Synthesis and Evaluation of Bis-quaternary-Based Surfactants as Additives for Water-Based Mud

Two series of cationic gemini surfactants, alkanediyl-α,ω-bis[N,N-dimethyl alkyl (octyl or dodecyl)ammonium] dibromide (R-s-R; s = 6, 10, 12 and R = 8 and 12) were prepared and evaluated as additives for water-based mud. The chemical structures of the prepared surfactants were confirmed using FTIR and mass spectroscopy. Surface activity of these compounds has been studied and their surface properties including surface tension, emulsification power, critical micelle concentration, effectiveness, maximum surface excess and minimum surface area were determined. The results showed that the prepared compounds have significant surface activity, especially those of longer hydrophobic chain length. The prepared cationic gemini surfactants were evaluated as viscosifiers and filter loss additives for water-based mud formulated from local Na-montmorillonite clay. XRD analysis was carried out to the Na-montmorillonite clay to determine the interaction of the surfactants with inter layers of the clay structure. Rheological properties, gel strength, thixotropy, filtration properties and the effect of temperature on rheological properties of the water-based mud were studied. The results indicated that the gemini surfactants have a positive effect on the rheological and filtration properties of the Na-montmorillonite clay according to American Petroleum Institute specifications.     

Green chemistry: microwave-assisted facile synthesis of 6-imino-1,3,4-thiadiazenes from reaction of thiocarbohydrazones with malononitrile dimer

The reactions of thiocarbohydrazones with malononitrile dimer under microwave irradiation are reported. These reactions give 6-imino-1,3,4-thiadiazines in good yields. The structures of products were elucidated by MS, IR and NMR spectra together with elemental analyses. The reaction mechanism was discussed.     

Direct Synthesis of Pyrazoles via reaction of C-ethoxycarbonyl-N-arylnitrilimines with benzalmalononitriles and some α-cyanocinnamic acid derivatives

Reaction of C-ethoxycarbonyl-N-arylnitrilimines ( 2a–d ) with α, β-disubstituted acrylonitriles ( 3a–f ) in refluxing benzene affords the corresponding substituted pyrazoles 5a–f and 6a–c respectively in good yield. However, reaction of 2a–e with 3g gives the 2-pyrazoline derivatives 7a–d . The assigned structures for the products 5–7 were confirmed by their spectra (i.r., ¹H-n.m.r.) and elemental analyses. Also the structures of the pyrazoles 5 were substantiated by comparison with their regioisomeres 8 .     

Barium aluminate hydrates. IV. α-BaO.Al2O3.4H2O

α-BaO.Al₂O₃.4H₂O has been synthesised and studied by infrared, X-ray and thermal analytical techniques. The compound of approximate formula BaO.Al₂O₃.0.5H₂O, described in Part III, forms as a dehydration product, and appears to be identical with the compound β-BAH₂ described by other workers. A possible explanation for the discrepancy in water content is discussed.     

Thermal modeling of plasma spray deposition of nanostructured ceramics

A thermal model for plasma spray deposition of ceramic materials onto metallic substrates has been developed. The enthalpy-based control volume formulation of the heat transfer processes has been used to study the temperature evolution in a two-dimensional substrate and in the coating as it is grown. In this paper, additional melting of ceramic splats after deposition is examined, with a view to predicting the retention of nanostructures in a spray consisting of agglomerated, nanometer-sized particles. Initial results for thin coatings indicate that when the mean temperature of the incoming particles is close to the fusion point of the ceramic material, the nanostructure distribution in the coating is largely determined by the composition of the spray. However, with thicker coatings, additional melting due to prolonged plasma gas heating combined with increased thermal resistance in the underlying coating leads to a loss of nanostructure.     

Self-assembled TiO₂ with increased photoelectron production, and improved conduction and transfer: enhancing photovoltaic performance of dye-sensitized solar cells

Highly crystalline mesoporous anatase TiO(2) is prepared through supramolecular self-assembly and by utilizing cetyltrimethylammonium bromide (CTAB) as templating material. Photoanodes of dye-sensitized solar cells (DSSCs) made from these TiO(2) nanoparticles are found to have a high specific surface area of 153 m(2)/g and high surface roughness. Optical absorption spectroscopy studies reveal that the photoanode films adsorb four times more dye than films made of commercial P25 TiO(2). Mercury porosimetry and field emission scanning electron microscope (FESEM) studies show hierarchical macro- and meso-porosity of the photoanode films leading to better dye and electrolyte percolation, combined with improved electron conduction pathways compared to P25 films. Electrochemical impedance studies confirm lower impedance and higher electron lifetime in the synthesized mesoporous TiO(2) films compared to P25 films. Higher photovoltaic efficiency was recorded of cells made from the synthesized mesoporous TiO(2) in comparison to the corresponding cells made from P25. Incident-photon-to-current efficiency data provided critical understanding of recombination kinetics, and provided proof of Mie scattering by the self-assembled submicrometer sized TiO(2) aggregates and the macropores in their structure. The scattering phenomenon was further corroborated by diffused reflectance studies. An in-depth analysis of CTAB-templated mesoporous TiO(2) has been conducted to show how it can be a good candidate photoanode material for enhancing the performance of DSSCs.     

Municipal solid waste compost application improves productivity, polyphenol content, and antioxidant capacity of Mesembryanthemum edule

Organic wastes were successfully used as soil amendment to improve agrosystems productivity. Yet, the effectiveness of this practice to enhance plant antioxidant capacities has received little attention. Here, we assess the effect of municipal solid waste (MSW) compost (at 40 t ha(-1)) on growth, polyphenol contents and antioxidant activities of Mesembryanthemum edule. MSW compost application significantly increased the soil contents of carbon, nitrogen, calcium, phosphorus and potassium. This was associated with higher nutrient (N, P, and K) uptake, which likely led to the significant improvement of the plant biomass and relative growth rate (RGR) (+93% on average) as compared to the control. In the same way, the fertilizing effect of the added organic matter significantly enhanced the antioxidant potential M. edule, assessed by radical scavenging activity, iron reducing power and β-carotene bleaching capacity. This was associated with significantly higher antioxidant contents, mainly total phenols and flavonoids. Heavy metal (Pb, Cd, Cu, and Zn) concentrations were slightly increased upon compost application, but remained lower than phytotoxic values. Overall, our results point out that short-term MSW compost application at 40 t ha(-1) is efficient in enhancing the productivity together with the antioxidant potentiality of M. edule without any adverse environmental impact.     

Surface enhanced Raman scattering of neurotransmitter release in neuronal cells using antibody conjugated gold nanoparticles

This study demonstrated the potential feasibility of using antibody-conjugated gold nanoparticles as highly sensitive and homogeneous sensing probes for biological monitoring of neurotransmitters in neuronal cells. Bands at 1152 and 1322 cm(-1) were also similar to SERS of metal catecholates, and could be assigned to catechol ring vibration and carbon-oxygen stretches.     

Niosomal encapsulation of the antitubercular drug, pyrazinamide

It is estimated that more than one-third of the world population is infected with Mycobacterium tuberculosis. Pyrazinamide (PZA) plays a unique role in shortening therapy because it kills a population of semilatent tubercle bacilli residing in an acidic environment. Niosomes are vesicles made up of non-ionic surfactant and exhibit behavior similar to liposomes in vivo. Preparation of PZA niosomes took place using different molar ratios of Span 60 and Span 85, with cholesterol (CH) i.e. Span: CH (1:1) and (4:2). Dicetyl phosphate and stearyl amine were used in preparation of negative and positively charged niosomes, respectively. Free PZA was separated by cooling centrifugation and estimated spectrophotometrically at 268.4 nm. Niosomes were characterized by electron microscopy and differential scanning calorimetry. The highest percentage PZA entrapped was obtained using Span 60 and the molar ratio (4:2:1) negatively charged niosomes. This was followed by the neutral PZA neutral (4:2) Span 60 niosomes. Biological evaluation of selected PZA niosomal formulations took place on guinea pigs infected with M. tuberculosis. The present work is an attempt to target maximum concentration of PZA to the affected site (lungs) and to exclude undesirable side effects and decrease toxicity. Macrophage targeting and overcoming drug resistance is our final goal.     

Localized in situ polymerization on graphene surfaces for stabilized graphene dispersions

We demonstrate a novel in situ polymerization technique to develop localized polymer coatings on the surface of dispersed pristine graphene sheets. Graphene sheets show great promise as strong, conductive fillers in polymer nanocomposites; however, difficulties in dispersion quality and interfacial strength between filler and matrix have been a persistent problem for graphene-based nanocomposites, particularly for pristine graphene. With this in mind, a physisorbed polymer layer is used to stabilize graphene sheets in solution. To create this protective layer, we formed an organic microenvironment around dispersed graphene sheets in surfactant solutions, and created a nylon 6, 10 or nylon 6, 6 coating via interfacial polymerization. Technique lies at the intersection of emulsion and admicellar polymerization; a similar technique was originally developed to protect luminescent properties of carbon nanotubes in solution. These coated graphene dispersions are aggregation-resistant and may be reversibly redispersed in water even after freeze-drying. The coated graphene holds promise for a number of applications, including multifunctional graphene-polymer nanocomposites.