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Voltammetric Method for Determining the Trace Moisture Content of Organic Solvents Based on Hydrogen-Bonding Interactions with Quinones
被引:55
|作者:
Hui, Yanlan
[1
]
Chng, Elaine Lay Khirn
[1
]
Chua, Louisa Pei-Lyn
[1
]
Liu, Wan Zhen
[1
]
Webster, Richard D.
[1
]
机构:
[1] Nanyang Technol Univ, Sch Math & Phys Sci, Div Chem & Biol Chem, Singapore 637371, Singapore
关键词:
ATTAINING EXPONENTIAL CONVERGENCE;
FINITE-DIFFERENCE EQUATIONS;
THIOIC S-ESTERS;
ELECTRON SPIN RESONANCE;
UNEQUALLY SPACED GRIDS;
N-ALKYL ESTERS;
ELECTROCHEMICAL REDUCTION;
APROTIC-SOLVENTS;
FLUX ERROR;
DIGITAL SIMULATIONS;
D O I:
10.1021/ac9026719
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Voltammetry experiments were performed on the natural quinone, vitamin K-1 (VK1), in a range of organic solvents of varying dielectric constant that are commonly used for electrochemical measurements [dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF), acetonitrile (MeCN), propionitrile (EtCN), butyronitrile (PrCN), 1,2-dichloroethane (DCE), dichloromethane (DCM), and 1,1,2,2-tetrachloroethane (TCE)]. The water content of the solvents was accurately measured using Karl Fischer (KF) coulometric titrations, and the voltammetric data were used to estimate the degree of hydrogen-bonding interactions between the reduced forms of VK1 and variable levels of water, thereby allowing a ranking of water-substrate interactions in the different solvents. The voltammetric data were analyzed based on interactions that occur between reduced forms of VK1 and the water, the solvent, and the supporting electrolyte. Calibration data were obtained that are independent of the nature of the reference electrode and allow the water content of the solvents to be calculated by performing a single voltammetric scant in the presence of VK1 and 0.2 M supporting electrolyte (Bu4NPF6).
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页码:1928 / 1934
页数:7
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