JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2018
·
IF 5.091
Yunqing Pi,Lingjia Ma,Peng Zhao,Yangdan Cao,Huiqin Gao,Chunfeng Wang,Qilu Li,Shuying Dong,Jianhui Sun
A kind of Co-Fe Prussian blue analogues (Co-Fe PBAs), cobalt hexacyanoferrate Co 3 [Fe(CN) 6 ] 2 , and graphene oxide (GO) were combined to synthesize magnetically separable Co-Fe PBAs@rGO nanocomposites through a simple two-step hydrothermal method. The crystalline structure, morphology and textural properties of the Co-Fe PBAs@rGO nanocomposites were characterized. The catalytic performance of the nanocomposites was evaluated by PMS activation, with Levofloxacin Hydrochloride (LVF) as the target contaminant. Synergistic interactions between the Co-Fe PBAs and rGO prevented the aggregation of the Co-Fe PBAs nanoparticles, which resulted in enhanced degradation efficiencies. The influence of several critical parameters was investigated, including the reaction temperature, PMS and Co-Fe PBAs@rGO catalyst concentrations, solution pH and salt content. LVF degradation was favored at higher catalyst and PMS concentrations, high temperatures, and in neutral or weak acidic solutions. Sulphate radicals were the dominant active species in the Co-Fe PBAs@rGO/PMS system. In addition, the Co-Fe PBAs@rGO exhibited no significant decrease in LVF degradation efficiency following five catalytic cycles. Thus, the as-prepared Co-Fe PBAs@rGO nanocomposite catalyst might be applied to the removal of hard-to-degrade organics owing to its high catalytic ability to activate PMS, as well as its good reusability and recyclability.
研究领域:
环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
SEPARATION SCIENCE AND TECHNOLOGY
·
2025
·
IF 2.3
Chunlai Wu,Aimaiti Gali,Chuanyun Peng,Yalei Miao,Juan Li,Xinyu Gao
The treatment of dye wastewater is of crucial significance for alleviating water pollution, ensuring ecological security and achieving the sustainable utilization of water resources. In this work, the 1-allyl-3-butylimidazolium chloride ionic liquid modified Co/Fe-LDH (Co/Fe-LDH@IL) was successfully synthesized and explored for elimination Methylene Blue (MB) from aqueous solutions. Characterizations revealed that the incorporation of ionic liquids notably increased the specific surface area from 5.37 m2.g−1 to 8.15 m2.g−1. Additionally, the number of surface active sites, was significantly enhanced. For a 25 mL MB solution with an initial concentration of 300 mg.L−1, the optimal dosage of Co/Fe-LDH@IL was determined to be 30 mg, achieving adsorption equilibrium within 20 min. Under these conditions, the maximum adsorption capacity was 517.43 mg.g−1. Kinetic studies indicated that the pseudo-second-order model accurately described the process. The Langmuir isotherm model provided a better fit than the Freundlich model, indicating a homogeneous monolayer adsorption mechanism. Column adsorption experiments further validated the superior performance of Co/Fe-LDH@IL in treating MB solutions of different concentrations. The adsorption mechanism involved electrostatic interactions, interface regulation by IL molecules, and monolayer π-π interaction adsorption on imidazole functional group. Co/Fe-LDH@IL exhibits outstanding adsorption performance and stability, showing great potential for efficiently treating MB-containing wastewater.
研究领域:
环境科学
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材料化学
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水处理技术
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吸附工程
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Fangxin Deng,Shoushu Wei,Xiangwei Zhang,Yanping Zhu,Qingze Chen,Zhiyi Deng,Runliang Zhu
A novel single-atom-like Co/Fe catalyst (i.e., Co/Fe-N-C) was synthesized by pyrolysis of a Zn/Co/Fe zeolitic imidazolate framework, and applied in peroxydisulfate (PDS) activation for removal of organic contaminants from wastewater. The isolated diatomic metal-nitrogen sites were detected by X-ray adsorption fine-structure. The degradation of four contaminants (i.e., phenol, bisphenol A, 2,4-dichlorophenol, and N-methyl-2-pyrrolidone) with a concentration of 100 mg/L could be degraded separately within 20 min by the Co/Fe-N-C system with 10 mmol/L of PDS, 0.5 g/L of catalyst dosage, and initial pH of 3. Besides, 79.2 % of phenol could be mineralized in 120 min, and the turn-over frequency value of the catalyst was calculated to be 27.17 min −1 , which was higher than the commonly reported homogeneous PS-AOPs. Moreover, the Co/Fe-N-C exhibited high stability (mineralization rate over 70 % after 5 cycles), a wide initial pH range (3−9), and high catalytic performance at 5–20 mmol/L of PDS concentrations. Based on the analysis of radical scavenging experiments and electron spin resonance spectra, the radical and non-radical pathways for PDS activation were proved in the system, and the contribution of phenol degradation by each pathway was clarified.
研究领域:
环境科学
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催化化学
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产品关联
DOI
高影响因子
ACS Catalysis
·
2024
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IF 11.3
Ying Zhang,Junjun Mao,Bo Zhang,Dan Wang,Chenchen Zhang,Yang Lou,Chengsi Pan,Yongfa Zhu
Electrochemical carboxylation of 1,3-dienes with carbon dioxide (CO2) is a feasible method to obtain dicarboxylic derivatives, which are important synthetic intermediates of polymers and pharmaceuticals. However, due to unavoidable byproducts and unfriendly conditions, the formation of pure dicarboxylic acids has been limited. In this work, we report that a bimetallic phosphating CoFeP catalyst on nickel foam (CoFeP/NF) served as a remarkable electrode, which transforms CO2 into multicarbon (C6+) dicarboxylic acids. The synergistic effects of CoFeP catalyst between Co and Fe allow activation of 1,3-dienes mainly, in which electron transfer easier to the 1,3-dienes proceeded to afford radical anion of the diene, pursuant carboxylation with CO2 and further electron transfer formed the ultimate carboxylated products. The reaction can occur in a commercial flow cell with gram-scale amplification. The dicarboxylic acid obtained was up to 1.08 g at a 5 mmol scale of 1,3-dienes, illustrating high electrocatalytic activity and practical application of CoFeP/NF.
研究领域:
化学
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材料科学
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环境科学
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2018
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IF 5.091
Bin Hu,Jin-Yun Yuan,Jia-Yue Tian,Minghua Wang,Xue Wang,Linghao He,Zhihong Zhang,Zhuo-Wei Wang,Chun-Sen Liu
A new bimetallic Co/Fe-MOF was synthesized and phosphatized to produce a visible-light-active Co/Fe binary metal phosphide embedded in a mesoporous carbon matrix (denoted by CoP/Fe 2 P@mC). The results of X-ray diffraction and photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy reveal the formation of CoP and Fe 2 P nanoparticles together with the Co and Fe metallic state. Combining the high electron–hole separation rate of Fe 2 P@mC, fast electron transfer of CoP@mC, and the strong adsorption of mesoporous carbon, the as-prepared CoP/Fe 2 P@mC catalyst exhibits substantially enhanced photocatalytic activity toward rhodamine B (RhB) degradation under visible light irradiation. Visible light harvesting efficiency is enhanced by the suitable bandgap structure of the CoP/Fe 2 P@mC photocatalyst. Moreover, the possible photocatalytic mechanism of CoP/Fe 2 P@mC toward RhB degradation was proposed on the basis of radical trapping and electron spin resonance results. This finding illustrates a potential utilization of bimetallic MOF-derived metal phosphide as a photocatalyst to remove dye pollutants in the environment.
研究领域:
材料科学
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环境科学
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产品关联
DOI
PubMed
高影响因子
CATALYSIS LETTERS
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2015
·Vol. 145
·期 3
·784-793
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IF 2.307
Zhang Xuejun,Zhang Peipei,Yu Hongbo,Ma Zhen,Zhou Shenghu
Abstract Bimetallic PdM (M = Ni, Co, Fe) nanoparticles were synthesized using butyllithium as a reductant, and were used to prepare Pd–M
x
O
y
/KIT-6 catalysts by appropriate oxidation and reduction treatments. These catalysts showed higher selectivity in the hydrogenation of p -chloronitrobenzene to p -chloroaniline than Pd/KIT-6. Relevant characterization was conducted using X-ray diffraction, transmission electron microscopy, N 2 adsorption–desorption, X-ray photoelectron spectroscopy, inductive coupled plasma emission spectrometer, and H 2 temperature-programmed reduction. Graphical Abstract
研究领域:
催化化学
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材料科学
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
Qian Zhao,Lei Liu,Ying Du,Sisi Jiang,Tingshun Jiang
Rational design of non-noble metal electrocatalyst with high stability and activity for OER is desirable for the production of renewable energy to solve the environmental crisis. Starting from Prussian blue analogues (PBAs) with special advantages, the trimetallic hollow structural Co-Fe-P/Cu 3 P/CF covered with extended nanosheets grown on nanorods was synthesized via ion exchange and calcination approaches in this study. The overpotential of the prepared electrode was only 205 mV at a current density of 100 mA cm − 2 , and it can maintain the stable catalytic activity for at least 60 h. The prominent electric performance is mainly attributed to the construction of the unique morphology, in which the rod-shaped structure can promote the transportation of the reactants, and the hollow structure as well as the nanosheets outside can expand the specific surface area. The electronic interaction between multiple metals can also improve the conductivity of the catalyst. The characterization analysis of the post electrode after long-term oxygen evolution reaction imply that the surface of the catalytic electrode was partially oxidized to the corresponding oxide, which can generate the new active sites to maintain the high catalytic activity together with the residual phosphide. Our research might provide a new reference for the deep exploration of PBA-based materials applied in electrochemical energy conversion and storage.
研究领域:
材料科学
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能源化学
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催化化学
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产品关联
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Shanhai Zhao,Yidan Luo,Chunhe Li,Kuankuan Ren,Yanyan Zhu,Weidong Dou
The synthesis of renewable fuel by CO 2 reduction is a promising research direction. The CO 2 reduction reaction may be promoted using photothermal catalysis to achieve efficient CO 2 conversion under mild conditions. In this context, designing efficient catalysts is urgent. In this work, ABO 3 (A = La, Ce; B = Ni, Co, Fe) perovskite catalysts were prepared by coprecipitation and calcination . Experimental results show that the A-site ions and B-site ions in ABO 3 perovskite nanomaterials have a great influence on their structure and photothermal catalytic performance. Among them, the LaNiO 3 catalyst shows excellent photothermal catalytic performance in the conversion of CO 2 to CO and CH 4 , which can generate 0.16 mmol g −1 h −1 CO and 1.38 mmol g −1 h −1 CH 4 at low CO 2 and H 2 concentrations. For the LaNiO 3 sample, its enhancement of catalytic performance mainly benefits from the largest number of active sites, the fastest carrier transport rate, and a relatively suitable band edge position compared with other catalysts. This study proposes a new method for improving the activity and selectivity of photothermal CO 2 reduction and offers a new direction for the recycling of waste gas.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
YuXin Zhao,Jiaxian Liu,Tong Zhang,FangXun Liu,Man Zheng,Kun Shi,JinPeng Liu,Yufan Zhang,Huan Wang
The exploration of an inexpensive catalyst with effective oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) activities to replace precious metal electrocatalysts has been of great interest in recent years. In this paper, CNT@Co-Fe/FePc composites were synthesized with high efficiency using a self-assembly strategy. In the synthesis process, carbon nanotubes (CNTs) were synthesized as the base material using crab shells as templates and honey as the carbon and nitrogen source. CoFe alloy nanoparticles derived from CoFe-based prussian blue analogs were self-assembled and anchored on CNTs, and then iron phthalocyanine with Fe-N 4 portion was coupled with CNTs by π-π stacking. Finally formed a homogeneous and stable composite material. The self-assembly method is simple and efficient to achieve good metal loading. The prepared CNT@Co 2 -Fe 1 /FePc exhibits excellent catalytic performance and stability for OER and ORR in alkaline electrolyte . The overpotential at 10 mA cm −2 of CNT@Co 2 -Fe 1 /FePc for OER is 343 mV with a very small Tafel slope of 43.59 mV dec −1 . CNT@Co 2 -Fe 1 /FePc has high methanol tolerance and persistence for ORR. This work provides a strategy for the construction of transition metal-carbon composite electrocatalytic materials with excellent catalytic performance and stability for OER and ORR reactions.
研究领域:
材料科学
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电催化
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能源化学
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产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2021
·
IF 5.316
Zhiliang Zhang,Deyao Xu,Junhua Li,Jinlong Liu,Xuanda Long,Kanda Su,Jiangnan Guo,Haixia Tong,Zeng Liu,Dong Qian
We rationally design and construct a heterostructured hybrid with reduced graphene oxide served as a platform to in-situ grow N-doped bamboo-like carbon nanotubes encapsulating bimetallic Co–Fe sulfide nanoparticles through a two-stage pyrolysis succeeded by an evaporating sulfurization process (denoted as Co x Fe 1- x S 2 @N-CNTs/rGO). By tuning the Co/Fe ratio, the optimal Co 0.6 Fe 0.4 S 2 @N-CNTs/rGO exhibits a remarkable oxygen evolution reaction (OER) performance in 1.0 M KOH, in which the overpotential at 10 mA cm −2 and Tafel slope are recorded as 248 mV ( vs . RHE) and 58.3 mV dec −1 , respectively, outmaneuvring commercial RuO 2 and most Co/Fe sulfide-based catalysts in recent peer reports. Comprehensive experiment results unravel that the outstanding OER electrocatalytic performance owes to the reinforced synergy between CoS 2 and FeS 2 , the heterostructures constituted by partial CoS 2 and FeS 2 , the confining effect of N-CNTs/rGO for CoS 2 and FeS 2 nanoparticles, and the high conductivity and large surface of N-CNTs/rGO.
研究领域:
材料科学
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能源化学
✓ 已验证
DOI
高影响因子
MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
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2025
·
IF 4.6
Yaqi Wu,Jianhua Qian,Jinjuan Xing,Junhua Li,He Huang,Yanan Wang,Xueming Kang,Lijuan Wang,Jiasheng Xu
Volatile organic compounds (VOCs), as hazardous environmental pollutants emitted from chemical industries, cause significant threats to human health and ecological environment owing to their inherent toxicity and carcinogenicity. Catalytic oxidation has emerged as a promising technology for VOC elimination, enabling complete degradation of pollutants into CO 2 and H 2 O. This study investigates transition metal oxide (TMO x , TM = Mn, Co, Fe, Ni, Cu, Zn)/TiO 2 catalysts for toluene degradation. Since the catalytic efficacy of TiO 2 -based catalysts critically depends on the quantity of surface oxygen vacancy (O v ) in heterogeneous processes, we engineered O v -rich interfaces by breaking atomic periodicity arrangements and generating unsaturated coordination sites. These structural modifications enhanced oxygen migration rates and increased reactive oxygen species availability. Among the synthesized catalysts, CuO/TiO 2 exhibited the highest performance, achieving 90 % toluene conversion (T 90 ) at 286 °C under a weight hourly space velocity (WHSV) of 20,000 mL/(g·h) with an initial toluene concentration of 1000 ppm. The measurement of in-situ DRIFTS suggested that toluene oxidation process abided by the path of toluene → benzaldehyde → benzoic acid → anhydride →CO 2 and H 2 O. Furthermore, the by CuO/TiO 2 catalyst demonstrated great reusability, and long-term stability, highlighting its potential for industrial-scale VOC abatement applications.
研究领域:
环境科学
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催化
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材料科学
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化学工程
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污染控制
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表面化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2021
·
IF 19.503
Weikang Zhu,Yabiao Pei,John C. Douglin,Junfeng Zhang,Haoyang Zhao,Jiandang Xue,Qingfa Wang,Ran Li,Yanzhou Qin,Yan Yin,Dario R. Dekel,Michael D. Guiver
Recently, much work has been devoted to designing catalysts with high porosity and efficient active sites. Although very promising results are achieved using Co/Fe–N–C catalysts based on rotating disk electrode (RDE) tests, actual fuel cell performance is below expectations, probably due to insufficient understanding of the catalyst layer (CL). Therefore, catalyst design should be considered holistically by taking into account CL performance, not only intrinsic activity. Here, Co/Fe–N–C with highly dispersed CoFe nanoalloy in the carbon network is obtained by careful design of Co/Fe-ZIF precursor, resulting in a high oxygen reduction reaction (ORR) site density with good stability. Concerning RDE test in the kinetic region and single cell test (SCT) with complex influence factors, the half-cell test (HCT) is introduced to more accurately evaluate the quality of the Co/Fe–CL. Multi-scale measurements (RDE, HCT and SCT) in different current density ranges allows targeting the key CL influence factors for fuel cell performance.
研究领域:
材料科学
·
能源科学
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DOI
高影响因子
危险品化学品经营许可证（带存储）