Preparation of Lithium Aluminum Layered Double Hydroxide from Ammonium Dawsonite and Lithium Carbonate

2012 ◽  
Vol 1481 ◽  
pp. 29-36
Author(s):  
C. A. Contreras Soto ◽  
E. Ramos-Ramírez ◽  
V. Reyes Zamudio ◽  
J. I. Macías
Keyword(s):  
Layered Double Hydroxide ◽  
Lithium Carbonate ◽  
Lithium Hydroxide ◽  
Lithium Aluminum ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Aluminum Lithium ◽  
Different Temperatures ◽  
Double Hydroxide

ABSTRACTAluminum lithium hydroxide carbonate hydrate, also known as Al/Li layered double hydroxide or Al-Li hydrotalcite-like compound [Al2Li(OH)6]2CO3•nH2O, was prepared by reaction of lithium carbonate with ammonium dawsonite [NH4Al(OH)2CO3]. The reaction of ammonium dawsonite with a lithium carbonate satured solution at different temperatures and lithium carbonate concentrations was studied. The obtained solids were characterized by differential thermal analysis (DTA), thermogravimetry (TGA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and transmission electron microscopy (TEM). By this method, crystalline Li/Al LDH [Al2Li(OH)6]2CO3·3H2O can be obtained at 60 °C and 4 h reaction time.

Preparation and Characterization of Aluminum Lithium Hydroxide Carbonate Hydrate Obtained From Basic Aluminum Sulfate

2012 ◽  
Vol 1372 ◽  
Author(s):  
César A. C. Soto ◽  
Aurora P. Delgado ◽  
Esthela R. Ramírez ◽  
Veridiana R. Zamudio
Keyword(s):  
Electron Microscopy ◽  
Aluminum Sulfate ◽  
Homogeneous Solution ◽  
Lithium Carbonate ◽  
Sodium Aluminate ◽  
Lithium Hydroxide ◽  
Transmission Electron ◽  
Aluminum Lithium ◽  
Double Hydroxide ◽  
Basic Aluminum

ABSTRACTAluminum lithium hydroxide carbonate hydrate, also known as Al-Li double hydroxide or Al-Li hydrotalcite-like compound [Al2Li(OH)6]2CO3•nH2O, was prepared from basic aluminum sulfate. This compound was prepared by precipitation in homogeneous solution of an aluminum bisulfite solution. A sodium aluminate aqueous solution was prepared by dissolving basic aluminum sulfate in 1M sodium hydroxide. The Al-Li double hydroxide was obtained after addition of lithium carbonate satured solution to the sodium aluminate solution, at 60 °C. The synthesized powder was characterized by thermal analysis (TG, DTG and DTA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). By this method crystalline Li-Al hydrotalcite like compound with composition near to Al4Li2(OH)12CO3 •3H2O was obtained.

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.

Intercalation of Collagen and Soybean Peptides into Zn–Al Layered Double Hydroxide

2008 ◽  
Vol 8 (1) ◽  
pp. 428-431 ◽  
Author(s):  
Sumio Aisawa ◽  
Aiko Yasutake ◽  
Satoshi Takahashi ◽  
Hidetoshi Hirahara ◽  
Eiichi Narita
Keyword(s):  
Layered Double Hydroxide ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Collagen Peptides ◽  
Transmission Electron ◽  
New Type ◽  
Diffraction Peaks ◽  
Xrd Patterns ◽  
Double Hydroxide

In order to develop a new type biocompatible organic/inorganic nanohybrid material, an intercalation of collagen peptides (CP) and soybean peptide (SP) into Zn–Al layered double hydroxide (LDH) by the coprecipitation reaction has been investigated. The peptide/LDH has been characterized by chemical analysis, powder X-ray diffraction (XRD), Raman spectroscopy, thermal gravimetric analysis (TG) and transmission electron microscopy (TEM). According to the XRD patterns and Raman spectra, the solid products were found to contain peptide and to show broad diffraction peaks with LDH structures. The CP/LDH and SP/LDH possess the expanding LDH structure, d00l = 2–3 nm, confirming that both peptides were intercalated into the LDH interlayer space with low organized stacking arrangement.

Characterization of Layered Double Hydroxide Modified with Sodium Dodecyl Sulfate and its Dispersion in Polyethylene

2013 ◽  
Vol 591 ◽  
pp. 138-141
Author(s):  
Zhi Dong Han ◽  
Xin Ke Zhang ◽  
Yue Wang ◽  
Zheng Quan Jiang ◽  
Peng Wang
Keyword(s):  
Sodium Dodecyl Sulfate ◽  
Layered Double Hydroxide ◽  
Sodium Dodecyl ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Dodecyl Sulfate ◽  
The Matrix ◽  
Mixing Method ◽  
Double Hydroxide

Mg-Al layered double hydroxide (LDH) was modified with sodium dodecyl sulfate (SDS) by regeneration method. The structure of modified LDH (SDS-LDH) was investigated by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The composites of SDS-LDH and polyethylene (PE) were prepared by melt blending and solution mixing method with maleated PE (PEgMA) as compatibilizer. The structure of the composites and the dispersion of SDS-LDH in the matrix were investigated by XRD and transmission electron microscopy (TEM), respectively. The results reveal that SDS was successfully intercalated into the interlayer space of LDH. SDS-LDH was hardly exfoliated in PE/PEgMA by melt blending. The nanocomposites of PE/(PEgMA/SDS-LDH) were successfully prepared by melt blending PE with SDS-LDH/PEgMA master-batch obtained by solution mixing. Homogeneous dispersion of SDS-LDH in the matrix was observed by TEM.

Fe–Cr/Al2O3 metal-ceramic composites: Nature and size of the metal particles formed during hydrogen reduction

1994 ◽  
Vol 9 (1) ◽  
pp. 229-235 ◽  
Author(s):  
Ch. Laurent ◽  
J.J. Demai ◽  
A. Rousset ◽  
K.R. Kannan ◽  
C.N.R. Rao
Keyword(s):  
Hydrogen Reduction ◽  
Ceramic Composites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Total Reduction ◽  
Transmission Electron ◽  
Combined Use ◽  
Metal Ceramic ◽  
Different Temperatures ◽  
Metallic Species

Fe-Cr/Al2O3 metal-ceramic composites prepared by hydrogen reduction at different temperatures and for different periods have been investigated by a combined use of Mössbauer spectroscopy, x-ray diffraction, transmission electron microscopy, and energy-dispersive x-ray spectroscopy in order to obtain information on the nature of the metallic species formed. Total reduction of Fe3+ does not occur by increasing the reduction time at 1320 K from 1 to 30 h, and the amount of superparamagnetic metallic species is essentially constant (about 10%). Temperatures higher than 1470 K are needed to achieve nearly total reduction of substitutional Fe3+. Interestingly, iron favors the reduction of chromium. The composition of the Fe-Cr particles is strongly dependent on their size, the Cr content being higher in particles smaller than 10 nm.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

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.

Effect of Calcination Temperature on the Morphological and Phase Structure of Hydrothermally Synthesized Copper Ion Doped TiO2 Nanotubes

2014 ◽  
Vol 1024 ◽  
pp. 7-10 ◽  
Author(s):  
Mohd Hasmizam Razali ◽  
M.N. Ahmad-Fauzi ◽  
Abdul Rahman Mohamed ◽  
Srimala Sreekantan
Keyword(s):  
Calcination Temperature ◽  
Morphological Evolution ◽  
Copper Ion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Scanning Electronmicroscopy ◽  
Higher Temperature ◽  
Uniform Diameter

Morphological evolution and phase transformations of copper ion doped TiO2nanotubes after being calcined at different temperatures were studied by field emission scanning electronmicroscopy, transmission electron microscopy, and X-ray diffraction. After calcination at 300°C, the nanotubes with uniform diameter and length wereobtained. At 400°C, the nanotube structures were maintained. Nevertheless the inner tube diameter became narrower, and in same instances disappeared due to aggregation of nanotubes. The copper ion doped TiO2nanotubes then transformed to nanorodsat 500°C and the length of the nanorodsshortens after calcination at 600 °C. When the calcination temperature was further increased to 700°C, the nanorodsdisintegrate to form nanoparticles. On the other hand the phase structures of copper ion doped TiO2nanotubes calcined at 300 and 400 °C were TiO2hexagonal. After calcined at higher temperature (600 and 700°C) they transformed to anatase TiO2(tetragonal).

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.

A new high-temperature inorganic–organic proton conductor: lanthanum sulfophenyl phosphate

2016 ◽  
Vol 70 (3) ◽  
Author(s):  
Ming-Feng Song ◽  
Zhong-Fang Li ◽  
Guo-Hong Liu ◽  
Su-Wen Wang ◽  
Xiao-Yan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Layered Structure ◽  
Proton Conductor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Transmission Electron ◽  
Good Crystallinity ◽  
Different Temperatures ◽  
Thermal Stability Of

AbstractLanthanum sulfophenyl phosphate (LaSPP) was synthesized by m-sulfophenyl phosphonic acid and lanthanum nitrate. UV-Vis spectrophotometry and Fourier-transform infrared spectroscopy indicate that the desired product was obtained and its elementary composition and typical layered structure were determined by energy dispersive X-ray spectroscopy and scanning electron microscopy. Transmission electron microscopy (TEM) proved its typical layered structure and X-ray diffraction spectroscopy indicated its good crystallinity and the interlayer distance of about 15.67 Å , which matches the value obtained by TEM (2.0 nm). Thermogravimetry and differential thermal analysis revealed good thermal stability of LaSPP. Proton conductivity of LaSPP was measured at different temperatures and relative humidities (RH), reaching values of 0.123 S cm

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