Daniela Ž. Popović, Tijana G. Ivanović, Jelena Miladinović, Zoran P. Miladinović, Ferenc T. Pastor, Mouad Arrad, Tijana Tomović
{"title":"通过电动势测量确定的 {yNaCl + (1 - y)NaH2PO4}(aq) AT T = 298.15 K 系统的活性系数","authors":"Daniela Ž. Popović, Tijana G. Ivanović, Jelena Miladinović, Zoran P. Miladinović, Ferenc T. Pastor, Mouad Arrad, Tijana Tomović","doi":"10.1007/s10953-024-01409-0","DOIUrl":null,"url":null,"abstract":"<p>The mean ionic activity coefficients of NaCl in the system {<i>y</i>NaCl + (1 − <i>y</i>) NaH<sub>2</sub>PO<sub>4</sub>}(aq) were determined by electromotive force measurements (EMF) in two series in which the NaCl ionic strength fraction was as follows: I series, <i>y</i> = (0.2368; 0.3101; 0.4101; 0.5051; 0.6090; 0.7775; 0.9039) and II series, <i>y</i> = (0.1998; 0.4005; 0.5993; 0.8105) in the range of total ionic strength of the solution <i>I</i><sub>m</sub> = (0.0887–1.0081) mol·kg<sup>−1</sup> at a temperature <i>T</i> = 298.15 K. A cell of the Na–ISE∣<span>\\({\\text{NaCl}(m}_{\\text{NaCl}})\\)</span>, <span>\\({\\text{Na}}{\\text{H}_{2}\\text{PO}}_{4}{(m}_{{\\text{Na}}{\\text{H}_{2}\\text{PO}}_{4}})\\)</span>∣Ag∣AgCl type was utilized for the EMF measurements. The standard electrode potential of the electrode pair was estimated as <i>E</i><sup>0</sup> = 23.2288 mV. The values of the mean ionic activity coefficient of NaCl in the mixed electrolyte solution, <span>\\({\\gamma }_{\\pm \\text{NaCl}}\\)</span>, were determined using the Nerst equation. The experimental results from this study were treated with the models proposed by Pitzer, Clegg and Scatchard to estimate the mixture parameters. A high degree of agreement was found between the experimental and calculated values of the mean ionic activity coefficients of NaCl with an average standard deviation of fit being <span>\\(\\text{s}.\\text{d}.\\left({\\gamma }_{\\pm }\\right)\\sim\\)</span> 2.5·10<sup>–3</sup> for each of the three models. The values of the osmotic coefficients of the system {<i>y</i>NaCl + (1 − <i>y</i>)NaH<sub>2</sub>PO<sub>4</sub>}(aq) were estimated based on the determined model parameters and compared with literature data. Negligible differences were found between the estimated and experimental values of the osmotic coefficients.</p>","PeriodicalId":666,"journal":{"name":"Journal of Solution Chemistry","volume":"100 1","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Activity Coefficients of the System {yNaCl + (1 − y)NaH2PO4}(aq) AT T = 298.15 K Determined by Electromotive Force Measurements\",\"authors\":\"Daniela Ž. Popović, Tijana G. Ivanović, Jelena Miladinović, Zoran P. Miladinović, Ferenc T. Pastor, Mouad Arrad, Tijana Tomović\",\"doi\":\"10.1007/s10953-024-01409-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The mean ionic activity coefficients of NaCl in the system {<i>y</i>NaCl + (1 − <i>y</i>) NaH<sub>2</sub>PO<sub>4</sub>}(aq) were determined by electromotive force measurements (EMF) in two series in which the NaCl ionic strength fraction was as follows: I series, <i>y</i> = (0.2368; 0.3101; 0.4101; 0.5051; 0.6090; 0.7775; 0.9039) and II series, <i>y</i> = (0.1998; 0.4005; 0.5993; 0.8105) in the range of total ionic strength of the solution <i>I</i><sub>m</sub> = (0.0887–1.0081) mol·kg<sup>−1</sup> at a temperature <i>T</i> = 298.15 K. A cell of the Na–ISE∣<span>\\\\({\\\\text{NaCl}(m}_{\\\\text{NaCl}})\\\\)</span>, <span>\\\\({\\\\text{Na}}{\\\\text{H}_{2}\\\\text{PO}}_{4}{(m}_{{\\\\text{Na}}{\\\\text{H}_{2}\\\\text{PO}}_{4}})\\\\)</span>∣Ag∣AgCl type was utilized for the EMF measurements. The standard electrode potential of the electrode pair was estimated as <i>E</i><sup>0</sup> = 23.2288 mV. The values of the mean ionic activity coefficient of NaCl in the mixed electrolyte solution, <span>\\\\({\\\\gamma }_{\\\\pm \\\\text{NaCl}}\\\\)</span>, were determined using the Nerst equation. The experimental results from this study were treated with the models proposed by Pitzer, Clegg and Scatchard to estimate the mixture parameters. A high degree of agreement was found between the experimental and calculated values of the mean ionic activity coefficients of NaCl with an average standard deviation of fit being <span>\\\\(\\\\text{s}.\\\\text{d}.\\\\left({\\\\gamma }_{\\\\pm }\\\\right)\\\\sim\\\\)</span> 2.5·10<sup>–3</sup> for each of the three models. The values of the osmotic coefficients of the system {<i>y</i>NaCl + (1 − <i>y</i>)NaH<sub>2</sub>PO<sub>4</sub>}(aq) were estimated based on the determined model parameters and compared with literature data. Negligible differences were found between the estimated and experimental values of the osmotic coefficients.</p>\",\"PeriodicalId\":666,\"journal\":{\"name\":\"Journal of Solution Chemistry\",\"volume\":\"100 1\",\"pages\":\"\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-08-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Solution Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s10953-024-01409-0\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solution Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s10953-024-01409-0","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Activity Coefficients of the System {yNaCl + (1 − y)NaH2PO4}(aq) AT T = 298.15 K Determined by Electromotive Force Measurements
The mean ionic activity coefficients of NaCl in the system {yNaCl + (1 − y) NaH2PO4}(aq) were determined by electromotive force measurements (EMF) in two series in which the NaCl ionic strength fraction was as follows: I series, y = (0.2368; 0.3101; 0.4101; 0.5051; 0.6090; 0.7775; 0.9039) and II series, y = (0.1998; 0.4005; 0.5993; 0.8105) in the range of total ionic strength of the solution Im = (0.0887–1.0081) mol·kg−1 at a temperature T = 298.15 K. A cell of the Na–ISE∣\({\text{NaCl}(m}_{\text{NaCl}})\), \({\text{Na}}{\text{H}_{2}\text{PO}}_{4}{(m}_{{\text{Na}}{\text{H}_{2}\text{PO}}_{4}})\)∣Ag∣AgCl type was utilized for the EMF measurements. The standard electrode potential of the electrode pair was estimated as E0 = 23.2288 mV. The values of the mean ionic activity coefficient of NaCl in the mixed electrolyte solution, \({\gamma }_{\pm \text{NaCl}}\), were determined using the Nerst equation. The experimental results from this study were treated with the models proposed by Pitzer, Clegg and Scatchard to estimate the mixture parameters. A high degree of agreement was found between the experimental and calculated values of the mean ionic activity coefficients of NaCl with an average standard deviation of fit being \(\text{s}.\text{d}.\left({\gamma }_{\pm }\right)\sim\) 2.5·10–3 for each of the three models. The values of the osmotic coefficients of the system {yNaCl + (1 − y)NaH2PO4}(aq) were estimated based on the determined model parameters and compared with literature data. Negligible differences were found between the estimated and experimental values of the osmotic coefficients.
期刊介绍:
Journal of Solution Chemistry offers a forum for research on the physical chemistry of liquid solutions in such fields as physical chemistry, chemical physics, molecular biology, statistical mechanics, biochemistry, and biophysics. The emphasis is on papers in which the solvent plays a dominant rather than incidental role. Featured topics include experimental investigations of the dielectric, spectroscopic, thermodynamic, transport, or relaxation properties of both electrolytes and nonelectrolytes in liquid solutions.