Influence of cell shape and aggregate formation on the optical properties of flowing whole blood

We studied the influence of shape and secondary, or intercellular, organization on the absorption and scattering properties of red blood cells to determine whether these properties are of any practical significance for optical evaluation of whole blood and its constituents. A series of measurements of transmittance and reflectance of light from bovine blood in a flow cuvette was conducted with a 650-900-nm integrating sphere at shear rates of 0-1600 s(-1), from which the influence of cell orientation, elongation, and aggregate formation on the absorption (mu(a)) and the reduced scattering (mu(s)') coefficients could be quantified. Aggregation was accompanied by a decrease of 4% in mu(s)' compared with the value in randomly oriented single cells. Increasing the degree of cell alignment and elongation as a result of increasing shear rate reduced mu(s)' by 6% and mu(a) by 3%, evaluated at a shear rate of 1600 s(-1). Comparison with T-matrix computations for oblate- and prolate-shaped cells with corresponding elongation and orientation indicates that the optical properties of whole blood are determined by those of its individual cells, though influenced by a collective scattering factor that depends on the cell-to-cell organization. We demonstrate that cell morphological changes must be taken into consideration when one is conducting whole blood spectroscopy.     

Comparison of methods to assess pigment dispersion

Two inks made with different red pigments were evaluated by common methods to assess the degree of pigment dispersion. One pigment is more difficult to disperse than the other in the vehicle used. The five methods that could detect changes in dispersion with each pass over a three-roll mill were a light scattering particle size distribution analyzer, a NPIRI fineness of grind gauge, gloss, contrast ratio measurements, and rheology. The gloss and contrast ratio measurements could detect changes with each pass over a three-roll mill only with a significant reduction in pigment particle size. Presented at the 78th Annual Meeting of the Federation of Societies for Coatings Technology, on October 16–20, 2000, in Chicago, IL. Commercial Graphics Division, 207-BN-03 3M Center, St. Paul, MN 55144. Retired from 3M Corp. before publication.     

Properties of a reactive‐graphitic‐carbon‐nanofibers‐reinforced epoxy

Our previous studies showed that herringbone graphitic GNFs surface‐derivatized with reactive linker molecules bearing pendant primary amino functional groups capable of binding covalently to epoxy resins. Of special importance, herringbone GNFs derivatized with 3,4′‐oxydianiline (GNF‐ODA) were found to react with neat butyl glycidyl ether to form mono‐, di‐, tri‐, and tetra‐glycidyl oligomers covalently coupled to the ODA pendant amino group. The resulting reactive GNF‐ODA (butyl glycidyl)_n nanofibers, r‐GNF‐ODA, are especially well suited for reactive, covalent incorporation into epoxy resins during thermal curing. Based on these studies, nanocomposites reinforced by the r‐GNF‐ODA nanofibers at nanofiber loadings of 0.15–1.3 wt% were prepared. Flexural property of cured r‐GNF‐ODA/epoxy nanocomposites were measured through three‐point‐bending tests. Thermal properties, including glass transition temperature (T_g) and coefficient of thermal expansion (CTE) for the nanocomposites, were investigated using thermal mechanical analysis. The nanocomposites containing 0.3 wt% of the nanofibers gives the highest mechanical properties. At this 0.3‐wt% fiber loading, the flexural strength, modulus and breaking strain of the particular nanocomposite are increased by about 26, 20, and 30%, respectively, compared to that of pure epoxy matrix. Moreover, the T_g value is the highest for this nanocomposite, 14°C higher than that of pure epoxy. The almost constant change in CTEs before and after T_g, and very close to the change of pure epoxy, is in agreement with our previous study results on a chemical bond existing between the r‐GNF‐ODA nanofibers and epoxy resin in the resulting nanocomposites. POLYM. COMPOS., 28:605–611, 2007. © 2007 Society of Plastics Engineers     

10 nm TriGate High k Underlap FinFETs: Scaling Effects and Analog Performance

Nano scale devices with improved performance than the conventional CMOS devices is of great need in recent days. The paper investigates the performance of     

Hot Deformation Behaviour of AA2014–10 wt% SiC Composite

The hot compression behaviour of AA2014 alloy having 10 wt% SiC particles was studied over a wide range of temperatures (ambient to 400 °C) and strain rates (0.01–10/s). The results were compared with those obtained from identical tests performed on the base alloy to understand the effect of the SiC particle reinforcement. Processing maps were generated using dynamic materials model from the flow stress of the samples. Microstructures of the deformed samples suggest the occurrence of dynamic recrystallization at high temperatures and low strain rate. Flow localization and adiabatic shear bands were observed at higher strain rates and temperatures. The lack of cohesion between SiC particles and the matrix was found to be responsible for the deteriorating deformation behavior of the composite over most of the processing domains. The activation energy for high temperature deformation in the presence of the SiC particles in the alloy was found to be significantly higher than that of the matrix. This makes deformation processing of the composite more difficult than that of the matrix.     

Electron-induced dissociation of singly charged organic cations as a tool for structural characterization of pharmaceutical type molecules

Collision-induced dissociation (CID) and electron-induced dissociation (EID) have been investigated for a selection of small, singly charged organic molecules of pharmaceutical interest. Comparison of these techniques has shown that EID carried out on an FTICR MS and CID performed on a linear ion trap MS produce complementary data. In a study of 33 molecule-cations, EID generated over 300 product ions compared to 190 product ions by CID with an average of only 3 product ions per precursor ion common to both tandem MS techniques. Even multiple stages of CID failed to generate many of the product ions observed following EID. The charge carrying species is also shown to have a very significant effect on the degree of fragmentation and types of product ion resulting from EID. Protonated species behave much like the ammonium adduct with suggestion of a hydrogen atom from the charge carrying species strongly affecting the fragmentation mechanism. Sodium and potassium are retained by nearly every product ion formed from [M + Na](+) or [M + K](+) and provide information to complement the EID of [M + H](+) or [M + NH(4)](+). In summary, EID is proven to be a fitting partner to CID in the structural elucidation of small singly charged ions and by studying EID of a molecule-ion holding different charge carrying species, an even greater depth of detail can be obtained for functional groups commonly used in synthetic chemistry.     

Preparation, characterization and properties of acid functionalized multi-walled carbon nanotube reinforced thermoplastic polyurethane nanocomposites

The multi-walled carbon nanotube (MWNT) reinforced thermoplastic polyurethane (TPU) nanocomposites were prepared through melt compounding method followed by compression molding. The spectroscopic study indicated that a strong interfacial interaction was developed between carbon nanotube (CNT) and the TPU matrix in the nanocomposites. The microscopic observation showed that the CNTs were homogeneously dispersed throughout the TPU matrix well apart from a few clusters. The results from thermal analysis indicated that the glass transition temperature (T_g) and storage modulus (E′) of the nanocomposites were increased with increase in CNTs content and their thermal stability were also improved in comparison with pure TPU matrix. The rheological analysis showed the low frequency plateau of shear modulus and the shear thinning behavior of the nanocomposites. The electrical behaviors of the nanocomposites are increased with increase in weight percent (wt%) of CNT loading. The mechanical properties of nanocomposites were substantially improved by the incorporation of CNTs into the TPU matrix.     

Health Benefits of Punicic Acid: A Review

Punicic acid (PA) is a polyunsaturated fatty acid (18:3 n‐5), which is classified as a conjugated linolenic acid. PA is also referred as a "super CLnA" whose effect is even more potent than that of an ordinary CLnA. It is found mainly in the seeds of pomegranate fruit (Punica granatum) and Trichoxanthes kirilowii and some other minor sources. It possesses a wide array of biological properties including antidiabetic, antiobesity, antiproliferative, and anticarcinogenic activity against various forms of cancer. In spite of this, PA has not been explored as a nutraceutical or as an ingredient of food products which can be aimed at specific consumer target groups. This review details the various health‐beneficial properties of PA and explores the possibilities of its utilization as an active ingredient in various food products.     

Effect of Interparticle Potentials and Sedimentation on Particle Packing Density of Bimodal Particle Distributions During Pressure Filtration

Effect of interparticle forces, bimodal particle size distribution, and slurry viscosity on particle packing in alumina bodies consolidated by pressure filtration is presented. The requirements for packing colloidal particles to their highest density are strong repulsive interparticle forces and optimum particle size distribution. Even though these conditions are met, the high packing density in consolidated bodies may be adversely affected by particle segregation resulting from sedimentation. Therefore, the slurry during consolidation must have a sufficiently high viscosity to prevent sedimentation.