The ever-increasing use of engineered nanomaterials will lead to heightened levels of these materials in the environment. The present review aims to provide a comprehensive overview of current knowledge regarding nanoparticle transport and aggregation in aquatic environments. Nanoparticle aggregation and deposition behavior will dictate particle transport potential and thus the environmental fate and potential ecotoxicological impacts of these materials. In this review, colloidal forces governing nanoparticle deposition and aggregation are outlined. Essential equations used to assess particle−particle and particle−surface interactions, along with Hamaker constants for specific nanoparticles and the attributes exclusive to nanoscale particle interactions, are described. Theoretical and experimental approaches for evaluating nanoparticle aggregation and deposition are presented, and the major findings of laboratory studies examining these processes are also summarized. Finally, we describe some of the chall...

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Aggregation and deposition of engineered nanomaterials in aquatic environments: role of physicochemical interactions.

Surface and structural characterization of multi-walled carbon nanotubes following different oxidative treatments

To utilize carbon nanotubes (CNTs) in various commercial and scientific applications, the graphene sheets that comprise CNT surfaces are often modified to tailor properties, such as dispersion. In this article, we provide a critical review of the techniques used to explore the chemical and structural characteristics of CNTs modified by covalent surface modification strategies that involve the direct incorporation of specific elements and inorganic or organic functional groups into the graphene sidewalls. Using examples from the literature, we discuss not only the popular techniques such as TEM, XPS, IR, and Raman spectroscopy but also more specialized techniques such as chemical derivatization, Boehm titrations, EELS, NEXAFS, TPD, and TGA. The chemical or structural information provided by each technique discussed, as well as their strengths and limitations. Particular emphasis is placed on XPS and the application of chemical derivatization in conjunction with XPS to quantify functional groups on CNT surfaces in situations where spectral deconvolution of XPS lineshapes is ambiguous.

/pdf/chemical-and-structural-characterization-of-carbon-nanotube-4unfwjdhsy.pdf

Chemical and structural characterization of carbon nanotube surfaces.

Stability of nanofluid: A review

Although graphene oxide (GO) has been used in many applications to improve human life quality, its environmental fate and behavior are still largely unknown. In this work, a novel approach that combines experimental measurements and theoretical calculations was used to determine the aggregation kinetics of GO sheets in aqueous solutions under different chemistry conditions (e.g., cation valence and pH). Experimental data showed that both cation valence and pH showed significant effect on the aggregation of GO sheets. The measured critical coagulation concentrations were in good agreement with the predictions of the extended Schulze–Hardy rule. Ca2+ and Mg2+ were more effective than Na+ in aggregating the GO sheets, which could be attributed to the cross-linking between GO sheets by the divalent cations through “bridging” the functional groups at the edges of the GO sheets. When solution pH increases, deprotonation of carboxylic groups was found to play a key role in increasing GO sheet stability and surfa...

Aggregation Kinetics of Graphene Oxides in Aqueous Solutions: Experiments, Mechanisms, and Modeling

Grafting oxygen-containing functional groups onto carbon nanotubes (CNTs) by acid treatment improves their dispersion in aqueous solutions, but there is a lack of quantitative information on the colloidal properties of oxidized CNTs. We have studied the influence that pH and electrolytes have in determining the colloidal stability of oxidized multiwalled carbon nanotubes (O-MWCNTs), prepared by refluxing pristine MWCNTs in nitric acid. The acid-treated MWCNTs contained oxygen predominantly in the form of carboxyl groups. Colloidal suspensions of O-MWCNTs were prepared by low-power sonication and contained negatively charged, individual MWCNTs with an average length of approximately 650 nm. Time-resolved dynamic light scattering revealed that the aggregation rate of O-MWCNTs exhibited both reaction and mass-transport limited regimes in the presence of different electrolytes and as a function of pH. Particle stability profiles constructed from aggregation rate data allowed for the determination of critical coagulation concentrations (CCC), a metric of colloidal stability. The CCC values of O-MWCNTs varied with counterion concentration and valence in a manner consistentwith DLVO theory. Potentiometric measurements of surface charge correlated well with the observed pH-dependent variations in the O-MWCNT's colloidal stability. Electrophoretic mobility was also a diagnostic of particle stability, but only in neutral and acidic conditions.

Colloidal Properties of Aqueous Suspensions of Acid-Treated, Multi-Walled Carbon Nanotubes

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Colloidal Properties of Aqueous Suspensions of Acid-Treated, Multi-Walled Carbon Nanotubes