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 language | English |
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Pages (from-to) | 6941-6951 |
Number of pages | 11 |
Journal | Crystal Growth and Design |
Volume | 22 |
Issue number | 12 |
DOIs | |
State | Published - 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.
Funders | Funder number |
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National Science Foundation | #NSF-HRD-1826745 |
U.S. Department of Energy | |
National Aeronautics and Space Administration | 12AL47G, 15AJ22G, -0841669, 1531243, 07AI520 |
Office of Science | |
Basic Energy Sciences | |
Argonne National Laboratory | DE-AC02–06CH11357 |
University of Arizona | |
Chemical Sciences, Geosciences, and Biosciences Division |