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Formation of Hydrophobic–Hydrophilic Associates in the N-Vinylpyrrolidone and Vinyl Propyl Ether Copolymer Aqueous Solutions

Sherniyaz KabdushevNational Engineering Academy of the Republic of Kazakhstan, Almaty 050010, KazakhstanGrigoriy A. MunDepartment of Chemistry & Technology of Organic Materials, Faculty of Chemistry and Chemical Technology, Polymers and Natural Compounds, Al Farabi Kazakh National University, Almaty 050040, KazakhstanIbragim SuleimenovNational Engineering Academy of the Republic of Kazakhstan, Almaty 050010, KazakhstanAdilet AlikulovDepartment of Chemistry & Technology of Organic Materials, Faculty of Chemistry and Chemical Technology, Polymers and Natural Compounds, Al Farabi Kazakh National University, Almaty 050040, KazakhstanRamazan ShaikhutdinovDepartment of Chemistry & Technology of Organic Materials, Faculty of Chemistry and Chemical Technology, Polymers and Natural Compounds, Al Farabi Kazakh National University, Almaty 050040, KazakhstanEldar KopishevDepartment of Chemistry, Faculty of Natural Sciences, L.N. Gumilyov Eurasian National University, Astana 010000, Kazakhstan
Polymersjournal2023en
ABI

Аннотация

Utilizing turbidimetry data, an examination is conducted on the behavior of solutions containing N-vinylpyrrolidone and vinyl propyl ether copolymer within a temperature range coinciding with the occurrence of a phase transition. The investigation reveals that within specific conditions prevailing in this domain, the emergence of entities denoted as hydrophobic-hydrophilic associates is conceivable. These entities are characterized by the presence of a relatively dense core, upheld by hydrophobic interplays, and they are proficient in effectively dispersing irradiation within the optical spectrum. Encircling this core is a hydrophilic periphery that impedes the formation of insoluble precipitates. The development of such associates transpires when hydrophobic interactions have attained a discernible prominence, although they remain inadequate to counteract the forces that drive the expansion of macromolecular coils. Under these circumstances, the energetically favored course of action entails the constitution of a core for the aforementioned associates, involving discrete segments from diverse macromolecules. Notably, the introduction of an additional constituent (ethanol) to the solution, which selectively mitigates hydrophobic interactions, serves to stabilize the hydrophobic-hydrophilic associations.

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