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  • 1
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: Online-Ressource (257 S., 9,48 MB) , Ill., graph. Darst
    Language: English , German
    Note: Förderkennzeichen BMBF 07ATF01 , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Auch als gedr. Ausg. vorh , Sonderband für "Atmospheric environment": "FEBUKO and MODMEP: a combined study of aerosol-cloud interaction by field experiments and model develepment" , Systemvoraussetzungen: Acrobat reader. , Beitr. teilw. engl. und dt., überw. engl.
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  • 2
    Publication Date: 2023-11-15
    Description: 〈title xmlns:mml="http://www.w3.org/1998/Math/MathML"〉Abstract〈/title〉〈p xmlns:mml="http://www.w3.org/1998/Math/MathML" xml:lang="en"〉Chemical processing of reactive nitrogen species, especially of NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 (= NO + NO〈sub〉2〈/sub〉) and nitrous acid (HONO), determines the photochemical ozone production and oxidation capacity in the troposphere. However, sources of HONO and NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 in the remote marine atmosphere are still poorly understood. In this work, the multiphase chemistry mechanism CAPRAM in the model framework SPACCIM was used to study HONO formation at Cape Verde (CVAO) in October 2017, adopted with the input of current parameterizations for various HONO sources. Three simulations were performed that adequately reproduced ambient HONO levels and its diurnal pattern. The model performance for NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 and O〈sub〉3〈/sub〉 improves significantly when considering dust‐surface‐photocatalytic conversions of reactive nitrogen compounds with high correlation coefficients up to 0.93, 0.56, and 0.89 for NO, NO〈sub〉2〈/sub〉, and O〈sub〉3〈/sub〉, respectively. Photocatalytic conversion of the adsorbed HNO〈sub〉3〈/sub〉 on dust is modeled to be the predominant contributor for daytime HONO at CVAO, that is, accounting for about 62% of the chemical formation rate at noontime. In contrast, the ocean‐surface‐mediated conversion of NO〈sub〉2〈/sub〉 to HONO and other discussed pathways are less important. The average OH levels at midday (9:00–16:00) modeled for cluster trajectory 1, 2, and 3 are 5.2, 5.1, and 5.2 × 10〈sup〉6〈/sup〉 molecules cm〈sup〉−3〈/sup〉, respectively. Main OH formation is driven by O〈sub〉3〈/sub〉 photolysis with a contribution of 74.6% to the total source rate, while HONO photolysis is negligible (∼1.8%). In summary, this study highlights the key role of dust aerosols for HONO formation and NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 cycling at CVAO and possibly in other dust‐affected regions, urgently calling for further investigations using field and model studies.〈/p〉
    Description: Plain Language Summary: Chemical processing of NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 (= NO + NO〈sub〉2〈/sub〉) and nitrous acid (HONO) is important for the tropospheric O〈sub〉3〈/sub〉 budget and oxidation capacity. However, the sources of HONO and cycling of NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 in the remote marine atmosphere are still poorly explored. A detailed multiphase chemistry model simulation showed a better performance of HONO, NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 and O〈sub〉3〈/sub〉 when considering dust‐surface‐photocatalytic conversions of reactive nitrogen compounds, especially the photocatalytic conversion of the adsorbed HNO〈sub〉3〈/sub〉 on dust. The simulations demonstrated that OH formation is mainly driven by the O〈sub〉3〈/sub〉 photolysis, while HONO photolysis is a negligible OH radical source due to its low concentration levels at Cape Verde. The study highlights the key role of dust aerosols for HONO and NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 chemistry in the remote marine boundary layer.〈/p〉
    Description: Key Points: 〈list list-type="bullet"〉 〈list-item〉 〈p xml:lang="en"〉The sources of HONO and NO〈sub〉〈italic〉x〈/italic〉〈/sub〉 at Cape Verde are well modeled with CAPRAM〈/p〉〈/list-item〉 〈list-item〉 〈p xml:lang="en"〉Photocatalytic conversion of adsorbed HNO〈sub〉3〈/sub〉 on dust is the predominant contributor for daytime HONO〈/p〉〈/list-item〉 〈list-item〉 〈p xml:lang="en"〉Photolysis of O〈sub〉3〈/sub〉 is the prevailing source of OH radical at Cape Verde, while HONO photolysis is a negligible OH radical source〈/p〉〈/list-item〉 〈/list〉 〈/p〉
    Description: Leibniz Association SAW
    Description: Horizon 2020 Framework Programme http://dx.doi.org/10.13039/100010661
    Description: National Key Research and Development Program of China http://dx.doi.org/10.13039/501100012166
    Description: National Natural Science Foundation of China http://dx.doi.org/10.13039/501100001809
    Description: https://doi.org/10.5281/zenodo.8070265
    Description: http://mcm.york.ac.uk/
    Description: https://capram.tropos.de/
    Description: https://ebas.nilu.no/
    Description: https://www.ready.noaa.gov/HYSPLIT_traj.php
    Keywords: ddc:551 ; HONO ; NOx ; CAPRAM ; heterogenous chemistry ; mineral dust ; OH radical ; marine boundary layer
    Language: English
    Type: doc-type:article
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 16641-16645 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Applied physics 64 (1997), S. 355-361 
    ISSN: 1432-0649
    Keywords: PACS:07.60; 42.20
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract. A series of atmospheric aerosol diffusion experiments combined with lidar detection was conducted to evaluate and calibrate an existing retrieval algorithm for aerosol backscatter lidar systems. The calibration experiments made use of two (almost) identical mini-lidar systems for aerosol cloud detection to test the reproducibility and uncertainty of lidars. Lidar data were obtained from both single-ended and double-ended lidar configurations. A backstop was introduced in one of the experiments and a new method was developed where information obtained from the backstop can be used in the inversion algorithm. Independent in-situ aerosol plume concentrations were obtained from a simultaneous tracer gas experiment with SF $_6$ , and comparisons with the two lidars were made. The study shows that the reproducibility of the lidars is within 15%, including measurements from both sides of a plume. The correspondence with in-situ measurements is excellent. Finally, the new backstop method is able to reveal information which can close the lidar equation by obtaining the relation between backscatter and extinction in an aerosol cloud.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0009-286X
    Keywords: Trennkurve ; Differenzenformel ; Fehleranalyse ; Meßwertausgleich ; Fehlerabschätzung ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 54 (1982), S. 62-63 
    ISSN: 0009-286X
    Keywords: Mengenausbringen ; Fehlerspektren ; gewichtete Ausgleichsrechnung ; mittlere Fehler ; Vertrauensintervalle ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 51 (1979), S. 1140-1141 
    ISSN: 0009-286X
    Keywords: Klassieren ; Partikelgrößenanalyse ; Verteilungssummenkurve ; Meßfehler ; Ausgleichsrechnung ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0009-286X
    Keywords: Partikelgrößenanalyse ; Fehlerspektren ; gewichtete Ausgleichsrechnung ; Potenzverteilung ; logarithmische Normalverteilung ; RRSB-Verteilung ; Meßwertkorrektur ; Trennkurve ; Mengenanteile ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
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    PANGAEA
    In:  Supplement to: van Pinxteren, Manuela; Müller, Conny; Iinuma, Yoshiteru; Stolle, Christian; Herrmann, Hartmut (2012): Chemical characterization of dissolved organic compounds from coastal sea surface microlayers (Baltic Sea, Germany). Environmental Science & Technology, 46(19), 10455-10462, https://doi.org/10.1021/es204492b
    Publication Date: 2023-05-12
    Description: The physicochemical properties of the sea surface microlayer (SML), i.e. the boundary layer between the air and the sea, and its impact on air-sea exchange processes have been investigated for decades. However, a detailed description about these processes remains incomplete. In order to obtain a better chemical characterization of the SML, in a case study three pairs of SML and corresponding bulk water samples were taken in the southern Baltic Sea. The samples were analyzed for dissolved organic carbon and dissolved total nitrogen, as well as for several organic nitrogen containing compounds and carbohydrates, namely aliphatic amines, dissolved free amino acids, dissolved free monosaccharides, sugar alcohols, and monosaccharide anhydrates. Therefore, reasonable analytical procedures with respect to desalting and enrichment were established. All aliphatic amines and the majority of the investigated amino acids (11 out of 18) were found in the samples with average concentrations between 53 ng/l and 1574 ng/l. The concentrations of carbohydrates were slightly higher, averaging 2900 ng/l. Calculation of the enrichment factor (EF) between the sea surface microlayer and the bulk water showed that dissolved total nitrogen was more enriched (EF: 1.1 and 1.2) in the SML than dissolved organic carbon (EF: 1.0 and 1.1). The nitrogen containing organic compounds were generally found to be enriched in the SML (EF: 1.9-9.2), whereas dissolved carbohydrates were not enriched or even depleted (EF: 0.7-1.2). Although the investigated compounds contributed on average only 0.3% to the dissolved organic carbon and 0.4% to the total dissolved nitrogen fraction, these results underline the importance of single compound analysis to determine SML structure, function, and its potential for a transfer of compounds into the atmosphere.
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 10
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    PANGAEA
    In:  Supplement to: van Pinxteren, Manuela; Herrmann, Hartmut (2013): Glyoxal and methylglyoxal in Atlantic seawater and marine aerosol particles: method development and first application during the Polarstern cruise ANT XXVII/4. Atmospheric Chemistry and Physics, 13(23), 11791-11802, https://doi.org/10.5194/acp-13-11791-2013
    Publication Date: 2023-05-12
    Description: An analytical method for the determination of the alpha dicarbonyls glyoxal (GLY) and methylglyoxal (MGLY) from seawater and marine aerosol particles is presented. The method is based on derivatization with o-(2,3,4,5,6-Pentafluorobenzyl)-hydroxylamine (PFBHA) reagent, solvent extraction and GC-MS (SIM) analysis. The method showed good precision (RSD 〈 10%), sensitivity (detection limits in the low ng/l range), and accuracy (good agreement between external calibration and standard addition). The method was applied to determine GLY and MGLY in oceanic water sampled during the Polarstern cruise ANT XXVII/4 from Capetown to Bremerhaven in spring 2011. GLY and MGLY were determined in the sea surface microlayer (SML) of the ocean and corresponding bulk water (BW) with average concentrations of 228 ng/l (GLY) and 196 ng/l (MGLY). The results show a significant enrichment (factor of 4) of GLY and MGLY in the SML. Furthermore, marine aerosol particles (PM1) were sampled during the cruise and analyzed for GLY (average concentration 0.19 ng/m**3) and MGLY (average concentration 0.15 ng/m**3). On aerosol particles, both carbonyls show a very good correlation with oxalate, supporting the idea of a secondary formation of oxalic acid via GLY and MGLY. Concentrations of GLY and MGLY in seawater and on aerosol particles were correlated to environmental parameters such as global radiation, temperature, distance to the coastline and biological activity. There are slight hints for a photochemical production of GLY and MGLY in the SML (significant enrichment in the SML, higher enrichment at higher temperature). However, a clear connection of GLY and MGLY to global radiation as well as to biological activity cannot be concluded from the data. A slight correlation between GLY and MGLY in the SML and in aerosol particles could be a hint for interactions, in particular of GLY, between seawater and the atmosphere.
    Type: Dataset
    Format: application/zip, 3 datasets
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