JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2019
·
IF 6.361
Zongchen Li,Xuemin Liu,Wei Jin,Qingsong Hu,Yaping Zhao
Arsenic species are regarded as typical water pollutants due to their toxicity. The chemical structures of arsenic species greatly influence their migration and transformation in the environment. Metal-organic frameworks (MOFs) are used as reliable adsorbents to control arsenic contamination, so it is urgently needed to study the effect of chemical structure of arsenic species during adsorption process. The adsorption behaviors of arsenate (As(V)) and its organic forms such as roxarsone (ROX), p-arsanilic acid (p-ASA) and dimethyl arsenate (DMA) by MIL-101(Fe), a type of highly porosity iron-based MOFs in aqueous environment were detailed investigated. The adsorption kinetics of those arsenic species on MIL-101(Fe) is rapid followed with pseudo-second-order kinetic model. MIL-101(Fe) exhibits excellent adsorption capacities for As(V), ROX, p-ASA and DMA with maximum adsorption capacities of 232.98, 507.97, 379.65 and 158.94 mg g −1 , respectively. The formed Fe O As inner-sphere coordination between arsenic species and the incomplete-coordinated cationic Fe in the MIL-101(Fe) cluster is the primary adsorption mechanism based on FTIR and XPS analysis. Substituent aromatic units in ROX and p-ASA strengthen the adsorption on MIL-101(Fe) through hydrogen bonds and π-π stacking interaction, resulting in higher adsorption capacities far beyond that of As(V) and DMA. The reusability of MIL-101(Fe) is limited by the strong Fe O As coordination. These results confirm MIL-101(Fe) a reliable adsorbent to control the aqueous arsenic species contamination and emphasize the significant role of the chemical structure of arsenic speciation on adsorption performances of MOFs.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
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2019
·
IF 8.355
Yunfei Zhang,Junfeng Niu,Jianhui Xu
In this study, it was demonstrated that the Fe ion was an effective promoter of bulk MoS 2 for the activation of peroxymonosulfate (PMS) to degrade acetaminophen (ACT). ACT removal rate constant in the presence of 5 mg/L FeSO 4 ·7H 2 O (0.1099 min −1 ) was approximately 20 times as that in the absence (0.0045 min −1 ) with 0.1 g/L MoS 2 of FeSO 4 ·7H 2 O at pH 0 3. Both electron paramagnetic resonance (EPR) characterization and quenching experiment suggested the key role of singlet oxygen ( 1 O 2 ), acting as dominant reactive species responsible for ACT degradation in the Fe 2+ /MoS 2 /PMS system. Besides, the chemical state and composition of MoS 2 , the ion (Fe and Mo) concentrations and the speciation of Mo(VI) were investigated. Results suggested that the promoting effect of Fe(II) ion originated from the regeneration of Fe 2+ mediated by MoS 2 , and the formation of molybdenum(VI) peroxo complex species in Fe 2+ /MoS 2 /PMS system. The present study not only provides an insight into PMS activation by MoS 2 accelerated by Fe(II) ion, but also suggests an high-efficiency, easy-to-handle and environmentally friendly method to treat refractory wastewater.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2019
·Vol. 54
·期 20
·13358-13367
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IF 3.442
Zhang Rui,Wu Yuanpeng,Zhang Haiyan,Xue Shishan,Guo Meiling,Zhang Tao
In this work, we present a hydrophobic–oleophilic Fe foam for oil–water separation. Hydrophobic–oleophilic Fe foam was fabricated simply through dip-coating with n -dodecyl mercaptan. The morphology, chemical composition and water contact angle of the Fe foam were characterized. The Fe foam could absorb a variety of oils, such as diesel, toluene, xylene, cyclohexane, dodecyl methacrylate, crude oil, 1,2-dichloroethane, hexane and chloroform, these oils could be underwater or on water surface, and it exhibited excellent durability, verified by the high separation efficiency (more than 98.8% for a cyclohexane–water mixture) after reusing for 48 times. Furthermore, oil collection with the Fe foam could be controlled remotely using external magnetic field, and the Fe foam displayed high flux, good anti-corrosion and wear resistance. The simple and low-cost fabrication method enabled the Fe foam to be a promising candidate for large-scale oil–water separation and for remotely controllable water purification.
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高影响因子
Frontiers of Chemical Science and Engineering
·
2017
·Vol. 11
·期 4
·613-623
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IF 1.712
Tang Honggui,Li Shuangshuang,Gong Dandan,Guan Yi,Liu Yuan
Carbon deposition and sintering of active components such as nano particles are great challenges for Ni-based catalysts for CO methanation to generate synthetic natural gas from syngas. Facing the challenges, bimetallic catalysts with different Fe content derived from layered double hydroxide containing Ni, Fe, Mg, Al elements were prepared by co-precipitation method. Nanoparticles of Ni-Fe alloy were supported on mixed oxides of aluminium and magnesium after calcination and reduction. The catalysts were characterized by Brunner-Emmett-Teller (BET), X-ray diffraction, hydrogen temperature programmed reduction, inductively coupled plasma, X-ray photoelectron spectroscopy, transmission electron microscopy and thermogravimetric techniques, and their catalytic activity for CO methanation was investigated. The results show that the Ni-Fe alloy catalysts exhibit better catalytic performance than monometallic catalysts except for the Ni4Fe-red catalyst. The Ni2Fe-red catalyst shows the highest CO conversion (100% at 260–350 °C), as well as the highest CH 4 selectivity (over 95% at 280–350 °C), owing to the formation of Ni-Fe alloy. In stability test, the Ni2Fe-red catalyst exhibits great improvement in both anti-sintering and resistance to carbon formation compared with the Ni0Fe-red catalyst. The strong interaction between Ni and Fe element in alloy and surface distribution of Fe element not only inhibits the sintering of nanoparticles but restrains the formation of Ni clusters.
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高影响因子
Catalysis Science & Technology
·
2024
·
IF 4.4
Xuewei Tu,Can Sun,Yang Hu,Yutong Chen,Shouxin Zhu,Jingyi Qu,Zhexiao Zhu,Xiang Zhang,Hui Zheng
Cycloaddition of CO2 and epoxides to synthesize cyclic carbonates via photothermal catalysis represents one of the effective strategies for achieving carbon neutrality. In this study, a facile one-step hydrothermal method was employed to synthesize a bimetallic photothermal catalyst FeCo@BPDC. This catalyst demonstrates remarkable efficiency in fixing CO2 to synthesize cyclic carbonates under atmospheric pressure and solvent-free conditions. Through comprehensive characterization and experimentation, the indispensability of bimetallic active sites has been convincingly demonstrated. Additionally, the incorporation of organic ligands significantly enhances the concentration of oxygen vacancies within the catalyst, thereby endowing it with excellent photocatalytic performance. This study presents a novel perspective for the design of photothermal catalysts that convert CO2 into value-added chemicals under mild conditions.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2024
·
IF 8.1
Haofan Jia,Liujing Yang,Hao Zhu,Yang Wang,Ying Chen,Kai Sun,Xinbao Li
In this study, a series of high-efficient catalyst, Co–Fe/Al 2 O 3 , were synthesized via the sol-gel method for low-temperature phenol steam reforming (PSR). The optimized catalyst, 15Co–2Fe/Al 2 O 3 , exhibited a remarkable phenol conversion of 95.3%, a H 2 yield of 92.1% at 450 °C, GHSV = 7500 h −1 and a steam-to-carbon (S/C) ratio of 10. Furthermore, the catalyst activity was maintained for 660 min before a gradual decline was observed. The NH 3 -TPD analysis revealed that the addition of Fe enhanced the surface acidity of the catalyst, providing more active sites for phenol adsorption and activation. This study aims to address the challenges associated with high reaction temperatures and poor catalyst stability in PSR. Various characterization techniques have been employed to investigate the reaction mechanisms of bimetallic catalysts in low-temperature PSR.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Chengcheng Qi,Yaqi Kong,Ziyin Yang
The regulation of the activity of single-atom nanozymes is crucial for the development of highly sensitive electrochemical sensors. The accessibility of single-atom nanozymes is an important factor limiting their activity. This study proposes a directional anchoring strategy to regulate the accessibility of single-atom nanozymes for boosting electrochemical nonenzymatic H 2 O 2 sensing. The directional anchoring of Fe single-atoms on the inner surface of nitrogen-doped carbon materials (In-Fe SAs/NC) and the outer surface of nitrogen-doped carbon materials (Out-Fe SAs/NC) was achieved via the hard template assisted method. The impact of the anchoring position of Fe SAs on the electrocatalytic reduction of H 2 O 2 was investigated. Density functional theory (DFT) calculations reveal that Fe SAs nanozymes are more likely to activate H 2 O 2 than the previously reported Fe 3 O 4 nanozymes. The anchoring of Fe SAs on the outer surface of NCs markedly enhances the accessibility of active sites in comparison to anchoring Fe SAs on the inner surface, thereby increasing the sensitivity for the detection of H 2 O 2 . The electrochemical sensor based on Out-Fe SAs/NC can be used to detect H 2 O 2 content in milk samples. The high accessibility and excellent intrinsic activity of Fe SAs render Out-Fe SAs/NC a highly effective sensing material.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·Vol. 48
·期 20
·9185-9195
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IF 2.7
Shikai Xue,Dongying Zhu,Qing Zuo,Shuangfeng Yang,Haiyan Wang,Qiujun Lu,Guoxing Yin,Guihua Ruan,Fuyou Du
A novel MIL-101(Fe)/ZnCrZr-LBMO heterojunction was successfully constructed and used for the removal of ciprofloxacin (CIP) in this work. The MIL-101(Fe)/ZnCrZr-LBMO composite exhibited significantly enhanced photocatalytic degradation activity, with reaction rates approximately 3.4 and 3.1 times faster than those observed with pristine MIL-101(Fe) and ZnCrZr-LBMO, respectively. The effect of different amounts of ZnCrZr-LBMO, sample pH, CIP concentration, inorganic cations, and anions on CIP removal was investigated, and the possible intermediates and degradation pathways of CIP were speculated. The·O2− radicals dominated CIP degradation, with minor contributions from 1O2, h+, and ·OH radicals. The composite exhibited high removal rates for CIP (94.7%), ofloxacin (86.8%), and tetracycline (96.3%), respectively, within 60 min of light irradiation, and excellent reusability, retaining over 85.1% CIP degradation rate after five cycles. Our work provides a new reference to construct highly efficient and easily recyclable MIL-101(Fe)/ZnCrZr-LBMO photocatalysts for the removal of antibiotic pollutants, promising advancements in real water treatment applications.
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高影响因子
Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Wenjin Ni,Sicheng Zhang,Lingling Cheng,Tiejun Luo,Hongyun Yang,Tengfei Duan,Dejian Yan
Developing efficient photoanodes for water oxidation is highly promising due to their critical role in producing green H 2 and harnessing solar energy. Herein, a metal-organic framework (MOF)/photoanode was successfully constructed by coating TiO 2 nanorods with MIL-88(Fe) MOF for photoelectrochemical (PEC) water splitting. The results demonstrated that MIL-88(Fe) was uniformly and tightly coated on TiO 2 and functioned as a cocatalyst. The MIL-88(Fe) MOF provides a large surface area and more Fe-O active sites, contributing to high PEC activity by reducing electron/hole recombination and enhancing light response capability. Moreover, the photoanode also exhibited an improved charge conductivity. As a result, the MIL-88(Fe)/TiO 2 photoanode exhibited an excellent photocurrent density of 1.06 mA cm −2 at 1.23 V RHE , which is approximately 2.6 times higher than the pristine TiO 2 . Charge transfer kinetics analyses and electrochemical tests were carried out and revealed that the improved PEC performance was attributed to the introduction of MIL-88(Fe), which promoted charge separation-transfer. This research provided new insights into the design of efficient semiconductor/MOF composite photoanodes for PEC water oxidation.
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高影响因子
RSC Advances
·
2016
·Vol. 6
·期 95
·92739-92747
·
IF 3.289
Li Zhang,Wei Wan,Qiang Wang,Wen-Chao Lu,Bei-Hua Hou,Ping Chen
Catalysts for the oxygen reduction reaction (ORR) are crucial in metal–air batteries, fuel cells and other electrochemical devices. Developing heteroatom-doped carbon catalysts with high performance and stability in alkaline media for practical application of metal–air batteries or in acidic media for practical application of proton exchange membrane fuel cells is still difficult and challenging. Here, we report the N-, Fe-doped carbon sphere/oriented carbon nanofiber nanocomposite (NFe-CS/CNF). N-, Fe-doped carbon spheres (NFe-CS) were derived from p-phenylenediamine and oriented N-, Fe-doped carbon nanofibers (NFe-CNF) were derived from o-phenylenediamine. 3.89 at% of N and 0.38 at% of Fe were doped in a typical product, which has high surface area. The typical product exhibits a high ORR activity and stability in acidic media and reveals superior stability and tolerance to methanol than Pt/C. In alkaline media, the typical product shows superior activity to Pt/C. The performance of a zinc–air full cell under real battery operation conditions indicates that the typical product is a competitive alternative to commercial PtC. The unique structure of NFe-CS/CNF could create strong interactions between the nanospheres and oriented nanofibers, promote charger transfer at the interface and improve the conductivity. This work provides a new fundamental understanding and design strategy for excellent carbon-based ORR catalysts.
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高影响因子
Journal of Nanomaterials
·
2016
·
IF 1.758
Yongli Zhang,Shujuan Dai,Yanbo Zhou,Kai Lin
Fe-Co-Ce composite catalysts were prepared by coprecipitation method using CO(NH2)2, NaOH, NH4HCO3, and NH3·H2O as precipitant agents. The effects of the precipitant agents on the physicochemical properties of the Fe-Co-Ce based catalysts were investigated by SEM, TEM, BET, TG-DTA, and XRD. It was found that the precipitant agents remarkably influenced the morphology and particle size of the catalysts and affected the COD removal efficiency, decolorization rate, and pH of methyl orange for catalytic wet air oxidation (CWAO). The specific surface area of the Fe-Co-Ce composite catalysts successively decreased in the order of NH3·H2O, NH4HCO3, NaOH, and CO(NH2)2, which correlated to an increasing particle size that increased for each catalyst. For the CWAO of a methyl orange aqueous solutions, the effects of precipitant agents NH3·H2O and NaOH were superior to those of CO(NH2)2 and NH4HCO3. The catalyst prepared using NH3·H2O as the precipitant agent was mostly composed of Fe2O3, CoO, and CeO2. The COD removal efficiency of methyl orange aqueous solution for NH3·H2O reached 92.9% in the catalytic wet air oxidation. Such a catalytic property was maintained for six runs.
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高影响因子
RSC Advances
·
2016
·Vol. 6
·期 74
·70271-70276
·
IF 3.289
Ying Huang,Zhaohui Wang,Changling Fang,Wenqian Liu,Xiaoyi Lou,Jianshe Liu
Addition order of reagents in the Acid Orange 7 (AO7) degradation process was investigated by varying the concentration of Fe(II), the Fe(II)/peroxymonosulfate (PMS) molar ratio and stepwise addition of Fe(II) and PMS. The importance of addition order of reagents was confirmed and an order of Fe(II)–PMS to improve the oxidation efficiency was recommended.
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高影响因子
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