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  • Electronic Resource  (11)
  • 1995-1999  (11)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 12413-12421 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 779-785 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Using the laser photolysis/laser-induced fluorescence (LIF) "pump-and-probe" technique, the dynamics of H atom formation in the photodissociation of CH3–CF2Cl (HCFC-142b) after excitation at 193 nm and the Lyman-α wavelength were studied under collision-free conditions in the gas-phase at room temperature. The H atoms produced were detected by (2p2P←1s2S)-LIF using tunable narrow-band Lyman-α laser radiation (λLα(approximate)121.6 nm) generated by resonant third-order sum-difference frequency conversion of pulsed dye laser radiation. In the VUV photodissociation experiments the Lyman-α laser radiation was used both to photodissociate the parent molecules and to detect the produced nascent H atoms via laser induced fluorescence. The following quantum yields ΦH for H atom formation were determined by a photolytic calibration method: ΦH(193 nm)=(0.06±0.02) and ΦH(Lα)=(0.53±0.12). From the measured H atom Doppler profiles the average H atom kinetic energy was determined to be ET(193 nm)=(51±10) kJ/mol and ET(Lα)=(72±4) kJ/mol, respectively. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 1359-1366 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The gas-phase dissociation dynamics of CH3Cl, CH2Cl2, and CHCl3 after photoexcitation at the Lyman-α wavelength (121.6 nm) were studied under collision-free conditions at room temperature. Narrow-band tunable Lyman-α laser radiation (λLα(approximate)121.6 nm) was generated by resonant third-order sum-difference frequency conversion of pulsed-dye-laser radiation and used both to photodissociate the parent molecules and to detect the nascent H atom products via (2p2P←1s2S) laser induced fluorescence. Absolute H atom quantum yields ΦH(CH3Cl)=(0.53±0.05), ΦH(CH2Cl2)=(0.28±0.03), and ΦH(CHCl3)=(0.23±0.03) were determined employing a photolytic calibration method where the Lyman-α photolysis of H2O was used as a reference source of well-defined H atom concentrations. H atom Doppler profiles were measured for all chlorinated methanes. In the case of CH3Cl the line shapes of the profiles indicate a pronounced bimodal translational energy distribution suggesting the presence of two H atom formation mechanisms leading to a markedly different H atom translational energy release. The observed "slow" component of the H atom translational energy distribution corresponds to an average kinetic energy of (55±5) kJ/mol, while the "fast" component leads to an average kinetic energy of (320±17) kJ/mol. The relative branching ratio between the "fast" and the "slow" H atom channel was determined to be (0.71±0.15). For CH2Cl2 and CHCl3 no bimodal translational energy distributions were observed. Here the translational energy distributions could each be well described by a single Maxwell–Boltzmann distribution, corresponding to an average translational energy of (81±9) kJ/mol and (75±4) kJ/mol, respectively. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0649
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract.  Using a confocal microscope with a single-photon avalanche photodiode as detector, we studied photon bursts of single Rhodamine 6G (R6G) and Rhodamin B-zwitterion (RB) molecules in aqueous solution by excitation of the lowest excited singlet state S 1 with a frequency-doubled titanium:sapphire laser. Multichannel scaler traces, the fluorescence autocorrelation function and fluorescence decay times determined by time-correlated single-photon counting have been measured simultaneously. The time-resolved fluorescence signals were analyzed with a maximum likelihood estimator. Fluorescence lifetime patterns in steps of 100 ps were generated by convolution with the excitation pulse. The lifetime of the S 1 state was derived from the Kullback-Leibler minimum discrimination information. We are able to demonstrate for the first time identification of two different single dye molecules via their characteristic fluorescence lifetimes of 1.79±0.33 ns (RB) and 3.79±0.38 ns (R6G) in aqueous solution.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0649
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Using a confocal microscope with a single-photon avalanche photodiode as detector, we studied photon bursts of single Rhodamine 6G (R6G) and Rhodamin B-zwitterion (RB) molecules in aqueous solution by excitation of the lowest excited singlet stateS 1 with a frequency-doubled titanium: sapphire laser. Multichannel scaler traces, the fluorescence autocorrelation function and fluorescence decay times determined by time-correlated single-photon counting have been measured simultaneously. The time-resolved fluorescence signals were analyzed with a maximum likelihood estimator. Fluorescence lifetime patterns in steps of 100 ps were generated by convolution with the excitation pulse. The lifetime of theS 1 state was derived from the Kullback-Leibler minimum discrimination information. We are able to demonstrate for the first time identification of two different single dye molecules via their characteristic fluorescence lifetimes of 1.79 ± 0.33 ns (RB) and 3.79 ± 0.38 ns (R6G) in aqueous solution.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0649
    Keywords: PACS: 42.80; 85.30; 878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: -11  M without separation steps.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0649
    Keywords: 33.50 ; 33.20 ; 34.90
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Laser-Induced Fluorescence (LIF) from the S1 state of acetone and 3-pentanone was studied as a function of temperature and pressure using excitation at 248 nm. Additionally, LIF of 3-pentanone was investigated using 277 and 312 nm excitation. Added gases were synthetic air, O2, and N2 respectively, in the range 0–50 bar. At 383 K and for excitation at 248 nm, all the chosen collision partners gave an initial enhancement in fluorescence intensity with added gas pressure. Thereafter, the signal intensity remained constant for N2 but decreased markedly for O2. For synthetic air, only a small decrease occurred beyond 25 bar. At longer excitation wavelengths (277 and 312 nm), the corresponding initial rise in signal with synthetic air pressure was less than that for 248 nm. The temperature dependence of the fluorescence intensity was determined in the range 383–640 K at a constant pressure of 1 bar synthetic air. For 248 nm excitation, a marked fall in the fluorescence signal was observed, whereas for 277 nm excitation the corresponding decrease was only half as strong. By contrast, exciting 3-pentanone at 312 nm, the signal intensity increased markedly in the same temperature range. These results are consistent with the observation of a red shift of the absorption spectra (≈9 nm) over this temperature range. Essentially, the same temperature dependence was obtained at 10 and 20 bar pressure of synthetic air. It is demonstrated that temperatures can be determined from the relative fluorescence intensities following excitation of 3-pentanone at 248 and 312 nm, respectively. This new approach could be of interest as a non-intrusive thermometry method, e.g., for the compression phase in combustion engines.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0649
    Keywords: 33.00 ; 42.65
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Polarization spectroscopy has been used to investigate the electronic bands of OH (A 2 Σ-X 2 Π) and NH (A 3 Π-X 3 Σ) radicals generated in atmospheric pressure flames. The pump-beam intensity dependence of the polarization-spectroscopy signals of isolated lines in theR branches has been studied. It was found that significant saturation is noticeable for pump-beam intensities as low as 0.1 MW/cm2. A detailed theoretical description inluding laser-bandwidth convolutions has been developed to model unsaturated polarization spectra of OH and NH. For OH, temperature evaluations have been performed in methane/air flames from fits to experimentalR 1 band head spectral structures. The results are critically dependent on the degree of saturation in experimental spectra, instrumental bandwidth and the assumed coupling cases in the calculation of line-strength parameters. It is shown that saturation leads to an error of more than 60% in the temperature evaluation when a pump-beam intensity of 1 MW/cm2 is used.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0649
    Keywords: PACS: 78.47
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 56 (1999), S. 1147-1154 
    ISSN: 1572-8943
    Keywords: composites ; DMTA ; glass transition temperature ; Round-Robin-test
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A sensitive method to characterize the thermomechanical behaviour of fiber reinforced composites is the dynamic mechanical thermoanalysis (DMTA) method. A Round-Robin-test with five different institutes was conducted to determine the role of the fiber orientation, processing conditions, test apparatus, the mode of loading, and the matrix materials on the determination of the glass transition temperature (Tg). The result shows that the DMTA is a suitable method to analyze Tg of long fiber composites. However, some major problems have to be taken into consideration: - A direct comparison of results from different DMTA-systems is not possible - The real temperatures in the specimens deviate from the temperatures displayed by the DMTA measuring system - There is no clear and common evaluation method for the glass transition temperature.
    Type of Medium: Electronic Resource
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