scholarly journals Preparation, Characterization and Applications of Chitosan-Nanosilica-Graphene Oxide Nanocomposite

2021 ◽  
Vol 33 (11) ◽  
pp. 2789-2795
Author(s):  
A. Sahila Grace ◽  
G.S. Prabha Littis Malar

In present study, a simple low cost method was used to prepare chitosan-nanosilica-graphene oxide (CS-NSi-GO) nanocomposite. Nanosilica and graphene oxide were synthesized from coconut husk ash and chitosan was synthesized from shrimp shell. Nanosilica was synthesized from coconut husk ash with alkaline extraction using sodium hydroxide followed by precipitation method using sulphuric acid. Graphene oxide was synthesized from the oxidative treatment of the raw material of coconut husk ash. After the synthesis of silica, the carbonized graphite was collected and treated by modified Hummer’s method. The CS-NSi-GO nanocomposite was prepared by condense polymerization method. Various analytical methods such as Fourier transform infrared (FTIR) spectroscopy, Fourier transform Raman (FT-Raman) spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX) and transmission electron microscopy (TEM) were used to characterize the CS-NSi-GO nanocomposite. Eventually antibacterial, antifungal, antioxidant and cytotoxicity of the prepared nanocomposite were also evaluated.

2016 ◽  
Vol 864 ◽  
pp. 112-116
Author(s):  
Rinlee Butch M. Cervera ◽  
Emie A. Salamangkit-Mirasol

Rice hull or rice husk (RH) is an agricultural waste obtained from milling rice grains. Since RH has no commercial value and is difficult to use in agriculture, its volume is often reduced through open field burning which is an environmental hazard. In this study, amorphous nanosilica from Philippine waste RH was prepared via acid precipitation method. The synthesized samples were fully characterized for its microstructural properties. X-ray diffraction pattern reveals that the structure of the prepared sample is amorphous in nature while Fourier transform infrared spectrum showed the different vibration bands of the synthesized sample. Scanning electron microscopy (SEM) and particle size analysis (PSA) confirmed the presence of agglomerated silica particles. On the other hand, transmission electron microscopy (TEM) revealed an amorphous sample with grain sizes of about 5 to 20 nanometer range and has about 95 % purity according to EDS analyses. The elemental mapping also suggests that leaching of rice hull ash effectively removed the metallic impurity such as potassium element in the material. Hence, amorphous nanosilica was successfully prepared via a low-cost acid precipitation method from Philippine waste rice hull.


2017 ◽  
Vol 751 ◽  
pp. 807-812
Author(s):  
Tuangphorn Prasitthikun ◽  
X. Wu ◽  
Tsugio Sato ◽  
Charusporn Mongkolkachit ◽  
Pornapa Sujaridworakun

High efficiency BiOBr/GO composites photocatalyst were successfully synthesized via a facile precipitation method. The precursors were prepared by dissolving Bi (NO3)3.5H2O and KBr in glycerol and distilled water, respectively. Various amounts (0.1-2 wt%) of graphene oxide were added into the mixed solution precursors, and stirred at room temperature to get precipitated powder without further heat treatment. The obtained products were characterized for phase, morphology, optical properties and surface area by X-ray diffraction (XRD), transmission electron microscopy (TEM), filed-emission scanning electron microscopy (FE-SEM), UV-Vis diffuse reflection spectroscopy (DRS) and Brunauer–Emmett–Teller (BET), respectively. The morphology and structure of as-synthesized samples were composed of numerous fine plates of BiOBr dispersed on the GO sheets. The photocatalytic activities of BiOBr/GO composites were evaluated by rhodamine B degradation under visible light irradiation. As the results, the significant increase in photodegradation of BiOBr/GO composite comparing with pure BiOBr was observed. Among all samples, the composite with 1 wt% of graphene oxide showed the highest photocatalytic performance.


2021 ◽  
Vol 4 (1) ◽  
pp. 26
Author(s):  
Sule Aytas ◽  
Sabriye Yusan ◽  
Senol Sert ◽  
Cem Gok

Magnetic graphene oxide nanocomposites (M-GO) were successfully synthesized by partial reduction co-precipitation method and used for removal of Sr(II) and Cs(I) ions from aqueous solutions. The structures and properties of the M-GO was investigated by X-ray diffraction, Fourier transformed infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, vibrating sample magnetometer (VSM) and N2-BET measurements. It is found that M-GO has 2.103 mg/g and 142.070 mg/g adsorption capacities for Sr(II) and Cs(I) ions, respectively. The adsorption isotherm matches well with the Freundlich for Sr(II) and Dubinin–Radushkevich model for Cs(I) and kinetic analysis suggests that the adsorption process is pseudo-second-ordered.


2010 ◽  
Vol 1266 ◽  
Author(s):  
Hongming Yu ◽  
Ruijun Pan ◽  
Xuefei Chen ◽  
Wentao Song ◽  
Jian Xie ◽  
...  

AbstractLiFePO4/graphene-oxide (GNO) composites were prepared by co-precipitation method. Their structure and morphology were investigated by X-ray diffraction, Fourier transform infrared spectra, field emission scanning electron microscopy, and transmission electron microscopy. A low content of GNO can be uniformly dispersed in the matrix of LiFePO4 nano particles, while at a higher content, GNO will aggregate severely and has a negative effect on the electrochemical performance of LiFePO4. Further heat treatment can improve the crystallinity of LiFePO4, and improve the electrochemical performance of LiFePO4 with a relatively low content of GNO.


2018 ◽  
Vol 7 (1) ◽  
Author(s):  
Sabriye Yusan

<p>Magnetic graphene oxide nanocomposites (M-GO) were successfully synthesized by partial reduction co-precipitation method and used for removal of Sr(II) and Cs(I) ions from aqueous solutions. The structures and properties of the M-GO was investigated by X-ray diffraction, Fourier transformed infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, vibrating sample magnetometer (VSM) and N<sub>2</sub>-BET measurements. It is found that M-GO has 2.103 mg/g and 142.070 mg/g adsorption capacities for Sr(II) and Cs(I) ions, respectively. The adsorption isotherm matches well with the Freundlich for Sr(II) and Dubinin–Radushkevich model for Cs(I) and kinetic analysis suggests that the adsorption process is pseudo-second-ordered.</p>


Author(s):  
T. P. Nolan

Thin film magnetic media are being used as low cost, high density forms of information storage. The development of this technology requires the study, at the sub-micron level, of morphological, crystallographic, and magnetic properties, throughout the depth of the deposited films. As the microstructure becomes increasingly fine, widi grain sizes approaching 100Å, the unique characterization capabilities of transmission electron microscopy (TEM) have become indispensable to the analysis of such thin film magnetic media.Films were deposited at 225°C, on two NiP plated Al substrates, one polished, and one circumferentially textured with a mean roughness of 55Å. Three layers, a 750Å chromium underlayer, a 600Å layer of magnetic alloy of composition Co84Cr14Ta2, and a 300Å amorphous carbon overcoat were then sputter deposited using a dc magnetron system at a power of 1kW, in a chamber evacuated below 10-6 torr and filled to 12μm Ar pressure. The textured medium is presently used in industry owing to its high coercivity, Hc, and relatively low noise. One important feature is that the coercivity in the circumferential read/write direction is significandy higher than that in the radial direction.


Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 122
Author(s):  
Karina J. Lagos ◽  
Bojan A. Marinkovic ◽  
Alexis Debut ◽  
Karla Vizuete ◽  
Víctor H. Guerrero ◽  
...  

Ecuadorian black mineral sands were used as starting material for the production of iron-titanium oxide nanostructures. For this purpose, two types of mineral processing were carried out, one incorporating a pre-treatment before conducting an alkaline hydrothermal synthesis (NaOH 10 M at 180 °C for 72 h), and the other prescinding this first step. Nanosheet-assembled flowers and nanoparticle agglomerates were obtained from the procedure including the pre-treatment. Conversely, nanobelts and plate-like particles were prepared by the single hydrothermal route. The nanoscale features of the product morphologies were observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. The ilmenite and hematite molar fractions, within the ilmenite-hematite solid solution, in the as-synthetized samples were estimated by Brown’s approach using the computed values of unit-cell volumes from Le Bail adjustments of X-ray powder diffraction (XRPD) patterns. The resulting materials were mainly composed of Fe-rich ilmenite-hematite solid solutions (hematite molar contents ≥0.6). Secondary phases, which possibly belong to lepidocrocite-like or corrugated titanate structures, were also identified. The current study demonstrated the feasibility of employing Ecuadorian mineral resources as low-cost precursors to synthesize high-added-value nanostructures with promising applications in several fields.


Coatings ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 257
Author(s):  
Mariam Khan ◽  
Naveed Kausar Janjua ◽  
Safia Khan ◽  
Ibrahim Qazi ◽  
Shafaqat Ali ◽  
...  

An Ag2O(x)−PrO2(y)/γ-Al2O3 electrocatalyst series (X:Y is for Ag:Pr from 0 to 10) was synthesized, to use synthesized samples in electrochemical applications, a step in fuel cells advancements. Ag2O(x)−PrO2(y)/γ-Al2O3/Glassy-Carbon was investigated for electrochemical oxidation of ammonia in alkaline medium and proved to be highly effective, having high potential utility, as compared to commonly used Pt-based electrocatalysts. In this study, gamma alumina as catalytic support was synthesized via precipitation method, and stoichiometric wt/wt.% compositions of Ag2O−PrO2 were loaded on γ-Al2O3 by co-impregnation method. The desired phase of γ-Al2O3 and supported nanocatalysts was obtained after heat treatment at 800 and 600 °C, respectively. The successful loadings of Ag2O−PrO2 nanocatalysts on surface of γ-Al2O3 was determined by X-rays diffraction (XRD), Fourier-transform Infrared Spectroscopy (FTIR), and energy dispersive analysis (EDX). The nano-sized domain of the sample powders sustained with particle sizes was calculated via XRD and scanning electron microscopy (SEM). The surface morphology and elemental compositions were examined by SEM, transmission electron microscopy (TEM) and EDX. The conductive and electron-transferring nature was investigated by cyclic voltammetry and electrochemical impedance (EIS). Cyclic voltammetric profiles were observed, and respective kinetic and thermodynamic parameters were calculated, which showed that these synthesized materials are potential catalysts for ammonia electro-oxidation. Ag2O(6)−PrO2(4)/γ-Al2O3 proved to be the most proficient catalyst among all the members of the series, having greater diffusion coefficient, heterogeneous rate constant and lesser Gibbs free energy for this system. The catalytic activity of these electrocatalysts is revealed from electrochemical studies which reflected their potentiality as electrode material in direct ammonia fuel cell technology for energy production.


2019 ◽  
Vol 56 ◽  
pp. 17-27
Author(s):  
Van Dat Doan ◽  
Van Thuan Le ◽  
Hoang Sinh Le ◽  
Dinh Hien Ta ◽  
Hoai Thuong Nguyen

In this work, nanosized calcium deficient hydroxyapatite (nCDHA) was synthesized by the precipitation method, and then utilized as an adsorbent for removal of Fe (II), Cu (II), Ni (II) and Cr (VI) ions from aqueous solutions after characterizing it by various techniques as scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX) and BET method. A possible structure of synthesized nCDHA was proposed. The adsorption study indicated that the adsorption equilibrium is well fitted with Langmuir isotherm model with the maximum adsorption capacities followed the order of Fe (II) > Cu (II) > Ni (II) > Cr (VI) with the values of 137.23, 128.02, 83.19 and 2.92 mg/g, respectively. The ion-exchange mechanism was dominant for the adsorption of metal ions onto nCDHA at initial metal concentrations lower than 0.01 mol/L. Along with the ion-exchange mechanism, there was an additional precipitation occurred on the surface of nCDHA in the case of Fe (II) and Cu (II) at initial concentrations higher than 0.01 mol/L.


Sign in / Sign up

Export Citation Format

Share Document