1.

point 2.2 is replaced by the following:

2.

in point 4, the title is replaced by the following title and subtitle:

‘4.   REFERENCE METHODS

3.

in paragraph 4a, the title is replaced by the following:

‘4–B   Measurement of the alcoholic strength of wines using a hydrostatic balance’;

4.

the following paragraph 4–C is inserted after paragraph 4–B:

‘4–C   Measurement of the alcoholic strength of wines by electronic densimetry using a frequency oscillator

1.   Method of measurement

1.1.   Title and introduction

The alcoholic strength by volume of wines must be measured before marketing, principally to comply with labelling rules.

Alcoholic strength by volume is defined in paragraph 1 of this chapter.

1.2.   Purpose and scope

The method of measurement described is electronic densimetry using a frequency oscillator.

For the purposes of the regulatory provisions in force, the trial temperature is set at 20 °C.

1.3.   Principle and definitions

The principle of this method is based on distilling wine volume by volume. The distilling method is described in paragraph 3 of this Chapter. Distillation eliminates non-volatile substances. Homologues of ethanol, together with ethanol and ethanol homologues in ethyl esters, are included in the alcoholic strength since they occur in the distillate.

The density of the distillate obtained is then measured. The density of a liquid at a given temperature is equal to the quotient of the mass over its volume:

ρ = m/V, for wine, it is expressed in g/ml.

For a hydroalcoholic solution such as a distillate, where the temperature is known, tables can be used to map density and alcoholic strength. This alcoholic strength corresponds to that of wine (distillation volume by volume).

In this method the density of the distillate is measured by electronic densimetry using a frequency oscillator. The principle consists of measuring the period of oscillation of a tube containing the sample subject to electromagnetic excitation. The density can then be calculated – it is linked to the period of oscillation by the following formula:

(1)

This link takes the form ρ = A T2 – B (2); hence there is a linear relationship between the density and the period squared. The constants A and B are specific to each oscillator and are estimated by measuring the period of fluids of known density.

1.4.   Reagents and products

1.4.1.   Reference fluids

Two reference fluids are used to adjust the densimeter. The densities of the reference fluids must encompass those of the distillates to be measured. A difference in the density of the reference fluids greater than 0,01000 g/ml is recommended. Their density must be known with a degree of uncertainty below +/- 0,00005 g/ml, at a temperature of 20,00 °C +/- 0,05 °C.

To measure the alcoholic strength by volume using an electronic densimeter, the reference fluids are:

1.4.2.   Cleaning and drying products

1.5.   Apparatus

1.5.1.   Electronic densimeter using a frequency oscillator

The electronic densimeter comprises the following:

The densimeter is placed on a perfectly stable stand that is insulated from all vibrations.

1.5.2.   Controlling the temperature in the measuring cell

The measuring tube is placed in a thermostatic chamber. The temperature stability must be +/- 0,02 °C or better.

Where possible, the temperature of the measuring cell should be checked as this has a strong impact on the measurement results. The density of a hydroalcoholic solution of 10 % vol is 0,98471 g/ml at 20 °C and 0,98447 g/ml at 21 °C, or a difference of 0,00024 g/ml.

The trial temperature is set at 20 °C. The temperature is measured in the cell using a thermometer with a resolution of below 0,01 °C in line with national standards. It should guarantee a temperature measurement with under +/- 0,07 °C uncertainty.

1.5.3.   Calibration of the apparatus

The apparatus must be calibrated before its first use, then every six months or if the check is unsatisfactory. Two reference fluids should be used to calculate the constants A and B (see above formula 2). Calibration should be carried out in line with the operating instructions for the apparatus. In principle, calibration is carried out using dry air (taking into account atmospheric pressure) and extremely pure water (twice distilled and/or micro-filtered with extremely high resistivity > 18 MΩ).

1.5.4.   Checking the calibration

To check the calibration, measure the density of the reference fluids.

The air density should be checked every day. A difference between the theoretical and the actual density greater than 0,00008 g/ml may indicate that the tube is blocked. It should therefore be cleaned. After cleaning, check the air density once again. If this check is not conclusive, the apparatus must be adjusted.

Check the water density also. If the difference between the theoretical and the actual density is greater than 0,00008 g/ml, the apparatus should be adjusted.

If it is difficult to check the temperature of the cell, the density of a hydroalcoholic solution with an alcoholic strength by volume comparable to that of the distillates analysed can be checked directly.

1.5.5.   Checks

If the difference between the theoretical density of a reference solution (known with under 0,00005 g/ml uncertainty) and the measurement is greater than 0,00008 g/ml, the temperature of the cell must be checked.

1.6.   Sampling and preparation of the samples

(see point 3 of this Chapter, “Method of obtaining distillate”).

1.7.   Procedure

After obtaining the distillate, measure its density or alcoholic strength by volume using densimetry.

First ensure the temperature stability of the measuring cell. The distillate in the densimeter cell must not contain air bubbles and must be homogeneous. If a lighting system is available which can help verify the absence of bubbles, it should quickly be switched off after carrying out the checks as the heat generated by the bulb affects the measuring temperature.

If the apparatus only gives the period, the density should be calculated using the constants A and B (see 1.3). If the apparatus does not give the alcoholic strength by volume directly, this can be obtained from the tables.

1.8.   Expression of results

The alcoholic strength by volume of the wine is that obtained for the distillate. It is expressed in “% vol”.

If the temperature conditions cannot be complied with, correct the result to express it at 20 °C. Give the result to two decimal places.

1.9.   Remarks

The volume placed in the measuring cell must be large enough to avoid any contamination by the previous sample. Consequently, at least two measurements should be carried out. If these do not give results within the repeatability limit, a third measurement is needed. The results of the last two measurements are normally homogeneous and the first value is eliminated.

1.10.   Precision

For samples with an alcoholic strength by volume of between 4 and 18 % vol

2.   Interlaboratory trials. Precision and accuracy on adjuncts

The method performance characteristics shown in paragraph 1.10 were obtained from an interlaboratory test carried out in accordance with established international procedures on six samples and by eleven laboratories.

All the details and repeatability and reproducibility calculations carried out in this test are described in the Chapter “TITRE ALCOOMETRIQUE VOLUMIQUE” (Alcoholic strength by volume) (point 4.B.2) of the OIV’s “Recueil International des Méthodes d’Analyse” (compendium of analysis methods – 2004 edition).’