Combining nuclear magnetic resonance and molecular dynamics simulations, we unravel the long-time dynamics of a paradigmatic colloid with strong dipole-dipole interactions. In a homogeneous magnetic field, ionic ferrofluids exhibit a stepwise association process from ensembles of monomers over stringlike chains to bundles of hexagonal zipped-chain patches. We demonstrate that attractive van der Waals interactions due to charge-density fluctuations in the magnetic particles play the key role for the dynamical stabilization of the hexagonal superstructures against thermal dissociation. Our results give insight into the dynamics of self-organization in systems dominated by dipolar interactions.

In this paper, we describe a method for measuring the average flow velocity of a sample by means of Nuclear Magnetic Resonance. This method is based on the Carr–Purcell–Meiboom–Gill (CPMG) sequence and does not require the application of any additional static or pulsed magnetic field gradients to the background magnetic field. The technique is based on analyzing the early-time behavior of the echo amplitudes of the CPMG sequence. Measurements of average flow velocity of water are presented. The experimental results show a linear relationship between the slope/y-intercept ratio of a linear fit of the first echoes in the CPMG sequence, and the average flow velocity of the flowing fluid. The proposed method can be implemented in low-cost Low-Field NMR spectrometers allowing a continuous monitoring of the average velocity of a fluid in almost real-time, even if the flow velocity changes rapidly.

A planar nuclear quadrupole resonance (NQR) sensor has been developed. The sensor is resilient to environmental noise and is capable of simultaneous independent multi-frequency operation. The device was constructed as an open multimodal birdcage structure, in which the higher modes, generally not used in magnetic resonance, are utilized for NQR detection. These modes have smooth distributions of the amplitudes of the corresponding radiofrequency magnetic fields everywhere along the sensor's surface. The phases of the fields, on the other hand, are cyclically shifted across the sensor's surface. Noise signals coming from distant sources, therefore, induce equal-magnitude cyclically phase-shifted currents in different parts of the sensor. When such cyclically phase-shifted currents arrive at the mode connection point, they destructively interfere with each other and are cancelled out. NQR signals of polycrystalline or disordered substances, however, are efficiently detected by these modes because they are insensitive to the phases of the excitation/detection. No blind spots exist along the sensor's surface. The sensor can be used for simultaneous detection of one or more substances in locations with environmental noise.

A birdcage coil capable of operating simultaneously and independently in three orthogonal dimensions has been developed. A co-rotational end-ring mode producing an RF field in the longitudinal direction was utilized in addition to the two common transverse orthogonal modes. Two conductor turns were used for each of the coil's windows, increasing its inductance by a factor of four, thereby, making the coil suitable for low-frequency applications. Two or three-frequency detection can be easily carried out with this device. Orthogonality of the coil's channels allows arbitrarily close frequency positioning of each resonant mode, potentially useful in wide-line NQR studies, in which simultaneous excitation/detection of signals from three adjacent regions of a single wide line can be performed. The coil's performance was evaluated using a three-dimensional scheme, in which a circularly polarized experiment was combined with a linearly polarized measurement at another frequency, resulting in SNR improvement by 55%.

Solid-state physical characterization of a pharmaceutical substance is necessary for successful development and approval of the final product. Different physical analytical techniques are available to do so: X-ray diffraction (XRD), IR, Raman, DSC, TG and NMR. Moreover, all of them detect the presence of excipients perturbing the analysis of the pure substance in low doses. In order to study polymorphism and pseudo polymorphism of drug, this paper introduces possible applications of pure nuclear quadrupole resonance, as a non-destructive technique in qualitative and quantitative approaches. Chlorpropamide and diclofenac sodium were used as examples. Unlike the mentioned techniques, the nuclear quadrupole resonance (NQR) signal of pharmaceutical compounds is not perturbed by the presence of solid excipient or other substances unless they possess resonance frequencies in the same frequency range of the compound studied.

A simple Q-damper device for active probe recovery time reduction is introduced along with a straightforward technique for the circuit's component value optimization. The device is inductively coupled to a probe through a coupling transformer positioned away from the main coil, which makes the design independent of the coil type being used. The Q-damper is a tuned circuit, which is resonant at the same frequency as the probe and can be actively interrupted. When the circuit is interrupted, it is detuned and, thereby, is uncoupled from the probe, which operates normally. Turning the device on leads to re-coupling of the circuits and causes splitting of the probe's resonance line, which can be observed through its drive port. A resistance of an appropriate value is introduced into the Q-damper circuit, resulting in smoothing of the resonance splitting into one broad line, representing the coupled system's low-Q state, in which the energy stored in the main coil is efficiently dissipated. The circuit's component values are optimized by monitoring the shape of this low-Q state. Probe recovery time reduction by, approximately, an order of magnitude has been obtained with this device. Application of the device during an NQR experiment led to an increase in the signal-to-noise ratio by a factor of 4.9.

Differential thermal analysis, and the 35Cl Nuclear Quadrupole Resonance frequency (νQ) and spin-lattice relaxation time (T1) were measured as a function of temperature in p-chlorofluorobenzene. Three different phases were found according to the thermal history of the sample and only one was stable up to the melting point. In one of the phases, the presence of molecular reorientations can be inferred from T1 data with activation energy of 3.7 kcal/mol. A value of 13.9 kJ/mol for the fusion heat of this compound has been obtained.