硅酸铋(BSO)晶体闪烁性能研究

报道对BSO晶体闪烁性能研究的若干结果. 包括晶体的激发光谱和荧光光谱、光产额、发光衰减时间和抗辐照能力等特性.     

Low-frequency modulation of distortion product otoacoustic emissions in humans

Low-frequency modulation of distortion product otoacoustic emissions (DPOAEs) was measured from the human ears. In the frequency domain, increasing the bias tone level resulted in a suppression of the cubic difference tone (CDT) and an increase in the magnitudes of the modulation sidebands. Higher-frequency bias tones were more efficient in producing the suppression and modulation. Quasi-static modulation patterns were derived from measuring the CDT amplitude at the peaks and troughs of bias tones with various amplitudes. The asymmetric bell-shaped pattern resembled the absolute value of the third derivative of a nonlinear cochlear transducer function. Temporal modulation patterns were obtained from inverse FFT of the spectral contents around the DPOAE. The period modulation pattern, averaged over multiple bias tone cycles, showed two CDT peaks each correlated with the zero-crossings of the bias tone. The typical period modulation pattern varied and the two CDT peaks emerged with the reduction in bias tone level. The present study replicated the previous experimental results in gerbils. This noninvasive technique is capable of revealing the static position and dynamic motion of the cochlear partition. Moreover, the results of the present study suggest that this technique could potentially be applied in the differential diagnosis of cochlear pathologies.     

离轴受限圆射流的三维湍流流场分析

利用原始变量,交叉网格的方法,以及采用κ-ε湍流模型,计算了离轴受限射流三维湍流流场,计算结果与用LDV测量结果作了比较,结果是满意的。计算结果提供了这样一个复杂的三维流场的清晰图象,为研究具有离轴射流的预燃室的稳燃机理提供了很多有用的信息,对计算结果作了详细的分析和讨论后,指出这样一个流场的重要三维特征是在θ方向梳线有大角度的扭曲。     

弱粘结的斜交铺设层合圆柱壳的柱形弯曲

导出了两端简文的具有弱粘结界面的任意斜交铺设层合圆柱壳柱形弯曲问题的一个精确弹性理论解。分析中采用线性弹簧模型来表征界面的弱粘结特性。引进新的物理量改写了基本方程,导出了对应的状态空间列式,并利用变量替换技术将该状态方程转换成常系数状态方程,从而方便求解。最后给出了数值算例,并讨论了弱界面的影响。     

铝合金等离子体淹没氮离子注入层的摩擦学性能研究

用等离子体淹没离子注入技术对ＬＹ１２和ＬＤ１０铝合金表面进行氮离子注入。用俄歇电子能谱分析离子注入层中氮的浓度分布，在此基础上进行了摩擦磨损试验。用扫描电观察和分析磨损表面特征。研究表明：氮离子注入铝合金形成细小，弥散的硬质ＡｌＮ析出相，铝合金表层的显微硬度增加，摩擦系数降低；耐磨性随着注入剂量和电压的增加而提高。磨损机制主要为粘着磨损，随离子注入剂量的增加，粘着磨损趋行减轻。     

Systematic chemical profiling of a multicomponent Chinese herbal formula Huo Luo Xiao Ling Dan by ultra high performance liquid chromatography coupled with electrospray ionization quadrupoletime‐of‐flight mass spectrometry

Huo Luo Xiao Ling Dan, a Chinese herbal formula consisting of 11 different herbs, has been used in folk medicine for the treatment of arthritis and other chronic inflammatory diseases. However, the chemical compositions of Huo Luo Xiao Ling Dan are not completely characterized. In the present study, an ultra high performance liquid chromatography coupled with electrospray ionization quadrupole time‐of‐flight mass spectrometry method in positive and negative ion modes was employed to identify biochemical constitutes in Huo Luo Xiao Ling Dan. As a result, a total of 76 compounds including alkaloids, monoterpene glycosides, iridoids, phenolic acids, and tanshinones, coumarins, lactones, flavones, and their glycosides, triterpenes, and triterpene saponins were characterized by comparing the retention time and mass spectrometry data with reference standards within 5 ppm error or by reference to the reference literature. These results would provide the basis for a further in vivo study of Huo Luo Xiao Ling Dan and information for potential new drug candidates for treating arthritis and other chronic inflammatory diseases.     

Two more pieces of the colibactin genotoxin puzzle from Escherichia coli show incorporation of an unusual 1-aminocyclopropanecarboxylic acid moiety

Colibactin represents a structurally undefined class of bacterial genotoxin inducing DNA damage and genomic instability in mammalian cells, thus promoting tumour development and exacerbating lymphopenia in animal models. The colibactin biosynthetic gene cluster (clb) has been known for ten years and it encodes a hybrid nonribosomal peptide synthetase (NRPS)/polyketide synthase (PKS) assembly line. Nevertheless, the final chemical product(s) remain unknown. Previously, we and others reported several colibactin pathway-related metabolites including N-myristoyl-d-asparagine (1) as part of a prodrug precursor that is cleaved from the putative precolibactin to form active colibactin by the peptidase ClbP. Herein, we report two new colibactin pathway-related metabolites (2 and 3) isolated from a clbP mutant of the probiotic E. coli Nissle 1917 strain. Their structures were established by HRMS and NMR. Compound 2 shows an additional 4-aminopenatanoic acid moiety with respect to 1, while 3 is characterized by the presence of an unusual 7-methyl-4-azaspiro[2.4]hept-6-en-5-one residue. Moreover, we propose the biosynthetic pathway towards both intermediates on the basis of extensive gene inactivation and feeding experiments. The identification of 2 and 3 provides further insight into colibactin biosynthesis including the involvement and formation of a rare 1-aminocyclopropanecarboxylic acid unit. Thus, our work establishes additional steps of the pathway forming the bacterial genotoxin colibactin.     

Bulk derivatization and cation exchange restricted access media-based trap-and-elute liquid chromatography–mass spectrometry method for determination of trace estrogens in serum

Estrone (E1), estradiols (α/β-E2), and estriol (E3) are four major metabolically active estrogens exerting strong biological activities at very low circulating concentrations. This paper reports a sensitive and efficient method with automated, on-line clean-up and detection to determine trace estrogens in a small volume of serum samples using liquid chromatography–electrospray ionization–tandem mass spectrometry directly, without off-line liquid–liquid or solid-phase extraction pretreatments. Serum aliquots (charcoal stripped fetal bovine serum, 100 μL) were spiked with four estrogen standards and their corresponding isotope-labeled internal standards, then bulk derivatized with 2-fluoro-1-methyl-pyridium p-toluenesulfonate (2-FMP) to establish the calibration curves and perform method validation. Calibration was established in the concentration ranges of 5–1000 pg mL⁻¹, and demonstrated good linearity of R² from 0.9944 to 0.9997 for the four derivatized estrogens. The lower detection limits obtained were 3–7 pg mL⁻¹. Good accuracy and precision in the range of 86–112% and 2.3–11.9%, respectively, were observed for the quality control (QC) samples at low, medium, and high concentration levels. The stability tests showed that the derivatized serum samples were stable 8 h after derivatization at room temperature and at least to 48 h if stored at −20 °C. The method was applied to measure trace estrogens in real human and bovine serum samples, and three of four estrogen compounds studied were observed and quantified.     

A photoelectrochemical cell for pollutant degradation and simultaneous H2 generation

A PEC cell with nanostructured BiVO₄ photoelectrode film presents outstanding azo dye degradation and simultaneous H₂ production performance.