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Aggregation behavior in water of new imidazolium and pyrrolidinium alkycarboxylates protic ionic liquids
Variation of the specific conductivity as a function of PIL concentration in water solutions for pyrrolidinium carboxylate PILs at 298 K. (○) 1a; (●) 2a. A novel class of anionic surfactants was prepared through the neutralization of pyrrolidine or imidazole by alkylcarboxylic acids. The compounds,...
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Published in: | Journal of colloid and interface science 2009-12, Vol.340 (1), p.104-111 |
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description | Variation of the specific conductivity as a function of PIL concentration in water solutions for pyrrolidinium carboxylate PILs at 298
K. (○)
1a; (●)
2a.
A novel class of anionic surfactants was prepared through the neutralization of pyrrolidine or imidazole by alkylcarboxylic acids. The compounds, namely the pyrrolidinium alkylcarboxylates ([Pyrr][C
n
H
2
n
+1COO]) and imidazolium alkylcarboxylates ([Im][C
n
H
2
n
+1COO]), were obtained as ionic liquids at room temperature. Their aggregation behavior has been examined as a function of the alkyl chain length (from
n
=
5 to 8) by surface tensiometry and conductivity. Decreases in the critical micelle concentration (cmc) were obtained, for both studied PIL families, when increasing the anionic alkyl chain length (
n). Surprisingly, a large effect of the alkyl chain length was observed on the minimum surface area per surfactant molecule (
A
min) and, hence the maximum surface excess concentration (
Γ
max) when the counterion was the pyrrolidinium cation. This unusual comportment has been interpreted in term of a balance between van der Waals and coulombic interactions. Conductimetric measurements permit determination of the degree of ionization of the micelle (a) and the molar conductivity (
Λ
M) of these surfactants as a function of
n. The molar conductivities at infinite dilution in water (
Λ
∞
) of the [Pyrr]
+ and [Im]
+ cations have been then determined by using the classical Kohlraush equation. Observed change in the physicochemical, surface, and micellar properties of these new protonic ionic liquid surfactants can be linked to the nature of the cation. By comparison with classical anionic surfactants having inorganic counterions, pyrrolidinium alkylcarboxylates and imidazolium alkylcarboxylates exhibit a higher ability to aggregate in aqueous solution, demonstrating their potential applicability as surfactant. |
doi_str_mv | 10.1016/j.jcis.2009.07.061 |
format | article |
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K. (○)
1a; (●)
2a.
A novel class of anionic surfactants was prepared through the neutralization of pyrrolidine or imidazole by alkylcarboxylic acids. The compounds, namely the pyrrolidinium alkylcarboxylates ([Pyrr][C
n
H
2
n
+1COO]) and imidazolium alkylcarboxylates ([Im][C
n
H
2
n
+1COO]), were obtained as ionic liquids at room temperature. Their aggregation behavior has been examined as a function of the alkyl chain length (from
n
=
5 to 8) by surface tensiometry and conductivity. Decreases in the critical micelle concentration (cmc) were obtained, for both studied PIL families, when increasing the anionic alkyl chain length (
n). Surprisingly, a large effect of the alkyl chain length was observed on the minimum surface area per surfactant molecule (
A
min) and, hence the maximum surface excess concentration (
Γ
max) when the counterion was the pyrrolidinium cation. This unusual comportment has been interpreted in term of a balance between van der Waals and coulombic interactions. Conductimetric measurements permit determination of the degree of ionization of the micelle (a) and the molar conductivity (
Λ
M) of these surfactants as a function of
n. The molar conductivities at infinite dilution in water (
Λ
∞
) of the [Pyrr]
+ and [Im]
+ cations have been then determined by using the classical Kohlraush equation. Observed change in the physicochemical, surface, and micellar properties of these new protonic ionic liquid surfactants can be linked to the nature of the cation. By comparison with classical anionic surfactants having inorganic counterions, pyrrolidinium alkylcarboxylates and imidazolium alkylcarboxylates exhibit a higher ability to aggregate in aqueous solution, demonstrating their potential applicability as surfactant.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2009.07.061</identifier><identifier>PMID: 19758596</identifier><identifier>CODEN: JCISA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Agglomeration ; Carboxylate ; Cations ; Chains ; Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; Imidazolium ; Infinity ; Ionic liquids ; Mathematical analysis ; Micelar properties ; Micelles ; Micelles. Thin films ; Protic ionic liquids ; Pyrrolidinium ; Surface physical chemistry ; Surface tension ; Surfactants</subject><ispartof>Journal of colloid and interface science, 2009-12, Vol.340 (1), p.104-111</ispartof><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-6ebed949d1493e006c81a7d1ed445884b00faecc0f7f7b792ccee8bb93e903053</citedby><cites>FETCH-LOGICAL-c483t-6ebed949d1493e006c81a7d1ed445884b00faecc0f7f7b792ccee8bb93e903053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22054100$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19758596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anouti, Meriem</creatorcontrib><creatorcontrib>Jones, Jennifer</creatorcontrib><creatorcontrib>Boisset, Aurélien</creatorcontrib><creatorcontrib>Jacquemin, Johan</creatorcontrib><creatorcontrib>Caillon-Caravanier, Magaly</creatorcontrib><creatorcontrib>Lemordant, Daniel</creatorcontrib><title>Aggregation behavior in water of new imidazolium and pyrrolidinium alkycarboxylates protic ionic liquids</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>Variation of the specific conductivity as a function of PIL concentration in water solutions for pyrrolidinium carboxylate PILs at 298
K. (○)
1a; (●)
2a.
A novel class of anionic surfactants was prepared through the neutralization of pyrrolidine or imidazole by alkylcarboxylic acids. The compounds, namely the pyrrolidinium alkylcarboxylates ([Pyrr][C
n
H
2
n
+1COO]) and imidazolium alkylcarboxylates ([Im][C
n
H
2
n
+1COO]), were obtained as ionic liquids at room temperature. Their aggregation behavior has been examined as a function of the alkyl chain length (from
n
=
5 to 8) by surface tensiometry and conductivity. Decreases in the critical micelle concentration (cmc) were obtained, for both studied PIL families, when increasing the anionic alkyl chain length (
n). Surprisingly, a large effect of the alkyl chain length was observed on the minimum surface area per surfactant molecule (
A
min) and, hence the maximum surface excess concentration (
Γ
max) when the counterion was the pyrrolidinium cation. This unusual comportment has been interpreted in term of a balance between van der Waals and coulombic interactions. Conductimetric measurements permit determination of the degree of ionization of the micelle (a) and the molar conductivity (
Λ
M) of these surfactants as a function of
n. The molar conductivities at infinite dilution in water (
Λ
∞
) of the [Pyrr]
+ and [Im]
+ cations have been then determined by using the classical Kohlraush equation. Observed change in the physicochemical, surface, and micellar properties of these new protonic ionic liquid surfactants can be linked to the nature of the cation. By comparison with classical anionic surfactants having inorganic counterions, pyrrolidinium alkylcarboxylates and imidazolium alkylcarboxylates exhibit a higher ability to aggregate in aqueous solution, demonstrating their potential applicability as surfactant.</description><subject>Agglomeration</subject><subject>Carboxylate</subject><subject>Cations</subject><subject>Chains</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Imidazolium</subject><subject>Infinity</subject><subject>Ionic liquids</subject><subject>Mathematical analysis</subject><subject>Micelar properties</subject><subject>Micelles</subject><subject>Micelles. Thin films</subject><subject>Protic ionic liquids</subject><subject>Pyrrolidinium</subject><subject>Surface physical chemistry</subject><subject>Surface tension</subject><subject>Surfactants</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EokvhC3BAviBOCeMkjmOJS1XxT6rEBc6WY0-2syTx1k5alk-Pl13EDS5jjfV7T6P3GHspoBQg2re7cucolRWALkGV0IpHbCNAy0IJqB-zDUAlCq20umDPUtoBCCGlfsouhFayk7rdsNur7Tbi1i4UZt7jrb2nEDnN_MEuGHkY-IwPnCby9mcYaZ24nT3fH2LMm6f598_4_eBs7MOPw5hVie9jWMjxbJnnSHcr-fScPRnsmPDF-b1k3z68_3r9qbj58vHz9dVN4ZquXooWe_S60V40ukaA1nXCKi_QN43suqYHGCw6B4MaVK905Rxi1_cZ1lCDrC_Zm5NvPuJuxbSYiZLDcbQzhjUZnZNrOyH1f0lVN9BBW9WZrE6kiyGliIPZR5psPBgB5liF2ZljFeZYhQFlchVZ9Opsv_YT-r-Sc_YZeH0GbHJ2HKKdjx5_uKoC2QiAzL07cZhjuyeMJjnC2aGniG4xPtC_7vgFwfyprQ</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Anouti, Meriem</creator><creator>Jones, Jennifer</creator><creator>Boisset, Aurélien</creator><creator>Jacquemin, Johan</creator><creator>Caillon-Caravanier, Magaly</creator><creator>Lemordant, Daniel</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20091201</creationdate><title>Aggregation behavior in water of new imidazolium and pyrrolidinium alkycarboxylates protic ionic liquids</title><author>Anouti, Meriem ; Jones, Jennifer ; Boisset, Aurélien ; Jacquemin, Johan ; Caillon-Caravanier, Magaly ; Lemordant, Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-6ebed949d1493e006c81a7d1ed445884b00faecc0f7f7b792ccee8bb93e903053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Agglomeration</topic><topic>Carboxylate</topic><topic>Cations</topic><topic>Chains</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Imidazolium</topic><topic>Infinity</topic><topic>Ionic liquids</topic><topic>Mathematical analysis</topic><topic>Micelar properties</topic><topic>Micelles</topic><topic>Micelles. Thin films</topic><topic>Protic ionic liquids</topic><topic>Pyrrolidinium</topic><topic>Surface physical chemistry</topic><topic>Surface tension</topic><topic>Surfactants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anouti, Meriem</creatorcontrib><creatorcontrib>Jones, Jennifer</creatorcontrib><creatorcontrib>Boisset, Aurélien</creatorcontrib><creatorcontrib>Jacquemin, Johan</creatorcontrib><creatorcontrib>Caillon-Caravanier, Magaly</creatorcontrib><creatorcontrib>Lemordant, Daniel</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anouti, Meriem</au><au>Jones, Jennifer</au><au>Boisset, Aurélien</au><au>Jacquemin, Johan</au><au>Caillon-Caravanier, Magaly</au><au>Lemordant, Daniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aggregation behavior in water of new imidazolium and pyrrolidinium alkycarboxylates protic ionic liquids</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>340</volume><issue>1</issue><spage>104</spage><epage>111</epage><pages>104-111</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><coden>JCISA5</coden><abstract>Variation of the specific conductivity as a function of PIL concentration in water solutions for pyrrolidinium carboxylate PILs at 298
K. (○)
1a; (●)
2a.
A novel class of anionic surfactants was prepared through the neutralization of pyrrolidine or imidazole by alkylcarboxylic acids. The compounds, namely the pyrrolidinium alkylcarboxylates ([Pyrr][C
n
H
2
n
+1COO]) and imidazolium alkylcarboxylates ([Im][C
n
H
2
n
+1COO]), were obtained as ionic liquids at room temperature. Their aggregation behavior has been examined as a function of the alkyl chain length (from
n
=
5 to 8) by surface tensiometry and conductivity. Decreases in the critical micelle concentration (cmc) were obtained, for both studied PIL families, when increasing the anionic alkyl chain length (
n). Surprisingly, a large effect of the alkyl chain length was observed on the minimum surface area per surfactant molecule (
A
min) and, hence the maximum surface excess concentration (
Γ
max) when the counterion was the pyrrolidinium cation. This unusual comportment has been interpreted in term of a balance between van der Waals and coulombic interactions. Conductimetric measurements permit determination of the degree of ionization of the micelle (a) and the molar conductivity (
Λ
M) of these surfactants as a function of
n. The molar conductivities at infinite dilution in water (
Λ
∞
) of the [Pyrr]
+ and [Im]
+ cations have been then determined by using the classical Kohlraush equation. Observed change in the physicochemical, surface, and micellar properties of these new protonic ionic liquid surfactants can be linked to the nature of the cation. By comparison with classical anionic surfactants having inorganic counterions, pyrrolidinium alkylcarboxylates and imidazolium alkylcarboxylates exhibit a higher ability to aggregate in aqueous solution, demonstrating their potential applicability as surfactant.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19758596</pmid><doi>10.1016/j.jcis.2009.07.061</doi><tpages>8</tpages></addata></record> |
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ispartof | Journal of colloid and interface science, 2009-12, Vol.340 (1), p.104-111 |
issn | 0021-9797 1095-7103 |
language | eng |
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source | ScienceDirect Journals |
subjects | Agglomeration Carboxylate Cations Chains Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry Imidazolium Infinity Ionic liquids Mathematical analysis Micelar properties Micelles Micelles. Thin films Protic ionic liquids Pyrrolidinium Surface physical chemistry Surface tension Surfactants |
title | Aggregation behavior in water of new imidazolium and pyrrolidinium alkycarboxylates protic ionic liquids |
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