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Wireless Networks - In Wireless Sensor Networks (WSNs), where power consumption is a huge concern, the improvement of the network’s lifetime is an area of constant study and innovation. The...  相似文献   
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Security is becoming an everyday concern for a wide range of electronic systems that manipulate, communicate, and store sensitive data. An important and emerging category of such electronic systems are battery-powered mobile appliances, such as personal digital assistants (PDAs) and cell phones, which are severely constrained in the resources they possess, namely, processor, battery, and memory. This work focuses on one important constraint of such devices-battery life-and examines how it is impacted by the use of various security mechanisms. In this paper, we first present a comprehensive analysis of the energy requirements of a wide range of cryptographic algorithms that form the building blocks of security mechanisms such as security protocols. We then study the energy consumption requirements of the most popular transport-layer security protocol: Secure Sockets Layer (SSL). We investigate the impact of various parameters at the protocol level (such as cipher suites, authentication mechanisms, and transaction sizes, etc.) and the cryptographic algorithm level (cipher modes, strength) on the overall energy consumption for secure data transactions. To our knowledge, this is the first comprehensive analysis of the energy requirements of SSL. For our studies, we have developed a measurement-based experimental testbed that consists of an iPAQ PDA connected to a wireless local area network (LAN) and running Linux, a PC-based data acquisition system for real-time current measurement, the OpenSSL implementation of the SSL protocol, and parameterizable SSL client and server test programs. Based on our results, we also discuss various opportunities for realizing energy-efficient implementations of security protocols. We believe such investigations to be an important first step toward addressing the challenges of energy-efficient security for battery-constrained systems.  相似文献   
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Laser induced plasma emission spectra from highT c superconducting samples of YBa2Cu3O7 and GdBa2Cu3O7 obtained with 1.06μm radiation from a Q switched Nd:YAG laser beam has been analysed. The results clearly show the presence of diatomic oxides in addition to ionized species of the constituent metals in the plasma thus produced.  相似文献   
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This article describes the formation and characterization of self‐assembled nanoparticles of controlled sizes based on amphiphilic block copolymers synthesized by ring‐opening metathesis polymerization. We synthesized a novel hydrophobic derivative of norbornene; this monomer could be polymerized using Grubbs' catalyst [Cl2Ru(CHPh)(PCy3)2] forming polymers of controlled molecular weight. We synthesized amphiphilic block copolymers of controlled composition and showed that they assemble into nanoparticles of controlled size. The nanoparticles were characterized using dynamic light scattering and transmission electron microscopy. Tuning the composition of the block copolymer enables the tuning of the diameters of the nanoparticles in the 30‐ to 80‐nm range. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3352–3359, 2004  相似文献   
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Polymerization of 2‐(diethylamino)ethyl methacrylate (DEAEMA) via homogeneous atom transfer radical polymerization under various reaction conditions is described. The effects of the initiators and solvents were examined. With 1,1,4,7,10,10‐hexamethyl triethylenetetramine/copper(I) chloride/p‐toluenesulfonyl chloride as the ligand/catalyst/initiator system in methanol, poly(DEAEMA) with a polydispersity index as low as 1.07 was synthesized. Kinetic studies demonstrated the polymerization was very well controlled and exhibited the living characteristic of the process. Well‐defined block copolymers of DEAEMA and tert‐butyl methacrylate (tBMA) were successfully synthesized. The copolymers could be synthesized with equally good results by starting with either p(DEAEMA) or p(tBMA) as the macroinitiators. However, only the macroinitiators terminated with chlorine should be used. The corresponding macroinitiators with bromine as a transferable group did not yield well‐defined copolymers. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2688–2695, 2003  相似文献   
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We have given design of a very small residual dispersion fiber system consisting of a small dispersion fiber(SDF) with flat modal field and a corresponding dual core coaxial dispersion compensating fiber (DCF).  相似文献   
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A series of symmetrical dimers consisting of salicylaldimine moieties connected by flexible alkylene central spacer via ether linkages has been synthesized. In order to validate the empirical rule suggested by Date et al. to account for the smectic behaviour of such dimers, the chain length of the terminal alkoxy chain has been kept constant (C8) while the number of methylene units in the central spacer was varied from C3 to C11. Another aim of the present investigation was to understand structure-property relationship in these dimers in which the salicylaldimine mesogenic segment has been used for the first time in dimers. The mesomorphic behaviour of these dimers was evaluated using optical microscopy and differential scanning calorimetry and the structure of some of the mesophases has been further investigated with the help of X-ray diffraction. Our studies reveal that the dimers consisting of 3 to 8 methylene units in the flexible spacer show only smectic (smectic C and smectic A) phases. For the dimers containing 4, 6 and 8 methylene units in the central spacer, a unique filament growth pattern has been observed in the smectic A phase while cooling from the isotropic phase. The dimers containing of C9 to C11 methylene groups exhibit the nematic phase in addition to smectic modifications. This observation indicates that when the terminal chains are shorter than the spacer, the tendency to form smectic phases is not fully extinguished but is perhaps reduced.  相似文献   
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