• Journal of the Korean Magnetic Resonance Society
• /
• v.23 no.2
• /
• pp.40-45
• /
• 2019

The phase transition temperatures and thermodynamic properties of $(NH_4)_2MnCl_4{\cdot}2H_2O$ grown by the slow evaporation method were studied using differential scanning calorimetry and thermogravimetric analysis. A structural phase transition occurred at temperature $T_{C1}$ (=264 K), whereas the changes at $T_{C2}$ (=460 K) and $T_{C3}$ (=475 K) seemed to be chemical changes caused by thermal decomposition. In addition, the chemical shift and the spin-lattice relaxation time $T_{1{\rho}}$ were investigated using $^1H$ magic-angle spinning nuclear magnetic resonance (MAS NMR), in order to understand the role of $NH_4{^+}$ and $H_2O$. The rise in $T_{1{\rho}}$ with temperature was related to variations in the symmetry of the surrounding $H_2O$ and $NH_4{^+}$.

• Journal of the Korean Magnetic Resonance Society
• /
• v.20 no.1
• /
• pp.1-6
• /
• 2016

The proton NMR line widths and spin-lattice relaxation rates, $T_1^{-1}$, of ferroelectric $LiH_3(SeO_3)_2$, $Li_2SO_4{\cdot}H_2O$, and $LiN_2H_5SO_4$ single crystals were measured as a function of temperature. The line width measurements reveal rigid lattice behavior of all the crystals at low temperatures and line narrowing due to molecular motion at higher temperatures. The temperature dependences of the proton $T_1^{-1}$ for these crystals exhibit maxima, which are attributed to the effects of molecular motion by the Bloembergen - Purcell - Pound theory. The activation energies for the molecular motions of $^1H$ in these crystals were obtained. From these analysis, $^1H$ in $LiH_3(SeO_3)_2$ undergoes molecular motion more easily than $^1H$ in $LiN_2H_5SO_4$ and $Li_2SO_4{\cdot}H_2O$ crystals.

• Journal of the Korean Magnetic Resonance Society
• /
• v.14 no.2
• /
• pp.76-87
• /
• 2010

The structural phase transition of $Cs_2MnCl_4{\cdot}2H_2O$ single crystals was investigated by determining the $^{133}Cs$ spin-lattice relaxation time $T_1$. The number of resonance lines in the $^{133}Cs$ spectrum changes from seven to one near 375 K, which means that above 375 K the Cs sites are symmetric. Further, the $T_1$ of the $^{133}Cs$ nucleus undergoes a significant change near 375 K, which coincides with the change in the splitting of the $^{133}Cs$ resonance lines. The change in $T_1$ near $T_C$ is related to the loss of $H_2O$, and means that the forms of the octahedra of water molecules surrounding $Cs^+$ are disrupted.

• Journal of applied mathematics & informatics
• /
• v.8 no.2
• /
• pp.539-550
• /
• 2001

In the present investigation, we study the influence of a transverse magnetic field through a porous medium. Laplace transform techniques are used to derive the solution in the Laplace transform domain. The inversion process is carried out using a numerical method based on Fourier series expansions. Numerical computations for the temperature, the microrotation and the velocity distributions as well as for the induced magnetic and electric fields and carried out and represented graphically.

• Journal of Magnetics
• /
• v.1 no.1
• /
• pp.1-3
• /
• 1996

The $YBa_2Cu_3O_{7-x}$ structure has been fluorinated by a gas phase exchange technique. The ${^19}F$NMR (nuclear magnetic resonance) spin-lattice relaxation rate (1/T1) measurements on a fluorinated sample gave superconducting energy gap of $2\Delta=4.6kT_c$.

• Bulletin of the Korean Chemical Society
• /
• v.4 no.1
• /
• pp.48-54
• /
• 1983

A magnetic nucleus located on an internal rotor can interact with magnetic fields arising from end-over-end molecular rotation as well as internal rotation. In this paper the expressions for spin-rotational relaxation times, $T_{1.SR}\;and\;T_{2.SR}$, are derived for such nucleus with the anisotropy of molecular rotation explicitly taken into consideration. The derived expressions are shown to be composed of two parts, the contribution from spin-overall-rotation coupling and that from spin-internal-rotation coupling. Some remarks on the use of derived expressions are also provided.

• Journal of the Korean Magnetic Resonance Society
• /
• v.20 no.4
• /
• pp.109-113
• /
• 2016

Resonance frequencies from the $^{113}Cd$ and $^{133}Cs$ nuclear magnetic resonance (NMR) spectra for the $CsCdBr_3$ single crystal were measured at varying temperatures by the static NMR method. The temperature-dependent changes of these frequencies are related to the changing structural geometry of the ${CdBr_6}^{4-}$ units, which affects the environment of $^{133}Cs$. The spin-lattice relaxation rates ($1/T_1$) for the $^{113}Cd$ and $^{133}Cs$ nuclei were measured in order to obtain detailed information about the dynamics of $CsCdBr_3$ crystals. The dominant relaxation mechanisms for $^{113}Cd$ and $^{133}Cs$ nuclei are direct single-phonon and Raman spin-phonon processes, respectively.

• Journal of the Korean Magnetic Resonance Society
• /
• v.19 no.1
• /
• pp.11-17
• /
• 2015

The Kubo formalism and utilizing the projection operator technique (POT) introduced by Kawabata, the electron spin resonance (ESR) line-shape formula for carbon nanotubes through the hyperfine interaction introduced earlier in terms of POT. We can see that the line-width decreases exponentially as the temperature increases. The spin relaxation time show gradual decrease as magnetic field becomes larger. The analysis reveals the peculiarities in spin relaxation inherent to one dimensional system at low temperature and weak magnetic fields. Thus, the present technique is considered to be more convenient to explain the carbon nanotubes as in the case of other optical transitions.

• Journal of the Korean Magnetic Resonance Society
• /
• v.22 no.4
• /
• pp.107-114
• /
• 2018

In this exploration, the nuclear magnetic resonance of the $^{207}Pb$ nucleus in $PbWO_4:Mn^{2+}$ and $PbWO_4:Dy^{3+}$ Single Crystals using FT-NMR spectrometer is investigated. The line width of the resonance line for the $^{207}Pb$ nucleus decreases as temperature increases due to motional narrowing. The chemical shift of $^{207}Pb$ NMR spectra also increases as temperature decreases for both crystals. The spinlattice relaxation times $T_1$ of $^{39}K$ nucleus were calculated as a function of temperature (180 K~400 K). The $T_1$ of $^{207}Pb$ nucleus decreases as temperature increases. The dominant relaxation mechanism at the studied temperature range can be deduced as the Raman process, which is the coupling between lattice vibrations and the nuclear spins. This deduction is substantiated by the fact that the nuclear spin-lattice relaxation rate $1/T_1$ of the $^{207}Pb$ nucleus in $PbWO_4:Mn^{2+}$ and $PbWO_4:Dy^{3+}$ single crystal is proportional to $T^2$, or temperature squared. The activation energies for the $^{207}Pb$ nucleus in $PbWO_4:Mn^{2+}$ and $PbWO_4:Dy^{3+}$ single crystals are $E_a=49{\pm}1meV$ and $E_a=47{\pm}2meV$, respectively.

• Proceedings of the Korean Magnetic Resonance Society Conference
• /
• 2002.08a
• /
• pp.35-35
• /
• 2002