Gaz inerte | EPFL Graph Search

vignette|Pour ne pas rancir, les paquets de chips sont remplis d'un gaz inerte. Un gaz inerte est un gaz qui ne participe à aucune réaction chimique (ou à très peu de réactions chimiques) dans des conditions données, généralement les conditions normales de température et de pression. Le plus souvent, un gaz n'est dit inerte que s'il s'agit d'un ensemble étendu de conditions. Les gaz inertes sont utilisés pour éviter que des réactions chimiques indésirables dégradent un échantillon, notamment des réactions d'oxydation et d'hydrolyse avec l'oxygène et l'humidité de l'air. Les gaz inertes les plus couramment utilisés sont l'azote et l'argon purifiés, en raison de leur forte abondance dans l'air (78,3 % , 1 % Ar) et de leur relativement faible coût. Historiquement, le terme désignait souvent les gaz nobles, qui effectivement ne réagissent qu'avec très peu de substances et dans des conditions très particulières. Ce sont les éléments du groupe 18 du tableau périodique : l'hélium, le néon, l

Assessment of microbial community changes and limiting factors during bioremediation of hydrocarbon-polluted soil with new miniaturized physiological methods

Karin Kaufmann

Due to human activities, organic pollutants are spilled to the environment where they threaten public health, often as contaminants of soil or groundwater. Living organisms are able to transform or mineralize many organic pollutants, and bioremediation techniques have been developed to remove pollutants from a contaminated site. However, fast and easy methods to document both the efficacy of bioremediation and the changes in soil microbial communities during bioremediation are not well developed. The major aim of this thesis was to develop miniaturized methods targeting the physiology of microbial communities during pollutant degradation in soil and to assess pollution-induced community changes. Furthermore, the methods should identify factors limiting efficient pollutant biodegradation. Petroleum hydrocarbons have been chosen as pollutants because these compounds are frequently spilled, readily water-soluble, partly toxic and carcinogenic, and therefore undesirable in soils and drinking water supplies. The influence of petroleum hydrocarbons on a microbial community in the vadose zone was assessed under field conditions. An artificial hydrocarbon mixture consisting of volatile and semi-volatile compounds similar to jet-fuel was emplaced in a previously uncontaminated vadose zone in nutrient-poor glacial melt water sand. The experiment included monitoring of microbial parameters and CO2 concentrations in soil gas over 3 months, in- and outside the hydrocarbon vapor plume that formed around the buried petroleum. Microbial and chemical analyses of vadose zone samples were performed on material from 9 cores drilled on 3 days at 3 distances from the buried petroleum mass to 3.3 m depth. Significantly elevated CO2 concentrations were observed after contamination. Total cell numbers as determined by fluorescence microscopy were strongly correlated with soil organic carbon and nitrogen content but varied little with contamination. Redundancy analysis (RDA) allowed direct analysis of effects of selected environmental variables or the artificial contamination on microbiological parameters. Variation in biomass and CO2 production was to 46 % explained by soil parameters and to 39.8 % by the duration of contamination. The microbial community structure was assessed by community-level physiological profile analysis using BiologTM EcoPlates. Only 35.9 % of variation in BiologTM data could be attributed to soil parameters and contamination, however, the samples with greatest exposure to hydrocarbons grouped together on RDA plots. It is concluded that at this nutrient-poor site, the microbial community was dominated by the natural heterogeneity and that the influence of petroleum hydrocarbon vapor was weak. BiologTM Eco-Plates combined with RDA were able to distinguish between samples with high and low hydrocarbon exposure. However, the method was not sensitive enough to produce consistent patterns in three replicates when extracts from subsurface soils with low cell numbers were inoculated. A more sensitive, MPN-based system was therefore developed and its ability to provide information about specific pollutant degraders was tested in alluvial sand. Eight dilutions of sand extracts were inoculated on medium- and substrate-containing polypropylene deep-well plates. To keep the concentrations of the volatile substrates constant over several days of incubation without intoxicating the soil community, a substrate-containing organic carrier phase was applied to each vial. The biochemically inert 2,2,4,4,6,8,8-heptamethylnonane (HMN) was appropriate for this purpose. Thus, the volatile substrates partition from HMN into the microorganism-containing soil water where they achieve relatively low concentrations. The sensitive watersoluble tetrazolium dye (WST-1) was added to each well after 7 days incubation to detect dehydrogenase activity. A dark yellow signal was developed for the substrates toluene, n-octane, n-dodecane, 1,2,4-trimethylbenzene and methylcyclohexane but not for isooctane, being strongest in n-alkane amended wells. With this method, more hydrocarbon degrading bacteria were detected in an alluvial sand exposed to kerosene for 72 hours compared to the community in the pristine sand. Both communities were mainly composed of n-alkane degraders. Although encouraging results were achieved, we noticed that the tetrazolium reduction was inhibited in some cases. Wells with high cell numbers, in which obvious growth occurred, did not produce a signal. In a next step, the two-liquid phase system with HMN was applied to modify a miniaturized respiration detection system using whole soil samples instead of soil extracts (Campbell et al., AEM 69, p. 3593). Soil was incubated in deep-well plates in presence of single volatile organic hydrocarbons. The carrier phase was added to the interstitial space in a bead layer on the bottom of the well (below the soil sample), and the hydrocarbons diffused into the soil-water. The soil activity was determined by means of an agar plate containing a pH indicator, which changes color as a function of the produced CO2. Physiological profiles specific to petroleum hydrocarbons in pristine and contaminated soils were assessed. The substrate concentrations, which induced highest microbial activity, as well as concentrations causing inhibition, were determined with effect-concentration curves. Community-level physiological profiles based on hydrocarbon degradation were obtained by applying multivariate analysis on the CO2 yields. The first measurement period of 0-6 hours after addition of relatively high hydrocarbon concentrations to the system yields values, which best separated soil types as well as pristine and contaminated soils. If low concentrations were applied, we obtained only significant separations after 24 hours incubation, probably after a growth step. The same micro-respiration system equipped with a 14CO2 detection plate was applied to study N and P limitation of aerobic mineralization of 14C-toluene in a soil previously exposed to petroleum. Significant nutrient limitation during short-term tests (24-48 hours) was identified and the optimized combination of nutrient addition was determined. Conclusively, miniaturized physiological methods have been proven to detect soil microbial community changes in petroleum hydrocarbon-contaminated soils. Adding an organic carrier phase to the miniaturized systems allowed assuring a volatile organic hydrocarbon supply in non-toxic concentrations in the soil water or the medium for several days. Thus simple, cost-effective systems to investigate the soil community during bioremediation and to address questions of nutrient shortage in soils have been provided with this thesis.

EPFL2004

Sputtered titanium oxynitride coatings for endosseous applications: Physical and chemical evaluation and first bioactivity assays

Oksana Banakh, Alessandro Pontearso, Rosendo Sanjines

Titanium oxynitride coatings (TiNxO3,) are considered a promising material for applications in dental implantology due to their high corrosion resistance, their biocompatibility and their superior hardness. Using the sputtering technique, TiNxO3, films with variable chemical compositions can be deposited. These films may then be set to a desired value by varying the process parameters, that is, the oxygen and nitrogen gas flows. To improve the control of the sputtering process with two reactive gases and to achieve a variable and controllable coating composition, the plasma characteristics were monitored in-situ by optical emission spectroscopy. TiNxO3, films were deposited onto commercially pure (ASTM 67) microroughened titanium plates by reactive magnetron sputtering. The nitrogen gas flow was kept constant while the oxygen gas flow was adjusted for each deposition run to obtain films with different oxygen and nitrogen contents. The physical and chemical properties of the deposited films were analyzed as a function of oxygen content in the titanium oxynitride. The potential application of the coatings in dental implantology was assessed by monitoring the proliferation and differentiation of human primary osteoblasts. (C) 2014 Elsevier B.V. All rights reserved.

Elsevier Science Bv2014

Dark curing kinetics of UV printing inks by real-time ATR-FTIR spectroscopy

Eric Jacques Nouzille

In UV-curable printing technology, an ink or a varnish is exposed to the UV-light source within a fraction of a second. Subsequent polymerization therefore proceeds in the dark, referred to as dark curing. Because dark curing can be critical and contributes to a large part of the overall conversion and to the final properties of the printed ink, the aim of this work was to get a better understanding of the dark curing process. Because an ink is a complex mixture of components, simpler systems representative of free radical and cationic chemistry were studied. Special attention was given to free radical polymerization with a detailed kinetic modeling. For cationic systems, the study was more application oriented. Attenuated-Total-Reflection Fourier-Transform Infrared (ATR-FTIR) spectroscopy was found to be the method of choice to follow in real-time the progress of the reaction under UV irradiation and in the dark. This technique allowed the study of curing conditions close to those encountered in industry. Dark curing of free radical was examined in systems consisting of a monomer (multifunctional acrylate) and a photoinitiator. The reactivities of different monomers were investigated and it was found that the chemistry of the spacer between the acrylate functional groups had an influence on the extent of dark curing. For example, TPGDA (tripropylene glycol diacrylate) led to higher overall conversion than HDDA (hexanediol diacrylate) although both are diacrylate monomers. Several explanations were put forward, such as the effect of dissolved oxygen, primary cyclization and initiation efficiency. The efficiency of photoinitiators (PIs) was examined and different behaviours were highlighted. For example, it was observed that DMPA (dimethoxyphenyl acetophenone) has a better quantum yield for α-cleavage compared to HCPK (1-hydroxycyclohexylphenyl ketone), whereas HCPK is more efficient in initiating the reaction, resulting in a better overall conversion in the dark. It is suggested that the two primary radicals resulting from the cleavage of the PI behave differently for DMPA and HCPK. One radical effectively initiates the reaction and the second is mainly involved in the termination process. These two different behaviours were observed under specific experimental conditions: (i) by covering the sample with a quartz plate and taking into account dissolved molecular oxygen and (ii) by curing under inert conditions with nitrogen. Photo-crosslinking polymerization reactions are strongly influenced by diffusion effects due to the formation of an infinite network. Therefore, it was proposed that a redistribution of reactivity within the system occurs, such as the diffusion of unreacted photoinitiators towards concentrations of unreacted monomers. This diffusion process has two positive effects: (i) for the same UV dose, but different intensities, a higher extent of conversion was reached with longer irradiation times under the condition investigated; (ii) multiple exposures led to a higher overall conversion than for a single exposure, for a fixed overall UV dose. Other parameters were explored, such as temperature and diffusing oxygen from air. With temperature, different trends were observed depending on the photoinitiator and the start of dark curing, either starting before the maximum rate of polymerization (Rp,max), or after Rp,max. The development of a kinetic model to describe dark curing of free radical polymerization was proposed. Existing models based on physical parameters, such as those incorporating diffusion-controlled phenomena and free-volume are relatively complex and require extensive information on the system studied. Therefore, a semi empirical approach was chosen in order to study the variation of fitting parameters when changing curing parameters, such as the photoinitiator concentration and type, the irradiation time, the UV light intensity and the temperature. The model was derived from kinetic data and it was assumed that rate coefficients are time-dependent and that termination, which was considered to be a first-order process, is propagation dependent. The kinetic equation has the form of a stretched exponential function and incorporates four fitting parameters. The model was evaluated for a large number of experimental data and very good fits were obtained with a random distribution of residuals. The exponent β was found to be sensitive to the termination process and reflected different reactivities in the dark as in the case of DMPA and HCPK. Dark curing of cationic systems continues until complete monomer conversion but at a slower rate. Thus systems with high reaction rates, both during UV irradiation and during the first seconds of the dark period, are of most importance for UV-curable printing technology. The most widely used diepoxide monomer in cationic ink formulation is 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate (DECC). In order to improve its reactivity during the first seconds of dark curing, the influence of several parameters was examined, such as the addition of an oxetane co-monomer (TMPO), the influence of relative humidity, UV dose, light intensity, temperature, and film thickness. The enhanced reactivity of DECC with TMPO was confirmed. During the cationic curing process, two reaction mechanisms compete; an activated chain end (ACE) mechanism and an activated monomer (AM) mechanism. It was observed that these two processes depend on the presence of hydroxyl containing compounds such as TMPO monomer, polyol compounds, and, most important, water. When the concentration of these components is increased the AM mechanism is enhanced, leading to higher conversion but at a slower curing rate, and a degradation of the mechanical properties. The presence of water is unavoidable and its concentration in the ink varies in presence of hydrophilic compounds, such as polyol. Furthermore, the water content increases with increasing relative humidity in air. It was shown that the reactivity of the system decreased as the percent of relative humidity increased. Moreover, although a higher overall conversion is achieved, the crosslink density of the film was severely reduced. This lower crosslink density was the result of the predominance of chain transfer reactions, leading to more pendant and short chains which were hydroxyl terminated. Moreover, the extent of conversion was thickness dependent since less water diffuses into the deeper layers occurred in thicker films.

EPFL2007