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Melting point: −22.0 to −22.7 °C (−7.6 to −8.9 °F; 251.2 to 250.5 K) ... Tetrachloroethylene, ... Most tetrachloroethylene is produced by high-temperature ...
Triple point: 250.81 K (–22.34 °C), ? Pa Critical point: 620 K (347 °C), 4760 kPa Std enthalpy change of fusion, Δ fus H o: 10.88 kJ/mol Std entropy change of fusion, Δ fus S o: 43.38 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o: 34.68 kJ/mol at 121 °C Std entropy change of vaporization, Δ vap S o: 102.8 J/(mol·K) at 25 ...
Melting point: −84.8 °C ... trichloroethylene and tetrachloroethylene are collected together and ... to its high heat transfer capabilities and its low-temperature ...
Boca Raton, Florida, 2003; Section 6, Fluid Properties; Critical Constants. Also agrees with Celsius values from Section 4: Properties of the Elements and Inorganic Compounds, Melting, Boiling, Triple, and Critical Point Temperatures of the Elements Estimated accuracy for Tc and Pc is indicated by the number of digits.
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.
Triple point [5] 188.4 K (−84.7 °C), ? Pa Critical point [5] 571 K (298 °C), 5016 kPa Std enthalpy change of fusion, Δ fus H o: 8.45 kJ/mol Std entropy change of fusion, Δ fus S o: 44.8 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o: 31.4 kJ/mol Std entropy change of vaporization, Δ vap S o? J/(mol·K) Solid properties Std ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
They have higher boiling and melting points compared to related hydrocarbons. Flammability reduces with increased chlorine substitution in hydrocarbons. [citation needed] Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage. [citation needed]