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Joseph F. Wild

Publications and source records attributed to Joseph F. Wild.

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Techno-economic Analysis of Light Isotope-enriched Elements for Lightweighting Applications

Lightweighting is critical to mass-sensitive applications such as aircraft and space transportation. Conventional lightweight strategies often rely on new designs of materials and structures. An alternative approach is to enrich the lightest stable isotopes in an element to reduce the elements atomic mass while having little effect on structural and chemical properties. However, the economic feasibility of this concept remains unclear. Here we present a techno-economic analysis of light isotope-enriched elements for lightweighting applications by estimating isotope enrichment cost and the economic gain from mass reduction. The enrichment cost is scaled from established large-scale processes. Twelve common aerospace-relevant elements are considered, including Li, B, C, Mg, Cl, Ti, Ni, Fe, Cu, Zn, Mo, and Sn. We find that nine elements, especially Li, B, Zn, Ni, Mo, and Sn, show potentially attractive economic benefit at moderate enrichment levels, whereas C, Mg, and Fe provide little or no benefit. With the optimized enrichment levels, an Airbus A380 is expected to save approximately USD 700 K over a 30-year operational lifetime, a SpaceX Falcon 9 could save USD 516 K, and a SpaceX Starship is expected to save USD 2.37 million over its whole lifetime. While the exact enrichment cost needs to be further investigated, these results provide an initial screening of promising candidate elements and highlight isotopic mass reduction as a potential drop-in lightweighting strategy.

cond-mat.mtrl-sci

Extreme breakdown of the Einstein relation in liquid water under centrifugation

We present evidence that the Einstein relation (ER) breaks down completely in pure water and dilute aqueous solutions under strong centrifugation fields at 40 oC. Isotopologues (e.g., H2O-18) and solutes migrate at a speed of only 5% of that predicted based on the ER. The ER is restored with the addition of solutes above a transition concentration (ct). We further discovered a new scaling law between the solute's partial molar density, the centrifugal acceleration, and ct, which can be quantitatively described by a two-phase model in analog to the Avrami model for phase transformation. The breakdown may stem from long-range dipole interactions or the hydrogen bond network in water, which are disrupted by the presence of solutes. This report shows that studying transport under centrifugation can be a new strategy to understand fundamental transport properties and complex interactions in liquids.

cond-mat.soft

Liquid solution centrifugation for safe, scalable, and efficient isotope separation

A general method of separating isotopes by centrifuging dissolved chemical compounds in a liquid solution is introduced. This technique can be applied to almost all elements and leads to large separation factors. The method has been demonstrated in several isotopic systems including Ca, Mo, O, and Li with single-stage selectivities of 1.046-1.067 per unit mass difference (e.g., 1.434 in 40Ca/48Ca, 1.134 in 16O/18O), which are beyond the capabilities of various conventional methods of isotope enrichment. Equations are derived to model the process and the results agree with those of the experiments. The scalability of the technique has been demonstrated by performing a three-stage enrichment of 48Ca, and the scalability is more broadly supported through analogies to the gas centrifuge, whereby countercurrent centrifugation can further multiply the separation factor by 5-10 times per stage in a continuous process. Optimal centrifuge conditions and solutions can achieve both high-throughput and highly efficient isotope separation.

nucl-ex