Publicado

2026-07-01

EFECTO DE LA TEMPERATURA EN EL EQUILIBRIO ÁCIDO-BASE DEL BICARBONATO

TEMPERATURE EFFECT ON THE BICARBONATE ACID-BASE EQUILIBRIUM

DOI:

https://doi.org/10.15446/rev.fac.cienc.v15n2.122472

Palabras clave:

Equilibrio químico, Ácido-base, Van't Hoff, Coeficiente de temperatura, Anfótero , Error analítico (es)
Chemical equilibrium, Acid-base, Van't Hoff, Temperature coefficient, Amphoteric, Analytic error (en)

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La constante de equilibrio químico, la escala de pH y la validez de las aproximaciones analíticas comunes en el estudio cuantitativo del equilibrio químico se ven afectadas por la temperatura. Sin embargo, en los cursos introductorios de química, el efecto cuantitativo de la temperatura sobre el equilibrio químico rara vez se aborda de manera explícita. Dado que el equilibrio ácido–base es esencial para comprender, modelar y llevar a cabo procesos químicos, biotecnológicos, biológicos y clínicos, el presente trabajo examina el equilibrio del bicarbonato en soluciones acuosas como un caso representativo desde el punto de vista didáctico. Mediante el uso de la ecuación de van’t Hoff, el estudio modela el efecto de la temperatura con el fin de mostrar cómo las variaciones dependientes de la temperatura pueden adquirir relevancia didáctica en la enseñanza y el aprendizaje del equilibrio químico. Se analizan tres modelos: un modelo exacto que incluye tanto el CO2 disuelto como el CO2 en fase gaseosa; un modelo intermedio basado únicamente en las reacciones anfóteras del bicarbonato, excluyendo el CO2; y un modelo aproximado que supone que el bicarbonato permanece como especie dominante mientras la concentración inicial se trata como constante, de modo que la acidez depende únicamente de las constantes de equilibrio. Los resultados muestran que el porcentaje de error en los cálculos de acidez para soluciones acuosas de bicarbonato, en función de la temperatura y de la concentración inicial, puede superar el intervalo típicamente considerado aceptable para los cálculos aproximados (1% a 5%). En consecuencia, la enseñanza del equilibrio químico en cursos introductorios debería incorporar explícitamente la dependencia con la temperatura de los cálculos analíticos, con el fin de promover el razonamiento crítico, hacer visible el carácter condicional de los métodos aproximados y fortalecer la articulación entre el formalismo matemático y el significado fisicoquímico del equilibrio.

The chemical equilibrium constant, the pH scale, and the validity of common analytical approximations in the quantitative study of chemical equilibrium are all affected by temperature. However, in introductory chemistry courses, the quantitative effect of temperature on chemical equilibrium is rarely addressed explicitly. Because acid–base equilibrium is essential for understanding, modeling, and carrying out chemical, biotechnological, biological, and clinical processes, the present work examines bicarbonate equilibrium in aqueous solutions as a representative instructional case. Using the van’t Hoff equation, the study models the effect of temperature in order to show how temperature-dependent variations can become instructionally significant in the teaching and learning of chemical equilibrium. Three models are analyzed: an exact model that includes both dissolved CO2 and CO2 in the gas phase; an intermediate model based only on the amphoteric reactions of bicarbonate, excluding CO2; and an approximate model that assumes bicarbonate remains the dominant species while the initial concentration is treated as constant, so that acidity depends only on the equilibrium constants. The results show that the error percentage in acidity calculations for aqueous bicarbonate solutions, as a function of temperature and initial concentration, can exceed the typically acceptable range for approximate calculations (1% to 5%). Consequently, the teaching of chemical equilibrium in introductory courses should explicitly incorporate the temperature dependence of analytical calculations to promote critical reasoning, make the conditional character of approximation methods visible, and strengthen the articulation between mathematical formalism and the physicochemical meaning of equilibrium.

Referencias

Adrogué, H. J., Gennari, F. J., Galla, J. H., & Madias, N. E. (2009). Assessing acid–base disorders. Kidney international, 76(12), 1239-1247.

Atasoy, B., Akkus, H., & Kadayifci, H. (2009). The effect of a conceptual change approach on understanding of students’ chemical equilibrium concepts. Research in Science & Technological Education, 27(3), 267-282.

Atkins, P. W. & Jones, L. (2012). Principios de Química, 5ed, Editorial Médica Panamericana.

Bandura, A. V. & Lvov, S.N. (2006), The Ionization Constant of Water Over Wide Ranges of Temperature and Density. J. Phys. Chem. Ref. Data, 35, 15-30.

Boron, W. F. (2004). Regulation of intracellular pH. Advances in physiology education, 28(4), 160-179.

Burton, G. W. (1965). Effects of the acid-base state upon the temperature coefficient of pH of blood. British Journal of Anaesthesia, 37(2), 89-102.

Carrero, J. I. (2024). Application of the van’t Hoff Equation to Phase Equilibria. ChemTexts, 10(3), 4-7.

Cheung, D. (2009). The adverse effects of Le Chatelier’s principle on teacher understanding of chemical equilibrium. Journal of Chemical Education, 86(4), 514.

Harms, P., Kostov, Y. & Rao, G. (2002). Bioprocess monitoring. Current opinion in biotechnology, 13(2), 124-127.

Harned, H. S., & Embree, N. D. (1934). The ionization constant of formic acid from 0 to 60. Journal of the American Chemical Society, 56(5), 1042-1044.

Harris, D. C. (2003). Análisis químico cuantitativo. Reverté.

Hu, Y. (2022). Temperature coefficient of seawater pH as a function of temperature, pH, DIC and salinity. Acta Oceanologica Sinica, 41(6), 114-118.

Jin, T., Kong, F. M., Yan, B. Y., Zhang, G. Z., Liu, Q., He, Q. Y., & Zhou, X. Y. (2022). Teaching and Learning Dialectical Relationship between Thermodynamic Equilibrium and Reaction Rate Constant. Educational Sciences: Theory & Practice, 22(2), 29-41.

Kajiya, D. (2021). Using Sodium Hydrogen Carbonate to Teach Chemical Concepts of Thermodynamics. Journal of Chemical Education, 98(12), 3968-3974.

Rosenberg, R. M., & Klotz, I. M. (2008). Chemical thermodynamics: basic concepts and methods. Wiley

Koga, N., Shigedomi, K., Kimura, T., Tatsuoka, T., & Mishima, S. (2013). Neutralization and acid dissociation of hydrogen carbonate ion: A thermochemical approach. Journal of Chemical Education, 90(5), 637-641.

Laidler, K. J. (2015). Van’t Hoff and the Scientific Imagination. In Culture of Chemistry: The Best Articles on the Human Side of 20th-Century Chemistry from the Archives of the Chemical Intelligencer (pp. 299-303). Boston, MA: Springer US.

Millero, F.J., Pierrot, D., Lee, K., Wanninkhofb, R., Feely, R., Sabine, C. L., Key, R.M. & Takahashie, T. (2002). Dissociation constants for carbonic acid determined from field measurements, Deep-Sea Res. I, 49, 1705-1723.

Mitchell, R. A., Herbert, D. A., & Carman, C. T. (1965). Acid-base constants and temperatura coefficients for cerebrospinal fluid. Journal of Applied Physiology, 20(1), 27-30.

Muradás, R. G., Ortega, C. S., Herrera, M. C., & Bosque, P. M. (2009). Concepciones alternativas, equilibrio químico y cambio conceptual. Enseñanza de las ciencias: revista de investigación y experiencias didácticas, Extra, 2406-2410.

Nagendrappa, G. (2007). Jacobus Henricus van’t Hoff: A short biographical sketch. Resonance, 12(5), 21-30.

Pedrosa, M. A., & Dias, M. H. (2000). Chemistry textbook approaches to chemical equilibrium and student alternative conceptions. Chemistry Education Research and Practice, 1(2), 227-236.

Pines, D., Ditkovich, J., Mukra, T., Miller, y., Kiefer, P. M., Daschakraborty, S., Hynes, J. T. & Pines, E. (2016). How Acidic Is Carbonic Acid?, J. Phys. Chem. B, 120, 2440-2451.

Rezsnyak, C. (2017). Determination of Thermodynamic Values (ΔS,ΔH, andΔG) from the Dissociation of a Weak Acid. World Journal of Chemical Education, 5(6), 193.

Riddle, H., & Lo-Fan-Hin, S. (2023). Students’ Misconceptions in Chemical Equilibria and Suggestions for Improved Instruction. New Directions in the Teaching of Natural Sciences, 18(1),1-13.

Sander, R. (2023). Compilation of Henry’s law constants (version 5.0.0) for water as solvent. Atmos. Chem. Phys., 23, 10901–12440.

Wenzel, T. J., Skoog, D. A., West, D. M., Holler, F. J., & Stanley R. Crouch, S. R. Fundamentals of analytical chemistry, International Ed.

Silbey, R. J., Alberty, R. A., Papadantonakis, G. A., & Bawendi, M. G. (2022). Physical chemistry. John Wiley & Sons.

Soli, A.L. & Byrne, R.H. (2002), CO2 System Hydration and Dehydration Kinetics and the Equilibrium CO2/H2CO3 Ratio in Aqueous NaCl Solution. Marine Chemistry, 78, 65-73.

Spear, F. S. (1996). The relationship between pH and PCO2 as the basis for simple classroom demonstration of chemical equilibrium in the carbonate system. Journal of Geoscience Education, 44(5), 565-568.

Stumm, W., Morgan, J. J. (2013). Aquatic chemistry: chemical equilibria and rates in natural waters. John Wiley & Sons.

Tang, D. (2025). Investigating Graduate Teaching Assistants’ Misconceptions in Chemical Equilibrium: Implications for Pedagogical Support. Doctoral dissertation, University of Oklahoma–Graduate College.

Wang, J. (2025). Reevaluating the van’t Hoff and Arrhenius Equations: How Temperature and Pressure Affect Chemical Reaction Thermodynamics, Equilibrium, and Kinetics. Civil, Architectural and Environmental Engineering Faculty Research & Creative Works. Missouri University of Science and Technology

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EFECTO DE LA TEMPERATURA EN EL EQUILIBRIO ÁCIDO-BASE DEL BICARBONATO. (2026). Revista De La Facultad De Ciencias, 15(2), 42-64. https://doi.org/10.15446/rev.fac.cienc.v15n2.122472