Perfluorochemicals are widely used in the manufacturing and processing of a vast array of consumer goods, including electrical wiring, clothing, household and automotive products. Furthermore, relatively small quantities of perfluorochemicals are also used in the manufacturing of food-contact substances that represent potential sources of oral exposure to these chemicals. The most recognizable products to consumers are the uses of perfluorochemicals in non-stick coatings (polytetrafluoroethylene (PTFE)) for cookware and also their use in paper coatings for oil and moisture resistance. Recent epidemiology studies have demonstrated the presence of two particular perfluorochemicals, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in human serum at very low part per billion levels. These perfluorochemicals are biopersistent and are the subject of numerous studies investigating the many possible sources of human exposure. Among the various uses of these two chemicals, PFOS is a residual impurity in some paper coatings used for food contact and PFOA is a processing aid in the manufacture of PTFE used for many purposes including non-stick cookware. Little information is available on the types of perfluorochemicals that have the potential to migrate from perfluoro coatings into food. One obstacle to studying migration is the difficulty in measuring perfluorochemicals by routine conventional analytical techniques such as GC/MS or LC-UV. Many perfluorochemicals used in food-contact substances are not detectable by these conventional methods. As liquid chromatography-mass spectrometry (LC/MS) develops into a routine analytical technique, potential migrants from perfluoro coatings can be more easily characterized. In this paper, data will be presented on the types of perfluoro chemicals that are used in food packaging and cookware. Additionally, research will be presented on the migration or potential for migration of these chemicals into foods or food simulating liquids. Results from migration tests show mg kg À1 amounts of perfluoro paper additives/coatings transfer to food oil. Analysis of PTFE cookware shows residual amounts of PFOA in the low mg kg À1 range. PFOA is present in microwave popcorn bag paper at amounts as high as 300 mg kg À1.

Molecular dynamics simulations and vibrational sum frequency generation (VSFG) experiments in the methyl-stretching spectral region have been used to study acetonitrile at the silica/liquid, silica/vapor, and liquid/vapor interfaces. Our simulations show that, at the silica/liquid interface, acetonitrile takes on a considerably different structure than in the bulk liquid. The interfacial structure is reminiscent of a lipid bilayer, and this type of ordering persists for tens of Ångstroms into the bulk liquid. This result has important implications for processes involving solid/acetonitrile interfaces, such as heterogeneous catalysis and chromatographic separations. Fitting of VSFG data that have an extremely low nonresonant background contribution provides strong evidence for interfacial populations pointing in opposite directions at these interfaces, in agreement with our simulations. The picture developed from our simulations and experiments reconciles conflicting interpretations of data from previous experimental studies of interfacial acetonitrile.

Molecular dynamics simulations have previously described how the physical properties across immiscible liquid-liquid interfaces should converge from aqueous to organic limits, but these predictions have largely gone untested, owing to difficulties associated with probing buried interfaces. X-ray and neutron scattering experiments have created detailed pictures of molecular structure at these boundaries, but such scattering studies cannot probe how surface-altered solvent structures affect interfacial solvating properties. Given that surface-mediated solvent properties control interfacial solute concentrations and reactivities, identifying the characteristic dimensions of interfacial solvation is essential for formulating predictive models of solution phase surface chemistry. Here we use specially synthesized solvatochromic surfactants that act as 'molecular rulers' and resonance-enhanced second-harmonic generation to measure the dipolar width of weakly and strongly associating liquid-liquid interfaces. Dipolar width describes the distance required for a dielectric environment to change from one phase to another. Our results show that polarity converges to a nonpolar limit on subnanometre length scales across a water-cyclohexane interface. However, polarity across the strongly associating, water-1-octanol interface is dominated by a nonpolar, alkane-like region. These data call into question the use of continuum descriptions of liquids to characterize interfacial solvation, and demonstrate that interfacial environments can vary in a non-additive manner from bulk solution limits.

Vibrational sum frequency spectroscopy has been used to examine the vibrational structure of phosphatidylcholine monolayers adsorbed to a water−carbon tetrachloride interface. The surfactants employed in this study belong to a family of saturated, symmetric phosphatidylcholines with acyl chain lengths ranging from C12 to C18 in increments of two methylene units. Vibrational spectra provide direct information about the orientation and degree of order among the acyl chains of the adsorbed phosphatidylcholines. Differences among spectra recorded under various polarization conditions show that acyl chains do not exhibit long range order or preferred tilt angle. Rather, acyl chains within a tightly packed monolayer stand up with their methyl C3 axes aligned perpendicular to the interface. Relative methyl and methylene symmetric stretch band intensities show that order within the monolayer increases with increasing surface coverage. Temperature-dependent studies of monolayer order suggest that a barrier exists to organic solvent penetration of the acyl chain network of a tightly packed, adsorbed monolayer. At a liquid−liquid interface, shorter chain phosphatidylcholine species form monolayers more ordered than those of longer chain species, although the dependence of monolayer order on acyl chain length is small. This trend reverses in monolayers at the air−water interface where longer chain phosphatidylcholines form monolayers dramatically more ordered than those of their shorter chain counterparts. The disparity in behavior between monolayers at the liquid−liquid and air−water interfaces is interpreted as evidence of acyl chain solvation by the organic CCl4 solvent.

Near-infrared imaging and vibrational Raman scattering have been used to measure the susceptibility of Ni-based cermet anodes to carbon formation in solid oxide fuel cells (SOFCs) operating with methane and methanol fuels at 715 °C. These two complementary optical methods afford previously unavailable opportunities to monitor chemical and physical processes occurring in situ and in real time with molecular specificity and spatial resolution. Imaging and spectroscopic data show that when the cell is held at open circuit voltage carbon forms within one minute of methanol or methane being introduced to the anode chamber. Raman spectra identify these deposits as highly ordered graphite based on a single sharp feature in the vibrational spectrum near 1580 cm−1. While graphite formed from methane remains highly ordered regardless of exposure duration, graphite formed from sustained exposure to methanol begins to show evidence of structural disorder inferred from the appearance of a weak feature at 1340 cm−1. This lower frequency vibrational band has been assigned previously to the presence of grain boundaries and/or site defects in a graphite lattice. Correlating the growth of intensity in the Raman spectra with exposure time quantifies the kinetics of carbon deposition and suggests that carbon formed from methanol grows via two distinct mechanisms. Thermal imaging data show that carbon deposition is endothermic and reduces anode temperatures. This effect is more pronounced for methanol (ΔT = −5.5 °C) than methane (ΔT = −0.5 °C). These results agree with data from vibrational Raman experiments showing that exposure to methanol leads to significantly more carbon deposition. Polarizing the cell reduces the amount of carbon deposited. This effect is reversible and more significant for methanol. The effects of the graphite formed from methanol are evident in electrochemical impedance data but less apparent in voltammetry experiments. In contrast, graphite formed from methane has only modest impact on device performance. Collectively, these studies address long-standing questions about the tendency of methanol to form carbon on eletrocatalytic SOFC anodes and the consequences of this chemistry on device performance.