W. El Fadel, S. El Hantati, Z. Nour, A. Dinane, A. Samaouali, B. Messnaoui
{"title":"298.15 K 时水/蔗糖/NH4H2PO4 系统的热力学行为以及 NH4H2PO4 在蔗糖溶液中的盐析作用","authors":"W. El Fadel, S. El Hantati, Z. Nour, A. Dinane, A. Samaouali, B. Messnaoui","doi":"10.1007/s10953-023-01343-7","DOIUrl":null,"url":null,"abstract":"<div><p>The hygrometric method is used to determine new thermodynamic data on water activity and saturated aqueous solution of the water/<span>d</span>-sucrose/ammonium dihydrogen phosphate (ADP) system in a wide range of NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> molality, ranging from 0.1 to 3 mol⋅kg<sup>−1</sup>, and for various <span>d</span>-sucrose contents from 0 to 4 mol⋅kg<sup>−1</sup>. Powder X-ray diffraction (XRD) and attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy were used to characterize the solid state. The Pitzer–Simonson–Clegg model (PSC) is used to fit the experimental data of osmotic coefficient obtained from water activities data. The predicted saturated aqueous solutions, with the PSC model, are in good agreement with experimental data. For the concentration inferior to 1 mol⋅kg<sup>−1</sup>, the negative deviation from ideality was shown with increasing the ADP concentrations. The estimated values of the activity coefficient of <span>d</span>-sucrose, activity coefficient of ADP, and the Gibbs energy of transfer of ADP from water to mixture (water/<span>d</span>-sucrose) show that both ADP and <span>d</span>-sucrose exert significant salting-out effects on the aqueous solution.</p></div>","PeriodicalId":666,"journal":{"name":"Journal of Solution Chemistry","volume":"53 6","pages":"790 - 814"},"PeriodicalIF":1.4000,"publicationDate":"2023-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thermodynamic Behavior of the System Water/d-Sucrose/NH4H2PO4 at 298.15 K, and Salting-Out of NH4H2PO4 on d-Sucrose Solutions\",\"authors\":\"W. El Fadel, S. El Hantati, Z. Nour, A. Dinane, A. Samaouali, B. Messnaoui\",\"doi\":\"10.1007/s10953-023-01343-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The hygrometric method is used to determine new thermodynamic data on water activity and saturated aqueous solution of the water/<span>d</span>-sucrose/ammonium dihydrogen phosphate (ADP) system in a wide range of NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> molality, ranging from 0.1 to 3 mol⋅kg<sup>−1</sup>, and for various <span>d</span>-sucrose contents from 0 to 4 mol⋅kg<sup>−1</sup>. Powder X-ray diffraction (XRD) and attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy were used to characterize the solid state. The Pitzer–Simonson–Clegg model (PSC) is used to fit the experimental data of osmotic coefficient obtained from water activities data. The predicted saturated aqueous solutions, with the PSC model, are in good agreement with experimental data. For the concentration inferior to 1 mol⋅kg<sup>−1</sup>, the negative deviation from ideality was shown with increasing the ADP concentrations. The estimated values of the activity coefficient of <span>d</span>-sucrose, activity coefficient of ADP, and the Gibbs energy of transfer of ADP from water to mixture (water/<span>d</span>-sucrose) show that both ADP and <span>d</span>-sucrose exert significant salting-out effects on the aqueous solution.</p></div>\",\"PeriodicalId\":666,\"journal\":{\"name\":\"Journal of Solution Chemistry\",\"volume\":\"53 6\",\"pages\":\"790 - 814\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2023-12-29\",\"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://link.springer.com/article/10.1007/s10953-023-01343-7\",\"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://link.springer.com/article/10.1007/s10953-023-01343-7","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Thermodynamic Behavior of the System Water/d-Sucrose/NH4H2PO4 at 298.15 K, and Salting-Out of NH4H2PO4 on d-Sucrose Solutions
The hygrometric method is used to determine new thermodynamic data on water activity and saturated aqueous solution of the water/d-sucrose/ammonium dihydrogen phosphate (ADP) system in a wide range of NH4H2PO4 molality, ranging from 0.1 to 3 mol⋅kg−1, and for various d-sucrose contents from 0 to 4 mol⋅kg−1. Powder X-ray diffraction (XRD) and attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy were used to characterize the solid state. The Pitzer–Simonson–Clegg model (PSC) is used to fit the experimental data of osmotic coefficient obtained from water activities data. The predicted saturated aqueous solutions, with the PSC model, are in good agreement with experimental data. For the concentration inferior to 1 mol⋅kg−1, the negative deviation from ideality was shown with increasing the ADP concentrations. The estimated values of the activity coefficient of d-sucrose, activity coefficient of ADP, and the Gibbs energy of transfer of ADP from water to mixture (water/d-sucrose) show that both ADP and d-sucrose exert significant salting-out effects on the aqueous solution.
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.