Chromatography is a method of analyzing the contents of a mixed substance. It is performed by dissolving the substance in a suitable solvent. A drop or spot of the resulting liquid is deposited near the edge of a piece of absorbent paper, such as blotting paper or special chromatography paper. The strip of paper with the spot at the bottom is then suspended over a solvent with the bottom edge of the paper in the solvent.
As the solvent soaks upwards, the solvent carries some particles upwards and away from the spot. Different compounds within the mixture will travel at different rates and eventually the strip of paper will show different bands of colors, separating out and indicating some of the various components that were in the original substance.
'Trailing a spot' is a short term for this laboratory process.
Tailing in chromatography can be caused by factors such as non-specific interactions between the analyte and the stationary phase, column overload, sample matrix effects, or inaccuracies in the injection process. These factors can lead to peak distortion, decreased resolution, and decreased sensitivity in chromatographic separations.
Tailing peaks are a known problem in chromatography (both HPLC and GC). It means the analytes are experiencing an out-drawn (extended) retention time and is usually due to one of these factors:Contaminated or active injector liner, seal or columnDead volume due to poorly installed liner or columnRagged column endA bad match between the polarities of the stationary phase and the solventA cold region in the sample flow path (GC)Debris in the liner or columnInjection takes too longSplit ratio is too low (GC)Overloading the inletSome types of compounds such as alcoholic amines, primary and secondary amines and carboxylic acids tend to tail
The chromatogram in paper chromatography is just the paper itself. You can look at the paper and see the dots that have risen due to the solvent. The appearance is just simply a piece of paper with dots that have risen from the baseline to a certain spot on the paper. see related link below for more info
In chromatography, if a spot is located at the baseline, it typically indicates that the substance being analyzed did not move with the mobile phase during the separation process. This can occur if the compound has a very strong affinity for the stationary phase or if it is not soluble in the mobile phase. As a result, the substance may not be effectively separated from other components, leading to poor resolution in the chromatogram.
Double-spotting chromatography paper helps ensure that the substance being analyzed is evenly distributed across the paper to enhance separation and analysis. It can also be used as a reference spot to track the movement of the solvent front during the chromatography process.
Fronting and tailing in chromatography are observed as distortions in the shape of the peaks on the chromatogram. Fronting occurs when the peak is broader and taller than expected, while tailing occurs when the peak is elongated and skewed. These distortions can be caused by factors such as sample overload, column overloading, or interactions between the sample and the stationary phase.
Tailing effect is an error that occurs when the spot is not allowed to dry hence leading increased diameter of the spot in a TLC plate. Nwando Ata.
Tailing in chromatography can be caused by factors such as non-specific interactions between the analyte and the stationary phase, column overload, sample matrix effects, or inaccuracies in the injection process. These factors can lead to peak distortion, decreased resolution, and decreased sensitivity in chromatographic separations.
Tailing in gas chromatography (GC) occurs when the analyte peak exhibits a longer tail on one side, often due to factors like column overload, inadequate column temperature, or interactions between the analyte and stationary phase. It can also result from the presence of impurities or degradation products that interfere with the separation process. Proper column selection, temperature optimization, and sample preparation can help mitigate tailing effects.
In chromatography, Rf is the distance the solute travels divided by the distance the mobile phase travels. For example, in thin layer chromatography, if the spot travels 7 cm, and the mobile phase travels 15 cm, the Rf value for that spot will be 7/15 = 0.47
Tailing peaks are a known problem in chromatography (both HPLC and GC). It means the analytes are experiencing an out-drawn (extended) retention time and is usually due to one of these factors:Contaminated or active injector liner, seal or columnDead volume due to poorly installed liner or columnRagged column endA bad match between the polarities of the stationary phase and the solventA cold region in the sample flow path (GC)Debris in the liner or columnInjection takes too longSplit ratio is too low (GC)Overloading the inletSome types of compounds such as alcoholic amines, primary and secondary amines and carboxylic acids tend to tail
explain in the trends in e-tailing in India
The chromatogram in paper chromatography is just the paper itself. You can look at the paper and see the dots that have risen due to the solvent. The appearance is just simply a piece of paper with dots that have risen from the baseline to a certain spot on the paper. see related link below for more info
That's a terrible question. Of course tailing ponds evaporate. Use your head before asking questions.
A ditch is made beside a tree and the tailing is dumped into it, and then, the tailing is covered with earth. This method is known as Phytostabilisation.
The cast of Tailing the Millennium - 2000 includes: Anna Zetchus as Herself - Narrator
In chromatography, if a spot is located at the baseline, it typically indicates that the substance being analyzed did not move with the mobile phase during the separation process. This can occur if the compound has a very strong affinity for the stationary phase or if it is not soluble in the mobile phase. As a result, the substance may not be effectively separated from other components, leading to poor resolution in the chromatogram.