Characterization of a Vortex Shaking Method for Aerosolizing Fibers

Generation of well-dispersed, well-characterized fibers is important in toxicology studies. A vortex-tube shaking method is investigated using glass fibers to characterize the generated aerosol. Controlling parameters that were studied included initial batch amounts of glass fibers, preparation of the powder (e.g., preshaking), humidity, and airflow rate. Total fiber number concentrations and aerodynamic size distributions were typically measured. The aerosol concentration is only stable for short times (t < 10 min) and then falls precipitously, with concomitant changes in the aerosol aerodynamic size distribution; the plateau concentration and its duration both increase with batch size. Preshaking enhances the initial aerosol concentration and enables the aerosolization of longer fibers. Higher humidity strongly affects the particle size distribution and the number concentration, resulting in a smaller modal diameter and a higher number concentration. Running the vortex shaker at higher flow rates (Q > 0.3 lpm), yields an aerosol with a particle size distribution representative of the batch powder; running the vortex shaker at a lower aerosol flow rate (Q ～ 0.1 lpm) only aerosolizes the shorter fibers. These results have implications for the use of the vortex shaker as a standard aerosol generator.

Copyright 2013 American Association for Aerosol Research     

Development of a Personal Sampler for Collecting Fungal Spores

Exposure to fungal aerosols is of concern in indoor environments. However, sampling limitations have previously made it difficult to assess exposures accurately, especially long-term exposures. A prototype personal aerosol sampler, based on cyclone principles and using a 1.5 ml microcentrifuge tube as a particle collection receptacle has been designed and fabricated. Collection efficiency for aerosol particles in the size range of fungal spores has been evaluated for different types of microcentrifuge tubes, together with the effect of a polyethylene glycol coating on the inside of the tube and the effect of adding water to the tube. Monodisperse, fluorescently tagged polymer microspheres with median diameters of 0.5, 1, 2, 3, 6, 11, and 16 μm were used to evaluate sampler performance with particle diameter. The microcentrifuge-tube sampler was tested at flow rates of 2 and 4 liters per minute (l/min). Experimental results indicate that the microcentrifuge-tube sampler has an aspiration efficiency of 100% in calm air for particles up to 16 μm. At 4 l/min, the microcentrifuge-tube sampler is able to collect nearly 100% of particles greater than 3 μm and > 90% of particles between 2.5 and 3 μm. The 50% cutoff size is 1.5 μm. The performance of the sampler did not vary with the different brands of tubes tested or with the presence or absence of a coating on the tube surface. Furthermore, the addition of water to the tube resulted in a slight increase in collection efficiency. A sampling time of 5 h was feasible at 45–50% relative humidity before evaporation led to significant water loss.

The cutoff size of 1.5 μm is comparable to many commercially available bioaerosol samplers. Besides being easy to use, simple to fabricate, and inexpensive, this novel sampler has several advantages over conventional samplers: long-term samples are possible (the limitation of impaction methods); there is no sample transfer loss since the transfer step has been eliminated (the limitation of filter cassettes); laboratory analyses are not dependent solely upon a single analysis method (the limitation of impaction methods), and there is no sampler adherence loss (the limitation of trying to wash microorganisms from filters). In addition, use of the sampler would be applicable in a variety of occupational settings from low bioaerosol concentrations (i.e., indoor environments) to high bioaerosol concentrations (i.e., agricultural setting) by varying sampling time periods and using sensitive analytical methods.     

Biobased adhesives,gums, emulsions,and binders: current trends and future prospects

Biopolymers derived from renewable resources are an emerging class of advanced materials that offer many useful properties for a wide range of food and nonfood applications. Current state of the art in research and development of renewable polymers as adhesives, gums, binders, and emulsions is the subject of this review. Much of the focus will be on major biopolymers such as starch, proteins, lignin, oils, and their derivatives found in both natural and modified forms, but other biopolymers of promising commercial interest will also be included where warranted. Polymers produced in nature are remarkably diverse in their chemistry, thermomechanical properties, rheology, plasticity, and chemical reactivity. In particular, their capacity to undergo a wide array of chemical modifications yields materials with tailored properties suitable for use as adhesives, gums, coatings, emulsions, and binders. Many such materials are now widely used in commercial products like building materials, lubricants, sealants, coatings, bonding aids, pharmaceuticals, paper, glues, flocculants, processed and frozen foods, as well as tissue engineering and bone repair products. This review provides a general overview of biobased polymers highlighting their source, availability, properties, and usage in industrial products along with the future prospects, challenges, and opportunities they offer.     

Comparison of Particle Size Distributions at Urban and Agricultural Sites in California's San Joaquin Valley

As part of the California Regional PM _2.5 and PM ₁₀ Air Quality Study (CRPAQS) particle size distributions were measured simultaneously at two sites; the city of Fresno and the agricultural site of Angiola. Reported here are data obtained by scanning mobility analysis over the size range from 10 nm to 400 nm for the intensive study period from December 1, 2000 through February 6, 2001. These high time resolution data show variability in the character of the distributions, as well as the in the total number concentrations. The most pronounced feature of the data set is a consistent, nighttime maxima in particle number concentrations with a modal diameter near 80 nm during the evening hours at the urban Fresno site. Although these maxima are correlated with CO, NO, and black carbon, the particle size is larger than the 30–40 nm modal diameters observed for traffic aerosols during the commute hours, and is attributed to a non-vehicle source. At the agricultural site, the morning maxima particle number concentration coincides with the maxima in NO concentration, but often precedes the morning maxima in black carbon. Values for the geometric mean particle diameter varied from day to day, but are correlated between the two sites, with somewhat larger particle sizes at Angiola during periods of stagnation.     

Variations in Tantalum Carbide Microstructures with Changing Carbon Content

A wide variety of microstructures have been obtained by vacuum plasma spraying (VPS) 39Ta:61C atomic percent feedstock powders. During processing, the powder feed was fed through a high energy VPS plasma plume, where altering nozzle angle changed the overall retained carbon concentration in the deposited material. The samples were subsequently sintered and hot isostatic pressed to homogenize and consolidate the microstructure. The microstructures consisted of grains that were either equiaxed or acicular. In the samples with less carbon loss, the equiaxed grains were either the TaC phase or a TaC matrix that encased fine laths of Ta₄C₃. In the sample with the most carbon loss, acicular grains were found containing layered and parallel TaC, Ta₂C, and Ta₄C₃ laths along the major‐axis of the grains. The phases of the compounds have been determined by using complimentary X‐ray diffraction and electron diffraction techniques. Focused ion beam serial sectioning and transmission electron microscopy tilt series tomography were performed to generate three‐dimensional reconstructions of the microstructure morphologies. This article addresses how tantalum carbide microstructures are controlled by the overall concentration and phase fraction content in each of these samples.     

Size-dependent mechanical behavior of nanoscale polymer particles through coarse-grained molecular dynamics simulation

Anisotropic conductive adhesives (ACAs) are promising materials used for producing ultra-thin liquid-crystal displays. Because the mechanical response of polymer particles can have a significant impact in the performance of ACAs, understanding of this apparent size effect is of fundamental importance in the electronics industry. The objective of this research is to use a coarse-grained molecular dynamics model to verify and gain physical insight into the observed size dependence effect in polymer particles. In agreement with experimental studies, the results of this study clearly indicate that there is a strong size effect in spherical polymer particles with diameters approaching the nanometer length scale. The results of the simulations also clearly indicate that the source for the increases in modulus is the increase in relative surface energy for decreasing particle sizes. Finally, the actual contact conditions at the surface of the polymer nanoparticles are shown to be similar to those predicted using Hertz and perfectly plastic contact theory. As ACA thicknesses are reduced in response to reductions in polymer particle size, it is expected that the overall compressive stiffness of the ACA will increase, thus influencing the manufacturing process.     

Effect of chain architecture on the compression behavior of nanoscale polyethylene particles

Polymeric particles with controlled internal molecular architectures play an important role as constituents in many composite materials for a number of emerging applications. In this study, classical molecular dynamics techniques are employed to predict the effect of chain architecture on the compression behavior of nanoscale polyethylene particles subjected to simulated flat-punch testing. Cross-linked, branched, and linear polyethylene chain architectures are each studied in the simulations. Results indicate that chain architecture has a significant influence on the mechanical properties of polyethylene nanoparticles, with the network configuration exhibiting higher compressive strengths than the branched and linear architectures. These findings are verified with simulations of bulk polyethylene. The compressive stress versus strain profiles of particles show four distinct regimes, differing with that of experimental micron-sized particles. The results of this study indicate that the mechanical response of polyethylene nanoparticles can be custom-tailored for specific applications by changing the molecular architecture.     

Strombus gigas inspired biomimetic ceramic composites via SHELL—Sequential Hierarchical Engineered Layer Lamination

Nature has produced remarkable structural designs based on many millennia of evolutionary optimization. Biological materials, such as the sea-shell, possess unique microstructures and properties that provide inspiration for the next generation of structural ceramics. Strombus gigas (Queen conch) shells contain a hierarchical, multilayered, crossed-lamellar architecture built with two natural materials (calcium carbonate and protein) with at least three identifiable scales (or orders) of structure. Drawing on Strombus gigas for inspiration, we have developed a new process to realize such complex micro-architectures in macroscopic form. SHELL (Sequential Hierarchical Engineered Layer Lamination) is a thermoplastic forming process that is capable of producing the third order structural complexity over the micron-millimeter length scales. We have fabricated silicon nitride—boron nitride ceramics via SHELL that are endowed with excellent damage tolerance, exhibit graceful failure, and exhibit toughening mechanisms similar to those observed in Strombus gigas.     

Single-molecule RNA folding

Single-molecule experiments significantly expand our capability to characterize complex dynamics of biological processes. This relatively new approach has contributed significantly to our understanding of the RNA folding problem. Recent single-molecule experiments, together with structural and biochemical characterizations of RNA at the ensemble level, show that RNA molecules typically fold across a highly rugged energy landscape. As a result, long-lived folding intermediates, multiple folding pathways, and heterogeneous conformational dynamics are commonly found for RNA enzymes. While initial results have suggested that stable secondary structures are partly responsible for the rugged energy landscape of RNA, a complete mechanistic understanding of the complex folding behavior has not yet been obtained. A combination of single-molecule experiments, which are well suited to analyze transient and heterogeneous dynamic behaviors, with ensemble characterizations that can provide structural information at a superior resolution will likely provide more answers.