Fluorine-Free Extinguishing of a Hydrocarbon Pool Fire with a Suspension of Glass Bubbles Grafted with Nanoscale Polymer Layers.

The current most efficient solution to extinguish liquid hydrocarbon (class B) pool fires involves fire-fighting foams containing fluorinated surfactants. However, fluorocarbon surfactants are unsafe due to their environmental persistence and negative toxicological/bioaccumulative impact. To this end, we show that fluorine-free aqueous suspensions of Glass Bubbles (GB) modified with hydrophilic polymer grafted layers can efficiently extinguish hydrocarbon pool fires. Namely, GB grafted with poly(oligo (ethylene glycol) methyl ether methacrylate) (POEGMA), GB-G was fabricated employing "grafting-through" and "grafting-from" methods and used to obtain the suspensions. It was found that the GB suspension, with a grafted layer of higher molecular weight and lower grafting density (GB-GL), proved superior to the more densely grafted GB-GH and nongrafted GB-0 system. The GB-GL suspensions displayed less negative spreading coefficients and viscosities lower than those of GB-GH/GB-0 compositions. When siloxane-polyoxyethylene surfactant was added to all GB suspensions, the interfacial properties were dominated by the surfactant, with all suspensions having the same positive spreading coefficient. However, the GB-GL-surfactant composition had the lowest viscosity among the suspensions studied in this work. Specifically, the viscosity of GB-GH and GB-0 suspensions at a shear rate of 77 s-1 was ∼110% and 70% higher than that of GB-GL. Due to the lower viscosity, the GB-GL suspension demonstrated the most efficient spreading over model hydrocarbon solid (polyethylene) and liquid (hexadecane) surfaces when the surfactant was added. The suspension also showed the best performance in the retardation of hexane evaporation when placed over the heated hexane pool. After 50 min, the amount of hexane that evaporated through GB-GH and GB-0 suspensions was ∼8 and 11 times higher, respectively, compared to the GB-GL suspension. We found that the GB-GL-surfactant system was the most efficient GB suspension in extinguishing the fire due to its superior spreading and sealing ability. It was within 10% of fluorine-containing foam's fire extinguishment performance. The GB suspensions are much safer in terms of burnback resistance as a torch applied directly to the suspension after extinguishment could not reignite the fire. The GB material is recyclable, since it can be collected and reused after application to a fire.

Biotechnology to reduce logistics burden and promote environmental stewardship for Air Force civil engineering requirements.

This review provides discussion of advances in biotechnology with specific application to civil engineering requirements for airfield and airbase operations. The broad objectives are soil stabilization, waste management, and environmental protection. The biotechnology focal areas address (1) treatment of soil and sand by biomineralization and biopolymer addition, (2) reduction of solid organic waste by anaerobic digestion, (3) application of microbes and higher plants for biological processing of contaminated wastewater, and (4) use of indigenous materials for airbase construction and repair. The consideration of these methods in military operating scenarios, including austere environments, involves comparison with conventional techniques. All four focal areas potentially reduce logistics burden, increase environmental sustainability, and may provide energy source, or energy-neutral practices that benefit military operations.

Insect antennae: Coupling blood pressure with cuticle deformation to control movement.

Insect antennae are hollow, blood-filled fibers with complex shape. Muscles in the two basal segments control antennal movement, but the rest (flagellum) is muscle-free. The insect can controllably flex, twist, and maneuver its antennae laterally. To explain this behavior, we performed a comparative study of structural and tensile properties of the antennae of Periplaneta americana (American cockroach), Manduca sexta (Carolina hawkmoth), and Vanessa cardui (painted lady butterfly). These antennae demonstrate a range of distinguishable tensile properties, responding either as brittle or strain-adaptive fibers that stiffen when stretched. Scanning electron microscopy and high-speed imaging of antennal breakup during stretching revealed complex coupling of blood pressure and cuticle deformation in antennae. A generalized Lamé theory of solid mechanics was developed to include the force-driven deformation of blood-filled antennal tubes. We validated the theory against experiments with artificial antennae with no adjustable parameters. Blood pressure increased when the insect inflated its antennae or decreased below ambient pressure when an external tensile load was applied to the antenna. The pressure-cuticle coupling can be controlled through changes of the blood volume in the antennal lumen. In insects that do not fill the antennal lumen with blood, this blood pressure control is lacking, and the antennae react only by muscular activation. We suggest that the principles we have discovered for insect antennae apply to other appendages that share a leg-derived ancestry. Our work offers promising new applications for multifunctional fiber-based microfluidics that could transport fluids and be manipulated by the same fluid on demand. STATEMENT OF SIGNIFICANCE: Insect antennae are blood-filled, segmented fibers with muscles in the two basal segments. The long terminal segment is muscle-free but can be flexed. To explain this behavior, we examined structure-function relationships of antennae of cockroaches, hawkmoths, and butterflies. Hawkmoth antennae behaved as brittle fibers, but butterfly and cockroach antennae showed strain-adaptive behavior like fibers that stiffen when stretched. Videomicroscopy of antennal breakup during stretching revealed complex coupling of blood pressure and cuticle deformation. Our solid mechanics model explains this behavior. Because antennae are leg-derived appendages, we suggest that the principles we found apply to other appendages of leg-derived ancestry. Our work offers new applications for multifunctional fiber-based microfluidics that could transport fluids and be manipulated by the fluid on demand.

Microwave Enhancement of Autocatalytic Growth of Nanometals.

The desire for designing efficient synthetic methods that lead to industrially important nanomaterials has led a desire to more fully understand the mechanism of growth and how modern synthetic techniques can be employed. Microwave (MW) synthesis is one such technique that has attracted attention as a green, sustainable method. The reports of enhancement of formation rates and improved quality for MW driven reactions are intriguing, but the lack of understanding of the reaction mechanism and how coupling to the MW field leads to these observations is concerning. In this manuscript, the growth of a metal nanoparticles (NPs) in a microwave cavity is spectroscopically analyzed and compared with the classical autocatalytic method of NP growth to elucidate the underpinnings for the observed enhanced growth behavior for metal NPs prepared in a MW field. The study illustrates that microwave synthesis of nickel and gold NPs below saturation conditions follows the Finke-Watzky mechanism of nucleation and growth. The enhancement of the reaction arises from the size-dependent increase in MW absorption cross section for the metal NPs. For Ni, the presence of oxides is considered via theoretical computations and compared to dielectric measurements of isolated nickel NPs. The study definitively shows that MW growth can be modeled by an autocatalytic mechanism that directly leads to the observed enhanced rates and improved quality widely reported in the nanomaterial community when MW irradiation is employed.

Specific effects in microwave chemistry explored through reactor vessel design, theory, and spectroscopy.

Microwave chemistry has revolutionized synthetic methodology for the preparation of organics, pharmaceuticals, materials, and peptides. The enhanced reaction rates commonly observed in a microwave have led to wide speculation about the function of molecular microwave absorption and whether the absorption leads to microwave specific effects and enhanced molecular heating. The comparison of theoretical modeling, reactor vessel design, and dielectric spectroscopy allows the nuance of the interaction to be directly understood. The study clearly shows an unaltered silicon carbide vessel allows measurable microwave penetration and therefore, molecular absorption of the microwave photons by the reactants within the reaction vessel cannot be ignored when discussing the role of molecular heating in enhanced molecular reactivity for microwave synthesis. The results of the study yield an improved microwave reactor vessel design that eliminates microwave leakage into the reaction volume by incorporating a noble metal surface layer onto a silicon carbide reaction vessel. The systematic study provides the necessary theory and measurements to better inform the arguments in the field.

Fabrication of liquid and vapor protective cotton fabrics.

Through microwave-assisted techniques, cotton textiles treated with heptadecafluoro-1,1,2,2-tetrahydrodecyltrimethoxysilane in the presence of high surface area silica nanoparticles create a material capable of repelling bulk liquid challenges while simultaneously adsorbing organic vapors from bulk liquid droplets. Characterizing the contradictory behavior of adsorption of vapors and repellency of liquids is the primary focus of this article. These procedures reveal a quick and simple method for a one-step deposition of a vapor-sorptive, liquid-repellent, Cassie-Baxter surface onto textiles. Packed column breakthrough and single swatch permeation experiments showed that treated materials possess a high affinity for 3-hepten-2-one vapor, while goniometry revealed contact angles in excess of 120° for surface-deposited, 5 µL droplets of several test liquids. Scanning electron micrograph images confirm a lotus-like, nanorough surface, while ATR-FTIR spectra confirm surface fluorocarbon moieties. The performance of so-treated materials lends itself to the application of chemical protective apparel, while the simplicity of the treatment bodes well for potential commercialization.

Controlled microwave-assisted growth of silica nanoparticles under acid catalysis.

In this work, we demonstrate the controlled synthesis of silica nanoparticles as small as 30 nm (±5 nm) and as large as 250 nm (±30 nm) in minutes using surfactant free, microwave-assisted synthetic techniques. Proper choice of solvent, silicic acid precursor, catalyst, and microwave irradiation time were the variables used to control nanoparticle size and, ultimately, overcome the previously reported shortcomings of using microwaves for silica nanoparticle synthesis. In these reactions acetone, a low-tan δ solvent, mediates the condensation reaction, while selective absorption of pulsed microwave radiation by the precursor promotes nanoparticle growth. Dynamic light scattering data, scanning electron micrographs, and transmission electron micrographs of the reaction products show that the size, shape, and granularity of the silica nanoparticles are highly dependent on reaction conditions. These microwave methods have utility for mass production of silica nanoparticles or other nanoparticles by flow-through microwave synthetic methods for industrial applications, as well as a facile method for encapsulating or embedding materials with silica for improved functionality and stability.

Magnetic rotational spectroscopy with nanorods to probe time-dependent rheology of microdroplets.

In situ characterization of minute amounts of fluids that rapidly change their rheological properties is a challenge. In this paper, the rheological properties of fluids were evaluated by examining the behavior of magnetic nanorods in a rotating magnetic field. We proposed a theory describing the rotation of a magnetic nanorod in a fluid when its viscosity increases with time exponentially fast. To confirm the theory, we studied the time-dependent rheology of microdroplets of 2-hydroxyethyl-methacrylate (HEMA)/diethylene glycol dimethacylate (DEGDMA)-based hydrogel during photopolymerization synthesis. We demonstrated that magnetic rotational spectroscopy provides rich physicochemical information about the gelation process. The method allows one to completely specify the time-dependent viscosity by directly measuring characteristic viscosity and characteristic time. Remarkably, one can analyze not only the polymer solution, but also the suspension enriched with the gel domains being formed. Since the probing nanorods are measured in nanometers, this method can be used for the in vivo mapping of the rheological properties of biofluids and polymers on a microscopic level at short time intervals when other methods fall short.

Methyl salicylate: a reactive chemical warfare agent surrogate to detect reaction with hypochlorite.

Methyl salicylate (MeS) has a rich history as an inert physical simulant for the chemical warfare agents sulfur mustard and soman, where it is used extensively for liquid- and vapor-permeation testing. Here we demonstrate possible utility of MeS as a reactivity simulant for chlorine-based decontaminants. In these experiments MeS was reacted with sodium hypochlorite varying stoichiometry, temperature, reaction time, and pH. No colored oxidation products were observed; however, chlorination of the aromatic ring occurred ortho (methyl 3-chlorosalicylate) and para (methyl 5-chlorosalicylate) to the position bearing the -OH group in both the mono- and disubstituted forms. The monosubstituted para product accumulated initially, and the ortho and 3,5-dichloro products formed over the next several hours. Yields from reactions conducted below pH 11 declined rapidly with decreasing pH. Reactions run at 40 °C produced predominantly para substitution, while those run at 0 °C produced lower yields of ortho- and para-substituted products. Reactions were also carried out on textile substrates of cotton, 50/50 nylon-cotton, and a meta aramid. The textile data broadly reproduced reaction times and stoichiometry observed in the liquid phase, but are complicated by physical and possibly chemical interactions with the fabric. These data indicate that, for hypochlorite-containing neutralizing agents operating at strongly alkaline pH, one can expect MeS to react stoichiometrically with the hypochlorite it encounters. This suggests utility of MeS in lieu of such highly hazardous surrogates as monochloroalkyl sulfides as a simulant for threat scenarios involving the stoichiometric decomposition of sulfur mustard. Specifically, the extent of coverage of the simulant on a fabric by the neutralizing agent can be directly measured. Similar reactivity toward other halogen oxidizing agents is likely but remains to be demonstrated.

Nanoporous artificial proboscis for probing minute amount of liquids.

We describe a method of fabrication of nanoporous flexible probes which work as artificial proboscises. The challenge of making probes with fast absorption rates and good retention capacity was addressed theoretically and experimentally. This work shows that the probe should possess two levels of pore hierarchy: nanopores are needed to enhance the capillary action and micrometer pores are required to speed up fluid transport. The model of controlled fluid absorption was verified in experiments. We also demonstrated that the artificial proboscises can be remotely controlled by electric or magnetic fields. Using an artificial proboscis, one can approach a drop of hazardous liquid, absorb it and safely deliver it to an analytical device. With these materials, the paradigm of a stationary microfluidic platform can be shifted to the flexible structures that would allow one to pack multiple microfluidic sensors into a single fiber.