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J. Cosmet. Sci., 60, 337–345 (May/June 2009) Accepted for publication December 29, 2008. Synopsis During hair coloring a number of disulfide bonds in cystine are oxidized (1) to create cysteic acid, forming binding sites for metal ions such as Ca2+ and Cu2+ from tap water (2). The increased uptake of these metals can have a detrimental impact on fiber properties—for example, reducing shine and causing a poor wet and dry feel (3). In addition, the increased uptake of copper can also contribute to further fiber damage during subsequent coloring due to its ability to take part in metal‐induced radical chemistry (4). It is important to know where in the fibers these metals are located in order to either effectively remove these metals or control their chemistry. Nanoscale secondary ion mass spectrometry (NanoSIMS) has been used to locate the calcium and copper within hair that has been treated with a colorant and washed multiple times in tap water containing these ions. Untreated hair is used as a baseline standard material. Images with up to 50‐nm spatial resolution of the preferential locations of calcium uptake were obtained, showing a high concentration of calcium in the cuticle region of colored hair, specifically in the sulfur‐rich regions (A‐layer and exocuticle).

Der Co‐Komplex (Ia) wurde durch Templat‐Kondensation von 2,6‐Diacetylpyridin und 2,9‐Di‐[ l‐methylhydrazino]‐ 1,10‐phenanthrolin in Gegenwart von CoCl2 in Wasser bei Rückflußtemp.

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