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Ammonia and ammonium over the southern Baltic Sea. Part 1. Preparation of aerosol and air samples for the determination of ammonia by the indophenol method

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
1997 saw the start of a study into the spatial and temporal changes in the chemical composition of the atmosphere over the littoral and offshore waters of the Baltic Sea. Collection of samples and their subsequent chemical analysis was preceded by meticulous laboratory experiments concerning the validation and adaptation of the analytical procedures. The colorimetric indophenol blue technique was used to analyse the aerosol samples for the concentration of ammonium ions and the air samples for their gaseous ammonia. The samples were collected with PTFE-filters and Whatman 41 filters coated with 5% orthophosphoric acid. This acid enhances the aerosol sampling efficacy but reduces the pH of the reaction in which indophenol is formed. The pH of the aerosol samples thus had to be raised, and this in turn required an alteration to the original procedure prior to ammonia determination. It was demonstrated that the addition of 0.1 N KOH to the filters coated with H3PO4 increases the pH of the reaction medium to the required level of pH = 8-11.5 and does not substantially influence the precision of the determination; the error of the modified procedure was of the order of 5.2%. Air samples for the determination of gaseous ammonia were collected with annular denuders. Oxalic acid and citric acid are the usual impregnating agents. In the present experiments oxalic acid was used for denuder impregnation; it turned out to be more effective than citric acid under the conditions of the southern Baltic Sea. The detection limit of the indophenol blue method in these laboratory experiments was 0.045 mmol dm-3. The respective relative standard deviations (RSD) within the range of higher and lower concentrations were 0.64% and 4.53%.
Słowa kluczowe
Czasopismo
Rocznik
Strony
175--184
Opis fizyczny
Bibliogr. 17 poz., fot., tab.
Twórcy
  • Institute of Oceanography, University of Gdańsk, al. Marszałka Piłsudskiego 46, PL-81-378 Gdynia, Poland
autor
  • Institute of Oceanography, University of Gdańsk, al. Marszałka Piłsudskiego 46, PL-81-378 Gdynia, Poland
Bibliografia
  • [1] Andersen H. V., Hovmand M. F., 1994, Measurements of ammonia and filter ammonium by denuder and filter pack, Atmos. Environ., 28 (21), 3495-3512.
  • [2] Appel B. R., Tokiwa Y., Haik M., Kothny E. L., 1984, Artifact particulate sulfate and nitrate formation on filter media, Atmos. Environ., 18 (2), 409-416.
  • [3] Appel B. R., Tokiwa Y., Kothny E. L., Wu R., Povard V., 1988, Evaluation of procedures for measuring atmospheric nitric acid and ammonia, Atmos. Environ., 22, 1565-1573.
  • [4] Behlen A., 1996, Reaktive Stickstoffverbindungen in der Atmosphäre – Konzentrationsbestimmungen und trockene Deposition auf Natursteine, Diss. FB Chemie, Univ. Hamburg, Schriften. Angew. Anal., (W. Dannecker, Hrsg.), 29, 7-50.
  • [5] Brauer M., Koutrakis P., Wolfson J. M., Spengler J. D., 1989, Evaluation of the gas collection of an annular denuder system under simulated atmospheric conditions, Atmos. Environ., 23, 1981-1986.
  • [6] Eatough N. L., McGregor S., Lewis E. A., Eatough D. J., Huang A. A., Ellis E., 1988, Comparison of six denuder methods and a filter pack for the collection of ambient HNO3(g), HNO2(g) and SO2(g) in the 1985 NSCM study, Atmos. Environ., 22, 1601-1618.
  • [7] EURACHEM, 2000, Quantifying uncertainty in analytical measurement, (2nd edn.) Lab. Govern. Chem., London, 1-126.
  • [8] Falkowska L., Bolałek J., Łysiak-Pastuszak E., 1999, Analiza chemiczna wody morskiej. 2. Pierwiastki biogeniczne N, P, Si, Fe, Wyd. Uniw. Gd., Gdańsk, 40-46.
  • [9] Ferm M., 1986, Concentration measurements and equilibrium studies of ammonium, nitrate and sulphur species in air and precipitation, Ph. D. thesis, Swed. Environ. Res. Inst., Göteborg.
  • [10] Grasshoff K., Ehrhardt M., Kremling K., 1983, Methods of seawater analysis, (2nd edn.) Verl. Chem., Weinheim, 419 pp.
  • [11] Harrison R. M., Kitto A.-M. N., 1990, Field intercomparison of filter pack and denuder sampling methods for reactive gaseous and particulate pollutants, Atmos. Environ., 24A, 2633-2640.
  • [12] Long G. L., Winefordner J. D., 1983, Limit of detection. A closer look at the IUPAC definition, Anal. Chem., 55 (7), 712-724.
  • [13] Markaki Z., Oikonomou K., Kocak M., Kouvarakis G., Chaniotaki A., Kubilay N., Mihalopoulos N., 2003, Atmospheric deposition of inorganic phosphorus in the Levantine Basin, eastern Mediterranean: spatial and temporal variability and its role in seawater productivity, Limnol. Oceanogr., 48 (4), 1557-1568.
  • [14] Perrino C., de Santis F., Febo A., 1988, Criteria for the choice of a denuder sampling technique devoted to the measurement of atmospheric nitrous and nitric acid, Atmos. Environ., 24A, 617-626.
  • [15] Possanzini M., Febo A., Liberti A., 1983, New design of a high- performance denuder for the sampling of atmospheric pollutants, Atmos. Environ., 17, 2605-2610.
  • [16] Sopauskiene D., Budvytyte D., 1993, Chemical characteristics of atmospheric aerosol in rural site of Lithuania, Atmos. Environ., 28, 1291-1296.
  • [17] Vossler T. L., Stevens R. K., Paur R. J., Baumgardner R. E., Bell J. P., 1988, Evaluation of improved inlets and annual denuder systems to measure inorganic air pollutants, Atmos. Environ., 22, 1729-1736.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUS5-0011-0057
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