Characterization of CeO2 Fine Particles Prepared by the Homogeneous Precipitation Method with a Mixed Solutionof Ethylene Glycol and Polyethylene Glycol

2004 ◽  
Vol 19 (4) ◽  
pp. 1087-1092 ◽  
Author(s):  
Naofumi Uekawa ◽  
Masayuki Ueta ◽  
Yong Jun Wu ◽  
Kazuyuki Kakegawa

Cerium oxide (CeO2) nanoparticles were obtained by heating a polyethylene glycol (PEG) solution of cerium nitrate hydrate [Ce(NO3)3 6H2O] at 383 K for 3 h. When the PEG, whose molecular weight was 20,000, was used for the preparation, the monodispersed CeO2, whose particle size was about 102 nm, was obtained. When the mixture of PEG20,000 and ethylene glycol (EG) was used to prepare the PEG solution of cerium nitrate hydrate, the average particle size increased from 102 nm to 660 nm with an increase in the EG content of the solution. The pore structure in the obtained CeO2 particles also depended on the weight ratio between EG and PEG20,000.

2013 ◽  
Vol 32 (5) ◽  
pp. 511-515 ◽  
Author(s):  
Xiao Guo Cao ◽  
Jia Wang ◽  
Qi Bai Wu ◽  
Hai Yan Zhang

AbstractYb:YAG transparent ceramic nano-powder was prepared by chemical co-precipitation method, with ammonium bicarbonate as the precipitant and polyethylene glycol as surfactant. The addition of polyethylene glycol can reduce the agglomeration and particle size of the prepared Yb:YAG powder. The morphology, thermal stability and phase structure of Yb:YAG nano-powder were charactered by scanning electron microscopy (SEM), thermogravimetry and differential thermal analysis (TG-DTA), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy. The results show that well-crystallized nano-powder was obtained by calcining the precursors at 900 °C for 3 h. The average particle size of Yb:YAG powder is about 100–200 nm. When the volume amount of polyethylene glycol is 2.0%, well-dispersed Yb:YAG powder with spherical particles of 100 nm diameter was obtained.


Author(s):  
Mohammed Sabar Al-lami ◽  
Malath H. Oudah ◽  
Firas A. Rahi

This study was carried out to prepare and characterize domperidone nanoparticles to enhance solubility and the release rate. Domperidone is practically insoluble in water and has low and an erratic bioavailability range from 13%-17%. The domperidone nanoparticles were prepared by solvent/antisolvent precipitation method at different polymer:drug ratios of 1:1 and 2:1 using different polymers and grades of poly vinyl pyrolidone, hydroxy propyl methyl cellulose and sodium carboxymethyl cellulose as stabilizers. The effect of polymer type, ratio of polymer:drug, solvent:antisolvent ratio, stirring rate and stirring time on the particle size, were investigated and found to have a significant (p? 0.05) effect on particle size. The best formula was obtained with lowest average particle size of 84.05. This formula was studied for compatibility by FTIR and DSC, surface morphology by FESEM and crystalline state by XRPD. Then domperidone nanoparticles were formulated into a simple capsule dosage form in order to study of the in vitro release of drug from nanoparticles in comparison raw drug and mixture of polymer:drug ratios of 2:1. The release of domperidone from best formula was highly improved with a significant (p? 0.05) increase.


2015 ◽  
Vol 752-753 ◽  
pp. 148-153
Author(s):  
M.M. Nassar ◽  
Taha Ebrahiem Farrag ◽  
M.S. Mahmoud ◽  
Sayed Abdelmonem

Calcium carbonate nanoparticles and nanorods were synthesized by precipitation from saturated sodium carbonate and calcium nitrate aqueous solutions through co precipitation method. A new rout of synthesis was done by both using pulsed mixing method and controlling the addition of calcium nitrate. The effect of the agitation speed, and the temperature on particle size and morphology were investigated. Particles were characterized using X-ray Microanalysis, X-ray analysis (XRD) and scanning electron microscopy (SEM). The results indicated that increasing the mixer rotation speed from 3425 to 15900 (rpm) decreases the average particle size to 64±7 nm. A rapid nucleation then aggregation induced by excessive shear force phenomena could explain this observation. Moreover, by increasing the reaction temperature, the products were converted from nanoparticle to nanorods. The maximum attainable aspect ratio was 6.23 at temperature of 75°C and rotation speed of 3425. Generally, temperature raise promoted a significant homoepitaxial growth in one direction toward the formation of calcite nanorods. Overall, this study can open new avenues to control the morphology of the calcium carbonate nanostructures.


2019 ◽  
Vol 19 (02) ◽  
pp. 1950014
Author(s):  
Sabereh Nazari ◽  
Sadegh Nazari ◽  
Fariba Mansourizadeh ◽  
Gholamreza Karimi

In this study, high purity gamma-alumina nanopowders with crystalline structures have been prepared via a sol–gel process by waste metal aluminum, HCl, NaOH, Polyethylene glycol (PEG) and polyvinyl alcohol (PVA). Polyethylene glycol and polyvinyl alcohol have been used as stabilizing agents. The characterization of the samples has been performed utilizing XRD, FTIR, SEM, N2 adsorption/desorption techniques. Prepared samples of gamma-alumina at 800∘C with PEG has an average crystallite size of 2.58[Formula: see text]nm, average particle size of 21[Formula: see text]nm, specific surface area (SSA) of 65.55[Formula: see text]m2/g, and pore volume of [Formula: see text]0.06[Formula: see text]cm3/g. The average crystallite size of 3.07[Formula: see text]nm, average particle size of 31[Formula: see text]nm, specific surface area of 131.25[Formula: see text]m2/g, and pore volume of [Formula: see text]0.14[Formula: see text]cm3/g, were obtained using PVA surfactant.


2013 ◽  
Vol 690-693 ◽  
pp. 454-457
Author(s):  
Hong Bo Li ◽  
Shu Yan Wu ◽  
Jing Wang ◽  
Chun Jie Li

Columnar crystaldendriteequiaxial dendritescolumnar crystalNanosized powder was synthesized by direct-reactive precipitation process using a stoichiometrical mixture of TiCl4, BaCl2 as the reactants while NaOH as precipitant. Under the ratio of Ba to Ti is 1.02, PH=13, three reaction temperature of 70°C, 80°C and 90°C were conducted respectively. Morphology and phase structure of powder were investigated, and the influence of reaction temperature on powder morphology was discussed. The result indicates that synthesized powder is single cubic BaTiO3 and contains no impurities. BaTiO3 powders generally show spherical, and average particle size decreases with increasing reaction temperature. When reaction temperature is 80°C, BaTiO3 powder has best uniformity and dispersivity with the diameter of 80-100nm. The influence of reaction temperature on powder particle size can be attributed to the corporate contribution of nucleation and growth rate. Polyglycol as surface active agent has a significant effect in restraining agglomeration.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Dinesh Patidar ◽  
Anusaiya Kaswan ◽  
N. S. Saxena ◽  
Kananbala Sharma

Monodispersed ZnO nanoparticles have been synthesised in ethylene glycol medium using zinc acetate and sodium hydroxide at room temperature through ultrasonic treatment. The monodispersed ZnO nanoparticles were characterized by XRD, TEM, SEM, and optical spectroscopy. The results indicate that ZnO shows the hexagonal wurtzite structure having 8 nm average particle size with the band gap of 3.93 eV. ZnO nanoparticles blended with P3HT show the improvement in the interchains and intrachains ordering as compared to pure P3HT. The power conversion efficiency of P3HT/ZnO solar cell is found to be 0.88%, which is comparable with the result obtained by other researchers.


2022 ◽  
Vol 951 (1) ◽  
pp. 012032
Author(s):  
R Ermawati ◽  
I Setiawati ◽  
Irwinanita ◽  
A Ariani

Abstract Particulate matter (PM) as one of the pollutants in the atmosphere needs to be studied. PM has physical and chemical characteristics and is called physicochemical properties. These properties vary depending on the source of the PM. PM samplers are used for air sampling to characterize some fine particles (PM2.5). The PM2.5 samples have collected from four sampling sites in the steel industry in Cilegon, Indonesia. The sampling sites are the main gate, the hot strip mill, the billet post, and the hot blast plant. The sampling period was four months. The physicochemical properties analysed are morphology, elements content, heavy metals, and particle size. The instruments used to analyse were Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometry (EDS), Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES), and Particle Size Analyzer (PSA). The morphology of PM2.5 detected varied, but the elements and the most elements found were F and C particles. The metals concentration was below the Indonesia Regulation. While the average particle size analysed was below 2,500 nm. The physicochemical properties of PM2.5 are affected by the type of production process in the industry.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2716
Author(s):  
Mona Ebadi ◽  
Kalaivani Buskaran ◽  
Saifullah Bullo ◽  
Mohd Zobir Hussein ◽  
Sharida Fakurazi ◽  
...  

In the last two decades, the development of novel approaches for cancer treatment has attracted intense attention due to the growing number of patients and the inefficiency of the available current conventional treatments. In this study, superparamagnetic iron oxide nanoparticles (SPIONs) were synthesized by the co-precipitation method in an alkaline medium. Then the nanoparticles were chemically modified by coating them with polyethylene glycol (PEG) and sorafenib (SO)–zinc/aluminum layered double hydroxide (ZLDH) to improve their biocompatibility. The SPIONs and their coated and drug-loaded nanoparticles, M-PEG–SO–ZLDH are of the crystalline phase with the presence of C, O, Al, Fe, Cl, Zn in the latter, indicating the presence of the coating layers on the surface of the SPIONs. The superparamagnetic properties of the bare SPIONs were found to be reduced but retained in its coated drug delivery nanoparticles, M-PEG–SO–ZLDH. The latter has an average particle size of 16 nm and the release of the drug from it was found to be governed by the pseudo-second-order kinetic. The cytotoxicity and biocompatibility evaluation of the drug-loaded magnetic nanoparticles using 3T3 and HepG2 cells using the diphenyltetrazolium bromide (MTT) assays shows that the synthesized nanoparticles were less toxic than the pure drug. This preliminary study indicates that the prepared nanoparticles are suitable to be used for the drug delivery system.


2016 ◽  
Vol 17 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Sujan Dhungana ◽  
Bhoj Raj Paudel ◽  
Surendra K. Gautam

In this work, we report the ZnTe semiconductor nanoparticles (NPs) prepared by aqueous chemical precipitation method using the tellurium precursor solution with different zinc compounds. Three batches of ZnTe NPs were synthesized to study the effect of dilution on the size and phase purity of ZnTe. The influence of source compounds and concentrations of the size and structure of NPs were studied. ZnTe NPs have great applications as field-effect transistors and photodetectors. The existing controversy regarding the crystalline structure of ZnTe NPs, whether it is cubic or hexagonal, has been resolved using X-ray Diffraction (XRD) data. The ZnTe NPs possess cubic structure, which is also confirmed by Electron Diffraction (ED) pattern. The average particle size determined from XRD data with the help of Debye-Scherrer equation is about 6 nm. The particle size can be further verified by Transmission Electron Microscopy (TEM) studies.  


Author(s):  
Amruta Papdiwal ◽  
Kishor Sagar ◽  
Vishal Pande

Poor water solubility and slow dissolution rate are major issues for the majority of upcoming and existing biologically active pharmaceutical compounds. Nateglinide is Biopharmaceutical Classification System Class-II drug that has low solubility and high permeability. The purpose of the present study was to improve the solubility and dissolution rate of Nateglinide by the preparation of nanosuspension by the nanoprecipitation technique. Nateglinide nanosuspension was evaluated for its particle size, in vitro dissolution study, and characterized by differential scanning calorimetry and scanning electron microscopy. The optimized formulation showed an average particle size of 207 nm and zeta potential of -25.8 mV. The rate of dissolution of the optimized nanosuspension was enhanced by 83% in 50 min relative to micronized suspension of nateglinide (37% in 50 min). This improvement was mainly due to the formulation of nanosized particles of Nateglinide. Stability study revealed that nanosuspension was more stable at room temperature and refrigerator condition with no significant change in particle size distribution. These results indicate that the nateglinide loaded nanosuspension may significantly improve in vitro dissolution rate and thereby possibly enhance the onset of therapeutic effect.


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