The existence of magnetic materials has been known almost since prehistoric times, but only in the 20th century has it been understood how and why the magnetic susceptibility is influenced by chemical composition or crystallographic structure. In the 19th century the pioneer work of Oersted, Ampere, Faraday and Joseph Henry revealed the intimate connection between electricity and magnetism. Maxwell's classical field equations paved the way for the wireless telegraph and the radio. At the turn of the present century Zeeman and Lorentz received the second Nobel Prize in physics for respectively observing and explaining in terms of classical theory the so-called normal Zeeman effect. The other outstanding early attempt to understand magnetism at the atomic level was provided by the semi-empirical theories of Langevin and Weiss. To account for paramagnetism, Langevin (1) in 1905 assumed in a purely ad hoc fashion that an atomic or molecular magnet carried a permanent moment µ, whose spatial distribution was determined by the Boltzmann factor. It seems today almost incredible that this elegantly simple idea had not occurred earlier to some other physicist inasmuch as Boltzmann had developed his celebrated statistics over a quarter of a century earlier. With the Langevin model, the average magnetization resulting from N elementary magnetic dipoles of strength µ in a field H is given by the expression (1) At ordinary temperatures and field strengths, the argument x of the Langevin function can be treated as small compared with unity. Then L(x) = :x, and Eq. (1) becomes perature, a relation observed experimentally for oxygen ten years earlier by Pierre Curie (2) and hence termed Curie's law.To explain diamagnetism, Langevin took into account the Larmor precession of the electrons about the magnetic field, and the resulting formula for the diamagnetic susceptibility is