From the instant of its creation, a silver-based image faces attack from a variety of sources. Some are internal and essential to the materials photographic papers are designed and manufactured with. They come in the form of chemicals, inherent or added to the paper, the emulsion or the coating. They either are a fundamental part of the paper characteristics or meant to improve them.
Other sources of attack are of external origin. Nevertheless, some are intrinsic to the photographic process and can be minimized but not completely avoided. Most processing chemicals fall into this category. In the very beginning of a print’s life, and only for a few minutes, we need them to be present to complete their designated tasks. Beyond that point, we like to rid the print of them quickly and entirely. Fortunately, these sources of image deterioration are under our control, but no matter how attentive our work might be, unavoidable traces of them will remain in the print forever, and given the right environmental conditions, they will have an opportunity to attack the very image they helped to create.
The remaining extrinsic sources of image attack are hiding patiently in our environment, ready to start their destructive work as soon as the print is processed and dry. They can broadly be separated into reducing and oxidizing agents. Roughly until the introduction of the automobile, reducing agents were the most common sources of image deterioration. Then, oxidizing agents like aldehyde, peroxide and ozone took over. Their presence peaked in the Western World around 1990 and fortunately began to decline since.
While stored in the dark, none of this may ever be visible, but when exposed to light print deterioration is highly accelerated. This is due to increased oxidation of the metallic image silver, caused either by internal oxidants from poor washing or by environmental gases, as found in atmospheric oxygen, ozone, curing paint and adhesive, new carpet, fossil fuel fumes, the resins from processed particle board and unfinished wood.
Image oxidation follows a pattern. Initially, image silver is oxidized into silver ions. Then, these mobile silver ions, supported by humidity and heat, migrate through the gelatin layer and, when the concentration is high enough, accumulate at the gelatin surface. Finally, the silver ions are reduced to silver atoms, which combine to colloidal silver particles. They are brownish in color, but at the print surface and viewed at a certain angle, they are visible in the form of small shiny patches. This more advanced defect is referred to as ‘mirroring’, and it occurs exclusively in the silver-rich shadows of the print.
There is evidence that RC prints are more susceptible to image oxidation than FB prints. One possible reason is that the polyethylene layer between emulsion and paper base in RC prints keeps the mobile silver ions from dissipating into the paper base, as they can in FB prints. In RC prints, the ions are more likely to travel to the emulsion surface, since they have no other place to go. Another reason for RC image oxidation is that light absorption by the titanium dioxide pigment in the polyethylene layer can cause the formation of titanium trioxide and oxygen. This will increase the rate of silver oxidation if the prints are mounted under glass, preventing the gases from escaping. As a preventive measure, modern RC papers made by the major manufacturers contain antioxidants to reduce the chance of premature oxidation. Proper toning and image stabilization practice will help to protect against image deterioration!