Quantification of carbonate carbon in aerosol filter samples using a modified thermal/optical carbon analyzer (M-TOCA)

2012 ◽  
Vol 4 (8) ◽  
pp. 2578 ◽  
Author(s):  
Steven Sai Hang Ho ◽  
Kin Fai Ho ◽  
Suixin Liu ◽  
Wandong Liu ◽  
Shun Cheng Lee ◽  
...  
2015 ◽  
Vol 52 (12) ◽  
pp. 1169-1181 ◽  
Author(s):  
Alyssa M. Bancroft ◽  
Frank R. Brunton ◽  
Mark A. Kleffner

The Moose River Basin in Ontario, Canada, contains nearly 1 km of Silurian marine strata, and although it has been studied for more than a century, its precise correlation globally has not been constrained. Herein, a core from the Victor Mine in the Moose River Basin was examined for conodont biostratigraphy and carbonate carbon (δ13Ccarb) isotope chemostratigraphy to provide a detailed chronostratigraphic framework for the Silurian strata (Severn River, Ekwan River, and Attawapiskat formations) in the Moose River Basin. The recovery of Aspelundia expansa, Aspelundia fluegeli fluegeli, Distomodus staurognathoides, Ozarkodina polinclinata estonica, Pterospathodus eopennatus, and Aulacognathus bullatus, as well as the lower Aeronian, upper Aeronian, lower Telychian (Valgu), and ascending limb of the Sheinwoodian (Ireviken) positive carbonate carbon (δ13Ccarb) isotope excursions provide significantly improved chronostratigraphic correlation of Llandovery strata in the Moose River Basin.


Radiocarbon ◽  
1978 ◽  
Vol 20 (3) ◽  
pp. 455-460 ◽  
Author(s):  
R A Parker ◽  
W M Sackett

Organic and carbonate carbon in sediments deposited in the Cariaco Basin and on the Mississippi River Delta and the total dissolved inorganic carbon in four water column profiles comprise the samples in this list. Except as noted below the samples were processed using the benzene synthesis and other procedures described by Mathews, et al (1972).


1998 ◽  
Vol 31 (17) ◽  
pp. 5818-5822 ◽  
Author(s):  
P. Robyr ◽  
M. Utz ◽  
Z. Gan ◽  
C. Scheurer ◽  
M. Tomaselli ◽  
...  

2014 ◽  
Vol 7 (7) ◽  
pp. 7397-7450 ◽  
Author(s):  
K. E. Yttri ◽  
J. Schnelle-Kreiss ◽  
W. Maenhaut ◽  
C. Alves ◽  
R. Bossi ◽  
...  

Abstract. The monosaccharide anhydrides (MAs) levoglucosan, galactosan and mannosan are products of incomplete combustion and pyrolysis of cellulose and hemicelluloses, and are found to be major constituents of biomass burning aerosol particles. Hence, ambient aerosol particle concentrations of levoglucosan are commonly used to study the influence of residential wood burning, agricultural waste burning and wild fire emissions on ambient air quality. A European-wide intercomparison on the analysis of the three monosaccharide anhydrides was conducted based on ambient aerosol quartz fiber filter samples collected at a Norwegian urban background site during winter. Thus, the samples' content of MAs is representative for biomass burning particles originating from residential wood burning. The purpose of the intercomparison was to examine the comparability of the great diversity of analytical methods used for analysis of levoglucosan, mannosan and galactosan in ambient aerosol filter samples. Thirteen laboratories participated, of which three applied High-Performance Anion-Exchange Chromatography (HPAEC), four used High-Performance Liquid Chromatography (HPLC) or Ultra-Performance Liquid Chromatography (UPLC), and six resorted to Gas Chromatography (GC). The analytical methods used were of such diversity that they should be considered as thirteen different analytical methods. All of the thirteen laboratories reported levels of levoglucosan, whereas nine reported data for mannosan and/or galactosan. Eight of the thirteen laboratories reported levels for all three isomers. The accuracy for levoglucosan, presented as the mean percentage error (PE) for each participating laboratory, varied from −63 to 23%; however, for 62% of the laboratories the mean PE was within ±10%, and for 85% the mean PE was within ±20%. For mannosan, the corresponding range was −60 to 69%, but as for levoglucosan, the range was substantially smaller for a subselection of the laboratories; i.e., for 33% of the laboratories the mean PE was within ±10%. For galactosan, the mean PE for the participating laboratories ranged from −84 to 593%, and as for mannosan 33% of the laboratories reported a mean PE within ±10%. The variability of the various analytical methods, as defined by their minimum and maximum PE value, was typically better for levoglucosan than for mannosan and galactosan, ranging from 3.2 to 41% for levoglucosan, from 10 to 67% for mannosan, and from 6 to 364% for galactosan. For the levoglucosan to mannosan ratio, which may be used to assess the relative importance of softwood vs. hardwood burning, the variability only ranged from 3.5 to 24%. To our knowledge, this is the first major intercomparison on analytical methods used to quantify monosaccharide anhydrides in ambient aerosol filter samples conducted and reported in the scientific literature. The results show that for levoglucosan the accuracy is only slightly lower than that reported for analysis of SO42− on filter samples, a constituent that has been analyzed by numerous laboratories for several decades, typically by ion chromatography, and which is considered a fairly easy constituent to measure. Hence, the results obtained for levoglucosan with respect to accuracy are encouraging and suggest that levels of levoglucosan, and to a lesser extent mannosan and galactosan, obtained by most of the analytical methods currently used to quantify monosaccharide anhydrides in ambient aerosol filter samples, are comparable. Finally, the various analytical methods used in the current study should be tested for other aerosol matrices and concentrations as well, the most obvious being summertime aerosol samples affected by wild fires and/or agricultural fires.


Atmosphere ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 661
Author(s):  
Denise C. Napolitano ◽  
Hilairy E. Hartnett ◽  
Pierre Herckes

Inorganic carbonate can be an important component of atmospheric particulate matter in arid environments where mineral dust components contribute significantly to air particulate matter. Carbonate carbon (CC) is only rarely quantified in atmospheric studies and methods to quantify carbonate in atmospheric samples are rare. In this manuscript, we present a novel protocol for quantifying carbonate carbon in atmospheric particulate matter samples, through the acidification of aerosol filters at ambient pressure and temperature and subsequent measurement of carbon dioxide (CO2) released upon acidification. This method is applicable to a variety of filter media used in air pollution studies, such as Teflon, cellulose, or glass fiber filters. The method allows the customization of the filter area used for analysis (up to 24 cm2) so that sufficient CO2 can be detected when released and to assure that the sample aliquot is representative of the whole filter. The resulting detection limits can be as low as 0.12 µg/cm2. The analysis of a known amount of sodium bicarbonate applied to a filter resulted in a relative error within 15% of the known mass of bicarbonate when measured 20 min after acidification. A particulate matter sample with aerodynamic diameter larger than 2.5 µm (PM>2.5) collected via cascade impaction on a high-volume aerosol sampler yielded good precision, with a CC concentration of 4.4 ± 0.3 µgC/cm2 for six replicates. The precision, accuracy, and reproducibility of this method of CC measurement make it a good alternative to existing quantification methods.


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