Hydration-Dependent Hierarchical Structures in Block Copolymer–Surfactant Complex Salts

2018 ◽  
Vol 51 (23) ◽  
pp. 9915-9924 ◽  
Author(s):  
Guilherme A. Ferreira ◽  
Lennart Piculell ◽  
Watson Loh
Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3265
Author(s):  
Guilherme A. Ferreira ◽  
Watson Loh ◽  
Daniel Topgaard ◽  
Olle Söderman ◽  
Lennart Piculell

Internally structured block copolymer-surfactant particles are formed when the complex salts of ionic-neutral block copolymers neutralized by surfactant counterions are dispersed in aqueous media. Here, we report the 1H NMR signal intensities and self-diffusion coefficients (D, from pulsed field gradient nuclear magnetic resonance, PFG NMR) of trimethyl alkylammonium surfactant ions and the poly(acrylamide)-block-poly(acrylate) (PAAm-b-PA) polyions forming such particles. The results reveal the presence of an “NMR-invisible” (slowly exchanging) fraction of aggregated surfactant ions in the particle core and an “NMR-visible” fraction consisting of surface surfactant ions in rapid exchange with the surfactant ions dissociated into the aqueous domain. They also confirm that the neutral PAAm blocks are exposed to water at the particle surface, while the PA blocks are buried in the particle core. The self-diffusion of the polyions closely agree with the self-diffusion of a hydrophobic probe molecule solubilized in the particles, showing that essentially all copolymer chains are incorporated in the aggregates. Through centrifugation, we prepared macroscopically phase-separated systems with a phase concentrated in particles separated from a clear dilute phase. D values for the surfactant and block copolymer indicated that the dilute phase contained small aggregates (ca. 5 nm) of surfactant ions and a few anionic-neutral block copolymer chains. Regardless of the overall concentration of the sample, the fraction of block copolymer found in the dilute phase was nearly constant. This indicates that the dilute fraction represented a tail of small particles created by the dispersion process rather than a true thermodynamic solubility of the complex salts.


2020 ◽  
Vol 11 (15) ◽  
pp. 2762-2762
Author(s):  
Alessandro Ianiro ◽  
Meng Chi ◽  
Marco M. R. M. Hendrix ◽  
Ali Vala Koç ◽  
E. Deniz Eren ◽  
...  

Correction for ‘Block copolymer hierarchical structures from the interplay of multiple assembly pathways’ by Alessandro Ianiro et al., Polym. Chem., 2020, DOI: 10.1039/d0py00081g.


Polymer ◽  
2011 ◽  
Vol 52 (4) ◽  
pp. 1180-1190 ◽  
Author(s):  
Ya-Sen Sun ◽  
Shih-Wei Chien ◽  
Jiun-You Liou ◽  
Chiu Hun Su ◽  
Kuei-Fen Liao

2014 ◽  
Vol 123 ◽  
pp. 679-684
Author(s):  
Eun Ju Jeong ◽  
Jin Wook Lee ◽  
Young-Je Kwark ◽  
Seung Hyun Kim ◽  
Kuen Yong Lee

2018 ◽  
Vol 209 ◽  
pp. 303-314 ◽  
Author(s):  
Valentina-Elena Musteata ◽  
Stefan Chisca ◽  
Florian Meneau ◽  
Detlef-M. Smilgies ◽  
Suzana P. Nunes

Hierarchical isotropic porous structures with spherical micrometer-sized cavities, interconnected by hexagonally ordered nanochannels, were prepared based on the phase separation of polystyrene-b-poly(t-butyl acrylate) block copolymers, following a nucleation and growth mechanism.


Langmuir ◽  
2014 ◽  
Vol 30 (39) ◽  
pp. 11493-11503 ◽  
Author(s):  
Ana Maria Percebom ◽  
Leandro Ramos Souza Barbosa ◽  
Rosangela Itri ◽  
Watson Loh

2020 ◽  
Vol 11 (13) ◽  
pp. 2305-2311
Author(s):  
Alessandro Ianiro ◽  
Meng Chi ◽  
Marco M. R. M. Hendrix ◽  
Ali Vala Koç ◽  
E. Deniz Eren ◽  
...  

Structurally complex hierarchical block copolymer assemblies can be formed in solution by controlling the interplay of phase separation, crystallization and block segregation with temperature.


2019 ◽  
Vol 10 (8) ◽  
pp. 991-999 ◽  
Author(s):  
Hongbing Pan ◽  
Wei Zhang ◽  
Anqi Xiao ◽  
Xiaolin Lyu ◽  
Pingping Hou ◽  
...  

Supramolecular liquid crystalline block copolymers prepared via hydrogen bonding exhibit hierarchical structures that can be tuned by varying the molar ratio of the discotic hydrogen-bonding acceptor to the block copolymer donor.


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