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Celesta Fong

Publications and source records attributed to Celesta Fong.

5 recordsLinked to original sources

Many protic ionic liquids mediate hydrocarbon-solvent interactions and promote amphiphile self-assembly.

A large number of protic ionic liquids (PILs) have been found to mediate solvent-hydrocarbon interactions and promote amphiphile self-assembly. Hexagonal, cubic, and lamellar lyotropic liquid crystalline phases were observed in PIL-hexadecyltrimethylammonium bromide systems. The driving force for the formation of the self-assembled aggregate structures has been attributed to an entropic contribution to the free energy of association, analogous to the hydrophobic effect in water. The specific aggregate structures formed depend upon the cationic and anionic components of the PIL and their interactions with the amphiphiles.

Anions↗

Protic ionic liquids: solvents with tunable phase behavior and physicochemical properties.

The phase behavior, including glass, devitrification, solid crystal melting, and liquid boiling transitions, and physicochemical properties, including density, refractive index, viscosity, conductivity, and air-liquid surface tension, of a series of 25 protic ionic liquids and protic fused salts are presented along with structure-property comparisons. The protic fused salts were mostly liquid at room temperature, and many exhibited a glass transition occurring at low temperatures between -114 and -44 degrees C, and high fragility, with many having low viscosities, down to as low as 17 mPa.s at 25 degrees C, and ionic conductivities up to 43.8 S/cm at 25 degrees C. These protic solvents are easily prepared through the stoichiometric combination of a primary amine and Brønsted acid. They have poor ionic behavior when compared to the far more studied aprotic ionic liquids. However, some of the other physicochemical properties possessed by these solvents are highly promising and it is anticipated that these, or analogous protic solvents, will find applications beyond those already identified for aprotic ionic liquids. This series of protic fused salts was employed to determine the effect of structural changes on the physicochemical properties, including the effect of hydroxyl groups, increasing alkyl chain lengths, branching, and the differences between inorganic and organic anions. It was found that simple structural modifications provide a mechanism to manipulate, over a wide range, the temperature at which phase transitions occur and to specifically tailor physicochemical properties for potential end-use applications.

Amines↗

Nonionic urea surfactants: formation of inverse hexagonal lyotropic liquid crystalline phases by introducing hydrocarbon chain unsaturation.

The homo-interaction between urea moieties residing in close proximity to each other generally results in very strong intermolecular hydrogen bonding. The bifurcated hydrogen bonding exhibited by n-alkyl substituted ureas means that for those urea surfactants possessing medium and long hydrocarbon chain substituents the crystal to isotropic liquid melting point is high and the solubility in water is very low, compared to other similar chain length nonionic surfactants. In addition, saturated n-alkyl urea surfactants do not form lyotropic liquid crystalline phases in water. In this work the strong intermolecular hydrogen bonding of the urea headgroup has been ameliorated through the introduction of unsaturated hydrocarbon chains, viz., oleyl (cis-octadec-9-enyl), linoleyl (cis, cis-octadec-9,12-dienyl), and linolenyl (cis, cis, cis-octadec-9,12,15-trienyl) with one, two, and three carbon double bonds, respectively. Unsaturation in the C18 urea surfactants lowers the melting point and promotes an inverse hexagonal phase, in oleyl urea-water and linoleyl urea-water systems, which is thermodynamically stable in excess water. As the degree of unsaturation is increased to three in linolenyl urea, there is a tendency for autoxidation/polymerization. The occurrence of an inverse hexagonal phase in the nonionic urea surfactant-water systems has been rationalized in terms of both local molecular and global self-assembled aggregate packing constraints.

Journal Article↗

Nonionic urea surfactants: influence of hydrocarbon chain length and positional isomerism on the thermotropic and lyotropic phase behavior.

The thermotropic and lyotropic phase behavior of 1- and 5-decyl urea, and 1-, 2-, 4-, and 6-dodecyl urea have been studied. This allowed the effect of positional isomerism to be examined. Intermolecular hydrogen bonding by the urea moiety is the dominant factor in determining the solid-state thermal behavior and crystal solubility boundary of these linear nonionic surfactants. The positional isomers where the urea moiety was not situated at the terminus of the hydrocarbon chain exhibited higher melting points than the 1-alkyl ureas. This has been rationalized by postulating interdigitated chains in the solid state. In the urea surfactant-water systems, three phases are observed, viz. crystalline solid, a dilute aqueous solution of the alkyl urea, and an isotropic liquid. The last two phases coexist in the low-surfactant, high-temperature region of the binary phase diagram. An overview of structure-property correlations for linear nonionic urea surfactants is presented in light of the new physicochemical data obtained for the decyl urea and dodecyl urea positional isomers.

Journal Article↗

X-ray and neutron reflectometry study of glow-discharge plasma polymer films.

Radio-frequency glow-discharge plasma polymer thin films of allylamine (AA) and hexamethyldisiloxane (HMDSO) were prepared on silicon wafers and analyzed by a combination of X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), X-ray reflectometry (XRR), and neutron reflectometry (NR). AFM and XRR measurements revealed uniform, smooth, defect-free films of 20-30 nm thickness. XPS measurements gave compositional data on all elements in the films with the exception of hydrogen. In combination with XRR and NR, the film composition and mass densities (1.46 and 1.09 g cm(-)(3) for AA and HMDSO, respectively) were estimated. Further NR measurements were conducted with the AA and HMDSO films in contact with water at neutral pH. Three different H(2)O/D(2)O mixtures were used to vary the contrast between the aqueous phase and the polymer. The amount of water penetrating the film, as well as the number of labile protons present, was determined. The AA film in contact with water was found to swell by approximately 5%, contain approximately 3% water, and have approximately 24% labile protons. The HDMSO polymer was found to have approximately 6% labile protons, no thickness increase when in contact with water, and essentially no solvent penetration into the film. The difference in the degree of proton exchange within the films was attributed to the substantially different surface and bulk chemistries of the two films.

Journal Article↗