Photocatalytic Degradation of 4,4′-Isopropylidenebis(2,6-dibromophenol) on Magnetite Catalysts vs. Ozonolysis Method: Process Efficiency and Toxicity Assessment of Disinfection By-Products

Flame retardants have attracted growing environmental concern. Recently, an increasing number of studies have been conducted worldwide to investigate flame-retardant sources, environmental distribution, living organisms’ exposure, and toxicity. The presented studies include the degradation of 4,4′-isopropylidenebis(2,6-dibromophenol) (TBBPA) by ozonolysis and photocatalysis. In the photocatalytic process, nano- and micro-magnetite (n-Fe₃O₄ and μ-Fe₃O₄) are used as a catalyst. Monitoring of TBBPA decay in the photocatalysis and ozonolysis showed photocatalysis to be more effective. Significant removal of TBBPA was achieved within 10 min in photocatalysis (ca. 90%), while for ozonation, a comparable effect was observed within 70 min. To determine the best method of TBBPA degradation concentration on COD and TOC, the removals were examined. The highest oxidation state was obtained for photocatalysis on μ-Fe₃O₄, whereas for n-Fe₃O₄ and ozonolysis, the COD/TOC ratio was lower. Acute toxicity results show noticeable differences in the toxicity of TBBPA and its degradation products to Artemia franciscana and Thamnocephalus platyurus. The EC₅₀ values indicate that TBBPA degradation products were toxic to harmful, whereas the TBPPA and post-reaction mixtures were toxic to the invertebrate species tested. The best efficiency in the removal and degradation of TBBPA was in the photocatalysis process on μ-Fe₃O₄ (reaction system 1). The examined crustaceans can be used as a sensitive test for acute toxicity evaluation.     

The performance of a distributed combat simulation with the time warp operating system

This paper analyzes the performance of a discrete-event combat simulation executed on a parallel processor under control of the Time Warp Operating System. Time Warp is in a class of distributed simulation methods called Optimistic methods which have proven to be useful over a wide range of simulations. The combat simulation used for this performance study, called STB88, is a division-corps model incorporating a number of different types of computations. The speed-up for three versions of this model on the Caltech/JPL Mark III Hypercube and the BBN Butterfly parallel processors was measured relative to an efficient sequential execution of the same model on the same hardware. The results indicate that STB88 version 1 achieves a speed-up of 28.6 on 60 Mark III processors, while STB88 version 2 achieves a speed-up of 36.8 on 100 Butterfly processors. Version 3 of STB88 achieved a speed-up of 38.5 on 128 Mark III processors. The versions differed only in their interface to Time Warp. On the Butterfly, the sequential execution completed in 2 hours, while the 100 processor execution completed in 3.2 minutes.     

Post-synthetic modification of conjugated microporous polymers

Control over the surface functionality and microporosity in conjugated microporous polymers (CMPs) has been achieved by the post-synthetic modification of amines into amides of with different alkyl chains, one of which was chiral. The surface areas, pore volumes, carbon dioxide uptakes and isosteric heat of adsorption for carbon dioxide can be rationally tuned.     

Synthesis and thermal decomposition of potassium tetraamidoboranealuminate,K[Al(NH2BH3)4]

A new potassium tetraamidoboranealuminate, K[Al(NH₂BH₃)₄], has been synthesized by a mechanochemical reaction between KAlH₄ and NH₃BH₃. The compound, K[Al(NH₂BH₃)₄], crystallizes in a triclinic unit cell with space group symmetry P?1. The crystal structure consists of [K(NH₂BH₃)₆]^5? octahedra which facilitate the bridging between K⁺ in 1D chains, while also bridging K⁺ to Al³⁺ to connect the 1D chains in a 3D network. Thermal analysis reveals that K[Al(NH₂BH₃)₄] decomposes in two exothermic steps at T ～ 94 and 138 °C and releases primarily hydrogen. The total gas release amounts to ～6.0 wt% H₂. The decomposition products are investigated ex situ by powder X-ray diffraction, infrared spectroscopy, and ¹¹B and ²⁷Al NMR and identified as KBH₄ and amorphous phases, possibly BN₃, N₂BH, and/or NBH₂ whereas aluminum is found in four-, five-, and six-fold coordination. Unfortunately, the decomposed sample shows no hydrogen absorption at T = 260 °C and p(H₂) = 110 bar.     

Potentiometric sensor for the indomethacin determination

A potentiometric indomethacin-selective sensor based on Rhodamine B indomethacinate ion-pair (IP) as a membrane carrier is reported. Influences of the membrane composition, pH, and possible interfering ions were investigated on the response properties of the electrode. The sensor exhibits significantly enhanced response toward indomethacinate ions over the concentration range 1 × 10^? 4 mol L^? 1 to 5 × 10^? 2 mol L^? 1 with a lower detection limit (LDL) of 3 × 10^? 5 mol L^? 1 and a slope of ? 60 mV decade^? 1. Fast and stable response, good reproducibility, long-term stability, applicability over a pH range of 6–10 is demonstrated. The proposed electrode shows good discrimination of indomethacin from several inorganic and organic ions. The proposed sensor has been applied for the direct potentiometric determination of indomethacin in pharmaceutical preparations.     

Variation of the Microwave Brightness Temperature of Sea Surfaces Covered with Mineral And Monomolecular Oil Films

Airborne microwave radiometer measurements over mineral and monomolecular oil films and adjacent clean sea surfaces are reported. An artificial crude-oil spill experiment in the New York Bight area showed a brightness temperature increase of the sea surface at 1.43 GHz as expected from a multilayered system with different dielectric constants. However, a monomolecular surface-film experiment with oleyl alcohol conducted in the North Sea during MARSEN in 1979 showed a strong brightness temperature depression at 1.43 GHz and no change in brightness temperature at 2.65 GHz. It is postulated that the monomolecular layer, because of its physical and chemical properties, polarized the underlying water molecules so strongly that the emissivity decreased from 0.31 to 0.016. It is estimated that the effective dielectric constant changed from 90 to 5.2 × 104. Because these phenomena occurred at 1.43 GHz it may be concluded that this frequency is very close to the center of a new anomalous dispersion region resulting from a restructuring of the water layer below the surface film.