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Overview of different strengthening techniques applied on walls used in historical structures
(2012)
Messung der empfundenen Geruchsintensität mit Multigas-Sensorsystemen, das Forschungsvorhaben SysPAQ
(2007)
Measuring perceived air quality and intensity by a Sensor System, the European Project SysPAQ
(2008)
Water-repellent renders were studied in order to evaluate their suitability for restoration applications. Water repellent admixtures, such as powdered siloxane-based products and metal soaps (zinc and calcium stearates), were mixed with a pozzolana-lime binder similar to historical binders with hydraulic properties. The chemical-physical and structural properties, the effectiveness and the durability of the water-repellent mortars in different environmental conditions were studied. The influence of the water repellent admixtures was evaluated by FT-IR analyses, by testing the mechanical properties and the behaviour in presence of water. The durability of the water-repellent mortars was evaluated after the exposure to artificial weathering (UV-light and water) and to immersion/drying cycles in saturated sodium sulphate solution. The nature of the water-repellent admixtures influenced both the hydration reactions and the chemical-physical properties of the mortars resulting in different resistance to the weathering and to salt crystallization.
The study evaluates Portland limestone cement mortars, natural hydraulic lime mortars and pozzolan-lime mortars modified with water-repellent admixtures (metal soaps and siloxanes) for their use in the maintenance of historic buildings. The chemical-physical characteristics, the durability and the resistance to artificial weathering (exposure to UV light and artificial rain) were examined. The exposure conditions used in the ageing test were chosen in order to simulate outdoor environmental conditions, in particular the processes caused by UV-light and thermal shock induced by rain water.
Aim: To observe the variation in accumulation of Fusarium and Alternaria mycotoxins across a topographically heterogeneous field and tested biotic (fungal and bacterial abundance) and abiotic (microclimate) parameters as explanatory variables.
Methods and Results: We selected a wheat field characterized by a diversified topography, to be responsible for variations in productivity and in canopy-driven microclimate. Fusarium and Alternaria mycotoxins where quantified in wheat ears at three sampling dates between flowering and harvest at 40 points.
Tenuazonic acid (TeA), alternariol (AOH), alternariol monomethyl ether (AME), tentoxin (TEN), deoxynivalenol (DON), zearalenone (ZEN) and deoxynivalenol-3-Glucoside (DON.3G) were quantified. In canopy temperature, air and soil humidity were recorded for each point with data-loggers. Fusarium spp. as trichothecene producers, Alternaria spp. and fungal abundances were assessed using qPCR. Pseudomonas fluorescens bacteria were quantified with a culture based method. We only found DON, DON.3G, TeA and TEN to be ubiquitous across the whole field, while AME, AOH and ZEN were only occasionally detected. Fusarium was more abundant in spots with high soil humidity, while Alternaria in warmer and drier spots. Mycotoxins correlated differently to the observed explanatory variables: positive correlations between DON accumulation, tri 5 gene and Fusarium abundance were clearly detected.
The correlations among the others observed variables, such as microclimatic conditions, varied among the sampling dates. The results of statistical model identification do not exclude that species coexistence could influence mycotoxin production.
Conclusions: Fusarium and Alternaria mycotoxins accumulation varies heavily across the field and the sampling dates, providing the realism of landscapescale studies. Mycotoxin concentrations appear to be partially explained by biotic and abiotic variables.
Significance and Impact of the Study: We provide a useful experimental design and useful data for understanding the dynamics of mycotoxin biosynthesis in wheat.
We propose a model to describe the sintering kinetics of polydispersed glass particles, having no adjustable parameter. The model is based on three sintering stages: a pure Frenkel' (F) first step, a mixed Frenkel/MackenzieShuttleworth' stage, and a third, pure MackenzieShuttleworth' (MS) step. The model considers sample shrinkage as the sum of the partial shrinkage of several clusters, each consisting of equally sized particles and each showing independent F or MS behavior. The overall set of clusters mimics the specimen's real particle size distribution. We then introduce the concept of neck forming ability, which allows the formation of necks among particles of different sizes, relaxing the clustering condition. Using experimental physical parameters: particle size distribution, viscosity, surface energy, and the theoretical neck forming ability, the model describes well the sintering kinetics of an alumino-borosilicate glass powder having polydispersed, irregular shaped particles in a variety of temperatures. The sintering kinetics of the real powder is slower, but not far from the calculated kinetics of a monodispersed distribution containing only particles of average size. Thus the model provides a tool for estimating the sintering kinetics of real glass powders, for any size distribution and temperature, thus minimizing the number of laboratory experiments.
Liquid adsorption chromatography at critical conditions (LACCC) in normal and in reversed-phase modes provides independent information on the molar mass distributions of both blocks of poly(methyl methacrylate)-block-poly(tert-butyl methacrylate), even if no information about the precursor is available. In addition, the amount of unreacted precursor can be determined, even if its molar mass is comparable to that of the total block copolymer. The reversal of elution order by changing of stationary and mobile phases makes it possible to independently characterize each block in the SEC mode of the LACCC system. Thus, complete structural information is obtained even without using two-dimensional chromatographic techniques.