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The temporal evolution of reactions is investigated using functional PCA, in which the functional loadings reflect the importance of reactions as a function of time.
Calculation of the standard molal thermodynamic properties of species and chemical reactions as a function of temperature and pressure is implemented in the primary function subcrt.
The purpose of this study was to investigate subcutaneous pressures and injection site reactions as a function of injection volume and flow rate.
The method was applied to study the kinetics of observed reactions as a function of both pyrite loading and concentration of Phe in order to gain additional insights into processes that control reaction rates.
Proof is given that formal potentials and formal temperature coefficients can be used with modified forms of the Nernst Equation to quantify the thermodynamics of flow cell reactions as a function of state-of-charge.
The energy available from the metabolic reactions as a function of temperature (equivalent to the mixing ratio) was calculated by multiplying the calculated Gibbs free energy for the reaction at each temperature by the concentrations of the reactants in the mixed fluid.
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Continuous sampling of the materials contained in a reaction vessel, followed by analysis with a mass spectrometer, has been used to identify and measure the quantity of intermediate species formed during a reaction as a function of time.
The threshold of launching of exothermic reaction as a function of the light absorbing coating layer thickness was studied.
As long as the water stays in the liquid state, the changes in the enthalpy of reaction as a function of temperature are minimal.
The EIS complex plane plots showed a drastic change in the charge transfer resistance of the probe redox reaction as a function of UO22+ concentration.
Sensitive measurements of the detector lifetime are achieved by monitoring the full-energy peak of the 3He(n, p 3H reaction as a function of time.
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