scholarly journals 4-Aminoacetophenone Intercalated CoAl Layered Double Hydroxides: Synthesis, Characterization and Adsorptive Removal of Cd(II) ions from Water Samples

2021 ◽  
Vol 22 (1) ◽  
pp. 139-149
Author(s):  
Abdul Rafay Bhatti
Keyword(s):  
Layered Double Hydroxides ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sorption Energy ◽  
Enolate Anion ◽  
Edx Analyses ◽  
Ft Ir ◽  
Wastewater Samples ◽  
Double Hydroxides ◽  
Ft Ir Spectroscopy

In the present study, CoAl-NO3 Layered Double Hydroxides (CoAl-NO3-LDH) was synthesized and an enolate anion of 4-Aminoacetophenone (AAP) was intercalated into LDH following the reconstruction approach. The CoAl-NO3-LDH and CoAl-AAP-LDH were characterized by Fourier-Transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscope (SEM) and energy dispersive X-ray (EDX) analyses. CoAl-AAP-LDH worked well for adsorption of Cd(II) ions from aqueous samples at optimum pH 7, adsorbent dosage 25 mg, concentration of Cd(II) ions 25 mg L-1 and shaking time 20 min at 25 °C. Different isotherms such as Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherms fitted well to adsorption data with correlation coefficient (R2) of 0.998, 0.982 and 0.992, respectively. Monolayered (Qm) and multi-layered (KF) capacities of CoAl-AAP-LDH for adsorption of Cd(II) ions were calculated and found to be 34.40 and 19.44 mg g-1, respectively. Sorption energy was calculated and found to be 9.13 kJ mol-1, indicating chemisorption or ion exchange sorption mechanism. The method worked well for the adsorption of Cd(II) ions from wastewater samples.

Characterization of Chromate-Intercalated Layered Double Hydroxides

2006 ◽  
Vol 514-516 ◽  
pp. 1541-1545 ◽  
Author(s):  
Margarita del Arco ◽  
Daniel Carriazo ◽  
Cristina Martín ◽  
Amalia M. Pérez Grueso ◽  
Vicente Rives
Keyword(s):  
Layered Double Hydroxides ◽  
Thermal Analyses ◽  
Basal Spacing ◽  
X Ray Diffraction ◽  
N2 Adsorption ◽  
Exchange Method ◽  
X Ray ◽  
Ft Ir ◽  
Double Hydroxides

PXRD (powder x-ray diffraction), FT-IR (Fourier Transform infrared), N2 adsorption at - 196 °C and TG/DTA (thermogravimetric and differential thermal analyses) techniques have been used for characterisation of MgAl- and ZnAl-CrO4 LDHs, which had been prepared by the ion exchange method from the corresponding chloride LDH (layered double hydroxides) precursors. The results indicates that the oxometalate intercalation in both systems produces interlayer microporosity and a basal spacing of 8.7 Å; This gallery height decreases when the samples are calcined in the temperature range 100-300 °C, due to a grafting process. A larger thermal stability is detected for MgAl-CrO4 sample than for the zinc-containing one.

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.

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.

scholarly journals Photocatalytic Degradation of 2,4,6-Trichlorophenol by MgO–MgFe2O4 Derived from Layered Double Hydroxide Structures

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 454 ◽  
Author(s):  
Esthela Ramos-Ramírez ◽  
Francisco Tzompantzi-Morales ◽  
Norma Gutiérrez-Ortega ◽  
Héctor G. Mojica-Calvillo ◽  
Julio Castillo-Rodríguez
Keyword(s):  
Photocatalytic Degradation ◽  
Layered Double Hydroxides ◽  
X Ray Diffraction ◽  
Application Study ◽  
Toxic Compounds ◽  
X Ray ◽  
Thermally Activated ◽  
Double Hydroxide ◽  
Double Hydroxides ◽  
Scanning Electron

In recent years, the search for solutions for the treatment of water pollution by toxic compounds such as phenols and chlorophenols has been increasing. Phenols and their derivatives are widely used in the manufacture of pesticides, insecticides, paper, and wood preservers, among other things. Chlorophenols are partially biodegradable but not directly photodegradable by sunlight and are extremely toxic—especially 2,4,6-trichlorophenol, which is considered to be potentially carcinogenic. As a viable proposal to be applied in the treatment of water contaminated with 2,4,6-trichlorophenol, this paper presents an application study of the thermally activated Mg/Fe layered double hydroxides as photocatalysts for the mineralization of this contaminant. Activated Mg/Fe layered double hydroxides were characterized by X-ray diffraction, thermal analysis, N2 physisorption, and scanning electron microscopy with X-ray dispersive energy. The results of the photocatalytic degradation of 2,4,6-trichlorophenol in aqueous solution showed good photocatalytic activity, with an efficiency of degradation of up to 93% and mineralization of 82%; degradation values which are higher than that of TiO2-P25, which only reached 18% degradation. The degradation capacity is attributed to the structure of the MgO–MgFe2O4 oxides derived from double laminate hydroxide Mg/Fe. A path of degradation based on a mechanism of superoxide and hollow radicals is proposed.

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.

Ball-Milling Stimulated Mechanochemical Processes in the System “Titanium-Toluene”

2019 ◽  
Vol 946 ◽  
pp. 351-356 ◽  
Author(s):  
Olga M. Kanunnikova ◽  
V.V. Aksenova ◽  
G.A. Dorofeev
Keyword(s):  
Ball Milling ◽  
Mechanical Energy ◽  
High Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Liquid Phases ◽  
Ft Ir ◽  
Titanium Powders ◽  
Solid Phases ◽  
Ft Ir Spectroscopy

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.

scholarly journals Two-Step Separation of Chitin from Shrimp Shells Using Citric Acid and Deep Eutectic Solvents with the Assistance of Microwave

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 409 ◽  
Author(s):  
Dandan Zhao ◽  
Wen-Can Huang ◽  
Na Guo ◽  
Shuye Zhang ◽  
Changhu Xue ◽  
...  
Keyword(s):  
Citric Acid ◽  
Deep Eutectic Solvents ◽  
Second Step ◽  
X Ray Diffraction ◽  
X Ray ◽  
Shrimp Shells ◽  
Ft Ir ◽  
Scanning Electron ◽  
Ft Ir Spectroscopy

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.

scholarly journals High efficient photocatalytic activity of Zn-Al-Ti layered double hydroxides nanocomposite

2018 ◽  
Vol 149 ◽  
pp. 01087 ◽  
Author(s):  
F. Amor ◽  
A. Diouri ◽  
I. Ellouzi ◽  
F. Ouanji ◽  
M. Kacimi
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Uv Irradiation ◽  
Layered Double Hydroxides ◽  
Removal Rate ◽  
X Ray Diffraction ◽  
Simple Method ◽  
X Ray ◽  
High Efficient ◽  
Double Hydroxides

This work establishes a simple method for synthesising layered double hydroxides (LDHs) powders with coprecipitation. The characteristics of the samples were investigated y X-ray diffraction (XRD), scanning electron microscopy (SEM) and spectrophotometer UV–Vis (DRS). Non-uniform distribution was shown for LDHs samples by SEM. Photocatalytic efficiencies were tested using methylene blue (MB) dye as a model contaminant under UV irradiation. In particular, Zn–Al-Ti LDH exhibited an excellent performance towards MB degradation compared with commercial TiO2 nanoparticles. Methylene blue removal percentage was reached at almost 100%, whereas commercial TiO2 reached a removal rate of only 66% under the same conditions within 20 min. The aim of the current work is to prepare Zn-Al-Ti layered double hydroxides nanocomposite and to evaluate their photocatalytic activity in the removal of methylene blue under UV irradiation.

scholarly journals Designing Magnetic Layered Double Hydroxides and Two-Dimensional Magnetic Nano-Nets of Cobalt Ferrite through a Novel Approach

2018 ◽  
Vol 8 (11) ◽  
pp. 2099 ◽  
Author(s):  
Osama Saber ◽  
Abdullah Aljaafari ◽  
Sarah Asiri ◽  
Khalid Batoo
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Layered Double Hydroxides ◽  
Cobalt Ferrite ◽  
High Coercivity ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Double Hydroxides

The present study has a dual aim of supporting magnetic nanoparticles over the nanolayers of LDHs and designing two-dimensional magnetic nano-nets of cobalt ferrite. In this trend, nanoparticles of CoFe2O4 were prepared and supported by Co-Fe LDH through urea hydrolysis. The nanolayered structures of Co-Fe LDH were confirmed by X-ray diffraction, energy-dispersive X-ray spectrometry, FT-IR spectra, thermal analyses, and transmission electron microscopy. In addition, they indicated that 13.2% CoFe2O4 were supported over Co-Fe LDH. Transformation of the nanolayered structures of Co-Fe LDH to nano-nets was achieved by the catalytic effect of the supported CoFe2O4 nanoparticles through solvent thermal technique. X-ray diffraction patterns and transmission electron microscopy images confirmed the transformation of the supported Co-Fe LDH to nano-nets of cobalt ferrite. In order to indicate the effect of the LDH for designing the nano-nets, nanoparticles of cobalt ferrite were prepared by the same technique without LDH. The magnetic behavior of the nano-nets and the supported Co-Fe LDH were measured and compared with the nanoparticles through vibrating sample magnetometer technique. The magnetic parameters indicated that the prepared nano-nets have ferromagnetic behavior and high coercivity. However, the prepared nanoparticles revealed a superparamagnetic state and low coercivity. The experimental results concluded that the incorporation of nanoparticles with nanowires into nano-net structures has been found to be an efficient way to improve their magnetic properties and prevent their agglomerations. Finally, layered double hydroxides are an important source for constructing magnetic nanolayered structures and nano-nets.

Two novel organic–inorganic hybrid materials from tetrachloridometallate(II) salts and 4-[(E)-2-(pyridin-1-ium-2-yl)ethenyl]pyridinium

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
Keyword(s):  
Three Dimensional ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Inorganic Hybrid ◽  
X Ray ◽  
Pyridinium Cation ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

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).

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