A Cross Layer Scheduling Framework for Supporting Bursty Data Applications in WCDMA Networks

In future wireless networks multimedia applications are expected to finally dominate the overall traffic volume. Shared channels are more suitable for the transmission of this type of traffic, as they are able to periodically adjust their transmission rate. In this paper, we introduce a cross-layer framework for WCDMA based networks which aims to make the packet scheduling procedure more efficient. In addition to that, we further propose a traffic scheduling scheme which serves the connections not only according to their delay sensitivity, but also according to the predicted state of their wireless channel. The efficiency of the proposed scheme, in terms of average packet delay and channel utilization is verified via simulations.     

Capability-Based Defenses Against DoS Attacks in Multi-path MANET Communications

We present the design, implementation, and evaluation of CapMan, a capability-based security mechanism that prevents denial-of-service (DoS) attacks against mobile ad-hoc networks (MANETs). In particular, our approach is designed to mitigate insider attacks that exploit multi-path routing to flood with packets on other participating nodes in the network. CapMan is instantiated on every node and enforces capability limits that effectively regulate the traffic for all end-to-end network flows. Each capability is issued and advertised by the capability distribution module, and is globally maintained via the capability enforcement logic. By periodically exchanging small usage summaries, all cooperating nodes are informed of the global network state in a scalable and consistent manner. The distribution of summaries empowers individual nodes to make informed decisions and regulate traffic as dictated by the per-flow capabilities across multiple dynamic routing paths. We implemented a prototype of CapMan as a module of the NS2 simulator. We conducted extensive simulations with the prototype using AOMDV as the underlying multi-path routing protocol. Both theoretical analysis and experimental results validate that our mechanism can effectively curtail sophisticated DoS attacks that target multi-path routing in MANETs. We can protect the overall network health even when both the initiator and the responder are malicious insiders and collude in an attempt to deprive the network of valuable resources. Finally, our results show that CapMan introduces relatively small and configurable network overhead and imposes minimal impact on non-attacking traffic flows.     

Smart Dust: Monte Carlo Simulation of Self-Organised Transport

Smart dust is envisaged as swarms of miniature communication/sensor devices useful for remote monitoring in space exploration. With diameters and densities comparable to sand particles the behaviour of passive dust will be identical to the movement of airborne sand. Here we examine algorithms for the adaptive shape change of smart dust modes that permits a change in drag coefficient depending on whether or not the random motion is in a favourable direction. Monte Carlo simulations are reported for swarms of smart dust devices transporting in the wind-dominated environment of the Martian landscape. It is concluded that relatively simple shape changing algorithms, activated through an electro-active polymer sheath, will permit self-organised transport over large distances.     

Low-temperature H2-SCR of NO on a novel Pt/MgO-CeO2 catalyst

The selective catalytic reduction of NO by H₂ under strongly oxidizing conditions (H₂-SCR) in the low-temperature range of 100–200 °C has been studied over Pt supported on a series of metal oxides (e.g., La₂O₃, MgO, Y₂O₃, CaO, CeO₂, TiO₂, SiO₂ and MgO-CeO₂). The Pt/MgO and Pt/CeO₂ solids showed the best catalytic behavior with respect to N₂ yield and the widest temperature window of operation compared with the other single metal oxide-supported Pt solids. An optimum 50 wt% MgO-50wt% CeO₂ support composition and 0.3 wt% Pt loading (in the 0.1–2.0 wt% range) were found in terms of specific reaction rate of N₂ production (mols N₂/g_cat s). High NO conversions (70–95%) and N₂ selectivities (80–85%) were also obtained in the 100–200 °C range at a GHSV of 80,000 h⁻¹ with the lowest 0.1 wt% Pt loading and using a feed stream of 0.25 vol% NO, 1 vol% H₂, 5 vol% O₂ and He as balance gas. Addition of 5 vol% H₂O in the latter feed stream had a positive influence on the catalytic performance and practically no effect on the stability of the 0.1 wt% Pt/MgO-CeO₂ during 24 h on reaction stream. Moreover, the latter catalytic system exhibited a high stability in the presence of 25–40 ppm SO₂ in the feed stream following a given support pretreatment. N₂ selectivity values in the 80–85% range were obtained over the 0.1 wt% Pt/MgO-CeO₂ catalyst in the 100–200 °C range in the presence of water and SO₂ in the feed stream. The above-mentioned results led to the obtainment of patents for the commercial exploitation of Pt/MgO-CeO₂ catalyst towards a new NO_x control technology in the low-temperature range of 100–200 °C using H₂ as reducing agent. Temperature-programmed desorption (TPD) of NO, and transient titration of the adsorbed surface intermediate NO_x species with H₂ experiments, following reaction, have revealed important information towards the understanding of basic mechanistic issues of the present catalytic system (e.g., surface coverage, number and location of active NO_x intermediate species, NO_x spillover).     

Mechanistic aspects of the water–gas shift reaction on alumina-supported noble metal catalysts: In situ DRIFTS and SSITKA-mass spectrometry studies

Steady-state isotopic transient kinetic analysis (SSITKA) experiments coupled with mass spectrometry were performed for the first time to study essential mechanistic aspects of the water–gas shift (WGS) reaction over alumina-supported Pt, Pd, and Rh catalysts. In particular, the concentrations (μmol g⁻¹) of active intermediate species found in the carbon-path from CO to the CO₂ product gas (use of ¹³CO), and in the hydrogen-path from H₂O to the H₂ product gas (use of D₂O) of the reaction mechanism were determined. It was found that by increasing the reaction temperature from 350 to 500 °C the concentration of active species in both the carbon-path and hydrogen-path increased significantly. Based on the large concentration of active species present in the hydrogen-path (OH/H located on the alumina support), the latter being larger than six equivalent monolayers based on the exposed noble metal surface area (θ > 6.0), the small concentration of OH groups along the periphery of metal-support interface, and the significantly smaller concentration (μmol g⁻¹) of active species present in the carbon-path (adsorbed CO on the noble metal and COOH species on the alumina support and/or the metal-support interface), it might be suggested that diffusion of OH/H species on the alumina support towards catalytic sites present in the hydrogen-path of reaction mechanism might be considered as a slow reaction step. The formation of labile OH/H species is the result of dissociative chemisorption of water on the alumina support, where the role of noble metal is to activate the CO chemisorption and likely to promote formate decomposition into CO₂ and H₂ products. It was found that there is a good correlation between the surface concentration and binding energy of CO on the noble metal (Pt, Pd or Rh) with the activity of alumina-supported noble metal towards the WGS reaction.     

Energy efficient network coding-based MAC for cooperative ARQ wireless networks

In this paper we introduce a network coding-aided energy efficient Medium Access Control (MAC) protocol that coordinates the transmissions among a set of relay nodes which act as helpers in cooperative Automatic Repeat reQuest-based (ARQ-based) wireless networks. Applying network coding techniques, we achieve to increase the energy efficiency of the network without compromising the system performance in terms of Quality of Service. Our proposed solution is evaluated by both analytical and simulation results.     

A molecular perspective of water at metal interfaces

Water/solid interfaces are relevant to a broad range of physicochemical phenomena and technological processes such as corrosion, lubrication, heterogeneous catalysis and electrochemistry. Although many fields have contributed to rapid progress in the fundamental knowledge of water at interfaces, detailed molecular-level understanding of water/solid interfaces comes mainly from studies on flat metal substrates. These studies have recently shown that a remarkably rich variety of structures form at the interface between water and even seemingly simple flat surfaces. In this Review we discuss the most exciting work in this area, in particular the emerging physical insight and general concepts about how water binds to metal surfaces. We also provide a perspective on outstanding problems, challenges and open questions.