10 research outputs found

    From M-ary Query to Bit Query: a new strategy for efficient large-scale RFID identification

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    The tag collision avoidance has been viewed as one of the most important research problems in RFID communications and bit tracking technology has been widely embedded in query tree (QT) based algorithms to tackle such challenge. Existing solutions show further opportunity to greatly improve the reading performance because collision queries and empty queries are not fully explored. In this paper, a bit query (BQ) strategy based Mary query tree protocol (BQMT) is presented, which can not only eliminate idle queries but also separate collided tags into many small subsets and make full use of the collided bits. To further optimize the reading performance, a modified dual prefixes matching (MDPM) mechanism is presented to allow multiple tags to respond in the same slot and thus significantly reduce the number of queries. Theoretical analysis and simulations are supplemented to validate the effectiveness of the proposed BQMT and MDPM, which outperform the existing QT-based algorithms. Also, the BQMT and MDPM can be combined to BQMDPM to improve the reading performance in system efficiency, total identification time, communication complexity and average energy cost

    Idle-slots elimination based binary splitting anti-collision algorithm for RFID

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    Tag collision avoidance is critical to the success of data communications in radio frequency identification (RFID) system. This paper presents an efficient idle-slots elimination based binary splitting (ISE-BS) algorithm to improve the performance of RFID system. In ISE-BS, by introducing 1 bit random number Q and 16-bits random number serial identifier (SID)which are transmitted before data exchange, tag collisions can be informed and unnecessary data exchange between reader and tags can be further eliminated. Moreover, ISE-BS exploits Q to separate conflicting tags into ‘0-1’ subsets randomly. Specifically, the tags in subset ‘0’ will start to transmit in the next period, where the success flag signal reflects the immediate data transmission. The tags in subset ‘1’ will wait in the pipeline. In such a way, the idle slots introduced by conventional binary splitting anti-collision algorithms can be removed with schedule of ISEBS. Extensive simulation results show that ISE-BS outperforms the existing proposed algorithms

    Capture-aware identification of mobile RFID tags with unreliable channels

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    Radio frequency identification (RFID) has been widely applied in large-scale applications such as logistics, merchandise and transportation. However, it is still a technical challenge to effectively estimate the number of tags in complex mobile environments. Most of existing tag identification protocols assume that readers and tags remain stationary throughout the whole identification process and ideal channel assumptions are typically considered between them. Hence, conventional algorithms may fail in mobile scenarios with unreliable channels. In this paper, we propose a novel RFID anti-collision algorithm for tag identification considering path loss. Based on a probabilistic identification model, we derive the collision, empty and success probabilities in a mobile RFID environment, which will be used to define the cardinality estimation method and the optimal frame length. Both simulation and experimental results of the proposed solution show noticeable performance improvement over the commercial solutions

    Uncertainty in Artificial Intelligence: Proceedings of the Thirty-Fourth Conference

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    Non-covalent interactions in organotin(IV) derivatives of 5,7-ditertbutyl- and 5,7-diphenyl-1,2,4-triazolo[1,5-a]pyrimidine as recognition motifs in crystalline self- assembly and their in vitro antistaphylococcal activity

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    Non-covalent interactions are known to play a key role in biological compounds due to their stabilization of the tertiary and quaternary structure of proteins [1]. Ligands similar to purine rings, such as triazolo pyrimidine ones, are very versatile in their interactions with metals and can act as model systems for natural bio-inorganic compounds [2]. A considerable series (twelve novel compounds are reported) of 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine (dbtp) and 5,7-diphenyl- 1,2,4-triazolo[1,5-a]pyrimidine (dptp) were synthesized and investigated by FT-IR and 119Sn M\uf6ssbauer in the solid state and by 1H and 13C NMR spectroscopy, in solution [3]. The X-ray crystal and molecular structures of Et2SnCl2(dbtp)2 and Ph2SnCl2(EtOH)2(dptp)2 were described, in this latter pyrimidine molecules are not directly bound to the metal center but strictly H-bonded, through N(3), to the -OH group of the ethanol moieties. The network of hydrogen bonding and aromatic interactions involving pyrimidine and phenyl rings in both complexes drives their self-assembly. Noncovalent interactions involving aromatic rings are key processes in both chemical and biological recognition, contributing to overall complex stability and forming recognition motifs. It is noteworthy that in Ph2SnCl2(EtOH)2(dptp)2 \u3c0\u2013\u3c0 stacking interactions between pairs of antiparallel triazolopyrimidine rings mimick basepair interactions physiologically occurring in DNA (Fig.1). M\uf6ssbauer spectra suggest for Et2SnCl2(dbtp)2 a distorted octahedral structure, with C-Sn-C bond angles lower than 180\ub0. The estimated angle for Et2SnCl2(dbtp)2 is virtually identical to that determined by X-ray diffraction. Ph2SnCl2(EtOH)2(dptp)2 is characterized by an essentially linear C-Sn-C fragment according to the X-ray all-trans structure. The compounds were screened for their in vitro antibacterial activity on a group of reference staphylococcal strains susceptible or resistant to methicillin and against two reference Gramnegative pathogens [4] . We tested the biological activity of all the specimen against a group of staphylococcal reference strains (S. aureus ATCC 25923, S. aureus ATCC 29213, methicillin resistant S. aureus 43866 and S. epidermidis RP62A) along with Gram-negative pathogens (P. aeruginosa ATCC9027 and E. coli ATCC25922). Ph2SnCl2(EtOH)2(dptp)2 showed good antibacterial activity with a MIC value of 5 \u3bcg mL-1 against S. aureus ATCC29213 and also resulted active against methicillin resistant S. epidermidis RP62A
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