Insights into the characteristics and sources of primary and secondary organic carbon: High time resolution observation in urban Shanghai

2018 ◽  
Vol 233 ◽  
pp. 1177-1187 ◽  
Author(s):  
Jian Xu ◽  
Qiongzhen Wang ◽  
Congrui Deng ◽  
V. Faye McNeill ◽  
Alison Fankhauser ◽  
...  
2020 ◽  
Vol 7 (9) ◽  
Author(s):  
Congcong Yu ◽  
Jinpei Yan ◽  
Honghai Zhang ◽  
Qi Lin ◽  
Hongguo Zheng ◽  
...  

2010 ◽  
Vol 3 (4) ◽  
pp. 1063-1074 ◽  
Author(s):  
H. Timonen ◽  
M. Aurela ◽  
S. Carbone ◽  
K. Saarnio ◽  
S. Saarikoski ◽  
...  

Abstract. A particle-into-liquid sampler (PILS) was coupled with a total organic carbon analyzer (TOC) and two ion chromatographs (IC) to enable high time-resolution measurements of water-soluble ions and water-soluble organic carbon (WSOC) by a single sampling and analytical set-up. The new high time-resolution measurement system, the PILS-TOC-IC, was able to provide essential chemical and physical information about fast changes in composition, concentrations and likely sources of the water-soluble fraction of atmospheric aerosol. The concentrations of major water-soluble ions and WSOC were measured by the PILS-TOC-IC system from 25 April to 28 May 2009. The data of the PILS-TOC-IC setup was compared with the data from the High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) data measured from 25 April to 8 May 2009. The measured water-soluble particulate organic matter (WSPOM) concentration varied typically from 0.10 to 8.8 μg m−3 (on average 1.5 μg m−3). The WSPOM contributed on average 51% to particulate organic matter (POM) measured with the AMS. The correlation between the data of all the online measurement devices (AMS, PILS-TOC-IC, semicontinuous EC/OC carbon analyzer and TEOM) was excellent. For sulfate, nitrate and ammonium the correlations between the PILS-TOC-IC and AMS were 0.93, 0.96 and 0.96, respectively. The correlation between WSPOM and POM was also strong (r = 0.88). The identified sources of WSPOM were long-range transported biomass burning and secondary organic aerosol (SOA) formation. WSPOM and oxalate produced in biomass burning were clearly correlated with carbon monoxide.


2020 ◽  
Vol 13 (8) ◽  
pp. 4333-4351
Author(s):  
Martin Rigler ◽  
Luka Drinovec ◽  
Gašper Lavrič ◽  
Athanasia Vlachou ◽  
André S. H. Prévôt ◽  
...  

Abstract. We present a newly developed total carbon analyzer (TCA08) and a method for online speciation of carbonaceous aerosol with a high time resolution. The total carbon content is determined by flash heating of a sample collected on a quartz-fiber filter with a time base between 20 min and 24 h. The limit of detection is approximately 0.3 µg C, which corresponds to a concentration of 0.3 µg C m−3 at a sample flow rate of 16.7 L min−1 and a 1 h sampling time base. The concentration of particulate equivalent organic carbon (OC) is determined by subtracting black carbon concentration, concurrently measured optically by an Aethalometer®, from the total carbon concentration measured by the TCA08. The combination of the TCA08 and Aethalometer (AE33) is an easy-to-deploy and low-maintenance continuous measurement technique for the high-time-resolution determination of equivalent organic and elemental carbon (EC) in different particulate matter size fractions, which avoids pyrolytic correction and the need for high-purity compressed gases. The performance of this online method relative to the standardized off-line thermo-optical OC–EC method and respective instruments was evaluated during a winter field campaign at an urban background location in Ljubljana, Slovenia. The organic-matter-to-organic-carbon ratio obtained from the comparison with an aerosol chemical speciation monitor (ACSM) was OM/OC=1.8, in the expected range.


2020 ◽  
Vol 223 ◽  
pp. 117241 ◽  
Author(s):  
Rosa M. Flores ◽  
Elif Mertoğlu ◽  
Hüseyin Özdemir ◽  
Bülent O. Akkoyunlu ◽  
Göksel Demir ◽  
...  

2019 ◽  
Author(s):  
Martin Rigler ◽  
Luka Drinovec ◽  
Gašper Lavrič ◽  
Athanasia Vlachou ◽  
André S. H. Prévôt ◽  
...  

Abstract. We present the newly developed Total Carbon Analyzer (TCA08), and a new method for online speciation of carbonaceous aerosol with a high time resolution. The total carbon content is determined by flash heating of a sample collected on a quartz-fiber filter with a time base between 20 min and 24 h. The limit of detection is approximately 0.3 μgC, which corresponds to a concentration of 0.3 μgC/m3 at a sample flow rate of 16.7 LPM and a 1-hour sampling time base. The concentration of particulate organic carbon (OC) is determined by subtracting black carbon concentration, concurrently measured optically by an Aethalometer®, from the total carbon concentration measured by the TCA08. The combination of TCA08 and Aethalometer (AE33) is an easy-to-deploy and low maintenance continuous measurement technique for the high time resolution determination of organic and elemental carbon (EC) in different particulate matter size fractions, which avoids pyrolytic correction and need for high purity compressed gases. The equivalence of this new online method to the standardized off-line thermo-optical OC-EC methods was evaluated during a winter field campaign at an urban background location in Ljubljana, Slovenia. The organic matter-to-organic carbon ratio obtained from the comparison with an Aerosol Chemical Speciation Monitor (ACSM) was OM/OC = 1.8, in the expected range.


2016 ◽  
Vol 16 (15) ◽  
pp. 9693-9710 ◽  
Author(s):  
Manuel Dall'Osto ◽  
David C. S. Beddows ◽  
Eoin J. McGillicuddy ◽  
Johanna K. Esser-Gietl ◽  
Roy M. Harrison ◽  
...  

Abstract. The aerosol time-of-flight mass spectrometer (ATOFMS) provides size-resolved information on the chemical composition of single particles with high time resolution. Within SAPUSS (Solving Aerosol Problems by Using Synergistic Strategies), continuous ATOFMS measurements of ambient particles were made simultaneously at two urban locations: urban background (UB) site and roadside (RS) site in the city of Barcelona (Spain) from 17 September to 18 October 2010. Two different instrumental configurations were used: ATOFMS (TSI 3800) with a converging nozzle inlet (high efficiency at about 800–2000 nm) at the UB site and ATOFMS (TSI 3800-100) with an aerodynamic lens inlet (high efficiency at about 300–700 nm) at the RS site. This is the first time, to our knowledge, that two ATOFMS instruments have been deployed in the same field study. The different instrument configurations had an impact on the observed particle types at the two sites. Nevertheless, 10 particle types were detected at both locations, including local and regional elemental carbon (22.7–58.9 % of total particles), fresh and aged sea salt (1.0–14.6 %), local and regional nitrate-containing aerosols (3–11.6 %), local lead-containing metallic particles (0.1–0.2 %), and transported Fe-nitrate particles (0.8–2.5 %). The ATOFMS at the UB also characterized four particle types: calcium-containing dust (0.9 %), Saharan dust (1.3 %), vanadium-containing particles (0.9 %), and vegetative debris (1.7 %). By contrast, the high statistical counts of fine particles detected at the RS allowed identification of eight particle types. Four of these contained organic nitrogen of primary and secondary origin, which highlights the complex nature of the sources and processes that contribute to this aerosol chemical component. Aminium salts were found related to coarse sulfate-rich particle types, suggesting heterogeneous reaction mechanisms for their formation. The other four particle types mainly containing organic carbon were found spiking at different types of the day, also showing a complex single-particle mixing state relationship between organic carbon and nitrate. This ATOFMS study clearly shows that the composition of atmospheric fine particles in Barcelona, and likely other Mediterranean urban areas, is complex, with a wide range of local and regional sources combining with chemical processing to produce at least 22 different particle types exhibiting different temporal behaviour. The advantage of using two ATOFMS instruments is also demonstrated, with the nozzle-skimmer configuration enabling detection of coarse dust particles and the aerodynamic lens configuration allowing better identification of particles rich in organic carbon and amines. Overall, we find that organic nitrogen is a considerable fraction of the single particles detected, especially at the traffic-dominated RS site. Further studies are needed, especially at high time resolution, to better understand the sources and properties of particulate organic nitrogen.


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