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Thermal entanglement

Recently, the concept of thermal entanglement was introduced and studied within one-dimensional spin systems [64-66]. The state of the system described by the Hamiltonian H at thermal equilibrium is p T) = exp —H/kT)/Z, where Z = Tr[exp(—7//feT)] is the partition function and k is Boltzmann s constant. As p T) represents a thermal state, the entanglement in the state is called the thermal entanglement [64]. [Pg.509]

For a two-qubit isotropic Heisenberg model, there exists thermal entanglement for the antiferromagnetic case and no thermal entanglement for the... [Pg.509]

The combined effects of a divalent Ca counterion and thermal treatment can be seen from studies of PMMA-based ionomers [16]. In thin films of Ca-salts of this ionomer cast from methylene chloride, and having an ion content of only 0.8 mol%, the only observed deformation was a series of long, localized crazes, similar to those seen in the PMMA homopolymer. When the ionomer samples were subject to an additional heat treatment (8 h at 100°C), the induced crazes were shorter in length and shear deformation zones were present. This behavior implies that the heat treatment enhanced the formation of ionic aggregates and increased the entanglement strand density. The deformation pattern attained is rather similar to that of Na salts having an ion content of about 6 mol% hence, substitution of divalent Ca for monovalent Na permits comparable deformation modes, including some shear, to be obtained at much lower ion contents. [Pg.149]

In Equation 1, t is a thermal vibration frequency, U and P are, respectively activation energy and volume whereas c is a local stress. The physical significance and values for these parameters are discussed in Reference 1. Processes (a)-(c) are performed with the help of a Monte-Carlo procedure which, at regular short time intervals, also relaxes the entanglement network to its minimum energy configuration (for more details, see Reference 1). [Pg.117]

Equation (2.53) is stating that the network modulus is the product of the thermal energy and the number of springs trapped by the entanglements. This is the result that is predicted for covalently crosslinked elastomers from the theory of rubber elasticity that will be discussed in a little more detail below. However, what we should focus on here is that there is a range of frequencies over which a polymer melt behaves as a crosslinked three-dimensional mesh. At low frequencies entanglements... [Pg.38]

Now that the entanglement of the XY Hamiltonian with impurities has been calculated at Y = 0, we can consider the case where the system is at thermal equilibrium at temperature T. The density matrix for the XY model at thermal equilibrium is given by the canonical ensemble p = jZ, where = l/k T, and Z = Tr is the partition function. The thermal density matrix is diag-... [Pg.510]

The zero-temperature calculations of the previous section Section, the XY model with impurities, represent a highly idealized situation however, it is unclear whether they have any relevance to the system at nonzero temperature. Since the properties of a quantum system for low temperatures are strongly influenced by nearby quantum critical points, it is tempting to attribute the effect of nearby critical points to persistent mixed-state entanglement in the thermal state. [Pg.511]


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See also in sourсe #XX -- [ Pg.509 , Pg.510 ]




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Entanglements

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