Preparation and characterization of a new sawdust/MNP/PEI nanocomposite and its applications for removing Pb (II) ions from aqueous solution

2018 ◽  
Vol 78 (12) ◽  
pp. 2469-2480
Author(s):  
Avat Ghasemi ◽  
Mahmoud Reza Sohrabi ◽  
Fereshteh Motiee
Keyword(s):  
Aqueous Solution ◽  
Contact Time ◽  
Adsorption Process ◽  
Aqueous Media ◽  
X Ray Diffraction ◽  
Phase Contact Time ◽  
X Ray ◽  
Langmuir Adsorption ◽  
Ft Ir

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.

scholarly journals Synthesis Fe3O4/Talc nanocomposite by coprecipition-ultrasonication method and advances in hexavalent chromium removal from aqueous solution

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 ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Adsorption Process ◽  
Low Cost ◽  
Batch Experiments ◽  
X Ray Diffraction ◽  
Order Model ◽  
X Ray ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Langmuir And Freundlich Equations

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.

Preparation and characterization of CTAB-HACC bentonite and its ability to adsorb phenol from aqueous solution

2011 ◽  
Vol 64 (1) ◽  
pp. 286-292 ◽  
Author(s):  
Ruihua Huang ◽  
Dongsheng Zheng ◽  
Bingchao Yang ◽  
Bo Wang ◽  
Zengqiang Zhang
Keyword(s):  
Aqueous Solution ◽  
Contact Time ◽  
Trimethyl Ammonium Chloride ◽  
Adsorption Efficiency ◽  
X Ray Diffraction ◽  
Phenol Solution ◽  
X Ray ◽  
Initial Ph ◽  
Lower Temperature

A novel type of adsorbent was prepared by modifying bentonite with N-2-hydroxypropyl trimethyl ammonium chloride chitosan (HACC) with cetyl trimethylammonium bromide (CTAB). The adsorbent was named CTAB-HACC bentonite. Its characteristics were investigated using thermogravimetric, Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction. The adsorption of phenol onto CTAB-HACC bentonite was evaluated by changing various parameters, such as contact time, adsorbent dosage, initial pH of the solution, and temperature. The maximum adsorption was observed at pH 12. Adsorption of phenol on CTAB-HACC bentonite favored at lower temperature and established the equilibrium in 30 min. The adsorption efficiency reached 82.1%, and the adsorption capacity was 7.12 mg/g from the phenol solution with a concentration of 500 mg/L at pH 12.0 and 20 °C.

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
Keyword(s):  
Aqueous Solution ◽  
Contact Time ◽  
Experimental Result ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
Factors Affecting ◽  
X Ray ◽  
Mixture Phase ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

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

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Microwave-assisted solvent-free synthesis and spectral and structural characterization of cyclotriphosphazene hexakis(o-tolylamide)

2018 ◽  
Vol 73 (12) ◽  
pp. 999-1003 ◽  
Author(s):  
Mohammad Hakimi ◽  
Homeyra Rezaei ◽  
Keyvan Moeini ◽  
Heidar Raissi ◽  
Vaclav Eigner ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Microwave Irradiation ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
X Ray ◽  
Microwave Assisted ◽  
Ft Ir ◽  
Solvent Free Synthesis

AbstractA new cyclotriphosphazene, 2,2,4,4,6,6-hexakis (o-tolylamono)-1,3,5,2λ5,4λ5,6λ5-triazatriphosphinine (MPAP), was prepared using microwave irradiation and identified by elemental analysis, FT-IR, Raman, 31P NMR spectroscopy, and single-crystal X-ray diffraction. In the crystal, in addition to hydrogen bonds, the network is further stabilized by inter- and intramolecular π–π stacking interactions between aromatic rings.

The Characterization of Bovine Bone-Derived Hydroxyapatite Isolated Using Novel Non-Hazardous Method

2020 ◽  
Vol 45 ◽  
pp. 49-56
Author(s):  
Aniek Setiya Budiatin ◽  
Samirah ◽  
Maria Apriliani Gani ◽  
Wenny Putri Nilamsari ◽  
Chrismawan Ardianto ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Extraction Method ◽  
Bovine Bone ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Novel Method ◽  
Scanning Electron

Bovine bone is a considerable source for the production of hydroxyapatite. The recent study reported a novel method to extract hydroxyapatite from bovine bone without producing hazardous residue. The bovine bones were cut and boiled in the opened chamber followed by boiling in pressurized tank. The bones were then soaked into 95% ethanol. Calcination was then conducted in 800°C, 900°C and 1,000°C, for 2 hours. The result was then grinded and sieved. The powder then was characterized using Fourier transform infrared (FT-IR), Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) to measure the purity of hydroxyapatite. It is concluded that the hydroxyapatite derived from this process showed 100% purity, resulting 35.34 ± 0.39% w/w from the wet bone weight and 72.3% w/w from the dried weight. The present extraction method has been proven to yield high amount of pure hydroxyapatite as well as reducing the use of hazardous reagent.

scholarly journals Synthesis, Crystal Structures, and Spectroscopic Characterization of Bis-aldehyde Monomers and Their Electrically Conductive Pristine Polyazomethines

Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1498 ◽  
Author(s):  
Abdul Hafeez ◽  
Zareen Akhter ◽  
John F. Gallagher ◽  
Nawazish Ali Khan ◽  
Asghari Gul ◽  
...  
Keyword(s):  
Electrical Conductivity ◽  
Spectroscopic Characterization ◽  
Spectroscopic Techniques ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
Electrically Conductive ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Ft Ir

Bis-aldehyde monomers 4-(4′-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4′-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4′-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4′-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal X-ray diffraction structures of 3b and 3c were determined. The structural characterization of the monomers and poly(azomethine)s was performed by FT-IR and NMR spectroscopic techniques and elemental analysis. Physicochemical properties of polymers were investigated by powder X-ray diffraction, thermogravimetric analysis (TGA), viscometry, UV–vis, spectroscopy and photoluminescence. These polymers were subjected to electrical conductivity measurements by the four-probe method, and their conductivities were found to be in the range 4.0 × 10−5 to 6.4 × 10−5 Scm−1, which was significantly higher than the values reported so far.

Characterization of Electrospun Poly(Lactic Acid)/polyaniline Blend Nanofibers

2011 ◽  
Vol 332-334 ◽  
pp. 317-320 ◽  
Author(s):  
Hui Qin Zhang
Keyword(s):  
Lactic Acid ◽  
Composite Nanofibers ◽  
Weight Ratio ◽  
Electrospinning Process ◽  
Poly Lactic Acid ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Ft Ir

In this study, composite nanofibers of polyaniline doped with dodecylbenzene sulfonic acid (PANI-DBSA) and Poly(lactic acid) (PLA) were prepared via an electrospinning process. The surface morphology, thermal properties and crystal structure of PLA/PANI-DBSA nanofibers are characterized using Fourier transform infrared spectroscopy (FT-IR), wide-angle x-ray diffraction (WAXD) and scanning electron microscopy (SEM). SEM images showed that the morphology and diameter of the nanofibers were affected by the weight ratio of blend solution.

Preparation and Electrical Characterization of Poly(Aniline) NanoClay Composites

2015 ◽  
Vol 34 (4) ◽  
Author(s):  
Esma Ahlatcioǧlu ◽  
Bahire Filiz şenkal ◽  
Mustafa Okutan
Keyword(s):  
Electrical Characterization ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Inorganic Hybrid ◽  
X Ray ◽  
Ft Ir ◽  
Doped Polyaniline ◽  
Poly Aniline ◽  
Scanning Electron

AbstractIn this work, synthesis and characterization of composite materials based on NanoClay(NC) and boric acid doped PolyAniline (PANI) is studied. PANI was successfully incorporated into NC to form PANI-NC composites. The resulting organic-inorganic hybrid material, PANI-NC was characterized by various physicochemical techniques. Formation of PANI inside the clay tactoid has been confirmed by X-ray diffraction studies (XRD), scanning electron microscope (SEM) and FT-IR. Also, conductivity and physical properties of the PANI-NC composites were investigated.

Structural and IR-spectroscopic characterization of magnesium acesulfamate

2016 ◽  
Vol 71 (1) ◽  
pp. 51-55 ◽  
Author(s):  
Oscar E. Piro ◽  
Gustavo A. Echeverría ◽  
Beatriz S. Parajón-Costa ◽  
Enrique J. Baran
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Elemental Analysis ◽  
Spectroscopic Characterization ◽  
Magnesium Carbonate ◽  
X Ray Diffraction ◽  
Triclinic Space Group ◽  
X Ray ◽  
Ir Spectroscopic

AbstractMagnesium acesulfamate, Mg(C4H4NO4S)2·6H2O, was prepared by the reaction of acesulfamic acid and magnesium carbonate in aqueous solution, and characterized by elemental analysis. Its crystal structure was determined by single crystal X-ray diffraction methods. The substance crystallizes in the triclinic space group P1̅ with one molecule per unit cell. The FTIR spectrum of the compound was also recorded and is briefly discussed. Some comparisons with other simple acesulfamate and saccharinate salts are also made.

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