Water Treatment By Adsorption with Electrochemical Regeneration
Bibliographic record
Abstract
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
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot 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.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
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.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
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".