Počet záznamů: 1
Effects of N-Alkanol Adsorption on Bubble Acceleration and Local Velocities in Solutions of the Homologous Series from Ethanol to N-Decanol
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SYSNO ASEP 0569767 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Effects of N-Alkanol Adsorption on Bubble Acceleration and Local Velocities in Solutions of the Homologous Series from Ethanol to N-Decanol Tvůrce(i) Krzan, M. (PL)
Chattopadhyay, P. (IN)
Orvalho, Sandra (UCHP-M) RID, ORCID, SAI
Zedníková, Mária (UCHP-M) RID, ORCID, SAIČíslo článku 2125 Zdroj.dok. Materials. - : MDPI
Roč. 16, č. 5 (2023)Poč.str. 18 s. Jazyk dok. eng - angličtina Země vyd. CH - Švýcarsko Klíč. slova bubble ; adsorption ; coverage ; alkanols Obor OECD Chemical process engineering Způsob publikování Open access Institucionální podpora UCHP-M - RVO:67985858 UT WOS 000947497400001 EID SCOPUS 85149869957 DOI 10.3390/ma16052125 Anotace The influence of n-alkanol (C2–C10) water solutions on bubble motion was studied in a wide range of concentrations. Initial bubble acceleration, as well as local, maximal and terminal velocities during motion were studied as a function of motion time. Generally, two types of velocity profiles were observed. For low surface-active alkanols (C2–C4), bubble acceleration and terminal velocities diminished with the increase in solution concentration and adsorption coverage. No maximum velocities were distinguished. The situation is much more complicated for higher surface-active alkanols (C5–C10). In low and medium solution concentrations, bubbles detached from the capillary with acceleration comparable to gravitational acceleration, and profiles of the local velocities showed maxima. The terminal velocity of bubbles decreased with increasing adsorption coverage. The heights and widths of the maximum diminished with increasing solution concentration. Much lower initial acceleration values and no maxima presence were observed in the case of the highest n-alkanol concentrations (C5–C10). Nevertheless, in these solutions, the observed terminal velocities were significantly higher than in the case of bubbles moving in solutions of lower concentration (C2–C4). The observed differences were explained by different states of the adsorption layer in the studied solutions, leading to varying degrees of immobilization of the bubble interface, which generates other hydrodynamic conditions of bubble motion. Pracoviště Ústav chemických procesů Kontakt Eva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227 Rok sběru 2024 Elektronická adresa https://www.mdpi.com/1996-1944/16/5/2125
Počet záznamů: 1