Preparation of ZnAl2O4 Spinel Directly from Zinc Aluminum Layered Double Hydroxide Precursor

2012 ◽  
Vol 567 ◽  
pp. 127-130
Author(s):  
Jian Ye Song ◽  
Ming Zhe Leng ◽  
Xing Qi Fu ◽  
Jian Qiang Liu
Keyword(s):  
Layered Double Hydroxide ◽  
Single Phase ◽  
Structural Characteristics ◽  
Atomic Level ◽  
X Ray Diffraction ◽  
Simple Route ◽  
X Ray ◽  
Znal2o4 Spinel ◽  
Double Hydroxide ◽  
Scanning Electron

Single-phase ZnAl2O4 spinel has been prepared by a novel simple route using layered double hydroxide as a precursor. ZnAl2O4 spinel is directly obtained by calcination of zinc aluminum layered double hydroxide (Zn/Al molar radio is 0.5) without further chemical treatment. The key feature of this method is that it affords uniform distribution of all metal cations on an atomic level in the precursor. The structural characteristics of the as-synthesized precursor and the resulted calcined products are obtained by X-ray diffraction and scanning electron microscope.

Influence of pH on Phosphate Intercalation in Zinc-Aluminum Layered Double Hydroxide

1998 ◽  
Vol 63 (5) ◽  
pp. 741-748 ◽  
Author(s):  
Mohamed Badreddine ◽  
Ahmed Legrouri ◽  
Allal Barroug ◽  
André De Roy ◽  
Jean-Pierre Besse
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Layered Double Hydroxide ◽  
Chloride Ion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Phosphate Ions ◽  
Double Hydroxide ◽  
Influence Of Ph ◽  
Scanning Electron

The exchange of chloride ion by phosphate ions in [Zn-Al-Cl] layered double hydroxide was investigated using X-ray diffraction and infrared spectroscopy. The effects of the pH of the solution containing the phosphate ions on the ion exchange was studied. The best sample in terms of crystallinity, was obtained at pH 8. This sample was further characterized by scanning electron microscopy and microanalysis.

scholarly journals Hydrothermal Synthesis of Ni/Al Layered Double Hydroxide Nanorods

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Yun Zhao ◽  
Fenfei Xiao ◽  
Qingze Jiao
Keyword(s):  
Electron Microscopy ◽  
Reaction Time ◽  
Layered Double Hydroxide ◽  
Hydrothermal Reaction ◽  
Ph Value ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Double Hydroxide ◽  
Scanning Electron

Ni/Al layered double hydroxide (LDH) nanorods were successfully synthesized by the hydrothermal reaction. The crystal structure of the products was characterized by X-ray diffraction (XRD). The morphology of the products was observed using transmission electron microscopy (TEM) and field emission scanning electron microscopy (SEM). The influences of reaction time and pH value on the morphology of the Ni/Al LDHs were investigated. The result showed that the well-crystallized nanorods of Ni/Al LDHs could be obtained when the pH value was about 10.0 with a long reaction time (12–18 h) at 180°C.

scholarly journals Nanocomposites of Magnetite and Layered Double Hydroxide for Recyclable Chromate Removal

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Gyeong-Hyeon Gwak ◽  
Min-Kyu Kim ◽  
Jae-Min Oh
Keyword(s):  
Layered Double Hydroxide ◽  
Magnetite Nanoparticles ◽  
X Ray Diffraction ◽  
Potential Measurement ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
House Of Cards ◽  
Double Hydroxide ◽  
Scanning Electron

Nanocomposites containing magnetic iron oxide (magnetite) nanoparticles and layered double hydroxide (LDH) nanosheets were prepared by two different methods, exfoliation-reassembly and coprecipitation, for aqueous chromate adsorbent. According to X-ray diffraction, scanning electron microscopy, and atomic force microscopy, both nanocomposites were determined to develop different nanostructures; LDH nanosheets well covered magnetite nanoparticles with house-of-cards-like structure in exfoliation-reassembly method, while coprecipitation resulted in LDH particle formation along with magnetite nanoparticles. Zeta-potential measurement also revealed that the magnetite surface was effectively covered by LDH moiety in exfoliation-reassembly compared with coprecipitation. Time, pH, concentration dependent chromate adsorption tests, and magnetic separation experiments exhibited that both nanocomposites effectively adsorb and easily collect chromate. However, exfoliation-reassembly nanocomposite was determined to be slightly effective in chromate removal by ~10%. Chromate adsorbed nanocomposites could be regenerated by treating with bicarbonate and the regenerated nanocomposites preserved ~80% of chromate adsorption efficacy after three times of recycling.

Study on optical and magnetic properties of FexNi1-xMn2O4 materials

2021 ◽  
Vol 66 (1) ◽  
pp. 57-64
Author(s):  
Hang Pham Vu Bich ◽  
Yen Nguyen Hai ◽  
Mai Phung Thi Thanh ◽  
Dung Dang Duc ◽  
Hung Nguyen Manh ◽  
...  
Keyword(s):  
Single Phase ◽  
Sol Gel ◽  
Vibrating Sample Magnetometer ◽  
Raman Scattering Spectrum ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scattering Spectrum ◽  
Diffraction Diagram ◽  
Optical And Magnetic Properties ◽  
Scanning Electron

In this study, we present the process of synthesis FexNi1-xMn2O4 (x = 0; 0.1; 0.3; 0.5; 0.7; 0.9; 1) by method sol-gel. Scanning electron microscope results shows that the particle size is about 50 nm. The X-ray diffraction diagram shows that the samples are single phase, changing structure clearly as the x ratio increases from 0 to 1. The lattice constant, the bond length also changes with x-value as shown on the Raman scattering spectrum. The results of the vibrating sample magnetometer show that the magnetism of the material FexNi1-xMn2O4 changes with the value of x and reaches a maximum in the range x from 0.5 to 0.7.

Crystal Chemistry and Phase Equilibrium Studies of the Bao(baco3)‐r2o3‐cuo Systems. V. Melting Relations in ba2(y,nd,eu)cu3o6+x

1989 ◽  
Vol 169 ◽  
Author(s):  
Winnie Wong‐Ng ◽  
Lawrence P. Cook ◽  
Michael D. Hill ◽  
Boris Paretzkin ◽  
E.R. Fuller
Keyword(s):  
Electron Microscopy ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Equilibrium Studies ◽  
X Ray ◽  
Helium Gas ◽  
Ionic Size ◽  
Differential Thermogravimetric Analysis ◽  
Melting Relations ◽  
Scanning Electron

AbstractThe influence of the ionic size of the lanthanides R on melting relations of Ba2RCu3O6+x, where R=Y, Eu and Nd, was studied and compared with that of a high Tc superconductor mixed‐lanthanide phase Ba2(Y.75Eu.125Nd 125)Cu3O6+xThese materials have been characterized by a variety of methods including differential thermogravimetric analysis (DTA), scanning electron microscopy (SEM) with energy dispersive X‐ray spectroscopy (EDX) and X‐ray powder diffraction. Single phase samples of Ba2(Y.75Eu.125Nd.125)Cu3O6+x were annealed at 1004, 1040, 1052, 1060, 1078, 1107 and 1160°C and quenched into a helium gas container cooled by liquid nitrogen. The SEM micrographs of these samples showed the progressive chnages in features of the microstructures from sintering and grain growth through melting and then recrystallization from the melt. The addition of the SEM technique in conjunction with X‐ray diffraction has been helpful in the study of phase equilibria in this system.

scholarly journals Photocatalytic Degradation of 2,4,6-Trichlorophenol by MgO–MgFe2O4 Derived from Layered Double Hydroxide Structures

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 454 ◽  
Author(s):  
Esthela Ramos-Ramírez ◽  
Francisco Tzompantzi-Morales ◽  
Norma Gutiérrez-Ortega ◽  
Héctor G. Mojica-Calvillo ◽  
Julio Castillo-Rodríguez
Keyword(s):  
Photocatalytic Degradation ◽  
Layered Double Hydroxides ◽  
X Ray Diffraction ◽  
Application Study ◽  
Toxic Compounds ◽  
X Ray ◽  
Thermally Activated ◽  
Double Hydroxide ◽  
Double Hydroxides ◽  
Scanning Electron

In recent years, the search for solutions for the treatment of water pollution by toxic compounds such as phenols and chlorophenols has been increasing. Phenols and their derivatives are widely used in the manufacture of pesticides, insecticides, paper, and wood preservers, among other things. Chlorophenols are partially biodegradable but not directly photodegradable by sunlight and are extremely toxic—especially 2,4,6-trichlorophenol, which is considered to be potentially carcinogenic. As a viable proposal to be applied in the treatment of water contaminated with 2,4,6-trichlorophenol, this paper presents an application study of the thermally activated Mg/Fe layered double hydroxides as photocatalysts for the mineralization of this contaminant. Activated Mg/Fe layered double hydroxides were characterized by X-ray diffraction, thermal analysis, N2 physisorption, and scanning electron microscopy with X-ray dispersive energy. The results of the photocatalytic degradation of 2,4,6-trichlorophenol in aqueous solution showed good photocatalytic activity, with an efficiency of degradation of up to 93% and mineralization of 82%; degradation values which are higher than that of TiO2-P25, which only reached 18% degradation. The degradation capacity is attributed to the structure of the MgO–MgFe2O4 oxides derived from double laminate hydroxide Mg/Fe. A path of degradation based on a mechanism of superoxide and hollow radicals is proposed.

scholarly journals Simple New Method for the Preparation of La(IO3)3 Nanoparticles

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2400 ◽  
Author(s):  
Zoulikha Hebboul ◽  
Amira Ghozlane ◽  
Robin Turnbull ◽  
Ali Benghia ◽  
Sara Allaoui ◽  
...  
Keyword(s):  
Single Phase ◽  
New Method ◽  
X Ray Diffraction ◽  
Chemical Route ◽  
X Ray ◽  
The Common ◽  
Controlled Preparation ◽  
Iodate Ions ◽  
Scanning Electron ◽  
Soft Chemical Route

We present a cost- and time-efficient method for the controlled preparation of single phase La(IO3)3 nanoparticles via a simple soft-chemical route, which takes a matter of hours, thereby providing an alternative to the common hydrothermal method, which takes days. Nanoparticles of pure α-La(IO3)3 and pure δ-La(IO3)3 were synthesised via the new method depending on the source of iodate ions, thereby demonstrating the versatility of the synthesis route. The crystal structure, nanoparticle size-dispersal, and chemical composition were characterised via angle- and energy-dispersive powder X-ray diffraction, scanning electron microscopy, and Fourier-transform infrared spectroscopy.

Nanocrystalline Barium Zirconium Titanate Synthesized by the Sonochemical Process

2013 ◽  
Vol 802 ◽  
pp. 119-123
Author(s):  
Supamas Wirunchit ◽  
Rangson Muanghlua ◽  
Supamas Wirunchit ◽  
Wanwilai Vittayakorn ◽  
Naratip Vittayakorn
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Reaction Time ◽  
Single Phase ◽  
Zirconium Titanate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Large Particles ◽  
Barium Zirconium Titanate ◽  
Scanning Electron

Nanocrystalline barium zirconium titanate, BaZr0.4Ti0.6O3, was synthesized successfully via the sonochemical process. The effects of reaction time on the precipitation of Ba(Zr,Ti)O3 particles were investigated briefly. The crystal structure as well as molecular vibrations and morphology were investigated. X-ray diffraction indicated that the powders exhibited a single phase perovskite structure, without the presence of pyrochlore or unwanted phases at the reaction time of 60 min. Nanocrystals were formed before being oriented and aggregated into large particles in aqueous solution under ultrasonic irradiation. A scanning electron microscopy (SEM) photograph showed the BZT powder as spherical in shape with uniform nanosized features.

Electrodeposition of Aluminum on 316L Stainless Steel from Molten Salts Based on Chlorides

2008 ◽  
Vol 373-374 ◽  
pp. 273-276 ◽  
Author(s):  
Yu Jiang Wang ◽  
Xin Xin Ma ◽  
Guang Wei Guo
Keyword(s):  
Stainless Steel ◽  
Cross Section ◽  
Molten Salts ◽  
Single Phase ◽  
316L Stainless Steel ◽  
Aluminum Layer ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Purity Aluminum ◽  
Scanning Electron

The electrodeposition of aluminum on 316L stainless steel from a molten salts based on chloride has been studied. The surface morphology of the aluminum layer has been examined through scanning electron microscope (SEM) and the structure of the aluminum layer has been analyzed by X-ray diffraction (XRD). The thickness of the deposited aluminum layer has been measured by the method of cross-section scan. It has been suggested that a white, smooth, non-porous and a high purity aluminum layer can be obtained on 316L stainless steel from the ternary chloride molten salts (AlCl3 – NaCl - KCl). And the structure of the aluminum layer was single-phase.

In Situ Polymerization and Characterization of Poly(ε-caprolactone)/Layered Double Hydroxide Nanocomposites

2012 ◽  
Vol 557-559 ◽  
pp. 371-374
Author(s):  
Lian Liu ◽  
Teng Yu ◽  
Pei Wang ◽  
Guang Shuo Wang
Keyword(s):  
Layered Double Hydroxide ◽  
In Situ Polymerization ◽  
X Ray Diffraction ◽  
Visible Spectroscopy ◽  
X Ray ◽  
Uv Visible ◽  
Absorbance Peak ◽  
Double Hydroxide

Nanocomposites of poly(ε-caprolactone) (PCL) and layered double hydroxide (LDH) were prepared by in situ polymerization at low LDHs loadings in this work. The resultants were characterized by FTIR spectroscopy, X-ray diffraction (XRD), differential scanning calorimeter (DSC) and UV-visible spectroscopy (UV-vis). FTIR showed that the PCL/LDHs nanocomposites were prepared successfully by in situ polymerization and XRD spectra showed that the crystal structure did not change greatly in the presence of LDHS. DSC results confirmed that LDHs could act as nucleating agents. UV-vis spectra showed that LDHs had stronger absorbance peak than LDH. Moreover, the PCL/LDHs nanocomposites had strong anti-ultraviolet effect by introduction of LDHs into polymer matrix.

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