Eine Apparatur zur Messung natürlicher 4C-Aktivitäten

Aufbau, Arbeitsweise und Eigenschaften einer Apparatur, mit der naturliche ^l4C-Aktiviäten in Grund- und Oberflächenwässern gemessen werden können, werden beschrieben.

Die Messung erfordert 3 Arbeitsschritte: Probenahme, Synthese von Benzol, welches dann den Probenkohlenstoff enthält, und Messung der ¹⁴C-Aktivität in einem Flüssigkeitsszintillationszähler.

Die Apparatur kann zur Datierung von Wasserproben im Altersbereich zwischen 200 und 37000 a verwendet werden.     

电枢超导型高温超导电机原理样机的温度场数值模拟研究

本文对一种电枢绕组部分采用高温超导线圈,转子励磁部分采用永磁体的新型高温超导原理样机进行了整体温度场的数值模拟计算,主要包括稳态冷却过程、瞬态冷却过程及零件配合面径向变形量计算三个方面的内容.通过对边界条件及传热条件的简化,建立了电机的近似平面轴对称传热模型,得出了高温超导线圈处冷却至工作温度(77K左右)所需的时间.另外还计算出零件配合面上的径向变形量,可据此制订低温尺寸公差,为零件的机械加工提供了指导.     

Simultaneous Determination of Acetylsalicylic Acid and Caffeine in Pharmaceutical Formulation by First Derivative Synchronous Fluorimetric Method

A sensitive, rapid, and specific assay has been developed for the simultaneous determination of acetylsalicylic acid and caffeine in commercial tablets based on their natural fluorescence. The mixture of these drugs was resolved by first derivative synchronous fluorimetric technique using two scans. At Δλ=106 nm, using first derivative synchronous scanning, only acetylsalicylic acid yields a detectable signal at 316 nm (peak to zero method) which is unaffected by caffeine. At Δλ=30 nm, the signal of caffeine at 288 nm (peak to zero method) is not affected by acetylsalicylic acid. The range of application is between 0.021 and 41.62 μg ml⁻¹ (correlation coefficient, R=0.9995) for acetylsalicylic acid and between 0.4486 and 44.86 μg ml⁻¹ (correlation coefficient, R=0.99786) for caffeine. The recovery range of 98.40–102% for acetylsalicylic acid and 90–100.5% for caffeine from their synthetic mixture was reported. Overall recovery of both compounds about 97–99% for acetylsalicylic acid and 97–98% for caffeine was obtained from real sample analysis. The detection limits are 0.0013 μg ml⁻¹ and 0.0306 μg ml⁻¹ for acetylsalicylic acid and caffeine, respectively. The relative standard deviation (n=10) for 20 μg ml⁻¹ of acetylsalicylic acid is 2.75% and for 2.2 μg ml⁻¹of caffeine is 1.7%.     

Detection

This review on second- and third-generation multidetectors devoted to heavy-ion collisions aims to cover the last twenty years. The presented list of devices is not exhaustive but regroups most of the techniques used during this period for nuclear reactions at intermediate energy (≃ 10A MeV to 1A GeV), both for charged-particle and neutron detection. The main part will be devoted to 4π multidetectors, projectile decay fragmentation, high-resolution magnetic spectrometers, auxiliary detectors and neutron detection. The last part will present the progress in electronics and detection in view of the construction of future-generation detectors.     

Development of neutron detectors and neutron radiography at Bhabha Atomic Research Centre

Design and development of neutron detectors and R&D work in neutron radiography (NR) for non-destructive evaluation are important parts of the neutron beam and allied research programme of Solid State Physics Division (SSPD) of Bhabha Atomic Research Centre (BARC). The detectors fabricated in the division not only meet the in-house requirement of neutron spectrometers but also the need of other divisions in BARC, Department of Atomic Energy units and some universities and research institutes in India and abroad for a variety of applications. The NR facility set up by SSPD at Apsara reactor has been used for a variety of applications in nuclear, aerospace, defense and metallurgical industries. The work done in the development of neutron detectors and neutron radiography is reported in this article.      

Performance studies on high pressure 1-D position sensitive neutron detectors

The powder diffractometer and Hi-Q diffractometer at Dhruva reactor make use of five identical 1-D position sensitive detectors (PSDs) to scan scattering angles in the range 3° to 140°. In order to improve the overall throughput of these spectrometers, it is planned to install a bank of 15 high-efficiency and high-resolution PSDs arranged in three layers with five PSDs in each layer. With each high pressure PSD (³He 10 bar + Kr 2 bar) showing the efficiency gain of 1.8 at 1.2 Å, detector bank is expected to show overall gain of 5.5 times the present detection efficiency and reduction in data collection time by equivalent factor. The 1-D PSDs are developed in batches of five, and are characterized so that all PSDs operate at uniform parameters such as position resolution, uniformity of efficiency and linearity of response. Position spectrum indicates the differential position resolution to be ～1 mm and integral position resolution to be 3–4 mm. Broadening of position spectrum at the extreme end of sensitive length of PSD is analysed using fine shift of the beam. Dependence of position resolution and dynamic range of output pulse on the input impedance of pre-amplifier is also presented.     

Simultaneous determination of yohimbine and boldine by first-derivative synchronous spectrofluorimetry

A method for the simultaneous determination of yohimbine and boldine in mixtures by first-derivative synchronous spectrofluorimetry has been developed. The method is based on their native fluorescence in 0.1N sulphuric acid medium. The constant wavelength difference chosen to optimize the determination was =_em -_em=82 nm. Yohimbine was measured at _ex//_em= 285/367 nm, and boldine at _ex/_em=272/354 nm. The range of application is 10–500 g/l for yohimbine and 1–50 g/l for boldine. The method was applied to the determination of yohimbine and boldine in synthetic mixtures and pharmaceuticals, with errors generally 2%. Relative standard deviations were about 2%.Dedicated to Professor Fermin Capitán on his 72th birthday     

胶束增敏导数—可变角同步荧光法同时测定两种羟基联苯

本文建立了２，２’－二羟基联苯（ＤＨＰ）和４－羟基联苯（ＨＰ）的胶束增敏导数－可变角同步荧光同时分析方法，可变角同步扫描所得到的ＤＨＰ和ＨＰ的谱峰位置均对应于常规光谱中的最佳激发－发射位置，经二阶求导后，消除分析谱带干扰，所得的二阶导数－可变角同步光谱即可用于两物质的同时测定，方法快速灵敏，ＤＨＰ测定范围为０．０５～０．５ｍｇ／Ｌ，ＨＰ测定范围为０．０７～２ｍｇ／Ｌ。     

二阶导数同步荧光光谱法同时直接测定厚朴酚及和厚朴酚

研究了厚朴酚与和厚朴酚及其混合溶液的二阶导数同步荧光光谱,结果两者的二阶导数同步荧光光谱得到完全分离,消除了彼此间的干扰,据此建立了一种二阶导数同步荧光光谱法同时直接测定混合物中厚朴酚与和厚朴酚的新方法.厚朴酚与和厚朴酚的线性范围分别为2.8～500.0 μg/L和4.3～560.0 μg/L;检出限分别为0.84和1.30 μg/L,回收率分别为94.65%～105.58%和95.09%～104.51%; 相对标准偏差均低于4.08%.本方法用于同时直接测定厚朴药材及其提取物中厚朴酚与和厚朴酚含量,结果令人满意.