Low-frequency proton NMR relaxometry of a polymer dispersed liquid crystal above TNI

Using proton NMR relaxometry in the kilohertz frequency range, we study dynamics of 5CB liquid crystal molecules dispersed in the form of spherical microdroplets in a PDLC material. The focus of the study is the spin-lattice relaxation in the rotating frame, T1rho(-1), measured above the nematic-isotropic transition TNI. We show that the relaxation rate T1rho(-1)--when induced by uniform molecular translational diffusion in a spherical cavity--depends on the strength of the rotating magnetic field as T1rho(-1) proportional to omega1(-alpha) where alpha varies between 0.7 and 1, depending on the thickness of the ordered surface layer. This relaxation mechanism governs mainly the transverse spin relaxation, whereas the measurements of the frequency and temperature dependence of T1rho(-1) indicate a strong effect of slowing-down of molecular translational diffusion in contact with the polymer surface and yield the average dwell-time of molecules at the surface of the order 10(-5) s.     

Chain dynamics in mesoscopically confined polymer melts. A field-cycling NMR relaxometry study

Polymer chain dynamics were studied with the aid of field-cycling NMR relaxometry (time scale: 10^-9s... 10^-4s) supplemented by field gradient NMR diffusometry (time scale: 10^-4s...10⁰s). Three sorts of samples of mesoscopically confined polymer melts were examined. In the first sample series, linear poly(ethylene oxide) was incorporated in strands embedded in a quasi-solid and impenetrable methacrylate matrix. The strand diameters ranged from 10 to 60 nm. It was shown that chain dynamics becomes dramatically different from bulk behavior. This so-called “corset effect” occurs both above and below the critical molecular mass and reveals dynamic features predicted for reptation. On the time scale of spin-lattice relaxation, the frequency and molecular weight, signature of reptation, T₁ ∼M⁰ ν^3/4, that is limit II of the Doi/Edwards formalism corresponding to the mean squared segment displacement law 〈r² 〉∼M⁰ t^1/4, showed up. A “tube” diameter of only 0.6 nm was concluded to be effective on this time scale even when the strand diameter was larger than the radius of gyration of the PEO random coils. The corset effect is traced back to the lack of the local fluctuation capacity of the free volume under nanoscopic confinements. The confinement dimension at which the cross-over from confined to bulk chain dynamics is expected was estimated to be micrometers. Using the so-called roll-coating technique, micrometer thick polymer melt layers between Kapton foils were prepared. Perceptible differences from the bulk materials were found. The polymer species studied in this case was perfluoropolyether with Flory radii in the order of 7 nm. Remarkably, the confinement effect was shown to reach polymer-wall distances of the order 100 Flory radii. As a third confinement system, melts of perfluoropolyether were filled into a porous silica glass (Vycor; 4 nm nominal pore size). In this case, a crossover from Rouse dynamics in the bulk to reptation in the Doi/Edwards limit III (T₁∼M^-1/2 ν^1/2 corresponding to 〈r² 〉∼M^-1/2 t^1/2) was observed.     

From a simple liquid to a polymer melt: NMR relaxometry study of polybutadiene

We utilize NMR field cycling relaxometry to study the crossover from glassy dynamics (t approximately > tau alpha) through Rouse to reptation behavior in a series of monodisperse polybutadienes with molecular weights M=355 to 817,000 g/mol. We separate characteristic polymer dynamics from the total spectrum dominated by glassy dynamics. The polymer dynamics show typical Rouse relaxation features that grow with M and saturate at high M. Comparing to Rouse theory, we determine the Rouse unit size MR approximately = 500 and entanglement weight Me approximately = 2000; the Rouse spectrum saturates at Mmax approximately = 4000. The local order parameter S approximately 0.11 is relatively large, indicating noticeable local packing already in the Rouse regime. The M dependence of the glass transition temperature Tg, obtained from dielectric relaxation spectra, shows distinctive kinks at MR and Me.     

Characterisation of magnetic resonance imaging (MRI) contrast agents using NMR relaxometry

ABSTRACT

This contribution describes the use of Fast Field-cycling relaxometry (FFC-NMR) for the characterisation of Gd(III)- and Mn(II)-based contrast agents for MRI. Through a series of selected examples, we analyse the role of different structural and dynamic parameters on ¹H relaxivity and on the shape of the ¹H Nuclear Magnetic Relaxation Dispersion (NMRD) profiles. The amplitude and shape of the profiles is affected by the number of water molecules coordinated to the metal ion, the water exchange rate, the rotational correlation time of the complex and the relaxation of the electron spin. As a result, ¹H NMRD profiles represent a powerful tool for the understanding of the properties of MRI contrast agent candidates at the molecular level.     

Investigations of polymer dynamics in nanoporous media by field cycling NMR relaxometry and the dipolar correlation effect

The chain dynamics of short-chain perfluoropolyether melts confined in Vycor nanoporous media has been characterized by field cycling nuclear magnetic resonance relaxometry and the dipolar correlation effect. The slowdown of motions under confinement, leading to larger residual dipolar couplings, has been probed by looking at the quotient of stimulated and primary echoes. Using field cycling relaxometry, it has been shown that there is strong evidence of reptation-like motion, even for such short-chain polymers as shown by the frequency and molecular weight dependences of the spin-lattice relaxation time.     

NMR imaging of falling water drops

The falling water drop is a simple model for studying phenomena related to chemical extraction, where two immiscible phases are dynamically blended to promote the transport of solute molecules from one phase to the other. Convective motion inside the drop significantly influences the extraction efficiency. Whereas optical and tracer methods are model bound or invasive, NMR imaging is noninvasive, direct, and applicable to nontransparent media. The first NMR measurements of a water drop falling through air are reported. It is shown that, in drops from pure water, large-scale convection rolls are observed in contrast to drops with the surface tension lowered by surfactants.     

Water dynamics in ionomer membranes by field-cycling NMR relaxometry

The dynamic behavior of water within two types of ionomer membranes, Nafion and sulfonated polyimides, has been investigated by field-cycling nuclear magnetic relaxation. This technique, applied to materials prepared at different hydration levels, allows to probe the proton motion on a time scale of the microsecond. The NMR longitudinal relaxation rate R(1) measured over three decades of Larmor angular frequencies omega is particularly sensitive to the host-water interactions and thus well suited to study fluid dynamics in restricted geometries. In the polyimide membranes, we have observed a strong dispersion of R(1)(omega) following closely a 1/sqrt[omega] law in a low-frequency range (correlation times from 0.1 to 10 micros). This is indicative of a strong interaction of water with "interfacial" hydrophilic groups of the polymeric matrix (wetting situation). On the contrary, in the Nafion, we observed weak variations of R(1)(omega) at low frequency. This is typical of a nonwetting behavior. At early hydration stages, the proton-proton inter-dipolar contribution to R(1)(omega) evolves logarithmically, suggesting a confined bidimensional diffusion of protons in the microsecond time range. Such an evolution is lost at higher swelling where a plateau related to 3D diffusion is observed.     

Study of magnetite nanoparticle suspensions by photometry and NMR relaxometry

A method has been described for preparation of suspensions of magnetite nanoparticles stabilized by porous silicon dioxide. The process of sedimentation of nanoparticles in suspensions of different compositions and concentrations has been analyzed by transmission coefficient measurements. Spectra of the transmission coefficient have been obtained for suspensions containing composite nanoparticles, the initial silicon dioxide, and macroscopic magnetite particles. The average effective radius of nanoparticles has been calculated from the time dependences of the transmission coefficient. It has been demonstrated that the synthesized nanoparticles possess magnetic-resonance contrast properties.     

NMR relaxometry study of gelatin based low-calorie soft candies

ABSTRACT

Soft candies are popular confectionery products. The most significant concern on the consumption of these products is the high amount of sugar and thus the high calories. The use of low-calorie sweeteners is a desirable trend in confectionery research. In this study, gelatin-based soft candies were formulated by using different sweeteners and their characterisation was performed using high and low field nuclear magnetic resonance (NMR) relaxation experiments. To complement the information obtained by NMR experiments, moisture content, water activity, texture analysis and differential scanning calorimeter experiments were also conducted. T₁ and T₂ relaxation times were measured at both low and high fields and also temperature-dependent measurements were conducted at the high field system. Candies were formulated by substitution of sucrose with maltitol, isomalt and stevia at 30%, 50% and 70% ratios. Significant difference was observed on relaxation times. T₁ values were best described by a mono-exponential model, whereas for T₂ relaxation times a bi-exponential model gave better results at both fields.     

Methods for peak assignment in low-resolution multidimensional NMR cross-correlation relaxometry

Several NMR protocols are presented for assigning peaks in complex T1-T2 spectra, including the effects of varying the spectrometer frequency and the CPMG pulsing rate. Extensions into a third dimension based on chemical-shift; diffusion- and field-cycled weighted T1-T2 cross-correlation methods are also explored as a means of peak assignment. We illustrate the power of these novel techniques with reference to simple aqueous sucrose solutions, but the methodology should be generally applicable.     

Quantitative evaluation of porous media wettability using NMR relaxometry

We propose a new method to determine wettability indices from NMR relaxometry. The new method uses the sensitivity of low field NMR relaxometry to the fluid distribution in oil-water saturated porous media. The model is based on the existence of a surface relaxivity for both oil and water, allowing the determination of the amount of surface wetted either by oil or by water. The proposed NMR wettability index requires the measurement of relaxation time distribution at four different saturation states. At the irreducible water saturation, we determine the dominant relaxation time of oil in the presence of a small amount of water, and at the oil residual saturation, we determine the dominant relaxation time of water in the presence of a small amount of oil. At 100% water and 100% oil saturation, we determine the surface relaxivity ratio. The interaction of oil with the surface is also evidenced by the comparison of the spin-lattice (T1) and spin-locking (T1rho) relaxation times. The new NMR index agrees with standard wettability measurements based on drainage-imbibition capillary pressure curves (USBM test) in the range [-0.3-1].     

High spatial resolution NMR imaging of polymer layers on metallic substrates

High spatial resolution NMR imaging techniques have been developed recently to measure the spatial inhomogeneity of a polymer coating film. However, the substrates of the polymer coatings for such experiments are generally required to be non-metallic, because metals can interact with static magnetic fields B(0) and RF fields B(1) giving rise to artifacts in NMR images. In this paper we present a systematic study on the effects of metallic substrates on 1D profiles obtained by high resolution NMR imaging. The off-resonance effect is discussed in detail in terms of the excitation profile of the RF pulses. We quantitatively show how the NMR signal intensities change with frequency offset at different RF pulse lengths. The complete NMR profiles were simulated using a Finite Element Analysis method by fully considering the inhomogeneities in both B(1) and B(0). The excellent agreement between the calculated and measured NMR profiles on both metallic and non-metallic substrates indicates that the experimental NMR profiles can be reproduced very well by numerical simulations. The metallic substrates can disturb the RF field of the coil by eddy current effect and therefore change the NMR profiles. To quantitatively interpret the NMR profile of a polymer layer on a metallic substrate, the profile has to be divided by the profile of a reference on the same metallic substrate located at the same distance from the coil.     

Field-cycling NMR relaxometry: the benefit of constructing master curves

ABSTRACT

The currently available field-cycling NMR relaxometers still suffer from a rather narrow frequency range; they facilitate measurements of the ¹H spin–lattice relaxation rate in the frequency of 10?kHz–30?MHz. This limit may be overcome by constructing master curves via exploiting frequency-temperature superposition, the latter being an intrinsic feature of the collective dynamics in many soft matter systems. It states that the shape of the motional time-correlation function is essentially temperature independent over a large temperature interval. As will be demonstrated, master curves may be built in the susceptibility or the spectral density representation of spin–lattice relaxation data. As a result, the effective frequency range is expanded up to ten decades, and the applied shift factors provide the temperature dependence of the corresponding correlation time. Three examples are presented: cyano adamantane in its plastically crystalline phase, the liquid glycerol, and the melt of poly(ethylene propylene). Advantages and limitations of the approach are discussed.     

Molecular dynamics of n-dodecylammonium chloride in aqueous solutions investigated by 2H NMR and 1H NMR relaxometry

Molecular dynamics in n-dodecylammonium chloride/water solutions for concentrations of 34 and 45 wt% was studied by 2H NMR and by 1H NMR dispersion of spin-lattice relaxation in the 2 kHz-90 MHz frequency range. The system exhibits a number of lyotropic liquid crystalline phases, which differ in symmetry and involve motions characterized by a wide frequency scale. The analysis of 2H NMR lineshapes of selectively deuterated DDACl molecules gave us an evidence for local trans-gauche conformational changes in the chains, whereas the dispersion of spin-lattice relaxation times T1 explored by fast field cycling method revealed fast local motions, translational diffusion and collective molecular dynamics of the chains. In particular, we have found that the order director fluctuation mechanism in smectic and nematic phases dominates spin-lattice relaxation below 1 MHz and that local motions and translational diffusion are responsible for the spin-lattice relaxation in the higher Larmor frequency range.     

Detecting columnar deformations in a supermesogenic octapode by proton NMR relaxometry

We used proton ( ¹H nuclear magnetic relaxation (NMR) dispersions to study the molecular dynamics in the isotropic phase and mesophases (nematic and columnar hexagonal) of a supermesogenic octapode formed by laterally connecting calamitic mesogens to an inorganic silsesquioxane cube through flexible spacers. The dispersions of the spin-lattice relaxation time (T₁) are interpreted through relaxation mechanisms used for the study of molecular dynamics in low-molar-mass liquid crystals but adapted to the case of liquid crystalline supermolecules. At high frequencies (above 10MHz) the behaviour of the T₁ with the Larmor frequency is similar for all phases and is ascribed to local reorientations and/or rotations. At intermediate and low frequencies (below 10MHz) our results show notable differences in the T₁ behaviour with respect to the mesophases. The nematic (N) and isotropic (Iso) phases’ low-frequency results are similar and are interpreted for both phases in terms of order director fluctuations (ODF), revealing that even in the isotropic phase local nematic order is detected by proton NMR relaxometry. Local nematic order in the Iso phase is interpreted in terms of the presence of nematic cybotactic clusters induced by the interdigitation of mesogens that is promoted by the silsesquioxane octapode molecular structure. In the columnar hexagonal (Col _h phase, the T₁ dispersions show that elastic columnar deformations (ECD) dominate the nuclear magnetic relaxation below 10MHz. This result shows that the columnar packing of the octapode clearly restricts the collective fluctuations of the mesogenic units inspite of their local nematic order.     

Fast field cycling NMR relaxometry studies of molten and cooled cocoa butter

ABSTRACT

Due to its relevance in the confectionery industry, cocoa butter (CB) has been extensively studied. However, most studies focus on its crystallisation properties, whilst studies of its liquid state are lacking. Here, and for the first time, a study of the self-diffusion of CB at different temperatures is presented, using fast field cycling (FFC) nuclear magnetic resonance (NMR) further validated using pulsed field gradient stimulated echo (PGSTE) NMR. Measurements were performed upon heating CB to either 50°C or 100°C and cooling it to 22°C. No hysteresis was found between the different thermal treatments. However, the activation energy (28.7 kJ/mol) estimated from the cooling protocol of the 100°C treatment, was the closest to that reported in the literature for similar systems. This suggests that measurements using a wider range of temperatures, and starting with a liquid material are advisable. Additionally, samples were measured during isothermal crystallisation at 22°C, showing that the region below 1 MHz is the most sensitive to phase changes.     

Flow-enhanced molecular reorientations and interfacial slip probed by field-cycling NMR relaxometry in microscopic pores

It is shown that hydrodynamic flow has an effect on spin-lattice relaxation in water filled into a porous monolithic silica material. This is a rotational analogue of translational hydrodynamic (or Taylor-Aris) dispersion arising from incoherent Brownian motion in combination with coherent flow. The effect is demonstrated with the aid of field-cycling NMR relaxometry and confirmed by theoretical considerations. The results directly verify bulk mediated surface diffusion and reveal interfacial slip at fluid-solid interfaces.