UV absorbance

The electrons of unsaturated bonds in many organic dmg molecules undergo energy transitions when UV light is absorbed. The intensity of absorption may be quantitatively expressed as an extinction coefficient , which has significance in analytical application of spectrophotometric methods. 

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Fig. 5. Anion-exchange separation of insulin and insulin A- and B-chains, over diethylaminoethyl (DEAF) in a 10.9 x 200 mm column having a volume of 18.7 mL. Sample volume is 0.5 mL and protein concentration ia 16.7 mAf Tris buffer at pH 7.3 is 1 mg/mL for each component ia the presence of EDTA. Eluent (also 16.7 mAf Tris buffer, pH 7.3) flow rate is 1.27 ml,/min, and protein detection is by uv absorbance at 280 nm. The straight line depicts the salt...

Reduction of the aromatic nuclei contained in catalytic C-9 resins has also been accomplished in the molten state (66). Continuous downward concurrent feeding of molten resin (120°C softening point) and hydrogen to a fixed bed of an alumina supported platinum—mthenium (1.75% Pt—0.25% Ru) catalyst has been shown to reduce approximately 100% of the aromatic nuclei present in the resin. The temperature and pressure required for this process are 295—300°C and 9.8 MPa (lOO kg/cni2), respectively. The extent of hydrogenation was monitored by the percent reduction in the uv absorbance at 274.5 nm. 

Miscellaneous. The reaction products of sahcylaldehyde with certain compounds containing active methylene groups, eg, acetylacetone, are excellent uv absorbers. Films containing these compounds can be used as uv filters to protect light-sensitive foods, wood products, paper, dyes, fibers, and plastics (95). 

Whereas the eadiest fluorescent-dye pigments would last only 20 days outdoors in a screen-ink film, fade resistance has been improved to such an extent that some modem daylight-fluorescent coated panels stiU have useful color after nine months or mote in Florida sunlight in a 45° exposure tack facing south. The fluorescent layer is usually coated with an acrylic film containing a uv absorber. Indoor-accelerated exposure equipment is, of course, invaluable in the development of such systems. Better dyes and resins very likely will make possible fat mote stable coatings in the future. 

Plastic Sheet. Poly(methyl methacrylate) plastic sheet is manufactured in a wide variety of types, including cleat and colored transparent, cleat and colored translucent, and colored semiopaque. Various surface textures ate also produced. Additionally, grades with improved weatherabiUty (added uv absorbers), mat resistance, crazing resistance, impact resistance, and flame resistance ate available. Selected physical properties of poly(methyl methacrylate) sheet ate Hsted in Table 12 (102). 

A major use for 2,4-di-/ f2 -amylphenol is in the production of uv stabilizers the principal one is a benzotriazole-based uv absorber, 2-(2 -hydroxy-3, 5 -di-/ f2 -amylphenyl)-5-chlorobenzotriazole [25973-55-17, which is widely used in polyolefin films, outdoor furniture, and clear coat automotive finishes (56). Another significant use for 2,4-di-/ f2 -amylphenol is in the photographic iadustry. A number of phenoxyacetic acid derivatives of... 

Cysteine is used as a reductant for cold wave treatment in place of thioglycoHc acid. A/-Lauroylarginine ethyl ester [48076-74-0] is appHed as the hydrochloride as a preservative. Urocanic acid [104-98-3] hich. is derived from histidine is used in skin cream as a uv absorber (235). 

Wea.ther lbillty. One of the more destmctive elements is exposure to sunlight specifically, ultraviolet (uv) light. AH sealants are affected by weathering, but there is much difference in the effect of weathering on different sealants. Most sHicones are stable with respect to uv exposure. Urethanes and polysulfides show effects of uv exposure, but can be formulated with uv absorbers to provide reasonable lifetimes in most appHcations. However, there are exceptions in aH classes of sealants and specifiers must be carehil to look for test data that has proven a specific sealant s durabHity. The source of the test data is also important data from an independent testing laboratory is generaHy apt to be more reHable. 

Derivatization of primary and secondary amines using 9-fluorenylmethyl chloroformate to form a nonpolar, uv-absorbing derivative has been reported (90,91). Amphetamine and catecholamine were used as probes to evaluate this procedure. The derivatives were well behaved and allowed separation in a short time. 

Numerous high pressure Hquid chromatographic techniques have been reported for specific sample forms vegetable oHs (55,56), animal feeds (57,58), seta (59,60), plasma (61,62), foods (63,64), and tissues (63). Some of the methods requite a saponification step to remove fats, to release tocopherols from ceHs, and/or to free tocopherols from their esters. AH requite an extraction step to remove the tocopherols from the sample matrix. The methods include both normal and reverse-phase hplc with either uv absorbance or fluorescence detection. AppHcation of supercritical fluid (qv) chromatography has been reported for analysis of tocopherols in marine oHs (65). 

A hst of uv absorbing substances found useful in protective sunscreen products is provided in Table 13. Some information on the levels permitted in products in both the United States and the EEC is included. Descriptions and specifications of sunscreens have been pubflshed (55). 

In principle, emulsified sunscreen products are similar to emollient skin-care products in which some of the emollient Hpids are replaced by uv absorbers. The formulation of an effective sunscreen product generally requites combination of a uvB and a uvA absorber if an SPF above about 12 is desired. Two or more of the sunscreens Hsted in Table 13 normally constitute about one-half of the nonvolatiles found in sunscreen lotions. The other half consists of an em ollient (solvent) and emulsifying and bodying agents. If water-resistant quaUties are desired, polymeric film formers, for example, acrylates—octylacrylamide copolymers [9002-93-1] or water-repellent Hpids, for example, dimetbicone [9006-65-9] are included. 

More recendy anhydrous sunscreens have become popular. Products of this type are based on blends of em ollient lipids and acceptable uv absorbers. Formulations of sunscreen products have beenpubHshed (56). 

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