Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures
Structure at the nanoscale in the organic phase of liquid-liquid extraction systems is often tied to separation performance. However, the weak interactions that drive extractant assembly lead to poorly defined structures that are challenging to identify. Here, we investigate the mechanism of water e...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2024-07, Vol.26 (26), p.1889-1811 |
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description | Structure at the nanoscale in the organic phase of liquid-liquid extraction systems is often tied to separation performance. However, the weak interactions that drive extractant assembly lead to poorly defined structures that are challenging to identify. Here, we investigate the mechanism of water extraction for a malonamide extractant commonly applied to f-element separations. We measure extractant concentration fluctuations in the organic phase with small angle X-ray scattering (SAXS) before and after contact with water at fine increments of extractant concentration, finding no qualitative changes upon water uptake that might suggest significant nanoscopic reorganization of the solution. The critical composition for maximum fluctuation intensity is consistent with small water-extractant adducts. The extractant concentration dependence of water extraction is consistent with a power law close to unity in the low concentration regime, suggesting the formation of 1 : 1 water-extractant adducts as the primary extraction mechanism at low concentration. At higher extractant concentrations, the power law slope increases slightly, which we find is consistent with activity effects modeled using Flory-Huggins theory without introduction of additional extractant-water species. Molecular dynamics simulations are consistent with these findings. The decrease in interfacial tension with increasing extractant concentration shows a narrow plateau region, but it is not correlated with any change in fluctuation or water extraction trends, further suggesting no supramolecular organization such as reverse micellization. This study suggests that water extraction in this system is particularly simple: it relies on a single mechanism at all extractant concentrations, and only slightly enhances the concentration fluctuations characteristic of the dry binary extractant/diluent mixture.
Structure, composition, and speciation in the organic phase of liquid-liquid extraction systems. |
doi_str_mv | 10.1039/d4cp01369g |
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Structure, composition, and speciation in the organic phase of liquid-liquid extraction systems.</description><subject>Adducts</subject><subject>Alkanes</subject><subject>Contact angle</subject><subject>Liquid-liquid extraction</subject><subject>Mixtures</subject><subject>Molecular dynamics</subject><subject>Power law</subject><subject>Surface tension</subject><subject>Water</subject><subject>X-ray scattering</subject><issn>1463-9076</issn><issn>1463-9084</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpd0UFPwyAUB3BiNG5OL941jV6MSRUKtPRops4lJnrQeGwQaGW2MIHG-e3Fbc7EE4_w4-W9_AE4RPACQVxeSiLmEOG8bLbAEJEcpyVkZHtTF_kA7Hk_gxAiivAuGGDGSsoIGYKXqfG6eQs-0SbY5JMH5RK1CI6LoK1JuJEJbxqnGr68d0q8caN95xNbJx1vreGdlirl7Ts3Kun0IvRO-X2wU_PWq4P1OQLPtzdP47v0_mEyHV_dpwJnOKQZkyIjCBclY6SsC0YLlmeKUiK5pIRTSblUBYk1LAl9lZAoRkVdlCT-qzEegZNVX-uDrrzQIQ4orDFKhCqjMC9oHtHZCs2d_eiVD1WnvVBtGye2va8wLCCDBFES6ek_OrO9M3GFH0VphiFDUZ2vlHDWe6fqau50x91XhWD1k0l1TcaPy0wmER-vW_avnZIb-htCBEcr4LzYvP6Fir8BluaPsw</recordid><startdate>20240703</startdate><enddate>20240703</enddate><creator>Bonnett, Brittany L</creator><creator>Rahman, Tasnim</creator><creator>Poe, Derrick</creator><creator>Seifert, Soenke</creator><creator>Stephenson, G. 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Brian</creatorcontrib><creatorcontrib>Servis, Michael J</creatorcontrib><creatorcontrib>Argonne National Laboratory (ANL), Argonne, IL (United States)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonnett, Brittany L</au><au>Rahman, Tasnim</au><au>Poe, Derrick</au><au>Seifert, Soenke</au><au>Stephenson, G. Brian</au><au>Servis, Michael J</au><aucorp>Argonne National Laboratory (ANL), Argonne, IL (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2024-07-03</date><risdate>2024</risdate><volume>26</volume><issue>26</issue><spage>1889</spage><epage>1811</epage><pages>1889-1811</pages><issn>1463-9076</issn><issn>1463-9084</issn><eissn>1463-9084</eissn><abstract>Structure at the nanoscale in the organic phase of liquid-liquid extraction systems is often tied to separation performance. However, the weak interactions that drive extractant assembly lead to poorly defined structures that are challenging to identify. Here, we investigate the mechanism of water extraction for a malonamide extractant commonly applied to f-element separations. We measure extractant concentration fluctuations in the organic phase with small angle X-ray scattering (SAXS) before and after contact with water at fine increments of extractant concentration, finding no qualitative changes upon water uptake that might suggest significant nanoscopic reorganization of the solution. The critical composition for maximum fluctuation intensity is consistent with small water-extractant adducts. The extractant concentration dependence of water extraction is consistent with a power law close to unity in the low concentration regime, suggesting the formation of 1 : 1 water-extractant adducts as the primary extraction mechanism at low concentration. At higher extractant concentrations, the power law slope increases slightly, which we find is consistent with activity effects modeled using Flory-Huggins theory without introduction of additional extractant-water species. Molecular dynamics simulations are consistent with these findings. The decrease in interfacial tension with increasing extractant concentration shows a narrow plateau region, but it is not correlated with any change in fluctuation or water extraction trends, further suggesting no supramolecular organization such as reverse micellization. This study suggests that water extraction in this system is particularly simple: it relies on a single mechanism at all extractant concentrations, and only slightly enhances the concentration fluctuations characteristic of the dry binary extractant/diluent mixture.
Structure, composition, and speciation in the organic phase of liquid-liquid extraction systems.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38895844</pmid><doi>10.1039/d4cp01369g</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-9984-3443</orcidid><orcidid>https://orcid.org/0000-0002-2404-1865</orcidid><orcidid>https://orcid.org/0000000224041865</orcidid><orcidid>https://orcid.org/0000000199843443</orcidid></addata></record> |
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subjects | Adducts Alkanes Contact angle Liquid-liquid extraction Mixtures Molecular dynamics Power law Surface tension Water X-ray scattering |
title | Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures |
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