The reactions of ozone with tertiary amines including the complexing agents nitrilotriacetic acid (NTA) and ethylenediaminetetraacetic acid (EDTA) in aqueous solution

2000 ◽  
pp. 2029-2033 ◽  
Author(s):  
Florinella Muñoz ◽  
Clemens von Sonntag
Keyword(s):  
Aqueous Solution ◽  
Ethylenediaminetetraacetic Acid ◽  
Nitrilotriacetic Acid ◽  
Complexing Agents ◽  
Tertiary Amines

The Extraction of Anionic Beryllium Complexes by Tri-iso-octylamine

1962 ◽  
Vol 15 (3) ◽  
pp. 457 ◽  
Author(s):  
HJ de Bruin ◽  
D Kairaitis ◽  
RB Temple
Keyword(s):  
Aqueous Solution ◽  
Stability Constants ◽  
Complexing Agents ◽  
Conditional Stability ◽  
Tertiary Amines ◽  
Ph Titration ◽  
Anionic Complexes ◽  
The Stability ◽  
Conditional Stability Constants ◽  
Beryllium Complexes

The extraction of beryllium from aqueous solution by long-chain tertiary amines has been observed in the presence of ligands giving rise to anionic complexes. The nature of the oxalate complex extracted by solutions of tri-iso-octylamine in chloroform has been studied in detail and the species formed in the organic phase were shown to have the composition Be(C2O4)2.{NH(i-C8H15)3}2. The complexes formed in aqueous solution between beryllium and several anionic complexing agents have been examined by the method of pH-titration. Conditional stability constants have been obtained for the complexes formed with oxalic, malonic, maleic, succinic, phthalic, and salicylic acids. Differences in their extractabilities can be explained semiquantitatively with the help of the stability constants and the acid association constants of the complexing agents.

Comparison of chelating ion exchange resins in sorption of copper(II) and zinc(II) complexes with ethylenediaminetetraacetic acid (EDTA) and nitrilotriacetic acid (NTA)

2008 ◽  
Vol 86 (10) ◽  
pp. 958-969 ◽  
Author(s):  
Dorota Kołodyńska ◽  
Zbigniew Hubicki
Keyword(s):  
Heavy Metal ◽  
Functional Groups ◽  
Heavy Metal Ions ◽  
Ethylenediaminetetraacetic Acid ◽  
Ph Value ◽  
Nitrilotriacetic Acid ◽  
Complexing Agents ◽  
Ion Exchange Resins ◽  
Ion Exchangers ◽  
Exchange Resins

This paper investigates the macroporous chelating ion exchangers with different functional groups for their sorption properties towards the copper(II) and zinc(II) ions. The investigations by the dynamic and static methods were carried out in the presence of traditional complexing agents. The differences in affinity of Cu(II) and Zn(II) complexes with these complexones result from the kind of functional groups of the chelating ion exchangers, such as thiourea, aminomethylphosphonate, iminodiacetate, and polyamine groups as well as from the pH value. The quantitative removal of studied heavy metal complexes using chelating ion exchangers is achieved in the case when resins compete successfully for the heavy metal ions against these chelators.Key words: chelating resins, heavy metals, EDTA, NTA.

Photooxidation at Platinum Colloidal TiO2 Aqueous-Solution Interfaces. I. Ethylenediaminetetraacetic Acid and Related-Compounds

1986 ◽  
Vol 39 (5) ◽  
pp. 757 ◽  
Author(s):  
DN Furlong ◽  
D Wells ◽  
WHF Sasse
Keyword(s):  
Carbon Dioxide ◽  
Aqueous Solution ◽  
Ethylenediaminetetraacetic Acid ◽  
Oxidation Potential ◽  
Illumination Time ◽  
Carbonium Ions ◽  
Production Of Hydrogen ◽  
Glycine Derivatives ◽  
Lactic Acids ◽  
Exhaustive Oxidation

The photooxidation of ethylenediaminetetraacetic acid ( edta ) and related glycine derivatives, at Pt/TiO2/aqueous solution interfaces, has been monitored via the production of hydrogen and carbon dioxide. Yields are consistent with the exhaustive oxidation of methoxycarbonyl groups and the rate varied with the number and distribution of such groups. A photooxidation pathway is proposed which involves the oxidation of intermediate carbonium ions. Plausible molecular intermediates, such as formic acid and formaldehyde in the case of edta , have been shown in separate experiments to be photooxidized according to the proposed pathway. The maximum rate of oxidation for each donor depends on its oxidation potential and its tendency to adsorb on TiO2 surfaces. Desorption due to pH increase, as well as consumption of the donor, causes the rate to decline rapidly with illumination time. Acetic and malonic acids gave some hydrogen but underwent mainly (> c. 80%) photo-Kolbe decarboxylation to yield carbon dioxide and methane. By contrast the oxidation of oxomalonic, pyruvic and lactic acids proceeded mainly via a H2 producing pathway similar to that established for edta. The oxidation of pyruvic and lactic acids ceased at a yield of one mole of CO2 per mole of acid.

EFFECTS OF COMPLEXING ON THE HOMOGENEOUS REDUCTION OF MERCURIC SALTS IN AQUEOUS SOLUTION BY MOLECULAR HYDROGEN

1956 ◽  
Vol 34 (10) ◽  
pp. 1372-1381 ◽  
Author(s):  
G. J. Korinek ◽  
J. Halpern
Keyword(s):  
Aqueous Solution ◽  
Molecular Hydrogen ◽  
Hydrogen Molecule ◽  
Bimolecular Reaction ◽  
Mercury Atom ◽  
Complexing Agents ◽  
Mercuric Ion ◽  
Rate Determining Step ◽  
Homogeneous Reduction

The effects of various complexing agents on the homogeneous reduction of mercuric salts by molecular hydrogen in aqueous solution were determined. In all cases the kinetics suggest that the rate-determining step is a bimolecular reaction between a mercuric ion or complex and a hydrogen molecule, probably leading to the formation of an intermediate mercury atom. The reactivity of various mercuric complexes was found to decrease in the following order: HgSO4 > Hg++ > HgAc2, HgPr2 > HgCl2 > HgBr2 > Hg(EDA)2++. Addition of anions such as OH−, CO3=, Ac−, Pr−, and Cl−, in excess of the amounts required to form stable mercuric complexes, was found to increase the rate. An interpretation of these effects is given.

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