
Instruction Manual
Model NGA2000 NDIR
Install the NDIR Analyzer Module in a clean,
NOTE
Unrestricted air flow in the rear of the Analyzer Module is critical to its performance and reliability..
a.Calibration Gases
All applications require a zero standard gas to set the zero point on the display and external data acquisition devices. if the factory provided Calibration and Data Sheet (in the rear of the manual) specifies a background gas, use this as a zero gas. If a background gas is not specified, use dry nitrogen.
negated if the same flow rate is used for sample, zero and span gases. But, if flow is high enough to cause elevated pressure, careful control (tighter tolerance) of flow rate is required to avoid errors.
If flow is kept at or below 2 SCFH (1 L/min), sample and instrument temperatures reach equilibrium regardless of stream temperature (within specifications; 0 to
55°C). At extremely high flow rates, this may not be true, although no such effect has been noted up to 18 SCFH (9 L/min).
See Table
c.Sample Pressure/Filtration
Sample should be introduced to the Analyzer Module at a maximum 690 hPa- gauge (10 psig). Pressurized applications are available, which require pressurized cells and careful control of flow rates, consult factory for these applications. Sample should be filtered for particulates down to two microns.
d.Leak Test
Span gas should be between 75% and | The Analyzer Module is completely tested | |
100% of fullscale span. Flowing reference | at the factory for gas leakage. The user is | |
(if used) should be dry nitrogen. | responsible for testing for leakage only at | |
| the inlet and outlet fittings on the rear panel. | |
| The user is also responsible for internal leak | |
b. Flow Rate | testing periodically and if any internal | |
Recommended sample flow rate is 1 to 2 | pneumatic components are adjusted or | |
replaced (with a test procedure chosen by | ||
SCFH (500 TO 1000 cc/min). A lower flow | ||
the user). | ||
rate will not affect readings but may result in | ||
| ||
an undesirable time lag. Excessive flow |
| |
can produce increases cell pressurization | ||
and reading error. | ||
| (See Figure | |
At higher cell pressures, the nonlinearity of | and outlet lines for sample/zero/span and | |
the calibration curve increases. Therefore, | flowing reference (if applicable) to | |
the calibration curve should be redrawn for | appropriately labeled fittings on the rear | |
higher flow rates. Also, the effect of | panel. All four connections are 1/4 inch | |
increased cell pressurization can be |
Rosemount Analytical Inc. A Division of Emerson Process Management |