scholarly journals Characterization of Fine Metallic Soap Particles by X-Ray Diffraction, Differential Scanning Calorimetry, and Specific Surface Area Analysis

2004 ◽  
Vol 53 (12) ◽  
pp. 627-640
Author(s):  
Kouhei SAWADA ◽  
Miki KONAKA
Keyword(s):  
Differential Scanning Calorimetry ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Metallic Soap ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

Preparation and Characterization of Flowerlike Nickel Oxide

2011 ◽  
Vol 121-126 ◽  
pp. 1044-1048
Author(s):  
Chang Yu Li ◽  
Shou Xin Liu ◽  
Li Li Liu
Keyword(s):  
Nickel Oxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Area Measurement ◽  
Simple Liquid ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Area Measurement

Flowerlike nickel oxide was synthesized by a simple liquid-phase process to obtain the hydroxide precursor and then calcined to form the nickel oxide. The precursor and the nickel oxide were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TG) , the scanning electron microscope(SEM) and Brunauer–Emmett–Teller-specific surface area measurement. The results indicated α-Nickel hydroxide was transferred to NiO with a cubic crystalline structure after being calcined at 450 °C; the NiO still kept the morphology of the precursors and the specific surface area of the NiO was 125.2m2/g.

PREPARATION AND CHARACTERIZATION OF TITANIA-PILLARED MONTMORILLONITE

2008 ◽  
Vol 15 (03) ◽  
pp. 329-336 ◽  
Author(s):  
YIMIN ZHANG ◽  
SHAOXIAN SONG ◽  
MIN ZHANG ◽  
BIYANG TUO
Keyword(s):  
Thermal Stability ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Thermal Stability ◽  
Basal Spacing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pillared Montmorillonite

In this work, a Ti -pillared montmorillonite with high thermal stability has been prepared by using a Na -montmorillonite as the host clay and polyhydroxy-titania ions as the pillaring precursor. The formation of Ti -pillared montmorillonite has been confirmed from the characterizations through X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric–differential scanning calorimeter, and specific surface area analyses. In the preparation of Ti -pillared montmorillonite several parameters, such as the type of solvent in which the synthesis is realized, the ratio of polyhydroxy-titania ions and montmorillonite, the intercalation time, the calcining temperature, and calcining time, were tested to understand their effects on the basal spacing. It was shown that this method could produce a Ti -pillared montmorillonite with the basal spacing of 3.74 nm, specific surface area of 409 m2/g, and mean pore size of 2.94 nm, as well as a high thermal stability up to 900°C.

Study of Heating Effect on Specific Surface Area, and Changing Optical Properties of ZnO Nanocrystals

2011 ◽  
Vol 403-408 ◽  
pp. 1205-1210
Author(s):  
Jaleh Babak ◽  
Ashrafi Ghazaleh ◽  
Gholami Nasim ◽  
Azizian Saeid ◽  
Golbedaghi Reza ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Energy Gap ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zno Nanocrystals ◽  
Transmission Electron ◽  
Zno Nanocrystal

In this work ZnO nanocrystal powders have been synthesized by using Zinc acetate dehydrate as a precursor and sol-gel method. Then the products have been annealed at temperature of 200-1050°C, for 2 hours. The powders were characterized using X-ray diffraction (XRD), UV-vis absorption and photoluminescence (PL) spectroscopy. The morphology of refrence ZnO nanoparticles have been studied using Transmission Electron Microscope (TEM). During the annealing process, increase in nanocrystal size, defects and energy gap quantitative, and decrease in specific surface area have been observed.

Fabrication and Characterization of Cu Doped CeO2 by Hydrothermal Process for Antimicrobial Activity

2019 ◽  
Vol 391 ◽  
pp. 114-119 ◽  
Author(s):  
Yeon Bin Choi ◽  
Jeong Hun Son ◽  
Dong Sik Bae
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Hydrothermal Process ◽  
Antibacterial Properties ◽  
Reaction Times ◽  
X Ray Diffraction ◽  
Spherical Type ◽  
Average Size

Cu doped CeO2 nanopowder was synthesized by hydrothermal process at 180°C for 2~10h. The average size and distribution of the synthesized Cu doped CeO2 nanopowder was controlled by reaction times. The crystallinity of the synthesized Cu doped CeO2 nanoparticles was investigated by X-ray diffraction (XRD). The morphology of the synthesized Cu doped CeO2 nanoparticles was observed by FE-SEM. The specific surface area of the synthesized Cu doped CeO2 nanoparticles was measured by BET. The crystal size of the synthesized Cu doped CeO2 nanoparticles decreased with decreasing reaction times. The average size of the synthesized Cu doped CeO2 nanoparticles was below 10nm and narrow, respectively. The shape of the synthesized Cu doped CeO2 nanoparticles was spherical type. The specific surface area of the synthesized Cu doped CeO2 nanoparticles increased with decreasing reaction times. Antibacterial properties of Cu doped CeO2 were analyzed by MIC method. The synthesized Cu doped CeO2 nanopowders showed antibacterial properties against E.coli and B.sub bacteria.

Study of Gamma Alumina Synthesis – Analysis of the Specific Surface Area

2014 ◽  
Vol 87 ◽  
pp. 54-60 ◽  
Author(s):  
A.H. Munhoz ◽  
H. de Paiva ◽  
L. Figueiredo de Miranda ◽  
E.C. de Oliveira ◽  
Raphael Cons Andrades ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ageing Time ◽  
Precursor Solution ◽  
Specific Area ◽  
Gamma Alumina ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dta And Tg

Different samples of pseudoboehmite (PB) were synthesized through the sol-gel process, using aluminum nitrate as precursor. The influence of variables on the synthesis and calcinations of the PB on the specific area of the obtained gamma-Alumina were studied. The variables were the ageing temperature (25 and 130o C), addition or not of polyvinyl alcohol to the precursor solution and the ageing time of the PB. The pH adjustment of the precursor solution was made by using ammonium carbonate. The products, which were obtained on different conditions, were then characterized by x-ray diffraction, specific area measurements through the BET process, and by thermal analysis (DTA and TG). After characterization, the synthesis products were calcined at 500°C; during this process the gamma-Alumina transformation was observed. The calcination products were characterized by the same methods (x-ray diffraction, BET, DTA and TG) and the desorption-absorption curves were obtained as well, in order to measure the pore volume of the samples. Finally, the results were analyzed through an experimental factorial planning, which showed that high specific surface area gamma-Al2O3 (around 330m²/g) can be obtained through this process.

scholarly journals Phase Transformation and Microstructure Characterization of Ceramic Porcelain with Different Ratio of Treated Fgd Sludge/Feldspar

2021 ◽  
Vol 2129 (1) ◽  
pp. 012092
Author(s):  
Suffi Irni Alias ◽  
Banjuraizah Johar ◽  
Syed Nuzul Fadzli Adam ◽  
Mustaffa Ali Azhar Taib ◽  
Fatin Fatini Othman ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Xrd Analysis ◽  
High Energy ◽  
Hydraulic Press ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Sludge Waste ◽  
Main Component

Abstract The porcelain formulation containing percentages of treated FGD sludge waste from 5% up to 15% in replacement of feldspar were prepared. The porcelain mixture formulation were mixed by high energy planatery mill at speed 300 rpm for 1 hours. The powder were compacted by using hydraulic press and sintered at temperature 1200 °C for 3 hours. The sintered samples were characterized using X-ray fluorescene (XRF), X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) and Thermogravimetry/Differential scanning calorimetry (TGA/DCS). The primary effect concerning the addition of treated FGD sludge was the change of intensity composition (gypsum and anhydrate) in porcelain formulation. The XRD analysis has shown that the main component in sludge waste were gypsum and anhydrate.

scholarly journals Preparation and photocatalytic activity of the layered titanates

2010 ◽  
Vol 4 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Marija Milanovic ◽  
Ivan Stijepovic ◽  
Ljubica Nikolic
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Bet Method ◽  
Ft Ir

Titanate structures were synthesized in highly alkaline solution using hydrothermal procedure. As-prepared powders were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). A specific surface area of the powders was measured by BET method. Results confirmed formation of layered trititanates, already after one hour of hydrothermal synthesis. To examine the photocatalytic activity of the as-prepared layered titanates, methylene blue (MB) was employed as a target compound in response to visible light at ambient temperature. It was observed that the specific surface area, size distribution and crystallinity are important factors to get high photocatalytic activity for the decomposition of MB. .

scholarly journals W-Sn Mixed Oxides and ZnO to Detect NOx and Ozone in Atmosphere

Proceedings ◽  
2018 ◽  
Vol 2 (13) ◽  
pp. 836
Author(s):  
Ambra Fioravanti ◽  
Sara Morandi ◽  
Alessia Amodio ◽  
Mauro Mazzocchi ◽  
Michele Sacerdoti ◽  
...  
Keyword(s):  
Zinc Oxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Mixed Oxides ◽  
Gas Sensing ◽  
Molar Fraction ◽  
Functional Materials ◽  
X Ray Diffraction ◽  
X Ray

Thick films of zinc oxide (ZnO) in form of nanospheres or hexagonal prisms and of tungsten-tin (W-Sn) mixed oxides at nominal Sn molar fraction (0.1, 0.3 and 0.5) were prepared. The functional materials were synthesized and characterized by SEM and TEM, X-ray diffraction, specific surface area measurements, UV-Vis-NIR and IR spectroscopies. The gas sensing measurements highlighted that ZnO is more performant in form of nanoprisms, while W-Sn sensors offer a better response towards NOx and ozone with respect to pure WO3.

Effects of dry grinding on pyrophyllite

Clay Minerals ◽  
1988 ◽  
Vol 23 (4) ◽  
pp. 399-410 ◽  
Author(s):  
J. L. Pérez-Rodríguez ◽  
L. Madrid Sánchez del Villar ◽  
P.J. Sánchez-Soto
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Grinding Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dry Grinding ◽  
Scanning Electron ◽  
Area Data

AbstractDry grinding of pyrophyllite (Hillsboro, USA) has been studied by X-ray diffraction (XRD), specific surface area measurements (BET) and scanning electron microscopy (SEM). At the beginning of the grinding process, some effects such as delamination, gliding and folding of the layers, and decrease in particle size were detected by SEM and XRD, resulting in a large increase in specific surface area, up to a maximum of ∼60 m2·g−1. Marked changes in the structure take place between 30 and 32 mins grinding. Longer grinding times increase the degree of disorder and SEM and specific surface area data suggest that aggregation occurs. XRD results indicate that some residual order persists in the degraded structure.

CO2 utilization by dry reforming of CH4 over mesoporous Ni/KIT-6 catalyst

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Congming Tang ◽  
Juan Huang ◽  
Dong Zhang ◽  
Qingqing Jiang ◽  
Guilin Zhou
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photoelectron Spectroscopy ◽  
Pore Diameter ◽  
Co2 Utilization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Catalytic Performances

Abstract The mesoporous Ni/KIT-6 catalysts with different composition were prepared by altering reduction temperatures. In addition, their physicochemical properties were characterized by X-ray diffraction, in-situ X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller techniques. The results shown that the specific surface area, composition and metallic Ni crystallinity of the Ni/KIT-6 catalyst were significantly affected by reduction temperatures. The catalytic performances of the prepared Ni/KIT-6 catalysts were evaluated via the CO2 reforming of CH4 into syngas and followed the order: RT0 < RT250 < RT300 < RT350 < RT400 < RT450 ≈ RT500. The specific surface area, pore volume, pore diameter, and Ni0 content of the most representative RT450 catalyst among of them were 646.7 m2 g−1, 0.92 cm3 g−1, 6.5 nm, and 30.9%, respectively. The CH4 and CO2 conversions of RT450 catalyst reached to 69.0 and 39.4% under a reaction temperature of 600 °C, respectively. The CO selectivity was greater than 49% and the RT450 catalyst had good stability.

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