Influence of chromatographic factors on remission measurements on thin-layer chromatograms. Part I. Choice of the method, properties of the stationary phase and application of substances Some introductory remarks are made concerning the choice of the determination method, and different methods are compared. Chromatographic factors affecting the spectrophotometric evaluation of thin-layer chromatograms are discussed. In connection with this, the layer thickness of the stationary phase, the grain-size distribution and the pore diameter of the adsorbent were investigated. In trace analyses using a stationary phase consisting of thin layers of finely granulated adsorbents having a small pore diameter, sensitivity can be increased by a factor of 10. It was found that there was no relationship between the direction in which the layer had been applied on the plates and that in which chromatography or measurement was carried out. The manner of applying the solutions to be examined is also discussed, and the advantages of applying the solution as streaks or round spots, respectively, are pointed out. For this purpose the polarity of the standard and test solutions should be considered so that no disturbances due to formation of zones differing in area will occur. To obtain calibration curves according to the Kubelka—Munk equation, the ratio of the measured area to the zone area should be kept constant.