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ACS Applied Nano Materials · 2024 · IF 5.3

3D MoS2/MgIn2S4 Nanoflower Heterojunctions for Photoreduction of Cr(VI): Mechanism, Influence, and Toxicity Evaluation

Xingrui Tong,Jinling Bao,Danfeng Chang,Dapeng Wang,Haibo Chang,Liquan Jing

Designing an efficient hole–electron separation method is essential to improving the photocatalytic efficiency of photocatalysts. Herein, we constructed a 3D MoS2/MgIn2S4 S-scheme heterojunction material using a solvothermal method. The built-in electric field formed by the interaction between MoS2 and MgIn2S4 promoted the separation of electrons and holes, significantly improving the photocatalytic activity of 3D MoS2/MgIn2S4. The 3% MoS2/MgIn2S4 composite photocatalyst successfully achieved a 100% reduction of Cr(VI) within 90 min and demonstrated good hydrogen production efficiency without using a sacrificial agent. Theoretical calculations confirmed the formation of S-scheme heterojunctions. Malondialdehyde and dehydrogenase tests showed that the Cr(VI) solution after reduction was not harmful to plant growth. Furthermore, we systematically investigated the effects of different Cr(VI) concentrations, catalyst dosages, ions, pH values, and organic acids on photocatalytic efficiency. The design of the S-scheme heterojunction photocatalysts provided a promising strategy for the photoreduction of Cr(VI).

研究领域: 环境科学 · 材料科学 · 化学工程
✓ 已验证 DOI 高影响因子
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ENVIRONMENTAL POLLUTION · 2016 · IF 4.839

Facile preparation of magnetic mesoporous MnFe2O4@SiO2−CTAB composites for Cr(VI) adsorption and reduction

Na Li,Fenglian Fu,Jianwei Lu,Zecong Ding,Bing Tang,Jiabin Pang

Chromium-contaminated water is regarded as one of the biggest threats to human health. In this study, a novel magnetic mesoporous MnFe 2 O 4 @SiO 2 −CTAB composite was prepared by a facile one-step modification method and applied to remove Cr(VI). X-ray diffraction, scanning electron microscopy, transmission electron microscopy , specific surface area, and vibrating sample magnetometer were used to characterize MnFe 2 O 4 @SiO 2 −CTAB composites. The morphology analysis showed that the composites displayed a core-shell structure. The outer shell was mesoporous silica with CTAB and the core was MnFe 2 O 4 nanoparticles , which ensured the easy separation by an external magnetic field. The performance of MnFe 2 O 4 @SiO 2 −CTAB composites in Cr(VI) removal was far better than that of bare MnFe 2 O 4 nanoparticles. There were two reasons for the effective removal of Cr(VI) by MnFe 2 O 4 @SiO 2 −CTAB composites: (1) mesoporous silica shell with abundant CTA + significantly enhanced the Cr(VI) adsorption capacity of the composites; (2) a portion of Cr(VI) was reduced to less toxic Cr(III) by MnFe 2 O 4 , followed by Cr(III) immobilized on MnFe 2 O 4 @SiO 2 −CTAB composites, which had been demonstrated by X-ray photoelectron spectroscopy results. The adsorption of Cr(VI) onto MnFe 2 O 4 @SiO 2 −CTAB followed the Freundlich isotherm model and pseudo-second-order model. Tests on the regeneration and reuse of the composites were performed. The removal efficiency of Cr(VI) still retained 92.4% in the sixth cycle. MnFe 2 O 4 @SiO 2 −CTAB composites exhibited a great potential for the removal of Cr(VI) from water.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI PubMed 高影响因子
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DALTON TRANSACTIONS · 2020 ·Vol. 49 ·期 14 ·4570-4577 · IF 4.174

Polyoxometalate-based crystalline materials as a highly sensitive electrochemical sensor for detecting trace Cr(VI)

Xing Xin,Na Hu,Yuanyuan Ma,Yali Wang,Lin Hou,Heng Zhang,Zhangang Han

It is crucial to find a convenient and sensitive method for quantitative determination of heavy metal chromium(VI) ions. Developing crystalline materials coupled with polyoxometalates as an electrochemical sensor is a promising approach to address the above issues. Here we reported two reductive polyoxometalate-based crystalline compounds with the formula of (H2bpp)2[Na4Fe(H2O)7][Fe(P4Mo6O31H6)2]·2H2O (1) and (H2bpp)6(bpp)2[Fe(P4Mo6O31H8)2]2·13H2O (2) (bpp = 1,3-bi(4-pyridyl)propane). Structural analysis indicated that both two compounds were composed of inorganic polyanionic clusters and organic protonated bpp cations. The difference lies in the arrangement mode of the inorganic moiety: crystal 1 shows a unique three-dimensional (3-D) inorganic porous skeleton, while crystal 2 consists of isolated 0-D polyanionic clusters. When used as electrochemical sensors in the determination of trace Cr(VI), crystal 1 shows a broad linearity range (2–2610 μM) with a low limit of detection (LOD) of 0.174 μM (9 ppb), which is superior to that of compound 2 (a LOD of 0.33 μM) and meets the standard of Cr(VI) in drinking water set by the WHO (less than 0.962 μM or 50 ppb). Importantly, crystal 1 showed benign selectivity to Cr(VI) in the presence of various heavy metal ions and good reproducibility in a real water sample, which prove its strong anti-interference ability. In addition, experimental results showed that the spatial arrangement of polyanionic clusters could affect the final electrochemical behavior of crystalline materials. This work provides some insights into the design of cost-effective POM-based electrochemical sensors at the molecular level.

研究领域: 材料科学 · 环境科学 · 分析化学
✓ 已验证 DOI 高影响因子
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PLASMA SCIENCE & TECHNOLOGY · 2025 · IF 1.8

Plasma modification of UiO-66-(OH)2 metal organic frameworks for photocatalytic Cr(VI) reduction

Ruiting Jian,Qirui Zou,Jianjun Yan,Bowen Liu,Lijun Sang,Zhongwei Liu

Cr(VI), a hazardous heavy metal pollutant found in wastewater, exerts detrimental effects on biological system and the human body. Efficient photocatalytic reduction of Cr(VI) to Cr(III) using high-performance materials offers a viable approach for chromium decontamination. In the current work, the defective UiO-66-(OH)2 with enhanced photocatalytic activity was developed by the plasma treatment. These defects not only triggered an expansion in mesoporous domains and increased the BET surface area of the UiO-66-(OH)2 system, thereby exposing more adsorption and photocatalytically active sites, but also created additional electron migration pathways, enhancing the separation of photogenerated e-/h+ pairs. When subjected to an operating power of 15 W, chamber pressure at 20 Pa, and a 300-second treatment period, UiO-66-(OH)2 exhibited a removal efficiency of 83 %. This work explored a novel way for the construction of the defective MOFs and broadened the utilizationation of MOFs in the fields of photoreduction of heavy metal ions in water.

研究领域: 环境科学 · 材料科学 · 化学工程
✓ 已验证 DOI 高影响因子
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ANALYTICAL CHEMISTRY · 2011 · IF 5.874

Metal–Organic Framework MIL-101(Cr) for High-Performance Liquid Chromatographic Separation of Substituted Aromatics

Cheng-Xiong Yang,Xiu-Ping Yan

The diverse structures and pore topologies, accessible cages and tunnels, and high surface areas make metal–organic frameworks attractive as novel media in separation sciences. Here we report the slurry-packed MIL-101(Cr) column for high-performance liquid chromatographic separation of substituted aromatics. The MIL-101(Cr) packed column (5 cm long × 4.6 mm i.d.) offered high-resolution separation of ethylbenzene (EB) and xylene, dichlorobenzene and chlorotoluene isomers, and EB and styrene. The typical impurities of toluene and o-xylene in EB and styrene mixtures were also efficiently separated on the MIL-101(Cr) packed column. The column efficiencies for EB, m-dichlorobenzene, and m-chlorotoluene are 20000, 13000, and 10000 plates m–1, respectively. The relative standard deviation for five replicate separations of the substituted aromatics was 0.2–0.7%, 0.9–2.9%, 0.5–2.1%, and 0.6–2.7% for the retention time, peak area, peak height, and half peak width, respectively. The MIL-101(Cr) offered high affinity for the ortho-isomer, allowing fast and selective separation of the ortho-isomer from the other isomers within 3 min using dichloromethane as the mobile phase. The effects of the mobile phase composition, injected sample mass, and temperature were investigated. The separation of xylene, dichlorobenzene, and chlorotoluene on MIL-101(Cr) was controlled by entropy change, while the separation of EB and styrene on MIL-101(Cr) was governed by enthalpy change.

研究领域: 分析化学 · 材料科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Enhanced Cr(VI) removal of zero-valent iron with high proton conductive FeC2O4·2H2O shell

Yue Hu,Guangming Zhan,Xing Peng,Xiufan Liu,Zhihui Ai,Falong Jia,Shiyu Cao,Fengjiao Quan,Wenjuan Shen,Lizhi Zhang

In this study, we coated a high proton conductive shell on the zero-valent iron (ZVI) surface by mechanically ball-milling ZVI with oxalic acid dihydrate (OX-ZVI), and demonstrated that the generated FeC 2 O 4 ·2H 2 O shell dramatically improved the Cr(VI) removal rate of ZVI by about 15–80 times. Owing to a higher proton conductivity of FeC 2 O 4 ·2H 2 O shell than that of Fe 2 O 3 shell, proton could easily transfer through FeC 2 O 4 ·2H 2 O shell into iron core and be reduced to H, accompanying with fast surface-bound Fe 2+ generation, resulting in high efficiency of Cr(VI) removal in a wide pH range. Meanwhile, the removed Cr(VI) was deposited on OX-ZVI surface in the formation of Fe x Cr 1-x (OH) 3 composites, accompanied by the appearance of typical hollow structure derived from iron core dissolution. This study clarifies the significance of proton transfer on the reactivity of zero-valent iron, and also provides a new strategy to prepare highly active zero-valent iron for Cr(VI) removal.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2016 ·Vol. 6 ·期 93 ·90232-90238 · IF 3.289

Efficient conversion of furfuryl alcohol to ethyl levulinate with sulfonic acid-functionalized MIL-101(Cr)

Xiao-Fang Liu,Hu Li,Heng Zhang,Hu Pan,Shan Huang,Kai-Li Yang,Song Yang

Catalytic ethanolysis of furfuryl alcohol (FA) to ethyl levulinate (EL) with MIL-101(Cr)–SO3H, prepared by simple one-pot hydrothermal treatment, is presented for the first time. The as-prepared catalyst with high surface area, hydrothermal and chemical stability, good dispersion, and feasible accessibility of –SO3H Brønsted acid sites was found to show superior performance to other sulfonic acid-functionalized solid catalysts. Besides the special textural properties, the obtained good catalytic activity of 79.2% EL yield and 100% FA conversion were also dependent on the density and strength of the Brønsted acid and the reaction parameters. A slight loss of catalytic activity after five consecutive recycles and the hot filtration experiment confirmed the good stability of MIL-101(Cr)–SO3H. Two coexisting reaction paths for the ethanolysis of FA to EL catalyzed by MIL-101(Cr)–SO3H were proposed, wherein 2-ethoxymethylfuran (2-EMF) was observed to be the dominant intermediate.

研究领域: 化学工程 · 催化科学
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Inorganics · 2022 ·Vol. 10 ·期 3 ·33 · IF 3.149

Low-Temperature and Additive-Free Synthesis of Spherical MIL-101(Cr) with Enhanced Dye Adsorption Performance

Tian Zhao,Hexin Zhu,Ming Dong,Minmin Zou,Songfan Tang,Mingliang Luo,Xianggang Li

The chromium-benzenedicarboxylate metal–organic framework (MOF), MIL-101(Cr), is one of the most well-investigated and widely used prototypical MOFs. Regarding its synthesis, the use of a toxic modulator (usually HF) and high reaction temperature (220 °C) are the main factors hindering its further expansion of production and utilization. In fact, high quality MIL-101(Cr) crystals can be prepared at a much lower temperature (160 °C) with spherical morphology via an additive-free approach. Compared to traditional octahedral MIL-101(Cr), the spherical MIL-101(Cr) possesses higher adsorption performance toward dye molecules, including methyl orange (MO) and rhodamine B (RB). The results suggest that toxic additives and high reaction temperatures are not essential in the synthesis of MIL-101(Cr), and the fabrication of spherical MIL-101(Cr) may offer a facile and effective pathway for the large-scale industrial application of MIL-101(Cr).

研究领域: 材料科学 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Efficient removal of Cr(VI) using recycled MgO from laterite nickel ore by fly ash doping

Liqing Zhang,Bo Li,Yonggang Wei,Haoyuan Xu

Environmental problems caused by Cr(VI) need to be solved urgently. As a green and safe adsorbent, magnesium oxide has the characteristics of strong adsorption capacity and safety, non-toxic and harmless. In this study, high-performance Cr(VI) adsorption material (F-MgO) was prepared by combination hydrothermal modification of recycling MgO and doping of solid waste fly ash with the MgO that was a by-product of high magnesium laterite nickel ore. The adsorption properties of F MgO composites for Cr(VI) were evaluated, and the maximum adsorption capacity of Cr(VI) by F MgO reaches 172.6 mg/g at pH = 2.0. The F-MgO also showed high stability and excellent cycle adsorption performance. The adsorption mechanism was extensively studied by adsorption kinetics and DFT theoretical calculation, and electrostatic adsorption and chemical interaction between Cr(VI) and F MgO active sites were demonstrated. The prepared F MgO composites from waste resources with a simple synthetic method have great potential in the treatment of chrome-containing wastewater to achieve the purpose of treating waste with waste.

研究领域: 环境科学 · 材料科学
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INORGANIC CHEMISTRY · 2024 · IF 4.3

Polyoxometalate Functionalized Cyclic Trinuclear Copper Compounds for Bifunctional Electrochemical Detection and Photocatalytic Reduction of Cr(VI)

Lin Yang,Zhou Yuan,Lufang He,Le Han,Bohan Li,Yan Xu

The design and intentional construction of crystalline materials containing two clusters with redox properties in one framework still remains challenging. Linking oxidative polyoxometalate (POM) clusters and a reductive cyclic trinuclear copper complex (Cu-CTC) to prepare stable catalysts is rarely reported. Herein, we successfully obtained two new polyoxometalate-based metal–organic compounds (POMOCs) [CuII3(PyCA)3(μ3-OH)(β-Mo8O26)0.5(H2O)2]·5H2O (1), [CuII3(PyCA)3(μ3-OH)]2(CuIIW12O40)[CuII(H2O)6] (2) (PyCA = 1H-pyrazole-4-carbaldehyde) by enabling precursors of Cu-CTC and POM cocrystallization in one pot via hydrothermal method. The [β-Mo8O26]4– cluster in compound 1 combined with Cu-CTC units to form a 1D structure, and the [CuW12O40]6– unit in compound 2 linked two Cu-CTC units to form a sandwich-like 0D structure. Also, Cu-CTC CuI3(PyCA)3·H2O (Cu3) was synthesized for performance comparison. A series of characterizations indicate that compound 1 is more conducive to electron transfer than compound 2. In addition, compounds 1 and 2 can act as bifunctional catalysts for the electrochemical detection and photocatalytic reduction of Cr(VI). Particularly, the photoreduction rates of Cr(VI) by compounds 1 and 2 are 96.7% and 96.3% for only 10 and 14 min under visible light, respectively, and it is better than that of Cu3 and most other reported photocatalysts. Furthermore, the active sites and mechanisms for electrochemical detection and photocatalytic reduction of Cr(VI) were discussed.

研究领域: 材料科学 · 环境科学 · 电化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Journal of Materiomics · 2025 · IF 9.6

Mechanical alloyed FeCoNiMoM (M=Cr, Cu) high-entropy alloy powders as electrocatalysts for oxygen evolution reaction

Caizhen Wu,Xin Zhang,Yingjie Zhang,Wensheng Ma,Degang Zhao,Bingbing Ren,Zhonghua Zhang,Yan Wang

Here, micron-sized high-entropy alloy (HEA) electrocatalysts (FeCoNiMoCr, Cr-HEA; FeCoNiMoCu, Cu-HEA) with dual-phase heterostructures were fabricated by mechanical alloying and subsequently loaded onto nickel foam (NF) to form the working electrode, exhibiting excellent oxygen evolution reaction (OER) performance. Specifically, the Cr-HEA/NF exhibits an overpotential of 271 mV at current density of 10 mA/cm 2 and a small Tafel slope of 69.1 mV/dec in 1 mol/L KOH solution, outperforming the performance of Cu-HEA/NF, commercial RuO 2 /NF and bare NF. HEA catalysts achieve outstanding long-term stability, as evidenced by chronopotentiometry (1 mol/L KOH for 48 h @10 mA/cm 2 and 6 mol/L KOH at 85 °C for 100 h @500 mA/cm 2 ) and chronoamperometry (1 mol/L KOH for 100 h @100 mA/cm 2 ). The impressive OER activity and stability of Cr-HEA can be attributed to the highly heterogeneous nested interfaces between amorphous and metastable nanocrystals, as well as the in-situ formation of multiphase structures. Notably, both density functional theory calculations and experimental results demonstrate that the synergistic interactions among the metal active sites in HEA collectively regulate the adsorption and desorption of oxygen-containing intermediates, thereby enhancing the OER catalytic activity. Specifically, the Cr-HEA presents a lower Gibbs free energy change during the transformation from O* to OOH*, resulting in a reduced overpotential.

CAS / MDL: 12036-10-1
研究领域: 材料科学 · 电化学
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2019 · IF 2.931

One-step synthesized fluorescent nitrogen doped carbon dots from thymidine for Cr (VI) detection in water

Fanglin Ming,Jingzhou Hou,Changjun Hou,Mei Yang,Xianfeng Wang,Jiawei Li,Danqun Huo,Qiang He

A novel, simple and low-cost nitrogen doped carbon dots (N-CDs) fluorescent sensor for sensitive detection of Cr (VI) was developed via one-step hydrothermal method using thymidine as carbon source. As-prepared N-CDs exhibited the ability of sensitive and selective detection of Cr (VI) through the inner filter effect (IFE). The performances of N-CDs were investigated with the characterization methods of transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Under the optimized conditions, a good logarithm correlation between the fluorescence intensity of N-CD S and the concentration of Cr (VI) was obtained ranging from 0.1 μM to 430 μM (R 2  = 0.992), with a low detection limit (LOD; S/N = 3) of 1.26 nM. The fluorescent sensor showed good repeatability, reproducibility and stability. Furthermore, N-CDs fluorescent sensor had a good applicability for Cr (VI) detection in real water samples with acceptable recoveries, and the detection results were consistent with the inductively coupled plasma mass spectrometry (ICP-MS) results, indicating this fluorescent sensor has a great potential for the environmental monitoring.

研究领域: 分析化学 · 环境科学 · 材料科学
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