Modeling Multicomponent Fuel Droplet Vaporization with Finite Liquid Diffusivity Using Coupled Algebraic-Dqmom with Delumping

Multicomponent fuel droplet vaporization models for use in combustion CFD codes often prioritize computational efficiency over model complexity. This leads to oversimplifying assumptions such as single component droplets or infinite liquid diffusivity. The previously developed Direct Quadrature Method of Moments (DQMoM) with delumping model demonstrated a computationally efficient and accurate approach to solve for every discrete species in a well-mixed vaporizing multicomponent droplet. To expand the method to less restrictive cases, a new solution technique is presented called the Coupled Algebraic-Direct Quadrature Method of Moments (CA-DQMoM). In contrast to previous moment methods for droplet vaporization, CA-DQMoM solves for the evolution of two liquid distributions by coupling a monovariate, homogeneous DQMoM approach with additional algebraic moment equations, allowing for a more complex droplet vaporization model with finite rates of liquid diffusion to be solved with computational efficiency. To further decrease computational expense, an approximation that employs the same nodes for both distributions can be used in certain cases. Finally, a delumping technique is adapted to the finite diffusivity model to reconstruct discrete species information at minimal computational cost. The model is proven to be accurate relative to a full discrete component model for both a kerosene droplet comprised of 36 species and a multicomponent droplet of 200 species while maintaining the computational efficiency of continuous thermodynamics models. The combined accuracy and computational efficiency demonstrated by the CA-DQMoM with delumping model for a multicomponent fuel droplet with finite liquid diffusivity makes it ideal for incorporation into CFD models for complex combustion process

Assessing technical candidates on the social web

This is the pre-print version of this Article. The official published version can be accessed from the link below - Copyright @ 2012 IEEEThe Social Web provides comprehensive and publicly available information about software developers: they can be identified as contributors to open source projects, as experts at maintaining weak ties on social network sites, or as active participants to knowledge sharing sites. These signals, when aggregated and summarized, could be used to define individual profiles of potential candidates: job seekers, even if lacking a formal degree or changing their career path, could be qualitatively evaluated by potential employers through their online contributions. At the same time, developers are aware of the Web’s public nature and the possible uses of published information when they determine what to share with the world. Some might even try to manipulate public signals of technical qualifications, soft skills, and reputation in their favor. Assessing candidates on the Web for technical positions presents challenges to recruiters and traditional selection procedures; the most serious being the interpretation of the provided signals. Through an in-depth discussion, we propose guidelines for software engineers and recruiters to help them interpret the value and trouble with the signals and metrics they use to assess a candidate’s characteristics and skills

A study of Na(x)Pt3O4 as an O2 electrode bifunctional electrocatalyst

The present study suggests that polytetrafluoroethylene (PTFE) bonded Na(X)Pt3O4 gas porous diffusion electrodes may be a viable candidate for bifunctional O2 reduction and evolution activity. The electrodes exhibited Tafel slopes of about 0.06 V/decade for both O2 reduction an evolution. For O2 reduction, the 0.06 slope doubled to 0.12 V/decade at larger current densities. Preliminary stability testing at 24 C suggest that the Na(x)Pt3O4 electrodes were relatively stable at reducing and oxidizing potentials typically encountered at the O2 electrodes in a regenerative fuel cell

Corrosion testing of candidates for the alkaline fuel cell cathode

It is desirable to employ a corrosion screening test for catalyst or support candidates for the fuel cell cathode before entering upon optimization of the candidate or of the catalytic electrode. To this end, corrosion test electrodes, intended for complete immersion and maximum wetting, have been made with 30 to 40 vol. pct Teflon; with perovskites this is about 10 to 15 pct. The candidates were synthesized by methods intended for single-phase product without special emphasis on high surface area, although the substances tested were no coarser than 2 m squared/g. A typical loading was 25 mg/cm sq of the pure substance, usually on gold screen, a few mm squared of which were left bare for contacting. Contact to the gold lead wire was made by welding with a micro-torch or a spot-welder. Corrosion testing consisted of obtaining current-voltage data under flowing inert gas in the potential region for reduction of O2. The electrode was immersed in 30 pct KOH. Observations were made at 20 C and 80 C, and the results compared with data from gold standards. Results with some perovskites, pyrochlores, spinels, and interstitial compounds will be discussed

O2 reduction at the IFC orbiter fuel cell O2 electrode

O2 reduction Tafel data were obtained for the IFC Orbiter fuel cell O2 electrode (Au-10 percent Pt catalyst) at temperatures between 24 and 81 C. BET measurements gave an electrode surface area of about 2040 sq cm per sq cm of geometric area. The Tafel data could be fitted to three straight line regions. For current densities less than 0.001 A/sq cm, the slope was essentially independent of temperature with a value of about 0.032 V/decade. Above 0.001 A/sq cm, the two regions, designated in the present study as the 0.04 and 0.12 V/decate regions, were temperature dependent. The apparent energies of activation for these two regions were about 9.3 and 6.5 kcal/mol, respectively. Tafel data (1 atmosphere O2) were extrapolated to 120 C for predicting changes in overpotential with increasing temperature. A mechanism is presented for O2 reduction

Corrosion testing of candidates for the alkaline fuel cell cathode

Current/voltage data was obtained for specially made corrosion electrodes of some oxides and of gold materials for the purpose of developing a screening test of catalysts and supports for use at the cathode of the alkaline fuel cell. The data consists of measurements of current at fixed potentials and cyclic voltammograms. These data will have to be correlated with longtime performance data in order to fully evaluate this approach to corrosion screening. Corrosion test screening of candidates for the oxygen reduction electrode of the alkaline fuel cell was applied to two substances, the pyrochlore Pb2Ru2O6.5 and the spinel NiCo2O4. The substrate gold screen and a sample of the IFC Orbiter Pt-Au performance electrode were included as blanks. The pyrochlore data indicate relative stability, although nothing yet can be said about long term stability. The spinel was plainly unstable. For this type of testing to be validated, comparisons will have to be made with long term performance tests

Special Quantum Field Theories In Eight And Other Dimensions

We build nearly topological quantum field theories in various dimensions. We give special attention to the case of 8 dimensions for which we first consider theories depending only on Yang-Mills fields. Two classes of gauge functions exist which correspond to the choices of two different holonomy groups in SO(8), namely SU(4) and Spin(7). The choice of SU(4) gives a quantum field theory for a Calabi-Yau fourfold. The expectation values for the observables are formally holomorphic Donaldson invariants. The choice of Spin(7) defines another eight dimensional theory for a Joyce manifold which could be of relevance in M- and F-theories. Relations to the eight dimensional supersymmetric Yang-Mills theory are presented. Then, by dimensional reduction, we obtain other theories, in particular a four dimensional one whose gauge conditions are identical to the non-abelian Seiberg-Witten equations. The latter are thus related to pure Yang-Mills self-duality equations in 8 dimensions as well as to the N=1, D=10 super Yang-Mills theory. We also exhibit a theory that couples 3-form gauge fields to the second Chern class in eight dimensions, and interesting theories in other dimensions.Comment: 36 pages, latex. References have been added together with a not

Solubility, stability, and electrochemical studies of sulfur-sulfide solutions in organic solvents

A preliminary study of the sulfur electrode in organic solvents suggests that the system warrants further investigation for use in a low temperature (100 deg to 120 C) Na-S secondary battery. A qualitative screening was undertaken at 120 C to determine the solubilities and stabilities of Na2S and Na2S2 in representatives of many classes of organic solvents. From the screening and quantitative studies, two classes of solvents were selected for work; amides and cyclic polyalcohols. Voltammetric and Na-S cell charge discharge studies of sulfide solutions in organic solvents (e.g., N, N-dimethylformamide) at 120 C suggested that the reversibilities of the reactions on Pt or high density graphite were moderately poor. However, the sulfur electrode was indeed reducible (and oxidizable) through the range of elemental sulfur to Na2S. Reactions and mechanisms are proposed for the oxidation reduction processes occurring at the sulfur electrode

Magnetic susceptibility variations in Loess sequences and their relationship to astronomical forcing

The long, well-exposed and often continuous sequences of loess found throughout the world are generally thought to provide an excellent opportunity for studying long-term, large-scale environmental change during the last few million years. In recent years, the most fruitful loess studies have been those involving the deposits of the loess in China. One of the most intriguing results of that work has been the discovery of an apparent correlation between variations in the magnetic susceptibility of the loess sequence and the oxygen isotope record of the deep sea. This correlation implies that magnetic susceptibility variations are being driven by astronomical parameters. However, the basic data have been interpreted in various ways by different authors, most of whom assumed that the magnetic minerals in the loess have not been affected by post-depositional processes. Using a chemical extraction procedure that allows us to separate the contribution of secondary pedogenic magnetic minerals from primary inherited magnetic minerals, we have found that the magnetic susceptibility of the Chinese paleosols is largely due to a pedogenic component which is present to a lesser degree in the loess. We have also found that the smaller inherited component of the magnetic susceptibility is about the same in the paleosols and the loess. These results demonstrate the need for additional study of the processes that create magnetic susceptibility variations in order to interpret properly the role of astronomical forcing in producing these variations