Fast Field-cycling Nuclear Magnetic Resonance Research Articles

Detecting soil hydrological connectivity in a badland area by fast field cycling nuclear magnetic resonance relaxometry

Detecting soil hydrological connectivity in a badland area by fast field cycling nuclear magnetic resonance relaxometry

Exploring Crystal-Phase Molecular Dynamics of the Low-Viscous Mesogen 6CHBT: A Combined FFC and High-Field NMR Relaxometry Investigation.

The molecular dynamics study of thermotropic mesogens exhibiting the crystal phases is valuable in unraveling the complex global (collective) and local (noncollective) motions executed by liquid crystal molecules, which would further advance the existing knowledge on orientationally disordered crystalline (ODIC) phases. Toward the fulfillment of such a task, a combined nuclear magnetic resonance (NMR) relaxometry approach employing the fast field cycling (FFC) NMR (10 kHz-30 MHz) and high-field pulsed NMR (400 MHz) techniques is utilized to sample the broad frequency range offered by molecular motions in the crystal phase of 4-(trans-4'-n-hexylcyclohexyl)-isothiocyanatobenzene (6CHBT). The validity of the observed relaxation data is tested and interpreted by the Bloembergen-Purcell-Pound (BPP) model involving the superposition of four mutually independent Lorentzian spectral densities, reflecting molecular dynamical processes on different time scales. The salient feature of the detailed analysis reveals that the lengthening of temporal dynamics in the crystal phase due to molecular rotations by jumps, which are of intermolecular origin, is evident and further supports the presence of collective-like local dynamics. The analysis does permit decoupling of the molecular reorientations about their short axes (∼100 ns) as well as long axes (∼50 ns) and methyl group rotations (∼0.5 ns) on distinct time scales. The activation energies for reorientations about the short axes and methyl group rotations are found to be 27.3 ± 2.7 and 15.8 ± 1.1 kJ/mol, respectively. The fast methyl rotations in the crystal phase of 6CHBT obtained from FFC NMR are further well complemented by high-field NMR, where 1H NMR line shapes are relatively narrow when compared to those of the nematic phase.

Water Dynamics in Dextran-Based Hydrogel Micro/Nanoparticles Studied by NMR Diffusometry and Relaxometry.

Water dynamics in mesoporous dextran hydrogel micro/nanoparticles was investigated by means of nuclear magnetic resonance (NMR) techniques. High-resolution 1H NMR spectra and pulsed field gradient (PFG) NMR diffusometry measurements obtained on swollen state dextran micro/nanogel revealed the existence of different fractions of water molecules based on their interaction with the gel matrix. In addition to the translational diffusion of bulk water, two more diffusion processes characterized with self-diffusion coefficients 1 and 2 orders of magnitude smaller than that of bulk water were identified. 1H spin-lattice relaxation dispersion profiles obtained for a broad range of Larmor frequencies using fast field cycling (FFC) and conventional NMR relaxometry techniques allowed us to further clarify the mechanisms of molecular motion. According to the water proton pool fractions and associated self-diffusion coefficients, it is shown that the relaxation contribution associated with reorientation-mediated translational motions (RMTDs) dominates the relaxation dispersion observed at intermediate frequencies. At very low frequencies, the spin-lattice relaxation rate is dominated by the slow solid-gel dynamics probed by the water molecules interacting with the pores' surface hydroxyl groups due to the rapid chemical exchange between surface hydroxyl groups and free water. The correlation time for the thumbling-like motion of the dextran gel was found to be in the submillisecond range. The values of the self-diffusion and coherence lengths associated with motion of water molecules interacting with the solid-gel particles are consistent with the particle size and pore size distributions obtained for the studied dextran gels.

Advanced insight on the water dynamics of anisotropic hydrogels by field-cycling nuclear magnetic resonance: Application of 3-Tau model

Fast field cycling (FFC) nuclear magnetic resonance (NMR) relaxometry is used to investigate an anisotropic polygalacturonate hydrogel formed by the diffusion of calcium ions from an external reservoir (external gelation). Such a hydrogel has a gradient of polymer density accompanied by a gradient of the mesh size of its 3D network. The NMR relaxation process is dominated by the interaction of proton spins between water molecules located at polymer interfaces and in nanoporous spaces. The FFC NMR experiment provides the spin-lattice relaxation rate R1ω as a function of Larmor frequency ω producing dispersion (NMRD) curves that are highly sensitive to the dynamics of the protons at the surfaces. The hydrogel is sliced into three parts and the NMR profile for each hydrogel slice is measured. The NMRD data for each slice is interpreted using the 3-Tau Model with the aid of user-friendly fitting software called 3TM. The key fit parameters include three nano-dynamical time constants and the average “mesh size” which collectively determine the bulk water and water surface layer contribution to the total relaxation rate. The results are consistent with independent studies where comparison is possible.

An automatic [formula omitted]-based regularization method for the analysis of FFC dispersion profiles with quadrupolar peaks

Fast Field-Cycling Nuclear Magnetic Resonance relaxometry is a non-destructive technique to investigate molecular dynamics and structure of systems having a wide range of applications such as environment, biology, and food. Besides a considerable amount of literature about modeling and application of such technique in specific areas, an algorithmic approach to the related parameter identification problem is still lacking. We believe that a robust algorithmic approach will allow a unified treatment of different samples in several application areas. In this paper, we model the parameters identification problem as a constrained L1-regularized non-linear least squares problem. Following the approach proposed in [Analytical Chemistry2021 93 (24)], the non-linear least squares term imposes data consistency by decomposing the acquired relaxation profiles into relaxation contributions associated with 1H−1H and 1H−14N dipole-dipole interactions. The data fitting and the L1-based regularization terms are balanced by the so-called regularization parameter. For the parameters identification, we propose an algorithm that computes, at each iteration, both the regularization parameter and the model parameters. In particular, the regularization parameter value is updated according to a Balancing Principle and the model parameters values are obtained by solving the corresponding L1-regularized non-linear least squares problem by means of the non-linear Gauss-Seidel method. We analyse the convergence properties of the proposed algorithm and run extensive testing on synthetic and real data. A Matlab software, implementing the presented algorithm, is available upon request to the authors.

Differentiation among dairy products by combination of fast field cycling NMR relaxometry data and chemometrics.

A set of commercial milk and Sicilian cheeses was analysed by a combination of fast field cycling (FFC) nuclear magnetic resonance (NMR) relaxometry and chemometrics. The NMR dispersion (NMRD) curves were successfully analysed with a mathematical model applied on Parmigiano-Reggiano (PR) cheese. Regression parameters were led back to the molecular components of cheeses (water trapped in casein micelles, proteins and fats) and milk samples (water belonging to hydration shells around dispersed colloidal particles of different sizes and bulk water). The application of chemometric analysis on relaxometric data enabled differentiating milk from cheeses and revealing differences within the two sample groups of either cheeses or milk samples. Marked differences among cheeses were evidenced by statistical analysis of the sole quadrupolar peaks parameters, suggesting that these contain information on the nature of the milk used during cheese production. Hence, combination of FFC NMR and chemometrics represents a powerful tool to investigate alterations in dairy products.

Design Overview of a Toroidal Fast-Field Cycling electromagnet

In this paper, the design and development of a novel Fast-Field Cycling (FFC) Nuclear Magnetic Resonance (NMR) relaxometer’s electromagnet is described. This magnet is tailored to increase the relaxometers’s usability, by increasing its portability capacities. It presents a compact toroidal shaped iron core, allowing to operate in a field range of 0 to 0.21 T, with high field homogeneity (less than 800 ppm in a volume of ≈ 0.57 cm3 ), low power consumption and reduced losses (about 40W). The simulation software COMSOL Multiphysics® is used to characterize the induced magnetic field, the heating and the cooling effects. The proposed optimized layout constitutes an innovative solution for FFC magnets.

Rheological and NMR Studies of Cellulose Dissolution in the Ionic Liquid BmimAc.

Solutions of two types of cellulose in the ionic liquid 1-butyl-3-methyl-imidazolium acetate (BmimAc) have been analyzed using rheology and fast-field cycling nuclear magnetic resonance (NMR) spectroscopy, in order to analyze the macroscopic (bulk) and microscopic environments, respectively. The degree of polymerization (DP) was observed to have a significant effect on both the overlap (c*) and entanglement (ce) concentrations and the intrinsic viscosity ([η]). For microcrystalline cellulose (MCC)/BmimAc solutions, [η] = 116 mL g-1, which is comparable to that of MCC/1-ethyl-3-methyl-imidazolium acetate (EmimAc) solutions, while [η] = 350 mL g-1 for the commercial cellulose (higher DP). Self-diffusion coefficients (D) obtained via the model-independent approach were found to decrease with cellulose concentration and increase with temperature, which can in part be explained by the changes in viscosity; however, ion interactions on a local level are also important. Both Stokes-Einstein and Stokes-Einstein-Debye analyses were carried out to directly compare rheological and relaxometry analyses. It was found that polymer entanglements affect the microscopic environment to a much lesser extent than for the macroscopic environment. Finally, the temperature dependencies of η, D, and relaxation time (T1) could be well described by Arrhenius relationships, and thus, activation energies (Ea) for flow, diffusion, and relaxation were determined. We demonstrate that temperature and cellulose concentration have different effects on short- and long-range interactions.

The Field-Frequency Lock for Fast Field Cycling Magnetic Resonance: From NMR to MRI

Magnetic field stability plays a fundamental role in Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging (MRI) experiments, guaranteeing accuracy and reproducibility of results. While high levels of stabilization can be achieved for standard NMR techniques, this task becomes particularly challenging for Fast Field Cycling (FFC) NMR and MRI, where the main magnetic field is switched to higher or lower levels during the pulse sequence, and field stabilization must be guaranteed within a very short time after switching. Recent works have addressed the problem with rigorous tools from control system theory, proposing a model based approach for the synthesis of magnetic field controllers for FFC-NMR. While an experimental proof of concept has underlined the correctness of the approach for a complete FFC-NMR setup, the application of the novel, model based Field-Frequency Lock (FFL) system to a FFC-MRI scanner requires proper handling of field encoding gradients. Furthermore, the proof of concept work has also stressed how further advances in the hardware and firmware could improve the overall performances of the magnetic field control loop. The main aim of this perspective paper is then discussing the key challenges that arise in the development of the FFL system suitable for a complete MRI scanner, as well as defining possible research directions by means of preliminary, simulated experiments, with the final goal of favoring the development of a novel, model based FFL system for FFC-MRI.

Heuristic Algorithm for the Analysis of Fast Field Cycling (FFC) NMR Dispersion Curves.

Evaluation of nuclear magnetic relaxation dispersion (NMRD) curves obtained by the fast field cycling nuclear magnetic resonance (FFC-NMR) relaxometry technique is a valuable tool for analyzing the microscopic dynamics of condensed matter systems. However, quantitative data analysis involves several conceptual and practical issues. Moving forward from previous literature approaches, we propose a new analysis method, relying on the elaboration of the inverse integral transform of the NMRD curve. Our approach results in a true heuristic method, able to unambiguously individuate the dynamic domains in the system, thereby avoiding the possible introduction of any element of discretion. The analysis of some data sets relevant to real samples suggests the possibility that the results obtained with the heuristic method may be actually led back to some distinct physical/chemical features of the systems.

Dynamical Comparison of Different Polymer Architectures-Bottlebrush vs Linear Polymer.

Different polymer architectures behave differently regarding their dynamics. We have used a combination of dielectric spectroscopy, and fast field cycling nuclear magnetic resonance (NMR) to compare the dynamical behavior of two different polymer architectures, with similar overall molecular weight. The systems of interest are a bottlebrush polymer and a linear one, both based on poly(dimethylsiloxane) (PDMS). To verify the structure of the PDMS-g-PDMS bottlebrush in the melt, small-angle neutron scattering was used, yielding a spherical shape. Information about the segmental dynamics was revealed by dielectric spectroscopy and extended to higher temperatures by fast field cycling NMR. One advantage of fast field cycling NMR is the detection of large-scale chain dynamics, which dielectric spectroscopy cannot probe for PDMS. While segmental relaxation seems to be independent of the architecture, the large-scale chain dynamics show substantial differences, as represented by the mean square displacement. Here, two regions are detected for each polymer. The linear polymer shows the Rouse regime, followed by reptation. In contrast, the bottlebrush polymer performs Rouse dynamics and diffusion in the available time window, and entanglement effects are completely missing.

NMR relaxometry analysis of molecular degradation in internal combustion engine lubricants.

A set of experimental techniques headed by proton fast field-cycling nuclear magnetic resonance (1 HFFC-NMR) were used to analyze the effects of degradation of lubricant oil used in an internal combustion engine (ICE). Its relaxometric, spectroscopic, and rheological properties were evaluated and interpreted in terms of changes in the chemical structure and the involved molecular dynamics. In order to better understand the relaxometric behavior, chemical changes induced by heat were investigated for selected n-alkanes, as model-systems due to their structural simplicity. Fourier transform infrared (FTIR) spectroscopy, viscosity measurements, and foaming were used to contrast NMR relaxometry experiments. Main observed changes associated with oil degradation can be attributed to molecular oxidation, fragmentation, and ramification. As an outstanding feature of this work, we show that the relaxometric analysis can be done without any special treatment of the sample, allowing results in less than 10 min.

Towards applying NMR relaxometry as a diagnostic tool for bone and soft tissue sarcomas: a pilot study

This work explores what Fast Field-Cycling Nuclear Magnetic Resonance (FFC-NMR) relaxometry brings for the study of sarcoma to guide future in vivo analyses of patients. We present the results of an ex vivo pilot study involving 10 cases of biopsy-proven sarcoma and we propose a quantitative method to analyse 1H NMR relaxation dispersion profiles based on a model-free approach describing the main dynamical processes in the tissues and assessing the amplitude of the Quadrupole Relaxation Enhancement effects due to 14N. This approach showed five distinct groups of dispersion profiles indicating five discrete categories of sarcoma, with differences attributable to microstructure and rigidity. Data from tissues surrounding sarcomas indicated very significant variations with the proximity to tumour, which may be attributed to varying water content but also to tissue remodelling processes due to the sarcoma. This pilot study illustrates the potential of FFC relaxometry for the detection and characterisation of sarcoma.

Nuclear Magnetic Resonance with Fast Field-Cycling Setup: A Valid Tool for Soil Quality Investigation

Nuclear magnetic resonance (NMR) techniques are largely employed in several fields. As an example, NMR spectroscopy is used to provide structural and conformational information on pure systems, while affording quantitative evaluation on the number of nuclei in a given chemical environment. When dealing with relaxation, NMR allows understanding of molecular dynamics, i.e., the time evolution of molecular motions. The analysis of relaxation times conducted on complex liquid–liquid and solid–liquid mixtures is directly related to the nature of the interactions among the components of the mixture. In the present review paper, the peculiarities of low resolution fast field-cycling (FFC) NMR relaxometry in soil science are reported. In particular, the general aspects of the typical FFC NMR relaxometry experiment are firstly provided. Afterwards, a discussion on the main mathematical models to be used to “read” and interpret experimental data on soils is given. Following this, an overview on the main results in soil science is supplied. Finally, new FFC NMR-based hypotheses on nutrient dynamics in soils are described

NMR Relaxometry and Diffusometry Analysis of Dynamics in Ionic Liquids and Ionogels for Use in Lithium-Ion Batteries.

We have investigated the charge transport dynamics of a novel solid-like electrolyte material based on mixtures of the ionic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM] TFSI) and various concentrations of lithium salt bis(trifluoromethylsulfonyl)imide (LiTFSI) confined within a SiO2 matrix, prepared via a sol-gel method. The translational diffusion coefficients of BMIM+, TFSI-, and Li+ in ILs and confined ILs (ionogels, IGs) with different concentrations of lithium salt have been measured at variable temperatures, covering the 20-100 °C range, using nuclear magnetic resonance (NMR) pulsed field gradient diffusion spectroscopy. The mobility of BMIM+, TFSI-, and Li+ was found to increase with the [BMIM] TFSI/LiTFSI ratio, exhibiting an almost liquid-like mobility in IGs. Additionally, the effect of confinement on IL rotational dynamics has been analyzed by measuring 1H, 19F, and 7Li spin-lattice relaxation rate dispersions of IGs at different temperatures, using fast field-cycling NMR relaxometry. The analysis of the experimental data was performed assuming the existence of two fractions of the liquid: a bulk fraction (at least several ionic radii from the silica particles) and a surface fraction (close to the silica particles) and using two different models based on translational and rotational diffusion and reorientation mediated by translational displacements. The existence and weighting of these two fractions of ions were obtained from the direct diffusion measurements. The results show that the ion dynamics slowed only modestly under confinement, which evidences that IGs preserve IL transport properties, and this behavior is an encouraging indication for using IGs as a solid electrolyte for Li+ batteries.

Temperature distribution of a Fast-Field Cycling Nuclear Magnetic Resonance relaxometer's electromagnet with reduced volume

Temperature distribution of a Fast-Field Cycling Nuclear Magnetic Resonance relaxometer's electromagnet with reduced volume

NMR studies of molecular ordering and molecular dynamics in a chiral liquid crystal with the SmC_{α}^{*} phase.

Molecular dynamics of the antiferroelectric liquid crystal 4'-(octyloxy)biphenyl-4-carboxylate2-fluoro-4-[(octyl-2-yloxy)carbonyl]phenyl (abbreviated as D16) was investigated using different nuclear magnetic resonance (NMR) techniques. D16 molecules form a smectic-C_{α}^{*} phase (SmC_{α}^{*}) in an extremely wide temperature range (∼10 °C). Due to a small tilt of the molecules, this phase is characterized by short switching times, important for new photonic applications. The proton spin-lattice relaxation times were measured in isotropic (Iso), smectic-A (SmA), and SmC_{α}^{*} phases over a wide frequency range of five decades, with conventional and fast field-cycling NMR techniques. This approach allowed a comparison of the essential processes of molecular dynamics taking place in these phases. On the basis of NMR relaxometry measurements, we present a description of the motional behavior of liquid crystal molecules forming SmC_{α}^{*}. Pretransitional effects were observed in wide temperature ranges in both the isotropic and SmA phases in D16. The ^{1}H fast field-cycling NMR measurements were supplemented with NMR diffusometry and ^{19}F NMR spectroscopy.

FFC NMR Relaxometer with Magnetic Flux Density Control

This paper describes an innovative solution for the power supply of a fast field cycling (FFC) nuclear magnetic resonance (NMR) spectrometer considering its low power consumption, portability and low cost. In FFC cores, the magnetic flux density must be controlled in order to perform magnetic flux density cycles with short transients, while maintaining the magnetic flux density levels with high accuracy and homogeneity. Typical solutions in the FFC NMR literature use current control to get the required magnetic flux density cycles, which correspond to an indirect magnetic flux density control. The main feature of this new relaxometer is the direct control of the magnetic flux density instead of the magnet current, in contrast with other equipment available in the market. This feature is a great progress because it improves the performance. With this solution it is possible to compensate magnetic field disturbances and parasitic magnetic fields guaranteeing, among other possibilities, a field control below the earth magnetic field. Experimental results validating the developed solution and illustrating the real operation of this type of equipment are shown.

Fast-Field Cycling Nuclear Magnetic Resonance relaxometer's electromagnet with optimized homogeneity and reduced volume

Fast-Field Cycling Nuclear Magnetic Resonance relaxometer's electromagnet with optimized homogeneity and reduced volume

Towards a Model-Based Field-Frequency Lock for Fast-Field Cycling NMR

Fast-field cycling nuclear magnetic resonance (FFC NMR) relaxometry allows to investigate molecular dynamics of complex materials. FFC relaxometry experiments require the magnetic field to reach different values in few milliseconds and field oscillations to stay within few ppms during signal acquisition. Such specifications require the introduction of a novel field-frequency lock (FFL) system. In fact, control schemes based only on current feedback may not guarantee field stability, while standard FFLs are designed to handle very slow field fluctuations, such as thermal derives, and may be ineffective in rejecting faster ones. The aim of this work is then to propose a methodology for the synthesis of a regulator that guarantees rejection of field fluctuations and short settling time. Experimental trials are performed for both model validation and evaluation of the closed-loop performances. Relaxometry experiments are performed to verify the improvement obtained with the new FFL. The results highlight the reliability of the model and the effectiveness of the overall approach.