scholarly journals A STUDY OF THE SYNTHESIS OF HYBRID ORGANOSILICATE NANOTUBES

2010 ◽  
Vol 5 (2) ◽  
pp. 83-86
Author(s):  
Eko Sri Kunarti ◽  
Grainne M Moran
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Room Temperature ◽  
Sol Gel ◽  
Tetraethyl Orthosilicate ◽  
Physical Characteristics ◽  
Ammonium Tartrate ◽  
Tube Forming ◽  
Controlled Hydrolysis ◽  
Scanning Electron

Hybrid organosilicate nanotubes have been prepared by sol-gel chemistry, using crystalline ammonium tartrate as the tube-forming template. The nanotubes were prepared by controlled hydrolysis and co-condensation of tetraethyl orthosilicate (TEOS) and methyltriethoxysilane (MTES) at room temperature. The synthetic conditions have been systematically studied. The physical characteristics of the materials were examined by scanning electron microscopy (SEM) and the aging times of the tubes due to slow post-gelation condensation reactions was investigated. The morphology and microstructure of the nanotubes are greatly influenced by the synthetic conditions.   Keywords: organosilicate, nanotube, ammonium tartrate crystals.

Antitumoral drug loaded in TEOS nanoparticles

2012 ◽  
Vol 1498 ◽  
pp. 9-14 ◽  
Author(s):  
Ana Paula V. Araújo ◽  
Claure N. Lunardi ◽  
Anderson J. Gomes
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Slow Release ◽  
Sol Gel ◽  
Aqueous Media ◽  
Tetraethyl Orthosilicate ◽  
Mean Diameter ◽  
Immunomodulating Drug ◽  
Distribution Studies ◽  
Scanning Electron

ABSTRACTMethotrexate (MTX), is a potent immunomodulating drug and widely used in the treatment of cancer, psoriasis and others disease. Despite its efficacy, the use of MTX is greatly limited due to its toxicity. To solve this problem, we prepared nanoparticles of tetraethyl orthosilicate (NP-TEOS) containing the compound methotrexate (MTX), by the sol-gel method. This drug delivery system (DDS) showed a loading efficiency of 39.7%. Size distribution studies were performed with dynamic light scattering and scanning electron microscopy revealing that these particles were spherical in shape, with a mean diameter between 140-430 nm and a low polydispersity (0.12 – 0.26). Also the particles displayed a low tendency toward aggregation which was confirmed by the low zeta potential -61.4 mV. Profile release showed a slow release loaded with MTX (PBS buffer pH = 7.4). The slow release can be attributed to the low porosity of the NP-TEOS and the extremely low diffusivity of MTX in aqueous media. B16-F10 cells were used to assay the toxicity and uptake of NP-TEOS showing to be nontoxic without MTX making a good candidate for DDS.

Influence of sintering technique on the characteristics of Li–Co nanoferrites

2017 ◽  
Vol 31 (33) ◽  
pp. 1750314 ◽  
Author(s):  
Maisnam Victory ◽  
Mamata Maisnam ◽  
Sumitra Phanjoubam
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Dielectric Constant ◽  
Room Temperature ◽  
Sol Gel ◽  
Conventional Technique ◽  
Vibrating Sample Magnetometer ◽  
Microstructural Properties ◽  
Room Temperature Dielectric Constant ◽  
Scanning Electron

Li–Co nanoferrites (Li[Formula: see text]Co[Formula: see text]Fe[Formula: see text]O4) with x = 0.00, 0.03, 0.06, 0.09, and 0.12, were synthesized by chemical sol–gel method. Two different sintering techniques viz. conventional technique (CT) and microwave technique (MT) were employed to heat treat the synthesized samples with an aim to study the effect of sintering technique on the properties of the nanoferrites. Structural and microstructural properties of the samples were investigated using XRD and scanning electron microscopy (SEM) technique, respectively. The variation of room temperature dielectric constant and dielectric loss were measured as a function of frequency in the range 100 Hz–1 MHz and the normal dispersive behavior was observed. Magnetic properties were investigated using Vibrating Sample Magnetometer (VSM), while Soohoo’s method was used to measure Curie temperature. The results obtained have been discussed in the paper.

Preparation of Silicon Dioxide Fiber via Sol-Gel Process

2008 ◽  
Vol 368-372 ◽  
pp. 794-796
Author(s):  
Xiao Hui Wang ◽  
Xiao Ping Liang ◽  
Shao Bo Xin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrochloric Acid ◽  
Silicon Dioxide ◽  
Sol Gel ◽  
Tetraethyl Orthosilicate ◽  
Molar Ratio ◽  
Sol Gel Process ◽  
Different Temperatures ◽  
Scanning Electron

Silicon dioxide gel fibers were prepared by hydrolysis reaction of tetraethyl orthosilicate (TEOS). TEOS was used as basic materials, anhydrous ethanol (EtOH) as solvent and hydrochloric acid (HCl) as the catalyst. The best proportion of the chosen materials (TEOS, EtOH, H2O and HCl) was 1:1:1.5:0.03(molar ratio).Gel fibers were investigated by thermogravimetry (TG). Silicon dioxide fibers were obtained by treating the gel fibers at different temperatures. The calcined fibers were characterized by scanning electron microscopy (SEM). The optimal sintering schedule was obtained. Silicon dioxide fiber dried at 200°C for 1 hour then calcined at 800°C for 3 hours was the best.

Scanning Electron Microscopy-cuticular Lesions on the Roundworm Ascaris Suum

1970 ◽  
Vol 28 ◽  
pp. 114-115
Author(s):  
P. A. Madden ◽  
W. R. Anderson
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Freeze Drying ◽  
Room Temperature ◽  
Secondary Electron ◽  
Distilled Water ◽  
Freeze Dried ◽  
Silver Paint ◽  
To Come ◽  
Scanning Electron

The intestinal roundworm of swine is pinkish in color and about the diameter of a lead pencil. Adult worms, taken from parasitized swine, frequently were observed with macroscopic lesions on their cuticule. Those possessing such lesions were rinsed in distilled water, and cylindrical segments of the affected areas were removed. Some of the segments were fixed in buffered formalin before freeze-drying; others were freeze-dried immediately. Initially, specimens were quenched in liquid freon followed by immersion in liquid nitrogen. They were then placed in ampuoles in a freezer at −45C and sublimated by vacuum until dry. After the specimens appeared dry, the freezer was allowed to come to room temperature slowly while the vacuum was maintained. The dried specimens were attached to metal pegs with conductive silver paint and placed in a vacuum evaporator on a rotating tilting stage. They were then coated by evaporating an alloy of 20% palladium and 80% gold to a thickness of approximately 300 A°. The specimens were examined by secondary electron emmission in a scanning electron microscope.

SEM Observations on the Germination of Euonymous Americanus

1985 ◽  
Vol 43 ◽  
pp. 508-509
Author(s):  
D.R. Hill ◽  
J.R. McCurry ◽  
L.P. Elliott ◽  
G. Howard
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Light Microscopy ◽  
Filter Paper ◽  
Room Temperature ◽  
Food Source ◽  
Environmental Chamber ◽  
Dormant Stage ◽  
Scanning Electron

Germination of Euonymous americanus in the laboratory has previously been unsuccessful. Ability to germinate Euonymous americanus. commonly known as the american strawberry bush, is important in that it represents a valuable food source for the white-tailed deer. Utilizing the knowledge that its seeds spend a period of time in the rumin fluid of deer during their dormant stage, we were successful in initiating germination. After a three month drying period, the seeds were placed in 25 ml of buffered rumin fluid, pH 8 at 40°C for 48 hrs anaerobically. They were then allowed to dry at room temperature for 24 hrs, placed on moistened filter paper and enclosed within an environmental chamber. Approximately four weeks later germination was detected and verified by scanning electron microscopy; light microscopy provided inadequate resolution. An important point to note in this procedure is that scarification, which was thought to be vital for germination, proved to be unnecessary for successful germination to occur. It is believed that germination was propagated by the secretion of enzymes or prescence of acids produced by microorganisms found in the rumin fluid since sterilized rumin failed to bring about germination.

scholarly journals Structural and optical properties of SnO2–Al2O3 nanocomposite synthesized via sol-gel route

2015 ◽  
Vol 33 (4) ◽  
pp. 714-718 ◽  
Author(s):  
Neeraj K. Mishra ◽  
Chaitnaya Kumar ◽  
Amit Kumar ◽  
Manish Kumar ◽  
Pratibha Chaudhary ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Properties ◽  
Sol Gel ◽  
Physical Interaction ◽  
X Ray Diffraction ◽  
Structural And Optical Properties ◽  
X Ray ◽  
Sensing Applications ◽  
Scanning Electron

AbstractA nanocomposite of 0.5SnO2–0.5Al2O3 has been synthesized using a sol-gel route. Structural and optical properties of the nanocomposite have been discussed in detail. Powder X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray diffraction spectroscopy confirm the phase purity and the particle size of the 0.5SnO2–0.5Al2O3 nanocomposite (13 to 15 nm). The scanning electron microscopy also confirms the porosity in the sample, useful in sensing applications. The FT-IR analysis confirms the presence of physical interaction between SnO2 and Al2O3 due to the slight shifting and broadening of characteristic bands. The UV-Vis analysis confirms the semiconducting nature because of direct transition of electrons into the 0.5SnO2–0.5Al2O3 nanocomposites.

Grain growth and sintering in Bi–(Pb)—Sr—Ca—Cu—O superconductors made by sol-gel

1994 ◽  
Vol 9 (2) ◽  
pp. 286-291 ◽  
Author(s):  
Kunsong Ma ◽  
Alain C. Pierre
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Citric Acid ◽  
Grain Growth ◽  
Sol Gel ◽  
Gel Processing ◽  
Scanning Electron

Bi—(Pb)—Sr—Ca—Cu—O superconductors were synthesized by sol-gel processing from nitrates by complexation with citric acid. Their grain growth and sintering above 800 °C were studied by Scanning Electron Microscopy (SEM) and Brunauer, Emmett, Teller (BET) porosimetry. The sintering was limited by anisotropic grain growth, and microcracks in 2212 phase grains were created due to the formation of 2223 phase.

Identification of Nd163 phase in melt-textured NdBa2Cu3O7−δ bulk samples

2003 ◽  
Vol 18 (9) ◽  
pp. 2050-2054 ◽  
Author(s):  
Marcello Gombos ◽  
Vicente Gomis ◽  
Anna Esther Carrillo ◽  
Antonio Vecchione ◽  
Sandro Pace ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscopy ◽  
Room Temperature ◽  
Polarized Light ◽  
Energy Dispersive ◽  
X Ray ◽  
Spontaneous Formation ◽  
The Stability ◽  
Scanning Electron

In this work, we report on the observation of Nd1Ba6Cu3O10,5 (Nd163) phase of the NdBaCuO system in melt-textured Nd123 bulk samples grown from a mixture of Nd123 and Nd210 phase powders. The observation was performed with polarized light optical microscopy and scanning electron microscopy–energy dispersive x-ray analyses. Images of the identified phase crystals show an aspect quite different from Nd422 crystals. Unexpectedly, Nd163 was individuated, even in “pure” Nd123 samples. Moreover, after long exposure to air, Nd163 disappeared completely in samples synthesized from powders containing Nd210. Thermogravimetry analyses of powders show that the stability of this phase in air is limited to temperatures higher than 900 °C, so Nd163 is unstable and highly reactive at room temperature. Moreover, an explanation of the observation of Nd163 in Nd210 free samples, based on the spontaneous formation of Nd163 phase in a Nd123 melt, is proposed.

Preparation of Borosilicate Xerogel and Research on its Mineralization

2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Ph Value ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Changes ◽  
Scanning Electron

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.

N-type Ba0.2Co4Sb11.5Te0.5: Optimization of thermoelectric properties by different pressures

2019 ◽  
Vol 33 (03) ◽  
pp. 1950027 ◽  
Author(s):  
Jiaxiang Chen ◽  
Xiaopeng Jia ◽  
Yuewen Zhang ◽  
Haiqiang Liu ◽  
Baomin Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Seebeck Coefficient ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Absolute Value ◽  
X Ray ◽  
Coefficient Increase ◽  
Maximum Power Factor ◽  
Scanning Electron

The polycrystalline skutterudite [Formula: see text] were successfully synthesized from 1.5 GPa to 3.5 GPa by the high pressure and high temperature (HPHT) method. Negative Seebeck coefficient confirmed the n-type conductivity of all samples. The phase compositions of samples were investigated by X-ray diffraction (XRD) and the microstructures were observed by scanning electron microscopy (SEM). It was found that the grains appeared smaller and the grain boundaries became more abundant when pressures were higher. We measured the electrical properties from room temperature to 723 K. Both the electrical resistivity and absolute value of Seebeck coefficient increase with the increasing synthetic pressure. At 723 K, the maximum power factor of [Formula: see text] was obtained for the sample synthesized under 3 GPa. The maximum ZT value of 0.61 was reached by [Formula: see text] synthesized under 3 GPa and measured at 723 K.

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