比色法测定纺织品中甲醛含量的确认研究

对纺织品中的甲醛含量测定的乙酰丙酮比色法中双甲酮确认试验进行了研究 ,发现在乙酰丙酮存在下双甲酮与甲醛的反应会发生逆反应 ,指出了文献方法中这一部分叙述的不准确之处     

对“微波共振跃迁法测量电子偶素2~3S_1-2~3P_1精细结构”实验拟合公式的探讨

本文对Michigan大学S.Hatamian等人在“微波共振跃迁法测量电子偶素2~3S_1-2~3P_J精细结构”实验中所用拟合公式进行了审慎的分析和推证,修正了该公式的功率增宽项,并就Mainz大学R.Ley等人对该公式的批评作了评价。最后,采用新、旧拟合公式对Michigan组实验数据进行拟合并讨论其结果。     

Fluorescence staining of yeast cells permeabilized by killer toxin K1: Determination of optimum conditions

Optimal assay conditions were established for the previously described method used to determine the activity ofSaccharomyces cerevisiae pore-forming killer toxin K1. The method is based on cell staining with bromocresol purple. Sensitive cells ofS. cerevisiae from the early exponential phase under nongrowth conditions and in the presence of glucose were the most convenient for determining the killer toxin activity. Maximum killing war reached when the suspension was buffered with 10 mM citrate-phosphate at pH 4.6.     

DFT study of NH3 dissociation on Si(1 1 1)-7 × 7. The role of intermolecular interactions

The adsorption of NH₃ molecule on the Si(1 1 1)-7 × 7 surface modelled with a cluster has been studied using density functional theory (DFT). The results indicate the existence of a precursor state for the non-dissociative chemisorption. The active site for the molecular chemisorption is the adatom; while the NH₃ molecule adsorbs on the Si restatom via this preadsorbed state, the adsorption on the Si adatom is produced practically without an energy barrier. The ammonia adsorption on the adatom induces an electron transfer from the dangling bond of this atom to the dangling bond of the adjacent Si restatom, hindering this site for the adsorption of a second NH₃ incoming molecule. However, this second molecule links strongly by means of two H-bonds. The dissociative chemisorption process was studied considering one and two ammonia molecules. For the dissociation of a lonely NH₃ molecule an energy barrier of ∼0.3 eV was calculated, yielding NH₂ on the adatom and H on the restatom. When two molecules are adsorbed, the NH₃-NH₃ interaction yields the weakening of a N-H bond of the ammonia molecule adsorbed closer the Si surface. As a consequence, the dissociation barrier practically disappears. Thus, the presence of a second NH₃ molecule at the adatom-restatom pair of the Si(1 1 1)-7 × 7 surface makes the dissociative reaction self-assisted, the total adsorption process elapsing with a negligible activation barrier (less than 0.01 eV).     

掺CdSxSe1-x玻璃波导分布反馈光学双稳器件

本文给出了掺CdS_xSe_1-x玻璃平面波导分布反馈(DFB)光学双稳器件的设计和制备方法,实现了低功耗、快速的本征光学双稳。     

南海一号出水景德镇窑与龙泉窑青瓷特征的无损分析研究

古代陶瓷产地研究是陶瓷考古的重要内容,也是科技考古工作者研究的重点。目前国内古代陶瓷产地研究主要依赖化学成分分析技术,对陶瓷釉层结构特征的无损分析研究却相对缺乏,难以对古代陶瓷进行全方位的认知。该研究首次将光学相干层析(OCT)与X射线荧光(XRF)光谱分析技术相结合,对南海一号沉船出水的南宋初期景德镇窑和龙泉窑青瓷瓷釉的断层结构特征和化学成分特征进行综合无损分析研究。首先采用扫频OCT成像系统对两个窑址青瓷瓷釉断层结构及装饰工艺特征进行了研究,分析了青瓷瓷釉类型、釉层厚度、釉层内气泡、包裹体、表面裂纹等特征及分布状况,对比了两窑址青瓷瓷釉断层结构特征,确定了可能采用的装饰工艺。其次,利用X射线荧光(XRF)光谱分析获得了两窑址青瓷胎釉的化学成分,对比研究了两个窑址青瓷胎釉化学成分差异,进而探讨了瓷釉断层OCT图像特征与釉层化学成分之间存在的联系。实验结果表明,景德镇青瓷和龙泉青瓷样品在釉层厚度、气泡、裂纹、包裹体等瓷釉断层结构特征上差异明显,在胎釉化学成分方面,两类青瓷在胎釉着色相关元素、釉层碱性氧化物等成分含量上也存在差异。同时,瓷釉断面结构特征差异与釉层化学成分差异存在紧密联系。实验证明,将OCT与XRF相结合是一种有效的辨别瓷器窑口的科学技术方法。     

铽－甲基吲哚乙酰丙酮三元配合物发光过程研究

测定和分析了ＲＥ．Ｌ１．Ｌ２（ＲＥ＝Ｔｂ（Ⅲ）、Ｇｄ（Ⅲ），Ｌ１＝３Ｍ（３甲基吲哚－１－乙酰基丙酮），Ｌ２＝ＴＰＰＯ、Ｐｈｅｎ、Ｄｉｐｙ）三元配合物的荧光光谱、磷光光谱、磷光寿命及变温荧光光谱等．讨论了Ｔｂ（Ⅲ）与配体之间的能级匹配和Ｌ１与Ｌ２的三重态之间传能的问题，说明了影响这些三元配合物荧光效率的主要因素及其发光过程．     

Chemisorption of 1,1-dichloroethene on the Si(1 1 1)-7 × 7 surface

Chemisorption of 1,1-dichloroethene (Cl₂CCH₂) to a Si(1 1 1)-7 × 7 surface was studied by means of X-ray photoelectron spectroscopy using synchrotron radiation, recording chlorine 2p and carbon 1s spectra. For carbon 1s, spectral assignment of the chemisorbed species is based on quantum chemical calculations of chemical shifts in model compounds.The results confirm the identity of covalently bonded 1-chlorovinyl (-CClCH₂) and vinylidene (CCH₂) adspecies. Upon chemisorption at room temperature it was found that about one-third of the molecules break one C-Cl bond while about two-thirds of the adsorbates break two C-Cl bonds. We do not, however, find evidence for isomerization of CCH₂ to di-bonded vinylene (-CHCH-).     

The rotational anisotropies in the ferromagnetism/antiferromagnetism 1/ antiferromagnetism 2 exchange bias structures

The rotational anisotropies in the exchange bias structures of ferromagnetism/antiferromagnetism 1/antiferromagnetism 2 are studied in this paper. Based on the model, in which the antiferromagnetism is treated with an Ising mean field theory and the rotational anisotropy is assumed to be related to the field created by the moment induced on the antiferromagnetic layer next to the ferromagnetic layer, we can explain why in experiments for ferromagnetism (FM)/antiferromagntism 1 (AFM1)/antiferromagnetism 2 (AFM2) systems the thickness-dependent rotational anisotropy value is non-monotonic, i.e. it reaches a minimum for this system at a specific thickness of the first antiferromagnetic layer and exhibits oscillatory behaviour. In addition, we find that the temperature-dependent rotational anisotropy value is in good agreement with the experimental result.     

Pressure-Induced Shifts of R1 and R2 Lines of YAG:Cr3+

By means of improved ligand-field theory, the "pure electronic" pressure-induced shifts (PS's) and the PS's due to electron-phonon interaction (EPI) of R1 line and R2 line of YAG:Cr3 have been calculated, respectively.The calculated results are in very good agreement with the experimental data. It is demonstrated that the admixture of |t22(3T1)e4T2> and |t322E> bases in the wavefunction of R1 level of YAG:Cr3 and its change with pressure play a key role for the PS of R1 line. The behaviors of the "pure electronic" PS of R1 line and the PS of R1 line due to EPI are different. It is the combined effect of them that gives rise to the total PS of R1 line, which has satisfactorily explained the experimental results. The systematic analyses and comparisons between the feature of R1-line PS of YAG:Cr3 and the ones of three laser crystals (GSGG:Cr3 , GGG:Cr3 and ruby) have been made, and the origin of the difference between them has been revealed.