Determination of total and available fractions of PAHs by SPME in oily wastewaters: overcoming interference from NAPL and NOM

Background, aim, and scope Polycyclic aromatic hydrocarbons (PAHs) are often found in oily wastewaters. Their presence is usually the result of human activities and has a negative effect on the environment. One important step in addressing this problem is to evaluate the effectiveness of PAH removal...

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Veröffentlicht in:Environmental science and pollution research international 2009-09, Vol.16 (6), p.671-678
Hauptverfasser: Gomes, Rui B, Nogueira, Regina, Oliveira, José M, Peixoto, João, Brito, António G
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container_issue 6
container_start_page 671
container_title Environmental science and pollution research international
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creator Gomes, Rui B
Nogueira, Regina
Oliveira, José M
Peixoto, João
Brito, António G
description Background, aim, and scope Polycyclic aromatic hydrocarbons (PAHs) are often found in oily wastewaters. Their presence is usually the result of human activities and has a negative effect on the environment. One important step in addressing this problem is to evaluate the effectiveness of PAH removal by biological processes since these are the most cost-effective treatments known today. Many techniques are presently available for PAH determination in wastewaters. Solid phase microextracion (SPME) is known to be one of the most effective techniques for this purpose. When analyzing complex matrices with substances such as natural organic matter (NOM) and non-aqueous phase liquids (NAPL), it is important to differentiate the free dissolved PAH from matrix-bonded PAH. PAHs associated with the bonded fraction are less susceptible to biological treatment. The present study concerns the development of a simple and suitable methodology for the determination of the freely dissolved and the total fraction of PAHs present in oily wastewaters. The methodology was then applied to an oily wastewater from a fuel station retention basin. Material and methods Headspace SPME was used for analyzing PAH since the presence of a complex or dirty matrix in direct contact with the fiber may damage it. Four model PAHs--anthracene, fluorene, phenanthrene, and pyrene--were analyzed by GC-MS. Negligible depletion SPME technique was used to determine the free fraction. Total PAH was determined by enhancing the mass transfer from the bonded phase to the freely dissolved phase by temperature optimization and the use of the method of standard additions. The PAH absorption kinetics were determined in order to define the optimal sampling conditions for this method. The fitting of the experimental data to a mathematical model was accomplished using Berkeley Madonna software. Humic acid and silicon oil were used as model NOM and NAPL, respectively, to study the effect of these compounds on the decrease of SPME response. Then, the method was evaluated with wastewater from a fuel station spill retention basin. Results The SPME kinetic parameters--k ₁ (uptake rate), k ₂ (desorption rate), and K SPME (partition coefficient)--were determined from experimental data modeling. The determination of the free fraction required 15-min sampling to ensure that PAH depletion from sample was below 1%. For total PAH, a 30-min extraction at 100°C ensured the maximum signal response in the GC-MS. For the determ
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Their presence is usually the result of human activities and has a negative effect on the environment. One important step in addressing this problem is to evaluate the effectiveness of PAH removal by biological processes since these are the most cost-effective treatments known today. Many techniques are presently available for PAH determination in wastewaters. Solid phase microextracion (SPME) is known to be one of the most effective techniques for this purpose. When analyzing complex matrices with substances such as natural organic matter (NOM) and non-aqueous phase liquids (NAPL), it is important to differentiate the free dissolved PAH from matrix-bonded PAH. PAHs associated with the bonded fraction are less susceptible to biological treatment. The present study concerns the development of a simple and suitable methodology for the determination of the freely dissolved and the total fraction of PAHs present in oily wastewaters. The methodology was then applied to an oily wastewater from a fuel station retention basin. Material and methods Headspace SPME was used for analyzing PAH since the presence of a complex or dirty matrix in direct contact with the fiber may damage it. Four model PAHs--anthracene, fluorene, phenanthrene, and pyrene--were analyzed by GC-MS. Negligible depletion SPME technique was used to determine the free fraction. Total PAH was determined by enhancing the mass transfer from the bonded phase to the freely dissolved phase by temperature optimization and the use of the method of standard additions. The PAH absorption kinetics were determined in order to define the optimal sampling conditions for this method. The fitting of the experimental data to a mathematical model was accomplished using Berkeley Madonna software. Humic acid and silicon oil were used as model NOM and NAPL, respectively, to study the effect of these compounds on the decrease of SPME response. Then, the method was evaluated with wastewater from a fuel station spill retention basin. Results The SPME kinetic parameters--k ₁ (uptake rate), k ₂ (desorption rate), and K SPME (partition coefficient)--were determined from experimental data modeling. The determination of the free fraction required 15-min sampling to ensure that PAH depletion from sample was below 1%. For total PAH, a 30-min extraction at 100°C ensured the maximum signal response in the GC-MS. For the determination of free and total PAHs, extractions were performed before reaching the SPME equilibrium. The wastewater used in this study had no free fraction of the analyzed PAHs. However, the four studied PAHs were found when the method for total PAH was used. Discussion The addition of NOM and NAPL dramatically decreased the efficiency of the SPME. This decrease was the result of a greater partition of the PAHs to the NAPL and NOM phases. This fact was also observed in the analysis of the fuel station spill retention basin, where no free PAH was measured. However, using the method of standard addition for the determination of total PAH, it was possible to quantify all four PAHs. Conclusions The method developed in the present study was found to be adequate to differentiate between free and total PAH present in oily wastewater. It was determined that the presence of NOM and NAPL had a negative effect on SPME efficiency. Recommendations and perspectives The presence of binding substances had a great influence on SPME kinetics. Therefore, it is of extreme importance to determine their degree of interference when analyzing oily wastewaters or results can otherwise be erroneous. Other factors influencing the total PAH determinations should be considered in further studies.</description><identifier>ISSN: 0944-1344</identifier><identifier>EISSN: 1614-7499</identifier><identifier>DOI: 10.1007/s11356-009-0118-4</identifier><identifier>PMID: 19290560</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Anthracene ; Aquatic Pollution ; Area 6.1 • Chemical Analytical Methods • Research Article ; Atmospheric Protection/Air Quality Control/Air Pollution ; Bioengineering ; Biological treatment ; Earth and Environmental Science ; Ecotoxicology ; Environment ; Environmental Chemistry ; Environmental effects ; Environmental Health ; Environmental impact ; Environmental Monitoring ; Equilibrium ; Experimental data ; Fluorene ; Headspace ; Humic acids ; Kinetics ; Mass transfer ; Mathematical models ; Nonaqueous phase liquids ; Organic Chemicals - analysis ; Organic matter ; Petroleum - analysis ; Phenanthrene ; Polycyclic aromatic hydrocarbons ; Polycyclic Aromatic Hydrocarbons - chemistry ; Retention ; Sampling ; Settling basins ; Solid phase methods ; Solid Phase Microextraction - methods ; Studies ; Temperature ; Waste Disposal, Fluid ; Waste Water Technology ; Wastewater ; Water Management ; Water Pollutants, Chemical - chemistry ; Water pollution ; Water Pollution Control</subject><ispartof>Environmental science and pollution research international, 2009-09, Vol.16 (6), p.671-678</ispartof><rights>Springer-Verlag 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-d83921966442df48c3f5321c288e35b6104e2f080374843dc314f5c9af0930243</citedby><cites>FETCH-LOGICAL-c486t-d83921966442df48c3f5321c288e35b6104e2f080374843dc314f5c9af0930243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11356-009-0118-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11356-009-0118-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19290560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomes, Rui B</creatorcontrib><creatorcontrib>Nogueira, Regina</creatorcontrib><creatorcontrib>Oliveira, José M</creatorcontrib><creatorcontrib>Peixoto, João</creatorcontrib><creatorcontrib>Brito, António G</creatorcontrib><title>Determination of total and available fractions of PAHs by SPME in oily wastewaters: overcoming interference from NAPL and NOM</title><title>Environmental science and pollution research international</title><addtitle>Environ Sci Pollut Res</addtitle><addtitle>Environ Sci Pollut Res Int</addtitle><description>Background, aim, and scope Polycyclic aromatic hydrocarbons (PAHs) are often found in oily wastewaters. Their presence is usually the result of human activities and has a negative effect on the environment. One important step in addressing this problem is to evaluate the effectiveness of PAH removal by biological processes since these are the most cost-effective treatments known today. Many techniques are presently available for PAH determination in wastewaters. Solid phase microextracion (SPME) is known to be one of the most effective techniques for this purpose. When analyzing complex matrices with substances such as natural organic matter (NOM) and non-aqueous phase liquids (NAPL), it is important to differentiate the free dissolved PAH from matrix-bonded PAH. PAHs associated with the bonded fraction are less susceptible to biological treatment. The present study concerns the development of a simple and suitable methodology for the determination of the freely dissolved and the total fraction of PAHs present in oily wastewaters. The methodology was then applied to an oily wastewater from a fuel station retention basin. Material and methods Headspace SPME was used for analyzing PAH since the presence of a complex or dirty matrix in direct contact with the fiber may damage it. Four model PAHs--anthracene, fluorene, phenanthrene, and pyrene--were analyzed by GC-MS. Negligible depletion SPME technique was used to determine the free fraction. Total PAH was determined by enhancing the mass transfer from the bonded phase to the freely dissolved phase by temperature optimization and the use of the method of standard additions. The PAH absorption kinetics were determined in order to define the optimal sampling conditions for this method. The fitting of the experimental data to a mathematical model was accomplished using Berkeley Madonna software. Humic acid and silicon oil were used as model NOM and NAPL, respectively, to study the effect of these compounds on the decrease of SPME response. Then, the method was evaluated with wastewater from a fuel station spill retention basin. Results The SPME kinetic parameters--k ₁ (uptake rate), k ₂ (desorption rate), and K SPME (partition coefficient)--were determined from experimental data modeling. The determination of the free fraction required 15-min sampling to ensure that PAH depletion from sample was below 1%. For total PAH, a 30-min extraction at 100°C ensured the maximum signal response in the GC-MS. For the determination of free and total PAHs, extractions were performed before reaching the SPME equilibrium. The wastewater used in this study had no free fraction of the analyzed PAHs. However, the four studied PAHs were found when the method for total PAH was used. Discussion The addition of NOM and NAPL dramatically decreased the efficiency of the SPME. This decrease was the result of a greater partition of the PAHs to the NAPL and NOM phases. This fact was also observed in the analysis of the fuel station spill retention basin, where no free PAH was measured. However, using the method of standard addition for the determination of total PAH, it was possible to quantify all four PAHs. Conclusions The method developed in the present study was found to be adequate to differentiate between free and total PAH present in oily wastewater. It was determined that the presence of NOM and NAPL had a negative effect on SPME efficiency. Recommendations and perspectives The presence of binding substances had a great influence on SPME kinetics. Therefore, it is of extreme importance to determine their degree of interference when analyzing oily wastewaters or results can otherwise be erroneous. Other factors influencing the total PAH determinations should be considered in further studies.</description><subject>Anthracene</subject><subject>Aquatic Pollution</subject><subject>Area 6.1 • Chemical Analytical Methods • Research Article</subject><subject>Atmospheric Protection/Air Quality Control/Air Pollution</subject><subject>Bioengineering</subject><subject>Biological treatment</subject><subject>Earth and Environmental Science</subject><subject>Ecotoxicology</subject><subject>Environment</subject><subject>Environmental Chemistry</subject><subject>Environmental effects</subject><subject>Environmental Health</subject><subject>Environmental impact</subject><subject>Environmental Monitoring</subject><subject>Equilibrium</subject><subject>Experimental data</subject><subject>Fluorene</subject><subject>Headspace</subject><subject>Humic acids</subject><subject>Kinetics</subject><subject>Mass transfer</subject><subject>Mathematical models</subject><subject>Nonaqueous phase liquids</subject><subject>Organic Chemicals - analysis</subject><subject>Organic matter</subject><subject>Petroleum - analysis</subject><subject>Phenanthrene</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>Polycyclic Aromatic Hydrocarbons - chemistry</subject><subject>Retention</subject><subject>Sampling</subject><subject>Settling basins</subject><subject>Solid phase methods</subject><subject>Solid Phase Microextraction - methods</subject><subject>Studies</subject><subject>Temperature</subject><subject>Waste Disposal, Fluid</subject><subject>Waste Water Technology</subject><subject>Wastewater</subject><subject>Water Management</subject><subject>Water Pollutants, Chemical - chemistry</subject><subject>Water pollution</subject><subject>Water Pollution Control</subject><issn>0944-1344</issn><issn>1614-7499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kcFu1DAURS1ERYeWD2ADFgt2oe_ZTmKzG5VCkabtSKVry-PYo1RJXOxMq1nw7zhkpEosurLkd-7xky8h7xG-IEB9lhB5WRUAqgBEWYhXZIEViqIWSr0mC1BCFMiFOCZvU7oHYKBY_YYco2IKygoW5M83N7rYt4MZ2zDQ4OkYRtNRMzTUPJq2M5vOUR-NneZpAtbLy0Q3e3q7vrqgbc603Z4-mTS6J5Nd6SsNjy7akKXbPM9X3kU32EkTenq9XK_-6a9vrk7JkTddcu8O5wm5-37x6_yyWN38-Hm-XBVWyGosGskVQ1VVQrDGC2m5LzlDy6R0vNxUCMIxDxJ4LaTgjeUofGmV8aA4MMFPyOfZ-xDD751Lo-7bZF3XmcGFXdIMmWLAygx--g-8D7s45N00Y1DWEmCy4QzZGFKKzuuH2PYm7jWCnorRczE6F6OnYvSU-XAQ7za9a54ThyYywGYg5dGwdfH55ZesH-eQN0GbbWyTvrtlgBywqvO3lPwvaNKfpg</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Gomes, Rui B</creator><creator>Nogueira, Regina</creator><creator>Oliveira, José M</creator><creator>Peixoto, João</creator><creator>Brito, António G</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7T7</scope><scope>7TV</scope><scope>7U7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>P64</scope><scope>PATMY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>7QH</scope><scope>7ST</scope><scope>7UA</scope><scope>SOI</scope></search><sort><creationdate>20090901</creationdate><title>Determination of total and available fractions of PAHs by SPME in oily wastewaters: overcoming interference from NAPL and NOM</title><author>Gomes, Rui B ; Nogueira, Regina ; Oliveira, José M ; Peixoto, João ; Brito, António G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-d83921966442df48c3f5321c288e35b6104e2f080374843dc314f5c9af0930243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anthracene</topic><topic>Aquatic Pollution</topic><topic>Area 6.1 • Chemical Analytical Methods • Research Article</topic><topic>Atmospheric Protection/Air Quality Control/Air Pollution</topic><topic>Bioengineering</topic><topic>Biological treatment</topic><topic>Earth and Environmental Science</topic><topic>Ecotoxicology</topic><topic>Environment</topic><topic>Environmental Chemistry</topic><topic>Environmental effects</topic><topic>Environmental Health</topic><topic>Environmental impact</topic><topic>Environmental Monitoring</topic><topic>Equilibrium</topic><topic>Experimental data</topic><topic>Fluorene</topic><topic>Headspace</topic><topic>Humic acids</topic><topic>Kinetics</topic><topic>Mass transfer</topic><topic>Mathematical models</topic><topic>Nonaqueous phase liquids</topic><topic>Organic Chemicals - analysis</topic><topic>Organic matter</topic><topic>Petroleum - analysis</topic><topic>Phenanthrene</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>Polycyclic Aromatic Hydrocarbons - chemistry</topic><topic>Retention</topic><topic>Sampling</topic><topic>Settling basins</topic><topic>Solid phase methods</topic><topic>Solid Phase Microextraction - methods</topic><topic>Studies</topic><topic>Temperature</topic><topic>Waste Disposal, Fluid</topic><topic>Waste Water Technology</topic><topic>Wastewater</topic><topic>Water Management</topic><topic>Water Pollutants, Chemical - chemistry</topic><topic>Water pollution</topic><topic>Water Pollution Control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes, Rui B</creatorcontrib><creatorcontrib>Nogueira, Regina</creatorcontrib><creatorcontrib>Oliveira, José M</creatorcontrib><creatorcontrib>Peixoto, João</creatorcontrib><creatorcontrib>Brito, António G</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Pollution Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health &amp; 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Their presence is usually the result of human activities and has a negative effect on the environment. One important step in addressing this problem is to evaluate the effectiveness of PAH removal by biological processes since these are the most cost-effective treatments known today. Many techniques are presently available for PAH determination in wastewaters. Solid phase microextracion (SPME) is known to be one of the most effective techniques for this purpose. When analyzing complex matrices with substances such as natural organic matter (NOM) and non-aqueous phase liquids (NAPL), it is important to differentiate the free dissolved PAH from matrix-bonded PAH. PAHs associated with the bonded fraction are less susceptible to biological treatment. The present study concerns the development of a simple and suitable methodology for the determination of the freely dissolved and the total fraction of PAHs present in oily wastewaters. The methodology was then applied to an oily wastewater from a fuel station retention basin. Material and methods Headspace SPME was used for analyzing PAH since the presence of a complex or dirty matrix in direct contact with the fiber may damage it. Four model PAHs--anthracene, fluorene, phenanthrene, and pyrene--were analyzed by GC-MS. Negligible depletion SPME technique was used to determine the free fraction. Total PAH was determined by enhancing the mass transfer from the bonded phase to the freely dissolved phase by temperature optimization and the use of the method of standard additions. The PAH absorption kinetics were determined in order to define the optimal sampling conditions for this method. The fitting of the experimental data to a mathematical model was accomplished using Berkeley Madonna software. Humic acid and silicon oil were used as model NOM and NAPL, respectively, to study the effect of these compounds on the decrease of SPME response. Then, the method was evaluated with wastewater from a fuel station spill retention basin. Results The SPME kinetic parameters--k ₁ (uptake rate), k ₂ (desorption rate), and K SPME (partition coefficient)--were determined from experimental data modeling. The determination of the free fraction required 15-min sampling to ensure that PAH depletion from sample was below 1%. For total PAH, a 30-min extraction at 100°C ensured the maximum signal response in the GC-MS. For the determination of free and total PAHs, extractions were performed before reaching the SPME equilibrium. The wastewater used in this study had no free fraction of the analyzed PAHs. However, the four studied PAHs were found when the method for total PAH was used. Discussion The addition of NOM and NAPL dramatically decreased the efficiency of the SPME. This decrease was the result of a greater partition of the PAHs to the NAPL and NOM phases. This fact was also observed in the analysis of the fuel station spill retention basin, where no free PAH was measured. However, using the method of standard addition for the determination of total PAH, it was possible to quantify all four PAHs. Conclusions The method developed in the present study was found to be adequate to differentiate between free and total PAH present in oily wastewater. It was determined that the presence of NOM and NAPL had a negative effect on SPME efficiency. Recommendations and perspectives The presence of binding substances had a great influence on SPME kinetics. Therefore, it is of extreme importance to determine their degree of interference when analyzing oily wastewaters or results can otherwise be erroneous. Other factors influencing the total PAH determinations should be considered in further studies.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>19290560</pmid><doi>10.1007/s11356-009-0118-4</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Anthracene
Aquatic Pollution
Area 6.1 • Chemical Analytical Methods • Research Article
Atmospheric Protection/Air Quality Control/Air Pollution
Bioengineering
Biological treatment
Earth and Environmental Science
Ecotoxicology
Environment
Environmental Chemistry
Environmental effects
Environmental Health
Environmental impact
Environmental Monitoring
Equilibrium
Experimental data
Fluorene
Headspace
Humic acids
Kinetics
Mass transfer
Mathematical models
Nonaqueous phase liquids
Organic Chemicals - analysis
Organic matter
Petroleum - analysis
Phenanthrene
Polycyclic aromatic hydrocarbons
Polycyclic Aromatic Hydrocarbons - chemistry
Retention
Sampling
Settling basins
Solid phase methods
Solid Phase Microextraction - methods
Studies
Temperature
Waste Disposal, Fluid
Waste Water Technology
Wastewater
Water Management
Water Pollutants, Chemical - chemistry
Water pollution
Water Pollution Control
title Determination of total and available fractions of PAHs by SPME in oily wastewaters: overcoming interference from NAPL and NOM
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