| Material | εr |
|---|---|
| Vacuum | 1 (by definition) |
| Air | 1.00058986±0.00000050 (atSTP, 900 kHz),[1] |
| PTFE/Teflon | 2.1 |
| Polyethylene/XLPE | 2.25 |
| Polyimide | 3.4 |
| Polypropylene | 2.2–2.36 |
| Polystyrene | 2.4–2.7 |
| Carbon disulfide | 2.6 |
| BoPET | 3.1[2] |
| Paper, printing | 1.4[3] (200 kHz) |
| Electroactive polymers | 2–12 |
| Mica | 3–6[2] |
| Silicon dioxide | 3.9[4] |
| Sapphire | 8.9–11.1 (anisotropic)[5] |
| Concrete | 4.5 |
| Pyrex (glass) | 4.7 (3.7–10) |
| Neoprene | 6.7[2] |
| Natural rubber | 7 |
| Diamond | 5.5–10 |
| Salt | 3–15 |
| Melamine resin | 7.2–8.4[6] |
| Graphite | 10–15 |
| Silicone rubber | 2.9–4[7] |
| Silicon | 11.68 |
| GaAs | 12.4[8] |
| Silicon nitride | 7–8 (polycrystalline, 1 MHz)[9][10] |
| Ammonia | 26, 22, 20, 17 (−80, −40, 0, +20 °C) |
| Methanol | 30 |
| Ethylene glycol | 37 |
| Furfural | 42.0 |
| Glycerol | 41.2, 47, 42.5 (0, 20, 25 °C) |
| Water | 87.9, 80.2, 55.5 (0, 20, 100 °C)[11] for visible light: 1.77 |
| Hydrofluoric acid | 175, 134, 111, 83.6 (−73, −42, −27, 0 °C), |
| Hydrazine | 52.0 (20 °C), |
| Formamide | 84.0 (20 °C) |
| Sulfuric acid | 84–100 (20–25 °C) |
| Hydrogen peroxide | 128aqueous–60 (−30–25 °C) |
| Hydrocyanic acid | 158.0–2.3 (0–21 °C) |
| Titanium dioxide | 86–173 |
| Strontium titanate | 310 |
| Barium strontium titanate | 500 |
| Barium titanate[12] | 1200–10,000 (20–120 °C) |
| Lead zirconate titanate | 500–6000 |
| Conjugated polymers | 1.8–6 up to 100,000[13] |
| Calcium copper titanate | >250,000[14] |

Therelative permittivity (in older texts,dielectric constant) is thepermittivity of a material expressed as a ratio with theelectric permittivity of a vacuum. Adielectric is an insulating material, and the dielectric constant of an insulator measures the ability of the insulator to store electric energy in an electrical field.
Permittivity is a material's property that affects theCoulomb force between two point charges in the material. Relative permittivity is the factor by which the electric field between the charges is decreased relative to vacuum.
Likewise, relative permittivity is the ratio of thecapacitance of acapacitor using that material as adielectric, compared with a similar capacitor that has vacuum as its dielectric. Relative permittivity is also commonly known as the dielectric constant, a term still used but deprecated by standards organizations in engineering[15] as well as in chemistry.[16]
Relative permittivity is typically denoted asεr(ω) (sometimesκ, lowercasekappa) and is defined as
whereε(ω) is thecomplex frequency-dependentpermittivity of the material, andε0 is thevacuum permittivity.
Relative permittivity is adimensionless number that is in generalcomplex-valued; its real and imaginary parts are denoted as:[17]
The relative permittivity of a medium is related to itselectric susceptibility,χe, asεr(ω) = 1 +χe.
In anisotropic media (such as non cubic crystals) the relative permittivity is a second ranktensor.
The relative permittivity of a material for afrequency of zero is known as itsstatic relative permittivity.
The historical term for the relative permittivity isdielectric constant. It is still commonly used, but has been deprecated by standards organizations,[15][16] because of its ambiguity, as some older reports used it for the absolute permittivityε.[15][18][19] The permittivity may be quoted either as a static property or as a frequency-dependent variant, in which case it is also known as thedielectric function. It has also been used to refer to only the real componentε′r of the complex-valued relative permittivity.[citation needed]
In the causal theory of waves, permittivity is a complex quantity. The imaginary part corresponds to a phase shift of the polarizationP relative toE and leads to the attenuation of electromagnetic waves passing through the medium. By definition, the linear relativepermittivity of vacuum is equal to 1,[19] that isε =ε0, although there are theoreticalnonlinear quantum effects in vacuum that become non-negligible at high field strengths.[20]
The following table gives some typical values.
| Solvent | Relative permittivity | Temperature | |
|---|---|---|---|
| C6H6 | benzene | 2.3 | 298 K (25 °C) |
| Et2O | diethyl ether | 4.3 | 293 K (20 °C) |
| (CH2)4O | tetrahydrofuran (THF) | 7.6 | 298 K (25 °C) |
| CH2Cl2 | dichloromethane | 9.1 | 293 K (20 °C) |
| NH3(liq) | liquid ammonia | 17 | 273 K (0 °C) |
| C2H5OH | ethanol | 24.3 | 298 K (25 °C) |
| CH3OH | methanol | 32.7 | 298 K (25 °C) |
| CH3NO2 | nitromethane | 35.9 | 303 K (30 °C) |
| HCONMe2 | dimethyl formamide (DMF) | 36.7 | 298 K (25 °C) |
| CH3CN | acetonitrile | 37.5 | 293 K (20 °C) |
| H2O | water | 78.4 | 298 K (25 °C) |
| HCONH2 | formamide | 109 | 293 K (20 °C) |
The relative low frequency permittivity ofice is ~96 at −10.8 °C, falling to 3.15 at high frequency, which is independent of temperature.[21] It remains in the range 3.12–3.19 for frequencies between about 1 MHz and the far infrared region.[22]
The relative static permittivity,εr, can be determined for staticelectric fields as follows: first thecapacitance of a testcapacitor,C0, is measured with vacuum between its plates. Then, using the same capacitor and distance between its plates, the capacitanceC with adielectric between the plates is measured. The relative permittivity can be then calculated as
For time-variantelectromagnetic fields, this quantity becomesfrequency-dependent. An indirect technique to calculateεr is conversion of radio frequencyS-parameter measurement results. A description of frequently used S-parameter conversions for determination of the frequency-dependentεr of dielectrics can be found in this bibliographic source.[23] Alternatively, resonance based effects may be employed at fixed frequencies.[24]
The relative permittivity is an essential piece of information when designingcapacitors, and in other circumstances where a material might be expected to introducecapacitance into a circuit. If a material with a high relative permittivity is placed in anelectric 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.
Dielectrics are used inradio frequency (RF) transmission lines. In acoaxial cable,polyethylene can be used between the center conductor and outside shield. It can also be placed inside waveguides to formfilters.Optical fibers are examples ofdielectricwaveguides. They consist of dielectric materials that are purposely doped with impurities so as to control the precise value ofεr within the cross-section. This controls therefractive 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.
The relative permittivity of air changes with temperature, humidity, and barometric pressure.[25] 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.
The relative static permittivity of a solvent is a relative measure of itschemical polarity. For example,water is very polar, and has a relative static permittivity of 80.10 at 20 °C whilen-hexane is non-polar, and has a relative static permittivity of 1.89 at 20 °C.[26] This information is important when designing separation,sample preparation andchromatography techniques inanalytical chemistry.
The correlation should, however, be treated with caution. For instance,dichloromethane has a value ofεr of9.08 (20 °C) and is rather poorly soluble in water (13 g/L or 9.8 mL/L at 20 °C); at the same time,tetrahydrofuran has itsεr =7.52 at 22 °C, but it is completely miscible with water. In the case of tetrahydrofuran, the oxygen atom can act as ahydrogen bond acceptor; whereas dichloromethane cannot form hydrogen bonds with water.
This is even more remarkable when comparing theεr values ofacetic acid (6.2528)[27] and that ofiodoethane (7.6177).[27] The large numerical value ofεr is not surprising in the second case, as theiodine atom is easily polarizable; nevertheless, this does not imply that it is polar, too (electronicpolarizability prevails over the orientational one in this case).
Again, similar as forabsolute permittivity, relative permittivity for lossy materials can be formulated as:
in terms of a "dielectric conductivity"σ (units S/m,siemens per meter), which "sums over all the dissipative effects of the material; it may represent an actual[electrical] conductivity caused by migrating charge carriers and it may also refer to an energy loss associated with the dispersion ofε′ [the real-valued permittivity]".[17]: 8 Expanding theangular frequencyω = 2πc / λ and theelectric constantε0 = 1 / μ0c2, which reduces to:
whereλ is the wavelength,c is the speed of light in vacuum andκ =μ0c / 2π = 59.95849 Ω ≈ 60.0 Ω is a newly introduced constant (unitsohms, or reciprocalsiemens, such thatσλκ =εr remains unitless).
Permittivity is typically associated withdielectric materials, however metals are described as having an effective permittivity, with real relative permittivity equal to one.[28] In the high-frequency region, which extends from radio frequencies to the farinfrared andterahertz region, the plasma frequency of the electron gas is much greater than the electromagnetic propagation frequency, so the refractive indexn of a metal is very nearly a purely imaginary number. In the low frequency regime, the effective relative permittivity is also almost purely imaginary: It has a very large imaginary value related to the conductivity and a comparatively insignificant real-value.[29]
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