Hanna Instruments HI 95725C User Manual

Page 4

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Absorption of Light is a typical phenomenon of interaction between electromagnetic radiation and
matter. When a light beam crosses a substance, some of the radiation may be absorbed by
atoms, molecules or crystal lattices.
If pure absorption occurs, the fraction of light absorbed depends both on the optical path length
through the matter and on the

physical

-chemical characteristics of the substance according to the

Lambert-Beer Law:

-log

I

/

I

o

=

ε

λ

c d

or

A

=

ε

λ

c d

Where:

-log

I

/

I

o

=

Absorbance (A)

I

o

=

intensity of incident light beam

I

=

intensity of light beam after absorption

ε

λ

=

molar extinction coefficient at wavelength

λ

c

=

molar concentration of the substance

d

=

optical path through the substance

Therefore, the concentration "c" can be calculated from the absorbance of the substance as the
other factors are known.
Photometric chemical analysis is based on the possibility to develop an absorbing compound
from a specific chemical reaction between sample and reagents. Given that the absorption of a
compound strictly depends on the wavelength of the incident light beam, a narrow spectral
bandwidth should be selected as well as a proper central wavelength to optimize measurements.
The optical system of Hanna's

HI 95000 series colorimeters is based on special subminiature

tungsten lamps and narrow-band interference filters to guarantee both high performance and
reliable results.

1) Liquid Crystal Display

2) Cuvet Holder
3) Cuvet alignment indicator
4) ON/OFF key

5) ZERO/SET key
6) READ key

7) CAL CHECK key

A microprocessor controlled special tungsten lamp emits radiation which is first optically
conditioned and beamed to the sample contained in the cuvet. The optical path is fixed by the
diameter of the cuvet. Then the light is spectrally filtered to a narrow spectral bandwidth, to
obtain a light beam of intensity

I

o

or

I.

The photoelectric cell collects the radiation

I

that is not absorbed by the sample and converts

it into an electric current, producing a potential in the mV range.
The microprocessor uses this potential to convert the incoming value into the desired measuring
unit and to display it on the LCD.
The measurement process is carried out in two phases: first the meter is zeroed and then the
actual measurement is performed.
The cuvet has a very important role because it is an optical element and thus requires particular
attention. It is important that both the measurement and the calibration (zeroing) cuvets are
optically identical to provide the same measurement conditions. Whenever possible use the same
cuvet for both. It is necessary that the surface of the cuvet is clean and not scratched. This to
avoid measurement interference due to unwanted reflection and absorption of light. It is
recommended not to touch the cuvet walls with hands.
Furthermore, in order to maintain the same conditions during the zeroing and the measuring
phases, it is necessary to close the cuvet to prevent any contamination.

Block diagram (optical layout)

PRINCIPLE OF OPERATION

FUNCTIONAL DESCRIPTION

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