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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
Main Authors: Anouti, Meriem, Jones, Jennifer, Boisset, Aurélien, Jacquemin, Johan, Caillon-Caravanier, Magaly, Lemordant, Daniel
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cited_by cdi_FETCH-LOGICAL-c483t-6ebed949d1493e006c81a7d1ed445884b00faecc0f7f7b792ccee8bb93e903053
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container_title Journal of colloid and interface science
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creator Anouti, Meriem
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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
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(○) 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. 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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
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1095-7103
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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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