水基流延工艺制备氧化铝生带材料研究

利用水基流延法,选用纯丙乳液作为粘结剂,成功制备出表面光滑、结构均匀、柔韧性良好、强度较高的Al2O3生带材料,并发现当分散剂聚丙烯酸铵(PAA-NH4)含量为2.5%(质量分数)、粘结剂纯丙乳液用量为27%～28%(体积分数)、pH值为9.5～10时可制备出稳定性良好、流动性适宜的α-Al2O3的水基流延浆料.对纯丙乳液进行了DTA和TGA热分析,在此基础上确定流延素片的排胶温度在500℃;将该工艺制备的α-Al2O3流延素片在1650℃并保温2 h的烧结条件下,获得了强度和致密度都较高的烧结体,其中烧结较好的流延片的相对密度达到94.5%.     

钇离子注入AZ31镁合金的氧化行为

研究了AZ31镁合金在钇离子剂量为5×10^16，1×10^17及5×10^17ions／cm^2注入条件下的氧化性能。纯氧气氛、500℃下的氧化实验结果表明，钇离子注入能提高AZ31镁合金的抗氧化性能，而且随着注入剂量的增大，合金表面抗氧化性能提高越大。俄歇电子能谱（AES）和X光电子能谱（XPS）分析表明：钇离子注入以后，在镁合金表面形成了具有双层结构的氧化层，外层主要由MgO组成，而内层主要由Y2O3，MgO构成。这一新形成的氧化层有利于提高AZ31镁合金的抗氧化性能。     

基于 Activiti 流程管理关键技术设计与实现

Activiti 是用于管理业务流程的工作流引擎,它的使用降低了复杂业务流程开发与维护的难度。但在实际应用中,流程节点无法自由跳转,给管理和使用带来诸多不便。本文研究了 Activiti 中的系统框架和接口,基于现有接口设计实现了流程节点自由跳转功能,并进行了框架整合。测试结果表明,该功能满足各项既定功能需求,具有一般性,可满足实际工作中相关要求。     

教学管理系统中报表设计与实现

通过VB程序设计和Excel软件相结合的方法,详细分析了生成各种数据报表的技术方法.     

基于单片机的小气候信息采集系统便携机设计

农业生产技术的快速发展,迫切需要一种适用于普及的、可靠、有效的针对农田小气候信息参数的实时采集系统,提高人们对作物生长与小气候之间关系的认识,为农业生产服务。本文介绍了基于PIC单片机的小气候信息采集系统便携机部分设计,文中详细描述了小气候信息采集方法和系统软硬件结构。便携机系统实现了包括温湿度、光照度、降雨量、蒸发量、大气压等15种小气候参数的自动、实时监测。通过实践证明该便携机设计合理、性能可靠,作为小气候信息采集系统的主体部分,是适合目前农田小气候信息自动监测的普及型设备。     

浅谈高职《计算机网络》课程教学改革

通过调查研究,对当前高职<计算机网络>的教学现状和存在的问题进行分析,本丈构建了高职<计算机网络>课程活动教学设计模式.     

一种改进的空间组合推举体制算法

详细分析了提升算法和空间组合推举体制算法,然后采用后拉伸变换的方法,对空间组合推举体制算法流程进行了改进,进一步降低了运算复杂度。实验中以CDF 9/7二维离散小波变换为例,对于JPEG 2000中推荐使用的5级小波分解,本文算法相对于原空间组合推举算法的缩放运算乘法量减少了34.3%,相对于标准L ifting算法总乘法量减少了44.53%。     

An efficient processing of a chain join with the minimum communication cost in distributed database systems

This paper investigates the optimization problem when executing a join in a distributed database environment. The minimization of the communication cost for sending data through links has been adopted as an optimization criterion. We explore in this paper the approach of judiciously using join operations as reducers in distributed query processing. In general, this problem is computationally intractable. A restriction of the execution of a join in a pre-defined combinatorial order leads to a possible solution in polynomial time. An algorithm for a chain query computation has been proposed in [21]. The time complexity of the algorithm isO(m ² n ²+m ³ n), wheren is the number of sites in the network, andm is the number of relations (fragments) involved in the join. In this paper, we firstly present a proof of the intuitively well understood fact—that the eigenorder of a chain join will be the best pre-defined combinatorial order to implement the algorithm in [21]. Secondly, we show a sufficient and necessary condition for a chain query with the eigenordering to be a simple query. For the process of the class of simple queries, we show a significant reduction of the time complexity fromO(m ² n ²+m ³ n) toO(mn+m ²). It is encouraging that, in practice, the most frequent queries belong to the category of simple queries. Editor: Peter Apers     

Stabilizing Redox-Active Hexaazatriphenylene in a 2D Conductive Metal–Organic Framework for Improved Lithium Storage Performance

Organic redox-active materials are promising electrode candidates for lithium-ion batteries by virtue of their designable structure and cost-effectiveness. However, their poor electrical conductivity and high solubility in organic electrolytes limit the device's performance and practical applications. Herein, the π-conjugated nitrogen-containing heteroaromatic molecule hexaazatriphenylene (HATN) is strategically embedded with redox-active centers in the skeleton of a Cu-based 2D conductive metal–organic framework (2D c-MOF) to optimize the lithium (Li) storage performance of organic electrodes, which delivers improved specific capacity (763 mAh g⁻¹ at 300 mA g⁻¹), long-term cycling stability (≈90% capacity retention after 600 cycles at 300 mA g⁻¹), and excellent rate performance. The correlation of experimental and computational results confirms that this high Li storage performance derives from the maximum number of active sites (CN sites in the HATN unit and CO sites in the CuO₄ unit), favorable electrical conductivity, and efficient mass transfer channels. This strategy of integrating multiple redox-active moieties into the 2D c-MOF opens up a new avenue for the design of high-performance electrode materials.