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jkqwzsoo | 2 years ago
There are no pores, so to speak. Polymer materials form amorphous solids with transient voids which open and close randomly due to thermal motion. They're not "pores" because they aren't permanent over long time scales. Rather, the polymer+water is modeled as a single fluid phase, the same as if you were modeling ethanol+water. The fact that the polymer is a "solid" doesn't affect the fact that it's actually a tangle of vibrating molecules just like any other mixture.
Other materials do have well defined pores, like MOFs and zeolites. In this case, the water does sorb as a liquid in the pore space, but is gated by transport between the pores in a similar manner.
This is made apparent because water does enter into polymers (even those which desalination) freely, with or without the presence of salt. It is not the case that "the pores are too small for water to cross normally". I can take a polymer that will swell with 50% of its own weight in water, and which has no "free" liquid water (as evidenced by the inability of the water in the polymer to form ice), yet make it reject >90% salt at very high pressures (>3000 psi). If you just let salt water sit on one side without pressure, salt and water will make their way through non-selectively. So it can't be that the water is being physically sieved from the ions to enter into the membrane. Rather, the pressure creates a change in the activity of water (due to the mechanical forces acting on the polymer near the low pressure/support material interface). Since the water is more soluble and more mobile in the polymer, it transports at a more rapid rate than the salt, resulting in desalination.
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