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Esters, carboxylic acid spectroscopic analysis

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]

The most characteristic feature in the spectroscopic analysis of ethers is the strong band of C-0 stretching. It occurs in the 1060-1300 cm range. In this region, many bands are present, but this alone does not establish the presence of an ether. For note, alcohols, carboxylic acids, and esters also show C-0 stretching. They can be eliminated as possibilities, however, by the fact alcohols would also show the strong and broad 0-H stretch in the 3200-3600 cm , car-... [Pg.610]


See other pages where Esters, carboxylic acid spectroscopic analysis is mentioned: [Pg.276]    [Pg.305]    [Pg.276]    [Pg.276]    [Pg.506]    [Pg.182]    [Pg.227]    [Pg.506]    [Pg.145]    [Pg.182]    [Pg.399]    [Pg.311]    [Pg.123]   
See also in sourсe #XX -- [ Pg.688 , Pg.689 ]

See also in sourсe #XX -- [ Pg.688 , Pg.689 ]




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Carboxyl analysis

Esters analysis

Spectroscopic analysis

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