Nested self-similar wrinkling patterns in skins

Stiff thin films on soft substrates are both ancient and commonplace in nature; for instance, animal skin comprises a stiff epidermis attached to a soft dermis. Although more recent and rare, artificial skins are increasingly used in a broad range of applications, including flexible electronics, tunable diffraction gratings, force spectroscopy in cells, modern metrology methods, and other devices. Here we show that model elastomeric artificial skins wrinkle in a hierarchical pattern consisting of self-similar buckles extending over five orders of magnitude in length scale, ranging from a few nanometres to a few millimetres. We provide a mechanism for the formation of this hierarchical wrinkling pattern, and quantify our experimental findings with both computations and a simple scaling theory. This allows us to harness the substrates for applications. In particular, we show how to use the multigeneration-wrinkled substrate for separating particles based on their size, while simultaneously forming linear chains of monodisperse particles.     

Managing the introduction of information security awareness programmes in organisations

Several studies explore information security awareness focusing on individual and/or organisational aspects. This paper argues that security awareness processes are associated with interrelated changes that occur at the organisational, the technological and the individual level. We introduce an integrated analytical framework that has been developed through action research in a public sector organisation, comprising actor-network theory (ANT), structuration theory and contextualism. We develop and use this framework to analyse and manage changes introduced by the implementation of a security awareness programme in the research setting. The paper illustrates the limitations of each theory (ANT, structuration theory and contextualism) to study multi-level changes when used individually, demonstrates the synergies of the three theories, and proposes how they can be used to study and manage awareness-related changes at the individual, organisational and technological level.     

Classification of Gait Patterns Using Kinematic and Kinetic Features,Gait Dynamics and Neural Networks in Patients with Unilateral Anterior Cruciate Ligament Deficiency

Neural Processing Letters - The anterior cruciate ligament (ACL) plays an important role in controlling knee joint stability. The literature provides conflicting information on whether patients...     

Inline method of droplet and particle size distribution analysis in dilute disperse systems

In the present article a measurement method of particle size distributions (PSD) in industrial installations which use a dispersed phase of low concentration (like spray dryers or spray scrubbers) is introduced. A new type of inline-measurement system has been developed and designed to work in spray drying conditions. A standard digital camera is used to record shadows of flowing particles inside the spray drying chamber. Collected images were analyzed by a newly developed software which recognizes particles only in the focus area and eliminates several types of artifacts. The constructed prototype of the PSD inline-analyzer was installed and used to monitor large laboratory scale spray dryer. All data collected by the designed system during the spray drying experiments were compared with data measured with an offline reference system to show accuracy of the new measurement technique.     

Rapid formation of soft hydrophilic silicone elastomer surfaces

We report on the rapid formation of hydrophilic silicone elastomer surfaces by ultraviolet/ozone (UVO) irradiation of poly(vinylmethyl siloxane) (PVMS) network films. Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes). We also provide evidence that the brief UVO irradiation treatment does not cause dramatic changes in the surface modulus of the PVMS network. We compare the rate of formation of hydrophilic silicone elastomer surfaces made of PVMS to those of model poly(dimethyl siloxane) (PDMS) and commercial-grade PDMS (Sylgard-184). We find that relative to PVMS, 20 times longer UVO treatment times are needed to oxidize the PDMS network surfaces in order to achieve a comparable density of surface-bound hydrophilic moieties. The longer UVO treatment times for PDMS are in turn responsible for the dramatic increase in surface modulus of UVO treated PDMS, relative to PVMS. We also study the formation of self-assembled monolayers (SAMs) made of semifluorinated organosilane precursors on the PVMS-UVO and PDMS-UVO network surfaces. By tuning the UVO treatment times and by utilizing mono- and tri-functional organosilanes we find that while mono-functionalized organosilanes attach directly to the substrate, SAMs of tri-functionalized organosilanes form in-plane networks on the underlying UVO-modified silicone elastomer surface, even with only short UVO exposure times.     

Release of Zn, Ni, Cu, SO4(2-) and CrO4(2-) as a function of pH from cement-based stabilized/solidified refinery oily sludge and ash from incineration of oily sludge

A framework for the evaluation of leaching behavior of inorganic constituents from stabilized/solidified refinery oily sludge and ash produced from incineration of oily sludge with cement was employed. Metal and anion release as a function of pH was investigated. The leaching test consisted of multiple parallel extractions at pH range from 2 to 12. Remarkably good immobilization >98% was observed for metals of solidified ash at pH>6 and >93% of solidified oily sludge at pH>7. Sulfate leaching was high at pH range 2-12. The leaching behavior of metals and anions was simulated by VMINTEQ. The calculations showed that leaching behavior of Zn, Ni and Cu was controlled by chemical equilibrium and surface complexation onto ferrihydrite, at the pH range 2-12. The dominant solid phases that controlled metal leachability were metal hydroxides. The dominant mechanism that described sulfate leaching was found to be chemical equilibrium. Sulfate and also chromate leachability was controlled by Ettringite and Cr(VI)Ettringite as the major minerals affecting their release.     

Cement-based stabilization/solidification of oil refinery sludge: Leaching behavior of alkanes and PAHs

Stabilization/solidification is a process widely applied for the immobilization of inorganic constituents of hazardous wastes, especially for metals. Cement is usually one of the most common binders for that purpose. However, limited results have been presented on immobilization of hydrocarbons in cement-based stabilized/solidified petroleum solid waste. In this study, real oil refinery sludge samples were stabilized and solidified with various additions of I42.5 and II42.5 cement (Portland and blended cement, respectively) and subject to leaching. The target analytes were total petroleum hydrocarbons, alkanes and 16 polycyclic aromatic hydrocarbons of the EPA priority pollutant list. The experiments showed that the waste was confined in the cement matrix by macroencapsulation. The rapture of the cement structure led to the increase of leachability for most of the hydrocarbons. Leaching of n-alkanes from II42.5 cement-solidified samples was lower than that from I42.5 solidified samples. Leaching of alkanes in the range of n-C(10) to n-C(27) was lower than that of long chain alkanes (>n-C(27)), regardless the amount of cement addition. Generally, increasing the cement content in the solidified waste samples, increased individual alkane leachability. This indicated that cement addition resulted in destabilization of the waste. Addition of I42.5 cement favored immobilization of anthracene, benzo[a]anthracene, benzo[b]fluoroanthene, benzo[k]fluoroanthene, benzo[a]pyrene and dibenzo[a,h]anthracene. However, addition of II42.5 favored 5 out of 16, i.e., naphthalene, anthracene, benzo[b]fluoroanthene, benzo[k]fluoroanthene and dibenzo[a,h]anthracene.     

On the kinematics of multiple manipulator space free-flyers and their computation

In this article, two basic approaches for kinematics modelling of multiple manipulator space free-flying robots (SFFRs) are developed. In the barycentric vector approach, the center of mass of the whole system is taken as a representative point for the translational motion of the system, and a set of body-fixed vectors which reflect both geometric configuration and mass distribution of the system are used. On the other hand, the direct path method relies on taking a point on the base body (preferably its center of mass) as the representative point for the translational motion of the system. The consequences of using each of the two approaches in deriving dynamics equations and in control design of SFFRs are discussed. It is revealed that the direct path method is a more appropriate approach for modelling multiple arm systems, in the presence of external forces/torques (i.e., free-flying mode). A 14 degree-of-freedom space free-flying system is considered as a benchmark system and a quantitative comparison between the two approaches is presented. The results show that the direct path method requires significantly less computations for position and velocity analyses. © 1998 John Wiley & Sons, Inc.     

Electron Holes in G-Quadruplexes: The Role of Adenine Ending Groups

The study deals with four-stranded DNA structures (G-Quadruplexes), known to undergo ionization upon direct absorption of low-energy UV photons. Combining quantum chemistry calculations and time-resolved absorption spectroscopy with 266 nm excitation, it focuses on the electron holes generated in tetramolecular systems with adenine groups at the ends. Our computations show that the electron hole is placed in a single guanine site, whose location depends on the position of the adenines at the 3′ or 5′ ends. This position also affects significantly the electronic absorption spectrum of (G⁺)^● radical cations. Their decay is highly anisotropic, composed of a fast process (<2 µs), followed by a slower one occurring in ~20 µs. On the one hand, they undergo deprotonation to (G-H2)^● radicals and, on the other, they give rise to a reaction product absorbing in the 300–500 nm spectral domain.