TEM observation of iron oxide pillars in montmorillonite

1990 ◽  
Vol 48 (4) ◽  
pp. 882-883
Author(s):  
H. Mori ◽  
Y. Murata ◽  
H. Yoneyama ◽  
H. Fujita
Keyword(s):  
Aqueous Solution ◽  
Iron Oxide ◽  
Fine Particles ◽  
Aqueous Suspension ◽  
Volume Ratio ◽  
Exchange Capacity ◽  
Nano Composites ◽  
Pillared Montmorillonite ◽  
Topographic Features ◽  
Transmission Electron

Recently, a new sort of nano-composites has been prepared by incorporating such fine particles as metal oxide microcrystallites and organic polymers into the interlayer space of montmorillonite. Owing to their extremely large specific surface area, the nano-composites are finding wide application[1∼3]. However, the topographic features of the microstructures have not been elucidated as yet In the present work, the microstructures of iron oxide-pillared montmorillonite have been investigated by high-resolution transmission electron microscopy.Iron oxide-pillared montmorillonite was prepared through the procedure essentially the same as that reported by Yamanaka et al. Firstly, 0.125 M aqueous solution of trinuclear acetato-hydroxo iron(III) nitrate, [Fe3(OCOCH3)7 OH.2H2O]NO3, was prepared and then the solution was mixed with an aqueous suspension of 1 wt% clay by continuously stirring at 308 K. The final volume ratio of the latter aqueous solution to the former was 0.4. The clay used was sodium montmorillonite (Kunimine Industrial Co.), having a cation exchange capacity of 100 mequiv/100g. The montmorillonite in the mixed suspension was then centrifuged, followed by washing with deionized water. The washed samples were spread on glass plates, air dried, and then annealed at 673 K for 72 ks in air. The resultant film products were approximately 20 μm in thickness and brown in color.

Synthesis and Characterization of Iron Oxide Nanostructured Particles in Na–Y Zeolite Matrix

2004 ◽  
Vol 19 (3) ◽  
pp. 930-936 ◽  
Author(s):  
Maxine Yee ◽  
Iskandar I. Yaacob
Keyword(s):  
Iron Oxide ◽  
Fine Particles ◽  
Gas Adsorption ◽  
Morphological Changes ◽  
X Ray Diffraction ◽  
Oxide Systems ◽  
Nanostructured Particles ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Adsorption Desorption

Formation of iron oxide nanoparticles within the internal cages of Na–Y zeolites was investigated. Sodium ions within the zeolites were replaced with iron(II) ions. Elemental composition studies showed a significant amount of iron in the exchanged sample. NaOH and dropwise additions of H2O2 at 60 °C triggered formation of zeolite–iron oxide systems. X-ray diffraction (XRD) patterns showed diminishing zeolite peaks along with evolution of peaks corresponding to γ-Fe2O3 and α-Fe2O3 with increasing NaOH concentration. Morphological changes from hexagonal-shaped zeolite to clusters of fine particles were observed under scanning electron microscope. Particles with about 15-nm diameter were detected by transmission electron microscopy. γ-Fe2O3 crystallites of 13.4 nm were determined from the broadening of XRD peaks. The magnetization curves of samples (precipitated using NaOH with concentrations of 2.0 M and above) showed absence of hysteresis and passed through the origin, indicating the particles are superparamagnetic. Gas adsorption–desorption measurement of the system precipitated with 2.0 M NaOH revealed a 26% increase in its specific surface area, indicating the presence of nanometer-sized particles within the zeolites.

Facile Enrichment and Photocatalytical Degradation of Low Concentration MB in Aqueous Solution

2011 ◽  
Vol 110-116 ◽  
pp. 2308-2315
Author(s):  
Liu Xue Zhang ◽  
Xiu Lian Wang
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Fine Particles ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Low Concentrations ◽  
Hydrolysis Of

Fine particles of photoactive anatase-type TiO2, prepared by hydrolysis of tetrabutyl orthotitanate and crystallized under microwave (MV) irradiation, were loaded on adsorbent support attapulgite (ATP). The prepared hybrids TiO2-ATP were characterized with transmission electron microscopy (TEM), selected-area electron diffraction (SAED), and X-ray diffraction (XRD) and photoactivity properties were evaluated separately. The substrates of target were adsorbed on the adsorbent support, and then a high concentration environments of the substrate was formed around the loaded TiO2, resulting in an increase in the photodestruction rate. One of the most interesting features of the resulting catalysts with low titania contain (<30%) is their fast decantability in comparison with that of TiO2. This way one of the most important drawbacks of photocatalysis, the catalysts separation from the solution, was overcome by simple sedimentation and decantation. The low concentrations MB may be removed through enrichment and photodegradation using the prepared TiO2-ATP photocatalyst.

scholarly journals Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy

Pharmaceutics ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1843
Author(s):  
Michał Żuk ◽  
Weronika Gawęda ◽  
Agnieszka Majkowska-Pilip ◽  
Magdalena Osial ◽  
Marcin Wolski ◽  
...  
Keyword(s):  
Iron Oxide ◽  
High Surface ◽  
Volume Ratio ◽  
Superparamagnetic Iron Oxide ◽  
Ovarian Cancer Cells ◽  
Shell Nanoparticles ◽  
Transmission Electron ◽  
Cancer Tissues ◽  
Core Shell Nanoparticles

Superparamagnetic iron oxide nanoparticles (SPIONs) are widely used for biomedical applications for their outstanding properties such as facile functionalization and doping with different metals, high surface-to-volume ratio, superparamagnetism, and biocompatibility. This study was designed to synthesize and investigate multifunctional nanoparticle conjugate to act as both a magnetic agent, anticancer immunological drug, and radiopharmaceutic for anticancer therapy. The carrier, 166Ho doped iron oxide, was coated with an Au layer, creating core-shell nanoparticles ([166Ho] Fe3O4@Au. These nanoparticles were subsequently modified with monoclonal antibody trastuzumab (Tmab) to target HER2+ receptors. We describe the radiobioconjugate preparation involving doping of a radioactive agent and attachment of the organic linker and drug to the SPIONs’ surface. The size of the SPIONs coated with an Au shell measured by transmission electron microscopy was about 15 nm. The bioconjugation of trastuzumab onto SPIONs was confirmed by thermogravimetric analysis, and the amount of two molecules per one nanoparticle was estimated with the use of radioiodinated [131I]Tmab. The synthesized bioconjugates showed that they are efficient heat mediators and also exhibit a cytotoxic effect toward SKOV-3 ovarian cancer cells expressing HER2 receptors. Prepared radiobioconjugates reveal the high potential for in vivo application of the proposed multimodal hybrid system, combined with magnetic hyperthermia and immunotherapy against cancer tissues.

Immobilization of ZnO Suspension on Glass Substrate to Remove Filtration During the Removal of Remazol Red R from Aqueous Solution

2016 ◽  
Vol 12 (6) ◽  
pp. 4127-4133
Author(s):  
Nazmul Kayes ◽  
Jalil Miah ◽  
Md. Obaidullah ◽  
Akter Hossain ◽  
Mufazzal Hossain
Keyword(s):  
Aqueous Solution ◽  
Glass Substrate ◽  
Uv Light ◽  
Aqueous Suspension ◽  
Light Irradiation ◽  
Zno Films ◽  
Light Sources ◽  
Zno Film ◽  
Semiconductor Oxides ◽  
Remazol Red

Photodegradation of textile dyes in the presence of an aqueous suspension of semiconductor oxides has been of growing interest. Although this method of destruction of dyes is efficient, the main obstacle of applying this technique in the industry is the time and cost involving separation of oxides from an aqueous suspension. In this research, an attempted was made to develop ZnO films on a glass substrate by simple immobilization method for the adsorption and photodegradation of a typical dye, Remazol Red R (RRR) from aqueous solution. Adsorption and photodegradation of  RRR were performed in the presence of glass supported ZnO film. Photodegradation of the dye was carried out by varying different parameters such as the catalyst dosage, initial concentrations of RRR, and light sources. The percentage of adsorption as well as photodegradation increased with the amount of ZnO, reaches a maximum and then decreased. Maximum degradation has been found under solar light irradiation as compared to UV-light irradiation. Removal efficiency was also found to be influenced by the pre-sonication of ZnO suspension.

scholarly journals Obtaining Silicon Oxide Nanoparticles Doped with Fluorine and Gold Particles by the Pulsed Plasma-Chemical Method

2019 ◽  
Vol 2019 ◽  
pp. 1-6
Author(s):  
Galina Kholodnaya ◽  
Roman Sazonov ◽  
Denis Ponomarev ◽  
Igor Zhirkov
Keyword(s):  
Chemical Synthesis ◽  
Silicon Oxide ◽  
Fine Particles ◽  
Chemical Reactor ◽  
Beam Diameter ◽  
Pulsed Plasma ◽  
Plasma Chemical ◽  
Plasma Chemical Synthesis ◽  
Transmission Electron ◽  
Average Size

This paper presents a study on pulsed plasma-chemical synthesis of fluorine- and gold-doped silicon oxide nanopowder. The gold- and fluorine-containing precursors were gold chloride (AuCl3) and sulphur hexafluoride (SF6). Pulsed plasma-chemical synthesis is realized on the laboratory stand, including a plasma-chemical reactor and TEA-500 electron accelerator. The parameters of the electron beam are as follows: 400–450 keV electron energy, 60 ns half-amplitude pulse duration, up to 200 J pulse energy, and 5 cm beam diameter. We confirmed the composite structure of SixOy@Au by using transmission electron microscopy and energy-dispersive spectroscopy. We determined the chemical composition and morphology of synthesized SixOy@Au and SixOy@F nanocomposites. The material contained a SixOy@Au carrier with an average size of 50–150 nm and a shell of fine particles with an average size of 5–10 nm.

scholarly journals Synthesis of a thermoresponsive crosslinked MEO2MA polymer coating on microclusters of iron oxide nanoparticles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Alejandro Lapresta-Fernández ◽  
Alfonso Salinas-Castillo ◽  
Luis Fermín Capitán-Vallvey
Keyword(s):  
Iron Oxide ◽  
Synthesis Temperature ◽  
Water Soluble ◽  
Covalent Attachment ◽  
Solution Temperature ◽  
Tetraethylene Glycol ◽  
Critical Solution Temperature ◽  
Large Size ◽  
Transmission Electron ◽  
Azo Initiator

AbstractEncapsulation of magnetic nanoparticles (MNPs) of iron (II, III) oxide (Fe3O4) with a thermopolymeric shell of a crosslinked poly(2-(2-methoxyethoxy)ethyl methacrylate) P(MEO2MA) is successfully developed. Magnetic aggregates of large size, around 150–200 nm are obtained during the functionalization of the iron oxide NPs with vinyl groups by using 3-butenoic acid in the presence of a water soluble azo-initiator and a surfactant, at 70 °C. These polymerizable groups provide a covalent attachment of the P(MEO2MA) shell on the surface of the MNPs while a crosslinked network is achieved by including tetraethylene glycol dimethacrylate in the precipitation polymerization synthesis. Temperature control is used to modulate the swelling-to-collapse transition volume until a maximum of around 21:1 ratio between the expanded: shrunk states (from 364 to 144 nm in diameter) between 9 and 49 °C. The hybrid Fe3O4@P(MEO2MA) microgel exhibits a lower critical solution temperature of 21.9 °C below the corresponding value for P(MEO2MA) (bulk, 26 °C). The MEO2MA coating performance in the hybrid microgel is characterized by dynamic light scattering and transmission electron microscopy. The content of preformed MNPs [up to 30.2 (wt%) vs. microgel] was established by thermogravimetric analysis while magnetic properties by vibrating sample magnetometry.

Preparation and Characterization of Ultrafine Monodisperse Iron Oxide Nanoparticles by Solvothermal Method

2015 ◽  
Vol 748 ◽  
pp. 93-96
Author(s):  
Cheng Mei Liu ◽  
Yu Xia Zhao ◽  
Jin Dong ◽  
Lu Hai Li ◽  
Yen Wei ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Iron Oxide Nanoparticles ◽  
Solvothermal Method ◽  
Physical Property Measurement System ◽  
Thermo Gravimetric Analysis ◽  
Physical Property ◽  
Oxide Nanoparticles ◽  
Gravimetric Analysis ◽  
Transmission Electron ◽  
Different Diameters

Using iron-oleate complex as a precursor, oleic acid as a stabilizer and 1-octadecene as a reductant, uniform-sized and highly monodisperse iron oxide nanoparitcles with different diameters were successfully synthesized via solvothermal method by changing reaction time. Transmission electron microscope (TEM), thermo-gravimetric analysis (TGA), fourier transform infrared spectroscopy (FT-IR), physical property measurement system (PPMS) and dynamic light scattering (DLS) was used to characterize obtained iron oxide nanoparticles. These results indicated that iron oxide nanoparitcles with the diameter ranging from 4 to 8 nm can be controllably synthesized.

High Cr(VI) Adsorption Performance of Coal-Based Activated Carbon in Aqueous Solution

2013 ◽  
Vol 798-799 ◽  
pp. 1123-1127
Author(s):  
Hua Lei Zhou ◽  
Qiong Qiong Zhu ◽  
Dong Hua Huang
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Pore Structure ◽  
Ph Value ◽  
High Surface ◽  
High Surface Area ◽  
Koh Activation ◽  
Transmission Electron ◽  
Mesoporous Adsorbent ◽  
Initial Ph

The activated carbon with high surface area was prepared by KOH activation from anthracite and used as adsorbent for removal of Cr (VI) from aqueous solution. The pore structure and surface properties were characterized by N2 adsorption at 77K, transmission electron microscope (TEM) and Fourier transform infrared spectroscopy ( FTIR). Effect of pH and isotherms at different temperature were investigated. Results show that the prepared carbon is a microporous-and mesoporous-adsorbent with developed pore structure and abundant surface oxygen-containing groups. PH value of the solution plays key function on the adsorption. The chemical adsorption dominates the adsorption process. The activated carbon exhibits much higher Cr adsorption capacity than the commercial activated carbon at initial pH of ~3. The equilibrium adsorption data are fitted by both Freundlich model and Langmuir model well.

Dissolution Characteristics and Morphology of Large-sized Scorodite Particles Synthesized from Fe(II) and As(V) in Aqueous Solution

2012 ◽  
Vol 31 (4-5) ◽  
pp. 451-458 ◽  
Author(s):  
S. Fujieda ◽  
K. Shinoda ◽  
T. Inanaga ◽  
M. Abumiya ◽  
S. Suzuki
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Surface Defects ◽  
Atmospheric Temperature ◽  
Orthorhombic Structure ◽  
X Ray ◽  
Long Term Storage ◽  
Transmission Electron ◽  
Term Storage

AbstractA novel process for preparing scorodite particles with a diameter of approximately 20 µm from Fe(II) and As(V) in aqueous solution has been developed by DOWA Metals and Mining. In the present study, the dissolution characteristics of iron and arsenic from the scorodite particles synthesized by this process have been investigated under different conditions. The results show that the concentration of arsenic dissolved from the particles in aqueous solution is very low, but it has a complicated dependence on the temperature and pH of the solution. Transmission electron microscopy (TEM) with an energy dispersive X-ray spectrometer (EDS) was used to analyze the morphology, structure, and composition of the scorodite particles. The results indicate that the scorodite particles exhibit a nearly octahedral shape with planes composed of almost (111) planes in the orthorhombic structure. The concentration of iron at the surface of the particles is higher than that of iron inside of the particles. This characteristic morphology, along with the minimal surface defects of the scorodite particles, is considered to be responsible for the low dissolution of arsenic from the particles in aqueous solution. Atmospheric temperature and solution conditions were also found to be important for the safe, long-term storage of arsenic using scorodite particles.

In-Situ Transmission Electron Microscopy of the Formation of Metal-Semiconductor Contacts

1990 ◽  
Vol 181 ◽  
Author(s):  
J. M. Gibson ◽  
D. Loretto ◽  
D. Cherns
Keyword(s):  
High Surface ◽  
High Vacuum ◽  
Volume Ratio ◽  
Ultra High Vacuum ◽  
Silicon Surfaces ◽  
Transmission Electron ◽  
Metal Silicides ◽  
Phase Sequence ◽  
Semiconductor Contacts

ABSTRACTWe have studied the formation of metal silicides in-situ in an ultra-high vacuum transmission electron microscope. Metals were deposited on in-situ cleaned, reconstructed silicon surfaces and annealed. For the metals Ni and Co, we find that the phase sequence in ultra-thin films is different from that seen in ≈1000 Å thick films, and attribute this to the high surface-to-volume ratio. In general reactions occur at room temperature, to form an epitaxial phase if possible. We report preliminary new results on the formation of Pd2Si.

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