Oxidation and removal of arsenic (III) from aerated groundwater by filtration through sand and zero-valent iron

Removing arsenic from contaminated groundwater in Bangladesh is challenging due to high concentrations of As(III), phosphate and silicate. Application of zero-valent iron as a promising removal method was investigated in detail with synthetic groundwater containing 500 microg/L As(III), 2-3mg/L P, 20mg/L Si, 8.2mM HCO3-, 2.5mM Ca2+, 1.6mM Mg2+ and pH 7.0. In a series of experiments, 1L was repeatedly passed through a mixture of 1.5 g iron filings and 3-4 g quartz sand in a vertical glass column (10mm diameter), allowing the water to re-aerate between each filtration. At a flow rate of 1L/h, up to 8 mg/L dissolved Fe(II) was released. During the subsequent oxidation of Fe(II) by dissolved oxygen, As(III) was partially oxidized and As(V) sorbed on the forming hydrous ferric oxides (HFO). HFO was retained in the next filtration step and was removed by shaking of the sand-iron mixture with water. Rapid phosphate removal provided optimal conditions for the sorption of As(V). Four filtrations lead to almost complete As(III) oxidation and removal of As(tot) to below 50 microg/L. In a prototype treatment with a succession of four filters, each containing 1.5 g iron and 60 g sand, 36 L could be treated to below 50 microg/L in one continuous filtration, without an added oxidant.     

Decreasing activated sludge thermal hydrolysis temperature reduces product colour, without decreasing degradability

Activated sludges are becoming more difficult to degrade in anaerobic digesters, due to the implementation of stricter nitrogen limits, longer sludge ages, and removal of primary sedimentation units. Thermal hydrolysis is a popular method to enhance degradability of long-age activated sludge, and involves pressure and heat treatment of the process fluid (150-160 degrees C saturated steam). However, as documented in this study, in a full-scale system, the use of thermal hydrolysis produces coloured, recalcitrant compounds that can have downstream impacts (e.g., failure of UV disinfection, and increased effluent nitrogen). The coloured compound formed during thermal hydrolysis was found to be melanoidins. These are coloured recalcitrant compounds produced by polymerisation of low molecular weight intermediates, such as carbohydrates and amino compounds at elevated temperature (Maillard reaction). By decreasing the THP operating temperature from 165 degrees C to 140 degrees C, THP effluent colour decreased from 12,677 mg-PtCo L(-1) to 3837 mg-PtCo L(-1). The change in THP operating temperature from 165 degrees C to 140 degrees C was shown to have no significant impact on anaerobic biodegradability of the sludge. The rate and extent of COD biodegradation remained largely unaffected by the temperature change with an average first order hydrolysis rate of 0.19 d(-1) and conversion extent of 0.43 g-COD(CH4)g-COD(-1).     

Presence of cancerostatic platinum compounds in hospital wastewater and possible elimination by adsorption to activated sludge

Platinum originating from the excreted cancerostatic platinum compounds (CPC) cisplatin, carboplatin and oxaliplatin was monitored over a period of 28 days in the wastewater of the oncologic ward of the Vienna University Hospital. Concentration levels ranging from 4.7 to 145 microg L(-1) were measured by inductively coupled plasma mass spectrometry (ICP-MS). An average ratio of weekly drug emission/drug consumption of 0.27+/-0.12 was assessed. Model studies were carried out for fundamental understanding of CPC interaction with the solid phases present at different stages of the water cycle. Wastewater and activated sludge were spiked with CPC at concentration levels as found in the sewer of the oncologic ward. The platinum concentration remaining in the tested solution was measured after 24 h of incubation. Depending on pH, the three substances exhibited considerably different adsorption rates in wastewater. At pH 7, cisplatin was adsorbed by 88%, whereas only 26% of carboplatin and 54% of oxaliplatin were removed from the aqueous phase. Adsorption by activated sludge was higher, less affected by pH variation and comparable for all investigated CPC (96% for cisplatin, 70% for carboplatin and 74% for oxaliplatin at pH 6.8). In a next step, the dependence of CPC adsorption was tested for wastewater and activated sludge of different sampling sites. Strong variations were found only for wastewater, whereas activated sludge showed more consistent elimination rates (average values: cisplatin 92%, carboplatin 72%, and oxaliplatin 78%). These findings indicate that the major part of the excreted CPC is adsorbed by the solid phase in the water cycle and is thus expected to be removed from the wastewater by sewage treatment plants.     

Electroless thin film CoNiFe-B alloys for integrated magnetics on Si

Electroless magnetic thin films have been deposited from borane-based baths suitable for use in integrated magnetics on Si applications. The baths were developed for compatibility with standard photoresist for microfabrication of integrated magnetics on Si. The specific formulations, which differ from those reported previously, yield uniform, high saturation magnetisation (up to 2.15 T) deposits with low coercivity (<2 Oe). The resistivity of the film can be increased to minimise eddy current losses by using higher dimethylamine borane (DMAB) content or the inclusion of a second reducing agent, hypophosphite, to facilitate phosphorus codeposition of up to 7 at.%. The Ni content in the plating bath has been shown to exert significant influence over the composition, deposition rate and coercivity. XRD analysis suggests that the deposits consist of nanocrystalline phase with grains <20 nm. Such small grains are consistent with the observed low coercivity of the deposits.     

Electrochemically stable gold nanoclusters in HOPG nanopits

Gold nanoparticles on highly oriented pyrolytic graphite (HOPG) electrodes are synthesized. They are stabilized in nanosized pits of well defined depth in the graphite surface. These pits are created by energetic cluster impact followed by etching under a well controlled oxygen atmosphere. We succeeded in the preparation of highly dispersed and stable Au electrodes with gold particles with a mean diameter smaller than 5 nm. The stability of the gold nanostructures for electrochemical applications has been tested by performing cyclic voltammetric measurements in 0.5 M H₂SO₄. While conventionally prepared sputter deposited electrodes show highly unstable structures in this size range, Au clusters stabilized in the nanosized containers are stable.     

Estimation of reinforcement in compatibilized polypropylene nanocomposites by extensional rheology

Structural characterization in polymer nanocomposites is usually performed using X‐ray scattering and microscopic techniques, whereas the improvements in processing and mechanical properties are commonly investigated by rotational rheometry and tensile testing. However, all of these techniques are time consuming and require quite expensive scientific equipment. It has been shown that a fast and efficient way of estimating the level of reinforcement in polymer nanocomposites can be performed by melt extensional rheology, because it is possible to correlate the level of melt strength with mechanical properties, which reflect both the 3D network formed by the clay platelets/polymer chains as well as final molecular structure in the filled system. The physical network made of silicate filler and polymer matrix has been evaluated by X‐ray diffraction and transmission electron microscopy. Extensional rheometry and tensile testing have been used to measure efficiency of the compatibilizer amount in a polypropylene‐nanoclay system. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Structurally Refined β‐Lactones as Potent Inhibitors of Devastating Bacterial Virulence Factors

Disarmed forces : Inhibition of the central virulence regulator ClpP by structurally refined β‐lactones resulted in dramatically reduced production of devastating virulence factors, including pyrogenic toxin superantigens derived from pathogenic multiresistant Staphylococcus aureus strains. Targeting of this virulence regulator could present an attractive strategy for neutralizing the harmful effects of bacterial pathogens, and help the host immune response to eliminate the disarmed bacteria.

     

Optimized dispersion of nanoparticles for biological in vitro and in vivo studies

Background

The aim of this study was to establish and validate a practical method to disperse nanoparticles in physiological solutions for biological in vitro and in vivo studies.

Results

TiO₂ (rutile) dispersions were prepared in distilled water, PBS, or RPMI 1640 cell culture medium. Different ultrasound energies, various dispersion stabilizers (human, bovine, and mouse serum albumin, Tween 80, and mouse serum), various concentrations of stabilizers, and different sequences of preparation steps were applied. The size distribution of dispersed nanoparticles was analyzed by dynamic light scattering and zeta potential was measured using phase analysis light scattering. Nanoparticle size was also verified by transmission electron microscopy. A specific ultrasound energy of 4.2 × 10⁵ kJ/m³ was sufficient to disaggregate TiO₂ (rutile) nanoparticles, whereas higher energy input did not further improve size reduction. The optimal sequence was first to sonicate the nanoparticles in water, then to add dispersion stabilizers, and finally to add buffered salt solution to the dispersion. The formation of coarse TiO₂ (rutile) agglomerates in PBS or RPMI was prevented by addition of 1.5 mg/ml of human, bovine or mouse serum albumin, or mouse serum. The required concentration of albumin to stabilize the nanoparticle dispersion depended on the concentration of the nanoparticles in the dispersion. TiO₂ (rutile) particle dispersions at a concentration lower than 0.2 mg/ml could be stabilized by the addition of 1.5 mg/ml albumin. TiO₂ (rutile) particle dispersions prepared by this method were stable for up to at least 1 week. This method was suitable for preparing dispersions without coarse agglomerates (average diameter < 290 nm) from nanosized TiO₂ (rutile), ZnO, Ag, SiO_x, SWNT, MWNT, and diesel SRM2975 particulate matter.

Conclusion

The optimized dispersion method presented here appears to be effective and practicable for preparing dispersions of nanoparticles in physiological solutions without creating coarse agglomerates.     

Electron Beam Crosslinking of Atactic Poly(propylene): Development of a Potential Novel Elastomer

Atactic amorphous poly(propylene) of various molecular weights has been modified with high energy electrons over an irradiation dose range of 0–200 kGy. Tri‐ and tetrafunctional monomers in varied concentrations have been used as crosslinking additives. A correlation between the original molecular weight and crosslinking behavior of the polymer was observed. A higher gel content is obtained with the tetrafunctional acrylate as compared to that with the trifunctional one, under the same treatment conditions. Electron irradiation treatment at elevated temperature gives rise to an increased gel content over that at room temperature. Similarly, the mechanical properties also enhance with gel content. Moreover, the stress‐strain behavior of the electron modified systems indicates a more pronounced elastomeric nature.

     

Experimental and numerical investigations regarding laser drop on demand jetting of Cu alloys

Active noise reduction, structural health monitoring and energy harvesting are possible applications of active structure components. An integration of piezoceramic modules into casted Al-structures can be defined as a long term goal to achieve high functional integration and thus to address lightweight construction. Since the liquidus temperature of standard electronic solder is not sufficient to withstand the thermal loads during Al die casting processes, a suitable wire bonding process is an enabling technology to generate active Al structures. In the scope of this work, a laser based drop on demand joining process is introduced. The process consists of four main steps. First a spherical CuSn12 braze preform of 600 µm diameter with a liquidus temperature of 1233 K is inserted into a ceramic capillary and being molten by a laser pulse. The droplet is subsequently ejected by gas overpressure and impinges on the joining area, consisting of the electrode structure of the piezo element and the Cu wire, where it forms a firm joint of the Cu wire and the electrode structure. In order to evaluate time–temperature profiles of the capillary during melting and detachment of the braze preform a simulation model was set up, indicating heating and cooling rates of 22,100 K/s. Further, the impact of the capillary geometry on the velocity fields of a passing medium was evaluated. By changing the capillary geometry, the gas flow velocity could be reduced by about 10% according to the simulation model, which resulted in a reduction of droplet height deviation of 7.5% and a reduction of the droplet diameter deviation of 32.2% in the experiment.