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RSC Advances · 2018 ·Vol. 8 ·期 22 ·12459-12470 · IF 2.936

Heterostructured Bi2S3@NH2-MIL-125(Ti) nanocomposite as a bifunctional photocatalyst for Cr(VI) reduction and rhodamine B degradation under visible light

Minghua Wang,Longyu Yang,Jinyun Yuan,Linghao He,Yingpan Song,Hongzhong Zhang,Zhihong Zhang,Shaoming Fang

A series of bismuth sulfide (Bi2S3) nanorods and amine-functionalized Ti-based metal–organic framework heterojunctions [denoted by Bi2S3@NH2-MIL-125(Ti)] were constructed and explored as bifunctional photocatalysts for Cr(VI) reduction and rhodamine B (RhB) degradation under visible light illumination. Compared with the individual NH2-MIL-125(Ti) and Bi2S3, the as-synthesized Bi2S3@NH2-MIL-125(Ti) photocatalyst exhibited an enhanced photocatalytic activity toward Cr(VI) and RhB owning to the synergetic effect between Bi2S3 and NH2-MIL-125(Ti). Moreover, the Bi2S3@NH2-MIL-125(Ti) heterojunctions showed increased Cr(VI) removal efficiency by adding RhB in the system. The photocatalytic mechanism was proposed based on the analysis of different scavenger for active species and electron spin resonance spectrometry. The introduction of Bi2S3 into NH2-MIL-125(Ti) can extend the light adsorption and improve the transfer and separation of photogenerated charge carriers through the Bi2S3@NH2-MIL-125(Ti) heterojunction with unique band gap structure. The synthesized Bi2S3@NH2-MIL-125(Ti) photocatalyst also exhibited good reusability and stability.

研究领域: 材料科学 · 环境科学 · 化学
✓ 已验证 DOI PubMed 高影响因子
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Low molecular weight organic acids strengthen the electron transfer of natural FeS2/biochar composite for Cr(VI) reduction: Experimental observations and governing mechanisms

Beibei Zhao,Jingchun Tang,Honghong Lyu,Feng Liu,Lan Wang

Low molecular weight organic acids with low cost and environmentally friendly characteristics can enhance the electron transfer between materials and contaminants. In this study, oxalic acid (OA), citric acid (CA), and ethylenediaminetetraacetic acid (EDTA) were selected to strengthen ball milled natural FeS 2 /biochar composite (FeS 2 /biochar) for aqueous Cr(VI) removal. 100% of Cr(VI) was removed when 5 mM of OA and 0.25 g·L −1 FeS 2 /biochar were used together. In contrast, the removal rate of Cr(VI) by the individual FeS 2 /biochar and OA was 57.9% and 6.3%, respectively. The experimental and characterization results suggested that OA was adsorbed on the surface of FeS 2 /biochar through the conjugated structure of pine biochar, thereby enhancing the dissolution rate of Fe(II) and S(-II) in the FeS 2 /biochar composite, and facilitating the conversion of Fe(II), S(-II), and Cr(VI) to Fe(III), SO 4 2- , and Cr(III), respectively. In addition, the complexation of OA with Fe(III) and Cr(III) reduced the formation of Fe(OH) 3 and Cr(OH) 3 , exposing more surface active site of FeS 2 /biochar for the reduction of Cr(VI). As an electron donor , the addition of OA enhanced the electron transfer process of FeS 2 /biochar to Cr(VI) on the one hand, and on the other hand promoted the redox cycle of Fe(II) through the electron transfer between OA and Fe ions . FeS 2 /biochar showed better stability even after 5 cycles (in 5 mM OA system). The present study demonstrated the promise of low molecular weight organic acids in strengthening materials for environmental remediation.

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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Small · 2022 ·Vol. 19 ·期 10 ·2205619 · IF 15.153

“Blockchain-Like” MIL-101(Cr)/Carbon Black Electrodes for Unprecedented Defluorination by Capacitive Deionization

Fei Yu,Xiaochen Zhang,Peng Liu,Bingbing Chen,Jie Ma

Metal-organic frameworks (MOF) have attracted extensive attention due to their ultra-high specific surface area and tunable structure, the mechanism of direct utilization for capacitive deionization (CDI) defluorination remains undefined. Here, MIL-101(Cr) with ultra-high specific surface area, high water stability, and open metal sites (OMSs) is prepared by a hydrothermal method for defluorination of CDI. Carbon black is used as a “chain” to connect F-stored in the holes of MIL-101(Cr) (Cr-MOF)as “blocks” to enhance the conductivity and ion storage capacity of MIL-101(Cr)/carbon black electrodes (Cr-MOF electrodes). This simple construction method avoids the process complexity of in situ synthesis and performs better. These easily constructed “blockchain-like” Cr-MOF electrodes exhibit excellent defluorination capacity (39.84 mg NaF g electrodes −1 ), low energy consumption (1.2 kWh kg NaF −1 ), and good stability. The coupling of the electrochemical redox reaction of Cr 3+ /Cr 4+ with confined water is investigated using in situ and ex situ analysis methods combined with density functional theory (DFT), resulting in an unprecedented defluorination mechanism for Cr-MOF electrodes. This study opens up new ideas for the application of MOF in CDI, clarifies the removal mechanism of MOF, and lays a foundation for further promoting the application of raw materials with poor conductivity in the field of CDI.

研究领域: 环境科学 · 材料科学 · 化学工程 · 电化学
✓ 已验证 DOI PubMed 高影响因子
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2025 · IF 5.4

Polysaccharide self-crosslinking and refrigerated air-drying interfacial modification: A new approach for konjac glucomannan-guar gum thin film loaded with NZVI for enhanced Cr(VI) removal

Xiangyu Wang,Fei Ge,Ping Ning,Zhiling Guo,Peng Zhang,Lisi Wu,Iseult Lynch

For facile fabrication of environmentally friendly nanoparticle film carriers, the present study utilized sodium periodate to oxidize and induce the self-crosslinking of konjac glucomannan (KGM) and guar gum (GG). Innovatively, the film preparation process involves refrigerated air-drying technique to simultaneously achieve interface modification. The dendritic structure and swelling characteristics produced by the refrigerated air-drying technique significantly increased the specific surface area and improved the dispersion and loading of NZVI. The biodegradable and swell-hydrolyzable characteristics of KGM-GG enabled the green treatment of the carriers. To evaluate the performance of the film, a composite material with highly dispersed nanoscale zero-valent iron (NZVI) was prepared to remove Cr(Ⅵ) in a wide pH range, especially under strongly acidic media. At room temperature and pH 2.0, Fe 0 /KGM-GG loaded with 1.2 mg of NZVI could completely remove Cr(Ⅵ) within 60 min. By characterization analysis, this rapid removal may be achieved by synergistic interactions such as adsorption, reduction, co-precipitation, and formation of bidentate-mononuclear complexes. The results showed that Fe 0 /KGM-GG had a good anti-interference ability in the presence of HA and coexisting ions. In this study, a new method for preparing environmentally friendly nanoparticle carriers with high loading and high dispersion through polysaccharide self-crosslinking and refrigerated air-drying film-making technology has been proposed, which provides a new way for green and sustainable synthesis of nanoparticle carrier materials.

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
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Journal of Materials Chemistry A · 2024 · IF 10.7

High-efficiency photocatalytic reduction of Cr(VI) by Z-scheme electron transfer in UiO-66-NH2@HDU-25 heterojunctions

Wen Lu,Chen Wang,Wenhui Song,Zhixiong Zhang,Chengde Xie,Jianjun Wang

The heavy metal ion hexavalent chromium (Cr(VI)) in wastewater significantly threatens public health. Heterojunction photocatalysts typically demonstrate high reduction efficiency in water for Cr(VI) contamination. Overcoming the drawbacks of single metal organic frameworks (MOFs) or covalent organic frameworks (COFs), MOF@COF heterostructures inherit the advantages of large porosity, high surface area, and multiple active sites of single components. Herein, we report novel hybrid UiO-66-NH2@HDU-25 heterojunctions based on a condensation reaction. The optimal ratio of UiO-66-NH2@HDU-25 presented significantly superior photocatalytic activity to most reported MOFs and COFs due to heterojunction formation, which promoted charge separation. Under identical conditions, the optimally formulated UiO-66-NH2@HDU-25 could remove over 99% of Cr(VI), approximately 1.8 and 2.6 times the original UiO-66-NH2 and HDU-25 levels. Furthermore, the UiO-66-NH2@HDU-25 (8 : 1) heterojunction demonstrated favorable reusability and stability over five reaction cycles. Various experiments and density functional theory (DFT) calculations investigated the charge carrier transport pathways and possible photocatalytic mechanisms. The Z-scheme mechanism for the photocatalytic Cr(VI) reduction by UiO-66-NH2@HDU-25 was proposed and validated. This work aims to open new horizons for preparing novel photocatalyst heterojunctions with excellent visible light responsiveness for environmental water remediation.

研究领域: 环境科学 · 材料科学 · 化学工程 · 光化学
✓ 已验证 DOI 高影响因子
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WATER RESEARCH · 2022 · IF 13.4

A process-based model for describing redox kinetics of Cr(VI) in natural sediments containing variable reactive Fe(II) species

Jingli Ren,Yutong Liu,Weimin Cao,Liyang Zhang,Fen Xu,Juan Liu,Yubo Wen,Jian Xiao,Lei Wang,Xiaoxiong Zhuo,Junfeng Ji,Yuanyuan Liu

Sediment-associated Fe(II) is a critical reductant for immobilizing groundwater contaminants, such as Cr(VI). The reduction reactivity of sediment-associated Fe(II) is dependent on its binding environment and influenced by the biogeochemical transformation of other elements (i.e., C, N and Mn), challenging the description and prediction of the reactivity of Fe(II) in natural sediments. Here, anaerobic batch experiments were conducted to study the variation in sediment-associated Fe(II) reactivity toward Cr(VI) in natural sediments collected from an intensive agricultural area located in Guangxi, China, where nitrate is a common surface water and groundwater contaminant. Then, a process-based model was developed to describe the coupled biogeochemical processes of C, N, Mn, Fe, and Cr. In the process-based model, Cr(VI) reduction by sediment-associated Fe(II) was described using a previously developed multirate model, which categorized the reactive Fe(II) into three fractions based on their extractabilities in sodium acetate and HCl solutions. The experimental results showed that Fe(II) generation was inhibited by NO 3 - and/or NO 2 − . After NO 3 − and NO 2 − were exhausted, the Fe(II) content and its reduction rate toward Cr(VI) increased rapidly. As the Fe(II) content increased, the three reactive Fe(II) fractions exhibited approximately linear correlations with aqueous Fe(II) concentrations ( C F e 2 + CFe2+ ), which was probably driven by sorptive equilibrium and redox equilibrium between aqueous and solid phases. The model results indicated that the reaction rate constants of the three Fe(II) fractions ( k n ) significantly increased with incubation time, and log( k n ) correlated well with C F e 2 + CFe2+ [ log ( k 1 ) = 2.84 C F e 2 + − 0.17 log(k1)=2.84CFe2+−0.17 , log ( k 2 ) = 5.90 C F e 2 + − 2.49 log(k2)=5.90CFe2+−2.49 and log ( k 3 ) = 3.09 C F e 2 + − 3.37 log(k3)=3.09CFe2+−3.37 ]. The numerical model developed in this study provides an applicable method to describe and predict Cr(VI) removal from groundwater under dynamic redox conditions .

研究领域: 环境科学 · 地球化学 · 水文地质学 · 生物地球化学
✓ 已验证 DOI 高影响因子
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Nanotechnology Reviews · 2021 ·Vol. 10 ·期 1 ·847-856 · IF 7.848

Triethanolamine interface modification of crystallized ZnO nanospheres enabling fast photocatalytic hazard-free treatment of Cr(vi) ions

Xiaowen Su,Zehua Wang,Yuan Huang,Zhenyu Miao,Shuhua Wang,Jianjun Wang,Xiao Li Zhang,Xiaomin Sun,Hong Liu,Yuanhua Sang

The hazard-free treatment of Cr( vi ) ions is critical in modern industry. Photocatalytic reduction and detoxification are high-potential strategies. Photocatalysts with high efficiency, low cost, environmental friendliness, and easy mass products are required. In this study, we report a facile strategy using triethanolamine (TEOA) as a capping ligand to modify the surface of ZnO nanospheres. The experimental and theoretical results reveal that the presence of TEOA on the surface was beneficial for electron enrichment on Zn and hole transfer to TEOA and can photocatalytically reduce Cr( vi ) by almost 100% in 5 min. The photocatalytic property of TEOA-modified ZnO could be renewed by the reabsorption of TEOA in solution. The great sedimental properties benefit photocatalyst recycling and renewal, which also provides high potential for water pollution and environmental emergency responses applications.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
✓ 已验证 DOI 高影响因子
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Food Science & Nutrition · 2022 ·Vol. 10 ·期 7 ·2224-2235 · IF 3.553

Fe3O4@PDA/MIL-101(Cr) as magnetic solid-phase extraction sorbent for mycotoxins in licorice prior to ultrahigh-performance liquid chromatography-tandem mass spectrometry analysis

Zhentao Tang,Qingrong Han,Gang Yu,Fei Liu,Yuzhu Tan,Cheng Peng

Magnetic solid-phase extraction (MSPE) strategy based on the Fe 3 O 4 @PDA/MIL-101(Cr) has been proposed to separate and purify five common mycotoxins in licorice, including aflatoxin B 1 , aflatoxin G 1 , sterigmatocystin, zearalenone, and ochratoxin A. Integrating the MSPE and solid–liquid extraction/partitioning, a modified QuEChERS was established to adapt to the complex licorice samples. The Fe 3 O 4 @PDA/MIL-101(Cr) was successfully synthesized and characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and nitrogen adsorption–desorption isotherms. Sorbents with superior advantages for exclusion of matrix interference and extraction of target analytes in a short time were obtained, according to their ability of magnetic separation, high surface area (287.75 m 2 /g), large pore volume (0.61 cm 3 /g), and nanosized structure with mesopores. Prior to analysis with ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS), several key parameters that would affect the sorbents’ extraction efficiency were extensively investigated. Under the optimized conditions, the practicality of the developed method for analysis of mycotoxins in licorice samples was confirmed by adequate linearity ( R 2 ≥ 0.9967), high sensitivity (LODs and LOQs, respectively, in the ranges 0.01–0.09 and 0.02–0.30 μg/kg), acceptable recovery (78.53%–116.28%), satisfactory reusability, and good interbatch precision of the sorbents (RSDs in the ranges 6.70%–11.20% and 6.02%–10.35%, respectively). The results indicated that the established method was feasible and reliable for the environment-friendly and rapid screening of mycotoxins in complex licorice samples.

研究领域: 分析化学 · 食品安全 · 中药学
✓ 已验证 DOI 高影响因子
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2024 · IF 3.5

Ultrasonic-assisted activation of clay for efficient removal of U(VI) and Cr(VI)

Yanxue Yue,Weiyu Zhu,Alhadi Ishag,Bo Zhang,Yubing Sun

The natural clay mineral was activated using the acid treatment under ultrasonic conditions to improve its adsorption performance. The acid-activated clay (AAC) was investigated to remove Cr(VI) from wasted lubricant and U(VI) from aqueous solution by batch, spectroscopy, and modeling. Batch experiments showed that the isotherms and adsorption kinetics of Cr(VI)/U(VI) on AAC were satisfactorily followed by Frenudlich and the pseudo-second-order model, respectively. The decreased adsorption of U(VI) on AAC with the increase of ion strength indicated the outer surface complexation of U(VI) on AAC. The interaction mechanism of Cr(VI)/U(VI) on AAC was demonstrated to be surface complexation by oxygenated functional groups (e.g., hydroxyl) according to X-ray photoelectron spectroscopy (XPS) analysis. According to fitting of surface complexation models using three approaches, the adsorption of U(VI) on AAC at different pH can be better fitted by the double-layer model compared to the constant-capacitance model and triple-layer model. These findings are great important for the application of acid activated clay in the removal of heavy metals and radionuclides from the environment.

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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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Rapid photocatalytic reduction of Cr(VI) with high concentration in wastewater by In2S3-ZnIn2S4 heterostructure hierarchical microtubes under visible light

Qian Chen,Xiao Wang,Wanyan Liu,Tao Luo,Zhen Jin,Yong Zhang,Jian Huang,Hua Zhang,Jinhua Wang,Fumin Peng

Currently, Cr(VI) poses a great threat to the human health and ecosystem due to its acute toxicity and potential carcinogenicity. In order to quickly and efficiently reduce Cr(VI) to Cr(III) by photocatalysis , a new In 2 S 3 -ZnIn 2 S 4 heterostructure hierarchical microtubes, which is based on the combination of the main three strategies for the enhancement of photocatalysts’ performance including semiconductor heterostructure, hierarchical microstructure, and hollow morphology, were designed and successfully synthesized via a facile liquid chemical treatment of metal-organic frameworks pre-synthesized as a self-sacrificing template. The microstructure, composition and photocatalytic properties of In 2 S 3 -ZnIn 2 S 4 composite were investigated by means of SEM, TEM, XRD , XPS, PL and electrochemical techniques . The photocatalytic reduction performance of In 2 S 3 -ZnIn 2 S 4 composites are much better than that of pure In 2 S 3 and ZnIn 2 S 4 under visible light irradiation . For the best photocatalytic activity of the as-prepared sample, the Cr(VI) with the initial concentration of 80 ​mg/L in the water can be photocatalytic reduced 93.4% in 10 ​min under visible light irradiation, which meet the requirement of design well.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
✓ 已验证 DOI 高影响因子
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Sewage sludge derived FeCl3-activated biochars as efficient adsorbents for the treatment of toxic As(III) and Cr(VI) wastewater

Chengcheng Shen,Li Gu,Sihao Chen,Yajuan Jiang,Peng Huang,Heng Li,Huayang Yu,Dong Xia

Effective utilization and resourcelization of sewage sludge into value-added by-products and insights into its environmental impacts during the fabrication process are urgent tasks to be tackled. Here, we adopt FeCl 3 to activate and functionalize sewage sludge to form FeCl 3 -activated biochars, which exhibited high adsorption capabilities for the treatment of toxic As(III) and Cr(VI) containing wastewaters. Kinetic studies suggested that the adsorption of As(III) and Cr(VI) species onto the biochar surface was attributed to physisorption and chemosorption, respectively. Equilibrium was reached after 3 h for the adsorption of Cr(VI), and slightly slower for that of As(III). Additionally, the structural stability of the adsorbent was maintained even in wastewater with high acidity (pH = 1), as corroborated by microscopic observations. Structural characterization of the adsorbents after adsorption showed that the excellent adsorption performance originated from adsorptive functionalities of the surface functional groups and the active Fe 3 O 4 particles forming Fe-O-As(III)/Fe-O-Cr(VI) complexes with the As(III)/Cr(VI) adsorbates. Evaluation via the green degree method demonstrated that transforming sewage sludge into biochar exerts very low impacts on the environment. Hence, this work offers a green alternative to convert the hazardous sewage sludge into value-added biochar materials, which can be further exploited as supporting frameworks for multifunctional catalysts or expanded to be investigated in reducing carbon footprints and energy conversion areas.

研究领域: 环境科学 · 废物管理 · 水处理 · 材料科学
✓ 已验证 DOI 高影响因子
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Nanomaterials · 2022 ·Vol. 12 ·期 21 ·3923 · IF 5.719

Surfactant-Modified CdS/CdCO3 Composite Photocatalyst Morphology Enhances Visible-Light-Driven Cr(VI) Reduction Performance

Wen-Yi Wang,Tian Sang,Yan Zhong,Chao-Hao Hu,Dian-Hui Wang,Jun-Chen Ye,Ni-Ni Wei,Hao Liu

The surfactant modification of catalyst morphology is considered as an effective method to improve photocatalytic performance. In this work, the visible-light-driven composite photocatalyst was obtained by growing CdS nanoparticles in the cubic crystal structure of CdCO3, which, after surfactant modification, led to the formation of CdCO3elliptical spheres. This reasonable composite-structure-modification design effectively increased the specific surface area, fully exposing the catalytic-activity check point. Cd2+from CdCO3can enter the CdS crystal structure to generate lattice distortion and form hole traps, which productively promoted the separation and transfer of CdS photogenerated electron-hole pairs. The prepared 5-CdS/CdCO3@SDS exhibited excellent Cr(VI) photocatalytic activity with a reduction efficiency of 86.9% within 30 min, and the reduction rate was 0.0675 min−1, which was 15.57 and 14.46 times that of CdS and CdCO3, respectively. Finally, the main active substances during the reduction process, the photogenerated charge transfer pathways related to heterojunctions and the catalytic mechanism were proposed and analyzed.Keywords:surfactant;CdS/CdCO3;photocatalytic;Cr(VI)

研究领域: 材料科学 · 环境科学 · 化学
✓ 已验证 DOI PubMed 高影响因子
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