Institute for Critical Technology and Applied Science (ICTAS)
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ICTAS Vision:
To be a premier institute to advance transformative, interdisciplinary research for a sustainable future.
ICTAS Mission:
To serve Virginia Tech, the Commonwealth of Virginia, the nation, and the world through high-impact research and scholarship at the intersections of engineering, the sciences -- physical, life, and social -- and the humanities. To this end, advance the frontiers of knowledge and education, enhance the educational experience of undergraduate, graduate, and professional students, and promote economic development through the creation and application of innovative research that enhances the quality of life and preserves our natural resources.
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Browsing Institute for Critical Technology and Applied Science (ICTAS) by Department "Civil and Environmental Engineering"
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- Aerosol microdroplets exhibit a stable pH gradientWei, Haoran; Vejerano, Eric P.; Leng, Weinan; Huang, Qishen; Willner, Marjorie R.; Marr, Linsey C.; Vikesland, Peter J. (2018-07-10)Suspended aqueous aerosol droplets (< 50 mu m) are microreactors for many important atmospheric reactions. In droplets and other aquatic environments, pH is arguably the key parameter dictating chemical and biological processes. The nature of the droplet air/water interface has the potential to significantly alter droplet pH relative to bulk water. Historically, it has been challenging to measure the pH of individual droplets because of their inaccessibility to conventional pH probes. In this study, we scanned droplets containing 4-mercaptobenzoic acid-functionalized gold nanoparticle pH nanoprobes by 2D and 3D laser confocal Raman microscopy. Using surface-enhanced Raman scattering, we acquired the pH distribution inside approximately 20-mu m-diameter phosphate-buffered aerosol droplets and found that the pH in the core of a droplet is higher than that of bulk solution by up to 3.6 pH units. This finding suggests the accumulation of protons at the air/water interface and is consistent with recent thermodynamic model results. The existence of this pH shift was corroborated by the observation that a catalytic reaction that occurs only under basic conditions (i.e., dimerization of 4-aminothiophenol to produce dimercaptoazobenzene) occurs within the high pH core of a droplet, but not in bulk solution. Our nanoparticle probe enables pH quantification through the cross-section of an aerosol droplet, revealing a spatial gradient that has implications for acid-base-catalyzed atmospheric chemistry.
- Nanomaterial enabled sensors for environmental contaminantsWillner, Marjorie R.; Vikesland, Peter J. (2018-11-22)The need and desire to understand the environment, especially the quality of one’s local water and air, has continued to expand with the emergence of the digital age. The bottleneck in understanding the environment has switched from being able to store all of the data collected to collecting enough data on a broad range of contaminants of environmental concern. Nanomaterial enabled sensors represent a suite of technologies developed over the last 15 years for the highly specific and sensitive detection of environmental contaminants. With the promise of facile, low cost, field-deployable technology, the ability to quantitatively understand nature in a systematic way will soon be a reality. In this review, we first introduce nanosensor design before exploring the application of nanosensors for the detection of three classes of environmental contaminants: pesticides, heavy metals, and pathogens.
- Plasmonic colorimetric and SERS sensors for environmental analysisWei, Haoran; Hossein Abtahi, Seyyed M.; Vikesland, Peter J. (The Royal Society of Chemistry, 2015-03-10)The potential for water pollution outbreaks requires the development of rapid, yet simple detection methods for water quality monitoring. Plasmonic nanostructures such as gold (AuNPs) and silver (AgNPs) nanoparticles are compelling candidates for the development of highly sensitive biosensors due to their unique localized surface plasmon resonances (LSPRs). The LSPR of AuNPs and AgNPs lies in the visible and infrared light range and is sensitive to the composition, size, shape, surrounding medium, and aggregation state of these NPs. This plasmonic behavior provides the basis for fabrication of colorimetric sensors for environmental analyses. Furthermore, the LSPR also enhances the electromagnetic field near the NP surface, which provides the basis for surface-enhanced Raman spectroscopy (SERS) based detection. Organic or inorganic pollutants and pathogens can be detected and differentiated based upon the finger-print spectra that arise when they enter SERS-active hot spots. In this tutorial review, we summarize progress made towards environmental analysis based on LSPR-based colorimetric and SERS detection. The problems and challenges that have hindered the development of LSPR-based nanosensors for real-world environmental pollutant monitoring are extensively discussed.
- Preparation and evaluation of nanocellulose-gold nanoparticle nanocomposites for SERS applicationsWei, Haoran; Rodriguez, Katia; Renneckar, Scott; Leng, Weinan; Vikesland, Peter J. (The Royal Society of Chemistry, 2015-06-09)Nanocellulose is of research interest due to its extraordinary optical, thermal, and mechanical properties. The incorporation of guest nanoparticles into nanocellulose substrates enables production of novel nanocomposites with a broad range of applications. In this study, gold nanoparticle/bacterial cellulose (AuNP/BC) nanocomposites were prepared and evaluated for their applicability as surface-enhanced Raman scattering (SERS) substrates. The nanocomposites were prepared by citrate mediated in situ reduction of Au3+ in the presence of a BC hydrogel at 303 K. Both the size and morphology of the AuNPs were functions of the HAuCl4 and citrate concentrations. At high HAuCl4 concentrations, Au nanoplates form within the nanocomposites and are responsible for high SERS enhancements. At lower HAuCl4 concentrations, uniform nanospheres form and the SERS enhancement is dependent on the nanosphere size. The time-resolved increase in the SERS signal was probed as a function of drying time with SERS ‘hot-spots’ primarily forming in the final minutes of nanocomposite drying. The application of the AuNP/BC nanocomposites for detection of the SERS active dyes MGITC and R6G as well as the environmental contaminant atrazine is illustrated as is its use under low and high pH conditions. The results indicate the broad applicability of this nanocomposite for analyte detection.
- Protein-aided formation of triangular silver nanoprisms with enhanced SERS performanceGeng, Xi; Leng, Weinan; Carter, Nathan A.; Vikesland, Peter J.; Grove, Tijana Z. (Royal Society of Chemistry, 2016-05-10)In this work, we present a modified seed-mediated synthetic strategy for the growth of silver nanoprisms with low shape polydispersity, narrow size distribution and tailored plasmonic absorbance. During the seed nucleation step, consensus sequence tetratricopeptide repeat (CTPR) proteins are utilized as potent stabilizers to facilitate the formation of planar-twinned Ag seeds. Ag nanoprisms were produced in high yield in a growth solution containing ascorbic acid and CTPR-stabilized Ag seeds. From the time-course UV-Vis and transmission electron microscopy (TEM) studies, we postulate that the growth mechanism is the combination of facet selective lateral growth and thermodynamically driven Ostwald ripening. The resultant Ag nanotriangles (NTs) exhibit excellent surface enhanced Raman spectroscopy (SERS) performance. The enhancement factor (EF) measured for the 4-mercapto benzoic acid (4-MBA) reporter is estimated to be 3.37 × 105 in solution and 2.8 × 106 for the SERS substrate.
- Role of coexisting tetragonal regions in the rhombohedral phase of Na0.5Bi0.5TiO3-xat.%BaTiO3 crystals on enhanced piezoelectric properties on approaching the morphotropic phase boundaryYao, Jianjun; Monsegue, Niven; Murayama, Mitsuhiro; Leng, W. N.; Reynolds, William T. Jr.; Zhang, Qinhui; Luo, Haosu; Li, Jiefang; Ge, Wenwei; Viehland, Dwight D. (AIP Publishing, 2012-01-01)The ferroelectric domain and local structures of Na0.5Bi0.5TiO3-xat.%BaTiO3 (NBT-x%BT) crystals for x = 0, 4.5, and 5.5 have been investigated by transmission electron microscopy. The results show that the size of polar nano-regions was refined with increasing xat. %BT. The tetragonal phase volume fraction, as identified by in-phase octahedral tilting, was found to be increased with BT. The findings indicate that the large electric field induced strains in morphotropic phase boundary compositions of NBT-x%BT originate not only from polarization rotation but also polarization extension. (C) 2012 American Institute of Physics. [doi: 10.1063/1.3673832]
- Toxicity of Silver Nanoparticles at the Air-Liquid InterfaceHolder, Amara L.; Marr, Linsey C. (Hindawi, 2013-01-01)Silver nanoparticles are one of the most prevalent nanomaterials in consumer products. Some of these products are likely to be aerosolized, making silver nanoparticles a high priority for inhalation toxicity assessment. To study the inhalation toxicity of silver nanoparticles, we have exposed cultured lung cells to them at the air-liquid interface. Cells were exposed to suspensions of silver or nickel oxide (positive control) nanoparticles at concentrations of 2.6, 6.6, and 13.2 μg cm⁻² (volume concentrations of 10, 25, and 50 μg ml⁻¹) and to 0.7 μg cm⁻² silver or 2.1 μg cm⁻² nickel oxide aerosol at the air-liquid interface. Unlike a number of in vitro studies employing suspensions of silver nanoparticles, which have shown strong toxic effects, both suspensions and aerosolized nanoparticles caused negligible cytotoxicity and only a mild inflammatory response, in agreement with animal exposures. Additionally, we have eveloped a novel method using a differential mobility analyzer to select aerosolized nanoparticles of a single diameter to assess the size-dependent toxicity of silver nanoparticles.
- Waste not want not: life cycle implications of gold recovery and recycling from nanowastePati, Paramjeet; McGinnis, Sean; Vikesland, Peter J. (Royal Society of Chemistry, 2016-08-24)Commercial-scale applications of nanotechnology are rapidly increasing. Enhanced production of nanomaterials and nano-enabled products and their resultant disposal lead to concomitant increases in the volume of nanomaterial wastes (i.e., nanowaste). Many nanotechnologies employ resource-limited materials, such as precious metals and rare earth elements that ultimately end up as nanowaste. To make nanotechnology more sustainable it is essential to develop strategies to recover these high-value, resource-limited materials. To address this complex issue, we developed laboratory-scale methods to recover nanowaste gold. To this end, α-cyclodextrin facilitated host–guest inclusion complex formation involving second-sphere coordination of [AuBr4]− and [K(OH2)6]+ was used for gold recovery and the recovered gold was then used to produce new nanoparticles. To quantify the environmental impacts of this gold recycling process we then produced life cycle assessments to compare nanoparticulate gold production scenarios with and without recycling. The LCA results indicate that recovery and recycling of nanowaste gold can significantly reduce the environmental impacts of gold nanoparticle synthesis.