Critical Casimir interactions of colloids in micellar critical solutions
| dc.contributor.author | Helden, Laurent | |
| dc.contributor.author | Knippenberg, Timo | |
| dc.contributor.author | Tian, Li | |
| dc.contributor.author | Archambault, Aubin | |
| dc.contributor.author | Ginot, Félix | |
| dc.contributor.author | Bechinger, Clemens | |
| dc.date.accessioned | 2021-02-10T09:59:45Z | |
| dc.date.available | 2021-02-10T09:59:45Z | |
| dc.date.issued | 2021-03-18 | |
| dc.description.abstract | We study the temperature-dependence of critical Casimir interactions in a critical micellar solution of the nonionic surfactant C12E5 dissolved in water. Experimentally, this is achieved with total internal reflection microscopy (TIRM) which measures the interaction between a single particle and a flat wall. For comparison, we also studied the pair interactions of a two dimensional layer of colloidal particles in the identical micellar system which yields good agreement with the TIRM results. Although, at the surfactant concentration considered here, the fluid forms a dynamical network of wormlike micelles whose structure is considerably more complex than that of simple critical molecular fluids, the temperature-dependence of the measured interactions is - for surface-to-surface distances above 160 nm - in excellent quantitative agreement with theory. Below 160 nm, deviations arise which we attribute to the adsorption of micelles to the interacting surfaces. | eng |
| dc.description.version | published | eng |
| dc.identifier.doi | 10.1039/d0sm02021d | eng |
| dc.identifier.pmid | 33533371 | eng |
| dc.identifier.ppn | 1757267980 | |
| dc.identifier.uri | https://kops.uni-konstanz.de/handle/123456789/52787 | |
| dc.language.iso | eng | eng |
| dc.rights | terms-of-use | |
| dc.rights.uri | https://rightsstatements.org/page/InC/1.0/ | |
| dc.subject.ddc | 530 | eng |
| dc.title | Critical Casimir interactions of colloids in micellar critical solutions | eng |
| dc.type | JOURNAL_ARTICLE | eng |
| dspace.entity.type | Publication | |
| kops.citation.bibtex | @article{Helden2021-03-18Criti-52787,
year={2021},
doi={10.1039/d0sm02021d},
title={Critical Casimir interactions of colloids in micellar critical solutions},
number={10},
volume={17},
issn={1744-683X},
journal={Soft Matter},
pages={2737--2741},
author={Helden, Laurent and Knippenberg, Timo and Tian, Li and Archambault, Aubin and Ginot, Félix and Bechinger, Clemens}
} | |
| kops.citation.iso690 | HELDEN, Laurent, Timo KNIPPENBERG, Li TIAN, Aubin ARCHAMBAULT, Félix GINOT, Clemens BECHINGER, 2021. Critical Casimir interactions of colloids in micellar critical solutions. In: Soft Matter. Royal Society of Chemistry (RSC). 2021, 17(10), pp. 2737-2741. ISSN 1744-683X. eISSN 1744-6848. Available under: doi: 10.1039/d0sm02021d | deu |
| kops.citation.iso690 | HELDEN, Laurent, Timo KNIPPENBERG, Li TIAN, Aubin ARCHAMBAULT, Félix GINOT, Clemens BECHINGER, 2021. Critical Casimir interactions of colloids in micellar critical solutions. In: Soft Matter. Royal Society of Chemistry (RSC). 2021, 17(10), pp. 2737-2741. ISSN 1744-683X. eISSN 1744-6848. Available under: doi: 10.1039/d0sm02021d | eng |
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<dcterms:abstract xml:lang="eng">We study the temperature-dependence of critical Casimir interactions in a critical micellar solution of the nonionic surfactant C<sub>12</sub>E<sub>5</sub> dissolved in water. Experimentally, this is achieved with total internal reflection microscopy (TIRM) which measures the interaction between a single particle and a flat wall. For comparison, we also studied the pair interactions of a two dimensional layer of colloidal particles in the identical micellar system which yields good agreement with the TIRM results. Although, at the surfactant concentration considered here, the fluid forms a dynamical network of wormlike micelles whose structure is considerably more complex than that of simple critical molecular fluids, the temperature-dependence of the measured interactions is - for surface-to-surface distances above 160 nm - in excellent quantitative agreement with theory. Below 160 nm, deviations arise which we attribute to the adsorption of micelles to the interacting surfaces.</dcterms:abstract>
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| source.publisher | Royal Society of Chemistry (RSC) | eng |
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