As mentioned earlier, it is of primary importance to migrate as little data as possible during mode changes to minimise the migration time and energy.
Acceptable reproducibilities of lower than 1.8% for migration time and 8.6% for peak areas were obtained.
values in the ranges of 0.01 0.11% and 0.54 1.60% for relative migration time and corrected peak area, respectively.
Tryptamine, tyramine, tryptophan, tyrosine and phenylalanine were identified by migration time and spiking in porcine decomposition fluids.
For the on-line analysis the migration time and detection limit were also found to be important parameters.
Intraday precision of migration time and peak area ratio were in the range of 0.17 0.44% and 1.64% and 6.25%, respectively.
For both modes, the relative standard deviation of migration time and peak intensity for consecutive injections was determined to be below 0.6 and 8%, respectively.
The amount migrated into the capillary, determined by the peak area, the resolution between the ofloxacin enantiomers, the migration time and the generated current were evaluated as responses.
In all these cases, inks were successfully differentiated on the basis of position (migration time) and shape of their characteristic peaks.
Experimental results demonstrate that compared with Xen, our system can significantly reduce downtime, total migration time, and total transferred data by 27.1%, 32%, and 68.8% respectively.
Secondly, we propose a triple-way pipeline to improve the performance of chunk mode data transfer and greatly reduce total migration time and downtime.
