Naslov
Interpolyelectrolyte interactions: relationship between formation of polyelectrolyte complexes in solution and polyelectrolyte multilayer build-up

Autori
Salopek, Jasmina ; Požar, Josip ; Kovačević, Davor

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
30th Conference of The European Colloid and Interface Society ; Book of Abstracts / Rovigatti, I. - Rim, 2016, Xx-xx

Skup
Conference of The European Colloid and Interface Society (30 ; 2016)

Mjesto i datum
Rim, Italija, 04.09.2016. - 09.09.2016

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
polyelectrolytes ; complexes ; multilayers ; QCM-D ; AFM

Sažetak
Interpolyelectrolyte interactions in solution and at surfaces lead to the formation of polyelectrolyte complexes (PECs) and polyelectrolyte multilayer (PEMs), respectively. Better knowledge of the relationship between the formation and properties of PEMs and PECs would enable the prediction and the control of deposition of a wide range of polyelectrolytes at various surfaces with important application possibilities. Therefore, we compared the results we obtained earlier1, 2 for the complexation of poly(allylammonium) chloride (PAH) and sodium poly(styrenesulfonate) (PSS) with the results obtained for PAH-PSS multilayer build-up. In order to do so, we studied the formation of PAH-PSS multilayers in aqueous solutions of various electrolytes by means of quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM). The QCM-D measurements indicated that the thickness of deposited layers depends on ionic strength and on the type of the type of salt used. The largest deposition of material was noticed in the case of nitrate and perchlorate anions. This is in accordance with the results obtained for PECs by means of DLS and spectrophotometric experiments which showed anion specific aggregation of positive complexes and the formation of precipitates containing larger amount of PAH with respect to PSS. The thickness of deposited films could be also correlated with the complexation enthalpies of used supporting electrolyte ions. The more enthalpically disfavourable complexation process in solution was, the larger was the amount of material deposited. The results can be explained by different counterion distributions around polyelectrolytes, caused by differences in the corresponding hydration enthalpies. The observed strong influence of counterion type on the composition of PAH/PSS nanoassemblies provides a path for the modification of multilayer properties simply be changing the type of salt during their preparation. Although the presented work was performed solely on the system PAH/PSS, the concepts and conclusions can be applied for various combinations of polyelectrolytes.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

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