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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 79 (1975), S. 1629-1632 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 80 (1976), S. 2057-2062 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 82 (1978), S. 2753-2754 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 76 (1972), S. 478-487 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 78 (1974), S. 2318-2320 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Water, air & soil pollution 27 (1986), S. 277-285 
    ISSN: 1573-2932
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Energietechnik
    Notizen: abstract The physical characterization of winter-time aerosol in the Detroit area studied over a 7-week period (January–March, 1983) is presented. Total suspended particle levels (〈15 μm) were 56 ± 29 μg m−3, with 66% of the material in the fine (〈2.5 μm) particle fraction. Coarse and fine particle masses were reasonably correlated, indicating that local sources, not long-range transport, influenced winter-time aerosol at the site. Mobile sources were responsible for a marked diurnal variation in the nuclei mode particle count and accounted for about 10% of the submicron aerosol mass. Decreases in submicron aerosol concentrations during precipitation appear to be associated with advection of clean air into the area during frontal passage rather than to precipitation scavenging.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 765-776 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Measurements of hydroxyl radical (HO) concentrations in ambient air by the technique of laser-induced fluorescence have been recently reported. The present study was undertaken to provide an independent test of the validity of those measurements. A photochemical reactor was used to provide a source of HO, and the concentration of HO in the reactor was determined by the laser-induced fluorescence technique. The HO concentration was also deduced from measured hydrocarbon decay rates in the reactor. There was agreement between the HO concentrations obtained by these two different methods, thus providing further validation of the fluorescence method. Some studies of HO fluorescence efficiency as well as of possible interferences with the fluorescence measurements are reported.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 665-671 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The relative rate technique has been used to measure rate constants for the reaction of chlorine atoms with nitro methane, nitro ethane, nitro propane, nitro butane, nitro pentane, ethyl nitrate, isopropyl nitrate, n-propyl nitrate, 2-pentyl nitrate, and 2-heptyl nitrate. Decay rates of these organic species were measured relative to one or more of the following reference compounds; n-butane, ethane, chloroethane, and methane. Using rate constants of 2.25 × 10-10 5.7 × 10-11, 8.04 × 10-12, and 1.0 × 10-13 cm3 molecule-1 s-1 for the reaction of Cl atoms with n-butane, ethane, chloroethane, and methane, respectively, the following rate constants were derived, in units of cm3 molecule-1 s-1: nitro methane, 〈7 × 10-15; nitro ethane, (2.05 ± 0.14) × 10-13; nitro propane, (1.13 ± 0.05) × 10-11; nitro butane, (5.13 ± 0.68) × 10-11; nitro pentane, (1.40 ± 0.14) × 10-10; ethyl nitrate, (3.70 ± 0.24) × 10-12; n-propyl nitrate, (2.15 ± 0.13) × 10-11; i-propyl nitrate, (3.94 ± 0.48) × 10-12; 2-pentyl nitrate, (1.00 ± 0.06) × 10-10; and 2-heptyl nitrate, (2.84 ± 0.50) × 10-10. Quoted errors represent 2σ and do not include possible systematic errors due to errors in the reference rate constants. Experiments were performed at 295 ± 2 K and atmospheric pressure (≃740 torr) of synthetic air. The results are discussed with respect to the previous literature data and to the modeling of these compounds in the atmosphere.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 1077-1089 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Fourier transform infrared spectroscopy was used to identify and quantify products of the self reaction of ethylperoxy radicals, C2H5O2, formed in the photolysis of Cl2/C2H6 mixtures in 700 torr total pressure of synthetic air at 295 K. From these measurements, branching ratios for the reaction channels of k1a/(k1a + k1b) = 0.68 and k1c/(k1a + k1b + k1c) ≤ 0.06 were established. Additionally, using the relative rate technique, the rate constant for the reaction of Cl atoms with C2H5OOH was determined to be (1.07 ± 0.07) × 10-10 × cm3 molecule-1 s-1. Results are discussed with respect to the previous kinetic and mechanistic studies of C2H5O2 radicals.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 1257-1269 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mechanisms for the Cl-initiated and OH-initiated atmospheric oxidation of t-butyl alcohol (TBA), methyl t-butyl ether (MTBE), and dimethyl ether (DME) have been determined. For TBA the only products observed are equimolar amounts of H2CO and acetone, and its atmospheric oxidation can be represented by (7), The mechanism for the atmospheric oxidation of DME is also straight forward, with the only observable product being methyl formate, The mechanism for the atmospheric oxidation of MTBE is more complex, with observable products being t-butyl formate (TBF) and H2CO. Evidence is presented also for the formation of 2-methoxy-2-methyl propanal (MMP), which is highly reactive and presumably oxidized to products. The atmospheric oxidation of MTBE can be represented by (9) and (10), In terms of atmospheric reactivity, DME, TBA, and MTBE all compare favorably with methanol. In terms of rate of reaction in the atmosphere, DME, MTBE, and TBA are 1.4, 0.40, and 0.28 times as reactive as CH3OH towards OH on a per carbon basis. With regard tochemistry, atmospheric oxidation of CH3OH yields highly reactive H2CO as the sole carbon-containing product. In contrast, only 25% of the carbon in TBA is converted to H2CO, with the balance yielding unreactive acetone. For DME, all the carbon is converted to methyl formate which is unreactive. Finally, for MTBE, 60% is converted to unreactive TBF while the remaining 40% produces highly reactive MMP.Final assessment of the impact of these materials on the atmospheric reactivity of vehicle emissions requires the determination of their emissions rates under realistic operating conditions.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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