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.

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.

Synthesis and Characterization of Nanocrystalline Hydroxyapatite Powder

2015 ◽  
Vol 1087 ◽  
pp. 142-146 ◽  
Author(s):  
Rosli Asmawi ◽  
Mohd Halim Irwan Ibrahim ◽  
Azriszul Mohd Amin ◽  
Najwa Mustapha ◽  
Iis Sopyan
Keyword(s):  
Particle Size ◽  
Calcium Phosphate ◽  
High Surface ◽  
High Surface Area ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Heating Process ◽  
X Ray Diffraction ◽  
Nanocrystalline Hydroxyapatite

Nanocrystalline hydroxyapatite (HA) powder was synthesized by a simple heating process involving simple chemical reaction. The characterization of the produced powder showed that the powder is nanosize with particle in the range of 30-70 mm in diameter and almost evenly spherical in shape. The powder also has a high surface area of 43.16 m2/g. Field Emission Scanning Electron Microscopy (FESEM) observation showed the crystallite and particle size become bigger with an increment of calcination temperature, indicating increasing of crystallinity.. FESEM observation showed the particle size become bigger with an increment of calcinations temperature. It is in agreement with the crystallite size analysis, obtained by Scherer’s formula and particle size analysis, measured by nanoSizer. X-ray Diffraction (XRD) and Fourier Transform Infra Red Spectroscopy (FTIR) analyses exhibited the same result, where HA phase was clearly observed at at various temperatures up to 600 ̊C. However, at temperature more than 600 ̊C, Tri calcium phosphate (TCP) phase appeared suppressing the HA phase, producing biphasic calcium phosphate.

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 CHARACTERIZATION OF KAPOK PERICARPIUM MICROCRYSTALLINE CELLULOSE PRODUCED OF ENZYMATIC HYDROLYSIS USING PURIFIED CELLULASE FROM TERMITE (MACROTERMES GILVUS)

2020 ◽  
pp. 7-14
Author(s):  
YULIANITA PRATIWI INDAH LESTARI ◽  
HERMAN SURYADI ◽  
MIRAJUNNISA ◽  
WIBOWO MANGUNWARDOYO ◽  
SUTRIYO ◽  
...  
Keyword(s):  
Particle Size ◽  
Enzymatic Hydrolysis ◽  
Microcrystalline Cellulose ◽  
Reference Product ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
Clear Zone ◽  
X Ray

Objective: This study aimed to increase the yield of microcrystalline cellulose (MCC) from kapok pericarpium alpha-cellulose produced by enzymatic hydrolysis using purified cellulase from Termites (Macrotermes gilvus) and to compare the characteristics with the reference product. Methods: In this research, MCC was prepared from kapok pericarpium powder through the chemical isolation process of alpha-cellulose, followed by enzymatic hydrolysis with purified cellulase from Macrotermes gilvus. The yield was improved by using purified cellulase in optimized temperature, pH, and hydrolysis time. Identification was carried out by using ZnCl and infrared spectrophotometry, followed by characterization of MCC include particle size analysis (PSA) and diffracto­gram pattern (X-Ray Diffraction). The results were compared with Avicel PH 101 as the reference product. Results: Purified cellulase from Macrotermes gilvus showed high cellulose activity. Cellulose in the concentration of 11.743 U/ml formed 49 mm clear zone area with cellulolytic index 7.16 that similar to the formed clear zone area of Trichoderma reesei (50 mm), the optimum hydrolysis condition was achieved at 50 °C, pH 6.0, in 2 h, which produced 80% yield of MCC. Produced MCC was analyzed with ZnCl and FTIR spectrum resulting in positive results, similar to reference. The results of the organoleptic test, particle size analysis, and diffracto­gram pattern (X-Ray Diffraction) showed crystalline characteristics of MCC is similar to the reference (Avicel PH 101). Conclusion: Cellulase Macrotermes gilvus yielded 80% MCC and higher enzymatic activity than Trichoderma reesei. Based on the organoleptic test, particle size analysis, and diffracto­gram pattern observation, MCC from kapok pericarpium has shown similar characteristics to reference (Avicel pH 101) and might be potential to be further developed.

scholarly journals POTENTIAL OF CELLULASE OF CHAETOMIUM GLOBOSUM FOR PREPARATION AND CHARACTERIZATION OF MICROCRYSTALLINE CELLULOSE FROM WATER HYACINTH (EICHHORNIA CRASSIPES)

2019 ◽  
pp. 140-146
Author(s):  
HERMAN SURYADI ◽  
YULIANITA PRATIWI INDAH LESTARI ◽  
MIRAJUNNISA ◽  
ARRY YANUAR
Keyword(s):  
Particle Size ◽  
Enzymatic Hydrolysis ◽  
Water Hyacinth ◽  
Particle Size Analysis ◽  
Chaetomium Globosum ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
Hydrolysis Time ◽  
X Ray

Objective: This study aimed to increase the yield of microcrystalline cellulose (MCC) made from water hyacinth ɑ-cellulose by enzymatic hydrolysis by using purified enzyme and to find it’s characteristics compared to the reference. Methods: In this research, MCC was prepared from water hyacinth powder through the chemical isolation process of ɑ-cellulose, followed by enzymatic hydrolysis with purified cellulase from Chaetomium globosum. The yield of MCC was improved by using purified enzyme and optimization of temperature, pH, and hydrolysis time. Identification was carried out by using ZnCl and infrared spectrophotometry, followed by characterization of MCC include particle size analysis (PSA) and diffracto­gram pattern (X-Ray Diffraction) compared to reference Avicel PH 101. Results: Purified enzyme from Chaetomium globosum has high activity with a clear zone area of 45 mm with cellulolytic index 6.5 that almost same as Trichoderma reesei (50 mm), with the cellulase enzyme activity of 6.691 U/ml. The optimum condition was at a temperature of 50⁰C and pH 6.0 with the hydrolysis time of 2 h, which produced 95% yield of MCC. Identification with ZnCl and FTIR spectrum showed positive results, similar to the reference. The results of organoleptic test, particle size analysis, and diffracto­gram pattern (X-Ray Diffraction) showed crystalline characteristic similar to reference (Avicel PH 101). Conclusion: Enzyme from Chaetomium globosum has a higher activity of cellulase than Trichoderma reesei with MCC obtained was 95%. Based on the comparison of the organoleptic test, particle size analysis, and diffracto­gram pattern, MCC from water hyacinth has a great potential which showed similar characteristic to reference (Avicel pH 101).

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.

Bentonite Clays Characterization in the Town of Sossego – Paraiba State

2015 ◽  
Vol 820 ◽  
pp. 65-70
Author(s):  
I.D.S. Pereira ◽  
V.N.F. Lisboa ◽  
I.A. Silva ◽  
J.M.R. Figueirêdo ◽  
G.A. Neves ◽  
...  
Keyword(s):  
Industrial Applications ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Drilling Fluids ◽  
X Ray Diffraction ◽  
Mineralogical Characterization ◽  
Bentonite Clays ◽  
The Town ◽  
Petroleum Drilling

Bentonite exhibt a range of industrial applications moving millions of dollars on the market per year. Among several applications if highlights it is use for petroleum drilling fluids. Thus, this work aims to characterize physical, mineralogical and technologically, the bentonitics clays of Sossego County, Paraíba, Brazil. Mineralogical characterization of clays was done through the following techniques: particle size analysis by laser diffraction, thermogravimetric and differential thermal analysis, chemical analysis and x-ray diffraction. The clays were turned in by treatment with sodium in Na2CO3 and then determined whether the apparent viscosity, plastic and volume of filtrate of clay-water dispersions. The results showed that the samples are of polycationic, showing levels of MgO, CaO and K2O, similar to those from Boa Vista County, Paraíba, Brazil, and consist of clay mineral kaolinite, quartz and esmec. The clays showed rheological properties that indicate potential for use in drilling fluids.

scholarly journals Synthesis of SnO2 Nanoparticles by High Potential Electrolysis

2017 ◽  
Vol 12 (2) ◽  
pp. 281 ◽  
Author(s):  
Fredy Kurniawan ◽  
Rahmi Rahmi
Keyword(s):  
Particle Size ◽  
Sno2 Nanoparticles ◽  
Particle Size Analysis ◽  
Reaction Engineering ◽  
High Potential ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nanoparticles Synthesis ◽  
The Fourier Transform

SnO2 nanoparticles have been synthesized by high voltage electrolysis. Tin bare was used for anode and cathode. The effect of potentials and electrolyte were studied. The particles obtained after electrolysis was characterized using X-ray Diffraction (XRD). The diffractogram is in agreement with the standard diffraction pattern of SnO2 which is identified as tetragonal structure. The Fourier Transform Infrared (FTIR) spectrum indicates that there is a vibration of Sn–O asymmetric at 580 cm-1. The optimum potential for SnO2 nanoparticles synthesis is 60 V at 0.06 M HCl which shows the highest UV-Vis spectrum. The absorption peak of SnO2 nanoparticles by UV-Vis spectrophotometer appears at about 207 nm. The particle size analysis shows that the SnO2 nanoparticles obtained have the size distribution in a range of 25-150 nm with the highest volume at 83.11 nm. Copyright © 2017 BCREC Group. All rights reservedReceived: 15th November 2016; Revised: 26th February 2017; Accepted: 27th February 2017How to Cite: Rahmi, R., Kurniawan, F. (2017). Synthesis of SnO2 Nanoparticles by High Potential Electrolysis. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (2): 281-286 (doi:10.9767/bcrec.12.2.773.281-286)Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.2.773.281-286 

scholarly journals Effect of Nanosized Colloidal Copper on Cotton Fabric

2010 ◽  
Vol 5 (3) ◽  
pp. 155892501000500 ◽  
Author(s):  
D.P. Chattopadhyay ◽  
B.H. Patel
Keyword(s):  
Particle Size ◽  
Cotton Fabric ◽  
Colloidal Solution ◽  
Chemical Reduction ◽  
Average Particle Size ◽  
Particle Size Analysis ◽  
Nano Particles ◽  
Size Analysis ◽  
Average Particle ◽  
Sem Images

This research deals with the synthesis of nanosized copper as colloidal solution and its application to cotton fabric. Copper nano colloids were prepared by chemical reduction of copper salt using sodium borohydride as reducing agent in presence of tri-sodium citrate. The size and size distribution of the particles were examined by particle size analyzer and the morphology of the synthesized particles was examined by SEM and AFM techniques. X-ray fluorescence spectroscopy detected the presence of copper in the treated fabric. The results of particle size analysis showed that the average particle size varied from 60 nm to 100 nm. The nano copper treated cotton was subjected to soil burial test for the assessment of its resistance towards microbial attack. SEM images of treated fabric indicate copper nano particles are well dispersed on the surface of the specimens. The treatments of nano copper colloidal solution on cotton not only improve its antimicrobial efficiency but also influenced the tensile strength of the fabric sample positively. The treatment was found to enhance the color depth and fastness properties of direct dyed cotton fabric samples.

scholarly journals PREPARATION AND CHARACTERIZATION OF ANTI-ACNE ETHOSOMES USING COLD AND THIN-LAYER HYDRATION METHODS

2018 ◽  
Vol 10 (1) ◽  
pp. 338
Author(s):  
Rachmawati Ramadhana Mustofa ◽  
Iskandarsyah .
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Thin Layer ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Multilamellar Vesicles ◽  
Zeta Potentials ◽  
Small Unilamellar Vesicles

Objective: This study aimed to prepare and characterize anti-acne ethosomes using the cold- and thin-layer hydration methods.Methods: A sonication step was included during ethosome preparation to improve the quality of the cold method. Azelaic acid, Phospholipon 90G,ethanol, propylene glycol, and phosphate buffer (pH 7.4) were used in the procedures. Prepared ethosomal suspensions were characterized usingtransmission electron microscopy, particle-size analysis, and spectrophotometry.Results: Ethosomes prepared using the thin-layer hydration method (F1) had small unilamellar vesicles, while those prepared using the cold methodwith 15-min sonication (F4) showed spherical, elliptical, unilamellar, and multilamellar vesicles. F1 ethosomes had a Dmean volume of 648.57±231.26,whereas those prepared using the cold method with 5- (F2), 10- (F3), and 15-min (F4) sonication had Dmean volumes of 2734.04±231.49 nm,948.90±394.52 nm, and 931.69±471.84 nm, respectively. Polydispersity indices of F2, F3, and F4 ethosomes were 0.74±0.21, 0.86±0.05, and 0.91±0.03,respectively, with a poor particle-size distribution, compared to that of F1 (0.39±0.01). Zeta potentials of F1–F4 ethosomes were −38.27±1.72 mV,−23.53±1.04 mV, −31.4±1.04 mV, and −34.3±1.61 mV, respectively. Entrapment efficiencies of F1–F4 ethosomes were 90.71±0.11%, 53.84±3.16%,72.56±0.28%, and 75.11±1.42%, respectively.Conclusion: Anti-acne ethosomes produced using the thin-layer hydration method had superior properties than those produced using the coldmethod with 15-min sonication.

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