Ocg Olaf Adan

Determination of moisture diffusivity in porous media using scanning neutron radiography

A technique for measuring moisture concentration profiles based on scanning neutron radiography is presented. With this technique moisture concentration profiles have been measured during drying of brick and kaolin clay. The isothermal moisture diffusivity as a function of moisture content could be determined directly from these profiles. An error analysis shows that the minimum spatial resolution for scanning should be 0.5 mm. If this condition is not satisfied, it is not possible, for example, to detect the minimum in the moisture diffusivity in the case of a receding drying front.

Determination of the liquid water diffusivity from transient moisture transfer experiments

The Boltzmann transformation method is used to determine the liquid water diffusivity from moisture content profiles as measured in a capillary water absorption experiment. An inter-laboratory comparison for analyzing the reliability of the determination method showed that the inaccuracy in the liquid water diffusivity is caused by scatter in the transformed data and by uncertainty in the boundary conditions at the intake surface and ahead of the steep moisture front. A methodology is proposed based on (1) the evaluation of the validity of the diffusion approach, (2) a simplified handling of the boundary conditions, (3) smoothing of the scattered data and (4) the evaluation of the quality of the determined liquid water diffusivity. For HAM (Heat-Air-Moisture transport) calculations values of the liquid water diffusivity for moisture contents higher than the capillary moisture content are disregarded. The liquid water diffusivity can be described by an exponential function limited at a lower moisture content bound. To describe the moisture diffusivity including liquid water and water vapour transports, a new parametric description of the moisture diffusivity is presented, which shows sufficient flexibility both in the hygroscopic and overhygroscopic ranges. When permeability is calculated from diffusivity, the permeability should monotonically increase with decreasing capillary pressure. In the hygroscopic region it should coincide with the measured water vapour permeabilities.

Determination of Liquid Water Transfer Properties of Porous Building Materials and Development of Numerical Assessment Methods: Introduction to the EC HAMSTAD Project

Implications of moisture in building and construction are of interest to the international community because of their huge economical consequences, including effects on health, maintenance and repair, retrofitting and conservation, as well as on common welfare. The present day knowledge offers a potential to tackle such problems, both in the design process and during the service life of building. In 2001, the European Commission initiated the project ‘‘HAMSTAD’’ (Heat Air and Moisture Standards Development) to propose a better modelling methodology than the traditional Glaser method. HAMSTAD focused on the development of draft standardisation procedures on determination methods of moisture transfer properties and a draft methodology for certification of advanced moisture modelling codes. To stimulate competitiveness and progress, the project was carried out following an ‘open methodology’ instead of a system of deterministic and prescriptive (pre-) standards. This paper outlines the project and highlights the main outputs, serving as an introduction to the following more detailed research papers resulting from that work.

T2 distribution spectra obtained by continuum fitting method using a mixed Gaussian and exponential kernel function

Static (1)H NMR Free Induction Decay (FID) signals of polymer solids contain a lot of information about the molecular dynamics. A T2 analysis of the FID has generally been performed in terms of discrete two- or three-component models. However, this requires a priori assumption of the number of proton species before analysis. This paper presents a method of analyzing the FIDs of the polymer solid samples in terms of a continuous T2 distribution. A mixed Gaussian and Exponential kernel function was used to represent the true characteristic of FIDs of the polymer solids. A simple and realistic assumption has been made to reduce the number of degrees of freedom in the continuum fitting and to make the fitting stable. An experimental static (1)H NMR FID of a typical polymer solid sample was analyzed as an example in the end to demonstrate the application of this method.

Production of an Extracellular Matrix as an Isotropic Growth Phase of Penicillium rubens on Gypsum

ABSTRACT Indoor mold represents an important environmental concern, but a fundamental knowledge of fungal growth stages is needed to limit indoor fungal proliferation on finishing materials used in buildings. The present study focused on the succession of germination stages of the common indoor fungus Penicillium rubens on a gypsum substrate. This substrate is used as a model system representing porous materials that are widely used in indoor environments. Imaging with cryo-scanning electron microscopy showed that the formation of an extracellular matrix (ECM) is a phase of the isotropic growth of P. rubens that is uniquely related to germinating conidia. Furthermore, the ECM is observed only when a dry-state inoculation of the surface is applied, i.e., applying conidia directly from a 7-day-old colony, mimicking airborne contamination of the surface. When inoculation is done by spraying an aqueous conidial suspension, no ECM is observed. Moreover, it is concluded that the formation of an ECM requires active processes in the fungal cell. The porosity of the substrate proved that the ECM substance has high-viscosity characteristics. The present results stress that studies of indoor fungal growth should consider the method of inoculation, knowing that the common aqueous suspension may obscure specific stages in the initial phases of germination.

Bound and free water distribution in wood during water uptake and drying as measured by 1D magnetic resonance imaging

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 (Deff). 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 Plasticizes Only a Small Part of the Amorphous Phase in Nylon-6

It is known that Polyamide 6 absorbs water in its amorphous phase. The exact composition of the amorphous phase will determine the uptake process. The heterogeneity in the amorphous phase with respect to plasticization by water uptake is quantified in this paper using NMR relaxometry. It is shown that water occupies and plasticizes only a small part (∼6%) of the nylon matrix. This part is located in between the crystalline domains where polymer chain mobility is higher. At low moisture content (<4%) water molecules are tightly bound to the polymer and have the same dynamics. A highly mobile pool of guest-hydrogen nuclei is detected starting at a moisture content of 4%. Here, water is absorbed in clusters and the interaction between the polymer chains and water molecules decreases, leading to decoupling of the dynamics of water and polymer.

A microscopy study of hyphal growth of Penicillium rubens on gypsum under dynamic humidity conditions.

To remediate indoor fungal growth, understanding the moisture relations of common indoor fungi is crucial. Indoor moisture conditions are commonly quantified by the relative humidity (RH). RH is a major determinant of the availability of water in porous indoor surfaces that fungi grow on. The influence of steady‐state RH on growth is well understood. Typically, however, the indoor RH constantly changes so that fungi have to endure frequent periods of alternating low and high RH. Knowledge of how common indoor fungi survive and are affected by the low‐RH periods is limited. In particular, the specific effects of a drop in RH on the growth of the mycelium remain unclear. In this work, video microscopy was used to monitor hyphal growth of Penicillium rubens on gypsum substrates under controlled dynamic humidity conditions. The effect of a single period of low RH (RH = 50–90%) interrupting favourable conditions (RH = 97%) was tested. It was found that hyphal tips ceased to extend when exposed to any tested decrease in RH. However, new hyphal growth always emerges, seemingly from the old mycelium, suggesting that this indoor fungus does not rely only on conidia to survive the humidity patterns considered. These findings are a fundamental step in unravelling the effect of RH on indoor fungal growth.

Wood staining fungi revealed taxonomic novelties in Pezizomycotina: new order Superstratomycetales and new species Cyanodermella oleoligni

A culture-based survey of staining fungi on oil-treated timber after outdoor exposure in Australia and the Netherlands uncovered new taxa in Pezizomycotina. Their taxonomic novelty was confirmed by phylogenetic analyses of multi-locus sequences (ITS, nrSSU, nrLSU, mitSSU, RPB1, RPB2, and EF-1α) using multiple reference data sets. These previously unknown taxa are recognised as part of a new order (Superstratomycetales) potentially closely related to Trypetheliales (Dothideomycetes), and as a new species of Cyanodermella, C. oleoligni in Stictidaceae (Ostropales) part of the mostly lichenised class Lecanoromycetes. Within Superstratomycetales a single genus named Superstratomyces with three putative species: S. flavomucosus, S. atroviridis, and S. albomucosus are formally described. Monophyly of each circumscribed Superstratomyces species was highly supported and the intraspecific genetic variation was substantially lower than interspecific differences detected among species based on the ITS, nrLSU, and EF-1α loci. Ribosomal loci for all members of Superstratomyces were noticeably different from all fungal sequences available in GenBank. All strains from this genus grow slowly in culture, have darkly pigmented mycelia and produce pycnidia. The strains of C. oleoligni form green colonies with slimy masses and develop green pycnidia on oatmeal agar. These new taxa could not be classified reliably at the class and lower taxonomic ranks by sequencing from the substrate directly or based solely on culture-dependent morphological investigations. Coupling phenotypic observations with multi-locus sequencing of fungi isolated in culture enabled these taxonomic discoveries. Outdoor situated timber provides a great potential for culturable undescribed fungal taxa, including higher rank lineages as revealed by this study, and therefore, should be further explored.

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.