Illustrated Physics
physics, drawn
Series

Attenuation — the series

6 essays on one idea, from the one that introduces it to the one that assumes the rest.
  1. An f² law that is right in shape and out by 30× in size. Two absorption curves for air against frequency, both logarithmic, in decibels per kilometre. The lower one is the classical Stokes–Kirchhoff result computed from air's viscosity and thermal conductivity alone, and it goes as f^2.000 — exactly two, because the loss per cycle is fixed and the number of cycles per metre is proportional to the frequency. The upper one is the measured atmospheric absorption at 20 °C and 50 per cent humidity, which fits f^1.42 and is 30 times larger at 1 kHz and 211 times at 125 Hz. The excess is not a correction to viscosity: it is nitrogen and oxygen storing energy in vibration and giving it back late, at a rate the water vapour sets, and it is the mechanism that actually removes the treble from a distant sound.

    The distance that takes the treble out

    Spreading treats every frequency alike; absorption does not. The loss per cycle is roughly fixed and the number of cycles per metre goes as the frequency, so absorption climbs as f² and a sound gets duller with distance as well as quieter — which is the whole account of why a nearby thunderclap cracks and a distant one rumbles.

    part 1 · waves
  2. Absorption and refraction, drawn as one function. The real and imaginary parts of a Lorentz oscillator's susceptibility against frequency, in units of the resonance. The imaginary part is the absorption: a symmetric line centred on the resonance, with a full width at half maximum equal to the damping — 0.05, 0.12, 0.30 here. The real part is the refraction, and it is what the same medium does to the speed of light. The two curves are not two facts about the medium: either one determines the other completely, by an integral over all frequencies, and that is a consequence of the medium responding after it is asked rather than before. Between x = 0.97 and x = 1.02 the refraction runs the wrong way — the index falls as the frequency rises, which is anomalous dispersion — and that region is exactly the width of the absorption line. Away from the line the index rises with frequency, which is ordinary dispersion and is why a prism separates colours in the order it does: every transparent material is on the low-frequency tail of an ultraviolet absorption it is not otherwise showing. A narrower line is a taller one, because the area under the absorption is fixed by how many electrons there are and by nothing else.

    The answer that cannot come first

    A medium absorbs at some frequencies and bends light at all of them, and those look like two separate facts to be measured separately. They are one fact. The requirement that a material respond after it is asked rather than before ties the absorption at every frequency to the refraction at every other, by an integral — and a material given the two halves independently answers before the question arrives.

    part 2 · waves
  3. A beam of sound has a weight. The force a fully absorbed acoustic beam exerts, against its power, for 3 media. It is the power divided by the speed of sound and nothing else — a watt in water gives 675 micronewtons, which is the weight of 68 milligrams, and a watt in air gives 2.9 millinewtons because the sound is slower there. This is not an analogy with light: it is the same statement, that a wave carrying energy carries momentum, with a much smaller speed in the denominator. The consequence is that acoustic power is measured by weighing. A radiation-force balance — an absorbing target on a laboratory balance, with the transducer beneath it — is the primary standard for ultrasonic output, and every therapeutic and diagnostic transducer is calibrated against one.

    Where the loudness goes

    An absorption coefficient removes energy from a wave, and energy removed has to appear somewhere. It appears twice, from the same coefficient: as heat, and as momentum. So a beam of sound has a weight — a watt absorbed in water weighs sixty-eight milligrams — and acoustic power is measured by putting an absorber on a balance. The ratio of the force to the heating contains no intensity at all.

    part 3 · waves
  4. An absorption that goes up when the photon gets harder. Mass attenuation coefficients for 4 materials against photon energy, both logarithmic, from tabulated measurements interpolated between. Away from a threshold every curve falls steeply — a harder photon is less easily absorbed, which is what makes X-rays penetrating. At a K edge the curve jumps upward: the photon has become able to eject an innermost electron, a whole new population becomes available, and the absorption multiplies by 4.4 for iodine at 33.17 keV and 4.0 for lead at 88 keV. That is a discontinuity in a material property as a function of frequency, and nothing in the classical description of absorption produces one. It exists because absorption at these energies is a transition of a bound electron rather than a loss in a medium.

    The steps in an absorption curve

    Every absorption law up to this point is smooth — a fixed loss per cycle, a relaxation, a power of frequency. Take the photon energy up to where it can eject an electron from an atom and the curve acquires steps, and they go the wrong way: the material becomes suddenly more opaque to a harder photon. Iodine absorbs four times as strongly at 33.4 keV as at 33.0, and that discontinuity is why it is injected into people.

    part 4 · waves
  5. The ripple that sits on top of an absorption edge. The Cu K absorption of copper foil, 293 K through its edge and for seven hundred electronvolts above it, with the smooth atomic background it would have if the absorbing atom were alone drawn beneath it. The difference between the two is the fine structure: a modulation reaching 11 per cent, dying away as the photon energy rises, and entirely absent from a free atom. It is there because the ejected electron is a wave that the neighbouring atoms scatter back onto the atom that emitted it, so the absorption depends on whether the returning wave arrives in step with the outgoing one — which depends on the distance to the neighbour and on nothing else about the sample.

    The ripple that counts the neighbours

    An absorption edge is drawn as a step and it is a step with a ripple on it — a modulation of eleven per cent in copper, five in a zinc site buried in a protein. The ripple is the ejected electron's own wave, scattered back onto the atom that emitted it, so its period is a distance. It is the only way of measuring where an atom's neighbours are that does not need a crystal.

    part 5 · waves
  6. The edge that is a straight line, not a step. The absorption of gallium arsenide near its own band gap of 1.424 electronvolts, on a logarithmic axis, at 4 temperatures. Below the gap the absorption does not stop; it falls exponentially, along a straight line whose slope is an energy, and the straightness holds over several decades. Raising the temperature makes the line shallower — the tail reaches further below the gap — and the slope runs from 5.6 millielectronvolts at 10 kelvin to 7.5 at 300, a factor of 1.33. The lines pivot about a point just above the gap rather than rotating about nothing, which is what makes the slope a single number worth quoting. The band gap's own shift with temperature has been removed here, so that the fan is the tail's doing and not the gap's.

    Below the gap, where there is nothing to absorb

    A semiconductor is supposed to be transparent below its band gap, and it is not. The absorption falls exponentially instead, over seven decades, along a straight line whose slope is an energy of a few millielectronvolts — and the description that produces that line has no states in the gap at all. What the slope measures is how much the gap itself is moving about.

    part 6 · waves

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