基于蛛状网拓扑智能变电站“三层一网”通信系统研究

在110kV及以下电压等级变电站中，“三层一网”架构虽然简化了二次系统接线，但实时性和可靠性难以保证。针对传统拓扑结构下的实时性和可靠性无法同时达到最优效果的问题，本文采用“三层一网”架构下蛛状网拓扑结构，仿真结果表明该结构下的通信系统实时性最佳，解决了传统拓扑结构实时性差的问题，并结合算例验证了其可行性；运用故障树分析法定量分析不同结构的可靠性，结果表明蛛状网结构的可靠性更好。为解决研究复杂的通信系统可靠性时传统故障树方法有一定的局限性的问题，本文引入T-S模糊故障理论，建立T-S故障树模型，计算结果表明蛛状网结构下通信系统可靠性最好。根据本文研究可以得到蛛状网拓扑结构能同时提高通信系统实时性和可靠性的结论。     

无模板剂法合成ZSM-35分子筛研究

在K+体系下研究了新型无模板剂无晶种法合成ZSM-35分子筛,并考察了SiO2/Al2O3、KOH/SiO2、H2O/SiO2、晶化时间、晶化温度对合成的影响.采用XRD(X射线衍射仪)、SEM(扫描电子显微镜)、XRF(X射线荧光衍射仪)等手段对分子筛的晶体结构和形貌进行表征.结果 表明,初始凝胶SiO2/Al2O3=37.3 ～ 45,KOH/SiO2=0.23 ～0.41,H2O/SiO2=24.1 ～ 34.2,晶化温度为160 ～170℃,晶化时间为4～8d可以合成出ZSM-35分子筛.当温度在160℃下合成7d所得样品的相对结晶度最高,当温度在170℃下合成4d为最佳合成条件.而且使用该方法合成出的ZSM-35分子筛形貌呈花瓣球状,片状花瓣大小介于358 nm～ 2.87 μm.     

节镍型奥氏体不锈钢的组织性能对比

针对200系J5A、J5两种牌号节镍型奥氏体不锈钢冷轧压延性能的差异,对比分析J5A、J5钢成分设计、组织、力学性能和马氏体含量,研究冷加工性能差异产生的机理。结果表明:由于J5A钢成分设计不合理,镍当量较低,奥氏体稳定性较差,马氏体转变点M_d(30/50)高,在轧制过程中产生大量冷加工变形诱变马氏体,加工硬化程度严重,压延性能差。     

基于介形类生态特征评价湖南某铀矿山地表水放射性环境

湖南某铀矿为我国一重要铀资源生产基地，长年的矿冶活动使该铀矿冶地域生态环境不可避免地遭到了一定程度破坏。本文以该铀矿冶地域介形类为研究对象，分析其分布与生态特征，并利用该生物评价本矿冶地域地表水放射性污染状况。结果表明，Cypridopsis vidua在溪流与河流中均有分布，Helerocypris incongruens仅发现于河流，两者丰度均不高。利用该两种介形类丰度及总丰度变化可指示水体铀浓度的变化，丰度越小，铀含量越大，反之亦然。Shannon-Wiener物种多样性指数与水体铀浓度呈明显负相关，表明也可利用介形类生物指数指示水体铀浓度。该生物指数明显偏低，说明该铀矿冶地域地表水环境质量需要改善，放射性污染应引起足够重视。     

Thermal-Disrupting Interface Mitigates Intercellular Cohesion Loss for Accurate Topical Antibacterial Therapy

Bacterial infections remain a leading threat to global health because of the misuse of antibiotics and the rise in drug-resistant pathogens. Although several strategies such as photothermal therapy and magneto-thermal therapy can suppress bacterial infections, excessive heat often damages host cells and lengthens the healing time. Here, a localized thermal managing strategy, thermal-disrupting interface induced mitigation (TRIM), is reported, to minimize intercellular cohesion loss for accurate antibacterial therapy. The TRIM dressing film is composed of alternative microscale arrangement of heat-responsive hydrogel regions and mechanical support regions, which enables the surface microtopography to have a significant effect on disrupting bacterial colonization upon infrared irradiation. The regulation of the interfacial contact to the attached skin confines the produced heat and minimizes the risk of skin damage during thermoablation. Quantitative mechanobiology studies demonstrate the TRIM dressing film with a critical dimension for surface features plays a critical role in maintaining intercellular cohesion of the epidermis during photothermal therapy. Finally, endowing wound dressing with the TRIM effect via in vivo studies in S. aureus infected mice demonstrates a promising strategy for mitigating the side effects of photothermal therapy against a wide spectrum of bacterial infections, promoting future biointerface design for antibacterial therapy.     

玉米秸秆衍生碳基固体酸的制备及其催化纤维素水解糖化

以玉米秸秆为原料，通过碳化-磺化法制备了碳基固体酸（CSA），采用XRD、FTIR、XPS、SEM、阳离子交换与返滴定法等手段对其结构形貌进行表征，并考察了制备条件对固体酸表面活性基团含量与催化活性的影响。以NaOH/尿素冻融预处理后的纤维素为底物，研究了CSA催化纤维素水解糖化的效果与条件。结果表明：NaOH/尿素冻融预处理能够有效辅助固体酸催化纤维素水解，在350℃碳化2h、100℃磺化5h条件下制备的CSA催化性能最好，其酸量达3.94mmol/g，其中磺酸基、羧基、酚羟基含量分别为1.09mmol/g、1.36mmol/g、1.49mmol/g。在m(CSA)∶m(纤维素)=3∶1、水解温度200℃、水解时间为0.5h的条件下，纤维素水解还原糖得率与转化率分别为47.1%和63%。CSA循环利用3次催化活性下降不大。本研究可为废弃生物质原料制备的固体酸催化纤维素水解转化利用提供科学参考。     

中国无机盐工业发展现状及展望

建国70 a以来中国无机盐工业发展迅猛,取得了巨大成就,中国已成为世界上最大的无机盐生产、出口和消费国。分析了中国无机盐工业生产现状和进出口情况,指出行业存在大宗产品产能过剩、产品精细化率偏低、产业集中度和资源配置率偏低、矿产资源保障能力不足、节能减排任务重、自主创新能力弱等问题,并提出未来发展建议及发展方向。新能源用无机材料、无机粉体功能材料、5G通迅用无机材料、电子化学品和电镀化学品等专用化学品将是未来无机盐工业发展的热点。随着产业链现代化水平的不断提升,将会逐渐实现行业规模化、绿色发展与安全生产。     

Robust Control of Permanent Magnet Synchronous Motors

In this paper, permanent magnet synchronous motors (PMSMs) are investigated. According to the feature of PMSMs, a novel state equation of PMSMs is obtained by choosing suitable state variables. Based on the state equation, robust controllers are designed via interval matrix and PI control idea. In terms of bilinear matrix inequations, sufficient conditions for the existence of the robust controller are derived. In order to reduce the conservation and the dependence on parameter, the control inputs of PMSMs are divided into two parts, a feedforward control input and a feedback control input, and relevant sufficient conditions for the existence of the controller are obtained. Because of the suitable choice of state variables, the proposed control strategies can cope with the load uncertainty and have robustness for disturbance. Finally, simulations are carried out via Matlab/Simulink soft to verify the effectiveness of the proposed control strategies. The performance of the proposed control strategies are demonstrated by the simulation results.      

Studies on one‐dimensional polyanilines prepared with n‐dodecylbenzenesulfonic and camphorsulfonic acids

Anilinium salts complexed with n‐dodecylbenzenesulfonic acid (DBSA) and camphorsulfonic acid (CSA) were found to self‐assemble into cylindrical micelles with bigger diameters than those complexed with only DBSA or CSA. These cylindrical micelles were polymerized into one‐dimensional copolyaniline nanotubes (PANIDBSACSA) via emulsion polymerization, demonstrating various morphologies depending on the ratio of DBSA to CSA. The UV?visible?NIR spectra of neat PANICSA and PANIDBSACSAs illustrate significant free carrier tails in the NIR region and conductivity 10–20 times higher than that of neat PANIDBSA whose UV?visible?NIR spectrum does not illustrate significant carrier tails. When the number of moles of DBSA is equivalent to or exceeds that of CSA in the polymerization mixture, SEM and TEM micrographs of the PANIDBSACSAs reveal that they have larger diameters than that of neat PANIDBSA. Besides, some of the surfaces of the big nanotubes were implanted and mounted with lots of small nanofibers of neat PANICSA polymerized from some of the CSA‐complexed aniliniums which were excluded from the cylindrical micelles before polymerization. TGA thermograms of PANIDBSACSAs show an intimate relationship between thermal deprotonation and the DBSA to CSA ratio. X‐ray diffraction patterns demonstrate a layered structure arrangement of polyaniline molecules of all one‐dimensional nanofibers. © 2015 Society of Chemical Industry