Structure and Properties of "Type IV" Lanthanide Nitrate Hydrate:Urea Deep Eutectic Solvents

被引:59
作者
Hammond, Oliver S. [1 ,2 ]
Bowron, Daniel T. [3 ]
Edler, Karen J. [1 ,2 ]
机构
[1] Univ Bath, Dept Chem, Claverton Down, Bath BA2 7AY, Avon, England
[2] Univ Bath, Ctr Sustainable Chem Technol, Claverton Down, Bath BA2 7AY, Avon, England
[3] Rutherford Appleton Lab, Sci & Technol Facil Council, ISIS Neutron & Muon Source, Didcot OX11 0QX, Oxon, England
基金
英国工程与自然科学研究理事会;
关键词
Deep eutectic solvents; Lanthanides; Neutron scattering; Ionic liquids; Nanostructure; Physical properties; TEMPERATURE MIXTURES LTTMS; SODIUM DODECYL-SULFATE; CHOLINE CHLORIDE; IONIC LIQUID; NEUTRON-DIFFRACTION; MOLTEN-SALTS; PHYSICAL-PROPERTIES; SURFACE-TENSION; LACTIC-ACID; HOLE THEORY;
D O I
10.1021/acssuschemeng.8b05548
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of lanthanide nitrate hydrate:urea "Type IV' deep eutectic solvents (DES; Ln = Ce, Pr, Nd) were prepared and their physical properties measured, showing very high surface tension and density, with low viscosity and glass transition temperatures. Calculated Gordon parameters were similar to water, with lower molecular volumes than "Type III" DES. The LnDES were used as reaction media for efficient combustion synthesis of lanthanide oxides. The nanostructure of the Ce(NO3)(3)center dot 6H(2)O:urea DES was measured using neutron and X-ray scattering and resolved with empirical potential structure refinement (EPSR) atomistic modeling. The models showed the existence of strongly bonded yet fluxional oligomeric [-Ce-NO3-] polyanions and polycations. Because of the excess of the molecular component in the mixture, an intercalating H-bonded nanostructure containing mainly water and urea was observed, which can be considered as a lubricating molecular pseudophase. This dichotomous structural observation helps to explain some of the unusual physical properties such as low viscosity and high surface tension, while also challenging the fundamental definitions of DES.
引用
收藏
页码:4932 / 4940
页数:17
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