scholarly journals Effect of calcination temperature on the properties and applications of bio extract mediated titania nano particles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
N. Saikumari ◽  
S. Monish Dev ◽  
S. Avinaash Dev
Keyword(s):  
Electron Microscopy ◽  
Calcination Temperature ◽  
Surface Properties ◽  
Economic Feasibility ◽  
Nano Particles ◽  
Textile Dye ◽  
Gravimetric Analysis ◽  
Anatase Titania ◽  
Nano Catalyst ◽  
Bet Analysis

AbstractIn order to deal with the arising environmental issues across the globe at present nano particles with unique properties laid a benchmark in the name of nano catalysis. In this work the significance of calcination temperature on the thermal, electronic, structural and surface properties of a nano catalyst produced by sol–gel method using ultrasonic radiation against the disposal of toxic textile pollutants is studied in detail. The extract of tea leaves has been used as a bio-template during the synthesis to revise the crystallite size, surface area, optical absorption potential, and rate of agglomeration of nano sized grains by regulating their physico-chemical and surface properties. The influence of calcination in the transformation of single phased anatase titania to mixed phase anatase–rutile titania and the corresponding outcome in its photocatalytic activity employed in water treatment applications have been verified. The nano catalyst obtained is characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transition electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), Thermo gravimetric analysis (TGA), Brunaueur Emmett Teller (BET) analysis, UV–Vis diffused reflectance spectroscopy (DRS-UV–Vis) etc. The mesoporosity of the particle was examined using Barrett Joyner Halenda (BJH) model. The enhanced photo catalytic efficiency (about 97.7%) of templated nano titania due to calcination is verified against Congo red, a textile dye under optimized conditions. The nano catalyst produced can be easily separated, recycled to support its economic feasibility.

Influence of Iron Oxide Nano Particles on Electrospun Poly (Vinylidene Fluride)-Based Carbon Nanofibers on Hydrogen Storage

2011 ◽  
Vol 471-472 ◽  
pp. 1184-1189 ◽  
Author(s):  
Samaneh Shahgaldi ◽  
Zahira Yaakob ◽  
Norazrina Mat Jali ◽  
Dariush Jafar Khadem ◽  
Wan Ramli Wan Daud ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Iron Oxide ◽  
Hydrogen Storage ◽  
Surface Area ◽  
Pore Volume ◽  
Vinylidene Fluoride ◽  
Thermo Gravimetric Analysis ◽  
Electrospinning Process ◽  
Nano Particles ◽  
Gravimetric Analysis

Electrospun Poly (vinylidene fluoride) (PVdF) fine fiber of 100-300 nm in diameter in ribbon shape was synthesized through the electrospinning process via sol-gel. In order to synthesize infusible nanofibers all processing of dehydrofluorination and carbonization was investigated. Iron nanoparticles was doped with PVDF nanofibers in order to be effective in surface area, and porosity to increase the hydrogen storage. The composition, morphology, structure and surface area of PVDF/Iron Oxide nanofibers were investigated by thermo gravimetric analysis (TGA) to determinate the temperature of possible decomposition and crystallinity, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Micromeritics (ASAP2020) used to study the textural properties of the sample, like surface area, total pore volume, and micro pore volume. The result shows that the PVDF without dehydrofluorination treatment for infusibility become melt at around 160 °C. By adding the iron oxide nanoparticles as a catalyst it can improve the characteristic of the carbon fiber for hydrogen storage. In best of our knowledge, PVDF doping with iron oxide investigated for first time.

Synthesis and Characterization of Titanium Dioxide Nanoparticles for Application in Enhanced Oil Recovery

2019 ◽  
Vol 391 ◽  
pp. 74-81 ◽  
Author(s):  
Hasnah Mohd Zaid ◽  
Hanan Fakhruldi ◽  
Foo Yoong Yow ◽  
Norzafirah Razali ◽  
Yaleeni Kanan Dasan
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Titanium Dioxide ◽  
Surface Area ◽  
Calcination Temperature ◽  
Enhanced Oil Recovery ◽  
Oil Recovery ◽  
Titanium Dioxide Nanoparticles ◽  
Average Particle ◽  
Bet Analysis

In this study, titanium dioxide nanoparticles were synthesized for possible application in enhanced oil recovery. Sol-gel method was employed with titanium (IV) isopropoxide as the precursor. The prepared materials were characterized using Powder X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), High-Resolution Transmission electron microscopy (HRTEM) and Brunauer–Emmet–Teller (BET) techniques. Reaction parameter such as calcination temperature was varied during the preparation to obtain the uniform TiO2 nanoparticles with the smallest particle size and high surface area. The results of study revealed that 400 °C is the optimum calcination temperature in preparing TiO2 nanoparticles producing the smallest crystallite and particle sizes. XRD results indicated that the nanoparticles have formed anatase phase at 400 °C and achieved low crystallite size of 7.27 nm with the smallest average particle size of 19.53 nm through FESEM and HRTEM observations. BET analysis had achieved the highest surface area 103.64 m2/g.

Collagen And Carbon-Ferrous Nanoparticles Used As A Green Energy Composite Material For Energy Storage Devices

2020 ◽  
Vol 13 ◽  
Author(s):  
Inbasekaran S. ◽  
G. Thiyagarajan ◽  
Ramesh C. Panda ◽  
S. Sankar
Keyword(s):  
Composite Material ◽  
Thermo Gravimetric Analysis ◽  
Value Added ◽  
Green Energy ◽  
Nano Particles ◽  
Hydroxyl Group ◽  
Gravimetric Analysis ◽  
Circuit Testing ◽  
Battery Cell ◽  
Dc Voltage

Background:: Chrome shavings, a bioactive material, are generated from tannery as waste material. These chrome shaving can be used for the preparation of many value-added products. Objective:: One such attempt is made to use these chrome shaving wastes as a composite bio-battery to produce DC voltage, an alternate green energy source and cleaner technology. Methods:: Chrome shavings are hydrolyzed to make collagen paste and mixed with the ferrous nanoparticles of Moringa oleifera leaves and Carbon nanoparticles of Onion peels to form electrolyte paste as base. Then, the electrolyte base was added to the aluminum paste and conducting gel, and mixed well to form composite material for bio-battery. Results:: The composite material of bio-battery has been characterized using Scanning Electron Microscopy (SEM), Fourier-Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC) and Thermo Gravimetric Analysis (TGA). Series and parallel circuit testing were done using Copper and Zinc electrodes or Carbon and Zinc electrodes as the battery terminals in the electrolyte paste. The surface area of these electrodes needs standardization from bench to pilot scale. The power generated, for an AA battery size, using a single bio-battery cell has produced a DC voltage of 1.5 V; current of 900 mA. Circuit testing on 1 ml of 80 well-cells connected in series has produced DC output of 18 V and 1100 mA whereas 48 V and 1500 mA were obtained from a series-parallel connection. Conclusion:: The glass transition temperature (Tg) of electrolyte of the bio-battery at 53°C indicates that, at this temperature, all the substances present in the bio-battery are well spread and contributing consistently to the electrolyte activity where Fe-C-Nano-Particles were able to form strong chemical bonds on the flanking hydroxyl group sites of the Collagen leading to reduced mobility of polymers and increase Tg. The results instigate promising trends for commercial exploitation of this composite for bio-battery production.

scholarly journals Solid-State Ball-Milling of Co3O4 Nano/Microspheres and Carbon Black Endorsed LaMnO3 Perovskite Catalyst for Bifunctional Oxygen Electrocatalysis

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 76
Author(s):  
Chelladurai Karuppiah ◽  
Balamurugan Thirumalraj ◽  
Srinivasan Alagar ◽  
Shakkthivel Piraman ◽  
Ying-Jeng Jame Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Energy Storage ◽  
Fuel Cell ◽  
Solid State ◽  
Carbon Black ◽  
Ball Milling ◽  
Potential Candidate ◽  
X Ray ◽  
Bifunctional Electrocatalyst ◽  
Bet Analysis

Developing a highly stable and non-precious, low-cost, bifunctional electrocatalyst is essential for energy storage and energy conversion devices due to the increasing demand from the consumers. Therefore, the fabrication of a bifunctional electrocatalyst is an emerging focus for the promotion and dissemination of energy storage/conversion devices. Spinel and perovskite transition metal oxides have been widely explored as efficient bifunctional electrocatalysts to replace the noble metals in fuel cell and metal-air batteries. In this work, we developed a bifunctional catalyst for oxygen reduction and oxygen evolution reaction (ORR/OER) study using the mechanochemical route coupling of cobalt oxide nano/microspheres and carbon black particles incorporated lanthanum manganite perovskite (LaMnO3@C-Co3O4) composite. It was synthesized through a simple and less-time consuming solid-state ball-milling method. The synthesized LaMnO3@C-Co3O4 composite was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction spectroscopy, and micro-Raman spectroscopy techniques. The electrocatalysis results showed excellent electrochemical activity towards ORR/OER kinetics using LaMnO3@C-Co3O4 catalyst, as compared with Pt/C, bare LaMnO3@C, and LaMnO3@C-RuO2 catalysts. The observed results suggested that the newly developed LaMnO3@C-Co3O4 electrocatalyst can be used as a potential candidate for air-cathodes in fuel cell and metal-air batteries.

scholarly journals Assessment of SnFe2O4 Nanoparticles for Potential Application in Theranostics: Synthesis, Characterization, In Vitro, and In Vivo Toxicity

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 825
Author(s):  
Saman Sargazi ◽  
Mohammad Reza Hajinezhad ◽  
Abbas Rahdar ◽  
Muhammad Nadeem Zafar ◽  
Aneesa Awan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
A549 Cells ◽  
In Vitro Cytotoxicity ◽  
Hek293 Cells ◽  
Hydrothermal Route ◽  
X Ray ◽  
Tin Chloride ◽  
Bet Analysis

In this research, tin ferrite (SnFe2O4) NPs were synthesized via hydrothermal route using ferric chloride and tin chloride as precursors and were then characterized in terms of morphology and structure using Fourier-transform infrared spectroscopy (FTIR), Ultraviolet–visible spectroscopy (UV-Vis), X-ray power diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET) method. The obtained UV-Vis spectra was used to measure band gap energy of as-prepared SnFe2O4 NPs. XRD confirmed the spinel structure of NPs, while SEM and TEM analyses disclosed the size of NPs in the range of 15–50 nm and revealed the spherical shape of NPs. Moreover, energy dispersive X-ray spectroscopy (EDS) and BET analysis was carried out to estimate elemental composition and specific surface area, respectively. In vitro cytotoxicity of the synthesized NPs were studied on normal (HUVEC, HEK293) and cancerous (A549) human cell lines. HUVEC cells were resistant to SnFe2O4 NPs; while a significant decrease in the viability of HEK293 cells was observed when treated with higher concentrations of SnFe2O4 NPs. Furthermore, SnFe2O4 NPs induced dramatic cytotoxicity against A549 cells. For in vivo study, rats received SnFe2O4 NPs at dosages of 0, 0.1, 1, and 10 mg/kg. The 10 mg/kg dose increased serum blood urea nitrogen and creatinine compared to the controls (P < 0.05). The pathology showed necrosis in the liver, heart, and lungs, and the greatest damages were related to the kidneys. Overall, the in vivo and in vitro experiments showed that SnFe2O4 NPs at high doses had toxic effects on lung, liver and kidney cells without inducing toxicity to HUVECs. Further studies are warranted to fully elucidate the side effects of SnFe2O4 NPs for their application in theranostics.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.

Synthesis and Luminescence Properties of Tris (8-Hydroxyquinoline) Iron Spindle-Like Structures at Room Temperature

2011 ◽  
Vol 391-392 ◽  
pp. 225-229 ◽  
Author(s):  
Qing Hong Kong ◽  
Hong Liu ◽  
Yun Long Zhang ◽  
Yong Sheng Yan
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Blue Shift ◽  
Solvent System ◽  
Iron Complex ◽  
Molecular Formula ◽  
Gravimetric Analysis ◽  
Element Analysis ◽  
Transmission Electron ◽  
Fourier Transformation Infrared Spectroscopy

Spindle-like bis (8-hydroxyquinoline) iron (FeQ3) complex has been synthesized with a facile method in a mixed solvent system at room temperature for 12 h. The molecular formula of the products is speculated by the C, H and N element analysis and thermal gravimetric analysis, and Fourier-transformation infrared spectroscopy was also utilized to measure its structure, which further confirm the molecular formula of the products. The observation of field emission scanning electron microscopy and transmission electron microscopy shows that the morphology of tris (8-hydroxyquinoline) iron complex is spindle-like structure. The photoluminescence of the products were also investigated. The results indicate that the photoluminescence emission of FeQ3spindles shows obvious blue shift contrasted with that of 8-hydroxyquinoline.

Effect of Synthesis Temperature on Particles Size and Morphology of Zirconium Oxide Nanoparticle

2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Zirconium Oxide ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Crystallite Sizes ◽  
Ft Ir

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.

scholarly journals Rapid Synthesis of Gold Nano-Particles Using Pulse Waved Potential in a Non-Aqueous Electrolyte

2017 ◽  
Vol 62 (2) ◽  
pp. 1389-1392
Author(s):  
J.G. Jang ◽  
J.-O. Lee ◽  
C.K. Lee
Keyword(s):  
Electron Microscopy ◽  
Size Distribution ◽  
Aqueous Electrolyte ◽  
Supporting Electrolyte ◽  
Nano Particles ◽  
Rapid Synthesis ◽  
Imidazolium Chloride ◽  
Transmission Electron ◽  
Potentiostatic Electrodeposition ◽  
Pulsed Electrodeposition

AbstractRapid synthesis of gold nanoparticles (AuNPs) by pulsed electrodeposition was investigated in the non-aqueous electrolyte, 1-ethyl-3-methyl-imidazoliumbis(trifluoro-methanesulfonyl)imide ([EMIM]TFSI) with gold trichloride (AuCl3). To aid the dissolution of AuCl3, 1-ethyl-3-methyl-imidazolium chloride ([EMIM]Cl) was used as a supporting electrolyte in [EMIM]TFSI. Cyclic voltammetry experiments revealed a cathodic reaction corresponding to the reduction of gold at −0.4 V vs. Pt-QRE. To confirm the electrodeposition process, potentiostatic electrodeposition of gold in the non-aqueous electrolyte was conducted at −0.4 V for 1 h at room temperature. To synthesize AuNPs, pulsed electrodeposition was conducted with controlled duty factor, pulse duration, and overpotential. The composition, particle-size distribution, and morphology of the AuNPs were confirmed by field-emission scanning electron microscopy (FE-SEM), energy-dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The electrodeposited AuNPs were uniformly distributed on the platinum electrode surface without any impurities arising from the non-aqueous electrolyte. The size distribution of AuNPs could be also controlled by the electrodeposition conditions.

Synthesis of Nanosized HMS Mesoporous Molecular Sieve in an Ionic Liquid-Water Mixture

2011 ◽  
Vol 236-238 ◽  
pp. 2110-2113
Author(s):  
Hong Liu ◽  
Meng Yang Wang ◽  
Wei Ran Cao
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Sol Gel ◽  
Mesoporous Molecular Sieve ◽  
Nano Particles ◽  
Water Mixture ◽  
X Ray ◽  
Transmission Electron ◽  
Adsorption Desorption ◽  
Synthesized Materials

The hexagonal mesoporous silica (HMS) nano-particles were prepared in mixture of 1-butyl-3-methyl-imidazolium tetrafluoroborate (BMIM+BF4-) ionic liquid and water by a sol-gel method. The structure and morphology of obtained materials were characterized by X-ray powder diffraction (XRD), N2adsorption-desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and dynamic light scattering (DLS). The influence of the amount of BMIM+BF4-was investigated. It was shown that the synthesized materials have discrete and uniform spherical morphology with the size in the range of 68-177 nm (obtained from DLS measurements), and the particle size of HMS can be controlled by varying the amount of BMIM+BF4-.

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