ENVIRONMENT INTERNATIONAL
·
2025
·
IF 9.7
Jiaqi Shi,Yan Li,Qi Wei,Xin Zhu,Shaohua Cao,Wenyi Xie,Yang Guo,Jing Wei,Zekai Li,Tao Long
The widely used rubber antioxidant N-(1,3-Dimethylbutyl)-N’-phenyl-p-phenylenediamine (6PPD) and its ozonated product, 6PPD-quinone (6PPD-Q), are highly toxic to aquatic life, yet understanding on their environmental behaviors is limited. This study comprehensively investigated their adsorption and transformation processes on natural Fe-Mn nodules (NFMN), which commonly exist in sediments and soils through a combination of diverse experimental and computational methods. The maximum adsorption capacity of 6PPD-Q (719.2 μg·g −1 ) is significantly higher than that of 6PPD (133.8 μg·g −1 ) at 293 K, and it is more difficult to desorb. They follow different kinetic and isothermal adsorption models, and environmental conditions (including temperature, pH, and anions) exert distinct influences on the adsorption of the two substances. Adsorption mechanisms involving electrostatic attraction, charge transfer, hydrogen bonding, and Lewis acid-base complexation were unveiled. For 6PPD, electrostatic adsorption and Lewis acid-base complexation contribute significantly to its adsorption. Conversely, for 6PPD-Q, the contribution of Lewis acid-base complexation outweighs that of hydrogen bonding, while the effect of electrostatic adsorption is relatively negligible. The stronger electrostatic attraction, more efficient charge transfer, and a greater number of binding sites for hydrogen bonding and Lewis acid-base complexation with NFMN results in more robust adsorption of 6PPD-Q. Furthermore, 6PPD can transform into 6PPD-Q on NFMN, facilitated by dissolved Mn(III). This study advances understanding of the adsorption behavior and mechanism of 6PPD and 6PPD-Q, and highlights a new pathway for 6PPD-Q formation, which provides valuable reference for assessing the water body exposure risks and formulating environmental remediation strategies for such pollutants. Environmental Implication This study offers the first comprehensive insight into the interactions between 6PPD/6PPD-Q and NFMN, illuminating their environmental behavior in water and soil systems. It reveals the adsorption discrepancy between 6PPD and 6PPD-Q, and elucidates the mechanisms underlying the difference in adsorption. Additionally, it uncovers a novel pathway for 6PPD-Q formation, offering valuable implications for risk assessment and environmental remediation strategies.
研究领域:
环境科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2019
·
IF 3.131
Nan Wang,Bin Han,Jianbo Wen,Mingwei Liu,Xinjun Li
A novel Mn-doped Fe 2 O 3 modified g-C 3 N 4 nanosheets composite has been prepared for overall water splitting. Structure characterizations reveal that the Mn are successfully doped in the Fe 2 O 3 nanoparticle and a close interface between g-C 3 N 4 and Mn-doped Fe 2 O 3 is obtained. The optimized FMC-10 photocatalyst has a H 2 evolution of 51 μmol h −1 . The improved photocatalytic performance can be ascribed to the synergy effect of both Mn-doped Fe 2 O 3 and g-C 3 N 4 . Doping Fe 2 O 3 with Mn promotes photo-induced charges and increases the charge transfer for the improved conductivity of the bulk Fe 2 O 3 , while favorable contacting with g-C 3 N 4 enhances the charge separation ability.
研究领域:
材料科学
·
化学
✓ 已验证
产品关联
DOI
高影响因子
IONICS
·
2019
·Vol. 25
·期 11
·5485-5494
·
IF 2.289
Wang Xiaoqing,Tian Songran,Zhang Xiaoqing,Li Guoyan,Liu Ying,Chen Botao,Cheng Bowen
A 3D Ni 3 S 2 @Mn-Co-OH/NF cross-linked nanosheet heterostructure composite electrode has been successfully fabricated by a facile two-step hydrothermal method. The as-prepared Ni 3 S 2 @Mn-Co-OH/NF composite electrode exhibits a high capacitance (3163 F g −1 at a current density of 3 mA cm −2 ), a superior rate performance (2071 F g −1 at a current rate of 30 mA cm −2 ), and stable cycling property (maintaining 96.6% of the initial capacitance after 4000 cycles at a current rate of 10 mA cm −2 ). This excellent electrochemical performance can be ascribed to the unique cross-linked nanosheet heterostructure formed directly on Ni foam current collector and the synergistic effect between Mn-Co-OH and Ni 3 S 2 of the composite electrode.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
Catalysts
·
2023
·Vol. 13
·期 7
·1031
·
IF 3.9
Jie Lin,Yihong Ding,Huile Jin,Tianbiao Zeng
Nickel, cobalt, and manganese oxides are easily obtainable non-noble metal catalysts for water splitting. However, the relationship between composition and catalysts’ performance still needs systematic studies. Herein, guided by theoretical calculations, a low overpotential, easily prepared Mn-doped Co3O4was deposited on graphite plates for water splitting. The 30% Mn-doped Co3O4(Co2.1Mn0.9O4) required the lowest overpotential for oxygen evolution reaction (OER), in which the Co2.1Mn0.9O4reached 20, 30, and 50 mA cm−2in the overpotentials of 425, 451, and 487 mV, respectively, with 90% IR compensation. Under overall water-splitting conditions, the current density reached 30 mA cm−2at an overpotential of 0.78 V without IR compensation. Charge density difference analysis illustrates that doped Mn provides electrons for O atoms, and that Mn doping also promotes the electron fluctuation of Co atoms. XPS analysis reveals that Mn-doping increases the chemical valence of the Co atom, and that the doped Mn atom also exhibits higher chemical valence than the Mn of Mn3O4, which is advantageous to boost the form of based-OOH* radical, then decrease the overpotential. Considering the particular simplicity of growing the Co2.1Mn0.9O4on graphite plates, this work is expected to provide a feasible way to develop the high-performance Co-Mn bimetallic oxide for water splitting.Keywords:water splitting;bimetallic oxides;Mn-doped Co3O4;DFT calculation
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF FLUORESCENCE
·
2024
·
IF 2.6
Zha Jiahao,He Chongjun,Chen Fangzhou,Wang Hongwei,Dong Biao,Liu Lijuan,Xia Mingjun,Deng Chenguang,Li Qian,Lu Yuangang,Chen Huiting
Oxide matrix red-emitting phosphors are deemed as excellent color converters for white light emitting diodes (WLEDs) and laser diodes (LDs). Manganese-doped MgAl 2 O 4 powder was synthesized by a solid-state reaction method at different sintering temperatures. Microstructure shows that grain size is mainly in the range of 0.2–5 μm, and grain agglomeration occurs with increased sintering temperature. XPS analysis indicates that the doped Mn ion exhibits a valence state of + 4 within the MgAl 2 O 4 matrix. The diffraction peak of the phosphors is shifted by the sintering temperature, which affects lattice constant. Upon excitation by 300 nm ultraviolet light, the samples emit asymmetric broadband red light within the range of 620–720 nm, attributed to Mn 4+ ion’s transition from 2 E g to 4 A 2g states. With the increasing temperature, the main emission peak shifts from 677 nm to 650 nm, ascribed to the change in energy level ( 2 E g ) resulting from the reduction of Al 2 O 3 phase. Crystal field theory confirmed that Mn 4+ ions are within a strong crystal field environment created by MgAl 2 O 4 matrix. By affecting particle size and crystallinity, the sintering temperature influences the fluorescence lifetime of the Mn 4+ ion. Notably, these red-emitting phosphors exhibits remarkable thermal stability as their emission intensity remains approximately at 58% of initial intensity even at elevated temperature (435 K). Consequently, Mn 4+ : MgAl 2 O 4 red-emitting phosphors with high thermal stability render them promising candidates for WLED applications.
研究领域:
材料科学
·
光学
✓ 已验证
DOI
高影响因子
Nanomaterials
·
2019
·Vol. 9
·期 5
·675
·
IF 4.034
Lei Zhu,Xi Li,Zhiying Liu,Lin Yao,Peng Yu,Ping Wei,Yanhua Xu,Xingmao Jiang
Mn-Ce-Zr-O catalysts doped with varying Mn content were prepared and assessed for the catalytic combustion of chlorobenzene (CB). Nanosized MCZ-0.67 catalyst with amorphous phase exhibited a high and stable catalytic activity among the studied catalysts, achieving 90% CB conversion at 226 °C and withstanding stability tests, including time-based stability and the successive influence of various operating conditions. Meanwhile, the MCZ-0.67 catalyst used showed good recyclability by calcination in air. Characterization results suggested that Mn doping played a dominant role in improving the catalytic performance, resulting in larger surface area, better redox properties and greater amounts of surface active oxygen. In addition, the introduction of Zr was also indispensable for maintaining the good catalytic performance of catalysts. Finally, trace amounts of polychlorinated by-products during CB oxidation were monitored and the oxidation process was discussed.Keywords:MnOx-CeO2-ZrO2;catalytic combustion;chlorobenzene;active oxygen;product analysis
研究领域:
环境科学
·
催化化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Wenhao Peng,Ningning Song,Zilong Su,Jiajun Wang,Kaixuan Chen,Shuji Li,Bingyan Wei,Shiping Luo,Aijuan Xie
A series of MoS 2 and Mn metal organic frameworks (Mn-MOF) were synthesized by hydrothermal method, and then MoS 2 , Mn-MOF and multi-walled carbon nanotubes (MWCNT) were mixed in different mass ratios and applied for supercapacitor. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge (GCD) are used to investigate the electrochemical performance of MoS 2 /Mn-MOF/MWCNT materials with different mass ratios. The experimental results show that when the mass ratio of m(MoS 2 ): m(Mn-MOF): m(MWCNT) is 1:4:1, the electrochemical performance of the MoS 2 /Mn-MOF/MWCNT composite is the best. The specific capacitance of optimal MoS 2 /Mn-MOF/MWCNT (1:4:1) reaches 862.73F g −1 , which is noticeable higher than that of MoS 2 (42.29F g −1 ), Mn-MOF (70.23F g −1 ) and MWCNT (347.27F g −1 ) materials. Moreover, the EIS test manifests that the MoS 2 /Mn-MOF/MWCNT (1:4:1) composite has a lower R ct value (2.566 Ω). Therefore, MoS 2 /Mn-MOF/MWCNT (1:4:1) has the best electrochemical performance among the all as-fabricated supercapacitor materials. This research provides an effective method for the development of Mn-based supercapacitor materials and improves the capacitance performance of MOFs materials.
研究领域:
材料科学
·
电化学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
Coatings
·
2024
·Vol. 14
·期 4
·453
·
IF 2.9
Ningning Xing,Lilin Yang,Li Wang,Yanxiang Lu,Hongkun Zhang,Xijun Sun,Min Zhao,Wenjie Tan,Jie Yang
The reliable detection of environmental contaminants can correctly forecast the degree of environmental pollution that has occurred, which contributes to improving the environmental purification rate and maintaining the ecological balance. Herein, a novel hierarchical biomimetic catalysis MnO2@CuAl-CLDHs was designed and synthesized using a facile method, which exhibited significantly enhanced peroxidase-like activity due to the unique composition and hierarchical mesoporous structure. Under optimized operational conditions, a visible colorimetric array based on the superior nanozyme activity of MnO2@CuAl-CLDHs was developed for the quantitative determination of hydroquinone with a wide linear detection range (1–100 μM) and a low detection limit (0.183 μM). Simultaneously, our presented strategy could analyze hydroquinone in real water samples with high accuracy. Therefore, the bimetallic co-catalyzed nanozymes are expected to be the perfect replacement for natural enzymes to develop convenient and efficient sensors.
研究领域:
环境科学
·
生物化学
✓ 已验证
产品关联
DOI
高影响因子
Processes
·
2022
·Vol. 10
·期 10
·1946
·
IF 3.352
Hong Shen,Zijun Tang,Xiang Xiao,Haiwen Wu,Hang Zhou,Ping Fang,Dingfang Zhu,Jianhua Ge
In this study, Mn-Ce/Al2O3/TiO2catalyst prepared by impregnation method was used for synergistic O3oxidation NO. The catalyst prepared by impregnating Al2O3/TiO2at a Mn:Ce molar ratio of 4:1 showed the best catalytic activity. The catalyst performance showed that when the molar ratio of Mn:Ce was 4:1 and the volume ratio of O3:NO was 1:4, the removal rate of NO could reach 63%, which could increase the removal rate by 40% compared with that of NO oxidized by O3alone. BET, XRD, and TEM characterization results showed that when the molar ratio of Mn:Ce was 4:1, the catalyst specific surface area, and pore capacity were the largest. A large amount of MnOx and CeOx were distributed on the catalyst surface. The XPS analysis showed that the oxidation-reduction and oxygen vacancy of Mn (IV)/Mn (III)/Mn (II) and Ce (IV)/Ce (III), had a synergistic effect on the decomposition of O3into reactive oxygen species(O*), thus improving the catalytic capacity of Mn-Ce/Al2O3/TiO2catalyst for O3. The O2-TPD analysis showed that the oxygen vacancies and oxygen species in the catalyst could be used as the active point of decomposition of O3into O*. The experimental results show that the prepared catalyst can significantly improve the efficiency of ozone oxidation of NO and reduce the amount of ozone. The catalyst can be applied to ozone oxidation denitrification technology.
研究领域:
环境科学
·
催化化学
✓ 已验证
DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
·
IF 4.3
Yuefeng Gao,Sai Xu,Yanbiao Li,Baojiu Chen
The low photoluminescence quantum yield (PLQY) of CsPbCl 3 perovskite quantum dots (PQDs) poses a significant challenge to their application as ion detection probes. To address this issue, we enhanced the PLQY of CsPbCl 3 PQDs through Mn doping. These enhanced PQDs were then employed as probes for the highly sensitive detection of Cu 2+ ions and temperature. CsPbCl 3 :Mn PQDs with varying Mn/Pb ratios were synthesized via hot injection. The Mn doping introduced an emission band near 600 nm, with intensity increasing alongside doping concentration. At an Mn/Pb ratio of 2.0, the PLQY was enhanced nearly tenfold, from 5.46 % for undoped CsPbCl 3 to 52.48 % for CsPbCl 3 :Mn. CsPbCl 3 :Mn PQDs with the highest PLQY were employed as luminescent probes, utilizing the fluorescence intensity ratio (FIR) technique for copper detection and temperature sensing. The experimental results demonstrated a linear relationship between the FIR and Cu 2+ concentration over the range of 22.12 nM–1600 nM, with 22.12 nM being the calculated limit of detection. Analysis of the emission spectra and fluorescence lifetimes at varying Cu 2+ concentrations revealed that electron transfer from CsPbCl 3 to Cu 2+ induced fluorescence quenching. CsPbCl 3 :Mn exhibits a high relative sensitivity of 15.89 % K −1 at 298 K, along with excellent reversibility. These findings highlight the potential application of CsPbCl 3 :Mn PQDs in both temperature sensing and the analysis of wear metals in engine lubricating oils.
研究领域:
材料科学
·
分析化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
FUEL PROCESSING TECHNOLOGY
·
2016
·
IF 3.847
Wei Li,Rui-tang Guo,Shu-xian Wang,Wei-guo Pan,Qi-lin Chen,Ming-yuan Li,Peng Sun,Shu-ming Liu
Heavy metals (such as Zn and Pb) have a deactivation effect on the catalyst for selective catalytic reduction of NO with NH 3 . In this study, it was found that the modification of Mn/TiO 2 catalyst by Nb could greatly enhance its Zn resistance. From the characterization results of BET, XRD, H 2 -TPR, NH 3 -TPD, it may be concluded that the introduction of Nb into Mn/TiO 2 catalyst would lead to its lower crystallinity , more acid sites and higher concentrations of Mn 4 + and surface chemisorbed oxygen. The results of in situ DRIFT study reveal that the NH 3 -SCR reactions over Mn/TiO 2 and Mn-Nb/TiO 2 all obey both the Langmuir-Hinshelwood mechanism and the Eley–Rideal mechanism, and the doping of Nb on Mn/TiO 2 catalyst could promote the adsorption of NH 3 and NOx species on it. All these features make a contribution to the high SCR activity and good Zn resistance of Mn-Nb/TiO 2 catalyst.
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
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2020
·
IF 3.99
Jiahui Deng,Yalin Cheng,Min Liu,Biyang Tu,Shan Xue,Haisheng Tao
In this study, Fe-Mn co-embed sodium alginate carbon spheres (Fe-Mn/SA-C) were prepared as a cost-effective adsorbent for aqueous Cd(II) removal by a facile pyrolysis method. The morphology and chemical composition of Fe-Mn/SA-C were explored with various characterized techniques. The results indicate that Fe-Mn/SA-C possess porous structures and abundant oxide-based functional groups. Fe-Mn/SA-C exhibits excellent adsorption properties for aqueous Cd(II) and the adsorption process is pH-dependent. The adsorption data could fit pseudo second-order and Langmuir models well, suggesting that chemisorption is a dominant adsorption mechanism and the maximum adsorption capacity is 280.11 mg −1 . Thermodynamic analysis demonstrates that the adsorption is spontaneous and endothermic. The adsorption mechanisms of Cd(II) include the complexation of Cd(II) with oxygen-based functional groups, precipitation, and ion exchange. Finally, the granulated and magnetic Fe-Mn/SA-C is an efficient and practical adsorbent for cadmium-containing wastewater treatment.
研究领域:
环境科学
·
材料科学
✓ 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）