This research provides new insights on the application of weak-base (WB) anion exchange resins (AERs) for groundwater treatment of six perfluoroalkyl acids (PFAAs) with different properties. Continuous-flow column adsorption and regeneration experiments involving WB, polyacrylic, and WB, polystyrene resins were conducted considering salt-only regeneration solutions and two representative strong-base (SB)-AERs of analogous polymer composition and a third solution of methanol/salt used as baseline for comparison. The WB, polyacrylic resin was regenerated using salt-only solutions of NaOH due to deprotonation of the tertiary amine functional group at alkaline pH. However, organic cosolvent was required to weaken the hydrophobic interactions between PFAAs and the nonpolar WB, polystyrene resin. Removal was predominantly influenced by polymer composition with free-base WB-AERs exhibiting similar selectivity and higher capacity as SB resin counterparts. This work highlights WB-AER selection based on PFAA-selective removal and more sustainable regeneration strategies.
{"title":"Removal of PFAS from groundwater using weak-base anion exchange resins","authors":"Christian Kassar, Treavor H. Boyer","doi":"10.1002/aws2.1325","DOIUrl":"https://doi.org/10.1002/aws2.1325","url":null,"abstract":"<p>This research provides new insights on the application of weak-base (WB) anion exchange resins (AERs) for groundwater treatment of six perfluoroalkyl acids (PFAAs) with different properties. Continuous-flow column adsorption and regeneration experiments involving WB, polyacrylic, and WB, polystyrene resins were conducted considering salt-only regeneration solutions and two representative strong-base (SB)-AERs of analogous polymer composition and a third solution of methanol/salt used as baseline for comparison. The WB, polyacrylic resin was regenerated using salt-only solutions of NaOH due to deprotonation of the tertiary amine functional group at alkaline pH. However, organic cosolvent was required to weaken the hydrophobic interactions between PFAAs and the nonpolar WB, polystyrene resin. Removal was predominantly influenced by polymer composition with free-base WB-AERs exhibiting similar selectivity and higher capacity as SB resin counterparts. This work highlights WB-AER selection based on PFAA-selective removal and more sustainable regeneration strategies.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1325","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50142741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Since publication of their article, Whelton et al. (2023) identified that a figure was referenced where the supplementary materials should have been referenced, and that the supplementary materials did not include important information.
The second paragraph of Section 4.3 read the following:
A drinking water chemical analysis “fire package” was proposed during the Marshall Fire response (Figure 1), and should be revised as more VOC and SVOC data becomes available.
The reference to Figure 1 for the “fire package” was incorrect and should have read the following:
A drinking water chemical analysis “fire package” was proposed during the Marshall Fire response (Appendix S1), and should be revised as more VOC and SVOC data becomes available.
The information provided in Appendix S1 was incomplete and was missing pages related to the S-3.2 enclosures. A file with the complete supporting information has replaced the previously published version.
{"title":"Corrigendum—The Marshall fire: Scientific and policy needs for water system disaster response","authors":"","doi":"10.1002/aws2.1323","DOIUrl":"https://doi.org/10.1002/aws2.1323","url":null,"abstract":"<p>Since publication of their article, Whelton et al. (<span>2023</span>) identified that a figure was referenced where the supplementary materials should have been referenced, and that the supplementary materials did not include important information.</p><p>The second paragraph of Section 4.3 read the following:</p><p>A drinking water chemical analysis “fire package” was proposed during the Marshall Fire response (Figure 1), and should be revised as more VOC and SVOC data becomes available.</p><p>The reference to Figure 1 for the “fire package” was incorrect and should have read the following:</p><p>A drinking water chemical analysis “fire package” was proposed during the Marshall Fire response (Appendix S1), and should be revised as more VOC and SVOC data becomes available.</p><p>The information provided in Appendix S1 was incomplete and was missing pages related to the S-3.2 enclosures. A file with the complete supporting information has replaced the previously published version.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1323","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50151630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Caroline Jankowski, Kristofer Isaacson, Madeline Larsen, Christian Ley, Myles Cook, Andrew J. Whelton
Following the 2021 Marshall Fire in Colorado, this study was conducted to better understand private well and plumbing damage and to develop public health guidance. More than 20 post-fire drinking water well guidance documents with varied recommendations were found. Approximately 227 wells were located in the fire footprint. Seventeen properties were visited, and a subset of wells were sampled for organic and inorganic contaminants. Property debris was also collected. Benzene, toluene, and 19 semi-volatile organic compounds (SVOCs) were detected in water extracts of property debris. No wells contained volatile organic compound contamination. Two shallow wells (12 and 15 ft) had debris contamination; one well contained notable SVOC contamination. One multi-home unregulated well system was extensively damaged, lost pressure, and had not been repressurized 11 months after the fire due to financial and technical challenges. Study results highlight the need for follow-up work to understand well system damage and household response.
{"title":"Wildfire damage and contamination to private drinking water wells","authors":"Caroline Jankowski, Kristofer Isaacson, Madeline Larsen, Christian Ley, Myles Cook, Andrew J. Whelton","doi":"10.1002/aws2.1319","DOIUrl":"https://doi.org/10.1002/aws2.1319","url":null,"abstract":"<p>Following the 2021 Marshall Fire in Colorado, this study was conducted to better understand private well and plumbing damage and to develop public health guidance. More than 20 post-fire drinking water well guidance documents with varied recommendations were found. Approximately 227 wells were located in the fire footprint. Seventeen properties were visited, and a subset of wells were sampled for organic and inorganic contaminants. Property debris was also collected. Benzene, toluene, and 19 semi-volatile organic compounds (SVOCs) were detected in water extracts of property debris. No wells contained volatile organic compound contamination. Two shallow wells (12 and 15 ft) had debris contamination; one well contained notable SVOC contamination. One multi-home unregulated well system was extensively damaged, lost pressure, and had not been repressurized 11 months after the fire due to financial and technical challenges. Study results highlight the need for follow-up work to understand well system damage and household response.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1319","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50150984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ashley N. Kent, Caroline G. Russell, Jason T. Carter, William A. Mitch, Raymond M. Hozalski, Peter M. Huck
Full-scale sampling at 16 facilities illustrated that NDMA precursor concentrations, measured by adding chloramine under Uniform Formation Conditions (NDMAUFC), increased across biofiltration at 7 of 16 facilities (by 3–48 ng/L or 12%–296%) but stayed the same or decreased (by up to 5 ng/L or 24%) at the other nine facilities. Increases in NDMAUFC concentrations were attributed to both particulate and soluble precursors. Only two facilities had an increase in NDMAUFC greater than 10 ng/L. However, NDMAUFC concentrations in the biofilter effluent from five facilities exceeded 10 ng/L during one or more sampling events. For these facilities, testing at multiple scales showed that mitigation steps could include pretreatment with ozone (which resulted in overall lower NDMAUFC), increased free chlorine contact time prior to ammonia addition, and/or optimized biofilter design and operation.
{"title":"Investigation of the formation of NDMAUFC across biofilters","authors":"Ashley N. Kent, Caroline G. Russell, Jason T. Carter, William A. Mitch, Raymond M. Hozalski, Peter M. Huck","doi":"10.1002/aws2.1322","DOIUrl":"https://doi.org/10.1002/aws2.1322","url":null,"abstract":"<p>Full-scale sampling at 16 facilities illustrated that NDMA precursor concentrations, measured by adding chloramine under Uniform Formation Conditions (NDMA<sub>UFC</sub>), increased across biofiltration at 7 of 16 facilities (by 3–48 ng/L or 12%–296%) but stayed the same or decreased (by up to 5 ng/L or 24%) at the other nine facilities. Increases in NDMA<sub>UFC</sub> concentrations were attributed to both particulate and soluble precursors. Only two facilities had an increase in NDMA<sub>UFC</sub> greater than 10 ng/L. However, NDMA<sub>UFC</sub> concentrations in the biofilter effluent from five facilities exceeded 10 ng/L during one or more sampling events. For these facilities, testing at multiple scales showed that mitigation steps could include pretreatment with ozone (which resulted in overall lower NDMA<sub>UFC</sub>), increased free chlorine contact time prior to ammonia addition, and/or optimized biofilter design and operation.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1322","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50140162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The formation of disinfection byproducts (DBPs) in finished drinking water is an ongoing challenge for public health agencies and water utilities. The Fourth Unregulated Contaminant Monitoring Rule data were used to assess the prevalence and drivers of haloacetic acids (HAAs)—a class of DBPs—in New York State's (NYS) public water systems, with a focus on total measured (HAA9), regulated (HAA5), brominated (HAA6Br), and unregulated (HAA4) HAAs. The concentrations of all HAA groups in NYS are found to be similar to those nationally, with HAA4 composing approximately 20% of HAA9. Concentrations of all HAA groups are lowest in groundwater and highest in surface waters across NYS systems. Higher total organic carbon (TOC) concentrations lead to elevated HAA9 and HAA5, while higher bromide concentrations favor more HAA4 and HAA6Br. HAA4 concentrations are well predicted with pre-oxidation/disinfection types, HAA5, TOC, and bromide concentrations, with an adjusted R2 of 70%.
{"title":"Characterization and drivers of haloacetic acids in New York State","authors":"Rassil Sayess, Scott Steinschneider","doi":"10.1002/aws2.1321","DOIUrl":"https://doi.org/10.1002/aws2.1321","url":null,"abstract":"<p>The formation of disinfection byproducts (DBPs) in finished drinking water is an ongoing challenge for public health agencies and water utilities. The Fourth Unregulated Contaminant Monitoring Rule data were used to assess the prevalence and drivers of haloacetic acids (HAAs)—a class of DBPs—in New York State's (NYS) public water systems, with a focus on total measured (HAA9), regulated (HAA5), brominated (HAA6Br), and unregulated (HAA4) HAAs. The concentrations of all HAA groups in NYS are found to be similar to those nationally, with HAA4 composing approximately 20% of HAA9. Concentrations of all HAA groups are lowest in groundwater and highest in surface waters across NYS systems. Higher total organic carbon (TOC) concentrations lead to elevated HAA9 and HAA5, while higher bromide concentrations favor more HAA4 and HAA6Br. HAA4 concentrations are well predicted with pre-oxidation/disinfection types, HAA5, TOC, and bromide concentrations, with an adjusted <i>R</i><sup>2</sup> of 70%.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1321","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50121495","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Madison Rasmus, Asher E. Keithley, Bryant A. Chambers, Grace Zhou, Greg Pope, Eric R. V. Dickenson, Bradley Bzdyra, Alisa Lu, Kerry A. Kinney, Mary Jo Kirisits
Hydraulic performance issues in drinking-water biofilters have sometimes been associated with phosphorus limitation and increased production of extracellular polymeric substances in previous bench-scale studies. However, field studies utilizing phosphorus supplementation to improve biofilter hydraulic performance have produced mixed results. Here, we determined the ratio of activities for phosphatase to glycosidase (PHO:GLY), which are enzymes involved in acquiring orthophosphate and biodegradable organic carbon from complex organic substrates, to assess phosphorus limitation in 21 pilot- and full-scale biofilters. Supplementation of the pilot-scale biofilter influents with 37 μg/L orthophosphate-P reduced the PHO:GLY from 1.8–40.3 (mean 14.8) to 0.3–15.9 (mean 5.3), demonstrating that increased orthophosphate availability decreases PHO:GLY. In the absence of phosphorus supplementation, the PHO:GLY of the pilot- and full-scale biofilters ranged from 0.3 to 40.3 (mean 10.1), and no hydraulic performance issues were noted. Thus, severe phosphorus limitation appears uncommon in the field, suggesting that phosphorus supplementation is unlikely to improve hydraulic performance in typical drinking water biofilters.
{"title":"Field evaluation of phosphorus limitation in drinking water biofilters","authors":"Madison Rasmus, Asher E. Keithley, Bryant A. Chambers, Grace Zhou, Greg Pope, Eric R. V. Dickenson, Bradley Bzdyra, Alisa Lu, Kerry A. Kinney, Mary Jo Kirisits","doi":"10.1002/aws2.1317","DOIUrl":"https://doi.org/10.1002/aws2.1317","url":null,"abstract":"<p>Hydraulic performance issues in drinking-water biofilters have sometimes been associated with phosphorus limitation and increased production of extracellular polymeric substances in previous bench-scale studies. However, field studies utilizing phosphorus supplementation to improve biofilter hydraulic performance have produced mixed results. Here, we determined the ratio of activities for phosphatase to glycosidase (PHO:GLY), which are enzymes involved in acquiring orthophosphate and biodegradable organic carbon from complex organic substrates, to assess phosphorus limitation in 21 pilot- and full-scale biofilters. Supplementation of the pilot-scale biofilter influents with 37 μg/L orthophosphate-P reduced the PHO:GLY from 1.8–40.3 (mean 14.8) to 0.3–15.9 (mean 5.3), demonstrating that increased orthophosphate availability decreases PHO:GLY. In the absence of phosphorus supplementation, the PHO:GLY of the pilot- and full-scale biofilters ranged from 0.3 to 40.3 (mean 10.1), and no hydraulic performance issues were noted. Thus, severe phosphorus limitation appears uncommon in the field, suggesting that phosphorus supplementation is unlikely to improve hydraulic performance in typical drinking water biofilters.</p>","PeriodicalId":101301,"journal":{"name":"AWWA water science","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aws2.1317","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50144708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andrew J. Whelton, Chad Seidel, Brad P. Wham, Erica C. Fischer, Kristofer Isaacson, Caroline Jankowski, Nathan MacArthur, Elizabeth McKenna, Christian Ley