Knowledge on moisture transport in wood is important for understanding its utilization, durability and product quality. Moisture transport processes in wood can be studied by Nuclear Magnetic Resonance (NMR) imaging. By combining NMR imaging with relaxometry, the state of water within wood can be identified, i.e. water bound to the cell wall, and free water in the cell lumen/vessel. This paper presents how the transport of water can be monitored and quantified in terms of bound and free water during water uptake and drying. Three types of wood from softwood to hardwood were selected covering a range of low to high density wood; pine sapwood and oak and teak. A calibration is performed to determine the different water states in each different wood type and to convert the NMR signal into moisture content. For all wood types, water transport appeared to be internally limited during both uptake and drying. In case of water uptake, free water was observed only after the cell walls were saturated with bound water. In case of drying, the loss of bound water starts only after vanishing of free water, irrespective of the position. Obviously, there is always a local thermodynamic equilibrium of bound and free water for both uptake and drying. Finally, we determined the effective diffusion coefficient (D eff ). Experimentally determined diffusion constants were compared with those derived by the diffusion models for conceptual understanding of transport mechanism. We found that diffusion in the cell wall fibers plays a critical role in the transport process.

Water uptake by multilayer films plays an important role in their performance. Individual layers may consist of different polymeric phases. Understanding the water uptake in such systems requires knowledge of the water distribution, its state in the polymer, and influence on the polymeric phases. This study illustrates the application of high-resolution NMR and relaxometry for measuring water distributions and evaluating water–polymer interactions. We studied water uptake in a two-layered base coat/top coat system, where the base coat consisted of acrylic, polyurethane, pigment particles, and a polymeric dispersant. Water and the polymer phases in the base coat were identified with NMR relaxometry. The water diffusivity in the base coat was determined. At high water contents water is highly mobile and is loosely bonded to the polymer. Reversible plasticization of the dispersant was observed. The polymeric dispersant seems to play a key role in the sorption of water by the coating.

The dynamics of the curing process of alkyd coatings is an important aspect for coating performance. The formation of cross links in an alkyd coating film has been followed in time using a microimaging nuclear magnetic resonance setup, having a spatial resolution of 5μm perpendicular to the film. During this cross-linking process a front has been observed inside the coating film. The position of this front varied with the square root of time. With the help of a simple reaction model, we have proven that this dynamics results from the fact that the curing rate is limited by the oxygen flux into the coating. This model can also explain, the differences in curing rates observed for various coatings.

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Collagen is an important component of the extracellular matrix (ECM) and plays an important role in normal tissue maturation and in pathological processes such as atherosclerosis and myocardial infarction. The diagnostics of the latter diseases using MRI could strongly benefit from the use of collagen-specific contrast agents. The current study aimed to develop a bimodal liposomal MR contrast agent that was functionalized with CNA35, a collagen adhesion protein of the Staphylococcus aureus bacterium. The liposomes were characterized in terms of CNA35 protein conjugation and loading. The overall morphology was assessed with DLS and cryo-TEM, while cryo-TEM tomography was used to visualize the protein coverage of the liposomes. The binding properties of the contrast agent were investigated using a fluorescence assay based on the rhodamine content of the liposomes. The bulk relaxivity was determined using regular relaxometry while the MR-properties of liposomes in their bound state were studied using NMR depth profiling. This CNA35 functionalized contrast agent and the set of in vitro experiments we performed indicate the potential of this technology for in vivo molecular imaging of collagen.

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The penetration of water into two-layer polymeric films of a hydrophilic base layer and hydrophobic top layer plays an important role in their performance. Little is known about the coupled effects of water uptake and stress in such films. To study such interactive phenomena, time-dependent distributions in the film are needed, which cannot be provided by traditional techniques. In this study, high-resolution NMR imaging was used to measure water profiles, showing that applied stress increased both the uptake rate and the amount of absorbed water. A model was formulated to describe the process, using the barrier properties of and the chemical potential differences over the top coat. On the basis of this, the diffusivity in the top layer and stress contribution were estimated. The results show that external stresses significantly influence water penetration into multilayer films.