中国紫胶树脂基本组成的研究

定量测定了紫胶树脂基本成分的含量；分离得到了紫胶树脂 状脂肪酸和环状萜烯酸的代表物－－紫胶桐酸和壳脑酸。研究发现国产紫胶中软树脂含量高于印度紫胶。结果证明国产紫胶与印度胶在组成和树脂分子构成方面基本一致。     

氮气中空心阴极放电条纹的发光特性

利用发射光谱法,在氮气环境下研究了圆柱型空心阴极放电条纹的特性。测量得到了气压为20 Pa,放电电流为1.3 mA时条纹区的发射光谱,结果表明发射光谱主要为氮分子的第一正带系(B3П_g →A3П_u)和 第二正带系(C3П_u→B3П_g )。利用双原子光谱发射理论,计算得到了氮分子振动温度的空间分布特性。结果表明光谱线强度呈周期性分布,明纹中心处的谱线强度高于暗纹中心处的谱线强度。明纹中心处的N₂分子振动温度为3 500～4 400 K,并且从阴极到阳极,明纹中心处光谱线强度和分子振动温度逐渐下降。同时测量得到了放电电流为1.0和1.5 mA时的发光条纹特性,研究了放电电流对条纹特性的影响。随着放电电流的增加,明纹中心处的分子振动温度升高,条纹间距增加。另外,利用测量得到的发光条纹,计算得到了条纹区的平均约化电场强度为44～49 m-1·Pa-1,并且由阴极向阳极逐渐降低。对于揭示气体放电中发光条纹的形成机理和促进空心阴极放电的稳定性有重要的参考价值。     

丙三醇溶液声致发光中的黑体辐射谱

利用U型管圆锥泡声致发光装置,测量到了丙三醇溶液中圆锥泡声致发光的光谱和光脉冲。结果表明,测量得到的发光光谱为光滑的连续谱,且与理论模拟得到的黑体辐射谱相吻合,拟合温度分布于2 600～3 500 K范围内。文章从空间和时间两方面分析了圆锥泡空化发光中存在黑体辐射的原因：较大的气泡体积(气泡塌缩半径为1.4 cm)与较长的发光时间(几十微秒)。另外,实验研究表明随着发光波长的增长,光脉冲宽度变宽,从而进一步证明了圆锥泡声致发光中的黑体辐射机制。最后,利用测量得到的发光光谱和脉冲计算得到了发光光强为0.18 J,远远高于其他方式得到的声致发光光强。     

溶液样品温度对ICP光源发射强度的影响

通过光电检测法研究了溶液样品温度在20,40和60 ℃条件下,对电感耦合等离子体(ICP)光源发射强度的影响。实验结果表明,随着溶液温度的提高,元素钡、铜和锌的谱线强度有明显的增强。观察了在不同溶液温度下,谱线强度随光源观察高度和载气压力的变化规律, 发现温度的提高使最佳观测高度位置降低,而最佳载气压力升高。     

防护板尺寸对Whipple防护结构撞击损伤影响的实验研究

通过高速撞击实验,探讨了采用小尺寸防护板的可行性。实验中采用的Whipple结构由尺寸变化的1 mm厚防护板（前板）和尺寸固定的3 mm厚舱壁板（后板）组成,防护板与舱壁板间隔10 cm。防护板为边长分别为8、12、16和20 cm的方形2A12铝合金板,舱壁板为边长为20 cm的方形5A06铝合金板。实验过程中均采用直径为4 mm的铝合金球形弹丸,撞击速度为1.45~1.71 km/s。实验结果表明:Whipple防护结构在舱壁板被击穿的概率大于0.8的条件下和击穿概率为0的条件下的极限速度以及舱壁板临界击穿条件下的速度都与防护板尺寸无关;并且,防护板前后表面击穿孔的直径及击穿孔侧壁的倾斜角也与防护板尺寸无关;但是,在速度相同的条件下随着板尺寸的增大,防护板板面的最大挠度增大,而且,防护板挠曲面的凸凹方向也由单一的凹向变成凸凹方向交替出现;随着速度的增加和板尺寸的增大,防护板最大挠度的增量减小。     

Biosynthesis of phycobilins. Formation of the chromophore of phytochrome, phycocyanin and phycoerythrin

Phycobiliproteins play important roles in photomorphogenesis and photosynthesis. The light-absorbing chromophores of the phycobiliproteins are linear tetrapyrroles (bilins) very similar in structure to the mammalian bile pigments. 5-Aminolaevulinate (5-ALA) is the first committed intermediate in phycobilin synthesis. The biosynthesis of 5-ALA, destined for phycobilins, occurs via the five-carbon pathway, now well established for tetrapyrrole synthesis in plants and distinct from the mammalian pathway. The phycobilins are formed by reduction of biliverdin which results from the synthesis and degradation of haem. This haem is an essential intermediate in the biosynthesis of phycobilins. Phycocyanobilin, the blue-green pigment found in certain algae and cyanobacteria, is formed from biliverdin via phytochromobilin, the chromophore of phytochrome. This leads to the likelihood that phytochromobilin is formed as an end product, or intermediate, in the synthesis of all phycobilins.     

大视角两步彩虹全息术

本文巧妙地运用了全息图的光路可逆性,采用两面反射镜与小面积全息图相结合,制得了视场角接近180°的大视角彩虹全息图.整个过程分两步完成,无需任何特殊的光学元件.文中给出了实验结果,并进行了讨论.     

The electrical properties of doped silicon,grown by Molecular-Beam-Epitaxy (MBE)

Measurements of the Hall coefficients and of the resistivity of MBE-grown Si, doped with P, As, Sb, B, and Ga in the concentration range 10¹⁴ to 10²⁰ cm^–3, were carried out at 77 K and at 300 K. With the exception of Ga-doped Si, the measured mobilities were close to or higher than those of bulk materials at both temperatures. The Mott metal/non-metal transition has been observed in the present epitaxial materials and the measured values for the critical impurity concentration at which the transition occurs, agree with values reported by other workers for bulk silicon.     

Comparison of the use of mass spectrometry and methylene unit values in the determination of the stereochemistry of estranediol, the major urinary metabolite of 19-nortestosterone in the horse

The stereochemistry of an isomer of 5-estrane-3,17 alpha-diol, the major metabolite of 19-nortestosterone in horse urine has been established by the use of methylene unit (MU) values. The empirical MU values of the bis-trimethylsilyl (TMS) derivatives of the eight available isomers of 5-androstane-3,17-diol and four isomers of 5-estrane-3,17 beta-diol were determined by capillary gas chromatography using three different columns. From this data the theoretical MU values for the bis-TMS derivatives of the four 5-estrane-3,17 alpha-diol isomers were predicted. Comparison of the experimentally determined MU value of the urinary metabolite with those of the theoretical values established the correct stereochemistry of the steroid. This method has been compared with the use of gas chromatography-mas spectrometry in the determination of the stereochemistry of unknown metabolites.