Characterization of Nanostructured Silica as Carrier for Insecticides Deltamethrin, Pyriproxyfen, and Chlorpyrifos and Testing the Insecticidal Efficacy Against Trogoderma granarium (Coleoptera: Dermestidae) Larvae

2019 ◽  
Vol 113 (1) ◽  
pp. 511-517
Author(s):  
Masumeh Ziaee ◽  
Asgar Babamir-Satehi
Keyword(s):  
Electron Microscopy ◽  
Silica Nanoparticles ◽  
Sol Gel ◽  
Sem Analysis ◽  
Efficient Treatment ◽  
Trogoderma Granarium ◽  
Transmission Electron ◽  
Insecticidal Efficacy ◽  
Sol Gel Process ◽  
Nanostructured Silica

Abstract Nanostructured silica can be used as a carrier of pesticides to enhance stability and controlled release of agrochemicals with an effective concentration on target pests. Silica nanoparticles (SNPs) were synthesized by sol–gel process and employed as a carrier of three different insecticides including deltamethrin, pyriproxyfen, and chlorpyrifos. The SNPs were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis and the insecticides-loaded in SNPs were characterized by transmission electron microscopy (TEM). The toxicity of insecticides alone and loaded in SNPs was evaluated against small and large larvae of Trogoderma granarium Everts on concrete surfaces. The immediate mortality was counted after 1, 3, and 7 d of exposure, and then surviving individuals were transferred to untreated surfaces for seven more days, with delayed mortality was recorded. Small larvae were more susceptible than large ones on all insecticide treatments. In addition, insecticides loaded in silica nanoparticles were more effective when compared with application of the insecticides alone. For immediate mortality, deltamethrin loaded in SNPs was the most efficient treatment causing 70.5% mortality on small and 55.5% mortality on large larvae after 7 d of exposure to the highest concentration. Pyriproxyfen loaded in SNPs caused low immediate mortality, but the mortality increased in delayed count indicated that the insecticide could control the larvae even after they have been removed from treated surfaces. It can be concluded that loading insecticides in SNPs could significantly increase their insecticidal efficiency, but this increase was compound-dependent.

An Experimental Study on Synthesis and Characterization of Silica Nanoparticles Prepared by Sol-Gel Method

2007 ◽  
Vol 553 ◽  
pp. 245-251
Author(s):  
Ali Shokuhfar ◽  
Tolou Shokuhfar ◽  
M. Ghazinejad ◽  
R. Babazade ◽  
S. Tabatabae
Keyword(s):  
Electron Microscopy ◽  
Silica Nanoparticles ◽  
Size Distribution ◽  
Sol Gel ◽  
Sio2 Nanoparticles ◽  
Industrial Applications ◽  
Silica Particles ◽  
Narrow Size Distribution ◽  
Molar Ratios ◽  
Transmission Electron

Monodispersed nanometer-sized particles proved to be very important and advantageous in many industrial applications. One of the notable groups of these particles is silica (SiO2) nanoparticles which are widely utilized in developing numerous products such as electrical and thermal insulators, humidity sensors, varnish, etc. Since the quality of some of these products depends highly on the purity and size distribution of the silica particles, it is necessary to produce silica nanoparticles of narrow size distribution and very high purity. In this research silica nanoparticles, with a relatively narrow size distribution, have been synthesized via the hydrolysis reaction of tetraethoxisilane (TEOS) in the solution of deionized water and ethanol (C2H5OH), and in the presence of ammonia (NH3) as a catalyst. The nature, morphology and the size of the silica particles has been studied using Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and X-ray diffraction. Results indicate that the morphology, structure and the diameter of silica particles depend strongly on the molar ratios of the reactants.

Synthesis and Characterization of SiO2@Y2MoO6:Eu3+ Core–Shell Structured Spherical Phosphors by Sol–Gel Process

2016 ◽  
Vol 16 (4) ◽  
pp. 3914-3920 ◽  
Author(s):  
G. Z Li ◽  
F. H Liu ◽  
Z. S Chu ◽  
D. M Wu ◽  
L. B Yang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Annealing Temperature ◽  
Uv Light ◽  
Sol Gel ◽  
Spherical Shape ◽  
Core Shell ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Average Size

SiO2@Y2MoO6:Eu3+ core–shell phosphors were prepared by the sol–gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core–shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core–shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eu3+ shows a strong PL emission (dominated by 5D0–7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.

scholarly journals Fabrication of TiO2Nanotanks Embedded in a Nanoporous Alumina Template

2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
C. Massard ◽  
S. Pairis ◽  
V. Raspal ◽  
Y. Sibaud ◽  
K. O. Awitor
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Thermal Treatments ◽  
X Ray Diffraction ◽  
Alumina Template ◽  
Nanoporous Alumina ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Sol Gel Process

The feasibility of surface nanopatterning with TiO2nanotanks embedded in a nanoporous alumina template was investigated. Self-assembled anodized aluminium oxide (AAO) template, in conjunction with sol gel process, was used to fabricate this nanocomposite object. Through hydrolysis and condensation of the titanium alkoxide, an inorganic TiO2gel was moulded within the nanopore cavities of the alumina template. The nanocomposite object underwent two thermal treatments to stabilize and crystallize the TiO2. The morphology of the nanocomposite object was characterized by Field Emission Scanning Electron Microscopy (FESEM). The TiO2nanotanks obtained have cylindrical shapes and are approximately 69 nm in diameter with a tank-to-tank distance of 26 nm. X-ray diffraction analyses performed by Transmission Electron Microscopy (TEM) with selected area electron diffraction (SAED) were used to investigate the TiO2structure. The optical properties were studied using UV-Vis spectroscopy.

Microstructural characteristics and photoluminescence performance of nanograined thermally treated CeO2-TiO2 xerogels

2007 ◽  
Vol 22 (5) ◽  
pp. 1182-1187
Author(s):  
Amita Verma ◽  
A.K. Srivastava ◽  
N. Karar ◽  
Harish Chander ◽  
S.A. Agnihotry
Keyword(s):  
Electron Microscopy ◽  
Crystallite Size ◽  
Sol Gel ◽  
Structural Features ◽  
X Ray Diffraction ◽  
Molar Ratios ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Crystallite Sizes ◽  
Thermally Treated

Nanostructured thermally treated xerogels have been synthesized using a sol-gel process involving cerium (Ce) chloride heptahydrate and titanium (Ti) propoxide mixed in different Ce:Ti molar ratios. Structural features of the xerogels have been correlated with their photoluminescence (PL) response. The crystallite sizes in the samples lie in the nanorange. The x-ray diffraction and transmission electron microscopy results have confirmed the coexistence of CeO2 and TiO2 nanocrystallites in these xerogels. In general, a decrease in the CeO2 crystallite size and an increase in the TiO2 crystallite size are observed in the xerogels as a function of Ti content. Scanning electron microscopy results have evidenced the evolution of ordered structure in the xerogels as a function of TiO2 content. Although both of the phases (CeO2 and TiO2) have exhibited PL in ultraviolet and visible regions, the major luminescence contribution has been made by the CeO2 phase. The largest sized CeO2 crystallites in 1:1 thermally treated xerogel have led to its highest PL response. PL emission in the xerogels is assigned to their nanocrystalline nature and oxygen vacancy-related defects.

TEM Study of Rutile-Phase TiO2 Nanosheets

2013 ◽  
Vol 850-851 ◽  
pp. 156-159
Author(s):  
Xin Yan Wu ◽  
Wei Xiong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photocatalytic Activity ◽  
Energy Dispersive Spectrometer ◽  
Sol Gel ◽  
Rutile Phase ◽  
High Photocatalytic Activity ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process

TiO2 nanosheets have been successfully synthesized via a simple sol-gel process. These nanostructures were characterized by transmission electron microscopy (TEM) and x-ray energy dispersive spectrometer (EDS). The sheet-shaped single-crystalline nanostructures are pure rutile-phase structure, with landscape dimension of 10-45 nm. EDS investigation confirms that the TiO2 nanosheets are only composed of Ti and O, and the atomic ration of Ti and O is close to 1:2. High photocatalytic activity might be expected for those TiO2 nanosheets due to their large surface area.

STUDY ON SYNTHESIS AND EVOLUTION OF NANOCRYSTALLINE Mg4Ta2O9 BY AQUEOUS SOL–GEL PROCESS

2012 ◽  
Vol 19 (03) ◽  
pp. 1250024 ◽  
Author(s):  
H. T. WU ◽  
C. H. YANG ◽  
W. B. WU ◽  
Y. L. YUE
Keyword(s):  
Electron Microscopy ◽  
Solid State ◽  
Sol Gel ◽  
Phase Evolution ◽  
Solid State Method ◽  
Conventional Solid State Method ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
State Method ◽  
Size And Morphology

Nanosized and highly reactive Mg4Ta2O9 were successfully synthesized by aqueous sol–gel method compared with conventional solid-state method. Ta-Mg-citric acid solution was first formed and then evaporated resulting in a dry gel for calcination in the temperature ranging from 600°C to 800°C for crystallization in oxygen atmosphere. The crystallization process from the gel to crystalline Mg4Ta2O9 was identified by thermal analysis and phase evolution of powders was studied using X-ray diffraction (XRD) technique during calcinations. Particle size and morphology were examined by transmission electron microscopy (TEM) and high resolution scanning electron microscopy (HR-SEM). The results revealed that sol–gel process showed great advantages over conventional solid-state method and Mg4Ta2O9 nanopowders with the size of 20–30 nm were obtained at 800°C.

Sol-gel Elaboration of Porous Oxide Coatings as Interphase in SiC/SiC Ceramic Matrix Composites

2003 ◽  
Vol 775 ◽  
Author(s):  
M. Verdenelli ◽  
S. Parola ◽  
F. Chassagneux ◽  
S. Jacques ◽  
H. Vincent ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Ceramic Matrix Composites ◽  
Matrix Composites ◽  
X Ray Diffraction ◽  
Brittle Behavior ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
The Matrix ◽  
Mesoporous Oxide

AbstractCombinations of meso-, macro- and microporous coatings with a chemical composition of 90%Al2O3-10%SiO2 were elaborated on SiC Hi-Nicalon fibers using the sol-gel process. They were evaluated as porous interphase for the reinforcement of CMC. The mesoporous oxide, in contact with the fiber, allows cracks deviation whereas the macroporous one, in contact with the matrix, avoids the gaseous infiltration of the mesopores during the SiC CVD matrix process. It also prevents from oxygen diffusion during high temperature under air. The characterization of the composites was performed by SEM (scanning electron microscopy), TEM (transmission electron microscopy), X-ray diffraction, and EDS (energy dispersive spectrometry). TEM evidenced the porosity gradient as expected. A tensile test on the composites revealed brittle behavior (fracture) and no fiber debonding was observed.

Effect of TiO2 addition on the preparation of β-spodumene powders by sol-gel process

1999 ◽  
Vol 14 (1) ◽  
pp. 196-203 ◽  
Author(s):  
Moo-Chin Wang ◽  
Ming-Hong Lin ◽  
Hok-Shing Liu
Keyword(s):  
Electron Microscopy ◽  
Ph Value ◽  
Sol Gel ◽  
Gelation Time ◽  
Glass Ceramics ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Fine Glass ◽  
A Minor

This study has shown the possibility of achieving two primary considerations for the advanced fabrication of spodumene with a composition of Li2O · Al2O3 · 4SiO2 · nTiO2 (LAST) glass-ceramics by a sol-gel process, namely, an enormous reduction of sintering temperature from 1600 to 1200 °C together with the appearance of simple phases of β-spodumene/rutile as opposed to products via the conventional melting-crystallization process. Fine glass-ceramic powders with a composition of Li2O · Al2O3 · 4SiO2 (LAS) have been synthesized by the sol-gel process using Si(OC2H5)4, Al(OC2H5)3, LiOCH3, and Ti(OC2H5)4 as the starting materials. The process included well-controlled hydrolysis polycondensation of the raw alkoxides. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electron diffraction (ED) analysis were utilized to study the effect of TiO2 addition on the preparation of β-spodumene powders by the sol-gel process. The gelation time of the LAST solution increases as the TiO2 content increases. For the low (<3) or high (>11) pH value, the gelation time was shortened. At pH = 5, regardless of the TiO2 content, the gel has the longest time of gelation. When the dried gels of the LAST system are heated from 800 to 1200 °C, the crystallized samples are composed of the major phase of β-spodumene and a minor phase of rutile (TiO2).

Preparation of Alumina Powders through Pyrocatechol, Resorcinol Mediated Sol-Gel Method

2016 ◽  
Vol 850 ◽  
pp. 742-747
Author(s):  
Xiang Zhang ◽  
Ping Yun Li ◽  
Xiao De Guo ◽  
Ting Yan
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
Xrd Study ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Scanning Electron ◽  
Organic Monomer

Ultrafine alumina powders were synthesized through pyrocatechol and resorcinol mediated sol-gel process. Aluminum nitrate was applied as the Al source and PVP was the dispersant. X-ray diffraction (XRD) study displayed that γ-Al2O3 powders formed in the range of 800-900 °C, and then γ-Al2O3 transformed to α-Al2O3 at higher temperatures, pure α-Al2O3 powders could be obtained at 1000 °C by using resorcinol as organic monomer. The results of transmission electron microscopy (TEM) revealed that Al2O3 nanoparticles with γ crystalline phase had grain sizes in the range of 5-40 nm. Scanning electron microscopy (SEM) observation displayed that the morphology of the prepared α-Al2O3 powders had aggregated bodies formed by Al2O3 grains in the range of 0.2-0.5μm. These results provide a new way of preparation of alumina powders.

scholarly journals Nanofabrication of Iron-Cobalt (FeCo) Alloy by Sol-gel Method

2021 ◽  
Vol 1 (1) ◽  
pp. 111-114
Author(s):  
Majid Farahmandjou ◽  
Parastoo Khalili
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Sem Analysis ◽  
The Body ◽  
X Ray Diffraction ◽  
Body Center Cubic ◽  
Transmission Electron ◽  
Structure Morphology ◽  
Bcc Structure ◽  
Body Center

Background and Introduction: Metal oxides (MOs) have been extensively used in a large range of engineering and medical applications. Methods: FeCo nanoparticles (NPs) were successfully synthesized by the solgel method in the presence of a powerful reducing agent-sodium borohydride (NaBH4). The structure, morphology, and optical properties of NPs were analyzed by X-ray diffraction (XRD), field effect scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR) at room temperature. Results: The XRD spectrum showed the body center cubic (BCC) structure of the samples after heat treatment at 500 °C. The SEM analysis exhibited that the particle size of as-synthesized and annealed samples was approximately 40 nm and 22 nm, respectively. Conclusion: The TEM investigations showed the rod-shaped sample of annealed NPs. The optical studies of the FTIR analysis revealed the starching bound of Fe-Co at the frequencies of 673 cm-1, 598 cm-1, and 478 cm-1.

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