Transformation of silver nanoparticles released from skin cream and mouth spray in artificial sweat and saliva solutions: particle size, dissolution, and surface area

The use of silver nanoparticles (Ag NPs) in consumer products can result in diffuse environmental dispersion of both NPs and ionic silver. This study investigated the transformation of Ag NPs present in two consumer products (skin cream, mouth spray) in terms of release of Ag NPs and ionic silver and changes in particle size in artificial sweat and saliva solutions. Large differences in silver release were observed with the smaller sized Ag NPs in mouth spray releasing more silver compared with the Ag NPs of the skin cream. Substantial particle agglomeration took place in both artificial sweat and saliva, forming large-sized agglomerates (> 100 nm). The amount of dissolved silver in solution after 24 h was less than 10% of the total amount of Ag NPs for both products. The results show that the Ag NPs of these consumer products will largely remain as NPs even after 24 h of skin or saliva contact. The use of normalization by geometric surface area of the particles was tested as a way to compare dissolution for Ag NPs of different characteristics, including pristine, bare, as well as PVP-capped Ag NPs. Normalization of silver dissolution with the geometric surface area was shown promising, but more extensive studies are required to unambiguously conclude whether it is a way forward to enable grouping of the dissolution behavior of Ag NPs released from consumer products.

Effect of Reduced Universal Adhesive Application Time on Enamel Bond Fatigue and Surface Morphology

SUMMARY Objective: The purpose of this study was to evaluate the effect of reduced application times of universal adhesives on enamel bond fatigue and surface morphology of the treated enamel with constant force atomic force microscopy (AFM). Methods: Four universal adhesives—Adhese Universal (AU), Clearfil Universal Bond Quick (CU), G-Premio Bond (GP), and Scotchbond Universal Adhesive (SU)—were evaluated in a laboratory for their ability to adhesively bond resin composite to enamel. Shear bond strengths were initially determined using 15 specimens per test group for each adhesive. Shear fatigue strengths were then determined using 20 specimens per test group for each the adhesives. The fatigue specimens were loaded using a sine wave at a frequency of 20 Hz for 50,000 cycles or until failure occurred. AFM observations, surface Ra roughness measurements, and geometric surface area evaluations of enamel surface treated with the adhesive agents were also conducted. Results: A strong relationship was found between the initial shear bond strength and shear fatigue strength for enamel surface Ra roughness but not for geometric surface area. The initial shear bond strength and shear fatigue strength of CU and GP were not influenced by different application times, unlike those of AU and SU. While the surface area of enamel treated with the adhesive agents was not significantly influenced by different application times and type of adhesive, surface Ra roughness of the enamel in the AU and SU groups significantly increased with increasing application time, unlike CU and GP. Conclusions: The results of this study suggest that universal adhesives, used with reduced application times, have adequate Ra surface roughness to provide sufficient resistance to enamel bond fatigue at application times from <1 second to 20 seconds, while the geometric surface area of adhesive-treated enamel did not show any significant changes at these different application times.

Total Oxidation of Dichloromethane over Silica Modified Alumina Catalysts Washcoated on Ceramic Monoliths

Silica modified alumina was used in this study for coating of a cordierite monolith substrate with two different channel densities. The performance of the prepared monolith catalysts was evaluated in catalytic total oxidation of dichloromethane before and after Pt impregnation. The characteristics similar to the powder form catalysts were kept rather successfully after washcoating the monolith as evidenced by electron microscopy (FESEM) and N2 physisorption. A dichloromethane (DCM) conversion of higher than 80% at 500 °C was reached over all the catalysts with 200 cpsi. The maximum conversion was obtained with the catalyst containing 10 mol % of silica. The total amount of major byproducts (CO, CH3Cl and CH2O) were slightly decreased by increasing the silica loading, and remarkably after Pt impregnation. After impregnation of Pt, the HCl yields were increased for two samples with the higher loading of silica (10 and 15 mol %) and reached the maximum when silica loading was 10%. Even though Pt impregnation did not significantly affect the DCM conversion, it improved the selectivity. Comparison between the two substrates (200 and 600 cpsi) evidenced that the key parameters of the monolith influencing the DCM oxidation are low value of open fraction area, hydraulic diameter, thermal integrity factor and high value of mechanical integrity factor and geometric surface area.

A Molecular Dynamics Study on the Effects of Nanostructural Clearances on Thermal Resistance at a Liquid-Solid Interface

The effects of the surface structures and the surface structural clearances at the nanometer scale on the thermal resistance at a liquid water-solid interface, as well as the self-diffusion behaviors of liquid molecules, were investigated directly by the non-equilibrium classical molecular dynamics simulations. When the potential parameter between liquid molecules and nanostructure atoms is equal to that between liquid molecules and solid wall atoms, the geometric surface area change depending on the nanostructures as well as their clearances and the self-diffusion coefficient change of the liquid molecules at the interface depending on the nanostructural clearances cause the thermal resistance change depending on the nanostructures at the liquid-solid interface. When the potential parameter between liquid molecules and nanostructure atoms is different from that between liquid molecules and solid wall atoms, the interfacial thermal resistance is dependent on the potential parameter between liquid molecules and nanostructure atoms itself rather than the geometric surface area in a molecular scale.