4.4 Article

Loss and Isotopic Fractionation of Alkali Elements during Diffusion-Limited Evaporation from Molten Silicate: Theory and Experiments

Journal

ACS EARTH AND SPACE CHEMISTRY
Volume 5, Issue 4, Pages 755-784

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsearthspacechem.0c00263

Keywords

diffusion; evaporation; K; Rb; isotope fractionation; Vesta

Funding

  1. NASA [NNX17AE86G, NNX17AE87G, 80NSSC17K0744, 80NSSC20K0821, 80NSSC20K1409, NNX17AE84G]
  2. NSF [EAR-2001098]
  3. NASA Earth and Space Science Fellowship [NNX15AQ97H]
  4. NSF Instrumentation and Facilities Program
  5. NASA [1002070, NNX17AE84G, 802392, NNX15AQ97H] Funding Source: Federal RePORTER

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Moderately volatile elements such as Na, K, and Rb are depleted differently in planetary bodies, and can be used as tracers to unravel the history of MVE depletion. Experimental studies at high temperatures have shown that diffusion plays a key role in governing the evaporation of K and Rb, leading to isotopic fractionation. Results suggest that the depletion of Na, Rb, and K in planetary bodies can be explained by evaporation from small, differentiated planetesimals under specific conditions.
Moderately volatile elements (MVEs) are variably depleted in planetary bodies, reflecting the imprints of nebular and planetary processes. Among MVEs, Na, K, and Rb are excellent tracers for unraveling the history of MVE depletion in planetary bodies because they have similar geochemical behaviors but can be chemically fractionated by evaporation and condensation processes. Furthermore, K and Rb are amenable to high-precision isotopic analyses, which can help constrain the conditions of evaporation and condensation. To quantitatively understand why Na, K, and Rb are depleted in planetary bodies, we have carried out vacuum evaporation experiments from basaltic melt at 1200 and 1400 degrees C to study their evaporation kinetics and isotopic fractionations. We chose this composition because it is relevant to evaporation from small differentiated planetesimals. The Rb isotopic compositions of the evaporation residues were measured by multicollector inductively coupled plasma mass spectrometry (MC-ICPMS), and the K isotopic compositions were measured along profiles across the residues by secondary ion mass spectrometry (SIMS). In the 1400 degrees C run products, we found that the concentrations of both K and Rb in the run products decreased from core to rim, which was accompanied by a heavy K isotope enrichment near the surface. This indicates that, in this run, evaporation was limited by diffusion. To use those data quantitatively, we derive analytical equations that describe the evaporation rate and isotopic fractionation associated with diffusion-limited evaporation from a sphere, slab, and cylinder in transient and quasi-steady state regimes. This model is used to tease out the roles that diffusive transport in the melt and evaporation at the melt/gas interface play in setting the elemental depletion and isotopic composition of the residue. Under our experimental conditions, volatility decreases in the order of Na, Rb, and K. Using our experimental results in a thermodynamic model, we have estimated the product gamma Gamma of activity coefficients x evaporation coefficients of Na, Rb, and K. The measured isotopic compositions of the residues are well explained using Rayleigh distillations, whereby the relative volatilities of K and Rb isotopes are given by the square root of their masses. We use our results and previously published data to predict how K and Rb could have been lost as a function of temperature, melt composition, oxygen fugacity, and saturation degree relevant to Vesta's building blocks. We find that the K and Rb depletions, K/Rb elemental fractionation, and delta K-41 and delta Rb-87 isotopic fractionations of Vesta (as sampled by howardite-eucrite-diogenite (HED) meteorites) are best explained by evaporation of submillimeter size objects for 0.1-10 years at moderate temperatures (similar to 1050 degrees C) in a medium similar to 98.8% saturated.

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