scholarly journals Chemical characterization of fine particular matter in Changzhou, China and source apportionment with offline aerosol mass spectrometry

2016 ◽  
Author(s):  
Zhaolian Ye ◽  
Jiashu Liu ◽  
Aijun Gu ◽  
Feifei Feng ◽  
Yuhai Liu ◽  
...  
Keyword(s):  
Trace Elements ◽  
Organic Matter ◽  
Organic Carbon ◽  
Source Apportionment ◽  
Major Ions ◽  
Chemical Properties ◽  
Chemical Characterization ◽  
Water Soluble ◽  
Traffic Emissions ◽  
Aerosol Mass

Abstract. Knowledge on aerosol chemistry in densely populated regions is critical for reduction of air pollution, while such studies haven't been conducted in Changzhou, an important manufacturing base and polluted city in the Yangtze River Delta (YRD), China. This work, for the first time, performed a thorough chemical characterization on the fine particular matter (PM2.5) samples, collected during July 2015 to April 2016 across four seasons in Changzhou city. A suite of analytical techniques were employed to characterize organic carbon / elemental carbon (OC / EC), water-soluble organic carbon (WSOC), water-soluble inorganic ions (WSIIs), trace elements, and polycyclic aromatic hydrocarbons (PAHs) in PM2.5; in particular, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was deployed to probe the chemical properties of water-soluble organic aerosols (WSOA). The average PM2.5 concentrations were found to be 108.3 μg m−3, and all identified species were able to reconstruct ~ 80 % of the PM2.5 mass. The WSIIs occupied about half of the PM2.5 mass (~ 52.1 %), with SO42−, NO3− and NH4+ as the major ions. On average, nitrate concentrations dominated over sulfate (mass ratio of 1.21), indicating influences from traffic emissions. OC and EC correlated well with each other and the highest OC / EC ratio (5.16) occurred in winter, suggesting complex OC sources likely including both secondarily formed and primarily emitted OA. Concentrations of eight trace elements (Mn, Zn, Al, B, Cr, Cu, Fe, Pb) can contribute up to 6.0 % of PM2.5 during winter. PAHs concentrations were also high in winter (140.25 ng m−3), which were predominated by median/high molecular weight PAHs with 5- and 6-rings. The organic matter including both water-soluble and water-insoluble species occupied ~ 20 % PM2.5 mass. SP-AMS determined that the WSOA had an average atomic oxygen-to-carbon (O / C), hydrogen-to-carbon (H / C), nitrogen-to-carbon (N / C) and organic matter-to-organic carbon (OM / OC) ratios of 0.36, 1.54, 0.11, and 1.74, respectively. Source apportionment of WSOA further identified two secondary OA (SOA) factors (a less oxidized and a more oxidized OA) and two primary OA (POA) factors (a nitrogen enriched hydrocarbon-like traffic OA and a cooking-related OA). On average, the POA contribution overweighed SOA (55 % vs. 45 %), indicating the important role of local anthropogenic emissions to the aerosol pollution in Changzhou. Our measurement also shows the abundance of organic nitrogen species in WSOA, and the source analyses suggest these species likely associated with traffic emissions, which warrants more investigations on PM samples from other locations.

scholarly journals Chemical characterization of fine particulate matter in Changzhou, China, and source apportionment with offline aerosol mass spectrometry

2017 ◽  
Vol 17 (4) ◽  
pp. 2573-2592 ◽  
Author(s):  
Zhaolian Ye ◽  
Jiashu Liu ◽  
Aijun Gu ◽  
Feifei Feng ◽  
Yuhai Liu ◽  
...  
Keyword(s):  
Trace Elements ◽  
Organic Matter ◽  
Particulate Matter ◽  
Organic Carbon ◽  
Source Apportionment ◽  
Fine Particulate Matter ◽  
Chemical Characterization ◽  
Water Soluble ◽  
Aerosol Mass ◽  
Fine Particulate

Abstract. Knowledge of aerosol chemistry in densely populated regions is critical for effective reduction of air pollution, while such studies have not been conducted in Changzhou, an important manufacturing base and populated city in the Yangtze River Delta (YRD), China. This work, for the first time, performed a thorough chemical characterization on the fine particulate matter (PM2.5) samples, collected during July 2015 to April 2016 across four seasons in this city. A suite of analytical techniques was employed to measure the organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), water-soluble inorganic ions (WSIIs), trace elements, and polycyclic aromatic hydrocarbons (PAHs) in PM2.5; in particular, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was deployed to probe the chemical properties of water-soluble organic aerosol (WSOA). The average PM2.5 concentration was found to be 108.3 µg m−3, and all identified species were able to reconstruct ∼ 80 % of the PM2.5 mass. The WSIIs occupied about half of the PM2.5 mass (∼ 52.1 %), with SO42−, NO3−, and NH4+ as the major ions. On average, nitrate concentrations dominated over sulfate (mass ratio of 1.21), indicating that traffic emissions were more important than stationary sources. OC and EC correlated well with each other and the highest OC ∕ EC ratio (5.16) occurred in winter, suggesting complex OC sources likely including both secondary and primary ones. Concentrations of eight trace elements (Mn, Zn, Al, B, Cr, Cu, Fe, Pb) can contribute up to ∼ 5.0 % of PM2.5 during winter. PAH concentrations were also high in winter (140.25 ng m−3), which were predominated by median/high molecular weight PAHs with five and six rings. The organic matter including both water-soluble and water-insoluble species occupied ∼ 21.5 % of the PM2.5 mass. SP-AMS determined that the WSOA had average atomic oxygen-to-carbon (O ∕ C), hydrogen-to-carbon (H ∕ C), nitrogen-to-carbon (N ∕ C), and organic matter-to-organic carbon (OM ∕ OC) ratios of 0.54, 1.69, 0.11, and 1.99, respectively. Source apportionment of WSOA further identified two secondary OA (SOA) factors (a less oxidized and a more oxidized oxygenated OA) and two primary OA (POA) factors (a nitrogen-enriched hydrocarbon-like traffic OA and a local primary OA likely including species from cooking, coal combustion, etc.). On average, the POA contribution outweighed SOA (55 % vs. 45 %), indicating the important role of local anthropogenic emissions in the aerosol pollution in Changzhou. Our measurement also shows the abundance of organic nitrogen species in WSOA, and the source analyses suggest these species are likely associated with traffic emissions, which warrants more investigations on PM samples from other locations.

scholarly journals Water-soluble organic carbon aerosols during a full New Delhi winter: Isotope-based source apportionment and optical properties

2014 ◽  
Vol 119 (6) ◽  
pp. 3476-3485 ◽  
Author(s):  
Elena N. Kirillova ◽  
August Andersson ◽  
Suresh Tiwari ◽  
Atul Kumar Srivastava ◽  
Deewan Singh Bisht ◽  
...  
Keyword(s):  
Optical Properties ◽  
Organic Carbon ◽  
Source Apportionment ◽  
Water Soluble ◽  
New Delhi ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon ◽  
Carbon Aerosols

scholarly journals Effect of Tillage System and Organic Matter Management Interactions on Soil Chemical Properties and Biological Activity in a Spring Wheat Short-Time Cultivation

Energies ◽  
2021 ◽  
Vol 14 (21) ◽  
pp. 7451
Author(s):  
Barbara Breza-Boruta ◽  
Karol Kotwica ◽  
Justyna Bauza-Kaszewska
Keyword(s):  
Organic Matter ◽  
Biological Activity ◽  
Organic Carbon ◽  
Spring Wheat ◽  
Chemical Properties ◽  
Soil Samples ◽  
Available Phosphorus ◽  
Organic Carbon Content ◽  
Tillage System ◽  
Short Time

Properly selected tillage methods and management of the available organic matter resources are considered important measures to enable farming in accordance with the principles of sustainable agriculture. Depending on the depth and intensity of cultivation, tillage practices affect soil chemical composition, structure and biological activity. The three-year experiment was performed on the soil under spring wheat (cv. Tybalt) short-time cultivation. The influence of different tillage systems and stubble management on the soil’s chemical and biological parameters was analyzed. Organic carbon content (OC); content of biologically available phosphorus (Pa), potassium (Ka), and magnesium (Mg); content of total nitrogen (TN), mineral nitrogen forms: N-NO3 and N-NH4 were determined in various soil samples. Moreover, the total number of microorganisms (TNM), bacteria (B), actinobacteria (A), fungi (F); soil respiratory activity (SR); and pH in 1 M KCl (pH) were also investigated. The results show that organic matter amendment is of greater influence on soil characteristics than the tillage system applied. Manure application, as well as leaving the straw in the field, resulted in higher amounts of organic carbon and biologically available potassium. A significant increase in the number of soil microorganisms was also observed in soil samples from the experimental plots including this procedure.

scholarly journals Status and Speciation of Silicon and Its Interaction with Physico-Chemical Properties

2021 ◽  
pp. 1-11
Author(s):  
Isaiah Ufuoma Efenudu ◽  
Ehi Robert Orhue ◽  
Ogochukwu Jennifer Ikeh ◽  
Michael Aimiesomon Erhayimwen ◽  
Blessing James
Keyword(s):  
Organic Matter ◽  
Acidic Medium ◽  
Soil Depth ◽  
Chemical Properties ◽  
Water Soluble ◽  
Sequential Fractionation ◽  
Soil Redox ◽  
Parent Materials ◽  
Physico Chemical ◽  
Negative Effect

The effectiveness of three different extractants soil mixtures—HCl, HCl + H2S04, and DTPA-TEA, in order to determine Si from soil and the forms of Silicon as influenced by different parent materials under acidic medium. Seven forms of Silicon; namely water soluble, specifically adsorbed, oxides bound, organic matter bound, exchangeable, residual, total viz sequential fractionation. Extractable Si value established in this study was (50.0 mg kg-1), indicating negative effect on plant physiology. The physico-chemical properties decreased significantly with increase in soil depth vs soil parent materials. In addition, the forms of Si in the parent materials decreased in the pattern RES, bound residual fractions > EXC, soluble & exchangeable fractions > OM, organic matter fraction. Among the properties the silt fraction, pH & OM significantly and positively correlated with the forms of silicon, with negative correlation vs clay which maybe due to silicon adsorption by clayey fraction of the soil (redox). Therefore the soil maybe be maintained and conserved for farming activities.

scholarly journals Contents, distribution, and fractionation of soil organic carbon and trace elements in soils under a green manure application

2020 ◽  
Vol 16 (No. 1) ◽  
pp. 50-58
Author(s):  
Yana Timofeeva ◽  
Lyudmila Purtova ◽  
Alexey Emelyanov ◽  
Maxim Burdukovskii ◽  
Irina Kiseleva ◽  
...  
Keyword(s):  
Trace Elements ◽  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Green Manure ◽  
Mineral Soil ◽  
Water Soluble ◽  
Household Waste ◽  
Nickel Ions ◽  
Low Degree ◽  
Soluble Components

We quantified the soluble fractions of the soil organic carbon (SOC) concentrations and the total and water-soluble trace elements in soils contaminated by household waste and remediated via the addition of green manure over 13 years and identified the main factors controlling the vertical distribution and accumulation of the trace elements. Green manure favoured the active formation of soil organic matter. The SOC of the examined soils was characterised by the active stabilisation by mineral soil compounds, but by a low degree of humification. The soils showed increased concentrations of Cr and Ni ions. The SOC and different soil compounds enriched by Si, Ca, and Mn ions were the important determinant for the distribution of Sr, V and Cu ions, as well as for the distribution of Pb and Cr ions bound to the water-soluble components of the soils. The low degree of SOC humification may be one of the main reasons of the high concentrations of Cu and Pb ions in the composition of the water-soluble soil compounds. The nickel ions were mainly associated with compounds enriched by the Al and Fe ions. The extremely high percentage concentration of the Ni ions in the water-soluble components of the soils may be result of the absence of the Ni ions adsorption by humic substances.

scholarly journals Source Apportionment of Fine Organic and Inorganic Atmospheric Aerosol in an Urban Background Area in Greece

Atmosphere ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 330 ◽  
Author(s):  
Manousos Ioannis Manousakas ◽  
Kalliopi Florou ◽  
Spyros N. Pandis
Keyword(s):  
Source Apportionment ◽  
Biomass Burning ◽  
Fine Particulate Matter ◽  
Organic Aerosols ◽  
Mitigation Strategies ◽  
Traffic Emissions ◽  
Aerosol Mass ◽  
Aerosol Mass Spectrometry ◽  
Five Factors ◽  
Potential Risks

Fine particulate matter (PM) originates from various emission sources and physicochemical processes. Quantification of the sources of PM is an important step during the planning of efficient mitigation strategies and the investigation of the potential risks to human health. Usually, source apportionment studies focus either on the organic or on the inorganic fraction of PM. In this study that took place in Patras, Greece, we address both PM fractions by combining measurements from a range of on- and off-line techniques, including elemental composition, organic and elemental carbon (OC and EC) measurements, and high-resolution Aerosol Mass Spectrometry (AMS) from different techniques. Six fine PM2.5 sources were identified based on the off-line measurements: secondary sulfate (34%), biomass burning (15%), exhaust traffic emissions (13%), nonexhaust traffic emissions (12%), mineral dust (10%), and sea salt (5%). The analysis of the AMS spectra quantified five factors: two oxygenated organic aerosols (OOA) factors (an OOA and a marine-related OOA, 52% of the total organic aerosols (OA)), cooking OA (COA, 11%) and two biomass burning OA (BBOA-I and BBOA-II, 37% in total) factors. The results of the two methods were synthesized, showcasing the complementarity of the two methodologies for fine PM source identification. The synthesis suggests that the contribution of biomass burning is quite robust, but that the exhaust traffic emissions are not due to local sources and may also include secondary OA from other sources.

scholarly journals Light absorption by polar and non-polar aerosol compounds from laboratory biomass combustion

2018 ◽  
Author(s):  
Deep Sengupta ◽  
Vera Samburova ◽  
Chiranjivi Bhattarai ◽  
Elena Kirillova ◽  
Lynn Mazzoleni ◽  
...  
Keyword(s):  
Light Absorption ◽  
Flow Reactor ◽  
Soluble Fraction ◽  
Chemical Properties ◽  
Water Soluble ◽  
Biomass Combustion ◽  
Absorption Properties ◽  
Oxidation Processes ◽  
Aerosol Mass ◽  
Physical Processing

Abstract. Fresh and atmospherically aged biomass-burning (BB) aerosol mass is mostly comprised of black carbon (BC) and organic carbon (OC) with its light-absorbing fraction – brown carbon (BrC). There is a lack of data on the physical and chemical properties of atmospheric BB aerosols, leading to high uncertainties in estimates of the BB impact on air quality and climate, especially for BrC. The polarity of chemical compounds influences their fate in the atmosphere including wet/dry deposition and chemical and physical processing. So far, most of the attention has been given to the water-soluble (polar) fraction of BrC, while the non-polar BrC fraction has been largely ignored. In the present study, the light absorption properties of polar and non-polar fractions of fresh and aged BB emissions were examined to estimate the contribution of different-polarity organic compounds to the light absorption properties of BB aerosols. In our experiments, four globally and regionally important fuels were burned under flaming and smoldering conditions in DRI’s combustion chamber. To mimic atmospheric oxidation processes (5–7 days), BB emissions were aged using an oxidation flow reactor (OFR). Fresh and OFR-aged BB aerosols were collected on filters and extracted with water and hexane to study absorption properties of polar and non-polar organic species. Spectrophotometric measurements over the 190 to 900 nm wavelength range showed that the non-polar (hexane-soluble) fraction is 2–3 times more absorbing than the polar (water-soluble) fraction. However, an increased absorbance was observed for the water extracts of oxidized/aged emissions while the absorption of the hexane extracts was lower for the aged emissions. Comparing the absorption Ångström Exponent (AAE) values, we observed changes in the light absorption properties of BB aerosols with aging that was dependent on the fuel types. The light absorption by HUmic LIke Substances (HULIS) was found to be higher in fuels characteristic of the southwestern USA. The absorption of the HULIS fraction was lower for OFR-aged BB emissions. Comparison of the light absorption properties of different polarity extracts (water, hexane, HULIS) provides insight into the chemical nature of BB BrC and its transformation during oxidation processes.

Soil organic carbon, permanganate fractions, and the chemical properties of acidic soils

Soil Research ◽  
1997 ◽  
Vol 35 (6) ◽  
pp. 1301 ◽  
Author(s):  
P. W. Moody ◽  
S. A. Yo ◽  
R. L. Aitken
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Chemical Properties ◽  
Soil Chemical Properties ◽  
Multiple Regression Equation ◽  
Organic C ◽  
Wide Range ◽  
Single Addition ◽  
Ph Buffer ◽  
Charge Curve

Total organic carbon (TC) in 32 acidic surface (0–10 cm) soils was divided into 3 fractions (C1, C2, and C3) based on oxidisability by different strengths of KMnO4 (33 mM and 167 mM). With the methodology used, ease of oxidation decreased in the order C1>C2>C3. Several fundamental soil chemical properties were also determined, i.e. ECEC, CEC at pH 6·5 (CEC6·5), slope of the charge curve (ΔCEC), pH buffer capacity, (pHBC), P sorption capacity using a single addition index (PSI150), and content of organically complexed Al. All soils had pH (1:5 water) <6·5, and comprised a wide range of soil types and clay contents. Multiple step-up regression indicated that C fractions were significantly (P < 0·05) correlated with ECEC, ΔCEC, CEC6·5, and pHBC. These results reinforce the critical importance of soil organic matter to the fundamental soil chemical properties of predominantly variable charge soils. The intercorrelations between the various oxidisable C fractions made it difficult to elucidate if degree of oxidisability had any bearing on the reactivity of the organic matter. ECEC was primarily correlated with C1, whereas all C fractions had highly significant (P < 0·01) effects on ΔCEC and pHBC. The fraction which was most difficult to oxidise, C3, made a significant (P < 0·01) contribution to CEC6·5 when combined with clay and ECEC in a multiple regression equation. Generally, one or other of the C fractions was better correlated with the fundamental soil chemical properties than TC. This simple empirical fractionation of soil organic C may therefore be a useful tool for assessing the effects of soil management on these properties.

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