Fine particle pH and gas–particle phase partitioning of inorganic species in Pasadena, California, during the 2010 CalNex campaign

pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1 and PM2. 5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (Cal...

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Published inAtmospheric chemistry and physics Vol. 17; no. 9; pp. 5703 - 5719
Main Authors Guo, Hongyu, Liu, Jiumeng, Froyd, Karl D., Roberts, James M., Veres, Patrick R., Hayes, Patrick L., Jimenez, Jose L., Nenes, Athanasios, Weber, Rodney J.
Format Journal Article
LanguageEnglish
Published Katlenburg-Lindau Copernicus GmbH 08.05.2017
Copernicus Publications
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Online AccessGet full text
ISSN1680-7324
1680-7316
1680-7324
DOI10.5194/acp-17-5703-2017

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Abstract pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1 and PM2. 5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (CalNex) study from 15 May to 15 June 2010 in Pasadena, CA. Particle pH and water were predicted with the ISORROPIA-II thermodynamic model and validated by comparing predicted to measured gas–particle partitioning of inorganic nitrate, ammonium, and chloride. The study mean ± standard deviation PM1 pH was 1.9 ± 0.5 for the SO42−–NO3−–NH4+–HNO3–NH3 system. For PM2. 5, internal mixing of sea salt components (SO42−–NO3−–NH4+–Na+–Cl−–K+–HNO3–NH3–HCl system) raised the bulk pH to 2.7 ± 0.3 and improved predicted nitric acid partitioning with PM2. 5 components. The results show little effect of sea salt on PM1 pH, but significant effects on PM2. 5 pH. A mean PM1 pH of 1.9 at Pasadena was approximately one unit higher than what we have reported in the southeastern US, despite similar temperature, relative humidity, and sulfate ranges, and is due to higher total nitrate concentrations (nitric acid plus nitrate) relative to sulfate, a situation where particle water is affected by semi-volatile nitrate concentrations. Under these conditions nitric acid partitioning can further promote nitrate formation by increasing aerosol water, which raises pH by dilution, further increasing nitric acid partitioning and resulting in a significant increase in fine particle nitrate and pH. This study provides insights into the complex interactions between particle pH and nitrate in a summertime coastal environment and a contrast to recently reported pH in the eastern US in summer and winter and the eastern Mediterranean. All studies have consistently found highly acidic PM1 with pH generally below 3.
AbstractList pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1 and PM2. 5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (CalNex) study from 15 May to 15 June 2010 in Pasadena, CA. Particle pH and water were predicted with the ISORROPIA-II thermodynamic model and validated by comparing predicted to measured gas–particle partitioning of inorganic nitrate, ammonium, and chloride. The study mean ± standard deviation PM1 pH was 1.9 ± 0.5 for the SO42−–NO3−–NH4+–HNO3–NH3 system. For PM2. 5, internal mixing of sea salt components (SO42−–NO3−–NH4+–Na+–Cl−–K+–HNO3–NH3–HCl system) raised the bulk pH to 2.7 ± 0.3 and improved predicted nitric acid partitioning with PM2. 5 components. The results show little effect of sea salt on PM1 pH, but significant effects on PM2. 5 pH. A mean PM1 pH of 1.9 at Pasadena was approximately one unit higher than what we have reported in the southeastern US, despite similar temperature, relative humidity, and sulfate ranges, and is due to higher total nitrate concentrations (nitric acid plus nitrate) relative to sulfate, a situation where particle water is affected by semi-volatile nitrate concentrations. Under these conditions nitric acid partitioning can further promote nitrate formation by increasing aerosol water, which raises pH by dilution, further increasing nitric acid partitioning and resulting in a significant increase in fine particle nitrate and pH. This study provides insights into the complex interactions between particle pH and nitrate in a summertime coastal environment and a contrast to recently reported pH in the eastern US in summer and winter and the eastern Mediterranean. All studies have consistently found highly acidic PM1 with pH generally below 3.
pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM.sub.1 and PM.sub.2. 5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (CalNex) study from 15 May to 15 June 2010 in Pasadena, CA. Particle pH and water were predicted with the ISORROPIA-II thermodynamic model and validated by comparing predicted to measured gas-particle partitioning of inorganic nitrate, ammonium, and chloride. The study mean ± standard deviation PM.sub.1 pH was 1.9 ± 0.5 for the SO.sub.4 .sup.2- -NO.sub.3 .sup.- -NH.sub.4 .sup.+ -HNO.sub.3 -NH.sub.3 system. For PM.sub.2. 5, internal mixing of sea salt components (SO.sub.4 .sup.2- -NO.sub.3 .sup.- -NH.sub.4 .sup.+ -Na.sup.+ -Cl.sup.- -K.sup.+ -HNO.sub.3 -NH.sub.3 -HCl system) raised the bulk pH to 2.7 ± 0.3 and improved predicted nitric acid partitioning with PM.sub.2. 5 components. The results show little effect of sea salt on PM.sub.1 pH, but significant effects on PM.sub.2. 5 pH. A mean PM.sub.1 pH of 1.9 at Pasadena was approximately one unit higher than what we have reported in the southeastern US, despite similar temperature, relative humidity, and sulfate ranges, and is due to higher total nitrate concentrations (nitric acid plus nitrate) relative to sulfate, a situation where particle water is affected by semi-volatile nitrate concentrations. Under these conditions nitric acid partitioning can further promote nitrate formation by increasing aerosol water, which raises pH by dilution, further increasing nitric acid partitioning and resulting in a significant increase in fine particle nitrate and pH. This study provides insights into the complex interactions between particle pH and nitrate in a summertime coastal environment and a contrast to recently reported pH in the eastern US in summer and winter and the eastern Mediterranean. All studies have consistently found highly acidic PM.sub.1 with pH generally below 3.
pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1 and PM2.5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (CalNex) study from 15 May to 15 June 2010 in Pasadena, CA. Particle pH and water were predicted with the ISORROPIA-II thermodynamic model and validated by comparing predicted to measured gas–particle partitioning of inorganic nitrate, ammonium, and chloride. The study mean ± standard deviation PM1 pH was 1.9 ± 0.5 for the SO42-–NO3-–NH4+–HNO3–NH3 system. For PM2.5, internal mixing of sea salt components (SO42-–NO3-–NH4+–Na+–Cl-–K+–HNO3–NH3–HCl system) raised the bulk pH to 2.7 ± 0.3 and improved predicted nitric acid partitioning with PM2.5 components. The results show little effect of sea salt on PM1 pH, but significant effects on PM2.5 pH. A mean PM1 pH of 1.9 at Pasadena was approximately one unit higher than what we have reported in the southeastern US, despite similar temperature, relative humidity, and sulfate ranges, and is due to higher total nitrate concentrations (nitric acid plus nitrate) relative to sulfate, a situation where particle water is affected by semi-volatile nitrate concentrations. Under these conditions nitric acid partitioning can further promote nitrate formation by increasing aerosol water, which raises pH by dilution, further increasing nitric acid partitioning and resulting in a significant increase in fine particle nitrate and pH. This study provides insights into the complex interactions between particle pH and nitrate in a summertime coastal environment and a contrast to recently reported pH in the eastern US in summer and winter and the eastern Mediterranean. All studies have consistently found highly acidic PM1 with pH generally below 3.
pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1 and PM2. 5 pH are calculated based on data from measurements during the California Research at the Nexus of Air Quality and Climate Change (CalNex) study from 15 May to 15 June 2010 in Pasadena, CA. Particle pH and water were predicted with the ISORROPIA-II thermodynamic model and validated by comparing predicted to measured gas–particle partitioning of inorganic nitrate, ammonium, and chloride. The study mean ± standard deviation PM1 pH was 1.9 ± 0.5 for the SO42−–NO3−–NH4+–HNO3–NH3 system. For PM2. 5, internal mixing of sea salt components (SO42−–NO3−–NH4+–Na+–Cl−–K+–HNO3–NH3–HCl system) raised the bulk pH to 2.7 ± 0.3 and improved predicted nitric acid partitioning with PM2. 5 components. The results show little effect of sea salt on PM1 pH, but significant effects on PM2. 5 pH. A mean PM1 pH of 1.9 at Pasadena was approximately one unit higher than what we have reported in the southeastern US, despite similar temperature, relative humidity, and sulfate ranges, and is due to higher total nitrate concentrations (nitric acid plus nitrate) relative to sulfate, a situation where particle water is affected by semi-volatile nitrate concentrations. Under these conditions nitric acid partitioning can further promote nitrate formation by increasing aerosol water, which raises pH by dilution, further increasing nitric acid partitioning and resulting in a significant increase in fine particle nitrate and pH. This study provides insights into the complex interactions between particle pH and nitrate in a summertime coastal environment and a contrast to recently reported pH in the eastern US in summer and winter and the eastern Mediterranean. All studies have consistently found highly acidic PM1 with pH generally below 3.
Audience Academic
Author Jimenez, Jose L.
Veres, Patrick R.
Roberts, James M.
Guo, Hongyu
Nenes, Athanasios
Weber, Rodney J.
Liu, Jiumeng
Froyd, Karl D.
Hayes, Patrick L.
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  orcidid: 0000-0003-0487-3610
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  fullname: Guo, Hongyu
– sequence: 2
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  orcidid: 0000-0001-7238-593X
  surname: Liu
  fullname: Liu, Jiumeng
– sequence: 3
  givenname: Karl D.
  orcidid: 0000-0002-0797-6028
  surname: Froyd
  fullname: Froyd, Karl D.
– sequence: 4
  givenname: James M.
  orcidid: 0000-0002-8485-8172
  surname: Roberts
  fullname: Roberts, James M.
– sequence: 5
  givenname: Patrick R.
  orcidid: 0000-0001-7539-353X
  surname: Veres
  fullname: Veres, Patrick R.
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  surname: Jimenez
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  givenname: Athanasios
  orcidid: 0000-0003-3873-9970
  surname: Nenes
  fullname: Nenes, Athanasios
– sequence: 9
  givenname: Rodney J.
  orcidid: 0000-0003-0765-8035
  surname: Weber
  fullname: Weber, Rodney J.
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Snippet pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here, PM1...
pH is a fundamental aerosol property that affects ambient particle concentration and composition, linking pH to all aerosol environmental impacts. Here,...
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SubjectTerms Aerosol effects
Aerosols
Air quality
Ammonium
Ammonium compounds
Chemical partition
Chemical properties
Chlorides
Climate
Climate change
Coastal environments
Coastal zone
Coastal zones
Components
Concentration (composition)
Dilution
Environmental aspects
Environmental impact
Gases
Humidity
Interactions
Lasers
Mathematical models
Measurement
Measurement techniques
Mercury cadmium telluride
Nitrates
Nitric acid
Nitric acids
Particle concentration
Particulate matter
Partitioning
pH effects
Relative humidity
Standard deviation
Sulfates
Summer
Temperature effects
Thermodynamic models
Winter
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Title Fine particle pH and gas–particle phase partitioning of inorganic species in Pasadena, California, during the 2010 CalNex campaign
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