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Hamed Salimi-Kenari

Hamed Salimi-Kenari

Academic rank: Assistant Professor
ORCID:
Education: PhD.
ScopusId:
Faculty: Faculty of Technology and Engineering
Address:
Phone: 01135305105

Research

Title
Synthesis and temperature-induced self-assembly of a positively charged symmetrical pentablock terpolymer in aqueous solutions
Type
JournalPaper
Keywords
Pentablock terpolymers Phase behavior Thermoresponsive polymers
Year
2017
Journal EUROPEAN POLYMER JOURNAL
DOI
Researchers Erfan Dashtimoghadam ، Hamed Salimi-Kenari ، Vahid Forooqi Motlaq ، Mohammad Mahdi Hasani-Sadrabadi ، Hamid Mirzadeh ، Kaizheng Zhu ، Kenneth Knudsen ، Bo Nyström

Abstract

A novel linear cationic ABCBA pentablock terpolymer composed of a positively charged poly (3-acrylamidopropyl) trimethyl ammonium chloride)) (PAMPTMA (+)) block at both ends and two thermoresponsive poly (Nisopropylacrylamide) (PNIPAAM) blocks separated by a hydrophilic poly(ethylene glycol) (PEG) block was synthesized via a “one-pot” atom transfer radical polymerization procedure (ATRP). The chemical composition of the pentablock terpolymer was confirmed by nuclear magnetic resonance (NMR) and asymmetric flow fieldflow fractionation (AFFFF). Depending on the polymer concentration in aqueous solution, this terpolymer forms unimers and self-assembled structures at elevated temperatures. The effect of concentration and temperatureinduced self-assembling behavior of the pentablock terpolymer in aqueous solution was examined by using turbidimetry, shear viscosity, rheo-small angle light scattering (rheo-SALS), dynamic light scattering (DLS), and small angle neutron scattering (SANS). The turbidity measurements demonstrated that the formation of intermicellar structures and compaction of the complexes are function of both polymer concentration and temperature. The viscosity and rheo-SALS experiments elucidated the intricate interplay between building-up and breaking-up of interchain complexes under the influence of shear flow. The DLS experiments show the coexistence of small entities and interchain complexes at low temperatures and the evolution of large intermicellar structures at higher temperatures. At the highest temperatures, compaction of the complexes occurred. The results from SANS revealed significant temperature-induced changes of the copolymer structure on a semi-local dimensional scale.