Effect of EDTA on the Morphology and Size of SrCO3 Particles during Crystallization

2010 ◽  
Vol 148-149 ◽  
pp. 1551-1555
Author(s):  
Yan Hong Zhao ◽  
Qing Yue Jia ◽  
You Gao ◽  
Xiao Jing Wang

Strontium carbonate particles with different morphologies and sizes were synthesized successfully by a precipitation method in the presence of ethylenediaminetetra-acetic acid disodium (abbreviate as EDTA) at 25 . The phase structure and morphology of these SrCO3 particles were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The XRD results showed that orthorhombic crystalline SrCO3 particles were prepared in the absence of and presence of EDTA. It was found that this additive played an important role in controlling the morphology and size of the particles, which changed from dendritic to spherical shape as EDTA was added.

2014 ◽  
Vol 977 ◽  
pp. 82-85
Author(s):  
Ming Li ◽  
Yan Zhen Yu ◽  
Juan Ting Wang

A new composite coagulant polymeric aluminum zinc ferric (PAZF) was synthesized from industrial wastes. The structure and morphology of the coagulant was characterized by X-ray Diffraction (XRD), Infrared Spectroscopy (IR) and Scanning Electron Microscopy (SEM) and the coagulation performances were evaluated by dyeing-printing wastewater treatment. The results show that new complex compounds are formed in PAZF. Compared with poly aluminum chloride (PAC), the contents of ionic polymerized bonds and the cross-copolymerization among Fe (III), Al (III) and Zn (II) hydroxyl polymerized bonds are increase obviously, and the surface morphology of PAZF presents a net-like structure with the longer molecular chain. Coagulation experiments indicate that PAZF exhibits better coagulation performance in removing turbidity, COD and chromaticity.


2021 ◽  
Vol 13 (1) ◽  
pp. 21
Author(s):  
Lilik Miftahul Khoiroh ◽  
Asmaul Dwi Ayu Sholekah ◽  
Eny Yulianti

Hematite coated PEG was synthesized by the sonication-calcination method. A variation of Na2CO3 is investigated to know the effect on structure and morphology. Characterization of samples are using X-ray fluorescence, X-ray diffraction, Scanning electron microscopy, and color reader techniques. XRF data showed that iron is the highest element in the precursor. The X-ray diffraction data confirm that Fe(OH)3, α-FeOOH, and Fe3O4 established at the sonication stage are then transformed into the α-Fe2O3 phase after calcination. The X-ray diffraction data also was found that α-Fe2O3 at 0.5 M formed with the highest crystallinity degree. The scanning electron microscopy showed that the particle's shape is spherical, bar-shaped, and aggregate. However, the distribution of particles is not uniform and still displays agglomeration. The Color reader shows the highest degree of lightness obtained is at 1 M variation.


2021 ◽  
Author(s):  
Fatma Unal

Abstract Terbium oxide (Tb2O3) particles (NPs) were synthesized by precipitation method using ammonium carbonate as precipitation agent. Effects of precursor molarity (0.1, 0.15 and 0.2 M) on photoluminescence (PL) behaviour of the NPs were investigated. The presence of the Tb2O3 phase was confirmed by X-Ray Diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR) analyses. Morphological investigations of the produced powders were made by Field Emission Gun-Scanning Electron Microscopy (FEG-SEM). It showed that the morphology of Tb2O3 particles transformed from the nanograin chain to bundles morphology of rod-like as the amount of precursor molarity increased. Emission spectrum were investigated by Photoluminescence (PL) Spectroscopy. All the Tb2O3 particles exhibited the strongest peak at 493 nm ascribed to 5D4-7F6 (magnetic dipole (MD), C2) transition. The increase in the number of C2 sites released from the MD transition with the increase of the precursor molarity caused a negative increase in the b* (yellowness/blueness of the emission) value in the CIE diagram, indicating that the colour shifted to the blue region. The Tb2O3 particles produced by the precipitation method exhibited novel strong cyan colour and the PL emission intensity increased with increasing molarity.


2014 ◽  
Vol 775-776 ◽  
pp. 450-454
Author(s):  
Mirele Costa da Silva ◽  
A.T.C. Silva ◽  
Ana Cristina F. Melo Costa ◽  
Normanda Lino de Freitas

The search of variations in the methodology for obtaining nanoferrites has attracted the interest of researchers in search of better results with regard to the structure and morphology of these materials. This study evaluates the effect of microwave power (50 and 70 W) in the structural and morphological characteristics of NiZn ferrite, using aniline as a fuel for combustion reaction. The aluminas were characterized by X-ray diffraction and scanning electron microscopy. The results showed that only the variation in microwave power is sufficient to change the structure of nanoferrites. The sample synthesized in power of 50 W was presented monophasic, illustrating the ferrite phase with crystallite size of 50.04 nm; and for 70 W, it was appeared, besides the ferrite phase, hematite and zinc oxide with a crystallite size of 17.07 nm. The morphology did not change significantly, the nanoferrites showed particles with similar geometry.


2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Rodholfo da Silva Barbosa Ferreira ◽  
Caio Henrique do Ó Pereira ◽  
Rene Anisio da Paz ◽  
Amanda Melissa Damião Leite ◽  
Edcleide Maria Araújo ◽  
...  

The nanocomposites have an extensive use in the current process of membrane preparation, taking into account their unique features as membranes. Thus, the study of nanocomposite processing to obtain membranes is highly important. In this work, Brazilian clay was used (Brasgel PA) for the preparation of polyamide/clay nanocomposite. The nanocomposites were produced in a high rotation homogenizer and in a twin screw extruder. From the nanocomposites and pure polymers processed in the two equipments, membranes were prepared by the immersion-precipitation method, using formic acid as solvent. By X-ray diffraction (XRD), the formation of exfoliated and/or partially exfoliated structures with changes in the crystalline phases of the polyamide was observed. From scanning electron microscopy images, it was observed that the processing clearly influenced the membrane morphology.


2013 ◽  
Vol 454 ◽  
pp. 288-291 ◽  
Author(s):  
Jian An Liu ◽  
Mei Mei Zhang ◽  
Xue Na Yang

A novel porous ferromagnetic glass-ceramic has been synthesized with glassceramic and hydroxyapatite for hyperthermia application. The glassceramic was obtained from a melt derived glass, and the hydroxyapatite was prepared via precipitation method with biological template (YEAST). Both components of such a mixture were sintered at 1000 °C for 1 hour in graphite. The sample was characterized by x-ray diffraction, scanning electron microscopy and magnetic measurements. This material exhibited magnetic behavior and porosity. The results show that porous ferromagnetic glass-ceramic, which saturation magnetization (Ms) of about 25 A·m2/kg and diameter of porous 30-50μm, was obtained.


2015 ◽  
Vol 71 (2) ◽  
pp. 89-92
Author(s):  
Ali Hejrani-Dalir ◽  
Masumeh Tabatabaee ◽  
Ali Sheibani

2-Amino-3-hydroxypyridinium dioxido(pyridine-2,6-dicarboxylato-κ3O2,N,O6)vanadate(V), (C5H7N2O)[V(C7H3NO4)O2] or [H(amino-3-OH-py)][VO2(dipic)], (I), was prepared by the reaction of VCl3with dipicolinic acid (dipicH2) and 2-amino-3-hydroxypyridine (amino-3-OH-py) in water. The compound was characterized by elemental analysis, IR spectroscopy and X-ray structure analysis, and consists of an anionic [VO2(dipic)]−complex and an H(amino-3-OH-py)+counter-cation. The VVion is five-coordinated by oneO,N,O′-tridentate dipic dianionic ligand and by two oxide ligands. Thermal decomposition of (I) in the presence of polyethylene glycol led to the formation of nanoparticles of V2O5. Powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) were used to characterize the structure and morphology of the synthesized powder.


2014 ◽  
Vol 938 ◽  
pp. 46-51 ◽  
Author(s):  
M. Nazri Abu Shah ◽  
S. Hanim Md Nor ◽  
Kamariah Noor Ismail ◽  
Abdul Hadi

A series of CexZr(1-x)O2 mixed oxides with different ratio (0 x 1) have been synthesized using microemulsion method. The structure and morphology of the mixed oxides have been investigated via X-ray Diffraction (XRD) and Field Emission Scanning Electron Microscopy (FESEM). The results showed that the synthesized mixed oxides were of nanoscale size and the cubic phase was obtained with the application of a ratio of x > 0.5. Additionally, it was found that the tetragonal phase existed with lower ceria content. The average crystallite size of the CexZr(1-x)O2 series were found to be in the 5 - 10 nm range. Moreover, the roughness of these mixed oxides had also decreased with increasing ceria content.


2008 ◽  
Vol 368-372 ◽  
pp. 409-411 ◽  
Author(s):  
Dao Yuan Yang ◽  
Fen Ling Qian ◽  
Kai Zhu ◽  
Zhan Ling Lu ◽  
Rui Zhang

Hexagonal MgAl2O4 spinel fibers were synthesized at 1500oC for 6h in nitrogen atmosphere. The structure and morphology of the fibers were investigated using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The fibers grew via vapor- liquid- solid mechanism. The twin mechanism was suggested to play a key role in the formation process of the hexagonal fibers.


2014 ◽  
Vol 25 (1) ◽  
pp. 43-46
Author(s):  
Cristina Ileana Covaliu ◽  
Gina Alina Traistaru ◽  
Gigel Paraschiv

Abstract Methane oxidation using different catalysts is an useful process for preventing air pollution. This study presents the methane oxidation by two types of catalysts: Pd-Sn/Al2O3 and spinel mixed oxide, CuFe2O4. The Pd-Sn/Al2O3 was successfully prepared by sol-gel method and CuFe2O4 by co-precipitation method. The catalysts obtained have been characterized structurally, morphologically and texturally by X-ray diffraction (XRD), scanning electron microscopy (SEM) and specific surface area (BET). The catalytic activity tests regarding methane oxidation were also performed.


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