Analysis of a turbulent boundary layer subjected to a strong adverse pressure gradient

We define two non-dimensional parameters $\text{Λ =}\text{τ}{}_{\mathrm{w}}\text{p}{}_{\mathrm{x}}\text{δ}$ and $\text{R}{}_{\mathrm{p}}\text{=}\text{U}{}_{\mathrm{p}}\text{δ}\text{ν}$ where τ_w is the wall stress, p_x(?0) is the pressure gradient to which the turbulent boundary layer (of thickness δ) is subjected, ν is the kinematic viscosity, $\text{U}{}_{\mathrm{p}}\text{= (}\text{νp}{}_{\mathrm{x}}\text{p}\text{)}{}^{\mathrm{<mtext>1</mtext><mtext>3</mtext>}}$ is a characteristic velocity and p is the density. The limit corresponding to the strong adverse pressure gradient is formulated as Λ → 0, R_p → ∞, ΛR_p finite. Using appropriate inner and outer asympcotic expansions, both above a wall layer possibly scaling with τ_w and ν, it is found by an application of Millikan's argument that there is an inertial sublayer where the streamwise velocity distribution obeys a half-power law, whose slope depends on Λ, and intercept on ΛR_p. Indeed comparison with available experimental data shows the inner law to be well represented by $\text{u}\text{Up}\text{= (3.5 + 19Λ)(}\text{yU}{}_{\mathrm{p}}\text{ν}\text{)}{}^{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{+ 2.5ΛR}{}_{\mathrm{p}}$. The outer flow obeys a generalized defect law; use of constant eddy viscosity closure yields results in good agreement with experiment.     

Pharmacokinetics and metabolic disposition of 14C-metronidazole-derived radioactivity in rat after intravenous and intravaginal administration

Urinary metabolites and the pharmacokinetics of radioactivity derived from 14C-metronidazole (14C-MTZ) were determined after intravenous (iv) or intravaginal (ivg) administration of 10 mg/kg to adult rats. Following iv or ivg administration, the disappearance of 14C from blood followed the kinetics of a two-compartment open-system model. The blood half-lives of 14C during the beta-phase were 10.9 +/- 1.6 and 13.6 +/- 4.2 hr, after iv and ivg administration, respectively. After ivg application, the MTZ-derived radioactivity was detected in tail blood at 5 min, peaked at 1 hr, declined rapidly to 6 hr and more slowly thereafter. The vaginal absorption half-life of 14C-MTZ was 0.28 +/- 0.09 hr. About 12% of the administered dose remained in the vagina after 1 hr and 1.5% after 24 hr. At 24 hr, the tissue distribution and concentration of 14C were similar in iv and ivg dosed rats, the highest 14C concentration being present in the kidneys and lowest in the fat. The percentages of the dose excreted in 24 hr in the urine and feces were 58 and 15 after iv administration, compared to 37 and 40 after the ivg route, respectively. Unchanged 14C-MTZ and five of its metabolites were detected in the urine irrespective of the route of administration. The results show that metronidazole is rapidly absorbed through the vaginal mucosa of the rat and the metabolism and excretion of this chemotherapeutic agent are influenced by the route of administration.     

Power Law Velocity Profile in Fully Developed Turbulent Pipe and Channel Flows

The power law velocity profile has been analyzed in terms of the envelope of the friction factor which gives the friction factor log law. The power law index α and prefactor C are shown as the function of the friction Reynolds number, as well as the function of the alternate variable the nondimensional friction velocity. The fully developed turbulent superpipe flow data of McKeon et al. and fully developed channel flow data of Zanoun et al. have been analyzed and the power law index α and prefactor C data have been estimated, first as a function of the friction Reynolds number and second as function of the nondimensional friction velocity. Based on analysis, several correlations have been proposed that have been supported by the data.     

SOME FUNDAMENTAL ATTRIBUTES OF FAR INFRARED RADIATION DRYING OF POTATO

Drying experiments were carried out using a far infrared heater to examine the drying characteristics of potato slices. The effect of several parameters e.g. radiation intensity, inlet air velocity and relative humidity on moisture and temperature history are presented. FIR drying of potato was observed to be a falling rate process. Drying rates were negatively correlated with air velocity. Relative humidity did not influence the drying rate. It was found that the modified exponential law describes the moisture removal of potato within an acceptable range.     

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities

A diverse family of protein 4.1R isoforms is encoded by a complex gene on human chromosome 1. Although the prototypical 80-kDa 4.1R in mature erythrocytes is a key component of the erythroid membrane skeleton that regulates erythrocyte morphology and mechanical stability, little is known about 4.1R function in nucleated cells. Using gene knockout technology, we have generated mice with complete deficiency of all 4.1R protein isoforms. These 4.1R-null mice were viable, with moderate hemolytic anemia but no gross abnormalities. Erythrocytes from these mice exhibited abnormal morphology, lowered membrane stability, and reduced expression of other skeletal proteins including spectrin and ankyrin, suggesting that loss of 4. 1R compromises membrane skeleton assembly in erythroid progenitors. Platelet morphology and function were essentially normal, indicating that 4.1R deficiency may have less impact on other hematopoietic lineages. Nonerythroid 4.1R expression patterns, viewed using histochemical staining for lacZ reporter activity incorporated into the targeted gene, revealed focal expression in specific neurons in the brain and in select cells of other major organs, challenging the view that 4.1R expression is widespread among nonerythroid cells. The 4.1R knockout mice represent a valuable animal model for exploring 4.1R function in nonerythroid cells and for determining pathophysiological sequelae to 4.1R deficiency.     

Pseudohalogenation of methyl 9-hydroxy-cis-12-and 12-hydroxy-cis-9-octadecenoate

Pseudohalogenation of methyl 9-hydroxy-cis-12-octadecenoate (I) and methyl 12-hydroxy-cis-9-octadecenoate (II) has been carried out with N,N-dibromobenzenesulfonamide (NNDBS). Compounds I and II, on reaction with NNDBS, formed four and three products, respectively. The interesting feature of these reactions was the formation of 1,4-epoxy compounds. The structures of individual compounds were established with the help of elemental and spectral analysis.     

Response of Different Genotypes of Faba Bean Plant to Drought Stress

Drought stress is one of the major abiotic stresses that are a threat to crop production worldwide. Drought stress impairs the plants growth and yield. Therefore, the aim of the present experiment was to select the tolerant genotype/s on the basis of moprpho-physiological and biochemical characteristics of 10 Vicia faba genotypes (Zafar 1, Zafar 2, Shebam, Makamora, Espan, Giza Blanka, Giza 3, C4, C5 and G853) under drought stress. We studied the effect of different levels of drought stress i.e., (i) normal irrigation (ii) mild stress (iii) moderate stress, and (iv) severe stress on plant height (PH) plant⁻¹, fresh weight (FW) and dry weight (DW) plant⁻¹, area leaf⁻¹, leaf relative water content (RWC), proline (Pro) content, total chlorophyll (Total Chl) content, electrolyte leakage (EL), malondialdehyde (MDA), hydrogen peroxide (H₂O₂) content, and activities of catalase (CAT), peroxidase (POD) and superoxide dismutase (SOD) of genotypes of faba bean. Drought stress reduced all growth parameters and Total Chl content of all genotypes. However, the deteriorating effect of drought stress on the growth performance of genotypes “C5” and “Zafar 1” were relatively low due to its better antioxidant enzymes activities (CAT, POD and SOD), and accumulation of Pro and Total Chl, and leaf RWC. In the study, genotype “C5” and “Zafar 1” were found to be relatively tolerant to drought stress and genotypes “G853” and “C4” were sensitive to drought stress.     

An Improved Method for Determining Medium- and Long-Chain FAMEs Using Gas Chromatography

The existing protocols for analyzing fatty acid methyl esters (FAMEs) using a one-step acetyl chloride (AC) catalyzed transesterification and extraction procedure cannot accurately determine the medium- and long-chain fatty acids simultaneously in clinical (enteral, parenteral) formulations. For example: (1) addition of AC at room temperature generates an exothermic reaction that often results in loss of sample and possible injury to the analyst; (2) certain polyunsaturated fatty acids (PUFAs) are less stable at elevated temperatures during the transesterification and contribute to the over-estimation of the C16:0 and C18:1 fatty acids; and (3) the flame-ionization detector (FID) response varies depending on the carbon chain length of the fatty acids, that consequently impacts the underestimation of medium-chain fatty acid (C6–C10) recoveries. To overcome these deficiencies and accurately determine FAMEs, we have developed an improved one-step transesterification method that employs the addition of AC in tubes kept on a dry ice bath, the transesterification at room temperature, and the data analysis using relative response factors. Using this modified protocol, we determined the fatty acid composition of lipid emulsions (Omegaven^® and Lipidem^®) on a Shimadzu GC2010 gas chromatography (GC) system using a capillary GC column (Zebron ZB-WAX plus, 30 m, 0.25 mm ID, 0.25 μm). Our data suggest that the improved method can be easily used to accurately determine fatty acids (C6–C24) in functional foods and lipid emulsions.     

Hydrolytic Depolymerization of PET in a Microwave Reactor

Recycling of PET was examined using hydrolytic depolymerization in an alkaline solution under microwave irradiation. The reaction was carried out in a sealed microwave reactor in which the pressure and temperature were controlled and recorded. The main products were the monomers TPA and EG. The effect of reaction temperature, time, amount of PET and alkaline concentration on the degree of PET depolymerization and TPA recovery was investigated. Microwave irradiation was found to reduce the time needed to achieve a specific degradation of PET significantly, with almost complete depolymerization occurring in 30 min at 180 °C and only 46 W of microwave power. Using a phase transfer catalyst (TOMAB) resulted in the same amount of unreacted PET but at significantly lower depolymerization temperatures.