Influence of drying conditions on the gelling properties of the 7S and 11S soy protein fractions

Soy protein fractions rich in β-conglycinin (7S) or glycinin (11S) were freeze dried or spray dried at temperatures of 120, 150 or 180 °C. The fractions were characterized for their particle size distribution, sorption isotherms and by scanning differential calorimetry. The gelling capacity of the protein fractions was studied at pH values of 3 and 7 using oscillatory measurements, mechanical properties and water holding capacity. The rheological measurements showed that viscous modulus (G″) predominated at low temperatures and the elastic modulus (G′) at high temperatures. At pH 3, the G′–G″ crossover occurred at lower temperatures when compared to pH 7. This behaviour was more accentuated for the 11S fractions due to its capacity to form stronger gels. An increase of drying temperature led to a displacement of the gel point to higher temperatures and decreased the elasticity modulus or gelling capacity of protein fractions. These results were confirmed by the mechanical properties, since at higher temperatures the gels were more fragile and brittle, especially when formed at pH 7.     

In Vitro Simultaneous Transfer of Lipids to HDL in Coronary Artery Disease and in Statin Treatment

The exchange of lipids with cells and other lipoproteins is a crucial process in HDL metabolism and for HDL antiatherogenic function. Here, we tested a practical method to quantify the simultaneous transfer to HDL of phospholipids, free-cholesterol, esterified cholesterol and triacylglycerols and to verify the lipid transfer in patients with coronary artery disease (CAD) or undergoing statin treatment. Twenty-eight control subjects without CAD, 27 with CAD and 25 CAD patients under simvastatin treatment were studied. Plasma samples were incubated with a donor nanoemulsion prepared by ultrasonication of the constituent lipids and labeled with radioactive lipids; % lipids transferred to HDL were quantified in the HDL-containing supernatant after chemical precipitation of non-HDL fractions and the nanoemulsion. The assay was precise and reproducible. Increase of temperature (4–37 °C), of incubation period (5 min to 2 h), of HDL-cholesterol concentration (33–244 mg/dL) and of mass of nanoemulsion lipids (0.075–0.3 mg/μL) resulted in increased lipid transfer from the nanoemulsion to HDL. In contrast, increasing pH (6.5–8.5) and albumin concentration (3.5–7.0 g/dL) did not affect lipid transfer. There was no difference between CAD and control non-CAD with regard to the lipid transfer, but statin treatment reduced the transfer to HDL of all four lipids. The test herein described is a valid and practical tool for exploring an important aspect of HDL metabolism.     

A genetic programming method for protein motif discovery and protein classification

Proteins can be grouped into families according to some features such as hydrophobicity, composition or structure, aiming to establish common biological functions. This paper presents MAHATMA—memetic algorithm-based highly adapted tool for motif ascertainment—a system that was conceived to discover features (particular sequences of amino acids, or motifs) that occur very often in proteins of a given family but rarely occur in proteins of other families. These features can be used for the classification of unknown proteins, that is, to predict their function by analyzing their primary structure. Experiments were done with a set of enzymes extracted from the Protein Data Bank. The heuristic method used was based on genetic programming using operators specially tailored for the target problem. The final performance was measured using sensitivity, specificity and hit rate. The best results obtained for the enzyme dataset suggest that the proposed evolutionary computation method is effective in finding predictive features (motifs) for protein classification.     

New developments in fire retardant non‐halogen aromatic phosphates

Akzo Nobel Chemicals has recently introduced on the market an aromatic oligomeric phosphate (BDP) based on Bisphenol A. This product shows higher thermal and hydrolytic stability than other aryl phosphates. It provides similar or better fire retardant performance than an oligomeric phosphate (RDP) based on resorcinol. Fire retardant formulations with BDP based on polycarbonate/ABS plastic (PC/ABS) blend, polyphenylene oxide/high impact polystyrene (PPO/HIPS) blend, and HIPS alone show similar or better physical properties than those obtained with RDP. Upon thermal decomposition of the fire retarded polymers containing BDP, phosphorus tends to accumulate in the solid residue, a result which indicates that the primary fire retardant action of BDP is likely to occur in the condensed phase.     

Comparison of the univariate and multivariate methods in the optimization of experimental conditions for determining Cu, Pb, Ni and Cd in biodiesel by GFAAS

Experimental design was used as a tool to define the optimum pyrolysis and atomization temperatures for four analytes (Cu, Pb, Ni and Cd) in biodiesel samples. Two chemical modifiers (Pd + Mg and W) and two distinct sample preparation procedures (microemulsion and wet digestion in a focused microwave system) were also investigated. The pyrolysis and atomization temperatures were optimized using 2⁴ factorial design for Cu, Pb, Ni and Cd, with 16 assays carried out for each analyte. The results for Cu and Pb indicated that variables of sample preparation for digestion by focused microwave was the most important one for both analytes. The pyrolysis and atomization temperatures applied were 1000 °C and 2200 °C for Cu and 500 °C and 2000 °C for Pb. None of the variables analyzed here were important for Ni, and the pyrolysis and atomization temperatures chosen for this element were 800 °C and 2300 °C. A different factorial design was used for Cd. The variables of medium and modifier were not important for this element, and the lowest temperatures, Tp-500 °C and Ta-1400 °C, were chosen based on this second design. The importance of factorial design in the simultaneous optimization of several variables studied by GFAAS was confirmed, for it involves fewer experiments and hence, lower costs, greater speed and higher efficiency.     

NETmix®, a new type of static mixer: Modeling,simulation, macromixing,and micromixing characterization

NETmix® is a new technology for static mixing based on a network of chambers connected by channels. The NETmix® model is the basis of a flow simulator coupled with chemical reaction used to characterize macro and micromixing in structured porous media. The chambers are modeled as perfectly mixing zones and the channels as plug flow perfect segregation zones. A segregation parameter is introduced as the ratio between the channels volume and the whole network volume. Different kinetics and reactants injection schemes can be implemented. Results show that the number of rows in the flow direction and the segregation parameter control both macro and micromixing, but the degree of micromixing is also controlled by the reactants injection scheme. The NETmix® model enables the systematic study of micromixing and macromixing for different network structures and reaction schemes, enabling the design of network structures to ensure the desired yield and selectivity. © 2009 American Institute of Chemical Engineers AIChE J, 2009     

Multiphase reacting flow studies of bubble column ozonation reactor for water remediation

A multiphase Volume‐of‐fluid (VOF) model was developed to gain further insights into the reactive flow parameters and electrical capacitance tomography (ECT) measurements on the remediation of hazardous organic pollutants. Low ozone bubble frequencies were obtained for high surface tension fluids, and the liquid viscosity affected the ozone bubbling frequency. The VOF model indicated that the increase of inlet gas velocity enriched the ozone bubble detachment and concomitantly generated larger ozone bubbles, decreasing the detoxification rates. VOF mappings and ECT visualizations of gas‐liquid unveiled preferential routes and highlighted the attenuation of the axisymmetric behavior of the ozonation bubble column under high‐interaction regimes.     

What's in a manner of speaking? Children's sensitivity to partner-specific referential precedents.

Do young children form “referential pacts”? If a person has referred to an object with a certain term (e.g., the horse), will children expect this person to use this term in the future but allow others to use a different expression (e.g., the pony)? One hundred twenty-eight children between 3 and 5 years old co-operated with an experimenter (E1) to move toys to new locations on a shelf. E1 established referential terms for all toys in a warm-up game. Then, either the original partner, E1, or a new partner, E2, played a second game with the same toys. In this game, the experimenters referred to toys using either their original terms from the warm-up game or new terms. Children were slower to react to new terms than old, and this difference in reaction times was greater in the original partner condition (but only on the first trial). Children sometimes protested at the use of new terms, doing so regardless of their interlocutor's identity. We contrast these findings with those for adults and discuss their implications for the debate regarding the nature of referential pacts. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Reduction and catalytic behaviour of heterobimetallic copper–lanthanide oxides

The reduction of the heterobimetallic copper–lanthanide oxides 2CuO·CeO₂ and 3CuO·Ln₂CuO₄ (Ln = La, Pr, Nd) was studied by H₂-TG/DTA and H₂-TPR. All systems exhibit two main reduction steps accompanied by mass losses in the temperature range 20–1000 °C. The first step was attributed to CuO reduction, whereas the second step is due either to copper reduction in the Ln₂CuO₄ phase with the concomitant formation of Ln₂O₃ or to the surface reduction of CeO₂. The products were characterized by XRD, SEM, EDX, and BET techniques and are better described as supported copper type materials. They were active for the mesityl oxide (4-methyl-2-penten-2-one) gas phase hydrogenation.