Bearings play a vital role in the operation of a two-axis system. Long-term bearing use inevitably produce bubbles and frictional damage. Therefore, the protection of bearings is critical for the stable operation of a two-axis system. In this study, a TiO₂ nanofilm is used to physically protect a bearing. The discretization method is used to analyse the cavitation process. Cavitation primarily occurs on the front surface of the pad during bearing operation. A finite element analysis of a bearing pad coated and not coated with TiO₂ nanofilms shows that TiO₂ nanofilms can effectively absorb the cavitation force exerted on pads, thereby reducing inflicted damage. Moreover, the TiO₂ nanofilm reduces the friction coefficient of the pad surface, promoting good bearing capacity of the bearing during rotation. The TiO₂ nanofilm serves as a protective layer that improves the anti-wear and bearing performance of a two-axis system.
{"title":"Study on Cavitation and Tribological of TiO₂ Nano-Film on Bearing Pads Surface.","authors":"Juan Zhang, Donghui Li, Bo Zhang","doi":"10.1166/jnn.2021.19506","DOIUrl":"https://doi.org/10.1166/jnn.2021.19506","url":null,"abstract":"<p><p>Bearings play a vital role in the operation of a two-axis system. Long-term bearing use inevitably produce bubbles and frictional damage. Therefore, the protection of bearings is critical for the stable operation of a two-axis system. In this study, a TiO₂ nanofilm is used to physically protect a bearing. The discretization method is used to analyse the cavitation process. Cavitation primarily occurs on the front surface of the pad during bearing operation. A finite element analysis of a bearing pad coated and not coated with TiO₂ nanofilms shows that TiO₂ nanofilms can effectively absorb the cavitation force exerted on pads, thereby reducing inflicted damage. Moreover, the TiO₂ nanofilm reduces the friction coefficient of the pad surface, promoting good bearing capacity of the bearing during rotation. The TiO₂ nanofilm serves as a protective layer that improves the anti-wear and bearing performance of a two-axis system.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Arenst Andreas Arie, Shealyn Lenora, Hans Kristianto, Ratna Frida Susanti, Joong Kee Lee
Lithium sulfur battery has become one of the promising rechargeable battery systems to replace the conventional lithium ion battery. Commonly, it uses carbon-sulfur composites as cathode materials. Biomass based carbons has an important role in enhancing its electrochemical characteristics due to the high conductivity and porous structures. Here, potato peel wastes have been utilized to prepare porous carbon lithium sulfur battery through hydrothermal carbonization followed by the chemical activation method using KOH. After sulfur loading, as prepared carbon-sulfur composite shows stable coulombic efficiencies of above 98% and a reversible specific capacity of 804 mAh g-1 after 100 cycles at current density of 100 mA g-1. These excellent electrochemical properties can be attributed to the unique structure of PPWC showing mesoporous structure with large specific surface areas. These results show the potential application of potato peel waste based porous carbon as electrode's materials for lithium sulfur battery.
锂硫电池已成为替代传统锂离子电池的极具发展前景的可充电电池系统之一。通常采用碳硫复合材料作为正极材料。生物质基碳具有高导电性和多孔结构,对提高其电化学性能具有重要作用。本课题以马铃薯皮废料为原料,通过水热炭化后KOH化学活化法制备多孔碳锂硫电池。负载硫后,碳硫复合材料的库仑效率稳定在98%以上,在100 mA g-1电流密度下循环100次后的可逆比容量为804 mAh g-1。这些优异的电化学性能可归因于PPWC独特的结构,具有较大的比表面积和介孔结构。这些结果显示了马铃薯皮废基多孔碳作为锂硫电池电极材料的潜在应用前景。
{"title":"Potato Peel Based Carbon-Sulfur Composite as Cathode Materials for Lithium Sulfur Battery.","authors":"Arenst Andreas Arie, Shealyn Lenora, Hans Kristianto, Ratna Frida Susanti, Joong Kee Lee","doi":"10.1166/jnn.2021.19288","DOIUrl":"https://doi.org/10.1166/jnn.2021.19288","url":null,"abstract":"<p><p>Lithium sulfur battery has become one of the promising rechargeable battery systems to replace the conventional lithium ion battery. Commonly, it uses carbon-sulfur composites as cathode materials. Biomass based carbons has an important role in enhancing its electrochemical characteristics due to the high conductivity and porous structures. Here, potato peel wastes have been utilized to prepare porous carbon lithium sulfur battery through hydrothermal carbonization followed by the chemical activation method using KOH. After sulfur loading, as prepared carbon-sulfur composite shows stable coulombic efficiencies of above 98% and a reversible specific capacity of 804 mAh g<sup>-1</sup> after 100 cycles at current density of 100 mA g<sup>-1</sup>. These excellent electrochemical properties can be attributed to the unique structure of PPWC showing mesoporous structure with large specific surface areas. These results show the potential application of potato peel waste based porous carbon as electrode's materials for lithium sulfur battery.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158896","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S Arockia Shyamala Paniyarasi, S Padmaja, M Pushpa Selvi, R M Gnanamuthu, R Nimma Elizabeth
The significant role of Tris(2,2,2-trifluoroethyl) phosphite (TTFP) as an efficient additive during cycling of the layered nanostructured LiNi0.1Mg0.1Co0.8O₂ and olivine LiFePO₄ cathode materials in EC/DMC and 1M LiPF6 electrolyte for Li-ion battery are extensively investigated in this work. The electrochemical characterization techniques such as cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy show that TTFP improves cycling stability and reduces the irreversible capacity of LiNi0.1Mg0.1Co0.8O₂ and LiFePO₄ electrodes. Also, the presence of TTFP in electrolyte solution reduces the impedance in LiNi0.1Mg0.1Co0.8O₂ and LiFePO₄ cathode materials at room temperature. A family of Nyquist plots was obtained from LiNi0.1Mg0.1Co0.8O₂ and LiFePO₄ electrodes for various potentials during the course of charging. The addition of TTFP in the electrolyte reduces the surface impedance of lithiated LiNi0.1Mg0.1Co0.8O₂ and LiFePO₄ which can be attributed to the reaction of the additive on the electrode's surface. Also, the presence of the additive TTFP in LiNi0.1Mg0.1Co0.8O₂ and LiFePO₄ cell enhances the lithium diffusion rate and improves the electronic conductivity of the cathode material.
{"title":"Elevated Electrochemical Performance of LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ Cathodes with Tris(2,2,2-trifluoroethyl) Phosphite as an Efficient Electrolyte Additive.","authors":"S Arockia Shyamala Paniyarasi, S Padmaja, M Pushpa Selvi, R M Gnanamuthu, R Nimma Elizabeth","doi":"10.1166/jnn.2021.19322","DOIUrl":"https://doi.org/10.1166/jnn.2021.19322","url":null,"abstract":"<p><p>The significant role of Tris(2,2,2-trifluoroethyl) phosphite (TTFP) as an efficient additive during cycling of the layered nanostructured LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and olivine LiFePO₄ cathode materials in EC/DMC and 1M LiPF<sub>6</sub> electrolyte for Li-ion battery are extensively investigated in this work. The electrochemical characterization techniques such as cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy show that TTFP improves cycling stability and reduces the irreversible capacity of LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ electrodes. Also, the presence of TTFP in electrolyte solution reduces the impedance in LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ cathode materials at room temperature. A family of Nyquist plots was obtained from LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ electrodes for various potentials during the course of charging. The addition of TTFP in the electrolyte reduces the surface impedance of lithiated LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ which can be attributed to the reaction of the additive on the electrode's surface. Also, the presence of the additive TTFP in LiNi<sub>0.1</sub>Mg<sub>0.1</sub>Co<sub>0.8</sub>O₂ and LiFePO₄ cell enhances the lithium diffusion rate and improves the electronic conductivity of the cathode material.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158965","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The application of electrochemical catalytic oxidation in wastewater treatment with powerful Cldoped graphene as an anode has been discussed as a novel approach to degrade acetaminophen effectively. The characteristics of Cl-doped graphene that were related to Cl loading content and microscopic morphology were analyzed by using several instruments, and the defects created by Cl doping were identified. Quenching experiments and electron paramagnetic resonance detection were proposed to clarify the mechanism underlying the production of active free radicals by Cldopedgraphene. The degradation results indicated that efficiency increased with the percentage of Cl atoms doped into the graphene. The best degradation efficiency of acetaminophen could reach 98% when Cl-GN-12 was used. In the process of electrocatalytic oxidation, O•-₂, and active chlorine, as the main active species, persistently attacked acetaminophen into open-ring intermediates, such as 4-chlororesorcinol, and finally into CO₂ and H²O.
{"title":"Facilely Prepared Cl-Doped Graphene as an Efficient Anode for the Electrochemical Catalytic Degradation of Acetaminophen.","authors":"Qian Zhang, Bingxin Wang, Jun-Ming Hong","doi":"10.1166/jnn.2021.19526","DOIUrl":"https://doi.org/10.1166/jnn.2021.19526","url":null,"abstract":"<p><p>The application of electrochemical catalytic oxidation in wastewater treatment with powerful Cldoped graphene as an anode has been discussed as a novel approach to degrade acetaminophen effectively. The characteristics of Cl-doped graphene that were related to Cl loading content and microscopic morphology were analyzed by using several instruments, and the defects created by Cl doping were identified. Quenching experiments and electron paramagnetic resonance detection were proposed to clarify the mechanism underlying the production of active free radicals by Cldopedgraphene. The degradation results indicated that efficiency increased with the percentage of Cl atoms doped into the graphene. The best degradation efficiency of acetaminophen could reach 98% when Cl-GN-12 was used. In the process of electrocatalytic oxidation, O<sup>•-</sup>₂, and active chlorine, as the main active species, persistently attacked acetaminophen into open-ring intermediates, such as 4-chlororesorcinol, and finally into CO₂ and H²O.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39159101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cadmium sulfide nanoparticles (CdS NPs) were synthesized by using cadmium acetate and thiourea as precursors and sodium oleate as the surfactant under different cadmium acetate concentrations in anhydrous ethanol. Cadmium (Cd) precursor concentration greatly affected the nucleation-growth of CdS NPs. In extremely dilute solution with a Cd precursor concentration of 0.1 mmol · L-1, an overlapped nucleation and growth corresponding to two pronounced absorption peaks at 310 nm and 350 nm, respectively, was observed. Unparalleled nucleation was dominant within very long reaction time until 10 hours. The nuclei and the resulting magic-sized CdS NPs may be used as seeds to prepare size and shape controllable nanoparticles. On the contrary, at a high Cd precursor concentration (5 mmol · L-1), nucleation and growth were separated. Only one first exciton absorption peak standing for the growth of regular CdS NPs appeared at 440 nm. Many techniques including transmission electron microscopy (TEM), X-ray powder diffraction (XRD), ultraviolet-visible (UV-Vis) absorption and photoluminescence (PL) spectrometers were applied to characterize the morphology, crystalline structure, and optical properties of CdS NPs.
{"title":"Observation of Dominant Nuclei and Magic-Sized CdS Nanoparticles in a Single-Phase System.","authors":"Xiaobo Nie, Yanming Chen","doi":"10.1166/jnn.2021.19504","DOIUrl":"https://doi.org/10.1166/jnn.2021.19504","url":null,"abstract":"<p><p>Cadmium sulfide nanoparticles (CdS NPs) were synthesized by using cadmium acetate and thiourea as precursors and sodium oleate as the surfactant under different cadmium acetate concentrations in anhydrous ethanol. Cadmium (Cd) precursor concentration greatly affected the nucleation-growth of CdS NPs. In extremely dilute solution with a Cd precursor concentration of 0.1 mmol · L<sup>-1</sup>, an overlapped nucleation and growth corresponding to two pronounced absorption peaks at 310 nm and 350 nm, respectively, was observed. Unparalleled nucleation was dominant within very long reaction time until 10 hours. The nuclei and the resulting magic-sized CdS NPs may be used as seeds to prepare size and shape controllable nanoparticles. On the contrary, at a high Cd precursor concentration (5 mmol · L<sup>-1</sup>), nucleation and growth were separated. Only one first exciton absorption peak standing for the growth of regular CdS NPs appeared at 440 nm. Many techniques including transmission electron microscopy (TEM), X-ray powder diffraction (XRD), ultraviolet-visible (UV-Vis) absorption and photoluminescence (PL) spectrometers were applied to characterize the morphology, crystalline structure, and optical properties of CdS NPs.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Manganese dioxide (α-MnO₂) and graphene oxide (GO nanocomposites were prepared and successfully characterized using Fourier-transform infrared (FT-IR), field emission scanning-electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDX) mapping methods and Xray diffraction (XRD) analyses. This reagent is an efficient catalyst for the aerobic oxidation of trimethylsilyl (TMS), tetrahedropyranyl (THP), and methoxymethyl ethers (MOM) to their corresponding carbonyl compounds in the presence of K₂CO₃. All reactions were performed in n-hexane under mild and completely heterogeneous reaction conditions. Our novel method has the advantages of excellent yields, short reaction times, availability and reusability of the catalyst and simple and easy work-up procedure compared to the conventional methods reported in the literature.
{"title":"Manganese Dioxide (<i>α</i>-MnO₂) and Graphene Oxide (GO) Nanocomposites: An Efficient Promotor for the Oxidative Deprotection of Trimethylsilyl, Tetrahydropyranyl and Methoxymethyl Ethers.","authors":"Pouran Pourayoob Foumani, Hassan Tajik, Farhad Shirini, Shahed Hassanpoor","doi":"10.1166/jnn.2021.19519","DOIUrl":"https://doi.org/10.1166/jnn.2021.19519","url":null,"abstract":"<p><p>Manganese dioxide (<i>α</i>-MnO₂) and graphene oxide (GO nanocomposites were prepared and successfully characterized using Fourier-transform infrared (FT-IR), field emission scanning-electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDX) mapping methods and Xray diffraction (XRD) analyses. This reagent is an efficient catalyst for the aerobic oxidation of trimethylsilyl (TMS), tetrahedropyranyl (THP), and methoxymethyl ethers (MOM) to their corresponding carbonyl compounds in the presence of K₂CO₃. All reactions were performed in <i>n</i>-hexane under mild and completely heterogeneous reaction conditions. Our novel method has the advantages of excellent yields, short reaction times, availability and reusability of the catalyst and simple and easy work-up procedure compared to the conventional methods reported in the literature.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158628","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this study, the ruthenium complexes, which is an organometallic N-3 and C-106 semiconductor material, was coated on indium tin oxide (ITO) by using the self-assembled technique and thus a diode containing an organometallic interface was produced. The effects of this interface on the electronic parameters of the diode were investigated. It is aimed to improve the heterogeneity problem of the inorganic/organic interface by chemically bonding these materials from COOH active parts to the ITO surface. In order to understand how the electronic parameters of the diode change with this modification, the Schottky diode electrical characterization approach has been used. The charge mobility of the diode was calculated using the current density-voltage curve (J-V) characteristic with Space Charge Limited Current (SCLC) technique. When the electrical field is applied to the diode, it can be said that the ruthenium complexes molecules create an electrical dipole and the tunneling current is transferred to the anode contact ITO through the ruthenium molecule through the charge carrier, thus contributing to the hole injection. The morphology of these interface modifications was examined by Atomic Force Microscope (AFM) and surface potential energy by KelvinProbe Force Microscope (KPFM). To investigate local conductivity of bare ITO and modified ITO surface, Scanning Spreading Resistance Microscopy (SSRM) that is a conductive AFM analyzing technique were performed by applying voltage to the conductive tip and to the sample. According to the results of this work the diode containing N-3 material shows the best performance in terms of charge injection to the ITO due to possess the lowest barrier height Φb as 0.43 eV.
{"title":"Electronic Parameters of Diode Based Organometallic Semiconductor Dyes Centered Ruthenium Complexes with Active COOH Terminals.","authors":"Ali Kemal Havare","doi":"10.1166/jnn.2021.19508","DOIUrl":"https://doi.org/10.1166/jnn.2021.19508","url":null,"abstract":"<p><p>In this study, the ruthenium complexes, which is an organometallic N-3 and C-106 semiconductor material, was coated on indium tin oxide (ITO) by using the self-assembled technique and thus a diode containing an organometallic interface was produced. The effects of this interface on the electronic parameters of the diode were investigated. It is aimed to improve the heterogeneity problem of the inorganic/organic interface by chemically bonding these materials from COOH active parts to the ITO surface. In order to understand how the electronic parameters of the diode change with this modification, the Schottky diode electrical characterization approach has been used. The charge mobility of the diode was calculated using the current density-voltage curve (<i>J-V</i>) characteristic with Space Charge Limited Current (SCLC) technique. When the electrical field is applied to the diode, it can be said that the ruthenium complexes molecules create an electrical dipole and the tunneling current is transferred to the anode contact ITO through the ruthenium molecule through the charge carrier, thus contributing to the hole injection. The morphology of these interface modifications was examined by Atomic Force Microscope (AFM) and surface potential energy by KelvinProbe Force Microscope (KPFM). To investigate local conductivity of bare ITO and modified ITO surface, Scanning Spreading Resistance Microscopy (SSRM) that is a conductive AFM analyzing technique were performed by applying voltage to the conductive tip and to the sample. According to the results of this work the diode containing N-3 material shows the best performance in terms of charge injection to the ITO due to possess the lowest barrier height Φ<sub>b</sub> as 0.43 eV.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The aim of this study was to explore the neurocognitive effects of dexmedetomidine-loaded gold nanoparticles (AuNPs-dexmedetomidine) on anesthetized rats. Sixty Sprague Dawley rats (age, 2-3 weeks; weight, 250-280 g) were randomly divided into three groups (n = 20): the control group and two groups that received intraperitoneal injection of AuNPs-dexmedetomidine at 50 and 100 μg/kg each. Western blotting and RT-PCR were used to determine the protein and mRNA expression of GSK-3β, respectively. Compared with that in the control group, GSK-3β expression in AuNP-dexmedetomidine groups increased (P < 0.05). The protein expression of GSK-3β was higher and mRNA expression was significantly lower in the 100 μg/kg AuNP-dexmedetomidine group (P < 0.05). AuNPs-dexmedetomidine reduced the neurocognitive effect on anesthetized rats through the regulation of the GSK-3β signaling pathway.
{"title":"Gold Nanoparticles with Dexmedetomidine Regulate GSK-3<i>β</i> to Reduce Neurocognitive Effects in Anesthetized Rats.","authors":"Xiaoxia Zhang, Zumin Xing, Jiyuan Li, Shuyi Tang, Yiwen Zhang","doi":"10.1166/jnn.2021.18745","DOIUrl":"https://doi.org/10.1166/jnn.2021.18745","url":null,"abstract":"<p><p>The aim of this study was to explore the neurocognitive effects of dexmedetomidine-loaded gold nanoparticles (AuNPs-dexmedetomidine) on anesthetized rats. Sixty Sprague Dawley rats (age, 2-3 weeks; weight, 250-280 g) were randomly divided into three groups (<i>n</i> = 20): the control group and two groups that received intraperitoneal injection of AuNPs-dexmedetomidine at 50 and 100 <i>μ</i>g/kg each. Western blotting and RT-PCR were used to determine the protein and mRNA expression of GSK-3<i>β</i>, respectively. Compared with that in the control group, GSK-3<i>β</i> expression in AuNP-dexmedetomidine groups increased (P < 0.05). The protein expression of GSK-3<i>β</i> was higher and mRNA expression was significantly lower in the 100 <i>μ</i>g/kg AuNP-dexmedetomidine group (P < 0.05). AuNPs-dexmedetomidine reduced the neurocognitive effect on anesthetized rats through the regulation of the GSK-3<i>β</i> signaling pathway.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39158962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Meiru Mao, Jianglong Kong, Kui Chen, Jiaxin Zhang, Ziteng Chen, Jiacheng Li, Yanan Chang, Hui Yuan, Xiaoyue Shi, Guogang Chen, Jian Zhang, Juan Li
Nano-particulate matters (NPM) induced the lung injury in mice were evaluated using quantitative micro-computed tomography in the present article. It is an important negative effect of health problems that NPM exposure provokes changes in the lung injury. The micro-computed tomography (CT) to assess lung injury in mouse models has been investigated. The dynamic structural changes in a NPM-induced lung injury mouse mode were monitored. Adults female BALB/C mice were repeatedly exposed to NPM, and micro-CT scans were performed at day 0, 3, 5 and 9. Lung samples were also collected for histological analysis at each time point. The total lung volume, the injured lung volume, and the normal lung volume were defined and calculated volume during the phase of NPM-exposure on the mice. The total and injured lung volumes of NPM-exposed mice were significantly larger than those of the mice at day 5 and 9. The data from micro-CT was consistent with alveolar enlargement and destruction by histological quantification from pathological section. The study for NPM-induced lung injury model by micro-CT may extend our understanding of the distinct pathophysiology of NPM induced lung injury in mice.
{"title":"Evaluation of Nano-Particulate-Matter-Induced Lung Injury in Mice Using Quantitative Micro-Computed Tomography.","authors":"Meiru Mao, Jianglong Kong, Kui Chen, Jiaxin Zhang, Ziteng Chen, Jiacheng Li, Yanan Chang, Hui Yuan, Xiaoyue Shi, Guogang Chen, Jian Zhang, Juan Li","doi":"10.1166/jnn.2021.19522","DOIUrl":"https://doi.org/10.1166/jnn.2021.19522","url":null,"abstract":"<p><p>Nano-particulate matters (NPM) induced the lung injury in mice were evaluated using quantitative micro-computed tomography in the present article. It is an important negative effect of health problems that NPM exposure provokes changes in the lung injury. The micro-computed tomography (CT) to assess lung injury in mouse models has been investigated. The dynamic structural changes in a NPM-induced lung injury mouse mode were monitored. Adults female BALB/C mice were repeatedly exposed to NPM, and micro-CT scans were performed at day 0, 3, 5 and 9. Lung samples were also collected for histological analysis at each time point. The total lung volume, the injured lung volume, and the normal lung volume were defined and calculated volume during the phase of NPM-exposure on the mice. The total and injured lung volumes of NPM-exposed mice were significantly larger than those of the mice at day 5 and 9. The data from micro-CT was consistent with alveolar enlargement and destruction by histological quantification from pathological section. The study for NPM-induced lung injury model by micro-CT may extend our understanding of the distinct pathophysiology of NPM induced lung injury in mice.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39159097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this article, we propose high-performance colorimetric detection of Hg+2 using silver nanoprisms. The spherical and triangular AgNPs were synthesized using varied concentration of NaBH4. Pristine AgNPs without any further modification were used for the detection of various metal ions including Hg2+, Pb2+, Cl-, Cd2+, Co2+, Cu2+, Ba2+, Pb2+, Cr3+, Cr₂O2-7 , Fe2+, Fe3+ etc. AgNPs were not only selective in detecting the ions of Cl- and Hg+2 ions but also highly sensitive. Minimum detection limit was observed to be as low as 10-7 ppm for both Hg+2 and Cl-. Water samples collected from various locations detected for the presence of various heavy metals. Silver nanoprisms owing to their surface plasmon resonance exhibit highly selective tendency towards detection against Hg+2.
{"title":"Silver Nanoprism for Selective and Sensitive Detection of Hg<sup>+2</sup> Ions.","authors":"Avneesh Mittal, Komal Gupta, Balaram Pani, Gulshan Kumar, Gopala Ram Bhadu, Sachin Kumar Godara, Ratyakshi Nain, Sidhharth Sirohi","doi":"10.1166/jnn.2021.19529","DOIUrl":"https://doi.org/10.1166/jnn.2021.19529","url":null,"abstract":"<p><p>In this article, we propose high-performance colorimetric detection of Hg<sup>+2</sup> using silver nanoprisms. The spherical and triangular AgNPs were synthesized using varied concentration of NaBH4. Pristine AgNPs without any further modification were used for the detection of various metal ions including Hg<sup>2+</sup>, Pb<sup>2+</sup>, Cl<sup>-</sup>, Cd<sup>2+</sup>, Co<sup>2+</sup>, Cu<sup>2+</sup>, Ba<sup>2+</sup>, Pb<sup>2+</sup>, Cr<sup>3+</sup>, Cr₂O<sup>2-</sup><sub>7</sub> , Fe<sup>2+</sup>, Fe<sup>3+</sup> etc. AgNPs were not only selective in detecting the ions of Cl<sup>-</sup> and Hg<sup>+2</sup> ions but also highly sensitive. Minimum detection limit was observed to be as low as 10<sup>-7</sup> ppm for both Hg<sup>+2</sup> and Cl<sup>-</sup>. Water samples collected from various locations detected for the presence of various heavy metals. Silver nanoprisms owing to their surface plasmon resonance exhibit highly selective tendency towards detection against Hg<sup>+2</sup>.</p>","PeriodicalId":16417,"journal":{"name":"Journal of nanoscience and nanotechnology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39159104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}