Wine Chemistry and Biochemistry

(Steven Felgate) #1

650 M. Dubernet


Automated methods frequently exhibit remarkable performance not only in terms


of sample throughput and cost, but in relation to the quality of results, especially in


relation to repeatability and reproducibility. Several systems are currently available


that enable simple automation of manual gestures; these include automatic titra-


tors, pH-meters with a circulating cell, etc., and involve approaches that are not


fundamentally different to the corresponding manual method. These techniques are


not, however, described in this chapter,nor are gas and liquid chromatography and


capillary electrophoresis, automated techniques, that may be present but are not


routinely used in oenological laboratories.


Four major families of automated analysers are routinely used today in oenology:


 Flow injection analysers

 Sequential analysers

 NIR (near infra-red) analysers

 FTIR (Fourier transform interferometer) analysers

For each of these families, the general principles, the particularities and limits of


their applications will be presented.


Note: The methods presented below are described in the OIV green document


Nā—¦1276ā€“2008 (Dubernet 2008).


12.2 Flow Injection (FIA) Analysers


The earliest studies on the automation of chemical analysis in oenology by FIA were


carried out by Sarris et al. (1970). However, it was only from 1974 onwards that this


technique started to become widely used in routine oenological determinations with


the development of reliable and repeatable analytical methods.


12.2.1 Composition and Principle of an FIA Analyser


FIA analysers are composed of separate modules, each of which has a specific


function.


12.2.1.1 The Sample Distributor


This module consists of a tray that can generally hold between 20 and 60 sample


vials whose volume is usually between 1 and 3ml. A pivoting arm to which is a


needle is attached aspirates an aliquot of each sample with a rinse step between each


sampling step. The needle is linked to the analytical circuit via a PVC tube. The


rinsing liquid, the sample, the rinsing liquid and the next sample are successively


aspirated by the needle. The rate of analysis is determined by the sample distributor.

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