scholarly journals Adsorptive Behavior of Kaolin for Amido Black Dye in Aqueous Solution

2018 ◽  
Vol 34 (3) ◽  
pp. 1233-1239 ◽  
Author(s):  
Olushola S. Ayanda ◽  
Kehinde O. Sodeinde ◽  
P. O. Okolo ◽  
Ayomitide A. Ajayi ◽  
Simphiwe M. Nelana ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Textile Wastewater ◽  
X Ray Diffraction ◽  
Order Model ◽  
Transmission Electron ◽  
Amido Black ◽  
Equilibrium Data ◽  
Adsorptive Behavior ◽  
Pseudo Second Order

In this study, the adsorption of amido black (AB) dye onto kaolin was investigated. The characterization of kaolin was carried out by powder x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR). Adsorption studies showed that the adsorption of AB onto kaolin increased with increasing adsorbent dosage, contact time, pH and temperature but decreased with increasing dye concentration. Equilibrium data fitted perfectly into the Langmuir and Freundlich equilibrium models, moreover, the kinetic data followed the pseudo-second order model. The adsorption process is endothermic and approximately 60.75% AB reduction was achieved when 0.75 g of kaolin was mixed with 20 mL of 40 mg/L AB for 60 min at 200 rpm. Therefore, this study shows that kaolin can be harnessed for the treatment of textile wastewater.

CuO/polypyrrole nanocomposites as a marker of toxic lead ions for ecological remediation in contrast with CuO and polypyrrole

2015 ◽  
Vol 38 (5-6) ◽  
Author(s):  
Asha Radhakrishnan ◽  
Padmavathiamma Rejani ◽  
Bhaskaran Beena
Keyword(s):  
Electron Microscopy ◽  
Selective Adsorption ◽  
X Ray Diffraction ◽  
Order Model ◽  
X Ray ◽  
Adsorption Performance ◽  
Transmission Electron ◽  
Pseudo Second Order ◽  
Hazardous Metal ◽  
Ecological Remediation

AbstractIn the present study, CuO, polypyrrole (PPy), and CuO/PPy nanocomposites were synthesized to compare the selective adsorption behavior of hazardous metal ions such as Pb(II) ions. The synthesized nanomaterials were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller surface area analysis, and energy dispersive X-ray spectroscopy. The adsorption studies clearly showed that CuO/PPy nanocomposites exhibited much higher adsorption performance than individual CuO and PPy. Kinetic data followed the pseudo-second-order model. The equilibrium attained at 120 min and isotherm follows the order Sips>Langmuir>Freundlich. The adsorbed Pb(II) is desorbed using 0.1

scholarly journals Investigation of nigrosine, alizarin, indigo and acid fuchsin removal by modification of CaO derived from eggshell with AgI: Adsorption, kinetic and photocatalytic studies

2019 ◽  
Vol 10 (1) ◽  
pp. 64-71
Author(s):  
Ibtighaa Kadhim Radhi ◽  
Mouayed Abdulaali Hussein ◽  
Zaki Naser Kadhim
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Kinetic Studies ◽  
Acid Fuchsin ◽  
X Ray Diffraction ◽  
Order Model ◽  
X Ray ◽  
Transmission Electron ◽  
Pseudo Second Order ◽  
Successful Removal

Successful removal of nigrosine, alizarin, indigo and acid fuchsin dyes from aqueous solutions using modified CaO nanoparticles has been investigated. The CaO was obtained from eggshells and modified with AgI. The adsorbents were characterized using X-ray diffraction, energy dispersive X-ray spectroscopy, scanning electron microscopy and transmission electron microscopy. The kinetic studies were also investigated, the results showed that the adsorption of alizarin dye follows the pseudo-first-order model, while the adsorption of the nigrosine, indigo, and acid fuchsin follow the pseudo-second-order model onto modified and unmodified CaO. Moreover, the photocatalytic activity of modified adsorbent was tested under sunlight. The modified adsorbent showed a strong photocatalytic activity, a 0.01 g modified adsorbent was sufficient to absorb 100% of acid fuchsin through only 5 min after exposes to sunlight.

scholarly journals Adsorptive Removal of Cd, Cu, Ni and Mn from Environmental Samples Using Fe3O4-Zro2@APS Nanocomposite: Kinetic and Equilibrium Isotherm Studies

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3209
Author(s):  
Aphiwe Siyasanga Gugushe ◽  
Anele Mpupa ◽  
Tshimangadzo Saddam Munonde ◽  
Luthando Nyaba ◽  
Philiswa Nosizo Nomngongo
Keyword(s):  
Electron Microscopy ◽  
Magnetic Nanomaterials ◽  
Batch Mode ◽  
X Ray ◽  
Freundlich Isotherms ◽  
Adsorption Capacities ◽  
Transmission Electron ◽  
Equilibrium Data ◽  
Pseudo Second Order ◽  
Wastewater Samples

In this study, Fe3O4-ZrO2 functionalized with 3-aminopropyltriethoxysilane (Fe3O4-ZrO2@APS) nanocomposite was investigated as a nanoadsorbent for the removal of Cd(II), Cu(II), Mn (II) and Ni(II) ions from aqueous solution and real samples in batch mode systems. The prepared magnetic nanomaterials were characterized using X-ray powder diffraction (XRD), scanning electron microscopy/energy dispersion x-ray (SEM/EDX) Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). Factors (such as adsorbent dose and sample pH) affecting the adsorption behavior of the removal process were studied using the response surface methodology. Under optimized condition, equilibrium data obtained were fitted into the Langmuir and Freundlich isotherms and the data fitted well with Langmuir isotherms. Langmuir adsorption capacities (mg/g) were found to be 113, 111, 128, and 123 mg/g for Cd, Cu, Ni and Mn, respectively. In addition, the adsorption kinetics was analyzed using five kinetic models, pseudo-first order, pseudo-second order, intraparticle diffusion and Boyd models. The adsorbent was successfully applied for removal of Cd(II), Cu(II), Mn (II) and Ni(II) ions in wastewater samples.

Detonation Synthesis of Nano-Size Materials

1995 ◽  
Vol 418 ◽  
Author(s):  
J. Forbes ◽  
J. Davis ◽  
C. Wong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Nucleation And Growth ◽  
Detonation Synthesis ◽  
X Ray Diffraction ◽  
Crystalline Materials ◽  
X Ray ◽  
Transmission Electron ◽  
Nano Size

AbstractThe detonation of explosives typically creates 100's of kbar pressures and 1000's K temperatures. These pressures and temperatures last for only a fraction of a microsecond as the products expand. Nucleation and growth of crystalline materials can occur under these conditions. Recovery of these materials is difficult but can occur in some circumstances. This paper describes the detonation synthesis facility, recovery of nano-size diamond, and plans to synthesize other nano-size materials by modifying the chemical composition of explosive compounds. The characterization of nano-size diamonds by transmission electron microscopy and electron diffraction, X-ray diffraction and Raman spectroscopy will also be reported.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

scholarly journals Preparation and Characterization of Polyhydroxybutyrate/Polycaprolactone Nanocomposites

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Cha Ping Liau ◽  
Mansor Bin Ahmad ◽  
Kamyar Shameli ◽  
Wan Md Zin Wan Yunus ◽  
Nor Azowa Ibrahim ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Basal Spacing ◽  
Cooh Group ◽  
Physical Interaction ◽  
X Ray Diffraction ◽  
Ion Exchange Reaction ◽  
Transmission Electron ◽  
Matrix Enhancement ◽  
Double Hydroxide

Polyhydroxybutyrate (PHB)/polycaprolactone (PCL)/stearate Mg-Al layered double hydroxide (LDH) nanocomposites were prepared via solution casting intercalation method. Coprecipitation method was used to prepare the anionic clay Mg-Al LDH from nitrate salt solution. Modification of nitrate anions by stearate anions between the LDH layers via ion exchange reaction. FTIR spectra showed the presence of carboxylic acid (COOH) group which indicates that stearate anions were successfully intercalated into the Mg-Al LDH. The formation of nanocomposites only involves physical interaction as there are no new functional groups or new bonding formed. X-ray diffraction (XRD) and transmission electron microscopy (TEM) indicated that the mixtures of nanocomposites are intercalated and exfoliated types. XRD results showed increasing of basal spacing from 8.66 to 32.97 Å in modified stearate Mg-Al LDH, and TEM results revealed that the stearate Mg-Al LDH layers are homogeneously distributed in the PHB/PCL polymer blends matrix. Enhancement in 300% elongation at break and 66% tensile strength in the presence of 1.0 wt % of the stearate Mg-Al LDH as compare with PHB/PCL blends. Scanning electron microscopy (SEM) proved that clay improves compatibility between polymer matrix and the best ratio 80PHB/20PCL/1stearate Mg-Al LDH surface is well dispersed and stretched before it breaks.

Synthesis and characterization of homogeneous lead-substituted tin oxide with the (110) face of rutile structure

2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Rutile Structure ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Synthesis of a rutile-type lead-substituted tin oxide with (110) face was investigated. The characterization was performed by x-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, infrared spectroscopy, x-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The homogeneous rutile-type lead-substituted tin oxide was obtained until 4.1 mol% of tin was substituted with lead. The surface of obtained oxide had a homogeneously lead-substituted (110) face.

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

Characterization of Fe–Ni(C) nanocapsules synthesized by arc discharge in methane

1999 ◽  
Vol 14 (5) ◽  
pp. 1782-1790 ◽  
Author(s):  
X. L. Dong ◽  
Z. D. Zhang ◽  
S. R. Jin ◽  
W. M. Sun ◽  
X. G. Zhao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Arc Discharge ◽  
Carbon Layer ◽  
Magnetization Measurement ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Energy Disperse Spectroscopy

Ultrafine Fe–Ni(C) particles of various compositions were prepared by arc discharge synthesis in a methane atmosphere. The particles were characterized by x-ray diffraction, transmission electron microscopy, energy disperse spectroscopy, chemical analysis, x-ray photoelectron spectroscopy, Mössbauer spectroscopy, and magnetization measurement. The carbon atoms solubilizing at interstitial sites in γ–(Fe, Ni, C) solution particles have the effects of forming austenite structure and changing microstructures as well as magnetic properties. A carbon layer covers the surface of Fe–Ni(C) particles to form the nanocapsules and protect them from oxidization. The mechanism of forming Fe–Ni(C) nanocapsules in the methane atmosphere was analyzed.

Microstructural Characterization of Pt/Ti and RuO2 Electrodes on SiO2/Si Annealed in the Oxygen Ambient

1996 ◽  
Vol 433 ◽  
Author(s):  
Jeong Soo Lee ◽  
Hyun JA Kwon ◽  
Young Woo Jeong ◽  
Hyun HA Kim ◽  
Kyu HO Park ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Film Surface ◽  
Microstructural Characterization ◽  
Silicide Phase ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Degree Of Oxidation ◽  
Thin Interlayer ◽  
Increasing Temperature

AbstractMicrostructures and interdiffusions of Pt/Ti/SiO2/Si and RuO2/SiO2/Si during annealing in O2 were investigated using x-ray diffraction, Auger electron spectroscopy, scanning electron microscopy, and transmission electron microscopy. The degree of oxidation and the interdiffusion of elements have remarkably increased with increasing temperature above 500 °C for the Pt/Ti/SiO2/Si case. The generation of Pt hillocks commenced at 500 °C. The Pt-silicide phase was also observed near the TiOx/SiO2 interface. The microstructural variations occurred to only a small amount for the RuO2/SiO2/Si case over the temperature range 300 – 700 °C. While there was no hillock formation, the RuO2 film surface was roughened by the thermal grooving phenomenon. A thin interlayer phase was found at the RuO2/SiO2 interface.

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