ABSTRACT
Adsorption of small ions such as phosphates to the surfaces of metal oxides can significantly alter the behavior of these materials, especially when present in the nanoscale form. Lithium cobalt oxide is a good model system for understanding small-molecule interactions with emerging nanomaterials because of its widespread use in lithium ion batteries and its known activity as a water oxidation catalyst. Here, we present a thermodynamic analysis of phosphate adsorption to LiCoO2 and corroborate the results with additional in situ techniques, including zeta potential measurements and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, at pH values relevant to potential environmental release scenarios. Flow microcalorimetry measurements of phosphate interaction with LiCoO2 at pH 7.4 show that there are two distinct exothermic processes taking place. Time-sequence in situ ATR-FTIR with two-dimensional correlation analysis reveals the spectroscopic signatures of these processes. We interpret the data as an interaction of phosphate with LiCoO2 that occurs through the release of two water molecules and is therefore, best described as a condensation process rather than a simple adsorption, consistent with prior studies, demonstrating that phosphate interaction with LiCoO2 is highly irreversible. Additional measurements for over longer times of 5 months show that phosphate adsorption terminates with one surface layer and that continued transformation over longer periods of time arises from H+/Li+ exchange and slow transformation to a cobalt hydroxide, with phosphate adsorbed to the surface only. To the best of our knowledge, this is the first time that flow microcalorimetry and two-dimensional correlation spectroscopy have been applied in tandem to clarify the specific chemical reactions that occur at the interface of solids and adsorbates.
ABSTRACT
Engineered nanoparticles are incorporated into numerous emerging technologies because of their unique physical and chemical properties. Many of these properties facilitate novel interactions, including both intentional and accidental effects on biological systems. Silver-containing particles are widely used as antimicrobial agents and recent evidence indicates that bacteria rapidly become resistant to these nanoparticles. Much less studied is the chronic exposure of bacteria to particles that were not designed to interact with microorganisms. For example, previous work has demonstrated that the lithium intercalated battery cathode nanosheet, nickel manganese cobalt oxide (NMC), is cytotoxic and causes a significant delay in growth of Shewanella oneidensis MR-1 upon acute exposure. Here, we report that S. oneidensis MR-1 rapidly adapts to chronic NMC exposure and is subsequently able to survive in much higher concentrations of these particles, providing the first evidence of permanent bacterial resistance following exposure to nanoparticles that were not intended as antibacterial agents. We also found that when NMC-adapted bacteria were subjected to only the metal ions released from this material, their specific growth rates were higher than when exposed to the nanoparticle. As such, we provide here the first demonstration of bacterial resistance to complex metal oxide nanoparticles with an adaptation mechanism that cannot be fully explained by multi-metal adaptation. Importantly, this adaptation persists even after the organism has been grown in pristine media for multiple generations, indicating that S. oneidensis MR-1 has developed permanent resistance to NMC.
ABSTRACT
A commonly overlooked and largely unknown aspect of assessing the environmental and biological safety of engineered nanomaterials is their transformation in aqueous systems. Complex metal oxides are an important class of materials for catalysis, energy storage, and water purification. However, the potential impact of nano complex metal oxides on the environment upon improper disposal is not well understood. We present a comprehensive analysis of the interaction of an environmentally relevant oxyanion, phosphate, with a complex metal oxide nanomaterial, lithium cobalt oxide. Our results show that adsorption of phosphate to the surface of these materials drastically impacts their surface charge, rendering them more stable in aqueous systems. The adsorbed phosphate remains on the surface over significant periods of time, suggesting that desorption is not kinetically favored. The implications of this interaction may be increased dispersibility and bioavailability of these materials in environmental water systems.
Subject(s)
Nanoparticles , Phosphates , Adsorption , Cobalt , OxidesABSTRACT
We report development of a mobile and easy-to-fabricate theta pipette microfluidic device for segmented flow sampling. The theta pipettes were also used as electrospray emitters for analysis of sub-nanoliter segments, which resulted in delivery of analyte to the vacuum inlet of the mass spectrometer without multiple transfer steps. Theta pipette probes enable sample collection with high spatial resolution due to micron or smaller sized probe inlets and can be used to manipulate aqueous segments in the range of 200 pL to tens of nanoliters. Optimized conditions can enable sampling with high spatial and temporal resolution, suitable for chemical monitoring in biological samples and studies of sample heterogeneity. Intercellular heterogeneity among Allium cepa cells was studied by collecting cytoplasm from multiple cells using a single probe. Extracted cytoplasm was analyzed in a fast and high throughput manner by direct electrospray mass spectrometry of segmented sample from the probe tip.
