Isotactic and syndiotactic polypropylene/multi-wall carbon nanotube composites: synthesis and properties

Isotactic polypropylene (iPP) and syndiotactic polypropylene (sPP) nanocomposites containing 0.1–3.5 wt.% multi-wall carbon nanotubes (MWCNTs) have been synthesized via in situ polymerization method with the use of C₂- and C_s- symmetry zirconocenes activated by methylaluminoxane (MAO) in liquid propylene medium. Fracture morphology studies by SEM reveal different MWCNT dispersion efficiency in various polymer matrices, which arises from the catalytic peculiarities of the composite synthesis. Considerable Young’s modulus enhancement of iPP and sPP (25–66%) takes place even at low MWCNT loadings (below 0.5 wt.%). The obtained nanocomposites can find use as efficient electromagnetic shielding materials and microwave absorbing filters due to relatively low permittivity values and considerable dielectric losses in microwave range. Calorimetry data demonstrate that MWCNTs exert evident influence as nucleating agents causing the rise of iPP and sPP crystallization temperature. Considerable retardation effect on iPP thermal oxidative degradation has been observed: the temperature of maximal weight loss rate rises by ~52 °C upon incorporating only 1.4 wt.% MWCNTs.     

Avalanche‐Discharge‐Induced Electrical Forming in Tantalum Oxide‐Based Metal–Insulator–Metal Structures

Oxide‐based metal–insulator–metal structures are of special interest for future resistive random‐access memories. In such cells, redox processes on the nanoscale occur during resistive switching, which are initiated by the reversible movement of native donors, such as oxygen vacancies. The formation of these filaments is mainly attributed to an enhanced oxygen diffusion due to Joule heating in an electric field or due to electrical breakdown. Here, the development of a dendrite‐like structure, which is induced by an avalanche discharge between the top electrode and the Ta₂O_5‐x layer, is presented, which occurs instead of a local breakdown between top and bottom electrode. The dendrite‐like structure evolves primarily at structures with a pronounced interface adsorbate layer. Furthermore, local conductive atomic force microscopy reveals that the entire dendrite region becomes conductive. Via spectromicroscopy it is demonstrated that the subsequent switching is caused by a valence change between Ta⁴⁺ and Ta⁵⁺, which takes place over the entire former Pt/Ta₂O_5‐x interface of the dendrite‐like structure.     

Stress update algorithm for the combined viscoplastic and plastic behaviours of single‐crystal superalloys

A crystallographic constitutive model is developed, which accounts for both rate‐sensitive and rate‐insensitive flow. Single‐crystal plasticity and viscoplasticity are the limiting cases of the model, so that it properly reflects the material response over a wide temperature range. A non‐linear dynamic recovery is included to properly describe ratchetting. We provide a robust integration scheme based on generalization of the return‐mapping algorithm and of the procedure for active set search. The implicit integration and consistent tangent are implemented through the UMAT subroutine in the ABAQUS finite element program. The capability of the model to account for both high and low strain rates is demonstrated in numerical examples. Finally, the stability of integration scheme and quadratic convergence of the global Newton–Raphson equilibrium iterations are demonstrated on the example of a notched bar under tension. Copyright © 2011 John Wiley & Sons, Ltd.     

Effect of temperature on aggregation/dissociation behavior of interpolymer complexes stabilized by hydrogen bonds

The effect of temperature on the aggregation/dissociation behavior of interpolymer complexes based on poly(acrylic acid) and various nonionic polymers—poly(vinyl pyrrolidone), poly(ethylene oxide), poly(acrylamide), hydroxypropylcellulose, hydroxyethylcellulose, poly(vinyl methyl ether), poly(vinyl ether of ethyleneglycol), and vinyl ether of ethyleneglycol‐co‐vinyl butyl ether—has been studied in aqueous solutions. It was shown that nonionic polymers could be classified into two groups according to the stability of their polycomplexes with respect to temperature. The first group of nonionic polymers forms interpolymer complexes, which are stable and undergo further aggregation upon increase in temperature. The second group forms polycomplexes, which dissociate at higher temperatures. The nature of forces stabilizing different interpolymer complexes in aqueous solutions is discussed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1946–1950, 2004     

Supramolecular Amphiphiles Based on Pillar[5]arene and Meroterpenoids: Synthesis,Self-Association and Interaction with Floxuridine

In recent years, meroterpenoids have found wide biomedical application due to their synthetic availability, low toxicity, and biocompatibility. However, these compounds are not used in targeted drug delivery systems due to their high affinity for cell membranes, both healthy and in cancer cells. Using the approach of creating supramolecular amphiphiles, we have developed self-assembling systems based on water-soluble pillar[5]arene and synthetic meroterpenoids containing geraniol, myrtenol, farnesol, and phytol fragments. The resulting systems can be used as universal drug delivery systems. It was shown by turbidimetry that the obtained pillar[5]arene/synthetic meroterpenoid systems do not interact with the model cell membrane at pH = 7.4, but the associates are destroyed at pH = 4.1. In this case, the synthetic meroterpenoid is incorporated into the lipid bilayer of the model membrane. The characteristics of supramolecular self-assembly, association constants and stoichiometry of the most stable pillar[5]arene/synthetic meroterpenoid complexes were established by UV-vis spectroscopy and dynamic light scattering (DLS). It was shown that supramolecular amphiphiles based on pillar[5]arene/synthetic meroterpenoid systems form monodisperse associates in a wide range of concentrations. The inclusion of the antitumor drug 5-fluoro-2′-deoxyuridine (floxuridine) into the structure of the supramolecular associate was demonstrated by DLS, 19F, 2D DOSY NMR spectroscopy.     

Open innovation in Russian state-owned enterprises

ABSTRACT

This paper studies open innovation practices in Russian state-owned enterprises (SOEs). In 2011, the Russian Government set ambitious goals in science, technology and innovation, and uses its large SOEs as channels to achieve these targets. These initiatives focus on the collaboration among innovation actors and introduce open innovation (OI) principles. Based on a large-scale innovation survey, we compare private enterprises to state-owned peers and present selected case studies. Our data support the claim that Russian SOEs are driving the demand for technology and mainly absorb incoming OI activities. Different to their peers, SOEs extend their OI activities to the country’s knowledge producers, such as research and technology organisations (RTOs), and leading universities. They work on incorporating scientific knowledge that could, indeed, hold the key to globally competitive technological innovations, but also have better capabilities to include business partners.

Abbreviation : OI: Open innovation; SOE: State-owned enterprise; RTO: Research and technology organisation; STI: Science, technology and innovation.     

Multi-physics modeling of doxorubicine binding to ion-exchange resin in blood filtration devices

A group of drugs used in intra-arterial chemotherapy (IAC) have intrinsic ionic properties, which can be used for filtering excessive drugs from blood in order to reduce systemic toxicity. The ion-exchange mechanism is utilized in an endovascular Chemofilter device which can be deployed during the IAC for capturing ionic drugs after they have had their effect on the tumor. In this study, the concentrated solution theory is used to account for the effect of electrochemical forces on the drug transport and adsorption by introducing an effective diffusion coefficient in the advection–diffusion–reaction equation. Consequently, a multi-physics model coupling hemodynamic and electrochemical forces is developed and applied to simulations of the transport and binding of doxorubicine in the Chemofilter device. A comparison of drug adsorption predicted by the computations to that measured in animal studies demonstrated the benefits of using the concentrated solution theory over the Nernst–Plank relations for modeling drug binding.     

Influence of addition of nanosize barium cerate on the microstructure and properties of top-seeded melt growth YBCO bulk superconductors

Barium cerate (BaCeO₃) is one of the possible additions to bulk YBa₂Cu₃O₇ single-grain superconductors to suppress the growth of Y₂BaCuO₅ (Y211) particles. This paper investigates the synthesis of barium cerate powder and its use in YBa₂Cu₃O₇ bulk superconductors. Crystalline barium cerate was synthesized by solid-state reaction, by co-precipitation of oxalates and by sol-gel method. Final calcination was held in air or in vacuum. It is shown that the most efficient in refining Y211 is nanocrystalline barium cerate prepared by sol-gel method calcined in vacuum. The effective refinement of Y211 particles occurred over the entire interval of nanocrystalline BaCeO₃ addition from 0.38 to 1.90 wt%. The optimal concentration of nanosize barium cerate was determined, microstructure and superconducting properties were characterized. The effect of Y211 content on trapped field in YBCO bulks with addition of nanocrystalline barium cerate is shown.     

Fluid Mixing for Low‐Power ‘Digital Microfluidics’ Using Electroactive Molecular Monolayers

A switchable electrode, which relies on an indium‐tin oxide conductive substrate coated with a self‐assembled monolayer terminated with an anthraquinone group (AQ), is reported as an electrowetting system. AQ electrochemical features confer the capability of yielding a significant modulation of surface wettability as high as 26° when its redox state is switched. Hence, an array of planar electrodes for droplets actuation is fabricated and integrated in a microfluidic device to perform mixing and dispensing on sub‐nanoliter scale. Vehiculation of cells across microfluidic compartments is made possible by taking full advantage of surface electrowetting in culture medium.     

Corrosion of YBCO bulk superconductor in air

A corrosion process caused by reaction of surfaces of oxygenation cracks of YBCO bulk single‐grain superconductor with air moisture was studied. X‐ray photo‐emission spectroscopy, done on air exposed (001) surfaces, confirmed oxygen bonds related to barium hydroxide. Thermal analyses and mass spectrometry of exposed samples has shown a release of water caused by decomposition of barium hydroxide hydrates during sample heating. The sample weight increase versus time was related to formation of barium hydroxide phases at the surfaces of oxygenation cracks. The morphological changes of these phases at heating were observed with scanning electron microscope.