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  • 2000-2004  (1)
  • 1990-1994  (2)
  • 1985-1989  (3)
  • Chemistry  (3)
  • Myocardial blood flow  (1)
  • alpha-adrenoceptor
  • frontal chromatography
Materialart
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Topics in catalysis 11-12 (2000), S. 263-270 
    ISSN: 1572-9028
    Schlagwort(e): nitric oxide ; selective catalytic reduction ; supported ruthenium catalysts ; frontal chromatography ; temperature-programmed surface reaction ; reaction mechanism
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Steady-state and transient kinetic experiments were performed in a versatile microreactor flow set-up with magnesia- and alumina-supported ruthenium catalysts in order to elucidate the mechanism of the selective catalytic reduction (SCR) of nitric oxide with hydrogen. Both Ru/MgO and Ru/γ-Al2O3 were found to be highly active catalysts converting NO and H2 into N2 and H2O with selectivities close to 100% at full conversion, although Ru-based catalysts are known to be active in the synthesis of NH3 from N2 and H2. Frontal chromatography experiments with NO at room temperature revealed that NO and its dissociation products displace adsorbed atomic hydrogen (H−*) almost completely from hydrogen-precovered Ru surfaces. Obviously, NO and H2 compete for the same adsorption sites, H−* being the weaker bound adsorbate. Temperature-programmed surface reaction (TPSR) experiments in H2 subsequent to NO exposure demonstrated that higher heating rates and lower partial pressures of H2 shift the selectivity from NH3 to N2. Therefore, the coverage of H−* is concluded to govern the branching ratio between the rate of associative desorption of N2 (2N−*→N2 + 2*) and the rate of hydrogenation of N−* (N−* + 3H–* →NH3 + 4*). Finally, the steady-state coverages of N- and O-containing adsorbates were derived by interrupting the SCR reaction and hydrogenating the adsorbates off as NH3 and H2O. By solving the site balance, the Ru surfaces were found to be essentially N2 is attributed to the very low coverage of H−* due to site blocking by a N + O coadsorbate layer, favouring the recombination of N−* instead of its hydrogenation to NH3.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Research in experimental medicine 185 (1985), S. 429-443 
    ISSN: 1433-8580
    Schlagwort(e): Myocardial blood flow ; Angiotensin II ; Saralasin ; Nephrectomy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The effect of hypoxia and the renin-angiotensin system on metabolic coronary regulation in hemorrhagic shock was studied in 22 anesthetized open-chest dogs. Left circumflex coronary blood flow was measured with an electromagnetic flowmeter. Dogs were ventilated with room air (n = 8) or 100% oxygen (n = 7). A third group of dogs was ventilated with room air and bilaterally nephrectomized 5 h prior to starting the experimental protocol (n = 7). After control data had been obtained, dogs were bled from the femoral arteries into a pressurized reservoir which maintained blood pressure at 45 ± 1 mm Hg. The angiotensin II receptor blocker, saralasin, was then infused i.v. (0.1, 1.0, 10.0 µg/kg per min). Coronary blood flow was reduced by hemorrhage, and no significant difference existed in coronary flow during hemorrhage among the three groups. Coronary sinus oxygen saturation was diminished in control animals during hemorrhage from 26% ± 1% to 17% ± 1% (P 〈 0.05) but normal in 100% oxygen ventilated animals (30% ± 3%) and in nephrectomized dogs (34% ± 4%). Coronary oxygen extraction was reduced by saralasin in intact but not in nephrectomized dogs. In six additional experiments, in which blood pressure was not artificially held constant during saralasin infusion, saralasin still significantly improved coronary sinus oxygen saturation and thus reduced coronary oxygen extraction. The data suggest that both hypoxia and the reninangiotensin system participate in the restriction of metabolic coronary regulation in hemorrhagic shock.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Basic research in cardiology 81 (1986), S. 29-39 
    ISSN: 1435-1803
    Schlagwort(e): atrial fibrillation ; coronary blood flow ; alpha-adrenoceptor ; coronary constriction
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The mechanism of coronary vasoconstriction induced by atrial fibrillation during maximal coronary dilatation was studied in 19 chloralose-urethane anesthetized dogs. Maximal coronary dilatation was achieved by carbochromene (5 mg/kg i.v.) or dipyridamole (0.2 mg/kg i.v.) Left circumflex coronary blood flow was measured with an electromagnetic flowmeter. Atrial fibrillation was compared with rhythmic atrial pacing at similar heart rates (207±12 vs. 204±12 beats/min). During maximal coronary dilatation, coronary resistance was 0.38±0.05 mm Hgxminx100 g/ml (RU) at sinus rhythm, 0.41±0.06 RU at atrial pacing, and 0.52±0.07 RU at atrial fibrillation, that was significantly (p〈0.005) higher than during sinus rhythm and atrial pacing. Accordingly, coronary oxygen extraction was 14±1% at sinus rhythm, 17±1% at atrial pacing (p〈0.005 vs. sinus rhythm) and 27±2% at atrial fibrillation (p〈0.001 vs sinus rhythm and atrial pacing). Beta-adrenoceptor blockade with propranolol (1 mg/kg i.v.) did not prevent this coronary vasoconstrictive effect. Following alpha-blockade with phenoxybenzamine (10 mg/kg i.v.), however, coronary resistance was 0.52±0.08 RU during sinus rhythm, 0.54±0.10 RU during atrial pacing and 0.57±0.09 RU during atrial fibrillation. The data suggest coronary vasoconstriction induced by atrial fibrillation mediated by an alpha-adrenoceptor mechanism.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 89-98 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: The occurrence of instabilities in chemically reacting systems, resulting in unsteady and spatially inhomogeneous reaction rates, is a widespread phenomenon. In this article, we use nonlinear signal processing techniques to extract a simple, but accurate, dynamic model from experimental data of a system with spatiotemporal variations. The approach consists of a combination of two steps. The proper orthogonal decomposition [POD or Karhunen-Loève (KL) expansion] allows us to determine active degrees of freedom (important spatial structures) of the system. Projection onto these “modes” reduces the data to a small number of time series. Processing these time series through an artificial neural network (ANN) results in a low-dimensional, nonlinear dynamic model with almost quantitative predictive capabilities.This approach is demonstrated using spatiotemporal data from CO oxidation on a Pt (110) crystal surface. In this special case, the dynamics of the two-dimensional reaction profile can be successfully described by four modes; the ANN-based model not only correctly predicts the spatiotemporal short-term behavior, but also accurately captures the long-term dynamics (the attractor). While this approach does not substitute for fundamental modeling, it provides a systematic framework for processing experimental data from a wide variety of spatiotemporally varying reaction engineering processes.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 12 (1988), S. 233-238 
    ISSN: 0142-2421
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: An X-ray photoelectron spectroscopic study is presented for an industrial catalyst surface, which is in its active form only accessible after reaction under technical conditions. A high pressure-high temperature reactor was attached to a surface analysis system. It allowed rapid transfer of a sample between the reaction environment and the UHV required for surface analysis. The active phase was identified as a ternary iron potassium oxide. No evidence was found for the previously suggested presence of a binary potassium hydroxide or carbonate phase in solid or liquid form. A new model of the active catalyst is proposed.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 18 (1992), S. 650-654 
    ISSN: 0142-2421
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: Na—Y zeolite was cation exchanged with Ru and tested in ammonia synthesis at atmospheric pressure. Activities up to ∼10% of the commercial iron catalyst scaled by the active surface area were observed. Characterization of the zeolites with XPS was complemented with reference thermal desorption spectroscopy data on a polycrystalline Ru metal surface. The catalysts showed high thermal stability in in situ reduction-oxidation cycles. The chemical state of the Ru will be discussed. From shift measurements the Ru is metallic in the active state, but line shape arguments point to a cluster-like particle morphology. The location of the Ru inside or outside the zeolite framework will be discussed.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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