Study on the Reaction Process of Ploy-High-Ferric-Silicic Coagulant

2010 ◽  
Vol 156-157 ◽  
pp. 1074-1077
Author(s):  
Yan Zhen Yu ◽  
Juan Tan ◽  
Yong Sun
Keyword(s):  
Particle Size ◽  
Electron Microscope ◽  
Theoretical Basis ◽  
Raw Materials ◽  
Particle Size Analysis ◽  
Synthesis Process ◽  
Size Analysis ◽  
Potassium Ferrate ◽  
Transmission Electron ◽  
Complexation Process

A new inorganic polymer coagulant，ploy-high-ferric-silicic coagulant with various Si/FeO42- ratios and salt-basicity, was prepared using the fly ash extract and potassium ferrate. The influence of both Si/FeO42- ratios and salt-basicity on the complexation process was explored with many analytical methods, such as transmission electron microscope (TEM), lased particle size analysis (LPSA) and infrared spectrum (IR). The results show that the ploy-high-ferric-silicic is a complexation compound, instead of a simple mixture of raw materials. The complexation process between Si and Fe may be different from various Si/FeO42- ratios and salt-basicity. The bonding can help revealing the high-ferric groups function in synthesis process. From analyzing the different ferrosilicon bonding modes, it can provide some theoretical basis to compound high-ferric coagulant.

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

The Evaporative Decomposition of Solutions Method (Eds) for the Production of Ultrafine Y1Ba2Cu3O7 from Nitrate and Mixed Anion Precursor Solutions

1989 ◽  
Vol 169 ◽  
Author(s):  
Rollin E. Lakis ◽  
Sidney R. Butler
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Barium Carbonate ◽  
Hollow Spheres ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

AbstractY1Ba2Cu3O7 has been prepared by the evaporative decomposition of solutions method. Nitrate and mixed anion solutions were atomized and decomposed at temperatures ranging from 300°C to 950°C. The resulting materials have been characterized using x-ray powder diffraction, Thermal Gravimetric Analysis (TGA), particle size analysis, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). The powder consists of 0.3 micron agglomerated hollow spheres with a primary particle size of 0.06 micron. TGA and x-ray diffraction indicate the presence of barium nitrate and barium carbonate due to incomplete decomposition and/or product contamination by the process environment.

Particle Size Analysis of the Synthesized Al2O3 by Dissolution and Alkali Fusion-Coprecipitation Methods

2020 ◽  
Vol 860 ◽  
pp. 128-134
Author(s):  
Cahyaning Fajar Kresna Murti ◽  
Malik Anjelh Baqiya ◽  
Endarko ◽  
Triwikantoro
Keyword(s):  
Particle Size ◽  
Ammonium Hydroxide ◽  
Particle Size Analysis ◽  
Fusion Product ◽  
Size Analysis ◽  
Particle Sizes ◽  
X Ray Diffraction ◽  
Bottom Up ◽  
Alkali Fusion ◽  
Transmission Electron

Particle size analysis of synthesized Al2O3 by dissolution and alkali fusion-coprecipitation methods has been conducted. The formation of nano- or microparticles can be synthesized by the top-down (physically) and bottom-up (chemically) methods. In this study, the commercial alumina (Merck) with the particle size of 63 µm was synthesized through the bottom-up method. The dissolution method was done by reacting to alumina with ammonium hydroxide (NH4OH). The alkali fusion method was carried out by reacting alumina with sodium hydroxide (NaOH) and it obtained by coprecipitation of the alkali fusion product with HCl and NH4OH. The result from both methods were calcined at 600°C. The phase of synthesized Al2O3 was identified by using X-ray diffraction (XRD), whereas the morphology observed using a transmission electron microscope (TEM), and the particle sizes measured by particle sizes analyzer (PSA). The XRD pattern shows the γ-Al2O3 phases with particle sizes of ~33 nm and ~25 nm from TEM observations, while the PSA results revealed agglomerated particles with particle sizes of 1263 nm and 477 nm for the dissolution and alkali fusion-coprecipitation method, respectively. Therefore, both methods can be used to reduce the particle size of γ-Al2O3.

scholarly journals Synthesis of ZnO-CdO Nanocomposites

2013 ◽  
Vol 1 (1) ◽  
pp. 11-14
Author(s):  
N. Sahu ◽  
◽  
R. K. Duchaniya ◽  
Keyword(s):  
Particle Size ◽  
Grain Size ◽  
Low Cost ◽  
Sol Gel ◽  
Particle Size Analysis ◽  
Synthesis Process ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The ZnO-CdO nanocomposite was prepared by sol-gel method by using their respective nitrates. It is a simple and low cost method to prepare nanocomposites. The drying temperature and drying period of prepared gel was varied during the synthesis process. The prepared samples were characterized by using scanning electron microscope (SEM), particle size analysis (PSA), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL) to get surface morphology, idea of getting particle of nanosized range so that further characterizations can be done, to study the optical property of synthesized nanocomposite and measure the band gap . The grain size determined by Scherrer’s formula was found to be between 30-50 nm.

Synthesis and Characterization of Polyimide/Silica Nanocomposites

2011 ◽  
Vol 311-313 ◽  
pp. 96-100
Author(s):  
Jian Li Cheng ◽  
Cun Zhou ◽  
Hao Peng ◽  
Huan Wang ◽  
Yu Sun
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Amic Acid ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Average Particle ◽  
Scanning Calorimetry ◽  
Silica Nanocomposites ◽  
Transmission Electron ◽  
Size Of Particles

Two kind of polyimide/silica nanocomposites which were recorded poly(amic acid)/ silica(PAA/SiO2) and SiO2in poly(amic acid) ammonium salt(PAS/SiO2) respectively, have been prepared for different methods. The size of SiO2in PAA/SiO2and PAS/SiO2are measured by Particle size analysis and the average particle size are 377nm and 53.7nm. Transmission electron microscopy(TEM) images of PAS/ SiO2confirm that the size of particles are ranged from 40 to 80nm. The stuctures of samples have been characterized by FT-IR spectra. The thermal stability of PAA/SiO2and PAS/SiO2are studied by thermogravimetric analysis (TGA) and the thermal behaviors were investigated by differential scanning calorimetry (DSC) in this paper. It is shown that PAA/SiO2have slightly better thermal properties than that of PAS/SiO2. The results obtained from Instron universal strength tester present the water-solube PAS/SiO2own the excellent mechanical prperties as same as PAA/SiO2.

Preparation, Characterization of Co3O4 Nano-Particles and its Catalytic Effect on the Combustion of Fuel Rich Propellants

2012 ◽  
Vol 560-561 ◽  
pp. 284-288 ◽  
Author(s):  
Wei Qiang Pang ◽  
Xiao Bing Shi ◽  
Yang Li
Keyword(s):  
Particle Size ◽  
Catalytic Effect ◽  
Solid Phase ◽  
Particle Size Analysis ◽  
Nano Particles ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Wide Size Distribution

The mono-dispersed Co3O4 nano-particles were prepared by means of solid phase synthetical method. The particle size, specific surface area, crystal structure and morphology of the samples were characterized by laser particle size analysis, x-ray diffraction (XRD) and transmission electron microscopy (TEM), respectively. The catalytic effects of nano-particles on the combustion of fuel rich propellant were investigated. The results show that the Co3O4 nano-particles prepared are uniform and with relatively wide size distribution curve. The catalytic effect of Co3O4 nano-particles on the fuel rich propellant is stronger than those of micro-sized Co3O4 particles and CuO nano-particles.

scholarly journals Preparation of the monodispersed carboxyl-functionalized polymer microspheres with disproportionated rosin moiety and adsorption of methylene blue

2018 ◽  
Vol 36 (5-6) ◽  
pp. 1260-1273 ◽  
Author(s):  
Cai-Li Yu ◽  
Feng Bian ◽  
Shu-Fen Zhang ◽  
Xu Xu ◽  
Peng Ren ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Particle Size ◽  
Raw Materials ◽  
Average Particle Size ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Average Particle ◽  
Polymer Microspheres ◽  
Carboxyl Content ◽  
Methylene Blue Adsorption

Carboxyl-functionalized polymer microspheres with a rosin moiety were prepared through dispersion polymerization using styrene, disproportionated rosin ester, and methylacrylic acid as raw materials. The effects of dispersion medium (ethanol/water) ratio, monomer mass proportion and initiator concentration on the polymer microspheres were studied. Scanning electron microscopy, laser particle size analysis, thermogravimetric analysis and Fourier transform infrared spectroscopy were used to characterize the microspheres, and their carboxyl contents were determined by the conductance titration method. The adsorption of methylene blue of the microspheres was also investigated. The results showed that rosin-based carboxyl-functionalized polymer microspheres were successfully synthesized. The microspheres exhibited smooth, spherical shapes with good monodispersity and high thermal stability. The carboxyl content of the microspheres prepared under optimum conditions was 0.089 mmol·g−1, with the average particle size approximately 950 nm. With increasing carboxyl contents of the polymer microspheres, their methylene blue adsorption capacities increased. The maximum methylene blue adsorption capacity of the microspheres was 59.55 mg·g−1 in the highest carboxyl content.

Large-Scale Fabrication of Ti3AlC2 Powder with High-Purity

2007 ◽  
Vol 336-338 ◽  
pp. 948-951
Author(s):  
Chang An Wang ◽  
Chun Qing Peng ◽  
Yang Song ◽  
Yong Huang
Keyword(s):  
Particle Size ◽  
High Purity ◽  
Mass Production ◽  
Large Scale ◽  
Raw Materials ◽  
Synthesis Method ◽  
Particle Size Analysis ◽  
Raw Material ◽  
Size Analysis ◽  
Sem Observation

A synthesis method of high-pure Ti3AlC2 powder with a large scale was presented as pressureless synthesis using TiC, Ti and Al powders as starting materials at 1300~1450°C in flow Ar. The different raw material scales were tested from 2 g to 1.0 kg, and the results showed that the purities of Ti3AlC2 powders could be kept around 97 wt% at different scales of raw materials. SEM observation and particle size analysis revealed that the synthesized Ti3AlC2 powders were uniform and around 5 μm in particle size. This method can be used for mass production of Ti3AlC2 powders with high-purity.

Development of Olanzapine Nano-Emulsion for Enhanced Brain Delivery

2012 ◽  
Vol 5 (1) ◽  
pp. 1648-1659
Author(s):  
Madhusudan Rao Y ◽  
Shailaja M ◽  
Ramakrishna S ◽  
Ramesh G ◽  
K H Reddy ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Research Work ◽  
Particle Size Analysis ◽  
Correlation Spectroscopy ◽  
Size Analysis ◽  
Uniform Size ◽  
Transmission Electron ◽  
Nano Emulsion

The main objective of the present research work was to design, optimize and characterize olanzapine loaded nano-emulsion for improved brain transport of the drug.   Olanzapine nano-emulsion was formulated using the ultrasonication method. The formulation variables (oil and surfactant) and process variables (ultrasonication time) were optimized by Response surface methodology using the Box-Behnken statistical method. Particle size, polydispersity index (PDI) and zeta potential were measured by photon correlation spectroscopy using a Malvern zeta sizer. Morphology of emulsion droplets was examined by transmission electron microscopy (TEM). Release study was performed and drug release was estimated by HPLC method. Stability studies were performed at 4oC-25oC for a period of three months. The optimized nano-emulsion obtained showed a uniform size distribution with an average size in the range of 65.1 nm to 74.21 nm and surface charge in the range of –18.9 mv to – 25.23 mv. The Transmission electron microscopy studies on olanzapine nano-emulsion revealed a spherical morphology of globules. An average of 91.91% of drug was released from the optimized formulation over a period of 24 hours. The particle size analysis after three months showed no significant change implying that the nano-emulsion was quite stable when stored at room temperature. Stable olanzapine nano-emulsion was formulated. The novel nanoformulation was found to be a potential vehicle for delivery of olanzapine to the brain.

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