Optimizing Transportation Problems with Multiple Objectives

Virtually all models developed for transportation problems have focused upon the optimization of a single objective criterion, namely the minimization of total transportation costs. They have generally neglected or often ignored the multiple conflicting objectives involved in the problem, the priority structure of these objectives, various environmental constraints, unique organizational values of the firm, and bureaucratic decision structures. However, in reality these are important factors which greatly influence the decision process of transportation problems. In this study the goal programming approach is utilized in order to allow for the optimization of multiple conflicting goals while permitting an explicit consideration of the existing decision environment.     

Properties of Calcium Phosphate Cements With Different Tetracalcium Phosphate and Dicalcium Phosphate Anhydrous Molar Ratios

Calcium phosphate cements (CPCs) were prepared using mixtures of tetracalcium phosphate (TTCP) and dicalcium phosphate anhydrous (DCPA), with TTCP/DCPA molar ratios of 1/1, 1/2, or 1/3, with the powder and water as the liquid. Diametral tensile strength (DTS), porosity, and phase composition (powder x-ray diffraction) were determined after the set specimens have been immersed in a physiological-like solution (PLS) for 1 d, 5 d, and 10 d. Cement dissolution rates in an acidified PLS were measured using a dual constant composition method. Setting times ((30 ± 1) min) were the same for all cements. DTS decreased with decreasing TTCP/DCPA ratio and, in some cases, also decreased with PLS immersion time. Porosity and hydroxyapatite (HA) formation increased with PLS immersion time. Cements with TTCP/DCPA ratios of 1/2 and 1/3, which formed calcium-deficient HA, dissolved more rapidly than the cement with a ratio of 1/1. In conclusion, cements may be prepared with a range of TTCP/DCPA ratios, and those with lower ratio had lower strengths but dissolved more rapidly in acidified PLS.     

Simultaneous determination of species-specific isotopic composition of Hg by gas chromatography coupled to multicollector ICPMS

This work presents the simultaneous online determination of the isotopic composition of different Hg species in a single sample by the hyphenation of gas chromatography (GC) with multicollector-inductively coupled plasma mass spectrometry (MC-ICPMS). With the use of commercially available instrumentation, precise and accurate species-specific Hg isotope delta values (per mil deviation of the Hg isotope ratio in the sample relative to a reference standard) have been obtained online from consecutive GC transient signals. The use of isothermal temperature programs to extend the elution of the Hg species, the proper selection of the peak integration window, as well as the preconcentration of real samples are critical to provide optimal counting statistics. Also, isotope ratio drift during transient signal elution was overcome by introducing a mixed Hg(II) and MeHg standard bracketing scheme and expressing all results using the delta-notation relative to SRM NIST-3133. Using the proposed methodology, we have obtained an external 2SD precision of 0.56 per thousand for delta (202)Hg that is more than 10 times smaller than the overall Hg stable isotope variation thus far observed in terrestrial samples. The measurement of species-specific Hg isotopic composition relative to SRM NIST-3133 has been validated versus two other analytical techniques, i.e., conventional nebulization (CN) of Hg(II) solution and cold vapor (CV) generation of Hg (0) vapor. A good agreement between the species-specific delta values obtained by the different techniques has been obtained in secondary fractionated reference standard (UM-Almaden) and environmental matrixes, i.e., BCR-CRM 464 (tuna fish) and IAEA-085 (human hair). The results show mass-dependent and mass-independent fractionation in environmental samples, i.e., mass-independent fractionation of odd isotopes (199)Hg and (201)Hg in tuna fish was observed. This methodology provides new possibilities for the future study of species-specific stable isotope geochemistry of Hg and other trace metals.     

Growth of one-dimensional Si/SiGe heterostructures by thermal CVD

The first results on a simple new process for the direct fabrication of one-dimensional superlattices using common CVD chambers are presented. The experiments were carried out in a 200?mm industrial Centura reactor (Applied Materials). Low dimensionality and superlattices allow a significant increase in the figure of merit of thermoelectrics by controlling the transport of phonons and electrons. The monocrystalline nanowires produced according to this process are both one-dimensional and present heterostructures, with very thin layers (40?nm) of Si and SiGe. Concentrations up to 30?at.% Ge were obtained in the SiGe parts. Complementary techniques including transmission electronic microscopy (TEM), selected area electron diffraction (SAED), energy dispersive x-ray spectroscopy (EDS), scanning transmission electron microscopy (STEM) in bright field and high angle annular dark field (HAADF STEM), and energy-filtered transmission electron microscopy (EF-TEM) were used to characterize the nanoheterostructures.     

Local pH variation as an initial step in bacterial surface-sensing and biofilm formation

The development of surface-associated layers of matrix-embedded microbial populations, called biofilms, is a serious problem in many medical and industrial settings. These contaminations are difficult to eradicate because of the high resistance level acquired by the cells in their particular environment. From the very beginning of the colonization process, modifications of gene expression are observed and could, at least partially, explain biofilm resistance. In order to develop anti-biofilm molecules and surface treatments, it is of pivotal importance to identify the physico-chemical parameters which activate the sensor systems of pioneering microbes when they come into contact with a surface. The aim of our study was to examine the pH variations in the local micro-environment created between the cell layer and the surface after bacteria adhesion. Using an ion-sensitive field effect transistor (ISFET), as a substratum, colonized by a curli hyperproducing strain known to form biofilms, we observed that the evolution of the pH change was significantly different in the micro-compartment in contact with the electrochemical sensor compared to that within the liquid phase.     

Solid fraction modelling for CO2 and CO2–THF hydrate slurries used as secondary refrigerants

In the present paper, the suitability of hydrate slurries in secondary refrigeration was investigated by the means of a new hydrate solid-fraction model. Considering the high melting enthalpy of CO₂-containing hydrates, slurries presenting high hydrate solid fractions can carry sufficient latent heat to be useful for a two-phase secondary-refrigerant application. The model presented in this paper allowed to calculate the solid fraction of CO₂ and CO₂–THF hydrate from thermodynamic conditions of pressure and temperature. Contrary to a previous work on single CO₂ hydrates in a closed system, the present model can take into account hydrate mixture and is well adapted to additional CO₂ injections (opened system). By relying on the hydrate-conversion model results, the study of hydrates in suspension in a carrying liquid was also studied in an experimental loop and was based on a formation process by CO₂ injection in a cooled aqueous solution.     

Synthesis of cadmium and zinc semiconductor compounds from an ionic liquid containing choline chloride and urea

A eutectic mixture of choline chloride and urea (commercially known as Reline) has been used as a medium from which CdS, CdSe, and ZnS thin films have been electrodeposited for the first time. Reline is a conductive room temperature ionic liquid (RTIL) with a wide electrochemical window, which is suitable for use as a medium for electrodeposition. The voltammetric behaviour of the Reline-Cd(II)-sulfur system has been investigated. Thin films of CdS deposited at constant potential were characterized by photocurrent and electrolyte electroabsorbance spectroscopies. Thin films of CdSe and ZnS have also been prepared, and their photocurrent excitation spectra have been measured.     

Prevalence of alcohol-impaired driving: An international comparison

This paper reports international differences in the extent of alcohol-impaired driving. These differences are then interpreted in the light of inducements and disincentives to drink and to drive.     

The Influence of C60 Powders On Cultured Human Leukocytes

In order to check its possible acute toxicity, C₆₀ was incorporated into living human phagocytes. It was observed that C₆₀ has no influence on the survival of human leukocytes.     

Resonance Raman spectroscopy of photolabile transition metal carbonyls: controlled photoalteration with continuous wave lasers to record spectra of reactants or transient species

A method has been developed that enables resonance Raman spectra of photolabile species in solution to be recorded under conditions where the level of photoalteration is controlled: a low level enables reactant spectra to be recorded, whereas a high level enables the spectra of short-lived transient species to be recorded in real time using continuous-wave (CW) lasers and standard Raman detection equipment. The design includes a sealed flow system, enabling air-sensitive species to be studied under an inert atmosphere. A simple theoretical model has been developed to aid the interpretation of experimental results, and its applicability is demonstrated. Controlled photoalteration and its theory are demonstrated with 413.1-nm excitation of carbonmonoxymyoglobin (MbCO), which generates deoxymyoglobin (deoxy-Mb) on photolysis, and for which the spectra of both species are well established. The methods have also been applied to two air-sensitive, photolabile transition metal carbonyls using 514.5-nm wavelength excitation: for Cp2Mo2(CO)6 (Cp = eta5-C5H5), increasing levels of photoalteration result only in a decrease in the parent band intensities, relative to the solvent bands; for Cp2Fe2(CO)4, increasing levels of photoalteration result in the appearance of additional bands that are assigned to the transient species CpFe(mu-CO)3FeCp, formed following the loss of a CO ligand.