scholarly journals SiO2 Coated Up-conversion Nanomaterial Doped with Ag Nanoparticles for Micro-CT Imaging

2021 ◽  
Author(s):  
Wei Zhang ◽  
Yanli Lu ◽  
YANG ZANG ◽  
Jinhui Han ◽  
Qingyun Xiong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Luminescence Intensity ◽  
Ag Nanoparticles ◽  
Fluorescence Spectra ◽  
Cell Counting ◽  
Micro Ct ◽  
Transmission Electron ◽  
Before And After ◽  
Sio2 Nanocomposites ◽  
Low Cytotoxicity

In this study, a new method for synthesizing Ag-NaYF4:Yb3+/Er3+ @ SiO2 nanocomposites was introduced. Using a hydrothermal method, the synthesized Yb3+- and Er3+-codoped NaYF4 upconversion luminescent materials and Ag nanoparticles were doped into upconversion nanomaterials and coated with SiO2 up-conversion nanomaterials. This material is known as Ag-UCNPs-SiO2’ it improves both the luminous intensity because of the doped Ag nanoparticles and has low cytotoxicity because of the SiO2 coating. The morphology of UCNPs was observed using scanning electron microscopy (SEM), and the mapping confirmed the successful doping of Ag nanoparticles. Successful coating of SiO2 was confirmed using transmission electron microscopy (TEM). Fluorescence spectra were used to compare changes in luminescence intensity before and after doping Ag nanoparticles. The reason for the increase in luminescence intensity after doping with Ag nanoparticles was simulated using first-principles calculations. The cytotoxicity of Ag-UCNPs-SiO2 was tested via the cell counting kit-8 (CCK-8) method, and its imaging ability was characterized using the micro-CT method.

scholarly journals SiO2 Coated Up-Conversion Nanomaterial Doped with Ag Nanoparticles for Micro-CT Imaging

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3395
Author(s):  
Wei Zhang ◽  
Yanli Lu ◽  
Yang Zang ◽  
Jinhui Han ◽  
Qingyun Xiong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Luminescence Intensity ◽  
Ag Nanoparticles ◽  
Fluorescence Spectra ◽  
Cell Counting ◽  
Micro Ct ◽  
Transmission Electron ◽  
Before And After ◽  
Sio2 Nanocomposites ◽  
Low Cytotoxicity

In this study, a new method for synthesizing Ag-NaYF4:Yb3+/Er3+ @ SiO2 nanocomposites was introduced. Using a hydrothermal method, the synthesized Yb3+- and Er3+-codoped NaYF4 up-conversion luminescent materials and Ag nanoparticles were doped into up-conversion nanomaterials and coated with SiO2 up-conversion nanomaterials. This material is known as Ag-UCNPs@SiO2, it improves both the luminous intensity because of the doped Ag nanoparticles and has low cytotoxicity because of the SiO2 coating. The morphology of UCNPs was observed using scanning electron microscopy (SEM), and the mapping confirmed the successful doping of Ag nanoparticles. Successful coating of SiO2 was confirmed using transmission electron microscopy (TEM). Fluorescence spectra were used to compare changes in luminescence intensity before and after doping Ag nanoparticles. The reason for the increase in luminescence intensity after doping with Ag nanoparticles was simulated using first-principles calculations. The cytotoxicity of Ag-UCNPs@SiO2 was tested via the cell counting kit-8 (CCK-8) method, and its imaging ability was characterized using the micro-CT method.

scholarly journals Up-Conversion Nanomaterial Doped With Au Nanoparticles With Photothermal Conversion for Multi-Modality Imaging

2021 ◽  
Author(s):  
Wei Zhang ◽  
Yanli Lu ◽  
Yang Zang ◽  
Qingyun Xiong ◽  
Jinping Xiong
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Near Infrared ◽  
Au Nanoparticles ◽  
Cell Counting ◽  
Infrared Light ◽  
Transmission Electron ◽  
Before And After ◽  
Low Cytotoxicity ◽  
Magnetic Resonance Imaging Mri

In this study, a new method for synthesizing Au-NaYF4:Yb3+/Er3+-DSPE-PEG2K nanocomposites was introduced. Using a hydrothermal method, the synthesized Yb3+- and Er3+-codoped NaYF4 upconversion luminescent materials and Au nanoparticles were doped into upconversion nanomaterials and modified with DSPE-PEG2k up-conversion nanomaterials. This material is known as Ag-UCNPs-DSPE-PEG2k, it improves both the luminous intensity because of the doped Au nanoparticles and has low cytotoxicity because of the DSPE-PEG2k modified. Exciting UCNPs with a wavelength of 980nm near-infrared light will emit light with a wavelength of 520nm to further excite gold nanoparticles to convert light energy into heat. Successful synthesized gold nanoparticles was confirmed using transmission electron microscopy (TEM). The morphology of UCNPs was observed using scanning electron microscopy (SEM), and the mapping confirmed the successful doping of Au nanoparticles. Fluorescence spectra were used to compare changes in luminescence intensity before and after doping Au nanoparticles. The cytotoxicity of Au-UCNPs-DSPE-PEG2K was tested via the cell counting kit-8 (CCK-8) method, and its imaging ability was characterized using the Magnetic Resonance Imaging (MRI) and Computed Tomography (CT) method.

scholarly journals Facile synthesis of Au/ZnO/Ag nanoparticles using Glechoma hederacea L. extract, and their activity against leukemia

2021 ◽  
Vol 23 (1) ◽  
Author(s):  
Renata Dobrucka ◽  
Aleksandra Romaniuk-Drapała ◽  
Mariusz Kaczmarek
Keyword(s):  
Electron Microscopy ◽  
Ag Nanoparticles ◽  
Mononuclear Cells ◽  
Leukemia Cell ◽  
Leukemia Cell Line ◽  
Mtt Test ◽  
Transmission Electron ◽  
Almost All ◽  
Glechoma Hederacea

AbstractMetal combinations have been attracting the attention of scientists for some time. They usually exhibit new characteristics that are different from the ones possessed by their components. In this work, Au/ZnO/Ag nanoparticles were synthesized biologically using Glechoma hederacea L. extract. The synthesized Au/ZnO/Ag nanoparticles were characterized by UV-Vis, Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM), and Atomic Force Microscopy (AFM). The microscopic methods confirmed the presence of spherical nanoparticles of 50–70 nm. The influence of biologically synthesized Au/ZnO/Ag nanoparticles on the vitality of human cells was evaluated in vitro with the use of established human Acute T Cell Leukemia cell line, Jurkat (ATCC® TIB-152™), as well as mononuclear cells isolated from peripheral blood (PBMC) of voluntary donors. Cell survival and the half-maximal inhibitory concentration index (IC50) were analyzed by the MTT test. The studies showed that the total loss of cell viability occurred at the Au/ZnO/Ag nanoparticle concentration range of 10 µmol–50 µmol. The use of Au/ZnO/Ag nanoparticles at the concentration of 100 µmol eliminated almost all living cells from the culture in 24h. The above observation confirms the result obtained during the MTT test.

scholarly journals Polystyrene/Montmorillonite Nanocomposites: Study of the Morphology and Effects of Sonication Time on Thermal Stability

2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Mashael Alshabanat ◽  
Amal Al-Arrash ◽  
Waffa Mekhamer
Keyword(s):  
Electron Microscopy ◽  
Thermal Stability ◽  
Solution Method ◽  
Sonication Time ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Polystyrene Matrix ◽  
Before And After ◽  
Silicate Layers ◽  
Thermal Stability Of

Polymer nanocomposites of polystyrene matrix containing 10% wt of organo-montmorillonite (organo-MMT) were prepared using the solution method with sonication times of 0.5, 1, 1.5, and 2 hours. Cetyltrimethylammonium bromide (CTAB) is used to modify the montmorillonite clay after saturating its surface with Na+ions. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to characterize the montmorillonite before and after modification by CTAB. The prepared nanocomposites were characterized using the same analysis methods. These results confirm the intercalation of PS in the interlamellar spaces of organo-MMT with a very small quantity of exfoliation of the silicate layers within the PS matrix of all samples at all studied times of sonication. The thermal stability of the nanocomposites was measured using thermogravimetric analysis (TGA). The results show clear improvement, and the effects of sonication time are noted.

scholarly journals Modification of Titanium Dioxide Nanoparticles with 3-(Trimethoxysilyl)propyl Methacrylate Silane Coupling Agent

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Thuy-Chinh Nguyen ◽  
Tien-Dung Nguyen ◽  
Duc-Toan Vu ◽  
Duc-Phuong Dinh ◽  
Anh-Hiep Nguyen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Tio2 Nanoparticles ◽  
Coupling Agent ◽  
Titanium Dioxide Nanoparticles ◽  
X Ray Diffraction ◽  
Nano Tio2 ◽  
Propyl Methacrylate ◽  
Transmission Electron ◽  
Before And After ◽  
Modification Of Titanium

This paper presents some characteristics, properties, and morphology of TiO2 nanoparticles (nano-TiO2) modified with various contents of 3-(trimethoxysilyl)propyl methacrylate (TMSPM) coupling agent. The treatment process was carried out in ethanol solvent at 50oC using ammonia as a catalyst for hydrolysis reaction of silane to silanol. Infrared spectroscopy, thermogravimetric analysis, transmission electron microscopy, field emission scanning electron microscopy, dynamic light scattering, ultraviolet-visible spectroscopy, and X-ray diffraction methods were used for determination of the characteristics, properties of nano-TiO2 before and after treatment. In addition, the contact angle and grafting efficiency of TMSPM on the surface of TiO2 nanoparticles was also evaluated. The obtained results confirmed that TMSPM was grafted to the TiO2 nanoparticles, the agglomeration of nano-TiO2 was decreased, and surface of TiO2 nanoparticles became hydrophobic after modification by TMSPM.

scholarly journals Barium-Encapsulated Biodegradable Polycaprolactone for Sulfate Removal

Water ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1789
Author(s):  
Changseok Han ◽  
Mallikarjuna Nadagouda
Keyword(s):  
Electron Microscopy ◽  
Barium Carbonate ◽  
High Capacity ◽  
Small Scale ◽  
Ohio River ◽  
Sulfate Removal ◽  
Transmission Electron ◽  
Before And After ◽  
High Resolution Tem ◽  
The Media

Various compositions of barium carbonate (BaCO3) loaded polycaprolactone (PCL) composites were prepared, including 2.5/97.5, 10/90, 30/70, 50/50 and 90/10 (PCL/BaCO3), via re-precipitation technique. Small-scale column tests were conducted to study the efficiency of sulfate removal using the PCL/BaCO3 composites. The composites before and after their use to remove sulfate were extensively characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), high-resolution TEM (HR-TEM), and thermogravimetric analysis (TGA). As PCL is a biodegradable polymer, these composites are environmentally friendly and have several advantages over barium sulfate precipitation in overcoming clogging issues in filters or resins due to collection of natural organic matter (NOM). The media used in this study exhibited high capacity and was able to remove more than 90% sulfate from synthetic sulfate containing waters and NOM samples collected from the Ohio River.

Study on Microstructure Differences of Coal Samples before and after Loading

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Jiajia Liu ◽  
Yingxiang Fang ◽  
Gaini Jia ◽  
Shouqi Chen ◽  
Jianmin Hu
Keyword(s):  
Electron Microscopy ◽  
Coal Seam ◽  
Coal Sample ◽  
Coal Seam Gas ◽  
Adsorbed Gas ◽  
Transmission Electron ◽  
Parallel Layer ◽  
Before And After ◽  
Spectrum Area ◽  
Nmr Techniques

The microscopic pore structure of coal affects the content of adsorbed gas. The microstructure of coal sample before and after loading is different, which will affect the adsorption and permeability of coal seam gas. In order to study this difference, the authors carried out mercury intrusion experiments on coal containing different coal samples and used nondestructive nuclear magnetic resonance (NMR) techniques, scanning electron microscopy, and transmission electron microscopy, to study the microstructure of coal samples before and after loading. The experimental results show that the pores of coal samples are mainly micropores and small pores, and the mesopores and macropores are relatively few. The T2 spectrum area of the coal sample is significantly increased after loading, and the parallel-layer coal samples’ T2 spectrum area is 46735, which is 9112 more than the vertical layer coal samples. The T2 spectrum of the vertical coalbed of saturated water samples shows a three-peak shape, the peak of the T2 spectrum is 12692, and the parallel bedding shows a bimodal morphology. The peak area of the T2 spectrum is 11277. The permeability of the parallel bedding coal sample is good, and the coal sample exhibits anisotropic properties. The pores and cracks of the coal samples increased after loading, and the localized area of the coal sample collapsed and formed a fracture zone, which was not conducive to the occurrence of coal seam gas. Further explanation of the changes in the permeability of the coal sample before and after loading will affect the gas storage and transportation.

scholarly journals Endothelium-derived hyperpolarizing factor in preeclampsia: heterogeneous contribution, mechanisms, and morphological prerequisites

2008 ◽  
Vol 294 (2) ◽  
pp. R510-R519 ◽  
Author(s):  
Leanid Luksha ◽  
Henry Nisell ◽  
Natallia Luksha ◽  
Marius Kublickas ◽  
Kjell Hultenby ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Subcutaneous Fat ◽  
Normal Pregnancy ◽  
Transmission Electron ◽  
Main Pathway ◽  
Before And After ◽  
Group 2 ◽  
Cytochrome P 450 ◽  
Group 1

We hypothesized that in preeclampsia (PE), contribution of endothelium-derived hyperpolarizing factor (EDHF) and the mechanism/s of its action differ from that in normal pregnancy (NP). We aimed to assess endothelial function and morphology in arteries from NP and PE with particular focus on EDHF. Arteries (≈200 μm) were dissected from subcutaneous fat biopsies obtained from women undergoing cesarean section. With the use of wire myography, responses to the endothelium-dependent agonist bradykinin (BK) were determined before and after inhibition of pathways relevant to EDHF activity. The overall responses to BK in arteries from PE ( n = 13) and NP ( n = 17) were similar. However, in PE, EDHF-mediated relaxation was reduced ( P < 0.05). All women within the PE group were divided into two subgroups: with more ( group 1) or less ( group 2) than 50% reduction of EDHF-typed responses after 18-α-glycyrrhetinic acid (an inhibitor of myoendothelial gap junctions, MEGJs). The division showed that 1) MEGJs are principally involved when the EDHF contribution is reduced; and 2) when the EDHF contribution is similar to that in NP, the H2O2 and/or cytochrome P-450 epoxygenase products of arachidonic acid (AA), along with MEGJs, confer EDHF-mediated relaxation. In contrast, MEGJs were the main pathway for EDHF in NP. The abundant presence of MEGJs in arteries from NP but deficiency of them in PE was observed using transmission electron microscopy. We conclude that PE is associated with heterogeneous contribution of EDHF, and the mechanism behind EDHF-typed responses is mediated either by MEGJs alone or in combination with H2O2 or cytochrome P-450 epoxygenase metabolites of AA.

Synthesis and Characterization of Porous Mo-W Oxide Nanostructures

2008 ◽  
Vol 8 (12) ◽  
pp. 6445-6450
Author(s):  
F. Paraguay-Delgado ◽  
Y. Verde ◽  
E. Cizniega ◽  
J. A. Lumbreras ◽  
G. Alonso-Nuñez
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Synthesis Method ◽  
Atomic Ratio ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Before And After

The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 °C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 °C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically.

Preparation, Characterization and Spectroscopy of Eu3+ in Gd2O3 Nanorods

2008 ◽  
Vol 8 (3) ◽  
pp. 1398-1403 ◽  
Author(s):  
Liqin Liu ◽  
En Ma ◽  
Renfu Li ◽  
Xueyuan Chen
Keyword(s):  
Electron Microscopy ◽  
Fluorescence Spectra ◽  
Filling Factor ◽  
Energy Levels ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
Excitation Spectra ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Eu3+:Gd2O3 nanorods were prepared by a hydrothermal method. X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, and Fourier transform-infrared spectroscopy were used to characterize the resulting samples. Emission and excitation spectra were studied using xenon excited spectroscopic experiments at 10 K. Energy transfer from Gd3+ to Eu3+, from the band gap of the host to Eu3+, and from Eu3+ (S6) to Eu3+ (C2) was observed. The energy levels of Eu3+ at the C2 site of cubic Gd2O3 were experimentally determined according to the fluorescence spectra at 10 K, and fit well with the theoretical values. The standard deviation for the optimal fit was 12.9 cm−1. The fluorescent lifetime of 5D0 (2.3 ms at 295 K) was unusually longer than that of the bulk counterparts (0.94 ms), indicating a small filling factor (0.55) for the nanorod volume. However the lifetime of 5D1 was much shorter than that of the bulk counterparts, 65 μs at 10 K, 37 μs at 295 K.

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