Some applications of polarography for investigation of equlibria in aqueous solutions of organic compounds

2009 ◽  
Vol 74 (11-12) ◽  
pp. 1777-1789 ◽  
Author(s):  
Petr Zuman
Keyword(s):  
Aqueous Solutions ◽  
Organic Compounds ◽  
Carbonyl Compounds ◽  
Limiting Current ◽  
Nitroso Compounds ◽  
Primary Amines ◽  
Acid Base ◽  
Fast Reactions ◽  
Half Wave

There are two possibilities how to follow equilibria of organic compounds established in aqueous solutions using polarography: for very fast reactions, information can be obtained from shifts of half-wave potentials. For slowly established equilibria, the changes in the limiting current are followed. In both cases variation of the half-wave potentials or limiting currents with concentration of a reactant, present in excess, is followed. The types of reactions, which had been followed in this way, are as follows: hydration–dehydration equilibria, additions of hydroxide ion to carbonyl and nitroso compounds, the role of slowly established acid–base equilibria involving C-acids; further also reactions involving the addition of ammonia, primary amines, hydroxylamine, and hydrazine to carbonyl compounds.

scholarly journals The role of the 2,7-dinitrozo-1,8-dihydroxynaphthalene-3,6-disulfonic acid reagent in determining the thorium ion (IV)

2021 ◽  
pp. 54-58
Keyword(s):  
Organic Reagent ◽  
Disulfonic Acid ◽  
Acid Base ◽  
Amperometric Titration ◽  
Amperometric Determination ◽  
Half Wave ◽  
Acid Reagent ◽  
Background Electrolytes

The aim is to develop a method for the amperometric determination of thorium (IV) ion with 2,7-dinitroso-1,8-dihydroxynaphthalene-3,6-disulfoxyl reagent. Methods of amperometric determination of thorium by solution of 2,7-dinitrozo-1,8-dihydroxynaphthalene-3,6-disulfonic acid on different acid-base properties of background electrolytes and buffer mixtures are considered. The half-wave potential of new reagent was found by logarithmic analysis equal 0.72 V at pH 2.82, which once again indicates on the irreversibility of the process of electrooxidation of the studied organic reagent in used acid-base medias. The conditions for amperometric titration of thorium are optimized, and the influence of outside accompanying metals on the shape of curves and the results of its determination are investigated.

scholarly journals Study of the factors that determine the transfer of water and organic compounds into the gas phase from aqueous solutions in a discharge with a liquid cathode

2021 ◽  
Vol 2100 (1) ◽  
pp. 012025
Author(s):  
A V Chistolinov ◽  
M A Khromov ◽  
R V Yakushin ◽  
M Kh Gadzhiev ◽  
A S Tyuftyaev
Keyword(s):  
Aqueous Solution ◽  
Free Surface ◽  
Aqueous Solutions ◽  
Gas Phase ◽  
Organic Compounds ◽  
Direct Current ◽  
Current Discharge ◽  
Liquid Cathode ◽  
Direct Current Discharge

Abstract A study was performed to investigate the transfer of organic compounds and water from an aqueous solution to the gas phase under the action of a direct current discharge, in which an aqueous solution that contains organic compounds plays the role of a cathode. The effect of the area of the free surface of a liquid in various reactors, as well as the effect of the stirring mode of a solution near the surface of a liquid on the rate of transfer of water and organic compounds under the action of a discharge of this type, have been investigated. It is shown that a change in the area of the free surface of a liquid has no significant effect on the rate of transfer of water and organic compounds from solution to the gas phase under the action of a direct current discharge with a liquid cathode. It is shown that the stirring mode and the temperature of the solution, on the contrary, have a very significant effect on the rate of nonequilibrium transfer of both water and organic compounds from solution to the gas phase under the action of a discharge with a liquid cathode.

Nitrogen excretion: three end products, many physiological roles.

1995 ◽  
Vol 198 (2) ◽  
pp. 273-281 ◽  
Author(s):  
P A Wright
Keyword(s):  
Uric Acid ◽  
Organic Compounds ◽  
Marine Invertebrates ◽  
Chemical Properties ◽  
Nitrogen Excretion ◽  
Acid Base ◽  
Ammonia Metabolism ◽  
Waste Products ◽  
End Products

There are diverse physiological functions of nitrogen end products in different animal groups, including excretion, acid-base regulation, osmoregulation and buoyancy. Animals excrete a variety of nitrogen waste products, but ammonia, urea and uric acid predominate. A major factor in determining the mode of nitrogen excretion is the availability of water in the environment. Generally, aquatic animals excrete mostly ammonia, whereas terrestrial animals excrete either urea or uric acid. Ammonia, urea and uric acid are transported across cell membranes by different mechanisms corresponding to their different chemical properties in solution. Ammonia metabolism and excretion are linked to acid-base regulation in the kidney, but the role of urea and uric acid is less clear. Both invertebrates and vertebrates use nitrogen-containing organic compounds as intracellular osmolytes. In some marine invertebrates, NH4+ is sequestered in specific compartments to increase buoyancy.

Estimation of the effect of NaCl on the solubility of organic compounds in aqueous solutions

2000 ◽  
Vol 89 (12) ◽  
pp. 1620-1625 ◽  
Author(s):  
Nina Ni ◽  
Mohamed M. El‐Sayed ◽  
Tapan Sanghvi ◽  
Samuel H. Yalkowsky
Keyword(s):  
Aqueous Solutions ◽  
Organic Compounds

On the Structure of Lead(II) Complexes in Aqueous Solutions. I. Trinuclear Clusters

1995 ◽  
Vol 60 (4) ◽  
pp. 527-536 ◽  
Author(s):  
Martin Breza ◽  
Alena Manová
Keyword(s):  
Quantum Chemistry ◽  
Aqueous Solutions ◽  
Electronic Structures ◽  
Mndo Method ◽  
Model Systems ◽  
Trinuclear Clusters ◽  
The Stability ◽  
Semiempirical Mndo

Using semiempirical MNDO method of quantum chemistry the optimal geometries and corresponding electronic structures of [Pb3(OH)n]6-n model systems as well as of their hydrated [Pb3(OH)n(H2O)8-n]6-n analogues (n = 4, 5) are investigated. The most stable trinuclear lead(II) complexes present in aqueous solutions correspond to cyclo-(μ3-OH)(μ2-OH)3Pb32+, Pb(μ-OH)2Pb(μ-OH)2Pb2+, cyclo-(μ3-OH)2(μ2-OH)3Pb3+, Pb(OH)(μ-OH)2Pb(μ-OH)Pb(OH)+ and Pb(OH)(μ-OH)2Pb(μ-OH)2Pb+ systems. The key role of OH bridges (by vanishing direct Pb-Pb bonds) on the stability of individual isomers is discussed.

scholarly journals Aging of atmospheric aerosols and the role of iron in catalyzing brown carbon formation

2021 ◽  
Author(s):  
Hind A. A. Al-Abadleh
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Atmospheric Aerosols ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Atmospheric Oxidation ◽  
Carbon Formation ◽  
Brown Carbon ◽  
Volatile Organic

Extensive research has been done on the processes that lead to the formation of secondary organic aerosol (SOA) including atmospheric oxidation of volatile organic compounds (VOCs) from biogenic and anthropogenic...

scholarly journals Conversion of Methanol on Rutile TiO2 (110) and Tungsten Oxide Clusters: 2. The Role of Defects and Electron Transfer in Bifunctional Oxidic Photocatalysts

2021 ◽  
Author(s):  
Lars Mohrhusen ◽  
Jessica Kräuter ◽  
Katharina Al-Shamery
Keyword(s):  
Electron Transfer ◽  
Transition Metal ◽  
Metal Oxide ◽  
Tungsten Oxide ◽  
Organic Compounds ◽  
Uv Irradiation ◽  
Organic P ◽  
Rutile Tio2 ◽  
Metal Oxide Surfaces

The photochemical conversion of organic compounds on tailored transition metal oxide surfaces by (UV) irradiation has found wide applications ranging from the production of chemicals to the degradation of organic...

scholarly journals Robust and efficient hydrogenation of carbonyl compounds catalysed by mixed donor Mn(I) pincer complexes

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Wenjun Yang ◽  
Ivan Yu. Chernyshov ◽  
Robin K. A. van Schendel ◽  
Manuela Weber ◽  
Christian Müller ◽  
...  
Keyword(s):  
Noble Metal ◽  
Crucial Role ◽  
Carbonyl Compounds ◽  
Catalytic Performance ◽  
Hydrogen Atmosphere ◽  
Pincer Complexes ◽  
Catalyst Activation ◽  
Hydrogenation Catalysts ◽  
Induction Times

AbstractAny catalyst should be efficient and stable to be implemented in practice. This requirement is particularly valid for manganese hydrogenation catalysts. While representing a more sustainable alternative to conventional noble metal-based systems, manganese hydrogenation catalysts are prone to degrade under catalytic conditions once operation temperatures are high. Herein, we report a highly efficient Mn(I)-CNP pre-catalyst which gives rise to the excellent productivity (TOF° up to 41 000 h−1) and stability (TON up to 200 000) in hydrogenation catalysis. This system enables near-quantitative hydrogenation of ketones, imines, aldehydes and formate esters at the catalyst loadings as low as 5–200 p.p.m. Our analysis points to the crucial role of the catalyst activation step for the catalytic performance and stability of the system. While conventional activation employing alkoxide bases can ultimately provide catalytically competent species under hydrogen atmosphere, activation of Mn(I) pre-catalyst with hydride donor promoters, e.g. KHBEt3, dramatically improves catalytic performance of the system and eliminates induction times associated with slow catalyst activation.

Ethanol conversion over Ga2O3-ZrO2 solid solution: empirical evidences of the reaction pathway, the surface acid–base property, and role of isolated gallium ion

2021 ◽  
Author(s):  
Takashi Yamamoto ◽  
Akihito Kurimoto ◽  
Riona Sato ◽  
Shoki Katada ◽  
Hirotaka Mine ◽  
...  
Keyword(s):  
Solid Solution ◽  
Reaction Pathway ◽  
Ethanol Conversion ◽  
Acid Base ◽  
Base Property ◽  
Temperature Range ◽  
Acid Base Property

Ethanol conversion by Ga2O3-ZrO2 solid solution was examined in the temperature range 573–773 K, and acetone/isobutene formation was confirmed under cofeeding of H2O vapor. The reaction pathway was empirically investigated...

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