942 resultados para ARM COORDINATION
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介绍了基于ARM和DSP的CSR主环磁场电源控制系统的设计和开发。系统以以太网作为连接各个单元的传输介质,以ARM板卡作为以太网中的一个通信节点,由DSP板卡完成实际的电源控制。实验表明控制效果良好,超过了预期的设计目标。
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以ARM(S3C4510B)、CPLD(XC95288XL)和微控制器(MSP430F149)为核心进行实时多路数据采集和控制的冷却储存环(CSR)真空控制系统设计。着重分析了控制系统组成、工作原理、功能实现、硬件电路和软件开发。该控制系统具有适应性与灵活性强、响应速度快、精度高、稳定性好、可靠性高、性价比优越、自我连锁保护等优点,现已成功应用于CSR真空控制系统中。
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门禁系统主要负责对出入通道进行管制,是社区楼宇安全监控系统的一部分。传统的门禁系统通常采用密码识别、卡片识别的方式进行验证,由于密码、卡片容易被盗用、丢失,系统安全性不高。在通信方式上传统门禁系统通常采用RS485或者RS232连接,传输距离、速度和连接终端数均受限制。本文提出的人像识别门禁系统解决方案采用ARM-Linux系统平台,依靠社区宽带综合业务网的传输和存储能力,结合密码、RFID和人像识别三种识别方式,利用网络技术和生物识别技术达到识别率高、响应速度快、扩展能力强的要求,并能够与驻地网的其它业务集成,提供业务级的联动服务。此外,该门禁系统还支持用户使用电话开门,由服务器完成对用户来电的识别和防伪验证。本文工作的主要贡献是:参与了ARM-Linux系统的裁剪、移植和声卡驱动的修改;建立了ARM-Linux交叉编译环境;完成了门禁前端软件系统的整体设计和实现;完成了服务器软件电话呼叫响应子系统的设计。
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Through tuning the length of flexible bis(triazole) ligands and different metal ion coordination geometries, four Wells-Dawson polyoxoanion-based hybrid compounds, [Cu-6(btp)(3)(P2W18O62)] center dot 3H(2)O (1) (btp = 1,3-bis(1,2,4-triazol-1-yl)propane), [Cu-6(btb)(3)((P2W18O62) center dot 2H(2)O (2), [Cu-3(btb)(6)(P2W18O62)] center dot 6H(2)O (btb = 1,4-bis(1,2,4-triazol-1-yl)butane) (3), and [Cu-3(btx)(5.5)((P2W18O62) center dot 4H(2)O (btx = 1,6-bis(1,2,4-triazol-1-yl)hexane) (4), were synthesized and structurally characterized. in compound 1, the metal-organic motif exhibits a ladder-like chain, which is further fused by the ennead-dentate [P2W18O62](6-) anions to construct a 3D structure. In compound 2, the metal-organic motif exhibits an interesting Cu-btb grid layer, and the ennead-dentate polyoxoanions are sandwiched by two Cu-btb layers to construct a 3D structure
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Reactions of zinc(II) or cadmium(II) salts with terephthalic acid (H(2)tp) and 1,3-bis(4-pyridyl) propane (bpp) have afforded four coordination polymers at room temperature, [Zn(mu-tp)(mu-bpp)](n)center dot 2nH(2)O (1), [Cd-2(mu-tp)(2)(mu-bpp)(3)](n)center dot 2nH(2)O (2), [Cd(mu-tp)(mu-bpp)(H2O)](n)center dot nH(2)O (3), and [Cd-2(mu-tp)(mu-bpp)(2)(bpp)(2)Br-2](n) (4). Single-crystal X-ray diffraction has revealed interesting topological features for these compounds.
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A novel porous material constructed from p-sulfonatocalix[4]arene molecules and a Ag-I coordination polymer has been structurally characterized. The porous supramolecular complex features a bilayer arrangement of p-sulfonatocalix[4]arene molecules linked by a Ag-I-hmt (hmt: hexamethylene- tetramine) coordination polymer through metal-ligand bonding, hydrogen bonding and host-guest interactions.
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A porous material with cobalt-oxygen cluster framework has been synthesized hydrothermally, which possesses large and rigid channels and manifests strong antiferromagnetic interactions, and the pyridinedicarboxylate ligand exhibits two types of rare coordination modes.
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Two highly connected cobalt(II) and zinc(II) coordination polymers with tetranuclear metal clusters as the nodes of network have been prepared, being the first example of an 8-connected self-penetrating net based on a cross-linked alpha-Po subnet.
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A supramolecular complex [Cu(phen)(2)H2O]{[Cu(phen)(H2O)](2)[C6AS]}center dot 2.5H(2)O (phen = 1,10'-phenanthroline and C6AS = p-sulfonatocalix[6]arene) has been synthesized under hydrothermal condition, and characterized by IR spectroscopy, TG analysis and single crystal X-ray diffraction. In the structure, unprecedented 1D ({[Cu(phen)(H2O)](2)[C(6)AS]}(2-))(n) coordination chains (exactly being belts) are stacked into some 2D layers by the pi center dot center dot center dot pi stacking interactions, which are further interconnected into a 3D extended structure by hydrogen bonding.
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A new approach to one-dimensional organization of gold nanoparticles (2-4 nm) is described, using poly(4-vinylpyridine) (P4VP) molecular chain as a template with the mediation of free Cu2+ ion coordination. The assembly was conducted on freshly prepared mica surfaces and in aqueous solution, respectively. The surface assembly was characterized by tapping mode atomic force microscopy (AFM), observing the physisorbed molecules in their chain-like conformation with an average height of 0.4 nm.