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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Improvement mechanism of NO photocatalytic degradation performance of self-cleaning synergistic photocatalytic coating under high humidity

Guanyu Liu,Huiyun Xia,Wenshuo Zhang,Lifang Song,Qiwei Chen,Yanhui Niu

Photocatalytic coating has been widely studied as a promising material to remove air pollutants. However, the effectiveness and long-term effect of photocatalysis in high relative humidity environment is still the main challenge in this field. In this study, a fluorinated WO 3 -TiO 2 nanorods/SiO 2 epoxy photocatalytic superamphiphobic coating (FTSE coating) was prepared using a simple spraying method. The micromorphology and chemical composition of FTSE coating was characterized by SEM , EDS, FT-IR, XPS and TGA techniques. The advanced contact angle and hysteresis angle test show that the FTSE coating had excellent superamphiphobicity. The mechanical abrasions , corrosion resistance and UV aging tests show that the FTSE coating exhibited reasonable durability. Besides, the NO degradation efficiency of hydrophilic and superamphiphobic coatings with contact angles of 20.19°, 87.74°, 162.93° and 164.47° was tested in different humidity environment. The results showed that the superamphiphobic coating exhibited more superior photocatalytic degradation efficiency (84.02%) than the hydrophilic coating (51.38%) at a high relative humidity (RH=98%). Finally, FTSE coating exhibited prominent photocatalytic stability and the synergistic effect of photocatalysis and self-cleaning. After 30 d outdoor weathering test, the NO degradation efficiency decreased by 13.07% and recovered to the original level after flushing. The improvement mechanism of NO degradation performance was proposed based on the characteristics of superamphiphobic surface.

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VACUUM · 2022 · IF 4.11

Chemiresistive gas sensor based on electrospun hollow SnO2 nanotubes for detecting NO at the ppb level

Peng Su,Wei Li,Jie Zhang,Xiaoling Xie

Detecting some appropriate target gases through the optimization of material structure is still applicable to some old sensing materials. In this work, we showed that hollow tin oxide (SnO 2 ) nanotubes (NTs) exhibited a remarkable sensing performance for nitric oxide (NO) at 160 °C. The sensing materials were prepared by direct annealing of electrospun precursor nanofibers , and hollow NTs can be obtained at an appropriate heating rate of 6 °C/min. Given the large surface area of hollow SnO 2 NTs, their sensing performance is better than that of solid SnO 2 NTs. The response of hollow SnO 2 NTs is approximately 33.3 upon exposure to 500 ppb of NO at 160 °C. The hollow SnO 2 NTs also exhibit good repeatability, long-term stability, and excellent selectivity . These remarkable sensing properties indicate that conventional SnO 2 still has great practical applications because of the fine design of the material structure and proper control of working conditions.

CAS / MDL: 9003-39-8
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

Ultrafine Cu nanoparticles decorated porous TiO2 for high-efficient electrocatalytic reduction of NO to synthesize NH3

Lei Chen,Wenting Sun,Zhiying Xu,Minghui Hao,Baojing Li,Xin Liu,Jingjing Ma,Liang Wang,Chunhu Li,Wentai Wang

Low-temperature electrocatalytic reduction of nitric oxide (NORR) is promising for the low-cost, high-efficiency removal and utilization of nitric oxide (NO), which couples the two crucial industrial processes of denitration and synthetic ammonia. We reported a binary catalyst of Cu/P–TiO 2 for NORR process, which took advantages of the Cu electrocatalysts and porous TiO 2 . The increase of surface areas and channels can improve the adsorption of NO molecules. The decoration of the ultrafine Cu nanoparticles on the porous TiO 2 may prevent the agglomeration of ultrafine Cu nanoparticles. The as-prepared Cu/P–TiO 2 electrode exhibits excellent electrocatalytic activity with a Faraday efficiency of 86.49% and NH 3 yield of 3520.80 μg·h −1 ·mg −1 in 0.1 M K 2 SO 4 at −0.3 V vs. RHE. The mechanism of the NORR reaction process with Cu/P–TiO2 catalysts was also discussed. This research may broaden the application areas of TiO 2 -based materials in the electrocatalysis and provide a new sight in the treatment of NO pollutants.

CAS / MDL: 100-10-7
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ACS Omega · 2022 · IF 4.132

Study on NO Removal Characteristics of the Fe(II)EDTA and Fe(II)PBTCA Composite System

Liwei Ma,Guoqiang Li,Youqian Wang,Siqi Chai,Guojie Zhang

Fe2+ complexation wet denitrification technology has become a research hotspot. It is very important to achieve efficient regeneration of the absorbent and increase NO absorption in the Fe2+ complexation system. They are the key to the industrial application of the Fe2+ complexation absorption process. In this paper, 2-phosphonate-butane-1,2,4-tricarboxylic acid and ethylenediamine tetraacetic acid were used as ligands to prepare a composite system for the first time. The characteristics of NO removal were investigated under different temperatures, pHs, Fe2+ concentrations, O2 contents, NO concentrations, CO2 contents, and SO2 concentrations. Compared with the single ligand, the results show that the denitrification performance of the solution with a complex ligand is significantly improved. In this system, pH 9, 40 °C temperature, and 20 mmol/L Fe2+ concentration are the economic ideal conditions for NO removal. The system can realize simultaneous removal of NO and SO2, but SO2 in flue gas has a dual effect on the NO removal reaction.

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Catalysis Science & Technology · 2022 ·Vol. 12 ·期 4 ·1245-1256 · IF 6.177

Time-resolved in situ DRIFTS study on NH3-SCR of NO on a CeO2/TiO2 catalyst

Jie Yang,Shan Ren,Mingming Wang,Zhichao Chen,Lin Chen,Lian Liu

Ce–Ti catalysts were considered as a promising replacement for V–Ti based catalysts for selective catalytic reduction (SCR) of nitrogen oxides (NO and NO2) with NH3. In this work, a CeO2/TiO2 catalyst was prepared by the impregnation method and studied by a series of in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) experiments. The results showed that CeO2 particles grew along TiO2 faces and amorphous cerium in the lattice of TiO2, both of which are present on the CeO2/TiO2 catalyst. NH4+ might adsorb on the Ti–O–Ce structures or TiO2–CeO2 interface as Brønsted acid sites, while two types of NH4+ species were distinguished by the time-resolved spectroscopic method due to the different increasing trends. Based on the temporal evolution transient in situ DRIFTS spectra, L-NH3 had higher activity than coordinated NH3 species, which suggested that gas phase NO reacted preferentially with L-NH3. The NH4NO3 intermediate dominated the SCR reactions over the CeO2/TiO2 catalyst, which followed the Eley–Rideal mechanism.

CAS / MDL: 13463-67-7 10294-41-4
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 14 ·16963-16971 · IF 3.056

A novel method of pH-buffered NaClO2-NaCl system for NO removal from marine diesel engine

Gong Pijian,Li Chunyu,Li Xinxue

Marine diesel engines produce a lot of exhaust gas (NO, SO 2 ). Based on the situation that wet scrubbing methods have been already applied to ship desulfurization and seawater is easily accessible around the ships, this paper proposed a novel AOP (advanced oxidation process) of NaClO 2 (sodium chlorite) with Cl − (abundant Cl − exist in seawater) to remove NO from the flue gases of marine engines. The buffer capacity of NaAC (sodium acetate), the effect of Cl − concentration, and Cl − promotion mechanism on NO removal were investigated. The result showed that the existence of NaAC in solution could inhibit the rapid decline of the solution pH. The addition of Cl − achieved a remarkable promotion to NO removal at lower NaClO 2 concentration, which was due to the fast generation of ClO 2 from the promotion decomposition of NaClO 2 by Cl − in acidic condition. Then, the thermodynamic and dynamic mechanism of the generation of ClO 2 was intensively analyzed. And the mechanism of NO removal was discussed finally.

CAS / MDL: 7758-19-2 127-09-3
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JOURNAL OF RARE EARTHS · 2020 · IF 3.104

Comparative study of La1–xCexMnO3+δ perovskites and Mn–Ce mixed oxides for NO catalytic oxidation

Baohuai Zhao,Rui Ran,Liu Yang,Xiaodong Wu,Zhichun Si,Duan Weng

A series of La 1– x Ce x MnO 3+ δ ( x  = 0, 0.05, 0.1, 0.2, and 0.3) perovskites and Mn–Ce mixed oxides were prepared. Their physico-chemical properties were systematically characterized and the NO oxidation activities of the catalysts were investigated. The La 0.9 Ce 0.1 MnO 3+ δ has the best activity among all of the catalysts, with a maximum NO conversion of 85% at 300 °C. The characterization results indicate that the doping of Ce improves the properties of the perovskites in terms of the specific surface area, the average valence state of Mn ions, the number of reactive oxygen species and the NO x desorption behaviors. The Mn–Ce mixed oxide calcined at 500 °C shows a similar NO oxidation activity with La 0.9 Ce 0.1 MnO 3+ δ . However, the activity of the mixed oxide obtained at 750 °C decreases a lot, which results from the loss of active sites and active oxygen species.

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ACS Applied Materials & Interfaces · 2023 · IF 9.5

Endothelium-Mimicking Bilayer Vascular Grafts with Dual-Releasing of NO/H2S for Anti-Inflammation and Anticalcification

Lijuan Wang,Fubang Liang,Yushuang Shang,Xu Liu,Meng Yin,Jian Shen,Jiang Yuan

Vascular complications caused by diabetes impair the activities of endothelial nitric oxide synthase (eNOS) and cystathionine γ-lyase (CSE), resulting in decreased physiological levels of nitric oxide (NO) and hydrogen sulfide (H2S). The low bioavailability of NO and H2S hinders the endothelialization of vascular grafts. In this study, endothelium-mimicking bilayer vascular grafts were designed with spatiotemporally controlled dual releases of NO and H2S for in situ endothelialization and angiogenesis. Keratin-based H2S donor was synthesized and electrospun with poly(l-lactide-co-ε-caprolactone) (PLCL) as the outer layer of the graft to release H2S. Hyaluronic acid, one of the major glycosaminoglycans in endothelial glycocalyx, was complexed with Cu ions as the inner layer to mimic glutathione peroxidase (GPx) and maintain long-term physiological NO flux. The synergistic effects of NO and H2S of bilayer grafts selectively promoted the regeneration and migration of human umbilical vascular endothelial cells (HUVECs), while inhibiting the overproliferation of human umbilical artery smooth muscle cells (HUASMCs). Bilayer grafts could effectively prevent vascular calcification, reduce inflammation, and alleviate endothelial dysfunction. The in vivo study in a rat abdominal aorta replacement model for 1 month showed that the graft had a good patency rate and had potential for vascular remodeling in situ.

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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Assessing variances in the impact of intrinsic minerals on NO and N2O precursors during sludge pyrolysis

Jiangtao Meng,Jing Wang,Fengling Yang,Fangqin Cheng

This study proposed a novel strategy to control nitrogen oxides (NOx) precursors by directing nitrogen to adhere to the fuel-N→NH 3 →N 2 pathway. The research aimed to illuminate the regulatory effects of CaO, Fe 2 O 3 , and their mixtures on NO and N 2 O precursors (NH 3 , HCN, and HNCO) during sludge pyrolysis, further sought to establish scientific correlations with varying temperatures and differentiate their impact. The findings indicated that unlike NH 3 , HNCO is generated from the cleavage of amides, sharing its origin with HCN. Notably, the sensitivities of three conditioners to different functional groups result in distinct impacts on precursor emissions. CaO interacted with –OH and N-H functional groups, releasing NH 3 . Fe 2 O 3 , being more responsive to C-H and C-C groups, contributed to HNCO emission. At 750 °C, a CaO-Fe 2 O 3 mixture created Ca x Fe y O z , which selectively reacted with N-H and C≡N, facilitating the conversion of HNCO and HCN to NH 3 . While temperature is a crucial factor in the performance of CaO, its impact on Fe 2 O 3 is primarily confined to transformation of heterocyclic and nitrile . Below 350 °C, Fe 2 O 3 favored the evolution of nitrogen into heterocyclic compounds within tar. Conversely, above 490 °C, it inhibited the formation of nitrile in char, promoting the dehydrogenation of tar into unsaturated aromatic structures. The CaO-Fe 2 O 3 mixtures exhibited a superposition of individual effects from CaO and Fe 2 O 3 , with Ca x Fe y O z stimulating N 2 emission. Importantly, among three conditioners, Fe 2 O 3 showed the most significant abatement effect on NOx precursors, primarily through nitrogen fixation in char, nitrogen enrichment in tar, and precursor oxidation. This research contributes innovative perspectives on nitrogen regulation in nitrogen-rich fuels, the utilization of NH 3 , and effective NO and N 2 O control.

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JOURNAL OF CATALYSIS · 2023 · IF 7.3

Pt/doped mullite catalysts with abundant oxygen vacancies and enhanced oxygen migration capacity for NO oxidation

Darong He,Xinmei Ding,Shanshan Li,Yaxin Liu,Ming Zhao,Jianli Wang,Yaoqiang Chen

Deep catalytic removal of nitrogen oxides is one of the widespread research topics, mainly limited by the low temperature activity and hydrothermal stability of the first step for NO oxidation. Oxygen vacancies (O v ) and oxygen migration capacity play a crucial role in this challenge. Particularly, tuning the Mn-O coordination environment according to the radius and valence differences of dopant ions can increase O v , while accelerate oxygen migration by constructing Pt/mullite interfaces. Here, based on the hydrothermal stability of Pt/mullite to NO oxidation, we designed Mg 2+ - and Ba 2+ -doped catalysts. And the NO oxidation performance of the Mg 2+ -doped catalyst was significantly enhanced compared to the undoped catalysts (After hydrothermal aging, turnover frequency = 1.9 s −1 at 150 °C and activation energy = 21 kJ/mol). Meanwhile, all catalysts tested with simulated diesel exhaust and the NO oxidation performance showed essentially no decrease after 16 h of hydrothermal aging at 800 °C. Furthermore, X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) demonstrated the O v content of doped catalysts increased significantly. In addition, O 2 temperature programmed desorption (O 2 -TPD) and Thermogravimetry (TG) proved that the oxygen migration capacity of doped catalysts was enhanced by several times. Notably, the simple doping method is general for the modification of other mullites and worthy of industrial application.

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Journal of Cleaner Production · 2023 · IF 11.1

Antifungal pentachloronitrobenzene/hydroxypropyl-beta-cyclodextrin inclusion complex nanofibers by electrospun with no polymer: Fabrication and characterization

Shuang Gao,Lei Zong,Yuhang Zhang,Yang Zhang,Xinyu Guo,Guanhua Guo,Lixia Zhao,Fei Ye,Ying Fu

Pentachloronitrobenzene (PCNB) is an organochlorine protective fungicide with poor water solubility. In this research, pentachloronitrobenzene/hydroxypropyl- β -cyclodextrin inclusion complex nanofibers (PCNB/HP β CD-IC-NF) with a stoichiometric ratio of 1:1 were prepared by polymer-free electrospinning for the establishment of a rapidly dissolving water-based drug delivery system. It was proved that the formation of PCNB/HP β CD-IC enhanced the water solubility and thermal stability of PCNB by phase solubility study and thermogravimetric analysis respectively. Specifically, the solubility of PCNB in 10 mM HP β CD solution enhanced about 2.83 times, while the initial thermal decomposition temperature of PCNB in PCNB/HP β CD-IC-NF was also increased from 124 °C to 235 °C. The antifungal activity experiment exhibited that the antifungal activity of PCNB/HP β CD-IC-NF against Rhizoctonia solani was 2.13 times higher than that of pure PCNB. In summary, the formulation of PCNB/HP β CD-IC-NF prepared in the present study could efficaciously improve the solvability, thermal stability and antifungal activity of PCNB, thereby promoting the development of PCNB dosage form to water-based and low-pollution, which had potential in reducing the harm of PCNB to the environment and developing clean pesticide formulations.

CAS / MDL: 82-68-8
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Synthesis of Tb2O3/ZnO composite nanofibers via electrospinning as chemiresistive gas sensor for detecting NO gas

Tao Wei,Wei Li,Jie Zhang,Xiaoling Xie

Forming nanocomposites among different metal oxide species may lead to gas sensors with superior gas sensing properties. In this work, terbium oxide (Tb 2 O 3 ) was used to form composite nanofibers with zinc oxide (ZnO) to detect nitric oxide (NO) gas. The Tb 2 O 3 /ZnO composite nanofibers were synthesized through a facile electrospinning and annealing treatment. The heterostructure was investigated by various techniques such as XRD , SEM, TEM , and XPS , whereas the gas sensing performance of the composite nanofibers was investigated with a static gas testing system. Results showed that the Tb 2 O 3 /ZnO composite nanofiber exhibited excellent sensing performance to NO at 180 °C. Specifically, the composite nanofiber with [Tb]/[Zn] molar ratio of 0.01 had a high response of 28.3 (resistance ratio) to 1 ppm NO gas at 180 °C, with low response to other interference gases. The sensor also exhibited good repeatability and long-term stability. These remarkable sensing properties indicate that conventional ZnO is still promising for real applications via material composition and structure.

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