On calculating the activity of components in binary silicate melts

2007 ◽  
Vol 33 (5) ◽  
pp. 459-463 ◽  
Author(s):  
N. I. Zalomov ◽  
V. N. Boronenkov ◽  
M. Zinigrad ◽  
S. M. Shanchurov
1971 ◽  
Vol 49 (5) ◽  
pp. 683-690 ◽  
Author(s):  
I. B. Smith ◽  
C. R. Masson

Activities of CoO in CoO–SiO2 melts were measured at 1450–1500 °C by equilibrating the melts, held in Pt–Rh containers, with atmospheres of known oxygen potential. Activities were calculated by the relationship[Formula: see text]where aCo, the activity of cobalt in the container, was determined in separate experiments.The results were compared with theoretical activity–composition curves based on the application of polymer theory to silicate melts. The results were in good agreement with theoretical curves calculated on the assumption of linear chains. In contrast, for all other binary silicate melts so far investigated the results are best represented in terms of theory in which all chain configurations are allowed. Ionic distributions and number average and weight average molecular weights were calculated as functions of the silica content from the experimental data. The calculated proportions of monomeric ion, SiO44−, dimer Si2O76−, and trimer Si3O108− were in reasonable agreement with experimental values based on trimethylsilylation and gas-chromatographic separation of the ionic constituents in quenched melts.


2004 ◽  
Vol 65 (8-9) ◽  
pp. 1609-1614 ◽  
Author(s):  
G. Ottonello ◽  
R. Moretti

1970 ◽  
Vol 48 (9) ◽  
pp. 1456-1464 ◽  
Author(s):  
C. R. Masson ◽  
I. B. Smith ◽  
S. G. Whiteway

Theoretical expressions derived previously for molecular size distributions in multichain polymers are applied to binary silicate melts. The treatment is an extension of a previous approach which was limited to the consideration of linear chains. When all configurations of the chain molecules are taken into consideration, the predicted variation of thermodynamic activity with composition agrees with experiment for all binary systems for which data are available. The effect of allowing for all chain configurations is largely to improve the fit between theory and experiment at high silica contents. Calculated ionic distributions for the system 'FeO'–SiO2 do not differ markedly from those previously reported. The mean chain length is unaffected. The results support previous views that principles of polymer chemistry can be applied usefully to silicate melts and glasses.


1970 ◽  
Vol 48 (1) ◽  
pp. 201-202 ◽  
Author(s):  
C. R. Masson ◽  
I. B. Smith ◽  
S. G. Whiteway

Expressions developed previously by Flory and by the authors for molecular size distributions in branched polymers were used to derive theoretical curves of activity vs. composition in binary silicate melts. In contrast with curves based on the Flory distribution those derived from our result were in good agreement with experiment over the entire range of compositions up to the maximum degree of polymerization allowed by the theory. The comparison is illustrated for the systems PbO–SiO2 and SnO–SiO2.


2012 ◽  
Vol 52 (10) ◽  
pp. 1902-1908 ◽  
Author(s):  
Masashi Nakamoto ◽  
Toshihiro Tanaka ◽  
Lauri Holappa ◽  
Takaiku Yamamoto

2020 ◽  
Vol 6 (1) ◽  
pp. 454-476
Author(s):  
Franco Foresta Martin ◽  
Silvio G. Rotolo ◽  
Manuela Nazzari ◽  
Maria Luisa Carapezza

Abstract Chlorine is a minor element present in obsidians in quantities greater than in average igneous rocks. The chlorine concentration in obsidians is generally low, of the order of tenths of wt %, but it exhibits an appreciable differentiation among geological sources. Despite these characteristics, chlorine has rarely been taken into consideration as a possible indicator of obsidian provenance and it does not appear in the chemical analytical tables accompanying the geochemical characterisation of obsidian samples. In this work, after an overview of chlorine geochemistry and cycle, we present thirty-one new electron microprobe (EPMA) analyses, including Cl, of geologic obsidians sampled from the four sources of the Central Mediterranean, exploited in prehistoric times (Monte Arci, Palmarola, Lipari and Pantelleria). The results are compared with 175 new EPMA analyses, including Cl, of archaeological obsidians already characterised in previous work and of known provenance. As such it was possible to ascertain that each source has a characteristic chlorine concentration, showing the utility of its use in the studies of obsidian provenance. Furthermore, given that the solubility of chlorine in silicate melts is correlated to its alkali content, in particular sodium, we assessed the efficacy of simple binary graphs Cl vs Na2O to better constrain the provenance of the obsidian samples.


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