Surface-dependent chemical equilibrium constants and capacitances for bare and 3-cyanopropyldimethylchlorosilane coated silica nanochannels

2011 ◽  
Vol 353 (1) ◽  
pp. 301-310 ◽  
Author(s):  
Mathias Bækbo Andersen ◽  
Jared Frey ◽  
Sumita Pennathur ◽  
Henrik Bruus
2014 ◽  
Vol 1665 ◽  
pp. 111-116 ◽  
Author(s):  
I. Puigdomènech ◽  
E. Colàs ◽  
M. Grivé ◽  
I. Campos ◽  
D. García

ABSTRACTA set of computer programs has been developed to draw chemical-equilibrium diagrams. This new software is the Java-language equivalent to the Medusa/Hydra software (developed some time ago in Visual basic at the Royal Institute of Technology, Stockholm, Sweden). The main program, now named “Spana” calls Java programs based on the HaltaFall algorithm. The equilibrium constants that are needed for the calculations may be retrieved from a database included in the software package (“Database” program). This new software is intended for undergraduate students as well as researchers and professionals.The “Spana” code can be easily applied to perform radionuclide speciation and solubility calculations of minerals, including solubility calculations relevant for the performance assessment of a nuclear waste repository. In order to handle ionic strength corrections in such calculations several approaches can be applied. The “Spana” code is able to perform calculations based on three models: the Davies equation; an approximation to the model by Helgeson et al. (HKF); and the Specific Ion-Interaction Theory (SIT). Default SIT-coefficients may be used, which widens the applicability of SIT significantly.A comparison is made here among the different ionic strength approaches used by “Spana” (Davies, HKF, SIT) when modelling the chemistry of radionuclides and minerals of interest under the conditions of a geological repository for nuclear waste. For this purpose, amorphous hydrous Thorium(IV) oxide (ThO2(am)), Gypsum (CaSO4·2H2O) and Portlandite (Ca(OH)2) solubility at high ionic strengths have been modelled and compared to experimental data from the literature. Results show a good fitting between the calculated values and the experimental data especially for the SIT approach in a wide range of ionic strengths (0-4 M).


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.


2018 ◽  
Vol 614 ◽  
pp. A1 ◽  
Author(s):  
P. Woitke ◽  
Ch. Helling ◽  
G. H. Hunter ◽  
J. D. Millard ◽  
G. E. Turner ◽  
...  

We have introduced a fast and versatile computer code, GGCHEM, to determine the chemical composition of gases in thermo-chemical equilibrium down to 100 K, with or without equilibrium condensation. We have reviewed the data for molecular equilibrium constants, kp(T), from several sources and discussed which functional fits are most suitable for low temperatures. We benchmarked our results against another chemical equilibrium code. We collected Gibbs free energies, ΔGf⊖, for about 200 solid and liquid species from the NIST-JANAF database and the geophysical database SUPCRTBL. We discussed the condensation sequence of the elements with solar abundances in phase equilibrium down to 100 K. Once the major magnesium silicates Mg2SiO4[s] and MgSiO3[s] have formed, the dust to gas mass ratio jumps to a value of about 0.0045 which is significantly lower than the often assumed value of 0.01. Silicate condensation is found to increase the carbon to oxygen ratio (C/O) in the gas from its solar value of ~0.55 up to ~0.71, and, by the additional intake of water and hydroxyl into the solid matrix, the formation of phyllosilicates at temperatures below ~400 K increases the gaseous C/O further to about 0.83. Metallic tungsten (W) is the first condensate found to become thermodynamically stable around 1600–2200 K (depending on pressure), several hundreds of Kelvin before subsequent materials such as zirconium dioxide (ZrO2) or corundum (Al2O3) can condense. We briefly discuss whether tungsten, despite its low abundance of ~2 × 10−7 times the silicon abundance, could provide the first seed particles for astrophysical dust formation.


2021 ◽  
Author(s):  
Raphael Kircher ◽  
Niklas Schmitz ◽  
Jürgen Berje ◽  
Kerstin Münnemann ◽  
Werner R. Thiel ◽  
...  

Formaldehyde reacts with solvents that contain hydroxyl groups (R–OH) in oligomerization reactions to oxymethylene oligomers (R–(OCH2)n–OH). The chemical equilibria of these reactions have been studied in the literature for water, for the mono-alcohols methanol, ethanol, and 1-butanol, as well as for the diols ethylene glycol and 1,4-butynediol. In the present work, the collective data were analyzed. It was found that the prolongation of the oxymethylene chains by the addition of formaldehyde can be described very well with a generalized chemical equilibrium constant Kx,n≥2R–OH, which is independent of the substructure (R) of the solvent. This holds for the oligomerization reactions leading to R–(OCH2)n–OH with n ≥ 2. The chemical equilibrium constant Kx,1R–OH of the reaction of formaldehyde with the solvent R–OH depends on the solvent, but simple trends are observed. The hypotheses of the existence of a generalized chemical equilibrium constant Kx,n≥2R–OH was tested for the reactions of formaldehyde with ethanol and 1-propanol, for which neither Kx,1R–OH nor Kx,nR–OH was previously available. The corresponding equilibria were studied by 13C NMR spectroscopy and the equilibrium constants were determined. A novel method was developed and used in these studies to obtain data on Kx,1R–OH by NMR spectroscopy, which is difficult because of the low amount of molecular formaldehyde. It was found that the generalized equilibrium constant is even valid for the acid-catalyzed formation of poly(oxymethylene) dimethyl ethers (OME).


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