3ulqflsohv ri &dorulphwulf 0hdvxuhphqw – IKA C 7000 Grundausstattung Set 2 User Manual

Page 21

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IKA

-WERKE C 7000

Ver. 07 09.07

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To make a calorimetric measurement, a sample of a substance is burnt. In order to

ignite the sample, energy must be supplied from an external source. An ignition

wire, which is heated to glowing point by passing an electric current through it, per-

forms this function. If the measurement is to be accurate, it is essential that the

sample is completely burnt. For this reason, combustion takes place in an atmos-

phere of oxygen at a pressure of 30 bar.

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In a calorimeter combustion takes place under defined conditions. A weighed sam-

ple of a substance is placed in the decomposition vessel, the sample is ignited, and

the increase in temperature of the decomposition vessel is measured. The gross

calorific value of a sample is calculated from:

temperature increase of the decomposition vessel

heat capacity (C value) of the calorimeter system

mass of the fuel sample

heat energy that is released by burning the ignition aid and auxiliary fuel, and

also by the formation of sulphuric and nitric acids (external energy).

To optimise the combustion process, the decomposition vessel is filled with pure

oxygen (99.95%). The pressure of the oxygen atmosphere in the decomposition

vessel is 30 bar. The fuel sample is weighed to an accuracy of 0.1 mg using an

analytical balance.

Precise determination of the calorific value of a substance demands that combustion

takes place under precisely defined conditions. The relevant standards make the

following assumptions:

any water contained in the fuel, and any water formed by the combustion of

compounds containing hydrogen in the fuel is present in a liquid state after

combustion;

no oxidation of atmospheric nitrogen has taken place;

gaseous products present after combustion consist of oxygen, nitrogen, carbon

dioxide and sulphur dioxide;

solids can also be formed (e.g. ash).

Frequently, other combustion products, not foreseen by the standards, are formed.

In such cases, analyses of the sample material and the combustion products are

required to supply data for correction calculations. The standard gross calorific value

is then determined from the measured value and the analysis data.

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