90 resultados para immunosuppressive agent
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软件开发过程的不可见是软件项目失败的主要原因之一。为了提高软件开发过程的可见性,研究人员从软件开发过程的表示、软件开发知识的管理和软件开发数据的挖掘等方面提出了相应理论、方法和工具,这些理论、方法和工具对提高软件过程的可见性提供了一定的帮助,但却都有自己的局限性,难以全面覆盖提高软件开发过程可见性的要素。 为此,我们需要进一步融合软件过程建模、知识管理和数据挖掘等领域各自的研究成果,探索一种不但支持从过程资产库提取知识,而且支持对这些知识进行描述和管理,同时还能将这些知识直接用于建立符合组织能力的软件过程模型,并可以根据该软件过程模型生成符合组织中人的能力的软件开发项目计划的完整方法,为提高软件开发过程的可见性提供全面、有力的支持,从而有效保障软件开发的质量和效率。 本文给出一种根据组织的软件过程资产库生成软件过程Agent知识的方法,该方法生成的软件过程Agent知识可被用于建立一种基于组织实体能力的软件过程模型。基于该方法,本文实现了一个软件过程Agent自动生成工具,该工具可以根据指定的软件过程资产库自动生成软件过程Agent实例及其知识。同时本文在应用实例研究中进行了实验验证,证明了该方法的有效性。 本文研究是对基于组织实体能力的软件过程建模方法的扩展和补充。该方法和基于组织实体能力的软件过程建模方法的集成,可有效支持根据组织过程资产库生成组织的软件开发知识并将这些知识进行描述,使其能够被用于建立符合组织能力的软件开发模型,并最终根据特定目标生成符合组织实际能力软件开发项目计划。
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本文从经济学和社会心理学角度出发 ,探讨了多种高级认知结构在社会活动中的作用 ,建立了多种高级认知结构的框架 ,研究了这些高级认知结构在多智能体代理系统环境中如何相互作用问题 ,并提出了三个系统模型来刻画这些相互作用。
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High-throughput screening is a promising new approach in analytical chemistry. Within the framework of an extended screening program (The German-Chinese Drug Screening Program), the enantioseparation of 86 drugs was investigated by capillary zone electrophoresis in the presence of the chiral solvating agent (CSA) octakis-(2,3,6-tri-O-methyl)-gamma-cyclodextrin (TM-gamma-CD). By this means, 15 drugs could be separated into enantiomeric pairs. Approximate measures for the degree of interaction (migration retardation factor, R-m) and for the degree of enantiomer recognition (migration separation factors, alpha(m)) revealed intriguing patterns that were compared with those found for native gamma-cyclodextrin (gamma-CD). Although there is a distinct influence of the analyte structure on the electrophoretic data, interpretation remains difficult. Most remarkably, permethylation of gamma-CD leads neither to a higher affinity nor to better chiral recognition, in contrast to the findings with alpha-CD.
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为了根据人力资源及项目信息进行资源调度,基于过程Agent的人力资源调度方法通过对软件过程中的人力资源建模,描述和定义了任务(目标)及联合体投标模型,并根据用户对目标的偏好生成调度计划,能够为软件企业在人力资源优化调度、项目进度安排等方面提供决策支持,进而提高软件企业的项目管理能力和资源利用效率。最后通过一个实例表明了该方法的可行性和有效性。
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为提高复杂网络环境和任务需求下器材保障的智能化水平,提出了一个数据驱动的多Agent器材保障决策支持系统DSS(decision support system),系统中的数据、模型以及Agent可分布在不同的网络节点上,高层Agent可由粒度更小的子Agent或Agent部件组合而成;系统中的各类智能Agent相互协作,共同完成异构数据集成、多维数据集构造、器材保障模型挖掘、复杂规划问题求解,以及保障方案自动生成等任务,从而有效降低了系统开发的难度,提高了Agent协作的灵活性。研究结果表明,该系统架构能够显著提升器材保障决策方案的质量和效率。
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Amphiphilic supramolecular miktoarm star copolymers linked by ionic bonds with controlled molecular weight and low polydispersity have been successfully synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization using an ion-bonded macromolecular RAFT agent (macro-RAFT agent). Firstly, a new tetrafunctional initiator, dimethyl 4,6-bis(bromomethyl)-isophthalate, was synthesized and used as an initiator for atom transfer radical polymerization (ATRP) of styrene to form polystyrene (PSt) containing two ester groups at the middle of polymer chain. Then, the ester groups were converted into tertiary amino groups and the ion-bonded supramolecular macro-RAFT agent was obtained through the interaction between the tertiary amino group and 2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl propionic acid (DMP). Finally, ion-bonded amphiphilic miktoarm star copolymer, (PSt)(2)-poly(N-isopropyl-acrylamide)(2), was prepared by RAFT polymerization of N-isopropylacrylamide (NIPAM) in the presence of the supramolecular macro-RAFT agent. The polymerization kinetics was investigated and the molecular weight and the architecture of the resulting star polymers were characterized by means of H-1-NMR, FTIR, and GPC techniques. (c) 2008 Wiley Periodicals, Inc.
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The influence of the concentration of a nucleating agent (NA), namely 1,3:2,4-di(3,4-dimethylbenzylidene) sorbitol (DMDBS), on the gamma phase content in a propylene/ethylene copolymer was investigated by means of Differential Scanning Calorimetry (DSC), Wide-Angle X-ray Diffraction (WAXD), Small- Angle X-ray Scatter (SAXS) and Polarized Optical Microscopy (POM).
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Selective extraction-separation of yttrium(Ill) from heavy lanthanides into 1-octyl-3-methylimidazolium hexafluorophosphate ([C(8)mim][PF6]) containing Cyanex 923 was achieved by adding a water-soluble complexing agent (EDTA) to aqueous phase. The simple and environmentally benign complexing method was proved to be an effective strategy for enhancing the selectivity of [C(n)mim] [PF6]/[Tf2N]-based extraction system without increasing the loss of [C(n)mim](+). (c) 2007 Elsevier B.V. All rights reserved.
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Amphiphilic biodegradable star-shaped polymer was conveniently prepared by the Sn(Oct)(2)-catalyzed ring opening polymerization of c-caprolactone (CL) with hyperbranched poly(ester amide) (PEA) as a macroinitiator. Various monomer/initiator ratios were employed to vary the length of the PCL arms. H-1 NMR and FTIR characterizations showed the successful synthesis of star polymer with high initiation efficiency. SEC analysis using triple detectors, RI, light scattering, and viscosity confirmed the controlled manner of polymerization and the star architecture.
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Well-defined polyacrylonitrile with a higher number-average molecular weight (R.) up to 200,000 and a lower polydispersity index (PDI, 1.7-2.0) was firstly obtained via reversible addition-fragmentation chain transfer (RAFT) process. This was achieved by selecting a stable, easy way to prepare disulfide compound intermediates including bis(thiobenzoyl) disulfide (BTBDS) and bis(thiophenylacetoyl) disulfide (BTPADS) to react with azobis(isobutyronitrile) to directly synthesize RAFT agents in situ.
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CdSe nanocrystals (NCs) are prepared in noncoordination solvents (1-octadecene (ODE) and paraffin liquid) with Ion g-chain primary alkylamine as the sole ligand, ODE-Se, and cadmium fatty acid salt as precursors. The obtained NCs meet the four fundamental parameters for high-quality NCs: high crystallinity, narrow size distribution, moderate photoluminescence quantum yield, and broad range size tunableness. Further, by simply regulating the relative molar ratio of alkylamine to cadmium precursor, the regular sized "nuclei" and final obtained NCs can be produced predictably within a certain size range.
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The microstructure and mechanical properties of beta-nucleated iPP before and after being annealed at different temperatures (90-160 degrees C) have been analyzed, Annealing induced different degrees of variation in fracture toughness of beta-nucleated iPP samples. namely, slight enhancement at relatively low annealing temperatures (< 110 degrees C) and great improvement at moderate temperatures (120-130 degrees C), whereas dramatic deterioration at relatively high temperatures ( > 140 degrees C) has been observed. The variation of fracture toughness of beta-nucleated iPP is observed to be dependent on the content of beta-NA. Experiments, including scanning electronic microscope (SEM), wide-angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), small-angle X-ray scattering (SAXS), and dynamic mechanical analysis (DMA), are performed to study the variations of microstructures as well as the toughening mechanism of the beta-nucleated iPP after being annealed.
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Finding a Suitable plasticizer for polylactide (PLA) is necessary to overcome its brittleness and enlarge its range of applications. In this study, commercial PLA was melt-blended with a new plasticizer, an ethylene glycol/propylene glycol random copolymer [poly(ethylene glycol-co-propylene glycol) (PEPG)] with a typical number-average molecular weight of 1.2 kDa and an ethylene glycol content of 78.7 mol %. The thermal properties, crystallization behavior, and mechanical properties of the quenched blends and the properties of the blends after storage for 2 months under the ambient conditions were investigated in detail. The advantage of using PEPG is that it does not crystallize at room temperature and has good compatibility with PLA. The quenched PLA/PEPG blends were homogeneous and amorphous systems. With an increase in the PEPG content (5-20%), the glass-transition temperature, tensile strength, and modulus of the blends decreased, whereas the elongation at break and crystallizability increased dramatically. The cold crystallization of PLA resulted in phase separation of the PLA/PEPG blends by annealing of the blends at the crystallization temperature.