<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-15T22:10:31Z</responseDate><request verb="GetRecord" identifier="oai:repository.ucc.edu.co:20.500.12494/15766" metadataPrefix="dim">https://repository.ucc.edu.co/server/oai/request</request><GetRecord><record><header><identifier>oai:repository.ucc.edu.co:20.500.12494/15766</identifier><datestamp>2024-08-11T01:59:16Z</datestamp><setSpec>com_20.500.12494_11</setSpec><setSpec>col_20.500.12494_247</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author">Romero Nieto, Alba Miledy</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Cerquera, Néstor Enrique</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Martínez, Fleming</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Delgado, Daniel Ricardo</dim:field>
   <dim:field mdschema="dc" element="coverage" qualifier="temporal" lang="spa">Vol. 287</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2019-12-16T22:57:43Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2019-12-16T22:57:43Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2019-08-01</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri" lang="spa">https://doi.org/10.1016/j.molliq.2019.110894</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/20.500.12494/15766</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="bibliographicCitation" lang="spa">Alba Miledy Romero-Nieto, Nestor Enrique Cerquera, Fleming Martínez, Daniel Ricardo Delgado, Thermodynamic study of the solubility of ethylparaben in acetonitrile+ water cosolvent mixtures at different temperatures, Journal of Molecular Liquids Volume 287, 1 August 2019, 110894</dim:field>
   <dim:field mdschema="dc" element="description" lang="spa">The thermodynamic analysis of the solubility of ethylparaben (1) in acetonitrile (1) + water (2) cosolvent mixtures at 9 temperatures, 10 cosolvent mixtures and the 2 pure solvents, water and acetonitrile, is reported herein. The solution thermodynamic functions were calculated from the experimental solubility data, using the van't Hoff and Gibbs equations, following the approach proposed by Krug et al. Thus, the solubility of ethylparaben is thermo-dependent, reaching its minimum value in pure water at 278.15 K and its maximum value in the cosolvent mixture w1 = 0.90 at 318.18 K. The enthalpy of solution is positive in all cases, which is an indication of the endothermic process, with an enthalpy-driven mixing process in mixtures rich in water and by entropy mixtures rich in acetonitrile.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="spa">The thermodynamic analysis of the solubility of ethylparaben (1) in acetonitrile (1) + water (2) cosolvent mixtures at 9 temperatures, 10 cosolvent mixtures and the 2 pure solvents, water and acetonitrile, is reported herein. The solution thermodynamic functions were calculated from the experimental solubility data, using the van't Hoff and Gibbs equations, following the approach proposed by Krug et al. Thus, the solubility of ethylparaben is thermo-dependent, reaching its minimum value in pure water at 278.15 K and its maximum value in the cosolvent mixture w1 = 0.90 at 318.18 K. The enthalpy of solution is positive in all cases, which is an indication of the endothermic process, with an enthalpy-driven mixing process in mixtures rich in water and by entropy mixtures rich in acetonitrile.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="tableofcontents" lang="spa">Highlights. --&#xd;
Abstract. --&#xd;
Keywords. --&#xd;
1. Introduction. --&#xd;
2. Experimental. --&#xd;
2.1. Reagents. --&#xd;
2.2. Preparation of the solvent mixture. --&#xd;
2.3. Determination of solubility. --&#xd;
3. Results and discussion. --&#xd;
3.1. Solubility of ethyl paraben in cosolvent mixtures of acetonitrile + water. --&#xd;
3.2. Activity coefficients of ethylparaben. --&#xd;
3.3. Thermodynamic functions of solution. --&#xd;
3.4. Thermodynamic functions of ethylparaben transfer. --&#xd;
3.5. Thermodynamic functions of the ethylparaben mixture. --&#xd;
3.6. Enthalpy–entropy compensation. --&#xd;
4. Conclusions. --&#xd;
Acknowledgements. --&#xd;
Declaration of competing interest. --&#xd;
References.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="cvlac" lang="spa">http://scienti.colciencias.gov.co:8081/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0001402116</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="orcid" lang="spa">https://orcid.org/0000-0002-4835-9739</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="gruplac" lang="spa">https://scienti.colciencias.gov.co/gruplac/jsp/visualiza/visualizagr.jsp?nro=00000000004151</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="email" lang="spa">danielr.delgado@campusucc.edu.co</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="gsid" lang="spa">https://scholar.google.com/citations?hl=es&amp;user=OW0mejcAAAAJ&amp;view_op=list_works</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="spa">10</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="spa">El sevier</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="spa">Universidad Cooperativa de Colombia, Facultad de Ingenierías, Ingeniería Industrial, Neiva</dim:field>
   <dim:field mdschema="dc" element="publisher" qualifier="program" lang="spa">Ingeniería Industrial</dim:field>
   <dim:field mdschema="dc" element="publisher" qualifier="place" lang="spa">Neiva</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="isversionof" lang="spa">https://www.sciencedirect.com/science/article/abs/pii/S0167732219313078</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="ispartofjournal" lang="spa">Journal of Molecular Liquids</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">J.F. Gomes, A. Lopes, M. Gmureka, R.M. Quinta-Ferreira, R.C. Martins Study of the influence of the matrix characteristics over the photocatalytic ozonation of parabens using Ag-TiO2 Sci. Total Environ., 646 (2019), pp. 1468-1477</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">T. Benijts, W. Lambert, A. Leenheer Analysis of multiple endocrine disruptors in environmental waters via wide-spectrum solid-phase extraction and dual-polarity ionization LC-Ion Trap-MS/MS Anal. Chem., 76 (2004), pp. 704-711</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">E.J. Routledge, J. Parker, J. Odum, J. Ashby, J.P. Sumpter Some alkyl hydroxy benzoate preservatives (parabens) are estrogenic Toxicol. Appl. Pharmacol., 153 (1998), pp. 12-19</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">P.D. Darbre, A. Aljarrah, W.R. Miller, N.G. Coldham, M.J. Sauer, G.S. Pope Concentrations of parabens in human breast tumours J. Appl. Toxicol., 24 (2004), pp. 5-13</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A. Jouyban Handbook of Solubility Data for Pharmaceuticals CRC Press, Boca Raton, FL (2010)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.N. Martin, P. Bustamante, A.H.C. Chun Physical Pharmacy: Physical Chemical Principles in the Pharmaceutical Sciences (4th ed.), Lea &amp; Febiger, Philadelphia (1993)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">J.K.H. Ma, B.W. Hadzija Basic Physical Pharmacy Jones &amp; Bartlett Learning, Burlington (2013)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">D. Bledzka, J. Gromadzińska, W. Wasowicz Parabens. From environmental studies to human health Environ. Int., 67 (2014), pp. 27-42</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">D.I. Caviedes Rubio, D.R. Delgado Regulación ambiental sobre los productos farmacéuticos residuales en ambientes acuáticos Entornos, 28 (2015), pp. 76-80</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">D.I. Caviedes Rubio, D.M. Camacho Feria, D.R. Delgado Tratamientos para la remoción de antibacteriales y agentes antimicrobiales presentes en aguas residuales Rev. Logos Cienc. Tecnol., 9 (2017), pp. 43-62</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">Z.J. Cárdenas, D.M. Jiménez, D.R. Delgado, O.A. Almanza, A. Jouyban, F. Martínez, W.E. Acree Jr. Solubility and preferential solvation of some n-alkyl-parabens in methanol + water mixtures at 298.15 K J. Chem. Thermodyn., 108 (2017), pp. 26-37</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">T. Higuchi, K.A. Connors Phase-solubility techniques Advances in Analytical Chemistry and Instrumentation, vol. 4, John Wiley &amp; Sons, Inc, New York (1965)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">D.M. Jiménez, Z.J. Cárdenas, D.R. Delgado, M.Á. Peña, F. Martínez Solubility temperature dependence and preferential solvation of sulfadiazine in 1, 4-dioxane+ water co-solvent mixtures Fluid Phase Equilib., 397 (2015), pp. 26-36</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">D.R. Delgado, E.F. Vargas, F. Martínez Thermodynamic study of the solubility of procaine HCl in some ethanol+ water cosolvent mixtures J. Chem. Eng. Data, 55 (2010), pp. 2900-2904</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.J. Parker The effects of solvation on the properties of anions in dipolar aprotic solvents Q. Rev. Chem. Soc. (2) (1962), pp. 163-187</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.N. Paruta, B.B. Sheth Solubility of parabens in syrup vehicles J. Pharm. Sci., 55 (1966), pp. 1208-1211</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.E. Beezer, S. Forster, W.-B. Park, G.J. Rimmer, G. Buckton Solution thermodynamics of 4-hydroxybenzoates in water, 95% ethanol-water, 1-octanol and hexane Thermochim. Acta, 178 (1991), pp. 59-65</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.F.M. Barton Solubility parameter Chem. Rev., 75 (1975), pp. 731-753</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">S.H. Yalkowsky Solubility and Solubilization in Aqueous Media American Chemical Society and Oxford University Press, New York (1999)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.N. Paruta, B.J. Sciarrone, N.G. Lordi Solubility of salicylic acid as a function of dielectric constant J. Pharm. Sci., 53 (1964), pp. 1349-1353</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.N. Paruta, B.J. Sciarrone, N.G. Lordi Solubility profiles for the xanthines in dioxane-water mixtures J. Pharm. Sci., 54 (1965), pp. 838-841</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">A.N. Paruta Solubility of the parabens in dioxane-water mixtures J. Pharm. Sci., 58 (1969), pp. 204-206</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">M.A. Peña, P. Bustamante, B. Escalera, A. Reíllo, J.M. Bosque-Sendra Solubility and phase separation of benzocaine and salicylic acid in 1,4-dioxane–water mixtures at several temperatures J. Pharm. Biomed. Anal., 36 (2004), pp. 571-578</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">J.H. Hildebrand The term “regular solution” Nature, 168 (1951), p. 868</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">J.H. Hildebrand, J.M. Prausnitz, R.L. Scott Regular and Related Solutions Van Nostrand Reinhold, New York (1970)</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">G.L. Perlovich, S.V. Rodionov, A. Bauer-Brandl Thermodynamics of solubility, sublimation and solvation processes of parabens Eur. J. Pharm. Sci., 24 (2005), pp. 25-33</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">R.J. Prankerd Solid-state properties of drugs. I. Estimation of heat capacities for fusion and thermodynamic functions for solution from aqueous solubility-temperature dependence measurements Int. J. Pharm., 84 (1992), pp. 233-244</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Thermodynamic analysis</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Cosolvent mixture</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Ethylparaben</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Acetonitrile</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Solubility</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Thermodynamic analysis</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Cosolvent mixture</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Ethylparaben</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Acetonitrile</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Solubility</dim:field>
   <dim:field mdschema="dc" element="title" lang="spa">Thermodynamic study of the solubility of ethylparaben in acetonitrile + water cosolvent mixtures at different temperatures</dim:field>
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