Color plates

With the permission of your instructor, carry out the following experiment. In a beaker, mix equal volumes of 0.001 M NH4SCN and 0.001 M FeCE (the latter solution must be acidified with concentrated HNO3 at a ratio of 4 drops/L to prevent the precipitation of Fe(OH)3). Divide solution in half, and add solid KNO3 to one portion at a ratio of 4 g per 100 mL. Compare the colors of the two solutions (see Color Plate 3), and explain why they are different. The relevant reaction is... 

Color Plate 5 shows the difference between a precipitate formed by direct precipitation and a precipitate formed by a homogeneous precipitation. 

Note These equations are from Doming, S. N. Morgan, S. L. Experimental Design A Chemometric Approach. Elsevier Amsterdam, 1987, and pseudo-three-dimensional plots of the response surfaces can be found in their figures 11.4, 11.5, and 11.14. The response surface for problem (a) also is shown in Color Plate 13. 

Color plate i shows ai external standards and th normal calibration ci... 

Black and colored plates can also be obtained from chromic acid baths. The plates are mostly oxides (177). Black chromium plating bath compositions are proprietary, but most do not contain sulfate. The deposit has been considered for use in solar panels because of its high absorptivity and low emissivity (175). 

Fuji Peel-Apart Film FP-100. In 1984 Fuji introduced FP-lOO, a peel-apart instant color film rated at ISO 100. The FP-lOO system uses a dye-release process similar to that used in the Fuji integral films. Figure 16b is a schematic cross section of FP-100, and Figure 11b (on the colored plate) is a micrograph of the unprocessed film in cross section. The negative stmcture includes a spacer layer between the red-sensitive layer and the cyan dye-releaser layer that it controls, similar to that shown in the FI-800 stmcture, but there are no spacers between the other emulsions and corresponding dye-releaser layers. 

The color plates for the chromatograms reproduced in the reagent monographs were produced using an Olympus OM-4 camera with 50 mm lens combined with a copying stand with TTL-Makroblitz T 28 (Olympus). 

We conclude this chapter with a few illustrative color plates. Simple B W graphics are sufficient for viewing CA only in the special case when sites take on one of two values. In all other cases, color is indispensable for visualizing the behavior of the system. The plates were produced using the freely available CA software packages MCell, Cellab and WinCA. See Appendix A CA Research Tools for a description of these programs and links to web sites from which they can be HnwnlnnHpH... 

Color plate I Elements and compounds, by Charles L. Finance. 

Figure 7. Example of space-resolved photoinduced microwave conductivity mapping of semiconductor interface distribution of photoconductivity in natural pyrite (from Murgul, Turkey, surface etched in acid solution). The overflow was adjusted to show patterns of low photoactivity. For color version please see color plates opposite p. 452.

Figure 8. Example of microwave conductivity transient map PMC relaxation time map taken from a 20- m thin silicon wafer onto which 11 droplets of zeolith suspension were deposited and dried. Reduced lifetimes are clearly observed in the region of droplets. For color version please see color plates opposite this page.

Figure 34. PMC lifetime map of n-type silicon/polymer (poly(epichlorhydrine-co-ethylenoxide-co-allyl-glycylether plus iodide) junction at -10 V potential (mostly dropping across the polymer layer), after Li+ insertion has changed the silicon interface. The statistical evaluation shows the drastic drop in the PMC lifetime. For color version please see color plates opposite p. 453.

Figure 4.4 The general protocol for information extraction from an herbal text (A-E) is paired with case examples from our work with the Ambonese Herbal by Rumphius. (A) Text is digitized. (B) Through either manual reading or automated extraction the plant name(s), plant part(s), and symptoms or disorders are identified. (C) These extracted data are then updated (as necessary) to reflect current names of the plants, using the International Plant Names Index (IPNI), and the pharmacological function(s) of the described medicinal plants are extrapolated from the mentioned symptoms and disorders. (D) The current botanical names are queried against a natural products database such as the NAPRALERT database to determine whether the plant has been previously examined. (E) Differential tables are generated that separate the plants examined in the literature from plants that may warrant further examination for bioactivity. (Adapted from Trends in Pharmacological Sciences, with permission.) See color plate.

Figure 7.6 The request for proposals life cycle. Used with kind permission from David Benton, GSK. See color plate.

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