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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2017 ·Vol. 17 ·期 12 ·8818-8826 · IF 1.483

Surface Basic Sites and Lattice Oxygen Sensitive Mn–Na2WO4/SiO2 Catalysts for Oxidative Coupling of Methane

Liu Jingwei,Huo Minfeng,Zhu Yan

Mn–Na2WO4/SiO2 synthesized by Urea-assisted hydrothermal-Impregnation route has more and stronger surface basic sites, and more surface lattice oxygen, leading to higher methane conversion with higher selectivity toward ethane and ethylene in oxidative coupling of methane reaction, compared to Mn–Na2WO4/SiO2 produced by Co-precipitation-Impregnation (CPI) and Sequential Impregnation (SI) methods.

研究领域: 催化化学 · 材料科学
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RSC Advances · 2017 ·Vol. 7 ·期 51 ·32146-32154 · IF 3.108

Mn/SAPO-34 as an efficient catalyst for the low-temperature selective catalytic reduction of NOx with NH3

Chengkai Pang,Yuqun Zhuo,Qiyu Weng

A series of Mn-exchanged SAPO-34 catalysts were synthesized and developed as catalysts for the low temperature selective catalytic reduction (SCR) of NO with ammonia in the presence of excess oxygen. 4Mn/SAPO-34 showed the highest SCR activity in the temperature range of 120–210 °C. The microstructure of zeolite supports, acidity, manganese species and reaction mechanism were investigated in detail by BET, NH3-TPD, UV-Vis, H2-TPR, XPS and in situ DRIFTS. Mn3+ and Mn4+ related species were proved to be the active sites for the SCR reaction. The Eley–Rideal mechanism was proved to be effective on 4Mn/SAPO-34 for the low temperature SCR reaction in which coordinated NH4+ species react with gas-phase NO to form an activated transition state and subsequently decomposed to N2 and H2O.

研究领域: 环境科学 · 催化化学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Photo-responsive Mn-doped TiO2-based superhydrophobic/ underwater superoleophobicity membrane for efficient oil-water separation and photothermal decontamination

Yujie Yang,Chengxin Li,Zhuwei Gao,Xinyu Qi,Lan He,Wei Huang,Jieqiong Wang,Zhongxin Liu

In recent years, oily wastewater has become an important factor in environmental pollution. As a transition metal element, manganese is able to introduce new impurity band gaps using d -orbital hybridization to extend the photoresponse range of TiO 2 , thus enabling TiO 2 to be self-cleaned under UV irradiation more easily. Therefore, we synthesized superhydrophobic/submerged superoleophobic Mn@TiO 2 -modified membranes which possess a self-cleaning property under UV light using manganese element-doped titanium dioxide and cotton fabric as the substrate by hydrothermal method and then investigated the relevance between the doping concentration of Mn and super-hydrophobicity. The results showed that water contact angles of prepared membranes with the Mn ions doping concentrations of 0.5 mol/L, 1.0 mol/L, and 1.5 mol/L were 147.89°, 150.43°, and 153.37°, respectively. The membrane with 1.5 mol/L was effective for the separation of the dichloromethane-water mixture. Under Xenon lamp irradiation, three membranes with different concentrations showed a significant temperature increase with the maximum rising to 53.1 ℃ within 2 min, reflecting an excellent photothermal conversion capability. In addition, the decontamination ability of the Mn@TiO 2 membrane was tested under UV light. The Mn@TiO 2 membrane was able to degrade the oil-red solution dripping on the surface, showing that the membrane had a good self-cleaning performance, which was significant for industrial applications.

CAS / MDL: 7220-79-3 61-73-4
研究领域: 环境科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

The photoactivity of complexation of DOM and Fe(Ⅱ)/Mn(Ⅱ) in aquatic system: Implication on the photodegradation of MCLR

Haishuo Wang,Xinke Tian,Zhichun Li,Jie Zhang,Shiyin Li,Heyong Huang

Lake eutrophication leads to the excessive proliferation of cyanobacteria in aquatic environments, resulting in microcystin-LR (MCLR) concentrations exceeding regulatory limits. The associated environmental risks and health concerns attract widespread attention. As one of the most active chemical substances in aquatic environments, dissolved organic matter (DOM) plays a critical role in the phototransformation of MCLR. In environments where Fe(II) and Mn(II) coexist, the phototransformation process of MCLR may be influenced. Among fulvic acid (FA), humic acid (HA), cyanobacteria-derived DOM (CDOM), and reed leaf-derived DOM (RDOM), FA has the highest apparent reaction rate constant for MCLR at 0.03567   h -1 . Using isopropanol, furfuryl alcohol, and sorbic acid as quenchers, the contributions of different photochemically produced reactive intermediates(PPRIs) to MCLR photodegradation follow the order: 3 DOM⁎ > ·OH > 1 O 2 . As pH increases, changes in the conformation and charge distribution of DOM and MCLR suppress MCLR photodegradation. The addition of Fe(II) or Mn(II) enhances the photodegradation of MCLR by DOM. Electron paramagnetic resonance tests and radical quenching experiments indicate that the introduction of Fe(II)/Mn(II) increases ·OH production. The enhanced ·OH promotes MCLR photodegradation more effectively than the suppression caused by Fe(II)/Mn(II) quenching of ³DOM⁎. Product analysis reveals that demethylation, hydroxylation, decarbonylation, decarboxylation, denitration, and bond cleavage are the main pathways of MCLR photodegradation. These findings provide valuable insights into the migration and transformation of MCLR in complex environments, contributing to a deeper understanding of the fate of pollutants in natural water systems, particularly in the presence of metal ions.

CAS / MDL: 68131-04-4
研究领域: 环境科学 · 水生生态学
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Catalysts · 2020 ·Vol. 10 ·期 11 ·1329 · IF 3.52

High Resistance of SO2 and H2O over Monolithic Mn-Fe-Ce-Al-O Catalyst for Low Temperature NH3-SCR

Shijie Hao,Yandi Cai,Chuanzhi Sun,Jingfang Sun,Changjin Tang,Lin Dong

Monolithic Mn-Fe-Ce-Al-O catalyst with honeycomb cordierite ceramic as a carrier was reported for the first time for low temperature deNOxapplication. In the reaction of selective catalytic reduction (SCR) of NO with NH3, a NO conversion of above 80% at 100 °C was obtained. Notably, the catalyst also showed excellent resistance against SO2and H2O. About 60% NO conversion was maintained after successive operation in the mixed stream of SO2and H2O for 168 h. The Brunner−Emmet−Teller (BET) measurement, SEM, EDS, thermogravimetric analysis (TG), FT-IR, and XPS results of the used catalysts indicated that certain amounts of ammonium sulfate was formed on the surface of the catalyst. XPS results revealed that partial of Fe2+was oxidized to Fe3+during the reaction process, and Fe2+species have strong redox ability, which can explain the decrease in activity after reaction. In addition, SO2and H2O induced a transformation of Ce from Ce4+to Ce3+on the surface of the catalyst, which increased the amount of chemisorbed oxygen. Owing to these factors, the addition of Ce and Fe species contributes to excellent resistance of the catalyst to SO2and H2O.Keywords:honeycomb catalyst;Mn-Fe-Ce-Al-O;low temperature denitration;water and sulfur resistance

研究领域: 环境科学 · 催化化学
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Nano Research · 2023 ·Vol. 16 ·期 8 ·10748-10755 · IF 9.9

Efficiently coupled glucose oxidation for high-value D-glucaric acid with ultradurable hydrogen via Mn(III) in acidic solution

Li Junhua,Jiang Yi,Zhang Xu,Huo Yidan,Du Fanglin,Tuo Yongxiao,Guo Zhiyan,Chen Dawei,Chen Shenghua

The electrooxidation of the alcohol and aldehyde molecules instead of water coupled with H 2 production has been proven to be effective for producing high-value fine chemicals under alkaline conditions. It is also noteworthy that under acidic conditions, the stability of non-noble metal water oxidation catalysts remains a great challenge due to the lattice oxygen mechanism. Hence, we coupled the biomass-derived glucose oxidation for high-value D-glucaric acid (GRA) with ultra-durable hydrogen in acid solution over a Yb-MnO 2 catalyst. The Mn 3+ regulated by Yb atoms doped in MnO 2 can effectively optimize the adsorption and desorption processes of the alcohol and aldehyde group and improve the intrinsic activity but cannot for H 2 O. The catalyst exhibited extremely high activity and stability after 50 h for glucose oxidation, inhibiting the lattice oxygen process and MnO 4− formation, while the activity was quickly lost within 0.5 h for water oxidation. Density functional theory (DFT) calculations further demonstrated that glucose oxidation reaction proceeds preferentially due to the oxidation of aldehyde group with lower adsorption-free energy (−0.4 eV) than water (Δ G > 0 eV), avoiding the lattice oxygen mechanism. This work suggests that biomass-derived glucose oxidation not only provides a cost-effective approach for high-value chemicals, but also shows an extremely potential as an alternative to acidic oxygen evolution reaction (OER) for ultradurable H 2 production.

CAS / MDL: 35725-34-9
研究领域: 生物化学 · 催化化学
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JOURNAL OF PHYSICS D-APPLIED PHYSICS · 2024 · IF 3.1

Mn Derived Growth of CsPbBr3 Nanoplatelets for Stable and Bright Orange Emission

Jinchan He,Cong Xie,Bo Wang,Ping Yang

Mn-doped perovskites have been extensively studied in optics, magnetism, and electronics due to their orange emission. However, successful Mn doping required a high Mn/Pb feed ratio. In this paper, Mn-doped CsPbBr3 nanoplatelets (NPLs) with bright orange emission were prepared by a two-step slow thermal injection synthesis. The slow injection of precursors effectively slow-down the crystal growth kinetic process and controls the growth of undoped CsPbBr3 NPLs. This process also significantly improves Mn doping efficiency. Mn doping induced the generation of numerous precursor clusters during the growth of CsPbBr3 NPLs, and the formation of these clusters was crucial for enhancing the doping efficiency. The maximum amount of Mn precursor in CsPb0.83Mn0.17Br3 was 50% of Pb precursors. The photoluminescence quantum yields (PLQYs) of CsPb0.94Mn0.06Br3 NPLs reached up to 80.6%, which was 3.1 times of that of CsPbBr3 NPLs. The PL properties of Mn-doped CsPbBr3 NPLs were significantly enhanced compared with pure CsPbBr3 NPLs. The growth process and luminescence mechanism of Mn-doped CsPbBr3 NPLs were discussed. High PLQYs and efficient Mn doping supplied an ideal approach for the preparation of various CsPbX3 (X = Cl, Br, and I) NCs for commercial applications.

研究领域: 材料科学 · 光学 · 纳米技术
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Surfaces and Interfaces · 2025 · IF 6.3

Alloying of Ni-Si intermetallic compounds and Co/Fe/Mn with enhanced CO oxidation activity

Jiangang Kang,Haihong Zhang,Yuehui He,Liang Wu,Hengdi Ye,Jinchao Wei

The novel Ni-Si intermetallic compounds are fabricated by elemental powder metallurgy. This study explores the synthesis of a series of catalysts (Ni-Si-M, M=Co, Fe, Mn) by alloying to augment the low-temperature efficiency of CO oxidation using Ni-Si intermetallic compounds. It is found the low-temperature catalytic activity of Ni-Si-Co, Ni-Si-Fe, and Ni-Si-Mn catalysts are significantly enhanced compared to the original Ni-Si. The catalytic activity among the catalysts ranks as follows: Ni-Si-Co > Ni-Si-Fe > Ni-Si-Mn > Ni-Si. The apparent activation energy (Ea) for Ni-Si-Co was the lowest at 57.3 kJ/mol, suggesting its efficient catalytic oxidation of CO. Additionally, the addition of Co, Fe and Mn elements actually promotes the generation of Ni 2+ as the CO adsorption site in the original Ni-Si. The addition of Co element also leads to the formation of Co 2+ as the adsorption site of O 2 in the process of CO oxidation reaction. The synergistic adsorption of Ni 2+ and Co 2+ to CO and O 2 promotes the CO oxidation reaction. Additionally, the catalysts demonstrate robust long-term stability in atmospheres containing H 2 O and SO 2 , with CO conversion initially suppressed but subsequently recovering and stabilizing at over 90%. This investigation offers novel insights into enhancing the low-temperature activity and stability of catalysts.

CAS / MDL: 63148-65-2
研究领域: 材料科学 · 催化化学
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Tungsten · 2024 · IF 5.6

A Mn-porphyrinic metal–organic framework immobilizing glucose oxidase for combined photodynamic/chemodynamic/starvation therapy

Sun Xin-Ran,Yuan Hao-Ming,Zhang Guo-Da,Wang Chao,Sun Shu-Juan,Shi Peng-Fei

The combination of photodynamic therapy (PDT) and chemodynamic therapy (CDT) in tumor treatment has attracted considerable attention. However, tumor hypoxia and glutathione (GSH) overproduction in the tumor tissue restricted the progress of their applications. Herein, a Mn-porphyrinic metal–organic framework (Mn-TCPP) was constructed by the one-pot method and further used for immobilizing glucose oxidase (GOx) to obtain GOx@Mn-TCPP. GOx would rapidly exhaust endogenous glucose into hydrogen peroxide (H 2 O 2 ) and gluconic acid, thus shutting off the energy supply of tumor cells for starvation treatment. Mn-TCPP catalyzed H 2 O 2 to produce oxygen, regulating the hypoxic tumor microenvironment and in turn improving 1 O 2 generation under laser irradiation. Interestingly, Mn-TCPP can reduce reactive oxygen species consumption owing to the redox reaction between Mn 3+ and GSH, thus greatly enhancing PDT. Furthermore, benefiting from GOx-mediated starvation therapy, Mn 2+ produced by Mn 3+ reduction can react with sufficient intracellular H 2 O 2 to generate ·OH with high cytotoxicity through a Fenton-like reaction. After treatment by GOx@Mn-TCPP under laser irradiation in vitro, the cell viability of 4T1 and A549 tumor cells reached to 20%, reflecting GOx@Mn-TCPP could give full play to the advantages of PDT/CDT/starvation therapy. The results in vivo demonstrated that GOx@Mn-TCPP mediated synergistic cascade therapy could significantly inhibit tumor growth and improve the therapeutic effect.

研究领域: 肿瘤学 · 生物医学工程 · 纳米医学
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RSC Advances · 2015 ·Vol. 5 ·期 20 ·15110-15117 · IF 3.84

Hydrothermal synthesis of Mn-doped CdS hollow sphere nanocomposites as efficient visible-light driven photocatalysts

Chunyan Zhang,Jiasheng Lai,Juncheng Hu

A series of Mn-doped CdS hollow sphere photocatalysts has been directly synthesized by a simple and facile hydrothermal route for the first time. It was demonstrated that GSH acts as the S source and a gas bubble-template in this process. The products were characterized by XRD, SEM, TEM, HRTEM, XPS, and UV-vis spectroscopy. The as-prepared CdS and Mn-doped CdS hollow spheres all showed much higher activity than P25 under visible light (λ > 420 nm) irradiation. Among them, the 2.0 mol% Mn-doped CdS sample exhibited the highest photoactivity for the removal of organic pollutant RhB, and about 99.2% MO was decomposed after 50 min of visible light irradiation. Moreover, this catalyst also showed good stability, and after four cycles, the degradation efficiency still remained at 85%. The excellent photoactivity of the as-prepared Mn-doped CdS hollow spheres could be attributed to the synergistic effects of its appropriate band-gap structure and the special porous spherical morphology. The unique hollow sphere structure may favor the harvesting of excited light due to its special multiple scattering effect within the interior space, and the doping of Mn2+ may facilitate the generation of photoinduced electrons and hole pairs, and inhibit their recombination rate by acting as temporary trapping sites. This material may have great application potentials in environmental remediation and energy harvesting.

CAS / MDL: 10022-68-1 70-18-8
研究领域: 材料科学 · 环境科学
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LWT-FOOD SCIENCE AND TECHNOLOGY · 2021 · IF 4.952

Oxidase-like Fe–Mn bimetallic nanozymes for colorimetric detection of ascorbic acid in kiwi fruit

Yaru Han,Linpin Luo,Liang Zhang,Yi Kang,Hao Sun,Jie Dan,Jing Sun,Wentao Zhang,Tianli Yue,Jianlong Wang

Nanozymes have become a frontier of research recently and possess broad application prospects in the field of analytical sensing. Herein, a Fe–Mn bimetallic nanozyme (FeMnzyme) was proposed for colorimetric analysis of ascorbic acid (AA). The FeMnzyme, with high specific surface area, consisted of Fe–Mn mixed oxide amorphous core and α-FeOOH nanorod shell characterized by scanning electron microscope (SEM) and Powder X-ray diffraction (XRD). It exhibits typical oxidase-like properties to catalyze oxidation of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to generate visible blue oxidized TMB (oxTMB) without exogenous H 2 O 2 . Due to the reducibility of AA to oxTMB, the FeMnzyme/oxTMB system can be employed as a promising colorimetric sensor for quantitative analysis of AA. The method has a good linear concentration range of 8 μmol L −1 to 56 μmol L −1 , and the detection limit is as low as 0.88 μmol L −1 (3σ). Finally, the proposed biosensor has been favorably put into use to determine AA content in kiwi fruit, indicating its reliability for practical application.

研究领域: 分析化学 · 生物传感 · 食品科学
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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS · 2024 · IF 2.5

Effect of Al3+ doping on magnetic properties of Zn-Mn ferrite nanoparticles for magnetic induction hyperthermia

Xiaogang Yu,Md Mostafezur Rahman,Renpeng Yang,Chengwei Wu,Abdelhakim Bouyahya,Wei Zhang

Magnetic induction hyperthermia with self-regulated temperature is an advanced technology capable of automatically regulating hyperthermia temperature through a magnetic phase transition, which has a promising application prospect. This paper investigated the effects of Al 3+ doping on the magnetic properties and Curie temperature of Zn-Mn ferrite. The specific saturation magnetization and Curie temperatures of Zn 0.5 Mn 0.5 Al x Fe 2-x O 4 (0 ≤ x ≤ 0.6) nanoparticles decrease linearly with increment of Al 3+ content. The magnetic heating experiments exhibit that the synthesized nanoparticles can raise the temperature of agar phantom to above 42 °C and self-regulate the temperature below their Curie temperatures, demonstrating their potential for self-regulated temperature hyperthermia. Additionally, in vitro cell experiments confirm the nanoparticles’ good biocompatibility.

研究领域: 材料科学 · 生物医学工程 · 纳米医学
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