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Addition of n-Alcohols Induces a Variety of Liquid-Crystalline Structures in Surfactant-Rich Cores of Dispersed Block Copolymer/Surfactant Nanoparticles

Ferreira, Guilherme A. (author)
University of Campinas
Piculell, Lennart (author)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
Loh, Watson (author)
University of Campinas
 (creator_code:org_t)
2016-12-05
2016
English 10 s.
In: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 1:6, s. 1104-1113
  • Journal article (peer-reviewed)
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  • Poly(acrylamide)-b-complex salts made from a symmetric poly(acrylate-b-acrylamide) block copolymer, where the acrylate charges are neutralized by cationic surfactant counterions, form kinetically stable aqueous dispersions of hierarchical aggregates with a liquid-crystalline complex salt core and a diffuse hydrated shell. By the addition of suitable amounts of long-chain alcohols, such as octanol or decanol, the structure of the internal phase can be varied, producing micellar cubic, hexagonal, lamellar, or reverse hexagonal liquid-crystalline phases. In addition, a disordered reverse micellar phase forms at the highest content of octanol. These core structures are the same as those previously obtained for macroscopic homopolymer poly(acrylate) complex salt/water/n-alcohol systems at the corresponding compositions. The poly(acrylamide)-b-complex salt dispersions are kinetically stable for several weeks, with their colloidal properties and internal structures remaining unchanged. The methodology described here establishes an easy and robust protocol for the preparation of colloidal nanoparticles with variable but controlled internal structures.

Subject headings

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)

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