Molecular Catalysis
·
2021
·
IF 5.062
Yu Guan,Yinhe Liu,Qiang Lv,Bo Wang
The selective catalytic reduction of nitrogen oxides (NO x ) by carbon monoxide (CO-SCR) is a promising way to deal with exhaust gasses. And Effective redox cycle and NO dissociation ability are crucial factors for catalytic reduction of NO x . Herein, Fe decorated CeO 2 microsphere catalysts with surface oxygen defect were synthesized by solvothermal and calcination method. Among all catalysts, 0.5Fe-CeO 2 sample showed excellent catalytic performance with efficiency near 96% for NO reduction under the condition of 550 ppmv NO, 1200 ppmv CO, and 40,000 h − 1 of GHSV. It was found that Fe doping could efficiently regulate Ce 4+ /Ce 3+ redox couple and oxygen vacancy for catalytic activity. XRD, Raman, XPS, EPR and H 2 -TPR etc. were employed to explore the physicochemical properties of samples. The results showed that Fe had been incorporated into CeO 2 by XRD, and the results of Raman spectrum and XPS indicated that Ce 4+ /Ce 3+ redox couple existed in 0.5Fe-CeO 2 catalyst. Furthermore, the H 2 -TPR spectrum displayed the formation of oxygen vacancy in the samples. N 2 adsorption-desorption isotherms indicated that the doping of Fe could enlarge the specific surface area, pore volume and pore dimeter of the samples, and thus greatly enhanced the NO adsorption and further NO catalytic reduction on catalysts. In addition, other characterization of physicochemical properties and density functional theory (DFT) calculation were performed to reveal the mechanism of NO + CO reaction. As a result, a mechanism was proposed to elucidate highly efficient NO reduction over the catalysts of Fe decorated CeO 2 microspheres. Finally, the synergistic effects of redox center and oxygen vacancy on catalytic activity enhancement were revealed. This work provides a promising way to the design of efficient catalysts for NO reduction.
研究领域:
催化化学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
PROGRESS IN ORGANIC COATINGS
·
2025
·
IF 7.3
Peng Xu,Tianguan Wang,Jingsha Tan,Wenfeng Ge,Huixuan Qian,Yanwei Zeng,Bing Lei,Honglei Guo,Zhiyuan Feng,Guozhe Meng
In this work, a new type of hollow mesoporous CeO 2 microsphere (HMCM), synthesized through a template-free approach, was utilized as both an inhibitor and a nanocontainer for loading the corrosion inhibitor benzotriazole (BTA). These microspheres were encapsulated with a co -deposition layer composed of polydopamine (PDA) and polyethyleneimine (PEI) to construct smart containers (PDA-PEI@HMCM-BTA) with pH-responsive release properties. The corrosion inhibition effect of PDA-PEI@HMCM-BTA nanocontainers was assessed and the release rate of BTA and Ce ions from the nanocontainers was greatly accelerated in the presence of acidic solutions. Electrochemical impedance spectroscopy (EIS) was conducted to evaluate the barrier properties and active anti-corrosion performance of the coatings. The results showed that the integration of nanocontainers within the waterborne epoxy coating significantly improved the corrosion resistance and self-healing capabilities, thereby providing efficient corrosion protection for carbon steels. The method offered a simplified synthesis route for Ce-based nanocontainers and presented a strategy for producing waterborne epoxy coatings with active anticorrosive properties.
研究领域:
材料科学
·
腐蚀与防护
·
纳米技术
✓ 已验证
产品关联
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2020
·
IF 4.551
Yapeng Xiang,Jie He,Na Sun,Yuteng Fan,Liming Yang,Caihong Fang,Long Kuai
The atomically dispersed catalysts have aroused great attention in the recent decade. However, the preparation of atomically dispersed Au catalysts presents more challenge than other atomically dispersed catalysts such as Pt, Pd, etc. From the aspect of support, this work contributes a novel hollow mesoporous CeO 2 microspheres (CeO 2 -hm) for efficient dispersion of single Au atoms (Au 1 ). Contributed by the high specific surface area and mesoporous structure, CeO 2 -hm possesses much higher capacity for undertaking Au 1 , than commercial CeO 2 particles (CeO 2 -c). Typically, with Au loading of 0.2 at%, CeO 2 -hm supported Au (Au 1 /CeO 2 -hm) presents atomic dispersion while CeO 2 -c supported Au (Au/CeO 2 -c) contains large amount of Au nanoparticles . Confirmed by catalyzing the water-gas shift (WGS) reaction, the obtained Au 1 /CeO 2 catalysts exhibit notably higher performance than the Au-based catalysts supported by CeO 2 -c and CeO 2 synthesized through co-precipitation and sol-gel strategies. For example, 0.2 at% Au 1 /CeO 2 -hm exhibits 9.1 times reactivity of equal Au loaded Au/CeO 2 -c catalyst. Besides, the CeO 2 -hm supported single-atom Au catalyst presents good tolerance under long-time WGS running.
研究领域:
催化化学
·
纳米材料科学
·
能源化学
·
表面科学
·
无机功能材料
✓ 已验证
DOI
高影响因子
Journal of Cleaner Production
·
2020
·
IF 7.246
Chengcheng Shi,Dachao Yuan,Luping Ma,Guangsheng Fu,Shufang Wang,Yaguang Li
Sunlight-driven toluene elimination system faces the problems of low reaction rate, secondary pollution, and especially tricky to large-scale production. In this work, we used a PVP assisted spray drying method to synthesize Cu doped CeO 2 microspheres with the merits of zero waste water and solids discharge, kilogram level yield, uniform dispersion of Cu, and high toluene combustion activity. Further, a new photothermal device was constructed to heat catalysts to 295 °C under one standard sunlight irradiation. As a result, the new photothermal device supported Cu doped CeO 2 microspheres showed a full oxidation of toluene at the rate of 59.82 mmol g −1 h −1 under 1 sun irradiation, 150 times higher than the advanced sunlight-driven toluene elimination. An industrial demonstration of this new system was developed, and this system was able to completely deal with 22.2 m 3 h −1 of exhaust with the toluene concentration of 1–10,000 ppm under 1 m 2 of outdoor sunlight irradiation in the daytime of winter, showing the potential on industrial applications.
研究领域:
环境科学
·
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）