scholarly journals Functionalized Porous Silica-Based Nano/Micro Particles for Environmental Remediation of Hazard Ions

Nanomaterials ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 247 ◽  
Author(s):  
Chun Li ◽  
Xin Wang ◽  
Zi Jiao ◽  
Yu Zhang ◽  
Xiang Yin ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Environmental Remediation ◽  
Direct Synthesis ◽  
Synthesis Method ◽  
Inorganic Materials ◽  
Synthesis Methods ◽  
Layer By Layer ◽  
Impregnation Method ◽  
Abrasive Resistance ◽  
Micro Particles

The adsorption and separation of hazard metal ions, radioactive nuclides, or minor actinides from wastewater and high-level radioactive waste liquids using functional silica-based nano/micro-particles modified with various inorganic materials or organic groups, has attracted significant attention since the discovery of ordered mesoporous silica-based substrates. Focusing on inorganic and organic modified materials, the synthesis methods and sorption performances for specific ions in aqueous solutions are summarized in this review. Three modification methods for silica-based particles, the direct synthesis method, wetness impregnation method, and layer-by-layer (LBL) deposition, are usually adopted to load inorganic material onto silica-based particles, while the wetness impregnation method is currently used for the preparation of functional silica-based particles modified with organic groups. Generally, the specific synthesis method is employed based on the properties of the loading materials and the silicon-based substrate. Adsorption of specific toxic ions onto modified silica-based particles depends on the properties of the loaded material. The silicon matrix only changes the thermodynamic and mechanical properties of the material, such as the abrasive resistance, dispersibility, and radiation resistance. In this paper, inorganic loads, such as metal phosphates, molybdophosphate, titanate-based materials, and hydrotalcite, in addition to organic loads, such as 1,3-[(2,4-diethylheptylethoxy)oxy]-2,4-crown-6-Calix{4}arene (Calix {4}) arene-R14 and functional 2,6-bis-(5,6-dialkyl-1,2,4-triazin-3-yl)-pyridines(BTP) are reviewed. More specifically, we emphasize on the synthesis methods of such materials, their structures in relation to their capacities, their selectivities for trapping specific ions from either single or multi-component aqueous solutions, and the possible retention mechanisms. Potential candidates for remediation uses are selected based on their sorption capacities and distribution coefficients for target cations and the pH window for an optimum cation capture.

scholarly journals A Review Paper on Heterogeneous Fenton Catalyst: Types of Preparation, Modification Techniques, Factors Affecting the Synthesis, Characterization, and Application in the Wastewater Treatment

2019 ◽  
Vol 15 (1) ◽  
pp. 1-34 ◽  
Author(s):  
Vijyendra Kumar ◽  
Titikshya Mohapatra ◽  
Sandeep Dharmadhikari ◽  
Prabir Ghosh
Keyword(s):  
Wastewater Treatment ◽  
Heterogeneous Catalyst ◽  
Synthesis Method ◽  
Effluent Treatment ◽  
Synthetic Wastewater ◽  
Precipitation Method ◽  
Synthesis Methods ◽  
Impregnation Method ◽  
Catalytic Method ◽  
Influence Of Process Parameters

This comprehensive review focuses on the different factors, modification in the synthesis method, characterization and application of heterogeneous catalyst in the wastewater treatment based on the Fenton process. The present review highlights the different catalyst preparation methods like wet impregnation method, hydrothermal method, sol-gel method, precipitation method and their application to treat different recalcitrant organic chemicals. Major heterogeneous catalyst synthesis methods were discussed with their excellent workability. The importance of modification through physical and chemical method  was  also reported. Different catalyst, pollutants and optimum parametric conditions available in the literature along with some relevant studies are summarized. The effect of factors like pH, calcination and some other modifiers on the synthesis and their efficiency in the wastewater treatment has been described. The important characterization of synthesized catalysts explaining their working efficiency has also been discussed. In the final section, the application of heterogeneous catalyst synthesized by different methods in the wastewater/effluent treatment has been investigated. The main aim of this review is to find out the influence of process parameters and catalytic method on degradation/decolorization of organic compounds present in industrial or synthetic wastewater. Copyright © 2020 BCREC Group. All rights reserved 

scholarly journals Interrelations of Synthesis Method, Polyethylene Glycol Coating, Physico-Chemical Characteristics, and Antimicrobial Activity of Silver Nanoparticles

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2475
Author(s):  
Amirah Shafilla Mohamad Kasim ◽  
Arbakariya Bin Ariff ◽  
Rosfarizan Mohamad ◽  
Fadzlie Wong Faizal Wong
Keyword(s):  
Antimicrobial Activity ◽  
Silver Nanoparticles ◽  
Polyethylene Glycol ◽  
Pathogenic Bacteria ◽  
Synthesis Method ◽  
Chemical Characteristics ◽  
Synthesis Methods ◽  
Uniform Size ◽  
Transmission Electron Microscopy Analysis ◽  
Physico Chemical

Silver nanoparticles (AgNPs) have been found to have extensive biomedical and biological applications. They can be synthesised using chemical and biological methods, and coated by polymer to enhance their stability. Hence, the changes in the physico-chemical characteristics of AgNPs must be scrutinised due to their importance for biological activity. The UV-Visible absorption spectra of polyethylene glycol (PEG) -coated AgNPs displayed a distinctive narrow peak compared to uncoated AgNPs. In addition, High-Resolution Transmission Electron Microscopy analysis revealed that the shapes of all AgNPs, were predominantly spherical, triangular, and rod-shaped. Fourier-Transform Infrared Spectroscopy analysis further confirmed the role of PEG molecules in the reduction and stabilisation of the AgNPs. Moreover, dynamic light scattering analysis also revealed that the polydispersity index values of PEG-coated AgNPs were lower than the uncoated AgNPs, implying a more uniform size distribution. Furthermore, the uncoated and PEG-coated biologically synthesised AgNPs demonstrated antagonisms activities towards tested pathogenic bacteria, whereas no antagonism activity was detected for the chemically synthesised AgNPs. Overall, generalisation on the interrelations of synthesis methods, PEG coating, characteristics, and antimicrobial activity of AgNPs were established in this study.

scholarly journals Sol-Gel Synthesis of the Double Perovskite Sr2FeMoO6 by Microwave Technique

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3876
Author(s):  
Jesús Valdés ◽  
Daniel Reséndiz ◽  
Ángeles Cuán ◽  
Rufino Nava ◽  
Bertha Aguilar ◽  
...  
Keyword(s):  
Particle Size ◽  
Hydrothermal Synthesis ◽  
Microwave Radiation ◽  
Structural Characteristics ◽  
Sol Gel ◽  
Synthesis Method ◽  
Double Perovskite ◽  
Synthesis Methods ◽  
X Ray ◽  
Sol Gel Synthesis

The effect of microwave radiation on the hydrothermal synthesis of the double perovskite Sr2FeMoO6 has been studied based on a comparison of the particle size and structural characteristics of products from both methods. A temperature, pressure, and pH condition screening was performed, and the most representative results of these are herein presented and discussed. Radiation of microwaves in the hydrothermal synthesis method led to a decrease in crystallite size, which is an effect from the reaction temperature. The particle size ranged from 378 to 318 nm when pH was 4.5 and pressure was kept under 40 bars. According to X-ray diffraction (XRD) results coupled with the size-strain plot method, the product obtained by both synthesis methods (with and without microwave radiation) have similar crystal purity. The Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) techniques showed that the morphology and the distribution of metal ions are uniform. The Curie temperature obtained by thermogravimetric analysis indicates that, in the presence of microwaves, the value was higher with respect to traditional synthesis from 335 K to 342.5 K. Consequently, microwave radiation enhances the diffusion and nucleation process of ionic precursors during the synthesis, which promotes a uniform heating in the reaction mixture leading to a reduction in the particle size, but keeping good crystallinity of the double perovskite. Precursor phases and the final purity of the Sr2FeMoO6 powder can be controlled via hydrothermal microwave heating on the first stages of the Sol-Gel method.

scholarly journals Microwave-Assisted vs. Conventional Hydrothermal Synthesis of MoS2 Nanosheets: Application towards Hydrogen Evolution Reaction

Crystals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1040 ◽  
Author(s):  
Getachew Solomon ◽  
Raffaello Mazzaro ◽  
Vittorio Morandi ◽  
Isabella Concina ◽  
Alberto Vomiero
Keyword(s):  
Hydrothermal Synthesis ◽  
Hydrothermal Method ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Current Density ◽  
Crystal Morphology ◽  
Synthesis Method ◽  
Synthesis Methods ◽  
Mos2 Nanosheets ◽  
Microwave Assisted

Molybdenum sulfide (MoS2) has emerged as a promising catalyst for hydrogen evolution applications. The synthesis method mainly employed is a conventional hydrothermal method. This method requires a longer time compared to other methods such as microwave synthesis methods. There is a lack of comparison of the two synthesis methods in terms of crystal morphology and its electrochemical activities. In this work, MoS2 nanosheets are synthesized using both hydrothermal (HT-MoS2) and advanced microwave methods (MW-MoS2), their crystal morphology, and catalytical efficiency towards hydrogen evolution reaction (HER) were compared. MoS2 nanosheet is obtained using microwave-assisted synthesis in a very short time (30 min) compared to the 24 h hydrothermal synthesis method. Both methods produce thin and aggregated nanosheets. However, the nanosheets synthesized by the microwave method have a less crumpled structure and smoother edges compared to the hydrothermal method. The as-prepared nanosheets are tested and used as a catalyst for hydrogen evolution results in nearly similar electrocatalytic performance. Experimental results showed that: HT-MoS2 displays a current density of 10 mA/cm2 at overpotential (−280 mV) compared to MW-MoS2 which requires −320 mV to produce a similar current density, suggesting that the HT-MoS2 more active towards hydrogen evolutions reaction.

Redox reaction mediated direct synthesis of hierarchical flower-like CuO spheres anchored on electrospun poly(vinylidene difluoride) fiber surfaces at low temperatures

RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 100228-100234 ◽  
Author(s):  
Yun-Yang Lee ◽  
Hsieh-Yu Li ◽  
Shih-Jiuan Chiu ◽  
Wen-Li Liang ◽  
Pi-Li Yeh ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Rhodamine B ◽  
Redox Reaction ◽  
Low Temperatures ◽  
Direct Synthesis ◽  
Catalytic Membranes ◽  
Vinylidene Difluoride

Flower-like CuO spheres anchored on electrospun PVDF fiber surfaces as catalytic membranes for the photodegradation of rhodamine B aqueous solutions.

Synthesis and Characterization of Alkeyl Imidazolium Ionic Liquids

2014 ◽  
Vol 1048 ◽  
pp. 452-455
Author(s):  
Qiang Wang ◽  
Shi Dong Wang ◽  
Ming Chen Qi ◽  
Shu Liang Zang
Keyword(s):  
Ionic Liquids ◽  
Chemical Structure ◽  
Direct Synthesis ◽  
Synthesis Method ◽  
Structure And Properties ◽  
Spectra Analysis ◽  
Infrared Spectrometer ◽  
Liquid Salts ◽  
Structure Of Matter

Two new imidazole ionic liquid salts, 1-allyl-3-methylimidazolium chloride ([AMIM]Cl) and 1-allyl-3-methy-imidazolium hydrogen sulfate ([EMIM]HSO4), were synthesized with direct synthesis and two-step synthesis method, using a viscosity meter, PH meter, conductivity meter, densitometer, infrared spectrometer determined its chemical structure and properties. The results show that two ionic liquids in the range is slightly different, the trend is roughly same. As the temperature increases, the viscosity decreases, PH gradually increased, the density decreases slightly, can be regarded as constant, the conductivity gradually increased. Ionic liquids of the two IR spectra analysis show its structure and synthetic route consistent with the structure of matter.

COMPARING AND IMPROVING THE SYNTHESIS OF STATE-BASED SPECIFICATIONS FROM SCENARIO-BASED SPECIFICATIONS

2012 ◽  
Vol 22 (07) ◽  
pp. 867-890
Author(s):  
ZHIJIAN WANG ◽  
WENRUI LI ◽  
PENGCHENG ZHANG
Keyword(s):  
Synthesis Method ◽  
The State ◽  
Experimental Comparison ◽  
Synthesis Methods ◽  
User Requirements ◽  
State Machines ◽  
Analysis Method ◽  
Improved Method ◽  
Local Synthesis ◽  
Novel Algorithm

The scenario-based specifications are popularly used to capture user requirements. The state-based specifications are very appropriate to capture system design. Recently, there has been increased research interest in connecting these two kinds of specifications, called synthesis. Synthesis is a way to automatically construct the state-based specifications from the scenario-based specifications. There are two kinds of synthesis methods: global synthesis and local synthesis. Global synthesis means constructing a state-based specification for the whole system from the scenario-based specifications, while local synthesis means constructing a state-based specification for each object in the system. The two different synthesis methods have different uses and need to be systematically compared. The contributions of this paper are twofold. Firstly, we propose an improved method supporting the global and the local synthesis of state machines (a kind of state-based specifications) by using a novel algorithm for state machine execution and an algorithm similar to operator priority analysis method, which can fully automate the process of synthesis. Our synthesis method also satisfies two important properties: completeness and soundness. Secondly, to the best of our knowledge, our work does the first attempt to systematically compare global synthesis with local synthesis, and shows some insightful results of the experimental comparison between the two kinds of synthesis methods, which are valuable for the practitioners to choose an appropriate synthesis method for the analysis and verification of the system.

General Synthesis Methods of Inorganic Materials for Supercapacitors

2021 ◽  
pp. 187-203
Author(s):  
Mehmet H. Calimli ◽  
Tugba G. Karahan ◽  
Anish Khan ◽  
Fatih Sen
Keyword(s):  
Inorganic Materials ◽  
Synthesis Methods ◽  
General Synthesis

Property of Cu2O-CuO/ZSM-5 nanocomposite and degradation process of azo dye AO7 without sacrificial agent (H2O2)

2016 ◽  
Vol 73 (11) ◽  
pp. 2747-2753 ◽  
Author(s):  
Wusong Kong ◽  
Hongxia Qu ◽  
Peng Chen ◽  
Weihua Ma ◽  
Huifang Xie
Keyword(s):  
Catalytic Activity ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Oxygen Demand ◽  
Operating Conditions ◽  
Surface Element ◽  
Impregnation Method ◽  
X Ray ◽  
Initial Ph ◽  
Sacrificial Agent

In this study, Cu2O-CuO/ZSM-5 nanocomposite was synthesized by the impregnation method, and its catalytic performance for the destruction of AO7 in aqueous solutions was investigated. The morphology, structure and surface element valence state of Cu2O-CuO/ZSM-5 were characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The operating conditions on the degradation of AO7 by Cu2O-CuO/ZSM-5, such as initial pH values, concentration of AO7 and catalyst dosage were investigated and optimized. The results showed that the sample had good catalytic activity for destruction of AO7 in the absence of a sacrificial agent (e.g. H2O2): it could degrade 91% AO7 in 140 min at 25 °C and was not restricted by the initial pH of the AO7 aqueous solutions. Cu2O-CuO/ZSM-5 exhibited stable catalytic activity with little loss after three successive runs. The total organic carbon and chemical oxygen demand removal efficiencies increased rapidly to 69.36% and 67.3% after 120 min of treatment by Cu2O-CuO/ZSM-5, respectively.

Highly efficient carbonaceous nanofiber/layered double hydroxide nanocomposites for removal of U(VI) from aqueous solutions

2019 ◽  
Vol 107 (4) ◽  
pp. 299-309
Author(s):  
Shuqi Yu ◽  
Xiangxue Wang ◽  
Shunyan Ning ◽  
Zhongshan Chen ◽  
Xiangke Wang
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Layered Double Hydroxide ◽  
Photoelectron Spectroscopy ◽  
Environmental Remediation ◽  
Three Dimensional ◽  
Order Kinetic ◽  
Surface Bonding ◽  
Double Hydroxide ◽  
Shed Light

Abstract The three-dimensional (3D) carbonaceous nanofiber and Ni-Al layered double hydroxide (CNF/LDH) nanocomposite was successfully prepared by a facile one-step hydrothermal methodology. Characterization of scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), XRD, and Fourier transformed infrared spectroscopy (FTIR) provided a demonstration that the modified CNF/LDH nanocomposite possessed abundant functional groups, for instance, metal-oxygen surface bonding sites (Ni–O as well as Al–O) and free-metal surface bonding sites (C–O, C–O–C, as well as O–C=O). The elimination of representative radionuclide (i.e. U(VI)) on the CNF/LDH nanocomposite from aqueous solutions was explored as a key function of pH, ionic strength, contact time, reaction temperature as well as radionuclide preliminary concentrations with the use of the batch methodology. As revealed by the findings, the sorption of radionuclides on CNF/LDH nanocomposite adhered to the pseudo-second-order kinetic model as well as Langmuir model. The maximum elimination capacity of U(VI) amounted to be 0.7 mmol/g. The independent of ionic strength shed light on the fact that inner-sphere surface complexation mainly overpowered radionuclide uptake by the CNF/LDH nanocomposite, which was further verified through the combination of FTIR and XPS spectral analyses. The abovementioned analyses shed light on the fact that the CNF/LDH nanocomposite can be regarded as a latent material to preconcentration radionuclides for environmental remediation.

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