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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Physical chemistry chemical physics : PCCP 2024-07, Vol.26 (26), p.1889-1811
Hauptverfasser: Bonnett, Brittany L, Rahman, Tasnim, Poe, Derrick, Seifert, Soenke, Stephenson, G. Brian, Servis, Michael J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1811
container_issue 26
container_start_page 1889
container_title Physical chemistry chemical physics : PCCP
container_volume 26
creator Bonnett, Brittany L
Rahman, Tasnim
Poe, Derrick
Seifert, Soenke
Stephenson, G. Brian
Servis, Michael J
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1039_D4CP01369G</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3075523081</sourcerecordid><originalsourceid>FETCH-LOGICAL-c323t-28dc2413798849f7857862e554dad54a5d5ade74d540945bd04e85cf794c24f33</originalsourceid><addsrcrecordid>eNpd0UFPwyAUB3BiNG5OL941jV6MSRUKtPRops4lJnrQeGwQaGW2MIHG-e3Fbc7EE4_w4-W9_AE4RPACQVxeSiLmEOG8bLbAEJEcpyVkZHtTF_kA7Hk_gxAiivAuGGDGSsoIGYKXqfG6eQs-0SbY5JMH5RK1CI6LoK1JuJEJbxqnGr68d0q8caN95xNbJx1vreGdlirl7Ts3Kun0IvRO-X2wU_PWq4P1OQLPtzdP47v0_mEyHV_dpwJnOKQZkyIjCBclY6SsC0YLlmeKUiK5pIRTSblUBYk1LAl9lZAoRkVdlCT-qzEegZNVX-uDrrzQIQ4orDFKhCqjMC9oHtHZCs2d_eiVD1WnvVBtGye2va8wLCCDBFES6ek_OrO9M3GFH0VphiFDUZ2vlHDWe6fqau50x91XhWD1k0l1TcaPy0wmER-vW_avnZIb-htCBEcr4LzYvP6Fir8BluaPsw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3075523081</pqid></control><display><type>article</type><title>Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Bonnett, Brittany L ; Rahman, Tasnim ; Poe, Derrick ; Seifert, Soenke ; Stephenson, G. Brian ; Servis, Michael J</creator><creatorcontrib>Bonnett, Brittany L ; Rahman, Tasnim ; Poe, Derrick ; Seifert, Soenke ; Stephenson, G. Brian ; Servis, Michael J ; Argonne National Laboratory (ANL), Argonne, IL (United States)</creatorcontrib><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.</description><identifier>ISSN: 1463-9076</identifier><identifier>ISSN: 1463-9084</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/d4cp01369g</identifier><identifier>PMID: 38895844</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Adducts ; Alkanes ; Contact angle ; Liquid-liquid extraction ; Mixtures ; Molecular dynamics ; Power law ; Surface tension ; Water ; X-ray scattering</subject><ispartof>Physical chemistry chemical physics : PCCP, 2024-07, Vol.26 (26), p.1889-1811</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c323t-28dc2413798849f7857862e554dad54a5d5ade74d540945bd04e85cf794c24f33</cites><orcidid>0000-0001-9984-3443 ; 0000-0002-2404-1865 ; 0000000224041865 ; 0000000199843443</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38895844$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/2506756$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonnett, Brittany L</creatorcontrib><creatorcontrib>Rahman, Tasnim</creatorcontrib><creatorcontrib>Poe, Derrick</creatorcontrib><creatorcontrib>Seifert, Soenke</creatorcontrib><creatorcontrib>Stephenson, G. Brian</creatorcontrib><creatorcontrib>Servis, Michael J</creatorcontrib><creatorcontrib>Argonne National Laboratory (ANL), Argonne, IL (United States)</creatorcontrib><title>Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><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.</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. Brian</creator><creator>Servis, Michael J</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>OTOTI</scope><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></search><sort><creationdate>20240703</creationdate><title>Insights into water extraction and aggregation mechanisms of malonamide-alkane mixtures</title><author>Bonnett, Brittany L ; Rahman, Tasnim ; Poe, Derrick ; Seifert, Soenke ; Stephenson, G. Brian ; Servis, Michael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-28dc2413798849f7857862e554dad54a5d5ade74d540945bd04e85cf794c24f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adducts</topic><topic>Alkanes</topic><topic>Contact angle</topic><topic>Liquid-liquid extraction</topic><topic>Mixtures</topic><topic>Molecular dynamics</topic><topic>Power law</topic><topic>Surface tension</topic><topic>Water</topic><topic>X-ray scattering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonnett, Brittany L</creatorcontrib><creatorcontrib>Rahman, Tasnim</creatorcontrib><creatorcontrib>Poe, Derrick</creatorcontrib><creatorcontrib>Seifert, Soenke</creatorcontrib><creatorcontrib>Stephenson, G. 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>
fulltext fulltext
identifier ISSN: 1463-9076
ispartof Physical chemistry chemical physics : PCCP, 2024-07, Vol.26 (26), p.1889-1811
issn 1463-9076
1463-9084
1463-9084
language eng
recordid cdi_crossref_primary_10_1039_D4CP01369G
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T20%3A17%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insights%20into%20water%20extraction%20and%20aggregation%20mechanisms%20of%20malonamide-alkane%20mixtures&rft.jtitle=Physical%20chemistry%20chemical%20physics%20:%20PCCP&rft.au=Bonnett,%20Brittany%20L&rft.aucorp=Argonne%20National%20Laboratory%20(ANL),%20Argonne,%20IL%20(United%20States)&rft.date=2024-07-03&rft.volume=26&rft.issue=26&rft.spage=1889&rft.epage=1811&rft.pages=1889-1811&rft.issn=1463-9076&rft.eissn=1463-9084&rft_id=info:doi/10.1039/d4cp01369g&rft_dat=%3Cproquest_cross%3E3075523081%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3075523081&rft_id=info:pmid/38895844&rfr_iscdi=true