scholarly journals NITROGEN THERMAL DESORPTION OF AS A CONTROL METHOD FOR DETERMINATION OF THE NANOPARTICLE SIZE IN COMPOSITIONS BASED ON ZINC OXIDE AND HYDROXYAPATITE

2021 ◽  
pp. 294-299
Author(s):  
Евгения Владимировна Мараева ◽  
Вячеслав Алексеевич Мошников
Keyword(s):  
Zinc Oxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Thermal Desorption ◽  
Control Method ◽  
Chemical Deposition ◽  
Bioactive Coatings ◽  
Sorption Method ◽  
Before And After

Работа посвящена анализу возможности применения метода тепловой десорбции азота для определения размеров наночастиц в композициях на основе гидроксиапатита и оксида цинка, изготовленных в форме таблеток с помощью ручного гидравлического пресса. Исходные порошки гидроксиапатита получены методом химического осаждения с использованием микроволнового излучения. С применением сорбционного метода БЭТ анализируется удельная поверхность порошков, составляющих композиции, до и после прессования, исследуется влияние состава композиций на удельную поверхность. Приводится расчет средних размеров наночастиц в композициях на основе результатов сорбционных измерений в рамках моделей сферических и стержневидных наночастиц. Область применения рассматриваемых материалов - медицина, в том числе использование в адресной доставке лекарств и в костной инженерии в качестве биоактивных покрытий, нанесенных на поверхность металлического биоимплантата. In this paper we consider the possibility of using the nitrogen thermal desorption method for determining the size of nanoparticles in compositions based on hydroxyapatite and zinc oxide. The compositions in the form of tablets were obtained using a manual water press. The initial powders of hydroxyapatite were obtained by chemical deposition using a microwave radiation. Using the BET sorption method, the specific surface area of the powders is analyzed before and after pressing, and the effect of the composition formulation on the specific surface area is investigated. The calculation of the average sizes of nanoparticles in composites is given on the basis of the results of sorption measurements within the framework of the models of spherical and rod-like nanoparticles. The field of application of the materials under consideration is medicine, including the use of nanocomposites in targeted drug delivery and in bone engineering as bioactive coatings applied to the surface of a metal bioimplant.

Size Analysis Based on Sorption Study Data for Hydroxyapatite Nanoparticles

2021 ◽  
Vol 1031 ◽  
pp. 172-177
Author(s):  
Evgeniya Maraeva ◽  
Kamilya Khalugarova
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Chemical Deposition ◽  
Study Data ◽  
Size Analysis ◽  
Hydroxyapatite Nanoparticles ◽  
Sorption Method ◽  
Sorption Study

This work is devoted to the study on the possibility of applying the method of analyzing the particle size of hydroxyapatite at various stages of synthesis. A series of hydroxyapatite powders obtained by chemical deposition using microwave radiation is considered. Determination of the size of hydroxyapatite nanorods is carried out on the basis of data on the density and specific surface area. The specific surface area is analyzed by the sorption method. Determination of the ratio "length / diameter" of nanorods is based on the analysis of images obtained by scanning electron microscopy.

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.

Effect of Crystals Size, Surface Area and Pore Size of Hydroxyapatite Microspheres on the Loading Ability of Bovine Serum Albumin

2011 ◽  
Vol 197-198 ◽  
pp. 17-20
Author(s):  
Jun Ming Li ◽  
Ai Juan Wang ◽  
Yu Peng Lv ◽  
Bai Ling Jiang
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Specific Surface ◽  
Pore Size ◽  
Surface Area ◽  
Specific Surface Area ◽  
Bovine Serum ◽  
Crystal Size ◽  
Adsorption Ability ◽  
Before And After

Effect of crystals size, surface area, pore size and porosity of hydroxyapatite microspheres on the loading ability of bovine serum albumin was studied in this paper. The surface morphology, specific surface area and porosity of hydroxyapatite microspheres were characterized by scanning electron microscope, specific surface area and pore size analyzer, respectively. The concentration of BSA in aqueous solutions both before and after adsorption was determined by ultraviolet-visible spectrophotometer. The results indicated that the adsorption behavior of bovine serum albumin appeared to obey the Langmuir-type isotherm model. Fast adsorption appeared at the beginning, and then decreased gradually. Hydroxyapatite microspheres calcined at 600°C had the maximum capacity, and those calcined at 800°C showed lower adsorption ability. The loading ability of hydroxyapatite microspheres depended on its crystal size, specific surface area, pore size and porosity, etc.

Synthesis and Characterization of Porous Mo-W Oxide Nanostructures

2008 ◽  
Vol 8 (12) ◽  
pp. 6445-6450
Author(s):  
F. Paraguay-Delgado ◽  
Y. Verde ◽  
E. Cizniega ◽  
J. A. Lumbreras ◽  
G. Alonso-Nuñez
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Synthesis Method ◽  
Atomic Ratio ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Before And After

The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 °C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 °C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically.

Effect of ZnO Particle Size on the Curing of Carboxylated NBR and Carboxylated SBR

2004 ◽  
Vol 77 (2) ◽  
pp. 214-226 ◽  
Author(s):  
G. R. Hamed ◽  
K.-C. Hua
Keyword(s):  
Zinc Oxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Cure Rate ◽  
Surface Areas ◽  
Diffusion Limited ◽  
Rate Of Dissolution ◽  
Oxide Particles ◽  
And Diffusion

Abstract A carboxylated nitrile rubber (XNBR) and a carboxylated SBR (XSBR) were mixed with zinc oxide particles of different specific surface areas (“S”, 35 m2/g; “M”, 3.5m2/g; “L”, 0.5 m2/g) and cure behavior at 165 ºC studied using oscillating disc rheometry. Without added zinc oxide, both raw rubbers slowly stiffen over many hours of heating. This is probably due to condensation of carboxyl groups to form anhydride crosslinks. XNBR compositions containing the finely divided “S” crosslink much more rapidly. Full cure is reached after about 10 minutes of heating. Cure rate decreases markedly as the specific surface area of the ZnO decreases. A composition containing “M” at twice stoichiometry requires about an hour to cure well, while with “L”, about 10 hours are required. In contrast, curing of the XSBR depends little on the specific surface area of the ZnO, either with “S” or “L”, curing is essentially complete after 30 minutes. After simply mixing ZnO into either rubber, it remains as a dispersed particulate. With XNBR, curing appears to be controlled by the rate of dissolution and diffusion of ZnO, while, with XSBR, reaction is not diffusion limited and may be confined to regions near particle surfaces.

Influence of Zinc Oxide Nanograins on Properties of Epoxidized Natural Rubber Vulcanizates

2017 ◽  
Vol 748 ◽  
pp. 79-83 ◽  
Author(s):  
Rudeerat Suntako
Keyword(s):  
Mechanical Properties ◽  
Zinc Oxide ◽  
Natural Rubber ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Epoxidized Natural Rubber ◽  
Precipitation Method ◽  
Cure Characteristics ◽  
Permanent Set

Zinc oxide (ZnO) nanograins are synthesized by precipitation method filled epoxidized natural rubber compared to conventional ZnO. The synthesized ZnO nanograins are characterized by X-ray diffraction and transmission electron microscopy and found that average primary size of ZnO synthesized around 40 nm and the specific surface area of 28.72 m2 g-1. Furthermore, the cure characteristics, rubber mechanical properties and permanent set were investigated. The obtained results are found that the ZnO nanograins significantly affected to cure characteristics, rubber mechanical properties and permanent set. This is due to small grain size and large specific surface area.

scholarly journals Polyamide-6 surface cracked forms nanofibers: A novel way for increasing the surface roughness, and porosity

2021 ◽  
Author(s):  
Sedigheh Aghayari
Keyword(s):  
Surface Roughness ◽  
Water Treatment ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Polyamide 6 ◽  
Bet Method ◽  
Before And After ◽  
The Web

Abstract Here away used to reduce the porosity of the nanofibers, which is removing PVA nanofibers from PVA/PA6 nanofibers by water treatment. Measuring the porosity of the electrospun web before and after treatment by the BET method proved this. The specific surface area of the web was 60 % reduced after water treatment. Surface roughness and pore volume have reduced after water treatment. Also, I introduced BET as the method for measuring the diameters of mesopores (or lower than 100nm). I used BET to prove that the cracks can make mesopores on the nanofibers.

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.

Finding the Specific Surface Area of an Organomineral Sorbent Produced by Electroplasma Treatment of Coal Flotation Waste

2021 ◽  
Vol 887 ◽  
pp. 603-609
Author(s):  
A.S. Kondratenko ◽  
S.L. Buyantuev ◽  
S.Yu. Shishulkin
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Thermal Activation ◽  
Thermal Destruction ◽  
Adsorption Model ◽  
Langmuir Adsorption ◽  
Coal Flotation ◽  
Solid Adsorbent ◽  
Before And After

This paper dwells upon finding the specific surface area of cake, a coal enrichment waste, exposed to electroplasma treatment; the goal is to make an organomineral porous material to be used as a sorbent for wastewater treatment. The research team used a monomolecular Langmuir adsorption model and surface tension of the surfactants before and after adsorption at the interface of solution and solid adsorbent. Another process considered herein was thermal activation of substances in the electroplasmic reactor for making organomineral porous materials from coal cakes. The paper presents the resulting specific surfaces area of the organomineral sorbent thus produced. Thus, the waste of flotation, i.e. coal cake, is fundamentally suitable for making porous substances by thermal destruction in an electroplasma reactor.

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