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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Magnetic Fe3O4/CeO2/g-C3N4 composites with a visible-light response as a high efficiency Fenton photocatalyst to synergistically degrade tetracycline

Shuai Wang,Jirong Long,Tian Jiang,Li Shao,Dan Li,Xianchuan Xie,Feigao Xu

Magnetic Fe 3 O 4 /CeO 2 /g-C 3 N 4 (FCG) composites with a visible-light response were successfully synthesized and characterized as a heterogeneous Fenton-like catalyst for tetracycline hydrochloride (TCH) degradation. The optimal mass ratio, pH value, catalyst addition, H 2 O 2 concentration, and temperature were explored. Photodegradation studies showed the best activity when the mass ratio of the composite was 1:0.75:0.75 (F 1 C 0.75 G 0.75 ) and the removal rate of TCH by F 1 C 0.75 G 0.75 reached 96.63% after 180 min. The first order kinetic constant of the reaction system was 0.0533 min −1 . According to the test of free radical scavenger and metal leaching tests, the Fenton-like degradation of TCH by F 1 C 0.75 G 0.75 composite was analyzed. g-C 3 N 4 effectively reduced the leaching of Fe and the location where TCH was attacked by hydroxyl radicals was mainly on the surface of the catalyst. The reusability of the F 1 C 0.75 G 0.75 composites was also studied after five cycles.

研究领域: 环境科学 · 材料科学 · 化学工程
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FUEL · 2022 · IF 8.035

Superior PbO-resistance of CeO2/ZrO2 catalyst promoted by solid superacid SO42−/ZrO2 for selective catalytic reduction of NOx with NH3

Xiaodi Li,Shan Ren,Lian Liu,Xiangdong Xing,Lin Chen,Jiangling Li,Jian Yang,Qingcai Liu

The serious deactivation of denitration catalysts caused by heavy metals still a thorny issue in the practical application of selective catalytic reduction of NO x with NH 3 . Herein, we proposed a novel anti-poisoning strategy by designing SO 4 2− /ZrO 2 superacid supported CeO 2 /ZrO 2 catalyst, and the effect of SO 4 2− /ZrO 2 supported CeO 2 /ZrO 2 for PbO-resistance NO x catalytic reduction was investigated. It was worthy to note that the introduction of solid superacid SO 4 2− /ZrO 2 significantly enhanced catalytic performance over the entire temperature range, with an exceptionally high NO x removal efficiency over 98 % during 250–500 °C. When 2 wt% PbO was deposited on the fresh catalyst, the catalytic activity of CeO 2 /ZrO 2 catalyst decreased obviously, while CeO 2 /ZrO 2 -S catalyst can still maintain a higher NO x conversion over 90 % from 275 to 500 °C. The characterization results confirmed that the introduction of solid superacid SO 4 2− /ZrO 2 enhanced the surface acidity and promoted the transformation from Ce 4+ to Ce 3+ . The results of in situ DRIFTS implied that the Eley-Rideal (E-R) mechanism was obeyed over CeO 2 /ZrO 2 catalyst, and both Eley-Rideal (E-R) and Langmuir-Hinshelwood (L-H) mechanisms were followed over CeO 2 /ZrO 2 -S catalyst in the SCR process. With regard to poisoned catalysts, the NH 3 adsorption was inhibited to some extent, while the reaction mechanism wasn’t changed by PbO poisoning.

CAS / MDL: 10294-41-4 206996-60-3
研究领域: 催化 · 环境科学 · 化学工程
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Theranostics · 2021 · IF 11.556

Catalytic patch with redox Cr/CeO2 nanozyme of noninvasive intervention for brain trauma

Shaofang Zhang,Ying Liu,Si Sun,Junying Wang,Qifeng Li,Ruijuan Yan,Yalong Gao,Haile Liu,Shuangjie Liu,Wenting Hao,Haitao Dai,Changlong Liu,Yuanming Sun,Wei Long,Xiaoyu Mu,Xiao-Dong Zhang

Traumatic brain injury (TBI) is a sudden injury to the brain, accompanied by the production of large amounts of reactive oxygen and nitrogen species (RONS) and acute neuroinflammation responses. Although traditional pharmacotherapy can effectively decrease the immune response of neuron cells via scavenging free radicals, it always involves in short reaction time as well as rigorous clinical trial. Therefore, a noninvasive topical treatment method that effectively eliminates free radicals still needs further investigation. Methods: In this study, a type of catalytic patch based on nanozymes with the excellent multienzyme-like activity is designed for noninvasive treatment of TBI. The enzyme-like activity, free radical scavenging ability and therapeutic efficacy of the designed catalytic patch were assessed in vitro and in vivo . The structural composition was characterized by the X-ray diffraction, X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy technology. Results: Herein, the prepared Cr-doped CeO 2 (Cr/CeO 2 ) nanozyme increases the reduced Ce 3+ states, resulting in its enzyme-like activity 3-5 times higher than undoped CeO 2 . Furthermore, Cr/CeO 2 nanozyme can improve the survival rate of LPS induced neuron cells via decreasing excessive RONS. The in vivo experiments show the Cr/CeO 2 nanozyme can promote wound healing and reduce neuroinflammation of mice following brain trauma. The catalytic patch based on nanozyme provides a noninvasive topical treatment route for TBI as well as other traumas diseases. Conclusions: The catalytic patch based on nanozyme provides a noninvasive topical treatment route for TBI as well as other traumas diseases.

研究领域: 神经科学 · 纳米技术 · 药理学 · 材料科学 · 生物医学工程
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INORGANIC CHEMISTRY COMMUNICATIONS · 2025 · IF 5.4

Rapid and efficient degradation of sulfadiazine in wastewater by activated peroxymonosulfate using CoWO4/CeO2 composite material

Shikun Song,Xi Tong,Jie Tan,Jingjing Xu,Mindong Chen,Li Sun

In this study, CoWO 4 /CeO 2 composites were synthesized by a hydrothermal method and used as activated peroxymonosulfate (PMS) catalysts for the degradation of antibiotic sulfadiazine (SDZ). The synthesized composites underwent systematic characterization on the synthesized composites to investigate the effects of Co: Ce atomic ratio, initial pH, PMS dosage, inorganic anions and other factors on the degradation performance. The results showed that 5 mg/L of SDZ could be degraded basically completely (99.8 % degradation rate) in 20 min by CWC-2/PMS system. Moreover, the degradation rate of SDZ was still more than 82 % after the composite was reused four times. The free radical quenching experiments and EPR tests confirm the redox potential difference between Co 3+ /Co 2+ and Ce 4+ /Ce 3+ was utilized for bimetallic cycling. And it could activate PMS to mainly produce SO 4 − • and O 2 − • radicals efficiently. Thus SDZ could be degraded effectively in this system.

研究领域: 环境科学 · 化学工程 · 材料科学 · 水处理技术 · 催化
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MEASUREMENT SCIENCE and TECHNOLOGY · 2025 ·Vol. 36 ·期 8 ·085104 · IF 3.4

Highly selective detection of trace methyl sec-butyl ether using cataluminescence sensor based on mesoporous CeO2 nanoparticles

Chengcheng Wan,Zhaoru Ban,Dan Zhang,Jiumei He,Yanju Chen,Shan Tang,Qianchun Zhang

Methyl sec-butyl ether (MSBE), a volatile organic compound, poses significant risks to both environmental safety and human health. Consequently, developing efficient sensors for the rapid and accurate detection of trace levels of MSBE is essential. In this study, we synthesized mesoporous CeO2 nanoparticles using carbon quantum dots as templates, resulting in the development of a highly sensitive cataluminescence sensor system. This sensor demonstrated an impressive linear detection range of 0.50–20 mg l−1 (R2 = 0.998) and a low detection limit of 0.08 mg l−1, coupled with a signal-to-noise ratio (S/N) of 3. We applied the mesoporous CeO2 nanoparticle sensor to measure MSBE levels in various environments, including a volatile medicine reagent freezer, laboratory gas, and a storage cabinet, which yielded concentrations of 2.07, 1.38, and 3.96 mg l−1, respectively. The sensor also exhibited excellent recovery rates, ranging from 91.1% to 110%, with relative standard deviations (RSD, n = 5) from 3.4% to 8.7%, indicating reliable performance. Additionally, gas chromatography-mass spectrometry was employed to elucidate the mechanism underlying the developed cataluminescence sensor. This study introduces a versatile approach for designing gas sensors for MSBE that not only exhibits high sensitivity and selectivity but also significantly enhances their potential applications in both industrial and environmental monitoring.

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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS · 2025 ·Vol. 113 ·期 9 ·e35646 · IF 3.4

PB/CeO2 Nanoparticles Regulating Reactive Oxygen Species for the Control of Enterococcus faecalis Infection in Root Canals

Huiwen Wang,Yuting Wu,Mingrui Dai,Tingting Zhu,Daming Wu,Diya Leng

To investigate the antibacterial effect, mechanism, and cytotoxicity of Prussian blue/Cerium dioxide (PB/CeO 2 ) nanoparticles against Enterococcus faecalis (E. faecalis) and biofilm. PB/CeO 2 nanoparticles were synthesized and characterized. The antibacterial mechanism of nanoparticles was explored through peroxidase (POD) activity assay, hydroxyl radicals (·OH) detection, and measurement of bacterial reactive oxygen species (ROS) and glutathione (GSH)/glutathione disulfide (GSSG) levels. The biocompatibility of PB/CeO 2 was evaluated by Cell Counting Kit-8 (CCK-8) assay and histological examination of the major visceral organs of rats. The antibacterial effect of PB/CeO 2 was assessed using the colony-forming unit (CFU) method. The impact of PB/CeO 2 on E. faecalis biofilm on dentin slices was further observed with CLSM and SEM. ANOVA and t -test were applied for statistical analysis ( p < 0.05). PB/CeO 2 demonstrated significant antibacterial activity against E. faecalis , mainly when used with H 2 O 2 , significantly enhancing its antibacterial effect and effectively disrupting E. faecalis biofilms on dentin slices. PB/CeO 2 nanoparticles catalyzed ROS production, disrupting the antioxidant defense system of E. faecalis cells, damaging bacterial cell membranes, and ultimately causing bacterial death. PB/CeO 2 nanoparticles exhibit good biocompatibility at appropriate concentrations in vivo and in vitro. The novel multifunctional nanocomposite shows great antibacterial effects against E. faecalis and its biofilm, with low cytotoxicity and good biocompatibility, offering a novel disinfection strategy for root canal treatment.

研究领域: 纳米技术 · 微生物学 · 牙科 · 材料科学 · 生物医学工程
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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Self-Assembly-Cooperating in Situ Construction of MXene–CeO2 as Hybrid Membrane Coating for Durable and High-Performance Proton Exchange Membrane Fuel Cell

Shengqiu Zhao,Rui Wang,Tian Tian,Hao Liu,Haining Zhang,Haolin Tang

The chemical durability of the membrane is a central issue in the development of proton exchange membrane fuel cells (PEMFCs), while incorporating cerium oxide as a free radical scavenger is one effective strategy to enhance durability. However, simultaneous dispersion and anchoring of cerium oxide in PEM have rarely been reported. Herein, MXene–CeO2 hybrids are prepared by self-assembly-cooperating in situ nucleation growth routes, then the MXene–CeO2 is sprayed on the cathode side of the r-PEM to fabricate a hybrid membrane with free radical resistance. The in situ nucleation growth of CeO2 on MXene nanosheets carriers effectively inhibits agglomeration and induces an anchoring effect through their interaction forces, forming CeO2 nanoparticles with a high specific surface and stable attachment, maximizing the free radical scavenging impact at the forefront of the membrane. The hybrid membrane with a loading of 0.1 mg cm–2 MXene–CeO2 exhibits a lower OCV decay rate (0.53 mV h–1), thickness variation (2.8%), and hydrogen crossover (2.6 mA cm–2) and higher maximum power density (1222.5 mW cm–2) than pristine r-PEM after accelerated degradation testing for 150 h.

CAS / MDL: 7789-24-4 9002-93-1
研究领域: 材料科学 · 能源工程 · 化学工程
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ChemistrySelect · 2023 ·Vol. 8 ·期 28 ·e202301088 · IF 2.1

Preparation of a Durable CuO/ZnO/CeO2/ZrO2 Catalyst on an SiC Support by an Inverse Microemulsion/Precipitation Method for Methanol Steam Reforming

Hui Zhou,Xiaoliang Sun,Wenming Guo,Tingting Bao,Yi Zhang,Chenxu Guo,Hanning Xiao,Hang Qin,Pengzhao Gao

Graphical [+] These authors contributed equally to this articleDurable CuO/ZnO/CeO 2 /ZrO 2 catalyst on SiC support for methanol steam reforming was prepared by the combination of inverse microemulsion method and precipitation method. The methanol conversion of the catalyst was still reached 98.8 % after 150 h, considerably higher than that of solution combustion method (70 %), without carbon deposition and pronounced sintering after the reaction. Durable CuO/ZnO/CeO 2 /ZrO 2 catalyst on SiC support for methanol steam reforming (MSR) was prepared by the combination of inverse microemulsion method and precipitation method which is termed as inverse microemulsion/precipitation method. The presence of Ce−O−Zr solid solution facilitated the production of oxygen vacancies and Ce 3+ species in the prepared CuO/ZnO/CeO 2 /ZrO 2 catalyst. Owing to the unique tiny reaction pool and the addition of precipitant for inverse microemulsion/precipitation method, the particle size of the prepared catalyst was principally between 2 and 6 nm, with an average size of 3.66 nm. Besides, the small particle size and the highly dispersed of Cu species boosted the reduction performance of the catalyst, enabling the reduction temperature to be only 201 °C. The methanol conversion of the reduced catalyst was still reached 98.8 % after 150 h, considerably higher than that of solution combustion method (70 %), without carbon deposition and pronounced sintering after MSR reaction.

研究领域: 催化化学 · 能源材料科学
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CRYSTENGCOMM · 2020 ·Vol. 22 ·期 23 ·4005-4013 · IF 3.117

Engineering CuOx–ZrO2–CeO2 nanocatalysts with abundant surface Cu species and oxygen vacancies toward high catalytic performance in CO oxidation and 4-nitrophenol reduction

Baolin Liu,Yizhao Li,Shaojun Qing,Kun Wang,Jing Xie,Yali Cao

Highly dispersed surface Cu species and oxygen vacancies are important for CuOx–CeO2 catalysts in many reactions, but it is difficult to increase the concentrations of highly dispersed Cu species and oxygen vacancies simultaneously by only adding a Cu component. Herein, CuOx–ZrO2–CeO2 (CZC) nanocatalysts with different ratios of Cu/Zr have been effectively produced by a simple solvent-free synthetic strategy. The effect of Zr doping on the structure and reactivity of the CuOx–CeO2 catalysts has been investigated with the help of carbon monoxide (CO) oxidation and 4-nitrophenol (4-NP) reduction as model reactions. It is revealed that the introduction of Zr relieved the agglomeration of surface Cu species, produced more oxygen vacancies in the interior and Cu+ species on the surface of the catalyst, and increased the reducibility of CuOx–CeO2. The CZC catalysts show remarkably enhanced catalytic activity due to the abundant surface active sites and the improved redox properties provided by the suitable doping of Zr into CuOx–CeO2. This work not only offers a practicable way to reconstruct the distribution of active metals on the metal oxide support but also provides a high-efficiency strategy to prepare oxide catalysts with excellent catalytic performance.

研究领域: 催化化学 · 材料科学
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PROGRESS IN ORGANIC COATINGS · 2022 · IF 6.206

Preparation of a novel IPDI/PUF@CeO2 bi-functional microcapsules and its improvement for the self-healing and anti-corrosion performance in epoxy coatings

Shuhui Liu,Hui Xie,Qingmin Cao,Yujie Ning,Yihan Song,Chengdong Zhang,Bin Liu

This research aims to improve the protective performance of coatings in harsh corrosive conditions by using functionalized self-healing microcapsules. CeO 2 /PUF MCs and PUF MCs were prepared via one-step emulsion polymerization . The microcapsules were implanted into epoxy coatings to investigate their self-healing performance. Multiple testing techniques, including SEM, FTIR, XRD , TGA , EIS , and NSS were used to characterize the morphology, crystal structure, chemical composition, thermal properties, and self-healing performance of the microcapsules and coatings. The experimental results indicated that the CeO 2 /PUF MCs had a spherical core-shell structure with a rough surface and an average diameter of 1583 nm. Meanwhile, the minimum corrosion products and the highest low-frequency impedance were found in CeO 2 /PUF MCs coating with artificial scratch, which demonstrated that the self-healing and anti-corrosion performance were significantly improved by the newly developed bi-functional microcapsules.

研究领域: 材料科学 · 涂层技术 · 腐蚀科学
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Advanced Composites and Hybrid Materials · 2024 ·Vol. 8 ·期 1 ·1-18 · IF 23.2

Facilely constructing physical-linked γ-Fe2O3/CeO2/cellulose nanofibril films for highly effective, recyclable, and multi-removal of heavy metals and dyes from wastewater

Yan Mengxing,Tan Yang,Dong Hanqi,Xu Huawei,Ling Zhe,Xiao Xiao,Huang Chen,Yong Qiang

The problems of heavy metal and dye contamination in wastewater urgently requires green, efficient, and convenient removal strategy. In this paper, a new type of γ-Fe 2 O 3 /CeO 2 /cellulose nanofibril (CNF) composite film (CNFMONP film) adsorbent based on nanocellulose was facilely prepared which is green, easy to be recycled, and has high-efficiency adsorption performance. The proposed CNFMONP films exhibited rough surface, excellent mechanical properties, and stability performance, as well as satisfying adsorption removal performance for Pb 2+ and Cu 2+ , with removal rates of 77.9% and 69.6%, respectively. In addition, a removal rate of up to 95.4% for the dye methylene blue (MB) was also achieved under UV illumination. The adsorption kinetics showed that the CNFMONP films were mainly chemisorbed for heavy metals. Besides, isotherm analysis indicated that monolayer adsorption is the adsorption behavior of the proposed film types adsorbent for heavy metals and dyes. Furthermore, the CNFMONP films still have excellent adsorption affinity after five rounds of cycles, with high adsorption efficiency of 75.0% for Pb 2+ in complex environment. Therefore, environmentally friendly CNFMONP films with excellent stabilization and adsorption properties were simply prepared, which may provide a highly efficient way for recyclable and multi adsorption of heavy metals and dyes.

研究领域: 环境科学 · 材料科学
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ACS Catalysis · 2020 · IF 12.35

Highly Efficient Hydrogenation of Nitrobenzene to Aniline over Pt/CeO2 Catalysts: The Shape Effect of the Support and Key Role of Additional Ce3+ Sites

Qingsong Zhang,Jiahao Bu,Jiandian Wang,Changyong Sun,Dongyang Zhao,Guangzhe Sheng,Xiaowei Xie,Ming Sun,Lin Yu

Pt/CeO2 catalysts with different support shapes and prereduction temperatures were prepared and tested in the liquid-phase hydrogenation of nitrobenzene. Detailed characterizations reveal that the support shape effect of Pt/CeO2 catalysts on nitrobenzene hydrogenation originates from the exposed crystal planes on CeO2 with different reducibilities. A high-energy surface is readily reduced to generate more Ce3+ surface sites and oxygen vacancies, not only favoring the dispersion and stabilization of Pt species due to stronger metal–support interaction but also providing more adsorption sites for reactants and intermediates. Reduction treatment at high temperatures has been proved to be an effective way to improve the performance of Pt/CeO2 catalysts by providing additional Ce3+ surface sites and high H-spillover capability. The additional Ce3+ far away from Pt, derived from a high-temperature reduction, can adsorb the N-phenylhydroxylamine intermediate more effectively due to its stronger electron-donating ability and in turn promote aniline formation. It is also found that Na ions with suitable content facilitate the generation and stabilization of surface Ce3+ by charge transfer and help Pt particles to maintain a smaller size. Consequently, a 0.25 wt % Pt catalyst, supported on Na-containing CeO2 nanorods and reduced at 600 °C, displays a high level of aniline productivity of 40.8 molAN/gPt/h and excellent stability in nitrobenzene hydrogenation at room temperature. A pathway of nitrobenzene hydrogenation catalyzed by Pt/CeO2 is also proposed.

CAS / MDL: 10294-41-4
研究领域: 催化化学 · 材料科学
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