scholarly journals Catalytic Properties of Phosphate-Coated CuFe2O4 Nanoparticles for Phenol Degradation

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Israa Othman ◽  
Mohammad Abu Haija ◽  
Fawzi Banat
Keyword(s):  
Catalytic Activity ◽  
Sol Gel ◽  
Phenol Degradation ◽  
Chemical Properties ◽  
Complete Removal ◽  
Catalytic Performance ◽  
Copper Ferrite ◽  
Experimental Conditions ◽  
Prepared Nanoparticles ◽  
And Chemical Properties

Copper ferrite (CuFe2O4) nanoparticles were prepared using the sol-gel autocombustion method and then coated with phosphate using different treatments with H3PO4. The structural and chemical properties of the phosphate-coated CuFe2O4 nanoparticles were controlled by changing the concentration of H3PO4 during the coating process. The prepared nanoparticles were characterized using XRD, FTIR, SEM, and EDS which provided information about the catalysts’ structure, chemical composition, purity, and morphology. The catalytic and photocatalytic activities of the phosphate-coated CuFe2O4 samples were tested and evaluated for the degradation of phenol using HPLC. The prepared nanoparticles successfully emerged as excellent heterogeneous Fenton-type catalysts for phenol degradation. The phosphate-coated CuFe2O4 catalysts exhibited a higher catalytic activity compared with the uncoated CuFe2O4 ones. Such a higher catalytic performance can be attributed to enhanced morphological, electronic, and chemical properties of the phosphate-coated CuFe2O4 nanoparticles. Additionally, the phosphate-coated CuFe2O4 nanoparticles also revealed a higher catalytic activity compared with TiO2 nanoparticles. Different experimental conditions were investigated, and complete removal of phenol was achieved under specific conditions.

Preparation and Photocatalytic Activity of Mixed Phase Anatase/rutile TiO2 Nanoparticles for Phenol Degradation

2014 ◽  
Vol 70 (2) ◽  
Author(s):  
Mohamad Azuwa Mohamed ◽  
Wan Norharyati Wan Salleh ◽  
Juhana Jaafar ◽  
Norhaniza Yusof
Keyword(s):  
Photocatalytic Activity ◽  
Tio2 Nanoparticles ◽  
High Performance ◽  
Sol Gel ◽  
Phenol Degradation ◽  
Chemical Properties ◽  
Mixed Phase ◽  
Rutile Tio2 ◽  
Physico Chemical ◽  
Degussa P25

The evolution of desirable physico-chemical properties in high performance photocatalyst materials involves steps that must be carefully designed, controlled, and optimized. This study investigated the role of key parameter in the preparation and photocatalytic activity analysis of the mixed phase of anatase/rutile TiO2 nanoparticles, prepared via sol-gel method containing titanium-n-butoxide Ti(OBu)4 as a precursor material, nitric acid as catalyst, and isopropanol as solvent. The prepared TiO2 nanoparticles were characterized by means of XRD, SEM, and BET analyses, and UV-Vis-NIR spectroscopy. The results indicated that the calcination temperature play an important role in the physico-chemical properties and photocatalytic activity of the resulting TiO2 nanoparticles. Different calcination temperatures would result in different composition of anatase and rutile. The photocatalytic activity of the prepared mixed phase of anatase/rutile TiO2 nanoparticles was measured by photodegradation of 50 ppm phenol in an aqueous solution. The commercial anatase from Sigma-Aldrich and Degussa P25 were used for comparison purpose. The mixed phase of anatase/rutile TiO2 nanoparticles (consists of 38.3% anatase and 61.7% rutile) that was prepared at 400°C exhibited the highest photocatalytic activity of 84.88% degradation of phenol. The result was comparable with photocatalytic activity demonstrated by Degussa P25 by 1.54% difference in phenol degradation. The results also suggested that the mixed phase of anatase/rutile TiO2 nanoparticles is a promising candidate for the phenol degradation process. The high performance of photocatalyst materials may be obtained by adopting a judicious combination of anatase/rutile and optimized calcination conditions.

Structuring-agent role in physical and chemical properties of Mo/SiO2 catalysts by sol-gel method

2018 ◽  
Vol 89 (2) ◽  
pp. 416-425
Author(s):  
William Giovanni Cortés-Ortiz ◽  
Alexander Baena-Novoa ◽  
Carlos Alberto Guerrero-Fajardo
Keyword(s):  
Sol Gel ◽  
Chemical Properties ◽  
Physical And Chemical Properties ◽  
Gel Method ◽  
Sol Gel Method ◽  
Physical And Chemical ◽  
And Chemical Properties

Infrared Characterization of PMMA-SiO2 Hybrid Glasses Obtained by Sol-Gel Process

2010 ◽  
Vol 1278 ◽  
Author(s):  
L.L. Díaz-Flores ◽  
A. S. López Rodríguez ◽  
P. SifuentesGallardo ◽  
M.A. Hernàndez Rivera ◽  
M.a Garnica Romo ◽  
...  
Keyword(s):  
Sol Gel ◽  
Chemical Properties ◽  
Hybrid Coatings ◽  
Force Microscopy ◽  
Air Atmosphere ◽  
Atomic Force ◽  
Sol Gel Process ◽  
Traditional Process ◽  
And Chemical Properties

AbstractThis work is about the production of hybrid coatings of the system SiO2-PMMA (PMMA, polymethylmethacrylate). These materials have interesting mechanical and chemical properties useful for anticorrosive and wear resistance applications. SiO2-PMMA hybrids were obtained by the sol-gel traditional process, using tetraethylorthosilicate (TEOS) and methylmethacrylate (MMA) by Aldrich Co, as starting reagents. The SiO2:PMMA ratio was varied from 0:1 to about 1:1 at air atmosphere deposition. The coatings were obtained on acrylic sheets and silicon wafers. A diversity of coatings with chemical composition ranging from SiO2 and PMMA to obtain the SiO2-PMMA hybrids were obtained. Infrared (IR) and atomic force microscopy (AFM), were performed to determinate structural and morphological behavior.

How does the Support Influence the Catalytic Activity of the Keggin Ion?

1996 ◽  
Vol 454 ◽  
Author(s):  
Zakiyyah Smith ◽  
Michael Palmieri ◽  
Nancy Buecheler ◽  
Susan A. Jansen
Keyword(s):  
Catalytic Activity ◽  
Carbon Materials ◽  
Solid Acid ◽  
Sol Gel ◽  
Catalytic Performance ◽  
Heteropoly Acids ◽  
Keggin Ion ◽  
Oxide Substrates ◽  
Silica Matrices

AbstractHeteropoly acids, HPA are well known solid acid and oxidation catalysts that find application in hetergeneous and homogeneous reactions. In the former, surface area and stability problems are diminshed by supporting the HPA. Typical supports include oxide substrates and porous carbon materials. The HPA's show some instability on these supports however. In this work, we demonstrate that HPA encapsulated in sol-gel silica matrices show enhanced catalytic performance without compromising the catalytic activity of the HPA. In addition, the specific role of the support in the catalytic process is described as well.

Properties of Nano-Hybrid Sol-Gel Materials Synthesized from Colloidal Silica-Silane Containing Epoxy Silane

2007 ◽  
Vol 336-338 ◽  
pp. 2278-2281 ◽  
Author(s):  
Moon Kyong Na ◽  
Dong Pil Kang ◽  
Hoy Yul Park ◽  
Myeong Sang Ahn ◽  
In Hye Myung
Keyword(s):  
Contact Angle ◽  
Colloidal Silica ◽  
Flat Surface ◽  
Coating Layer ◽  
Sol Gel ◽  
Chemical Properties ◽  
Coating Films ◽  
Initial Stage ◽  
Physical And Chemical ◽  
And Chemical Properties

Three kinds of colloidal silica (CS)/silane sol solutions were synthesized in variation with parameters such as different acidity and reaction time. Sol solutions were prepared from HSA CS/ methyltrimethoxysilane (MTMS), LS CS/MTMS and LS CS/MTMS/γ -Glycidoxypropyltri methoxysilane (ES) solutions. In order to understand their physical and chemical properties, sol-gel coating films were fabricated on glass. Coating films on glass, obtained from LS/MTMS sol, had high contact angle, also, much enhanced flat surface in the case of LS/MTMS sol was observed in comparison with HSA/ MTMS sol. From all sol-gel solutions, seasoning effect of for enhancing properties of sol-gel coating layer on glass was observed while such sol-gel solutions were left for 7days. In initial stage of sol-gel reaction, all most of sol solutions used in this work seem to be unstable, formation of coating films was a little hazy and rough. However, improved coating films as observed in 4days later. LS/MTMS/ES sol solutions were synthesized with ES, adding to LS/MTMS sol. Contact angle of LS/MTMS/ES sol-gel coating films decreased, since ES played a role in forming hydrophilic hydroxyl sol. The elastic portion of coating films prepared from LS/MTMS/ES sol increased with addition of ES, but thermal stability decreased a little.

Ru/TiO2 Nanostructured Catalysts: Synthesis, Characterization and Catalytic Activity Towards Hydrogenation of Ethyl Levulinate

2021 ◽  
Vol 21 (12) ◽  
pp. 6160-6167
Author(s):  
Sakthivel Kumaravel ◽  
Sivakumar Thiripuranthagan ◽  
Elangovan Erusappan ◽  
Aishwarya Sivakumar ◽  
Saranraj Kumaravel ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Inductively Coupled Plasma ◽  
Sol Gel ◽  
Nanostructured Catalysts ◽  
Optical Emission ◽  
Morphological Properties ◽  
Emission Spectrometry ◽  
Experimental Conditions ◽  
Ethyl Levulinate ◽  
Ru Nanoparticles

Pristine TiO2 and x% Ru/TiO2 catalysts with different wt.% of Ru (x%= 1.5%, 2%, 2.5% and 3%) were synthesized using sol–gel and simple impregnation methods. Different characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), High-resolution transmission electron microscope (HR-TEM), Inductively coupled plasma-optical emission spectrometry (ICP-OES) and Thermogravimetry/Differential thermal analysis (TG/DTA) were used to study the physicochemical and morphological properties. The XRD patterns of the as-prepared pristine TiO2 catalyst showed high crystalline nature. The HR-TEM images revealed that the Ru nanoparticles (NPs) were evenly dispersed on the TiO2 surface. The prepared catalysts were evaluated for their catalytic activity towards the liquid phase hydrogenation of ethyl levulinate under mild reaction conditions (ambient H2 pressure). Among the various catalysts, 2.5% Ru/TiO2 catalyst showed the maximum catalytic activity of 79% ethyl levulinate (EL) conversion with 82% selectivity of γ-valerolactone (GVL). The recyclability test revealed that the most active 2.5% Ru/TiO2 also showed the highest stability of the catalyst under optimized experimental conditions.

Tuning Packing, Structural Flexibility, and Porosity in 2D Metal–Organic Frameworks by Metal Node Choice

2019 ◽  
Vol 72 (10) ◽  
pp. 797 ◽  
Author(s):  
Witold M. Bloch ◽  
Christian J. Doonan ◽  
Christopher J. Sumby
Keyword(s):  
Structural Changes ◽  
Metal Organic Frameworks ◽  
Chemical Properties ◽  
Complete Removal ◽  
Structural Flexibility ◽  
X Ray Diffraction ◽  
Metal Centre ◽  
Metal Organic ◽  
Physical And Chemical ◽  
And Chemical Properties

Understanding the key features that determine structural flexibility in metal–organic frameworks (MOFs) is key to exploiting their dynamic physical and chemical properties. We have previously reported a 2D MOF material, CuL1, comprising five-coordinate metal nodes that displays exceptional CO2/N2 selectively (L1=bis(4-(4-carboxyphenyl)-1H-pyrazolyl)methane). Here we examine the effect of utilising six-coordinate metal centres (CoII and NiII) in the synthesis of isostructural MOFs from L1, namely CoL1 and NiL1. The octahedral geometry of the metal centre within the MOF analogues precludes an ideal eclipse of the 2D layers, resulting in an offset stacking, and in certain cases, the formation of 2-fold interpenetrated analogues β-CoL1 and β-NiL1. We used a combination of thermogravimetric analysis (TGA), and powder and single crystal X-ray diffraction (PXRD and SCXRD) to show that desolvation is accompanied by a structural change for NiL1, and complete removal of the coordinated H2O ligands results in a reduction in long-range order. The offset nature of the 2D layers in combination with the structural changes impedes the adsorption of meaningful quantities of gases (N2, CO2), highlighting the importance of a five-coordinate metal centre in achieving optimal pore accessibility for this family of flexible materials.

The Ceramist as Chemist - Opportunities for New Materials

1984 ◽  
Vol 32 ◽  
Author(s):  
D. R. Uhlmann ◽  
B.J.J. Zelinski ◽  
G.E. Wnek
Keyword(s):  
Wide Spectrum ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Glass Ceramics ◽  
Chemical Properties ◽  
Ceramic Materials ◽  
Process Technology ◽  
Chemical Homogeneity ◽  
And Chemical Properties

ABSTRACTThe use of sol-gel techniques to prepare glasses and crystalline ceramics offers outstanding opportunity for breakthroughs in technology. The areas of particular promise include novel glasses; crystallineceramics with exceptional microstructures; coatings for modification of electrical, optical, mechanical and chemical properties; porous media with high surface area and tailored chemistry; ceramic powders with high chemical homogeneity and narrow distributions of particle size; matrix materials in ceramicceramic composites; and a wide spectrum of specialty ceramic materials, ranging from abrasives and fibers to glass ceramics and films. Opportunities in each of these areas will be discussed and related to the advances in understanding and process technology required for their achievement. The theses will be advanced that creative chemistry provides the key to many of these advances, that ceramists simply MUST learn more chemistry, but that we dare not rest from our labors when the chemistry is done.

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