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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 1492-1496 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 1Σ+←X 1Σ+ electronic transition of the C2nH− and C2n−1N− (n=4–7) anion chains has been observed following mass selection and codeposition with excess neon at 6 K. Photodetachment of the electron resulted in the detection of a band system due to the neutral C2n−1N radical. The spectra suggest that C7N, like C5N, has a 2Σ ground state. The B 2Π←X 2Π transition is detected for the larger C2n−1N (n=5–7) chains. These appear at slightly higher energies than those of the isoelectronic C2nH radicals and show similar spectral features. Several infrared transitions of the anions have also been observed. © 1999 American Institute of 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 111 (1999), S. 7397-7401 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic absorption spectra of the even-numbered carbon molecules C6–C14 have been measured in neon matrices. Bare carbon anions were produced in a cesium sputter source, mass selected, codeposited with neon at 6 K, and neutralized. The spectra show, apart from the known (1) 3Σu−←X 3Σg− transition of linear C6, C8, and C10 in the visible, absorption bands in the UV region. The spectral data when considered in conjunction with ab initio calculations show that the linear forms of C6 and C8 have the next strong (2) 3Σu−←X 3Σg− transition with band maximum near 238 and 277 nm, respectively, whereas the band systems of C10, C12, and C14 at 316, 332, and 347 nm are due to the monocyclic species. © 1999 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 107 (1997), S. 22-27 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The absorption spectra of the electronic transitions A 2Σg+←X 2Πg, B 2Σu+←X 2Πg, (2) 2Πu←X 2Πg, and (3) 2Πu←X 2Πg of C4−, as well as A 2Σg+←X 2Πu, (2) 2Πg←X 2Πu, and (3) 2Πg←X 2Πu of C6− have been obtained in neon matrices. The spectra were measured after mass-selected deposition of the anions with excess of neon at 5 K. The assignments are based on mass-selection, spectroscopic evidence, photobleaching behavior, and ab initio calculations. Vibrational frequencies in the electronically excited states have been inferred. © 1997 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 2261-2261 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 5356-5360 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Annealing reactions of carbon atoms, molecules, and their anions, trapped in noble gas matrices, were studied spectroscopically. To this aim Cn− (n=1–4) anions were mass-selected and codeposited with argon or neon to form matrices at low temperatures. The charged species were neutralized by uv irradiation. Carbon chain elongation is observed only if neutral or charged atomic carbon is present in the matrix. Spectra of linear carbon clusters up to C11 were observed after C− deposition, electron detachment, and subsequent annealing. The reaction between two Cn (n≥2) species in solid argon or neon was studied and can be disregarded even at temperatures near the point of matrix sublimation. © 1997 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 4468-4472 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electronic transitions, (2)2Π←X 2Π (n=4–7), 2Σ←X 2Π (n=4,5) in addition to the known one C 2Π←X 2Π (n=4–7) of linear carbon anions C2n− have been observed in neon matrices. Absorption spectra were measured after mass-selected deposition of the anions with excess of neon at 5 K. The assignments are based on mass-selection, wavelength dependence of the 000 transition on size, photobleaching behavior, and ab initiocalculations. Vibrational frequencies in the excited electronic states have been inferred. The band system attributed previously to the 3Σu−←X 3Σg− transition of C10, C12, and C14 is shown to be the (2)2Π←X 2Π transition of their anions. Another set of weak bands is assigned to the 3Σu−←X 3Σg− system of C10 but none were discernible for C12 or C14. This is experimental evidence for the predicted change from linear to nonlinear geometries for the even numbered carbon species larger than C10. © 1997 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 4954-4960 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 1Σ+u←X 1Σ+g electronic absorption system of the carbon chains C2n+1 (n=3–7) trapped in 5 K neon matrices has been identified. The 1Πu←X 1Σ+g transition has also been observed for C5 and C7, as well as a dipole forbidden one for all the species. The spectroscopic information was derived from absorption spectra recorded after neutralization of mass-selected anions and cations that were codeposited with an excess of neon to form a matrix. The assignment is based on the mass-selection, theoretical predictions, and trends observed for this homologous series. These results are related to published absorption spectra of graphite vapor trapped in rare gas matrices. The suggestion that such species may be potential carriers of diffuse interstellar bands is considered. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Publication Date: 2020-03-05
    Description: Since 2016, a UV camera records images of the Popocatépetl Volcano for continuous monitoring of the SO2 plume. Five band-pass filters (300a, 300b, 307, 310, 330) with the different bandwidth (BW) of 10 and 25nm with transmissions centered at 300nm (BW=10) nm), 300nm (BW=25 nm), 307nm (BW=25 nm), 310nm (BW=10 nm)and 330nm (BW=10 nm) are used for the analysis. In order to fully characterize the filters and improve our knowledge of the errors affecting the results, the UV camera was used together with a UV spectrometer for experiments and measurements. Gas cells with different concentrations were prepared to simulate field conditions and to calibrate the SO2 column images when measuring from a fixed site. Our study is focused on a) applying the required corrections due to vignetting by the instrumentation as well as flattening the light intensity gradients in the field of view, b) determining the effect on the results when using different interference filters, c) applying a simplified light dilution correction and d) performing an a posteriori calibration correction using four interference filters. Our results show that a permanently installed and well-characterized camera, even with the rather long distance from the crater (11.3 km), can provide valuable and reliable information of the SO2 emissions from the Popocatépetl Volcano.
    Description: Published
    Description: 82-94
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 9
    Publication Date: 2020-07-10
    Description: TROPOMI (the TROPOspheric Monitoring Instrument), on board the Sentinel-5 Precursor (S5P) satellite, has been monitoring the Earth's atmosphere since October 2017 with an unprecedented horizontal resolution (initially 7 km2×3.5 km2, upgraded to 5.5 km2×3.5 km2 in August 2019). Monitoring air quality is one of the main objectives of TROPOMI; it obtains measurements of important pollutants such as nitrogen dioxide, carbon monoxide, and formaldehyde (HCHO). In this paper we assess the quality of the latest HCHO TROPOMI products versions 1.1.(5-7), using ground-based solar-absorption FTIR (Fourier-transform infrared) measurements of HCHO from 25 stations around the world, including high-, mid-, and low-latitude sites. Most of these stations are part of the Network for the Detection of Atmospheric Composition Change (NDACC), and they provide a wide range of observation conditions, from very clean remote sites to those with high HCHO levels from anthropogenic or biogenic emissions. The ground-based HCHO retrieval settings have been optimized and harmonized at all the stations, ensuring a consistent validation among the sites. In this validation work, we first assess the accuracy of TROPOMI HCHO tropospheric columns using the median of the relative differences between TROPOMI and FTIR ground-based data (BIAS). The pre-launch accuracy requirements of TROPOMI HCHO are 40 %–80 %. We observe that these requirements are well reached, with the BIAS found below 80 % at all the sites and below 40 % at 20 of the 25 sites. The provided TROPOMI systematic uncertainties are well in agreement with the observed biases at most of the stations except for the highest-HCHO-level site, where it is found to be underestimated. We find that while the BIAS has no latitudinal dependence, it is dependent on the HCHO concentration levels: an overestimation (+26±5 %) of TROPOMI is observed for very low HCHO levels (8.0×1015 molec. cm−2). This demonstrates the great value of such a harmonized network covering a wide range of concentration levels, the sites with high HCHO concentrations being crucial for the determination of the satellite bias in the regions of emissions and the clean sites allowing a small TROPOMI offset to be determined. The wide range of sampled HCHO levels within the network allows the robust determination of the significant constant and proportional TROPOMI HCHO biases (TROPOMI =+1.10±0.05 ×1015+0.64±0.03 × FTIR; in molecules per square centimetre). Second, the precision of TROPOMI HCHO data is estimated by the median absolute deviation (MAD) of the relative differences between TROPOMI and FTIR ground-based data. The clean sites are especially useful for minimizing a possible additional collocation error. The precision requirement of 1.2×1016 molec. cm−2 for a single pixel is reached at most of the clean sites, where it is found that the TROPOMI precision can even be 2 times better (0.5–0.8×1015 molec. cm−2 for a single pixel). However, we find that the provided TROPOMI random uncertainties may be underestimated by a factor of 1.6 (for clean sites) to 2.3 (for high HCHO levels). The correlation is very good between TROPOMI and FTIR data (R=0.88 for 3 h mean coincidences; R=0.91 for monthly means coincidences). Using about 17 months of data (from May 2018 to September 2019), we show that the TROPOMI seasonal variability is in very good agreement at all of the FTIR sites. The FTIR network demonstrates the very good quality of the TROPOMI HCHO products, which is well within the pre-launch requirements for both accuracy and precision. This paper makes suggestions for the refinement of the TROPOMI random uncertainty budget and TROPOMI quality assurance values for a better filtering of the remaining outliers.
    Print ISSN: 1867-1381
    Electronic ISSN: 1867-8548
    Topics: Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 10
    Publication Date: 1997-07-01
    Print ISSN: 1089-5639
    Electronic ISSN: 1520-5215
    Topics: Chemistry and Pharmacology , Physics
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