Dynamic mechanical properties for polyurethane elastomers applied in elastomeric mortar

Dynamic mechanical properties of a polyurethane (PU) elastomer and a mortar processed with the same elastomer (modified polytetramethylene ether glycol (PTMEG)) were studied. The results obtained showed that the liquid aromatic amine ETHACURE® 300, used as cure agent, can be used to substitute the aromatic amine MOCA®, which is usually used as cure agent in high performance elastomers. The resulting mortar produced with ETHACURE® 300 presents similar dynamic‐mechanical thermal properties when compared with MOCA ®. However, dynamic‐mechanical thermal analysis studies showed that the mortar developed with ETHACURE® 300 presents some advantages such as the low values of tan δ, indicating a good capacity of recovery of the strain after retreating an applied force. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Thermal characteristics of louvered fins with a low-reynolds number flow

A heat recovery system is crucial for the effective use of energy where heat rejection from production processes is unavoidable and must be reused. The response of the louvered fins to the low-Reynolds number hot gas is yet to be reported in the literature for the application of a heat exchanger on low-speed hot plume arising from heat sources in production processes. This study focuses on the effects of the louvered fin heat exchanger’s design parameters, which include the louver pitch and louver angle, on the convective heat transfer, which defines the thermal interaction between the hot, buoyant, naturally-induced air and the louvered fins. The resulting Colburn factors (j) are compared with those derived under forced convection with a similar range of low Reynolds number (233 to 1024). All experiments are done on a 15:1 scaled-up model. The fin aspect ratios between the fin spacing and louver pitch are set at 0.75, 1, and 1.5, while the louver angles are set at 18°, 23°, 30°, 35°, and 40°. The Colburn factor strongly depends on the louver angle, especially at the lower range of the Reynolds number. The decreasing aspect ratio induces more hot buoyant air into the louver-formed channels, increasing the heat transfer rate. When the fin angle increases towards 30°, a larger Colburn factor is produced. However, the heat transfer characteristic drops as the angle goes beyond 30°. The highest j for the low speed flow is attained when the louver angle is 30° and the fin aspect ratio is 1.     

Lipase/acyltransferase‐catalysed interesterification of fat blends containing n‐3 polyunsaturated fatty acids

The lipase/acyltransferase from Candida parapsilosis is an original biocatalyst that preferentially catalyses alcoholysis over hydrolysis in biphasic aqueous/organic media. In this study, the performance of the immobilised biocatalyst in the interesterification in solvent‐free media of fat blends rich in n‐3 polyunsaturated fatty acids (n‐3 PUFA) was investigated. The interesterification activity of this biocatalyst at a water activity (a_w) of 0.97 was similar to that of commercial immobilised lipases at a_w values lower than 0.5. Thus, the biocatalyst was further used at an a_w of 0.97. Response surface modelling of interesterification was carried out as a function of medium formulation, reaction temperature (55–75 °C) and time (30–120 min). Reaction media were blends of palm stearin (PS), palm kernel oil and triacylglycerols (TAG) rich in n‐3 PUFA (“EPAX 4510TG”; EPAX AS, Norway). The best results in terms of decrease in solid fat content were observed for longer reaction time (>80 min), lower temperature (55–65 °C), higher “EPAX 4510TG” content and lower PS concentration. Reactions at higher temperature led to final interesterified fat blends with lower free fatty acid contents. TAG with high equivalent carbon number (ECN) were consumed while acylglycerols of lower ECN were produced.     

4,9-Diaminoacridines and 4-Aminoacridines as Dual-Stage Antiplasmodial Hits

Multi-stage drugs have been prioritized in antimalarial drug discovery, as targeting more than one process in the Plasmodium life cycle is likely to increase efficiency, while decreasing the chances of emergence of resistance by the parasite. Herein, we disclose two novel acridine-based families of compounds that combine the structural features of primaquine and chloroquine. Compounds prepared and studied thus far retained the in vitro activity displayed by the parent drugs against the erythrocytic stages of chloroquine-sensitive and -resistant Plasmodium falciparum strains, and against the hepatic stages of Plasmodium berghei, hence acting as dual-stage antiplasmodial hits.     

Understanding the Rate‐Limiting Step of Glycogenolysis by Using QM/MM Calculations on Human Glycogen Phosphorylase

Liver glycogen phosphorylase (GP) is a key enzyme for human health, as its increased activity is associated with type 2 diabetes. The GP catalytic mechanism has been explored by quantum mechanics/molecular mechanics (QM/MM) methods. Herein, we propose a mechanism that proceeds by three steps: 1) it begins with transfer of a hydrogen atom from the phosphate group of the pyridoxal 5′‐phosphate (HPO₄^2?‐PLP) cofactor to the phosphate substrate; 2) the glycosidic linkage is then cleaved through protonation of the glycosidic oxygen atom by a hydroxy group of the inorganic phosphate group; and 3) an oxygen atom of the phosphate performs a nucleophilic attack on the anomeric carbon atom of glucose, concomitant with the return of a proton from phosphate to PO₄^3?‐PLP, which finally leads to formation of the glucose‐1‐phosphate product and recovers the initial state of the PLP cofactor. The glycosidic bond cleavage and nucleophilic attack from the phosphate group to the glycosyl molecule have the highest activation free energies. The structural properties of the hereby characterized transition states could be very useful in structure‐based drug design studies against liver GP.     

Mechanisms of manganese bioremediation by microbes: an overview

Although an important micronutrient for many living organisms, manganese (Mn) can become a health and environmental problem at high concentrations. The element is usually found in wastewaters and drainages of different industrial sectors and its removal is notoriously difficult because of the high stability of the Mn (II) ion in aqueous solutions. The treatment of Mn‐laden wastewaters may include microorganisms that catalyze Mn oxidation by either enzymatic or non‐enzymatic pathways. In this context, this mini‐review discusses the mechanisms by which fungi and bacteria promote Mn bioremediation. © 2016 Society of Chemical Industry