Evaluating the solute-solvent interactions of glycine in aqueous solution of choline based ionic liquids through volumetric properties at T= (293.15 to 313.15 K)
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作者:
Panda, Somenath
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Durban Univ Technol, Dept Chem, ZA-4001 Durban, South Africa
Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, IndiaDurban Univ Technol, Dept Chem, ZA-4001 Durban, South Africa
Panda, Somenath
[1
,2
]
Gardas, Ramesh L.
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Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, IndiaDurban Univ Technol, Dept Chem, ZA-4001 Durban, South Africa
Gardas, Ramesh L.
[2
]
Deenadayalu, Nirmala
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Durban Univ Technol, Dept Chem, ZA-4001 Durban, South AfricaDurban Univ Technol, Dept Chem, ZA-4001 Durban, South Africa
Deenadayalu, Nirmala
[1
]
机构:
[1] Durban Univ Technol, Dept Chem, ZA-4001 Durban, South Africa
[2] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India
The molecular interactions of amino acids with the different ionic liquids (ILs) are important in order to study the stability and behavior of the amino acids. In this study, we have examined the interactions of glycine in the aqueous solutions with two aprotic ionic liquids based on cholinium cation, namely, cholinium propanoate [Chl][Pro] and cholinium hexanoate [Chl][Hex]. The different interactions were quantified through their partial molar volumes (V-phi) where it was found that the shorter chained [Chl][Pro] interacts more with the molecules of the glycine, compared to [Chl][Hex]. The derivation of infinite dilution parameter through the application of the Masson equation revealed further insights into the different types of interactions. The calculated limiting partial molar volume of transfer, (Delta V-phi(0) values for water to aqueous solutions of ILs indicated that hydrophobic-hydrophobic interactions dominates over other attractive interactions in longer chain [Chl][Hex] than in [Chl][Pro]. The calculation of hydration number (n(H)) revealed that with increasing IL concentrations, lesser number of water molecules remain attached to the glycine, indicating the structure breaking nature of the ILs, which were further confirmed from the Hepler equation. (C) 2019 Elsevier B.V. All rights reserved.
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VelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, IndiaVelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, India
Losetty, Venkatramana
Hazarathaiah Yadav, C.
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VelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, IndiaVelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, India
Hazarathaiah Yadav, C.
Devi Wilfred, Cecilia
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Univ Teknol PETRONAS, Fac Fundamental & Appl Sci, Bandar Seri Iskandar 32610, Perak, MalaysiaVelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, India
Devi Wilfred, Cecilia
Gardas, Ramesh L.
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Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, IndiaVelTech Rangarajan Dr Sagunthala R&D Inst Sci & T, Dept Chem, Chennai 600062, Tamil Nadu, India
机构:
Massey Univ, Inst Fundamental Sci Chem, Private Bag 11 222, Palmerston North, New ZealandMassey Univ, Inst Fundamental Sci Chem, Private Bag 11 222, Palmerston North, New Zealand
Hedwig, Gavin R.
Jameson, Geoffrey B.
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Massey Univ, Inst Fundamental Sci Chem, Private Bag 11 222, Palmerston North, New ZealandMassey Univ, Inst Fundamental Sci Chem, Private Bag 11 222, Palmerston North, New Zealand
Jameson, Geoffrey B.
Hoiland, Harald
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Univ Bergen, Dept Chem, N-5020 Bergen, NorwayMassey Univ, Inst Fundamental Sci Chem, Private Bag 11 222, Palmerston North, New Zealand