The results presented in
Section 3 demonstrate that the deformations of the PCF and OCF observed after immersion are almost completely reversible. For the ACF within the solutions DIW, CEM, and NaCl, a chemical hysteresis is discernible, which is not fully reversible, at least within the measured time periods of 24
and 48
(
Figure 5). It remains to be determined whether this reversibility is still present after several immersion-extraction cycles, or, in the case of ACF, whether the hysteresis is further increased. Furthermore, the test results and the deviation from the measured values in DIW, as ascertained by [
29,
30], indicate that preconditioning may exert a significant influence on both the amplitude and the type of deformation. However, the potential for preconditioning with higher moisture contents or temperatures to result in positive deformation in the case of magnesium chloride, for instance, remains uncertain. It is also probable that preconditioning exerts a non-linear influence on the process and, as a consequence, on strain and temperature measurements. In general, further investigations by [
37,
38] demonstrate that thermodynamic changes influence the swelling effect. In [
28], it is claimed that the pH value can influence the swelling of polymers within solutions. However, this could not be confirmed based on the results. A slight deviation in the measured strains between CEM (pH 12.6) and DIW of 23
was observed, but this could also be attributed to general measurement fluctuations. For all liquids, the OCF showed a significant time delay after immersion to reach maximum deformation compared to PCF and ACF. The incorporation of the liquid into the polymer structure appears to take longer. After removal, however, a similar evolution was observed as for PCF. Although there is variation in the amount of deformation in different solutions (as shown in
Figure 3 to
Figure 5), there is a general pattern in the order of strain deviation in response to different liquids when the fibers are similarly preconditioned in air. The highest positive strains were observed in DIW and CEM, followed by the NaCl and NaNO
2 solutions. In contrast, the MgCl
2 solution exhibited negative strains for all coating materials. This dependency can also be interpreted as an increasing influence of the salt solutions relative to the reference condition of placement in distilled water (DIW). This remarkable finding suggests that the measured strain variations are governed by more fundamental processes that are independent of the type of coating observed. It is hypothesized that this strain effect is related to the affinity of the materials for the salt solution and the resulting enhancement of water in the coating layer. The order of the strain deviation (DIW > NaCl > NaNO
2 > MgCl
2) correlates with the relative humidity determined over the saturated electrolyte solutions in the equilibrium state. The relative humidities are 75, 66 and 33 for NaCl, NaNO
2 and MgCl
2, respectively [
39,
40,
41,
42]. For CEM, no corresponding value for relative humidity could be found in the literature. Therefore, it can be postulated that the phase transition of water molecules from the bulk liquid phase into the polymer coatings is controlled by analogous principles as for the transition of water from the liquid to the gaseous phase. Consequently, the activity of water molecules is reduced by the addition of ions, which can be described by Raoult’s law [
43,
44]. In the case of MgCl
2, the direction of the phase transition is reversed, resulting in the transport of water molecules absorbed during preconditioning from the polymer to the electrolyte. When polar polymers, especially polyacrylates, are exposed to water, hydrogels can form. These are also known as superabsorbent polymers. They are used in a variety of applications, including the self-sealing of pipes and the production of water-absorbing fillers [
46,
47,
48]. According to the literature, the degree of swelling depends on two factors: the degree of cross-linking within the polymer and the salt content of the absorbent [
47]. The degree of swelling is inversely proportional to the concentration of cations shielding the stationary anions in the polar polymer [
45]. This results in a lower strain for electrolyte solutions compared to DIW. Furthermore, the Donnan theory [
48] states that the higher the charge density of the cations in the electrolyte solution, the lower the swelling pressure in the hydrogel. As an illustrative example, a comparison can be made between saturated MgCl
2 and NaCl solutions. In these solutions, the charge density of Mg
2+ is significantly higher than that of Na
+, resulting in a significantly lower swelling pressure. The difference in the degree of strain deviation observed in the ACF for the two sodium salt solutions can be attributed to their disparate saturation concentrations (5.5/
for NaCl and 11.9/
for NaNO
2). According to Donnan’s theory, the swelling pressure is increased in the NaCl solution due to its lower charge density.