Pre- and Postapplication Thermal Treatment Strategies for Sorption Enhancement and Reactivation of Biochars for Removal of Per- and Polyfluoroalkyl Substances from Water
被引:22
作者:
Wang, Zhengyang
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Connecticut Agr Expt Stn, Dept Environm Sci & Forestry, New Haven, CT 06504 USAUniv North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Wang, Zhengyang
[3
]
Alinezhad, Ali
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Univ North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USAUniv North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Alinezhad, Ali
[1
]
Sun, Runze
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Univ North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USAUniv North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Sun, Runze
[1
]
Xiao, Feng
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机构:
Univ North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Univ Missouri, Dept Civil & Environm Engn, Columbia, MO 65211 USAUniv North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Xiao, Feng
[1
,2
]
Pignatello, Joseph J.
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Connecticut Agr Expt Stn, Dept Environm Sci & Forestry, New Haven, CT 06504 USAUniv North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
Pignatello, Joseph J.
[3
]
机构:
[1] Univ North Dakota, Dept Civil Engn, Grand Forks, ND 58202 USA
[2] Univ Missouri, Dept Civil & Environm Engn, Columbia, MO 65211 USA
[3] Connecticut Agr Expt Stn, Dept Environm Sci & Forestry, New Haven, CT 06504 USA
Exposure to per- and polyfluoroalkyl substances (PFAS) in drinking water poses a major public health threat. Commercial granular activated carbon (GAC) has been used for the sorptive removal of PFAS in practical applications. Biochar is a possible cheaper alternative to GAC for small-scale water treatment systems. Here, we report a strategy for employing biochar for PFAS removal that combines post-pyrolysis modification, which greatly improves performance, with a reactivation step that enables its reuse. Modification entails brief postpyrolysis air oxidation at 400 degrees C, which considerably enlarges pore size and specific surface area and thereby increases the solid-to-water distribution ratio, KD, of individual PFAS by as much as 3 orders of magnitude. In some cases (e.g., perfluorooctanoic acid) the KD was comparable to that of commercial GAC. The sorbed PFAS could be decomposed by brief thermal reactivation of the spent biochar at 500 degrees C in N-2 or air. After thermal reactivation in air, the biochars exhibited even greater PFAS KD values in a second cycle. While thermal reactivation of a GAC in air could be achieved, as well, sorption affinity for the shorter-chain PFAS was noticeably reduced. Overall, this study points to a new strategy of using biochars for PFAS removal.
机构:
Shandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Li, Mingjun
Zhao, Xin
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Shandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Beijing Normal Univ, Coll Water Sci, Beijing 100875, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Zhao, Xin
Yan, Peihao
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Shandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Yan, Peihao
Xie, Huijun
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Shandong Univ, Environm Res Inst, Qingdao 266237, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Xie, Huijun
Zhang, Jian
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Shandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Jinan 250014, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Zhang, Jian
Wu, Suqing
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机构:
Wenzhou Univ, Sch Life & Environm Sci, Wenzhou 325035, Zhejiang, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
Wu, Suqing
Wu, Haiming
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Shandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R ChinaShandong Univ, Sch Environm Sci & Engn, Key Lab Water Pollut Control & Resource Reuse, Qingdao 266237, Peoples R China
机构:
Univ N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Manning, Irene M.
Chew, Nick Guan Pin
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Univ N Carolina, Dept Environm Sci & Engn, Gillings Sch Global Publ Hlth, 135 Dauer Dr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Chew, Nick Guan Pin
Macdonald, Haley P.
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Univ N Carolina, Dept Environm Sci & Engn, Gillings Sch Global Publ Hlth, 135 Dauer Dr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Macdonald, Haley P.
Miller, Kelsey E.
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US EPA, Off Res & Dev, Ctr Environm Measurement & Modeling, Res Triangle Pk, NC 27709 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Miller, Kelsey E.
Strynar, Mark J.
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US EPA, Off Res & Dev, Ctr Environm Measurement & Modeling, Res Triangle Pk, NC 27709 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Strynar, Mark J.
Coronell, Orlando
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Univ N Carolina, Dept Environm Sci & Engn, Gillings Sch Global Publ Hlth, 135 Dauer Dr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA
Coronell, Orlando
Leibfarth, Frank A.
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Univ N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, 131 South Rd, Chapel Hill, NC 27599 USA