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The tracking of a moving object with a mobile robot has been implemented based on the detected sound from the moving object using a microphone array. The difference between the travel times of the sound source to each of the three microphones mounted to the robot has been used to calculate the distance and orientation of the sound source. The cross-correlations between the received signals have been used to detect the individual sound signal from the object and to calculate the time difference between two signals. This provides reliable and precise time differences among the sound signals arrived at the microphones compared to the conventional method. In order to determine the tracking direction to the sound source, Fuzzy rules have been applied; the results are used for real-time control of the mobile robot. The efficiency of the proposed algorithm has been demonstrated through real-world experiments and compared to the conventional approach.  相似文献   
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The atom transfer radical polymerization (ATRP) of methyl methacrylate catalyzed by copper–tripodal complexes with ferrocene moieties (CuX/TRENFcImine, where X is Br or Cl, and TRENFcImine is tris‐[2‐(ferrocenylmethyleneimino)ethyl]amine) was investigated to understand the effect of redox active moieties on the performance of ATRP catalysts. The CuBr/TRENFcImine system was highly active, with 82% conversion in 2 h. However, the polymerization became slower at higher molar ratios of monomer to catalyst. The polydispersity index was broad, and the initiation efficiency was relatively low. On the basis of the conformational analysis, the highly active and less controlled polymerization was probably caused by the electronic effect rather than the steric effect on the ferrocene moieties, which led to the higher and lower values in the activation and deactivation steps, respectively. The polydispersity index was improved by the addition of CuBr2, but this led to slower rates of polymerization. The effect of halide groups on ATRP caused a faster rate in the CuBr/TRENFcImine polymerization system than in the CuCl/TRENFcImine system. The higher molar ratio of monomer to catalyst had no significant effect on the CuCl/TRENFcImine system. Nonetheless, the trace of water in the CuCl2·2H2O system accelerated the rate of propagation, which led to a higher molecular weight. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   
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A series of tris(R‐methyltriazolylmethyl)amines [R = C6H5 ( 1 ), 4‐FC6H4 ( 2 ), 4‐MeOC6H4 ( 3 ), Fc ( 4 )] were prepared and used as ligands for catalytic ATRP of methyl methacrylate (MMA). Despite a lower activity, the CuBr/ 4 catalyst promoted relatively well controlled polymerization compared to CuBr/ 1 , as evidenced by narrower polydispersity indices. Meanwhile, no polymerization activity was observed with CuBr/ 2 and CuBr/ 3 under the catalytic conditions investigated. The CV measurements of CuBr2 complexes supported 1 and 4 in DMSO showed E1/2 values of –0.206 and –0.224 V, respectively, confirming the more electron‐rich nature of CuBr/ 4 . Although both CuBr/ 1 and CuBr/ 4 catalysts were only partially soluble in several organic solvents used, kinetic studies revealed a pseudo first order linear plot of ln[M]0/[M]t versus time. Addition of CuBr2 into the polymerization systems led to a decrease in polymer polydispersities and the observed rate constants (kobs). © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   
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