Algorithm for Calculating the Protolytic Equilibrium Constants of Organic Acids in Isopropyl Alcohol

2021 ◽  
Vol 95 (9) ◽  
pp. 1826-1830
Author(s):  
S. S. Lysova ◽  
T. A. Skripnikova ◽  
Yu. E. Zevatsky
2020 ◽  
Vol 94 (10) ◽  
pp. 2030-2033
Author(s):  
N. N. Kuranova ◽  
N. A. Chesnokova ◽  
A. S. Gushchina ◽  
K. V. Grazhdan ◽  
V. A. Sharnin

Soil Research ◽  
2000 ◽  
Vol 38 (4) ◽  
pp. 807 ◽  
Author(s):  
Sahta Ginting ◽  
Bruce B. Johnson ◽  
Sabine Wilkens

The effect of 5 organic anions (citrate, malate, malonate, oxalate, and tartrate) on the concentration of Al measured with 2 colorimetric reagents [pyrocatechol violet (PCV) and aluminon] was determined as a function of reaction time. The results are compared with concentrations of reactive Al [Al3+ + AlOH2+ + Al(OH)2+ ] predicted from stability constants. The PCV reagent was found to overestimate this fraction, i.e. to underestimate the extent of complexation by oxalate, malonate, and malate, even when the shortest reaction time of 30 s was applied. However, the aluminon reagent provided a good estimate of ‘reactive’ Al at the 30 s reaction time in the presence of all organic anions studied. At a citrate and tartrate to Al ratio of 1 : 2, the ‘reactive’ Al concentration, determined from stability constant data, underestimated the extent of Al complexation. These deviations could be modelled by the addition of a further complex, with the composition Al2 (OH)L2+ for citrate and Al2(OH)2L2+ for tartrate. Tentative equilibrium constants for these species are presented.


Author(s):  
Fabien Thomas ◽  
Armand Masion

Aluminum is the most abundant metal of the Earth’s crust, of which it represents approximately 8%, ranking after oxygen and silicon. It exists mainly as oxides. In terrestrial environments, aluminum commonly exists as secondary (authigenic) hydroxide or aluminosilicate minerals, mainly clays. These minerals are highly insoluble at neutral pH. However, aluminum occurs in detectable amounts in natural waters, due to leaching of the soil minerals in acidic conditions. Soil acidity may have a natural origin, such as an acidic (silicic) mother rock, melted snow, dissolved carbonic acid, or biologically generated organic acids. During the past two decades, it has been demonstrated that one of the major origins of increased aluminum mobilization and transport in forested soils is introduction of strong acid through atmospheric sulfur and nitrogen deposition. It has also been shown that aqueous aluminum is the biogeochemical link between atmospheric pollution and damage caused to tree roots and aquatic organisms such as plankton, crustaceans, insects, and fish. Biological studies have shown that the different aluminum species exhibit various toxicities: the most toxic are the monomeric and the polynuclear species; complexation with organic acids results in low toxicity. The significance of aluminum to human health has long been regarded as negligible. There is a possible link between high-level aluminum contamination by renal dialysis or hemodialysis, and neurodegenerative health disorders such as Parkinson’s or Alzheimer’s diseases, but the part played by aluminum is not clear. However, since aluminum salts are used on an industrial level as coagulants and flocculants in water treatment, the aluminum concentration and speciation in drinking water deserve careful monitoring. Because of the specific toxicity of the aluminum species, there has been considerable concern in the past two decades over the speciation of aqueous aluminum present in soils and aquatic systems. To this end, several techniques have been developed in order to partition the aluminum species. The most common among them are chromatographic separation and categorization methods such as timed ferron reaction, and computational methods derived from thermodynamic equilibrium constants. However, significant discrepancies between the results have been noticed, and attributed to the dramatic interference of organic and inorganic anions in the Al fractionation.


1975 ◽  
Vol 30 (5-6) ◽  
pp. 393-398 ◽  
Author(s):  
J. Zsakó ◽  
Cs. Várhelyi ◽  
Z. Finta ◽  
J. Kiss-Jakab

In aqueous solutions the nonelectrolyte [Co(DH)2(NO2)(H2O)] participates in protolytic eqilibria and thus it exists in 7 different forms. Rate constants of the aquation, which leads to the substitution of the nitro group, have been measured in the pH-range between 3.72 and 8 at various temperatures. From these data rate constants, activation energies and entropy values of the aquation of 2 ionic species have been derived, as well as equilibrium constants for the protolytic equilibrium between these species. The kinetic parameters obtained have been compared to those of the aquation of the ionic species which exist in acid and basic solutions and the correlation between structure and activation energy of the aquation has been discussed.


In spite of the numerous industrial processes developed for the hydrogenation of various organic substances with the aid of catalytic materials, but little work has been accomplished on the determination of the mass action equilibrium constants of organic substances which undergo thermal dissociation. Thus in the dissociation of ethyl alcohol into acetaldehyde and hydrogen, or of isopropyl alcohol into acetone and hydrogen, two reactions widely employed, the dependance of the degree of the dissociation on the temperature is unknown. Sabatier (‘La Catalyse en Chimie Organique’) states (p. 82) that acetaldehyde is easily hydrogenated at 140°C. and acetone at a temperature of 115° to 125°C. utilising nickel as a catalytic agent. At higher temperatures, however, 200° to 350°C., acetone is not hydrogenated to isopropyl alcohol, but methyl isobutylketone and diisobutylketone are produced. Again (p. 161) ethyl alcohol undergoes rapid dehydrogenation at a copper surface within the temperature range 200° to 350°C.; at 420°C. the acetaldehyde produced undergoes decomposition. Isopropyl alcohol in contact with the same catalytic agent slowly commences to undergo dehydrogenation at 150°C., dehydrogenation being rapid at 250° to 430°C.


Author(s):  
J.M. Guilemany ◽  
F. Peregrin

The shape memory effect (SME) shown by Cu-Al-Mn alloys stems from the thermoelastic martensitic transformation occuring between a β (L2,) metastable phase and a martensitic phase. The TEM study of both phases in single and polycrystalline Cu-Al-Mn alloys give us greater knowledge of the structure, order and defects.The alloys were obtained by vacuum melting of Cu, Al and Mn and single crystals were obtained from polycrystalline alloys using a modified Bridgman method. Four different alloys were used with (e/a) ranging from 1.41 to 1.46 . Two different heat treatments were used and the alloys also underwent thermal cycling throughout their characteristic temperature range -Ms, Mf, As, Af-. The specimens were cut using a low speed diamond saw and discs were mechanically thinned to 100 μm and then ion milled to perforation at 4 kV. Some thin foils were also prepared by twin-jet electropolishing, using a (1:10:50:50) urea: isopropyl alcohol: orthophosphoric acid: ethanol solution at 20°C. The foils were examinated on a TEM operated at 200 kV.


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