UV degradables

Tetrahydrofurfuryl alcohol also has been cleared for use in California under Rule 66. It meets the rigid specifications for uv degradation in environmentally sensitive areas. In addition to domestic use, a substantial amount of tetrahydrofurfuryl alcohol is used as a solvent for agricultural chemicals in Europe. 

Acryhc polymers are fairly iasensitive to normal uv degradation siace the primary uv absorption of acryhcs occurs below the solar spectmm (59). The iacorporation of absorbers, such as i9-hydroxyben2ophenone [117-99-7] further improves the uv stabihty (59). Under normal use conditions acryhc polymers have superior resistance to degradation and show remarkable retention of their original properties. 

Other polymers used in the PSA industry include synthetic polyisoprenes and polybutadienes, styrene-butadiene rubbers, butadiene-acrylonitrile rubbers, polychloroprenes, and some polyisobutylenes. With the exception of pure polyisobutylenes, these polymer backbones retain some unsaturation, which makes them susceptible to oxidation and UV degradation. The rubbers require compounding with tackifiers and, if desired, plasticizers or oils to make them tacky. To improve performance and to make them more processible, diene-based polymers are typically compounded with additional stabilizers, chemical crosslinkers, and solvents for coating. Emulsion polymerized styrene butadiene rubbers (SBRs) are a common basis for PSA formulation [121]. The tackified SBR PSAs show improved cohesive strength as the Mooney viscosity and percent bound styrene in the rubber increases. The peel performance typically is best with 24—40% bound styrene in the rubber. To increase adhesion to polar surfaces, carboxylated SBRs have been used for PSA formulation. Blends of SBR and natural rubber are commonly used to improve long-term stability of the adhesives. 

All polyethylenes are soft, flexible and resistant to acids and alkalis up to 60°C. They retain this flexibility down to —40°C. Hence they have good resistance to impact even at low temperatures. However, unless correctly formulated they can suffer from environmental stress cracking (ESC), poor adhesion and UV degradation. ESC is the phenomenon which occurs when a thermoplastic is put under stress, e.g. bent, in a particular environment and prematurely cracks or crazes. Alcohol and detergent are examples of agents that can cause ESC in polyethylenes. 

Bis(tributyltin) oxide is known to break down to inorganic tin under UV irradiation in laboratory conditions (509, 510), and the decomposition may be accelerated by absorbing the organotin compound on a cel-lulosic matrix (511). As bis(tributyltin) oxide is known to react rapidly with carbon dioxide (atmospheric, or trapped in various cellulosic materials, such as cotton or wood) (512), to form bis(tributyltin) carbonate, (BusSnO)2CO, the observed UV degradation pattern may be rationalized in terms of more-ready breakdown of the carbonate than of the oxide, due to the presence of the carbonyl chromophore. The half-life of bis(tributyltin) oxide in pond water has recently been given as 16 days (513). Diorganotin compounds have also been shown to decompose to inorganic tin under UV irradiation (514, 515). 

Since the UV degraded C-PVC still contains substantial amounts of the initial CHC1-CHC1 structure, one can expect the chlorine radicals evolved to also initiate the zip-dehydrochlorination of these structures. The resulting chlorinated polyenes will then be further destroyed by the laser irradiation, so that finally all the C-PVC polymer is converted into a purely carbon material within a fraction of a second. 

The formation of the major UV degradation peak at about 287 nm in the weathered PC appears to correlate well with the formation of the yellow color in the weathered sample. In Figure 8 the formation of both the peak at 287 nm and the yellow color have been assumed to be products of a first order reaction. This figure shows a plot of the log of the percentage of a scaling constant minus the yellowness index divided by the constant, versus a measurement of the exposure. In this case, the exposure is expressed as cal/cm2, obtained from ENC0N data. 

UV degradation is a chemical destruction process which leads, under short-wave light, to the direct oxidation of the binder by means of atmospheric oxygen. The reaction takes place mainly via photo-activated states of the binder macromolecules. 

A further consequence of our photocatalytic oxidation cycle is the protective function which rutile pigments exert against UV degradation. This effect can be shown by several methods ... 

Choosing the most stable TiO modification. It has been shown that chalking is the result of two main processes UV degradation and the photocatalytic oxidation cycle. What can be done to stabilize Ti02 pigments in such a way that they cause as little chalking as possible A few possibilities have already been mentioned ... 

There are various requirements for impact-modified PVC. The most demanding is for outdoor sidings and window frames, where lifetimes of 20 years are expected. Because butadiene polymers or copolymers (e.g., acrylonitrile/butadiene/styrene (ABS), methyl methacrylate/butadiene/styrene (MBS)) are susceptible to UV degradation these polymers are usually not employed instead acrylate polymers are used for these applications. 

Differential photocalorimetry (DPC) is included here since the instrument used is essentially an adaptation of DSC instrumentation. The photocalorimeter comprises a DSC instrument with a UV/visible source mounted on top, such that light of appropriate wavelength or wavelength region from the source is focused onto the measuring head (both reference and sample pans). The most frequent use of DPC is in the study of polymer cure reactions, but it may also be used to follow such as UV degradation. 

Sections of several packages were tested by dilute solution viscometry in decahydronaphthalene at 135°C to determine if the failures are consistent with UV degradation. The top surface of each package was partially covered by a paper label. This label should have shielded the underlying film from UV exposure, and there should be a difference in the solution viscosity of material taken from the shielded center of the package and material taken from the UV-exposed edge. Sections from the center and edge of three samples were... 

This type of degradation can also be referred to as photodegradation or ultraviolet (UV) degradation. It includes photo-oxidation. It produces some of the more familiar signs of degradation of plastics embrittlement, discoloration and loss of transparency. 

Table 3.13 Examples of UV degradation according to the polymer and exposnre location...

COPEs are handicapped by a lower elasticity than conventional rubbers, the more so the greater the hardness certain risks of creep, relaxation and permanent set, the more so the higher the temperature high cost risks of hydrolysis especially for the polyester-ester types risks of UV degradation lack of soft grades density inherent flammability, but FR grades are marketed. 

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