GF17608529
Tungsten
foil, not light tested, 25x25mm, thickness 0.003mm, 99.95%
Sinónimos:
Tungsten, W 000090, W
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About This Item
Productos recomendados
assay
99.95%
form
foil
manufacturer/tradename
Goodfellow 176-085-29
resistivity
4.9 μΩ-cm, 20°C
size × thickness
25 x 25 mm × 0.003 mm
bp
5660 °C (lit.)
mp
3410 °C (lit.)
density
19.3 g/mL at 25 °C (lit.)
SMILES string
[W]
InChI
1S/W
InChI key
WFKWXMTUELFFGS-UHFFFAOYSA-N
General description
For updated SDS information please visit www.goodfellow.com.
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Ultramicroscopy, 119, 106-110 (2011-11-15)
Thermionic electron emission from 200 to 500 nm thick coatings of scandium oxide on tungsten foil have been examined in thermionic emission microscopy, spectroscopic photoelectron microcopy, synchrotron radiation and ultraviolet photoelectron spectroscopy (UPS). A clear dependence of the scandium oxide-W
Physics in medicine and biology, 26(3), 435-443 (1981-05-01)
Curves relating beam energy, scattering foil thickness, central-axis depth-dose, and beam flatness have been generated using data taken on a Siemens 200A betatron. The curve set allows a single combination of tungsten foil thickness and electron beam energy to be
Chemical record (New York, N.Y.), 5(5), 308-320 (2005-10-08)
The reaction of M2(O2CBu(t))4 (M = Mo, W) with a dicarboxylic acid in toluene yields compounds of general formula [M2]-O2C-X-CO2-[M2] ([M2] = M2(O2CBu(t))3; X = conjugated spacer). The M2 units are electronically coupled via interactions between the M2 delta and
Biological trace element research, 88(2), 97-112 (2002-09-26)
Tungstate is an oxyanion that has biological similarities to vanadate. In recent years, a number of studies have shown the antidiabetic effects of oral tungstate in animal models of diabetes. However, because of the tissue accumulation and potential toxicity derived
Biological chemistry, 386(10), 999-1006 (2005-10-13)
The molybdenum enzymes 4-hydroxybenzoyl-CoA reductase and pyrogallol-phloroglucinol transhydroxylase and the tungsten enzyme acetylene hydratase catalyze reductive dehydroxylation reactions, i.e., transhydroxylation between phenolic residues and the addition of water to a triple bond. Such activities are unusual for this class of
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