Search results for "Oxide"
showing 10 items of 6424 documents
Photoelectrochemical Synthesis of Polypyrrole on Anodic Ta[sub 2]O[sub 5] Films
2007
Polypyrrole film was photoelectrochemically grown on insulating Ta 2 O 5 anodic film in acetonitrile solution. A characterization by photocurrent spectroscopy (PCS) of metal/oxide/polypyrrole interface was carried out. The PCS results suggest that a metallic-like PPy is formed under illumination at constant anodic potential. By polarizing the polypyrrole at cathodic potentials a photocurrent spectrum typical of p-type semiconducting film was recorded. A scanning electron microscopy study of PPy surfaces solution side and oxide side allowed us to obtain information on the morphology of the polymer as well as a rough estimate of the film thickness and of the diameter of PPy globules at the tw…
Coping with Oxygen
2010
Sometime before 2.7 BYA, a new and biologically toxic substance began to appear in the environment. Biologically produced dioxygen, O2, probably first began to accumulate in small pools or layers above cyanobacterial mats. These photosynthesizers must have already developed ways to at least partially deal with dioxygen and, with greater difficulty, the reactive oxygen species (ROS) derived from it (see Chap. 1 and below). But for primitive anaerobes in the vicinity, these new substances must have been especially toxic. Nevertheless, it is clear that they evolved ways to cope with the new threats. One way was to simply avoid dioxygen altogether.
Detoxication Strategy of Epoxide Hydrolase—The Basis for a Novel Threshold for Definable Genotoxic Carcinogens
2004
From our recent work on the three-dimensional structure of epoxide hydrolases we theoretically deduced the likelihood of a two-step catalytic mechanism that we and others have subsequently experimentally confirmed. Analysis of the rate of the two steps by us and by others show that the first step—responsible for removal of the reactive epoxide from the system—works extraordinarily fast (typically three orders of magnitude faster than the second step), sucking up the epoxide like a sponge. Regeneration of the free enzyme (the second step of the catalytic mechanism) is slow. This becomes a toxicological problem only at doses of the epoxide that titrate the enzyme out. Our genotoxicity work s…
Significance of various enzymes in the control of reactive metabolites
1987
Most chemical carcinogens are relatively inert and need metabolic activation to the ultimately carcinogenic species. The concentration of such species is controlled by several different enzymes. Especially well studied is the important group of enzymes responsible for the control of reactive epoxides. Many natural, as well as man-made foreign compounds, including pharmaceuticals, possess olefinic or aromatic double bonds. Such compounds can be transformed to epoxides by microsomal monooxygenases present in many mammalian organs. By virtue of their electrophilic reactivity, such epoxides may spontaneously react with nucleophilic centres in the cell and thus covalently bind to DNA, RNA and pr…
The catalytic-thermometric determination of molybdenum in steels based on the hydrogen peroxide-iodide indicator reaction
1990
Abstract The Mo VI -catalysed hydrogen peroxide-iodide reaction has been optimised for thermometry in an HCl medium using the initial slope method. The substitution of sodium perborate by H 2 O 2 and the conversion of the reaction to a process showing a Landolt effect are considered and discussed. The linear range extended from 0.2 μg Mo VI ml −1 to 1.2 μg Mo VI ml −1 with a detection limit of 0.06 μg Mo VI ml −1 . Interferences were also studied. The optimised procedure was applied to the evaluation of molybdenum in steels after extraction with α-benzoinoxime in chloroform.
High yield recombinant production of a self-assembling polycationic peptide for silica biomineralization.
2015
We report the recombinant bacterial expression and purification at high yields of a polycationic oligopeptide, P5S3. The sequence of P5S3 was inspired by a diatom silaffin, a silica precipitating peptide. Like its native model, P5S3 exhibits silica biomineralizing activity, but furthermore has unusual self-assembling properties. P5S3 is efficiently expressed in Escherichia coli as fusion with ketosteroid isomerase (KSI), which causes deposition in inclusion bodies. After breaking the fusion by cyanogen bromide reaction, P5S3 was purified by cation exchange chromatography, taking advantage of the exceptionally high content of basic amino acids. The numerous cationic charges do not prevent, b…
A continuous reaction system to investigate dispersion polymerization of vinyl monomers in supercritical carbon dioxide
2006
A laboratory-scale continuous reaction system using a stirred tank reac- tor was assembled in our laboratory to study the dispersion polymerization of vinyl monomers in supercritical carbon dioxide (scCO2). The apparatus was equipped with a suitable downstream separation section to collect solid particles entrained in the effluent stream from the reactor, whose monomer concentration could be measured online with a gas chromatograph. The dispersion polymerization of methyl methacry- late in scCO2 was selected as a model process to be investigated in the apparatus. The experiments were performed at 65 8C and 25 MPa with 2,2 0 -azobisisobutyroni- trile as the initiator and a reactive polysilox…
Polymerization of vinylidene fluoride with perfluoropolyether surfactants in supercritical carbon dioxide as a dispersing medium
2006
The heterogeneous polymerization of vinylidene fluoride (VDF) was investigated at 50 °C with supercritical carbon dioxide (scCO 2 ) as a dispersing medium and diethylperoxidicarbonate as an initiator in the presence of different perfluoropolyether surfactants. When FLK 7004A ammonium carboxylate salts were used at a 5% (w/w) concentration with respect to VDF, with an initial pressure of 31-45 MPa and with an olefin concentration of about 5.5 mol/L, monomer conversions up to 63% were obtained, corresponding to a final solid content higher than 200 g/L, and the polymer was collected at the end of the process in the form of a white powder completely composed of microspheres. The effects of the…
Tin compounds interaction with membranes of egg lecithin liposomes.
2007
This work is a continuation of earlier research concerning the influence of tin compounds on the dynamic properties of liposome membranes produced with lecithin hen egg yolks (EYL). The experiments were carried out at room temperature (about 25 ∞C). Four tin compounds were chosen, including three organic ones, (CH3)4Sn, (C2H5)4Sn and (C3H7)3SnCl, and one inorganic, SnCl2. The investigated compounds were admixed to water dispersions of liposomes. The content of the admixture changed within the range 0 mol-% to 11mol-% in proportion to EYL. Two spin probes were used in the experiment: 2,2,6,6-tetramethylpiperidine- 1-oxyl (TEMPO) and 2-ethyl-2-(15-methoxy-15-oxopentadecyl)-4,4-dimethyl-3-oxaz…
CO2 as a C1-organic building block: Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate an…
2006
The purpose of this work is to establish and discuss quantitative relationships between the selectivity in preparative scale electrolysis and intrinsic and operational parameters for the electrocarboxylation of aromatic ketones. For the investigated ketones, under appopriate experimental conditions the selectivity of the process is mainly determined by the competition between carboxylation and protonation, de-halogenation reactions (when an halogenated ketone is involved), and possibly dimerizations involving the electrogenerated radical anion. A simple model was proposed to account for these unwanted side paths which allows to predict the dependence of the selectivity as a function of the …