ChemCatChem
·
2026
·Vol. 18
·期 13
·e70894
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IF 4.1
Siqi Tan,Jie Gu,Kexin Sha,Yihan Jiao,Yanxi Wu,Yiru Wang,Hongjian Yu,Jie Han
Niobates have emerged as promising candidates for environmental catalysis, particularly in the realm of piezocatalysis, owing to their distinctive layered architectures and robust physicochemical performance. In this study, we report the successful fabrication of A-site cation-tailored ABi 2 Nb 2 O 9 (A = Sr, Ca, and Ba) layered oxides via a molten salt strategy. Notably, the molten salt-synthesized SrBi 2 Nb 2 O 9 exhibits superior piezocatalytic performance in H 2 O 2 evolution with a yield reaching 1836.1 µmol g −1 h −1 , approximately 2.1 times higher than that of SrBi 2 Nb 2 O 9 prepared by the solid-state method. Furthermore, this material demonstrates exceptional piezocatalytic activity, degrading 98.0% of Rhodamine B within 75 min, with a reaction rate constant of 0.04966 min −1 . In addition, the catalyst shows durable stability, maintaining 97% of its original activity after four cycles. The influence of environmental factors, including solution pH and inorganic anions (Cl − and CO 3 2− ), was also systematically evaluated. This work elucidates that the synergistic integration of A-site cation engineering and molten salt synthesis effectively modulates the piezoelectric response of ABi 2 Nb 2 O 9 (A = Sr, Ca, and Ba), offering new insights and a viable pathway for the design of novel, high-performance piezocatalysts for environmental remediation. Graphical Molten salt-mediated A-site cation engineering of ABi 2 Nb 2 O 9 effectively modulates piezoelectric response, achieving superior piezocatalytic H 2 O 2 production and pollutant degradation. This work provides a viable pathway for designing high-performance piezocatalysts for environmental remediation.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2022
·
IF 4.598
Shuang Wu,Zheni Wang,Lei Wan,Chenghui Luo,Shams Ali Baig,Xinhua Xu
In the present study, Pd/Ni foam electrode was prepared by improved impregnation method for electrocatalytic hydrodechlorination (ECH) of clofibric acid (CA). The effects of complexing agent addition into the impregnation solution for the formation of Ni(OH) 2 and the ECH activity of Pd/Ni foam electrode were investigated. Results revealed that the introduction of sodium acetate (the complexing agent) greatly enhanced the ECH activity as compared to common impregnation liquid. Characterizations analyses demonstrated that the addition of sodium acetate did not change the phase of the electrode’s surface, but effectively reduced the deposition of Ni(OH) 2 . The surface morphology of the electrode was changed simultaneously by the addition of sodium acetate and the interlacing structure of Ni(OH) 2 and Pd catalyst was formed. NaAc before -Pd/Ni and NaAc after -Pd/Ni foam electrodes were used to perform ECH experiments on CA, and the combined Pd/Ni foam 15 min electrode was compared with the Pd/Ni foam 6 h electrode. After 2 h of electrolysis, the NaAc after -Pd/Ni foam electrode was found to remove the CA (∼100%) in the solution, which was 1.3 times the removal rate of the Pd/Ni foam 6 h electrode to CA and exceeded the Pd/Ni foam 15 min electrode. Findings from the present study demonstrated that adding the complexing agent into the impregnation solution can improve the ECH activity of Pd/Ni foam electrode and achieve a faster and more efficient dechlorination effect of CA.
研究领域:
环境化学
·
电化学
·
催化
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 19
·54556-54567
·
IF 5.8
Zhang Ge,Yang Huifen,Li Xuan,Zhou Yichen,Guo Song,Zhao Tong
The control of multiple heavy metals (HMs) pollution in solid wastes, especially the co-contamination of As and other heavy metal cations, is of great importance to ecological and environmental health. To address this problem, the preparation and application of multifunctional materials have attracted wide attention. In this work, a novel Ca-Fe-Si-S composite (CFSS) was applied to stabilize As, Zn, Cu, and Cd in acid arsenic slag (ASS). The CFSS exhibited synchronous stabilization ability for As, Zn, Cu, Cd and owned strong acid neutralization capacity. Under simulated field conditions, the acid rain extracted HMs in ASS successfully decreased below the emission standard (GB 3838–2002-IV category in China) after incubated by 5% CFSS for 90 days. Meanwhile, the application of CFSS promoted the transformation of leachable HMs into less accessible forms, which was conductive to the long-term stabilization for HMs. There was competitive relation among the three heavy metal cations, following the stabilization sequence of Cu > Zn > Cd during incubation. And the stabilization mechanisms of HMs by CFSS were proposed as chemical precipitation, surface complexation, and ion/anion exchange. The research will be greatly conducive to the remediation and governance of field multiple HMs contaminated sites.
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PubMed
高影响因子
JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY
·
2022
·Vol. 103
·期 3
·865-875
·
IF 2.606
Jia Jiannan,He Mengting,Wang Yunpeng,Zhang Wei,Wan Jun,Zhang Yuting,Xu Qiang,Chen Shiguo,Qiao Xvsheng,Fan Xianping
A propylene oxide (PO)-driven fast sol-gel route followed with a post high temperature calcination were utilized to synthesize Ca x Sr 1- x Al 2 O 4 : Eu 2+ cationic solid solution phosphors with micro-spherical morphologies and improved internal quantum efficiencies. The polyethylene oxide (PEO) was also employed to induce the phase separation of Ca x Sr 1- x Al 2 O 4 : Eu 2+ precursors to get monodispersed spherical morphologies in the sol-gel system. Benefit from uniform copolymerization of each chemical components and pyrolysis of organic matter, Ca, Sr, Al and O were homogenously distributed in the produced Ca x Sr 1- x Al 2 O 4 : Eu 2+ cage like microspheres. It helps to efficiently trap incident light and to improve the PL efficiencies. By changing the ratio of Ca/Sr, infinite solid solution polycrystalline phosphors, Ca x Sr 1- x Al 2 O 4 : Eu 2+ microspheres with x = 0~1, can be obtained and their PL emission can be gradually tuned from green to white to blue. Micro-spherical SrAl 2 O 4 : Eu 2+ , Ca x Sr 1- x Al 2 O 4 : Eu 2+ and CaAl 2 O 4 : Eu 2+ phosphors exhibited internal quantum efficiencies as high as 71.1, 35.3~45.9 and 75.3%, respectively.
Graphical abstract
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Frontiers in Chemistry
·
2022
·
IF 5.545
Wang Huan,Fan Yanmiao,Yang Qiaoli,Sun Xiaoyu,Liu Hao,Chen Wei,Aziz Ayesha,Wang Shenqi
Redox activity is an important indicator for evaluating electrochemical biosensors. In this work, we have successfully polymerized indole-5-carboxylic acid into poly-5-carboxyindole nanomaterials (PI-5-CA), using its superior redox activity, and introduced carboxylated single-walled carbon nanotubes (C-SWCNTs) to synthesize a composite material. Finally, a synthesized composite material was used for the modification of the glass carbon electrode to fabricate the PI-5-CA/C-SWCNTs/GCE-based immunosensor and was successfully applied for the sensitive detection of E. coli O157:H7. The fabricated immunosensor exhibited an outstanding electrocatalytic activity toward the detection of E. coli O157:H7 with a remarkably lowest limit of detection (2.5 CFU/ml, LOD = 3 SD/k, n = 3) and has a wide linear range from 2.98×101 to 2.98×107 CFU/ml. Inspired from the excellent results, the fabricated electrode was applied for the detection of bacteria from real samples (water samples) with a good recovery rate (98.13–107.69%) as well as an excellent stability and specificity. Owing to its simple preparation, excellent performance, and detection time within 30 min, our proposed immunosensor will open a new horizon in different fields for the sensitive detection of bacteria from real samples.
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JOURNAL OF POWER SOURCES
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2020
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IF 8.247
Jun Li,Jie Hou,Ying Lu,Qi Wang,Xiuan Xi,Yun Fan,Xian-Zhu Fu,Jing-Li Luo
CO 2 -poisoning effect on cathodes is an unnegligible problem for commercial application of solid oxide fuel cells (SOFCs). In order to enhance CO 2 tolerance of cathodes, partial replacement of Ba by Ca in BaCo 0·4 Fe 0·4 Zr 0·1 Y 0·1 O 3-δ (BCFZY) cathode is proposed in this study. The stability of Ba 0·95 Ca 0·05 Co 0·4 Fe 0·4 Zr 0·1 Y 0·1 O 3-δ (BCaCFZY) and BCFZY in CO 2 -containing atmosphere is investigated comparably. When tested in a symmetrical cell and exposed to air with 1% CO 2 or 10% CO 2 , the electrochemical performance of BCFZY cathode shows obviously degradation and carbonate particles are formed on the cathode surface . Exhilaratingly, the polarization resistance of BCaCFZY cathode is more stable and the cathode surface remains clean. The durability test in proton-conducting single cells further proves that the fine stability of BCaCFZY cathode can be achieved in air with 1% CO 2 atmosphere. In addition, thermodynamic analysis reveals the mechanism of Ca doping to improve stability. Ca dopant itself has a high CO 2 resistance and the introduction of Ca element reduces Ba segregation on surface. Base on the experimental results above, the BCaCFZY cathode is a promising candidate for SOFC applications .
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SENSORS AND ACTUATORS B-CHEMICAL
·
2019
·
IF 6.393
Xin Xiong,Yao Zhang,YinFang Wang,HaiFeng Sha,Nengqin Jia
By virtue of the metal organic framework UiO-66-NH 2, an ingenious electrochemiluminescence immunosensor was successfully constructed for subtle exploration of the breast cancer biomarker CA 15-3. In this protocol, Ru(bpy) 3 Cl 2 ·6H 2 O (Ru(bpy) 3 2+ ), as a conventional luminescent reagent, provides a stable and strong luminescent signal. The UiO-66-NH 2 serves as a carrier to provide a large specific surface area for enhancing the electrochemical luminescence signal response of Ru(bpy) 3 2+ . UiO-66-NH 2 , Ru(bpy) 3 2+ are fixed together with Nafion membrane, and CA 15-3 antibody is covalently conjugated onto the membrane through the amide reaction. Ru(bpy) 3 2+ @UiO-66-NH 2 is used as the detection system. The experimental results reveal that the ECL signal decreased obviously after the CA 15-3 antigen molecule is captured on the immunosensor, with the capture of manifesting the principle of electrochemical luminescence quenching detection. Under optimal conditions, the sensor is sensitive and selective for detecting CA 15-3 with the detection range from 5 × 10 −4 to 5 × 10 2 U mL -1 and the low LOD (1.7705 × 10 -5 U mL -1 ). Furthermore, multiple experiments elucidate that the as-prepared sensor could be used for susceptibly detect CA 15-3 in actual samples, which has underlying application prospects in biological analysis.
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POLYMER DEGRADATION AND STABILITY
·
2016
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IF 3.12
Mei Wang,Jianling Xia,Jianchun Jiang,Shouhai Li,Kun Huang,Wei Mao,Mei Li
A novel liquid Ca/Zn thermal stabilizer was synthesized from tung-maleic anhydride (TMA) as feedstock and evaluated for its stabilizing effects on poly (vinyl chloride) (PVC). First, N -(3-amino-benzoic acid) tung-maleamic acid (ABTMA) was prepared from the ammonolysis of TMA and para -aminobenzoic acid (PABA). Then its complex calcium salt (ABTMA-Ca) and zinc salt (ABTMA-Zn) were synthesized through a one-step method, and investigated by Fourier transform infrared spectroscopy and elemental analysis . ABTMA-Ca and ABTMA-Zn were separately treated with diethylene glycol monobutyl ether at 120 °C for 3 h to form liquid ABTMA-Ca (LABTMA-Ca) and liquid ABTMA-Zn (LABTMA-Zn). The effects of LABTMA-Ca/LABTMA-Zn, CaSt 2 /ZnSt 2 and C36DA-Ca/C36DA-Zn on thermal stability of PVC were studied through Congo Red test, discoloration tests and dynamic thermal stability analysis. The LABTMA-Ca/LABTMA-Zn thermal stabilizer exhibit excellent long-term stability. Analysis of tensile and dynamic mechanical properties shows PVC samples stabilized with LABTMA-Ca/LABTMA-Zn and the other two Ca/Zn systems all display comparable strength , modulus and glass transition. A common stabilizing mechanism of LABTMA-Ca/LABTMA-Zn system and its radical mechanism were presented, respectively.
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Journal of Materials Research and Technology-JMR&T
·
2025
·
IF 6.6
Geng Tang,Hong Yang,Bingqing Zhao,Dunying Wang,Fangfang Zeng,Qibin Liu
The rapid repair of bone defects remains a challenging clinical goal, with bio-piezoelectric composites emerging as promising materials due to their ability to replicate bone’s natural composition and electrical functionality. This study developed hydroxyapatite (HA)-based composites incorporating (Ba,Ca)(Ti,Sn)O3-based piezoceramics, achieving piezoelectric coefficients of 28.7 ± 2.48 pC/N, 11.1 ± 0.57 pC/N, and 5.7 ± 0.98 pC/N at HA mass fractions of 10%, 20%, and 30%, respectively, with a porosity around 20%. The composites were synthesized with a solid-state sintering method. The phase structure, surface morphology, and ferroelectric domain configuration of the composites were characterized. Electrical properties, compressive strengthen, hydrophilicity, in vitro bioactivity, biocompatibility and osteogenic ability were assessed. X-ray diffraction (XRD) analysis confirmed that all composites consisted of perovskite structure and HA phases. Microscopic observations revealed the (Ba,Ca)(Ti,Sn)O 3 -based piezoceramics particles embedded within the HA matrix. Evenly dispersed, irregular pores were formed, and pore size decreased as the HA content increased. The composite with 20 wt.% HA exhibited dense, small wedge-shaped domains and ferroelectric orthogonal (O) phase. Importantly, these composites demonstrated favorable compressive strength, surface wettability and biocompatibility, along with enhanced bioactivity and osteogenic differentiation ability in vitro , underscoring their potential in bone tissue engineering applications.
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CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Linjia Li,Yiran Zhang,Xiaochao Wang,Junfeng Lu,Jiaqi Feng,Shu Zhao,Wei Qiu,Zhen Huang,He Lin
Integrated carbon capture and utilization (ICCU) technology based on Ca-Ni-based dual-function materials (DFMs) is an important carbon reduction measure. However, the severe performance degradation of DFMs caused by H 2 O is a challenge for ICCU. This study aims to improve the H 2 O resistance of Ce-doped Ni-Ca-based DFMs by Mg-Y co-doping. After 10 cycles with H 2 O, the carbon capture capacity, methane yield, and methane production rate were maintained at 11 mmol/g, 10.5 mmol/g, and 121.18 μmol/g·min, respectively. Changing the water vapor content (0 ∼ 10 %) has little effect on its performance. Characterizations (XRD, TEM, XPS, H 2 -TPR, CO 2 -TPD, NH 3 -TPD, H 2 -TPSR, and in-situ DRIFTS) and experiments (carbonation and conversion by H 2 O experiments) revealed a directional induced hydrogen spillover mechanism: The strong interactions of Ni-Mg and Ni-Y reduce the particle size and inhibit agglomeration; meanwhile, H 2 O can activate the Y-doped Ni-based catalyst in the carbonation process, inducing hydrogen spillover into the methanation reaction path during the subsequent conversion process, where Mg-promoted generated formaldehyde species act as a vital intermediate. It provides a novel idea to enhance the H 2 O resistance of DMFs to achieve stable ICCU performances.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·
IF 2.7
Xuhui Wang,Guojie Zhang,Huanhuan Dong,Yong Zhang
Maltitol, a natural compound, offers a potentially eco-friendly alternative to conventional auxiliary thermal stabilizers. Its auxiliary stabilization effect was studied by discoloration tests, Congo red tests, thermogravimetric analysis, and UV–visible spectroscopy. Additionally, x-ray photoelectron spectroscopy and discoloration tests were used to study the stabilizing mechanisms of maltitol. Compared to dipentaerythritol, commonly used in the PVC industry, maltitol as an auxiliary stabilizer exhibits better improvement in thermal stability. This improvement is related to its melting point, ability to complex with zinc chloride, and content of hydroxyl groups. Furthermore, the addition of maltitol in PVC not only maintains good transparency of PVC basically unchanged but also improves the mechanical properties. Maltitol, as a natural, eco-friendly, and efficient auxiliary thermal stabilizer, exhibits a promising application prospect in PVC materials.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Bingbing Liu,Yifei Zhang,Peidong Yang,Yanfang Huang,Yubin Xue,Hu Sun,Shuzhen Yang,Guihong Han
Zinc electrolyte crystallization sediment (ZECS) generated in the zinc hydrometallugy industry contains valuable metals of strontium (Sr), manganese (Mn), and zinc (Zn), which has economical value but poses potential detrimental to the environment. However, the extraction and recovery of Sr is extremely difficult due to the thermodynamically stable Ca and Sr sulfate cocrystallization structure in ZECS. The destruction of refractory sulfate cocrystallization structure is a prerequisite for Sr extraction, and the carbothermal reduction roasting method is demonstrated to be efficient for the phase reconstruction. In this study, a stepwise Sr, Mn, and Zn recovery process from ZECS via carbothermal reduction roasting-acid leaching-selective precipitation-multistage extraction was proposed. In the reduction roasting procedure, all the sulfates including CaSO 4 , SrSO 4 , and Ca 0.7 Sr 0.3 SO 4 are reduced to soluble sulfides. Meanwhile, most MnO 2 is converted to a low-valence Mn product (MnO) that is soluble in acid, and the reduced Zn (g) is volatilized which can be collected from the flue dust. In the acid leaching procedure, the leaching efficiencies of Sr, Ca, and Mn are as high as 97.34%, 97.44%, and 95.49% respectively, while 99.50% Si in the form of silica is enriched in the leaching residue. After that, high-purity Sr solution was obtained after selective precipitation for Mn removal and D2EHPA multistage extraction for Ca removal. 97.41% Mn in the leaching solution is precipitated by adjusting the pH value to 9.5 with NaOH solution. After four-stage extraction, 79.60% Sr and only 0.35% Ca are retained in the aqueous phase. The purified solution contains 2.88 g/L Sr, 0.052 g/L Ca, and 0.014 g/L Mn, which can be used to prepare industrial SrCO 3 product via the carbonation operation. Thermodynamic behavior and reduction roasting reconstruction mechanism of Ca and Sr sulfate cocrystallization structure in ZECS were discussed in this work. The distributions of main metal elements (Sr, Ca, Mn, and Zn) in ZECS during the carbothermal reduction roasting-acid leaching-selective precipitation-multistage extraction process were also systematically studied.
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