DETERMINATION OF THE VOLATILE COMPONENTS OF BEER

A method relying on headspace sampling and gas chromatography for the determination of the lower boiling point volatile compounds (fusel oils) in beer, has been approved by the Analysis Committee of the Institute of Brewing (IOB), for inclusion in Recommended Methods of Analysis. In view of the large values obtained for precision in terms of repeatability (r₉₅) and reproducibility (R₉₅) and the differences in gas chromatographic equipment used by individual brewing laboratories, the method is considered not to be ideal, but is given as a guideline only. The IOB Analysis Committee has recommended a method relying on gas chromatography and flame photometric detection for the determination of dimethyl sulphide in beer. Repeatability (r₉₅) and reproducibility (R₉₅) values of 3.3 μg/litre and 3.66+0.168 m μg/litre (where m is concentration), respectively, were obtained over the range 20–50 μg/litre. Methods currently used in brewing laboratories, for the measurement of vicinal diketones, are being surveyed with a view to obtaining a suitable method for collaborative testing by the Analysis Committee.     

THE DETERMINATION OF DIMETHYL SULPHIDE IN BEER BY HEADSPACE GAS CHROMATOGRAPHY — A COLLABORATIVE INVESTIGATION OF PRECISION

A method for the determination of dimethyl sulphide in beer by headspace gas chromatography has been collaboratively tested within ten laboratories of one brewing group at 3 levels from 19.8 to 52.4 μg/litre. The repeatability values (r₃₅ were found to be independent of concentration, but a strong linear relationship was found between the mean values (m) and the reproducibility value (R₃₅). The precision data can be summarised as r₃₅ = 3.3 μg/litre, R₃₅ = 3.66 + 0.168 μg/litre .     

DETERMINATION OF VICINAL DIKETONES IN BEER BY GAS CHROMATOGRAPHY (HEADSPACE TECHNIQUE)—COLLABORATIVE TRIAL

Two methods for the determination of vicinal diketones in beer have been collaboratively tested by the Analysis Committee of the Institute of Brewing and are recommended for use. Both methods employ gas chromatography and are essentially the same, except that one relies on the use of a packed column and the other on a capillary column. For diacetyl it was judged that repeatability (r₉₅) values were independent of concentration over the range 0.04 to 0.19 mg/litre. Over this range, r₉₅ values for diacetyl of 0.028, 0.020 and 0.026 mg/litre were obtained for capillary, packed columns and combined results respectively. Values for reproducibility (R₉₅) were judged to be dependent on the mean level (m). R₉₅ values were 0.032 + 0.68 m, 0.01 + 0.47 m and 0.005 + 0.67 m were obtained for capillary, packed columns and combined results respectively. For both methods the r₉₅ and R₉₅ values for 2,3-pentanedione were judged to be independent of concentration over the range 0.02 to 0.07 mg/litre. For capillary columns, packed columns and combined results respectively, r₉₅ values were 0.009, 0.009, 0.010 mg/litre and R₉₅ values were 0.037, 0.042 and 0.038 mg/litre.     

DETERMINATION OF LOWER BOILING POINT VOLATILE COMPOUNDS IN BEER BY HEADSPACE GAS CHROMATOGRAPHY — COLLABORATIVE TRIAL

The Analysis Committee has collaboratively tested local routine headspace gas chromatographic methods for the determination of the lower boiling point volatile compounds in beer. The repeatability values (r₉₅) were dependent upon mean concentration (m) for acetaldehyde and alcohols but not for esters, whilst reproducibility values (R₉₅) were dependent upon concentration in all cases. The range of values of m and the estimates of r₉₅ and R₉₅ (mg/litre) for each compound were, respectively: acetaldehyde (5–8, 0.21m, 0.60m); propanol (9–23, 0.25m, 2.5+0.57m); isobutanol (5–22, 0.56+0.085m, 1.7+0.15m); methylbutanols (45–105, 0.14m, 0.22m); ethyl acetate (10–54, 3.1, 2.1+0.29m); isoamyl acetate (0.8–4.7, 0.36, 0.20+0.58m); and ethyl hexanoate (0.13–0.36, 0.073, 0.10+0.91m). No advantage was gained by diluting beer samples containing 9% V/V ethanol to 4% ethanol (used for the calibration mixtures) prior to analysis, but use of a standard method of sample preparation decreased most of the R₉₅ values. No recommendation is made in this interim report.     

DETERMINATION OF ALUMINIUM IN BEER BY GF-AAS

A method for the determination of aluminum in beer, has been collaboratively tested. The method tested relies on atomic absorption spectrometry with atomization in a graphite furnace. Five pairs of beers, with concentrations ranging from 96 to 1000 μg/litre, were analysed by eleven laboratories. The repeatability (r₉₅) values ranged from 10 to 69 μg/l, and the reproducibility (R₉₅) values ranged from 70 to 465 μg/l,. A second collaborative trial with a slightly different method protocol gave no improvement. Due to the high reproducibility values the method was not adopted for inclusion in Analytica-EBC.     

ESTIMATION OF ISO-ALPHA-ACIDS IN BEER BY HPLC-COLLABORATIVE TRIAL

A procedure relying on high performance liquid chromatography for the estimation of iso-alpha-acids in beer has been collaboratively tested by the IOB Analysis Committee. In addition the trial samples were analysed by the IOB Recommended Method for the measurement of bitterness (BU). It was judged that the results obtained by the HPLC method were not sufficiently precise to permit adoption as a Recommended Method. However, since the method has the advantage of measuring bitterness in terms of iso-alpha-acids, it is suggested as an alternative to that of the Recommended Method. The iso-alpha-acids are absorbed from beer on to a C₁₈ Bond Elut column and then selectively desorbed prior to isocratic analysis by HPLC using an eluting solvent of methanol/water/phosphoric acid/tetrabutylammonium hydroxide and a C₁₈ radialpak cartridge. For both methods the repeatability values (r₉₅) were not dependent upon mean concentration (m) whereas the reproducibility values (R₉₅) were dependent upon concentration. The values of (r₅₃) and (R₉₅) obtained were 2.11 and (1.38 + 0.134 m) over the concentration range 13.8 to 34.0 mg/litre for the HPLC procedure and 1.20 and (0.76 + 0.122 m) over the concentration range 15.4 to 38.6 BU for the Recommended Method.     

THE DETERMINATION OF SULPHUR DIOXIDE IN BEER—COLLABORATIVE TRIAL OF FOUR METHODS

The Institute of Brewing Analysis Committee has collaboratively tested four methods for the determination of sulphur dioxide in beer over the range 1 to 40 mg/litre. The p-rosaniline method (r₉₅ = 0.51 + 0.10 m. R₉₅ = 0.63 + 0.26 m) was found to have the best precision and is recommended as an alternative to the Monier Williams method (r₉₅ = 0.43 + 0.15 m, R₉₅ = 1.86 + 0.27 m) where high precision at low sulphur dioxide levels is required. The dithiobisnitrobenzoic acid (DTNB) method and the IOB rapid distillation method showed considerably worse precisions.     

DETERMINATION OF NITRATE IN BEER BY ION CHROMATOGRAPHY

¹A method, relying on ion chromatography, for the determination of nitrate in beer, has been collaboratively tested by members of the European Brewery Convention (EBC) and the Brewery Convention of Japan (BCOJ). Precision values were judged to be acceptable. Repeatability (r₉₅) and reproducibility (R₉₅) values were 1.5, 0.96, 5.1, and 9.3, 10.4, 13.5 respectively for corresponding mean levels of 6.5, 26.2 and 52.8 mg/litre. However, r₉₅ and R₉₅ values of 1.5 and 2.3 respectively were obtained for an aqueous solution of nitrate ions at a mean level of 20.7 mg/litre. The determination of nitrate is recommended for use and inclusion in Analytica-EBC, as an additional analyte in the International Method which relies on ion chromatography for estimating chloride, sulphate and phosphate.     

THE DETERMINATION OF ALCOHOL IN BEER USING THE SCABA AUTOMATED METHOD (COLLABORATIVE TRIAL)

The Institute of Brewing Analysis Committee has organised two collaborative trials for the analysis of alcohol using the ServoChem Automatic Beer Analyser (SCABA). The mean repeatability (r₉₅) values for the two trials were 0.051% and 0.034% V/V respectively. The value for the second trial could however be judged to be dependent on concentration (m) at 0.008m% V/V. The Reproducibility (R₉₅) values of both trials were judged to be dependent on concentration at 0.027m% V/V and 0.025m% V/V respectively. The combined data for the two trials gave r₉₅ = 0.044% V/V and R₉₅ = 0.026m% V/V.     

DETERMINATION OF HOT WATER EXTRACT

The Analysis Committee of the European Brewery Convention has recommended that the Hot Water Extract procedure for malt, which relies on a coarse grind and single temperature mash (65°C), is included in Analytica-EBC, as an additional method to that of the EBC Extract procedure. The Committee accepted the precision values obtained by the Institute of Brewing on the 1984 Check Malt. Repeatability (r₉₅) and reproducibility (R₉₅) values in litre degrees/kg were 2.14 and 3.48 respectively, for mean value of 295.3 at a Miag 0.7 mm setting, and 1.93 and 2.90 respectively, for a mean value of 298.2 at a Miag 0.2 mm setting.     

DETERMINATION OF ANIONS IN BEER BY ION CHROMATOGRAPHY

A method relying on ion chromatography, with suppressed ion detection, for the determination of anions in beer, has been collaboratively tested by members of the American Society of Brewing Chemists, the European Brewery Convention and the Brewery Convention of Japan. Precision values obtained for the determination of chloride, sulphate and phosphate in beer were judged to be acceptable. Repeatability (r₉₈) and reproducibility (R₉₈) values for chloride were 5.7, 12.6, 12.5 and 15.0, 38.4, 36.8 respectively at corresponding mean levels of 68.7, 218.6 and 322.5 mg/litre. r₉₈ and R₉₈ values for sulphate were 7.5, 6.2, 7.6 and 44.8, 54.0, 46.5 respectively at corresponding mean levels of 101.4, 205.1 and 122.6 mg/litre. r₉₈ and R₉₉ values for phosphate were 14.1, 11.9, 24.9 and 78.7, 53.8, 84.0 at corresponding mean levels of 411.5, 224.1 and 397.5 mg/litre. Whilst the r₉₈ value for nitrate was acceptable, the value for R₉₈ was unsatisfactory. The ion chromatographic method for determining chloride, sulphate and phosphate in beer is recommended for use and inclusion in Analytica -EBC as an International Method.     

DETERMINATION OF THE MOISTURE CONTENT OF BARLEY

The method of the International Organization for Standardization, (ISO 712–1985) for the determination of moisture in cereals and cereal products, has been tested by members of the Analysis Committee of the European Brewery Convention on samples of barley. The method, which relies on loss in mass on drying at 130–133°C for 2 h, is recommended for use as a replacement for the current method, based on loss in mass on drying at 105–107°C for 3 h. It was judged that precision values were independent of concentration over the range 11 to 13% m/m. Repeatability (r₉₅) and Reproducibility R₉₅) values of 0.13 and 0.55 respectively were obtained over this range. At a mean level of 21.7% m/m, the r₉₅ and R₉₅ values were 0.27 and 2.6 respectively. This was probably due to errors associated with the double drying technique which is necessary for samples at this moisture content.     

ESTIMATION OF FERMENTABLE CARBOHYDRATES — COLLABORATIVE TRIAL

A procedure relying on high performance liquid chromatography, for the estimation of fermentable carbohydrates in wort, has been tested collaboratively and adopted by the Institute of Brewing Analysis Committee as a Recommended Method. A radially compressed cartridge containing silica modified with tetraethylenepentamine is used with an eluting solvent of acetonitrile/water. The results of a preliminary trial indicated that better precision is achieved using manual measurements of peak height and omitting an internal standard. In the main trial where 5 laboratories analysed 5 sample pairs the repeatability (r₉₅) and reproducibility (R₉₅) values found with their mean concentration levels (m) to which they are applicable were: fructose (0.0256 + 0.0660m) and (0.0711 + 0.0691m) for 0.17–1.01 g/100 ml; glucose 0.090m and 0.139m for 0.80–2.07 g/100 ml; sucrose 0.095 and (0.0746 + 0.1663m) for 0.12–3.88 g/100 ml; maltose 0.219 and 0.917 for 4.17–6.09 g/100 ml; maltotriose 0.122 and 0.236 for 0.97–1.19 g/100 ml. The precision values for the sums of the total fermentable sugars were 0.578 and 1.040 for 6.71–14.24 g/100 ml.     

DETERMINATION OF MOISTURE,TOTAL AVAILABLE EXTRACT AND SOLUBLE EXTRACT IN SPENT GRAINS

The methods for the determination of moisture⁴, total available^3,4 and soluble extracts⁴ in spent grains have been collaboratively tested by members of the Analysis Committee of the European Brewery Convention to obtain repeatability (r₉₅) and reproducibility (R₉₅) values . Repeatability and reproducibility values of 0.1 and 0.67 respectively were obtained for spent grain moisture's ranging between 4 and 8% m/m in pre-dried and pro-milled samples. In a pro-dried and unmilled sample containing 3.4% m/m moisture the values obtained were 0.3 and 1.5 respectively . For total available extract (MEBAK) these values were 0.5 and (2.2+0.045 m) respectively, with total available extract ranging from 9 to 42% m/m dry matter, where m refers to the actual value. The values for the pre-dried and unmilled sample containing an extract of 41.2% m/m were 0.5 and 4.6 respectively . The precision values for soluble extract were dependent on the extract level of the sample over the range 6 to 40% m/m dry matter. A repeatability value of 0.13+0.007 m and a reproducibility value of 0.2+0.06 m were obtained over this range. Values for the same pre-dried and unmilled sample with a soluble extract of 38.7% m/m were 1.3 and 3.8% m/m respectively .     

DETERMINATION OF THE SOLUBLE IRON CONTENT OF FILTER AIDS: A COLLABORATIVE TRIAL

The international method for the determination of the soluble iron content of filter aids has been collaboratively tested by members of the Analysis Committee of the European Brewery Convention to obtain repeatability (r₉₈) and reproducibility (R₉₈) values. It was Judged that precision values were dependent on the quantity of the soluble iron content of the filter aids over the range 32 to 220 mg/kg. Repeatability (r₉₈) value of 0.050 m and reproducibility value (R₉₈) of 0.255 m were obtained over this range.     

DETERMINATION OF ETHANOL IN BEER BY DIRECT INJECTION GAS CHROMATOGRAPHY: A COMPARISON OF SIX IDENTICAL SYSTEMS

Six identical gas chromatographic (GC) systems from the same manufacturer were evaluated for the determination of ethanol in beers. Each system was assessed for detector linearity and drift using standard ethanol solutions. Repeatability (r₉₅) of each machine, repeatability (r₉₅) of the GC method and reproducibility (R₉₅) of the method over a range of ethanol concentrations (1–11% V/V) was determined using commercial beers. All six instruments were linear over the ethanol range 0–12% V/V and were in good agreement. Drift of the machines was negligible over the period of the analysis. Over the ethanol range 0.95 to 6.32% V/V the repeatability (r₉₅) and reproducibility (R95) values were 0.050 and 0.083 respectively. Over the ethanol range 9.48 to 11.15% V/V the repeatability (r₉₅) and reproducibility (R₉₅) values were 0.153 and 0.227 respectively. Comparison of the precision values and those obtained in a recent IOB Analysis Committee Collaborative¹ for the determination of ethanol by gas chromatography showed no significant differences between the two methods. The reported method is suitable for determination of ethanol in beers.     

DETERMINATION OF ETHANOL IN BEER BY GAS CHROMATOGRAPHY (DIRECT INJECTION)—COLLABORATIVE TRIAL

A method employing gas chromatography for the determination of ethanol in beer has been collaboratively tested by the Analysis Committee of the Institute of Brewing. It was judged that precision values were independent of concentration over the range 0.93 to 6.05% V/V ethanol. Repeatability (r₉₅) and reproducibility (R₉₅) values of 0.061 and 0.136 respectively, were obtained over this range. At a mean level of 9.17% V/V, the r₉₅ and R₉₅ values were 0.154 and 0.284 respectively. This was probably due to dilution errors as the sample had to be diluted to bring it within the linear range of the method. A comparison of the precision values given by the gas chromatographic method, with those obtained in 1991/1992 by 8 laboratories in a major brewing company using 12 sample pairs, for the IOB Recommended Distillation Method, revealed that there is no significant difference between the precision data for the two methods.     

EXTRACT AND COLOUR DETERMINATION OF TORREFIED PRODUCTS (WHEAT,BARLEY AND RYE)—COLLABORATIVE TRIAL

A procedure for preparing torrefied products for analysis has been examined and the effects of this procedure on the determination of laboratory extract and colour have been collaboratively tested by the Analysis Committee of the Institute of Brewing. White malts of DP levels 50° and 100° IOB were used as the sources of enzymes in the mixed mash procedure. With these malts r₉₅ and R₉₅ values for extract of the torrefied products ranged from 1.7 to 10.2 and 12.4 to 21.9 resp. on mean extracts ranging from 244 to 270 litre °/kg. The r₉₅ and R₉₅ values for colour ranged from 1.6 to 2.3 and 2.2 to 3.8 resp. on mean colours ranging from 2.7 to 3.5 EBC units.     

A GAS CHROMATOGRAPHIC METHOD FOR THE ACCURATE DETERMINATION OF LOW CONCENTRATIONS OF VOLATILE SULPHUR COMPOUNDS IN ALCOHOLIC BEVERAGES

By using a new sensitive method the contents of dimethyl sulphide, dimethyl disulphide and dimethyl trisulphide have been determined in beers and wines, and the contents of these sulphides and diethyl sulphite measured in distilled beverages. The head-space volatiles are swept out from the beverage in a stream of nitrogen and adsorbed in a tube containing porous polymer. The volatiles are desorbed directly onto the column of a gas chromatograph by connecting the tube to the column and sliding the free end of the tube into the hot injection block from the oven side. The sulphur-sensitive flame photometric detector is used and the peak areas and identifications are collected on cassette and processed by computer to give the content of volatile sulphur compounds directly in μg/litre beverage. The detection limits are 2 μg/litre for dimethyl sulphide, 0.1 μg/litre for dimethyl disulphide and trisulphide, and 5 μg/litre for diethyl sulphite. The analysis time for each sample is 30 min and the coefficient of variation is 5%.     

Effect of modifiers on thermal behaviour of Se in acid digestates and slurries of vegetables by graphite furnace atomic absorption spectrometry

The influence of sample preparation strategy of vegetables on the electrothermal behaviour of Se without and with chemical modifiers such as Pd(NO₃)₂, Pd(NO₃)₂ + Mg(NO₃)₂, Pd(NO₃)₂ + Cd(NO₃)₂, pre-reduced Pd, Mg(NO₃)₂, and Ni(NO₃)₂ was investigated. Acid digestates and slurries of vegetables (0.1% m/v in 1% v/v HNO₃ + 0.005% v/v of Triton X-100) were used to prepare reference solutions or slurries. For 10 μl of each modifier tested, pyrolysis and atomization temperatures were evaluated using pyrolysis and atomization curves, respectively. Best conditions, such as thermal stability, signal profile, repeatability and sensitivity were attained using Pd(NO₃)₂ as chemical modifier. The following heating program (temperature, ramp/hold time) of the graphite tube of the Varian SpectrAA-800Z atomic absorption spectrometer was used: dry step (85 °C, 5/0 s; 95 °C, 40/0 s; 120 °C, 10/5 s); pyrolysis step (1400 °C, 10/3s); atomization step (2200 °C, 1/2 s); clean step (2600 °C, 2/0 s). This pyrolysis temperature is 800 °C higher than when measuring without any modifier. For 20 μL sample volume and 10 μg Pd(NO₃)₂, analytical curves in the 3.0–30 μg Se l⁻¹ range were obtained. The method was applied for Se determination in acid digestates and slurries of 10 vegetable samples and one standard reference material (rice flower) and results were in agreement at 95% confidence level. Recoveries varied from 89 to 95% for spiked samples. The lifetime of the graphite tube was ca. 250 firings and the relative standard deviations (n=12) for a typical acid digestate and slurry containing 20 μg Se l⁻¹ were 3.8% and 8.3%, respectively. The limits of detection were 2.0 μg Se l⁻¹ and 0.6 μg Se l⁻¹ Se for digestates and slurries, respectively.