In ion chromatography, each spike on the chromatogram represents the detection of a specific ion or ionic species as it elutes from the column. The position of the spike corresponds to the retention time of that ion, while the area under the spike is proportional to its concentration in the sample. By comparing these spikes to calibration standards, the concentration of each ion in the sample can be quantified.
Each spike on an ion chromatograph represents a distinct ion or ion species detected in the sample as it passes through the chromatographic column. The position of the spike on the time axis indicates the retention time of that specific ion, while the height or area of the spike correlates with the concentration of the ion in the sample. By analyzing these spikes, one can identify and quantify the various ions present in the sample.
there are different types like gas chrom. and thinlayer chrom Answer: There are two types of chromatography:liquid chromatography gas chromatography
The Dionex company manufactures chromatography, ion chromatography, and extraction systems for identifying components of chemical mixtures. Chromatography is the process of separating different kinds of mixtures.
Formic acid can be determined by ion chromatography.
In ion chromatography, "prime" typically refers to the process of preparing and conditioning the ion exchange column to ensure optimal performance. This involves flushing the column with a suitable eluent to remove impurities and equilibrate the stationary phase before sample analysis. Proper priming enhances resolution and sensitivity, allowing for accurate separation and quantification of ions in the sample.
Each spike on an ion chromatograph represents a distinct ion or ion species detected in the sample as it passes through the chromatographic column. The position of the spike on the time axis indicates the retention time of that specific ion, while the height or area of the spike correlates with the concentration of the ion in the sample. By analyzing these spikes, one can identify and quantify the various ions present in the sample.
Yes they are the same
Douglas T. Gjerde has written: 'Ion chromatography' -- subject(s): Ion exchange chromatography 'DNA chromatography' -- subject(s): Analysis, Chromatographic analysis, DNA, Genetic Techniques, High Pressure Liquid Chromatography, Isolation & purification
Ion chromatography involves the separation of ions and polar molecules and is used for protein purification, among other things. Information about this process can be found at Wikipedia or InnovaTech.
there are different types like gas chrom. and thinlayer chrom Answer: There are two types of chromatography:liquid chromatography gas chromatography
The Dionex company manufactures chromatography, ion chromatography, and extraction systems for identifying components of chemical mixtures. Chromatography is the process of separating different kinds of mixtures.
Formic acid can be determined by ion chromatography.
Shahab A Shamsi has written: 'Reversed phase /ion chromatography and capillary electrophoresis of ionic compounds with indirect detection' -- subject(s): Chemistry, Ion exchange chromatography, Capillary electrophoresis
T. R Acciani has written: 'Chemical analysis of wet scrubbers utilizing ion chromatography' -- subject(s): Analysis, Ion exchange chromatography, Scrubber (Chemical technology)
Single column depends upon small differences in conductivity between sample ions and elutent ions. Suppressor based ion exchange has a second ion exchange column, (suppressor) after the original ion exchanger that converts ions to a limited charged product.
Examples: distillation, ion-exchange, chromatography, decantation, extraction.
chromatography has many varieties -paper chromatography, sometime complexe mixtures cant be separated, TLC plates do not have long stationary phases -gaz chromatography: the molecule should be volatile -Chiral Chromatography can be expensive - Ion Exchange or Ion Chromatography: Turbidity should be low below 10ppm -Size Exclusion Chromatography: low resolution technique which gives few peaks and requires large differences in molecular weight for resolution -Gel chromatography: the target protein frequently becomes an abundant substrate for proteases that may also be present in the mixture. Another disadvantage is low sample handling.