Reaction Kinetics and Combustion Dynamics of I4O9 and Aluminum Mixtures.

Tetraiodine nonoxide (I4O9) has been synthesized using a dry approach that combines elemental oxygen and iodine without the introduction of hydrated species. The synthesis approach inhibits the topochemical effect promoting rapid hydration when exposed to the relative humidity of ambient air. This stable, amorphous, nano-particle material was analyzed using differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) and showed an exothermic energy release at low temperature (i.e., 180 °C) for the transformation of I4O9 into I2O5. This additional exothermic energy release contributes to an increase in overall reactivity of I4O9 when dry mixed with nano-aluminum (Al) powder, resulting in a minimum of 150% increase in flame speed compared to Al + I2O5. This study shows that as an oxidizer, I4O9 has more reactive potential than other forms of iodine(V) oxide when combined with Al, especially if I4O9 can be passivated to inhibit absorption of water from its surrounding environment.

Arsenic removal by electrocoagulation using combined Al-Fe electrode system and characterization of products.

Combination of electrodes, such as aluminum and iron in a single electrochemical cell provide an alternative method for removal of arsenic from water by electrocoagulation. The removal process has been studied with a wide range of arsenic concentration (1-1000 ppm) at different pH (4-10). Analysis of the electrochemically generated by-products by XRD, XPS, SEM/EDAX, FT-IR, and Mössbauer Spectroscopy revealed the expected crystalline iron oxides (magnetite (Fe3O4), lepidocrocite (FeO(OH)), iron oxide (FeO)) and aluminum oxides (bayerite (Al(OH)3), diaspore (AlO(OH)), mansfieldite (AlAsO(4).2(H2O)), as well as some interaction between the two phases. The amorphous or very fine particular phase was also found in the floc. The substitution of Fe3+ ions by Al3+ ions in the solid surface has been observed, indicating an alternative removal mechanism of arsenic in these metal hydroxides and oxyhydroxides by providing larger surface area for arsenic adsorption via retarding the crystalline formation of iron oxides.

Experimental and theoretical study of the atmospherically important O2-H2O complex.

The theoretically predicted water-oxygen van der Waals adduct has been experimentally confirmed by vibrational characterization using matrix isolation spectroscopic studies at 10 K. Vibrational bands for asymmetric and symmetric OH-stretching for this adduct have been found at 3728 cm(-1) and 3639 cm(-1), respectively. Theoretical calculations performed with Gaussian 98 software at the MP2/6-311++G(2d,2p) level of theory support the alternative structure of the hydrated complex proposed by this study.

Arsenic removal via electrocoagulation from heavy metal contaminated groundwater in La Comarca Lagunera México.

Arsenic contamination is an enormous worldwide problem. A large number of people dwelling in Comarca Lagunera, situated in the central part of northern México, use well water with arsenic in excess of the water standard regulated by the Secretary of Environment and Natural Resources of México (SEMARNAT), to be suitable for human health. Individuals with lifetime exposure to arsenic develop the classic symptoms of arsenic poisoning. Among several options available for removal of arsenic from well water, electrocoagulation (EC) is a very promising electrochemical treatment technique that does not require the addition of chemicals or regeneration. First, this study will provide an introduction to the fundamental concepts of the EC method. In this study, powder X-ray diffraction, scanning electron microscopy, transmission Mössbauer spectroscopy and Fourier transform infrared spectroscopy were used to characterize the solid products formed at iron electrodes during the EC process. The results suggest that magnetite particles and amorphous iron oxyhydroxides present in the EC products remove arsenic(III) and arsenic(V) with an efficiency of more than 99% from groundwater in a field pilot scale study.

Fundamentals, present and future perspectives of electrocoagulation.

Electrocoagulation is an electrochemical wastewater treatment technology that is currently experiencing both increased popularity and considerable technical improvements. There has been relatively little effort to better understand the fundamental mechanisms of the processes, particularly those that could provide design parameters to optimize the performances of this relatively simple and inexpensive technique. In a research programme to delineate the mechanisms of the fundamental processes involved in, the authors have realized that the technology has been insufficiently reviewed with emphasis on the fundamentals and their relationship to the performance of this technology. This paper presents an in-depth discussion and consideration of the factors that need to be addressed for optimum performance of this technology. Recent improvements of this technique and the theoretical model studies are also reviewed.

Treatment of orange II azo-dye by electrocoagulation (EC) technique in a continuous flow cell using sacrificial iron electrodes.

This paper describes the EC treatment of orange II dye solution in a flow cell using sodium chloride as an internal electrolyte. In this technique dye solutions were passed through a flow-through EC apparatus consisting of a flow-through cell, the electrode assembly, the feed pump and the DC power supply unit. The cell contained five parallel iron electrodes, which form four parallel cells. Experiments were run at 25 degrees C under various electrolyte concentrations, dye concentrations, current density, flow rate of the solution, and pH at dc current range of 2-5A. Various number of recycles of the treated dye solution were also performed at the same dc current range. Optimum conditions to get high removal efficiency were experimentally determined. It was found that 98.5% of the dye was removed from the solution under the optimum conditions. The residue from a blank run (pH = 7.3) and a dye added run (pH = 8.5) were collected by vacuum filtration and analyzed by XRD after drying in a vacuum desiccator. The XRD data indicated the presence of mainly maghemite (gamma-Fe2O3) and magnetite (Fe3O4) in the residue. However, there is not much difference between the X-ray diffractograms of the blank sample and the dye-containing residue to warrant any conclusions therefrom with regard to the interactions between the oxides and the dye molecules.

An X-ray diffraction (XRD) and Fourier transform infrared spectroscopic (FT-IR) investigation of the long-term effect on the solidification/stabilization (S/S) of arsenic(V) in Portland cement type-V.

The long-term effects on solidification/stabilization (S/S) of As5+-bearing oxyanions (AsO4(3)-) in Portland cement type-V (OPC) have been investigated by X-ray diffraction (XRD) and Fourier transform infrared spectroscopic (FT-IR) techniques. The results of this study confirm our previous results that the early hydration of cement is inhibited by the presence of AsO4(3)-, and that the inhibition is mainly caused by the formation of highly insoluble Ca3(AsO4)2 on the surface of hydrating cement particles. Arsenate analog of ettringite [Ca6(Al2O6)(SO4)3 x 32H2O] was identified in the early stages of hydration of pure Portland cement and As(V)-treated Portland cement [OPC-As(V)], but not in 10-year-old similar samples. The XRD and FT-IR results indicated interactions of oxyanions and cement particles to produce minor quantities of As5+-bearing compounds in fresh as well as in 10-year-old samples. New As5+-bearing phases, NaCaAsO4 x 7.5H2O and Ca5(AsO4)3OH were identified in the 10-year-old OPC-As(V) samples by XRD analyses. Based on these results it is concluded that Portland cement may be considered as a potential matrix to immobilize As5+-bearing wastes.