Abstract
Two BC(black carbon) samples,BC700 and BC400,were prepared from China fir wood by pyrolytic charring at 700 and 400 ℃,respectively.The sorption behavior and mechanisms of tributyltin(TBT) on the two BC samples were evaluated as a function of seawater pH and salinity.The results indicated that BC700 had a higher specific surface area but lower content of organic matter than BC400.TBT sorption on BC700 was primarily a physical adsorption process while hydrophobic partitioning also significantly contributed to TBT sorption on BC400.Increasing salinity from 5 to 35 g/kg facilitated TBT sorption by 1.03—2.12 times as an overall result of the enhancing effective concentration of TBT because of 'salting-out' and the reducing role of electrostatic interaction because of BC surface charge neutralization.Environmental pH had a significant influence to TBT forms in the solution.It was found that TBT existed in both cationic(TBT+) and uncharged species at pH=4.00 and 6.25 but mostly in uncharged species(TBT) at pH=8.00.TBT sorption reached maximum at pH=6.25,as compared to pH=4.00 and 8.00,due presumably to multiple mechanisms involving electrostatic interaction,physical adsorption and hydrophobic partitioning between TBT and BC.In addition,XPS spectra showed that the binding energy of Sn3d5/2 peak shifted higher with decreasing pH,confirming the TBT-BC electrostatic interaction.Therefore,sorption of TBT on the BC700 was mainly physical adsorption and electrostatic interaction while hydrophobic partitioning also significantly contributed to TBT sorption on BC400.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.