Synthesis and Characterisation of Tb4L3(Phen)0.75•7H2O Nanorods

2011 ◽  
Vol 194-196 ◽  
pp. 878-881
Author(s):  
Hui Juan Ren ◽  
Zhen Feng Cui ◽  
De Hui Sun ◽  
Guang Yan Hong

The rare earth complex terbium (III)-pyromellitic acid (H4L)-1,10-phenanthroline (phen) nanorod was synthesized in the polyvinylpyrrolidone (PVP) matrix by a co-precipitation method. The chemical composition of the as-synthesized sample was speculated to be PVP/Tb4L3(phen)0.75∙7H2O by elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES), and Fourier transform infrared spectroscopy (FTIR). The transmission electron microscopy (TEM) result exhibited that the as-synthesized sample was nanorods with diameters of ca. 150 nm. The X-ray diffraction pattern (XRD) of the sample showed that it was a crystalline complex. The thermogravimetric curve (TGA) analysis exhibited that the sample is stable below 450 °C. UV–Vis diffuse reflectance spectra exhibited that there is a broad and strong absorption band in the range of 280-350 nm. The photoluminescence analyses (PLA) indicated that the as-synthesized sample emitted the characteristic green fluorescence of Tb (III) ions under ultraviolet light excitation.

2011 ◽  
Vol 284-286 ◽  
pp. 806-810
Author(s):  
Jun Wan ◽  
Jing Zhao ◽  
Ming Qiao Zhu ◽  
Huan Dai ◽  
Lei Wang

Au/Co3O4catalysts were prepared by a co-precipitation method and characterized by inductively coupled plasma-atomic emission spectrometry (ICP-AES), transmission electron microscope (TEM) and X-ray diffraction (XRD). The selective oxidation of cyclohexane to cyclohexanone and cyclohexanol was investigated over Au/Co3O4catalysts using molecular oxygen as oxidant. These catalysts showed higher activities as compared to the pure Co3O4under the same reaction conditions.


2021 ◽  
Vol 947 (1) ◽  
pp. 012026
Author(s):  
Trung Dang-Bao ◽  
Hoa-Hung Lam ◽  
Thi-Hoai-Linh Dang

Abstract In the present work, Ce-Ti and Ce-Ti/Fe3O4 hybrid oxides were prepared by co-precipitation method and then characterized by X-ray diffraction (XRD), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and scanning electron microscope (SEM) techniques. The nano-adsorbents were applied to remove fluoride (with the concentration range of 10–30 mg L−1) from aqueous solution, reaching the adsorption equilibrium within 30–60 minutes. Practically, the fluoride removal onto both nanomaterials was efficient at the neutral pH (pH 5–7) and obeyed the Langmuir adsorption isotherm with the maximum adsorption capacities of 22.78 mg g–1 (Ce-Ti) and 20.28 mg g–1 (Ce-Ti/Fe3O4) at room temperature.


2011 ◽  
Vol 239-242 ◽  
pp. 2488-2491
Author(s):  
Hui Juan Ren ◽  
De Hui Sun ◽  
Zhen Feng Cui ◽  
Guang Yan Hong

The europium(III)-benzoic acid(HL)-1,10-phenanthroline(phen) complex was synthesized in the ethanol-H2O system by a precipitation method. The morphology of the minicrystal complex with diameters of ca. 1.0 µm is characterized by scanning electron microscopy (SEM). Elemental analysis and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) are used to determine the chemical composition of the complex. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction analysis (XRD) are used to examine the structure of the complex. The results show that the complex is a new kind of crystalline complex and the composition of the complex is speculated to be EuL3(phen). The thermogravimetric curve (TGA) analysis indicates that the complex is stable below 232 °C in air. The photoluminescence analyses (PLA) exhibit that the complex emits the characteristic red fluorescence of Eu (III) ions at 613nm under ultraviolet light excitation.


2011 ◽  
Vol 121-126 ◽  
pp. 1500-1503
Author(s):  
Hui Juan Ren ◽  
Hua Yang ◽  
De Hui Sun ◽  
Zhen Feng Cui ◽  
Guang Yan Hong

Rare earth europium (Eu(III))-pyromellitic acid (H4L)-1,10-phenanthroline (phen) ternary luminescent complex has been synthesized in polyvinylpyrrolidone (PVP) matrix by precipitation method. The chemical constitution of the complex has been demonstrated as PVP/EuL4/3L(phen)•2H2O by a combination of elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and Fourier-transform infrared spectroscopy (FT-IR). X-ray diffraction analysis (XRD) has shown that the complex is a new kind of crystal whose structure is totally different from two ligands. The morphology of the complex has been investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results have shown that the complex has a rodlike crystal structure and the diameter of the rod is about 400 nm. Thermogravimetric analysis (TG) has indicated that the luminescent complex is thermally stable below 300 °C. Photoluminescence spectra (PL) have revealed that the complex can emit Eu3+ characteristic red fluorescence under ultraviolet excitation.


2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
K. Elen ◽  
A. Kelchtermans ◽  
H. Van den Rul ◽  
R. Peeters ◽  
J. Mullens ◽  
...  

Due to a dominant one-dimensional growth rate, nanoparticles of zinc oxide often show a rodlike morphology. As a result, the synthesis of small spherical nanoparticles of undoped ZnO remains challenging. This paper presents two procedures that successfully produce a powder consisting of equiaxed zinc oxide nanoparticles: one using a polyethylene glycol- (PEG-) assisted solvothermal method and the other by calcination of zinc oxalate obtained from a microemulsion-mediated method. In the latter, zinc-substituted aerosol OT (AOT) is used as a surfactant. The samples are characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), thermogravimetric analysis (TGA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), photon correlation spectroscopy (PCS), and photoluminescence (PL) spectroscopy. Both synthesis techniques produce nanoparticles with similar sizes in the range of 10 to 20 nm. Dense aggregates observed in the calcined powder are infrequent in the case of the solvothermal method.


2019 ◽  
Vol 20 (1) ◽  
pp. 175
Author(s):  
Zobair El Afia ◽  
Mohamed Youssef Messous ◽  
Mohamed Cherkaoui ◽  
Mounia Tahri

The synthesis of TiO2 co-doped by (Ce, Yb) rare earth couple has been realized. This couple of rare earth can convert a high-energy photon to two low energy photons to enhance the energy efficiency of silicon solar cells. The undoped, 2% Ce doped- and (2% Ce, 4% Yb) Codoped- Titanium oxide were prepared by the co-precipitation method. The Infrared spectroscopy FTIR-ATR analysis indicates a continuous visible absorption in the 750–400 cm–1 region, confirming the formation of a titanium-oxygen bond. The X-Ray Diffraction characterization showed the dominance of the rutile crystalline phase with the presence of anatase one and the calculated crystallite size is between 7 to 13 nm. The X-Ray Fluorescence confirms the insertion of the dopants while the Inductively Coupled Plasma Mass Spectrometry ICP-MS showed the ratio 2 between Ce and Yb concentration. The thermogravimetric analysis indicated that Ce/Yb doped titanium was thermally stable. The absorption in the UV-visible (200 and 1000 nm) has been improved proportionally with the dopants.


2012 ◽  
Vol 554-556 ◽  
pp. 575-579 ◽  
Author(s):  
Yun Chuan Yang ◽  
Hong Hao Yu ◽  
Xin Ying Wang

The preparation of different morphological basic magnesium carbonate particles with hollow rod-like, hull of peanut and leaf from the pyrogenation of magnesium carbonate trihydrate were described. The morphology, crystal phase and purity of basic magnesium carbonate were characterized by scanning electron microscopy(SEM), transmission electron microscopy(TEM), X-ray diffraction (XRD) and inductively coupled plasma atomic emission spectrometer (ICP-AES). The results indicated that the formation of three morphological basic magnesium carbonates were obtained via platelike particles of magnesium carbonate trihydrate under certain conditions where the temperature and stirring rate were properly controlled. The length of the hollow rod means up to 6~7µm, and its diameter means up to 1~2µm.


2015 ◽  
Vol 7 (2) ◽  
pp. 1393-1403
Author(s):  
Dr R.P VIJAYALAKSHMI ◽  
N. Manjula ◽  
S. Ramu ◽  
Amaranatha Reddy

Single crystalline nano-sized multiferroic BiFeO3 (BFO) powders were synthesized through simple chemical co-precipitation method using polyethylene glycol (PEG) as capping agent. We obtained pure phase BiFeO3 powder by controlling pHand calcination temperature. From X-ray diffraction studies the nanoparticles were unambiguously identified to have a rhombohedrally distorted perovskite structure belonging to the space group of R3c. No secondary phases were detected. It indicates single phase structure. EDX spectra indicated the appearance of three elements Bi, Fe, O in 1:1:3. From the UV-Vis diffuse reflectance spectrum, the absorption cut-off wavelength of the BFO sample is around 558nm corresponding to the energy band gap of 2.2 eV. The size (60-70 nm) and morphology of the nanoparticles have been analyzed using transmission electron microscopy (TEM).   Linear M−H behaviour and slight hysteresis at lower magnetic field is observed for BiFeO3 nanoparticles from Vibrating sample magnetometer studies. It indicates weak ferromagnetic behaviour at room temperature. From dielectric studies, the conductivity value is calculated from the relation s = L/RbA Sm-1 and it is around 7.2 x 10-9 S/m.


2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.


MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.


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