Bi(III)4-methylpiperidinedithiocarbamate coprecipitation procedure for separation--pre-concentration of trace metal ions in water samples by flame atomic absorption spectrometric determination

A pre-concentration method was developed for determination of trace amounts of cadmium, copper and lead in water samples by FAAS after coprecipitation by using potassium 4-methylpiperidinedithiocarbamate (K4-MPDC) as a chelating agent and Bi(III) as a carrier element. This procedure is based on filtration of the solution containing precipitate on a cellulose nitrate membrane filter following Cd(II), Cu(II) and Pb(II) coprecipitation with Bi(III)4-MPDC and then the precipitates together with membrane filter were dissolved in concentrated nitric acid. The metal contents of the final solution were determined by FAAS. Several parameters including pH of sample solution, amount of carrier element and reagent, standing time, sample volume for precipitation and the effects of diverse ions were examined. The accuracy of the method was tested with standard reference material (MBH, C31XB20 and CRM BCR-32) and Cd, Cu and Pb added samples. Determination of Cd, Cu and Pb was carried out in sea water, river water and tap water samples. The recoveries were >95%. The relative standard deviations of determination were less than 10%.     

Morphological and Thermal Properties of ABS/Montmorillonite Nanocomposites Using ABS with Different AN Contents

Acrylonitrile‐butadiene‐styrene (ABS)/clay nanocomposites have been prepared using two types of ABS with different AN contents and a chemically modified clay, Cloisite 20A. The composites were prepared by melt mixing in a twin‐screw extruder. Their morphological properties were characterized by XRD and TEM. The thermal stability of the polymer nanocomposites was studied using TGA and flammability tests. The results were analyzed in terms of the effect of the clay content and the type of ABS used on the clay dispersion and the thermal stability of the nanocomposites. Experimental results confirmed that better dispersion and intercalation and/or exfoliation can be obtained when using an ABS with a higher AN content. The study using TGA and flammability tests showed that the nanodispersed layers of silicate enhanced the thermal stability of the ABS matrix, and that an ABS with higher AN content was more effective in providing fire retardancy. This suggests that when using higher AN contents, more polar groups are present within the polymer matrix, allowing a more homogeneous dispersion and intercalation of the chain polymers into the organomodified montmorillonite clay (MMT), and even some exfoliation of the nanoclay. <figure> <picture> <source srcset="https://wol-prod-cdn.literatumonline.com/cms/attachment/da7b62bb-9121-4ac1-920d-6b3166631b46/mgra001.jpg" media="(min-width: 1650px)"></source><img class="figure__image-full" src="https://wol-prod-cdn.literatumonline.com/cms/attachment/86290c58-58c1-4fe0-8973-5a8470094357/mgra001.jpg" data-lg-src="https://wol-prod-cdn.literatumonline.com/cms/attachment/da7b62bb-9121-4ac1-920d-6b3166631b46/mgra001.jpg" alt="image" title="image"></picture> <p class="caption-style">     

Artificial reconstruction of two cryptic angucycline antibiotic biosynthetic pathways

Genome-sequencing projects have revealed that Streptomyces bacteria have the genetic potential to produce considerably larger numbers of natural products than can be observed under standard laboratory conditions. Cryptic angucycline-type aromatic polyketide gene clusters are particularly abundant. Sequencing of two such clusters from Streptomyces sp. PGA64 and H021 revealed the presence of several open reading frames that could be involved in processing the basic angucyclic carbon skeleton. The pga gene cluster contains one putative FAD-dependant monooxygenase (pgaE) and a putatively bifunctional monooxygenase/short chain alcohol reductase (pgaM), whereas the cab cluster contains two similar monooxygenases (cabE and cabM) and an independent reductase (cabV). In this study we have reconstructed the biosynthetic pathways for aglycone synthesis by cloning and sequentially expressing the angucycline tailoring genes with genes required for the synthesis of the unmodified angucycline metabolite-UWM6-in Streptomyces lividans TK24. The expression studies unequivocally showed that, after the production of UWM6, the pathways proceed through the action of the similar monooxygenases PgaE and CabE, followed by reactions catalysed by PgaM and CabMV. Analysis of the metabolites produced revealed that addition of pgaE and cabE genes directs both pathways to a known shunt product, rabelomycin, whereas expression of all genes from a given pathway results in the production of the novel angucycline metabolites gaudimycin A and B. However, one of the end products is most probably further modified by endogenous S. lividans TK24 enzymes. These experiments demonstrate that genes that are either inactive or cryptic in their native host can be used as biosynthetic tools to generate new compounds.     

Mechanical and Morphological Studies of Poly(propylene)‐Filled Eggshell Composites

Poly(propylene) (PP) composites were prepared by using eggshell (ES) as filler and their mechanical properties were compared with those using talc (TA) and calcium carbonate (CC) of different grain sizes (<i>X</i><sub>50</sub>). A decrease in impact strength and deformation at break with increase in filler content was observed. The PP composite with ES (<i>X</i><sub>50</sub> = 8.4 µm) was stiffer than those with CC (<i>X</i><sub>50</sub> = 0.7 µm). The hybrid composite PP‐ES‐TA showed a similar stiffness as the PP‐TA composites due to the similar morphology of TA (<i>X</i><sub>50</sub> = 0.5 µm) and ES, when TA was replaced up to 75 wt.‐% by ES. SEM study revealed evidence of improved interfacial bonding between PP and ES in theirs composites. <figure> <picture> <source srcset="https://wol-prod-cdn.literatumonline.com/cms/attachment/dd387483-44cd-49a1-9948-27328c462499/mgra001.jpg" media="(min-width: 1650px)"></source><img class="figure__image-full" src="https://wol-prod-cdn.literatumonline.com/cms/attachment/dfbe5dab-c674-4333-8a09-aa6494f3dbeb/mgra001.jpg" data-lg-src="https://wol-prod-cdn.literatumonline.com/cms/attachment/dd387483-44cd-49a1-9948-27328c462499/mgra001.jpg" alt="image" title="image"></picture> <p class="caption-style">     

Tunnel junctions with multiferroic barriers

Multiferroics are singular materials that can exhibit simultaneously electric and magnetic orders. Some are ferroelectric and ferromagnetic and provide the opportunity to encode information in electric polarization and magnetization to obtain four logic states. However, such materials are rare and schemes allowing a simple electrical readout of these states have not been demonstrated in the same device. Here, we show that films of La(0.1)Bi(0.9)MnO(3) (LBMO) are ferromagnetic and ferroelectric, and retain both ferroic properties down to a thickness of 2 nm. We have integrated such ultrathin multiferroic films as barriers in spin-filter-type tunnel junctions that exploit the magnetic and ferroelectric degrees of freedom of LBMO. Whereas ferromagnetism permits read operations reminiscent of magnetic random access memories (MRAM), the electrical switching evokes a ferroelectric RAM write operation. Significantly, our device does not require the destructive ferroelectric readout, and therefore represents an advance over the original four-state memory concept based on multiferroics.     

Cyanobacteria as bioreactors for the synthesis of Au, Ag, Pd, and Pt nanoparticles via an enzyme-mediated route

Common Anabaena, Calothrix, and Leptolyngbya cyanobacteria are shown to form Au, Ag, Pd, and Pt nanoparticles of well-controlled size. These nanoparticles are synthesized intra-cellularly, and naturally released in the culture medium, where they are stabilized by algal polysaccharides, allowing their easy recovery. The size of the recovered particles as well as the reaction yield is shown to depend on the cyanobacteria genus. Investigations of nanoparticle formation indicate that the intracellular nitrogenase enzyme is responsible for the metal reduction but that the cellular environment is involved in the colloid growth process.     

Differential effects of pharmacological doses of melatonin on malondialdehyde and glutathione levels in young and old rats

BACKGROUND: The free radical theory of aging suggests the oxygen-derived species as the causative agents and free radical scavengers as the defense systems in aging process. The exact role of the free radical scavenging effects of melatonin in aging remains to be clarified. OBJECTIVE: In this experimental study, we investigated the age-related changes of malondialdehyde (MDA), a lipid peroxidation product, and glutathione (GSH) and the effects of exogenous melatonin. METHODS: Plasma, liver, and lung MDA and GSH levels of 9- and 28-month-old rats were measured. RESULTS: Plasma, lung, and liver MDA levels of old rats were significantly higher than those of the young ones (p = 0.024, p = 0.005, and p = 0.0007, respectively). However, while the lung GSH levels were found to be significantly decreased in the control group of old rats as compared with young ones (p = 0.005), the liver GSH levels were unchanged. Plasma MDA levels were found to be significantly lower in the melatonin group of old rats as compared with the control group (p = 0.020) but lung and liver MDA levels were not significantly different. There were no significant differences in the levels of measured parameters between both groups of young rats. CONCLUSION: Our results suggest that increased levels of lipid peroxidation products may have a role in aging, and exogenous melatonin may delay the aging process of tissues by means of its free radical scavenging effects.     

Neutral lipids of chickpea flour and protein isolates

The neutral lipids composition of defatted chickpea flour and two types of protein isolates has been studied. The main compounds in neutral lipids are triacylglycerols, free fatty acids, and diacylglycerols. Other compounds present are wax esters, free fatty alcohols, and free sterols. The main fatty acids in neutral lipids are C<sub>18:2</sub> and C<sub>18:1</sub> among the unsaturated, and C<sub>16:0</sub> and C<sub>18:0</sub> among the saturated acids. Free and esterified alcohols range from C<sub>16:0</sub> to C<sub>28:0</sub>, the majority being those with an even number of carbon atoms. Sterols observed are β-sito-sterol, campesterol, stigmasterol, and δ-5-avenasterol. Triacyl-glycerols are partially hydrolyzed, and the amounts of unsaturated sterols and unsaturated fatty acids are reduced as a result of the chemical treatment during production of the protein isolates.     

Adhesion of edible oils to food contact surfaces

Adhesion of oils and fatty food products to packages is an important storage problem, because it increases product-package interactions that alter quality. Reducing such adhesion would also allow savings in recycling and cleaning processes. The aim of our work was to test if some thermodynamical adhesion models were correlated to edible oils’ bulk adhesion as measured experimentally. Food-contact surfaces were low-density polyethylene, polyethylene teraphthalate, stainless steel, and glass. The Young-Dupré equation and five models of adhesion from the literature were used to calculate solids’ surface tension and the thermodynamical work of adhesion (Wa). The dispersive, polar, acid-base, and hydrogen surface tension components of oils and solids were calculated. The experimental adhesion, or amount of edible oils remaining on solid surfaces after contact, was found to be correlated to Young-Dupré Wa, involving contact angle measured by specially designed image analysis technique. Two models, involving, respectively, surface tension’s hydrogen component and a linear dependence of Wa<sup>p</sup> on the liquid polar surface tension component, fitted best with oil bulk adhesion as measured experimentally. Our theoretical approach to fatty food material adhesion seems, so far, consistent to predict global residues of edible oils on solid surfaces.     

Greffage de molécules à la surface du silicium par voie électrochimique

The hydrogentated surface of silicon exhibits remarkable properties, but poor resistance to oxidation. To improve its stability, surface hydrogen has been replaced by several organic groups. Such grafting can be carried out chemically by a multi-step reaction scheme. However, an electrochemical approach allows direct reaction with the hydrogenated surface. The porous-silicon surface has been partially methoxylated by a controlled anodic dissolution. If has also been methylated using a non-destructive anodic process, with a yield of 80%, limited only by steric hindrance. The methylated surface of porous silicon exhibits a stability against oxidation increased by an order of magnitude.