Mass Attenuation Coefficient Calculator
Mass Attenuation Coefficient Calculator
NIST photon attenuation data as a reference: μ/ρ and μen/ρ for eight materials from 1 keV to 20 MeV, with the linear coefficients, the mean free path, every absorption edge and a derived split of the three interaction processes.
This is narrow-beam attenuation through uniform material: the physics, not a shielding design. Real geometry scatters, and the scattered photons a narrow-beam calculation ignores can add tens of per cent to the dose behind a thick shield — that is what a build-up factor is for, and where a page omits one it says so on the page. A shield arrived at from a figure here has not been designed: shielding is specified by a qualified expert against the regulation that applies, and then verified by measurement.
Mass attenuation coefficient
Lead at caesium-137 — 661.7 keV — with both coefficients, the interaction split and the K edge
One coefficient per gram, three processes inside it, and a step where a shell switches on
- μ/ρ
- the mass attenuation coefficient, cm²/g. A cross-section per gram, so it depends on the composition and the photon energy and NOT on the density — which is exactly why NIST tabulates it this way and why the density on this page is a separate, editable input
- μen/ρ
- the mass energy-absorption coefficient, the energy actually deposited locally per gram per unit fluence. Always smaller than μ/ρ, because a Compton scatter removes a photon from the beam while carrying most of its energy onward. Dose and kerma want this one; transmission wants the other, and the ratio between them runs from 0.141 to 0.997 in water alone, and not monotonically
- σ_pe
- photoelectric absorption. Scales roughly as Z to the fourth or fifth power and falls roughly as the cube of the energy, which is why it dominates the left of the curve and why atomic number is everything there. It is also the process with the EDGES: each electron shell has a binding energy, and the shell becomes available the moment the photon can eject an electron from it
- σ_incoh
- Compton scattering. Depends on the number of ELECTRONS and almost not at all on which element they belong to, so in the Compton region all materials converge when compared per gram. The figure on this page is the Klein–Nishina free-electron cross-section times NIST’s ⟨Z/A⟩, which is an upper bound below about 100 keV because it ignores electron binding
- σ_pair
- electron–positron pair production. Impossible below 1.022 MeV, which is twice the electron rest energy, and growing as the square of the atomic number above it — which is why lead’s coefficient turns back upward at 4 MeV while water’s does not until 20
- λ = 1/μ
- the mean free path, the average distance to the first interaction. It is 1/ln2 = 1.4427 times the half-value layer, always, and the two get confused. One mean free path transmits 1/e, about 36.8 per cent
- a K edge
- the step. Lead’s is at 88.0045 keV and multiplies μ/ρ by 4.02 across a few electronvolts, which makes lead at 90 keV three and a half times the absorber it is at 85. No smooth function of energy can represent that, which is why these pages interpolate between NIST’s tabulated points rather than fitting a curve to them
Worked example
Lead at caesium-137 — 661.7 keV — with both coefficients, the interaction split and the K edge
THE TWO COEFFICIENTS. Log-log interpolated between NIST's 600 and 800 keV rows: μ/ρ = 0.111120 cm²/g and μen/ρ = 0.059841. Their ratio is 0.5385, so of every photon lead removes from this beam, only 54 per cent of the energy stays in the lead and the rest leaves as scattered radiation. For water the same ratio is 0.3801 — a water shield passes on nearly two thirds of what it takes out of the beam
AND THE LINEAR ONES. Multiply by 11.35 g/cm³: μ = 1.261213 per cm, μen = 0.679190 per cm. The mean free path is 1/μ = 7.9289 mm — the average distance a photon goes before its first interaction — which is 1.4427 times the half-value layer of 5.4959 mm. Those two get swapped and the error is 44 per cent
HOW MANY ELECTRONS ARE IN A GRAM OF IT, which is the number that explains the next step. NIST's 〈Z/A〉 for lead is 0.39575, so a gram holds 238,300,000,000 Telectrons. Water's 〈Z/A〉 is 0.55508 — so a gram of WATER holds 40 per cent MORE electrons than a gram of lead. Lead is a heavy element, not an electron-rich one
WHICH PROCESS IS DOING IT. The Klein–Nishina cross-section at 661.7 keV is 0.25620 barn per electron, which times the electrons per gram gives a Compton coefficient of 0.061059 cm²/g — 54.9 per cent of lead's total. The other 45.1 per cent is photoelectric absorption and coherent scattering, since 661.7 keV is below the 1.022 MeV pair threshold. In WATER at the same energy the Compton share is 99.94 per cent: there is essentially nothing else happening
THE SPLIT IS DERIVED, NOT TABULATED, and that matters. NIST's table carries the total coefficient and not the five partial cross-sections, so the Compton figure above is Klein–Nishina for a FREE electron and the remainder is whatever is left over. Free electrons are the wrong model below about 100 keV, where binding suppresses incoherent scattering, so down there the Compton share printed here is an upper bound. Through the Compton region, which is where it is used, it is good to a few per cent
AND THE EDGE, which is the reason this page exists. Lead's K edge is at 88.0045 keV and the coefficient across it goes from 1.911 to 7.682 cm²/g — a factor of 4.020 over twenty electronvolts. Below the edge a photon cannot eject a K-shell electron at all and the whole K shell is unavailable; above it, the most tightly bound shell in the atom switches on. The practical consequence runs the wrong way round from every intuition about radiation: lead's half-value layer is 0.293 mm at 85 keV and 0.084 mm at 90 keV, so a HIGHER energy is easier to shield. It is the only place on the curve where that is true
WHAT THE CURVE LOOKS LIKE WHEN YOU DRAW IT. The chart on this page sweeps 10 keV to 20 MeV on log axes. For lead: a steep photoelectric fall interrupted by the L edges at 13 to 16 keV and the K edge at 88, a Compton plateau through the hundreds of keV and the low MeV, a minimum at 4 MeV where μ/ρ is 0.04197 — the least absorbing lead ever gets — and then a rise as pair production takes over. Water's minimum is not until the 20 MeV end of the table, because pair production grows as the square of the atomic number
μ/ρ at six source energies, with μen/ρ and the ratio at caesium-137
| Material | Density (g/cm³) | ⟨Z/A⟩ | Tc-99m (cm²/g) | I-131 (cm²/g) | Ir-192 (cm²/g) | F-18 (cm²/g) | Cs-137 (cm²/g) | Co-60 (cm²/g) | μen/ρ at Cs-137 | μen/ρ ÷ μ/ρ |
|---|---|---|---|---|---|---|---|---|---|---|
| Lead (Pb) | 11.3500 | 0.39575 | 2.37137 | 0.27759 | 0.25629 | 0.15652 | 0.11112 | 0.05876 | 0.05984 | 0.5385 |
| Concrete, ordinary | 2.3000 | 0.50932 | 0.14809 | 0.10152 | 0.09985 | 0.08831 | 0.07878 | 0.05807 | 0.02989 | 0.3794 |
| Water | 1.0000 | 0.55508 | 0.15359 | 0.10999 | 0.10823 | 0.09597 | 0.08569 | 0.06323 | 0.03257 | 0.3801 |
| Iron / mild steel (Fe) | 7.8740 | 0.46556 | 0.21767 | 0.09887 | 0.09666 | 0.08326 | 0.07346 | 0.05350 | 0.02794 | 0.3803 |
| Tungsten (W) | 19.3000 | 0.40250 | 1.86714 | 0.22773 | 0.21120 | 0.13404 | 0.09857 | 0.05577 | 0.05049 | 0.5123 |
| Aluminium (Al) | 2.6990 | 0.48181 | 0.14260 | 0.09631 | 0.09470 | 0.08366 | 0.07461 | 0.05496 | 0.02826 | 0.3788 |
| Soft tissue (ICRU-44) | 1.0600 | 0.54996 | 0.15227 | 0.10903 | 0.10729 | 0.09508 | 0.08490 | 0.06265 | 0.03227 | 0.3801 |
| Air, dry (sea level) | 0.0012 | 0.49919 | 0.13842 | 0.09898 | 0.09740 | 0.08631 | 0.07707 | 0.05687 | 0.02929 | 0.3800 |
Every absorption edge in the eight materials, with the size of the step
| Material | Edge | Energy (keV) | μ/ρ just below | μ/ρ just above | Jump | What it is |
|---|---|---|---|---|---|---|
| Lead (Pb) | M5 | 2.4840 | 800.602 | 1,397.029 | 1.745× | an M subshell edge |
| Lead (Pb) | M4 | 2.5856 | 1,943.988 | 2,457.993 | 1.264× | an M subshell edge |
| Lead (Pb) | M3 | 3.0664 | 1,857.005 | 2,145.990 | 1.156× | an M subshell edge |
| Lead (Pb) | M2 | 3.5542 | 1,496.004 | 1,584.993 | 1.059× | an M subshell edge |
| Lead (Pb) | M1 | 3.8507 | 1,311.003 | 1,367.994 | 1.043× | an M subshell edge |
| Lead (Pb) | L3 | 13.0352 | 67.010 | 162.099 | 2.419× | an L subshell edge |
| Lead (Pb) | L2 | 15.2000 | 107.800 | 148.499 | 1.378× | an L subshell edge |
| Lead (Pb) | L1 | 15.8608 | 134.400 | 154.799 | 1.152× | an L subshell edge |
| Lead (Pb) | K | 88.0046 | 1.910 | 7.683 | 4.022× | the K edge, and the one that matters for shielding |
| Concrete, ordinary | Na-K | 1.0721 | 2,889.008 | 2,977.984 | 1.031× | the K edge of Na in the mixture |
| Concrete, ordinary | Mg-K | 1.3050 | 1,775.005 | 1,780.990 | 1.003× | an M subshell edge |
| Concrete, ordinary | Al-K | 1.5596 | 1,104.003 | 1,175.994 | 1.065× | the K edge of Al in the mixture |
| Concrete, ordinary | Si-K | 1.8389 | 752.502 | 1,630.993 | 2.167× | the K edge of Si in the mixture |
| Concrete, ordinary | K-K | 3.6074 | 280.401 | 291.098 | 1.038× | the K edge of K in the mixture |
| Concrete, ordinary | Ca-K | 4.0381 | 213.101 | 251.999 | 1.183× | the K edge of Ca in the mixture |
| Concrete, ordinary | Fe-K | 7.1120 | 51.870 | 54.150 | 1.044× | the K edge of Fe in the mixture |
| Water | none in the tabulated range | — | — | — | — | its elements are all too light — the K edges of hydrogen and oxygen are at 13.6 and 543 eV, below the 1 keV start of the table |
| Iron / mild steel (Fe) | K | 7.1120 | 53.190 | 407.598 | 7.663× | the K edge, and the one that matters for shielding |
| Tungsten (W) | M5 | 1.8092 | 1,108.002 | 1,327.057 | 1.198× | an M subshell edge |
| Tungsten (W) | M4 | 1.8716 | 2,900.929 | 3,170.020 | 1.093× | an M subshell edge |
| Tungsten (W) | M3 | 2.2810 | 2,828.007 | 3,278.984 | 1.159× | an M subshell edge |
| Tungsten (W) | M2 | 2.5749 | 2,445.006 | 2,598.988 | 1.063× | an M subshell edge |
| Tungsten (W) | M1 | 2.8196 | 2,104.005 | 2,193.990 | 1.043× | an M subshell edge |
| Tungsten (W) | L3 | 10.2068 | 92.010 | 233.399 | 2.537× | an L subshell edge |
| Tungsten (W) | L2 | 11.5440 | 168.900 | 231.200 | 1.369× | an L subshell edge |
| Tungsten (W) | L1 | 12.0998 | 206.501 | 238.199 | 1.154× | an L subshell edge |
| Tungsten (W) | K | 69.5251 | 2.552 | 11.230 | 4.400× | the K edge, and the one that matters for shielding |
| Aluminium (Al) | K | 1.5596 | 362.101 | 3,956.982 | 10.928× | the K edge, and the one that matters for shielding |
| Soft tissue (ICRU-44) | Na-K | 1.0721 | 3,087.008 | 3,098.983 | 1.004× | the K edge of Na in the mixture |
| Soft tissue (ICRU-44) | P-K | 2.1455 | 458.301 | 464.997 | 1.015× | the K edge of P in the mixture |
| Soft tissue (ICRU-44) | S-K | 2.4720 | 310.201 | 315.798 | 1.018× | the K edge of S in the mixture |
| Soft tissue (ICRU-44) | Cl-K | 2.8224 | 215.801 | 218.799 | 1.014× | the K edge of Cl in the mixture |
| Soft tissue (ICRU-44) | K-K | 3.6074 | 107.300 | 110.499 | 1.030× | the K edge of K in the mixture |
| Air, dry (sea level) | Ar-K | 3.2029 | 134.000 | 148.499 | 1.108× | the K edge of Ar in the mixture |
Where Compton scattering takes over, and where pair production takes it back
| Material | Compton reaches half the total at (keV) | Compton share at 30 keV (%) | Compton share at 100 keV (%) | Compton share at 511 keV (%) | Compton share at 1.25 MeV (%) | Compton share at 5 MeV (%) | Compton share at 10 MeV (%) | Coefficient bottoms out at |
|---|---|---|---|---|---|---|---|---|
| Lead (Pb) | 587.0 | 0.5 | 2.1 | 43.6 | 76.6 | 46.2 | 24.4 | 4 MeV |
| Concrete, ordinary | 49.7 | 19.1 | 87.0 | 99.5 | 99.7 | 87.4 | 68.7 | 20 MeV |
| Water | 29.0 | 53.2 | 96.5 | 99.8 | 99.8 | 91.4 | 76.8 | 20 MeV |
| Iron / mild steel (Fe) | 125.1 | 2.0 | 37.2 | 96.5 | 99.0 | 73.8 | 47.7 | 8 MeV |
| Tungsten (W) | 492.1 | 0.6 | 2.7 | 51.8 | 82.1 | 49.0 | 26.0 | 4 MeV |
| Aluminium (Al) | 54.6 | 15.4 | 83.9 | 99.4 | 99.7 | 84.8 | 63.8 | 20 MeV |
| Soft tissue (ICRU-44) | 29.3 | 52.2 | 96.4 | 99.8 | 99.8 | 91.5 | 77.0 | 20 MeV |
| Air, dry (sea level) | 29.8 | 50.8 | 96.1 | 99.8 | 99.8 | 90.6 | 75.0 | 20 MeV |
Four coefficients that get mistaken for each other
| Quantity | Symbol and unit | What it counts | Use it for | Do NOT use it for |
|---|---|---|---|---|
| Mass attenuation coefficient | μ/ρ, cm²/g | Every interaction that removes a photon from the beam, including the ones that only deflect it | Transmission, half-value layers, shield thickness — anything about how much beam survives | Dose or kerma. It counts a Compton scatter that carried 95 per cent of the energy onward as a complete removal |
| Mass energy-transfer coefficient | μtr/ρ, cm²/g | The fraction of the photon energy handed to electrons | Kerma, and as the step before the next row | Transmission. It is smaller than μ/ρ, so it under-states how much a centimetre attenuates and therefore over-specifies the shield |
| Mass energy-absorption coefficient | μen/ρ, cm²/g | The energy actually deposited locally — energy transfer minus what the electrons radiate away as bremsstrahlung | Absorbed dose, air kerma rate constants, detector response | Transmission. In water at caesium-137 it is 38 per cent of μ/ρ, so using it in the exponential would ask for 2.6 times the thickness actually needed — expensive rather than dangerous, which is why the mistake survives |
| Linear attenuation coefficient | μ, per cm | The same interactions as the first row, per centimetre instead of per gram | The exponential itself, and the half-value layer | Anything where the density is uncertain. μ inherits the density error directly; μ/ρ does not have one |
Two coefficients that get swapped, one step where a shell switches on, and three processes in three regions
There are two coefficients on this page and they answer different questions. μ/ρ counts every interaction that removes a photon from the beam, including a Compton scatter that deflects it by two degrees and carries 99 per cent of its energy onward. μen/ρ counts the energy that actually stays behind. In lead at caesium-137 the ratio is 0.539 and in water it is 0.380 — so a water shield passes on 62 per cent of what it takes out of the beam. Transmission, half-value layers and shield thicknesses all want μ/ρ. Absorbed dose, air kerma rate constants and detector response all want μen/ρ. Swapping them is a factor of two to three, and the direction of the error is not the one people expect: μen/ρ is the SMALLER, so putting it in the exponential under-states how much each centimetre attenuates and asks for too much shielding — in water at caesium-137 it would ask for 2.6 times the thickness actually needed. Expensive rather than dangerous, which is exactly why the mistake survives. The ratio is not a constant you can remember either, and it is not even monotone: in water it is 0.997 at 1.5 keV, bottoms out at 0.141 at 80 keV, and climbs back to 0.76 at 20 MeV.
The K edge is why lead is wonderful at 100 keV and poor at 85. Photoelectric absorption needs the photon to eject a bound electron, and each shell has a threshold. Below 88.0045 keV a photon cannot touch lead’s K shell at all, so the atom is absorbing with its L and M shells only; a few electronvolts above, the most tightly bound shell in the atom switches on and the coefficient QUADRUPLES — 1.910 cm²/g below, 7.683 above, a factor of 4.02 across a step that is essentially vertical. The half-value layer falls from 0.293 mm at 85 keV to 0.084 mm at 90 keV. This is the one place on the whole attenuation curve where a HIGHER photon energy is easier to shield, and it has real consequences: a filtered 150 kV X-ray beam behaves in lead like a monoenergetic 84 keV beam, sitting just under the edge where lead is at its weakest in that band, and tungsten — whose K edge is at 69.5 keV — beats it between 69.5 and 88 keV for exactly that reason. No smooth fit to this data can represent an edge, which is why the lookup behind these pages interpolates between NIST’s tabulated points instead.
Three processes, three regions, and the shape of the curve is the argument. On the left, photoelectric absorption: falling roughly as the cube of the energy and rising as the fourth or fifth power of atomic number, which is where lead is worth fifteen to thirty times its weight in concrete and where the edges live. In the middle, Compton scattering off individual electrons, which depends on the number of electrons per gram and essentially not at all on which element they belong to — so in this region all eight materials converge to within a factor of 1.3 of one another per gram, and lead’s advantage evaporates completely. On the right, pair production, which cannot happen below 1.022 MeV and then grows as the square of the atomic number, so every curve has a minimum and the heavy elements reach theirs first: 4 MeV for lead and tungsten, 8 for iron, and past the end of the table for water. The energy at which Compton takes over is the single most useful number on the page, and it rises from 29 keV in water to 587 keV in lead.
Lead has fewer electrons per gram than water, and that is not a trick. NIST’s 〈Z/A〉 column gives lead 0.39575 electrons per nucleon and water 0.55508, so a gram of water holds 40 per cent MORE electrons than a gram of lead. Wherever attenuation is Compton scattering and nothing else, that is the whole story: per unit mass, lead beats water below 1.012 MeV, LOSES to it from 1.012 to 2.471 MeV, and wins again above that as pair production takes over. The often-quoted claim that lead is “20 to 30 per cent better than an equal mass of low-Z material” is true at diagnostic energies and false at cobalt-60. What is never in doubt is the DENSITY: lead is 11.35 g/cm³ against water’s 1.00, so even where it loses per gram it wins per centimetre by a factor of ten. Lead buys space.
The interaction split on this page is derived, not tabulated, and that is stated rather than implied. NIST’s table carries the total μ/ρ and the total μen/ρ, not the five partial cross-sections its methodology section sums. So the Compton column here is computed from the Klein–Nishina cross-section per FREE electron — which reproduces the two standard check values, 0.6652 barn in the Thomson limit and 0.2112 barn at 1 MeV — multiplied by NIST’s own 〈Z/A〉, and the remainder is whatever is left over. Free electrons are the wrong model at low energy, where binding suppresses incoherent scattering, so below about 100 keV the Compton share printed here is an UPPER bound and the remainder a lower one. Through the Compton region, which is where the split is actually read, it is good to a few per cent. If you need the partial coefficients properly, NIST’s XCOM program publishes them.
What this page is for, and what it is not. It is the reference the other shielding pages on this site read from: a half-value layer, a shield thickness and a layered stack are all this coefficient with a density and an exponential attached. It is also the page to come to when a number elsewhere looks wrong, because it prints the raw quantity rather than a result derived from it. What it is not is a dose calculation, a shield design or a statement about anything being safe: a coefficient is a property of a material, and every number on this page would be the same whether the beam were a millisievert an hour or a thousand. The thicknesses it prints are narrow-beam, like everything in this category, and a real shield needs 11 to 33 per cent more than ln2/μ for the reason the half-value layer page sets out at length.
Frequently asked questions
What is the difference between μ/ρ and μen/ρ?
μ/ρ is about the BEAM and μen/ρ is about the ENERGY. μ/ρ counts every interaction that takes a photon out of the beam, including a Compton scatter that deflects it slightly and carries nearly all its energy away with it; μen/ρ counts only the energy deposited locally. μen/ρ is therefore always the smaller, and the ratio is not a constant: in water it is 0.380 at caesium-137, 0.997 at 1.5 keV, and a minimum of 0.141 at 80 keV — so it is not monotone and cannot be remembered as a rule. At a few keV nearly every interaction is a photoelectric absorption that deposits everything; at 80 keV nearly every interaction is a Compton scatter that carries the energy away; at many MeV the Compton electron keeps most of the energy and deposits it locally after all. Use μ/ρ for transmission and shielding, μen/ρ for dose and kerma. Putting the second one in the exponential would ask for 2.6 times the thickness needed in water at caesium-137 — expensive rather than dangerous, which is why the mistake is easy to live with and hard to notice.
Why does lead’s attenuation jump at 88 keV?
Because that is the binding energy of lead’s K-shell electrons, and photoelectric absorption needs the photon to be able to eject the electron it interacts with. Below 88.0045 keV a photon cannot eject a K electron at all, so the entire K shell — the most tightly bound and most effective absorber in the atom — is unavailable, and lead absorbs with its L and M shells only. A few electronvolts above, the K shell switches on and μ/ρ goes from 1.910 to 7.683 cm²/g, a factor of 4.02. The practical consequence is counter-intuitive and real: lead’s half-value layer is 0.293 mm at 85 keV and 0.084 mm at 90 keV, so a higher-energy photon is easier to stop. It is the only place on the curve where that happens.
Is lead always the best gamma shield?
Per centimetre, nearly always. Per gram, no, and the exception is in the energy range people use most. Lead’s 〈Z/A〉 is 0.39575 against water’s 0.55508, so a gram of lead holds 29 per cent fewer electrons than a gram of water — and where attenuation is Compton scattering, electrons per gram is all that matters. Per unit mass, lead beats water below 1.012 MeV, loses to it from 1.012 to 2.471 MeV, and wins again above that as pair production takes over. Tungsten beats lead throughout on thickness, at considerably more money, which is why it is used in collimators and syringe shields and not in walls. And concrete beats both on cost and holds the building up, which is why most shielding in the world is concrete.
Why does the coefficient start rising again above a few MeV?
Pair production. Above 1.022 MeV — twice the electron rest energy — a photon can convert into an electron and a positron in the field of a nucleus, and the cross-section for that grows as the SQUARE of the atomic number and with the energy. So every attenuation curve falls, bottoms out, and rises, and the heavy elements turn first: lead and tungsten at 4 MeV, iron at 8, while water, air, tissue, concrete and aluminium do not reach their minimum before the 20 MeV end of the NIST table. One thing NOT in these numbers: photonuclear absorption, which NIST’s methodology section says can contribute 5 to 10 per cent of the total in a narrow band somewhere between 5 and 40 MeV, is excluded from the tabulation.
Where do the interaction percentages come from?
From a derivation, not from NIST, and the page says so because the distinction matters. NIST’s table carries the total μ/ρ and the total μen/ρ, not the five partial cross-sections. The Compton figure here is the Klein–Nishina total cross-section per FREE electron — which checks out against the Thomson limit of 0.6652 barn at low energy and the standard 0.2112 barn at 1 MeV — multiplied by NIST’s 〈Z/A〉 and the Avogadro constant, and the remainder is everything else. The weakness is at low energy: free electrons are the wrong model where binding matters, so below about 100 keV the Compton share is an upper bound, by roughly ten per cent in water at 30 keV and more below. Through the Compton region it is good to a few per cent. For properly separated partials, NIST’s XCOM program is the source.
How accurate is the interpolation between NIST’s energies?
Measured by leave-one-out on the grid — drop a tabulated point, rebuild it from its neighbours in log-log space, compare — the median error is 0.3 to 1.4 per cent and the mean about 1.6 across all eight materials. The worst cases are the steep photoelectric region: 20 to 40 keV in water, air and soft tissue reaches 11 to 13 per cent, and lead and tungsten peak at 5.6 to 6.5 per cent near 300 keV. At the energies these pages are actually used at it is 1 to 4 per cent, and three of them carry no error at all because they are exact grid points: 40 keV, 60 keV and 1.25 MeV. The interpolation is done in log-log space on purpose; done linearly it would be 2.3 per cent high on μ for lead at caesium-137, which is 2.3 per cent low on the half-value layer and therefore wrong in the unsafe direction.
What is the mean free path, and is it the same as the half-value layer?
No, and it is the longer of the two by 44 per cent. The mean free path is 1/μ, the average distance a photon travels before its first interaction; the half-value layer is ln2/μ, the thickness that removes half of them. The ratio is 1/ln2 = 1.4427 for every material at every energy. For lead at caesium-137 the mean free path is 7.93 mm and the half-value layer is 5.50 mm. One mean free path transmits 1/e, about 36.8 per cent. Substituting one for the other gives a thickness wrong by 44 per cent, and in the thin direction if you use the half-value layer where the mean free path belongs.
Can I use these coefficients for a material that is not in the list?
Only with care, and the right way depends on what you have. If your material is the SAME composition at a different density — a denser pour of the same concrete mix — then μ/ρ is unchanged and you need only type the density, which is what the override on this page is for. If the COMPOSITION differs, μ/ρ differs too and scaling the density is not enough: barytes and magnetite concretes have much larger coefficients at low energy than ordinary concrete, because the heavy aggregate raises the effective atomic number. For a mixture, μ/ρ is the mass-weighted sum of the elements’ own values, which is how NIST computes the compound rows here, and NIST’s own tables and its XCOM program will do an arbitrary mixture for you.
Related calculators
References
- J. H. Hubbell and S. M. Seltzer, Tables of X-Ray Mass Attenuation Coefficients and Mass Energy-Absorption Coefficients, NIST Standard Reference Database 126, physics.nist.gov/PhysRefData/XrayMassCoef/ (read 7 October 2026). Every coefficient on these pages comes from here: eight materials, 1 keV to 20 MeV, 369 tabulated rows. A work of the United States Government and therefore free of domestic copyright, which is the reason this vertical exists in the form it does — the alternative sources for the same numbers are copyrighted standards. Three things were checked against it before anything was written: every absorption edge sits at its published energy (lead K at 88.0045 keV, tungsten K at 69.525, iron K at 7.112); μ/ρ at 1 MeV reproduces the published spot value for all eight materials to the last printed digit; and μen/ρ is at or below μ/ρ in every one of the 369 rows, as it must be.
- Table 1: Values of <Z/A>, I and Densities for Elemental Media and Table 2: … for Compounds and Mixtures, NIST X-Ray Mass Attenuation Coefficients (read 7 October 2026). Two things are taken from these. The <Z/A> column, which is what turns a Klein–Nishina cross-section per electron into a coefficient per gram: lead 0.39575, tungsten 0.40250, iron 0.46556, aluminium 0.48181, ordinary concrete 0.50932, dry air 0.49919, ICRU-44 soft tissue 0.54996, water 0.55508. And the density column, which matters because a mass attenuation coefficient is per gram and cannot become a thickness without one: 11.35, 19.30, 7.874, 2.699, 2.300, 1.205×10−3, 1.060 and 1.000 g/cm3. Note what the <Z/A> column shows on its own: lead carries 0.396 electrons per nucleon against water’s 0.555, so a gram of lead holds 29 per cent FEWER electrons than a gram of water. Where attenuation is Compton scattering and nothing else, which for these two materials is 1.01 MeV to 2.47 MeV, that makes lead the worse material per gram, and only its density rescues it.
- X-Ray Mass Attenuation Coefficients — Section 2: Methodology, NIST (read 7 October 2026). Cited for the composition of the total cross-section, which is the structure of the interaction-share figures on the coefficient page: NIST’s equation sums five processes — the photoelectric effect, coherent (Rayleigh) scattering, incoherent (Compton) scattering, electron–positron pair production and triplet production — and notes that photonuclear absorption, which is not in the sum, “can contribute as much as 5 % to 10 % to the total photon interaction cross section in a fairly narrow energy region usually occurring somewhere between 5 MeV and 40 MeV”. It also says that the photoelectric cross-sections were calculated over 1 keV to 1.5 MeV, which is why these pages treat the residual above a couple of MeV as pair production. The partial coefficients themselves are NOT in the table these pages use, and the split printed on the coefficient page is therefore derived rather than tabulated — which the page states.
- CODATA recommended values of the fundamental physical constants, as adopted in the 2019 SI. Used for three numbers in the Klein–Nishina cross-section on the coefficient page: the classical electron radius re = 2.8179403262×10−13 cm, the electron rest energy mec2 = 0.510 998 950 MeV, and the Avogadro constant NA = 6.022 140 76×1023 mol−1, which is now exact by definition. The cross-section computed from them reproduces the two standard check values: the Thomson limit 8πre2/3 = 0.6652 barn as the energy goes to zero, and 0.2112 barn at 1 MeV.
- Ionizing Radiation — Shielding Layer Examples, Occupational Safety and Health Administration, osha.gov/ionizing-radiation/introduction/shielding-layer-examples (read 7 October 2026). A US Government work and reproduced here. Two rows, six materials-worth of numbers, all in centimetres: caesium-137 at 0.66 MeV, HVL 4.8 concrete / 1.6 steel / 0.7 lead and TVL 15.7 / 5.3 / 2.1; cobalt-60 at 1.17 and 1.33 MeV, HVL 6.6 / 2.1 / 1.2 and TVL 20.8 / 6.9 / 4.0. These are BROAD-BEAM figures and every one of them is larger than ln2/μ from the NIST coefficient. At caesium-137 the excess is 25 per cent for concrete, 33 for steel and 27 for lead; at cobalt-60 it is 27, 28 and 15. The ratio of TVL to HVL in the table is also worth reading: narrow-beam it would be exactly ln10/ln2 = 3.322 for every entry, and here it runs 3.27, 3.31, 3.00, 3.15, 3.29 and 3.33, which is the rounding of one-significant-figure entries rather than physics.
- Lead shielding thickness — what are the lead codes?, IonActive Consulting radiation protection resource hub (read 7 October 2026). The source for the six BS EN 12588 rolled lead sheet codes and for the practical advice around them: Code 3 is 1.32 mm, Code 4 1.80, Code 5 2.24, Code 6 2.65, Code 7 3.15 and Code 8 3.55, with “a ± 5% tolerance”. Three statements are taken from it directly. Sheet lead codes “tend to be used for relatively low energy applications (i.e. up to about 150 kVp)”. “Where significantly thick lead is required (e.g. 10’s – 100’s mm), lead bricks are often the better option”. And “since lead codes relate to specific thickness dimensions there is often a compromise required, so you may need to use a lead code above what you actually require” — which is the reason the shield-thickness page prints the code at or above the answer rather than the nearest one. It also gives a useful anchor at the diagnostic end: “at 150 kV it is often reported that the TVT is 0.95 mm lead (so practically 1 mm lead)”.
- Gamma ray, Wikipedia (read 7 October 2026). Read for the shielding section and quoted for one comparison that is worth having because it is in the units people actually think in: “gamma rays that require 1 cm (0.4 inch) of lead to reduce their intensity by 50% will also have their intensity reduced in half by 4.1 cm of granite rock, 6 cm (2.5 inches) of concrete, or 9 cm (3.5 inches) of packed soil”, and for the statement that “a lead (high Z) shield is 20–30% better as a gamma shield than an equal mass of a low-Z shielding material”. Both are consistent with the NIST coefficients at around 1 MeV, with one correction. The energy at which lead’s narrow-beam half-value layer is exactly 1.000 cm is 1.194 MeV, and concrete’s there is 5.07 cm, not 6 — so the quoted pairing is about 18 per cent generous to concrete, which is roughly the size of a build-up correction and may be where it came from. The second statement needs more care still: per unit MASS lead beats water below 1.012 MeV, LOSES to it from 1.012 to 2.471 MeV, and wins again above that as pair production takes over. “20–30% better” is true at diagnostic energies and false at cobalt-60.
