NMR-measurements for determination of local moisture content of coated wood

Local increased moisture content (MC) in wood constructions may result in different kinds of mechanical and, especially, biological degrading problems. Therefore, it is of great importance to control the MC of the material. However, there is at present no appropriate method for determining local MC in wood without destroying the product itself. Nondestructive measurements of local MC in wood is significant for the possibility of, for instance, monitoring the in situ MC in wood constructions over time, and thereby predicting potential problems. The nuclear magnetic resonance (NMR) technique has been shown to be valuable for the measurement of MC in wood. In this study, the possibility of utilizing this technique for local MC measurement in wood has been tested on wood samples exposed to water absorption for 72 h. The samples came from three different wood species treated with paint systems available on the market. In the wood samples an artificial “crack” had been created in the paint to introduce an area where the water could easily gain access to the wood. The results show the possibility of using the NMR technique for local MC measurements in wood. The measurement area, however, must be related to the properties of the material. In the case of wood, the measurement spot must be related to the early/latewood proportions. Further, a calibration of the NMR measurement must be made in relation to the expected density variations of the material.     

Wear study of field worn clutch actuators and evaluation of a model test

Pneumatic clutch actuators, employed in trucks, have been investigated. The surfaces of the inside of the anodised aluminium cylinders, of the lip seals and of the guiding rings have been studied by SEM and optical microscopy. For most of the actuators no significant wear was revealed. However, one actuator, with leakage problems, was severely worn. An extensive amount of scratches was found on the cylinder surface, the thickness of the guiding ring had decreased and large parts were missing from the lip seal. A possible explanation is that particles have entered the system thus altering the contact conditions. A test setup was developed to investigate how particles present in the system affect the wear. A part of the piston, with lip seal and guiding ring, slides against a part of the anodised aluminium cylinder in a back- and forward motion. Pure silicone grease lubricated tests resulted in no wear. Tests with added dust particles resulted in distinct scratches on the aluminium surface and embedded particles in the guiding ring and the lip seal. These tests provide results in good agreement with the wear revealed in the investigations of used actuators and support the theory that wear is caused by particles.     

The importance of SO2 and SO3 for sulphation of gaseous KCl - An experimental investigation in a biomass fired CFB boiler

This paper is based on results obtained during co-combustion of wood pellets and straw in a 12 MW circulating fluidised bed (CFB) boiler. Elemental sulphur (S) and ammonium sulphate ((NH₄)₂SO₄) were used as additives to convert the alkali chlorides (mainly KCl) to less corrosive alkali sulphates. Their performance was then evaluated using several measurement tools including, IACM (on-line measurements of gaseous alkali chlorides), a low-pressure impactor (particle size distribution and chemical composition of extracted fly ash particles), and deposit probes (chemical composition in deposits collected). The importance of the presence of either SO₂ or SO₃ for gas phase sulphation of KCl is also discussed. Ammonium sulphate performed significantly better than elemental sulphur. A more efficient sulphation of gaseous KCl was achieved with (NH₄)₂SO₄ even when the S/Cl molar ratio was less than half compared to sulphur. Thus the presence of gaseous SO₃ is of greater importance than that of SO₂ for the sulphation of gaseous KCl.     

Power-based control of physical systems

It is well known that energy-balancing control is stymied by the presence of pervasive dissipation. To overcome this problem in electrical circuits, the alternative paradigm of power shaping was introduced in Ortega, Jeltsema, and Scherpen (2003) —where, as suggested by its name, stabilization is achieved shaping a function akin to the power instead of the energy function. In this paper we extend this technique to general nonlinear systems. The method relies on the solution of a PDE, which identifies the open-loop storage function. We show through some physical examples, that the power-shaping methodology yields storage functions which have units of power. To motivate the application of this control technique we illustrate the procedure with two case studies: a tunnel diode circuit and a two-tanks system.     

Essential elements and contaminants in edible tissues of European and American lobsters

In several European countries clawed lobsters, such as the European (Homarus gammarus) and American (H. americanus) ones are widely consumed. Yet, information about essential elements and contaminants in both species is still scarce. Therefore, the aim of this work was to characterise the elemental content in the edible part (muscle, hepatopancreas, gonads and roe) of both homarids and to compare them with the daily intake recommendations and maximum allowed levels. Two techniques were employed: energy-dispersive X-ray fluorescence (EDXRF) to quantify Cl, S, K, Ca, Fe, Cu, Zn, As, Se, Br and Sr; and flame atomic-absorption spectrometry (FAAS) to analyse Na, Mg, Mn, Cd, Hg and Pb. Significant differences were found in the elemental composition of edible tissues of both species, likely reflecting the distinct physiological role of those tissues: muscle (higher: Na, Mg, Ca and Sr; lower: Fe, Se, Cd); hepatopancreas (higher: Fe, Cu, Br and Cd); gonads (lower: Cl, Ca, Zn and Hg); and roe (higher: Na and Br; lower: K and As). Statistical differences in the elemental composition of each tissue were found between both homarids: Muscle (Na, Se, As and Hg); Hepatopancreas (Na, Mg, Fe, Cu, Se, Br and Hg); and gonads (S and Zn). Since the geographical distribution of both species is different, the differences likely reflect distinct elemental composition in the aquatic environment and, consequently in the feed chain. Both lobster species were rich sources of Na, Cl, Cu, Zn and Se for human consumption. Regarding contaminants, only Cd was detected at high concentrations in the hepatopancreas of both homarids. Despite Cd values were well above the maximum allowed level set by the European Commission for crustaceans’ muscle, so far any limit value was set for crustaceans’ hepatopancreas. Nonetheless, the present study recommends avoiding or moderately consuming this tissue in homarids.     

Exploration of the two‐photon excitation spectrum of fluorescent dyes at wavelengths below the range of the Ti:Sapphire laser

We have studied the wavelength dependence of the two‐photon excitation efficiency for a number of common UV excitable fluorescent dyes; the nuclear stains DAPI, Hoechst and SYTOX Green, chitin‐ and cellulose‐staining dye Calcofluor White and Alexa Fluor 350, in the visible and near‐infrared wavelength range (540–800 nm). For several of the dyes, we observe a substantial increase in the fluorescence emission intensity for shorter excitation wavelengths than the 680 nm which is the shortest wavelength usually available for two‐photon microscopy. We also find that although the rate of photo‐bleaching increases at shorter wavelengths, it is still possible to acquire many images with higher fluorescence intensity. This is particularly useful for applications where the aim is to image the structure, rather than monitoring changes in emission intensity over extended periods of time. We measure the excitation spectrum when the dyes are used to stain biological specimens to get a more accurate representation of the spectrum of the dye in a cell environment as compared to solution‐based measurements.     

Biobased composites prepared by compression molding with a novel thermoset resin from soybean oil and a natural‐fiber reinforcement

Biobased composites were manufactured with a compression‐molding technique. Novel thermoset resins from soybean oil were used as a matrix, and flax fibers were used as reinforcements. The air‐laid fibers were stacked randomly, the woven fabrics were stacked crosswise (0/90°), and impregnation was performed manually. The fiber/resin ratio was 60 : 40. The prepared biobased composites were characterized by impact and flexural testing. Scanning electron microscopy of knife‐cut cross sections of the specimens was also done to investigate the fiber–matrix interface. Thermogravimetric analysis of the composites was carried out to provide indications of thermal stability. Three resins from soybean oil [methacrylated soybean oil, methacrylic anhydride modified soybean oil (MMSO), and acetic anhydride modified soybean oil] were used as matrices. The impact strength of the composites with MMSO resin reinforced with air‐laid flax fibers was 24 kJ/m², whereas that of the MMSO resin reinforced with woven flax fabric was between 24 and 29 kJ/m². The flexural strength of the MMSO resin reinforced with air‐laid flax fibers was between 83 and 118 MPa, and the flexural modulus was between 4 and 6 GPa, whereas the flexural strength of the MMSO resin reinforced with woven fabric was between 90 and 110 MPa, and the flexural modulus was between 4.87 and 6.1 GPa. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Decomposition of belowground litter and metal dynamics in salt marshes (Tagus Estuary, Portugal)

The concentrations of C, Fe, Mn, Zn, Cu, Pb and Cd were determined monthly in decomposing roots of Halimione portulacoides, using litterbag experiments, in two salt marshes of the Tagus estuary with different levels of contamination. Although carbon concentrations varied within a narrow interval during the experiment, litter decomposed rapidly in the first month (weight loss between 0.051 and 0.065 g d(-1)). The time variation of metals was examined in terms of Me/C ratios and metal stocks. Ratios of Fe/C and Mn/C and their metal stocks increased in spring, presumably due to the precipitation of oxides in the surface of decomposing roots. Subsequent decrease of Fe/C and Mn/C ratios suggests the use of Fe and Mn oxides, as electron acceptors, in the organic matter oxidation. Zinc, Cu, Pb and Cd ratios to C were, in general, higher than at initial conditions implying that metal that leached out was slower than carbon. However, metal stocks decreased during the experiment indicating that incorporation or sorption of metals in Fe and Mn oxides did not counterbalance the amount of Zn, Pb and Cd released from decomposing litter. An exception was observed for Cu, since stock in the less contaminated marsh (Pancas) increased during the decomposition, indicating that litter was efficient on Cu binding under more oxidising conditions. These results emphasize the importance of litter decomposition and sediment characteristics on metal cycling in salt marshes.     

Oxidatively Derived Volatile Compounds in Microencapsulated Fish Oil Monitored by Solid-phase Microextraction (SPME)

The stability of microencapsulated fish oil was studied during storage at 4 °C for up to 20 wk. Different coating mixtures consisting of gelatin or caseinate in blends with carbohydrates (sucrose, lactose, maltodextrin) were investigated. Oxidative stability of the microencapsulated fish oil was monitored by analysis of volatile compounds using gas chromatography olfactometry (GC‐O) or GC flame ionization (GC‐FID) (SPME‐HS‐GC/O or GC/ FID and HS‐GC/MS), Oxipres test, thiobarbituric acid‐reactive substances (TBARS), and sensory analysis. Coating mixture of caseinate and lactose showed slightly better stability than the sucrose and maltodextrin caseinate mixtures. Combination of fish gelatin and maltodextrin did not show as good oxidative stability as the coating blend of caseinate, lactose, and lecithin. Hexanal, 2‐nonenal and 2,4‐decadienals were selected as quality indicators to monitor the lipid oxidation during storage of the samples. SPME‐GC‐O analysis of these indicators showed that they were representative for the oxidation occurring in the microencapsulated fish oil. SPME‐GC‐FID analysis was sensitive enough to detect oxidative changes during storage. Oxidative stability test, TBARS results, and sensory analysis were in agreement with the SPME, indicating that SPME (polydimethylsiloxane/divinylbenzene [PDMS/ DVB] fiber) can be a useful tool for rapid analysis of lipid oxidation in microencapsulated fish oil.