SYNTHESIS AND CHARACTERIZATION OF n-BUTYL 4-(3,4-DIMETHOXYPHENYL)-6-METHYL-2-THIOXO-1,2,3,4 TETRAHYDROPYRIMIDINE-5-CARBOXYLATE NANOCRYSTALLINE PARTICLES BY WATER/OIL MICROEMULSION METHOD

2011 ◽  
Vol 10 (06) ◽  
pp. 1237-1244 ◽  
Author(s):  
POORVESH M. VYAS ◽  
MIHIR J. JOSHI ◽  
AKSHAY M. PANSURIYA ◽  
YOGESH T. NALIAPARA

Various pyrimidine derivatives are well known for their different pharmaceutical applications. The n-butyl 4-(3, 4-dimethoxyphenyl)-6-methyl-2-thioxo-1,2,3,4 tetrahydropyrimidine-5-carboxylate (n-butyl THPM) was synthesized by using n-butylacetoacetate. The n-butyl acetoacetate was obtained by transesterification of ethyl acetoacetate with n-butyl alcohol using Biginelli condensation. The synthesized powder was used to obtain the nanoparticles of n-butyl THPM by using water/oil microemulsion technique. The average particle size was calculated from the powder XRD pattern by applying Scherrer's formula. The nanoparticles of n-butyl THPM were observed by Transmission Electron Microscope (TEM). The diameter of the nanoparticles varied from 15 nm to 65 nm. The nanoparticles were also characterized by FT–IR spectroscopy, TG–DTA–DSC and mass spectroscopy. The n-butyl THPM nanoparticles were stable up to 280°C. Thermodynamic and kinetic parameters of decomposition were obtained by applying Coats and Redfern relation to the thermogram. The dielectric study was carried out in the frequency range of 50 Hz to 5 MHz. The dielectric constant, dielectric loss and ac conductivity decreased as the frequency of applied field increased.

Author(s):  
Harish Kumar ◽  
Renu Rani

ZnO nanoparticles were synthesized by microemulsion route in W/S ratio of 5 at room temperature. X-ray diffraction (XRD) pattern reveals wurtzite structure of ZnO nanoparticles. Rod shape of ZnO nanoparticles of average particle size 10.0 to 12.0 nm were observed by transmission electron microscopy. FT-IR spectra confirmed the adsorption of surfactant molecules at the surface of ZnO nanoparticles and presence of Zn-O bonding. Thermal studies were carried out by the differential scanning calorimeter (DSC) techniques. In addition, UV-Visible spectra were employed to estimate the band gap energy of ZnO nanoparticles.


2011 ◽  
Vol 415-417 ◽  
pp. 617-620 ◽  
Author(s):  
Yan Su ◽  
Ying Yun Lin ◽  
Yu Li Fu ◽  
Fan Qian ◽  
Xiu Pei Yang ◽  
...  

Water-soluble gold nanoparticles (AuNPs) were prepared using 2-mercapto-4-methyl-5- thiazoleacetic acid (MMTA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The AuNPs product was analyzed by transmission electron microscopy (TEM), UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy (FTIR). The TEM image shows that the particles were well-dispersed and their average particle size is about 5 nm. The UV-vis absorption and FTIR spectra confirm that the MMTA-AuNPs was stabilized by the carboxylate ions present on the surface of the AuNPs.


2017 ◽  
Vol 263 ◽  
pp. 165-169
Author(s):  
Silvia Chowdhury ◽  
Faridah Yusof ◽  
Nadzril Sulaiman ◽  
Mohammad Omer Faruck

In this article, we have studied the process of silver nanoparticles (AgNPs) aggregation and to stop aggregation 0.3% Polyvinylpyrrolidone (PVP) was used. Aggregation study carried out via UV-vis spectroscopy and it is reported that the absorption spectrum of spherical silver nanoparticles were found a maximum peak at 420 nm wavelength. Furthermore, Transmission Electron Microscopy (TEM) were used to characterized the size and shape of AgNPs, where the average particle size is around 10 to 25 nm in diameter and the AgNPs shape is spherical. Next, Dynamic Light Scattering (DLS) were used, owing to observed size distribution and self-correlation of AgNPs.


2019 ◽  
Vol 11 (11) ◽  
pp. 1064-1070 ◽  
Author(s):  
Nkosinathi G. Dlamini ◽  
Albertus K. Basson ◽  
V. S. R. Rajasekhar Pullabhotla

Bioflocculant from Alcaligenis faecalis HCB2 was used in the eco-friendly synthesis of the copper nanoparticles. Nanoparticles were characterized using a scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-visible spectroscopy, thermo gravimetric analysis (TGA) and Fourier Transform Infrared Spectroscopy (FT-IR). The transmission electron microscopy images showed close to spherical shapes with an average particle size of ∼53 nm. Energy-dispersive X-ray spectroscopy analysis confirmed the presence of the Cu nanopartilces and also the other elements such as O, C, P, Ca, Cl, Na, K, Mg, and S originated from the bioflocculant. FT-IR results showed the presence of the –OH and –NH2 groups, aliphatic bonds, amide and Cu–O bonds. Powder X-ray diffraction peaks confirmed the presence of (111) and (220) planes of fcc structure at 2 of 33° and 47° respectively with no other impurity peaks.


2012 ◽  
Vol 500 ◽  
pp. 104-107
Author(s):  
Zhi Qin Chen ◽  
Xiang Liang Chen ◽  
Shu Juan Zhang ◽  
Jun Xi Hu ◽  
Wen Kui Li

Uniform nanocrystalline pure anatase has been synthesized and characterized using tetrabutyl titanate aqueous solution as starting precursors by microwave hydrothermal method. The influences of synthesis conditions (reaction time and temperature) on the formation, crystal phase and crystallite size of TiO2has been investigated. A mixture solution of tetrabutyl titanate and normal butyl alcohol in 1:4 molar ratio is processed in a microwave hydrothermal autoclave at low temperature 120°C for different durations, at 200°C for 20 min to precipitate titania powders, respectively. It was revealed that uniformly dispersed and granulous single phase anatase prepared at 120°C for 180 min with the average particle size of 10 nm was formed by means of XRD and TEM.


2017 ◽  
Vol 35 (1) ◽  
pp. 50-57 ◽  
Author(s):  
M. Jamshidiyan ◽  
A.S. Shirani ◽  
Gh. Alahyarizadeh

AbstractFour different magnetic Fe3O4 nanoparticles were synthesized and characterized by solvothermal method based on different sodium salts. Sodium salts which were used to synthesize the nanoparticles were NaOAc, Na2CO3, a mixture of NaOAc and Na3Cit, and a mixture of NaOAc and Na2C2O4. The structural and optical properties of the synthesized nanoparticles were examined by XRF, XRD, SEM and FT-IR. The results estimated from XRD pattern and SEM image indicated that the second sample (Na2CO3) had the lowest average particle and crystallite size around 29 nm and 43 nm. It was also shown that the first (NaOAc) and second (Na2CO3) samples had the best FT-IR spectra, similar to the available commercial sample which was provided by Merck. At last, the prepared Fe3O4 nanoparticles were applied as sorbents to sorb uranium ions (U(VI)) from radioactive wastewater. The adsorption results showed that the highest U(VI) adsorption was obtained for the second sample in the solution with pH around 10.


2011 ◽  
Vol 228-229 ◽  
pp. 639-644 ◽  
Author(s):  
Jian Lin Xu ◽  
Shu Hua Yang ◽  
Li Hui Zhang ◽  
Zhao Kang ◽  
Qiang Guo

The nano-antimony particles with different shape, size and stability are prepared by electrochemical method under the dilute hydrochloric acid electrolyte including the surface dispersant OP-10 and different current densities. The influences of current density on the shape and size of nanometer antimony particles prepared by electrochemical method are analyzed by using X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FT-IR). The results show that nano-antimony powder can be prepared by electrochemical method, and the antimony powder possesses the crystal structure with orthorhombic hexahedron. The current density has a significant impact on the agglomeration, shape and size of antimony powder. The size and shape of antimony powder are determined by the nucleation rate of nano-antimony and combination capacity of antimony ions and OP-10 surface dispersing agents affected by current density. When the current density is 25mA/cm2, the average particle size is 12nm or so, the shape is spherical, and the nano-antimony particles are well dispersed and no agglomeration.


2011 ◽  
Vol 284-286 ◽  
pp. 839-843 ◽  
Author(s):  
Li Li Wang ◽  
Jin Chen ◽  
Guang Cheng Yang ◽  
Fu De Nie

A carbonate precursor with high sintering activity was prepared by co-precipitation method under ultrasonic radiation. This precursor precipitant completely transformed to pure YAG phase after being calcined at 900 °C for 4 h. The properties of YAG nanopowders obtained under different synthetic process were studied by XRD, TG-DSC, FT-IR and SEM. The results show that the ultrasonic radiation can fine the precursor and reduce its agglomeration. YAG nanopowders with an average particle size of about 60 nm were obtained and particles were sphere-shaped with good dispersity.


2021 ◽  
pp. 1873-1878
Author(s):  
Omar Abdulsada Ali ◽  
Sarmed S.M. Al-Awadi

Well dispersed Cu2FeSnSe4 (CFTSe) nanofilms were synthesized by hot-injection method. The structural and morphological measurements were characterized using XRD (X-ray diffraction), Raman spectroscopy, SEM (scanning electron microscopy), and TEM (transmission electron microscopy). Chemical composition and optical properties of as-synthesized CFTSe nanoparticles were characterized using EDS (energy dispersive spectroscopy) and UV-Vis spectrophotometry. The average particle size of the nanoparticles was about 7-10 nm. The UV-Vis absorption spectra showed that the synthesized CFTS nanofilms have a band gap (Eg) of about 1.16 eV. Photo-electrochemical characteristics of CFTSe nanoparticles were studied and indicated their potential application in photovoltaic applications.


2012 ◽  
Vol 15 (2) ◽  
pp. 27-34
Author(s):  
Nguyet Thi Thuy Dao ◽  
Duong Phuc Nguyen ◽  
Hien Duc Than

This paper presents the synthesis and characterization of Y3Fe5O12, Gd3Fe5O12 and Dy3Fe5O12 nanoparticles by sol-gel method using initial salts solution of Y(NO3)3, Gd(NO3)3, Dy(NO3)3, Fe(NO3). The lattice constant, crystallite size and particle morphology of these ferrite garnet nanoparticles were studied by using X-ray diffraction and transmission electron microscopy (TEM). The results showed that the garnet samples prepared by this method were formed at 800oC, which is lower than the sintering temperature for ceramic bulk samples (1400oC). The particle size is in the range 25- 40 nm as observed via TEM image and the average particle size was found to be 37nm using Debye- Scherrer formula.


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