M. Van der Waals has sought out the modifications which must be introduced into the simple characteristic equation to bring it nearer to reality. He extends to the case of gases the considerations by which Laplace, in his famous theory of capillarity, reduced the effect of the molecular attraction to a perpendicular pressure exercised on the surface of a liquid. This leads him to add to the external pressure, that due to the reciprocal attractions of the gaseous particles. On the other hand, when we attribute finite dimensions to these particles, we must give a higher value to the number of shocks produced in a given time, since the effect of these dimensions is to diminish the mean path they traverse in the time which elapses between two consecutive shocks. The calculation thus pursued leads to our adding to the pressure in the simple equation a term which is designated the internal pressure, and which is the quotient of a constant by the square of the volume; also to our deducting from the volume a constant which is the quadruple of the total and invariable volume which the gaseous molecules would occupy did they touch one another. The experiments fit in fairly well with the formula of Van der Waals, but considerable discrepancies occur when we extend its limits, particularly when the pressures throughout a rather wider interval are considered; so that other and rather more complex formulas, on which there is no advantage in dwelling, have been proposed, and, in certain cases, better represent the facts. But the most remarkable result of M. Van der Waals' calculations is the discovery of corresponding states. For a long time physicists spoke of bodies taken in a comparable state. Dalton, for example, pointed out that liquids have vapour-pressures equal to the temperatures equally distant from their boiling-point; but that if, in this particular property, liquids were comparable under these conditions of temperature, as regards other properties the parallelism was no longer to be verified. No general rule was found until M. Van der Waals first enunciated a primary law, viz., that if the pressure, the volume, and the temperature are estimated by taking as units the critical quantities, the constants special to each body disappear in the characteristic equation, which thus becomes the same for all fluids. The words corresponding states thus take a perfectly precise signification. Corresponding states are those for which the numerical values of the pressure, volume, and temperature, expressed by taking as units the values corresponding to the critical point, are equal; and, in corresponding states any two fluids have exactly the same properties.