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51.
中药配方颗粒红外光谱法的快速鉴别   总被引:14,自引:0,他引:14  
周群  李静  孙素琴  梁曦云 《分析化学》2003,31(3):292-295
采用红外光谱法对中药配方颗粒及其辅料进行了鉴别研究。结果表明:不同生产厂商的配方颗粒中所添加的辅料类型及用量有较大差别;不同种的配方颗粒在辅料含量较低的情况下有较明显的指纹性,而辅料含量较高时,采用差谱技术可以提高谱图的指纹性,达到中药配方颗粒--鉴别的目的。该法简便、快速、可靠,是中药配方颗粒宏观质控的一个强有力的手段。  相似文献   
52.
采用改进颗粒床模型的CFD方法模拟了实验室规模冷模装置内鼓泡床的流体流动时空特性。模拟结果表明表观气速是影响气固动态特征和压力波动的主要因素之一:随表观气速的增大,气泡数目增加,气泡体积增大,压力波动增强;气速越高时均压降越大;在内循环鼓泡流化床内固体颗粒呈“单室”流型。上述与实验观察相吻合的模拟结果将有助于放大和设计商业化的内循环流化床生物质气化炉。  相似文献   
53.
通过吸附在铂纳米颗粒表面的氢交替还原氯金酸和氯铂酸,得到了复合型纳米颗粒Pt@Au/Pt,用UV-Vis光谱、TEM和XRD对其进行了表征.  相似文献   
54.
单分散磁性纳米颗粒的制备及生物高分子在其上的组装   总被引:3,自引:0,他引:3  
磁性纳米颗粒因其潜在的生物医学应用价值而成为纳米生物材料领域研究的前沿。本文综述了单分散磁性纳米颗粒的制备方法以及生物高分子在磁性纳米颗粒上的组装的研究进展。  相似文献   
55.
The composites with nano-particles of Ni-Fe alloys dispersed on the nano-layers of expanded graphite (EG) were prepared by the impregnation of EG with ethanol solutions of nickel and iron acetates, followed by drying and reduction in H2. The square nano-particles of Ni-Fe alloys with particle sizes of mainly 20~40 nm were found to be well spread on the layers of EG. The alloy nano-particles exhibited high shielding effectiveness (SE) for electromagnetic radiations at low frequencies due to their high magnetic conductivity. Since EG is electronically conductive and displayed high SE at high frequencies, the composites exhibited good SE at wide range of frequencies. The electric and magnetic conductivities of the composites could be monitored through regulating the loadings of alloy nano-particles on EG, and it was found that the composites with 20%~40% of the alloys exhibited good SE. Specifically, the composite 27%Ni-3%Fe-EG showed the excellent SE from 66 to 110 dB at the frequencies from 300 kHz to 1.5 GHz.  相似文献   
56.
报道了一种单颗粒微电极制备新方法, 并研究了LaNi4.7Al0.3球形单颗粒微电极的电化学行为.  相似文献   
57.
反相高效液相色谱法测定3种中成药中的葛根素   总被引:7,自引:0,他引:7  
田菁  黄阁  赵怀清  李发美 《色谱》2001,19(5):457-460
 建立了测定小儿清感灵片、步长新脑心通胶囊和感冒清热颗粒 3种中成药中葛根素含量的反相高效液相色谱方法。采用APEXODS色谱柱 ,以醋酸铵缓冲液 (10 0mmol/L ,pH 5 0 ) 甲醇 (体积比为 75∶2 5 )的混合溶液为流动相 ,检测波长为 2 5 0nm ,流速为 0 8mL/min。葛根素在 2mg/L~ 2 0mg/L时其色谱峰面积与质量浓度的线性关系良好 (r =0 9999) ;上述 3种中成药中的葛根素含量分别为 3 48mg/g ,1 0 8mg/ g及 1 5 2mg/ g(蔗糖型 ) ;其加样回收率分别为 99 0 % ,93 4%和 97 5 %。该法简便、快速、专属性强 ,可以作为多种中药制剂中葛根素含量的测定方法。  相似文献   
58.
Stable poly(styrene-co-sodium styrene sulfonate) (P(St-NaSS) nanoparticles with broader size distribution were synthesized by thermal emulsion polymerization without any conventional initiators and emulsifiers. The obtained polymer nanoparticles have higher ξ potential, and the particle sizes have broad distribution. The stability of polymer particles originated from the addition of small amounts of ionic comonomer, NaSS, which can act as an emulsifier in somewhat. The monomer conversion could reach up to about 28 wt% in 48 h, and did not increase by further polymerization when higher polymerization temperature (120 ℃) was employed. This polymerization system may be give some further understand for mechanism of emulsion polymerization.  相似文献   
59.
Oleic acid (OA)-modified SiO2 (OA-m-SiO2) nanoparticles were prepared using surface modification method. Infrared spectroscopy (IR) was used to investigate the structure of the OA-m-SiO2 nanoparticles, and the result showed that OA attached onto the surface of SiO2 nanoparticles through esterification. Effect of OA concentration on the dispersion stability of OA-m-SiO2 in heptane was also studied, and the result indicated that OA-m-SiO2 nanoparticles were dispersed in heptane more stably than the unmodified ones. OA-m-SiO2 nanoparticles can also be dispersed in polypropylene (PP) matrix in nano-scale. The effect of OA-m-SiO2 on crystallization of PP was studied by means of DSC. It was found that the introduction of OA-m-SiO2 resulted in significant increase in the crystallization temperature, crystallization degree and crystallization rate of PP, and OA-m-SiO2 could effectively induce the formation of β-crystal PP. Effect of OA-m-SiO2 content on mechanical properties of PP/OA-m-SiO2 nanocomposites was also studied. The results show that OA-m-SiO2 can significantly improve the mechanical properties of PP.  相似文献   
60.
The introduction of mesoporous nanosize zirconia to the catalyst for methanol synthesis dedicates the nanosized catalyst and mesoporous duplicated properties. The catalyst bears the larger surface area, larger mesoporous volume and more uniform diameter, more surface metal atoms and oxygen vacancies than the catalyst prepared with the conventional coprecipitation method. The modification of microstructure and electronic effect could result in the change of the reduced chemical state and decrease of reducuction temperature of copper, donating the higher activity and methanol selectivity to the catalyst. The results of methanol synthesis demonstrate that the Cu^+ is the optimum active site. Also, the interaction between the copper and zirconia shows the synergistic effect to fulfil the methanol synthesis.  相似文献   
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