853 resultados para Mineral Retention


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Reversed-phase high performance liquid chromatography (RP-HPLC) was employed to develop predictive models for fish bioconcentration factors (BCF) of organic compounds. Estimation of BCF from RP-HPLC retention parameters on octadecyl-bonded silica gel (ODS), cyanopropyl-bonded silica gel (CN), and phenyl-bonded silica gel (Ph) columns were investigated. The results show that, for a set of compounds belonging to different chemical classes, the CN stationary phase is the best one among the three columns and better than n-octanol/water model for BCF estimation. A multi-column RP-HPLC model, using the retention parameters on the CN and Ph columns as the variables of multiple linear regression equations, was further evaluated to estimate BCF of organic compounds belonging to different chemical classes, and the results show that the multi-column RP-HPLC model is better than that of any single RP-HPLC column for BCF estimation.

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A new numerical emulation algorithm was established to calculate retention parameters in RP-HPLC with several retention times under different linear or nonlinear binary gradient elution conditions and further predict the retention time under any other binary gradient conditions. A program was written according to this algorithm and nine solutes were used to test the program. The prediction results were excellent. The maximum relative error of predicted retention time was less than 0.45%. (C) 2002 Elsevier Science B.V. All rights reserved.

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A novel approach is proposed for the simultaneous optimization of mobile phase pH and gradient steepness in RP-HPLC using artificial neural networks. By presetting the initial and final concentration of the organic solvent, a limited number of experiments with different gradient time and pH value of mobile phase are arranged in the two-dimensional space of mobile phase parameters. The retention behavior of each solute is modeled using an individual artificial neural network. An "early stopping" strategy is adopted to ensure the predicting capability of neural networks. The trained neural networks can be used to predict the retention time of solutes under arbitrary mobile phase conditions in the optimization region. Finally, the optimal separation conditions can be found according to a global resolution function. The effectiveness of this method is validated by optimization of separation conditions for amino acids derivatised by a new fluorescent reagent.

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A novel method for the optimization of pH value and composition of mobile phase in HPLC using artificial neural networks and uniform design is proposed. As the first step. seven initial experiments were arranged and run according to uniform design. Then the retention behavior of the solutes is modeled using back-propagation neural networks. A trial method is used to ensure the predicting capability of neural networks. Finally, the optimal separation conditions can be found according to a global resolution function. The effectiveness of this method is validated by optimization of separation conditions for both basic and acidic samples.

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Polymethacrylate-based monolithic columns were prepared for capillary electrochromatography (CEC) by in situ copolymerization of butyl methacrylate (BMA), 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS), and ethylene dimethacrylate (EDMA) in the presence of a porogen in fused-silica capillaries of 100 mum I.D. The abnormal phenomenon that retention factors for neutral species decreases with applied voltage in CEC was observed. Capillary electrophoresis (CE) instruments usually require a period of time to increase voltage from 0 kV to desired value, which is called as ramp time. Such ramp time and any error in the determination of dead time should be taken into account during the accurate calculation of retention factors. After the correction of the retention factors, the plots of the corrected factors for alkylbenzene versus applied voltage were made, the absolute value of the plot slopes are less than 1.8 X 10(-4), Which indicates that the corrected retention times for neutral species do not show any dependence on applied voltage. Further, the plots of the corrected retention times for acidic and basic compounds versus the reciprocal of applied voltage were drawn, where the target compounds were eluted in neutral form. The very nice linearity of the plots was obtained. The linear correlation coefficients are over 0.999. Here, the slopes of the plots represent

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在试验过程中,通常采用一个土样进行连续试验来测定土壤的持水特征。此时,土样的有机质、黏粒矿物类型和阳离子交换量等性质基本保持不变,而土壤的容重在水力学和机械压力共同作用下会发生很大的变化。因此,我们认为实测的土壤持水特征不再是土壤吸力和含水量相对应的一条曲线,而是由土壤质量含水量、吸力和容重三变量共同确定的一个曲面。本文在Brooks-Corey土壤水分特征曲线模型的基础上,提出了两种描述土壤质量含水量、吸力和容重三变量关系的曲面模型,分析了模型的优缺点和适用条件,并采用离心机石蜡控容重法实测了四种质地填装土壤的三变量特征曲面。研究结果表明:土壤持水特征是由土壤质量含水量、吸力和容重三变量共同确定的一个曲面这一假设是合理的;类似于Brooks-Corey模型的两种幂函数经验曲面模型能够合理地描述填装土壤的实测数据,决定系数均大于0.94;模型Ⅰ的拟合效果略好于模型Ⅱ,但模型Ⅱ包含两个物理意义明确的参数,具有一定的优势。这一研究将为校正容重变化对土壤水力学参数的影响提供新的途径。

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采用田间取样与室内分析相结合的方法,研究了黄土高原坡地苹果园肥力状况与矿质氮累积。结果表明,坡地苹果园土壤肥力低,氮、磷严重缺乏,钾相对丰富,土壤属于砂壤土,通气性强,保肥、保水性差。0—60cm土层土壤有机质含量为9.24~28.12g/kg,全氮为0.22~0.60g/kg,速效磷为0.17~16.08mg/kg,速效钾为80.06~168.39mg/kg;黄土高原坡地苹果园中NO3-—N有深层累积分布,累积深度大于2m,在180—200cm层最高累积量达249.61kg/hm2,而NH4+—N无深层累积。不同施肥处理对土壤剖面中的NH4+—N和NO3-—N含量分布影响不同,对NH4+—N含量和分布影响不明显,但不同施肥方式对NO3-—N含量分布影响显著。施加氮肥促进NO3-—N深层累积,施加磷肥有助于降低土层中的NO3-—N含量,缩小富集量的分布范围。

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Thematic Mapper (TM) and Enhanced Thematic Mapper (ETM)+ data have been successfully employed in the field of mineral exploration to identify key minerals over arid and semi-arid terrains. However, redundant vegetation and cloud may seriously interfere with the discrimination of the minerals with diagnostic features. Therefore, in this study, we use masking technique to eliminate the negative influence of vegetation and cloud and Crosta technique to identify the diagnostic features of hydroxyl-minerals, carbonate-minerals and iron oxides. Then the anomalies were endowed with special colours and overlapped with the remote-sensing and geochemical data, overlaying images as remote-sensing anomalies. The mineral exploration work was carried through by synthetic analysis of the remote-sensing images, geochemical data and structures. Finally, areas with high correlation between the occurrence of hydrothermal alteration and presence of main faults and geochemical anomalies were considered as mineral exploration targets worthy of further detailed exploration programmes.