Characterization of superficial modification of ferrous rusted substrates subjected to dechlorination-electrochemical process

Preservation of archaeological artefacts after their removal from saline media is a difficult task due to the chloride content of the oxide layers which are unstable in atmospheric conditions, especially if the relative humidity exceeds 85%. For this reason, removal of chlorides from rust layers is one of the priorities of conservationists or restorers of historical artefacts. However, removal of chloride ions is not an easy procedure because of the many considerations involved in the process. In this research, artificially pre-rusted iron samples and an actual historical cannonball were subject to a dechlorination process in a potassium hydroxide solution to measure constant chloride release in a bulk solution. After the chloride removal process, a commercial protective layer was applied to the rust for stabilization purposes. It was calculated that the kinetics of the dechlorination process is driven by diffusion behaviour following Fick’s second law. When this diffusion process prevails, the dechlorination extraction affects the integrity of rust layers as is demonstrated with scanning electron microscopy and X-ray diffraction analyses. It was proven that the chloride removal procedure causes the studied iron layers to stiffen, provoking superficial modification and, in some cases, fractures of the rust. By means of electrochemical impedance spectroscopy it was calculated that the magnitude of the positive effect of the dechlorinated samples depends on the protective features of the rust. Therefore, this research reveals that an efficient chloride removal procedure depends on the electrochemical properties of the dechlorination process and the initial morphology of the iron rust.     

Facile preparation of highly dispersed Pt nanoparticles supported on heteroatom-containing porous carbon nanospheres and their catalytic properties for the reduction of 4-nitrophenol

Heteroatom-containing porous carbon nanospheres with a high surface area were firstly fabricated by pyrolysis of poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) (PZS) nanospheres which were fabricated by a facile polycondensation between hexachlorocyclotriphosphazene and 4,4′-sulfonydiphenol. Then the porous carbon nanosphere-supported Pt nanoparticles (Pt NPs@C-PZS) were synthesized by a simple microwave reduction method, during which Pt NPs were highly dispersed on the surface of carbon supports. The surface morphologies and chemical composition of the as-obtained C-PZS and Pt NPs@C-PZS nanocomposites were characterized by SEM, TEM, XRD, XPS, and Raman spectroscopy. Characterization results showed that the Pt NPs with an average diameter of 2 nm was well anchored onto the surface of C-PZS nanospheres. In addition, the as-prepared Pt NPs@C-PZS nanocomposites exhibited an excellent catalytic capability towards the reduction of 4-nitrophenol to 4-aminophenol by excessive sodium borohydride (NaBH₄) at room temperature.     

Conjugated heat transfer investigation with racetrack-shaped jet hole and double swirling chamber in rotating jet impingement

A numerical study is performed to investigate the effects of jet hole shape and channel geometry on impingement cooling for both stationary and rotating condition. Two hole shapes and two channel geometries are introduced to counteract the adverse effects of centrifugal force and Coriolis force which are induced by rotation. Both the fluid and solid part are considered for realizing the conjugate heat transfer simulation. The unsteady k-ω SST turbulence model was employed to obtain the time-averaged Nusselt number distributions, time-averaged temperature and temperature gradient fields and the turbulent flow structure. The results show that the cooling jet from the racetrack-shaped hole can effectively withstand the intensive streamwise crossflow to enhance the heat transfer. The double swirling chamber (DSC) channel significantly improves the heat transfer characteristics on the cambered surface and diminishes the adverse effects of the Coriolis force. The high Nu number region is expanded while the temperature uniformity is improved. The combination of the racetrack-shaped hole and DSC channel provides the highest heat transfer among the four cases. The averaged Nu numbers on both the leading and trailing sides for all tested cases show obvious downtrend as rotation number increases, especially at high Reynolds number.     

Use of polymers for taste-masking pediatric drug products

Many drugs are bitter and overcoming this bitter taste is a major barrier in developing a successful product, especially for pediatric patients. Approaches to mask taste include changing taste perception, creating a physical barrier to separate the drug from interacting with taste buds, and changing drug solubility. This review is focused on polymers and the different ways these materials are used to achieve taste masking. Attention is given to systems that are easily swallowed, as swallowability is another concern in developing palatable products for pediatrics. Variables that should be considered when selecting a taste-masking approach are also presented.     

Partitioning of PCBs from air to clothing materials in a Danish apartment

Polychlorinated biphenyl (PCB) contamination of buildings continues to pose an exposure threat, even decades after their application in the form of calks and other building materials. In this research, we investigate the ability of clothing to sorb PCBs from contaminated air and thereby influence exposure. The equilibrium concentration of PCB‐28 and PCB‐52 was quantified for nine used clothing fabrics exposed for 56 days to air in a Danish apartment contaminated with PCBs. Fabric materials included pure materials such as cotton and polyester, or blends of polyester, cotton, viscose/rayon, and/or elastane. Air concentrations were fairly stable over the experimental period, with PCB‐28 ranging from 350 to 430 ng/m³ and PCB‐52 ranging from 460 to 550 ng/m³. Mass accumulated in fabric ranged from below detection limits to 4.5 mg/g of fabric. Cotton or materials containing elastane sorbed more than polyester materials on a mass basis. Mass‐normalized partition coefficients above detection limits ranged from 10^5.7 to 10^7.0 L/kg. Clothing acts as a reservoir for PCBs that extends dermal exposure, even when outside or in uncontaminated buildings.     

Oxygenated VOCs,aqueous chemistry,and potential impacts on residential indoor air composition

Dampness affects a substantial percentage of homes and is associated with increased risk of respiratory ailments; yet, the effects of dampness on indoor chemistry are largely unknown. We hypothesize that the presence of water‐soluble gases and their aqueous processing alters the chemical composition of indoor air and thereby affects inhalation and dermal exposures in damp homes. Herein, we use the existing literature and new measurements to examine the plausibility of this hypothesis, summarize existing evidence, and identify key knowledge gaps. While measurements of indoor volatile organic compounds (VOCs) are abundant, measurements of water‐soluble organic gases (WSOGs) are not. We found that concentrations of total WSOGs were, on average, 15 times higher inside homes than immediately outside (N = 13). We provide insights into WSOG compounds likely to be present indoors using peer‐reviewed literature and insights from atmospheric chemistry. Finally, we discuss types of aqueous chemistry that may occur on indoor surfaces and speculate how this chemistry could affect indoor exposures. Liquid water quantities, identities of water‐soluble compounds, the dominant chemistry, and fate of aqueous products are poorly understood. These limitations hamper our ability to determine the effects of aqueous indoor chemistry on dermal and inhalation exposures in damp homes.