Rate of Effusion Calculator

Compare two gases' effusion or diffusion rates from their molar masses.

Solves every direction of Graham's law in mol/s and g/mol.

Updated October 15, 2026
Frank Zhao - Creator
CreatorFrank Zhao
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Introduction

Two gases, one small hole, one question: given how heavy each gas is, how much faster does the lighter one escape — or spread — than the heavier one? This page answers that from the molar masses alone, and it answers the reverse question too: hand it a measured pair of rates and it returns the molar mass of the gas you have not identified yet.

Graham's law is a single statement containing four quantities — the two rates and the two molar masses. Any three of them fix the fourth, so the same page predicts a rate from the masses, checks a ratio you measured in the lab, or turns a rate pair into an identification. You choose the process first: effusion through a small opening, or diffusion of one gas into another. The two molar masses describe the gas pair and stay put when you switch; each process keeps its own pair of rate boxes.

That makes it useful in three fairly different situations: coursework and lab work where an unknown gas has to be narrowed down; reasoning about leaks and gas handling, where the practical question is whether one gas escapes appreciably faster than another; and the industrial case below, where two molecules differ by three mass units and a single pass through a barrier separates them by less than half a percent.

Any of the four boxes

Fill in three and the missing one follows

mol/s and g/mol

Rates in moles per second, molar masses in grams per mole

One ratio, two processes

Effusion and diffusion follow the same square-root law

Quick start

1

Choose the process you measured

Effusion is a gas escaping through a small opening — a pinhole, a porous plug, the rubber wall of a balloon that slowly deflates. Diffusion is one gas spreading into another, with no hole involved. Pick the one that matches your experiment: the molar masses you type stay with the gas pair either way, but the rate boxes belong to the process, so a rate measured one way is never mixed with a rate measured the other way.

2

Enter the two molar masses in grams per mole

Hydrogen is 2.016 g/mol, nitrogen 28.014, oxygen 31.998, carbon dioxide 44.009, uranium hexafluoride about 352. These come from the standard atomic weights published by the Commission on Isotopic Abundances and Atomic Weights, which is also the place to look up a value when you are adding up a compound rather than typing a familiar gas.

3

Enter whichever rate you already know

If you are predicting, one rate is enough — anything measured in moles per second on your apparatus. Leave the other rate box empty. If instead both rates came off the instrument, leave a molar mass empty and the page works that out.

4

Read the derived number

Hydrogen against oxygen, with hydrogen effusing at 1 mol/s and the two molar masses at 2.016 and 31.998 g/mol, returns 0.2510059 mol/s for oxygen:

r2r_2==r1M1M2r_1 \sqrt{\frac{M_1}{M_2}}==1×2.01631.9981 \times \sqrt{\frac{2.016}{31.998}}==0.2510059 mol/s0.2510059\ \mathrm{mol/s}

The empty box fills in, and the three boxes you typed stay as you left them. Nothing about the hole, the pressure or the temperature is needed for this number, because those cancel out of the ratio.

5

Turn it into a sentence about the two gases

Oxygen at 0.2510059 mol/s per 1 mol/s of hydrogen means hydrogen leaves about four times faster: the ratio is 1/0.2510059=3.9841 / 0.2510059 = 3.984, the same number you get straight from 31.998/2.016\sqrt{31.998/2.016}. State it that way to a colleague and it means something; state a bare rate in mol/s and you are also describing the size of your hole.

The law and what it assumes

Graham's law says that the rate at which a gas effuses is inversely proportional to the square root of its molar mass. Put two gases through the same opening under the same conditions and the constants drop out, leaving a ratio that depends on nothing but the two masses.

r1r2=M2M1\frac{r_1}{r_2} = \sqrt{\frac{M_2}{M_1}}

r1r_1 and r2r_2 are the two rates in moles per second, and M1M_1 and M2M_2 the two molar masses in grams per mole. Squaring both sides gives r12M1=r22M2r_1^{2} M_1 = r_2^{2} M_2, which is the form that shows why the mass direction is the sensitive one: the ratio of the rates enters twice.

Why the ratio has no units of its own

r1frater2frate\frac{r_1 f_{\mathrm{rate}}}{r_2 f_{\mathrm{rate}}}==r1r2\frac{r_1}{r_2}\qquadM2fmassM1fmass\frac{M_2 f_{\mathrm{mass}}}{M_1 f_{\mathrm{mass}}}==M2M1\frac{M_2}{M_1}

Both rates are read on the same scale and both molar masses on the same scale, so the conversion factors sit above and below the line and cancel. That is why the page asks only that the two rates match each other and the two molar masses match each other — as long as you are consistent, the ratios behave.

Both processes, one ratio — but not one rate

Effusion and diffusion are described by the same square-root law, and for a given pair of gases they give the same ratio. The absolute rates are not interchangeable: an effusion rate counts molecules crossing a hole per second, while a diffusion measurement follows one gas spreading into another over a distance, and the two numbers for the same gas are different. That is why the process choice in this calculator swaps in its own pair of rate boxes rather than reusing one, and why an effusion rate should never be typed next to a diffusion rate.

The three other directions

Rearranging the same relation gives every box in terms of the other three. The two rate directions are gentle; the two molar-mass directions square the rate ratio:

r1=r2M2M1r_1 = r_2 \sqrt{\frac{M_2}{M_1}}\qquadM1=M2(r2r1)2M_1 = M_2 \left( \frac{r_2}{r_1} \right)^{2}\qquadM2=M1(r1r2)2M_2 = M_1 \left( \frac{r_1}{r_2} \right)^{2}

Because that last pair squares the ratio, a small error in a measured rate roughly doubles in the molar mass it produces. A 1% slip shows the effect: with rates of 0.99 and 1.00 mol/s and a reference gas of 28.014 g/mol, the page returns 27.45652 g/mol instead of 28.014 — a 1% rate error turned into a 2% mass error. When you are identifying an unknown gas from two measured rates, the rates are the part worth repeating.

What the relation assumes

Both gases at the same temperature and pressure, behaving as ideal gases, passing through the same small opening — small enough that molecules cross one at a time rather than being swept through in a stream. Under those conditions the ratio is set by the masses alone. Real measurements drift from it when the opening is wide, the pressure is high, the temperature differs between the two readings, or the gas is heavy enough for its own molecules to interact noticeably — uranium hexafluoride is the standard example of the last case.

Worked examples

1

Identify an unknown gas against nitrogen

Situation: An unknown gas and nitrogen are effused through the same pinhole at the same temperature. Over the same interval the unknown comes through at 0.8374 times the rate of nitrogen.

Entered

Rate of effusion of Gas 1 (nitrogen)1 mol/s
Rate of effusion of Gas 2 (unknown)0.8374 mol/s
Molar mass of Gas 128.014 g/mol
Molar mass of Gas 2left empty

Returned

M2M_2==M1(r1r2)2M_1 \left( \frac{r_1}{r_2} \right)^{2}==28.014×(10.8374)228.014 \times \left( \frac{1}{0.8374} \right)^{2}==39.9493 g/mol39.9493\ \mathrm{g/mol}

That is argon. CIAAW gives argon a standard-atomic-weight interval of 39.792 to 39.963 g/mol, and 39.9493 falls inside it — so the reading is consistent with argon and inconsistent with anything much lighter or heavier.

In practice: Compare the answer with the gases you actually had on the bench. A 5% error in the rate ratio would move this mass by about 4 g/mol, which is the whole distance from here to carbon dioxide at 44.009 g/mol — so treat a single pair of readings as a shortlist, not as an identification.

2

How much faster does the lighter uranium isotope effuse?

Situation: Uranium hexafluoride is the gas used to separate uranium isotopes, because fluorine has only one naturally occurring isotope and therefore does not add to the mass difference. Using nominal mass numbers, the two forms are about 349.0 g/mol (uranium-235) and 352.0 g/mol (uranium-238).

Entered

Rate of effusion of Gas 1 (uranium-235 hexafluoride)1 mol/s
Molar mass of Gas 1349.0 g/mol
Molar mass of Gas 2352.0 g/mol
Rate of effusion of Gas 2left empty

Returned

r2r_2==r1M1M2r_1 \sqrt{\frac{M_1}{M_2}}==1×349.0352.01 \times \sqrt{\frac{349.0}{352.0}}==0.99573 mol/s0.99573\ \mathrm{mol/s}

The heavier molecule leaves at 0.99573 mol/s for every 1 mol/s of the lighter one, so the single-stage separation factor is 1/0.99573=1.004291 / 0.99573 = 1.00429: a 0.43% difference in rate from a three-unit difference in mass. The U.S. Nuclear Regulatory Commission describes that process and why uranium hexafluoride is the gas it runs on.

In practice: One pass through one barrier buys 0.43%. The NRC describes the gaseous diffusion process as needing many hundreds of barriers in series to lift the uranium-235 content from the 0.7% found in nature to the few per cent a reactor needs — which is the gap between a ratio on this page and an enrichment plant.

Practical tips

Take both readings in one run

The ratio cancels the size of the opening, the temperature and the amount of gas only when those really are the same for both readings. Two runs on two days, or a different fill pressure, put those differences straight into the ratio — and into any molar mass you back-solve, where the error doubles.

Times are not rates — invert them first

If your measurement is how long a fixed amount of gas takes, remember that the faster gas takes less time, so the rate ratio is the inverse of the time ratio. Enter 1/t1/t in each rate box with equal amounts of both gases, or convert to moles per second first. Typing the times themselves turns the answer upside down.

Use the real molar mass

Hydrogen is 2.016 g/mol rather than a round 2, and a compound is the sum of its atoms: carbon dioxide is 12.011+2×15.999=44.009 g/mol12.011 + 2 \times 15.999 = 44.009\ \mathrm{g/mol}. If what you have is a density, or a mass and a volume rather than a formula, the molar mass of gas calculator turns it into the number this page wants.

Keep the two processes apart

Effusion and diffusion give the same ratio for the same pair of gases, but a rate measured one way is not a rate measured the other way. Both rate boxes in one calculation must come from the same process; mixing them produces a ratio of two different kinds of measurement, and no amount of care with the molar masses will rescue it.

What the red molar mass warning means

If a molar mass comes out below 1 g/mol or above 1000 g/mol, the page keeps the number on screen and marks the box instead of hiding it. The lower bound is set by monatomic hydrogen at 1.008 g/mol — the lightest species that can exist as a gas — so anything under 1 g/mol is impossible. The upper bound sits far above the heaviest gases that are handled as gases; uranium hexafluoride, at about 352 g/mol, is the usual yardstick. Either warning almost always means a swapped rate, a wrong unit or a misplaced decimal point, so recheck the rate pair before the molar mass.

Questions

Q

Why are zero and negative rates refused?

A rate of zero means no gas left the container, which is not an effusion measurement, and a negative rate has no meaning at all. The relation also divides by the rate ratio, so a zero would leave the question without an answer. Any positive rate works, however small; the same applies to the molar masses, which must be above zero.

Q

Can I use it for a mixture?

Not directly. The law compares one gas with one other gas, and a mixture changes while it effuses: the lighter component leaves first, so both the composition and the rate drift during the measurement. Treat the result as belonging to a pure gas, or to a single component you can follow on its own.

Q

Does it matter which gas I call Gas 1?

No. Swapping the two labels flips the rate ratio and the molar-mass ratio together, so the pair is described just as well either way round. What does matter is that the rate and the molar mass in each box belong to the same gas — a rate for nitrogen sitting next to the molar mass of oxygen is the mistake that produces a confidently wrong answer.

Q

Can I get an absolute rate, or a diffusion coefficient?

This page works from ratios, so it always needs one measured rate for one of the gases; it cannot invent the opening size, temperature and pressure that set an absolute rate. A diffusion coefficient is a different quantity altogether: it describes how fast a substance spreads through a medium, in square metres per second, and it is covered by the diffusion coefficient calculator. Use the two together when you have both a rate ratio and a spreading measurement to make sense of.

Limitations and scope

  • An ideal-gas picture. The relation assumes both gases are at the same temperature and pressure, behave ideally, and pass through an opening small enough for molecules to cross one at a time. Wide openings, high pressures, and gases close to their boiling points all pull real rates away from the number shown here.
  • A rate in mol/s describes the apparatus as much as the gas. Hole area, temperature and pressure difference all set the absolute number, so the same gas reads very differently in two setups. The law compares two gases inside one setup; it is not a specification of a leak rate.
  • The molar-mass direction doubles your measurement error. Because that direction squares the rate ratio, the page can confirm that a back-solved molar mass is physically possible, but it cannot tell you whether your rates were accurate.
  • Real separations are cascades, not single stages. The uranium hexafluoride example returns a 0.43% advantage per pass; industrial enrichment reaches useful concentrations only by repeating that pass many hundreds of times. One number from this page is not a design calculation for a separation plant.
  • Not a basis for safety or process decisions. For flammable, toxic or radioactive gases, for pressure-vessel work and for any plant design, verify against measured data and have the decision reviewed by a qualified engineer. Treat the output here as an educational and estimating tool.
Rate of Effusion Calculator - Graham's Law of Effusion and Diffusion