Ultraviolet Luminescence in Mg0.12Zn0.88O Alloy Films

We investigate the origin of ultraviolet （UV） emission from Mg0.12 Zn0.88 O alloy thin films with a wurtzite structure fabricated on c-plane Al2O3 substrates by plasma assisted molecular beam epitaxy. At room temperature, the absorption edge and UV emission band of the Mg0.12Zn0.88O film shift to high-energy side compared with ZnO films. Temperature dependence of the photoluminescence spectra shows that the UV emission is composed of free exciton and neutral donor bound exciton emissions. Two-step dissociation processes of the UV emission are observed with the increasing temperature. The thermal quenching mechanism is attributed to the dissociation of the free exciton from the neutral donor bound exciton in the low temperature region and the dissociation of free electron and hole from the free exciton in the high temperature region.     

防紫外线伞ATR-OMNI采样器的FTIR分析

本实验使用OMNI采样器，直接对伞面内外进行单反射ATR的分析，快速、简便、不破坏样品，得到分辨率很好的红外图谱，再配合红外谱库的谱图检索，可以分别得到匹配率95％以上的尼龙－6和聚酯型聚氨酯的分析结果。     

Eu^2＋：BaFCl光激励发光过程中紫外线的激发与漂白效应

通过改变紫外线的辐射照能量范围，研究了Ｅｕ＾２＋：ＢａＦＣｌ的光激励发光性质。发现紫外线能量大于Ｅｕ＾２＋的最低激发态能量及紫外线的能量小于Ｅｕ＾２＋最低激发态的能量两种情况下，光激励发光具有明显的差异，分析了产生差异的原因，给出了紫外线的辐照能量发生转时所对应的能级位置。     

3,4,5-三甲氧基苯甲酰甲壳素的制备与表征

在甲磺酸体系中，将具有较好紫外吸收性能的3，4，5—三甲氧基苯甲酸分子键接到甲壳素的分子链上，制得了3，4，5—三甲氧基苯甲酰甲壳素。采用红外光谱、^1H-NMR、广角X—射线衍射、紫外光谱等表征方法对改性产物进行了结构表征。通过对改性产物的紫外光谱表征发现产物具有一定的吸收紫外线能力。产物在有机溶剂中有一定的溶解性能。     

硬脂酸稀土对PVC热稳定效能的递变

研究了钪、钷外其他稀土金属硬脂酸皂对PVC热稳定作用. 结果表明 它们均属长期型热稳定剂, 与少量硬脂酸锌并用可有效改善其抑制PVC初期着色的效能;不同硬脂酸稀土与硬脂酸锌并用稳定的PVC具有相似的初期色相, 但中、长期热稳定性不同, 其中镧系金属皂的中、长期热稳定性随原子序数呈现明显的奇偶效应递变规律性;硬脂酸稀土具有类似于碱土金属皂的热稳定作用机制.     

聚氯乙烯复合热稳定剂中铅镉钡的同时测定

聚氯乙烯（PVC）材料广泛应用于建筑、电讯、交通、电子、化工、包装等行业。然而，PVC加工时存在着一个致命的弱点，就是其流动温度为136℃，分解温度为140℃，两者相差仅4℃，给加工带来很大难度，为了能顺利加工就必须加入热稳定剂，热稳定剂是PVC加工不可缺少的主要助剂之一。热稳定剂种类繁多，我国目前大量使用的稳定剂为铅盐及金属皂等稳定剂，产量高达4．5万吨。由于铅、镉、钡等金属元素具有一定的毒性，使用中易造成环境污染，有害于人体健康，因此必须严格加以控制。     

三苄基氯化锡及其衍生物的合成

三苄基氯化锡最初用格氏法制得。Keiti等曾报道由锡和苄基氯直接制备,这时溶剂对反应的影响很大:用水作溶剂时得到三苄基锡;用甲苯作溶剂时得到二苄基二氯化锡;用正丁醇作溶剂时三苄基氯化锡的产率只有61％。在反应体系中加入KI、KBr或H_3PO_4等催化剂,三苄基氯化锡的产率也只有60％。本文用DMF作溶剂,AlCl_3-I_2作催化剂,并首次在反应体系中加入镁、锌、铝和钠等使副产物氯化亚锡还原成活性很高的金属锡,后者再与等基氯反应,可使三苄基氯化锡的产率提高到91.3％。文中还报导三种尚     

有机锡聚醚的合成及性质的研究

利用界面缩聚技术,将二烷基二氯化锡、二(β-烷氧羰乙基)二氯化锡与有机二元醇、酚、硫醇反应,制成了一系列新的有机锡大分子化合物.对这些新化合物进行了分子量、红外光谱、TG/DTG测试.对有机锡大分子化合物阻止聚氯乙烯(PVC)热分解性能进行了测定.结果表明,新合成的有机锡聚醚化合物可作为PVC热稳定剂使用.     

分散聚合水基聚苯胺乳胶微球制备与表征

水溶性空间稳定剂聚乙烯吡咯烷酮（PVP）存在时，采用分散聚合制备水溶性单分散的聚苯胺(PAn)乳胶粒子，采用透射电子显微镜（TEM）观察粒子形态及尺寸；利用紫外-可见吸收光谱对胶体分散体系进行表征.实验结果表明，当PAn含量较少（w< 16.78％）时， PAn-PVP复合乳胶粒子呈米粒状；当PAn含量较大（w >23.22％）时， PAn-PVP复合乳胶粒子呈球形.     

Determination of Tetracyclines in Honey Using Liquid Chromatography with Ultraviolet Absorbance Detection and Residue Confirmation by Mass Spectrometry

A determination method has been optimized and validated for the simultaneous analysis of tetracycline （TC）, oxytetracycline （OTC）, chlortetracycline （CTC） and doxycycline （DC） in honey. Tetracyclines （TCs） were removed from honey samples by chelation with metal ions bound to small Chelating Sepharose Fast Flow columns and eluted with Na2EDTA-Mcllvaine pH 4.0 buffers. Extracts were further cleaned up by Oasis HLB solid-phase extraction （SPE）, while other solid-phase extraction cartridges were compared. Chromatographic separation was achieved using a polar end-capped C 18 column with an isocratic mobile phase consisting of oxalic acid, acetonitrile and methanol. LC with ultraviolet absorbance at 355 nm resulted in the quantitation of all four tetracycline residues from honey samples fortified at 15, 50, and 100 ng/g, with liner ranges for tetracyclines of 0.05 to 2 μg/mL. Mean recoveries for tetracyclines were greater than 50% with R.S.D. values less than 10% （n= 18）. Detection limits of 5, 5, 10, 10 ng/g for oxytetracycline, tetracycline, chlortetracycline and doxycycline, respectively and quantitation limits of 15 ng/g for all the four tetracyclines were determined. Direct confirmation of the four residues in honey （2-50 ng/g） was realized by liquid chromatography-tandem mass spectrometry （LC/MS/MS）. The linear ranges of tetracyclines determined by LC/MS/MS were between 5 to 300 ng/mL, with the linear correlation coefficient r〉 0.995. The limits of detection of 1 to 2 ng/g were obtained for the analysis of the TCs in honey.