JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
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2021
·Vol. 331
·期 1
·365-373
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IF 1.371
Li Chunhui,He Hui,He Mingjian,Gao Yang,Zhang Meng,Jiao Caishan
A detailed extraction equilibrium study is experimentally performed to understand the extraction mechanisms of Ce(IV) by 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (C 4 mimNTf 2 ) in 1,2-dichloroethane. Further, the influence of adding TBP on the distribution ratio is investigated and demonstrated. The ceric aqueous chemistry in the nitric acid solution and slope analysis are combined to reveal the extraction mechanism. The monovalent anionic complex HCe(NO 3 ) 6 − is the dominant species, which extracted by C 4 mimNTf 2 . Importantly, this study demonstrates the antagonistic effect between TBP and C 4 mimNTf 2 on the extraction process.
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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DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2022
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IF 4.831
Haiping Zhao,Ziyi Zhang,Yong Han,Weixia Yang,Wenzhi Tang,Tianli Yue,Zhonghong Li
A nanocomposite (UiO-66/Ce-MnO 2 ) was fabricated by combining UiO-66 with cerium-doped manganese dioxide (Ce-MnO 2 ) for colorimetric detecting vitamin C (Vc). Compared with traditional artificial enzymes, the as-synthesized UiO-66/Ce-MnO 2 were simple to prepare and did not require the participation of other active substances. The doping of cerium increased the oxygen vacancies and the UiO-66 as a carrier improved the dispersibility. The formation of superoxide anion (O 2 − ) and the inside Ce 4+ /Ce 3+ and Mn 4+ /Mn 3+ redox couples of UiO-66/Ce-MnO 2 endowed UiO-66/Ce-MnO 2 with a high catalytic capability, which could catalytically oxidize 3, 3′, 5, 5′-tetramethylbenzidine (TMB) into oxidation state TMB (oxTMB) without H 2 O 2 , accompanying with color change and a prominent peak at 652 nm in UV–vis spectra. Based on the inhibitory effects of Vc on catalytic oxidation of TMB, detection of Vc can be achieved, exhibiting a linear relationship in the concentration of 1.13–17.01 μmol L −1 with a low detection limit of 65.82 nmol L −1 . This system can also be detected by smartphone, the linear detection range is 12.47–22.67 μmol L −1 . Vc contents in fruits and vegetables detected by the sensor were in good agreement with the 2, 4-Dinitrophenylhydrazine colorimetry method ( P > 0.05), indicating a reliable sensor for Vc detection.
研究领域:
生物化学
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食品科学
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材料科学
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DOI
PubMed
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2025
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IF 11.3
Liang Chu,Zhaokun Wang,Teng Zhao,Mu Yang,Ge Wang
Metal-organic frameworks (MOFs) as host-guest catalyst in oxidative desulfurization (ODS) face challenges due to limited access to active sites through their microporosity. Herein, hierarchical porous Ce-UiO-66 (HCU) was synthesized through a templating method in an aqueous environment to enhance host accessibility; phosphotungstic acid (PW) was uniformly loaded within the mesopores of HCU via post-impregnation; Ce sites were exposed by selective removing the coordinated acetate from the HCU with the acid post-treatment, these synergistically optimized the catalytic potential of the composite. The resulting HCU@5PW-H demonstrates outstanding desulfurization performance (1000 ppm sulfur removal) within 16 minutes under mild conditions (40 °C, O/S molar ratio = 5) and maintains high efficiency over at least eight cycles. The catalytic mechanism involves the decomposition of H 2 O 2 to reactive oxygen species (ROS) and the formation of W VI -peroxo intermediates that determine the ODS activity. This synergistic mechanism offers a promising strategy to enhance the oxidation potential of hierarchical porous MOF-based host-guest catalysts under mild conditions.
研究领域:
材料科学
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催化化学
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产品关联
DOI
PubMed
高影响因子
PROGRESS IN ORGANIC COATINGS
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2025
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IF 7.3
Chenkai Xu,Yujie Yuan,Valeryia Kasneryk,Maria Serdechnova,Carsten Blawert,Yuankun Wei,Dongmei Zeng,Mengke Wang,Dahai Gao,Hao Wang,Mikhail L. Zheludkevich,You Zhang
Corrosion protection of high-strength aluminum alloys remains a critical challenge, especially for applications in marine and aerospace environments. This work reports BIPT-6, a new cerium-based metal-organic framework designed for sustainable corrosion protection of AA2024 aluminum alloy. BIPT-6 contains both Ce(III) and Ce(IV) ions and is constructed with 2,5-furandicarboxylate (FDA 2− ), a biomass-derived ligand, through a simple one-pot solvothermal method. The structure and composition were verified by a series of advanced characterization methods. BIPT-6 crystallizes in a monoclinic system with space group P 2 1/ n . The protective ability of novel BIPT-6 was evaluated by electrochemical impedance spectroscopy (EIS). It demonstrated good corrosion inhibition efficiency for the AA2024 aluminum alloy samples immersed in 0.05 mol/L NaCl solution containing 5 × 10 −4 mol/L BIPT-6. Finally, BIPT-6 was applied as an additive to epoxy resin to prepare anti-corrosive coatings. The EIS results show that BIPT-6@Epoxy coating system provides a superior corrosion protection and stability to aluminum alloy AA2024 compared to blank coating. The corrosion inhibition mechanism of BIPT-6 was also investigated, highlighting its synergistic effect from dual corrosion inhibitors. This work showcased BIPT-6 as a promising approach for sustainable, smart corrosion protection strategies in aluminum alloys.
研究领域:
材料科学
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腐蚀工程
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金属有机框架
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表面工程
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电化学
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产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Xuebi Du,Dawei Shao,Shichao Feng,Yinhua Wan
Two-dimensional (2D) metal–organic framework nanosheets (MONs) materials exhibit significant potential in achieving high CO 2 separation performance. This study presents a demonstration of the rapid synthesis of Ce 6 BTB nanosheets at a low temperature of 80 °C and atmosphere pressure of approximately 1 atm. The resulting Ce 6 BTB nanosheets possess notable characteristics, such as high aspect ratios and 1D diamond shaped channels, which facilitate the fast rapid transport of CO 2 molecules. The Ce 6 BTB was firstly blended into PIM-1 with different loadings to form PIM/Ce 6 BTB mixed matrix membranes (MMMs). The incorporation of well-dispersed Ce 6 BTB fillers enhances the efficiency of CO 2 transport by inter-flake nano-channels and intra-flake pores. Moreover, the increased crystallinity, dense chain spacing, and hydrogen bonding contribute to enhanced sieving ability, resulting in high gas selectivity. Consequently, the MMMs containing 2 wt% Ce 6 BTB demonstrate high CO 2 permeability of 5930 Barrer and CO 2 /N 2 selectivity of 23.2, which is far surpasses 2008 upper bound from Robeson and approaches the refined 2019 upper bound from MeKenow. Furthermore, the PIM/Ce 6 BTB-2 MMMs present relatively good anti-pressure properties and long-term operation stability, which is advantageous in terms of industrial applications.
研究领域:
材料科学
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化学工程
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DOI
高影响因子
ACS ES&T Engineering
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2023
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IF 7.1
Junna Yan,Mengyu Ma,Keyi Liu,Yang Bao,Feihu Li
Efficient removal and recovery of phosphorus (P) from wastewater is critical for addressing both phosphate rock depletion and eutrophication-related deterioration of surface water quality. Herein, we present a promising platform approach integrating cerium-doped NH2-MIL-101(Fe) with melamine sponge (MS) scaffolds for rapid and high-efficiency recovery of P from wastewater. The as-prepared MIL-101@sponge composites (denoted as MIL-101@CS, MIL-101@PVDF, and MIL-101@SDBS, respectively) are featured by flexibility and stability according to many characterization techniques. Batch adsorption of P over these composite adsorbents indicates that these MIL-101@sponge composites exhibit a maximum adsorption capacity (e.g., 253.66 mg g–1 for MIL-101@CS) at the optimum pH of 6.0 and that adsorption equilibrium can be attained within 150 min and well described by the pseudo-second-order kinetic model. In addition, these composites show a high selectivity for P over carbonate and other common monovalent anions under environmentally relevant conditions. The results of desorption and recycling tests indicate that MIL-101@CS retains good adsorption and desorption efficiency even in a much short operating time (i.e., 5 min), which allows such a composite to be applied in enriching and recovering P efficiently from wastewater via a rapid adsorption/desorption operation. Moreover, the high feasibility of MIL-101@CS in actual scenarios was validated by efficiently enriching the P from a sludge dewatering liquid. Furthermore, the main mechanisms for P adsorption are elucidated from various microstructural characterizations. Overall, this work presents a strategy of integrating MIL-101 with sponge scaffolds for rapidly and efficiently recovering P from wastewater, which may be potentially extended to the recovery of other value-added elements of interest from waste streams.
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
高影响因子
JOURNAL OF RARE EARTHS
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2017
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IF 2.429
Feng WANG,Wenbo WANG,Yongfeng ZHU,Aiqin WANG
CTS- g -(AA- co -SS)/ISC hybrid hydrogel adsorbent with crosslinked network structure and superior adsorption performance for rare-earth metal ions was successfully synthesized in aqueous solution by a simple one-step free-radical grafting polymerization reaction among acrylic acid (AA), sodium p -styrenesulfonate (SS) and chitosan (CTS) using illite/smectite clay (ISC) as the inorganic additive. The structure of the as-prepared CTS- g -(AA- co -SS)/ISC hydrogel adsorbent was characterized, and the reaction parameters such as AA/SS molar ratio and ISC content were optimized, and the effects of pH values, initial concentration and contact time on the adsorption performance for Ce(III) and Gd(III) were systematically evaluated. It was found that the maximum adsorption capacities of the hydrogel adsorbent toward Ce(III) and Gd(III) reached 174.05 and 223.79 mg/g, respectively, and the adsorption quickly achieved equilibrium within 15–20 min. The adsorbed Ce(III) and Gd(III) could be easily desorbed for recovery, and the used adsorbent was able to be regenerated for reuse. After five adsorption-desorption cycles, the regenerated adsorbent could still retain the adsorption capacities that were close to the initial value. The adsorption process was well described by pseudo-second-order kinetic mode and the Langmuir isotherm model, and the chemical complexation between ions and –COO – was mainly responsible for the high adsorption capacity. As a whole, the hybrid hydrogel adsorbent was potential to be used for the adsorption and recovery of Ce(III) and Gd(III) from water.
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
高影响因子
Journal of Nanomaterials
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2016
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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.
研究领域:
化学工程
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环境科学
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产品关联
DOI
高影响因子
Catalysts
·
2023
·Vol. 13
·期 3
·626
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IF 3.9
Dengmao Wu,Xianyan Lv,Xiurong Ren,Changming Hou,Qianwei Ma,Junxuan Yao,Jiangliang Hu
The catalytic oxidation of VOCs is widely acknowledged as the most available technology to reduce air pollution. Among the catalysts for VOCs, 1 wt%-Pt/TiO2catalysts using metal as a doping element have shown amazing potential in many fields. However, achieving high catalytic performance at relatively low temperatures based on the activation of molecules is still a formidable challenge owing to the catalytic activity being highly dependent on temperature. Here, the role of the rare earth metal Ce in the catalytic oxidation of ethane was studied by preparing Pt/CexTi1−xO2(x = 0, 0.002, 0.005, 0.01, 0.02, and 0.05) catalysts. When the Ce/(Ce+Ti) molar ratio was 0.01, Pt/Ce0.01Ti0.99O2achieved 90% ethane conversion at 436 °C. This reaction temperature is 15% lower than that for Pt/TiO2. The characterization results show that the doping of Ce caused lattice expansion of TiO2and its distortion brought about by oxygen vacancies. Additionally, the appropriate amount of Ce-doping can alter the interaction between the active component Pt and the carrier TiO2, thereby improving the activity and concentration of the active surface lattice oxygen species of the catalyst. These results provide a foundation for the design of the catalytic oxidation of VOCs under mild operating conditions.Keywords:VOCs;Pt-based catalyst;catalyst carrier;catalysis;oxidation;Ce-doping
研究领域:
环境科学
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化学工程
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材料科学
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产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2024
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IF 3.8
Ci Li,Conghui Che,Fang Li,Wei Xue,Jing Li,Xinqiang Zhao,Yanji Wang
Ce-based composite oxides were used for catalyzing the methyl N-phenyl carbamate (MPC) synthesis from aniline and dimethyl carbonate. Among them, CuO–CeO2 exhibited the best catalytic performance. Characterization results showed that the second metal (Cu, Zn, Mn, Co, and Zr) can be doped into the CeO2 lattice and led to strong interactions, modifying the content of Ce3+, oxygen vacancy, and acidity of the catalyst. Notably, Ce3+, oxygen vacancies, and weak Lewis acid sites are beneficial to MPC synthesis. Additionally, CuO–CeO2–M, prepared by mechanical mixing, exhibited better catalytic activity than CuO–CeO2–C prepared by co-precipitation. This was due to the preparation method affecting the interaction between CuO and CeO2. CuO primarily interacted with CeO2 through interfacial contact in CuO–CeO2–C, whereas the interaction in CuO–CeO2–M involves both this interfacial contact effect and the presence of solid solution structures, thereby influencing the content of Ce3+, oxygen vacancy, and acidity.
研究领域:
化学
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催化材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Shaoxia Yang,Qing Wang,Huazhang Zhao,Daoqing Liu
The intrinsic properties of metal-based adsorbents originate from multiples factors such as surface functional groups, electronic and dimensional structures. However, the synthetic strategies are limited to top-down methods, which inhibited the improvement of adsorbent performance. Herein, Fe-Ce bimetal oxide composites are prepared by a bottom-up modified MOF template method. MOF template-directed nano rod-like morphology can expose more active sites and facilitate phosphate access to active sites. The introduction of citric acid effectively increased the amount of surface –OH groups and greatly improved the phosphate adsorption capacity. Furthermore, the Fe dopant enables the high Ce(III) fraction and generate magnetic property for Fe-Ce bimetal oxide composites, which are capable of enhancing the intrinsic phosphate adsorption performance. The results show that the optimized Fe-Ce bimetal adsorbent showed remarkably high phosphate adsorption capacity, achieving a maximum phosphate adsorption capacity of 357 mg g −1 by Langmuir model. High adsorption capacity and high magnetic separation efficiency characteristics make this adsorbent a promising material for phosphate treatment. The above results further prove the effectiveness of the bottom-up strategy in the design process of environmental functional materials.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
Waste and Biomass Valorization
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2024
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IF 2.6
Luo Bo,Liu Huiyu,Shan Rui,Zhang Jun,Yuan Haoran,Chen Yong
Purpose This work aims to investigate the thermal behavior and kinetic characteristics of polyethylene (PE) pyrolysis over Cu/Ce modified ZSM-5. The influences of metal types, particles size of active center and interaction of Cu–Ce species on products distribution are elucidated. Methods Metal-modified ZSM-5 catalysts were prepared by negative pressure impregnation method. Catalytic fast pyrolysis and thermogravimetric experiments were conducted using Py–GC/MS and TG/MS for the qualitative and quantitative analysis of pyrolysis products. Results Morphology characterization indicated the interaction of Cu–Ce species facilitated the regulation of active center size into a nanoparticle scale. The final products were restricted to a carbon number of less than 9 over CuCe/ZSM-5. Cu–Ce modification increased the aliphatic content from 58.5 to 76.1%. Kinetic analysis revealed a remarkable reduction in activation energies during both the intermediate and final stages, where an average decrease of 30% was achieved. Conclusion The synergistic effects of Cu 0 and CeO x facilitated the formation of more short chain olefins by enhancing C–C bonds cleavage activity. Undesired polycyclic aromatic hydrocarbons (PAHs) were avoided by the optimal steric hindrance of CuCe/ZSM-5. Graphical Abstract
研究领域:
能源化学
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催化材料科学
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）