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SUBJECTS sebacic acid

SIMUL5 has been used to study oscillation patterns that occur in background electrolytes with complex eigenmobilities when they are subjected to an electric field [91]. For a system composed of 0.21 mM sebacic acid and 0.323 mM imidazole, simulation revealed the production of local 10 mM perturbations of the imidazole concentration, which exponentially grew as long as the system was in the region of complex eigenmobilities. This unusual behavior could be experimentally validated and is thus not a simulation artifact. [Pg.534]

The low-volatility, flame-resistant phosphoric acid esters have maintained their position in products subjected to high levels of mechanical strain such as conveyor belts. Triphenyl phosphate, used only for molding compounds made of cellulose esters, is a practically noncombustible product that is not soluble in benzine. Tricresyl phosphate (TCP) is a flame-retardant plasticizer for PVC products subjected to heavy mechanical stress. The esters of the aliphatic dicarboxylic acids (adipic, azelaic, and sebacic acid) are used as plasticizers for PVC and PVAC. These products are resistant to cold and light. The esters of higher fatty acids such as pelargonates, laurates, palmitates, stearates, and ricinoleates are, strictly speaking, not plasticizers, but are rather used as extenders, secondary plasticizers, or lubricants. [Pg.131]

As displayed in Figure 10.4, the ricinoleic acid (here the saponification product, pure ricinoleic acid) is subjected to a further alkaline treatment. At elevated temperatures (180-270 °C) the ricinoleic acid is subjected to a strong soda (with NaOH or KOH) treatment to cleave 2-octanol and sebacic acid. The 2-octanol side product could be a source for various eight carbon products, but is currently marketed in low-end applications areas such as plasticizers, if not directly combusted. [Pg.283]

A biodegradable polyanhydride has been prepared by polycondensation of a lithocholic acid dimer (Scheme 11b). The homopolymer has a Tg of 85°C and a melting point of >250°C, both of which can be lowered by the incorporation of a comonomer (sebacic acid). The polymers have been subjected to degradation and release studies, using p-nitroanUine as the model drug. The degradation and release rates are found to be dependent on the copolymer composition, and no apparent toxicity is observed in vivo [110]. [Pg.168]

Detection and result The chromatogram was dried in a stream of warm air for 10 min, immersed in the reagent solution for 3 s and then subjected to intense UV radiation (high pressure lamp, A = 365 nm) for up to 10 min. Terephthalic (hRf 0 - 5), pimelic (hRf 55), suberic (hRf 60), sebacic (hRf 65 — 70) and benzoic acids (hRf 70 — 75) together with sorbic, malic, adipic, citric, tartaric, lactic and fumaric acids only exhibited a reaction on silica gel layers at higher concentrations. 4-Hydroxybenzoic, salicylic and acetylsalicylic acids fluoresced light blue after irradiation. The detection limit per chromatogram zone was 0.5 pg for salicylic acid and more than 5 pg for benzoic acid. [Pg.308]

Synthetic esters, (a) primarily esters of dibasic acids such as adipic and sebacic, though in Europe some monobasic acid esters have been prepared and used (h) organic esiers of phosphoric and silicic acid, which have some advantage of being more lire-resislant than Ihe other organic compounds bm which are subject to hydrolysis on exposure to water,... [Pg.944]

The skin has two layers, the outer layer is called the epidermis and the inner the dermis. The epidermis has a protective function. It consists of densely packed flat cells, thicker in some areas, like the palms of the hands, which are more subject to injury. It is covered by a moist film known as an acid mantle, made up of secretions from sweat and sebaceous glands, that helps to protect from acids, alkalis, excessive water, heat and friction by preventing the skin from drying out. The natural grease of the skin can be removed by solvents. In the deeper layer of the epidermis are pigment cells which produce the tan following exposure to sunlight and protect the body from ultraviolet radiation. [Pg.455]


See other pages where SUBJECTS sebacic acid is mentioned: [Pg.78]    [Pg.461]    [Pg.37]    [Pg.284]    [Pg.377]    [Pg.149]    [Pg.308]    [Pg.146]    [Pg.270]    [Pg.23]    [Pg.157]    [Pg.48]    [Pg.346]    [Pg.33]    [Pg.231]   
See also in sourсe #XX -- [ Pg.599 ]




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