کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
201093 460533 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Volumetric properties of ionic liquids, 1-Ethyl-3-ethylimidazolium chloride [Emim][Cl] and 1-Ethyl-3-methylimidazolium hydrogen sulfate [Emim][HSO4] in sucrose aqueous solutions at T = (293.15–313.15) K and ambient pressure
ترجمه فارسی عنوان
خواص حجمی مایعات یونی، 1-متیل-3-ethylimidazolium کلرید [Emim] [CL] و 1-متیل 3-متیل سولفات هیدروژن [Emim] [HSO4] در محلول های آبی ساکارز در T = (293.15-313.15) K و فشار محیط
کلمات کلیدی
مایع یونی؛ سوکروز؛ تراکم؛ حجم مولی ظاهری؛ Expansibility؛ ساختار ساز
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• Densities for ternary solutions of (Sucrose + IL + H2O) are measured.
• [Emim][Cl] and [Emim][HSO4] at temperatures T=(293.15–313.15) K are considered.
• Vφ values for ILs increased with concentration of IL and temperature.
• ΔtVφ0, for both ionic liquids were negative which decreased with sucrose concentration.
• Both ionic liquids were structure maker in aqueous sucrose solutions.

The solute – solvent interactions considered in ternary systems ([Emim][Cl] + sucrose + H2O), ([Emim][HSO4] + sucrose + H2O) and binary systems ([Emim][Cl] + H2O), ([Emim][HSO4] + H2O). For this purpose, the apparent molar volumes, Vφ calculated from experimental density data. To obtain limiting apparent molar volumes Vφ0, the Redlich-Meyer type of equation fitted to apparent molar volume values. Then the limiting apparent molar volumes of transfer, ΔtVφ0, for studied ionic liquids (ILs) from water to aqueous solutions of sucrose calculated and their values were negative for all systems. The values of limiting apparent molar expansibility, Eφ0, obtained from first derivative of limiting apparent molar volumes with respect to temperature. The values of second derivative of limiting apparent molar volumes with respect to temperature indicated that both ionic liquids act as structure maker in studied solutions. Also results confirm that ion-ion interactions are stronger than ion-solvent interactions in these solutions.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fluid Phase Equilibria - Volume 425, 15 October 2016, Pages 120–126
نویسندگان
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