. The FAPbBr 3 /A-SiO 2 composites show the significantly enhanced visible-light-driven NO removal activity (70%) compared to the pristine FAPbBr 3 (30%) in half an hour at room temperature, revealing that the increased active sites and efficient charge carrier separation contribute to the absorption and activation of reactant molecules. This work would open the new possibilities for improving the photocatalytic ability of perovskite quantum dots.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2020
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IF 16.683
Xiaoshu Lv,Jingyuan Zhang,Xingan Dong,Jian Pan,Wendong Zhang,Weilu Wang,Guangming Jiang,Fan Dong
We demonstrated the partial Ni 2+ substitution for Mg 2+ in Mg 2 Al-layered double hydroxide nanosheet (Ni/LDH) significantly improved its photocatalytic performance in removing the ppb-level NO pollutant from air. With 25 % of Mg 2+ substituted, the Ni/LDH delivered the highest NO removal efficiency of 42.10 % (87.2 % of them were mineralized to nitrate) under UV-light irradiation. Such a robust performance with the low energy input (8 W) made Ni/LDH among the top photocatalysts for NO removal. We evidenced the OH − carried by Ni/LDH transformed to · OH radicals by trapping the photoexcited holes. This unique feature was intriguing as the OH − at layer surfaces of LDH were abundant, fully exposed and dynamically supplemented by atmospheric water, which endowed Ni/LDH with superior · OH production capability even under low atmospheric moistures. The positive contribution of Ni 2+ arose from its function in optimizing band structure and activating the OH − of LDH, leading to enhanced reactive oxidative species production.
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JOURNAL OF HAZARDOUS MATERIALS
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2020
·
IF 9.038
Hongyuan Xi,Song Zhou,Jinxi Zhou,Zhao Zhang
The novel combined system using Na 2 S 2 O 8 /urea was used to simultaneously absorb nitric oxide and sulfur dioxide emissions from marine diesel engines as well as inhibit the formation of nitrate in cleaning wastewater to meet the increasingly stringent requirements of regulations. The influences of reaction temperature, Na 2 S 2 O 8 concentration, urea concentration, SO 2 concentration, NO concentration and pH value on SO 2 removal efficiency, NO removal efficiency and nitrate concentration were investigated. The experimental results showed that different reaction temperatures had different influences on SO 2 removal efficiency, NO removal efficiency and nitrate concentration. An increase in Na 2 S 2 O 8 could improve the absorption of NO. The addition of urea could effectively improve the removal efficiency of NO and reduce the nitrate concentration. The removal efficiencies of 1000 ppm NO and 1000 ppm SO 2 achieved 100 % with 0.2 mol/L Na 2 S 2 O 8 and 2 mol/L urea at 70℃, and the nitrate content was 8.56 mg/L which was far lower than the regulatory requirement of 60 mg/L. The acidic condition (pH ≤ 5.5) not only facilitated the absorption of NO but also reduced the generation of nitrate. According to the experimental results, the novel combined system was promising to be applied to the control technology of marine diesel engine exhaust.
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JOURNAL OF HAZARDOUS MATERIALS
·
2020
·
IF 9.038
Fanyu Meng,Lina Guo,Haocheng Zou,Boming Zhu,Fayang Zhou,Yiqing Zeng,Jiayou Han,Jun Yang,Shule Zhang,Qin Zhong
To achieve high NO oxidation efficiency, excessive O 3 must be used, which would lead to the high cost and escape of ozone. Herein, we adopted low cost and environmental-friendly TiO 2 as the catalyst of low concentration O 3 and H 2 O 2 system for high-efficiency NO x oxidation. The Ti sites on TiO 2 were the deprotonation sites of H 2 O 2 and H 2 O into Ti-OOH and Ti-OH species, respectively. We found that the surface of rutile phase TiO 2 had a low concentration Ti-OOH component but a large amount of Ti-OH after contacting with H 2 O 2 solution, thus lots of ·OH and a few O 2 − radicals formed with introducing O 3 molecules. H 2 O 2 solution induced the formation of a large amount of Ti-OOH and Ti-OH species on the anatase phase TiO 2 surface, thus lots of O 2 − generated in the O 3 /H 2 O 2 system. O 2 − and O H radicals could efficiently oxidize NO, in which O 2 − radicals could oxidize NO to NO 3 − in one step with high selectively. Therefore, anatase TiO 2 had better performance in NO x oxidation than rutile phase TiO 2 . The effect of temperature and SO 2 concentration on NO oxidation was also investigated, the results showed that TiO 2 -A/O 3 /H 2 O 2 system promoted NO oxidation at a low temperature and a low concentration of SO 2 .
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
·
IF 7.489
Runping Wu,Qing Ye,Kai Wu,Shuiyuan Cheng,Tianfang Kang,Hongxing Dai
The alkali metal (M = Na, K, Rb, and Cs)-modified C-FDU-15 (M-C-FDU-15( x ); x was the M/C-FDU-15 M ratio, and equal to 0.01–0.03) samples were prepared through an in situ process, and characterized by means of the TG, XRD, TEM, EDS, N 2 adsorption–desorption, O 2 -TPD, and CO 2 -TPD techniques. The (NO + O 2 ) adsorption mechanism was investigated using the (NO + O 2 )-TPD and DRIFTS techniques. The results show that the sequence of (NO + O 2 ) adsorption performance was Na-C-FDU-15(0.01) (104.1 mg/g) > K-C-FDU-15(0.01) (92.4 mg/g) > C-FDU-15 (76.2 mg/g) > Rb-C-FDU-15(0.01) (65.1 mg/g) > Cs-C-FDU-15(0.01) (62.3 mg/g). The alkali metal was uniformly distributed in C-FDU-15 and its doping enhanced the amount of the basic sites in the sample. Moreover, the optimal Na/C-FDU-15 M ratio was 0.02. (NO + O 2 ) were chemically adsorbed mainly in the forms of nitrite (NO 2 − ) and nitrate (NO 3 − ) on M-C-FDU-15( x ). A more amount of NO was converted to nitrate than to nitrite. There were three key factors of enhancing the (NO + O 2 ) adsorption capacity of C-FDU-15 due to alkali metal doping: the first factor was the increasing of surface area and pore volume of the sample, the second one was the enhancement in amount of the active sites in the sample, and the third one was the smaller alkali metal ionic radius in the sample.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2020
·
IF 3.573
Meijuan Chen,Xiaoyan Wei,Liaoliao Zhao,Yu Huang,Shun-cheng Lee,Wingkei Ho,Kehao Chen
Highly efficient and stable photocatalysts were synthesized at room temperature by modifying MIL-125(Ti) with N-doped carbon quantum dots (N/CM(Ti)). The N/CM(Ti) with 2.5 vol % N doped carbon quantum dots (N/CQDs) had the best light absorption and visible-light photocatalytic nitrogen oxide (NO) removal efficiency (approximately 49%). It was found through X-ray photoelectron spectroscopy analysis that a N–Ti–O bond was formed in the 2.5 vol % N/CM(Ti), which is more conducive to charge transfer. Photocurrent and electrochemical impedance data also showed that the carrier separation efficiency of 2.5 vol % N/CM(Ti) was significantly superior to that of MIL-125(Ti). In addition, the TiIII–TiIV of MIL-125(Ti) acts as the active center for photocatalytic removal of NO. Two possible electron migration paths were proposed: electron transfer from N/CQDs to TiIII–TiIV center of MIL-125(Ti) due to the photoinduced electron transfer property of N/CQDs, and absorption of UV light generated from the N/CQDs by the terephthalic acid ligand followed by electron transfer to metal active sites for photocatalytic removal of NO.
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