Chroma+GAS: An Expedited Solution for the Chemical Equilibrium for Cool Stellar Atmospheres

2021 ◽  
Vol 133 (1024) ◽  
pp. 064501
Author(s):  
C. Ian Short ◽  
Philip D. Bennett
1976 ◽  
Vol 72 ◽  
pp. 21-22
Author(s):  
A. J. Sauval

In cool stars, the determination of abundances of elements requires the resolution of the chemical equilibrium for each element even if atomic lines only are used. In the past, several authors have solved the well-known system of equations for a limited number of elements and of molecules. New calculations have been performed with special emphasis on the completeness of the system. Thus, all stable elements (83) have been included and a lot of molecules have been selected in order to omit no abundant compound. Owing to the lack of data (since many molecules are as yet not known spectroscopically), it appeared necessary to estimate many molecular parameters. Approximate equilibrium constants have been determined from analogies found among known molecules.It has been shown once more that the dissociation energy is by far the most important parameter, which yields alone the final accuracy.Our calculations include about 1200 molecules, of which more than half are new compounds never introduced in earlier investigations. We have found that, for about twenty elements such as Ti, Zr, La and most of the lanthanides, the new molecules play an important role in the chemical equilibrium. The cases of titanium, zirconium and lanthanum have been particularly investigated owing to the use of several bands of their oxides in the spectral classification of M- and S-type stars. We have noted that the experimental determinations of the dissociation energy of most monoxides and dioxides are as yet rather inaccurate. Furthermore, neither the spectrum nor the heat of atomization of hydroxides are known in the laboratory. It has appeared that estimating the dissociation energy of hydroxides was particularly difficult in consequence of the lack of data for such molecular compounds.For oxygen-rich stars, we have investigated the influence of uncertainties of the dissociation energy of the most abundant species on the march of the molecular concentrations. In the case of titanium, we have found that the concentration of TiO strongly changes at low temperature (T <2520 K) according to the adopted Doo- values for TiO, TiOH and TiO2. Therefore, the interpretation of the TiO bands in the coolest stars has to take this new effect into account. In any way, we have checked that the TiO concentration always increases from early K- to late M-type stars. We have also shown that the depletion factor for Ti presents a final uncertainty of a factor of about ten at 2520 K, which still increases at lower temperature. That is due to the cumulative effect of the inaccuracies of molecular data. Therefore, in late M-type stars, the determination of the abundance of titanium remains rather uncertain even if it is derived from Ti I or Ti II lines. The present inaccuracy will only be reduced from very precise measurements of the dissociation energy of the relevant molecules. For Zr and La, we have found similar results to that for Ti. Furthermore, we have noted that there is no determination of absolute transition probabilities for the ZrO and LaO bands (contrary to TiO bands) which are both of first importance for the spectral classification of cool stars.For carbon-rich stars as well as for S-type stars (i.e. O/C very near unity), we have checked that the molecules always play a much less important role that in oxygen-rich stars, as it was first noted by Tsuji (Astron. Astrophys.23, 411, 1973).Our conclusion is that there is an urgent need of accurate measurements of the dissociation energy of many molecules and also of band oscillator strengths for most of the transitions of stellar interest. Furthermore, several new selected compounds have to be investigated in the laboratory, especially the dioxides and hydroxides. Such accurate molecular data are necessary in order to get a better knowledge of the physical conditions in cool stellar atmospheres.


1985 ◽  
Vol 10 (6) ◽  
pp. 883-891 ◽  
Author(s):  
M. Allegrini ◽  
G. Alzetta ◽  
P. Bicchi ◽  
S. Gozzini ◽  
L. Moi

2020 ◽  
Vol 31 (3) ◽  
pp. 84
Author(s):  
J. Jusniar ◽  
E. Effendy ◽  
Endang Budiasih ◽  
S. Sutrisno

<p class="p1"><span class="s1">This study aims to develop a Three-tier Diagnostic Instrument on Chemical Equilibrium (TT-DICE) to diagnose high school students’ misconceptions related to this topic. TT-DICE consists of thirty items, asking for students’ answers, reasonings, and levels of confidence. Three-stages development models developed by Treagust applied in developing TT-DICE. First-stage was a literature study to analyze the main concepts and students’ misconceptions in CE. The next step is the development of the TT-DICE prototype, consisting of item development, preliminary experiments, interviews, and revisions. The third stage of validity checking starts with content validation by experts and practitioners. A field test conducted to determine the reliability and quality variables are supporting TT-DICE items. These variables are Item Validity (IV), Difficulty Level (DL), Discrimination Index (DI), and effectiveness of distractors. Content validity by validators showed that the TT-DICE is valid with a very high category (96.1%). The results of item validity show that 88.9% of the items are valid. Testing of DL, DI, and the effectiveness of distractors in general, shows a good category. The Reliability of the three-tiers TTDICE using Alpha Cronbach is a high and very high category, respectively (0.83, 0.81 &amp; 0.91). The overall validity test results also concluded if the TT-DICE is valid, reliable, and suitable to diagnose misconceptions of Chemical Equilibrium.</span></p>


1980 ◽  
Vol 45 (3) ◽  
pp. 777-782 ◽  
Author(s):  
Milan Šolc

The establishment of chemical equilibrium in a system with a reversible first order reaction is characterized in terms of the distribution of first passage times for the state of exact chemical equilibrium. The mean first passage time of this state is a linear function of the logarithm of the total number of particles in the system. The equilibrium fluctuations of composition in the system are characterized by the distribution of the recurrence times for the state of exact chemical equilibrium. The mean recurrence time is inversely proportional to the square root of the total number of particles in the system.


Author(s):  
Dennis Sherwood ◽  
Paul Dalby

Building on the previous chapter, this chapter examines gas phase chemical equilibrium, and the equilibrium constant. This chapter takes a rigorous, yet very clear, ‘first principles’ approach, expressing the total Gibbs free energy of a reaction mixture at any time as the sum of the instantaneous Gibbs free energies of each component, as expressed in terms of the extent-of-reaction. The equilibrium reaction mixture is then defined as the point at which the total system Gibbs free energy is a minimum, from which concepts such as the equilibrium constant emerge. The chapter also explores the temperature dependence of equilibrium, this being one example of Le Chatelier’s principle. Finally, the chapter links thermodynamics to chemical kinetics by showing how the equilibrium constant is the ratio of the forward and backward rate constants. We also introduce the Arrhenius equation, closing with a discussion of the overall effect of temperature on chemical equilibrium.


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