Significant Figures Calculator and Counter
Count significant figures, round numbers to a specified precision, convert scientific notation, and solve mathematical operations using significant-figure rules with clear explanations.
Calculate partial pressures with Dalton's law from mole fractions, gas mixtures or the ideal gas law, add partial pressures to a total, and convert between atm, kPa, Pa, bar and mmHg.
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This partial pressure calculator applies Dalton's law in four ways. It can turn a mole fraction and a total pressure into a partial pressure, split a total pressure across a mixture of gases from their amounts in moles, add separate partial pressures to get a total, or find the pressure of a single gas from the ideal gas law. Every answer is shown in atm, kPa, Pa, bar and mmHg, with the working written out step by step so you can check it against a textbook or a lab sheet.
Dry air is about 20.95% oxygen by volume, so its mole fraction is about 0.2095. At a total pressure of 1 atm, P(O₂) = 0.2095 × 1 atm = 0.2095 atm, which is 21.23 kPa or 159.2 mmHg.
A cylinder at 200 kPa holds 3.0 mol of nitrogen, 1.5 mol of oxygen and 0.5 mol of argon, 5.0 mol in total. The mole fractions are 0.60, 0.30 and 0.10, so the partial pressures are 120 kPa, 60 kPa and 20 kPa. They add back to 200 kPa.
Hydrogen is collected over water at 25 °C with a total pressure of 755.0 mmHg. Water's vapour pressure at 25 °C is about 23.8 mmHg, so the dry hydrogen pressure is 755.0 − 23.8 = 731.2 mmHg. Use the total-from-partials mode in reverse by checking that 731.2 + 23.8 returns 755.0 mmHg.
0.500 mol of gas at 25 °C in a 10.0 L flask: T = 298.15 K and V = 0.0100 m³, so P = 0.500 × 8.314462618 × 298.15 ÷ 0.0100 = 123,948 Pa, about 124.0 kPa or 1.223 atm.
Dalton's law of partial pressures says that in a mixture of gases that do not react, each gas pushes on the container walls as if it were alone, and the total pressure is the sum of those separate pushes. Because pressure in an ideal mixture is proportional to the number of molecules, each gas's share of the total pressure equals its share of the moles.
Mole fraction mode uses Pᵢ = Xᵢ × P_total. The fraction must be at least 0 and no more than 1, and the total pressure must be greater than zero.
Mixture mode first adds the moles: n_total = n₁ + n₂ + … . Each mole fraction is Xᵢ = nᵢ ÷ n_total, and each partial pressure is Xᵢ × P_total. The tool also adds the fractions and shows the sum, which should be 1 apart from rounding.
Total mode uses P_total = P₁ + P₂ + … + Pₙ, with every value in the same unit.
Ideal gas mode uses P = nRT ÷ V with R = 8.314462618 J/(mol·K). Celsius is converted with T(K) = T(°C) + 273.15, litres are divided by 1,000 to get cubic metres, and the answer comes out in pascals before conversion.
Unit conversion goes through pascals: 1 atm = 101,325 Pa, 1 bar = 100,000 Pa, 1 kPa = 1,000 Pa and 1 mmHg = 101,325 ÷ 760 Pa, about 133.322 Pa. Results are rounded to six significant figures for display only.
A mole fraction is a ratio of part to whole, so it cannot be negative and cannot exceed 1. If you type a percentage such as 21 instead of 0.21, the calculator stops and asks for a decimal rather than returning a partial pressure 21 times larger than the total. In mixture mode the fractions are computed from the moles, so they always add to 1 and you do not have to normalise them yourself.
A diver breathes air at 30 metres of seawater, where the absolute pressure is about 4.0 bar. With an oxygen fraction of 0.21, P(O₂) = 0.21 × 4.0 = 0.84 bar, and with a nitrogen fraction of 0.79, P(N₂) = 0.79 × 4.0 = 3.16 bar. The two add back to 4.0 bar. This is the same calculation dive planners use to check oxygen exposure, although real dive planning needs proper training, tables or a dive computer, not a web calculator.
Mixing units is the most frequent error: adding a value in kPa to a value in mmHg gives a meaningless total. Another is using Celsius directly in P = nRT/V, which can even give a negative pressure. A third is forgetting that a gas collected over water is wet, so the measured total includes water vapour.
The law is very accurate for gases at ordinary pressures and temperatures, such as air, breathing mixtures, combustion gases and most classroom problems. It becomes less exact at high pressure or low temperature, where molecules take up a noticeable share of the volume and attract one another, and for gases that react, dissolve or condense.
The calculator assumes ideal gases that do not react with each other. It does not apply van der Waals or other real-gas corrections, it does not look up vapour pressures, and it does not handle gas solubility in liquids (Henry's law). Results are shown to six significant figures, which can be more precision than your measurements support, so round the final answer to match your data.
See the disclaimer for what these tools do not cover.
Count significant figures, round numbers to a specified precision, convert scientific notation, and solve mathematical operations using significant-figure rules with clear explanations.
입력하는 대로 길이, 무게, 온도를 변환합니다. 통화, 면적, 부피는 포함되지 않습니다. 절대 영도보다 낮은 온도는 거부됩니다.
퍼센트, 증가율, 감소율, 그리고 한 숫자가 다른 숫자의 몇 퍼센트인지 계산합니다.
쉼표나 공백으로 구분한 숫자 목록의 평균, 중앙값, 최빈값을 구합니다.
이전 값과 새 값을 비교해 변화율을 확인하세요. 80에서 100은 +25%, 100에서 80은 −20%입니다. 시작 값 0은 허용되지 않습니다.
가격에 할인율을 적용해 절약 금액과 결제 금액을 확인하세요. 숫자만 입력하세요. 통화 기호는 사용할 수 없고 100%를 넘는 할인은 거부됩니다.
A value from 0 to 1, e.g. 0.21 for 21%.