Analysis of transport phenomena within PEM fuel cells – An analytical solution

Transport phenomena within PEM fuel cells are investigated and a comprehensive analytical solution is presented. The methodology couples the transport within the fuel cell supply channels and the substrate which is composed of five different layers. The layers are all treated as macroscopically homogeneous porous media with uniform morphological properties such as porosity and permeability. The locally volume-averaged equations are employed to solve for transport through the porous layers. The problem encompasses complex interfacial transport phenomena involving several porous–porous as well as porous–fluid interfaces. Chemical reactions within the catalyst layers are also included. The method of matched asymptotic expansions is employed to solve for the flow field and species concentration distributions. Throughout the analysis, the choice of the gauge parameters involved in the perturbation solutions for velocity and concentration is found to be inherently tied to the physics of the problem and therefore an important physical metric. The analytical solution is found to be in excellent agreement with prior computational simulations. The analytical results are used to investigate several aspects of transport phenomena and their substantial role in PEM fuel cell operation. The solution presented in this work provides the first comprehensive analytical solution representing fuel cell transport phenomena.     

Putative mechanism for anticancer properties of Ag–PP (NPs) extract

One of the most important challenges in treating cancer is the invasion and the angiogenesis of cancer cells. The synthesis of green nanoparticles (NPs) and their use in therapeutic fields is one of the most effective methods with minimal side effects in cancer treatment. In this study, cytotoxic and anti‐angiogenic effects of silver NPs (AgNPs) coated with palm pollen extract [Ag–PP(NPs)] were evaluated. For this purpose, the cells were treated with NPs and then were subjected to trypan blue testing (48 h). Then, the cancer invasion was evaluated by the scratch procedure and the expressions of the vascular endothelial growth factor (VEGF) and its receptor (VEGF‐R) genes were estimated using real‐time PCR assay. Also, the angiogenesis effect of the NPs was investigated with chick chorioallantoic membrane (CAM) assay. The Ag–PP(NPs) induced cytotoxicity on MCF7 cells. The findings also showed that Ag–PP(NPs) inhibit invasive cancer cells and reduce the expression of VEGF and VEGF‐R and significantly reduced the number and vessels lengths and the lengths and weights of the embryos in CAM assay. Ag–PP(NPs) with the induction of cytotoxic effects, metastatic inhibition and anti‐angiogenesis properties should be considered as an appropriate option for treatment of cancerInspec keywords: nanomedicine, genetics, cellular biophysics, toxicology, patient treatment, silver, cancer, biochemistry, biomedical materials, nanoparticles, nanofabrication, membranesOther keywords: minimal side effects, cancer treatment, silver NPs, cancer invasion, vascular endothelial growth factor, receptor genes, VEGF‐R, real‐time polymerase chain reaction assay, angiogenesis effect, chick chorioallantoic membrane assay, MCF7 cells, invasive cancer cells, cytotoxic effects, putative mechanism, anticancer properties, antiangiogenic effects, antiangiogenesis properties, Ag–PP‐induced cytotoxicity, metastatic inhibition, palm pollen extraction, trypan blue testing, time 48.0 hour, Ag     

A new stress-updating algorithm for viscoplasticity

Material behavior beyond the elastic limit can be rate-dependent, and this rate sensitivity can be captured by the viscoplastic material models. To describe the viscoplastic material behavior in structural analysis, an efficient numerical framework is necessary. In this paper an algorithm is proposed for metals for which von Mises yield surface along with Peri?’s viscoplastic model is employed. The efficiency and accuracy of the technique is examined by comparison with different numerical studies. The convergence rate of the proposed algorithm is investigated. Characteristics of the viscoplastic behavior such as relaxation are illustrated in the selected case studies. Finally, application of the algorithm in practice is demonstrated by a boundary value problem.

     

Respiratory burst activity of blood and milk neutrophils in dairy cows during different stages of lactation.

The non-stimulated and phorbol 12-myristate 13-acetate (PMA)-stimulated luminol-augmented cellular chemiluminescence (CL) response and viability of milk and blood polymorphonuclear leukocytes (PMN) were determined in lactating dairy cows during different stages of lactation. In the first study, ten healthy cows each in early, mid and late lactation were compared. In a second study, the same measurements as in the first study were evaluated longitudinally in 12 cows during 1 month following parturition. The CL activity and myeloperoxidase (MPO) content of milk PMN and macrophages (M) were also compared. Milk M did not possess MPO activity and were devoid of any luminol-enhanced CL. The CL activity of milk and blood PMN was significantly lower in early lactation than in mid and late lactation (P < 0.001). Whereas little changes were observed in viability of blood PMN, the viability of milk PMN was lower in early lactation than in mid and late lactation (P < 0.001). The percentage of PMN in isolated milk cells was also lower during early lactation than during mid and late lactation (P < 0.001). The CL activity in response to PMA during early, mid and late lactation increased 13, 59 and 42-fold in blood PMN and 1.7, 2.6 and 2.4-fold in milk PMN, respectively, in comparison with non-stimulated PMN. The CL activity, both in milk and blood PMN. the milk PMN viability and the percentage of milk PMN were lowest between 3 d and 11 d post partum. These observed changes immediately after calving could contribute to a higher susceptibility to mastitis in that period.     

Characteristics of date pit oil

Date pit oils of three Iranian varieties of dates were examined for their fatty acid composition and some of their characteristics. The properties and compositions of the pit oils did not differ significantly from each other or from previously published literature values.     

Increase in Escherichia coli inoculum dose accelerates CD8+ T-cell trafficking in the primiparous bovine mammary gland

Although migration of leukocytes into the mammary gland is pivotal for a cow's response against intramammary invading pathogens, the contribution of lymphocyte subsets to this response remains unclear. To investigate the dynamics of lymphocyte populations during Escherichia coli mastitis, T-lymphocyte subsets, CD4⁺/CD8⁺ ratio, CD21⁺ cells, and lymphoproliferation were studied in blood and milk of primiparous cows exposed to different quantities of bacteria. The cows were intramammarily inoculated with 10⁴ cfu of E. coli (group A) and 10⁶ cfu (group B). Compared with group A, a much greater number of lymphocytes migrated into the infected quarters at postinfection hour (PIH) 6 to 24 in group B, and the CD8⁺ cells were the first-recruited T cells in the milk. There was a significant decline in the CD4⁺/CD8⁺ ratios at PIH 6 to 24 in group B. The decrease of CD4⁺/CD8⁺ ratios at PIH 6 to 24 resulted mainly from greater CD8⁺ cell concentrations in milk. In contrast, at PIH 72, CD4⁺/CD8⁺ ratios increased about 2-fold in both groups. This increase was mainly due to the increase in CD4⁺ cell concentration. The increased concentration of CD4⁺ cells coincided with an increase in the CD21⁺ cell population in the milk. In blood, the increase of CD8⁺ cells appeared much faster in group B (PIH 6 and 12) than in group A. The results from lymphoproliferation also indicated a greater increase in the proliferative response in both blood and milk lymphocytes of group B. Our study demonstrates for the first time that an increase of E. coli inoculum dose accelerates the trafficking of CD8+ cells during initiation of E. coli mastitis, and these cells are the predominant T cells in milk during the early hours of bovine E. coli mastitis.     

Application of Exponential-Based Methods in Integrating the Constitutive Equations with Multicomponent Nonlinear Kinematic Hardening

The von-Mises plasticity model, in the small strain regime, along with a class of multicomponent nonlinear kinematic hardening rules is considered. The material is assumed to be stabilized after several load cycles and therefore, isotropic hardening will not be accounted for. Application of exponential-based methods in integrating plasticity equations is provided, which is based on defining an augmented stress vector and using exponential maps to solve a system of quasi-linear differential equations. The solutions obtained by this new technique give very accurate updated stress values that are consistent with the yield surface. The classical forward Euler method is reformulated in details and applied to the multicomponent form of the nonlinear kinematic hardening in order to provide a comparison for the suggested technique. Moreover, a consistent tangent operator for the exponential-based integration strategy and also for the classical forward Euler algorithm is presented. In order to show the robustness and performance of the proposed formulation, an extensive numerical investigation is carried out.     

Proteases involved in mammary tissue damage during endotoxin-induced mastitis in dairy cows

During and after diapedesis, milk polymorphonu-clear neutrophils (PMN) release many proteases that have the potential of degrading extracellular matrix proteins and milk proteins. However, the kinetics of milk proteolysis during inflammation and the underlying mechanisms are poorly defined. The enzymes involved in bovine mammary tissue destruction were investigated in this study using an endotoxin-induced mastitis model. Using zymography techniques, the proteolytic activity of milk and mammary tissue during mastitis was examined. Mastitic milk produced 6 caseolysis bands, 4 of which differed from the ones produced by plasmin. Peak proteolytic activity, bovine serum albumin contents, and mammary tissue damage occurred between 6 and 12 h postchallenge. Mastitic milk proteases hydrolyzed casein, gelatin, collagen, hemoglobin, mammary gland membrane proteins, and lactoferrin. These results confirm that mastitic milk proteases have a broad spectrum of activity. The hydrolytic activity of mastitic milk was partially inhibited by aprotinin, EDTA, 1,10-phenanthroline, leupeptin, and pefabloc. When cocultured with normal mammary tissue, mastitic milk, but not normal milk, caused mammary tissue degradation. In situ zymography of mammary gland showed increased proteolytic activity in mastitic tissue compared with normal tissue. The similarity of zymograms of mastitic milk, blood PMN, milk somatic cells, and PMN strongly suggests that proteases in mastitic milk mainly originate from milk PMN. These results suggest that proteases released by PMN are actively involved in udder tissue damage during mastitis.     

Differential leukocyte count method for bovine low somatic cell count milk

Whereas many differential leukocyte count methods for high somatic cell count (SCC) milk from mastitic cows are available, only a few have been developed for low SCC milk. We have developed a flow cytometric differential leukocyte count method for low SCC milk. The procedure consists of 1) 1.5 ml of diluted milk sample (30%, vol/vol dilution with PBS), 2) centrifugation, 3) leukocyte labeling with SYTO 13 and 4) flow cytometric analysis. Four major leukocyte populations can be clearly identified in the green fluorescence-side scatter dot plot: lymphocytes and monocytes (LM), polymorphonuclear neutrophils (PMN), mature macrophages (Mphi), and cells with apoptotic features based on chromatin condensation and nuclear fragmentation. The optimal processing temperature was 20 degrees C. Significant differences among samples with similar differential leukocyte counts were found. Storage of milk samples during 2 d at 7 degrees C had no effect on differential leukocyte count. Using the new method, differential leukocyte count was performed in low SCC milk samples from cows in early, mid, and late lactation. In accordance with previous studies, PMN and Mphi percentages were lower and LM percentages were higher in early lactation than in the other stages of lactation. The percentage of cells with apoptotic features was higher in early lactation than in mid and late lactation. In conclusion, a rapid, simple, accurate, and reproducible standard procedure was developed to determine the differential leukocyte count (Mphi, PMN, LM, and cells with apoptotic features) of bovine low SCC milk.