Exchangeable calcium, magnesium and sodium and the dispersion of illites in water. I. Characterization of illites and exchange reactions

Soil Research ◽  
1977 ◽  
Vol 15 (3) ◽  
pp. 243 ◽  
Author(s):  
CL Chi ◽  
WW Emerson ◽  
DG Lewis
Keyword(s):  
Surface Area ◽  
Divalent Cations ◽  
Average Particle Size ◽  
Type Equation ◽  
Direct Calculation ◽  
Double Layers ◽  
Average Particle ◽  
Exchange Reactions ◽  
Fine Grained ◽  
Calcium Magnesium

Three 'pure' illites were studied. Two, extracted from soils, were fine grained, and the other coarse, extracted from a shale. The average particle size of each clay was determined from electron micrographs and a specific surface area calculated. For the two soil illites any difference in the surface area deduced from water vapour sorption as compared with nitrogen sorption or by direct calculation, was consistent with the purity of the clay as determined by X-ray diffraction. For the shale, there was a large discrepancy, which is attributed to this illite having a greater surface density of charge. For the two soil illites, the exchange of calcium or magnesium for sodium, over the ESP range 0-12 and the calcium-magnesium exchange isotherms were determined. The exchange of sodium followed the same Gapon-type equation for both clays, and was independent of whether calcium or magnesium was the dominant cation. The calcium-magnesium isotherms were also symmetrical. No evidence was therefore found for calcium ions being more strongly held at exchange sites than magnesium ions. It was shown that in the solutions used to equilibrate the clays, which were 1 mM in divalent cations, diffuse double layers were not formed.

Study on the kinetics of process for obtaining cobalt nanopowder by hydrogen reduction under isothermal conditions

2021 ◽  
Vol 1 (1) ◽  
pp. 49-56
Author(s):  
Hieр Nguyen Tien
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Hydrogen Reduction ◽  
Average Particle Size ◽  
Chemical Deposition ◽  
Average Particle ◽  
Isothermal Conditions ◽  
Electron Microscopes ◽  
Kinetics Of

The kinetics of metallic cobalt nanopowder synthesizing by hydrogen reduction from Co(OH)2 nanopowder under isothermal conditions were studied. Co(OH)2 nanopowder was prepared in advance by chemical deposition from aqueous solutions of Co(NO3)2 cobalt nitrate (10 wt.%) and NaOH alkali (10 wt.%) at room temperature, pH = 9 under continuous stirring. The hydrogen reduction of Co(OH)2 nanopowder under isothermal conditions was carried out in a tube furnace in the temperature range from 270 to 310 °C. The crystal structure and composition of powders was studied by X-ray phase analysis. The specific surface area of samples was measured using the BET method by low-temperature nitrogen adsorption. The average particle size of powders was determined by the measured specific surface area. Particles size characteristics and morphology were investigated by transmission and scanning electron microscopes. Kinetic parameters of Co(OH)2 hydrogen reduction under isothermal conditions were calculated using the Gray–Weddington model and Arrhenius equation. It was found that the rate constant of reduction at t = 310 °C is approximately 1.93 times higher than at 270 °C, so the process accelerates by 1.58 times for 40 min of reduction. The activation energy of cobalt nanopowder synthesizing from Co(OH)2 by hydrogen reduction is ~40 kJ/mol, which indicates a mixed reaction mode. It was shown that cobalt nanoparticles obtained by the hydrogen reduction of its hydroxide at 280 °C are aggregates of equiaxed particles up to 100 nm in size where individual particles are connected to several neighboring particles by contact isthmuses.

Preparation and Antibacterial Performances of Electrocatalytic Zinc Oxide Nanoparticles with Diverse Morphologies

2021 ◽  
Vol 17 (9) ◽  
pp. 1824-1829
Author(s):  
Junlin Li ◽  
Xiangfei Li ◽  
Dong Liang ◽  
Xiaojuan Zhang ◽  
Qing Lin ◽  
...  
Keyword(s):  
Zinc Oxide ◽  
Surface Area ◽  
Zinc Oxide Nanoparticles ◽  
Average Particle Size ◽  
Three Dimensional ◽  
Diffusion Method ◽  
Oxide Nanoparticles ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Zno Nps

This study exploits the potential of zinc oxide nanoparticles (ZnO-NPs) with diverse morphologies as catalysts and antibacterial agent. Spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were prepared by microemulsion method, solvent heat method and hydrothermal method, respectively. The structural characterizations of samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. XRD results revealed the formation of spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were all wurtzite crystal structure. SEM results showed that spherical ZnO-NPs had an average particle size of 30–40 nm, rod-shaped ZnO-NPs were about 500 nm long and 100 nm wide with obvious hexagonal crystals. Flower-shaped ZnO-NPs had a three-dimensional appearance with obvious petals. Results of electrochemical HER (Hydrogen evolution reaction) experiments revealed that spherical ZnO-NPs exhibited the highest electrocatalytic activity at the lowest potential voltage due to their largest specific surface area. The antibacterial property of ZnO-NPs samples were studied by the optical density method and disc diffusion method. All samples had antibacterial effects against E. coli. and flower-shaped ZnO-NPs showed the best antibacterial activity due to the largest surface area in comparison with spherical ZnO-NPs and rod-shaped ZnO-NPs, which promised the maximum Zn2+ release as bactericide mechanism that registered in the case of different ZnO-NPs morphologies.

scholarly journals SiO2:MgMnO3: An Efficient Heterogeneous Catalyst for One Pot Synthesis of 1H-Pyrazolo[1,2-b]phthalazine-5,10-dione Derivatives

2020 ◽  
Vol 32 (10) ◽  
pp. 2489-2494
Author(s):  
S.S. Sagar ◽  
R.P. Chavan
Keyword(s):  
Surface Area ◽  
Average Particle Size ◽  
Bet Surface Area ◽  
High Yield ◽  
Average Particle ◽  
One Pot ◽  
Short Reaction Time ◽  
Investigative Techniques ◽  
Current Procedure ◽  
Efficient Heterogeneous Catalyst

The present study deals with hydrothermal synthesis of SiO2 composite MgMnO3 catalyst. The obtained polycrystalline product was analyzed by using physical investigative techniques including XRD, SEM, EDAX, TEM, SAED and BET surface area. The product corresponded to average particle size of 100 nm by TEM images. The BET surface area was found 234.38 cm2/g for SiO2 composite MgMnO3 catalyst which indicates a good catalytic property. The synthesized catalyst was applied for the synthesis of 1H-pyrazolo[1,2-b]-phthalazine-5,10-dione in presence of ethanol as a solvent at 80 ºC. The current procedure and catalyst offers the gains of clean reaction, short reaction time, high yield, easy purification and financial availability of the catalyst.

scholarly journals Microwave solvothermal synthesis and characterization of manganese-doped ZnO nanoparticles

2016 ◽  
Vol 7 ◽  
pp. 721-732 ◽  
Author(s):  
Jacek Wojnarowicz ◽  
Roman Mukhovskyi ◽  
Elzbieta Pietrzykowska ◽  
Sylwia Kusnieruk ◽  
Jan Mizeracki ◽  
...  
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Solvothermal Synthesis ◽  
Web Application ◽  
Zinc Acetate Dihydrate ◽  
Average Particle Size ◽  
Average Particle ◽  
Sem Images

Mn-doped zinc oxide nanoparticles were prepared by using the microwave solvothermal synthesis (MSS) technique. The nanoparticles were produced from a solution of zinc acetate dihydrate and manganese(II) acetate tetrahydrate using ethylene glycol as solvent. The content of Mn2+ in Zn1− x Mn x O ranged from 1 to 25 mol %. The following properties of the nanostructures were investigated: skeleton density, specific surface area (SSA), phase purity (XRD), lattice parameters, dopant content, average particle size, crystallite size distribution, morphology. The average particle size of Zn1− x Mn x O was determined using Scherrer’s formula, the Nanopowder XRD Processor Demo web application and by converting the specific surface area results. X-ray diffraction of synthesized samples shows a single-phase wurtzite crystal structure of ZnO without any indication of additional phases. Spherical Zn1− x Mn x O particles were obtained with monocrystalline structure and average particle sizes from 17 to 30 nm depending on the content of dopant. SEM images showed an impact of the dopant concentration on the morphology of the nanoparticles.

Preparation and Particle Size Characterization of Cu Nanoparticles Prepared by Anodic Arc Plasma

2010 ◽  
Vol 92 ◽  
pp. 163-169
Author(s):  
Hong Xia Qiao ◽  
Zhi Qiang Wei ◽  
Ming Ru Zhou ◽  
Zhong Mao He
Keyword(s):  
Crystal Structure ◽  
Particle Size ◽  
Specific Surface ◽  
Size Distribution ◽  
Surface Area ◽  
Specific Surface Area ◽  
Average Particle Size ◽  
Spherical Shape ◽  
Average Particle ◽  
Uniform Size

Copper nanoparticles were successfully prepared in large scales by means of anodic arc discharging plasma method in inert atmosphere. The particle size, specific surface area, crystal structure and morphology of the samples were characterized by X-ray diffraction (XRD), BET equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED). The experiment results indicate that the crystal structure of the samples is fcc structure as same as that of the bulk materials. The specific surface area is is 11 m2/g, with the particle size distribution ranging from 30 to 90 nm, the average particle size about 67nm obtained from TEM and confirmed from XRD and BET results. The nanoparticles have uniform size, higher purity, narrow size distribution and spherical shape can be prepared by this convenient and effective method.

Preparation of fine-grained MgO and Gd2O3 stabilized ZrO2 thin films by electron beam physical vapor deposition co-evaporation

1997 ◽  
Vol 12 (12) ◽  
pp. 3260-3265 ◽  
Author(s):  
F. Tcheliebou ◽  
M. Boulouz ◽  
A. Boyer
Keyword(s):  
Thin Films ◽  
Electron Beam ◽  
Average Particle Size ◽  
Electron Gun ◽  
Cubic Phase ◽  
Crystallographic Structure ◽  
Average Particle ◽  
Scanning Electron Micrographs ◽  
Dopant Content ◽  
Fine Grained

Thin films of ZrO2 doped with MgO and Gd2O3, 1–1.5 μm in thickness are formed onto nickel substrates by reactive thermal evaporation using a dual-hearth electron gun. X-ray diffraction patterns of the deposits show changes in the crystallographic structure and average particle size as a function of the dopant content. A mixture of monoclinic and tetragonal phases gradually disappears to become a single cubic phase with increasing dopant molar fraction. The average crystallite size deduced from diffraction line broadening decreases as the dopant content increases. This observation is strongly confirmed by scanning electron micrographs which reveal a smooth surface topography. Fine-grained materials obtained here are interpreted in terms of high nucleation rate and kinetically limited grain growth. It appears that composition, crystallographic structure, and microstructure relations are of paramount importance in ZrO2-based films prepared by electron-beam evaporation.

scholarly journals The Properties of Screen Printed (Bi,Pb)-Sr-Ca-Cu-O Thick Films Based On Decomposed Oxalate Powders

1993 ◽  
Vol 15 (3-4) ◽  
pp. 155-163
Author(s):  
J. Hagberg
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Mixed Oxide ◽  
Thick Films ◽  
Average Particle Size ◽  
Nominal Composition ◽  
Average Particle ◽  
Transmission Electron ◽  
Screen Printed

The significance of powder and paste characteristics was studied in order to improve the morphology and structure of superconducting (Bi,Pb)-Sr-Ca-Cu-O screen printed thick films. Powder with nominal composition of Bi1.75Pb0.4Sr1.9Ca2.1Cu3.2Oywas prepared via the oxalate route and decomposed at 430 to 795℃. The decomposed powders were characterized by X-ray diffraction, transmission electron microscopy and specific surface area measurements. These studies showed a variation of specific surface area from 16.5 to 0.9 m2/g and a variation of the average particle size from 100 nm to 800 nm in the studied temperature interval. The phase structure showed three distinct temperature areas; between 430 to 620, 620 to 715, and at 795℃.Thick-film pastes were made by the addition of an organic vehicle at 500, 620, 650 and 795℃ to decompose annealed oxalate synthesized powders and, for comparison, the vehicle was also added to sintered mixed-oxide/carbonate-based powder in weight ratios from 0.42 to 0.54:1. Films were screen printed on single crystal MgO (100) substrates and melt annealed at 890 to 895℃ for 3 min and subsequently, for prolonged diffusion, annealed at 852℃. After firing, the films were mainly composed of the (001) textured (Bi,Pb)2Sr2Ca2Cu3Oyphase. The reference films, made from mixed oxide/carbonate powder, resembled the films based on oxalate powders decomposed at 795℃. Films based on oxalate powders, decomposed at lower temperatures, were smoother and were able to carry noticeably higher currents than films based on powders decomposed at higher temperatures.

scholarly journals Growth of significantly low dimensional zinc orthotitanate (Zn2TiO4) nanoparticles by solid state reaction method

2018 ◽  
Vol 50 (1) ◽  
pp. 133-138 ◽  
Author(s):  
Lizina Khatua ◽  
Rudrashish Panda ◽  
Avanendra Singh ◽  
Arpan Nayak ◽  
Pravakar Satapathy ◽  
...  
Keyword(s):  
Particle Size ◽  
Solid State ◽  
Surface Area ◽  
Solid State Reaction ◽  
Average Particle Size ◽  
Cost Effective ◽  
Solid State Reaction Method ◽  
Average Particle ◽  
Reaction Method ◽  
Low Dimensional

In this work, the ZnO-TiO2 mixed phase nanoparticles were prepared by solid state reaction method by using ZnO and TiO2 powder as precursors. The X-ray diffraction pattern shows a dominant phase of Zinc Orthotitanate (Zn2TiO4). The average particle size (58?18 nm) calculated by the analysing FESEM data closely matches with the particle size calculated by Scherrer?s equation. The calculated average particle size is significantly smaller than the previously published results of nanoparticles, prepared by same method. In the Brunauer-Emmett-Teller (BET) study the specific surface area of the nanoparticles was found as 8.78 m2/g which is similar to the surface area reported in this material prepared by mechanochemical method. The method which we report is simpler and cost effective unlike the previous reported.

scholarly journals Sol-gel synthesis of anatase nanopowders for efficient photocatalytic degradation of herbicide Clomazone in aqueous media

2017 ◽  
Vol 49 (3) ◽  
pp. 319-330
Author(s):  
Aleksandar Golubovic ◽  
Bojana Simovic ◽  
Slavica Gasic ◽  
Dusan Mijin ◽  
Aleksandar Matkovic ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Surface Area ◽  
Active Substance ◽  
Anatase Phase ◽  
Sol Gel ◽  
Aqueous Media ◽  
Average Particle Size ◽  
Commercial Product ◽  
Average Particle ◽  
Developed Surface

TiO2 nanopowders were produced by sol-gel technique using TiCl4 as a starting material. For the preparation of crystalline anatase with developed surface area, this aqueous solution has been mixed with 0.05 M or 0.07 M (NH4)2SO4 solution in a temperature-controlled bath. The pH values of the suspension were 7, 8 or 9. According to the x-ray diffraction (XRD) analysis the anatase crystallite sizes were about 12 nm, which coincided with the average particle size revealed by scanning electron microscopy (SEM). The Raman scattering measurements have shown the presence of a small amount of highly disordered brookite phase in addition to dominant anatase phase with similar nanostructure in all synthesized powders. BET measurements revealed that all synthesized catalysts were fully mesoporous, except the sample synthesized with 0.07 M (NH4)2SO4 at pH=9, which had small amount of micropores. The photocatalytic degradation of herbicide Clomazone was carried out for both the pure active substance and as the commercial product (GAMIT 4-EC) under UV irradiation. The best photocatalytic efficiency was obtained for the catalyst with the largest specific surface area, confirming this parameter as crucial for enhanced photocatalytic degradation of the pure active substance and commercial product of herbicide Clomazone.

Development of Heterostructured Ferroelectric SrZrO3/CdS Photocatalysts with Enhanced Surface Area and Photocatalytic Activity

2020 ◽  
Vol 20 (6) ◽  
pp. 3770-3779 ◽  
Author(s):  
Umar Farooq ◽  
Farheen Naz ◽  
Ruby Phul ◽  
Nayeem Ahmad Pandit ◽  
Sapan Kumar Jain ◽  
...  
Keyword(s):  
Particle Size ◽  
Dielectric Constant ◽  
Photocatalytic Activity ◽  
Surface Area ◽  
Room Temperature ◽  
Average Particle Size ◽  
Chemical Deposition ◽  
Bet Surface Area ◽  
Cds Nanoparticles ◽  
Average Particle

This paper reports the attempt to develop an efficient heterostructure photocatalyst by employing SrZrO3 as ferroelectric substrate with deposited nanostructured CdS semiconductor on the surface. Primarily bare SrZrO3 and CdS nanoparticles were synthesized by using polymeric citrate precursor and co-precipitation routes, respectively. The chemical deposition technique was used to develop the CdS over the surface of the pre-synthesized SrZrO3 nanoparticles. The synthesized bare nanoparticles and their heterostructure were characterized by XRD which shows the formation of orthorhombic and face centred cubic (FCC) phases of SrZrO3 and CdS, respectively. TEM was used to estimate the morphology and particle size of as-synthesized nanoparticles, which shows the average particle size of 14, 24 and 25 nm for SrZrO3, CdS and SrZrO3/CdS, respectively. The BET surface area of SrZrO3, CdS and SrZrO3/CdS samples was found to be 299, 304 and 312 m2/g respectively. Methylene blue was used as model pollutant to determine the photocatalytic activity of the synthesized nanomaterials. The heterostructure shows an enhanced activity as compared to bare nanoparticles. Dielectric constant and dielectric loss of the nanoparticles was investigated as a function of frequency at room temperature and as a function of temperature at 500 kHz. The room temperature dielectric constant for SrZrO3, CdS and SrZrO3/CdS was found to be 13.2, 17.8 and 25.5 respectively at 100 kHz.

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