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991.
针对无线传感器网络中节点因干扰过大导致重传能耗增加, 进而节点过早失效、网络生命期缩短的问题, 根据网络拓扑信息和路由信息设计节点的负载模型, 从而构建了节点的生命期模型. 然后利用博弈论将路径增益、交叉干扰和节点生命期等性能参数融入到效益函数中, 构建信道分配博弈模型. 理论分析证明该博弈模型存在纳什均衡. 进而运用最佳回应策略, 在所构建的信道分配博弈模型的基础上, 设计了一种优化网络生命期的抗干扰信道分配算法. 该算法使节点在选择信道时避免与网络中交叉干扰较大的节点和生命期较小的节点使用相同信道, 实现干扰小、能耗低且均衡的信道选择. 理论分析与仿真结果证明该算法最终能够快速地收敛到纳什均衡, 且具有较小的信息复杂度, 从而减小算法本身的通信能耗. 同时, 该算法具有良好的抗干扰性和信道均衡性, 能够有效地延长网络生命期. 相似文献
992.
Highly selective label free colorimetric sensor based on AgNPs stabilized by phenolic chelating ligand, N,N′-bis(2-hydroxybenzyl)-1,2-diaminobenzene (1), for NO2− anions has been developed. Addition of NO2− showed selective decolourisation of brownish yellow colour of 1-AgNPs with the detection limit of 10−7 M. Absorption studies showed the complete disappearance of 1-AgNPs peak at 426 nm due to the conversion of AgNPs to silver ions. The presence silver ions were confirmed by white precipitates of AgCl formation with NaCl. The interference studies confirmed the high selectivity of NO2− sensing in presence of anions as well as cations by 1-AgNPs. A linear relationship was observed between the change of absorption and concentration of NO2−. The present approach could be performed at room temperature and ambient conditions. The practical applications of 1-AgNPs for selective sensing of NO2− in different water samples such as ground, river, pond and tap water have also been demonstrated. 相似文献
993.
Shan Liu Maochao WeiAuthor Vitae Xiangli ZhengAuthor VitaeShuai XuAuthor Vitae Changli Zhou 《Analytica chimica acta》2014
We are just beginning to exploit the fascinating potential of thionine, called electrochemical probe that can selectively recognize specific polycyclic aromatic hydrocarbons (PAHs), as tools for the detection of tricyclic aromatic hydrocarbons phenanthrene (PHE) and anthracene (ANT). A novel electrochemical sensing platform by modification of electroactive thionine functionalized graphene onto glass carbon electrode (Th/GRs/GCE) surface was constructed. The immobilized thionine showed a remarkable stability, which may benefit from the π–π stacking force with graphene. Under optimum conditions, the proposed electrochemical sensor exhibited high sensitivity and low detection limit for detecting PHE and ANT. The total amount of PHE and ANT could be quantified in a wide range of 10 pM–0.1 μM with a good linearity (R2 = 0.9979) and a low detection limit of 0.1 pM (S/N = 3). Compounds which possess one or two benzene rings or PAHs with more than three rings, such as benzene, naphthalene (NAP), benzo[a]pyrene (BaP) and pyrene (PYR) show little interference on the detection. Consequently, a simple and sensitive electrochemical method was proposed for the determination of PHE and ANT, which was used to determine PHE and ANT in waste water samples. The electrochemical method provides a general tool that complements the commonly used spectroscopic methods and immune method for the detection of PAHs. 相似文献
994.
María Cuartero Jonathan Sabaté del Río Pascal Blondeau Joaquín A. Ortuño F. Xavier Rius Francisco J. Andrade 《Analytica chimica acta》2014
The development of a solid-contact potentiometric sensor based on conducting rubbers using a carbon nanotubes ink is described here. Commercial rubbers are turned into conductive ones by a simple and versatile method, i.e. painting an aqueous dispersion of single-walled carbon nanotubes on the polymer surface. On this substrate, both the working ion-selective electrode and the reference electrode are built in order to form an integrated potentiometric cell. As a proof-of-principle, selective potassium electrodes are fully characterized giving comparable performances to conventional electrodes (sensitivity, selectivity, stability, linear range, limit of detection and reproducibility). As an application of the rubber-based electrodes, a bracelet was constructed to measure potassium levels in artificial sweat. Since rubbers are ubiquitous in our quotidian life, this approach offers great promise for the generation of chemical information through daily objects. 相似文献
995.
Kundan Tayade Amanpreet Kaur Sandesh Tetgure G. Krishana Chaitanya Narinder Singh Anil Kuwar 《Analytica chimica acta》2014
The (13E,19E)-N1′,N3′-bis[4-(diethylamino)-2-hydroxybenzylidene]malonohydrazide (L) has been developed for the detection of Th4+ ions using dual channel signalling system. The UV–vis absorbance and fluorescence spectroscopic data revealed the formation of L–Th4+ complex in 1:1 equilibrium. The density functional theory (DFT) also confirms the optimum binding cavity for the recognition of metal ion. The binding constant computed from different mathematical models for an assembly of L–Th4+. The detection limit of L for Th4+ recognition is to a concentration down to 0.1 μM (0.023 μg g−1). The present sensing system is also successfully applied for the detection of Th4+ ion present in soil near nuclear atomic plants. 相似文献
996.
Sanjukta A. Kumar Neha Thakur Harshala J. Parab Shailaja P. Pandey Rakesh N. Shinde Ashok K. Pandey Sangita D. Kumar A.V.R. Reddy 《Analytica chimica acta》2014
A visual strip has been developed for sensing iron in different aqueous samples like natural water and fruit juices. The sensor has been synthesized by UV-radiation induced graft polymerization of acrylamide monomer in microporous poly(propylene) base. For physical immobilization of iron selective reagent, the in situ polymerization of acrylamide has been carried out in the presence of 1,10-phenanthroline. The loaded strip on interaction with Fe(II) in aqueous solution turned into orange red color and the intensity of the color was found to be directly proportional to the amount of Fe(II) in the aqueous sample. The minimal sensor response with naked eye was found for 50 ng mL−1 of Fe in 15 min of interaction. However, as low as 20 ng mL−1 Fe could be quantified using a spectrophotometer. The detection limit calculated using the 3s/S criteria, where ‘s’ is the standard deviation of the absorbance of blank reagent loaded strip and ‘S’ is the slope of the linear calibration plot, was 1.0 ng mL−1. The strip was applied to measure Fe in a variety of samples such as ground water and fruit juices. 相似文献
997.
A molecularly imprinted copolymer, poly(o-phenylenediamine-co-o-aminophenol) (PoPDoAP), was prepared as a new ascorbic acid (AA) sensor. The copolymer was synthesized by incorporation of AA as template molecules during the electrochemical copolymerization of o-phenylenediamine and o-aminophenol, and complementary sites were formed after the copolymer was electrochemically reduced in ammonium aqueous solution. The molecularly imprinted copolymer sensor exhibited a high sensitivity and selectivity toward AA. Differential pulse voltammograms (DPVs) showed a linear concentration range of AA from 0.1 to 10 mM, and the detection limit was calculated to be 36.4 μM. Compared to conventional polyaniline-based AA sensors, the analytical performance of the imprinted copolymer sensor was improved due to the broadened usable pH range of PoPDoAP (from pH 1.0 to pH 8.0). The sensor also exhibited a good reproducibility and stability. And it has been successfully applied in the determination of AA in real samples, including vitamin C tablet and orange juices, with satisfactory results. 相似文献
998.
Construction and Validation of New Electrochemical Carbon Nanotubes Sensors for Determination of Acebutolol Hydrochloride in Pharmaceuticals and Biological Fluids
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A simple, rapid and a highly selective method for direct electrochemical determination of acebutolol hydrochloride (AC) was developed. The developed method was based on the construction of three types of sensors conventional polymer (I), carbon paste (II) and modified carbon nanotubes (MCNTs) carbon paste (III). The fabricated sensors depend mainly on the incorporation of acebutolol hydrochloride with phosphotungstic acid (PTA) forming ion exchange acebutolol‐phosphotungstate (AC‐PT). The performance characteristics of the proposed sensors were studied. The sensors exhibited Nernstian responses (55.6 ± 0.5, 57.14 ± 0.2 and 58.6 ± 0.4 mV mol L?1) at 25 °C over drug concentration ranges (1.0 × 10?6‐1.0 × 10?2, 1.0 × 10?7‐1.0 × 10?2 and 5.0 × 10?8‐1.0 × 10?2 mol L?1 with lower detection limits of (5.0 × 10?7, 5.0 × 10?8 and 2.5 × 10?8 mol L?1 for sensors (I), (II) and (III), respectively. The influence of common and possible interfering species, pharmaceutical additives and some related pharmacological action drugs was investigated using separate solution method and no interference was found. The stability indicating using forced degradation of acebutolol hydrochloride was studied. The standard addition method was used for determination of the investigated drug in its pharmaceutical dosage forms and biological fluids. The results were validated and statistically analysed and compared with those from previously reported methods. 相似文献
999.
1000.
Manoj K. KesharwaniMoorthy Suresh Amitava Das Bishwajit Ganguly 《Tetrahedron letters》2011,52(28):3636-3639
The computational and experimental studies have revealed that even simple molecule like borazine can act as a sensor for fluoride ions. This study further reported the various binding modes of analytes using quantum chemical calculations and the nature of such interactions have been examined using electron density surface analysis. Total charge transfer analysis (qCT) correlates well with the binding affinities of analytes with the borazine receptor. 相似文献