In Situ Observations of Barium Sulfate Nucleation in Nanopores

Alexander B. Brady, Juliane Weber, Ke Yuan, Lawrence F. Allard, Omar Avina, Ramon Ogaz, Yao Jen Chang, Nikhil Rampal, Vitalii Starchenko, Gernot Rother, Lawrence M. Anovitz, Jose L. Bañuelos, Hsiu Wen Wang, Andrew G. Stack

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The nucleation and growth of barium sulfate in nanoporous silica was investigated using in situ small-angle X-ray scattering and X-ray pair distribution function analysis, together with ex situ transmission and scanning transmission electron microscopy (TEM and STEM) imaging. We found that crystalline barite formation in micropores is likely preceded by a nonbulk barite phase in the nanopores, indicating a possible nonclassical nucleation pathway for barium sulfate under confinement. The nucleation of barium sulfate inside the nanopores stopped at ∼12% of the pores filled and was seemingly limited by the formation of crystals near the exterior of the silica particles, which likely blocked subsequent solute transport into the interior of the nanopores. The growth rate of barium sulfate was fit using the Johnson-Mehl-Avrami-Kolmogorov equation and constrained using a growth rate of barite of ∼1.0 × 10-7 mol/m2/s, obtained from previous studies, but is consistent with TEM and STEM observations made here. The inferred nucleation rate of barium sulfate inside nanopores is estimated to be on the order of 1.0 × 109 nuclei/m2/s, which is 2 orders of magnitude higher than previous measurements on a planar silica substrate (∼1.0 × 107 nuclei/m2/s). This implies that the ability of silica nanopores to promote barium sulfate nucleation is sufficiently high as to create a potentially self-limiting condition, where the nucleation reaction is shut down prematurely because rapid growth blocks reactant transport.

Original languageEnglish
Pages (from-to)6941-6951
Number of pages11
JournalCrystal Growth and Design
Volume22
Issue number12
DOIs
StatePublished - Dec 7 2022

Funding

This material is primarily based upon work supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. This research also used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02–06CH11357. Part of the TEM characterization was performed at the Kuiper Materials Imaging and Characterization Facility at the University of Arizona with financial support of the Core Facility Pilot Project Grant Program awarded to Dr. Tom Zega (PI) and J.W. (Co-PI). O.A., R.O., and J.L.B. were supported by the National Science Foundation under Grant #NSF-HRD-1826745. The authors acknowledge NASA grants #NNX12AL47G, #NNX15AJ22G, and #NNX07AI520, and NSF grants #1531243 and #EAR-0841669 for funding of the instrumentation in the Kuiper Materials Imaging and Characterization Facility at the University of Arizona. The authors thank Tiffany Kinnibrugh and Soenke Seiffert for their help with the data acquisition.

FundersFunder number
National Science Foundation#NSF-HRD-1826745
U.S. Department of Energy
National Aeronautics and Space Administration12AL47G, 15AJ22G, -0841669, 1531243, 07AI520
Office of Science
Basic Energy Sciences
Argonne National LaboratoryDE-AC02–06CH11357
University of Arizona
Chemical Sciences, Geosciences, and Biosciences Division

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