JOURNAL OF HAZARDOUS MATERIALS
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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 .
研究领域:
环境科学
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催化化学
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DOI
PubMed
高影响因子
CANADIAN JOURNAL OF CHEMICAL ENGINEERING
·
2017
·Vol. 96
·期 1
·27-32
·
IF 1.356
Haiqian Zhao,Xingcun Gao,Chenghao Liu,Zhonghua Wang,Hanbing Qi
Basic rules of NO oxidation by a Fe 2+ /H 2 O 2 /AA directional decomposition system were researched based on the technical background of flue gas NO x removal. Effects of gas-liquid interfacial area, main gas, and solution parameters on NO oxidation efficiency ( η ) were analyzed. The results showed that adequate contact area was the precondition for high η by a Fe 2+ /H 2 O 2 /AA system. η decreased with the increase in NO concentration, which illustrated that this method would be efficient in oxidizing NO at a low concentration. η tended to decrease linearly with the growth in gas flow, however, the NO oxidation rate ( v ) rose with the increase in NO concentration and gas flow. η increased with the initial concentrations of H 2 O 2 and Fe 2+ , but the amplitude decreased. Controlling the initial concentrations of H 2 O 2 and Fe 2+ to achieve reasonable synergies between generation rate and consumption rate of ·OH could weaken the invalid consumption of reactants. η increased with the increase in temperature in the range 30–60 °C, but it nearly did not change with temperature after 60 °C. This oxidation technology and the traditional wet flue gas desulphurization technology exhibited temperature synergy. Under typical pH of wet desulphurization, η and H 2 O 2 consumption rate did not change obviously.
研究领域:
环境科学
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化学工程
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DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2022
·
IF 14.224
Yanshan Wan,Jibiao Li,Jiupai Ni,Chong Wang,Chengsheng Ni,Hong Chen
Photocatalysis is believed to be an important way of reducing NO pollutant in air and the facet engineering of semiconducting oxides could enhance the efficiency of the photocatalysis. ZnO nanoparticles with different exposed crystalline facets were successfully synthesized using a hydrothermal method and their photocatalytic degradation towards NO was investigated. The crystals from ZnCl 2 precursor were hexagonal mesoporous ones with exposed (0002) facet, while those from zinc acetate were in the form of flakes or wheat ears with enhanced exposure of (10 1 ( − ) 1) facet. Calcination in air imparted an enhanced the textural coefficient of the orientated facets as well as the oxygen defects. The nanocrystals with enhanced (0002) facet and lower flat-band energy did better in photoelectrochemical water-oxidation than those with exposed (10 1 ( − ) 1) facet that showed superior photocatalytic activity (approaching 76.7 ± 0.6% under 365 nm photons) for NO oxidation. According to theoretical calculations, (10 1 ( − ) 1) facet with O termination showed much higher affinity to NO molecules than other configurations, and the oxygen vacancy in ZnO played an minor role in the photocatalytic oxidation of NO. A high quantum efficiency approaching 97.5 ± 1.4% under 275 nm photons was obtained for the ZnO crystals from zinc acetate with mixed (0002) and (10 1 ( − ) 1) facets. This research explores the special characteristics of ZnO with different exposed facets and is important for the future design of highly efficient photocatalyst for hazardous material removal.
研究领域:
材料科学
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环境科学
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DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 19
·56188-56197
·
IF 5.8
Chen Jingwen,Wu Menglin,Ni Jiupai,Ni Chengsheng
Photocatalysis using the visible light of the sun is an environmentally friendly method of eliminating the NOx pollutant from the ambient air. Although Cs 3 Bi 2 Br 9 , a semiconductor with a band gap of 2.54 eV, may be a strong absorber of visible light, its photocatalysis towards the abatement of NOx is unknown. In this study, Cs 3 Bi 2-x Pb x Br 9-x (0 ≤ x ≤ 0.0789) are used for the photocatalytic oxidation of NOx. A significant NO oxidation efficiency (80%) is observed over Cs 3 Bi 2-x Pb x Br 9-x (x = 0.0443) under visible light, which is attributable to the Br vacancy ( V Br ) brought about by Pb 2+ doping. The presence of V Br increased the ionic selectivity of in the oxidized NO. At higher Pb doping level, two HONOs adsorbed on the V Br , linked, and then reduced by hot electrons to produce N 2 O 2 2− . The di-azo coupling could passivate the activation of NO on the V Br . This work advances the defect engineering of halide for the photo-driving solid–gas reaction in air.
研究领域:
材料科学
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环境科学
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DOI
PubMed
高影响因子
Catalysts
·
2019
·Vol. 9
·期 6
·519
·
IF 3.444
Jiaming Shao,Fawei Lin,Yan Li,Hairong Tang,Zhihua Wang,Peixi Liu,Guanyi Chen
NO oxidation was conducted over MnOx-CeO2catalysts, which were synthesized by the co-precipitation method. The calcination temperature and third metal doping were the main considerations. MnCe catalysts calcined at 350 °C and 450 °C attained the highest NO conversion efficiency, compared to 550 °C. XRD results suggested that the higher the calcination temperature, the higher the crystallization degree, which led to a negative effect on catalytic activity. Subsequently, Sn, Fe, Co, Cr, and Cu were separately doped into MnCe composites, but no improvement was observed for these trimetallic catalysts in NO conversion. Nevertheless, MnCeSn, MnCeFe, and MnCeCo still exhibited a desirable NO conversion efficiency, so they were tested under SO2addition together with MnCe catalyst. Among them, MnCeFe exhibited the highest NO conversion after whole poisoning testing. XPS results indicated that Fe could protect Mn and Ce metal oxides from being reduced during SO2poisoning process. Furthermore, in in-situ DRIFTS measurement, part of nitrate species maintained undestroyed on the MnCeFe catalyst surface after SO2poisoning. These characteristics reinforced that Fe dropping would achieve better performance under SO2atmosphere.Keywords:MnOx-CeO2;co-precipitation;NO oxidation;SO2resistance;metal addition
研究领域:
环境科学
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催化化学
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DOI
高影响因子
Heliyon
·
2024
·
IF 3.4
Yige Guo,Xiaoxue Niu,Huaiyu Yang,Liwen Chen,Yizhen Ren,Huining Guo,Bo Wu
The oxidation rate of NO to NO 2 is a critical parameter in the removal of NO x within selective catalytic reduction (SCR) systems. LaCoO 3-δ is a kind of potential catalyst to enhance the oxidation of NO to NO 2 , it may offers an economic and stable alternative to noble metal catalysts, particularly at elevated temperatures. This study aimed to enhance the catalytic efficiency of LaCoO 3-δ through strontium (Sr) doping. La 1-x Sr x CoO 3-δ (with varying x values of 0.1, 0.2, 0.3, 0.4) was synthesized using a sol-gel method. La 1-x Sr x CoO 3-δ exhibited superior NO oxidation catalytic activity compared to LaCoO 3-δ , with the most notable enhancement observed at x = 0.3 (84 % conversion). This improvement can be attributed to the substitution of La 3+ with Sr 2+ , which induces lattice distortion and charge imbalance, thereby creating more oxygen vacancies that enhance the catalytic oxidation capability of La 1-x Sr x CoO 3-δ . However, it's important to note that an excessive amount of Sr can result in the formation of SrCO 3 deposits on the surface of La 1-x Sr x CoO 3-δ , thereby diminishing its catalytic oxidation performance. The catalytic oxidation reaction behavior adhered most closely to the O 2 -adsorbed E-R model, the surface defects in La 1-x Sr x CoO 3-δ playing a pivotal role in the catalytic reaction.
研究领域:
化学
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环境科学
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材料科学
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DOI
PubMed
高影响因子
CATALYSIS LETTERS
·
2020
·Vol. 151
·期 6
·1755-1765
·
IF 2.482
Meng Fanyu,Zhang Mingjia,Zhou Fayang,Zou Haocheng,Zhu Boming,Zeng Yiqing,Zhang Shule,Zhong Qin
Abstract CrO x /black-TiO 2 catalysts were prepared by ligand-assisted (citric acid, oxalic acid and ethylenediaminetetraacetic acid) impregnation method. These catalysts were characterized in detail by means of X-ray diffraction, Raman, BET, X-ray photoelectron spectroscopy, H 2 and O 2 (NO) temperature programmed reduction or desorption and in-suit DFTIR spectra. The results indicated that ligands assistance was beneficial for CrO x interacted with oxygen vacancies and O–Ti–O structures. Among all the catalysts, CrO x /black-TiO 2 /CA (modified by citric acid) revealed excellent catalytic activity and stability for NO oxidation in the temperature range of 200–450 °C. The characterization results exhibited that the interaction existed between CrO x and oxygen vacancies resulting in more Cr 6+ . Moreover, the strong interaction between CrO x and O–Ti–O was attributed to the modification of carboxylic acid, which increased the content of Cr 3+ and chemical adsorption oxygen. High content of chemical adsorption oxygen promoted the adsorption ability of O 2 , and Cr 6+ enhanced the adsorption capacity of NO. Hence, chemical adsorption oxygen and Cr 6+ synergistically promoted the NO oxidation. Graphic Abstract
研究领域:
催化材料科学
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环境化学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2015
·
IF 4.321
Shifa Zhong,Yuanyuan Sun,Hongchuan Xin,Chunpeng Yang,Lei Chen,Xuebing Li
LaNi 1 − x Co x O 3 ( x = 0, 0.1, 0.3, 0.7, 1.0) perovskite catalysts were prepared by co-precipitation method and investigated in the catalytic oxidation of NO. LaNi 0.7 Co 0.3 O 3 showed the best catalytic activity among all the samples, confirming the potential of LaNi 0.7 Co 0.3 O 3 as a cheap and efficient NO oxidation catalyst. The high reactivity of LaNi 0.7 Co 0.3 O 3 was mainly due to the moderate amount of adsorbed NO and O 2 and their moderate adsorption strength on the surface of the catalyst, as determined by the XRD, H 2 -TPR, NO-TPD, O 2 -TPD and XPS studies.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2025
·
IF 9.7
Zixun Fang,Yao Zhou,Yang Yang,Yidong Hou,Can Yang,Jinshui Zhang
Artificial Z-scheme photocatalytic systems, inspired by natural photosynthesis, have been widely employed for pollutant removal. In this study, we fabricated a ternary Z-scheme Bi 2 O 3 /Bi/porous carbon nitride (PCN) heterojunction with an intimately coupled interface through a simple EG-assisted solvothermal approach to improving photocatalytic performance of NO oxidation. The in-situ generated metallic Bi acts as an electron mediator, effectively accelerating the separation and transfer of photoexcited carriers. The unique Z-scheme charge transfer mechanism provides the strong redox abilities and isolates the active sites for specific reactions, thus promoting photocatalytic NO oxidation activity. As a result, the optimized Bi 2 O 3 /Bi/PCN sample achieved a NO removal efficiency of 94.6%, outperforming single-component catalysts and most previously reported heterojunction-based photocatalysts. Additionally, in-situ Fourier transform infrared spectroscopy was employed to propose the NO removal mechanism, offering valuable insight into the conversion pathway. Such a heterogeneous Z-scheme photocatalytic system with a strong redox ability, high charge-separation efficiency, and long-term stability, demonstrates significantly enhanced photoactivity for pollutant removal and is expected to attract increasing interest for other photocatalytic applications.
研究领域:
环境科学
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材料科学
·
光催化技术
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产品关联
DOI
PubMed
高影响因子
PLoS One
·
2018
·Vol. 13
·期 4
·e0192324
·
IF 2.766
Hai-qian Zhao,Zhong-hua Wang,Xing-cun Gao,Cheng-hao Liu,Han-bing Qi
H 2 O 2 was adopted to oxidize NO in simulated flue gas at 100–500°C. The effects of the H 2 O 2 evaporation conditions, gas temperature, initial NO concentration, H 2 O 2 concentration, and H 2 O 2 :NO molar ratio on the oxidation efficiency of NO were investigated. The reason for the narrow NO oxidation temperature range near 500°C was determined. The NO oxidation products were analyzed. The removal of NO x using NaOH solution at a moderate oxidation ratio was studied. It was proven that rapid evaporation of the H 2 O 2 solution was critical to increase the NO oxidation efficiency and broaden the oxidation temperature range. the NO oxidation efficiency was above 50% at 300–500°C by contacting the outlet of the syringe needle and the stainless-steel gas pipe together to spread H 2 O 2 solution into a thin film on the surface of the stainless-steel gas pipe, which greatly accelerated the evaporation of H 2 O 2 . The NO oxidation efficiency and the NO oxidation rate increased with increasing initial NO concentration. This method was more effective for the oxidation of NO at high concentrations. H 2 O 2 solution with a concentration higher than 15% was more efficient in oxidizing NO. High temperatures decreased the influence of the H 2 O 2 concentration on the NO oxidation efficiency. The oxidation efficiency of NO increased with an increase in the H 2 O 2 :NO molar ratio, but the ratio of H 2 O 2 to oxidized NO decreased. Over 80% of the NO oxidation product was NO 2 , which indicated that the oxidation ratio of NO did not need to be very high. An 86.7% NO removal efficiency was obtained at an oxidation ratio of only 53.8% when combined with alkali absorption.
研究领域:
环境科学
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化学工程
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产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Tianjiao Wu,Bibo Ma,Huanhuan Bai,Lin Wang,Yumei Zhang,Qingzhi Luo,Jing An,Huiying Mu,Desong Wang,Yandong Duan
Developing highly efficient photocatalysts that selectively convert NO pollutants to NO 3 ¯ while storing metabolic nitrogen for crops remains a great challenge. Simultaneously, there is a dearth of research investigating the relationship between the chemical environment and the activity of catalytic sites. Herein, an efficient impregnation approach to access atomically dispersed Sr single atoms supported on Nb 2 O 5 is reported; meanwhile, various ligands (-Cl, -Br, -OH) are employed to customize the local structure. The results show that Cl-Sr/Nb 2 O 5 exhibits excellent catalytic performance in eliminating NO, which is significantly superior to other catalysts. The introduction of Sr atom and ligand increases the energy barrier of NO 2 formation, thus improving the selectivity of converting NO to NO 3 ¯. This study highlights the importance of precisely designing the catalytic site at the atomic level, and the obtained insights may serve as a valuable guide for developing future catalyst designs.
研究领域:
环境科学
·
材料科学
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产品关联
DOI
高影响因子
Processes
·
2022
·Vol. 10
·期 12
·2562
·
IF 3.352
Yuxi Gao,Baofang Jin,Xiaodong Wu,Zhenguo Li,Rui Ran,Duan Weng
Two Mn0.15Ce0.85O2−δmixed oxides were synthesized by a co-precipitation method using Mn(NO3)2and KMnO4as the manganese precursors, respectively. Structural analyses by X-ray powder diffraction and Raman spectroscopy reveal the formation of MnOx-CeO2solid solutions. The Mn0.15Ce0.85O2−δcatalyst prepared from the high-valent manganese precursor exhibits higher activity for the catalytic oxidation of NO. The advantage of KMnO4is related to the improved redox property of the catalyst as supported by H2temperature-programmed reduction (TPR) and O2temperature-programmed desorption (TPD). The Mn-Ce interactions create more Mn4+, Ce3+and oxygen vacancies on the KMnO4-synthesized mixed oxides based on the Raman and X-ray photoelectron spectra (XPS).Keywords:solid solutions;precursor;oxidation state;lattice defects;NO oxidation
研究领域:
催化化学
·
材料科学
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）