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61.
本文对垂直低温两相流管底部液氮汽泡的上升速度运用高速摄像机进行了可视化实验研究,对所采集的实时图像进行处理.在Cole和Mendelson汽泡上升速度经验公式的基础上,通过对液氮汽泡的上升速度的分析,提出了圆管管路底部液氮汽泡的上升速度的拟合公式,分析研究其变化规律,为进一步探求圆管内液氮弹状汽泡的生成机理提供依据. 相似文献
62.
S. Pedersen-Bjergaard T. N. Asp J. Vedde G. E. Carlberg T. Greibrokk 《Chromatographia》1993,35(3-4):193-198
Summary Three chlorinated dimethyl sulfones and five chlorinated thiophenes have been identified in the alkaline extraction liquor from a bleach plant by gas chromatography with atomic emission detection (GC-AED) and with mass spectrometry (GC-MS). The information on elemental content obtained by GC-AED enabled a rapid screening of the sulfur compounds and provided important structural information complementary to the mass spectral data. Quantitation was accomplished by GC-AED based on universal calibration. 相似文献
63.
人工神经网络方法预测气相色谱保留值 总被引:8,自引:2,他引:8
本文运用一典型的人工神经网络模型-“反向传播“模型的改进形式,研究了诱导效应指数I,摩尔折射度Ro,疏水亲脂参数IgP,以及分子联通性指数与气象色谱保留行为的关系,实现了对色谱保留植的预测。神经网络预测模型的最大相对误差不超过8.7%。结果表明,该方法性能良好,可望成为色谱保留值预测的有效手段。 相似文献
64.
Summary Chiral recognition of many enantiomeric solutes by a chiral amide stationary phase is based mainly on hydrogen bonding. A
chiral-recognition-factor CHI is proposed, given by the difference of the enthalpy change in the enantiomer discrimination,
standardized with respect to the specific interaction of the solutes with the diamide core of the stationary phase. The r?le
of the entropy part is also discussed. By extrapolation of the retention behaviour to elevated temperature, peak inversion
of enantiomers is predicted.
Presented at the 15th International Symposium on Chromatography, Nürnberg, October 1984 相似文献
65.
66.
The application of the recently introduced ethylchloroformate derivatization method for the separation and determination of selenomethionine and selenocystein in selenium-enriched yeast and yeast-free tablets by means of a gas chromatography-mass spectrometry (GC-MS) system has been studied. The efficiency of three methods for the extraction of selenomethionine from the tablets were compared. Total selenium content of the same tablets were measured using inductively coupled plasma (ICP)-MS and it was found that in the selenized yeast tablets about 80% of the total selenium is present as selenomethionine. The results were in agreement with the values in the labels and with the literature. The accuracy of the total selenium analysis was controlled by the analysis of a reference material. 相似文献
67.
Summary An analytical GC method was developed which uses a single packed column consisting of three packings in series prepared with the following liquid phases: dimethyl sulfolane, propylene carbonate, and silver nitrate. This system provides satisfactory resolution of mixtures of C1–C5 hydrocarbons and dimethyl ether obtained when converting methanol to gasoline. Due to the high capacity of the column it is possible to inject larger sample amounts permitting trace analysis. 相似文献
68.
Evaluation of gas chromatography-tandem quadrupole mass spectrometry for the determination of organochlorine pesticides in fats and oils 总被引:1,自引:0,他引:1
Patel K Fussell RJ Hetmanski M Goodall DM Keely BJ 《Journal of chromatography. A》2005,1068(2):289-296
A gas chromatography-tandem quadrupole mass spectrometry multi-residue method for the analysis of 19 organochlorine pesticides in fats and oils has been developed. Gel permeation chromatography was employed to remove lipid material prior to GC-MS/MS analysis. Average recoveries of the pesticides spiked at 10 and 50 microg kg(-1) into fish oil, pork fat, olive oil and hydrogenated vegetable oil were typically in the range 70-110% with relative standard deviations generally less than 10%. Calculated limits of detection are between 0.1 and 2.0 microg kg(-1) and results obtained for the analysis of proficiency test materials are in good agreement with assigned values. The higher selectivity of the GC-MS/MS compared to electron capture detection and GC-MS in selective ion monitoring mode allowed unambiguous identification and confirmation of all the target pesticides at low microg kg(-1) levels in fats and oils in a single analysis. 相似文献
69.
Summary A method for the gas chromatographic trace analysis of underivatized nitrophenols in ground-water is presented. Using a highly
de-activated separation system a satisfactory precision for their quantitative GC analysis could be achieved by avoiding condensation
of the solvent and by fast injection of the sample. The reproducibility of the peak areas of eleven nitrophenols in ethylacetate
was <5 % RSD. Using a nitrogen-phosphorus detector detection limits were in a range from 10 to 30 pg. Within the concentration
range from 0.1 to 10 ng μl−1 the calibrations were linear with correlation coefficients >0.992.
The approach described was applied to the analysis of nitrophenols in ground-water near a former ammunition plant, after preconcentration
by continuous liquid/liquid extraction with ethylacetate. Using a GC-MS technique and retention times various nitrophenols
were identified and then quantified in the μg/L-range by applying NPD. 相似文献
70.
气相色谱-质谱法测定电子电气产品中多溴二苯醚及多溴联苯 总被引:14,自引:0,他引:14
建立了利用气相色谱-质谱测定电子、电气产品中多溴二苯醚及多溴苯的方法。对样品的粉碎、提取方法、色谱柱的选择、测定条件进行研究,并自建标准质谱图库;采用保留时间、Br同位素规则、质谱特征离子、谱库检索等4种方式相结合进行定性,避免了假阳性及漏检的情况,结果更加准确可靠。本法检出限为5mg/kg,PBDEs的回收率为91.3%,PBBs的回收率为92.5%,相对标准偏差(RSD)为4.3%。与现有方法相比,本法分离时间最短(6min),具有简便快速、实用性强、灵敏度高、准确可靠等特点,适用于电子电气产品、塑料、橡胶、汽车内饰材料等的溴系阻燃剂分析,满足欧盟RoHS指令检测的要求。 相似文献