Protonated Hydroxylamine‐Assisted Iron Catalytic Activation of Persulfate for the Rapid Removal of Persistent Organics from Wastewater. Issue 3 (17th July 2022)
- Record Type:
- Journal Article
- Title:
- Protonated Hydroxylamine‐Assisted Iron Catalytic Activation of Persulfate for the Rapid Removal of Persistent Organics from Wastewater. Issue 3 (17th July 2022)
- Main Title:
- Protonated Hydroxylamine‐Assisted Iron Catalytic Activation of Persulfate for the Rapid Removal of Persistent Organics from Wastewater
- Authors:
- Merouani, Slimane
Dehane, Aissa
Belghit, Aouattef
Hamdaoui, Oualid
Tobba, Yasser A.
Lahlou, Chouaib
Shah, Maulin P. - Other Names:
- Shah Maulin P. guestEditor.
Rodriguez Couto Susana guestEditor. - Abstract:
- Abstract: This research aims at optimizing the effects of processing conditions, salts, natural organic materials, and water matrices quality on the effectiveness of the Fe(II)/K2 S2 O8 /hydroxylamine process in the degradation of pararosaniline. Assisting the Fe(II)/KPS (potassium persulfate) treatment with protonated hydroxylamine (H3 NOH + ) increases the degradation rate of pararosaniline by more than 100%. Radical scavenger experiments show that the SO4 ●− radical dominates pararosaniline degradation in the Fe(II)/KPS system, whereas ● OH is the dominant reactive species in the presence of H3 NOH + . The disparity in pararosaniline removal effectiveness upon the Fe(II)/KPS/H3 NOH + and Fe(II)/KPS systems gets more significant with increasing reactants doses (i.e., H3 NOH +, H2 O2, Fe(II)) and solution pH (2–7). Interestingly, H3 NOH + increased the working pH to 6 instead of pH 4 for the Fe(II)/KPS process. Moreover, mineral anions such as Cl −, NO3 −, NO2 −, and SO4 − (up to 10 × 10 −3 m ) do not affect the efficiency of the Fe(II)/KPS/H3 NOH + process. In contrast, acid humic decreases the performance of the process by ≈20%. In natural mineral water, treated wastewater, and river water samples, the Fe(II)/KPS/H3 NOH + process maintains higher degradation performance (≈95%), whereas the process efficiency is greatly amortized in seawater. The efficiency of the Fe(II)/KPS process was drastically decreased in the various water matrices. Abstract : ProtonatedAbstract: This research aims at optimizing the effects of processing conditions, salts, natural organic materials, and water matrices quality on the effectiveness of the Fe(II)/K2 S2 O8 /hydroxylamine process in the degradation of pararosaniline. Assisting the Fe(II)/KPS (potassium persulfate) treatment with protonated hydroxylamine (H3 NOH + ) increases the degradation rate of pararosaniline by more than 100%. Radical scavenger experiments show that the SO4 ●− radical dominates pararosaniline degradation in the Fe(II)/KPS system, whereas ● OH is the dominant reactive species in the presence of H3 NOH + . The disparity in pararosaniline removal effectiveness upon the Fe(II)/KPS/H3 NOH + and Fe(II)/KPS systems gets more significant with increasing reactants doses (i.e., H3 NOH +, H2 O2, Fe(II)) and solution pH (2–7). Interestingly, H3 NOH + increased the working pH to 6 instead of pH 4 for the Fe(II)/KPS process. Moreover, mineral anions such as Cl −, NO3 −, NO2 −, and SO4 − (up to 10 × 10 −3 m ) do not affect the efficiency of the Fe(II)/KPS/H3 NOH + process. In contrast, acid humic decreases the performance of the process by ≈20%. In natural mineral water, treated wastewater, and river water samples, the Fe(II)/KPS/H3 NOH + process maintains higher degradation performance (≈95%), whereas the process efficiency is greatly amortized in seawater. The efficiency of the Fe(II)/KPS process was drastically decreased in the various water matrices. Abstract : Protonated hydroxylamine (H3 NOH + ) is an efficient accelerator of the Fe(III)/Fe(II) redox cycle. It exhibits significant promotion of the degradation of pararosaniline by the Fe(II)/persulfate system. Addition of H3 NOH + results in an increase of the working pH for the Fe(II)/persulfate system up to pH 6. The efficiency of the Fe(II)/persulfate/H3 NOH + ternary system is high in various water matrices. … (more)
- Is Part Of:
- Clean. Volume 51:Issue 3(2023)
- Journal:
- Clean
- Issue:
- Volume 51:Issue 3(2023)
- Issue Display:
- Volume 51, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 51
- Issue:
- 3
- Issue Sort Value:
- 2023-0051-0003-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-07-17
- Subjects:
- degradation -- Fe(II)/KPS/H3NOH+ process -- radicals -- textile wastewater -- water quality
Water quality -- Periodicals
Water -- Pollution -- Periodicals
Pollution -- Periodicals
Bioremediation -- Periodicals
Sewage -- Periodicals
Water chemistry -- Periodicals
333.7205 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1863-0669 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/clen.202100304 ↗
- Languages:
- English
- ISSNs:
- 1863-0650
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3278.424500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26383.xml