<?xml version="1.0" encoding="utf-8" standalone="yes"?><feed xmlns="http://www.w3.org/2005/Atom"><generator uri="https://gohugo.io" version="0.141.0">Hugo v0.141.0</generator><id>https://millironx.millironx.page/@indiewebpub/tags/diffusion/</id><link rel="self" type="application/atom+xml" href="https://millironx.millironx.page/@indiewebpub/tags/diffusion/feed.xml"/><link rel="alternate" type="text/html" href="https://millironx.millironx.page/@indiewebpub/tags/diffusion/"/><updated>2025-03-31T00:14:19+00:00</updated><title>All content tagged "diffusion" on Milliron X</title><entry><id>https://millironx.millironx.page/@indiewebpub/academia/hydronium-pva/</id><link rel="alternate" href="https://doi.org/10.1021/acsestengg.2c00107"/><title>Investigation of Hydronium Diffusion in Poly(vinyl alcohol) Hydrogels: A Critical First Step to Describe Acid Transport for Encapsulated Bioremediation</title><published>2022-09-02T00:00:00+00:00</published><updated>2022-09-02T00:00:00+00:00</updated><author><name>Carson J. Silsby</name><uri>https://millironx.millironx.page/@indiewebpub/people/carson-j.-silsby/</uri></author><author><name>Jonathan R. Counts</name><uri>https://millironx.millironx.page/@indiewebpub/people/jonathan-r.-counts/</uri></author><author><name>Thomas A. Christensen II</name><uri>https://millironx.millironx.page/@indiewebpub/people/thomas-a.-christensen-ii/</uri></author><author><name>Mark F. Roll</name><uri>https://millironx.millironx.page/@indiewebpub/people/mark-f.-roll/</uri></author><author><name>Kristopher v. Waynant</name><uri>https://millironx.millironx.page/@indiewebpub/people/kristopher-v.-waynant/</uri></author><author><name>James G. Moberly</name><uri>https://millironx.millironx.page/@indiewebpub/people/james-g.-moberly/</uri></author><category term="paper"/><category term="diffusion"/><category term="hydrogels"/><category term="ionic strength"/><category term="polymers"/><category term="transport properties"/><summary type="text">
Bioremediation of chlorinated aliphatic hydrocarbon-contaminated aquifers can be hindered by high contaminant concentrations and acids generated during remediation. Encapsulating microbes in hydrogels may provide a protective, tunable environment from inhibiting compounds; however, current approaches to formulate successful encapsulated systems rely on trial and error rather than engineering approaches because fundamental information on mass-transfer coefficients is lacking. To address this knowledge gap, hydronium ion mass-transfer rates through two commonly used hydrogel materials, poly(vinyl alcohol) and alginic acid, under two solidification methods (chemical and cryogenic) were measured. Variations in hydrogel crosslinking conditions, polymer composition, and solvent ionic strength were investigated to understand how each influenced hydronium ion diffusivity. A three-way ANOVA indicated that the ionic strength, membrane type, and crosslinking method significantly (p &lt; 0.001) contributed to changes in hydronium ion mass transfer. Hydronium ion diffusion increased with ionic strength, counter to what is observed in aqueous-only (no polymer) solutions. Co-occurring mechanisms correlated to increased hydronium ion diffusion with ionic strength included an increased water fraction within hydrogel matrices and hydrogel contraction. Measured diffusion rates determined in this study provide first principal design information to further optimize encapsulating hydrogels for bioremediation.</summary><content type="html" xml:lang="en" xml:base="https://millironx.millironx.page/@indiewebpub/">
&lt;p>Bioremediation of chlorinated aliphatic hydrocarbon-contaminated aquifers can be
hindered by high contaminant concentrations and acids generated during
remediation. Encapsulating microbes in hydrogels may provide a protective,
tunable environment from inhibiting compounds; however, current approaches to
formulate successful encapsulated systems rely on trial and error rather than
engineering approaches because fundamental information on mass-transfer
coefficients is lacking. To address this knowledge gap, hydronium ion
mass-transfer rates through two commonly used hydrogel materials, poly(vinyl
alcohol) and alginic acid, under two solidification methods (chemical and
cryogenic) were measured. Variations in hydrogel crosslinking conditions,
polymer composition, and solvent ionic strength were investigated to understand
how each influenced hydronium ion diffusivity. A three-way ANOVA indicated that
the ionic strength, membrane type, and crosslinking method significantly (&lt;em>p&lt;/em> &amp;lt;
0.001) contributed to changes in hydronium ion mass transfer. Hydronium ion
diffusion increased with ionic strength, counter to what is observed in
aqueous-only (no polymer) solutions. Co-occurring mechanisms correlated to
increased hydronium ion diffusion with ionic strength included an increased
water fraction within hydrogel matrices and hydrogel contraction. Measured
diffusion rates determined in this study provide first principal design
information to further optimize encapsulating hydrogels for bioremediation.&lt;/p>
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