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ADP5072 bảng dữ liệu(PDF) 3 Page - Analog Devices

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Giải thích chi tiết về linh kiện  Fully Automatic High Performance Conductivity Measurement System
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ADP5072 bảng dữ liệu(HTML) 3 Page - Analog Devices

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Circuit Note
CN-0359
analog.com
Rev. C | 3 of 10
CIRCUIT DESCRIPTION
CONDUCTIVITY THEORY
The resistivity of a material or liquid is defined as the resistance of a
cube of the material with perfectly conductive contacts on opposite
faces. The resistance can be calculated using Equation 1:
R=ρLA
(1)
where:
R is the resistance.
ρ is the resistivity of the material.
L is the distance between the contacts.
A is the area of the contacts.
Resistivity is measured in units of Ω cm. A 1 Ω cm material has a
resistance of 1 Ω when contacted on opposite faces of a 1 cm × 1
cm × 1 cm cube.
Conductance is the reciprocal of resistance, and conductivity is the
reciprocal of resistivity. The unit of measurement of conductance is
Siemens (S), and the unit of measurement of conductivity is S/cm,
mS/cm, or μS/cm.
All aqueous solutions conduct electricity to some degree. Adding
electrolytes such as salts, acids, or bases to pure water increases
the conductivity (and decreases resistivity).
For the purposes of this circuit note, Y is the general symbol for
conductivity measured in S/cm, mS/cm, or μS/cm. However, in
many cases, the distance term is dropped for convenience, and the
conductivity is simply expressed as S, mS, or μS.
A conductivity system measures conductivity by means of electron-
ics connected to a sensor called a conductivity cell immersed in a
solution, as shown in Figure 2.
Figure 2. Conductivity Cell Geometry and Electrical Connections
The electronic circuitry applies an alternating voltage on the sensor
and measures the resulting current, which is related to the conduc-
tivity. Because conductivity has a large temperature coefficient (up
to 4%/°C), a temperature sensor is incorporated into the circuitry
to adjust the reading to a standard temperature, usually 25°C
(77°F). When measuring solutions, the temperature coefficient of
the conductivity of the water itself must be considered.
A basic conductivity sensor typically consists of two electrodes that
are insulated from one another. The electrodes, typically Type 316
stainless steel, titanium palladium alloy, or graphite, are specifically
sized and spaced to provide a known cell constant. Theoretically, a
cell constant of 1.0/cm describes two electrodes, each sized 1 cm2
in area, and spaced 1 cm apart. Cell constants must be matched to
the measurement system for a given range of operation.
For instance, if a sensor with a cell constant of 1.0/cm is used in
pure water with a conductivity of 1 μS/cm, the cell has a resistance
of 1 MΩ. Conversely, the same cell in seawater has a resistance
of 30 Ω. Because the resistance ratio is so large, it is difficult for
ordinary instruments to accurately measure such extremes with
only one cell constant.
When measuring the 1 μS/cm solution, the cell is configured with
large area electrodes spaced a small distance apart. For example,
a cell with a cell constant of 0.01/cm results in a measured cell re-
sistance of approximately 10,000 Ω rather than 1 MΩ. It is easier to
accurately measure 10,000 Ω than 1 MΩ; therefore, the measuring
instrument can operate over the same range of cell resistance for
both ultrapure water and high conductivity seawater by using cells
with different cell constants.
The cell constant is defined as the ratio of the distance between the
electrodes to the area of the electrodes, which can be calculated
using Equation 2:
K=LA
(2)
where:
K is the cell constant in cm-1.
L is the distance between electrodes in cm.
A is the area of electrode surface in cm2.
The instrumentation then measures the cell conductance using
Equation 3:
Y=IV
(3)
Y is the measured cell conductance in S.
I is the cell current.
V is the excitation voltage.
The conductivity of the liquid is then calculated using Equation 4:
Yx=K×Y
(4)
Yx is the conductivity of the liquid in S/cm.
K is the cell constant in cm-1.
Y is measured conductance in S.
There are two types of conductivity cells: those with two electrodes,
and those with four electrodes, as shown in Figure 3. The electro-
des are often referred to as poles.



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