高速列车转向架故障信号的聚合经验模态分解和 模糊熵特征分析

为了对高速列车转向架关键部件进行状态监测,利用转向架故障振动信号的特点,提出了一种结合聚合经验模态分解和模糊熵的特征提取方法.对故障信号进行聚合经验模态分解,得到一系列具有不同物理意义的简单成分信号,采用相关分析法选取最能反映原信号特征的本征模态函数.对这些本征模态函数和原信号分别计算模糊熵值构成多尺度复杂性度量的特征向量,输入最小二乘支持向量机中进行分类识别,与模糊熵特征相比得到了更好的识别效果,证明了算法的有效性.     

Synthesis and characterization of new aromatic polyimides containing well‐defined conjugation units

A series of aromatic polyimides composed of well‐defined conjugation units were synthesized form 5,5′‐bis(4‐aminophenyl)‐2,2′‐bifuryl (PFDA) and 2,2′‐bis(furyl) benzidine (FurylBZ) with various dianhydrides. The synthesized polyimides emit blue to green light with a quantum yield of 7.3–14.9%, depending on the polymer backbone. In particular, PFDA‐based polymers exhibit extremely narrow photo‐luminescence. The structure, thermal stability, refractive index and dielectric properties of the polymer films were also determined.     

聚苯胺/涤纶导电织物再掺杂及洗涤性能的研究

采用现场吸附聚合法制备了聚苯胺 /涤纶导电织物 ,采用不同种类的酸对其进行再掺杂 ,研究了酸的种类对织物导电性能的影响 ,并对导电织物进行了洗涤实验及洗涤牢度实验。结果表明 :无机酸对导电织物的掺杂效果优于大多数有机酸。导电涤纶织物的导电性能受洗涤液酸碱度的影响 ,其中碱性洗涤液使导电性能降低 2个数量级 ,酸性洗涤液使导电性能下降 1个数量级 ,而且聚苯胺在涤纶织物表面具有良好的附着性     

抗人IgG-抗HRP双特异性单克隆抗体的研制及初步应用

用8－AG（8－氮杂鸟嘌呤）驯化的HRP－MCAb（抗辣根过氧化物酶单克隆抗体）杂交瘤细胞HAT（次黄嘌呤氨基喋呤胸苷）敏感株与人IgG免疫的BALB／c小鼠脾细胞进行二次融合，获得5株能稳定分泌抗人IgG－抗HRP的BsMcAb（双特异性单克隆抗体）杂交－杂交癌细胞，用其混合腹水经HRP亲和层析纯化的BsMcAb制备BsMcAbPAP（双特异性单抗过氧化物酶-抗过氧化物酶复合物）试剂代替丙肝诊断试剂盒中酶标二抗，比较结果初步表明两者差异无显著意义，将为IgG的检测提供有用试剂。     

聚(L-谷氨酸-γ-苯甲酯)接枝共聚物的合成

以溶液聚合直接合成聚丙烯酸,通过接枝反应将疏水的聚肽链接到聚丙烯酸亲水链段上形成两亲性共聚物,合成了新型聚肽接枝共聚物。用核磁共振等方法表征了接枝共聚物的存在。实验结果表明其在含有钠离子的水溶液中能自行组装成为高聚物纳米胶束。     

2000m3低温丙烯球罐球壳板型式和材料的选择

大型球罐球壳板型式和材料的选择是设计的首要环节,从这两方面论述了设计时选择的过程。     

注射成型模具排气槽的设计

塑料注射成型模具的排气方式和排气槽结构直接影响塑料制品质量。介绍了塑料注射成型模具的排气方式、排气槽设计经验以及切实可行的排气方案和排气槽结构。     

卡尔曼滤波在核脉冲全谱数据采集系统中的应用

针对核脉冲全谱数据采集技术中采用的深度加权滤波法在数据量少时平滑效果差、滞后大的缺点,设计了卡尔曼滤波算法替代传统滤波算法进行解谱的方案。滤波算法首先根据信号与噪声的状态空间模型,建立状态方程和测量方程,然后根据广义卡尔曼滤波对测量方程进行更新,最后根据现场的标准刻度井测量数据确定测量矩阵,对测量数据进行滤波。实测结果表明,该滤波算法相对于传统滤波算法,能够消除谱图的统计涨落,提高光滑度,遏制滞后,并保证滤波后曲线不失真。     

The role of the WO x ad-component to Pt and PtRu catalysts in the electrochemical CH3OH oxidation reaction

High surface area carbon-supported platinum-based catalysts, Pt/C, PtWO _x /C, PtRu/C and PtRuWO _x /C, were prepared via a chemical reduction route using single metal precursor salts. The catalyst particles were found to be in the nanoscale range, and the addition of Ru clearly decreased the particle size. The Ru was found to be partially incorporated into the face centered cubic lattice of Pt and to form a single Ru catalyst component. X-ray diffraction and X-ray photon spectroscopy did not provide evidence for electronic interactions between WO _x and Pt as well as WO _x and Ru. However, the addition of tungsten to the PtRuWO _x /C catalyst resulted in a high degree of catalyst particle agglomeration. Both Ru containing catalysts showed significantly higher activities for the CH₃OH oxidation reaction in terms of Pt + Ru mass as well as electroactive Pt + Ru surface area than the Pt/C and PtWO _x /C catalysts. The addition of tungsten appeared to mainly result in some ‘physical’ modification of the catalytically active Pt and Ru surface components such as differences in electroactive surface area rather than promotion of the CH₃OH oxidation reaction via a true catalytic mechanism.     

Ligand-binding domain of farnesoid X receptor (FXR) had the highest sensitivity and activity among FXR variants in a fluorescence-based assay

The farnesoid X receptor (FXR, NR1H4) has been recognized as an attractive therapeutic target because it is a nuclear hormone receptor that controls the expression level of cholesterol-7α-hydroxylase, which in turn regulates bile acid production and cholesterol excretion. To compare receptor activity between each domain and the full-length protein, human FXR cDNA was cloned from a human liver cDNA library. Three human FXR cDNA, designated FXR₂₀, FXR₃₃, and FXR₅₃ cDNA, were subcloned and ligated into a pET28a expression vector. Each protein was expressed in Escherichia coli (BL21) and purified by nickel-nitrilotriacetic acid column chromatography. Approximately 5 mg of FXR₃₃ (1–182 amino acids deleted from FXR, 37 kDa) and 2 mg of FXR₅₃ (the full-length protein of FXR, 59 kDa) was purified from 1 L of Luria-Bertani culture, achieving at least 90% purity. The coactivator recruitment assay for FXR activation was carried out with the three variants of the FXR protein by using dissociation-enhanced lanthanide fluoroimmunoassay-europium-N¹-labeled anti-His antibody. From an optimized assay, a saturated hyperbolic fluorescence signal curve was produced when 250 nM of FXR₃₃ and 100 nM of steroid receptor coactivator-1 peptide, a coactivator of FXR consisting of 26 amino acids, were used with a concentration dependence on chenodeoxycholic acid (from 0 to 200 μM). The ligand-binding domain of FXR (FXR₃₃) was the most suitable protein for studying the activation of FXR with a fluorescence-based assay, because it showed better structural stability than either the full length of FXR (FXR₅₃) or the DNA-binding domain of FXR (FXR₂₀).