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|Field of application|
|Description of techniques, methods and equipment|
|a) Alcoholic fermentation|
|b) Lactic acid fermentation|
|Field of application|
|Description of processing techniques, methods and equipment|
C6H12O6 = 2 C2H5OH + 2 CO2 (Glucose) = (Ethyl alcohol) + (Carbon dioxide)
This is an anaerobic process, i.e. it does not require the presence of oxygen. The temperature of fermentation is usually in the range 8 -30°C. The temperature affects the rate of fermentation, the efficiency of conversion and the flavour and aroma of the finished product. Selected strains of yeasts are often used to optimise the alcohol yield and the production of aromatics as secondary components.
Nitrogen, vitamins and trace elements are usually added as yeast nutrients. The pH may also be adjusted. This ensures that the fermentation is efficient and produces the required flavour. The type of yeast species used affects the rate, efficiency, flavour and aroma and is therefore carefully selected to give the desired results. Traditionally, fermentation in beer and wine making has been carried out in open fermentation vessels. These are now being replaced by cylindrical closed fermenters, making recovery of the CO2 possible.
yoghurt and other fermented dairy products, fermented meat products (certain types of sausages) and vegetables (i.e. sauerkraut). To start the fermentation, bacteria cultures known as starters are added to the raw material to be fermented. In lactic acid fermentation, lactose or other sugars are converted into lactic acid and small amounts of other components. Lactic acid formation is accompanied by a decrease in pH, which is important for the taste, the aroma and the preservation of the product. There are several species of bacteria which are able to produce lactic acid. Each species gives its own typical taste and aroma.
Lactic acid fermentation is an anaerobic process. It is sometimes necessary to remove as much of the oxygen as possible to enhance the fermentation process. Lactic acid fermentation is carried out at 20 – 40°C. The preparation of starter cultures is a sensitive process since the risk of airborne infection must be reduced to an absolute minimum. Starter cultures must therefore be prepared in a separate room supplied with filtered air at a slight positive pressure compared to normal atmospheric pressure. The equipment cleaning system must also be carefully designed to prevent detergent and sterilant residues from coming into contact with the cultures and spoiling them. These very high hygiene constraints, coupled with the requirements of the temperature regulation (heat treatment of the substrate first and then cooling) require a specific energy consumption and use of cooling water.