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 28,634 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A range of uranium oxide-based catalysts, derived from UO2(NO3)2.6H2O and UCl4 precursors, and supported on gamma-Al2O3, SiO2 and mesoporous H1SiO2, have been synthesized and then characterized using the following methods: isothermal nitrogen adsorption/desorption measurements, diffuse reflectance infrared spectroscopy (DRIFTS), gas titration of surface hydroxyl groups using Grignard reagents, U L(III) extended X-ray absorption fine structure (EXAFS), powder X-ray diffraction (PXRD), and thermogravimetric and differential thermal analysis. Brij76-templated H1SiO2 mesoporous silicas are found to be essentially stable under flowing oxygen after 16 h at 1073 K. At temperatures above this, however, extensive structural collapse, together with extensive dehydroxylation, ensues. Titration of the accessible hydroxyl group concentrations shows that in these materials the density of OH groups is considerably lower than in their amorphous counterparts. The adsorption of uranyl nitrate onto these dispersants results in a supported, and partially dehydrated, phase of the parent molecule with little obvious structural distortion; however, the adsorption of UCl4 leads to a complex adstructure which may best be described as U(O)2Cl2. The subsequent formation of the uranium oxide phase, nominally active for the oxidation of CO and selective reduction of NO (generally accepted to be U3O8), is found to be a considerable function of both the precursor and support system employed. Calcination of such systems to 1073 K results in extensive extrusion of the supported uranium phase from mesoporous supports, resulting in the formation of very large orthorhombic U3O8 domains. PXRD, however, shows that on amorphous SiO2 and gamma-Al2O3 similar treatment results in the formation of a hexagonal phase of U3O8. The formation of U3O8 is found to be promoted in mesoporous systems and by the presence of Cl in the catalyst make up. Some evidence is also found that suggests that a persistence of Cl limits the growth of U3O8 domains.
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PMID:Effects of precursor and support variation in the genesis of uranium oxide catalysts for CO oxidation and selective reduction of NO: Synthesis and characterization. 1685 1

The capability of three dimensionally ordered macroporous (3DOM) hydroxyapatite, Ca10(PO4)6(OH)2 (HAp), to capture cadmium and lead ions from their respective salt solutions was studied as a function of temperature. Synthesis of 3DOM material was achieved by colloidal crystal templating of polystyrene spheres (1 microm diameter) using calcium nitrate (Ca(NO3)2) and orthophosphoric acid (H3PO4) as precursors. The macroporous product consisted primarily of HAp (>80% depending on the sintering temperature) together with amorphous calcium phosphate. The sorption ability of 3DOM material to Cd/Pb ion was benchmarked against HAp powder prepared via the same route without the template. On the basis of quantitative X-ray diffraction (XRD) and analytical transmission electron microscopy(ATEM) 3DOM HAp demonstrated a higher uptake of cadmium, viz. x = 0.71 in Ca10-xCdx(PO4)6(OH)2 than nonporous HAp (x = 0.42). The incorporation of Cd was homogeneous in the 3DOM HAp crystals (as compared to the powder) leading to a decrease in lattice parameters as Cd2+ has a smaller ionic radius compared to Ca2+. A preference for Cd to enter the Ca" tunnel site of HAp was consistent with this being the readily exchangeable site. The lead-bearing solution acted to collapse the macropores through the rapid crystallization of pyromorphite (Pb10(P04)6(OH)2) via a dissolution-precipitation mechanism, possibly promoted by the amorphous component, that overwhelmed HAp ion exchange. The rapid crystallochemical incorporation of Cd and fixation of Pb by 3DOM HAp demonstrates the potential of thin-walled porous structures for the treatment of contaminated waters.
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PMID:Cadmium and lead ion capture with Three dimensionally ordered macroporous hydroxyapatite. 1715 16

The N,N',N'',N'''-1,2,4,5-tetra(ethylhexanoate) pyromellitamide is found to be capable of both intermolecular aggregation and binding to small anions. It is synthesized by aminolysis of pyromellitic anhydride with ethanolamine, followed by a reaction with hexanoyl chloride. The single-crystal X-ray structure of the pyromellitamide shows that it forms one-dimensional columnar stacks through an intermolecular hydrogen-bonding network. It also forms self-assembled gels in nonpolar solvents, presumably by a hydrogen-bonding network similar to the solid-state structure as shown by IR and XRD studies. Aggregation by intermolecular hydrogen bonding of the pyromellitamide is also observed by NMR and IR in solution. Fitting of NMR dilution data for pyromellitamide in d6-acetone to a cooperative aggregation model gave KE=232 M-1 and positive cooperativity of aggregation (rho=0.22). The pyromellitamide binds to a range of small anions with the binding strength decreasing in the order chloride>acetate>bromide>nitrate approximately iodide. The data indicate that the pyromellitamide binds two anions and that it displays negative cooperativity. The intermolecular aggregation of the pyromellitamide can also be altered using small anion stimuli; anion addition to preformed self-assembled pyromellitamide gels causes their collapse. The kinetics of anion-induced gel collapse are qualitatively correlated to the binding affinities of the same anions in solution. The cooperative anion binding properties and the sensitivity of the self-assembled gels formed by pyromellitamide toward anions could be useful in the development of sensors and switching/releasing devices.
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PMID:Pyromellitamide aggregates and their response to anion stimuli. 1749 82

Metal nanoparticles combined with environmentally sensitive polymers can lead to enhanced nanometer-sized switches. We present a silver nanoparticle synthesis method that uses poly(N-isopropylacrylamide) (PNIPAM) as the nucleating, capping, and stabilizing agent. The synthesis is performed at room temperature by sodium borohydride-mediated reduction of silver nitrate in the presence of a fully hydrated polymer. The resulting metal nanoparticles have a narrow size distribution comparable to or better than those achieved with other synthesis methods. The silver particles can be thermally precipitated by the collapse of the PNIPAM shell and resolubilized with fast response times, as shown by surface plasmon spectroscopy. The silver-PNIPAM composite allows for combined surface plasmon and thermal switching applications.
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PMID:Environmentally sensitive silver nanoparticles of controlled size synthesized with PNIPAM as a nucleating and capping agent. 1759 29

The products isolated from the reaction between Cd(NO3)2 x 4H2O and 1,4-benzenedicarboxylic acid (H2bdc) in DMF are very dependent on the conditions. At 115 degrees C, the reaction gives [Cd(bdc)(DMF)]infinity, which has a three-dimensional network structure, whereas at 95 degrees C, 1 is formed alongside [Cd3(bdc)3(DMF)4]infinity 2, which has a two-dimensional network structure. When the reaction is carried out under pressure, it yields [Cd3(bdc)3(DMF)4]infinity 3, which is a supramolecular isomer of 2. The structure of 3 differs from that of 2 regarding the way the Cd3(O2CR)6 units are interlinked to form layers. When the reaction was carried out in DMF that had undergone partial hydrolysis, the only isolated product was [(NMe2H2)2[Cd(bdc)2] x 2DMF]infinity 4. Compound 4 has a three-dimensional triply-interpenetrated diamondoid structure, with dimethylammonium cations and DMF molecules included within the pores. The reaction between Cd(NO3)2 x 4H2O and H2bdc in DEF gave [Cd(bdc)(DEF)]infinity 5, regardless of the solvent quality. Compound 5 has a three-dimensional network structure. The reaction of Cd(NO3)2 x 4H2O and 1,3-benzenedicarboxylic acid (H2mbdc) in DMF gave [Cd(mbdc)(DMF)]infinity 6 which has a bilayer structure. The thermal properties of the new materials have been investigated, and the coordinated DEF molecules from 5 can be removed on heating to 400 degrees C without any change in the powder X-ray diffraction pattern. The H2 sorption isotherm for the desolvated material shows marked hysteresis between adsorption and desorption, and less adsorption than predicted by simulations. Kinetic data indicate that the hysteresis is not due to mass transfer limitations, and the most likely explanation for this behaviour lies in partial collapse of the framework to an amorphous phase under the conditions of activation.
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PMID:Syntheses, structures and properties of cadmium benzenedicarboxylate metal-organic frameworks. 1846 Dec 2

The sessile lifestyle of plants constrains their ability to acquire mobile nutrients such as nitrate. Whereas proliferation of roots might help in the longer term, nitrate-rich patches can shift rapidly with mass flow of water in the soil. A mechanism that allows roots to follow and capture this source of mobile nitrogen would be highly desirable. Here, we report that variation in nitrate concentration around roots induces an immediate alteration of root hydraulic properties such that water is preferentially absorbed from the nitrate-rich patch. Further, we show that this coupling between nitrate availability and water acquisition results from changes in cell membrane hydraulic properties and is directly related to intracellular nitrate concentrations. Split-root experiments in which nitrate was applied to a portion of the root system showed that the response is both localized and reversible, resulting in rapid changes in water uptake to the portions of the roots exposed to the nitrate-rich patch. At the same time, water uptake by roots not supplied with nitrate was reduced. We believe that the increase in root hydraulic conductance in one part causes a decline of water uptake in the other part due to a collapse in the water potential gradient driving uptake. The translation of local information, in this case nitrate concentration, into a hydraulic signal that can be transmitted rapidly throughout the plant and thus coordinate responses at the whole plant level, represents an unexpected, higher level physiological interaction that precedes the level of gene expression.
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PMID:Nitrate control of root hydraulic properties in plants: translating local information to whole plant response. 1875 87

ABSTRACT Conidia of Cercospora zeae-maydis are the primary inoculum causing gray leaf spot of maize. On nutrient-deficient substrates, but not on water on the leaf surface, conidia germinate and develop secondary conidia on conidiophores produced from germ tubes or conidial cells. A population of conidia increases its numbers more than twofold by 2 days on the surface of a water droplet and by fourfold on trichomes. This microcycle conidiation is suppressed by hydrogen peroxide and ammonium compounds but not by nitrate compounds, amino acids, or simple sugars. Microcycle conidiation is sensitive to alpha-amanitin and cycloheximide, suggesting that new RNA and proteins must be synthesized. Upon transfer from a humid to a dry atmosphere, secondary conidia and conidiophores dehydrate and collapse. Mature, dehydrated, secondary conidia are liberated by wind speeds approximately one-third those required to liberate hydrated conidia. The dispersed secondary conidia can rehydrate and germinate normally. Because this microcycle conidiation occurs at the expense of endogenous reserves, the ability to produce secondary conidia is lost after four successive cycles without a period of growth on nutrient media. This alternative method of maintaining inoculum potential during periods of fluctuating relative humidity may have epidemiological consequences when primary conidia fail to infect.
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PMID:Microcycle Conidiation in Cercospora zeae-maydis. 1894 34

Acute liver failure (ALF) can be complicated by lung dysfunction. The aim of this study was to test the hypothesis that inhibition of oxidative stress through iron chelation with desferrioxamine (DFX) attenuates pulmonary injury caused by ALF. 14 adult female domestic pigs were subjected to surgical devascularisation of the liver and were randomised to a study group (DFX group, n = 7), which received post-operative intravenous infusion of DFX (14.5 mg x kg(-1) x h(-1) for the first 6 h post-operatively and 2.4 mg x kg(-1) x h(-1) until completion of 24 h), and a control group (n = 7). Post-operative lung damage was evaluated by histological and bronchoalveolar lavage fluid (BALF) analysis. DFX resulted in reduced BALF protein levels and tissue phospholipase (PL)A(2) activity. Plasma malondialdehyde and BALF nitrate and nitrite concentrations were lower, while catalase activity in the lung was higher after DFX treatment. PLA(2), platelet-activating factor acetylhydrolase and total cell counts in BALF did not differ between groups. Histological examination revealed reduced alveolar collapse, pneumonocyte necrosis and total lung injury in the DFX-treated animals. DFX reduced systemic and pulmonary oxidative stress during ALF. The limited activity of PLA(2) and the attenuation of pneumonocyte necrosis could represent beneficial mechanisms by which DFX improves alveolar-capillary membrane permeability and prevents alveolar space collapse.
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PMID:Desferrioxamine attenuates minor lung injury following surgical acute liver failure. 1904 11

Anion effluxes are amongst the earliest reactions of plant cells to elicitors of defence responses. However, their properties and their role in disease resistance remain almost unknown. We previously demonstrated that cryptogein, an elicitor of tobacco defence responses, induces a nitrate (NO(3) (-)) efflux. This efflux is an early prerequisite to the cryptogein-triggered hypersensitive response (HR). Here, we analyzed the electrophysiological properties of the elicitor-mediated NO(3) (-) efflux and clarified the mechanisms through which it contributes to cell death. Application of the discontinuous single electrode voltage-clamp technique in tobacco cells elicited with cryptogein enabled us to record the activation of slow-type deactivating anion channel currents. Cryptogein-induced plasma membrane depolarization and Ca(2+) influx, an essential component of elicitor signalling for HR cell death, were prevented by inhibiting the NO(3) (-) efflux. Similarly, pharmacological blocking of the anion efflux suppressed vacuolar collapse, a hallmark of cell death. The role of NO(3) (-) efflux in mediating proteases activation was further assessed. It is shown that cryptogein induced the activation of three proteases with apparent molecular masses of 95, 190 and 240 kDa. Their activation occurred independently on the anion efflux and, together with cell death, was strongly reduced by cycloheximide and the protease inhibitor PMSF. In contrast, the NO(3) (-) efflux was shown to promote the accumulation of transcripts encoding vacuolar processing enzymes, a family of proteases previously reported to contribute to the disruption of vacuole integrity observed during the HR. Collectively, our data indicate that anion efflux is an early prerequisite to morphological and biochemical events participating to cell death.
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PMID:Cryptogein-induced anion effluxes: electrophysiological properties and analysis of the mechanisms through which they contribute to the elicitor-triggered cell death. 1951 73

We present novel results on thermocavitation using a CW medium-power near infrared laser (lambda=975 nm) focused into a saturated copper nitrate saline solution. Due to the large absorption coefficient at the laser wavelength, the solution can be heated to its superheat limit (T(sh) approximately 270-300 degrees C). Superheated water undergoes explosive phase transition around T(sh) producing approximately half-hemispheric bubbles (gamma approximately 0.5) in close contact with the substrate. We report the temporal dynamic of the cavitation bubble, which is much shorter than previously reported under similar conditions. It was found that the bubble radius and pressure wave amplitude emitted on bubble collapse decreases exponentially with the power laser. Thermocavitation can be a useful tool for the generation of ultrasonic waves and controlled ablation for use in high-resolution lithography.
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PMID:Time-resolved analysis of cavitation induced by CW lasers in absorbing liquids. 2058 17


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