scholarly journals Synergistic effect of antitumor activity of doxorubicin and bicomponent nanostructures based on aluminum oxide

2020 ◽  
Vol 19 (2) ◽  
pp. 82-89
Author(s):  
O. V. Bakina ◽  
N. V. Svarovskaya ◽  
A. A. Miller ◽  
A. S. Lozhkomoev ◽  
A. V. Avgustinovich ◽  
...  
Keyword(s):  
Synergistic Effect ◽  
Biomedical Application ◽  
Chemical Properties ◽  
Integrated System ◽  
X Ray Diffraction ◽  
Joint Application ◽  
Transmission Electron ◽  
Combined Use ◽  
Low Toxicity ◽  
Physical And Chemical

Introduction. There are high-thech methods of nanoparticle production with controlled morphology and physical and chemical properties. Alumina-based mesoporous nanostructures have low toxicity and biocompatibility. FDI recommends alumina for biomedical application. Alumina inhibits the grow of cancer due to positive zeta-potential and low solubility in water. We observed the synergistic effect of joint application of doxorubicin and nanostructures. This approach reduces drug concentration and its toxicity.Purpose: to synthesize nanostructures with different surface potentials and to study toxicity of these nanostructures alone and in combination with doxorubicin.Material and Methods. The alumina-based nanostructures were obtained by the hydrolysis of nanopowder. The morphology of nanostructures was investigated by transmission electron microscopy with an integrated system of energy dispersive analysis. The phase composition of the particles was determined by x-ray diffraction. The effect of the synthesized nanostructures on the viability of cell lines was determined using the MTT test.Results. The synthesized nanostructures have a low toxicity and can be used as an adjuvant for doxorubicin.Conclusion. The combined use of doxorubicin and bicomponent nanostructures leads to an increase in the damaging effect of doxorubicin on Neuro-2a cells.

scholarly journals The Influence Of NO/O2 On The NOx Storage Properties Over A Pt-Ba-Ce/γ-Al2O3 Catalyst

2019 ◽  
Vol 17 (1) ◽  
pp. 1459-1465
Author(s):  
Xuedong Feng ◽  
Jing Yi ◽  
Peng Luo
Keyword(s):  
Sol Gel ◽  
Chemical Properties ◽  
No Oxidation ◽  
Test Results ◽  
X Ray Diffraction ◽  
Storage Performance ◽  
Transmission Electron ◽  
Temperature Programmed ◽  
Physical And Chemical ◽  
Al2o3 Catalyst

AbstractWith the purpose of studying the influence of NO/O2 on the NOx storage activity, a Pt-Ba-Ce/γ-Al2O3 catalyst was synthesized by an acid-aided sol-gel method. The physical and chemical properties of the catalyst were characterized by X-ray diffraction (XRD) and Transmission Electron Microscope (TEM) methods. The results showed that the composition of the catalyst was well-crystallized and the crystalline size of CeO2 (111) was about 5.7 nm. The mechanism of NO and NO2 storage and NOx temperature programmed desorption (NO-TPD) experiments were investigated to evaluate the NOx storage capacity of the catalyst. Pt-Ba-Ce/γ-Al2O3 catalyst presented the supreme NOx storage performance at 350℃, and the maximum value reached to 668.8 μmol / gcat. Compared with O2-free condition, NO oxidation to NO2 by O2 had a beneficial effect on the storage performance of NOx. NO-TPD test results showed that the NOx species stored on the catalyst surface still kept relatively stable even below 350℃.

Synthesis and Characterization of Cassava Starch Nanocrystals by Hydrolysis Method

2015 ◽  
Vol 1113 ◽  
pp. 446-452 ◽  
Author(s):  
Nur Shazrynda Md Shahrodin ◽  
Abdul Razak Rahmat ◽  
Agus Arsad
Keyword(s):  
Chemical Properties ◽  
Cassava Starch ◽  
High Yield ◽  
X Ray Diffraction ◽  
Hydrolysis Method ◽  
Transmission Electron ◽  
Hydrolysis Process ◽  
20 Nm ◽  
Physical And Chemical ◽  
Starch Nanocrystals

Cassava starch nanocrystals (CSN) has not been reported in open literature, although other starches such as rice, corn, potato and bean were widely used as the main material. Thus, the objective of this research was to investigate the possibility of synthesizing high yield of CSN at different concentration of sulphuric acid (H2SO4). The physical and chemical properties of synthesize CSN was also investigated. Synthesized CSN was prepared by hydrolysing native cassava starch (NCS) with several concentration of H2SO4 (2.8 M, 3.0 M, 3.2 M and 3.4 M). The acid hydrolysis process took five days with continuous stirring speed of 300 to 400 rpm, with constant temperature of 37 °C. The hydrolysed solution of CSN underwent centrifuging process with distilled water until neutral to make sure that no acid residues remain in the CSN solution. The CSN precipitate was dried in an oven over night at 60 °C. The highest yield (1.1 %) produced was from 3.4 M CSN. Morphology test by Transmission Electron Microscopy indicated that the samples have been destructed and degraded to be nanocrystals with a size range of 5 - 20 nm. X-ray Diffraction (XRD) and 13C Nuclear Magnetic Resonance (NMR) were used to indicate the type of crystallinity for both NCS and CSN.

Preparation of Pd/γ-Al2O3 Nanocatalyst and Characterization by X-Ray Diffraction and Transmission Electron Microscope

2013 ◽  
Vol 685 ◽  
pp. 312-315
Author(s):  
Karim. H. Hassan
Keyword(s):  
Electron Microscope ◽  
Transmission Electron Microscope ◽  
Selective Hydrogenation ◽  
Chemical Properties ◽  
Impregnation Method ◽  
Activated Alumina ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Physical And Chemical

In petrochemical industry, and mainly in ethylene production plants, acetylene presents in trace amount in ethylene gas and causes a serous problems owing to it is higher activity and being explosive at certain concentration limits with air, so it has to be converted to ethylene in selective hydrogenation. Three selective hydrogenation nanocatalysts Pd/γ-Al2O3 that contain 0.03 %, 0.05% and 0.07 wt % of palladium loaded on activated alumina were prepared by impregnation method. They were characterized for physical and chemical properties and structurally by X-ray diffraction, metal dispersion, and transmission electron microscope.

Mineralogy of volcanically derived alluvial soils at Moshi, Tanzania

Soil Research ◽  
2016 ◽  
Vol 54 (8) ◽  
pp. 926
Author(s):  
T. S. Taylor ◽  
J. C. Hughes ◽  
L. W. Titshall
Keyword(s):  
Electron Microscopy ◽  
Clay Fraction ◽  
Chemical Properties ◽  
Volcanic Glass ◽  
X Ray Diffraction ◽  
Surface Areas ◽  
Transmission Electron ◽  
Physical And Chemical ◽  
Extractable Iron ◽  
And Chemical Properties

Despite intensive commercial agriculture in the rift zone of Tanzania, mineralogical studies on the soils influenced by volcanic parent materials are scarce. A mineralogical investigation of the soils and two buried ash layers from an irrigated sugar estate was undertaken using X-ray diffraction, transmission electron microscopy and measurements of extractable iron, aluminium and silicon and the specific surface area (SSA) of the clay fraction. The dominant mineral in the sand and silt fractions was sanidine. The clay fractions contained mainly high-defect kaolin, illite and K-feldspar, with small amounts of calcite, talc and gibbsite in some samples. Electron microscopy revealed the presence of tubular and spheroidal halloysite and <0.5µm kaolinite crystals, as well as nanocrystalline material, probably allophane, and volcanic glass. The amounts of ferrihydrite (0.34–1.84%) and allophane (0.52–6.84%) were low in the soils but higher in the buried ash layers. The surface areas of the clay fractions were high (up to 145m2g–1) and it was calculated that 5% allophane constituted 22% of the total SSA. Although all soils were dominated by halloysite and small kaolinite particles, it is likely that the small amounts of allophane with high SSA has a strong effect on their physical and chemical properties.

Synthesis and Properties of Iron-Based Magnetic Nanoparticles

2016 ◽  
Vol 712 ◽  
pp. 282-287
Author(s):  
Nikita Sashko ◽  
Elena Vaitulevich ◽  
Tatiana Yurmazova
Keyword(s):  
Magnetic Field ◽  
Magnetic Measurements ◽  
Water Solution ◽  
Chemical Properties ◽  
Drug Carriers ◽  
Field Analysis ◽  
X Ray Diffraction ◽  
Magnetic Field Analysis ◽  
Transmission Electron ◽  
Physical And Chemical

We have obtained magnetite nanoparticles (MNP) by using chemical coprecipitation of Fe2+ and Fe3+ in water solution. The size of these particles was less than 9 nm, and they possessed corresponding physical and chemical properties. Citric acid was used to stabilize magnetite particles suspension. The acid was affixed to the surface of the particles by adding it in fresh MNP solution during synthesis. Affixing carboxyl groups on the surface of MNP not only does improve particles' dispersion in solvent, but also allows adding further modifications to their surface. The properties of the particles' microstructure and morphology were determined with X-Ray diffraction (XRD) and transmission electron microscopy (TEM), whereas their magnetic properties were determined by means of automated pulse magnetic field analysis equipment. Magnetic measurements have shown that saturation magnetization was 94 emu/g with nanoparticles being at room temperature. We have also researched possible application of these particles as drug carriers by determining doxorubicin sorption capacity on the surface of MNPs. These MNPs have proven to have perspective ability to be a magnetic field-controlled carrier for cancer-treating drugs. The obtained particles can also potentially be used as a contrast medium for MRI.

scholarly journals Structural Characterizations of Palladium Clusters Prepared by Polyol Reduction of [PdCl4]2−Ions

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Loredana Schiavo ◽  
Lucrezia Aversa ◽  
Roberta Tatti ◽  
Roberto Verucchi ◽  
Gianfranco Carotenuto
Keyword(s):  
Photoelectron Spectroscopy ◽  
Chemical Properties ◽  
Nucleating Agent ◽  
X Ray Diffraction ◽  
Palladium Clusters ◽  
X Ray ◽  
Transmission Electron ◽  
Hydrogen Technology ◽  
Physical And Chemical

Palladium nanoparticles are of great interest in many industrial fields, ranging from catalysis and hydrogen technology to microelectronics, thanks to their unique physical and chemical properties. In this work, palladium clusters have been prepared by reduction of [PdCl4]2−ions with ethylene glycol, in the presence of poly(N-vinyl-2-pyrrolidone) (PVP) as stabilizer. The stabilizer performs the important role of nucleating agent for the Pd atoms with a fast phase separation, since palladium atoms coordinated to the polymer side-groups are forced at short distances during nucleation. Quasispherical palladium clusters with a diameter of ca. 2.6 nm were obtained by reaction in air at 90°C for 2 hours. An extensive materials characterization by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and other characterizations (TGA, SEM, EDS-SEM, and UV-Vis) has been performed in order to evaluate the structure and oxidation state of nanopalladium.

Influence of tungsten sources on the synthesis and properties of ammonium dioxothiotungstate

2010 ◽  
Vol 64 (1) ◽  
Author(s):  
Yunfei Bi ◽  
Shuangqin Zeng ◽  
Dadong Li ◽  
Hong Nie
Keyword(s):  
Tungsten Oxide ◽  
Chemical Properties ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Detailed Characteristic ◽  
Temperature Programmed ◽  
Physical And Chemical ◽  
And Chemical Properties

AbstractAmmonium dioxothiotungstate was synthesized using different tungsten sources and characterized in detail by powder X-ray diffraction, energy dispersive X-ray spectrometry, transmission electron microscopy, nitrogen adsorption, and temperature-programmed sulfidation. It was found that tungsten oxide nanobelts are superior to ammonium metatungstate as tungsten source for the synthesis of ammonium dioxothiotungstate due to a time-consuming aging step being excluded from the synthesis route. Moreover, detailed characteristic data reveal that, when tungsten oxide nanobelts are used, the physical and chemical properties of the resulting ammonium dioxothiotungstate including particles size, specific surface area, and sulfidation pattern were improved. Also, the hydrodesulfurization measurements showed higher catalytic activity and balanced selectivity of the resulting ammonium dioxothiotungstate.

Synthesis of Cadmium Telluride Nanoparticles Using Thioglycolic Acid, Thioglycerol, and L-Cysteine

2021 ◽  
Vol 21 (7) ◽  
pp. 4073-4076
Author(s):  
Insol Jo ◽  
Jeong Won Kang ◽  
Ki-Sub Kim
Keyword(s):  
Cadmium Telluride ◽  
Thioglycolic Acid ◽  
Chemical Properties ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Cdte Nanoparticles ◽  
Transmission Electron ◽  
Face Centered ◽  
Physical And Chemical

Cadmium telluride (CdTe) nanoparticles (NPs) are known for their unique physical and chemical properties. NP synthesis via a size-controlled procedure has become an intriguing research topic because NPs exhibit novel optical and physical properties depending on their size. Their sizes and properties can vary depending on the types and concentrations of stabilizers, which are bound to the surface of the NPs and protect the NPs from aggregation. In this study, we synthesized CdTe NPs stabilized by thioglycolic acid (TGA), 1-thioglycerol (TGC), and L-cysteine (L-C). The ratio of stabilizer to Cd2+ was 1:2.4. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and photoluminescence (PL) were employed for characterization of the NPs. The average sizes of the synthesized NPs were 4.2, 4.1, and 3.7 nm for TGA, TGC, and L-C, respectively. The maximum fluorescent emission peaks of the three NP solutions were at 554.9, 551.6, and 538.3 nm for TGA, TGC, and L-C, respectively. The produced particles were crystalline in structure with a face-centered cubic (fcc) system.

Synthesis and Characterization of Zn doped Li(Li0.21Mn0.54Ni0.125Co0.125)O2 as the Layer Materials For Battery Applications

2018 ◽  
Vol 21 (2) ◽  
pp. 127-131
Author(s):  
S. Rumh. Kadhim ◽  
Reihan Etefagh ◽  
H. Arabi
Keyword(s):  
Infrared Spectroscopy ◽  
Chemical Elements ◽  
Sol Gel ◽  
Chemical Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Physical And Chemical ◽  
And Chemical Properties

In this paper, pure and impure nanopowders of Li(Li0.021Mn0.54Ni0.125Co0.125)O2 were prepared with different percentages (x=0.02%, 0.05%, 0.075%, 0.10%) of Zn impurity by sol-gel method, and the effect of different percentages were investigated on the structural, physical and chemical properties of the samples. These properties of samples characterized by X-ray diffraction (XRD), field-scattering microscopy (FESEM), X-ray energy spectroscopy (EDS), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential thermal analysis (DTA), infrared spectroscopy (FTIR), and the results of characterization were investigation. All the reflection peaks indicate that the samples have standard α-NaFeO2 layered structure with the space group R3m, except for the super lattice ordering between 22°-25°.The FESEM images have shown that these nanoparticles have Hexagonal structures for doped and undoped nanopowders. The particle size of nanopowders in the range of 30-80 nm the chemical analysis of EDS has proven the presence of Zn in the samples. TG /DTA measurements showed weight loss in pure and impure of nanopowders. In infrared spectroscopy (FTIR), the connection bonds and chemical elements used in these nanopowders have been investigated.

Monitoring of Fluctuations in the Physical and Chemical Properties of a High-Calcium Fly Ash

1987 ◽  
Vol 113 ◽  
Author(s):  
Scott Schlorholtz ◽  
Ken Bergeson ◽  
Turgut Demirel
Keyword(s):  
Fly Ash ◽  
Chemical Properties ◽  
Operating Conditions ◽  
Physical And Chemical Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Morphological Studies ◽  
High Calcium ◽  
Physical And Chemical ◽  
And Chemical Properties

ABSTRACTThe physical and chemical properties of fly ash produced at Ottumwa Generating Station have been monitored since April, 1985. The fly ash is produced from burning a low sulfur, sub-bituminous coal obtained from the Powder River Basin near Gillette, Wyoming. One-hundred and sixty samples of fly ash were obtained during the two year period. All of the samples were subjected to physical testing as specified by ASTM C 311. About one-hundred of the samples were also subjected to a series of tests designed to monitor the self-cementing properties of the fly ash. Many of the fly ash samples were subjected to x-ray diffraction and fluorescence analysis to define the mineralogical and chemical composition of the bulk fly ash as a function of sampling date. Hydration products in selected hardened fly ash pastes, were studied by x-ray diffraction and scanning electron microscopy. The studies indicated that power plant operating conditions influenced the compressive strength of the fly ash paste specimens. Mineralogical and morphological studies of the fly ash pastes indicated that stratlingite formation occurred in the highstrength specimens, while ettringite was the major hydration product evident in the low-strength specimens.

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