Multiyear Performance of a Pervious Concrete Infiltration Basin BMP

The use of infiltration storm-water best management practices (BMPs) has become a more commonly used approach as a means of reducing postdevelopment runoff volumes in many areas throughout the United States. Although studies regarding the performance of infiltration BMPs are emerging, much remains to be learned about their design, construction, and operation. The increase in knowledge will improve the performance and longevity of these BMPs. The performance of one such infiltration basin over a 2-year cycle is presented in this paper. The study site is a pervious concrete infiltration basin BMP built in 2002 in a courtyard common area at Villanova University. The system consists of three linked infiltration beds lined with geotextile filter fabric, filled with coarse aggregate, and overlaid with pervious concrete. The natural soil beneath the infiltration BMP is a silty sand. The BMP is extensively instrumented to facilitate water quantity and quality research. Both water-quantity and -quality results are presented. The water-quantity analysis showed that the performance of the basin was directly related to its infiltration characteristics. The infiltration rate of the silty sand is cyclic, with higher rates during warmer periods and lower rates during colder periods. The water quality analysis investigated the pollutant reduction for chloride, copper, nitrogen, and phosphorus from the inlet to the surface-water outlet of the structure, as well as differences in pollutant concentration levels between the basin, surrounding ground, and varying soil layer elevations beneath the basin. In general, the pollutant reduction to the surface waters was greater than 90% from inlet to outlet, primarily influenced by the infiltration of the storm water into the natural soils below the BMP. The pollutant concentration of the infiltrating runoff was found to be higher than expected in the area adjacent to the bed when compared to concentration levels found at a similar depth beneath the infiltration bed. Comparison of pollutant concentration levels, as the water moved from within the storage bed to the soil beneath the bed, were shown to vary, with statistical differences found for mean concentration levels of both pH and copper levels; and no statistical differences were found for conductivity, total phosphorous, and chloride at each elevation.     

Impact of selective oxidation during inline annealing prior to hot-dip galvanizing on Zn wetting and hydrogen-induced delayed cracking of austenitic FeMnC steel

The present study discusses the impact of selective oxidation during in-line annealing of Fe–23%Mn–0.6%C–0.3%Si steel on surface and sub-surface properties and is focused on hot-dip galvanizability and susceptibility to hydrogen-induced delayed cracking. Annealing temperature (700–1100 °C) and dewpoint DP (? 15/?30/?50 °C) of the 5%H₂–N₂ annealing atmosphere were varied in order to investigate Zn wetting in dependence on selective oxidation of Mn and Si. Sub-surface microplasticity (hardness, pop-in frequency, pop-in activation load) was examined by electrochemical nanoindentation in-situ to hydrogen charging (ECNI) to assess hydrogen/material interactions. Zn wetting fails if external Mn and Si oxidation is not avoided by performing high reductive bright annealing (1100 °C/DP ? 50 °C). Zn wetting will however turn to increase if a roughly globular MnO layer appears and Si is internally oxidized (700–900 °C/DP ? 15 °C). Selective oxidation further affects hydrogen/material interactions by influencing the local distribution of solid-soluted Mn: ECNI results indicate hydrogen-induced dislocation demobilization (HEDE mechanism) or dislocation mobilization (HELP mechanism) in dependence on the local amount of solid-soluted Mn within the sub-surface. Macroscopic delayed cracking seems to occur earlier if HELP is predominating. The gained results benefit understanding the impact of selective oxidation on galvanizability and susceptibility to hydrogen-induced failure of austenitic FeMnC steel and advance further developments in processing high Mn alloyed steels.     

Five decades of Computer-Aided Ship Design

This article will present a synoptical review of key developments in Computer-Aided Ship Design since its inception about five decades ago. Milestone events and major innovations will be identified in several categories of ship design application with the principal emphasis on the methodologies, the modeling and the integration of the ship design process. The discussion will address many specific subtasks of ship design on the common platform of a human-guided, computer-based decision process.     

Similarity K-d tree method for sparse point pattern matching with underlying non-rigidity

We propose a method for matching non-affinely related sparse model and data point-sets of identical cardinality, similar spatial distribution and orientation. To establish a one-to-one match, we introduce a new similarity K-dimensional tree. We construct the tree for the model set using spatial sparsity priority order. A corresponding tree for the data set is then constructed, following the sparsity information embedded in the model tree. A matching sequence between the two point sets is generated by traversing the identically structured trees. Experiments on synthetic and real data confirm that this method is applicable to robust spatial matching of sparse point-sets under moderate non-rigid distortion and arbitrary scaling, thus contributing to non-rigid point-pattern matching.     

Effect of a variety of organic additives on retention and efficiency in micellar liquid chromatography

The effect of 21 organic additives (alkanols, alkane diols, dipolar aprotic solvents, alkanes) on the chromatographic behavior (retention, elution strength, efficiency) of probe solutes of widely differing hydrophobicity, such as benzene and 2-ethylanthraquinone, have been examined using a C18 stationary phase and sodium dodecyl sulfate (SDS) micellar mobile phases. The mobile-phase elution strength parallels the octanol-water partition coefficients of the additives or their ability to bind to the SDS micellar system, due to the increased solubility in the mobile phase and reduced affinity for the additive-modified surfactant-coated stationary phase. The comparison of the elution strength of micellar mobile phases with that of a reference acetonitrile-water system indicates that the elution strength is lower for micellar systems and depends on the nature of the eluted solute. The displacement of the solute-micelle and solute-stationary phase binding equilibria is quantified for several probe solutes eluted with micellar mobile phases in the presence of 1-propanol, 1-butanol, 1-pentanol, and acetonitrile. A correlation was also observed between the number of theoretical plates and the hydrophobicity of the alcohol additives: the efficiency initially increased steeply and reached a plateau. Compared to benzene, a more hydrophobic additive was needed to attain the maximum efficiency for the more hydrophobic 2-ethylanthraquinone analyte. Dipolar aprotic solvents appear to be somewhat more effective in enhancing the efficiency than alcohols. The results are rationalized in terms of the ability of the organic additives to alter the composition, structure, dynamics, and properties of the micelles and the surfactant-coated stationary phase.