Application Note No. 193/2015

Similar documents
COMPENDIUM OF INTERNATIONAL METHODS OF ANALYSIS - OIV Volatile acidity. Volatile Acidity

Application Note No. 184/2015

LABORATORY PRACTICES IN WINE ANALYSIS. Dpto. Nutrición y Bromatología II. Facultad de Farmacia. UCM

Acidity and ph Analysis

Find out all you need to know about measuring SO 2. in wine making

Winemaking and Sulfur Dioxide

Royal Society of Chemistry Analytical Division East Anglia Region National Schools' Analyst Competition

Volume NaOH ph ph/ Vol (ml)

RESOLUTION OIV-OENO ANALYSIS OF VOLATILE COMPOUNDS IN WINES BY GAS CHROMATOGRAPHY

Harvest Series 2017: Wine Analysis. Jasha Karasek. Winemaking Specialist Enartis USA

Activity Sheet Chapter 6, Lesson 6 Using Chemical Change to Identify an Unknown

Student Handout Procedure

Separation of a Mixture

Determination of Alcohol Content of Wine by Distillation followed by Density Determination by Hydrometry

Application Note. Hydrolysis Unit E-416, Extraction Unit E-816 Soxhlet. Fat determination according to Weibull-Stoldt - Standard application

Acidity and Blending. The art of using Titratable Acidity as a tool for blending consistency

ISO INTERNATIONAL STANDARD. Oilseed residues Determination of oil content Part 2: Rapid extraction method

Methanol (Resolution Oeno 377/2009, Revised by OIV-OENO 480/2014)

HI Titratable Total Acidity Mini Titrator for Wine Analysis

15. Extraction: Isolation of Caffeine from Tea

HOW MUCH DYE IS IN DRINK?

Making Hard Cider. A Guide for Small-Scale Producers. Lee Elliot Williams. Bellevue College. Technical Writing Certificate Program

Notes on acid adjustments:

Science Project for ICCE General Level

Analytical Method for Coumaphos (Targeted to agricultural, animal and fishery products)

Setting up your fermentation

Measuring Sulfur Dioxide: A Perennial Issue. Tom Collins Fosters Wine Estates Americas

HI Formol Number Mini Titrator for Wine and Fruit Juice Analysis

FOOD FOR THOUGHT Topical Insights from our Subject Matter Experts LEVERAGING AGITATING RETORT PROCESSING TO OPTIMIZE PRODUCT QUALITY

LAB ANALYSES for BEGINNERS to INTERMEDIATES

Lab 2: Phase transitions & ice cream

Experiment 7: The Clock Reaction

Copyright JnF Specialties, LLC. All rights reserved worldwide.

Bromine Containing Fumigants Determined as Total Inorganic Bromide

EU Legal framework Wine Council Regulation (EC) 1234/207 integrating Regulation (EC) 479/2008 Commission Regulation (EC) 606/2006 Amendments of this r

The sugar determination in the winemaking process

National Food Safety Standard

GB Translated English of Chinese Standard: GB NATIONAL STANDARD

Chemistry 212 MOLAR MASS OF A VOLATILE LIQUID USING THE IDEAL GAS LAW

Chapter 14 Tex-619-J, Analysis of Water for Chloride and Sulfate Ions

Specific Heat of a Metal

FAT, TOTAL (Hydrolysis)

Practical 1 - Determination of Quinine in Tonic Water

INSTRUCTION MANUAL Mi456

The Separation of a Mixture into Pure Substances

Problem How does solute concentration affect the movement of water across a biological membrane?

WINEWORKS LABORATORY PRODUCTS & SERVICES

1. Determine which types of fruit are susceptible to enzymatic browning.

Preparation 1: Chloroform

CHEM Experiment 4 Introduction to Separation Techniques I. Objectives

Rapid Analysis of Soft Drinks Using the ACQUITY UPLC H-Class System with the Waters Beverage Analysis Kit

Separating the Components of a Mixture

THE MAGIC OF CHEMISTRY SHOW

EXTRACTION. Extraction is a very common laboratory procedure used when isolating or purifying a product.

SVENSK STANDARD SS-EN Surface active agents Determination of primary, secondary and tertiary amino nitrogen Potentiometric titration

Dry Ice Rainbow of Colors Weak Acids and Bases

DRAFT EAST AFRICAN STANDARD

Biology 30S Unit #1 Wellness & Homeostasis

Introduction to Measurement and Error Analysis: Measuring the Density of a Solution

PRODUCT SELECTION GUIDE

Gravimetric Analysis

Laboratory Performance Assessment. Report. Analysis of Pesticides and Anthraquinone. in Black Tea

Determination of Melamine Residue in Milk Powder and Egg Using Agilent SampliQ Polymer SCX Solid Phase Extraction and the Agilent 1200 Series HPLC/UV

Official Journal of the European Union L 154/39

Assessment of the CDR BeerLab Touch Analyser. March Report for: QuadraChem Laboratories Ltd. Campden BRI Group contracting company:

SYNTHESIS OF SALICYLIC ACID

PECTINASE Product Code: P129

WINERY LABORATORY MANUAL

Application Note FP High Sensitivity Coumarin Analysis. Introduction. Keywords

Gravimetric Analysis

Prototocatechualdehyde methylenation. Photo-essay.

HI FREE & TOTAL SULPHUR DIOXIDE MINITITRATOR for wine analysis

INSTRUCTION MANUAL Mi455

Validation Report: Free Sulfite Assay Kit (cat. no. K-FSULPH)

CHEMISTRY INVESTIGATORY PROJECT

Proficiency Testing and Determination of Standard Parameters in Wine

Correlation of the free amino nitrogen and nitrogen by O-phthaldialdehyde methods in the assay of beer

RESOLUTION OIV-OENO BEVERAGES WITH LOW ALCOHOL CONTENT UPDATE TO METHOD OIV-MA-AS312-01A

Separating the Components of a Mixture

ION FORCE DNA EXTRACTOR FAST Cat. N. EXD001

SO 2 and You: Understanding the When, Why, and How of SO 2 Management in Your Winery. NGP Webinar Tuesday, May 8, 2018

Introduction to the General Chemistry II Laboratory. Lab Apparatus and Glassware

THIN LAYER CHROMATOGRAPHY AND MELTING POINT DETERMINATION: DETECTION OF CAFFEINE IN VARIOUS SAMPLES

The Purpose of Certificates of Analysis

Diffusion, Osmosis, and Water Potential Lab Report

LAB: One Tube Reaction Part 1

Introduction. Question. Hypothesis. Materials. Procedure

Objective: To observe fermentation and discuss the process. Problem: Will yeast give off significant amounts of gas to inflate a balloon?

Validation Report: Total Sulfite Assay Kit (cat. no. K-TSULPH)

Introducing the Automated Fiber Analyzer

Allergens in wine a specific detection of Casein, Egg and Lysozyme

Dry Ice Color Show Dry Ice Demonstrations

depend,: upon the temperature, the strain of

Diffusion & Osmosis Labs

Automation of AOAC for the Identification of FD&C Color Additives in Foods using Solid Phase Extraction

COMPARATIVE EVALUATION OF CLARIFYING REAGENTS OCTAPOL AND LEAD SUB ACETATE FOR USE WITH MASSECUITES AND MOLASSES. Niconor Reece and Sydney Roman

OenoFoss. Instant quality control throughout the winemaking process. Dedicated Analytical Solutions

CAUTION!!! Do not eat anything (Skittles, cylinders, dishes, etc.) associated with the lab!!!

The fermentation of glucose can be described by the following equation: C6H12O6 2 CH3CH2OH + 2 CO2 + energy glucose ethanol carbon dioxide.

EXPERIMENT 6. Molecular Fluorescence Spectroscopy: Quinine Assay

Transcription:

Application Note No. 193/2015 Determination of volatile acids in wine and juice Distillation Unit K-355: Volatile acids determination according to Schenk SA

1 Introduction The main part (>95 %) of the volatile acidity in wine and juice is acetic acid which is formed by oxidative or anaerobic fermentation. The average level of acetic acid in a new dry table wine is less than 400 mg/l, though levels may range from undetectable up to 3 g/l. A too high level of volatile acids is an indicator for a low quality and acetous product. In Switzerland, for example, the tolerance level of volatile acids is 1200 mg/kg [1]. In the USA the legal limits are 1200 mg/kg volatile acids for white wine and 1400 mg/kg for red wine [2]. Here a method for the volatile acid determination, based on steam distillation and performed in the laboratories of Schenk SA in Rolle Switzerland, is presented. Steam distillation is the preferred method for volatile acid determination and described in detail in normative procedures [3, 4]. Importantly, the used distillation equipment can be used for volatile acids and alcohol determination [5]. 2 Equipment Distillation Unit K-355 (alternatively also the K-360 can be utilized for distillation) External titrator Sample tubes 500 ml (043982) Beaker for sample collection Water aspirator vacuum pump Vacuum flask 3 Chemicals and Materials Chemicals: Tartaric acid, crystalline Sodium hydroxide solution, 0.1 M Phenolphthalein solution, 1 %, in neutral alcohol, 70 % (m/v) Sulfuric acid (96 %) : water solution (1:4) Iodine solution, 1/64 N (1/128 mol/l) Starch solution, 25 g/l; Preparation according to SLMB 30A 4.2: A mixture of 500 ml glycerine and 500 ml water are heated to 70 C. 25 g starch are added in small portions, heated up to 90 C and then cooled. The solution is stable for at least 6 months. For safe handling please pay attention to the corresponding MSDS. Samples: Red wine and white wine samples used for an interlaboratory test with 31 participating laboratories as well as eight characteristic Swiss wine samples. Application Note 193/2015 May 2015 2/5

4 Procedure The procedure was done according to Schenk SA, Rolle Switzerland. The volatile acidity is derived from the acetic acid present in wine in the free state and combined as salts. The official analysis method requires a separation of volatile acids by steam distillation of water and then condensation of the vapors. In case that carbon dioxide is present in wine it has to be eliminated prior to the distillation. Sulfur dioxide and sorbic acid are also distilled and would increase the results. Therefore, it is necessary to determine both and correct the volatile acid results by deducting the sulfur dioxide content. Preparation of sample For the elimination of carbon dioxide place about 50 ml of wine in a vacuum flask and apply vacuum to the flask with the water pump for one to two minutes while continuously shaking. Steam distillation Preheating of the distillation unit: Distill for 5:30 minutes with 100 % steam power and an empty glass tube. Pipette 20 ml of wine or juice in the 500 ml sample tube. Add about 0.5 g of tartaric acid. A 500 ml beaker is attached to the outlet tube and filled with a small amount of distilled water in order to immerse the tube outlet in water and assure the complete collection of volatile acids. The sample is then distilled for 10 minutes by applying 100 % steam power. Between each sample distillation a cleaning step is performed including 3 minutes distillation with 100 % steam power. Depending on the sample volume, the amount of volatile acids, the distillation time and the sodium hydroxide factor (Equation 1) the parameters have been optimized as shown in Table 1. The choice of 20 ml sample volume is in accordance with the OIV method [3], while 10 ml sample are suggested in the SLMB [4]. Table 1: Optimal parameters depending on the sample volume. Sample volume [ml] Destillation time [min] Factor (F) NaOH 0.1 M Volume of distillate [ml] 10 8 0.6 About 300 20 10 0.3 About 400 50 14 0.1 About 500 Titration To quantify the volatile acids content add 3 drops of phenolphthalein to the distillate. Titrate with 0.1 M NaOH solution until the pink color remains stable for 10 seconds. Since sulfur dioxide is co-distilled with volatile acids during steam distillation the determined volatile acid content has to be corrected for its sulfur dioxide content by a second - iodometric - titration. Therefore, the distillate is acidified with 5 ml sulfuric acid (1:4). Titrate the sulfur dioxide with the 1/64 N iodine solution according to Reaction 1. To visually determine the SO 2 content a few ml of the starch solution are added. Starch and iodide form an intense blue iodine-starch complex, indicating the end of the titration. SO 2 + I 2 + 2 H 2O 2 I - + 4 H + + SO 4 2- Reaction 1 5 Calculation The content of volatile acids in wine and juice is determined according to Equation 1 [4]. The factor F in Equation 1 is dependent on the sample volume as listed in Table 1. Volatile acidity = F (a t 1-10/64 b t 2) Equation 1 Application Note 193/2015 May 2015 3/5

Volatile acidity g acetic acid / L a titrated volume of NaOH 0.1 M [ml] b titrated volume of iodine solution 1/64 N [ml] t 1 titer of NaOH solution 0.1 M t 2 titer of iodine solution 1/64 N F factor NaOH Example: Sample volume: 20 ml Titrated volume of NaOH 0.1 M: 2.7 ml Titrated volume of iodine solution 1/64 N: 0.92 ml Volatile acidity = 0.3 (2.7 1 10/64 0.92 1) = 0.77 g/l The precision of the method according to [4]: Repeatability r (all wines) = 0.04 g/l acetic acid Reproducibility R (all wines) = 0.08 g/l acetic acid NOTE: Some wines include sorbic acid as a preservative. Since 96 % of sorbic acid is steam distilled with a distillate volume of 250 ml, its acidity must be subtracted from the volatile acidity. 100 mg of sorbic acid corresponds to an acidity of 0.89 ml NaOH 1 M or 0.053 g of acetic acid [3]. 6 Results and Discussion For this study Schenk SA tested two unknown wine samples, a red and a withe wine, within a proficiency testing campaign with 31 participating laboratories as well as eight characteristic Swiss wine samples. The volatile acid content was determined in a single measurement for each sample. The volatile acid content is given in g acetic acid per liter wine. Measured volatile acid contents were in line with the average content determined by the 31 laboratories that performed the proficiency testing. The allowed accuracy limit was 0.05. From the tested samples one sample (Dunkel (Red)) was above the tolerance level [1] while the others were well below. Table 2: Results of the volatile acidity determination in red wine. Average labs (31 labs) 0.49 Result determined with K-355 0.49 Table 3: Results of volatile acidity determination in white wine. Average labs (31 labs) 0.63 Result determined with K-355 0.63 Table 4: Results of volatile acidity determination in red and white wine samples. Samples Garanoir (Red wine) 0.75 Dunkel (Red) 2.33 Garanoir (white) 0.29 Gewurtz (Red) 0.6 Chasselas (Red) 0.48 Gamay (Red) 0.36 Gewurtz (White) 0.72 Chasselas (White) 0.41 Application Note 193/2015 May 2015 4/5

7 Conclusion The determination of volatile acids in wine using the Distillation Unit K-355 provides reliable and well comparable results. With the method described, Schenk SA reported volatile acid concentrations in test samples that exactly represent the average value of the 31 testing labs. In addition, the K-355 used for steam distillation of volatile acids is also employed for the determination of the alcohol content in the mentioned samples. Hence, the K-355 * has a broad application range in the wine and juice analysis. 8 Acknowledgement Büchi Labortechnik AG would like to thank Schenk SA in Rolle, Switzerland, for sharing experience and providing the data shown in chapter 6. 9 References [1] Verordnung über Fremd- und Inhaltsstoffe in Lebensmittel. [2] 27 CFR 4.21 - The standards of identity, (a) Class 1; grape wine (iv) [3] Compendium of the international methods of analysis OIV, Method OIV-MA-AS313-02:R 2009. [4] Bestimmung der flüchtigen Säuren durch Wasserdampfdestillation, Schweizer Lebensmittelbuch, SLMB, 30 A Wein aus Trauben, Untersuchungsmethode 5.2,1993. [5] Application Note 176/2014 Determination of alcohol in wine, BUCHI Operation Manual for the Distillation Unit K-355 *The K-360 can also be used for alcohol and volatile acid determinations as this distillation unit fulfills the same requirements. Application Note 193/2015 May 2015 5/5