Ilias Iliopoulos

ORCID: 0000-0002-9368-2906
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Research Areas
  • Surfactants and Colloidal Systems
  • Advanced Polymer Synthesis and Characterization
  • Electrostatics and Colloid Interactions
  • Hydrogels: synthesis, properties, applications
  • Polymer Nanocomposites and Properties
  • Polymer crystallization and properties
  • Rheology and Fluid Dynamics Studies
  • biodegradable polymer synthesis and properties
  • Particle Dynamics in Fluid Flows
  • Block Copolymer Self-Assembly
  • Synthesis and properties of polymers
  • Polymer Surface Interaction Studies
  • Enhanced Oil Recovery Techniques
  • Polymer composites and self-healing
  • Advanced Sensor and Energy Harvesting Materials
  • Machine Learning in Materials Science
  • Wind and Air Flow Studies
  • Material Dynamics and Properties
  • Fluid Dynamics and Turbulent Flows
  • Advanced Battery Materials and Technologies
  • Dielectric materials and actuators
  • Analytical Chemistry and Chromatography
  • Fiber-reinforced polymer composites
  • NMR spectroscopy and applications
  • Conducting polymers and applications

Centre National de la Recherche Scientifique
2009-2024

École nationale supérieure d'arts et métiers
2017-2024

HESAM Université
2021-2024

Laboratoire Procédés et Ingénierie en Mécanique et Matériaux
2021-2023

Conservatoire National des Arts et Métiers
2017-2021

Arkema (France)
2014-2016

Chimie Moléculaire, Macromoléculaire, Matériaux
2002-2013

ESPCI Paris
1995-2013

ParisTech
2008-2013

Sorbonne Université
1991-2007

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTMixed Micelles Formed by Cationic Surfactants and Anionic Hydrophobically Modified PolyelectrolytesBenoit Magny, Ilias Iliopoulos, Raoul Zana, Roland AudebertCite this: Langmuir 1994, 10, 9, 3180–3187Publication Date (Print):September 1, 1994Publication History Published online1 May 2002Published inissue 1 September 1994https://pubs.acs.org/doi/10.1021/la00021a047https://doi.org/10.1021/la00021a047research-articleACS PublicationsRequest reuse...

10.1021/la00021a047 article EN Langmuir 1994-09-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTViscometric evidence of interactions between hydrophobically modified poly(sodium acrylate) and sodium dodecyl sulfateI. Iliopoulos, T. K. Wang, R. AudebertCite this: Langmuir 1991, 7, 4, 617–619Publication Date (Print):April 1, 1991Publication History Published online1 May 2002Published inissue 1 April 1991https://pubs.acs.org/doi/10.1021/la00052a003https://doi.org/10.1021/la00052a003research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/la00052a003 article EN Langmuir 1991-04-01

Polystyrene (PS) end-capped polyelectrolytes were prepared by modification of polystyrene−poly(tert-butyl acrylate)−polystyrene triblock copolymers synthesized via anionic polymerization. These amphiphilic polymers are associated in dilute aqueous solutions forming loose multimicellar clusters. At higher polymer concentrations an extensive intermicellar bridging occurs, leading to the formation a transient network as revealed viscoelastic response system. The so-formed gel is characterized...

10.1021/ma991410e article EN Macromolecules 2000-03-24

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTReversible Thermal Gelation in Polymer/Surfactant Systems. Control of the TemperatureK. Loyen, I. Iliopoulos, R. Audebert, and U. OlssonCite this: Langmuir 1995, 11, 4, 1053–1056Publication Date (Print):April 1, 1995Publication History Published online1 May 2002Published inissue 1 April 1995https://pubs.acs.org/doi/10.1021/la00004a002https://doi.org/10.1021/la00004a002research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/la00004a002 article EN Langmuir 1995-04-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAssociation and Thermal Gelation in Mixtures of Hydrophobically Modified Polyelectrolytes Nonionic SurfactantsAnne Sarrazin-Cartalas, Ilias Iliopoulos, Roland Audebert, Ulf OlssonCite this: Langmuir 1994, 10, 5, 1421–1426Publication Date (Print):May 1, 1994Publication History Published online1 May 2002Published inissue 1 1994https://pubs.acs.org/doi/10.1021/la00017a018https://doi.org/10.1021/la00017a018research-articleACS PublicationsRequest reuse...

10.1021/la00017a018 article EN Langmuir 1994-05-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTComplexation of acrylic acid copolymers with polybases: importance cooperative effectsI. Iliopoulos and R. AudebertCite this: Macromolecules 1991, 24, 9, 2566–2575Publication Date (Print):April 29, 1991Publication History Published online1 May 2002Published inissue 29 April 1991https://pubs.acs.org/doi/10.1021/ma00009a066https://doi.org/10.1021/ma00009a066research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ma00009a066 article EN Macromolecules 1991-04-01

The crosslinking of epoxidized natural rubber with dodecanedioic acid and the mechanism its acceleration by 1,2-dimethylimidazole (DMI) are investigated using nuclear magnetic resonance spectroscopy. Solid-state NMR experiments (1H, 1H → 13C cross-polarization direct polarization) used to analyse crosslinked samples, whereas solution provides information about liquid species. solid-state demonstrates ester nature crosslinks, confirms that DMI acts through formation imidazolium dicarboxylate...

10.1039/c2py00591c article EN Polymer Chemistry 2012-01-01

Derivatives of poly(sodium acrylate) bearing a few mole percent perfluoroalkyl side chains were synthesized. Their solution properties investigated by rheology and compared to those their hydrogenated analogues. As the modified polymers, these new materials display an associating behavior. In semidilute polymer exhibits viscosities several orders magnitude higher than unmodified acrylate). However, this viscosifying effect is more pronounced for perfluorinated derivatives. By comparing...

10.1021/la970003y article EN Langmuir 1997-08-01

The phase behavior and rheological properties of hydrophobically modified copolymers based on a thermosensitive N-isopropylacrylamide backbone are reported. These polymers bear rather high fraction (5−25 mol %) octyl, dodecyl, or octadecyl side groups, their solubility in water is ensured by positive charges, introduced to the same unit as alkyl group. Their governed competition between hydrophilic character charges hydrophobic groups. Thus, cloud point temperature, TCP, turbidity level...

10.1021/ma991409f article EN Macromolecules 2000-03-24

The interactions between poly(N-isopropylacrylamide), PNIPAM, and poly(sodium acrylate) hydrophobically modified with octadecyl groups, HMPA, in aqueous solutions, were studied by using viscometry turbidimetry. viscosity of mixtures the two polymers, at 25 °C, may be several orders magnitude higher than corresponding PNIPAM unmodified precursor acrylate). modification degree greater enhancement. Furthermore, increasing molar mass leads to a more pronounced increase. elevation phase...

10.1021/ma970884f article EN Macromolecules 1997-12-01

The association mechanism of several hydrophobically modified sodium polyacrylates (HMPA) in aqueous solutions has been investigated by fluorescence probing with pyrene as the fluorescent probe, electrical conductivity, and 13C NMR. HMPAs differed molecular weight poly(acrylic acid) precursor, degree hydrophobe substitution, carbon number (alkyl chain). results showed that is less cooperative than micellization conventional surfactants there a concentration below which no micelle-like...

10.1021/la000709j article EN Langmuir 2000-11-11

We report on the viscoelastic response of a physical gel formed in aqueous solutions poly(sodium acrylate) end-capped with short polystyrene (PS) blocks. Above percolation threshold (cgel = 0.2 wt %) transient network is constituted PS hydrophobic domains (cross-links) interconnected via fully charged polyelctrolyte chains. Oscillatory shear and step-strain experiments were employed to study properties. The stretched conformation middle blocks (bridges) high hydrophobicity ends have...

10.1021/ma011391k article EN Macromolecules 2002-03-28

Abstract The structure of polymer complexes stabilized through hydrogen bonds can be much influenced by the presence nonactive groups (structure defects) on chains. In this paper two very simple homopolymer/copolymer systems are studied: homopolymer is a polybase, polyoxyethylene (PEO) or polyvinylpyrrolidone (PVP), and copolymer partially neutralized poly(acrylic acid) (PAA). acrylate PAA chain behave as defects. Viscometry provides information about macroscopic complex in solution while...

10.1002/pola.1988.080260127 article EN Journal of Polymer Science Part A Polymer Chemistry 1988-01-01

We studied the effect of neutral polymer poly(vinyl alcohol) on rheological properties and microstructure highly charged mixed wormlike micelles anionic cationic surfactants, potassium oleate n-octyltrimethylammonium bromide, without adding salt. It was shown that induces a hundredfold increase viscosity longest relaxation time appearance well-defined plateau modulus, which assigned to interlacing micellar chains. When amount added exceeds 2 wt %, characteristics (the viscosity, time,...

10.1021/acs.macromol.6b02385 article EN Macromolecules 2016-12-20

Poly(ether ketone ketone) (PEKK) is a semicrystalline polymer investigated for highly demanding applications in aerospace, transportation, electronics, and oil & gas industries. The properties required these applications, such as thermomechanical chemical stability, are intimately linked to the crystalline state of material. PEKK exhibits polymorphism that depends, among other factors, on its thermal history. control quantification subject this study. Amorphous (T/I = 60/40, where T stands...

10.1021/acsapm.0c01380 article EN ACS Applied Polymer Materials 2021-03-09

10.1016/s1359-0294(98)80023-x article EN Current Opinion in Colloid & Interface Science 1998-10-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTInterpolymer association between acrylic acid copolymers and polyethylene glycol: effects of the copolymer natureG. Bokias, G. Staikos, I. Iliopoulos, R. AudebertCite this: Macromolecules 1994, 27, 2, 427–431Publication Date (Print):January 1, 1994Publication History Published online1 May 2002Published inissue 1 January 1994https://pubs.acs.org/doi/10.1021/ma00080a016https://doi.org/10.1021/ma00080a016research-articleACS PublicationsRequest reuse...

10.1021/ma00080a016 article EN Macromolecules 1994-01-01
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