The bond dissociation energy (enthalpy) is also referred to as bond disruption energy, bond energy, bond strength, or binding energy (abbreviation: BDE, BE, or D) . It is defined as the standard enthalpy change of the following fission: R−X → R + X . The BDE, denoted by Do(R−X), is usually derived by the thermochemical equation, Do(R−X) = ∆fH o(R) + ∆fH o(X) – ∆fH o(RX) . The enthalpy of format...

Near-surface air moisture observations from Phoenix and Curiosity display diurnal adsorption, which appears insensitive to mineralogy of regolith. To study this, adsorptive column model simulations are made for midsummer at Phoenix, validated against recalibrated TECP water vapor pressures p. Two standard-form (= obeying the van't Hoff equilibrium law) adsorption isotherms with quite different ...

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Equations are set up to calculate the observed standard free energy change for the hydrolysis of ATP (namely, AGobs, the quantity evaluated on the basis of total ATP, ADP, and orthophosphate concentrations at equilibrium, irrespective of the state of ionization or complex formation, or both) as a function of pH and Mg2+ ion concentration. The variation of AGobs is analyzed in terms of AG, the s...

Equations are set up to calculate the observed standard free energy change for the hydrolysis of ATP (namely, AGobs, the quantity evaluated on the basis of total ATP, ADP, and orthophosphate concentrations at equilibrium, irrespective of the state of ionization or complex formation, or both) as a function of pH and Mg2+ ion concentration. The variation of AGobs is analyzed in terms of AG, the s...

A direct calorimetric measurement of the overall enthalpy change associated with self-assembly of organic monolayers at the liquid-solid interface is for most systems of interest practically impossible. In previous work we proposed an adapted Born-Haber cycle for an indirect assessment of the overall enthalpy change by using terephthalic acid monolayers at the nonanoic acid-graphite interface a...