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Dibenzylideneacetone or dibenzalacetone, often abbreviated dba, is an organic compound with the formula C 17 H 14 O. It is a pale-yellow solid insoluble in water, but soluble in ethanol. It is a pale-yellow solid insoluble in water, but soluble in ethanol.
The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.
The bulk compounds should be contrasted with nanoparticles which exhibit melting-point depression, meaning that they have significantly lower melting points than the bulk material, and correspondingly lower Tammann and Hüttig temperatures. [4] For instance, 2 nm gold nanoparticles melt at only about 327 °C, in contrast to 1065 °C for a bulk ...
Transition temperatures for the constituent elements have dashes ----- in the first column in a blank row, such as at 922 K, the melting point of Mg. Transition temperatures for the substance have two blank rows with dashes, and a center row with the defined transition and the enthalpy change, such as the melting point of MgCl 2 at 980 K. The ...
Values refer to the enthalpy change in the conversion of liquid to gas at the boiling point (normal, 101.325 kPa). References
For example, the melting point of silicon at ambient pressure (0.1 MPa) is 1415 °C, but at pressures in excess of 10 GPa it decreases to 1000 °C. [13] Melting points are often used to characterize organic and inorganic compounds and to ascertain their purity. The melting point of a pure substance is always higher and has a smaller range than ...
It has a melting point of 450 °C and a boiling point of 988 °C. Tellurium has a polyatomic (CN 2) hexagonal crystalline structure. It is a semiconductor with a band gap of 0.32 to 0.38 eV. Tellurium has a moderate ionisation energy (869.3 kJ/mol), high electron affinity (190 kJ/mol), and moderate electronegativity (2.1).
N.B. Pilling and R.E. Bedworth [2] suggested in 1923 that metals can be classed into two categories: those that form protective oxides, and those that cannot. They ascribed the protectiveness of the oxide to the volume the oxide takes in comparison to the volume of the metal used to produce this oxide in a corrosion process in dry air.