AI Article Synopsis

  • Hydroxypropyl methylcellulose (HPMC) is a cellulose ether made with both hydrophobic methyl and hydrophilic hydroxypropyl groups, affecting its interactions with water.
  • The study explored how HPMC cryogels interacted with water and surfactants using sorption tests and nuclear magnetic resonance, discovering most water molecules behaved like intermediate water.
  • Key findings showed that HPMC with high degrees of substitution produced slower swelling rates and higher contact angles, while the addition of surfactants increased swelling rates and altered the hydrophobic characteristics, which is important for controlling reactions in various applications.

Article Abstract

Hydroxypropyl methylcellulose (HPMC) belongs to the cellulose ether family that has hydroxyl groups substituted by hydrophobic methyl groups (DS) and hydrophilic hydroxypropyl groups (MS). Herein, the interactions between water molecules and cryogels prepared with HPMC in the presence and absence of a linear nonionic surfactant, as well as CaO microparticles, which react with water producing O, were systematically investigated by sorption experiments and Time-Domain Nuclear Magnetic Resonance. Regardless of the DS and MS, most water molecules presented transverse relaxation time t2 typical of intermediate water and a small population of more tightly bound water. HPMC cryogels with the highest DS of 1.9 presented the slowest swelling rate of 0.519 ± 0.053 g/(g.s) and the highest contact angle values 85.250 ± 0.004, providing the best conditions for a slow reaction between CaO and water. The presence of surfactant favored hydrophobic interactions that allowed the polar head of the surfactant to be exposed to the medium, resulting in a higher swelling rate and lower contact angle values. The HPMC with the highest MS presented the fastest swelling rate and the lowest contact angle. These findings are relevant for the formulations and reactions, where tuning the swelling kinetics is crucial for the final application.

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http://dx.doi.org/10.1016/j.carbpol.2023.121029DOI Listing

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