摘要：这的确是解决交通拥堵的一种方法。这项叫作“3D快速巴士”的创新设计是由深圳华世未来泊车设备工程公司提出的，用以缓解中国过度拥挤的交通。这些大型巴土的离地净高将惊人地达到4到4．5米，

摘要：德国Thyssen机械设计有限公司用模型原理在泵主要构件保持不变情况下,精心设计超排理和部分排量范围叶轮系列,不但能够节约能量,而且提高了可靠性、降低了噪音。用不同蜗壳与9个叶轮组合进行测算,为新泵设计确立参数,给出了设计方案,论述了设计的原理、特点和方法。

摘要：Disease and sufferings lead religious persons nearer to almighty in search of mercy. Not much is known about how to design and disseminate programs of spiritual exercises and spiritual indicators for persons suffering with some disease (sufferers). Research is required to advance the understanding of prioritized internal and external indicators responsible for spiritual awakening among these sufferers. In this paper, an attempt is made to compute OFDP (overall futuristic decision priority) weights to generate spiritual scenarios for spiritual awakening by using MCFDM (multi-criteria futuristic decision-making) methodology. The generated prioritized spiritual scenarios responsible for spiritual awakening among sufferers were then used to assess the effect of some kind of disease (physical problem, suffering, disorder, etc.) on strengthening their religious faith and defining their optimal spiritual trajectories towards ultimate reality. In this research work, a two-phased DRFI (disease-religious faith-interaction) experiment is also designed and developed. The results derived from Phase-I pilot research study based on prioritized spiritual scenarios on 20 male and female sufferers are also presented.

摘要：通过应用 Pane 的板理论,对 U 形管换热器整体管板的两侧进行了分析。考虑了实心环板及管板与壳、管箱壳体的相互作用影响。在以前的分析法基础上,提出了一个新的设计方法。采用 Osweiller 假定的弹性系数,以及 Slot 和O'Donnell 的有效弹性系数;应用 ASMEⅧ-2分篇的应力分类概念,分析了管板系统的变形、内力,以及在节距、对角线两个方向上评价了一次应力强度。把这个方法获得的设计厚度与 ASMEⅧ-1、TEMA 和 BS-5500得到的厚度相比较,并且这个方法能够使我们计算连接区域的壳体、管箱的应力。本文的分析设计方法,全面研究了管板的特性,并可以获得较薄的管板厚度,尽管这些规范的方法都是依据 Gardner 以前的安全可靠、有效的设计规则,作为坚实的基础,但管板的设计厚度仍然可降低10%左右。

摘要：Transketolase, the most critical enzyme of the non-oxidative branch of the pentose phosphate pathway, has been reported as a novel target in Plasmodium falciparum as it has least homology with the human host. Homology model of P. falciparum transketolase (PfTk) was constructed using the crystal structure of S. cervisiae transketolase as a template, and used for the identification and prioritization of potential compounds targeted against Plasmodium falciparum transketolase. The docking studies with fructose-6-phosphate and thiamine pyrophosphate showed that His31, Asp473, Ser388, Arg361 and His465 formed hydrogen bonds with fructose-6-phosphate while pyrimidine ring of coenzyme interacted with conserved residues of protein viz., Leu121, Glu415, Gly119. The major interacting residues involved in binding of oxythiamine pyrophosphate were similar to cofactor binding site of PfTk. An integrated pharmacophore, co-factor ThDP and substrate fructose-6-pho- sphate, based virtual screening of a small mo- lecule database retrieved eight and thirteen compounds respectively. When screened for their activity against P. falciparum transketolase, one compound in case of ThDP and three compounds in case of fructose-6-phosphate based screening were found active against PfTk. Identification of these novel and chemically diverse inhibitors provides initial leads for optimization of more potent and efficacious drug candidates to treat malarial infection.