Effects of carbon materials on the formation of disinfection byproducts during chlorination: Pore structure and functional groups.
Clicks: 325
ID: 2792
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
65.9
/100
325 views
262 readers
Trending
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #43 of 168 articles by views in Water research
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 168 in total.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Release of carbon materials (CMs) into water and wastewater treatment systems occurs due to their increasing utilization as adsorbents for water treatment. When the CMs, mixed with natural organic matter (NOM), interact with disinfectants used during water treatment (e.g. chlorine), the released CMs can affect the formation of disinfection byproducts (DBPs). In this study, three common CMs were investigated to reveal their possible effects and the mechanisms of DBP formation during the chlorination of NOM. The experimental results indicate that DBPs generation decreased by 10-40% in the presence of CMs when Suwannee River humic acid (SRHA) was chlorinated. The adsorption of SRHA by CMs was hypothesized as the major cause for the DBPs inhibition. CMs could irreversibly adsorb DBP precursors in their mesopores through π-π bonding and hydrophobic effects. OH groups on the surface of CMs were shown to be critical for DBPs inhibition through linking with the OH or COOH groups on the surface of NOM via hydrogen bonding. The study also showed that water chemistry parameters, such as pH and salinity, can affect DBP formation by changing the adsorption of NOM onto CMs. With diverse NOM components, the presence of CMs resulted in decreased formation of trichloromethane from 57.1 μg/L to 23.8, 38.4, and 40.4 μg/L when coal-made activated carbon (CAC), wheat straw-made BC pyrolyzed at 300 °C (WSBC300), and multiwalled carbon nanotubes (MWCNTs), respectively, were added to surface water; and from 30.6 μg/L to 20.0, 19.2, and 13.2 μg/L when CAC, WSBC300, and MWCNTs, respectively, were added to wastewater.
| Reference Key |
zhang2019effectswater
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Zhang, Min;Wang, Xuan;Du, Tingting;Wang, Huihui;Hao, Huizhi;Wang, Yingying;Li, Yao;Hao, Tianwei; |
| Journal | Water research |
| Year | 2019 |
| DOI |
S0043-1354(19)30572-X
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.