Aggregation of oxidized multi-walled carbon nanotubes: Interplay of nanomaterial surface O-functional groups and solution chemistry factors. (August 2019)

• Record Type: Journal Article
• Authors: Xia, Tianjiao; Guo, Xuetao; Lin, Yixuan; Xin, Bo; Li, Shunli; Yan, Ni; Zhu, Lingyan
• Is Part Of: Environmental pollution. Volume 251(2019)
• Page Start: 921
• Page End: 929
• Publication Date: 2019-08
• Subjects: Carbon nanotubes -- Colloidal stability -- Hamaker constant -- DLVO interaction -- Oxidation; Pollution -- Periodicals; Pollution -- Environmental aspects -- Periodicals; Environmental Pollution -- Periodicals; Pollution -- Périodiques; Pollution -- Aspect de l'environnement -- Périodiques; Pollution -- Effets physiologiques -- Périodiques; Pollution; Pollution -- Environmental aspects; Periodicals; Electronic journals; 363.73
• DOI: 10.1016/j.envpol.2019.05.079
• Languages: English
• ISSNs: 0269-7491

Abstract

Abstract: The fast-growing production and application of carbon nanotube (CNT) materials in a variety of industrial products inevitably lead to their release to wastewater and surface water. CNT would experience oxidization in wastewater treatment plant due to the presence of large amount of disinfectants, such as H2 O2 and O3, which in turn affects the environmental fates and risks of CNT. In this study, oxidized CNT materials (O-CNTs) were prepared by treating CNT with H2 O2 /UV and O3 (denoting as H2 O2 -CNT and O3 -CNT, respectively). A variety of characterizations indicated that oxygen containing groups were generated on CNT surface upon the oxidation, and the O/C ratio increased in the order of pristine CNT < H2 O2 -CNT < O3 -CNT. In the presence of Na +, K + and Mg 2+, the O-CNTs displayed better colloidal stability than the pristine CNT, and the stability increased with the oxidation degree (indicated by O/C ratio). This could be explained by the more negative surface charge and stronger hydrophilicity of the O-CNTs. Unexpectedly, in the presence of Ca 2+, the most oxidized O3 -CNT exhibited the poorest colloidal stability. The abundant carboxyl groups in O3 -CNT provided effective binding sites for cation bridging effect through Ca 2+ and led to stronger aggregation. Increasing pH was more favorable to disperse CNTs (both O-CNT and pristine CNT) in the presence of Na +, but much less effective in inhibiting the aggregation of O3 -CNT in presence of Ca 2+ . This could be explained by the stronger cation bridging effect due to enhanced deprotonation the –COOH groups at higher pH conditions. The calculated Hamaker constants of the CNTs decreased with the oxidation degree, implying that there was lower van der Waals force between the O-CNTs. The Derjaguin–Landau–Verwey–Overbeek (DLVO) calculation confirmed that O-CNTs had to overcome higher energy barrier and thus showed better colloidal stability than the pristine CNT in the presence of Na + . Graphical abstract: Image 1 Highlights: Oxidation treatments introduced oxygen containing functional groups on CNTs. The O/C ratio and oxidation degree increased in the order of pristine CNT < H2 O2 -CNT < O3 -CNT. O-CNTs displayed better colloidal stability than pristine CNT in solutions containing Na +, K + or Mg 2+ . Increased hydrophilcity and more negative surface charges promoted the colloidal stability of O-CNTs. In presence of Ca 2+, O3 -CNT exhibited the poorest colloidal stability due to cation-bridging effect. Abstract : Capsule : Colloidal stability of CNTs relays on the intricate interplay between their surface O-functional groups and solution chemistry factors.