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The response of polysiloxane materials to volatile organic compounds (VOCs) including benzene, toluene, ethylbenzene, and toluene (BTEX), as well as cyclohexane, acetone, methanol and isopropanol is studied using thin film large-angle refractometry. Refractive index and thickness changes are measured to quantify the diffusion rate and partition coefficients associated with the absorption and desorption of VOC vapours into polydimethylsiloxane (PDMS) and polydiphenylsiloxane (PDPS) - PDMS copolymer films. Absorption of volatile solvent vapours into siloxane polymers is found to follow two distinct mechanisms with different absorption rates. These mechanisms are also associated with different excess volumes of mixing and may be accompanied by a polymer restructuring step.

Langmuir 34(49), 14858 - 14868 (2018). doi:10.1021/acs.langmuir.8b01635 special issue: "Nucleic Acids Nanoscience at Interfaces", Colloidal nucleic acid carrier systems based on cationic lipids are a promising pharmaceutical tool in the implementation of gene therapeutic strategies. This study demonstrates the complex behavior of DNA at the lipid–solvent interface facilitating structural changes of the lyotropic liquid-crystalline phases. For this study, the structural properties of six malonic acid based cationic lipids were determined using small- and wide-angle X-ray scattering (SAXS and WAXS) as well as differential scanning calorimetry (DSC). Selected lipids (lipid 3 and lipid 6) with high nucleic acid transfer activity have been investigated in detail because of the strong influence of the zwitterionic helper lipid 1,2-di(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine (DOPE) on the structural properties as well as of the complex formation of lipid–DNA complexes (lipoplexes). In the case of lipid 3, DNA stabilizes a metastable cubic mesophase with Im3m symmetry and an Im3m Q$_{α}^c$ lipoplex is formed, which is rarely described for DNA lipoplexes in literature. In the case of lipid 6, a cubic mesophase with Im3m symmetry turns into a fluid lamellar phase while mixing with DOPE and complexing DNA., Published by ACS Publ., Washington, DC

The uptake and release of sorbates into films and coatings is typically accompanied by changes of the films' refractive index and thickness. We provide a comprehensive model to calculate the concentration of the sorbate from the average refractive index and the film thickness, and validate the model experimentally. The mass fraction of the analyte partitioned into a film is described quantitatively by the Lorentz-Lorenz equation and the Clausius-Mosotti equation. To validate the model, the uptake kinetics of water and other solvents into SU-8 films (d = 40-45 μm) were explored. Large-angle interferometric refractometry measurements can be used to characterize films that are between 15 μm to 150 μm thick and, Fourier analysis, is used to determine independently the thickness, the average refractive index and the refractive index at the film-substrate interface at one-second time intervals. From these values the mass fraction of water in SU-8 was calculated. The kinetics were best described by two independent uptake processes having different rates. Each process followed one-dimensional Fickian diffusion kinetics with diffusion coefficients for water into SU-8 photoresist film of 5.67 × 10(-9) cm(2) s(-1) and 61.2 × 10(-9) cm(2) s(-1).