1,048 research outputs found
Finite element analysis of a fluid-structure interaction in flexible pipe line
This paper describes the basic theory and computing method for transient flow of liquid in flexible pipe such as rubber tubing and arterial system. A mathematical model taking into account tube wall axial and radial motion (in which the dynamic fluid pressure causes circumferential and axial motion of the tube wall) is presented. The tube wall is assumed to be elastic material and the compressibility of the liquid is neglected. Circumferential and axial strain-stress relationships for the tube are considered. The obtained mathematical system is constituted of four non-linear hyperbolic partial differential equations describing the wave propagation in both pipe wall and liquid flow. The fluid-structure interaction is found to be governed by Poisson’s ratio. In this steady finite element method based on Galerkin formulation is applied. Numerical results show a good similarity with those of the literature obtained by the characteristics method.Key words : Fluid-structure interaction, flexible pipe, rubber, finite element method
Cognitive Radio Networks: Realistic or Not?
A large volume of research has been conducted in the cognitive radio (CR)
area the last decade. However, the deployment of a commercial CR network is yet
to emerge. A large portion of the existing literature does not build on real
world scenarios, hence, neglecting various important interactions of the
research with commercial telecommunication networks. For instance, a lot of
attention has been paid to spectrum sensing as the front line functionality
that needs to be completed in an efficient and accurate manner to enable an
opportunistic CR network architecture. This is necessary to detect the
existence of spectrum holes without which no other procedure can be fulfilled.
However, simply sensing (cooperatively or not) the energy received from a
primary transmitter cannot enable correct dynamic spectrum access. For example,
the low strength of a primary transmitter's signal does not assure that there
will be no interference to a nearby primary receiver. In addition, the presence
of a primary transmitter's signal does not mean that CR network users cannot
access the spectrum since there might not be any primary receiver in the
vicinity. Despite the existing elegant and clever solutions to the DSA problem
no robust, implementable scheme has emerged. In this paper, we challenge the
basic premises of the proposed schemes. We further argue that addressing the
technical challenges we face in deploying robust CR networks can only be
achieved if we radically change the way we design their basic functionalities.
In support of our argument, we present a set of real-world scenarios, inspired
by realistic settings in commercial telecommunications networks, focusing on
spectrum sensing as a basic and critical functionality in the deployment of
CRs. We use these scenarios to show why existing DSA paradigms are not amenable
to realistic deployment in complex wireless environments.Comment: Work in progres
Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation
The analysis of some extra- and intragenic markers within or closely linked to the cystic fibrosis transmembrane regulator (CFTR) gene is useful as a molecular method in clinical linkage analysis. Indeed, knowing that the molecular basis of cystic fibrosis (CF) is highly heterogeneous in our population, the study of haplotype association with normal and CF chromosomes could be very helpful in cases where one or both mutations remain unidentified. In this study, we analysed with PCR-RFLP and capillary electrophoresis some extra (pJ3.11, KM19 and XV2C) and intragenic (IVS8CA, IVS17bTA and IVS17bCA) polymorphic markers in 50 normal and 10 Tunisian patients carrying the rare E1104X mutation in order to determine the haplotype associated with this mutation. For the extragenic markers, 8 haplotypes were identified. The most frequent of them are the 221 and 112 accounting for 80% of total haplotypes. For the intragenic markers, five haplotypes were present on the E1104X chromosomes. One of them 16-31-13 accounted for 50%. To our knowledge, this is the first work to be interested to the haplotypes linked to the E1104X mutation. This preliminary study of haplotypes could be a helpful method to determine the molecular lesions responsible of this pathology
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