Degradation film photodegradation

In 1994, it is apparent that time has largely borne out these predictions. Where there has been no legislation the use of photodegradants appears to be diminishing. However, in at least one major industrial country legislation has taken place which will prevent use of non-degradable packaging films. 

We also note two reports on the degradation of stacked films of oriented PET. In the first [36], photodegradation is said to be two-step in nature with weak links cleaving first followed by a much slower cleaving of the strong links . The chain scission process was tracked versus exposure time by measurement of solution viscosity [37], In the second paper [38], the surface nature of the degradation was reported and the rationale elucidated for why surface degradation causes overall mechanical failure limited by that layer, much as we have discussed in the impact properties of the PECT (see above). 

Photodegradation. The photochemical degradation products of diflubenzuron in strictly aqueous solution are unreported, perhaps because of the compound s refractory solubility. Exposure of thin films on glass or a 0.1 ppm aqueous solution to sunlight... 

Desai et al. [86] reported on the photolytic degradation of the anti-viral, sorivudine, which formed the inactive Z-isomer. On the basis of extensive dmg-excipient compatibility studies it was found that the incorporation of iron oxide pigments into the blends (direct compression or wet granulated) stabilised the dmg to photodegradation indeed, so much so that the tablet was found not to require a film coat. The data are summarised in Table 2.6. 

Investigations, related to the photoprotection of nifedipine tablets using films containing titanium dioxide and/or tartrazine, revealed that the photoprotective effect of a film could be evaluated by using its concentration of colorant (C) and thickness (L) value. This value is the product of concentration of the colorant C and the film thickness L. Tablets coated with films having the same CL value had the same photodegradation rates. Degradation rates were found to be proportional to the CL value for every colorant system tested (18). 

Fundamental questions related to the electronic configuration of the open or colored forms and the number and structures of the photomerocyanine isomers are considered on the basis of the results of continuous-wave (stationary) and time-resolved (picosecond, nanosecond, and millisecond) Raman experiments. For spironaphthoxazine photochromic compounds, the Raman spectra may be attributed to the TTC (trans-trans-cis) isomer having a dominant quinoidal electronic configuration. Surface-enhanced resonance Raman spectroscopy (SERRS) is demonstrated as a new analytical method for the study of the photodegradation process in solution for nitro-BIPS derivatives. The development of this method could lead to the identification of the photoproducts in thin polymer films or sol-gel matrices and ultimately to control of degradation. 

Christensen, P.A. Dilks, A. Egerton, T.A. Tem-perley, J. Infrared spectroscopic evaluation of the photodegradation of paint. Part 1. The UV degradation of acrylic films pigmented with titanium dioxide. J. Mater. Sci. 1999, 34, 5689-5700. 

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