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81.
In this Letter, we propose general optimization methods to design broadband high-efficiency grating couplers for planar waveguides. We attribute the coupling bandwidth to the mismatch of effective indices between the diffracted beam and the actual grating structure around the operation wavelength for fiber to waveguide excitation. The coupling bandwidth formula is deduced. A simple parameter-separate optimization procedure is proposed for general layered grating couplers for high coupling efficiency. Using our principle, we optimized a grating coupler for a horizontal slot waveguide operating at wavelength 1.55 μm for TM polarization. The grating coupler has 1 dB bandwidth of 60 nm and coupling efficiency of 65% with incident light from single-mode optical fiber (SMF) at 8°. 相似文献
82.
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。 相似文献
83.
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. 相似文献
84.
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. 相似文献
85.
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. 相似文献
86.
Development of a method using high‐performance liquid chromatographic fingerprint and multi‐ingredients quantitative analysis for the quality control of Yangxinshi Pian
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Yerui Li Kai Yang Bowen Liu Ye Jin Xuesong Liu Zuolin Jiang Lianjun Luan Yongjiang Wu 《Journal of separation science》2015,38(17):2989-2994
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. 相似文献
87.
In this paper, we find some new explicit examples of Hamiltonian minimal Lagrangian submanifolds among the Lagrangian isometric immersions of a real space form in a complex space form. 相似文献
88.
Hongtao Liu Ling Liu Yiquan Xiong Xuemei Yang Tiangang Luan 《Journal of chromatography. A》2010,1217(43):6747-6753
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. 相似文献
89.
制备了苯基甲苯基二苯并富烯(phenyltolyldibenzofulvene,1)并研究了其发光性能.化合物1具有聚集诱导发光(aggregation induced emission,AIE)及结晶诱导荧光增强(crystallization enhanced emission,CEE)的性质,且化合物1可形成蓝色、蓝绿色荧光的晶体以及黄绿色荧光的无定形态.因化合物1分子为扭曲的螺旋桨构象,分子在聚集态中以较疏松的形式堆积,故化合物1可在热、溶剂气氛以及外力刺激下发生多种聚集态间的可逆转变,从而实现在三种不同发光状态间的可逆转变.我们尝试将化合物1用于光学记录,以单一化合物1为发光材料,其可在蓝绿及蓝色荧光颜色背景上以暗黄绿色字迹记录,可通过研磨、加热及溶剂气氛处理擦除字迹,并将记录纸分别转变为蓝色、蓝绿色及黄绿色,因此化合物1有望用于光存储材料. 相似文献
90.