侧面预电离氟化氪激光器研制

采用侧面紫外火花隙自动预电离代替小极上小孔预电离，使放电泵浦氟化氪激光器的主放电均匀性大为改善。输出激光能量由１４０ｍＪ提高到２５０ｍＪ，增益区光能密度为２．３Ｊ／１，同时电极寿命和气体寿命也大为提高。     

Simultaneous Determination of Three Flavonoids in Rat Plasma by RP-LC After Oral Administration of the Total Flavonoids of Scutellaria barbata

A liquid chromatographic method for the simultaneous determination of three flavonoids, scutellarin (SCU), isoscutellarein-8-O-glucuronide (ISO) and luteolin (LUT) in rat plasma was developed and validated. Following a single-step liquid–liquid extraction with ethyl acetate, the analytes and internal standard (IS) (rutin) were successfully separated on a Diamonsil C₁₈ column using a mobile phase composed of acetonitrile (A)–0.2% phosphoric acid aqueous solution (B) (0–5 min, 20% A–29% A; 5–25 min, 29% A, v/v) at a flow rate of 1.0 mL min^?1. The linear range was 0.044–2.20 μg mL^?1 for SCU, 0.042–2.08 μg mL^?1 for ISO, and 0.056–2.80 μg mL^?1 for LUT, with the correlation coefficients of 0.9995, 0.9989 and 0.9963, respectively. The limit of quantification of SCU, ISO and LUT were 44, 41.6 and 56 ng mL^?1, respectively. The accuracy of assay was between 88.4 and 103.0%. The inter-day and intra-day precisions (RSD) were less than 10.5%. The developed method was simple, rapid and applied successfully to study the pharmacokinetics of SCU, ISO and LUT after oral administration of the total flavonoids of Scutellaria barbata.     

Simultaneous determination of four alkaloids in Lindera aggregata by ultra-high-pressure liquid chromatography-tandem mass spectrometry

A new separation and quantification method using liquid chromatography under ultra-high-pressure in combination with tandem mass spectrometry (MS/MS) was developed for simultaneous determination of four alkaloids in Lindera aggregata. The analysis was performed on an Acquity UPLC BEH C(18) column (50mmx2.1mm, 1.7microm particle size; Waters, Milford, MA, USA) utilizing a gradient elution profile and a mobile phase consisting of (A) water containing 10mM ammonium acetate adjusted to pH 3 with acetic acid and (B) acetonitrile. An electrospray ionization (ESI)-tandem interface in the positive mode was employed prior to mass spectrometric detection. The calibration curve was linear over the range of 17.1-856ng for boldine, 42.4-2652ng for norboldine, 6.1-304ng for reticuline and 0.5-50ng for linderegatine, respectively. The average recoveries ranged from 99.2 to 101.4% with RSDs< or =2.7%. Then, four L. aggregata samples from different batches were analyzed using the established method. The results indicated that ultra-high-pressure liquid chromatography-tandem mass spectrometry provided improved chromatographic parameters resulting in significantly increased sample throughput including lower solvent consumption and lower limits of quantitation (LOQs) for most of target analytes compared to previous method employing conventional high-performance liquid chromatography (HPLC) separation. So, the established method was validated, sensitive and reliable for the determination of four alkaloids in L. aggregata.     

Global existence and bounds for blow‐up time in a class of nonlinear pseudo‐parabolic equations with a memory term

In this article, we consider the initial boundary value problem for a class of nonlinear pseudo‐parabolic equations with a memory term: Under suitable assumptions, we obtain the local and global existence of the solution by Galerkin method. We prove finite‐time blow‐up of the solution for initial data at arbitrary energy level and obtain upper bounds for blow‐up time by using the concavity method. In addition, by means of differential inequality technique, we obtain a lower bound for blow‐up time of the solution if blow‐up occurs.     

Development of a method using high‐performance liquid chromatographic fingerprint and multi‐ingredients quantitative analysis for the quality control of Yangxinshi Pian

A simple and reliable method of high‐performance liquid chromatography with diode array detection method was developed for fingerprint analysis and simultaneous determination of six compounds including puerarin, salvianolic acid B, berberine hydrochloride, palmatine chloride, dehydrocorydaline, and icariin in the Chinese medicine preparation Yangxinshi Pian. The separation was performed on an Agilent Eclipse XDB‐C₁₈ reserved‐phase column (250 mm × 4.6mm I.D., 5 μm) using gradient elution with 50 mmol/L monopotassium phosphate aqueous solution and methanol as mobile phase at a flow rate of 1.0 mL/min. The column operating temperature was set at 30°C, and the detection wavelength was 280 nm. The method was validated by linearity, precision, accuracy, stability, and recovery. For fingerprint analysis, 25 peaks were selected as the common peaks, and four kinds of similarities including cosine similarity (S), ratio of similarity (S′), projection content similarity (C), and content similarity (P) were applied to evaluate the quality consistency of different batches of Yangxinshi Pian. The results showed that the developed method was an efficient tool for quality evaluation of Yangxinshi Pian.     

Simultaneous determination of UV filters and polycyclic musks in aqueous samples by solid-phase microextraction and gas chromatography–mass spectrometry

A simple, precise and accurate method for the simultaneous determination of four UV filters and five polycyclic musks (PCMs) in aqueous samples was developed by solid-phase microextraction coupled with gas chromatography–mass spectrometry (SPME-GC–MS). The operating conditions affecting the performance of SPME-GC–MS, including fiber thickness, desorption time, pH, salinity, extraction time and temperature have been carefully studied. Under optimum conditions (30 μm PDMS fiber, 7 min desorption time, pH 7, 10% NaCl, 90 min extraction time at 24 °C), the correlation coefficients (r²) of the calibration curves of target compounds ranged from 0.9993 to 0.9999. The limit of detection (LOD) and limit of quantification (LOQ) ranged from 0.2 to 9.6 ng L⁻¹ and 0.7 to 32.0 ng L⁻¹, respectively. The developed procedure was applied to the determinations of four UV filters and five PCMs in river water samples and internal standard was used for calibration to compensate the matrix effect. Good relative recoveries were obtained for spiked river water at low, medium and high levels. The proposed SPME method was compared with traditional SPE procedure and the results found in river water using both methods were in the same order of magnitude and both are quite agreeable.     

Origin7．5软件在大学物理综合设计性实验教学中的应用探讨

本文采用origin7．5软件对大学物理综合设计性实验数据的处理进行了探讨。实验结果揭示出了热敏电阻温度特性、光敏电阻伏安特性和光照特性。     

On comparison of jump point detection for an exchange rate series

The main purpose of this paper is to investigate the detection of jump points of a discontinuous function in the presence of a noise by the wavelet approach. A computing algorithm of our method is proposed and then applied to the daily exchange rate of US Dollar against Deutsche Mark. All the points detected by our method reflect very strong economic and political impacts. Other statistical methods to detect jump points have also been applied to the same exchange rate data. Our proposed method has produced more convincing empirical results than others.     

Att-U-Net：融合注意力机制的U-Net骨导语声增强*

近年来大量全卷积网络、U-Net等编解码网络结构应用于语音增强,它们具有计算复杂度低、模型参数少等优势。然而,与长短时记忆模型等方法相比,这些编解码结构仍存在不能充分利用先后时间之间和高低频率之间的关联信息等缺点,尤其对于长序列数据的输入,编解码结构存在信息丢失的问题。为保持计算效率的同时考虑更充分的时频关联信息建模,本文提出一种融合注意力机制的U-Net网络的骨导语音增强方法（Att-U-Net）,通过在跳跃连接中引入注意力机制,生成一个权重矩阵,将编码层中的全局信息根据权重融入对应的解码层中,使网络在编解码过程中能够关注输入数据中与增强目标相关程度高的重要信息,同时抑制不相关的信息。在骨导语音数据集上的实验表明,融合注意力机制的U-Net网络能在保持模型轻量化的同时有效提升骨导语音的增强效果,增强后的语音在各项客观评价指标上均优于基线模型。通过对编解码网络中间层的可视化分析发现,在解码过程中注意力机制有效地保留了有声段的信息,滤除了骨导语音由于骨导传声特性带来的中频共振,从而使得增强后的骨导语音具有较好的听觉效果。