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Introduction to Soil Chemistry

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color measurement: the spectropho<strong>to</strong>meter 159<br />

organic matter may have dark-colored components that are released in<strong>to</strong> the<br />

extracting solution and cause interference with the spectropho<strong>to</strong>metric<br />

analysis. Thus extracts must be analyzed <strong>to</strong> make sure that they are free of<br />

interference.<br />

8.8. COLOR MEASUREMENT: THE SPECTROPHOTOMETER<br />

Color measurement is based on the Beer–Lambert law, which can be<br />

expressed as follows:<br />

I<br />

A = log10 I<br />

In this equation A is the absorbence also called the optical density, I is the<br />

intensity of the bean of light entering the sample, and I ex is the intensity of the<br />

beam of light exiting the sample. The absorbance is proportional <strong>to</strong> both<br />

the concentration of absorbing species and the pathlength of the light through<br />

the sample. Normally standard-size sample cells are used, and so the pathlength<br />

is constant for all samples.<br />

This type of analysis involves colored solutions; thus the spectropho<strong>to</strong>meter<br />

need function only in the visible range of the spectrum. A visible light source<br />

is used <strong>to</strong> provide light that passes through the sample in a cuvette, <strong>to</strong> a grating<br />

where it is dispersed in<strong>to</strong> its respective wavelengths. The analytical wavelength,<br />

that is, the wavelength absorbed by the colored compound, is isolated<br />

and directed <strong>to</strong> the detec<strong>to</strong>r, where the amount of light at this wavelength is<br />

measured and displayed on the readout.A diagram of a spectrometer is shown<br />

in Figure 8.8. Note that there are many different ways <strong>to</strong> design a spectropho<strong>to</strong>meter<br />

and its light path. The diagram given is simply a general representation<br />

of how a spectropho<strong>to</strong>meter works.<br />

Cuvettes used with the spectropho<strong>to</strong>meter are not simply test tubes. They<br />

are specially made tubes and are often matched such that a set of tubes will<br />

all have the same absorbence characteristics. Cuvettes should never be used<br />

as test tubes; they must be kept clean at all times, and care must be taken not<br />

Slit<br />

Light source<br />

Sample<br />

cuvette<br />

Read out<br />

0.55<br />

ex<br />

Detec<strong>to</strong>r<br />

Grating<br />

Figure 8.8. Diagram of the light path in a spectropho<strong>to</strong>meter.

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