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  2. Curie's law - Wikipedia

    en.wikipedia.org/wiki/Curie's_law

    H {\displaystyle H} is the magnitude of the applied magnetic field (A/m), T {\displaystyle T} is absolute temperature (K), C {\displaystyle C} is a material-specific Curie constant (K). Pierre Curie discovered this relation, now known as Curie's law, by fitting data from experiment. It only holds for high temperatures and weak magnetic fields.

  3. Curie temperature - Wikipedia

    en.wikipedia.org/wiki/Curie_temperature

    In physics and materials science, the Curie temperature (T C), or Curie point, is the temperature above which certain materials lose their permanent magnetic properties, which can (in most cases) be replaced by induced magnetism. The Curie temperature is named after Pierre Curie, who showed that magnetism is lost at a critical temperature. [1]

  4. Table of thermodynamic equations - Wikipedia

    en.wikipedia.org/wiki/Table_of_thermodynamic...

    m = mass of each molecule (all molecules are identical in kinetic theory), γ (p) = Lorentz factor as function of momentum (see below) Ratio of thermal to rest mass-energy of each molecule: θ = k B T / m c 2 {\displaystyle \theta =k_ {\text {B}}T/mc^ {2}} K2 is the modified Bessel function of the second kind.

  5. Curie–Weiss law - Wikipedia

    en.wikipedia.org/wiki/Curie–Weiss_law

    In magnetism, the Curie–Weiss law describes the magnetic susceptibility χ of a ferromagnet in the paramagnetic region above the Curie temperature: where C is a material-specific Curie constant, T is the absolute temperature, and TC is the Curie temperature, both measured in kelvin. The law predicts a singularity in the susceptibility at T = TC.

  6. Fundamental thermodynamic relation - Wikipedia

    en.wikipedia.org/wiki/Fundamental_thermodynamic...

    The first law of thermodynamics states that: where and are infinitesimal amounts of heat supplied to the system by its surroundings and work done by the system on its surroundings, respectively. According to the second law of thermodynamics we have for a reversible process: Q {\displaystyle \mathrm {d} S= {\frac {\delta Q} {T}}\,} Hence:

  7. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...

  8. Thermodynamic limit - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_limit

    In statistical mechanics, the thermodynamic limit or macroscopic limit, [1] of a system is the limit for a large number N of particles (e.g., atoms or molecules) where the volume V is taken to grow in proportion with the number of particles. [2] The thermodynamic limit is defined as the limit of a system with a large volume, with the particle ...

  9. Magnetochemistry - Wikipedia

    en.wikipedia.org/wiki/Magnetochemistry

    Magnetochemistry. Magnetochemistry is concerned with the magnetic properties of chemical compounds and elements. Magnetic properties arise from the spin and orbital angular momentum of the electrons contained in a compound. Compounds are diamagnetic when they contain no unpaired electrons. Molecular compounds that contain one or more unpaired ...