Reviewing Integrated Science and Mathematics: The Search for Evidence and Definitions From New Perspectives

Based upon current research needs indicated from recent literature reviews, this integrative review concentrates on two of the perceived major impediments to integrating science and mathematics: The lack of evidence to support integration and the lack of a definition for integration. Using mixed methodology, this review found quantitative evidence favoring integration from a meta-analysis of 31 studies of student achievement, qualitative evidence revealing the existence of multiple forms of integration, and historical evidence of publishing patterns from across the 20th century. The forms of integration were identified and defined; differential effects were identified both between forms and between science and mathematics when the forms were analyzed by effect size. Additional research implications and suggestions for future research were also identified.     

An improved method for determination of uranium isotopic composition in urine by alpha spectrometry

A comparative study of source preparation techniques to determine uranium isotopic composition by alpha spectrometry, namely electrodeposition and chemical stripping with polymeric membranae containing trioctylphosphine oxide (TOPO), is presented. The mean yield obtained for electrodeposition and TOPO deposition were 85% and 74%, respectively. The mean activity ratio²³⁵U/²³⁸U were 0.044 and 0.042 and the ratio²³⁴U/²³⁸U were 0.994 and 1.009, using electrodeposition and TOPO deposition techniques, respectively. The method of uranium separation from urine using an ion-exchange resin Dowex 1×8, chloride form and citrate form, was also studied. The obtained global yields of these methods were 50% and 41%, respectively.     

Experimental investigation of effects of variation in heating rate,temperature and heat flux on fire properties of a non-charring polymer

Journal of Thermal Analysis and Calorimetry - Differential scanning calorimetry (DSC) technique is used to study the solid reactions in the 2024 Al–Cu–Mg and 2014...     

On the Behavior of [Zn(Propyltetrazole)6](BF4)2 Single Crystal Under High-Vacuum Conditions

We studied the long-term (190 hours) behaviour of [Zn(propyltetrazole)₆](BF₄)₂ single crystal under high-vacuum (HV) conditions (10^–8 torr) with a depth-sensitive technique of positron annihilation spectroscopy (PAS). The obtained data indicate the slow formation of a new near-surface structure which is formed by the decomposition of the [Zn(propyltetrazole)₆]²⁺ ions. The assumption of such a decomposition process was confirmed by additional mass spectroscopic measurements.     

Effects of Surfactant Volume Fraction on the Antioxidant Efficiency and on The Interfacial Concentrations of Octyl and Tetradecyl p-Coumarates in Corn Oil-in-Water Emulsions

Surfactants have been used for decades in the food industry for the preparation of lipid-based emulsified food stuffs. They play two main roles in the emulsification processes: first they decrease the interfacial tension between the oil and water, facilitating droplet deformation and rupture; second, they reduce droplet coalescence by forming steric barriers. However, addition of surfactants to binary oil-water mixtures also brings up the formation of three-dimensional interfacial layers, surrounding each emulsion droplet, that significantly alter chemical reactivity. This is the case, for instance, in the inhibition reaction between antioxidants and the lipid radicals formed in the course of the spontaneous oxidation reaction of unsaturated lipids, which are commonly employed in the preparation of food-grade emulsions. The rate of the inhibition reaction depends on the effective concentrations of antioxidants, which are mostly controlled by the amount of surfactant employed in the preparation of the emulsion. In this work, we analyze the effects of the surfactant Tween 20 on the oxidative stability and on the effective concentrations of two model antioxidants derived from cinnamic acid, determining their interfacial concentrations in the intact emulsions to avoid disrupting the existing equilibria and biasing results. For this purpose, a recently developed methodology was employed, and experimental results were interpreted on the grounds of a pseudophase kinetic model.     

Influence of Perfluorinated End Groups on the SFRD of [Pt(cod)Me(CnF2n+1)] onto Porous Al2O3 in CO2 under Reductive Conditions

The optimized synthesis of a range of cyclooctadiene‐stabilized Pt complexes that contained different perfluoro‐alkane chains, [Pt(cod)Me(C_nF_2n+1)], is presented. These metal–organic compounds were employed in the so‐called supercritical fluid reactive deposition (SFRD) in CO₂ under reductive conditions to generate metallic nanoparticles on aluminum oxide as a porous support. Thus, Al₂O₃‐supported Pt nanoparticles with a narrow particle‐size distribution were obtained. At a reduction pressure of 15.5 MPa and a temperature of 353 K, particle diameters of d₅₀=2.3–2.8 nm were generated. Decreasing the pressure during the reduction reaction led to slightly larger particles whilst decreasing the amount of organometallic precursor in CO₂ yielded a decrease in the particle size from x₅₀=3.2 nm to 2.6 nm and a particle‐size distribution of 2.2 nm. Furthermore, substitution of the CH₃ end group by the C_nF_2n+1 end groups led to a significant drop in Pt loading of about 50 %. Within the series of perfluorinated end groups that were considered, the Pt complex that contained a branched perfluoro‐isopropyl group showed the most‐interesting results when compared to the control precursor, [Pt(cod)Me₂] ( 1 ).     

Use of Magnetic Resonance Imaging as a Tool for the Study of Foamy Oil Behavior for an Extra‐Heavy Crude Oil. T2 /Viscosity Correlation with Respect to Pressure

The purpose of this work is to present the results of the phase behavior study for a live heavy oil during a pressure depletion process using magnetic resonance imaging (MRI) as a tool to characterize foamy oil phenomena. The experiments were carried out in the pressure range of 13.1 to 1.4MPa. Signal intensity images were obtained at each pressure and with respect to time, that is, approximately for a total time of 3h after each pressure change. It is possible to see a variation in intensity across the sample. These changes can be associated with changes in mobility as well as segregation of the oil. It was also possible to observe that what we trust is the formation of gas channels at the last two pressure values, as it comes out of solution. A correlation between the transverse relaxation time T2 and temperature was established with the aim of producing one between T2 and viscosity. In this way viscosity maps for the live oil were obtained as a function of pressure and time. It was observed that above the bubble point, the viscosity maps varied from low to high to low with respect to time for the same pressure. Below the bubble point the situation is reverse. The viscosity map changes from high to low to high with respect to time for the same pressure. The study shows the potential use of MRI to follow viscosity changes during pressure depletion test in a PVT MRI cell.