Effect of organic and inorganic ions on the lower critical solution transition and aggregation of PNIPAM. Issue 38 (26th September 2018)

• Record Type: Journal Article
• Authors: Pérez-Fuentes, Leonor; Bastos-González, Delfi; Faraudo, Jordi; Drummond, Carlos
• Is Part Of: Soft matter. Volume 14:Issue 38(2018)
• Page Start: 7818
• Page End: 7828
• Publication Date: 2018-09-26
• Subjects: Soft condensed matter -- Periodicals; 530.413
• DOI: 10.1039/c8sm01679h
• Languages: English
• ISSNs: 1744-683X

Abstract

Abstract : We have studied the effect of different ions belonging to the extended Hofmeister series on the thermosensitive polymer poly( N -isopropylacrylamide) (PNIPAM), by combining Differential Scanning Calorimetry (DSC) and Dynamic Light Scattering (DLS). Abstract : We have studied the effect of different ions belonging to the extended Hofmeister series on the thermosensitive polymer poly( N -isopropylacrylamide) (PNIPAM), by combining Differential Scanning Calorimetry (DSC) and Dynamic Light Scattering (DLS). The variations in the lower critical solution temperature ( T LCS ) and enthalpy change during PNIPAM phase separation evidence the importance of considering both hydration and hydrophobicity to explain the interaction of ions with interfaces. The results obtained in the presence of inorganic ions can be explained by the tendency of water molecules to preferentially hydrate the PNIPAM chains or the ions, depending on the kosmotropic (highly hydrated) or chaotropic (poorly hydrated) character of the ions. On the contrary, tetraphenyl organic ions (Ph4 B − and Ph4 As + ) interact with the hydrophobic moieties of PNIPAM chains, inducing a significant reduction of the T LCS . DLS results show that the aggregation state of PNIPAM above the T LCS is also strongly influenced by the presence of ions. While macroscopic phase separation (formation of a polymer-rich phase insoluble in water) was apparent in the presence of inorganic ions, we observed the formation of submicron PNIPAM aggregates at temperatures above the T LCS in the presence of the hydrophobic ions. Kinetically arrested monodisperse PNIPAM nanoparticles were formed in the presence of the Ph4 B − anion, while a rather polydisperse distribution of particle sizes was observed in the presence of Ph4 As + . These results show that ionic specificity influences both the static (thermodynamic) and dynamic (kinetically controlled aggregation) states of PNIPAM in an aqueous environment.