Recovery of recycled paper in the removal of the textile dye basic yellow 28: characterization and adsorption studies

2019 ◽  
Vol 34 (2) ◽  
pp. 218-227
Author(s):  
Radouane Laib ◽  
Samira Amokrane-Nibou ◽  
Djamel Nibou ◽  
Mohamed Trari
Keyword(s):  
Oxygen Demand ◽  
Textile Dye ◽  
X Ray Diffraction ◽  
Order Model ◽  
Recycled Paper ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Ph Range ◽  
Best Fit ◽  
Ft Ir Spectroscopy

Abstract A recycled newspaper pulp (NPP) was used in the adsorption of a basic textile dye (Sandocryl gold yellow, basic yellow 28: BY28). NPP was deinked and bleached for the homogeneity of the adsorbent and elimination of the anchor. The release of NPP was followed by measuring the absorbance and chemical oxygen demand (COD) in water. The NPP samples were characterized by X-ray diffraction and FT-IR spectroscopy while the morphology was visualized by the SEM technique and the chemical composition determined by the energy dispersive spectroscopy (EDS). The adsorption of BY28 on NPP was investigated by varying the contact time (0–160 min), pH (2–6), biosorbent dose (1–8 g) and initial BY28 concentration (25–200 mg L−1); the results show a good yield in the pH range (4–7). The adsorption isotherms were studied by the Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Tempkin models. A maximal NPP adsorption capacity of 91.21 mg g−1 at 20 °C was obtained. The kinetic study showed that the best fit is obtained with the pseudo second order model that correlates suitably the experimental data well.

scholarly journals Adsorption of strontium on different sodium-enriched bentonites

2017 ◽  
Vol 82 (4) ◽  
pp. 449-463 ◽  
Author(s):  
Sanja Marinovic ◽  
Marija Ajdukovic ◽  
Natasa Jovic-Jovicic ◽  
Tihana Mudrinic ◽  
Bojana Nedic-Vasiljevic ◽  
...  
Keyword(s):  
Cation Exchange ◽  
Adsorption Capacity ◽  
Textural Properties ◽  
X Ray Diffraction ◽  
Order Model ◽  
Surface Areas ◽  
Alkaline Conditions ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ph Range

Bentonites from three different deposits (Wyoming, TX, USA and Bogovina, Serbia) with similar cation exchange capacities were sodium enriched and tested as adsorbents for Sr2+ in aqueous solutions. X-Ray diffraction analysis confirmed successful Na-exchange. The textural properties of the bentonite samples were determined using low-temperature the nitrogen physisorption method. Significant differences in the textural properties between the different sodium enriched bentonites were found. Adsorption was investigated with respect to adsorbent dosage, pH, contact time and the initial concentration of Sr2+. The adsorption capacity increased with pH. In the pH range from 4.0?8.5, the amount of adsorbed Sr2+ was almost constant but 2?3 times smaller than at pH ?11. Further experiments were performed at the unadjusted pH since extreme alkaline conditions are environmentally hostile and inapplicable in real systems. The adsorption capacity of all the investigated adsorbents toward Sr2+ was similar under the investigated conditions, regardless of significant differences in the specific surface areas. It was shown and confirmed by the Dubinin?Radushkevich model that the cation exchange mechanism was the dominant mechanism of Sr2+ adsorption. Their developed microporous structures contributed to the Sr2+ adsorption process. The adsorption kinetics obeyed the pseudo-second-order model. The isotherm data were best fitted with the Langmuir isotherm model.

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.

pH Controlled Reversible Interaction of Remazol Orange with Chitin

2017 ◽  
Vol 75 ◽  
pp. 25-36 ◽  
Author(s):  
Muhammad Mominur Rahman ◽  
Abdullah Muhammad Zakaria ◽  
Shaikat Chandra Dey ◽  
Md Ashaduzzaman ◽  
Sayed Md Shamsuddin
Keyword(s):  
Polymeric Materials ◽  
Textile Dye ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Separation Science ◽  
Sustainable Environment ◽  
Effects Of Ph ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Ph Controlled

Biomaterials offer alternative opportunities to build sustainable environment compared to synthetic polymeric materials. Here, we utilized a naturally occurring and plentiful biopolymer, chitin, for the studies on interactive phenomena of a reactive textile dye, Remazol Orange (RO), from aqueous solution. The functional groups and crystallinity of chitin were examined by Fourier transform infrared spectroscopy (FT-IR) and x-ray diffraction (XRD) study. Scanning electron microscopy (SEM) and thermogravimetric analysis (TGA) were employed for the exploration of morphology and thermal stability of chitin. In order to investigate the effects of pH, contact time and initial RO concentration, batch studies were performed at room temperature of 25°C. Chitin exhibited a highly pH controlled reversible interaction with RO. RO was bounded 116.3 milligram per gram of chitin at pH 2.0 within 90 minutes of continuous shaking whereas 98.45% (w/w) RO were immediately unbounded from the chitin surface when the in-situ environment was changed at pH 10. Langmuir adsorption isotherm and pseudo-second order kinetic plot indicate homogeneous chemisorption and uniform monolayer of dye molecules on chitin surface. The findings from this study will certainly add value to analytical research leading to advanced applications in separation science and technology.

Competitive Biosorption of Pb(II) and Cu(II) by Functionalised Micropogonias undulates Scales

2020 ◽  
Vol 13 ◽  
Author(s):  
Joshua O. Ighalo ◽  
Ibrahim O. Tijani ◽  
Oluwaseun J. Ajala ◽  
Fisayo O. Ayandele ◽  
Omodele A. Eletta ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Low Cost ◽  
Fish Scales ◽  
Wet Impregnation ◽  
Monolayer Adsorption ◽  
Competitive Biosorption ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Best Fit

Background: Modified bio-based adsorbents from plant sources can be used for pollution remediation by adsorption due to their low cost and availability in large quantities. Objective: In this study, the competitive biosorption of Pb(II) and Cu(II) by Micropogonias undulates functionalised fish scales (FFS) was conducted. The functionalisation was done by wet impregnation with Fe2+. Method: The biosorbent was characterised by Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (SEM-EDS) and Branueur–Emmett–Teller (BET) analyses. Results: The major constituents in the FFS were calcium and phosphorus from the collagen and apatite on the scales. Optimum removal efficiency for both metals was >99% at 10 g/l dosage. It was observed that the Langmuir isotherm model and the pseudo second order kinetics model were the best fit for the experimental data. The monolayer adsorption capacity of FFS for Pb(II) and Cu(II) was observed to be 96.15 mg/g and 100 mg/g respectively. Conclusion: The study revealed that the competitive biosorption of heavy metals can be achieved (at a good adsorption capacity) using functionalised Micropogonias undulates fish scales.

scholarly journals Multidimensional Ln-Aminophthalate Photoluminescent Coordination Polymers

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  
Keyword(s):  
Water Content ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Low Cost ◽  
Microwave Assisted Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

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.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

Hydrothermal synthesis, crystal structure and properties of a two-dimensional uranyl coordination polymer based on a flexible zwitterionic ligand

2018 ◽  
Vol 74 (3) ◽  
pp. 366-371 ◽  
Author(s):  
Wen Cui ◽  
Ruyu Wang ◽  
Xi Shu ◽  
Yu Fan ◽  
Yang Liu ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Hydrothermal Reaction ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Uranyl Compounds ◽  
X Ray ◽  
Potential Applications ◽  
Ft Ir ◽  
Fuel Reprocessing ◽  
Ft Ir Spectroscopy

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.

Study on Nano- and Microcrystallites in Urines of Uric Acid Stone Patients

2013 ◽  
Vol 655-657 ◽  
pp. 1927-1930 ◽  
Author(s):  
Guang Na Zhang ◽  
Zhi Yue Xia ◽  
Jian Ming Ouyang ◽  
Li Kuan
Keyword(s):  
Electron Microscopy ◽  
Uric Acid ◽  
X Ray Diffraction ◽  
Uric Acid Stone ◽  
Urine Ph ◽  
Stone Formers ◽  
Transmission Electron ◽  
Close Relationship ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The presence of crystallites in urine is closely related to stones formation. In this article, the components, morphology of nano- and micro-crystallites in urines of 20 uric acid (UA) stone formers as well as their relationship with the formation of UAstones were comparatively studied using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The main constituent of urinary crystallites was uric acid. Their particle size distribution was highly uneven, ranging from several nanometers to several tens of micrometers, and obvious aggregation was observed. These results showed that there was close relationship among stone components, urinary crystallites composition and urine pH.

Preparation and Characterization of Cefradine/Montmorillionite Composites

2012 ◽  
Vol 560-561 ◽  
pp. 434-437 ◽  
Author(s):  
Lan Wang ◽  
Wen Ji Guo ◽  
Yan Zhao Zhao
Keyword(s):  
Gastric Fluid ◽  
Simulated Gastric Fluid ◽  
X Ray Diffraction ◽  
Simulated Intestinal Fluid ◽  
Solution Intercalation ◽  
Method Of Solution ◽  
Ft Ir ◽  
In The Beginning ◽  
Ft Ir Spectroscopy

The objective of this paper was to prepare the composite of crefradine/montmorillionite in the method of solution intercalation. The drug load and intercalation rate varied with the drug concentration. X-ray diffraction (XRD), Fourier transformed infrared (FT-IR) Spectroscopy, and thermal analysis (TG-DSC) were applied to characterize composite mentioned above. Together with drug release tests, results indicate cefradine intercalated into montmorillionite.The release profiles of cefradine/MMT in simulated gastric fluid (pH 1.2) and simulated intestinal fluid (pH 7.4) at 37°Cduring 10h are shown in Fig. 4. The amount of cefradine in the beginning 2h came up to 35% and 50%, and in the following time, cefradine released slowly. The release behaviors met the requirements of sustained release.

scholarly journals The Bio-fabrication of Gold Nanoparticles (AuNPs) by Green Method and Study of its Electrochemical Applications

2020 ◽  
Vol 1 (4) ◽  
pp. 22-25
Author(s):  
Azwan Morni
Keyword(s):  
Gold Nanoparticles ◽  
Ir Spectroscopy ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Green Method ◽  
Oh Groups ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

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.

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