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641.
The use of micellar electrokinetic capillary chromatography (MECC) with electrochemical detection is described for the determination of puerarin and daidzein in Puerariae radix and its medicinal preparations. Operated in a wall-jet configuration, a 300 μm diameter carbon-disk electrode was used as the working electrode, which exhibits good responses at +900 mV (versus SCE) for the two analytes. Under the optimum conditions, the analytes were base-line separated within 11 min in a sodium dodecyl sulphate—borax (pH 7.8) running buffer, and excellent linearity was obtained in the concentration range from 5.0×10−4 to 5.0×10−6 mol/l. The detection limit (S/N=3) was 6×10−7 and 1.1×10−6 mol/l for puerarin and daidzein, respectively. This work provides a useful method for the analysis of traditional Chinese medicines.  相似文献   
642.
杨毓华  李三喜 《应用化学》1997,14(1):104-106
线性低密度聚乙烯/乙烯醋酸乙烯共聚物共混体系的相容性及性能杨毓华*白春霞花荣于李三喜(中国科学院长春应用化学研究所长春130022)(沈阳化工学院高分子科学与工程系沈阳)关键词线性低密度聚乙烯,乙烯醋酸乙烯共聚物,共混,相容性,DSC,WAXD,力...  相似文献   
643.
The decomposition of methoxy on Cu(111), Ag(111), Au(111), Ni(111), Pt(111), Pd(111), and Rh(111) has been studied in detail by the density functional theory calculations. The calculated activation barriers were successfully correlated with the coupling matrix element V 2 ad and the d-band center (ε d ) for the group IB metals and group VIII metals, respectively. By comparison of the activation energy barriers of the methoxy decomposition on different metals, it was found that Pt is the best catalyst for methoxy decomposition. The possible reason why the metallic Pt is the best catalyst has been analyzed from both the energetic data and the electronic structure information, that is, methoxy decomposition on Pt(111) has the largest exothermic behavior due to the closest p-band center of the CH 3 O among all metals after the adsorption.  相似文献   
644.
The time-domain ABCD matrix formalism is based on the propagation of a Gaussian pulse which is characterized by the pulsewidth and chirp. In this paper, we will perfect this method and derive time-domain ABCD matrices for more optical devices. Especially, we extend this perfected theory to analyze the principle of passive mode-locking by reasonable approximation though, as we know, the output pulse generated from passive mode-locking fiber laser is of sech-shape. It is attractive because it can present a fairly apparent view to understand the mechanism of fiber lasers as well as analytic results to understand the pulse characteristics.  相似文献   
645.
麦裕华  陈徽  钱扬义 《化学教育》2009,30(8):22-24,80
"图像类比"是通过日常事物或生活情景图像实现类比科学概念的有效学习工具.使用文本分析法探讨人教版高中化学选修模块教科书中图像类比的使用情况,发现图像类比的使用率低和使用范围狭窄,内部结构简单而良好,具有充分的解释性语句.提出在化学教科书中使用图像类比的3项原则及使用图像类比进行教学活动的建议.  相似文献   
646.
This paper reports a simple method to prepare barium sulphate nanoparticles by use of tetradecanoic acid, hexadecanoic acid and stearic acid as modifier. The barium sulphate nanoparticles obtained are characterized by using Fourier transform infra-red spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic laser light scatter (DLLS) and thermogravimetric analysis (TGA), respectively. The results show that the BaSO4 particles are all spherical and in the nano-scale. Our method has a better dispersion and controllable diameter dependent on the length of the chain of organic acid and the pH value of the system. A possible mechanism is also discussed.  相似文献   
647.
By making use of Clark duality, perturbation technique and dual least action principle, some results on the existence of subharmonic solutions with minimal period to second-order subquadratic discrete Hamiltonian systems are obtained.  相似文献   
648.
考虑一类具有分布偏差变元的偶数阶中立型阻尼泛函微分方程的振动性,利用积分平均技巧和Riccati变换,获得了该类方程振动的几个准则,推广了现有文献的一些结果,并给出了几个应用实例.  相似文献   
649.
李静  郭展辰  赵旭  马玉花  韩萍  封顺 《色谱》2015,33(11):1210-1213
建立了一种高效液相色谱同时测定尿液中4种肾脏病常用药物依那普利、氨苯蝶啶、呋塞米及缬沙坦含量的方法。色谱分离选用WondaSil C18-WR (150 mm×4.6 mm, 5 μ m);以10.0 mmol/L乙酸铵溶液(pH 3.90)和乙腈为流动相进行梯度洗脱,流速为1.0 mL/min,于254 nm波长下检测,18 min内实现了4种药物的分离分析。结果表明依那普利、氨苯蝶啶、呋塞米、缬沙坦分别在0.15~300 mg/L、0.05~100 mg/L、0.75~750 mg/L、0.05~100 mg/L范围内线性良好,检出限依次为1.38×10-2、7.67×10-3、3.69×10-2、1.16×10-2mg/L,平均加标回收率在89.49%~99.20%之间,相对标准偏差(RSD, n=3)在4.12%~9.44%之间。结果表明该方法样品处理简便、快速,结果准确可靠,为肾脏病患者尿液中的治疗药物浓度监测提供了一种新方法。  相似文献   
650.
A simple and rapid sample preparation method of dispersive liquid-liquid microextraction(DLLME) was applied in the simultaneous determination of six parabens in the aqueous cosmetics. The analysis was performed on gas chromatography coupled with a flame ionization detection(GC-FID). The mixed solution containing 30 μL of chloroform(extraction solvent) and 300 μL of tetrahydrofuran(dispersive solvent) was rapidly injected into the sample solution for the purpose of microextraction. After that, the solution mentioned above was centrifuged at 4000 r/min for 10 min, and then the organic sediment phase was detected by GC-FID. The effects of experimental parameters, such as the extraction solvent and the volume of it, and the dispersive solvent and the volume of it, on the yield of the extraction were studied in detail. Under the optimum conditions, the enrichment factors of the target analytes range from 87 to 214. Linearity ranges are 0.05-10.0μg/mL for methylparaben and 0.025--5.0 μg/mL for the other five parabens. The relative standard deviations(RSDs) are lower than 8.2%(n=6). The proposed method was applied to the analysis of six parabens in eleven aqueous cosmetics. The recoveries of the target analytes in the spiked real samples are in the range of 81.0%-103%.  相似文献   
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