基于区间犹豫模糊语言集的水资源多目标决策

以鄂北水资源配置工程为对象,研究大型调水工程背景下的多水源多目标优化配置。将鄂北地区水库分为充蓄水库、补偿水库与在线水库等3类,根据各类水库特点对鄂北水资源配置工程进行系统概化,建立以年缺水量最小和调水成本最低为目标函数的多水源多目标优化配置模型。采用权重系数法进行求解得到非劣解集。最后采用基于区间犹豫模糊语言与TOPSIS的多目标决策方法对各方案的缺水量与调水量作出评价并遴选出最优方案。研究结果表明:对鄂北水资源配置工程而言,缺水量与调水量的权重比为7∶3的方案综合评价最优,重视缺水的同时兼顾调水成本;基于区间犹豫模糊语言集与TOPSIS的水资源多目标决策方法经本文实例验证具有较高的稳定性与可行性。     

时间效应在悬滴法测定表面张力中的影响

表面张力是流体重要的物理性质,测定表面张力的方法通常包括毛细管上升法、最大气泡压力法、拉环法、旋滴法和悬滴法等。目前,最普遍的表面张力的测定方法为国家标准推荐的平板法或拉环法。然而,悬滴法作为一项成熟的表面张力测定方法且具备静态表面张力及动态表面张力测定功能,目前使用该法测定的较少。文章使用悬滴法测定较低含量的表面活性剂溶液静态表面张力时发现结果与拉环法差异较大,而测定单组分液体及含量较大的表面活性剂溶液,悬滴法与拉环法的测定数据差异较小,这种情况的相关报道较少。另外,使用动态表面张力测定探索了静态测定时出现差异的原因,并对应用悬滴法进行表面张力测定的适用范围进行了总结。使用悬滴法测定表面张力时,应注意时间效应的影响。     

FPGA互连测试中的反馈桥接故障覆盖问题

现场可编程门阵列(FPGA)内部资源众多,其中互连资源出现故障的概率远远高于片内其他资源,而在以往许多互连测试研究中,所生成的测试配置存在无法覆盖反馈桥接故障的难题,所以较难有测试配置实现故障列表的100%覆盖。因此通过约束桥接故障只发生在单个查找表(LUT)内的信号线上,并结合单项函数,对反馈桥接故障模型进行优化改进,从根本上解决难题；然后对优化后的反馈桥接故障设置相应的约束条件,再使用布尔可满足性理论(SAT)生成满足约束条件的测试配置。采用优化后的故障模型对ISCAS"89基准电路进行了测试配置生成实验,结果表明生成的测试向量解决了反馈桥接故障的覆盖难题,并且在实现故障列表的100%覆盖下,优化后的故障模型所需要的测试配置数最少。     

Gelatinised and hydrolysed corn starch is a cost-effective carbon source with higher production of L-lactic acid by Bacillus coagulans compared with glucose

L-lactic acid is an important organic acid widely used in pharmaceutical, food and textile industries. Bacillus coagulans BCS13002 can efficiently produce L-lactic acid with two kinds of carbon sources. BCS13002 produced L-lactic acid at a content of 10.23 ± 0.16 g/L and 11.67 ± 0.22 g/L, when glucose and gelatinised and hydrolysed corn starch （GHCS） were used, respectively. GHCS exhibits several advantages, including high yield of L-lactic acid and low cost. Proteomics analyses identified several key enzymes, which contributed to the higher production of L-lactic acid when GHCS was used as the carbon source. Those key enzymes were involved in the two-component system (SpoOF), pantothenate and CoA biosynthesis (pantothenate synthetase, 1.584-fold; dihydroxy-acid dehydratase, 1.517-fold), beta-alanine metabolism (1.605-fold) and valine, leucine and isoleucine biosynthesis (1.517-fold) pathways. This study provides a biological basis for using GHCS as a substitute of glucose in the production of L-lactic acid.     

泵站系统停机过渡过程研究进展

泵站系统停机过渡过程主要是由于泵站中水泵的突然停机,而造成的泵站系统中管道内液体的流速发生突然变化,继而引起压力的急剧变化而产生水锤的过程.文章通过对泵站系统停机过渡过程中水锤的国内外研究现状的分析和了解,介绍了计算过渡过程水锤的两种常用方法,并且提出了三种水锤防护措施,为泵站系统停机过渡过程水锤防护提供参考.     

城市空间精细化体验路线设置初探 ——以杭州运河卖鱼桥至大关桥路段为例

文章以教学及学术研究内容为基础,阐释对城市空间进行精细化体验路线设置的探索,表达尝试通过具体场景节点设置和丰富历史建筑信息,为本地居民和外来参观者提供专业角度的城市空间体验完整线路的努力.这是一个持续的系列研究,教学中的散点历史建筑通过城市空间体验路线设置串联起来,共同构成为城市发展历程的见证者和体现者.具体的城市生活附着在抽象的城市空间体验路线中,最终整体输出为立体丰富的杭州城市文化名片.     

The dehydrogenation kinetics and reversibility improvements of Mg(BH4)2 doped with Ti nano-particles under mild conditions

Magnesium borohydride, Mg(BH₄)₂, is ball-milled with Ti nano-particles. Such catalyzed Mg(BH₄)₂ releases more hydrogen than pristine Mg(BH₄)₂ does during isothermal dehydrogenation at 270, 280, and 290 °C. The catalyzed Mg(BH₄)₂ also exhibits better dehydrogenation kinetics than the pristine Mg(BH₄)₂. Based on kinetics model fitting, the activation energy (E_a) of the catalyzed Mg(BH₄)₂ is calculated to be lower than pristine Mg(BH₄)₂. During partial dehydrogenation, the catalyzed Mg(BH₄)₂ releases 4.23 wt % (wt%) H₂ for the second dehydrogenation at 270 °C, comparing to 4.05, and 3.75 wt% H₂ at 280, and 290 °C. The reversibility of 4.23 wt% capacity is also one of the highest for Mg(BH₄)₂ dehydrogenation under mild conditions such as 270 °C as reported. 4 cycles of Mg(BH₄)₂ dehydrogenation are conducted at 270 °C. The capacities degrade during 4 cycles and tend to be stable at about 3.0 wt% for the last two cycles. By analyzing the hydrogen de/absorption products of the catalyzed sample, Mg(BH₄)₂ is found to be regenerated after rehydrogenation according to Fourier Transform Infrared (FTIR) spectroscopy. Ti nano-particles can react with Mg(BH₄)₂ during ball-milling and de/rehydrogenation. The products include TiH_1.924, TiB, and TiB₂, which can improve the dehydrogenation properties of Mg(BH₄)₂ from a multiple aspect.     

Towards performance improved anion exchange membrane: Cross-linking with multi-cations oligomer modified graphene oxide

Cross-linking structure has been proven to be an effective approach to address the balance issue between ionic conductivity, dimensional stability and other properties of anion exchange membranes (AEMs). Here, a novel multi-cationic oligomer was synthesized from 1,4-diazabicyclo [2,2,2]octane and 1,6-dibromohexane, and subsequently used to prepare multi-cationic oligomer brushes-decorated graphene oxide (QBGO). The obtained QBGO was employed as the cross-linker to form cross-linked poly (arylene ether sulfone) (QPAES) AEMs by end-cap tertiary amine coupling reaction. Benefiting from the introduction of the multi-cations and flexible long-chain cross-linker structure, the cross-linked QPAES/QBGO membranes formed hydrophilic/hydrophobic phase-separation microstructures and well-defined ionic channels which are responsible for water uptake and ion transfer. As a result, the cross-linked QPAES/QBGO-2.0 membrane exhibited 1.90-fold higher ionic conductivity and better chemical stability than the control QPAES membrane. The QPAES/QBGO-2.0 membrane displayed a higher power density of 75.7 mW cm^?2 than that of the control QPAES membrane (53.1 mW cm^?2) in a H₂/O₂ fuel cell test. In a word, we propose that this novel design strategy holds broad prospects for the design of new polymer electrolyte membrane materials.