Energy The relative permittivity is an essential piece of information when designing
capacitors, and in other circumstances where a material might be expected to introduce
capacitance into a circuit. If a material with a high relative permittivity is placed in an
electric field, the magnitude of that field will be measurably reduced within the volume of the dielectric. This fact is commonly used to increase the capacitance of a particular capacitor design. The layers beneath etched conductors in printed circuit boards (
PCBs) also act as dielectrics.
Communication Dielectrics are used in
radio frequency (RF) transmission lines. In a
coaxial cable,
polyethylene can be used between the center conductor and outside shield. It can also be placed inside waveguides to form
filters.
Optical fibers are examples of
dielectric waveguides. They consist of dielectric materials that are purposely doped with impurities so as to control the precise value of
εr within the cross-section. This controls the
refractive index of the material and therefore also the optical modes of transmission. However, in these cases it is technically the relative permittivity that matters, as they are not operated in the electrostatic limit.
Environment The relative permittivity of air changes with temperature, humidity, and barometric pressure. Sensors can be constructed to detect changes in capacitance caused by changes in the relative permittivity. Most of this change is due to effects of temperature and humidity as the barometric pressure is fairly stable. Using the capacitance change, along with the measured temperature, the relative humidity can be obtained using engineering formulas.
Chemistry The relative static permittivity of a solvent is a relative measure of its
chemical polarity. For example,
water is very polar, and has a relative static permittivity of 80.10 at 20 °C while
n-
hexane is non-polar, and has a relative static permittivity of 1.89 at 20 °C. This information is important when designing separation,
sample preparation and
chromatography techniques in
analytical chemistry. The correlation should, however, be treated with caution. For instance,
dichloromethane has a value of
εr of
9.08 (20 °C) and is rather poorly soluble in water (13g/L or 9.8mL/L at 20 °C); at the same time,
tetrahydrofuran has its
εr =
7.52 at 22 °C, but it is completely miscible with water. In the case of tetrahydrofuran, the oxygen atom can act as a
hydrogen bond acceptor; whereas dichloromethane cannot form hydrogen bonds with water. This is even more remarkable when comparing the
εr values of
acetic acid (6.2528) and that of
iodoethane (7.6177). The large numerical value of
εr is not surprising in the second case, as the
iodine atom is easily polarizable; nevertheless, this does not imply that it is polar, too (electronic
polarizability prevails over the orientational one in this case). == Lossy medium ==