Interstellar Polycyclic Aromatic Compounds and Astrophysics

Over the past 15 years, thanks to significant, parallel advancements in observational, experimental, and theoretical techniques, tremendous strides have been made in our understanding of the role polycyclic aromatic compounds (PACs) in the interstellar medium (ISM). Twenty years ago, the notion of an abundant population of large, carbon-rich molecules in the ISM was considered preposterous. Today, the unmistakable spectroscopic signatures of PACs--shockingly large molecules by previous interstellar chemistry standards--are recognized throughout the universe. In this article, we will examine the interstellar PAC model and its importance to astrophysics, including: (a) the evidence which led to inception of the model, (b) the ensuing laboratory and theoretical studies of the fundamental spectroscopic properties of PAC by which the model has been refined and extended, and (c) a few examples of how the model is being exploited to derive insight into the nature of the interstellar PAC population.     

Airborne Dust Capture and Induced Airflow of Various Spray Nozzle Designs

Water spray characteristics, including droplet size and velocity, airborne dust capture potential, and induced airflow quantity for various spray nozzle designs were evaluated to provide basic information for improving spray applications. Water droplet size and velocity characteristics were initially measured by a Phase Doppler Particle Analyzer (PDPA) for hollow cone, full cone, flat fan, and air atomized spray nozzles at similar operating parameters. Airflow inducement and dust capture experiments were also conducted under the same operating parameters to examine any salient features of the spray nozzle type, droplet characteristics, induced airflow, and airborne dust capture.

Test results indicate that there are trade offs between airflow inducement and dust capture efficiency. A spray nozzle with a wider discharge angle was observed to induce more airflow, but at reduced dust capture efficiencies. Increasing spray nozzle fluid pressure(s) generally reduced water droplet sizes with concurrent increases in droplet velocity, airflow inducement, and airborne dust capture. Placing a three-sided barrier around the spray nozzles normally reduced spray air induction and increased dust capture efficiency. A direct relationship between airborne dust capture efficiency and spray input power normalized per unit of airflow induced was observed. This information can be utilized to improve the performance of water sprays for reducing airborne dust levels.     

Investigation of a Novel Condensation Aerosol Generator: Solute and Solvent Effects

Part I of this article presents results of an experimental study on gas-phase nucleation for three model solutes and their solvent, propylene glycol (PG), with variables being solute concentration and the nature of the solute substance. A single manifestation of an aerosol generator, which forms condensation aerosols by cooling of hot vapor issuing from an electrically heated, pumped capillary, is described and used for all experiments. The effects of solute concentration and solute type were studied for deoxycorticosterone (DOC), benzil (BZ), and phenyl salicylate (PhS). Suppression of homogeneous nucleation and occurrence of heterogeneous condensation of the solvent was observed at different solute concentrations for BZ, PhS, and DOC. The nature and concentration of the solute dissolved in the solvent was shown to determine the final particle size distribution of the condensed aerosol. In the case of the least volatile solute, DOC, solute aerosol and total aerosol size distributions were identical at low solute concentrations. A transitional concentration region then existed in which a bimodal solute aerosol was formed, followed at high concentrations by increasing separation of the solvent-dominated aerosol size distribution and that of the solute. In Part II of this article, the effect of DOC dissolution in different solvents was studied at fixed solute concentration. The effects of six glycol solvents--i.e., PG, ethylene glycol (EG), dipropylene glycol (DPG), diethylene glycol (DEG), triethylene glycol (TEG), and tetraethylene glycol (TetEG)--and three nonglycol solvents--i.e., dimethyl sulfoxide (DMSO), formamide (FORM), and oleyl alcohol (OA)--were studied, as these affected the resultant aerosol sizes. Suppression of total aerosol mass median aerodynamic diameter (MMAD) was observed on dissolution of 0.5% w/w DOC in each solvent, although suppression occurred to different extents. It was shown that the boiling point or volatility of the solvent used to dissolve the less volatile DOC had an effect on the final particle size distribution of the condensed aerosol and whether the aerodynamic size distributions for the solute and the total aerosol were the same or different.     

Solid-State Phase Relationships in the Calcia-Titania-Zirconia System at 1200°C

Phase relationships were investigated in the CaO–TiO₂–ZrO₂ system at 1200°C for compositions containing <50 mol% CaO using X-ray diffraction and electron probe microanalysis. The existence of two previously reported ternary phases, zirconolite (CaZrTi₂O₇) and calzirtite (Ca₂Zr₅Ti₂O₁₆), was confirmed. Each of these phases exhibited a significant range of homogeneity between TiO₂ and ZrO₂, while maintaining a nearly constant concentration of CaO. The ternary solubilities of the constituent binary phases were found to be small (typically <1 mol%), with the exceptions of the perovskites (CaTiO₃ and CaZrO₃). These latter phases displayed mutual solubilities of at least 22 mol% but exhibited significant variations in composition from grain to grain. Thermodynamic equilibrium was clearly not established in several samples, although most of the phase relationship information obtained was self-consistent.     

Intuitive robust stability metric for PID control of self-regulating processes

Published methods establish how plant-model mismatch in the process gain and dead time impacts closed-loop stability. However, these methods assume no plant-model mismatch in the process time constant. The work presented here proposes the robust stability factor metric, RSF, to examine the effect of plant-model mismatch in the process gain, dead time, and time constant. The RSF is presented in two forms: an equation form and a visual form displayed on robustness plots derived from the Bode and Nyquist stability criteria. This understanding of robust stability is reinforced through visual examples of how closed-loop performance changes with various levels of plant-model mismatch. One example shows how plant-model mismatch in the time constant can impact closed-loop stability as much as plant-model mismatch in the gain and/or dead time. Theoretical discussion shows that the impact is greater for small dead time to time constant ratios. As the closed-loop time constant used in Internal Model Control (IMC) tuning decreases, the impact becomes significant for a larger range of dead time to time constant ratios. To complete the presentation, the RSF is used to compare the robust stability of IMC-PI tuning to other PI, PID, and PID with Filter tuning correlations.     

Rowlinson's concept of an effective hard sphere diameter

Attention is drawn to John Rowlinson's idea that the repulsive portion of the intermolecular interaction may be replaced by a temperature-dependent hard sphere diameter. It is this approximation that made the development of perturbation theory possible for realistic fluids whose intermolecular interactions have a steep, but finite, repulsion at short separations.     

Modeling and characterization of dynamic failure of borosilicate glass under compression/shear loading

In this paper, we study the impact-induced dynamic failure of a borosilicate glass block using an integrated experimental/analytical approach. Previous experimental studies on dynamic failure of borosilicate glass have been reported by Nie et al. [Nie X, Chen WW, Sun X, Templeton DW. Dynamic failure of borosilicate glass under compression/shear loading – experiments. J Am Ceram Soc, in press.] using the split Hopkinson pressure bar (SHPB) technique. The damage growth patterns and stress histories have been reported for various glass specimen designs. In this study, we propose to use a continuum damage mechanics (CDM)-based constitutive model to describe the initial failure and subsequent stiffness reduction of glass. Explicit finite element analyses are used to simulate the glass specimen impact event. A maximum shear stress-based damage evolution law is used in describing the glass damage process under combined compression/shear loading. The impact test results are used in quantifying the critical shear stress for the borosilicate glass under examination. It is shown that with only two modeling parameters, reasonably good comparisons between the predicted and the experimentally measured failure maps can be obtained for various glass sample geometries. Comparisons between the predicted stress histories for different sample designs are also used as model validations.     

High-efficiency, solid-state, dye-sensitized solar cells using hierarchically structured TiO₂ nanofibers

High-performance, room-temperature (RT), solid-state dye-sensitized solar cells (DSSCs) were fabricated using hierarchically structured TiO? nanofiber (HS-NF) electrodes and plastic crystal (PC)-based solid-state electrolytes. The electrospun HS-NF photoelectrodes possessed a unique morphology in which submicrometer-scale core fibers are interconnected and the nanorods are dendrited onto the fibers. This nanorod-in-nanofiber morphology yielded porosity at both the mesopore and macropore level. The macropores, steming from the interfiber space, afforded high pore volumes to facilitate the infiltration of the PC electrolytes, whereas the mesoporous nanorod dendrites offered high surface area for enhanced dye loading. The solid-state DSSCs using HS-NFs (DSSC-NF) demonstrated improved power conversion efficiency (PCE) compared to conventional TiO? nanoparticle (NP) based DSSCs (DSSC-NP). The improved performance (>2-fold) of the DSSC-NFs was due to the reduced internal series resistance (R(s)) and the enhanced charge recombination lifetime (τ(r)) determined by electrochemical impedance spectroscopy and intensity modulated photocurrent/photovoltage spectroscopy. The easy penetration of the PC electrolytes into HS-NF layers via the macropores reduces R(s) significantly, improving the fill factor (FF) of the resulting DSSC-NFs. The τ(r) difference between the DSSC-NF and DSSC-NP in the PC electrolytes was extraordinary (~14 times) compared to reported results in conventional organic liquid electrolytes. The optimized PCE of DSSC-NF using the PC electrolytes was 6.54, 7.69, and 7.93% at the light intensity of 100, 50, and 30 mW cm?2, respectively, with increased charge collection efficiency (>40%). This is the best performing RT solid-state DSSC using a PC electrolyte. Considering the fact that most reported quasi-solid state or nonvolatile electrolytes require higher iodine contents for efficient ion transport, our HS-NFs are a promising morphology for such electrolytes that have limited ion mass transport.     

Empirical rock physics relationships on carbonate dry-frame elastic properties

Laboratory tests were conducted to analyze the ultrasonic velocity response to the pressure change in dry carbonate rocks from the Weyburn oilfield,Canada.Twent...     

Direct current testing to measure corrosiveness of wood preservatives

A qualitative test that mimics the corrosion behaviour of metals in contact with treated wood without using wood specimens would be of great value in rapidly evaluating the corrosiveness of new wood preservatives. The objective of this study was to determine whether the linear polarisation resistance of metals immersed in a solution of preservative chemicals is related to corrosion of metals in wood. This technique was used to measure the corrosion rate of four types of metals in three different aqueous solutions of wood preservatives. The four metals were UNS G10180 (SAE 1018 steel), UNS S30400 (AISI 304 stainless steel), UNS S43000 (AISI 430 stainless steel), and UNS Z15001 (zinc). The metals were subjected to various concentrations of alkaline copper quat (ACQ-D), ammoniacal copper citrate (CC), and chromated copper arsenate type C (CCA-C). It was found that the corrosion of metals in the solutions of the wood preservatives did not correlate well to what is known about the corrosion of metals in contact with wood.