谐波齿轮系统的快慢振荡机制研究

谐波齿轮减速器是一种新型的传动装置, 因其具有诸多的优点, 因而得到了广泛应用. 谐波齿轮减速器涉及不同振荡尺度之间的耦合作用, 这通常会诱发复杂的快慢振荡, 严重影响了谐波齿轮系统的正常工作. 本文考虑涉及扭转刚度非线性因素的谐波齿轮系统, 旨在研究系统的快慢动力学, 揭示新型的快慢振荡机制. 首先, 构建了非线性扭转刚度下的谐波齿轮系统的快慢动力学模型. 然后, 通过改变扭转刚度系数, 得到了系统从常规振荡向快慢振荡的转迁过程. 接着, 简要地论述了有关快慢系统的基础理论. 在此基础上, 采用快慢分析法研究了快子系统的动力学特性, 揭示了快慢振荡的产生机制. 研究表明, 当系统参数改变时, 快子系统的平衡点曲线并未发生失稳或分岔; 然而, 在某一点附近, 平衡点曲线能够产生急剧量变, 其特征是平衡点在局部小范围内可以在正坐标值与负坐标值之间快速转迁. 在此基础上, 揭示了一种诱发快慢振荡的新型动力学机制, 比较了这种诱发机制与其他相关机制之间的区别. 本文丰富了系统通向快慢振荡的路径, 为实际谐波齿轮传动系统中的快慢振荡机理与控制研究提供参考.      

基于车桥耦合理论的梁式桥阻尼比识别研究

提出一种基于车桥耦合动力学理论的梁式桥阻尼比识别方法. 首先按照动力学理论将测试车设计为单自由度体系, 然后利用安装在测试车上的传感器采集信号, 从测试车与桥梁接触点响应信号中得到梁式桥响应的信号, 基于车桥耦合动力学原理滤波处理得到包含梁式桥第一阶频率的信号, 最后假定梁式桥阻尼比值, 通过假定的梁式桥阻尼比值获取假定的梁式桥第一阶振型, 不断循环直至假定的阻尼比值下计算的第一阶振型最大值点居中, 即为识别的梁式桥真实阻尼比. 本文首先从车桥耦合动力学理论推导上说明了该方法的可行性, 然后考虑在不同车速与非恒定车速、路面粗糙度、环境噪音等影响因素下进行车桥耦合动力学模型分析, 最后通过实桥试验进行了初步验证. 研究结果表明: 该方法能一定程度上克服外界不利因素的影响, 达到识别梁式桥阻尼比的目的, 为识别梁式桥阻尼比提供一种更优方法, 其具有参数设置较少、操作简单方便以及更高测试精度等优点, 同时有助于推动基于车桥耦合的车桥耦合动力学理论技术在梁式桥模态参数识别工作中的实际工程应用.      

万古霉素手性固定相分离曼尼希碱类化合物对映体

采用大环抗生素类万古霉素手性固定相高效液相色谱法研究了一系列曼尼希碱类化合物的手性分离情况,并讨论了流动相中有机相的种类和比例、缓冲盐的种类和浓度、pH和柱温对该类化合物手性分离的影响。最佳实验条件为:乙腈:硝酸铵(35mmol/L,pH3.8)=15∶85(V/V),柱温15℃,流速0.6mL/min,检测波长300nm;四氢呋喃:硝酸铵(20mmol/L,pH4)=15∶85(V/V),柱温15℃,流速0.6mL/min,检测波长350nm。通过对比研究8种曼尼希碱类化合物的色谱行为,从结构上讨论了化合物中各种官能团对手性分离的影响,并探讨了手性分离的内在机制。     

Identification of Pharmacophoric Fragments of DYRK1A Inhibitors Using Machine Learning Classification Models

Dual-specific tyrosine phosphorylation regulated kinase 1 (DYRK1A) has been regarded as a potential therapeutic target of neurodegenerative diseases, and considerable progress has been made in the discovery of DYRK1A inhibitors. Identification of pharmacophoric fragments provides valuable information for structure- and fragment-based design of potent and selective DYRK1A inhibitors. In this study, seven machine learning methods along with five molecular fingerprints were employed to develop qualitative classification models of DYRK1A inhibitors, which were evaluated by cross-validation, test set, and external validation set with four performance indicators of predictive classification accuracy (CA), the area under receiver operating characteristic (AUC), Matthews correlation coefficient (MCC), and balanced accuracy (BA). The PubChem fingerprint-support vector machine model (CA = 0.909, AUC = 0.933, MCC = 0.717, BA = 0.855) and PubChem fingerprint along with the artificial neural model (CA = 0.862, AUC = 0.911, MCC = 0.705, BA = 0.870) were considered as the optimal modes for training set and test set, respectively. A hybrid data balancing method SMOTETL, a combination of synthetic minority over-sampling technique (SMOTE) and Tomek link (TL) algorithms, was applied to explore the impact of balanced learning on the performance of models. Based on the frequency analysis and information gain, pharmacophoric fragments related to DYRK1A inhibition were also identified. All the results will provide theoretical supports and clues for the screening and design of novel DYRK1A inhibitors.     

Investigating bottom-quark Yukawa interaction at Higgs factory

Measuring the fermion Yukawa coupling constants is important for understanding the origin of the fermion masses and their relationship with spontaneously electroweak symmetry breaking.In contrast,some new physics(NP)models change the Lorentz structure of the Yukawa interactions between standard model(SM)fermions and the SM-like Higgs boson,even in their decoupling limit.Thus,the precise measurement of the fermion Yukawa interactions is a powerful tool of NP searching in the decoupling limit.In this work,we show the possibility of investigating the Lorentz structure of the bottom-quark Yukawa interaction with the 125 GeV SM-like Higgs boson for future e^+e^- colliders.     

新型PTP 1B抑制剂喹啉腙及酰腙化合物的合成与活性研究

喹啉腙及喹啉酰腙类化合物具有广泛的生物活性.本文设计合成了29个未见报道的4-(2-芳基)喹啉芳腙和芳酰腙类化合物,采用光吸收检测法测试所合成化合物对蛋白酪氨酸磷酸酶PTP 1B的抑制作用.结果 表明,喹啉腙类化合物对PTP 1B具有显著的酶抑制作用,在20μ g/mL浓度时,有21个化合物对PTP 1B抑制率在80％...     

大气颗粒物中总碳含量的测量不确定度评定

分析了元素分析仪测定大气颗粒物中碳质组分的测量不确定度来源,对总碳含量的测量不确定度进行了评估。测定咖啡碱标准样品中的碳含量,称样量为1 500~2 500μg时,测定结果为(49.27±0.26)%;测定大气颗粒物样品中的总碳含量,样品面积为3.14 cm2时,测定结果为(106±3)μg/cm2。     

低温液体无损贮存压力升高的实验与计算

准确、简单地预测低温液体无损贮存时的压力升高具有重要的实用价值。对一低温容器利用液氮为介质进行了多次无损贮存实验,利用多元线性回归方法对实验数据进行分析和检验。分析表明无损贮存时间、初始充满率对压力升高的影响较大,而环境温度的影响可以忽略,并拟合出了压力升高的计算公式。计算结果和实验结果在很大范围内能够较好地吻合。该种计算方法在预测低温液体无损贮存压力升高时有较高的准确性与可靠性。     

The Biological Fate of Pharmaceutical Excipient β-Cyclodextrin: Pharmacokinetics,Tissue Distribution,Excretion, and Metabolism of β-Cyclodextrin in Rats

β-cyclodextrin has a unique annular hollow ultrastructure that allows encapsulation of various poorly water-soluble drugs in the resulting cavity, thereby increasing drug stability. As a bioactive molecule, the metabolism of β-cyclodextrin is mainly completed by the flora in the colon, which can interact with API. In this study, understanding the in vivo fate of β-cyclodextrin, a LC-MS/MS method was developed to facilitate simultaneous quantitative analysis of pharmaceutical excipient β-cyclodextrin and API dextromethorphan hydrobromide. The established method had been effectively used to study the pharmacokinetics, tissue distribution, excretion, and metabolism of β-cyclodextrin after oral administration in rats. Results showed that β-cyclodextrin was almost wholly removed from rat plasma within 36 h, and high concentrations of β-cyclodextrin distributed hastily to organs with increased blood flow velocities such as the spleen, liver, and kidney after administration. The excretion of intact β-cyclodextrin to urine and feces was lower than the administration dose. It can be speculated that β-cyclodextrin metabolized to maltodextrin, which was further metabolized, absorbed, and eventually discharged in the form of CO₂ and H₂O. Results proved that β-cyclodextrin, with relative low accumulation in the body, had good safety. The results will assist further study of the design and safety evaluation of adjuvant β-cyclodextrin and promote its clinical development.     

溶剂浮选-气相色谱法测定铝酸钠溶液中的硬脂酸钠

用溶剂浮选-气相色谱法测定铝酸钠溶液中的硬脂酸钠。选择环己酮为浮选溶剂,样品经1∶1(V/V)的盐酸酸化后,以40 mL/m in的速度通入氮气并以环己酮为浮选溶剂浮选30 m in进行富集,用CH3OH/BF3在80℃水浴中加热3 m in进行甲酯化,以毛细管色谱柱PEG-20M(30 m×0.32 mm,i.d.)分离,邻苯二甲酸二乙酯为内标,氢火焰离子化检测器检测。方法在硬脂酸与内标的质量比在0.1~10范围内呈良好的线性关系(r=0.9997);硬脂酸钠的相对标准偏差为1.35%(n=7);回收率为96.9%~98.1%。