SULFUR DIOXIDE INTERACTION WITH MONOETHANOLAMMONIUM AND POLYETHYLENEPOLYAMMONIUM CITRATES AQUEOUS SOLUTIONS PRODUCTS COMPOSITION AND THE RELATIVE STABILITY

The paper presents the results of pH, redox, and conductometric studies on the acid-base interaction during sulfur dioxide chemisorption by aqueous solutions containing 0.1 mol/L monoethanolammonium (MEA·1/3CA) and polyethylenepolyammonium (PEPA·1/3CA) citrates, as well as buffer solutions of monoethanolamine–monoethanolammonium citrate (MEA·1/6CA) and polyethylenepolyamine–polyethylenepolyammonium citrate (PEPA·1/6CA), in comparison with sodium citrate. The composition of the compounds formed during SO2 absorption by Na3Cit, MEA·1/3CA, PEPA·1/3CA, MEA·1/6CA, and PEPA·1/6CA solutions at 273–313 K was determined.For the same amount of absorbed sulfur dioxide, an increase in specific electrical conductivity (æ) with rising temperature was observed in SO2–Na3Cit–H2O and SO2–MEA×1/3CA–H2O solutions within the 273–313 K range. However, in the SO2–MEA×1/3CA–H2O, SO2–PEPA×1/3CA–H2O, SO2–MEA×1/6CA–H2O, and SO2–PEPA×1/6CA–H2O systems, a decrease in Δæ was noted upon heating to 303 K, which is attributed to their ion-molecular composition. Based on developed mathematical models, the ion-molecular component composition of SO2–MEA×1/3CA–H2O and SO2–MEA×1/6CA–H2O solutions was determined at 283–313 K. The concentration and thermodynamic constants for the formation of ionic associates were calculated:(NH3CH2CH2OH)2SO3, {H3CH2CH2OH}{HOC3H4(COOH)2(COO-)} (Ia), {H3CH2CH2OH}2{HOC3H4(COOH)(COO-)2} (IIa), {H3CH2CH2OH}2{HOC3H4(COOH)2(COO-)} (IIb), {H3CH2CH2OH}3{HOC3H4(COO-)3} (IIIa), as well as ion-molecular associates:{H3CH2CH2OH}{HOC3H4(COOH)3} (Ib), {NH2CH2CH2OH}3{H3CH2CH2OH}3{HOC3H4(COO-)3} (IVa), {NH2CH2CH2OH}2{H3CH2CH2OH}4{HOC3H4(COO-)3} (IVb). In SO2–MEA×1/3CA–H2O solutions, as the temperature increases, bond rearrangement occurs in ionic associates IIa and Ib, as indicated by the absence of a clear temperature dependence ofp, along with the strengthening of IIa and Ib. Conversely, in SO2–MEA×1/6CA–H2O solutions, increasing temperature leads to the weakening of the bonds in compounds Ia, IIIa, IVa, and IVb, while in compound Ib, the bonds strengthen.

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Journal
Ukrainian Chemistry Journal
Published
2025-04-25
DOI
https://doi.org/10.33609/2708-129x.91.3.2025.3-24
Primary Topic
Extraction and Separation Processes
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article
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article

SULFUR DIOXIDE INTERACTION WITH MONOETHANOLAMMONIUM AND POLYETHYLENEPOLYAMMONIUM CITRATES AQUEOUS SOLUTIONS PRODUCTS COMPOSITION AND THE RELATIVE STABILITY

T. S. Bіenkovska, Р. Е. Хома, С. В. Водзинский
Ukrainian Chemistry Journal
Extraction and Separation Processes
article

SULFUR DIOXIDE INTERACTION WITH MONOETHANOLAMMONIUM AND POLYETHYLENEPOLYAMMONIUM CITRATES AQUEOUS SOLUTIONS PRODUCTS COMPOSITION AND THE RELATIVE STABILITY

T. S. Bіenkovska, Р. Е. Хома, С. В. Водзинский
article en

Abstract

The paper presents the results of pH, redox, and conductometric studies on the acid-base interaction during sulfur dioxide chemisorption by aqueous solutions containing 0.1 mol/L monoethanolammonium (MEA·1/3CA) and polyethylenepolyammonium (PEPA·1/3CA) citrates, as well as buffer solutions of monoethanolamine–monoethanolammonium citrate (MEA·1/6CA) and polyethylenepolyamine–polyethylenepolyammonium citrate (PEPA·1/6CA), in comparison with sodium citrate. The composition of the compounds formed during SO2 absorption by Na3Cit, MEA·1/3CA, PEPA·1/3CA, MEA·1/6CA, and PEPA·1/6CA solutions at 273–313 K was determined.For the same amount of absorbed sulfur dioxide, an increase in specific electrical conductivity (æ) with rising temperature was observed in SO2–Na3Cit–H2O and SO2–MEA×1/3CA–H2O solutions within the 273–313 K range. However, in the SO2–MEA×1/3CA–H2O, SO2–PEPA×1/3CA–H2O, SO2–MEA×1/6CA–H2O, and SO2–PEPA×1/6CA–H2O systems, a decrease in Δæ was noted upon heating to 303 K, which is attributed to their ion-molecular composition. Based on developed mathematical models, the ion-molecular component composition of SO2–MEA×1/3CA–H2O and SO2–MEA×1/6CA–H2O solutions was determined at 283–313 K. The concentration and thermodynamic constants for the formation of ionic associates were calculated:(NH3CH2CH2OH)2SO3, {H3CH2CH2OH}{HOC3H4(COOH)2(COO-)} (Ia), {H3CH2CH2OH}2{HOC3H4(COOH)(COO-)2} (IIa), {H3CH2CH2OH}2{HOC3H4(COOH)2(COO-)} (IIb), {H3CH2CH2OH}3{HOC3H4(COO-)3} (IIIa), as well as ion-molecular associates:{H3CH2CH2OH}{HOC3H4(COOH)3} (Ib), {NH2CH2CH2OH}3{H3CH2CH2OH}3{HOC3H4(COO-)3} (IVa), {NH2CH2CH2OH}2{H3CH2CH2OH}4{HOC3H4(COO-)3} (IVb). In SO2–MEA×1/3CA–H2O solutions, as the temperature increases, bond rearrangement occurs in ionic associates IIa and Ib, as indicated by the absence of a clear temperature dependence ofp, along with the strengthening of IIa and Ib. Conversely, in SO2–MEA×1/6CA–H2O solutions, increasing temperature leads to the weakening of the bonds in compounds Ia, IIIa, IVa, and IVb, while in compound Ib, the bonds strengthen.

Ukrainian Chemistry JournalVol. 91(3)
Institute of Environmental Protection (PL)
Openalex Percentile: Top 91%
Extraction and Separation Processes
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