Using Aerosol Light Absorption Measurements for the Quantitative Determination of Wood Burning and Traffic Emission Contributions to Particulate Matter

2008 ◽  
Vol 42 (9) ◽  
pp. 3316-3323 ◽  
Author(s):  
Jisca Sandradewi ◽  
Andre S. H. Prévôt ◽  
Sönke Szidat ◽  
Nolwenn Perron ◽  
M. Rami Alfarra ◽  
...  
1972 ◽  
Vol 55 (5) ◽  
pp. 1145-1149
Author(s):  
Lueangier Moten

Abstract A quantitative method is presented for the determination of cadmium at low levels (5–20 ppm) in water-soluble color additives by atomic absorption spectroscopy. Absorption measurements were made on aqueous solutions of typical color additives to which known amounts of cadmium had been added. The method requires no pretreatment of sample and should be applicable to all water-soluble color additives.


1971 ◽  
Vol 54 (4) ◽  
pp. 790-795
Author(s):  
C E Jones ◽  
L E Pracht

Abstract This collaborative study represents an attempt to validate the ion exchange zincon method for the quantitative determination of zinc in fertilizers. The values of the standard deviations Sd, Sr, and Sb and the results of the F- and t-tests are presented as an estimate of the precision, accuracy, and dependability. Atomic absorption measurements were also made and provided reference data for evaluation purposes. In its present form, the method falls short of expectations as an alternative wet approach to the dithizone method. It is recommended that the methods for determining zinc in fertilizers be studied further.


2016 ◽  
Author(s):  
Peter Zotter ◽  
Hanna Herich ◽  
Martin Gysel ◽  
Imad El-Haddad ◽  
Yanlin Zhang ◽  
...  

Abstract. Black carbon (BC) measured by a multi-wavelength Aethalometer can be apportioned to traffic and wood burning. The method is based on the differences in the dependence of aerosol absorption on the wavelength of light used to investigate the sample, parameterized by the source-specific Ångström absorption exponent (α). While the spectral dependence (defined as α values) of the traffic-related BC light absorption is low, wood smoke particles feature enhanced light absorption in the blue and near ultraviolet. Source apportionment results using this methodology are hence strongly dependent on the α values assumed for both types of emissions: traffic αTR, and wood burning αWB. Most studies use a single αTR and αWB pair in the Aethalometer model, derived from previous work. However, an accurate determination of the source specific α values is currently lacking and in some recent publications the applicability of the Aethalometer model was questioned. Here we present an indirect methodology for the determination of WB and αTR by comparing the source apportionment of BC using the Aethalometer model with 14C measurements of the EC fraction on 16 to 40 h filter samples from several locations and campaigns across Switzerland during 2005–2012, mainly in winter. The data obtained at eight stations with different source characteristics also enabled the evaluation of the performance and the uncertainties of the Aethalometer model in different environments. The best combination of αTR and αWB (0.9 and 1.68, respectively) was obtained by fitting the Aethalometer model outputs (calculated with the absorption coefficients at 470 nm and 950 nm) against the fossil fraction of EC (ECF/EC) derived from 14C measurements. Aethalometer and 14C source apportionment results are well correlated (r = 0.81) and the fitting residuals exhibit only a minor positive bias of 1.6 % and an average precision of 9.3 %. This indicates that the Aethalometer model reproduces reasonably well the 14C results for all stations investigated in this study using our best estimate of a single αWB and αTR pair. Combining the EC, 14C and Aethalometer measurements further allowed assessing the dependence of the mass absorption cross section (MAC) of BC on its source. Results indicate no significant difference in MAC at 880 nm between BC originating from traffic or wood burning emissions. Using ECF/EC as reference and constant a priori selected αTR values, αWB was also calculated for each individual data point. No clear station-to-station or season-to-season differences in αWB were observed, but αTR and αWB values are interdependent. For example, an increase in αTR by 0.1 results in a decrease in αWB by 0.1. The fitting residuals of different αTR and αWB combinations depend on ECF/EC such that a good agreement cannot be obtained over the entire ECF/EC range using other α pairs. Additional combinations of αTR = 0.8, and 1.0 and αWB = 1.8 and 1.6, respectively, are possible but only for ECF/EC between ~ 40 % and 85 %. Applying α values previously used in literature such as αWB of ~ 2 or any αWB in combination with αTR = 1.1 to our data set results in large residuals. Therefore we recommend to use the best α combination as obtained here (αTR = 0.9 and αWB = 1.68) in future studies when no or only limited additional information like 14C measurements are available. However, these results were obtained for locations impacted by BC mainly from traffic consisting of a modern car fleet and residential wood combustion with well-constrained combustion efficiencies. For regions of the world with different combustion conditions, additional BC sources or fuels used further investigations are needed.


2012 ◽  
Vol 12 (10) ◽  
pp. 27367-27393
Author(s):  
S. Canepari ◽  
C. Farao ◽  
E. Marconi ◽  
C. Giovannelli ◽  
C. Perrino

Abstract. This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C). The analytical performance of the method was verified by using standard materials containing 5.55% and 1% by weight of water. The recovery was greater than 95%; the detection limit was about 20 μg. The method was then applied to NIST reference materials (NIST1649a, urban particulate matter) and to real PM10 samples collected in different geographical areas. In all cases the repeatability was satisfactory (10–15%). When analyzing the reference material, the separation of four different types of water was obtained. In real PM10 samples the amount of water and its thermal profile differed as a function of the chemical composition of the dust. Mass percentages of 3–4% of water were obtained in most samples, but values up to about 15% were reached in areas where the chemical composition of PM is dominated by secondary inorganic ions and organic matter. High percentages of water were also observed in areas where PM is characterized by the presence of desert dust. A possible identification of the quality of water released from the samples was tried by applying the method to some hygroscopic compounds that are likely contained in PM (pure SiO2, Al2O3, ammonium salts, carbohydrates and dicarboxylic acids) and by comparing the results with those obtained from field samples.


2007 ◽  
Vol 5 (4) ◽  
Author(s):  
Marie-Christine Fournier-Salaün ◽  
Philippe Salaün

AbstractIn the last decade, different methods have been developed for the determination of chromium(VI) concentration in water. These methods use high cost equipment or they require a long preparation time. Because of their drawbacks, this paper describes an on-line, rapid and sensitive procedure for the determination of Cr(VI) concentrations in aqueous solutions via pH and absorption measurements. Only four Cr(VI) species are considered. The effects of pH and of total amount of chromium on the Cr(VI) speciation are investigated. The molar absorptivities of four chromium species at 371 nm are determined by minimising an objective function. The knowledge of these molar absorptivities and the measurements of pH and absorption at 371 nm lead to a rapid determination of total Cr(VI) concentration. The reliability and applicability of the method were confirmed using synthetic water samples.


2017 ◽  
Vol 17 (6) ◽  
pp. 4229-4249 ◽  
Author(s):  
Peter Zotter ◽  
Hanna Herich ◽  
Martin Gysel ◽  
Imad El-Haddad ◽  
Yanlin Zhang ◽  
...  

Abstract. Equivalent black carbon (EBC) measured by a multi-wavelength Aethalometer can be apportioned to traffic and wood burning. The method is based on the differences in the dependence of aerosol absorption on the wavelength of light used to investigate the sample, parameterized by the source-specific absorption Ångström exponent (α). While the spectral dependence (defined as α values) of the traffic-related EBC light absorption is low, wood smoke particles feature enhanced light absorption in the blue and near ultraviolet. Source apportionment results using this methodology are hence strongly dependent on the α values assumed for both types of emissions: traffic αTR, and wood burning αWB. Most studies use a single αTR and αWB pair in the Aethalometer model, derived from previous work. However, an accurate determination of the source specific α values is currently lacking and in some recent publications the applicability of the Aethalometer model was questioned.Here we present an indirect methodology for the determination of αWB and αTR by comparing the source apportionment of EBC using the Aethalometer model with 14C measurements of the EC fraction on 16 to 40 h filter samples from several locations and campaigns across Switzerland during 2005–2012, mainly in winter. The data obtained at eight stations with different source characteristics also enabled the evaluation of the performance and the uncertainties of the Aethalometer model in different environments. The best combination of αTR and αWB (0.9 and 1.68, respectively) was obtained by fitting the Aethalometer model outputs (calculated with the absorption coefficients at 470 and 950 nm) against the fossil fraction of EC (ECF ∕ EC) derived from 14C measurements. Aethalometer and 14C source apportionment results are well correlated (r  =  0.81) and the fitting residuals exhibit only a minor positive bias of 1.6 % and an average precision of 9.3 %. This indicates that the Aethalometer model reproduces reasonably well the 14C results for all stations investigated in this study using our best estimate of a single αWB and αTR pair. Combining the EC, 14C, and Aethalometer measurements further allowed assessing the dependence of the mass absorption cross section (MAC) of EBC on its source. Results indicate no significant difference in MAC at 880 nm between EBC originating from traffic or wood-burning emissions. Using ECF ∕ EC as reference and constant a priori selected αTR values, αWB was also calculated for each individual data point. No clear station-to-station or season-to-season differences in αWB were observed, but αTR and αWB values are interdependent. For example, an increase in αTR by 0.1 results in a decrease in αWB by 0.1. The fitting residuals of different αTR and αWB combinations depend on ECF ∕ EC such that a good agreement cannot be obtained over the entire ECF ∕ EC range using other α pairs. Additional combinations of αTR  =  0.8, and 1.0 and αWB  =  1.8 and 1.6, respectively, are possible but only for ECF ∕ EC between  ∼  40 and 85 %. Applying α values previously used in the literature such as αWB of  ∼  2 or any αWB in combination with αTR  =  1.1 to our data set results in large residuals. Therefore we recommend to use the best α combination as obtained here (αTR  =  0.9 and αWB  =  1.68) in future studies when no or only limited additional information like 14C measurements are available. However, these results were obtained for locations impacted by black carbon (BC) mainly from traffic consisting of a modern car fleet and residential wood combustion with well-constrained combustion efficiencies. For regions of the world with different combustion conditions, additional BC sources, or fuels used, further investigations are needed.


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