INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2025
·
IF 3.9
Lantong Gou,Xiandong Hao,Zhiyong Xu,Wenbo Zhao
Nitric oxide (NO), a major air pollutant from coal-fired power plants, demands an efficient capture for environmental and industrial applications. Ferrous-based absorbents exhibit promising potential for NO capture due to rapid Fe2+-NO complexation. Herein, a novel nonaqueous FeCl2/PEG200 mixture absorbent was designed by employing FeCl2 as the Fe2+ source and PEG200 as the solvent. The FTIR/UV–vis spectrum confirmed Fe2+-NO complex formation and suggested possible reaction mechanisms. Dynamic sorption experiments were systematically conducted to evaluate sorption performance. Kinetic and thermodynamic analyses obtained activation energy, enthalpy change, and entropy change information. Most importantly, a new sorption kinetic model has been established, which can be used to predict the NO sorption capacity at any temperature and partial pressure. Cyclic sorption─desorption testing demonstrated a high desorption efficiency (>91%) and robust cyclic stability over 4 consecutive cycles. This work establishes the FeCl2/PEG200 system as an efficient, reusable, and scalable candidate for industrial NO capture.
研究领域:
环境工程
·
化学工程
·
工业化学
·
大气污染控制
·
材料科学
✓ 已验证
产品关联
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
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
·
2020
·
IF 3.442
Li Wang,Junbo Wang,Xiaona Liu,Yaxin Chen,Heping Cheng,Yabin Wu,Hui Peng,Zhen Ma
An FeCeO x solid solution with an Fe/Ce molar ratio of 1 was obtained via a modified sol-gel method. The promotional effect of Fe 3+ ions in the lattice of cubic CeO 2 for catalytic reduction of NO with NH 3 was studied. The NO conversion over the FeCeO x catalyst was obviously higher than those over CeO 2 and Fe 2 O 3 catalysts. FeCeO x was characterized by using XRD , TEM, and XANES , etc. The experimental results revealed that Fe substituted Ce in CeO 2 to form an Fe–O–Ce solid solution with high activity for catalytic reduction of NO. The atomic and electric structures of the FeCeO x catalyst were studied to explain the enhanced catalytic activity.
研究领域:
材料科学
·
环境催化
✓ 已验证
DOI
高影响因子
Frontiers of Environmental Science & Engineering
·
2025
·Vol. 19
·期 3
·1-15
·
IF 6.4
Zhang Xiang,Tian Jian,Hu Tanghui,Yue Guangyong,Liu Xianlong,Zhou Wen,Liu Xiaohong,Wang Xinye
Combining pulverized coal gasifiers with cement kiln production is promising for application in low-cost and efficient NO reduction. This paper presents a pulverized coal gasifier catalytic denitration technique and investigates the homogeneous reduction (by CO and CH 4 ) and heterogeneous catalytic reduction (by coke, CaO, MgO, and Fe 2 O 3 ) of NO. A combination of Chemkin simulations and fixed-bed experiments is used to elucidate the reaction pathways and key intermediates of NO reduction by carbon-based gases. In addition, the activation energies for different catalyst combinations were analyzed via reaction kinetics. The results demonstrate that the presence of small amounts of O 2 inhibits NO reduction by CO but promotes NO reduction by CH 4 . The NCO• radical is essential for the NO reduction process, and the generation of this radical depends on the CH 4 cleavage intermediate and O• radical. CaO and Fe 2 O 3 exhibit more significant catalytic effects on NO reduction by carbon-based gases than the other catalysts tested. The presence of a small amount of O 2 in the reacting gas mixtures facilitates the NO reduction reaction. The activation energy is reduced to 1.02 kJ/mol, and the NO conversion reaches 99.80% when the catalyst is C + CaO + MgO + Fe 2 O 3 and the gas composition is CO + CH 4 + O 2 . This work provides theoretical support and data recommendations for the use of pulverized coal gasifiers for the denitrification of cement kilns.
研究领域:
化学工程
·
环境科学
✓ 已验证
DOI
高影响因子
Nanomaterials
·
2023
·Vol. 13
·期 5
·908
·
IF 5.3
Renjun Si,Yan Li,Jie Tian,Changshu Tan,Shaofeng Chen,Ming Lei,Feng Xie,Xin Guo,Shunping Zhang
In this work, we studied the influence of cross-interference effects between VOCs and NO on the performance of SnO2and Pt-SnO2-based gas sensors. Sensing films were fabricated by screen printing. The results show that the response of the SnO2sensors to NO under air is higher than that of Pt-SnO2, but the response to VOCs is lower than that of Pt-SnO2. The Pt-SnO2sensor was significantly more responsive to VOCs in the NO background than in air. In the traditional single-component gas test, the pure SnO2sensor showed good selectivity to VOCs and NO at 300 °C and 150 °C, respectively. Loading noble metal Pt improved the sensitivity to VOCs at high temperature, but also significantly increased the interference to NO sensitivity at low temperature. The explanation for this phenomenon is that the noble metal Pt can catalyze the reaction between NO and VOCs to generate more O−, which further promotes the adsorption of VOCs. Therefore, selectivity cannot be simply determined by single-component gas testing alone. Mutual interference between mixed gases needs to be taken into account.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMISTRY OF MATERIALS
·
2023
·
IF 8.6
Xingyu Fan,Botao Chen,Hui Xu,Anqiang Pan,Shuquan Liang,Songwen Tan,Yongju He
Depleting intracellular glutathione (GSH) has emerged as a potent strategy to combat cancer. However, the existing GSH-depleting agents are too toxic or ineffective and standalone GSH depletion fails to yield a satisfactory curative effect. Herein, we present an intelligent nanoparticle that possesses GSH depletion, glucose consumption accompanied with H2O2 production, and NO generation properties for multimodal cancer therapy. The nanoparticle is constructed by synthesis of tetrasulfide bond-doped mesoporous silica nanoparticles followed by conjugating glucose oxidase (GOx) on the surface and loading l-arginine (l-Arg) into the mesopores. In this nanoparticle, the doped tetrasulfide bonds can quickly deplete GSH, which increases the cellular reactive oxygen species concentration to induce ferroptosis and meanwhile triggers particle biodegradation to expose the loaded l-Arg. Moreover, the elevated H2O2 level activates l-Arg to release NO for NO therapy. GOx consumes glucose to initiate starvation therapy and simultaneously produces a large amount of H2O2. Importantly, the produced H2O2 can not only potentiate ferroptosis but also promote NO release to enhance NO therapy. Besides, NO could in turn improve the efficacy of starvation therapy by damaging the mitochondria to block energy supply. In vitro and in vivo studies demonstrate that the nanoparticles show a great synergistic effect of ferroptosis/starvation/NO therapy, which can significantly kill cancer cells and remarkably inhibit tumor growth without obvious side effects. Therefore, we think that the designed nanoparticles may provide a promising paradigm for synergistic cancer therapy and hold a prospect in clinical trials.
研究领域:
纳米技术
·
癌症生物学
·
药学
·
治疗学
✓ 已验证
DOI
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
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
ACS Catalysis
·
2016
·
IF 9.307
Xianwei Wang,Nobutaka Maeda,Alfons Baiker
Promotion of Au/TiO2 by FeOx addition is shown to result in a very strong enhancement of activity and selectivity in the NO reduction with CO. The nanocomposite Au-FeOx/TiO2 catalysts were prepared by deposition–precipitation (Au/TiO2) and subsequent impregnation (FeOx). Structural characterization of the nanocomposite catalysts using XRD, TEM, TPR, XPS, and DRIFTS revealed that they consist of titania-supported Au particles of about 4.4–4.8 nm size, which were partially covered with a thin layer of FeOx,, mainly made up of Fe2+ (FeO), in addition to a small fraction of Fe3+ (Fe2O3). In situ DRIFTS studies showed that, in comparison to Au/TiO2, on the Au-FeOx/TiO2 nanocomposites new adsorption sites were created, which led to enrichment of CO and NO molecules on the Au surface and at its interfaces with FeOx and TiO2. At the reaction temperature (250 °C), a new surface NO–CO complex, where both Fe and Au are proposed to be involved in the adsorptive interaction, was discovered. The titania-supported Au-FeOx nanocomposites considerably facilitated the formation of this complex and contributed to the striking enhancement of the catalytic performance (activity and selectivity) of the Au-based catalyst.
研究领域:
催化化学
·
材料科学
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Xiaoyan Li,Rui Zhao,Hongfang Li,Jing Jiang,Lunhong Ai,Xuejuan Cao,Juanli Liu,Hanjun Zou,Youyu Duan
Suffering from inefficient separation and transfer of photogenerated carriers, the deeply photocatalytic oxidation of NO-to-NO 3 – over g-C 3 N 4 is still a daunting challenge. Well-designed heterojunction photocatalysts have been proven to be effective in steering charge transfer for achieving a particular migration path and more active sites, which hold huge promise in further performance stimulation. Herein, in-situ face-to-face hydrothermal approach is developed to prepare a multilayer heterostructure O doping g-C 3 N 4 (O-g-C 3 N 4 ) with W 18 O 49 (O-g-C 3 N 4 @W 18 O 49 ). The experimental and theoretical results show that the unique multilayer heterostructure can improve the separation efficiency of carriers by changing the electron migration path. Moreover, doping O atoms are identified as the newly formed active centers to largely facilitate the activation of NO. Impressively, the O-g-C 3 N 4 @W 18 O 49 photocatalyst thus exhibits largely improved photocatalytic NO removal rate (56.7 %, 0.1 g of sample) and high selectivity of NO to NO 3 – (98.3 %). It outperforms the reported photocatalysts materials in visible light. This study not only provides a facile strategy for experimentally screening advanced photocatalytic materials, but also paves the way for the deep oxidation of NO.
研究领域:
材料科学
·
环境科学
·
催化化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
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
·
环境科学
✓ 已验证
DOI
高影响因子
JOURNAL OF CATALYSIS
·
2024
·
IF 6.5
Yuxi Meng,Shaomian Liu,Yixi Wang,Wenqing Xu,Jiajian Gao,Sansan Yu,Fabing Su,Tingyu Zhu
Selective catalytic reduction of NO using CO (CO-SCR) is a promising technology for the purification of NO in the flue gas. However, the presence of O 2 significantly inhibits the activity of the CO-SCR catalyst. Herein, we synthesize a hollow Mn-doped CeO 2 @Co 3 O 4 catalyst (Mn-CeO 2 @Co 3 O 4 ), which achieved 82% NO conversion, 100% CO conversion, and 78% N 2 selectivity under 5 vol% O 2 at 200 °C, superior to those of CeO 2 @Co 3 O 4 and Co 3 O 4 @CeO 2 catalysts. The characterization results indicate that the strong electronic interaction at the heterointerfaces between Co 3 O 4 and CeO 2 plays a crucial role in promoting selective adsorption of NO. Furthermore, the Mn doping into the Co 3 O 4 lattice of the catalyst facilitates the conversion of N 2 O intermediates, thereby enhancing the overall activity. This research provides a new strategy for the design and synthesis of CO-SCR catalysts.
研究领域:
催化
·
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
International Journal of Environmental Research and Public Health
·
2023
·Vol. 20
·期 5
·4009
·
IF 4.614
Han Chen,Yutao Hu,Zanyun Ying,Yinfeng Xia,Jiexu Ye,Jingkai Zhao,Shihan Zhang
The efficient, stable, and selective photocatalytic conversion of nitric oxide (NO) into harmless products such as nitrate (NO3−) is greatly desired but remains an enormous challenge. In this work, a series of BiOI/SnO2heterojunctions (denoted asX%B-S, whereX% is the mass portion of BiOI compared with the mass of SnO2) were synthesized for the efficient transformation of NO into harmless NO3−. The best performance was achieved by the 30%B-S catalyst, whose NO removal efficiency was 96.3% and 47.2% higher than that of 15%B-S and 75%B-S, respectively. Moreover, 30%B-S also exhibited good stability and recyclability. This enhanced performance was mainly caused by the heterojunction structure, which facilitated charge transport and electron-hole separation. Under visible light irradiation, the electrons gathered in SnO2transformed O2to ·O2−and ·OH, while the holes generated in BiOI oxidized H2O to produce ·OH. The abundantly generated ·OH, ·O2−, and1O2species effectively converted NO to NO−and NO2−, thus promoting the oxidation of NO to NO3−. Overall, the heterojunction formation between p-type BiOI and n-type SnO2significantly reduced the recombination of photo-induced electron-hole pairs and promoted the photocatalytic activity. This work reveals the critical role of heterojunctions during photocatalytic degradation and provides some insight into NO removal.Keywords:NO removal;photocatalysis;BiOI/SnO2;heterojunction;enhanced mechanism
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
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