Sulfur Dioxide by Ripper Titration2
Sulfur Dioxide by Ripper Titration2
Sulfur Dioxide by Ripper Titration2
This method is based on the redox reaction where sulfur dioxide, in the form of the bisulphite ion,
reacts with iodine as follows:
Unreacted iodine forms a blue complex with starch indicator to signify the endpoint.
The addition of sodium bicarbonate prior to commencing the titration creates an inert blanket of
carbon dioxide gas to prevent interference caused by oxygen in air.
Red wines may require decolourising with activated carbon prior to performing the titration in order
for the endpoint colour change to be observed. Colour pigments in red wines may also interfere
with the result, so this method is best suited to pale coloured or white wines only.
When determining total sulfur dioxide, the sample is pretreated with sodium hydroxide solution to
adjust the pH. This causes chemically bound forms of sulfur dioxide to be released in solution as
free sulphur dioxide.
It is essential to titrate to an endpoint where the blue colour persists for 30 seconds to ensure that all
forms of sulfur dioxide in solution have reacted.
Equipment Required:
Reagent Preparation:
It is strongly advised that solutions be prepared by laboratory technicians due to the
corrosive nature of the acids and alkalis involved.
0.01M iodine solution: (Accurate) Prepare from commercially available ampoules as per the
instructions provided. Standardise before use (method attached). Store in brown glass in the dark.
Solution is stable for 3 months.
1M sodium hydroxide: (accuracy not necessary) Carefully and slowly add 40g of solid sodium
hydroxide, with stirring, to a large beaker of around 800mL cold distilled water. Allow to cool and
dilute to 1 litre with distilled water.. Caution: considerable heat is evolved from this dissolution.
25% v/v sulfuric acid: (accuracy not necessary) Measure 250mL of concentrated sulfuric acid in a
graduated cylinder. Carefully and slowly, with constant stirring, add the acid to 750mL of cold
distilled water. Caution: it may be necessary to stand the mixture in an ice bath during the addition
and mixing operation, as considerable heat is involved with this dilution. Allow to cool completely
and dilute to 1 litre with distilled water.
Vitex – Commercially available starch indicator
Method:
• The addition of the sodium carbonate causes a reaction that releases carbon dioxide gas. The
carbon dioxide acts as an inert blanket that prevents interference due to oxygen. The titration
must be completed quickly before the carbon dioxide disperses to the atmosphere. It is
advisable to do a few practice titrations first.
• At low pH (for example, once the acid addition step has occurred) a portion of the free
sulphite is present in the volatile (SO2 gas) form. To prevent erroneous results from the loss
of SO2 from volatilisation, it is essential that the titration is carried out as rapidly as
possible.
• The colour change may be easier to detect if a strong light source is used to illuminate the
solution.
• For best accuracy use a 10mL burette.
• The analysis for total SO2 involves the addition of 1M NaOH to hydrolyse bisulphite
addition compounds (bound SO2). The completeness of this reaction is pH dependent. It has
been determined that above pH 12 almost total dissociation of bound sulphites occurs. This
is a timed reaction, allowing less or more time to elapse than instructed will introduce error.
• Ascorbic acid and other substances that react with iodine (including phenols, sugars and
aldehydes) interfere with the determination. The result should therefore be treated as a good
estimate of the amount of sulphites present. For a more accurate result the aspiration
(Rankine) method should be used.
Appendix:
Method for standardising 0.01M iodine solution against standard sodium thiosulphate solution:
References:
Iland, Ewart, Sitters, Markides & Bruer, Techinques for Chemical Analysis and Quality
Monitoring during Winemaking, 2000
Zoeckein, Fugelsang, Gump & Nury, Production Wine Analysis,1990