Effects of Iron on Optical Properties of Dissolved Organic Matter
Iron is a source of interference in the spectroscopic analysis of dissolved organic matter (DOM); however, its effects on commonly employed ultraviolet and visible (UV–vis) light adsorption and fluorescence measurements are poorly defined. Here, we describe the effects of iron(II) and iron(III) on...
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Veröffentlicht in: | Environmental science & technology 2014-09, Vol.48 (17), p.10098-10106 |
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description | Iron is a source of interference in the spectroscopic analysis of dissolved organic matter (DOM); however, its effects on commonly employed ultraviolet and visible (UV–vis) light adsorption and fluorescence measurements are poorly defined. Here, we describe the effects of iron(II) and iron(III) on the UV–vis absorption and fluorescence of solutions containing two DOM fractions and two surface water samples. In each case, regardless of DOM composition, UV–vis absorption increased linearly with increasing iron(III). Correction factors were derived using iron(III) absorption coefficients determined at wavelengths commonly used to characterize DOM. Iron(III) addition increased specific UV absorbances (SUVA) and decreased the absorption ratios (E 2:E 3) and spectral slope ratios (S R) of DOM samples. Both iron(II) and iron(III) quenched DOM fluorescence at pH 6.7. The degree and region of fluorescence quenching varied with the iron:DOC concentration ratio, DOM composition, and pH. Regions of the fluorescence spectra associated with greater DOM conjugation were more susceptible to iron quenching, and DOM fluorescence indices were sensitive to the presence of both forms of iron. Analyses of the excitation–emission matrices using a 7- and 13-component parallel factor analysis (PARAFAC) model showed low PARAFAC sensitivity to iron addition. |
doi_str_mv | 10.1021/es502670r |
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Here, we describe the effects of iron(II) and iron(III) on the UV–vis absorption and fluorescence of solutions containing two DOM fractions and two surface water samples. In each case, regardless of DOM composition, UV–vis absorption increased linearly with increasing iron(III). Correction factors were derived using iron(III) absorption coefficients determined at wavelengths commonly used to characterize DOM. Iron(III) addition increased specific UV absorbances (SUVA) and decreased the absorption ratios (E 2:E 3) and spectral slope ratios (S R) of DOM samples. Both iron(II) and iron(III) quenched DOM fluorescence at pH 6.7. The degree and region of fluorescence quenching varied with the iron:DOC concentration ratio, DOM composition, and pH. Regions of the fluorescence spectra associated with greater DOM conjugation were more susceptible to iron quenching, and DOM fluorescence indices were sensitive to the presence of both forms of iron. 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Sci. Technol</addtitle><description>Iron is a source of interference in the spectroscopic analysis of dissolved organic matter (DOM); however, its effects on commonly employed ultraviolet and visible (UV–vis) light adsorption and fluorescence measurements are poorly defined. Here, we describe the effects of iron(II) and iron(III) on the UV–vis absorption and fluorescence of solutions containing two DOM fractions and two surface water samples. In each case, regardless of DOM composition, UV–vis absorption increased linearly with increasing iron(III). Correction factors were derived using iron(III) absorption coefficients determined at wavelengths commonly used to characterize DOM. Iron(III) addition increased specific UV absorbances (SUVA) and decreased the absorption ratios (E 2:E 3) and spectral slope ratios (S R) of DOM samples. Both iron(II) and iron(III) quenched DOM fluorescence at pH 6.7. The degree and region of fluorescence quenching varied with the iron:DOC concentration ratio, DOM composition, and pH. Regions of the fluorescence spectra associated with greater DOM conjugation were more susceptible to iron quenching, and DOM fluorescence indices were sensitive to the presence of both forms of iron. Analyses of the excitation–emission matrices using a 7- and 13-component parallel factor analysis (PARAFAC) model showed low PARAFAC sensitivity to iron addition.</description><subject>Adsorption</subject><subject>Fluorescence</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Iron</subject><subject>Iron - chemistry</subject><subject>Optical Phenomena</subject><subject>Organic Chemicals - chemistry</subject><subject>Oxidation-Reduction</subject><subject>Rivers - chemistry</subject><subject>Solubility</subject><subject>Solutions</subject><subject>Spectrometry, Fluorescence</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Surface Properties</subject><subject>Surface water</subject><subject>Ultraviolet radiation</subject><subject>Water - chemistry</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1Lw0AQhhdRbK0e_AMSEEEP0f1O9lhq1YJSDwrewu5mIilpNu4mgv_e1NYiehEG5jAPzzDzInRM8CXBlFxBEJjKBPsdNCSC4likguyiIcaExYrJlwE6CGGBMaYMp_toQAVOOePJEI2nRQG2DZEropl3ddTXvGlLq6vo0bsGfFvC1_S6DMFV75BHc_-q69JGD7ptwR-ivUJXAY42fYSeb6ZPk7v4fn47m4zvY805bWNpjcgFA5EqXeSJMIZyDkIRBZIzZQjlhlllZUINtQkpwIAiRlpGtLJasBE6X3sb7946CG22LIOFqtI1uC5kREiZcpqI5B-oUJJila6sp7_Qhet83R-yEhLCmZC4py7WlPUuBA9F1vhyqf1HRnC2iiDbRtCzJxtjZ5aQb8nvn_fA2RrQNvzY9kf0CetLisg</recordid><startdate>20140902</startdate><enddate>20140902</enddate><creator>Poulin, Brett A</creator><creator>Ryan, Joseph N</creator><creator>Aiken, George R</creator><general>American Chemical Society</general><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>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope><scope>7QH</scope><scope>7TV</scope><scope>7UA</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope></search><sort><creationdate>20140902</creationdate><title>Effects of Iron on Optical Properties of Dissolved Organic Matter</title><author>Poulin, Brett A ; Ryan, Joseph N ; Aiken, George R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a442t-6cb5d53e589afd75bb244e5919e6439b124b3c9c672b2c71febe91b6c31a9ca53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adsorption</topic><topic>Fluorescence</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Iron</topic><topic>Iron - chemistry</topic><topic>Optical Phenomena</topic><topic>Organic Chemicals - chemistry</topic><topic>Oxidation-Reduction</topic><topic>Rivers - chemistry</topic><topic>Solubility</topic><topic>Solutions</topic><topic>Spectrometry, Fluorescence</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Surface Properties</topic><topic>Surface water</topic><topic>Ultraviolet radiation</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poulin, Brett A</creatorcontrib><creatorcontrib>Ryan, Joseph N</creatorcontrib><creatorcontrib>Aiken, George R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poulin, Brett A</au><au>Ryan, Joseph N</au><au>Aiken, George R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Iron on Optical Properties of Dissolved Organic Matter</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2014-09-02</date><risdate>2014</risdate><volume>48</volume><issue>17</issue><spage>10098</spage><epage>10106</epage><pages>10098-10106</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Iron is a source of interference in the spectroscopic analysis of dissolved organic matter (DOM); however, its effects on commonly employed ultraviolet and visible (UV–vis) light adsorption and fluorescence measurements are poorly defined. Here, we describe the effects of iron(II) and iron(III) on the UV–vis absorption and fluorescence of solutions containing two DOM fractions and two surface water samples. In each case, regardless of DOM composition, UV–vis absorption increased linearly with increasing iron(III). Correction factors were derived using iron(III) absorption coefficients determined at wavelengths commonly used to characterize DOM. Iron(III) addition increased specific UV absorbances (SUVA) and decreased the absorption ratios (E 2:E 3) and spectral slope ratios (S R) of DOM samples. Both iron(II) and iron(III) quenched DOM fluorescence at pH 6.7. The degree and region of fluorescence quenching varied with the iron:DOC concentration ratio, DOM composition, and pH. Regions of the fluorescence spectra associated with greater DOM conjugation were more susceptible to iron quenching, and DOM fluorescence indices were sensitive to the presence of both forms of iron. Analyses of the excitation–emission matrices using a 7- and 13-component parallel factor analysis (PARAFAC) model showed low PARAFAC sensitivity to iron addition.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25084347</pmid><doi>10.1021/es502670r</doi><tpages>9</tpages></addata></record> |
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subjects | Adsorption Fluorescence Hydrogen-Ion Concentration Hydrophobic and Hydrophilic Interactions Iron Iron - chemistry Optical Phenomena Organic Chemicals - chemistry Oxidation-Reduction Rivers - chemistry Solubility Solutions Spectrometry, Fluorescence Spectrophotometry, Ultraviolet Surface Properties Surface water Ultraviolet radiation Water - chemistry |
title | Effects of Iron on Optical Properties of Dissolved Organic Matter |
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