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1.
Water Res ; 92: 149-55, 2016 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-26852288

RESUMO

Sales of bottled drinking water have shown a large growth during the last two decades due to the general belief that this kind of water is healthier, its flavour is better and its consumption risk is lower than that of tap water. Due to the previous points, consumers are more demanding with bottled mineral water, especially when dealing with its organoleptic properties, like taste and odour. This work studies the compounds that can generate obnoxious smells, and that consumers have described like swampy, rotten eggs, sulphurous, cooked vegetable or cabbage. Closed loop stripping analysis (CLSA) has been used as a pre-concentration method for the analysis of off-flavour compounds in water followed by identification and quantification by means of GC-MS. Several bottled water with the aforementioned smells showed the presence of volatile dimethyl selenides and dimethyl sulphides, whose concentrations ranged, respectively, from 4 to 20 ng/L and from 1 to 63 ng/L. The low odour threshold concentrations (OTCs) of both organic selenide and sulphide derivatives prove that several objectionable odours in bottled waters arise from them. Microbial loads inherent to water sources, along with some critical conditions in water processing, could contribute to the formation of these compounds. There are few studies about volatile organic compounds in bottled drinking water and, at the best of our knowledge, this is the first study reporting the presence of dimethyl selenides and dimethyl sulphides causing odour problems in bottled waters.


Assuntos
Água Potável/química , Águas Minerais/análise , Compostos Organosselênicos/análise , Sulfetos/análise , Paladar , Cromatografia Gasosa-Espectrometria de Massas , Limite de Detecção
2.
J Chromatogr A ; 1125(1): 117-23, 2006 Aug 25.
Artigo em Inglês | MEDLINE | ID: mdl-16756984

RESUMO

In the present article, a headspace solid-phase microextraction method coupled to GC/MS was developed and applied for the simultaneous determination of mono- and sesquiterpenic hydrocarbons in virgin olive oils of different olive variety and geographical origin. Analysis of various oils resulted in the simultaneous detection of 15 monoterpenes and 30 sesquiterpenes. Some of these hydrocarbons were previously reported to be constituents of virgin olive oil terpenoid fraction, although we also detected some terpenic hydrocarbons that have not previously been documented as present in virgin olive oil. Significant differences were detected in the proportion of terpenic compounds in oils obtained from different olive varieties grown in different geographical areas. The monoterpene, and particularly the sesquiterpene composition of olive oil may be used to distinguish samples from different cultivar and geographical areas.


Assuntos
Cromatografia Gasosa-Espectrometria de Massas/métodos , Monoterpenos/análise , Óleos de Plantas/análise , Sesquiterpenos/análise , Monoterpenos/isolamento & purificação , Azeite de Oliva , Óleos de Plantas/química , Reprodutibilidade dos Testes , Sesquiterpenos/isolamento & purificação , Temperatura , Fatores de Tempo
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