Dendrite growth direction measurements : understanding the solute advancement in continuous casting of steel

Maintaining competitiveness in steel manufacturing requires improving process efficiency and production volume whilst enhancing product quality and performance. This is particularly challenging for producing value-added advanced steel grades such as advanced high strength steels and electrical steels. These grades due to higher weight percentage of alloying elements cause difficulties in various stages of upstream and downstream processing, and this includes continuous casting, wherein high solute levels are critical towards macro-segregation. Interface growth direction in systems with more than one component is dictated by the solute profile ahead of the moving solidification front. Understanding the profile of growth direction with casting process parameters during the progress of casting will provide an important perspective towards reducing the macro-segregation in the cast product. In the present study, two steel slab samples from conventional slab caster under the influence of electromagnetic brake (EMBR) at Tata Steel in IJmuiden (The Netherlands) have been investigated for dendrite deflection measurements. The samples showed a transition zone where a change in the deflection behavior occurs. Also, the magnitude of the deflection angle decreases away from the slab surface. Correlating these experimental data with modeled fluid flow profile will help in improving the understanding of the dynamic nature of the solute advancement so that the casting parameters can be optimized to improve product quality

Sugar-Sweetened Beverage Intake Trends in US Adolescents and Their Association with Insulin Resistance-Related Parameters

The purpose of this study was to evaluate current sugar-sweetened beverage (SSB) consumption trends and their association with insulin resistance-related metabolic parameters and anthropometric measurements by performing a cross-sectional analysis of the NHANES data during the years 1988–1994 and 1999–2004. Main outcome measures included SSB consumption trends, a homeostasis model assessment of insulin resistance, blood pressure, waist circumference, body mass index, and fasting concentrations of total cholesterol, HDL-cholesterol, LDL-cholesterol, and triglycerides. Although overall SSB consumption has increased, our data suggest that this increase was primarily due to an increase in the amount of SSBs consumed by males in the high-SSB intake group alone. Multivariate linear regression analyses also showed that increased SSB consumption was independently associated with many adverse health parameters. Factors other than SSB consumption must therefore be contributing to the increasing prevalence of obesity and metabolic syndrome in the majority of US children

Effect of nanoparticle size on the near-surface pH-distribution in aqueous and carbonate buffered solutions

An analytical solution for the effect of particle size on the current density and near-surface ion distribution around spherical nanoparticles is presented in this work. With the long-term aim to support predictions on corrosion reactions in the human body, the spherical diffusion equation was solved for a set of differential equations and algebraic relations for pure unbuffered and carbonate buffered solutions. It was shown that current densities increase significantly with a decrease in particle size, suggesting this will lead to an increased dissolution rate. Near-surface ion distributions show the formation of a steep pH-gradient near the nanoparticle surface (\u3c6 μm) which is further enhanced in the presence of a carbonate buffer (\u3c2 μm). Results suggest that nanoparticles in pure electrolytes not only dissolve faster than bigger particles but that local pH-gradients may influence interactions with the biological environment, which should be considered in future studies

Electrochemical Estimations of the Gold Nanoparticle Size Effect on Cysteine-Gold Oxidation,

Gold nanoparticles are interesting for nanobiomedical applications, such as for drug delivery and as diagnostic imaging contrast agents. However, their stability and reactivity in-vivo are influenced by their surface properties and size. Here, we investigate the electrochemical oxidation of differently sized citrate-coated gold nanoparticles in the presence and absence of L-cysteine, a thiol-containing amino acid with high binding affinity to gold. We found that smaller sized (5, 10 nm) gold nanoparticles were significantly more susceptible to electrochemical L-cysteine interactions and/or L-cysteine-facilitated gold oxidation than larger (20, 50 nm) sized gold nanoparticles, both for the same mass and nominal surface area, under the conditions investigated (pH 7.4, room temperature, stagnant solutions, and scan rates of 0.5 to 450 mV s−1). The electrochemical measurements of drop-casted gold nanoparticle suspensions on paraffin-impregnated graphite electrodes were susceptible to the quality of the electrode. Increased cycling resulted in irreversible oxidation and detachment/oxidation of gold into solution. Our results suggest that L-cysteine-gold interactions are stronger for smaller nanoparticles

The algebra of adjacency patterns: Rees matrix semigroups with reversion

We establish a surprisingly close relationship between universal Horn classes of directed graphs and varieties generated by so-called adjacency semigroups which are Rees matrix semigroups over the trivial group with the unary operation of reversion. In particular, the lattice of subvarieties of the variety generated by adjacency semigroups that are regular unary semigroups is essentially the same as the lattice of universal Horn classes of reflexive directed graphs. A number of examples follow, including a limit variety of regular unary semigroups and finite unary semigroups with NP-hard variety membership problems.Comment: 30 pages, 9 figure

Effect of nanoparticle size on the near-surface pH-distribution in aqueous and carbonate buffered solutions

An analytical solution for the effect of particle size on the current density and near-surface ion distribution around spherical nanoparticles is presented in this work. With the long-term aim to support predictions on corrosion reactions in the human body, the spherical diffusion equation was solved for a set of differential equations and algebraic relations for pure unbuffered and carbonate buffered solutions. It was shown that current densities increase significantly with a decrease in particle size, suggesting this will lead to an increased dissolution rate. Near-surface ion distributions show the formation of a steep pH-gradient near the nanoparticle surface (<6 m) which is further enhanced in the presence of a carbonate buffer (<2 m). Results suggest that nanoparticles in pure electrolytes not only dissolve faster than bigger particles but that local pH-gradients may influence interactions with the biological environment, which should be considered in future studies

Electrochemical estimations of the gold nanoparticle size effect on cysteine-gold oxidation

Gold nanoparticles are interesting for nanobiomedical applications, such as for drug delivery and as diagnostic imaging contrast agents. However, their stability and reactivity in-vivo are influenced by their surface properties and size. Here, we investigate the electrochemical oxidation of differently sized citrate-coated gold nanoparticles in the presence and absence of L-cysteine, a thiol-containing amino acid with high binding affinity to gold. We found that smaller sized (5, 10 nm) gold nanoparticles were significantly more susceptible to electrochemical L-cysteine interactions and/or L-cysteine-facilitated gold oxidation than larger (20, 50 nm) sized gold nanoparticles, both for the same mass and nominal surface area, under the conditions investigated (pH 7.4, room temperature, stagnant solutions, and scan rates of 0.5 to 450 mV s−1). The electrochemical measurements of drop-casted gold nanoparticle suspensions on paraffin-impregnated graphite electrodes were susceptible to the quality of the electrode. Increased cycling resulted in irreversible oxidation and detachment/oxidation of gold into solution. Our results suggest that L-cysteine-gold interactions are stronger for smaller nanoparticles