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Ultraviolet stabilization

Several coats of resin are applied to the prepared substrate at approximately 4- to 6-hour intervals, with one or more coats being dressed with colored paint flakes which are sealed in by the next coat and then lightly sanded. This type of flooring was widely marketed about ten years ago but, in the main, they were considered unsatisfactory due to rapid discoloration of the floor because of the lack of ultraviolet stability of the urethane resins used, which rapidly turned yellow-brown and looked dirty. However, ultraviolet-stable urethane resins that do not suffer this discoloration are now available, and this type of durable decorative flooring is gaining re-acceptance (for example, for kitchens, toilets and reception areas). [Pg.103]

Photophysical Studies of Ultraviolet Stabilizers, Particularly in the 2-Hydroxyphenyl Benzotriazole Class... [Pg.1]

The photodegradation of synthetic polymers can be considerably reduced upon addition of ultraviolet stabilizers. The UV stabilizers (preferably derivatives of o-hydroxy-benzophenone or of 2-(2 -hydroxys -methylphenyl)benzotriazole (Tinuvin) transform the absorbed light energy into thermal energy thus preventing all sorts of photochemically initiated reactions. For review articles see the papers of Otter-stedt (.l), Heller and Blattmann ( 2, 2), Kloepffer (jl, j ), Gysling (JS) and Trozzolo (19 ) ... [Pg.1]

Mechanisms of Photodegradation of Ultraviolet Stabilizers and Stabilized Polymers... [Pg.27]

Photochemical changes in both II and the acetoxy derivative have been monitored in fluid solution and incorporated in a polymer film. Fig. 5 shows the spectral changes accompanying photochemical transformation of the acetoxy derivative. Then changes may be interpreted in terms of scheme 3, which proposes a photochemical 1,3 acyl shift to form "in situ" an ultraviolet stabilizer chromophore which also has a carbonyl functionality. [Pg.36]

It is primarily the prospect of reduced mobility and volatility, with the expected improvement in long-term performance, which motivates the preparation of polymeric ultraviolet stabilizers. Work in this area was reviewed thoroughly by Bailey and Vogl in 1976 (1), and more recently by the author (2). The present paper describes recent synthetic work involving four classes of effective ultraviolet stabilizers salicylate esters (I), 2-hydroxybenzophenones (II), a-cyano-3-phenyl-cinnamates (III) and hydroxyphenylbenzotriazoles (IV). In each... [Pg.43]

Radical polymerizations of vinyl-substituted ultraviolet stabilizers were accomplished with azobisisobutyronitrile (AIBN) as initiator, with careful exclusion of oxygen. Copolymerization was also readily achieved. The following sections describe in detail the preparation of polymeric ultraviolet stabilizers from salicylate esters, 2-hydroxybenzophenones, a-cyano-p-phenyl-cinnamates and hydroxyphenylbenzotriazoles. [Pg.44]

The incorporation of four different classes of important ultraviolet stabilizers into high polymer chains has been accomplished by synthesis of polymerizable, vinyl-substituted stabilizer derivatives followed by radical polymerization. [Pg.50]

Each of the derivatives may be regarded as a substituted styrene, and classical styrene syntheses have been employed. Radical polymerization of the phenolic monomers (salicylate esters, 2-hydroxybenzophenones and hydroxyphenylbenzotriazoles) proceeds normally with AIBN as initiator, at least when oxygen is carefully excluded. It is expected that polymeric ultraviolet stabilizers, perhaps in combination with conventional stabilizer will make an important contribution to photostabilization technology. [Pg.50]

Certain metal salts effectively reduce the photoactivity of titanium dioxide pigments. Combination of these salts with an appropriate antioxidant and/or ultraviolet stabilizer provided highly efficient stabilization of polypropylene. The deactivation/ stabilization performance of the metal salts is adequately explained on the basis of their decomposition of hydrogen peroxide at the pigment surface and by annihilation of positive holes in the pigment crystal lattice. [Pg.161]

Hydroxybenzophenones represent the largest and most versatile class of ultraviolet stabilizers that are used to protect materials from the degradative effects of ultraviolet radiation. They function by absorbing ultraviolet radiation and by quenching electronically excited states. [Pg.1280]

A maximum flexural stress of 9,500 psi is assumed for polycarbonate. This conservative stress value should account for degradation in ultraviolet stabilized polycarbonate exposed to long term solar exposure. While more research is required in this area, it is reasonable to expect at least a ten year useful life for ultraviolet stabilized polycarbonate. A Young s modulus of 345,000 psi and a Poisson s ratio of 0.38 are also assumed for polycarbonate. [Pg.131]

Figures 2 through 9 are design charts for ultraviolet stabilized polycarbonate under blast load. Charts are provided for pane thicknesses of 1/4, 3/8, 1/2, and 1 inch for pane areas up to 25 ft at pane aspect ratios (pane length to width ratios) of 1.00, 1.50, 2.00 and 4.00. The charts relate the peak experienced blast overpressure capacity, B, for convenient pane dimensions across the spectrum of encountered blast durations. Depending on the orientation of the window to the charge, the blast overpressure may either be incident or reflected. The pane dimensions (measured across the span from the gasket centerline) peak blast capacity at 1000 msec, B, static frame design pressure, r, and the required bite are printed to the right... Figures 2 through 9 are design charts for ultraviolet stabilized polycarbonate under blast load. Charts are provided for pane thicknesses of 1/4, 3/8, 1/2, and 1 inch for pane areas up to 25 ft at pane aspect ratios (pane length to width ratios) of 1.00, 1.50, 2.00 and 4.00. The charts relate the peak experienced blast overpressure capacity, B, for convenient pane dimensions across the spectrum of encountered blast durations. Depending on the orientation of the window to the charge, the blast overpressure may either be incident or reflected. The pane dimensions (measured across the span from the gasket centerline) peak blast capacity at 1000 msec, B, static frame design pressure, r, and the required bite are printed to the right...
USP acid test analy chem A United States Pharmacopoeia test to determine the carbonizable substances present In petroleum white oils. yti es pe as ad. test) UV stabilizer chem Any chemical compound that, admixed with a thermoplastic resin, selectively absorbs ultraviolet rays used to prevent ultraviolet degradation of polymers. Also known as ultraviolet stabilizer. yu ve sta ba.iTz ar)... [Pg.394]

Uses. In ultraviolet stabilizers and smoke depressants for polymers to increase the burn rate of rocket propellants to prevent erosion of space capsule shields to improve the viscosity of lubricants to catalyze polymerization reactions to catalyze combustion some derivatives used as hematinic agents... [Pg.242]

Uses. As a raw material in chemical syntheses as ultraviolet stabilizers in plastics found in solvents and as a constituent of gasoline... [Pg.712]

In most applications, polyester and vinyl ester resins are used as the matrix materials. Epoxies are also used, although they require longer cure times and do not release easily from the pultrusion dies. Hence, thermosetting resins are most commonly used with pultrusion, although some high-performance thermoplastics such as PEEK and polysulfone can also be accommodated. In addition to the resin, the resin bath may contain a curing agent (initiator, cf. Section 3.3.1.2), colorants, ultraviolet stabilizer, and fire retardant. [Pg.796]


See other pages where Ultraviolet stabilization is mentioned: [Pg.1005]    [Pg.1011]    [Pg.1037]    [Pg.373]    [Pg.732]    [Pg.327]    [Pg.399]    [Pg.401]    [Pg.403]    [Pg.405]    [Pg.407]    [Pg.409]    [Pg.1]    [Pg.40]    [Pg.43]    [Pg.43]    [Pg.154]    [Pg.157]    [Pg.239]    [Pg.1274]    [Pg.1280]    [Pg.982]    [Pg.58]    [Pg.144]    [Pg.129]    [Pg.391]    [Pg.48]    [Pg.148]    [Pg.17]    [Pg.489]   
See also in sourсe #XX -- [ Pg.7 ]




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Polymerizable ultraviolet stabilizers

Stability to Light and Ultraviolet Rays

Stabilizers polymeric ultraviolet

Stabilizers ultraviolet absorbers

Ultraviolet Light Protection and Stabilization

Ultraviolet absorbers, polymeric material stabilization

Ultraviolet light stability

Ultraviolet light stability polymers

Ultraviolet light stabilization

Ultraviolet light stabilization carbon black

Ultraviolet light stabilization interactions

Ultraviolet light stabilization mechanism

Ultraviolet light stabilization stabilizer

Ultraviolet light stabilization varieties

Ultraviolet light stabilizers

Ultraviolet protectant stabilizer

Ultraviolet radiation polymer coating stabilization

Ultraviolet radiation-stabilizers

Ultraviolet stability

Ultraviolet stability

Ultraviolet stability additive coloring effects

Ultraviolet stability carbon black pigments

Ultraviolet stability dispersability

Ultraviolet stabilizer

Ultraviolet stabilizer

Ultraviolet stabilizers epoxies

Ultraviolet stabilizers mechanisms

Ultraviolet stabilizers polyurethanes

Ultraviolet-stabilized polycarbonate

Ultraviolet/sunlight stability

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