电力系统动态消息编码技术

为方便通信双方在未协商通信内容情况下动态、高效地交换模型和数据,提出了电力系统动态消息编码技术。该编码技术采用二进制自描述方式描述大型电力系统模型和数据,共有四种编码方式:M0用于兼容抽象语法标记(ASN.1);M1在ASN.1的基础上加入名字选项,用于少量数据的结构化描述;M2扩展编码头部,编码效率高;M3扩展编码头部,描述类信息。实际使用中,首次通信时使用M3发送类型和结构信息,其后通信使用M2发送数据;当类型和结构发生变化时,再次发送类型和结构信息,有效地解决了数据量和维护的矛盾问题。     

Fundamental Theories on a Combined Energy Cycle of an Electrostatic Induction Hydrogen Electrolytic Cell and Fuel Cell to Produce Fully Sustainable Hydrogen Energy

A hydrogen electrolyzer for decomposition of stable compound H₂O is essentially an electronic device that uses mainly electrostatic‐to‐chemical energy conversion to produce a stoichiometric H₂+O₂ fuel. To achieve a breakthrough in the practical hydrogen electrolytic cell, we demonstrate the electrostatic induction potential superposed electrolyzer. This system operates on a mechanism in which, on a theoretical basis, the power used is 17% of the total electrical energy required, while the remaining 83% can be provided by electrostatic energy free of power. Because H₂O is placed in its decomposition state in the electrostatic field where no current flows, the decomposition voltage is identified as a barrier potential that the electrolytic current must overcome by expending the major part of the total system power. The potential superposition method for supplying energy to the cell was found to avoid the barrier potential effect within the laws of thermodynamics. Combining a fuel cell for producing power from pure H₂ and O₂ in stoichiometric proportions with this type of hydrogen electrolytic cell in a closed energy cycle can achieve a highly positive H₂ balance.     

换流站站用电备自投装置设计及整定

为了保证直流输电工程换流站站用电设备安全稳定运行,必须合理设计站用电系统及备用电源自动投入装置的动作逻辑。以糯扎渡直流输电工程普洱换流站为例,根据主接线形式、运行要求和具体运行工况,对10 k V备自投的五种运行工况分别设计了备自投充放电逻辑和十三种动作投切逻辑,对400 V备自投单母分段运行方式设计了两种动作投切逻辑。同时,对备自投装置的定值整定原则及定值配合相关问题进行了研究,给出了推荐定值。所提出的备自投方案经现场实际运行证明:通过10 k V和400 V两级备自投装置的配合,在各种运行工况下某路或某两路站用电源失电时备自投装置都能快速动作投切至备用电源,无需降低直流输送功率或停运,大大提高了直流系统的可靠性。     

Development of a superporous hydroxyethyl cellulose‐based hydrogel by anionic surfactant micelle templating with fast swelling and superabsorbent properties

The self‐assembling anionic surfactant, sodium n‐dodecyl sulfonate (SDS) micelles were used as pore‐forming templating for fabricating novel superporous hydroxyethyl cellulose‐grafting‐poly(sodium acrylate)/attapulgite (HEC‐g‐PNaA/APT) hydrogels. The network characteristics, morphologies of the hydrogels and removing of SDS micelles from the final product by washing with ethanol/water (v/v, 7 : 3) procedure were determined by Fourier transform infrared spectroscopy and scanning electron microscopy, as well as by determination of swelling ratio, swelling rate, and stimuli response to salts and pHs. The results showed that the added‐SDS concentration significantly affected the morphologies and pore structure of the hydrogel, and 2 mM SDS facilitates to form a homogeneous and well‐defined pore structure in the gel network to extremely improve the swelling ratio and swelling rate. The 2 mM SDS‐added superporous HEC‐based hydrogel not only had highest equilibrium swelling ratio (Q_eq, 1118, 102 g g^?1 in distilled water and 0.9 wt % NaCl solution), rapid swelling rate (k_is, 5.2840 g g s^?1), also showed multistimulus responses to salts and pHs, which may allow its applications in several areas such as adsorption, separation and biomedical materials. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42027.     

Intelligent micellar polymeric nanocarriers for therapeutics and diagnosis

Polymeric micelles can be designed and synthesized to bear polymeric blocks with different hydrophilicities; this triggers their self‐assembly into micellar aggregates similar to those generated with traditional surfactants. The basic structure consists of a hydrophobic core, capable of containing guest substances, and a hydrophilic shell, which stabilizes the payload and protects it from external degradation or prevents its quick elimination from the body. The accumulation of block copolymer micelles (BCMs) in a target cell or tissue can be accomplished by two main mechanisms, passive and active targeting; this allows the payload release at the site of action when desired. Hence, in this general overview, we pay special attention to newly developed single‐stimulus‐ and multi‐stimuli‐responsive delivery systems capable of disassembling and reassembling (in some cases) as a response to changes in their physicochemical properties. Also, special interest is also devoted to multifunctional BCMs incorporating multiple therapeutic agents and/or multiple imaging contrast agents, which can be considered the new generation (third generation) of drug‐delivery systems, that is, nanotheranostic platforms. Finally, a summary of BCM‐based drug‐delivery systems currently under clinical trials is given. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42650.     

Multiscale approach to the morphology,structure, and segmental dynamics of complex degradable aliphatic polyurethanes

A multiscale approach spanning from the segmental (subnanometer) up to micrometer level was applied for detailed study of the self‐assembly of aliphatic block polyurethane (PU) elastomers. To understand the principles of the self‐organization of hard and soft segments in the complex multi‐component systems, several two‐component model PU samples, that is, the products of 1,6‐diisocyanatohexane (HDI) with three diols differing in the length and constitution were also prepared, characterized, and investigated: (i) polycarbonate‐based macrodiol (MD), (ii) biodegradable oligomeric diol (DL‐L; product of butane‐1,4‐diol and D,L‐lactide), and (iii) butane‐1,4‐diol (BD). The study (particularly ¹³C‐¹H PILGRIM NMR spectra) reveals complex internal organization and interesting (application appealing) behavior of multi‐component PUs. Hard segments (HDI+BD products) feature self‐assembled and significantly folded chain conformations with interdomain spacing 15–22 nm (small‐angle X‐ray scattering analysis). The small domains are hierarchically assembled in various structural formations of µm size (spherulites) depending on PU composition, as detected by transmission electron microscopy and atomic force microscopy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41590.     

Preparation and monovalent selective properties of multilayer polyelectrolyte modified cation‐exchange membranes

This study reports the modification of commercial cation‐exchange membrane by layer‐by‐layer adsorption of polyethyleneimine and poly(acrylic acid) (PAA) to endow them with monovalent ion selectivity. The chemical and morphological changes of the modified membrane surface were examined by ATR‐FTIR and SEM, respectively. The permselectivity for monovalent cations of the membranes was investigated by electrodialysis experiments. The effects of deposited bilayer number, the salt concentration, and pH of the dipping polyelectrolyte solutions on selectivity were investigated. Meanwhile, the resistance of membranes was measured taking energy consumption into consideration. The polyelectrolyte multilayer was crosslinked using epichlorohydrin to improve stability, and the durability of the composite membrane was studied. Separation mechanism of the composite membrane was also investigated. It is demonstrated that the bivalent cations are mainly rejected by electrostatic repulsion from the positive charge on the surface of the composite membranes. The sieving effect of the dense structure of skin layer becomes more pronounced with the number of deposited layers increased. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41488.     

Use of a CO2‐switchable hydrophobic associating polymer to enhance viscosity–response

A series of copolymers, poly(acrylamide)‐co‐poly(N,N‐dimethylaminoethyl methacrylate)‐co‐poly(N‐cetyl DMAEMA) (abbreviation PDAMCn), was synthesized with different monomer ratios. The resulting copolymer solution shows pronounced viscosity–response property which is CO₂‐triggered and N₂‐enabled. Electrical conductivity experiment shows that tertiary amine group on DMAEMA experiences a protonate and deprotonate transition upon CO₂ addition and its removal. In addition, different incorporation rates of DMAEMA leads to two kinds of morphological change in the presence of CO₂ and thus induces different rheological behaviors. PDAMCn incorporating longer hydrophobic monomer (C₁₈DM) show more pronounced initial viscosity and higher critical stress required to cause network deformation, which consequently enhances the viscosity–response property of the solution. The addition of NaCl could also tune the viscosity of PDAMCn solution. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41468.