Ozonation of oil sands process-affected water accelerates microbial bioremediation

Ozonation can degrade toxic naphthenic acids (NAs) in oil sands process-affected water (OSPW), but even after extensive treatment a residual NA fraction remains. Here we hypothesized that mild ozonation would selectively oxidize the most biopersistent NA fraction, thereby accelerating subsequent NA biodegradation and toxicity removal by indigenous microbes. OSPW was ozonated to achieve approximately 50% and 75% NA degradation, and the major ozonation byproducts included oxidized NAs (i.e., hydroxy- or keto-NAs). However, oxidized NAs are already present in untreated OSPW and were shown to be formed during the microbial biodegradation of NAs. Ozonation alone did not affect OSPW toxicity, based on Microtox; however, there was a significant acceleration of toxicity removal in ozonated OSPW following inoculation with native microbes. Furthermore, all residual NAs biodegraded significantly faster in ozonated OSPW. The opposite trend was found for ozonated commercial NAs, which are known to contain no significant biopersistent fraction. Thus, we suggest that ozonation preferentially degraded the most biopersistent OSPW NA fraction, and that ozonation is complementary to the biodegradation capacity of microbial populations in OSPW. The toxicity of ozonated OSPW to higher organisms needs to be assessed, but there is promise that this technique could be applied to accelerate the bioremediation of large volumes of OSPW in Northern Alberta, Canada.     

Poly[ethylene‐co‐(vinyl alcohol)]‐graft‐poly(ε‐caprolactone) Synthesis by Reactive Extrusion, 1 ‐ Structural and Kinetic Study

Chemical modification of EVOH in the molten state at 185 °C by a grafting from process of poly(ε‐caprolactone) in batch was studied. ¹H NMR was used to characterize the structure evolutions of PCL grafts. In addition to grafting reactions, dynamic covalent transesterification reactions between EVOH residual alcohols and the polyester grafts led to a redistribution of the PCL grafts length. up to 27 and SR up to 80% were obtained. Experiments made in a corotating mini twin‐screw extruder also confirmed these results. The effect of the alcohol to caprolactone ratio and catalyst concentration (SnOct₂) on kinetic evolution showed that few minutes were necessary to complete the polymerization. A kinetic model was proposed and adequate conditions for the synthesis by reactive extrusion were defined.

     

Estimation method for determining surface film conductance during cooling of fish packages

This paper presents an alternative method for determining the surface film conductance of an infinite fish slab subjected to the cooling process. Many methods have been published, but their solutions have inherent appreciable inaccuracy and limitations. The present authors used the temperature histories of five locations within a slab sample of fish, obtained by the experimental investigation part of this work, along with the inverse heat conduction problem (IHCP) technique to develop a correlation for variable surface film conductance. When the above correlation was used for temperature predictions, the predicted and experimentally measured temperature distribution profiles were compared numerically. Better agreement than that implemented by other investigators was achieved. This revealed the accuracy and superiority of the present method, and the limitations of other methods are overcome in this method.     

Effect of organic chelates on the performance of hybrid sol–gel coated AA 2024-T3 aluminium alloys

Sol–gels are organic–inorganic polymers formed by hydrolysis/condensation reactions of alkoxide precursors, primarily silanes, which have found applications as electronic, optical and protective coatings. These coatings possess important characteristics such as chemical stability, physical strength and scratch resistance. Further performance improvement is achieved through the incorporation of zirconium and titanium based nanoparticles, also formed through the sol–gel process. However due to the inherent difference in the reactivity of the precursors, the hydrolysis of each precursor must be carried out separately before being combined for final condensation. Zirconium precursors are commonly chelated using acetic acids, prior to hydrolysis, to lower the hydrolysis rate.In this body of work various ligands such as organic acids, acetyl acetone (AcAc) and 2,2′-bipyridine (Bipy) were used to control the zirconium hydrolysis reaction and form nanoparticles within the silane sol matrix.Nanoparticle modified coatings formed from the silane sol on AA 2024-T3 aluminium were characterised spectroscopically, electrochemically and calorimetrically to evaluate the potential effect of the different chelates on the final film properties while neutral salt spray tests were performed to study their anti-corrosion performance. Results indicate that the acid ligand modified coatings provided the best performance followed by AcAc, while Bipy was the poorest. In all cases the zirconium nanoparticle improved the protective properties of the sol–gel coating.     

Adsorption of some heavy metal ions from aqueous solutions on Nafion 117 membrane

Nafion 117 membrane was investigated for the removal of Ni(II), Co(II), Pb(II), Cu(II) and Ag(I) metal ions from their synthesized aqueous solutions. The different variables affecting the adsorption capacity of the membrane such as contact time, initial metal ion concentration in the feed solution, pH of the sorption medium and temperature of the solution were investigated on a batch sorption basis. The affinity of Nafion 117 membrane towards heavy metal ions was found to increase in the sequence of Cu(II), Ni(II), Co(II), Pb(II), and Ag(I) with adsorption equilibrium achieved after 30 min for all metal ions. Among all parameters, pH has the most significant effect on the adsorption capacity, particularly in the range of 3.1-5.9. The variation of temperature in the range of 25-65 °C was found to have no significant effect on the adsorption capacity. Nafion 117 membrane was found to have high stability combined with repeated regeneration ability and can be suggested for effective removal of heavy metal ions such as Cu(II), Ni(II) and Co(II) from aqueous solutions.     

Confinement effect of stiffened and unstiffened concrete-filled stainless steel tubular stub columns

This paper presents a comparative study between stiffened and unstiffened concrete-filled stainless steel hollow tubular stub columns using the austenitic stainless steel grade EN 1.4301 (304). Finite element analysis of concrete-filled stainless steel unstiffened tubular stub columns is constructed herein based on the confined concrete model recently available in the literature. It is then compared with the experimental results of concrete-filled stainless steel stiffened tubular stub columns. The stiffened stainless steel tubular sections were fabricated by welding four lipped angles or two lipped channels at the lips. The longitudinal stiffener of the column plate was formed to avoid shrinkage of the concrete and to act as a continuous connector between the concrete core and the stainless steel tube. The behavior of the columns was investigated using two different nominal concrete cubic strengths of 30 and 60 MPa. The overall depth-to-width ratios (aspect ratio) varied from 1.0 to 1.8. The depth-to-plate thickness ratio of the tube sections varied from 60 to 90. The stiffened and unstiffened concrete-filled stainless steel tube specimens were subjected to uniform axial compression over the concrete and stainless steel tube to force the entire section to undergo the same deformations by blocking action. The ABAQUS 6.6 program, as a finite element package, is used in the current work. The results of the comparative study showed that the stainless steel tubes in stiffened concrete-filled columns offered a high average of increase in the confinement of the concrete core than that of the unstiffened concrete-filled columns.     

Improved Tricyclic Inhibitors of Trypanothione Reductase by Screening and Chemical Synthesis

Trypanothione reductase (TryR) is a key validated enzyme in the trypanothione‐based redox metabolism of pathogenic trypanosomes and leishmania parasites. This system is absent in humans, being replaced with glutathione and glutathione reductase, and as such offers a target for selective inhibition. As part of a program to discover antiparasitic drugs, the LOPAC1280 library of 1266 compounds was screened against TryR and the top hits evaluated against glutathione reductase and T. brucei parasites. The top hits included a number of known tricyclic neuroleptic drugs along with other new scaffolds for TryR. Three novel druglike hits were identified and SAR studies on one of these using information from the tricyclic neuroleptic agents led to the discovery of a competitive inhibitor (K_i=330 nM ) with an improved potency against T. brucei (EC₅₀=775 nM ).     

Fabrication of porous polymer monoliths in polymeric microfluidic chips as an electrospray emitter for direct coupling to mass spectrometry

Coupling of polymeric microfluidic devices to mass spectrometry is reported using porous polymer monoliths (PPM) as nanoelectrospray emitters. Lauryl acrylate-co-ethylene dimethacrylate porous polymer monolith was photopatterned for 5 mm at the end of the channel of microfluidic devices fabricated from three different polymeric substrate materials, including the following: poly(dimethylsiloxane) (PDMS), poly(methyl methacrylate) (PMMA), and cyclic olefin copolymer (COC). Spraying directly from the end of the chip removes any dead volume associated with inserted emitters or transfer lines, and the presence of multiple pathways in the PPM prevents the clogging of the channels, which is a common problem in conventional nanospray emitters. Spraying from a microfluidic channel having a PPM emitter produced a substantial increase in TIC stability and increased sensitivity by as much as 70x compared to spraying from an open end chip with no PPM. The performance of PPM emitter in COC, PMMA, and PDMS chips was compared in terms of stability and reproducibility of the electrospray. COC chips showed the highest reproducibility in terms of chip-to-chip performance, which can be attributed to the ease and reproducibility of the PPM formation due to the favorable optical and chemical properties of COC. We have further tested the performance of the COC chips by constant infusion of poly(propylene glycol) solution at organic content ranging from 10 to 90% methanol and at flow rates ranging from 50 to 1000 nL/min, showing optimum spraying conditions (RSD < 5%) at 50-70% organic content and at flow rates from 100 to 500 nL/min. The PPM sprayer was also used for protein preconcentration and desalting prior to mass spectrometric detection, and results were comparable with a chip spraying from an electrospray tip.     

A study on the behaviour of TLD-100 glow peaks at extreme ambient temperatures in Riyadh, Saudi Arabia

In this study, the temperature-induced variations in the TLD-100 response and the modifications in its glow peaks are investigated in real environmental exposure conditions in Riyadh, Saudi Arabia, where ambient temperatures during summer reach >45 degrees C and with relative humidity of <10%. Three groups of 12 TLD-100 cards in Harshaw type 8814 TLD cardholders were deployed as environmental dosemeters for a period of approximately 1 month for 12 consecutive months. One group was irradiated to 5 mGy 137Cs prior to deployment; another was irradiated to the same dose after deployment, while the last group was left unirradiated. Analysis of glow curves was done using commercially available glow curve deconvolution software (CGCD). Monthly variations in peak 3, 4 and 5 areas relative to the corresponding peak areas of a prompt glow curve are presented. Results of this study show good TL signal compensation between peaks 4 and 5 at all ambient temperatures encountered in this experiment, despite the observed individual variations experienced by each of these peaks. The sum of peak 4 and 5 areas is constant to within approximately 10%, for both pre- and post-irradiated dosemeters, during this 12-month cycle.