137 resultados para ION EXCHANGE CHROMATOGRAPHY


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介绍了采用光刻离子交换工艺制作平面交叉型微透镜阵列的方法。利用积分形式的光线方程式讨论了平面交叉型微透镜的近轴光学特性,研究了微透镜的光线轨迹方程式和一些重要的近轴成像特性,利用ABCD定理得到了平面交叉型微透镜像距、焦距、像高、横向放大率和主平面位置的数学表达式,焦距的理论计算结果和实验数据吻合得很好。

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对离子交换波导制备过程中掺铒磷酸盐玻璃表面的侵蚀问题进行了研究,分析了产生侵蚀的原因,提出镀K9玻璃薄膜的方法,对掺铒磷酸盐玻璃表面进行保护.采用光学显微镜和原子力显微镜对波导表面特性进行了表征。同时对平板波导的光学特性进行了测试.研究表明K9玻璃薄膜不仅能够对掺铒磷酸盐玻璃起到保护作用,同时允许交换离子透过进入磷酸盐玻璃形成波导层.

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采用镀K9玻璃薄膜方法来解决离子交换掺铒磷酸盐玻璃波导表面的侵蚀问题,对K9玻璃薄膜的厚度进行了优化研究。测量分析了样品的荧光光谱和荧光寿命,采用光学显微镜和棱镜耦合技术对不同K9玻璃薄膜厚度下制备波导的表面形貌和导光特性进行了表征和测试。结果表明,与掺铒磷酸盐玻璃原材料相比,镀K9玻璃薄膜后荧光光谱保持不变,荧光寿命稍有下降(约0.2 ms);K9玻璃薄膜的厚度在60~80 nm的范围内保护效果最佳。为下一步制备掺铒有源玻璃光波导器件奠定了良好的实验基础。

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制备了用于离子交换法制备光波导器件的掺铒碲-钨-钠玻璃基质。应用扎得-奥菲而特(Judd—Ofelt)理论计算了玻璃样品的三个强度参量,由强度参量计算了Er^3+离子的自发跃迁几率、荧光分支比等光谱参量;应用麦克库玻(McCumber)理论,计算了Er^3+离子在1.5μm的受激发射截面,荧光测试发现Er^3+离子的荧光半峰全宽可达65nm。比较了Er^3+离子在不同玻璃基质中的光谱特性。结果表明,Er^3+离子在碲-钨-钠玻璃中具有较高的受激发射截面和较宽的荧光半峰全宽,可以用于宽带光波导器件的制备。

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研制了一种用于宽带波导放大器的掺铒碲钨酸盐激光玻璃材料,对玻璃热稳定性、光谱性质进行了表征,并在其上采用离子交换法制作了平面光波导.掺铒碲钨酸盐玻璃的转变温度Tg和析品开始温度Tx分别为377.1和488.5℃;荧光半高宽为52nm;应用McCumber理论,计算得出Er^3+离子4I13/2→^4I15/2跃迁在峰值波长1532nm的受激发射截面为0.91×10^-20cm^2.不同条件下制作了在632.8nm处多模的平面光波导,通过拟合得到Ag^+离子在300℃的有效扩散系数De为2.82×10^-1

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A novel Vb(3+)-Er-(3+) codoped phosphate glass for high power flashlamp pumping and high repetition rate laser at 1.54 mu m, designated EAT5-2, is developed. The weight-loss rate of is 1.3 x 10(-5) gcm(-2) h(-1) in boiling water, which is comparable to Kigre's QX-Er glass. Some spectroscopic parameters are analysed by Judd-Ofelt theory and McCumber theory The emission cross section is calculated to be 0.73 x 10(-20) cm(2). The thermo-mechanical properties of EAT5-2 are modified after an ion-exchange chemical strengthening process in a KNO3/NaNO3 molten salt bath. The thresholds for optical damage from the flashlamp pumping are tested on glass rods. A repetition rate of 15 Hz is achieved for chemically strengthened glass. The laser experimental results at. 1.54 mu m from flashlamp pumping are also reported.

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制备了化学稳定的Er^3+/Yb^3+共掺的磷酸盐玻璃,并在其中制作了用于光放大器和激光器的平面光波导.这种磷酸盐玻璃的失重速率为4.7×10^-5g·cm^-2·hr^-1,小于Kigre公司商业化的磷酸盐玻璃QX/Er的失重速率.采用Ag^+-Li^+交换技术制作了平面光波导并用m-线光谱在632.8nm测量了平面光波导的有效折射率.根据反WKB法得到折射率形貌,计算了离子交换参数如:离子交换深度、表面折射率,折射率改变和扩散系数等.

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A new Er(3+)/Yb(3+) co-doped phosphate glass has been prepared, which exhibits good chemical durability and spectralproperties. Planar graded index waveguides have been fabricated in the glass by (Ag+)-Na(+) ion exchange in a mixed melt of silver nitrate and potassium nitrate. Ion exchange is carried out by varying the process parameters such as temperature, diffusion time, and molten salt compositions. The diffusion parameters, diffusion coefficients, and activation energy are determined by the guidelines of fabricated waveguides, which are determined by the input prism coupling technique.

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A waveguide amplifier is fabricated by Ag+-Na+ two-step ion exchange on Er/Yb-doped phosphate glass. The spectroscopic performance of glass and the properties of channel waveguide are characterized. A double-pass configuration is adopted to measure the gain and noise figure (NF) of the waveguide amplifier, and the comparison of gain and NF for the single and double-pass configuration of the waveguide amplifier is presented. The results show that the double-pass configuration can make the gain increase from 8.8dB (net gain 2.2dB/cm) of the single-pass one to 14.6 dB (net gain 3.65 dB/cm) for small input power at 1534 nm, and the NF are all lower than 5.5dB for both the configurations.

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研究了退火和二次离子交换对Er^3+/Yb^3+共掺的磷酸盐玻璃平面光波导传输特性的影响。在退火过程中,由于热效应和波导层Ag^+离子的浓度差使得Ag^+离子重新分布;随着退火时间的延长和温度的升高,光波导模式数目逐渐增加,波导层深度加深,且波导表面折射率与玻璃基质折射率差减小,退火扩散深度与退火时间的平方根成正比。电子探针结果显示在二次离子交换后形成了掩埋式的光波导,Ag^+离子浓度接近二次方分布,而掩埋式的光波导有助于降低光波导的传输损耗。

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通过优化熔融条件和玻璃组份,成功开发出一种新的Er^3+/Yb^3+共掺磷酸盐玻璃,其在沸水和熔盐中均表现出很好的化学稳定性。通过分析室温下Er^3+/Yb^3+共掺磷酸盐玻璃的吸收光谱,计算得到了Er^3+离子在波长1533nm处的峰值发射截面和杜得-奥菲而特强度参数;其中Er^3+离子在波长1533nm处的峰值发射截面为0.72×10^20cm^2,大于Schott的IOG1玻璃中Er^3+离子的峰值发射截面0.67×10^-20cm^2。通过改变离子交换的条件,获得了1.55μm单模光波导的制作条件

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Several biochemical and biological activities such as phospholipase A(2), arginine esterase, proteolytic, L-amino acid oxidase, 5'nucleotidase, acetylcholinesterase, thrombin-like, anticoagulant, and hemorrhagic activities were determined for whole desiccated venom of Trimeresurus jerdonii. An acidic phospholipase (named TJ-PLA(2)) was purified by anionic exchange chromatography, gel filtration, and reverse phase HPLC. TJ-PLA(2) had a molecular weight of 16,000 and a pI of 4.8. TJ-PLA(2) was non-lethal to mice up to an i.p. dose of 15 mg/kg body weight and lacked neurotoxicity and myotoxicity. It induced edema in the footpads of mice. The purified enzyme inhibited ADP- and collagen-induced human platelet aggregation in a manner which was both dose- and time-dependent.

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A hemorrhagic proteinase, jerdohagin, was purified from Trimeresurus jerdonii venom by gel filtration and ion-exchange chromatographies. It was a single chain polypeptide with an apparent molecular weight of 96 kDa as estimated by SDS-PAGE under the non-reducing and reducing conditions. Internal peptide sequencing indicated that it consisted of metalloproteinase, disintegrin-like and cysteine-rich domains and belonged to the class III snake venom metalloproteinases (class P-III SVMPs). Like other typical metalloproteinases, hemorrhagic activities of jerdohagin were completely inhibited by EDTA, but not by PMSF. Jerdohagin preferentially degraded a-chain of human fibrinogen. Interestingly, jerdohagin did not activate human prothrombin, whereas it cleaved human prothrombin and fragment F1 of activated human prothrombin. (C) 2004 Elsevier Ltd. All rights reserved.

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A new L-amino acid oxidase (designated as DRS-LAAO) was purified from Daboia russellii siamensis venom by ion-exchange, gel filtration and affinity chromatographies. DRS-LAAO is a homodimeric enzyme with a molecular weight of 120.0 kDa as measured by size

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Ovulation in the Bactrian camel depends upon ovulation-inducing factors in the seminal plasma. The present study was conducted to isolate and purify the bioactive fractions from the seminal plasma of these camels. The seminal plasma was fractionated by anion-exchange chromatography, and six fractions were obtained. The bioactive potential of each fraction was estimated from its effect on rat pituitary tissue cultured in vitro and by the effect of an intramuscular injection of the fraction into female camels in vivo. Both the third fraction (F3) and the fifth fraction (F5) stimulated the release of LH in vitro and in vivo. In addition, female camels ovulated within 48 h after intramuscular injection of F3. However, neither F3 nor F5 had any significant effect on the secretion of FSH, either in vitro or in vivo. When F3 was further fractionated into four subfractions, the third subfraction (F3-3) still stimulated the in vitro release of LH, but not of FSH. An attempt to further purify the ovulation-inducing factors in F3-3 failed owing to the similarity of the molecular characters.