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At least 1,783 records · Page 99
All sourcesNASA NTRSDOE OSTI
DOE OSTI2018

May reversible water uptake/release by hydrates explain the thermal expansion of cement paste? ÔÇö Arguments from an inverse multiscale analysis

Quasi-instantaneous thermal expansion of cement pastes is governed by the relative humidity (RH) within their air-filled pores and by the decrease/increase of this internal RH resulting from a temperature decrease/increase. The latter effect is traced back to quasi-instantaneous water uptake/release by cement hydrates, using microporomechanics and a three-scale representation of mature cement pastes. Partially saturated gel and capillary pores are considered to be connected and spherical, with radii following exponential distributions. The Mori-Tanaka scheme provides the scale transition from effective pore pressures to eigenstrains at the cement paste level. This modeling approach, together with considering mass conservation of water, allows for downscaling macroscopic thermal expansion coefficients, so as to identify the molecular water uptake/release characteristics of the hydrates. The latter characteristics are mixture-independent, as shown by their use for predicting the thermal expansion coefficients of different mature cement pastes, with w/c-ratios ranging from 0.50 to 0.70.

36 MATERIALS SCIENCE↗
DOE OSTI2023

Separation of rare earth element radioisotopes by reverse-phase high-speed counter-current chromatography

Analytical scale purification of rare earth element (REE) radioisotopes is typically accomplished using cation-exchange resins (e.g. AG 50W-X8) and high-performance liquid chromatography (HPLC). Despite the variety of improvements made since the development of this separation process in the 1950s, nearest neighbor separations remain a challenge, as does the issue of irreversible sample adsorption. Herein, we report a study that evaluates the potential of high-speed counter-current chromatography (HSCCC) as an alternative method for purifying REE elements, with specific reference to separations of fission product REE of interest to nuclear forensics. Complementary HSCCC REE separation experiments, one spiked with radiotracer and REE fission product activity, allowed for in depth analysis of resulting fractions from both an elemental (inductively coupled plasma atomic emission spectroscopy, ICP-AES) and radiological (gamma-ray spectrometry, beta counting) purity perspective. The highly reproducible nature of separation profiles generated from HSCCC instruments was leveraged to simplify work-up of samples containing radioisotopes. Subsequent radioanalytical evaluation revealed minimal carryover of Eu into neighboring Sm and Tb fractions (as indicated by presence of 150Eu), and trace contamination of the Tb fraction with Y (as indicated by presence of 91Y). Subtle differences in stationary phase retention across the two columns were reflected in significant variations in decontamination factors of duplicate parallel separations. Furthermore, these differences paired with obtained distribution of radioisotopes provided valuable insights into future improvements. Collectively, this study represents a significant step forward in development of HSCCC technology for task specific REE radioisotope purification.

07 ISOTOPE AND RADIATION SOURCES↗