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Gas Solubility (gas + solubility)
Selected AbstractsHigher Gas Solubility in Nanoliquids?CHEMPHYSCHEM, Issue 1 2008Sylvain Miachon Dr. Beyond Henry's law: In nanometer-confining media, gas solubility increases widely (see figure). H2, CH4 and C2H6 solubility values in two solvents are obtained by quantitative 1H NMR spectroscopy. A mass-balance model involving the gas,liquid interface zone agrees well with the observed variation. [source] The Presence of Functional Groups Key for Biodegradation in Ionic Liquids: Effect on Gas SolubilityCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 3 2010Yun Deng Abstract The effect of the incorporation of either ester or ester and ether functions into the side chain of an 1-alkyl-3-methylimidazolium cation on the physico-chemical properties of ionic liquids containing bis(trifluoromethylsulfonyl)imide or octylsulfate anions is studied. It is believed that the introduction of an ester function into the cation of the ionic liquids greatly increases their biodegradability. The density of three such ionic liquids is measured as a function of temperature, and the solubility of four gases,carbon dioxide, ethane, methane, and hydrogen,is determined between 303,K and 343,K and at pressures close to atmospheric level. Carbon dioxide is the most soluble gas, followed by ethane and methane; the mole fraction solubilities vary from 1.8×10,3 to 3.7×10,2. These solubilities are of the same order of magnitude as those determined for alkylimidazolium-based ionic liquids. The chemical modification of the alkyl side chain does not result in a significant change of the solvation properties of the ionic liquid. All of the solubilities decrease with increasing temperature, corresponding to an exothermal solvation process. From the variation of this property with temperature, the thermodynamic functions of solvation (Gibbs energy, enthalpy, and entropy) are calculated and provide information about the solute,solvent interactions and the molecular structure of the solutions. [source] Increased gas solubility in nanoliquids: Improved performance in interfacial catalytic membrane contactorsAICHE JOURNAL, Issue 2 2009Marc Pera-Titus Abstract The kinetics of gas-liquid catalytic reactions can be strongly promoted when these are performed in interfacial catalytic membrane reactors instead of other three-phase reactors such as slurry stirrers or trickle beds. The well-defined gas-liquid-catalyst contact in this system avoiding diffusional limitations is usually argued as the main reason for such enhancement. In this work, using nitrobenzene hydrogenation as a model reaction, we propose that this increased catalytic performance might also be attributed, at least partially, to increased gas solubilities in mesoconfined solvents (or simply "nanoliquids") in interfacial contactors overcoming the values predicted by Henry's Law. To support this hypothesis, we provide experimental evidence of a dramatic increase of H2 solubility in confined ethanol using mesoporous ,-Al2O3 as confining solid. Gas-liquid solubilities can be enhanced up to five times over the corresponding bulk values for nanoliquid sizes lower than 15 nm as long as the gas-liquid interface is confined in a mesoporous array. In such a situation, the volume of the gas-liquid interface is no longer negligible compared to the total volume of the confined liquid, and the high surface excess concentrations of the gas adsorbed on the liquid surface make solubility grow up dramatically. According to these measurements, we discuss how nanoliquids might form in catalytic membrane contactors, which gas-liquid configuration in the reactor appears to be more appropriate, and how the structure of the mesoporous catalytic layer contributes to their increased gas solubilization performance. © 2008 American Institute of Chemical Engineers AIChE J, 2009 [source] Perfluorocarbons: Life sciences and biomedical uses Dedicated to the memory of Professor Guy Ourisson, a true RENAISSANCE man.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 7 2007Marie Pierre Krafft Abstract Perfluorocarbons are primarily characterized by outstanding chemical and biological inertness, and intense hydrophobic and lipophobic effects. The latter effects provide a powerful noncovalent, labile binding interaction that can promote selective self- assembly. Perfluoro compounds do not mimic nature, yet they can offer abiotic building blocks for the de novo design of functional biopolymers and alternative solutions to physiologically vital issues. They offer new tags useful for molecular recognition, selective sorting, and templated binding (e.g., selective peptide and nucleic acid pairing). They also stabilize membranes and provide micro- and nanocompartmented fluorous environments. Perfluorocarbons provide inert, apolar carrier fluids for lab-on-a-chip experiments and assays using microfluidic technologies. Low water solubility, combined with high vapor pressure, allows stabilization of injectable microbubbles that serve as contrast agents for diagnostic ultrasound imaging. High gas solubilities are the basis for an abiotic means for intravascular oxygen delivery. Other biomedical applications of fluorocarbons include lung surfactant replacement and ophthalmologic aids. Diverse colloids with fluorocarbon phases and/or shells are being investigated for molecular imaging using ultrasound or magnetic resonance, and for targeted drug delivery. Highly fluorinated polymers provide a range of inert materials (e.g., fluorosilicons, expanded polytetrafluoroethylene) for contact lenses, reconstructive surgery (e.g., vascular grafts), and other devices. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1185,1198, 2007. [source] Increased gas solubility in nanoliquids: Improved performance in interfacial catalytic membrane contactorsAICHE JOURNAL, Issue 2 2009Marc Pera-Titus Abstract The kinetics of gas-liquid catalytic reactions can be strongly promoted when these are performed in interfacial catalytic membrane reactors instead of other three-phase reactors such as slurry stirrers or trickle beds. The well-defined gas-liquid-catalyst contact in this system avoiding diffusional limitations is usually argued as the main reason for such enhancement. In this work, using nitrobenzene hydrogenation as a model reaction, we propose that this increased catalytic performance might also be attributed, at least partially, to increased gas solubilities in mesoconfined solvents (or simply "nanoliquids") in interfacial contactors overcoming the values predicted by Henry's Law. To support this hypothesis, we provide experimental evidence of a dramatic increase of H2 solubility in confined ethanol using mesoporous ,-Al2O3 as confining solid. Gas-liquid solubilities can be enhanced up to five times over the corresponding bulk values for nanoliquid sizes lower than 15 nm as long as the gas-liquid interface is confined in a mesoporous array. In such a situation, the volume of the gas-liquid interface is no longer negligible compared to the total volume of the confined liquid, and the high surface excess concentrations of the gas adsorbed on the liquid surface make solubility grow up dramatically. According to these measurements, we discuss how nanoliquids might form in catalytic membrane contactors, which gas-liquid configuration in the reactor appears to be more appropriate, and how the structure of the mesoporous catalytic layer contributes to their increased gas solubilization performance. © 2008 American Institute of Chemical Engineers AIChE J, 2009 [source] Parameters of gas dissolution in liquids obtained by isothermal pressure decayAICHE JOURNAL, Issue 1 2009Maurice L. Rasmussen Abstract A rapid and effective data analysis and interpretation approach is developed and validated for simultaneous determination of the film-mass-transfer and diffusion coefficients from time-limited experimental data obtained by dissolving gas in liquids by the pressure-decay method under isothermal conditions. Whereas previous approaches require experimental data until equilibrium and only determine the diffusion coefficient, accurate and rapid estimation of both parameters are achieved using a shorter set of time-limited data, thereby reducing the errors owing to swelling by significant gas dissolution at later times. The equilibrium conditions can be predicted theoretically stemming from an analysis of the time-limited data. This provides the estimates of the equilibrium pressure and gas solubility. This methodology not only yields accurate parameter values, but also alleviates the sufficiently large-time collection of pressure-decay data needed to essentially achieve equilibrium. © 2008 American Institute of Chemical Engineers AIChE J, 2009 [source] Direct Volumetric Measurement of Gas Oversolubility in Nanoliquids: Beyond Henry's LawCHEMPHYSCHEM, Issue 12 2009Marc Pera-Titus Dr. Abstract The properties of condensed matter are strongly affected by confinement and size effects at the nanoscale. Herein, we measured by microvolumetry the increased solubility of H2 in a series of solvents (CHCl3, CCl4, n -hexane, ethanol, and water) when confined in the cavities of mesoporous solids (,-alumina, silica, and MCM-41). Gas/liquid solubilities are enhanced by up to 15 times over the corresponding bulk values for nanoliquid sizes smaller than 15 nm as long as gas/liquid interfaces are mesoconfined in a porous network. Although Henry's law constant apparently no longer applies under these confinement, the concentration of dissolved H2 still increases linearly with increasing pressure in the range 1,5 bar. We discuss the role and main implications of surface excess concentrations at mesoconfined gas/liquid interfaces in enhancing gas solubility. [source] Higher Gas Solubility in Nanoliquids?CHEMPHYSCHEM, Issue 1 2008Sylvain Miachon Dr. Beyond Henry's law: In nanometer-confining media, gas solubility increases widely (see figure). H2, CH4 and C2H6 solubility values in two solvents are obtained by quantitative 1H NMR spectroscopy. A mass-balance model involving the gas,liquid interface zone agrees well with the observed variation. [source] | ||||||||||