Wet air regeneration of PAC: Comparison of carbons with different surface oxygen characteristics

Surface oxygen has an important effect on the wet air regeneration (WAR) of powdered activated carbons (PAC) and on the adsorption properties of the regenerated PAC. Virgin and phenanthrene-loaded PACs were regenerated in a bench-scale reactor, and then analyzed to determine surface oxygen content, adsorption capacity, and extent of phenanthrene oxidation.Even though the virgin wood-base (WB) and lignite-base (LB) PACs had about the same oxygen content, the oxygen content of the WB PAC increased more than twice as much as the LB PAC during regeneration. The difference was caused by the larger amount of CO₂-evolving oxides that formed on the WB PAC. WAR reduces the capacity of PAC for p-nitrophenol (PNP). Removing the surface oxides had varying effects on the carbon's capacity for PNP. Also, adsorbed phenanthrene was more easily oxidized on the WB PAC than on the LB PAC during regeneration.     

Effects of primary sludge particulate (PSP) entrapment on ultrasonic (20 kHz) disinfection of Escherichia coli

The role of primary sludge particulates (PSPs) in ultrasonic disinfection of Escherichia coli (E. coli) was investigated. Entrapment of E. coli by PSP was directly observed through scanning electron microscope (SEM) after E. coli and PSP were incubated together in water for 24 h at 35 °C. Entrapment coefficient was proposed for the first time to reflect the ability of PSP to entrap E. coli and was estimated as 1.4 × 10³ CFU/mg PSP under our experimental conditions. Ultrasonication (20 kHz) of different E. coli-PSPs solutions showed that the entrapped E. coli cells were protected by PSP from ultrasonication and the unentrapped cells were not. However, the protection of entrapped E. coli cells gradually decreased as ultrasonication proceeded, suggesting the ability of power ultrasonication to deprotect the entrapped E. coli cells. SEM studies suggested a two-step mechanism for ultrasonic (20 kHz) disinfection of entrapped E. coli: breakdown of the protective PSP refugia and disinfection of the exposed E. coli cells. This research will enable more informed decisions about disinfection of aqueous samples where porous PSP are present.     

Future directions in physiochemical modeling of the thermodynamics of polyelectrolyte coacervates

We review theories of polyelectrolyte (PE) coacervation, which is the spontaneous association of oppositely charged units of PEs and phase separation into a polymer-dense phase in aqueous solution. The simplest theories can be divided into “physics-based” and “chemistry-based” approaches. In the former, PEs are treated as charged, long-chain, molecules, defined by charge level, chain length, and chain flexibility, but otherwise lacking chemical identity, with electrostatic interactions driving coacervation. The “chemistry-based” approaches focus on the local interactions between the species for which chemical identity is critical, and describe coacervation as the result of competitive local binding interactions of monomers and salts. In this article, we show how these approaches complement each other by presenting recent approaches that take both physical and chemical effects into account. Finally, we suggest future directions toward producing theories that are made quantitatively predictive by accounting for both long range electrostatic and local chemically specific interactions.     

Topical safety and vasoconstrictive assay-based bioequivalence of a new reformulated mometasone cream

Objectives: A new improved mometasone furoate (Elocon?) cream with an emulsification system that produces a stable emulsion has been developed. In order to register the product in various markets, it was essential to ensure the cream was topically well tolerated and that it was bioequivalent to the reference product.

Methods: Phase I clinical studies were performed to assess the local safety and tolerability upon multiple dosing of this new cream as well as to assess the single-dose bioequivalence relative to the marketed product. Bioequivalence was assessed using a vasoconstrictive assay (VCA) after a dose-duration pilot study was completed with the marketed Elocon cream.

Key findings: The new mometasone cream and its vehicle were nonirritating in healthy subjects during 21-day patch application (MCII <0.025). The positive control was moderately irritating in the same study. The pivotal VCA study enrolled 162 subjects with 105 detectors included in the analysis of bioequivalence. In the 105 detectors, the ratio (×100%) of AUEC values at ED₅₀ for test vs. standard (90% CI) was 112.91% (105.55, 120.87), within the bioequivalence criteria of (80, 125).

Conclusions: These studies supported the registration of reformulated mometasone cream in various markets.