scholarly journals Effects of water-soluble organic carbon on aerosol pH

2019 ◽  
Vol 19 (23) ◽  
pp. 14607-14620 ◽  
Author(s):  
Michael A. Battaglia Jr. ◽  
Rodney J. Weber ◽  
Athanasios Nenes ◽  
Christopher J. Hennigan

Abstract. Water-soluble organic carbon (WSOC) is a ubiquitous and significant fraction of fine particulate matter. Despite advances in aerosol thermodynamic equilibrium models, there is limited understanding on the comprehensive impacts of WSOC on aerosol acidity (pH). We address this limitation by studying submicron aerosols that represent the two extremes in acidity levels found in the atmosphere: strongly acidic aerosol from Baltimore, MD, and weakly acidic conditions characteristic of Beijing, China. These cases are then used to construct mixed inorganic–organic single-phase aqueous particles and thermodynamically analyzed by the Extended Aerosol Inorganics Model (E-AIM) and ISORROPIA models in combination with activity coefficient model AIOMFAC (Aerosol Inorganic–Organic Mixtures Functional groups Activity Coefficient) to evaluate the effects of WSOC on the H+ ion activity coefficients (γH+) and activity (pH). We find that addition of organic acids and nonacid organic species concurrently increases γH+ and aerosol liquid water. Under the highly acidic conditions typical of the eastern US (inorganic-only pH ∼1), these effects mostly offset each other, giving pH changes of < 0.5 pH units even at organic aerosol dry mass fractions in excess of 60 %. Under conditions with weaker acidity typical of Beijing (inorganic-only pH ∼4.5), the nonacidic WSOC compounds had similarly minor effects on aerosol pH, but organic acids imparted the largest changes in pH compared to the inorganic-only simulations. Organic acids affect pH in the order of their pKa values (oxalic acid > malonic acid > glutaric acid). Although the inorganic-only pH was above the pKa value of all three organic acids investigated, pH changes in excess of 1 pH unit were only observed at unrealistic organic acid levels (aerosol organic acid concentrations > 35 µg m−3) in Beijing. The model simulations were run at 70 %, 80 %, and 90 % relative humidity (RH) levels and the effect of WSOC was inversely related to RH. At 90 % RH, WSOC altered aerosol pH by up to ∼0.2 pH units, though the effect was up to ∼0.6 pH units at 70 % RH. The somewhat offsetting nature of these effects suggests that aerosol pH is sufficiently constrained by the inorganic constituents alone under conditions where liquid–liquid phase separation is not anticipated to occur.

2020 ◽  
Author(s):  
Christopher Hennigan ◽  
Michael Battaglia, Jr. ◽  
Rodney Weber ◽  
Athanasios Nenes

&lt;p&gt;Water soluble organic carbon (WSOC) is a ubiquitous and significant fraction of fine particulate matter.&amp;#160; Despite advances in aerosol thermodynamic equilibrium models, there is limited understanding on the comprehensive impacts of WSOC on aerosol acidity (pH).&amp;#160; We address this limitation by studying submicron aerosol that represent the two extremes in acidity levels found in the atmosphere: strongly acidic aerosol from Baltimore, MD, and weakly acidic conditions characteristic of Beijing, China. These cases are then used to construct mixed inorganic/organic single-phase aqueous particles, and thermodynamically analyzed by the E-AIM and ISORROPIA models in combination with activity coefficient model AIOMFAC to evaluate the effects of WSOC on the H&lt;sup&gt;+&lt;/sup&gt; ion activity coefficients (&amp;#947;&lt;sub&gt;H+&lt;/sub&gt;) and activity (pH).&amp;#160; We find that addition of organic acids and non-acid organic species concurrently increases &amp;#947;&lt;sub&gt;H+&lt;/sub&gt; and aerosol liquid water.&amp;#160; Under the highly acidic conditions typical of the eastern U.S. (inorganic-only pH ~1), these effects mostly offset each other, giving pH changes of &lt; 0.5 pH units even at organic aerosol dry mass fractions in excess of 60%.&amp;#160; Under conditions with weaker acidity typical of Beijing (inorganic-only pH ~4.5), the non-acidic WSOC compounds had similarly minor effects on aerosol pH, but organic acids imparted the largest changes in pH compared to the inorganic-only simulations.&amp;#160; Organic acids affect pH in the order of their pKa values (oxalic acid &gt; malonic acid &gt; glutaric acid).&amp;#160; Although the inorganic-only pH was above the pK&lt;sub&gt;a&lt;/sub&gt; value of all three organic acids investigated, pH changes in excess of 1 pH unit were only observed at unrealistic organic acid levels (aerosol organic acid concentrations &gt; 35 &amp;#181;g m&lt;sup&gt;-3&lt;/sup&gt;) in Beijing.&amp;#160; The model simulations were run at 70%, 80%, and 90% relative humidity (RH) levels and the effect of WSOC was inversely related to RH.&amp;#160; At 90% RH, WSOC altered aerosol pH by up to ~0.2 pH units, though the effect was up to ~0.6 pH units at 70% RH.&amp;#160; The somewhat offsetting nature of these effects suggests that aerosol pH is sufficiently constrained by the inorganic constituents alone under conditions where liquid-liquid phase separation is not anticipated to occur.&lt;/p&gt;


2019 ◽  
Author(s):  
Michael A. Battaglia Jr. ◽  
Rodney J. Weber ◽  
Athanasios Nenes ◽  
Christopher J. Hennigan

Abstract. Water soluble organic carbon (WSOC) is a ubiquitous and significant fraction of fine particulate matter. Despite advances in aerosol thermodynamic equilibrium models, there is limited understanding on the comprehensive impacts of WSOC on aerosol acidity (pH). We address this limitation by studying submicron aerosol that represent the two extremes in acidity levels found in the atmosphere: strongly acidic aerosol from Baltimore, MD, and weakly acidic conditions characteristic of Beijing, China. These cases are then used to construct mixed inorganic/organic single-phase aqueous particles, and thermodynamically analyzed by the E-AIM and ISORROPIA models (in combination with activity coefficient model AIOMFAC) to evaluate the effects of WSOC on the H+ ion activity coefficients (γH+) and activity (pH). We find that addition of organic acids and non-acid organic species concurrently increases γH+ and aerosol liquid water. When allowed to modulate pH, these effects mostly offset each other, giving pH changes of


2009 ◽  
Vol 43 (11) ◽  
pp. 1099-1107 ◽  
Author(s):  
David C. Snyder ◽  
Andrew P. Rutter ◽  
Ryan Collins ◽  
Chris Worley ◽  
James J. Schauer

Atmosphere ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 395
Author(s):  
Yali Jin ◽  
Caiqing Yan ◽  
Amy P. Sullivan ◽  
Yue Liu ◽  
Xinming Wang ◽  
...  

Despite the significant role water-soluble organic carbon (WSOC) plays in climate and human health, sources and formation mechanisms of atmospheric WSOC are still unclear; especially in some heavily polluted areas. In this study, near real-time WSOC measurement was conducted in Beijing for the first time with a particle-into-liquid-sampler coupled to a total organic carbon analyzer during the springtime, together with collocated online measurements of other chemical components in fine particulate matter with a 1 h time resolution, including elemental carbon (EC), organic carbon (OC), multiple metals, and water-soluble ions. Good correlations of WSOC with primary OC, as well as carbon monoxide, indicated that major sources of WSOC were primary instead of secondary during the study period. The positive matrix factorization model-based source apportionment results quantified that 68 ± 19% of WSOC could be attributed to primary sources, with predominant contributions by biomass burning during the study period. This finding was further confirmed by the estimate with the modified EC-tracer method, suggesting significant contribution of primary sources to WSOC. However, the relative contribution of secondary source to WSOC increased during haze episodes. The WSOC/OC ratio exhibited similar diurnal distributions with O3 and correlated well with secondary WSOC, suggesting that the WSOC/OC ratio might act as an indicator of secondary formation when WSOC was dominated by primary sources. This study provided evidence that primary sources could be major sources of WSOC in some polluted megacities, such as Beijing. From this study, it can be seen that WSOC cannot be simply used as a surrogate of secondary organic aerosol, and its major sources could vary by season and location.


2014 ◽  
Vol 119 (6) ◽  
pp. 3476-3485 ◽  
Author(s):  
Elena N. Kirillova ◽  
August Andersson ◽  
Suresh Tiwari ◽  
Atul Kumar Srivastava ◽  
Deewan Singh Bisht ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document