JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2024
·
IF 9.4
Zheng Wang,Hui Li,Chuang Jiang,Wenya Liu,Siyu Zhang,Yibin Zhou,Kang Liu,Yaqing Xiao,Ruyan Hou,Xiaochun Wan,Yingnan Liu
Herein, a novel dual-mode probe for organophosphorus pesticides (OPs) colorimetric and photothermal detection was developed based on manganese modified porphyrin metal–organic framework (PCN-224-Mn). PCN-224-Mn had excellent oxidase-like activity and oxidized colorless 3,3,5,5-tetramethylbenzidine (TMB) to blue–green oxidation state TMB (oxTMB), which exhibited high temperature under near-infrared irradiation. l -ascorbate-2-phosphate was hydrolyzed by acid phosphatase to produce ascorbic acid, which weakened colorimetric and photothermal signals by impacting oxTMB generation. The presence of OPs blocked the production of ascorbic acid by irreversibly inhibiting the activity of acid phosphatase, causing the restoration of chromogenic reaction and the increase of temperature. Under the optimal conditions, the probe showed a good linear response to OPs in the concentration range of 5 ∼ 10000 ng/mL, using glyphosate as the analog. The detection limits of glyphosate in colorimetric mode and photothermal mode were 1.47 ng/mL and 2.00 ng/mL, respectively. The probe was successfully used for sensitive identification of OPs residues in tea, brown rice, and wheat flour. This work proposes a simple and reliable colorimetric/photothermal platform for OPs identification, which overcomes the problem that single-mode detection probes are susceptible to external factors, and has broad application potential in the field of food safety.
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MICROCHEMICAL JOURNAL
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2024
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IF 4.9
Fang Li,Nuotong Shen,Qingcheng Li,Chen Yang,Limin Zhang,Mingjin Wang
The development of microfluidic flow injection analysis (FIA) system for simultaneous and real-time detection of multiple metal ions is of great importance for environmental monitoring, food safety and industrial field. In this work, a multiplexed microfluidic chip based FIA system was fabricated for simultaneous determination of three metal ions, by using Fe(III), Mn(II) and Cu(II) as models. The multiplexed microfluidic chip based FIA system is composed of three parts, including a multi-channel FIA system for solution manipulation, a group of microfluidic chips for reagents mixing and reaction, and one fiber optic spectrometer for fast and real-time absorbance signal detection. The sample solution and chromogenic reagents were injected into the microfluidic chips to carry out specific colorimetric reactions. Fe(III), Mn(II) and Cu(II) reacts with 5-sulfosalicylic acid, formaldoxime, and bis(cyclohexanone) oxalyldihydrazone, respectively, to generate orange, ember and blue colored solution with peak absorbance at 420 nm, 450 nm, and 600 nm, respectively. The absorbance signal of the generated three channels of solution can be sequentially detected by using only one mini spectrometer. The linear detection range for Fe(III), Mn(II) and Cu(II) is 0.1–20 mg/L, 0.1–12 mg/L and 0.2–12 mg/L, respectively. The limit of detection for Fe(III), Mn(II) and Cu(II) is 0.07, 0.02 and 0.1 mg/L respectively. And the limit of quantification for Fe(III), Mn(II) and Cu(II) is 0.2, 0.07 and 0.3 mg/L, respectively. The recoveries of spiked Fe (III), Mn (II), and Cu (II) in real water samples are between 95.3 % to 106 %. Finally, the developed microfluidic chip based FIA system was successfully applied to simultaneous determination of three metal ions in environmental water samples and zinc smelting solution from zinc hydrometallurgy industry with satisfied results.
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TRANSACTIONS OF TIANJIN UNIVERSITY
·
2018
·Vol. 24
·期 4
·361-369
·
IF 0
Zhang Xubin,Dong Jianxin,Hao Zhencheng,Cai Wangfeng,Wang Fumin
Active Fe- and Mn-loaded MCM-41 (Fe–Mn/MCM-41), which was synthesized via a hydrothermal reaction followed by impregnation, is used in the heterogeneous Fenton reaction to degrade methyl orange (MO) in aqueous solution. The synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, N 2 adsorption–desorption isotherm analysis, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Compared with Fe/MCM-41 and Mn/MCM-41, Fe–Mn/MCM-41 showed higher activity for MO degradation and mineralization. Effects of various operating parameters, such as pH, Mn content, and H 2 O 2 dosage, on the degradation process were subsequently investigated. Results of experiments on the effect of radical scavengers revealed that the degradation of MO could be attributed to oxidation by HO·. The synergy of Fe and Mn species in the Fenton oxidation process was also explained.
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Applied Sciences-Basel
·
2018
·Vol. 8
·期 1
·95
·
IF 1.689
Chengzhi Wang,Cheng Zhang,Yonggang Zhao,Xin Yan,Peng Cao
Honeycomb cordierite-based Mn–Ce/Al2O3catalysts were prepared by the impregnation method and used for low-temperature selective catalytic reduction (SCR) of NOxwith NH3, with and without SO2and/or H2O in a homemade fixed-bed tubular reactor. The catalyst reached nearly 80% NOxconversion at 100 °C in the absence of SO2. However, SO2reduces the catalytic activity (80% to 72%) of the honeycomb cordierite-based Mn–Ce/Al2O3catalysts under identical conditions. This finding demonstrated that the catalyst exhibited high activity at low temperature and excellent SO2resistance in the presence of 50 ppm SO2. The fresh and sulfated honeycomb cordierite-based Mn–Ce/Al2O3catalysts were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), N2adsorption–desorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetry and differential thermal analysis (TG-DTA), and Fourier transform infrared (FT-IR) spectroscopy. Characterization results indicated that the deactivation by SO2was primarily the result of the deposition of ammonium hydrogen sulfate and sulfated CeO2on the catalyst surface during the SCR process. The formed sulfates depressed the catalytic activity via the blocking of pores and the occupation of active sites. Additionally, the competitive adsorption between SO2and NH3always decreased the catalytic activity.Keywords:Mn–Ce/Al2O3catalyst;low temperature selective catalytic reduction;honeycomb cordierite;SO2resistance
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Journal of Environmental Chemical Engineering
·
2024
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IF 7.4
Ying Huang,Juan Lei,Baobao Bai,Xiaoli Ren,Lijun Cheng,Yu Cao,Shuang Wang,Jinping Li
Traditional powder catalysts are not suitable for industrial applications due to low utilization of active phase and easy sintering. Therefore, monolithic catalyst MCCF with good stability and water-resistance was designed for the catalytic oxidation of toluene-acetone mixture, in which amorphous MnO x derived via pyrolysis of Mn-MOFs loaded on copper foam (CF) and different transition layers were employed between MnO x and CF to regulate Cu-Mn interaction. The combined action of amorphous MnO x and the Cu-Mn strong interaction enhanced the catalytic degradation of toluene-acetone mixture. The existence of amorphous MnO x and the impacts of Cu-Mn interaction on weakening Mn-O bonds and stimulating reactive oxygen species were verified by various characterizations. Furthermore, the reaction pathways of toluene and acetone on catalyst MCCF were revealed as well as their interactions within the mixture.
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Chemistry-An Asian Journal
·
2024
·Vol. 19
·期 15
·e202400482
·
IF 3.5
Jiahua Wu,Xuan Yang,Dong Xu,Say Leong Ong,Jiangyong Hu
While numerous persulfate-based advanced oxidation processes (AOPs) have been studied based on fancy catalysts, the practical combination of Fe or Mn modified granular activated carbon (GAC) has seldom been investigated. The present study focused on a green and readily synthesized Fe−Mn bimetallic oxide doped GAC (Fe−Mn@GAC), to uncover its catalytic kinetics and mechanism when used in the peroxydisulfate (PDS)-based oxidation process for degrading Rhodamine B (RhB), a representative xenobiotic dye. The synthesized Fe−Mn@GAC was characterized by SEM-EDS, XRD, ICP-OES and XPS analyses to confirm its physicochemical properties. The catalytic kinetics of Fe−Mn@GAC+PDS system were evaluated under varying conditions, including PDS and catalyst dosages, solution pH, and the presence of anions. It was found Fe−Mn@GAC exhibited robust catalytic performance, being insensitive to a wide pH range from 3 to 11, and the presence of anions such as Cl − , SO 4 2− , NO 3 − and CO 3 2− . The catalytic mechanism was investigated by EPR and quenching experiments. The results indicated the catalytic system processed a non-radical oxidation pathway, dominated by direct electron transfer between RhB and Fe−Mn@GAC, with singlet oxygen ( 1 O 2 ) playing a secondary role. The catalytic system also managed to maintain a RhB removal above 81 % in successive 10 cycles, and recover to 89.5 % after simple DI water rinse, showing great reusability. The catalytic system was further challenged by real dye-containing wastewater, achieving a decolorization rate of 84.5 %. This work not only provides fresh insight into the kinetics and mechanism of the Fe−Mn@GAC+PDS catalytic system, but also demonstrates its potential in the practical application in real dye-containing wastewater treatment.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Shuangjun Li,Xiangping Xiao,Luyang Zuo,Rui Li,Lijun Liu,Huitao Fan,Bo Li,Liya Wang
Designing semiconductor photocatalysts with unique structures can improve the transfer efficiency of solar energy to hydrogen (H 2 ). In this study, a dual modification method of element doping and morphological control was used. The Mn-doped hollow octahedron ZnIn 2 S 4 (ZHO-Mn) was synthesized by a simple one-pot solvothermal method using the octahedral Mn-based metal–organic framework (Mn-MOF) as a template. Experiments and theoretical calculations show that the ZHO-Mn has additional active sites, strong light absorption ability and good photoelectric performance. The H 2 production performance of optimized ZHO-Mn10 was the best (11.9 mmol h −1 g −1 ), which was 7.4 times that of monomer ZnIn 2 S 4 (1.6 mmol h −1 g −1 ). This study provides a new one-step method for the dual control of doping and morphology of ZnIn 2 S 4 photocatalyst
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ACS Omega
·
2024
·
IF 3.7
Qingjing Liu,Ruisheng Wang,Ranjia Li,Xiaosheng Wang,Suoqi Zhao,Changchun Yu
Mn–Na2WO4-based catalysts with different supports were prepared using the incipient wetness impregnation method and evaluated for their oxidative coupling of methane (OCM) reaction performance. The results demonstrated that the SiO2- supported catalyst exhibited the best catalytic performance, and the introduction of H2O further enhanced its activity. Under the conditions of a feed gas mixture of CH4/O2/H2O = 6:1:24 at 800 °C and atmospheric pressure, the CH4 conversion and C2+ selectivity over the Mn–Na2WO4/SiO2 catalyst increased from 28.4% and 77.4% (without H2O) to 33.2% and 84.9%, respectively. In contrast, the catalytic activity using TiO2 and MgO supports drastically declined. Characterizations using X-ray diffraction (XRD), in situ infrared spectroscopy (In-situ IR), X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H2-TPR), and oxygen temperature-programmed desorption (O2-TPD) revealed that the introduction of steam not only served as a diluent to decrease the partial pressures of the reactants CH4 and O2, thereby reducing deep oxidation reactions in the gas phase, but also interacted with surface oxygen species (O22–) and silica to form adjacent surface-bonded disilanol free radicals Si–OIH. This interaction facilitated the dehydrogenation and coupling of two methane molecules on the catalyst surface, resulting in the generation of C2+ products, significantly enhancing the catalytic activity and selectivity of OCM.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Mingfu Li,Shuanglan Hu,Yingchuan Zhang,Jiannan Qin,Douyong Min,Chunlin Chen,Pingjun Zhang,Liqun Jiang,Jian Zhang
The green oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) is a crucial step in the development of sustainable and degradable plastics. Here, a series of MnCO 3 -Mn x Co 3-x O 4 -Ov composite oxides are synthesized by a simple solid-state grinding and carbonization method, exhibiting a 100 % HMF conversion rate and 98.7 % FDCA yield directly using air as the oxygen source. Physicochemical characterizations indicate that the introduced carbon promotes the diffusion of Mn species and reduction of Co 3 + /Co 4+ , resulting in more unsaturated coordination of Co–O and the enhanced formation of oxygen vacancies (O v ). The kinetic analysis suggests that the oxidation of HMF to FDCA can be effectively promoted by regulating the O v content in the catalyst after changing the Mn/Co ratio. Moreover, density functional theory (DFT) calculations demonstrate the crucial role of O v in reducing the adsorption energy of HMF on the catalyst surface and activation of O 2 molecules to replenish lattice oxygens during the completion of the catalytic cycle. This work provides a promising strategy to engineer transition metals as alternatives to noble metal-based catalysts towards catalytic oxidation for the production of biofuels and bioplastics.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
·
IF 9
Nan Li,Haibo Liu,Bin Yang,Bo Xie,Yangtao Wu,Lingjun Bu,Shiqing Zhou
This study establishes a manganese-activated ferrate (Mn(II)/Fe(VI)) process for autonomous Microcystis aeruginosa removal, addressing the critical challenge of additive dependency and secondary pollution in conventional algal control strategies. System performance was critically governed by Mn/Fe stoichiometric ratios and total oxidant dosages, with near-complete algal elimination (>98 %) achieved at Mn/Fe = 1:1 (≥200 μM total dosage) while maintaining cell integrity. TOC analysis revealed dosage-dependent control over cellular lysis and intracellular organic matter (IOM) releasing. Spectroscopic characterization demonstrated process efficacy in degrading dissolved organics through decreased UV 254 absorbance (unsaturation reduction), declining SUVA (aromaticity loss), and elevated E2/E3 ratios (molecular weight reduction). Comparative analyses identified dissolved organic carbon as a more sensitive cellular stress indicator than K + release, attributed to MnO 2 adsorptive sequestration of released intracellular constituents. Mechanistic investigations revealed dual role of Mn(II) that rapid surface accumulation provided oxidative protection, while subsequent Fe(VI)-driven MnO x formation enabled floc growth through particle bridging. Water matrix effects followed valence-specific modulation, where divalent cations (Ca 2+ /Mg 2+ ) enhanced removal via charge screening, and excessive monovalent ions (Na + /NH 4 + ) impaired efficiency through ionic strength interference. This work pioneers a green oxidation-coagulation synergy that eliminates supplemental additives, offering a sustainable paradigm for mitigating cell rupture and IOM release in algae-laden water treatment.
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Materials Today Chemistry
·
2025
·
IF 6.7
Qing Chen,Xinyu Zou,Ling Shi,Maocong Hu,Mao Peng,Zhenhua Yao
While bifunctional electrocatalysts enabling both oxygen reduction (ORR) and oxygen evolution (OER) reactions are recognized as pivotal chemical steps for next-generation energy devices, their practical implementation persists as a formidable scientific challenge. In this study, hetero-structured catalyst (CrFeCoNiCu/Mn 3 O 4 /MnO/NC) was successfully synthesized in situ containing both high-entropy alloy and spinel manganese-based oxide by a simple heat treatment process while two control samples (CrFeCoNiCu/Mn 3 O 4 /NC and CrFeCoNiCu/NC) were also prepared. It exhibited excellent catalytic performance and stability for both ORR and OER compared with commercial Pt/C and RuO 2 catalysts. The superior bifunctional performance was further observed with the overpotential gaps (ΔE gap ) of the three electrodes being 0.634 V, 0.655 V, and 0.698 V, respectively, which were lower than those of the combination of RuO 2 and Pt/C at 0.723 V. The enhanced catalytic performance was subsequently corroborated by density-functional theory (DFT). This study proposes an alternative method for the synthesis and design of high-performance bifunctional electrocatalysts.
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2025
·
IF 1.6
Liu Xinying,Lei Yuhan,Shi Jialin,Wang Zixuan,Zhang Wenxiu,Zhang Guanghui,Gu Ping
A novel adsorbent, Mn-MOF-74, was synthesized using a room-temperature, water-based method by assembling Mn 2+ metal nodes with 2,5-dihydroxyterephthalic acid ligands, and was further applied for Co 2+ removal. Mn-MOF-74 exhibited minimal pH dependence within a pH range of 3–8.5, achieving Co 2+ removal efficiencies between 92.5 and 96.3%, with a distribution coefficient of up to 2.9 × 10 4 mL·g −1 . A function relationship between the Co 2+ removal efficiency and the adsorbent dosage or initial concentration was proposed. The dominant removal mechanism was identified as ion exchange between Mn 2+ and Co 2+ , with chemisorption being the primary rate-limiting step.
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