Biosolids leachate variability, stabilization surrogates, and optical metric selection
文献情報
Michael Gonsior, Jon Chorover, Leanne C. Powers, Amanda Hamilton, Mark Ramirez
Sludge and biosolids organic matter (OM) are increasingly assessed via optical measurements of associated leachates – especially at pilot and bench scales. Limited work has systematically characterized optical and size exclusion chromatography (SEC) based properties of leachable OM from full-scale solid stabilization processes, however. In this study, leachable OM of biosolids from nine full-scale facilities with lime treatment (LT), anaerobic digestion, or aerobic digestion (AeD) (n = 3 facilities per type), was sampled for three sampling dates per facility and multiple extractions per biosolid (n = 54 leachates). Leachates were characterized by high-performance size exclusion chromatography (HP-SEC-UV), ultraviolet (UV)-visible absorbance spectra, and excitation emission matrix (EEM) spectroscopies, pH, and leachable DOC/kg solid. AnD and AeD biosolids-DOM consistently exhibited higher molecular weight DOM (1360 Da) and fluorescence emissions >380 nm after digestion. This suggested higher molecular-weight, heterogeneous OM is released into soluble phases after biological treatment. Fluorescent emission peaks >450 nm were present only in AnD-biosolids leachates (n = 27), providing a consistent signature for anaerobically digested material. Given the agreement of these trends with pilot scale studies, strategies detecting fluorescence emissions >380 nm are proposed stabilization surrogates at full-scale facilities. Prior to this study, there was limited literature consensus for which optical metrics best quantified sludge and biosolids-DOM transformations, however. Critical analysis of ten optical metrics indicated that not all pre-established metrics captured unique spectral differences in biosolids-DOM spectra, as optical metrics were first developed for aquatic DOM. Absorption (E2 : E3, SUVA254, SR), and fluorescence metrics (HIX, BIX, and fluorescence regional integration (FRI)) were less adaptable to biosolids-DOM spectra. Principal component analysis (PCA) confirmed that targeted peak ratio assessment (i.e. B : T or A : C peak maxima analysis) best differentiated intrinsic fluorescent DOM changes by treatment. Three independent parallel factor analysis (PARAFAC) models for major treatment types of LT, AnD, and AeD biosolids-DOM also validated treatment differences captured by peak picking surrogates. PARAFAC models described new components in the OpenFluor spectral database. Overall, targeted fluorescence peak picking represents a surrogate strategy to monitor leachate quality changes across full-scale treatment trains. These findings may advance optical approaches for process engineering and advanced stabilization research.
おすすめジャーナル

Drug Discovery Today

Organic Process Research & Development

Journal of Peptide Science

Acta Materialia

New Journal of Chemistry

Saudi Pharmaceutical Journal

Russian Journal of Coordination Chemistry

Journal of Saudi Chemical Society

Russian Journal of Organic Chemistry

Current Opinion in Colloid & Interface Science
関連文献
Vacancy-triggered and dopant-assisted NO electrocatalytic reduction over MoS2
Chao Wu
DOI: 10.1039/D1CP02764F
Experimental and computational investigation of the bond energy of thorium dicarbonyl cation and theoretical elucidation of its isomerization mechanism to the thermodynamically most stable isomer, thorium oxide ketenylidene cation, OTh+CCO
Arjun Kafle, P. B. Armentrout
DOI: 10.1039/D1CP04263G
DPD simulations on mixed polymeric DOX-loaded micelles assembled from PCL-SS-PPEGMA/PDEA–PPEGMA and their dual pH/reduction-responsive release
Zexiong Yang, Haiqian Zhao, Delin Wang, Li Yin, Kenxiang Cai, Zehua Lin, Tao Chen, Chufen Yang
DOI: 10.1039/D1CP02750F
Steered molecular dynamics and stability analysis on PAH dimerisation and condensation on fullerene and soot surfaces
Wenjun Kong, Jun Xia
DOI: 10.1039/D1CP01019K
Adsorption of water in Na-LTA zeolites: an ab initio molecular dynamics investigation
Joharimanitra Randrianandraina, Michael Badawi, Bruno Cardey, Manuel Grivet, Jean-Emmanuel Groetz, Christophe Ramseyer, Freddy Torrealba Anzola, Caroline Chambelland, Didier Ducret
DOI: 10.1039/D1CP02624K
Correction: Flexible lipid nanomaterials studied by NMR spectroscopy
Jacob J. Kinnun, Horia I. Petrache
DOI: 10.1039/D1CP90155A
Fluorescence band exchange narrowing in a series of squaraine oligomers: energetic vs. structural disorder
Arthur Turkin, Pavel Malý
DOI: 10.1039/D1CP02136B
Covalent photofunctionalization and electronic repair of 2H-MoS2via nitrogen incorporation
Helena Osthues, Christian Schwermann, Johann A. Preuß, Thorsten Deilmann, Rudolf Bratschitsch, Michael Rohlfing, Nikos L. Doltsinis
DOI: 10.1039/D1CP02313F
Effect of Hf doping on He behavior in tritium storage material ZrCo
You Yu, Yanhong Shen, Jiangfeng Song
DOI: 10.1039/D1CP01803E
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...

![1-[(4-Methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile structure 1-[(4-Methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile structure](https://static.chemtradehub.com/structs/143/1434747-57-5-fc0d.webp)



