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相关论文: Aggregation of hydrophobic-amphiphilic block copol…

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Amphiphilic block copolymer solutions form various micellar structures including micelles and vesicles. We applied the density functional theory for block copolymers which we have proposed to amphiphilic block copolymer systems. The 3…

软凝聚态物质 · 物理学 2007-05-23 Takashi Uneyama , Masao Doi

The interaction of amphiphilic polymers with small colloids, capable to reversibly stick onto the chains, is studied. Adhesive small colloids in solution are able to dynamically bind two polymer segments. This association leads to…

软凝聚态物质 · 物理学 2010-11-10 Vladimir A. Baulin , Albert Johner , Josep Bonet Avalos

Binary mixtures of amphiphiles in solution can self-assemble into a wide range of structures when the two species individually form aggregates of different curvatures. In this paper, we focus on small, spherically-symmetric aggregates in a…

软凝聚态物质 · 物理学 2012-07-02 M. J. Greenall , G. Gompper

Using the self-consistent field lattice model, polymer concentration $\bar{\phi}_{{P}}$ and chain length $N$ (keeping the length ratio of hydrophobic to hydrophilic blocks constant) the effects on temperature-dependent behavior of micelles…

软凝聚态物质 · 物理学 2014-07-10 X. -G. Han , Y. -H. Ma

The phase behaviour of amphiphilic multiblock copolymers with a large number of blocks in semidilute solutions is studied by lattice Monte Carlo simulations. The influence on the resulting structures of the concentration, the solvent…

软凝聚态物质 · 物理学 2016-08-18 Virginie Hugouvieux , Monique A. V. Axelos , Max Kolb

We perform off-lattice, canonical ensemble molecular dynamics simulations of the self-assembly of long segmented copolymers consisting of alternating, tunably attractive and hydrophobic {\em binder} domains, connected by hydrophilic {\em…

软凝聚态物质 · 物理学 2015-07-21 Hamed Mortazavi , Cornelis Storm

Using detailed atomistic simulations,we explore the conformational landscape of aggregates formed by biomimetic antimicrobial(AM) binary methacrylate copolymers,with hydrophobic and charged functional groups and the role of inclusion of…

软凝聚态物质 · 物理学 2020-02-25 Garima Rani , Kenichi Kuroda , Satyavani Vemparala

We present an extensive computer simulation study of structure formation in amphiphilic block copolymer solutions after a quench from a homogeneous state. By using a mesoscopic field-based simulation method, we are able to access time…

软凝聚态物质 · 物理学 2009-11-13 Xuehao He , Friederike Schmid

Mixtures of micelle-forming and lamella-forming amphiphiles in solution can form disk-shaped bilayers, sometimes referred to as bicelles. Using self-consistent field theory (SCFT), we investigate the structure and stability of these…

软凝聚态物质 · 物理学 2016-01-11 M. J. Greenall

We have linked the structural and dynamic properties in aqueous solution of amphiphilic charged diblock copolymers poly(butyl acrylate)-b-poly(acrylic acid), PBA-b-PAA, synthesized by controlled radical polymerization, with the…

软凝聚态物质 · 物理学 2007-08-28 M. Jacquin , P. Muller , R. Talingting-Pabalan , H. Cottet , J. -F. Berret , T. Futterer , O. Theodoly

Amphiphilic block copolymers self-assemble into diverse nanoscale morphologies with significant implications for drug delivery. This work presents systematic Brownian dynamics simulations of multi-chain diblock and triblock copolymers…

软凝聚态物质 · 物理学 2026-04-21 Ehsan Kamali Ahangar , Dominic Robe , Elnaz Hajizadeh

Aggregation of amphiphiles through the action of hydrophobic interactions is a common feature in soft condensed matter systems and is of particular importance in the context of biophysics as it underlies both the generation of functional…

We present a model for the joint self-assembly of amphiphilic polymers and small amphiphilic molecules (surfactants) in a dilute aqueous solution. The polymer is assumed to consist of a hydrophilic backbone and a large number of hydrophobic…

软凝聚态物质 · 物理学 2007-05-23 H. Diamant , D. Andelman

The interaction between a flexible polymer in good solvent and smaller associating solute molecules such as amphiphiles (surfactants) is considered theoretically. Attractive correlations, induced in the polymer because of the interaction,…

软凝聚态物质 · 物理学 2007-05-23 H. Diamant , D. Andelman

We report on the formation of colloidal complexes resulting from the electrostatic self-assembly of polyelectrolyte-neutral block copolymers and oppositely charged surfactants. The copolymers investigated are asymmetric and characterized by…

软凝聚态物质 · 物理学 2007-05-23 Jean-Francois Berret , Pascal Herve , Isabelle Grillo

From dumbbells to FCC crystals, we study the self-assembly pathway of amphiphatic, spherical colloidal particles as a function of the size of the hydrophobic region using molecular dynamics simulations. Specifically, we analyze how local…

软凝聚态物质 · 物理学 2015-05-13 William L. Miller , Angelo Cacciuto

In recent experiments involving PNIPAM copolymers it has been observed that stable spherical nanoparticles are being formed by association of several chains in poor aqueous solution instead of aggregation. This type of mesoscopic structures…

软凝聚态物质 · 物理学 2007-05-23 E. G. Timoshenko , R. Basovsky , Yu. A. Kuznetsov

Isoporous membranes made from diblock copolymers have numerous applications, including water treatment and protein separation, and are successfully produced at a laboratory scale under controlled conditions. However, achieving optimal…

软凝聚态物质 · 物理学 2023-04-11 Nicolas Moreno , Suzana Nunes , Victor Calo

We study the effect of the molecular architecture of amphiphilic star polymers on the shape of aggregates they form in water. Both solute and solvent are considered at a coarse-grained level by means of dissipative particle dynamics…

软凝聚态物质 · 物理学 2017-03-31 O. Y. Kalyuzhnyi , J. M. Ilnytskyi , C. von Ferber

We present a combined experimental and theoretical study on the role of copolymer architecture in the self-assembly of binary PEO-PCL mixtures in water-THF, and show that altering the chain geometry and composition of the copolymers can…

软凝聚态物质 · 物理学 2011-07-06 M. J. Greenall , P. Schuetz , S. Furzeland , D. Atkins , D. M. A. Buzza , M. F. Butler , T. C. B. McLeish
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