A study has been made of the elution behavior of curium(III), americium(III), plutonium(III), actinium(III), plutonium(IV), neptunium(IV), uraniuM(IV), thorium(IV), neptunium(V), plutonium (VI), uranium (VI), lanthanum(III), cerium(III), europium(III), ytterbium(III), ytterium(III), strontium(II), barium(II), radium(II), cesium(I) with 3.2 M, 6.2 M, 9.3 M, and 12.2 M HCl solutions from Dowex-50 cation exchange resin columns. These elutions show that in high concentrations of hydrochloric acid the actinides form complex ions with chloride ion to a much greater extent than the lanthanides. The strengths of the tripositive actinide complex ions apparently go in the order plutonium > americium> curium, although their ionic radii also decrease in this same order. To explain these results, a partial covalent character may be ascribed to the bonding in the transuranium complex ions. It is shown that a reasonable structure for such covalent bonding involves hybridization of the 5f orbitals in the actinide elements.

During his distinguished career spanning more than 50 years, Nobel laureate (Chemistry) Glenn T Seaborg published over 500 works. This volume puts together about 100 of his selected papers. The papers are divided into five categories. Category I consists of papers which detail the discovery of 10 transuranium elements and numerous heavy isotopes of special importance. Category II papers describe the discovery of a number of isotopes which became the workhorses of nuclear medicine or found other applications. Papers in Category III describe how the chemical properties of transuranium elements were originally determined, how chemistry is applied in nuclear sciences, and other chemical investigations, including early work done with the great chemist G N Lewis. Papers in Category IV cover radioactive decay chains and nuclear systematics. Lastly, papers in Category V illustrate how the powerful methods of chemistry are used to explain nuclear reactions in low, intermediate and high energy nuclear physics.

This volume will capture transformational changes in both the chemistry and engineering side of solvent extraction, creating new directions and deepening our understanding of the structure and dynamics of liquid-liquid systems from the molecular- to nano- to meso- to bulk-scale. Reviews will cover advances in microfluidics, new tools for understanding the structure and dynamics of the liquid-liquid interface, ionic liquids in liquid-liquid extraction, molecular dynamics to visualize interactions in the solvent phase, liquid-liquid electrochemistry to interrogate the energetics of interfacial transport and complexation, design of new extractants, and the streamlining of process applications.