Hydration pressure of a homologous series of nonionic alkyl hydroxyoligo(ethylene oxide) surfactants
文献情報
Helge Pfeiffer, Hans Binder, Gotthard Klose, Karel Heremans
The hydration pressure of a homologous series of nonionic surfactants of the type CH3(CH2)n−1(OCH2CH2)mOH (CnEm) was determined by using sorption gravimetry. The hydration pressure shows a non-exponential decay on hydration and the curves are best fitted with a rational function. The non-exponential character is explained by contributions arising from the bending energy of non-lamellar liquid crystalline phases. The parameters obtained show that hydration of pure nonionic surfactants is correlated with the number of the oxyethylene groups in the headgroup. However, they are almost independent of the length of the alkyl chain. Exceptions are surfactants in the solid crystalline state that almost prevent hydration. Furthermore, the respective mesophase structures do not dominate the hydration behaviour. The Gibbs free energy (free enthalpy) of hydration is −1.1 kJ mol−1 per oxyethylene group.
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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.












![(2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure (2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure](https://static.chemtradehub.com/structs/173/173867-04-4-d2d3.webp)

