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Light exposure

These are systems in which multilayer stmctures are fonned from molecules containing one or more double bonds and in which polymerization is subsequently initiated by appropriate means such as electron beam or UV light exposure. [Pg.2618]

Tables 2—5 Hst some typical properties or ranges of properties for the more common film and sheet products. Although these values are good for comparative purposes, actual performance tests are best to determine suitabiHty for use. Properties of multiple-layer films or sheets in laminar stmctures cannot always be predicted from values for the individual polymer layers. Use conditions of stress, temperature, humidity, and light exposure all strongly influence performance. Film and sheet manufacturers can recommend product combinations or variations that may provide significant performance advantages to the user. Tables 2—5 Hst some typical properties or ranges of properties for the more common film and sheet products. Although these values are good for comparative purposes, actual performance tests are best to determine suitabiHty for use. Properties of multiple-layer films or sheets in laminar stmctures cannot always be predicted from values for the individual polymer layers. Use conditions of stress, temperature, humidity, and light exposure all strongly influence performance. Film and sheet manufacturers can recommend product combinations or variations that may provide significant performance advantages to the user.
Plutonium(IV) polymer is a product of Pu(IV) hydrolysis and is formed in aqueous solutions at low acid concentrations. Depolymerization generally is accomplished by acid reaction to form ionic Pu(IV), but acid degradation of polymer is strongly dependent on the age of the polymer and the conditions under which the polymer was formed (12). Photoenhancement of Pu(IV) depolymerization was first observed with a freshly prepared polymer material in 0.5 HClOh, Fig. 3 (3 ). Depolymerization proceeded in dark conditions until after 140 h, 18% of the polymer remained. Four rather mild 1-h illuminations of identical samples at 5, 25, 52, and 76 h enhanced the depolymerization rates so that only 1% polymer remained after the fourth light exposure (Fig. 3). [Pg.270]

The effects of four 1 h, low intensity, UV light exposures to enhance the degradation of freshly prepared Pu(IV) polymer. The darkened line represents depolymerization under dark conditions. The solution contained 0.0093 M total Pu and 0.47 11 HClOi at 22°C (3). [Pg.271]

Preparations of DNA and bacterial suspensions irradiated using a germicidal bulb (Osram, Germany) through an optical filter of 254 nm with a power light exposure of 6.7 W/m as determined by UV radiometer (TKA-PKM, Russia). [Pg.186]

Historically, photoaging has been defined as the superimposed effects of photodamage on intrinsically aging skin. It is a consequence of chronic ultraviolet light exposure. Photodam-... [Pg.161]

Based on the photoresistivity levels of certain crystals like Se, Ge, Si, CdS, and PbS, photoconductors are constructed. Under light impact, they reduce their electrical resistance up to about 10" times. They are used in portable instruments like light exposure meters. [Pg.16]

Regarding the data concerning the stability of curcumin in solution, it is advisable to perform extraction under acidic conditions and to avoid direct light exposure. However, it will also depend on the material from which curcumin has to be extracted. [Pg.78]

Only 6% of the iifitial total lycopene prepared as a thin film on the surface of each vial remained after 144 hr under fluorescent light (2000 to 3000 lux) at 25°C under N2. Lycopene degradation occurred as a first-order reaction at 2.93 x 10" /min, and the concentration of aU lycopene mono-c isomers already present in the sample, 5-cis-, 9-cis-, l3-cis- and 15-d5 -, showed an inconsistent change in this period. Nevertheless, formation of lycopene di-c isomers was observed after 32 hr of light exposure and when considering relative percentage, loss of 13% of all-trani-lycopene occurred while an increase of 11% for total cis isomers was found after 144 hr. ... [Pg.233]

Nishi, J., Ogura, R, Sugiyama, M., Hidaka, T. and Kohno, M. (1991). Involvement of active oxygen in lipid peroxide radical reaction of epidermal homogenate following ultra-violet light exposure. J. Invest. Dermatol. 97, 115-119. [Pg.123]

An important drawback of a-Si H is its intrinsic metastability the electronic properties degrade upon light exposure. This was discovered by Staebler and Wron-ski [87, 88], and is therefore known as the Staebler-Wronski effect (SWE). This effect manifests itself by an increase in the density of neutral dangling bonds, A db, upon illumination, according to N, (t) oc where G is the generation rate... [Pg.10]

The most common risk factors for skin cancer development after transplantation include increased age, excessive ultraviolet (UV) light exposure, high degree of immunosuppression, Fitzpatrick skin types I, II and III, history of skin cancers, and infection by human papillomavirus.77... [Pg.850]

Obviously, use of such databases often fails in case of interaction between additives. As an example we mention additive/antistat interaction in PP, as observed by Dieckmann et al. [166], In this case analysis and performance data demonstrate chemical interaction between glycerol esters and acid neutralisers. This phenomenon is pronounced when the additive is a strong base, like synthetic hydrotalcite, or a metal carboxylate. Similar problems may arise after ageing of a polymer. A common request in a technical support analytical laboratory is to analyse the additives in a sample that has prematurely failed in an exposure test, when at best an unexposed control sample is available. Under some circumstances, heat or light exposure may have transformed the additive into other products. Reaction product identification then usually requires a general library of their spectroscopic or mass spectrometric profiles. For example, Bell et al. [167] have focused attention on the degradation of light stabilisers and antioxidants... [Pg.21]

Light-exposure meter based on selenium upon illumination, the conductivity can increase by a factor of 1000. [Pg.52]

For many decades, the standard technique for measuring carotenoids has been high-pressure liquid chromatography (HPLC). This time consuming and expensive chemical method works well for the measurement of carotenoids in serum, but it is difficult to perform in human tissue since it requires biopsies of relatively large tissue volumes. Additionally, serum antioxidant measurements are more indicative of short-term dietary intakes of antioxidants rather than steady-state accumulations in body tissues exposed to external oxidative stress factors such as smoking and UV-light exposure. [Pg.89]


See other pages where Light exposure is mentioned: [Pg.429]    [Pg.223]    [Pg.547]    [Pg.259]    [Pg.215]    [Pg.503]    [Pg.493]    [Pg.373]    [Pg.31]    [Pg.97]    [Pg.334]    [Pg.370]    [Pg.47]    [Pg.170]    [Pg.162]    [Pg.162]    [Pg.316]    [Pg.65]    [Pg.89]    [Pg.288]    [Pg.331]    [Pg.490]    [Pg.561]    [Pg.588]    [Pg.137]    [Pg.96]    [Pg.781]    [Pg.188]    [Pg.52]    [Pg.162]    [Pg.162]    [Pg.53]    [Pg.94]    [Pg.97]   
See also in sourсe #XX -- [ Pg.316 ]

See also in sourсe #XX -- [ Pg.360 ]

See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.283 ]




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Bright light exposure

Color Changes Upon Exposure to Light

Color, light exposure effects

Effect of exposure to light

Exposure to light

Exposure to light sources

Food processing light exposure

Hindered amine light stabilizers exposure

Light exposure colourant

Light exposure tests

Light exposure time

Light exposure, surface changes

Operating light- and water-exposure

Operating light- and water-exposure apparatus (fluorescent UV-condensation

Radiation Exposure (Including Light)

TL and OSL after Exposure to UV Light

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