Synthesis Of Highly Ordered Macroporous Minerals: Extension of the Synthetic Method to Other Metal Oxides and Organic-Inorganic Composites

1998 ◽  
Vol 549 ◽  
Author(s):  
C.F. Blanford ◽  
T.N. Do ◽  
B.T. Holland ◽  
A. Stein
Keyword(s):  
Electron Microscopy ◽  
Metal Oxides ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Wide Range ◽  
Ordered Macroporous ◽  
Lower Temperature

AbstractThe facile synthesis of three-dimensional macroporous arrays of titania, zirconia and alumina was recently reported [1]. The synthesis of these materials has now been extended to the oxides of iron, tungsten, and antimony, as well as a mixed yttrium-zirconium system and organically modi- fied silicates. These materials were characterized by Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), X-ray energy dispersive spectrometry (EDS), and powder X-ray diffraction (XRD). Ordered structures of iron, tungsten, and antimony were formed from alkoxide precursors as in the originally reported synthesis, but the template was removed at a lower temperature. Samples of vinyl- and 2-cyanoethyl-modified silicates were formed from a mixture of organotrialkoxysilane and tetraalkoxysilane precursors; the polystyrene template was removed by extraction with a THF/acetone mixture. These results show the ease of extending the original syn- thesis to a wide range of systems. Also, the ability to form homogenous mixed-metal oxides will be important for tailoring the dielectric and photonic properties of these materials.

Synthesis and characterization of 3D Cu0.45Mn0.55O2 nanoflowers with novel photoluminescence and magnetic properties

2014 ◽  
Vol 28 (09) ◽  
pp. 1450071
Author(s):  
Arbab Mohammad Toufiq ◽  
Fengping Wang ◽  
Qurat-ul-ain Javed ◽  
Quanshui Li ◽  
Yan Li
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Three Dimensional ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Growth Method ◽  
First Time

In this paper, three-dimensional (3D) Cu 0.45 Mn 0.55 O 2 nanoflowers self-assembled by interconnecting dense stacked single-crystalline nanoplates have been prepared using the template-free hydrothermal growth method. The morphology, phase structure and composition of the as-prepared nanomaterial were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) with selected area electron diffraction (SAED) and energy-dispersive X-ray spectroscopy (EDX). FESEM and TEM analyses show that the size of 3D Cu 0.45 Mn 0.55 O 2 nanoflowers is in the range of 1–1.5 μm and the thickness of interconnected nanoplates is about 40 nm on the average. The photoluminescence (PL) spectra of the as-prepared Cu 0.45 Mn 0.55 O 2 nanostructures at room temperature exhibits prominent emission bands located in red–violet spectral region. Moreover, magnetic investigations revealed the weak ferromagnetic behavior of the as-prepared Cu 0.45 Mn 0.55 O 2 nanoflowers and reported for the first time using vibrating sample magnetometer (VSM).

Synthesis and Photoluminescence Properties of Novel SnO2 Zigzag Nanoribbons

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Vapour Deposition ◽  
Chemical Vapour ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Ceramic Boat

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.

scholarly journals Synthesis of Three-Dimensional Fe3O4/Graphene Aerogels for the Removal of Arsenic Ions from Water

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Yan Ye ◽  
Da Yin ◽  
Bin Wang ◽  
Qingwen Zhang
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
3D Structure ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Aerogels ◽  
Transmission Electron ◽  
Potential Applications ◽  
Removal Of Arsenic

We report the synthesis of three-dimensional Fe3O4/graphene aerogels (GAs) and their application for the removal of arsenic (As) ions from water. The morphology and properties of Fe3O4/GAs have been characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and superconducting quantum inference device. The 3D nanostructure shows that iron oxide nanoparticles are decorated on graphene with an interconnected network structure. It is found that Fe3O4/GAs own a capacity of As(V) ions adsorption up to 40.048 mg/g due to their remarkable 3D structure and existence of magnetic Fe3O4nanoparticles for separation. The adsorption isotherm matches well with the Langmuir model and kinetic analysis suggests that the adsorption process is pseudo-second-ordered. In addition to the excellent adsorption capability, Fe3O4/GAs can be easily and effectively separated from water, indicating potential applications in water treatment.

On the destruction of kaolinite and gibbsite by phenylphosphonic, phenylphosphinic and phenylarsonic acids: evidence for the formation of new Al compounds

Clay Minerals ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 391-404 ◽  
Author(s):  
J. E. F. C. Gardolinski ◽  
G. Lagaly ◽  
M. Czank
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Transmission Electron Microscopy ◽  
Fourier Transform ◽  
Linear Chain ◽  
X Ray Diffraction ◽  
Phenylphosphonic Acid ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron

AbstractKaolinite and synthetic γ-Al(OH)3 (gibbsite or hydrargillite) were reacted with phenylphosphonic, phenylphosphinic and 2-nitrophenol-4-arsonic acids. The products were studied by powder X-ray diffraction, transmission electron microscopy/selected area electron diffraction/ energy dispersive X-ray/Fourier transform infrared and simultaneous thermogravimetric/differential thermal analysis. The acids were not intercalated but, instead, easily destroyed the structure of the minerals. Lamellar Al phenylphosphonate and aluminium phenylphosphinate and phenylarsonate with polymeric linear-chain structures were formed from kaolinite. The reaction between gibbsite and the same acids yielded almost identical products. No evidence of formation of grafted kaolinite derivatives after the reaction with phenylphosphonic acid was found.

Synthesis of Fe2O3/CNTs for the Fast Removal of Tetracycline from Aqueous Solutions

2014 ◽  
Vol 915-916 ◽  
pp. 933-941 ◽  
Author(s):  
Zhong Jie Zhang ◽  
Chang Yu Lu ◽  
Wei Huang ◽  
Wei Sheng Guan ◽  
Yue Xin Peng
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Magnetic Measurements ◽  
Ferrite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Wide Range ◽  
Fast Removal ◽  
Scanning Electron

The effective remove to tetracycline still remains a big challenge for scientists. In this work, we used a new method for preparing functional magnetic CNTS with ferrite nanoparticles. A wide range of techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and magnetic measurements were applied to characterize the obtained Fe2O3/CNTs. Moreover, we have also studied the properties of adsorbent to tetracycline. In addition, we have found that the Fe2O3/CNTs are better reusable adsorbent than other traditional adsorbents by magnetic separation recycling method.

Preparation and Characterization of Helical Structure ZnS by Solvothermal Method

2011 ◽  
Vol 233-235 ◽  
pp. 1954-1957
Author(s):  
Xiao Yan Yan ◽  
Zhi Qiang Wei ◽  
Li Gang Liu ◽  
Xiao Juan Wu ◽  
Ge Zhang
Keyword(s):  
Electron Microscopy ◽  
Solvothermal Method ◽  
Helical Structure ◽  
Sodium Sulphide ◽  
X Ray Diffraction ◽  
Hexagonal Crystal ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron

Helical structure ZnS were successfully prepared via solvothermal method by the reaction of zinc acetate and sodium sulphide. The composition, morphology, and microstructure of the sample were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), the corresponding selected area electron diffraction (SAED) and X-ray energy spectrum (EDS). The experiment results show that the sample is 1-D hexagonal crystal ZnS and grows along the [002] direction, and is helical structure, with lengths in the range of 100-200 nm, the diameter about 5-15 nm, and pitch about 20nm.

FABRICATION AND CHARACTERISTICS OF ALN NANOWIRES

2001 ◽  
Vol 15 (30) ◽  
pp. 1455-1458 ◽  
Author(s):  
H. CHEN ◽  
X. K. LU ◽  
S. Q. ZHOU ◽  
X. H. HAO ◽  
Z. X. WANG
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Sublimation Method ◽  
Scanning Electron

Single phase AlN nanowires are fabricated by a sublimation method. They were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), typical selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM). The SEM and TEM images show that most of the nanowires have diameters of about 10–60 nm. The crystal structure of AlN nanowires revealed by XRD, SAED and HRTEM shows the AlN nanowires have a wurtzite structure.

scholarly journals Synthesis of NiW Supported on an Al-Modified Cubic Ia3d Mesoporous KIT-5 Catalyst and Its Hydrodenitrogenation Performance of Quinoline

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1183
Author(s):  
Xing Liu ◽  
Shaoqing Guo ◽  
Xin Li ◽  
Lijing Yuan ◽  
Hongyu Dong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Fourier Transform ◽  
Three Dimensional ◽  
Fourier Transform Infrared ◽  
Photoelectron Spectra ◽  
Sulfide Catalysts ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Large Pore Size

Pure KIT-5 and a series of Al-KT-X materials modified by different amounts of aluminum were synthesized by a direct hydrothermal method and acted as supports for the catalysts of a quinoline hydrodenitrification reaction with the NiW active phases supported. The results of X-ray diffraction (XRD), N2 isotherm absorption-desorption, scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) for the supports indicated that Al species were embedded into the framework of the KIT-5 materials with a large pore size, pore volume, and specific surface area. The Pyridine-Fourier transform infrared spectroscopy (Py-IR) result of the catalysts demonstrated that the addition of aluminum atoms enhanced the acidity of the catalysts. The results of the high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectra (XPS) characterizations for the sulfide catalysts indicated that the embedded Al species could facilitate the dispersion of active metals and the formation of the active phases. Among all the catalysts, NiW/Al-KT-40 showed the maximal hydrodenitrogenation conversion (HDNC) due to its open three-dimensional pore structure, appropriate acidity, and good dispersion of active metals.

scholarly journals Solvent-Mediated Eco-Friendly Synthesis and Characterization of Monodispersed Bimetallic Ag/Pd Nanocomposites for Sensing and Raman Scattering Applications

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
G. Sathiyadevi ◽  
B. Loganathan ◽  
B. Karthikeyan
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Dimethyl Formamide ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Bimetallic Nanocomposites ◽  
Ft Ir

The solvent-mediated eco-friendly monodispersed Ag/Pd bimetallic nanocomposites (BNCs) having thick core and thin shell have been prepared through novel green chemical solvent reduction method. Reducing solvent, dimethyl formamide (DMF) is employed for the controlled green synthesis. Characterization of the synthesized Ag/Pd BNCs has been done by x-ray diffraction (XRD) studies, high-resolution scanning electron microscopy (HR-SEM), energy-dispersive X-ray analysis (EDX), and high-resolution transmission electron microscopy (HR-TEM) with selected area electron diffraction (SAED) pattern. The nature of the interaction of L-cysteine with Ag/Pd BNCs has been studied by using surface plasmon spectroscopy, Fourier transform-infrared spectroscopy (FT-IR), cyclic voltammetry (CV), and theoretical methods.

scholarly journals Oxalic Acid-Assisted Hydrothermal Synthesis and Luminescent of Hexagonal NaYF4:Ln3+ (Ln = Sm, Eu, Yb/Er) Micro/Nanoplates

2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Feng Tao ◽  
Zhishun Shen ◽  
Zhijun Wang ◽  
Da Shu ◽  
Qi Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Oxalic Acid ◽  
Molar Ratio ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ph Values ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Display Systems

Hexagonal NaYF4:Ln3+ micro/nanoplates were successfully synthesized via a hydrothermal method using oxalic acid as a shape modifier. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) have been used to study the morphologies and crystal structure of the products. The effects of the pH values and the molar ratio of oxalic acid to NaOH on the crystal growth have been investigated in detail. The time-dependent experiments have been conducted to investigate the morphology evolution process, and based on the results, a possible growth mechanism was proposed. The photoluminescence properties of 5 mol% Eu3+ and 3 mol% Sm3+ doped NaYF4 and 20 mol% Yb3+/2 mol% Er3+ codoped NaYF4 micro/nanoplates were investigated. The experimental results showed that NaYF4:Ln3+ micro/nanoplates have excellent luminescence and can be potential application in the field of light display systems, lasers, and optoelectronic devices.

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