Reyes Isabella, Palacio Maria M, Yarce Cristhian J, Oñate-Garzón Jose, Salamanca Constain H
Laboratorio de Diseño y Formulación de Productos Químicos y Derivados, Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Naturales, Universidad ICESI, Calle 18 No. 122-135, Cali 760035, Colombia.
Grupo de Investigación en Química y Biotecnología (QUIBIO), Facultad de Ciencias Básicas, Universidad Santiago de Cali, calle 5 No. 62-00, Cali 760035, Colombia.
Polymers (Basel). 2020 May 2;12(5):1036. doi: 10.3390/polym12051036.
Alternating amphiphilic copolymers are macromolecular systems with a polarity duality in their structure, since they are generally formed by alternating segments corresponding to a potential electrolyte group and an alkyl (aliphatic or aromatic) group. These systems, depending on the ionization degree, as well as the time, may form different types of intra and interpolymeric aggregates in aqueous media. Therefore, this study, which in fact is the continuation of a previously reported work, is focused on establishing how the ionization degree of the sodium and potassium salts of the poly(maleic acid--octadecene) affect zeta potential, pH, electrical conductivity, particle size, polydispersity index, and surface tension over time. The results showed that polymeric salts with a high ionization degree in aqueous media formed homogeneous systems with bimodal sizes and high zeta potential values, which tended to quickly become less negative, lowering the pH and slightly increasing the electrical conductivity; while systems with low ionization degree lead to the opposite, forming heterodispersed systems with several populations of particle sizes, high polydispersity, low zeta potential values, neutral and invariable pH values, and high electrical conductivity values. Consequently, these results suggest that the values of particle size, polydispersity index, zeta potential, pH, and electrical conductivity change regarding the polymeric ionization degree, as well as the time. Therefore, such variables should be considered and controlled when working with this kind of polymeric materials.
交替两亲共聚物是一类在结构上具有极性二元性的大分子体系,因为它们通常由对应于潜在电解质基团和烷基(脂肪族或芳香族)基团的交替链段组成。这些体系根据电离程度以及时间的不同,在水性介质中可能形成不同类型的分子内和分子间聚集体。因此,本研究实际上是之前一项报道工作的延续,重点在于确定聚(马来酸 - 十八碳烯)的钠盐和钾盐的电离程度如何随时间影响zeta电位、pH值、电导率、粒径、多分散指数和表面张力。结果表明,在水性介质中具有高电离程度的聚合物盐形成具有双峰尺寸和高zeta电位值的均相体系,其zeta电位值往往会迅速减小负值,降低pH值并略微增加电导率;而低电离程度的体系则产生相反的结果,形成具有多种粒径分布、高多分散性、低zeta电位值、pH值中性且不变以及高电导率值的多分散体系。因此,这些结果表明,粒径、多分散指数、zeta电位、pH值和电导率的值会随着聚合物的电离程度以及时间而变化。所以,在使用这类聚合物材料时应考虑并控制这些变量。