scholarly journals Extraction and Characterization of Chitosan from Crab Shells: Kinetic and Thermodynamic Studies of Arsenic and Copper Adsorption from Electroplating Wastewater

2020 ◽  
pp. 2156-2171
Author(s):  
Sumaila A. ◽  
Ndamitso M. M. ◽  
Iyaka Y. A. ◽  
Abdulkareem, A. S. ◽  
Tijani J. O. ◽  
...  

Crab shells were used to produce chitosan via the three stages of deproteinization, demineralization and deacetylation using sodium hydroxide and hydrochloric acid under different treatment conditions of temperature and time. The produced chitosan was characterized using Fourier transform infrared spectroscopy (FTIRS), X-ray diffraction (XRD), high – resolution scanning electron microscopy (HRSEM), electron dispersion spectroscopy (EDS), dynamic light scattering (DLS), Brunauer Emmett Teller (BET) and Thermogravimetric analysis (TGA). The adsorption behavior of chitosan to remove arsenic (As) and copper (Cu) from electroplating wastewater was examined by batch adsorption process as a function of adsorbent dose, contact time and temperature. The FTIR, XRD, HRSEM and EDS analyses confirmed, respectively, the presence of –NH2 and –OH functional groups, with amorphous/crystalline phases, crystallinity index of 69.54%, needle-like morphology and Carbon (C), Oxygen (O) and Nitrogen N) in the produced chitosan. While DLS, BET and TGA showed, respectively, that the produced chitosan has an average particle size of 729nm, is moderately polydisperse, has12.67 m2/g surface area, mesoporous in nature, and with thermal stability of up to 1430C. The optimum adsorbent dose, contact time and temperature values to remove As and Cu by chitosan were 15mg, 45 minutes, 333K and25mg, 60 minutes, 349K,respectively. Under the employed conditions, chitosan though has a low surface area, displaying high adsorption capacity for both metal ions. The adsorption isotherm data were better fitted to the Jovanovic isotherm model while the kinetic data fitted best to the pseudo-second order model. The thermodynamic studies established that the adsorption was feasible but endothermic in nature. This study shows that chitosan adsorbents purify electroplating wastewater.

Author(s):  
Hieр Nguyen Tien

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.


2018 ◽  
Vol 36 (3-4) ◽  
pp. 1112-1143 ◽  
Author(s):  
Mohammad Hossein Karimi Darvanjooghi ◽  
Seyyed Mohammadreza Davoodi ◽  
Arzu Y Dursun ◽  
Mohammad Reza Ehsani ◽  
Iman Karimpour ◽  
...  

In this study, treated eggplant peel was used as an adsorbent to remove Pb2+ from aqueous solution. For this purpose batch adsorption experiments were performed for investigating the effect of contact time, pH, adsorbent dose, solute concentrations, and temperature. In order to assess adsorbent’s physical and chemical properties, Fourier transform infrared spectroscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy were used. The results showed that the adsorption parameters for reaching maximum removal were found to be contact time of 110 min, adsorbent dose of 0.01 g/ml, initial lead(II) concentration of 70 ppm, pH of 4, and temperature of 25°C. Moreover, for the experiments carried out at pH > 4 the removal occurred by means of significant precipitation as well as adsorption. Furthermore, these results indicated that the adsorption followed pseudo-second-order kinetics model implying that during the adsorption process strong bond between lead(II) and chemical functional groups of adsorbent surface took place. The process was described by Langmuir model (R2 = 0.99; maximum adsorption capacity 88.33 mg/g). Also thermodynamics of adsorption was studied at various temperatures and the thermodynamic parameters including equilibrium constant (K), standard enthalpy change, standard entropy change, and standard free energy changes were obtained from experimental data.


2021 ◽  
Vol 17 (9) ◽  
pp. 1824-1829
Author(s):  
Junlin Li ◽  
Xiangfei Li ◽  
Dong Liang ◽  
Xiaojuan Zhang ◽  
Qing Lin ◽  
...  

This study exploits the potential of zinc oxide nanoparticles (ZnO-NPs) with diverse morphologies as catalysts and antibacterial agent. Spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were prepared by microemulsion method, solvent heat method and hydrothermal method, respectively. The structural characterizations of samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. XRD results revealed the formation of spherical ZnO-NPs, rod-shaped ZnO-NPs and flower-shaped ZnO-NPs were all wurtzite crystal structure. SEM results showed that spherical ZnO-NPs had an average particle size of 30–40 nm, rod-shaped ZnO-NPs were about 500 nm long and 100 nm wide with obvious hexagonal crystals. Flower-shaped ZnO-NPs had a three-dimensional appearance with obvious petals. Results of electrochemical HER (Hydrogen evolution reaction) experiments revealed that spherical ZnO-NPs exhibited the highest electrocatalytic activity at the lowest potential voltage due to their largest specific surface area. The antibacterial property of ZnO-NPs samples were studied by the optical density method and disc diffusion method. All samples had antibacterial effects against E. coli. and flower-shaped ZnO-NPs showed the best antibacterial activity due to the largest surface area in comparison with spherical ZnO-NPs and rod-shaped ZnO-NPs, which promised the maximum Zn2+ release as bactericide mechanism that registered in the case of different ZnO-NPs morphologies.


2015 ◽  
Vol 43 (3) ◽  
pp. 277-281 ◽  
Author(s):  
M Rahman ◽  
S Gul ◽  
M Ajmal ◽  
A Iqbal ◽  
Akk Achakzai

Removal of cadmium from aqueous solution was studied by using Quetta pine (Pinus halepensis Mill.) leaves. Batch adsorption experiments were performed as a function of appropriate equilibrium time, pH, concentration of adsorbate and amount of adsorbent. The optimum pH required for maximum adsorption was found to be 7.0 and the maximum contact time for the equilibrium was 30 minutes at adsorbent dose of 10 g. The maximum adsorption efficiency of cadmium removal was 98.50%. The results were better fitted by Langmuir than Freundlich isotherm. The separation factor of equilibrium 0.12 and 0.67 showed that Quetta pine leaves are good adsorbent of cadmium from aqueous solution DOI: http://dx.doi.org/10.3329/bjb.v43i3.21598 Bangladesh J. Bot. 43(3): 277-281, 2014 (December)


2020 ◽  
Vol 32 (10) ◽  
pp. 2489-2494
Author(s):  
S.S. Sagar ◽  
R.P. Chavan

The present study deals with hydrothermal synthesis of SiO2 composite MgMnO3 catalyst. The obtained polycrystalline product was analyzed by using physical investigative techniques including XRD, SEM, EDAX, TEM, SAED and BET surface area. The product corresponded to average particle size of 100 nm by TEM images. The BET surface area was found 234.38 cm2/g for SiO2 composite MgMnO3 catalyst which indicates a good catalytic property. The synthesized catalyst was applied for the synthesis of 1H-pyrazolo[1,2-b]-phthalazine-5,10-dione in presence of ethanol as a solvent at 80 ºC. The current procedure and catalyst offers the gains of clean reaction, short reaction time, high yield, easy purification and financial availability of the catalyst.


2016 ◽  
Vol 7 ◽  
pp. 721-732 ◽  
Author(s):  
Jacek Wojnarowicz ◽  
Roman Mukhovskyi ◽  
Elzbieta Pietrzykowska ◽  
Sylwia Kusnieruk ◽  
Jan Mizeracki ◽  
...  

Mn-doped zinc oxide nanoparticles were prepared by using the microwave solvothermal synthesis (MSS) technique. The nanoparticles were produced from a solution of zinc acetate dihydrate and manganese(II) acetate tetrahydrate using ethylene glycol as solvent. The content of Mn2+ in Zn1− x Mn x O ranged from 1 to 25 mol %. The following properties of the nanostructures were investigated: skeleton density, specific surface area (SSA), phase purity (XRD), lattice parameters, dopant content, average particle size, crystallite size distribution, morphology. The average particle size of Zn1− x Mn x O was determined using Scherrer’s formula, the Nanopowder XRD Processor Demo web application and by converting the specific surface area results. X-ray diffraction of synthesized samples shows a single-phase wurtzite crystal structure of ZnO without any indication of additional phases. Spherical Zn1− x Mn x O particles were obtained with monocrystalline structure and average particle sizes from 17 to 30 nm depending on the content of dopant. SEM images showed an impact of the dopant concentration on the morphology of the nanoparticles.


2010 ◽  
Vol 92 ◽  
pp. 163-169
Author(s):  
Hong Xia Qiao ◽  
Zhi Qiang Wei ◽  
Ming Ru Zhou ◽  
Zhong Mao He

Copper nanoparticles were successfully prepared in large scales by means of anodic arc discharging plasma method in inert atmosphere. The particle size, specific surface area, crystal structure and morphology of the samples were characterized by X-ray diffraction (XRD), BET equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED). The experiment results indicate that the crystal structure of the samples is fcc structure as same as that of the bulk materials. The specific surface area is is 11 m2/g, with the particle size distribution ranging from 30 to 90 nm, the average particle size about 67nm obtained from TEM and confirmed from XRD and BET results. The nanoparticles have uniform size, higher purity, narrow size distribution and spherical shape can be prepared by this convenient and effective method.


1993 ◽  
Vol 15 (3-4) ◽  
pp. 155-163
Author(s):  
J. Hagberg

The significance of powder and paste characteristics was studied in order to improve the morphology and structure of superconducting (Bi,Pb)-Sr-Ca-Cu-O screen printed thick films. Powder with nominal composition of Bi1.75Pb0.4Sr1.9Ca2.1Cu3.2Oywas prepared via the oxalate route and decomposed at 430 to 795℃. The decomposed powders were characterized by X-ray diffraction, transmission electron microscopy and specific surface area measurements. These studies showed a variation of specific surface area from 16.5 to 0.9 m2/g and a variation of the average particle size from 100 nm to 800 nm in the studied temperature interval. The phase structure showed three distinct temperature areas; between 430 to 620, 620 to 715, and at 795℃.Thick-film pastes were made by the addition of an organic vehicle at 500, 620, 650 and 795℃ to decompose annealed oxalate synthesized powders and, for comparison, the vehicle was also added to sintered mixed-oxide/carbonate-based powder in weight ratios from 0.42 to 0.54:1. Films were screen printed on single crystal MgO (100) substrates and melt annealed at 890 to 895℃ for 3 min and subsequently, for prolonged diffusion, annealed at 852℃. After firing, the films were mainly composed of the (001) textured (Bi,Pb)2Sr2Ca2Cu3Oyphase. The reference films, made from mixed oxide/carbonate powder, resembled the films based on oxalate powders decomposed at 795℃. Films based on oxalate powders, decomposed at lower temperatures, were smoother and were able to carry noticeably higher currents than films based on powders decomposed at higher temperatures.


Soil Research ◽  
1977 ◽  
Vol 15 (3) ◽  
pp. 243 ◽  
Author(s):  
CL Chi ◽  
WW Emerson ◽  
DG Lewis

Three 'pure' illites were studied. Two, extracted from soils, were fine grained, and the other coarse, extracted from a shale. The average particle size of each clay was determined from electron micrographs and a specific surface area calculated. For the two soil illites any difference in the surface area deduced from water vapour sorption as compared with nitrogen sorption or by direct calculation, was consistent with the purity of the clay as determined by X-ray diffraction. For the shale, there was a large discrepancy, which is attributed to this illite having a greater surface density of charge. For the two soil illites, the exchange of calcium or magnesium for sodium, over the ESP range 0-12 and the calcium-magnesium exchange isotherms were determined. The exchange of sodium followed the same Gapon-type equation for both clays, and was independent of whether calcium or magnesium was the dominant cation. The calcium-magnesium isotherms were also symmetrical. No evidence was therefore found for calcium ions being more strongly held at exchange sites than magnesium ions. It was shown that in the solutions used to equilibrate the clays, which were 1 mM in divalent cations, diffuse double layers were not formed.


Author(s):  
Dang Tan Hiep ◽  
Bui Thi Hoa ◽  
Ngo Thi My Thanh ◽  
Nguyen Viet Long ◽  
Le Hong Phuc ◽  
...  

The ferromagnetic Fe3O4 nanoparticles with the average particle size of about 10 nm were used to adsorb chromium (VI) in aqueous solution. The equilibrium of Cr(VI) adsorption can be achieved at the pH value of 2.5, in the contact time of 120 minutes. The mechanisms of Cr(VI) adsorption were evaluated by 4 isothermal adsorption models Langmuir, Freundlich, Redlich-Peterson, and Temkin. The results showed that all four models are satisfied; especially, Redlich-Peterson is the most suitable model to describe the adsorption kinetic of Cr(VI) on ferromagnetic Fe3O4 nanoparticles.


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