JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2014
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IF 3.552
Hang Long,Pingxiao Wu,Lin Yang,Zhujian Huang,Nengwu Zhu,Zhixian Hu
Ethylamine modified vermiculite (Ethyl-VER) with high specific surface area and excellent pore structure was prepared to remove cesium from aqueous solution. The physic-chemical properties of the pristine and modified vermiculite were analyzed by X-ray diffraction (XRD), Fourier-transform infrared (FTIR), specific surface area (BET) and scanning electron microscopy/energy disperse spectroscopy (SEM/EDS). The corroding effect of ethylamine increased the specific surface area of vermiculite from 4.35 to 15.59 m 2 g −1 , and the average pore diameter decreased from 6.8 to 5.34 nm. Batch adsorption experiments were conducted as a function of pH, initial Cs + concentration, contact time, coexisting cations (K + , Na + , Ca 2+ ) and low-molecular-weight organic acids (acetic acid, oxalic acid, citric acid) to illustrate the adsorption behavior. The study found that the adsorption capacity of cesium in aqueous solution was improved from 56.92 to 78.17 mg g −1 after modification. The formation of micropores and mesopores and the increased surface area played a critical role in the enhancement of cesium adsorption. Kinetic experiments indicated that the adsorption process can be simulated well with a pseudo-second-order model. The presence of cations or low-molecular-weight organic acids inhibited cesium adsorption in different degrees. On the basis of our results, Ethyl-VER with good surface characteristics and high adsorption capacity is a suitable adsorbent for cesium removal from aqueous solution.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2022
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IF 6.371
Zhengdao Li,Yan Xiong,Dongqin Bi,Qi Liu,Chuanyun Yang,Jia Zhang
To optimize the structure and composition of the metal oxide semiconductor is one of effective approaches to improve its gas-sensing performance. In this paper, Zn 2 SnO 4 solid octahedrons were first synthesized by a hydrothermal method , then converted to hollow structures with a shape preserved through a simple and practical acid etching process. Ultimately, the hierarchical ZnSnO 3 /Zn 2 SnO 4 hollow composite with porous structure was designed and prepared by in situ growth of ZnSnO 3 nanosheets on the surface of Zn 2 SnO 4 hollow octahedrons in the seed mediated wet-chemical way. It was found that through the structure evolution from solid octahedron to hollow structure, the sensitivity of gas sensor toward triethylamine (TEA) was visibly improved. Significantly, superior TEA-sensing properties, such as lower optimal working temperature, higher sensitivity, wider linear response range, more rapid response/recovery speed and more excellent selectivity were further achieved by decorating Zn 2 SnO 4 hollow octahedrons with ZnSnO 3 nanosheets. It was remarkable that the sensor based on hierarchical ZnSnO 3 /Zn 2 SnO 4 porous hollow octahedrons displayed long-term stability to TEA and anti-humidity property, suggesting its potential practical applications in detection of highly toxic TEA. The improved sensing mechanism on the strength of structure and composition evolution for the gas sensor was discussed in detail.
研究领域:
材料科学
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传感器技术
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
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2023
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IF 5.2
Xuehua Chen,Chao Qin,Zicheng Zheng,Hanwen Chi,Zhizhen Ye,Liping Zhu
Gas sensors with good repeatability and controllable fabrication method are extremely desired for practical applications. Co-MOF-derived Co 3 O 4 is a promising gas-sensing material candidate because of its large surface area, ultrahigh porosities, and abundant oxygen defects. However, the advantages of Co-MOF precursor were limited by the traditional sensor fabrication methods. Moreover, the high resistance and poor surface activity of Co 3 O 4 resulted in low gas-sensing performance at room temperature (RT). To overcome these challenges, in-situ sensors based on Co 3 O 4 porous films with controlled nanoscale thickness were directly prepared on ceramic substrates by using Co-MOF films as precursors. To further improve the conductivity, SnO 2 catalytic overlayers were introduced on top of Co 3 O 4 sensors to construct SnO 2 /Co 3 O 4 bilayer sensors, which were promising for triethylamine (TEA) detection at RT. As a result, the optimized SnO 2 /Co 3 O 4 sensor exhibited a fast response/recovery rate (11 s/16 s), high selectivity, and a satisfactory sensitivity (150%) to TEA at RT. The enhanced gas-sensing performance could be attributed to the unique bilayer structures, improved conductivity, and synergistic effects of the SnO 2 catalytic overlayers and Co 3 O 4 sensing layers.
研究领域:
材料科学
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化学传感器
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纳米技术
✓ 已验证
产品关联
DOI
高影响因子
Molecular Catalysis
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2025
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IF 4.9
Kai Zhang,Shuwei Chen,Zhaohui Guo,Yingxiong Wang,Yan Qiao
As a renewable resource, the catalytic conversion of xylose has attracted much attention. The epimerization of xylose to lyxose is an important way to obtain the rare sugar lyxose. Current approaches to xylose epimerization encounter several challenges, including the requirement for high temperatures, the use of costly catalysts and a propensity for side reactions that favor the formation of ketoses. CaCl 2 is an environmentally friendly and naturally abundant metal salt that can act as a Lewis acid in catalytic processes. Herein, we demonstrate that CaCl 2 and Et 3 N work synergistically to achieve 68 % lyxose yield under mild conditions. Compared to conventional approaches, which often require harsh conditions or expensive catalysts, our system demonstrates a cost-effective and selective strategy. Moreover, through a combined experimental and computational approach (NMR, isotope tracing and DFT), we provide unprecedented mechanistic insights into the role of calcium complexation in facilitating epimerization. Complexation between xylose and calcium ion was confirmed by NMR titration and Diffusion Ordered NMR Spectroscopy (DOSY-NMR). Isotope experiments further demonstrated that the C1-C2 migration caused the turnover of the hydroxyl group at C2 in the presence of calcium ions. The frontier orbital analysis and deprotonation energy calculation showed that the hydroxyl group at C1 had the lowest deprotonation energy, which initiated the ring-opening process. The DFT calculations reveal that the calcium ions preferentially complex with the hydroxyl groups of xylose, thereby reducing the energy barrier for the C1 proton dissociation and facilitating the epimerization. These findings offer a new perspective on xylose epimerization with Ca-based catalyst.
研究领域:
生物化学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
ACS Sensors
·
2025
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IF 9.1
Tianrun Zheng,Yi Lu,Yilin Wang,Hong Zhou,Kang Yang,Mingxue Zhang,Yueying Liu,Fengmin Liu,Geyu Lu
Optimizing and improving the surface activity of Co3O4 sensing materials are crucial for applications in triethylamine detection. Herein, indium-doped Co3O4 hollow microflowers (InCo HMfs), assembled from ultrathin nanosheets, were prepared via a hydrolysis reaction. Three distinct crystal facets─{1 1 0}, {1 1 1}, and {0 0 1}─were observed in 2-InCo HMfs. Results from TEM, XPS, and XAS characterization show that the increase of Co2+ content induced by indium doping promotes the formation of highly active crystal planes in Co3O4. DFT calculations revealed the reasons for the improvement in the gas sensing performance of 2-InCo HMfs and the multiple effects of In ions. Our dual strategy of doping with indium and hydrolysis markedly improved the intrinsic TEA sensing performance of Co3O4, offering a novel avenue for designing high-performance TEA sensors.
研究领域:
材料科学
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化学传感器
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表面化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2023
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IF 6.2
Xiaoyan Xiong,Lijiu Cao,Siyi Li,Xuqi Hu,Guoqiang Liu,Yunpeng Gong,Yufang Chen,Tao Jin
In this study, a composite heterojunction material of Ti 3 C 2 Tx MXene nanosheets with Co 9 S 8 @In 2 S 3 nanoparticles , named (Co 9 S 8 @In 2 S 3 )/MXene, was constructed using a hydrothermal method . The materials were characterized and analyzed in terms of morphology, structure, and selective response properties to triethylamine gas. The materials were characterized by SEM, TEM, HAADF, STEM, XRD , XPS, BET, and other tests. The results showed a response value of 44.9 for (Co 9 S 8 @In 2 S 3 )/20% MXene at 350 °C and 20 ppm triethylamine (TEA), with a response/recovery time of 63 s/115 s respectively. In particular, (Co 9 S 8 @In 2 S 3 )/MXene exhibits excellent immunity to interference and a highly stable adsorption/desorption process with almost no noise interference. In addition, the (Co 9 S 8 @In 2 S 3 )/MXene material showed stable and fast selective response to TEA in different types of gas mixtures compared with the commonly used single TEA selective response study method. The results of this study provide valuable techniques and theories for the Environmental protection application of TEA selective response materials. Finally, this article performs a comparative analysis on the mechanism of selection response and stability of (Co 9 S 8 @In 2 S 3 )/MXene materials, and concludes that the process determining the specific response of (Co 9 S 8 @In 2 S 3 )/MXene materials to particular gas molecules includes three processes: shape-selective adsorption, redox reaction , and charge carrier conduction.
研究领域:
材料科学
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环境科学
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化学
✓ 已验证
产品关联
DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2020
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IF 3.232
Angxin Tong,Xiaojun Tang,Feng Zhang,Bin Wang
In this study, we mainly focused on predictable regularities of the red shift of ultraviolet spectra for β-phenylethylamine (PEA), NaCl and NaOH in aqueous solution. The absorption peaks of the UV spectra near 191 nm of NaCl, NaOH and PEA in aqueous solution moved in the direction of a red shift while the molar absorption coefficient at the peak increased regularly with the increasing solution concentration. These shifts were obtained for solutions with concentrations ranging from 3.68 to 1000 mmol/L for NaCl, from 0.762 to 2000 mmol/L for NaOH, and from 0.0515 to 8.91 mmol/L for PEA. The plots of the logarithm of the solution concentration for NaCl and PEA versus the absorbance at 191 nm and at the peak were linear, and the plots of the logarithm of the solution concentration for NaCl and PEA versus the wavelength at the peak (shifted from 191 nm) were also linear. In addition, the plots of the logarithm of the solution concentration for NaOH that ranged from 0.762 to 1.96 mmol/L versus the absorbance at 191 nm and at the peak were linear as well as the plots of the logarithm of the solution concentration for NaOH that ranged from 1.96 to 2000 mmol/L versus the wavelength at the peak. The slopes of the absorbance at 191 nm of PEA, NaCl and NaOH were somewhat similar to the absorbance at the peak separately, whereas the slopes of the wavelengths at the peak were different from them. Finally, in order to obtain the predictable regularity of the red shift of the UV spectrum for the mixture, 22 ternary mixtures were prepared. The results indicate that the inhibiting effect of hydroxide ions (OH-) caused the wavelength near 206 nm to remain unchanged when the solution concentration of NaOH in the mixture was more than 0.762 mmol/L.
研究领域:
化学
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光谱学
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分析化学
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2025
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IF 9
Miao-Miao Jia,Si-Yuan Yang,Ke-Ke Chen,Pan-Pan Zhang,Wei Shao,Zhen Chen,Zi-Meng Xu,Qing-Yun Wu,Yi Li,Ming Xue
Thin-film composite (TFC) reverse osmosis (RO) membranes, fabricated by interfacial polymerization, have achieved significant success in addressing the global water scarcity. Over the past three decades, the camphor sulfonic acid (CSA)/triethylamine (TEA) has been widely used in fabrication of TFC RO membranes. However, the mechanism of this unique formula remains elusive and contentious. In this work, for the first time, deciphering that introducing CSA/TEA into the aqueous phase has negligible impact on the selective polyamide (PA) layer but facilitate the aqueous solution impregnating of porous polysulfone (PSf) support. Specifically, the acidic CSA significantly hinders amine diffusion yet preserves the porosity of the PSf support during high-temperature curing. TEA is essential in modulating the pH changes and balancing the monomer diffusion rate that results from CSA. The COMSOL simulations have further elucidated that the presence of an aqueous solution within the porous support can mitigate the thermal expansion of the PSf, consequently inhibiting the shrinkage of surface pores. The TFC membrane demonstrated a substantial improvement in water permeance due to the preservation of its pore structure. The obtained TFC membrane demonstrated an exceptional NaCl rejection of 99.3 % and a high water flux of 76.8 L m –2 h −1 (2000 ppm NaCl, 15.5 bar), exceeding that of the state-of-the-art TFC RO membranes. Moreover, the RO membrane manifested with long-term stability and good fouling resistance. The mechanistic insights have important implications to more efficient membrane-based desalination and water reuse, thereby reducing energy consumption and minimizing environmental carbon footprint.
研究领域:
材料科学
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环境工程
✓ 已验证
产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
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2024
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IF 8
Weining Liu,Hairong Li,Dandan Huang,Xi Tan,Mingyang Zhao,Qionglin Cheng,Ming Yi,Qi Ding,Yaqian Ren,Guohan Liu
Triethylamine (TEA) poses severe safety hazards to industrial production and human health. To accurately detect TEA concentrations and rapidly warn of leakage, a simple reflux condensation method was deployed to successfully incorporate Zn 2+ in situ into Mo-MOFs precursor in a green, safe, and time-efficient synthesis condition. Subsequently, through calcination, MoO 3 /ZnMoO 4 -X (MMZ-X) were prepared, which exhibited an increased number of defects and enriched porosity, facilitating the access and interaction of TEA with adsorption sites. Simultaneously, rationally built in situ MoO 3 /ZnMoO 4 heterostructures accelerated carrier migration and induced a drastic resistive change. MMZ-2 demonstrated outstanding TEA sensing performance, exhibiting extremely high sensitivity ( R = 572.3, 100 ppm), along with superior selectivity, repeatability and stability, rapid response and recovery times, and a low detection limit. Moreover, the key intrinsic parameters of the heterostructure on the atomic scale were determined by density functional theory (DFT) calculations, providing a detailed elucidation of the sensing enhancement mechanism of the MoO 3 /ZnMoO 4 heterostructure. The simple and efficient synthesis method and the related mechanistic analysis pave a new path for designing high-performance TEA gas sensors with practical applications.
研究领域:
材料科学
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化学传感器
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环境监测
✓ 已验证
产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2024
·
IF 8
Shenman Yao,Dehua Wang,Jiahao Li,Jianxian You,Yulin Zhu,Wufei Gong,Keng Xu,Yan Liang,Yanxing Yang,Yong Yang
Crystal facets engineering emerges as a potent strategy for modulating the surface properties and gas sensing performance of semiconductor metal oxides. However, related studies have primarily focused on conventional binary metal oxides gas sensing materials, while few studies have investigated the crystal facets-dependent gas sensing activity of recently developed ternary metal oxides. Herein, the effect of crystal facets on the gas sensing activity of Aurivillius-type layered perovskite structure material Bi 2 MoO 6 was studied. It was shown that Bi 2 MoO 6 nanosheets with {001} crystal facets exhibited significantly enhanced gas sensing activity with a high response value of 72 (R a /R g ) towards 100 ppm of triethylamine at relatively low working temperature of 250 °C, which was about 10 times higher than that of Bi 2 MoO 6 nanosheets with {010} crystal facets. The gas mechanism was elucidated at the atomic and electronic levels through first principles calculation combined with experimental characterization. On the one hand, the synergistic effect of Mo/Bi bimetallic sites makes the adsorption/charge transfer between {001} facets and triethylamine much stronger. On the other hand, {001} facets have abundant chemically adsorbed oxygen and oxygen vacancy on the surface, which act as the active species in gas sensing. These results not only significantly broaden the application scope of Aurivillius-type layered perovskite structure materials in the realm of gas sensing, but also provide important guidance for the study of gas sensing mechanism in ternary metal oxides.
研究领域:
材料科学
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气体传感技术
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2024
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IF 12.2
Huixuan Chen,Jiayu Li,Siwen Tao,Xinhua Tian,Xikun Sun,Ruiqin Gao,Ni Bai,Guo-Dong Li
Developing fast, accurate and sensitive triethylamine gas sensors with low detection limits is paramount to ensure the safety of workers and the public. However, sensors based on single metal oxide materials still suffer from drawbacks such as low response sensitivity and long response and recovery times. To address these challenges, in this work, a series of mesoporous CdO/CdGa 2 O 4 microspheres were synthesized. We optimized the sensor's sensing performance to triethylamine by fine-tuning the ratio of CdO to CdGa 2 O 4 . Among them, CdO:3CdGa 2 O 4 -based sensor demonstrates a rapid response time of 2 s to detect 100 ppm of triethylamine, with a high response value of 211 and exceptional selectivity. Furthermore, it exhibits a low detection limit of 20 ppb for triethylamine, making it suitable for practically testing fish freshness. Crucially, electron transfer between the heterojunctions increases the chemically adsorbed oxygen on the materials’ surface, thereby enhancing the sensor's response sensitivity to triethylamine. This discovery provides new insights and methodologies for the design of highly efficient triethylamine gas sensors.
研究领域:
材料科学
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化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2024
·
IF 5.7
Qilin Yang,Yitao Bai,Shuangping Liu,Xiao Han,Tiantian Liu,Dongna Ma,Jian Mao
Elevated levels of biogenic amines (BAs) in fermented food can have negative effects on both the flavor and health. Mining enzymes that degrade BAs is an effective strategy for controlling their content. The study screened a strain of Lactobacillus hilgardii 1614 from fermented food system that can degrade BAs. The multiple copper oxidase genes LHMCO1614 were successfully mined after the whole genome protein sequences of homologous strains were clustered and followed by homology modeling. The enzyme molecules can interact with BAs to stabilize composite structures for catalytic degradation, as shown by molecular docking results. Ingeniously, the kinetic data showed that purified LHMCO1614 was less sensitive to the substrate inhibition of tyramine and phenylethylamine. The degradation rates of tyramine and phenylethylamine in huangjiu (18% vol) after adding LHMCO1614 were 41.35 and 40.21%, respectively. Furthermore, LHMCO1614 demonstrated universality in degrading tyramine and phenylethylamine present in other fermented foods as well. HS-SPME-GC-MS analysis revealed that, except for aldehydes, the addition of enzyme treatment did not significantly alter the levels of major flavor compounds in enzymatically treated fermented foods (p > 0.05). This study presents an enzymatic approach for regulating tyramine and phenylethylamine levels in fermented foods with potential applications both targeted and universal.
研究领域:
微生物学
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食品安全
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酶学
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）