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91.
Donnet JB Ridaoui H Balard H Barthel H Gottschalk-Gaudig T 《Journal of colloid and interface science》2008,325(1):101-106
The interactions of water, hexamethyldisiloxane, and dodecane with pyrogenic silica samples, modified by a controlled partial silylation with dimethyldichlorosilane, were studied by microcalorimetry and wettability measurements. The samples, having a coverage ratio lower than dimethylsilyl (DMS) monolayer capacity ( approximately 2.6 DMS/nm(2)), show a regular and linear decrease of their heat of immersion into water with the coverage ratio and correlate with the increase of residual silanol groups. Two critical coverage ratios were evidenced at about 25 and 50% of the DMS monolayer capacity, the grafted silica remaining hydrophilic, below 25% being strongly hydrophobic beyond. The heat of immersion into hexamethyldisiloxane decreases until 50% of the DMS monolayer whereas that of dodecane remains independent of the grafting ratio. This study demonstrates that the water/residual free silica surface plays the main role in the stabilization of the W/O Pickering's emulsions. 相似文献
92.
Donnet JB Balard H Nedjari N Hamdi B Barthel H Gottschalk-Gaudig T 《Journal of colloid and interface science》2008,328(1):15-19
The heat of immersion and the surface properties of pyrogenic silicas were examined using microcalorimetry and inverse gas chromatography at finite concentration (FC-IGC). The microcalorimetric measurements showed a regular decrease of the heat of immersion, in water, per area unit with an increase in the surface areas. The desorption isotherms were established using FC-IGC. It is observed that BET constant value goes through a minimum, whereas the shapes of distribution function of the adsorption energies of isopropanol are changing. All results could be interpreted using a model of formation of the pyrogenic silica in the flame, which explains the change of surface functionality and geometry occurring around 200 m2/g. 相似文献
93.
The exit of a wetting fluid from a thin microchannel into a sudden expansion is studied experimentally. In the case of the exit from a single channel, the advancing interface converges to a parabolic shape after an initial transient, in accordance with the lubrication limit analysis of a spreading drop. The experiments are then repeated for the exit from two parallel channels. At early times, the two exiting drops behave independently and display the same evolution as a single exiting droplet, while at late times we recover a single parabolic profile. The transition between the early and late states is due to the merging of the two drops, which is associated with a sudden increase in the flow rate. This is the signature of a collective effect which acts to redistribute the fluid spatially. Finally, the experiment is generalized to the case of seven parallel channels where a cascade of two-by-two mergings is observed, indicating that local interactions dominate the dynamics which lead to the global state of the system. 相似文献
94.
Multiresidue analytical methods for the ultra-trace quantification of 33 priority substances present in the list of REACH in real water samples 总被引:1,自引:0,他引:1
Baugros JB Giroud B Dessalces G Grenier-Loustalot MF Cren-Olivé C 《Analytica chimica acta》2008,607(2):191-203
Innovative and simultaneous multiresidue analytical methods of 33 multi-class pollutants in wastewaters, surface and ground waters, using solid phase extraction (SPE) followed by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) are presented. Target compounds include several groups of emerging and persistent contaminants derived from the European priority list of the registration evaluation and authorisation of chemicals system (REACH): organochlorine (8) and organophosphorus (2) pesticides, carbamates (2), fungicides (8), phthalates (2), alkylphenols (10) and bisphenol A.The recovery rates of the SPE gave levels ranged from 84 to 118% with exception of some compounds that yielded lower (methamidophos (50%), p,p′-DDT (60%) and o,p′-DDT (72%)) but all recoveries were acceptable. Low limits of detection (LOD) varied between 0.2 and 88.9 ng L−1 (except for HPTE and 4n-octylphenol giving 161 and 220 ng L−1, respectively). A study of matrix effects was performed in order to evaluate the best and reliable calibration approach.The developed analytical method was successfully applied to the analysis of the 33 substances in wastewater effluents as well as surface and ground waters. The most frequently detected families were alkylphenols and industrial endocrine disrupting compounds (phthalates and bisphenol A). 相似文献
95.
Bossa JB Borget F Duvernay F Theulé P Chiavassa T 《The journal of physical chemistry. A》2008,112(23):5113-5120
We study low temperature reactivity of methylamine (CH3NH2) and carbon dioxide (CO2) mixed within different ratios, using FTIR spectroscopy and mass spectrometry. We report experimental evidence that the methylammonium methylcarbamate [CH3NH3(+)][C3NHCO2(-)] and methylcarbamic acid (CH3NHCOOH) are formed when the initial mixture CH3NH2:CO2 is warmed up to temperatures above 40 K. An excess of CH3NH2 favors the carbamate formation while an excess of CO2 leads to a mixture of both methylammonium methylcarbamate and methylcarbamic acid. Quantum calculations show that methylcarbamic acid molecules are associated into centrosymmetric dimers. Above 230 K, the carbamate breaks down into CH3NH2 and CH3NHCOOH, then this latter dissociates into CH3NH2 and CO2. After 260 K, it remains on the substrate a solid residue made of a well-organized structure coming from the association between the remaining methylcarbamic acid dimers. This study shows that amines can react at low temperature in interstellar ices rich in carbon dioxide which are a privileged place of complex molecules formation, before being later released into "hot core" regions. 相似文献
96.
Clare JP Ayling AJ Joos JB Sisson AL Magro G Pérez-Payán MN Lambert TN Shukla R Smith BD Davis AP 《Journal of the American Chemical Society》2005,127(30):10739-10746
Cholapod anion receptors can achieve high affinities while maintaining compatibility with nonpolar media. Previously they have been shown to transport anions across cell and vesicle membranes. In the present work, the scope of the architecture is expanded and structure-selectivity relationships are investigated. Eight new receptors have been synthesized, with up to six H-bond donor centers. Using Cram's extraction method, these compounds plus five known examples have been tested for binding to seven monovalent anions (tetraethylammonium salts, wet chloroform as solvent). Association constants in excess of 10(10) M(-1) have been measured for several pairings. Selectivities vary with receptor geometry, as expected. More remarkably, they also depend on receptor strength: more powerful receptors show a wider range of binding free energies, and therefore a greater spread of Ka(X-)/Ka(Y-). This "affinity-selectivity" effect can be derived from empirical relationships for H-bond strengths, and could prove widely operative in supramolecular chemistry. 相似文献
97.
We give in this paper topological and dynamical characterizations of mathematical quasicrystals. Let denote the space of uniformly discrete subsets of the Euclidean space. Let denote the elements of that admit an autocorrelation measure. A Patterson set is an element of such that the Fourier transform of its autocorrelation measure is discrete. Patterson sets are mathematical idealizations of quasicrystals. We prove that S is a Patterson set if and only if S is almost periodic in (,), where denotes the Besicovitch topology. Let be an ergodic random element of . We prove that is almost surely a Patterson set if and only if the dynamical system has a discrete spectrum. As an illustration, we study deformed model sets. 相似文献
98.
Barberon F Baroghel-Bouny V Zanni H Bresson B d'Espinose de la Caillerie JB Malosse L Gan Z 《Magnetic resonance imaging》2005,23(2):267-272
The durability of cement-based materials with respect to exterior aggressions is one of the current priorities in civil engineering. Depending on their use, the cement-based materials can be exposed to different types of aggressive environments. For instance, damages to concrete structures in contact with a saline environment (sea water on bridges, deicing salts on roads, etc.) are of utmost importance. Upon exposure to saline water, Cl- ions penetrate into the structures and subsequently lead to reinforcement corrosion. Chloride attack is often combined with other aggressive influences such as temperature (e.g., freezing) or the ingress of other ions (e.g., sulfates in sea water). We therefore aim to explore the effect of sodium chloride (NaCl) on the structural chemistry of cement paste. Existing studies about reinforcement corrosion by chloride have focused on the penetration of Cl- ions and the comparison between "free" ions (water-soluble ions) and bound ones. However, little is known about the fixation mechanisms, the localization of Cl in the cement matrix and the structural interaction between Cl and the silicate and aluminate hydrate phases present in cement paste. We present here results of a multinuclear nuclear magnetic resonance study on the fixation of chloride in the hydration products and the characterization of new phases potentially appearing due to chloride ingress. 相似文献
99.
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