high sodium concentration
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2018 ◽  
Vol 36 (Supplement 1) ◽  
pp. e111
Author(s):  
S. Al-Hajj ◽  
A. Goumard ◽  
A. Heraud ◽  
S. Georgeault ◽  
J. Burlaud-Gaillard ◽  
...  

The non-dispersive interaction energy between glass and water as a function of pH is expected to reflect the surface charge generated by the exposed chemical functions on the clean glas s surface. The variations in surface charge, generated by the exposed SiOH and aluminum oxide groups, is expected to give rise to fea-tures representing the surface chemistry of the clean glass. The scatter i n the data shown in Figures 4 and 5 allows only general trends to be discerned. The p.z.c.'s at pH 3 and 9 have been described in the preceding paragraphs. It is interesting to note that the chromic acid cleaned glass surfaces behave in a similar manner, showing virtually identical trends. The pyrolysis cleaned glass surfaces show dif-ferences in their behavior across the different glass compositions. These trends correlate with those observed for organic contamination of these surfaces, as de-scribed in Section 3.1, where the chromic acid cleaned glass surfaces all showed similar behavior, while the pyrolyzed glass showed significant differences in its sensitivity to contamination. In particular, the pyrolyzed silica surface shows far lower non-dispersive interaction energy with water than the pyrolyzed Corning code 1737 or sodalime glasses. This features correlates with the high degree of adsorbed contamination, described in Section 3.1, for the pyrolyzed silica surface. The datum in Figure 5 for the non-dispersive interaction energy between a py-rolyzed silica surface and water at pH 7 corresponds to a contact angle of 31°. This is significantly higher than the contact angle of water on a pyrolyzed silica surface freshly immersed into liquid octane. While the surface cleanliness was measured after cleaning, it was not measured after substrate immersion in the acidic or alkaline solutions. It is possible that the comparatively low non-dispersive interaction energy observed for pyrolyzed silica is partially an artifact caused by contamination of the cleaned silica before immersion into liquid oc-tane. Figure 4 shows similar behavior fo r the glass surfaces, suggesting that the alu-minoborosilicate and sodalime glasses show behavior similar to that of a silica surface. This phenomenon may be due to the leaching of soluble alkaline oxides from the glass surfaces during chromic acid cleaning, leaving a surface enriched in silica that behaves essentially in the same way as a chromic acid cleaned silica surface. In Figure 5, the minimum in the non-dispersive interaction energy between glass and water at pH 9 is not present for pyrolyzed sodalime glass. This mini-mum was presumed to be associated with a high sodium ion concentration in solution, neutralizing the SiO" groups at the glass surface. The presence of sodium oxide (see Table 1) in the sodalime glass composition may generate a high so-dium environment for the the silano l groups at the glass surface. The high sodium concentration in the glass may thus be equivalent to a high sodium concentration in solution, neutralizing the p.z.c.

2003 ◽  
pp. 111-113

1982 ◽  
Vol 34 (1) ◽  
pp. 107-110 ◽  
Author(s):  
M. A. Lindeman ◽  
T. D. A. Brigstocke ◽  
P. N. Wilson

ABSTRACTTwo trials were conducted at the BOCM Silcock Development Unit at Stoke Mandeville. The first trial evaluated the response on doe and progeny, from mating to 8 weeks after parturition, of rabbit compound diets containing 0, 100, 200 and 300 g sodium hydroxide-treated straw per kg. Performance data showed no detrimental effect of inclusion levels up to 300 g sodium hydroxide-treated straw per kg despite its high sodium concentration.A second trial was made to ascertain whether these findings were due to the treated straw itself or to increasing sodium concentrations. A standard rabbit compound diet containing 2·5 g sodium per kg was compared with diets containing either 5·0 or 10·0 g sodium per kg, and with experimental compound diets containing either 80 g sodium hydroxide-treated straw or 80 g untreated straw per kg and both containing 2·5 g sodium per kg. Peak food conversion was estimated to occur at a dietary sodium concentration of 4·6g/kg, although the slope of the dose response curve was not statistically significant at the P ≤ level.The results indicate that compound diets containing up to 80 to lOOg sodium hydroxide-treated straw per kg may be fed to rabbits and that inclusion of levels of up to 300 g sodium hydroxide-treated straw per kg are not detrimental to performance. On the other hand, an inclusion of 80 g untreated ground straw per kg in compound diets for rabbits had a growth-depressing effect.


1967 ◽  
Vol 50 (3) ◽  
pp. 505-517 ◽  
Author(s):  
Issei Seyama ◽  
Hiroshi Irisawa

It already has been well documented that the maximum rate of depolarization and amplitude of action potentials are directly dependent on [Na+]o in the vertebrate myocardium. Almost all studies have been carried out at low sodium concentration ranges by substituting NaCl for other substances. Action potentials should be demonstrable in higher sodium concentrations, but cells are inevitably damaged by osmotic changes. The blood of elasmobranchs is nearly isosmotic with sea water, but NaCl accounts for 54.5% of the osmotic pressure and 38.7% of it is maintained by urea molecules. Utilizing this special situation in elasmobranchs, the effect of high sodium concentration was studied up to 170% of normal sodium concentration, while still retaining isosmotic condition. The rate of depolarization, amplitude, and duration of the myocardial action potential all increased in direct proportion to [Na+]o, and no depressant effect on transmembrane action potentials was observed in solutions of high sodium concentration. With regard to depolarization rate, the regression curve fitted by the least squares method passed through zero within two standard errors. At high sodium levels, the overshoot changed as expected theoretically, but at lower ranges it deviated from the theoretical values. [Na+]i, and [K+]i, in this tissue have been determined, and these data are explained on the basis of the Na theory.


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