Transient and steady-state deformations and breakup of dispersed-phase droplets of immiscible polymer blends in steady shear flow

Transient and steady-state deformations and breakup of viscoelastic polystyrene droplets dispersed in viscoelastic high-density polyethylene matrices were observed in a simple steady shear flow between two transparent parallel disks. By separately varying the elasticities of the individual blend components, the matrix shear viscosity, and the viscosity ratio, their effects on the transient deformation, steady-state droplet size, and the breakup sequence were determined. After the startup of a steady shear flow, the viscoelastic droplet initially exhibits oscillations of its length in the flow direction, but eventually stretches preferentially in the vorticity direction. We find that at fixed capillary number, the oscillation amplitude decreases with increasing droplet elasticity, while the oscillation period depends primarily on, and increases with, the viscosity ratio. At steady-state, the droplet length along the vorticity direction increases with increasing capillary number, viscosity ratio, and droplet elasticity. Remarkably, at a viscosity ratio of unity, the droplets remain in a nearly undeformed state as the capillary number is varied between 2 and 8, apparently because under these conditions a tendency for the droplets to widen in the vorticity direction counteracts their tendency to stretch in the flow direction. When a critical capillary number, Ca_c, is exceeded, the droplet finally stretches in the vorticity direction and forms a string which becomes thinner and finally breaks up, provided that the droplet elasticity is sufficiently high. For a fixed matrix shear stress and droplet elasticity, the steady-state deformation along the vorticity direction and the critical capillary number for breakup both increase with increasing viscosity ratio.     

Evaluation of sampling units and sampling plans for adults of Cryptolestes ferrugineus (Coleoptea: Laemophloeidae) in stored wheat under different temperatures, moisture contents, and adult densities

Development and evaluation of optimum size and number of sample units is required for cost-effective management of stored grain beetles. In this study, we evaluated the sampling parameters and accuracy of insect density detection and estimation, developed the optimum size and number of sample units, and conducted a feasibility study of the insect detection and density estimation. The measured insect densities in 92% of random samples were less than the introduced insect densities and 67.4 ± 10.8% of random samples did not contain adults when the introduced insect density was 0.1 A/kg (adult/kg). If the random sampling technique was used and 15% of the stored wheat bulk was sampled, 72% of determined means of insect densities of the sampling sets were lower than the introduced insect densities. Increasing the size of sample units did not improve the accuracy of the estimation of insect densities; however, it did considerably increase the probability of insect detection when insect densities were lower than 1.0 A/kg. We recommend at least 7 kg per sample unit for insect detection (especially when insect densities < 0.1 A/kg) and the optimum number of sample units with 15 kg grain per unit should be >24 for a fixed precision of 0.35 when insect densities < 0.1 A/kg. This might be a challenge for grain storage practice. Therefore, using sampling technique to estimate insect densities and detect insects at low insect densities (<0.1 A/kg) might not be practicable.     

The affinity of cholera toxin for Ni2+ ion

Cholera toxin (CT) was shown to bind to immobilized Ni2+ ion. The affinityof CT for the complex required the presence of the Ni2+ ion, since CT wasunable to bind in its absence. Binding was mediated by the B-subunit (CTB)as both CT and CTB bound to the resin, but not the A- subunit (CTA).Binding was reversible in the presence of imidazole and suggested that theaffinity of CT for the Ni2+ ion was mediated by His residues. Theheat-labile enterotoxin of Escherichia coli (LT), which is closely relatedto CT, was unable to bind to the Ni2+ ion. Comparison of amino acidsequences revealed the presence of three His residues in CT (positions 13,57 and 94), but only one in LT (position 57). To confirm that the residuesat positions 13 and 94 of CTB were responsible for the binding, they werechanged to residues found in LTB. Changing His13-->Arg completelyabrogated the ability of CTB to bind to Ni2+ ion. In contrast, the mutationof His 94-->Asn reduced, but did not abrogate, the ability of CTB tobind to Ni2+ ion. Based on calculated interatomic distances, it is unlikelythat His13 and His94 are part of the same complex. There appear to be twoseparate binding sites, with the principal site involving His13 and a muchweaker site involving His94. This latter site can only participate inbinding if the complex involving His13 has formed.     

Model for reaction‐assisted polymer dissolution in LIGA

A new chemically oriented mathematical model for the development step of the LIGA process is presented (LIGA is an acronym for the German words Lithographie, Galvanoformung, and Abformung). The key assumption is that the developer can react with the polymeric resist material to increase the solubility of the latter, thereby partially overcoming the need to reduce the polymer size. The ease with which this reaction takes place is assumed to be determined by the number of side‐chain scissions that occur during the X‐ray exposure phase of the process. The dynamics of the dissolution process are simulated by the solution of the reaction diffusion equations for this three‐component, two‐phase system, the three species being the unreacted and reacted polymers and the solvent. The mass fluxes are described by multicomponent diffusion (Stefan–Maxwell) equations, and the chemical potentials are assumed to be given by the Flory–Huggins theory. Sample calculations are used to determine the dependence of the dissolution rate on key system parameters such as the reaction rate constant, polymer size, solid‐phase diffusivity, and Flory–Huggins interaction parameters. A simple photochemistry model is used to relate the reaction rate constant and the polymer size to the absorbed X‐ray dose. The resulting formula for the dissolution rate as a function of the dose and temperature is fit to an extensive experimental database to evaluate a set of unknown global parameters. The results suggest that reaction‐assisted dissolution is very important at low doses and low temperatures, the solubility of the unreacted polymer being too small for it to be dissolved at an appreciable rate. However, at high doses or at higher temperatures, the solubility is such that the reaction is no longer needed, and dissolution can take place via the conventional route. These results provide an explanation for the observed dependences of both the rate of dissolution and its activation energy on the absorbed dose. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 25–37, 2005     

Future directions in physiochemical modeling of the thermodynamics of polyelectrolyte coacervates

We review theories of polyelectrolyte (PE) coacervation, which is the spontaneous association of oppositely charged units of PEs and phase separation into a polymer-dense phase in aqueous solution. The simplest theories can be divided into “physics-based” and “chemistry-based” approaches. In the former, PEs are treated as charged, long-chain, molecules, defined by charge level, chain length, and chain flexibility, but otherwise lacking chemical identity, with electrostatic interactions driving coacervation. The “chemistry-based” approaches focus on the local interactions between the species for which chemical identity is critical, and describe coacervation as the result of competitive local binding interactions of monomers and salts. In this article, we show how these approaches complement each other by presenting recent approaches that take both physical and chemical effects into account. Finally, we suggest future directions toward producing theories that are made quantitatively predictive by accounting for both long range electrostatic and local chemically specific interactions.     

The formation of nanostructured surfaces by electrochemical techniques: a range of emerging surface finishes. Part 2: examples of nanostructured surfaces by plating and anodising with their applications

In part 1 of this review, emerging practice to realise nanostructured metallic coatings by electrodeposition, anodising and electrophoresis has been considered. Conventional, aqueous electrolytes may be utilised in some cases if workpiece preparation and process conditions are well controlled. Such coatings can provide wear and corrosion resistance or a catalytic or high active area compared to more conventional coatings. An overview of the principles involved in deploying electrochemical techniques to produce nanostructured surfaces and factors influencing developments in this rapidly emerging field were considered. The strategies, which can be adopted to electrodeposit nanostructured metallic coatings, include grain refinement, application of a pulsed current, inclusion of nanoparticles into the coating and the use of nanoporous templates. In part 2, examples of nanostructured coatings and their properties are illustrated with research findings from the authors’ laboratory and the literature. Nanostructured metallic coatings include nanocrystalline, functionally graded, nanocomposite and recently introduced hierarchical structures. The potential uses for these coatings in engineering industries (including tribology and energy conversion) are summarised. Finally, future developments necessary to realise and deploy the coatings in increasingly demanding environments are considered.     

A guide to the crystallographic analysis of icosahedral viruses

Determining the structure of an icosahedral virus crystal by X-ray diffraction follows very much the same course as conventional protein crystallography. The major differences arise from the relatively large sizes of the particles, which significantly affect the data collection process, data processing and management, and later, the refinement of a model. Most of the other differences are due to the high 5 3 2 point group symmetry of icosahedral viruses. This alters dramatically the means by which initial phases are obtained by molecular substitution, extended to higher resolution by electron density averaging and density modification, and the refinement of the structure in the light of high non-crystallographic symmetry. In this review, we attempt to lead the investigator through the various steps involved in solving the structure of a virus crystal. These steps include the purification of viruses, their crystallization, the recording of X-ray diffraction data, and its reduction to structure amplitudes. It further addresses the problems attending phase determination and ultimately the refinement of a model. Finally, we describe the unique properties of virus crystals and the factors that influence their physical and diffraction properties.     

The view from the top

The challenge of integrating large amounts of renewable energy resources into the electric sector requires updated transmission analysis techniques. Economic planning, primarily in the form of value-based planning over interconnectionwide areas, is needed before performing the traditional single-hour, capacity-based reliability analyses.     

Clinical management of carpal tunnel syndrome: a 12-year review of outcomes

Carpal tunnel syndrome (CTS) is a disorder frequently encountered by occupational health care specialists. The health care management of this disorder has involved a diverse set of clinical procedures. The present article is a review of the literature related to CTS with an emphasis on occupational-related CTS. MEDLINE, Cumulative Index to Nursing and Allied Health Literature, PsycLIT, and NIOSHTIC databases from 1985-1997 were searched for treatment outcome studies related to CTS. Treatments of interest included surgery, physical therapy, drug therapy, chiropractic treatment, biobehavioral interventions, and occupational rehabilitation. A systematic review of the effects of these interventions on symptoms, medical status, function, return to work, psychological well-being, and patient satisfaction was completed. Compared to other treatments, the majority of studies assessed the effects of surgical interventions. Endoscopic release was associated with higher levels of physical functioning and fewer days to return to work when compared to open release. Limited evidence indicated: 1) steroid injections and oral use of B6 were associated with pain reduction; 2) in comparison to splinting, range of motion exercises appeared to be associated with less pain and fewer days to return to work; 3) cognitive behavior therapy yielded reductions in pain, anxiety, and depression; and, 4) multidisciplinary occupational rehabilitation was associated with a higher percentage of chronic cases returning to work than usual care. Workers' compensation status was associated with increased time to return to work following surgery. Conclusions are preliminary due to the small number of well-controlled studies, variability in duration of symptoms and disability, and the broad range of reported outcome measures. While there are several opinions regarding effective treatment, there is very little scientific support for the range of options currently used in practice. Despite the emerging evidence of the multivariate nature of CTS, the majority of outcome studies have focused on single interventions directed at individual etiological factors or symptoms and functional limitations secondary to CTS.