The Study of the Removal of Cu(II) from Aqueous Solution by Papia undulates Shell

2016 ◽  
Vol 675-676 ◽  
pp. 664-666
Author(s):  
Noppadon Chamchoi ◽  
Narong Sangwaranatee ◽  
Jakrapong Kaewkhao ◽  
K. Teanchai ◽  
Wichian Siriprom

In present study, the removal of Cu (II) ions from aqueous solution was investigated by both biosorption and investigated by X-ray Diffraction (XRD), Energy Dispersive X-ray Fluorescence (EDXRF) and Fourier transform infrared (FT-IR) spectroscopy. The variable of the batch experiment include solution pH, content time, were conducted to determine the factors affecting capacities sorption of Cu (II). The experimental result explored that that the maximum pH for efficient sorption of Cu (II) was 9. The optimum condition of sorption were found to be contact time of 180 min, and initial Cu concentration 200 mg/L, while the result of XRD reveal that the Paphia undulate shell have aragonite phase and change to mixture phase after sorption which corresponding, with the result of EDXRF which increasing the concentration of Cu

2016 ◽  
Vol 675-676 ◽  
pp. 7-10
Author(s):  
K. Chantarasunthon ◽  
Kanyakorn Teanchai ◽  
Wichian Siriprom

In this study, the experimental investigation and assessment the absorption capacity for Zn ion with Amusium Pleuronectes shell. The investigations were carried out by batch method and variables of the batch experiment include solution pH, Contact time, were determind. The mechanism of bisorption is chemisorption or/and physical adsorption was confirmed by X-ray Diffraction (XRD) and Energy Dispersive X-ray Fluorescence (EDXRF). The results showed that the Amusium Pleuronectes shell has a high level of absorption capacity for Zn (II) ions. Another that result of mechanism of biosorption suggests and confirm with the result of XRD and EDXRF.


2018 ◽  
Vol 78 (12) ◽  
pp. 2469-2480
Author(s):  
Avat Ghasemi ◽  
Mahmoud Reza Sohrabi ◽  
Fereshteh Motiee

Abstract A new sawdust/magnetite nanoparticles/polyethyleneimine (SD/MNP/PEI) nanocomposite was synthesized by grafting polyethyleneimine (PEI) to magnetic sawdust. Features of SD/MNP/PEI were characterized using Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD), vibrating sample magnetometer (VSM) and scanning electron microscopy (SEM). SD/MNP/PEI was used as an adsorbent for the removal of lead (Pb (II)) from aqueous solution. The effects of independent variables including pH of solution, adsorbent dose and contact time were performed and adsorption isotherms were obtained. Experimental results show that priority effective variables were pH and the amount of nanocomposite, and it was found that the sorption capacity increases with the increasing phase contact time. The adsorption process followed the Langmuir adsorption isotherm. Although SD and SD/MNP do not show a high affinity for the adsorption of Pb (II) in aqueous media, polyethyleneimine cross-linked on SD/MNP showed 40 and 66% increases, respectively, in the adsorption of Pb (II) compared to the SD and SD/MNP. It was found that SD/MNP/PEI removes more efficiently lead ions from aqueous solutions than the SD, SD/MNP. Desorption of the lead from the SD/MNP/PEI was conducted. It was proved that SD/MNP/PEI has excellent properties and can be used as a sorbent of multi-use.


Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  

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.


2018 ◽  
Vol 74 (3) ◽  
pp. 366-371 ◽  
Author(s):  
Wen Cui ◽  
Ruyu Wang ◽  
Xi Shu ◽  
Yu Fan ◽  
Yang Liu ◽  
...  

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.


2020 ◽  
Vol 1 (4) ◽  
pp. 22-25
Author(s):  
Azwan Morni

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.


2020 ◽  
Vol 38 (9-10) ◽  
pp. 483-501
Author(s):  
Nguyen Thi Huong ◽  
Nguyen Ngoc Son ◽  
Vo Hoang Phuong ◽  
Cong Tien Dung ◽  
Pham Thi Mai Huong ◽  
...  

The Fe3O4/Talc nanocomposite was synthesized by the coprecipitation-ultrasonication method. The reaction was carried out under a inert gas environment. The nanoparticles were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), fourier-transform infrared spectroscopy (FT-IR) and vibrating sample magnetometry techniques (VSM), the surface area of the nanoparticles was determined to be 77.92 m2/g by Brunauer-Emmett-Teller method (BET). The kinetic data showed that the adsorption process fitted with the pseudo-second order model. Batch experiments were carried out to determine the adsorption kinetics and mechanisms of Cr(VI) by Fe3O4/Talc nanocomposite. The adsorption process was found to be highly pH-dependent, which made the material selectively adsorb these metals from aqueous solution. The isotherms of adsorption were also studied using Langmuir and Freundlich equations in linear forms. It is found that the Langmuir equation showed better linear correlation with the experimental data than the Freundlich. The thermodynamics of Cr(VI) adsorption onto the Fe3O4/Talc nanocomposite indicated that the adsorption was exothermic. The reusability study has proven that Fe3O4/Talc nanocomposite can be employed as a low-cost and easy to separate.


2019 ◽  
Vol 946 ◽  
pp. 351-356 ◽  
Author(s):  
Olga M. Kanunnikova ◽  
V.V. Aksenova ◽  
G.A. Dorofeev

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.


Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 409 ◽  
Author(s):  
Dandan Zhao ◽  
Wen-Can Huang ◽  
Na Guo ◽  
Shuye Zhang ◽  
Changhu Xue ◽  
...  

In this research, a two-step extraction approach was developed for chitin preparation from shrimp shells by utilizing citric acids and deep eutectic solvents (DESs), which effectively removed minerals and proteins. In the first step, minerals of shrimp shells were removed by citric acid, and the demineralization efficiency reached more than 98%. In the second step, the removal of protein was carried out using deep eutectic solvents with the assistance of microwave, and the deproteinization efficiency was more than 88%. The results of scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction analysis (XRD), and thermogravimetric analysis (TGA) showed that the quality of DES-prepared chitin was comparable to that of traditional acid/alkali-prepared chitin. These results were realized without utilizing hazardous chemicals, which are detrimental to the environment. This research indicates that a DES-based preparation approach has the potential for application in the recovery of biopolymers from natural resources.


2015 ◽  
Vol 71 (1) ◽  
pp. 48-52 ◽  
Author(s):  
José J. Campos-Gaxiola ◽  
Susana P. Arredondo Rea ◽  
Ramón Corral Higuera ◽  
Herbert Höpfl ◽  
Adriana Cruz Enríquez

Two organic–inorganic hybrid compounds have been prepared by the combination of the 4-[(E)-2-(pyridin-1-ium-2-yl)ethenyl]pyridinium cation with perhalometallate anions to give 4-[(E)-2-(pyridin-1-ium-2-yl)ethenyl]pyridinium tetrachloridocobaltate(II), (C12H12N2)[CoCl4], (I), and 4-[(E)-2-(pyridin-1-ium-2-yl)ethenyl]pyridinium tetrachloridozincate(II), (C12H12N2)[ZnCl4], (II). The compounds have been structurally characterized by single-crystal X-ray diffraction analysis, showing the formation of a three-dimensional network throughX—H...ClnM−(X= C, N+;n= 1, 2;M= CoII, ZnII) hydrogen-bonding interactions and π–π stacking interactions. The title compounds were also characterized by FT–IR spectroscopy and thermogravimetric analysis (TGA).


2016 ◽  
Vol 3 (10) ◽  
pp. 1306-1316 ◽  
Author(s):  
M. Węcławik ◽  
A. Gągor ◽  
R. Jakubas ◽  
A. Piecha-Bisiorek ◽  
W. Medycki ◽  
...  

Two hybrid crystals imidazolium iodoantimonate(iii) and iodobismuthate(iii) have been synthesized and characterized in a wide temperature range (100–350 K) by means of X-ray diffraction, dielectric spectroscopy, proton magnetic resonance, FT-IR spectroscopy and optical observations.


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