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Record W2344122715 · doi:10.1149/ma2015-01/16/1201

Water Treatment By Adsorption with Electrochemical Regeneration

2015· article· en· W2344122715 on OpenAlexaff
Edward P.L. Roberts, N.W. Brown, Syed Nadir Hussain, Hussain Mohammad, A. Martin

Bibliographic record

VenueECS Meeting Abstracts · 2015
Typearticle
Languageen
FieldEngineering
TopicMembrane-based Ion Separation Techniques
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsAdsorptionElectrochemistryAnodeChemistryPhenolActivated carbonEffluentChemical engineeringElectrodeOrganic chemistryWaste management

Abstract

fetched live from OpenAlex

There have been several studies of electrochemical regeneration of activated carbon adsorbents used for removal of organic contaminants [1], including both cathodic and anodic treatment. The process offers advantages over thermal regeneration including in-situ (on-site) regeneration and minimal adsorbent losses [2]. However, long regeneration times, high energy costs and in some cases poor regeneration efficiencies have constrained implementation [2]. An alternative approach has been developed using graphite intercalation compound (GIC) adsorbents [3], that have low adsorption capacities but are amenable to rapid electrochemical regeneration. The electrochemical regeneration using GIC adsorbents is achieved through the anodic oxidation of the adsorbed species whereby a packed bed of the loaded GIC adsorbent is used as the anode within an electrochemical cell. The regenerated adsorbent, including any water trapped in the bed of adsorbent, is transferred without additional treatment to the next adsorption cycle. This means that no secondary waste is generated in the process. However, partially oxidized organics could be released into the treated water causing contamination with potentially more toxic compounds. In addition, some studies have suggested that phenol can polymerise during electrochemical oxidation, especially on the surface of graphite electrodes. The nature and concentrations of the breakdown products generated during electrochemical oxidation determines the toxicity of the treated effluent. In this context, the breakdown products released in the liquid phase has been studied [4, 5]. Phenol was chosen as a model pollutant in these studies. A variety of oxidation intermediates including aromatics, aliphatic acids and chlorinated species have been observed during electrochemical regeneration of the GIC adsorbent in treating the aqueous solution of phenol. However, the concentrations of the breakdown products were fairly low compared to the initial concentration of phenol to be treated. The main mechanism responsible for the formation of breakdown products was found to be associated with indirect oxidation of phenol in solution i.e phenolic oxidation from solution as opposed to the oxidation of sorbed phenolics and therefore, the phenol adsorbed onto the surface of GIC adsorbent was not observed to contribute to the formation of these products [4]. The present study is concerned with the formation of gaseous breakdown products generated during electrochemical regeneration of GIC adsorbents. Carbon dioxide and carbon monoxide were detected as the main gaseous breakdown products formed in the during the regeneration process under a range of conditions. When electrochemical regeneration was carried out galvanostatically, both the volume and CO 2 concentration of the gas evolved during regeneration of phenol loaded adsorbent were higher than the volume and CO 2 concentration of the gas obtained when no phenol was present. In order to show that the CO 2 formed is from the phenol, experiments using a 13 C labelled phenol were carried out. These experiments confirm that a significant proportion of the adsorbed phenol was oxidized to CO 2 . The results suggest that about 50 to 60% of the adsorbed phenol is accounted for by the measured carbon dioxide in the evolved gas. This does not account for any carbon dioxide dissolved in the water during regeneration, and dynamic analysis suggests that this could be a significant fraction of CO 2 in the evolved gases. Work is on-going to investigate the amount of carbon dioxide dissolved in the treated water. This study confirms that electrochemical mineralization of adsorbed organics on GIC adsorbents is achievable. This is an important finding for the development of practical water treatment processes. [1] R.M. Narbaitz, J. Cen, Electrochemical regeneration of granular activated carbon. Wat. Res , 28(1994),1771. [2] R.M. Narbaitz, A. Karimi‐Jashni, Electrochemical regeneration of granular activated carbons loaded with phenol and natural organic matter. Environ. Technol, 30 (2009), 27. [3] K.T. Eccleston, A.J. Eccleston, N.W. Brown, E.P.L. Roberts, Apparatus for the electrochemical regeneration of adsorbents. US Patent 7790024 B2, 2010. [4] S.N. Hussain, E.P.L. Roberts, H.M.A. Asghar, A.K. Campen, N.W. Brown, Oxidation of phenol and adsorption of breakdown products using a graphite adsorbent with electrochemical regeneration, Electrochim. Acta. 92 (2013) 20 [5] S.N. Hussain, H.M.A. Asghar, A.K. Campen, N.W. Brown, E.P.L. RobertS, Breakdown products formed due to oxidation of adsorbed phenol by electrochemical regeneration of a graphite adsorbent,Electrochim. Acta. 110 (2013) 550

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.024
Threshold uncertainty score0.440

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.229
Teacher spread0.214 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2015
Admission routes1
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