Morpho-Structural and Chemical Composition Properties of PVP-Capped ZnO Nanoparticles Synthesized via a Simple-Polyol Method

2019 ◽  
Vol 286 ◽  
pp. 15-22
Author(s):  
Gregorio Flores-Carrasco ◽  
J.R. Mora ◽  
R. Ramírez ◽  
Carlos Bueno ◽  
Salvador Alcántara-Iniesta ◽  
...  
Keyword(s):  
Zno Nanoparticles ◽  
Single Step ◽  
Polyol Method ◽  
X Ray Diffraction ◽  
Physico Chemical ◽  
Precursor Synthesis ◽  
Primary Particles ◽  
Ft Ir ◽  
Composition Properties ◽  
Ft Ir Spectroscopy

In this work, we report on the processing of PVP-capped ZnO nanoparticles employing a simple-polyol method, varying only the molar concentration (0.01 and 0.1 M) of Zn(CH3COO)2•2H2O used as zinc precursor. Synthesis is performed using ethylene glycol (EG) as solvent and polyvinylpyrrolidone (PVP) as capping agent. Physico-chemical characteristics of the as-synthesized particles were studied by X-Ray Diffraction (XRD), Fourier Transform Infrared (FT-IR) spectroscopy, Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). SEM micrographs revealed formation of quasi-spherical secondary particles formed by aggregation of primary nanosized subunits crystallized from 0.01 M precursor. When precursor with a higher concentration is used, no aggregation occurs and only tiny primary particles in the nanosized range are obtained. XRD confirmed that ZnO nanoparticles have the hexagonal wurtzite-type structure. SEM, EDS and FT-IR showed that applied route produced ZnO nanoparticles with functionalized surface. Presented results imply clear dependence of the particles morphology and size from precursor concentration which could be used for rapid, continuous, single-step preparation of PVP-capped ZnO nanoparticles tailored in accordance to application demands.

Consequences of Fluoride Incorporation on Properties of Apatites

2006 ◽  
Vol 309-311 ◽  
pp. 697-700 ◽  
Author(s):  
Racquel Z. LeGeros ◽  
Dindo Q. Mijares ◽  
Fang Yao ◽  
John P. LeGeros ◽  
T. Bromage ◽  
...  
Keyword(s):  
Crystal Size ◽  
Chemical Properties ◽  
Calcium Deficiency ◽  
X Ray Diffraction ◽  
X Ray ◽  
Physico Chemical ◽  
Lower Solubility ◽  
Ft Ir ◽  
Hydrolysis Of ◽  
Ft Ir Spectroscopy

Fluoride, when incorporated in the apatite, stabilizes the structure. The purpose of this study was to determine the consequences of fluoride (F) substitution on the physico-chemical properties of apatites. F-containing apatites were prepared by precipitation or by hydrolysis of CaHPO4 in solutions containing different F concentrations and characterized using x-ray diffraction, FT-IR spectroscopy, scanning electron microscopy, thermogravimetry and chemical analyses. Results showed that F incorporation have the following effects: (a) decrease in a-axis dimension, (b) increase in crystal size and thickness, (c) decrease in calcium deficiency, and (d) lower solubility.

scholarly journals Experimental and Physico-Chemical Comparison of ZnO Nanoparticles’ Activity for Photocatalytic Applications in Wastewater Treatment

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 678
Author(s):  
Stefano Alberti ◽  
Irene Basciu ◽  
Marco Vocciante ◽  
Maurizio Ferretti
Keyword(s):  
Wastewater Treatment ◽  
Zno Nanoparticles ◽  
Energy Dispersive Spectrometer ◽  
Chemical Properties ◽  
X Ray Diffraction ◽  
Commercial Sample ◽  
Synthetic Process ◽  
Physico Chemical ◽  
Photocatalytic Applications ◽  
Reflectance Measurements

In this contribution, the photoactivity upon activation by simulated sunlight of zinc oxide (ZnO) obtained from two different synthetic pathways (Acetate and Nitrate) is investigated for water purification. Different reagents and processes were exploited to obtain ZnO nanoparticles. Products have been characterized by means of X-Ray Diffraction, Scanning Electron Microscopy along with Energy Dispersive Spectrometer, Dynamic Light Scattering, and Diffuse Reflectance Measurements, to highlight the different outcomes ascribable to each synthesis. A comparison of characteristics and performances was also carried out with respect to commercial ZnO. Nanoparticles of this semiconductor can be obtained as aggregates with different degrees of purity, porosity, and shape, and their physical-chemical properties have been addressed to the specific use in wastewater treatment, testing their effectiveness on the photocatalytic degradation of methylene blue (MB) as a model pollutant. Excluding the commercial sample, experimental results evidenced a better photocatalytic behavior for the ZnO Nitrate sample annealed at 500 °C, which was found to be pure and stable in water, suggesting that ZnO could be effectively exploited as a heterogeneous photocatalyst for the degradation of emerging pollutants in water, provided that thermal treatment is included in the synthetic process.

scholarly journals Multidimensional Ln-Aminophthalate Photoluminescent Coordination Polymers

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  
Keyword(s):  
Water Content ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Low Cost ◽  
Microwave Assisted Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The development of straightforward reproducible methods for the preparation of new photoluminescent coordination polymers (CPs) is an important goal in luminescence and chemical sensing fields. Isophthalic acid derivatives have been reported for a wide range of applications, and in addition to their relatively low cost, have encouraged its use in the preparation of novel lanthanide-based coordination polymers (LnCPs). Considering that the photoluminescent properties of these CPs are highly dependent on the existence of water molecules in the crystal structure, our research efforts are now focused on the preparation of CP with the lowest water content possible, while considering a green chemistry approach. One- and two-dimensional (1D and 2D) LnCPs were prepared from 5-aminoisophthalic acid and Sm3+/Tb3+ using hydrothermal and/or microwave-assisted synthesis. The unprecedented LnCPs were characterized by single-crystal X-ray diffraction (SCRXD), powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM), and their photoluminescence (PL) properties were studied in the solid state, at room temperature, using the CPs as powders and encapsulated in poly(methyl methacrylate (PMMA) films, envisaging the potential preparation of devices for sensing. The materials revealed interesting PL properties that depend on the dimensionality, metal ion, co-ligand used and water content.

Hydrothermal synthesis, crystal structure and properties of a two-dimensional uranyl coordination polymer based on a flexible zwitterionic ligand

2018 ◽  
Vol 74 (3) ◽  
pp. 366-371 ◽  
Author(s):  
Wen Cui ◽  
Ruyu Wang ◽  
Xi Shu ◽  
Yu Fan ◽  
Yang Liu ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Hydrothermal Reaction ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Uranyl Compounds ◽  
X Ray ◽  
Potential Applications ◽  
Ft Ir ◽  
Fuel Reprocessing ◽  
Ft Ir Spectroscopy

The interaction between the uranyl cation, (UO2)2+, and organic species is of interest due to the potential applications of the resulting compounds with regard to nuclear waste disposal and nuclear fuel reprocessing. The hydrothermal reaction of various uranyl compounds with flexible zwitterionic 1,1′-[1,4-phenylenebis(methylene)]bis(pyridin-1-ium-4-carboxylate) dihydrochloride (Bpmb·2HCl) in deionized water containing drops of H2SO4resulted in the formation of a novel two-dimensional uranyl coordination polymer, namely poly[tetraoxido{μ2-1,1′-[1,4-phenylenebis(methylene)]bis(pyridin-1-ium-4-carboxylate)}di-μ3-sulfato-diuranium(VI)], [(UO2)2(SO4)2(C20H16N2O4)]n, (1). Single-crystal X-ray diffraction reveals that this coordination polymer exhibits a layered arrangement and the (UO2)2+centre is coordinated by five equatorial O atoms. The structure was further characterized by FT–IR spectroscopy, powder X-ray diffraction (PXRD) and thermogravimetric analysis (TGA). The polymer shows high thermal stability up to 696 K. Furthermore, the photoluminescence properties of (1) has also been studied, showing it to exhibit a typical uranyl fluorescence.

Study on Nano- and Microcrystallites in Urines of Uric Acid Stone Patients

2013 ◽  
Vol 655-657 ◽  
pp. 1927-1930 ◽  
Author(s):  
Guang Na Zhang ◽  
Zhi Yue Xia ◽  
Jian Ming Ouyang ◽  
Li Kuan
Keyword(s):  
Electron Microscopy ◽  
Uric Acid ◽  
X Ray Diffraction ◽  
Uric Acid Stone ◽  
Urine Ph ◽  
Stone Formers ◽  
Transmission Electron ◽  
Close Relationship ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The presence of crystallites in urine is closely related to stones formation. In this article, the components, morphology of nano- and micro-crystallites in urines of 20 uric acid (UA) stone formers as well as their relationship with the formation of UAstones were comparatively studied using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The main constituent of urinary crystallites was uric acid. Their particle size distribution was highly uneven, ranging from several nanometers to several tens of micrometers, and obvious aggregation was observed. These results showed that there was close relationship among stone components, urinary crystallites composition and urine pH.

Preparation and Characterization of Cefradine/Montmorillionite Composites

2012 ◽  
Vol 560-561 ◽  
pp. 434-437 ◽  
Author(s):  
Lan Wang ◽  
Wen Ji Guo ◽  
Yan Zhao Zhao
Keyword(s):  
Gastric Fluid ◽  
Simulated Gastric Fluid ◽  
X Ray Diffraction ◽  
Simulated Intestinal Fluid ◽  
Solution Intercalation ◽  
Method Of Solution ◽  
Ft Ir ◽  
In The Beginning ◽  
Ft Ir Spectroscopy

The objective of this paper was to prepare the composite of crefradine/montmorillionite in the method of solution intercalation. The drug load and intercalation rate varied with the drug concentration. X-ray diffraction (XRD), Fourier transformed infrared (FT-IR) Spectroscopy, and thermal analysis (TG-DSC) were applied to characterize composite mentioned above. Together with drug release tests, results indicate cefradine intercalated into montmorillionite.The release profiles of cefradine/MMT in simulated gastric fluid (pH 1.2) and simulated intestinal fluid (pH 7.4) at 37°Cduring 10h are shown in Fig. 4. The amount of cefradine in the beginning 2h came up to 35% and 50%, and in the following time, cefradine released slowly. The release behaviors met the requirements of sustained release.

scholarly journals The Bio-fabrication of Gold Nanoparticles (AuNPs) by Green Method and Study of its Electrochemical Applications

2020 ◽  
Vol 1 (4) ◽  
pp. 22-25
Author(s):  
Azwan Morni
Keyword(s):  
Gold Nanoparticles ◽  
Ir Spectroscopy ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Green Method ◽  
Oh Groups ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

This study reports a green method for the synthesis of gold nanoparticles (AuNPs) using the aqueous extract of Salix aegyptiaca extract. The effects of gold salt concentration, extract concentration and extract quantity were investigated on nanoparticles synthesis. Novel methods of ideally synthesizing AuNPs are thus thought that are formed at ambient temperatures, neutral pH, low costs and environmentally friendly fashion. AuNPs were characterized with different techniques such as UV–vis spectroscopy, FT-IR spectroscopy, X-ray diffraction, and TEM. FT-IR spectroscopy revealed that gold nanoparticles were functionalized with biomolecules that have primary carbonyl group, -OH groups and other stabilizing functional groups. TEM experiments showed that these nanoparticles are formed with various shapes and X-ray diffraction pattern showed high purity and face centered cubic structure of AuNPs. For electrochemical properties of AuNPs, a modified glassy carbon electrode using AuNPs (AuNPs/GCE) was investigated. The results show that electronic transmission rate between the modified electrode and [Fe (CN)6]3-/4- increased.

scholarly journals Nanosized MoO3 as a reusable heterogeneous catalyst for the synthesis of 2,6-bis(benzylidene)cyclohexanones

2015 ◽  
Vol 33 (1) ◽  
pp. 163-168 ◽  
Author(s):  
Nitin R. Dighore ◽  
Priyanka L. Anandgaonker ◽  
Suresh T. Gaikwad ◽  
Anjali S. Rajbhoj
Keyword(s):  
Heterogeneous Catalyst ◽  
Product Yield ◽  
Synthesis Process ◽  
X Ray Diffraction ◽  
Structure Directing Agent ◽  
Vis Spectroscopy ◽  
Solvent Formation ◽  
Ft Ir ◽  
Work Up ◽  
Ft Ir Spectroscopy

AbstractCrystalline MoO3 nanoparticles were obtained by electrochemical synthesis process using tetrapropylammonium bromide as a stabilizer and structure-directing agent in ACN:THF(4:1) solvent. Formation of MoO3 nanoparticles took place at a constant supply current of 14 mA/cm2. These synthesized MoO3 nanoparticles were characterized by UV-Vis spectroscopy, FT-IR spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM). So prepared MoO3 nanoparticles were used as a heterogeneous catalyst for the synthesis of 2,6-bis(benzylidene)cyclohexanone derivatives. This protocol offers several advantages, such as simple work-up procedure, recyclability of the catalyst, excellent product yield in a short reaction time and purification of products with a non-chromatographic method.

Ball-Milling Stimulated Mechanochemical Processes in the System “Titanium-Toluene”

2019 ◽  
Vol 946 ◽  
pp. 351-356 ◽  
Author(s):  
Olga M. Kanunnikova ◽  
V.V. Aksenova ◽  
G.A. Dorofeev
Keyword(s):  
Ball Milling ◽  
Mechanical Energy ◽  
High Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Liquid Phases ◽  
Ft Ir ◽  
Titanium Powders ◽  
Solid Phases ◽  
Ft Ir Spectroscopy

The present work deals with the investigation of the transformations of the solid and liquid phases at high energy planetary ball milling of toluene together with titanium powder. The sequence of structural toluene transformations using FT-IR spectroscopy was investigated. Phase constitutions and morphology of ball milled titanium powders were studied by X-ray diffraction and scanning electron microscopy. It is shown that mechanically induced destruction of toluene occurs by the mechanism of catalytic cracking. During ball milling, concentration of aromatic hydrocarbons in the liquid phase decreases, at the same time the content of alkenes, cycloalkanes, and isoalkanes increases. The main solid products of the mechanosynthesis were cubic and hexagonal titanium carbo-hydrides.Evolution of lattice parameters, crystallites sizes, and micro-stresses of the solid phases during ball milling as a function of the mechanical energy dose have been discussed.

scholarly journals An Efficient and Novel Ammonia Sensor Based on Polypyrrole/Tin Oxide/MWCNT Nanocomposite

2020 ◽  
Vol 32 (6) ◽  
pp. 1505-1510
Author(s):  
Ahmad Husain ◽  
Mohd Urooj Shariq ◽  
Anees Ahmad
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Charge Carriers ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Ammonia Sensing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

In present study, the synthesis and characterization of a novel polypyrrole (PPy)/tin oxide (SnO2)/MWCNT nanocomposite along with pristine polypyrrole is reported. These materials have been studied for their structural and morphological properties by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. PPy/SnO2/MWCNT nanocomposite has been converted into a pellet-shaped sensor, and its ammonia sensing studies were carried out by calculating the variation in the DC electrical conductivity at different concentration of ammonia ranging from 10 to 1500 ppm. The sensing response of the sensor was determined at 1500, 1000, 500, 200, 100 and 10 ppm and found to be 70.4, 66.1, 62.2, 55.4, 50.8 and 39.7%, respectively The sensor showed a complete reversibility at lower concentrations along with excellent selectivity and stability. Finally, a sensing mechanism was also proposed involving polarons (charge carriers) of polypyrrole and lone pairs of ammonia molecules

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