Preparation of Chrysotile Nanotubes under Hydrothermal Condition

2011 ◽  
Vol 284-286 ◽  
pp. 688-691 ◽  
Author(s):  
Yang Feng Huang ◽  
Ye Bin Cai ◽  
Hao Liu
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Condition ◽  
Xrd Analysis ◽  
Outer Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structure And Morphology ◽  
Transmission Electron ◽  
Inner Diameter ◽  
Temperature And Pressure

In a neutral environment, Chrysotile nanotubes have been synthesized by hydrothermal method, with MgO and SiO2powder as the starting materials. X-Ray Diffraction(XRD), Scanning Electron Microscopy(SEM), Transmission Electron Microscopy(TEM) are used to characterize the crystal structure and morphology of the as-prepared samples. We found that the diameter of Chrysotile is uniform. Their outer diameter is about 30~50 nm and the inner diameter is about 6~8 nm. The length of them is a few hundred nanometers. The XRD analysis indicates that the as-prepared Chrysotile is a Rhombohedral structures. The results of HRTEM and SAED showed that the {006} planes of serpentine roll up along the [600] direction to form the tubular structure. In addition, the curves of temperature and pressure with time showed that the water might participate in the reaction.

Efficient synthesis of carbon nanotubes with improved surface area by low-temperature solvothermal route from dichlorobenzene

2013 ◽  
Vol 67 (11) ◽  
Author(s):  
Gantigaiah Krishnamurthy ◽  
Sarika Agarwal
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Carbon Source ◽  
Surface Area ◽  
Heating Temperature ◽  
Outer Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

AbstractThe synthesis of well-aggregated carbon nanotubes in the form of bundles was achieved by the catalytic reduction of 1,2-dichlorobenzene by a solvothermal approach. The use of 1,2-dichlorobenzene as a carbon source yielded a comparably good percentage of carbon nanotubes in the range of 60–70 %, at a low reaction temperature of 200°C. The products obtained were analysed by X-ray diffraction, Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy techniques. The X-ray diffraction studies implied the presence of pure, crystalline, and well-ordered carbon nanotubes. The scanning electron and transmission electron microscopic images revealed the surface morphology, dimensions and the bundled form of the tubes. These micrographs showed the presence of multi-walled carbon nanotubes with an outer diameter of 30–55 nm, inner diameter of 15–30 nm, and lengths of several hundreds of nanometers. Brunauer-Emmett-Teller-based N2 gas adsorption studies were performed to determine the surface area and pore volume of the carbon nanotubes. These carbon nanotubes exhibit a better surface area of 385.30 m2 g−1. In addition, the effects of heating temperature, heating time, amount of catalyst and amount of carbon source on the product yield were investigated.

Fabrication and Characterization of Titanium Based Nanotubes

2009 ◽  
Vol 79-82 ◽  
pp. 581-584 ◽  
Author(s):  
Li Ang Song ◽  
Li Xin Cao ◽  
Ge Su ◽  
Wei Liu ◽  
Hui Liu ◽  
...  
Keyword(s):  
Diffuse Reflectance Spectroscopy ◽  
Cost Effective ◽  
Outer Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Amorphous Phases ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Inner Diameter

Titanium based nanotubes (8-12nm outer diameter and 4-6nm inner diameter) were successfully fabricated by a simple and cost-effective hydrothermal method. The nanotube-like amorphous phases TNT(Na) and TNT(H) were obtained with different post treatment. The samples were characterized by means of high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), selected area electron diffraction (SAED), energy dispersive X-ray spectrum (EDS) and UV-Vis diffuse reflectance spectroscopy (DRS). The photocatalytic activities of the nanotubes were evaluated using photo-oxidation of methyl orange.

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

scholarly journals Hydrothermal Synthesis of MnWO4@GO Composite as Non-Precious Electrocatalyst for Urea Oxidation

Nanomaterials ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 85
Author(s):  
Patnamsetty Chidanandha Nagajyothi ◽  
Kisoo Yoo ◽  
Rajavaram Ramaraghavulu ◽  
Jaesool Shim
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Photoelectron Spectroscopy ◽  
Xrd Analysis ◽  
Morphological Characterization ◽  
Energy Storage And Conversion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Density Values

In this study, manganese tungstate (MW) and MW/graphene oxide (GO) composites were prepared by a facile hydrothermal synthesis at pH values of 7 and 12. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy were used for the structural, compositional, and morphological characterization of the nanoparticles (NPs). The XRD analysis revealed that the formation of monoclinic MnWO4 did not have impurities. The SEM and TEM analyses showed that the synthesized NPs were rod-shaped and well-distributed on the GO. The as-synthesized samples can be used as electrocatalysts for the urea oxidation reaction (UOR). The MW@GO-12 electrocatalyst exhibited higher current density values compared to other electrocatalysts. This study provides a new platform for synthesizing inexpensive nanocomposites as promising electrocatalysts for energy storage and conversion applications.

Enhancement of durability of NIR emission of Ag2S@ZnS QDs in water

2017 ◽  
Vol 31 (32) ◽  
pp. 1750297 ◽  
Author(s):  
M. Karimipour ◽  
M. Bagheri ◽  
M. Molaei
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Xrd Analysis ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Nir Emission ◽  
Core Shell Structure ◽  
Phase Transmission

Stability of Ag2S@ZnS QDs in water is a crucial concern for their application in biology. In this work, both physical sustainability and emission stability of Ag2S QDs were enhanced using parameter optimization of a pulsed microwave irradiation (MI) method up to 105 days after their preparation. UV–Vis and photoluminescence spectroscopies depicted an absorption and emission about 817 nm and 878 nm, respectively. X-ray diffraction (XRD) analysis showed a growth of Ag2S acanthite phase. Transmission Electron Microscopy (TEM) images revealed a clear formation of Ag2S@ZnS core–shell structure.

Simultaneous phase- and morphology-controlled synthesis of MnO2 crystals through controlled release of cuprous ions in hydrothermal condition

2009 ◽  
Vol 24 (1) ◽  
pp. 58-65 ◽  
Author(s):  
Yange Zhang ◽  
Zhi Zheng ◽  
Ka Wai Wong ◽  
Fengling Yang ◽  
Zude Zhang
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Condition ◽  
Redox System ◽  
Controlled Synthesis ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron ◽  
Cuprous Ions

The α-, β-, and δ-MnO2 with various morphologies have been synthesized by a novel redox system of KMnO4 and CuCl with HCl added under a hydrothermal condition. The resultant MnO2 products have been characterized by x-ray diffraction, scanning electron microscopy, and transmission electron microscopy. Upon control of reaction temperature and duration, it was observed that MnO2 polymorphs of different morphology (e.g., flowery δ-MnO2, β-MnO2 nanowires and octahedrons, α-MnO2 nanowires) can be prepared in an adjustable manner. The phenomenon is mainly attributed to the effect of cuprous ions controllably released from CuCl by the action of HCl at different experimental conditions. The corresponding formation mechanism for the MnO2 crystals will also be proposed and discussed.

Synthesis and Characterization of Nano Hydroxylapatite by Reaction Precipitation in Impinging Streams

2010 ◽  
Vol 160-162 ◽  
pp. 1301-1308 ◽  
Author(s):  
Jun Yuan ◽  
Yuan Wu ◽  
Qi Xin Zheng ◽  
Xiao Lin Xie
Keyword(s):  
Electron Microscopy ◽  
Xrd Analysis ◽  
Synthesis And Characterization ◽  
Preparation Process ◽  
X Ray Diffraction ◽  
Excellent Performance ◽  
X Ray ◽  
Operation Conditions ◽  
Transmission Electron

Hydroxylapatite(HAP) nano-whiskers are prepared by reaction-precipitation in the submerged circulative impinging stream reactor(SCISR), with (NH4)2HPO4 and Ca(NO3)2 as the reagents; and the products are characterized by X-ray diffraction (XRD) analysis, Fourier transform infrared (FTIR) spectroscopy, Scanning electron microscopy (SEM) and Transmission electron microscopy (TEM). The results TEM measured indicate that the product prepared under typical operation conditions is average-sized 15nm and 50-70nm long. Multiply repeated experiments illustrates that, because of the excellent performance of the reactor, the preparation process can be easily controlled to yield nano rod/whisker hydroxylapatite with very narrow size distribution.

scholarly journals Investigation of Lithiated Carbons by Transmission Electron Microscopy and X-Ray Diffraction Analysis

1998 ◽  
Vol 548 ◽  
Author(s):  
T. D. Tran ◽  
X. Y. Song ◽  
K. Kinoshita
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Carbon Black ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Lattice Image ◽  
X Ray ◽  
Storage Mechanism ◽  
Transmission Electron ◽  
Diffraction Patterns

ABSTRACTThe microstructures of lithiated synthetic graphite and carbon black were studied by high- resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD) analysis. Information about the crystal structure of carbon containing various Li compositions can provide useful insights to our understanding of the Li storage mechanism in carbonaceous materials. Samples with compositions of Li0.93C6or Li0.45C6 were found to contain both stage-one and stage-two compounds. These observations are consistent with XRD data. The changes in sample microstructure as the results of lithiation and exposure to electron irradiation were observed by TEM and recorded over several minutes in the microscope environment. Selected area electron diffraction patterns indicated that the lithiated samples quickly changed composition to LiC 24, which appeared to dominate during the brief analysis period. The layer planes in the lattice image of a disordered carbon black after Li insertion are poorly defined, and changes in the microstructure of these lithiated carbons was not readily apparent. Observations on these lithium intercalation compounds as well as the limitation of the experimental procedure will be presented.

Synthesis of Ultra-Fine Conducting Polyaniline Micro/Nanotubes Using Fiber Template and Their NH3 Gas Sensitivity

2007 ◽  
Vol 7 (12) ◽  
pp. 4515-4521 ◽  
Author(s):  
Bo Xue ◽  
Shaoyan Qi ◽  
Jian Gong ◽  
Yu Gao ◽  
Shuang Yao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Wide Angle ◽  
X Ray Diffraction ◽  
Gas Sensitivity ◽  
X Ray ◽  
Transmission Electron ◽  
Conducting Polyaniline ◽  
Inner Diameter ◽  
Scanning Electron

We have recently fabricated ultra-fine conducting polyaniline (PANI) tubes with high gas sensitivity. This route includes two steps. Firstly, aniline polymerizes on the surface of a suitable fiber template prepared by electrospun nitrocellulose (NC). Then, the NC fiber template is dissolved and the ultra-fine PANI tubes are obtained. The structure of the conducting PANI tubes is characterized by IR spectrum and wide-angle X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results indicate that the PANI shows the shape of ultra-fine tubes with average inner diameter of 250–350 nm. The wall thickness of the ultra-fine PANI tubes increases with increasing the content of oxidant. The conductivity of the doped PANI tubes is about 6 9 × 10−2 S. The results of gas sensitivity of the ultra-fine PANI tubes indicate that the PANI tubes can act as "electronic nose" to detect toxic NH3 gas below 20 ppm.

scholarly journals Preparation and Photocatalytic Activity of Magnetic Fe3O4/SiO2/TiO2Composites

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Rijing Wang ◽  
Xiaohong Wang ◽  
Xiaoguang Xi ◽  
Ruanbing Hu ◽  
Guohua Jiang
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Separation And Purification ◽  
X Ray Diffraction ◽  
Magnetic Composites ◽  
X Ray ◽  
Structure And Morphology ◽  
Transmission Electron ◽  
Potential Applications ◽  
Ft Ir

A simple sol-gel method was used to prepare magnetic Fe3O4/SiO2/TiO2composites with core-shell structure. Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM) have been applied to investigate the structure and morphology of the resultant composites. The obtained composites showed excellent magnetism and higher photodegradation ability than pure TiO2. The photocatalytic mechanism was also discussed. The magnetic composites should be extended to various potential applications, such as photodegradation, catalysis, separation, and purification processes.

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