HJ 692-2014Stationary source emission. Determination of nitrogen oxides. Non-dispersive infrared absorption method (English PDF)
固定污染源废气 氮氧化物的测定 非分散红外吸收法
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Issued by
Ministry of Ecology and Environment
Level / Type
National · Mandatory
Issue date
February 7, 2014
Implementation date
April 15, 2014
Scope
HJ 692-2014 is the English-translated version of 固定污染源废气 氮氧化物的测定 非分散红外吸收法.
HJ 692-2014 — This standard specifies the determination of stationary sources of nitrogen oxides in the exhaust gas Central Africa dispersive infrared absorption method.
This standard applies to the determination of stationary sources of nitrogen oxides in the exhaust gas. This method of nitric oxide (as NO2) detection limit of 3mg/m3, measured lower limit of 12mg/m3.
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Document preview — HJ 692-2014
National Standard of the People's Republic of China
- ICS
- 13.040.40
- Classification
- Z 25
Issued by: Ministry of Ecology and Environment
Contents
- Preface
- 1 Scope
- 2 Normative references
- 3 Terms and definitions
- 4 Principle of the method
- 5 Interference and eliminate
- 6 Reagents and materials
- 7 2 instruments and equipment
- 8 Sample .2
- 9 Step 2 Analysis
- 10 Results Calculation and representation .3
- 11 Precision and accuracy .3
- 12 Quality assurance and quality control
- 13 Precautions .4
- Appendix A (informative) measured before and after the performance of the instrument Checklist .5
Foreword
To implement the "People's Republic of China Environmental Protection Law" and "People's Republic of China Air Pollution Prevention Law," guard ring Environment, protect people's health, specifications fixed monitoring methods source emission of nitrogen oxides, the development of this standard.
This standard specifies the determination of stationary sources of nitrogen oxides in the exhaust gas Central Africa dispersive infrared absorption method.
This standard is the first release.
This standard is developed by the Ministry of Environmental Protection Science, Technology organization.
This standard drafting units. China National Environmental Monitoring Center, Shanghai Environmental Monitoring Center, Hebei Province Environmental Monitoring Center.
The standard verification unit. Environmental Monitoring Center Station of Hebei Province, Shenyang Environmental Monitoring Central Station, Hubei environmental monitoring Heart Station, Guiyang Municipal Environmental Monitoring Center, Tianjin Environmental Monitoring Center, Qinhuangdao City environmental protection monitoring station this standard MEP February 7, 2014 for approval.
This standard since April 15, 2014 implementation.
The standard explanation by the Ministry of Environmental Protection.
Determination of Non-Stationary source emission of nitrogen oxides dispersive infrared absorption method
1 Scope
This standard specifies the determination of stationary sources of nitrogen oxides in the exhaust gas Central Africa dispersive infrared absorption method.
This standard applies to the determination of stationary sources of nitrogen oxides in the exhaust gas.
This method of nitric oxide (as NO2) detection limit of 3mg/m3, measured lower limit of 12mg/m3.
2 Normative references
This standard refers to the contents of the following documents or the terms. For undated references, the effective version applies to this standard.
GB/T 16157 Stationary source emission-Determination of particulates and gaseous pollutants sampling methods HJ/T 75 stationary sources Continuous Emission Monitoring Technical Specification (Trial) HJ/T 76 stationary sources Continuous Emission Monitoring system technical requirements and test methods (Trial) HJ/T 373 stationary sources Monitoring Quality Assurance and Quality Control Technical Specifications HJ/T 397 stationary source emission monitoring and technical specifications
3 Terms and Definitions
3.1 Nitrogen oxides nitrogen oxides
It refers to stationary sources of nitrogen oxides present in exhaust gas to nitric oxide (NO) and nitrogen dioxide (NO2) forms.
3.2 Calibration span calibration span
The upper limit of the instrument calibration, the calibration standard gas concentration value (if multi-point calibration, compared with the highest standards of calibration gas concentration values). calibration Range (hereinafter referred to by CS) is selected to be appropriate, the average concentration of gaseous pollutants measured should be between 20% ~ 100% CS shall not exceed Over CS. When the determination of low concentrations of nitrogen oxides (NOx), in order to achieve the data quality objectives, do not choose too high CS. CS should be small Than or equal to the instrument's full scale.
3.3 Zero drift zero drift
Before and after the determination of the percentage deviation of the calibration range of the instrument measurement results for the same zero gas.
3.4 Span drift span drift
Before and after the determination of the percentage deviation of the calibration range of the instrument measurement results of the same standard gas.
3.5 System deviation system bias
Standard gas directly into the host instrument air intake (direct measurement mode) and the measurement results obtained by the standard gas sampling tube end into instrument the percentage deviation of calibrated span measurement result is (system measurement mode) or obtained absolute error.
4 Principle of the method
The use of NO gas infrared spectral regions, particularly selective 5.3µm wavelength of light absorbed by the Lambert - NO Beer law quantitative exhaust and NO2 in the exhaust gas through the converter for the reduction of the concentration of NO after.
5 and elimination of interference this method can eliminate the interference of interfering gases by tandem-type pneumatic detectors or gas filter correlation technique. Exhaust gas particulate matter and water vapor Interference, as well as the impact on the measured temperature of the exhaust gas through the filter dust, desiccant cooling means to cool the exhaust gas and the rapid addition of water to reduce or eliminate Interference to an acceptable level.
6 Reagents and materials
6.1 of nitric oxide, nitrogen dioxide standard gas Gas certified environmental standards, uncertainty of not more than 2% of the current uncertainty or attainable. Check the indication error and standard deviation system Quasi-gas concentration is 40% ~ 60% CS or equal to CS.
6.2 Nitrogen
Purity greater than 99.99%.
7 Instruments and equipment
7.1 Non-dispersive infrared absorption method nitrogen oxides analyzer
7.1.1 Composition
Non-dispersive infrared absorption method nitrogen oxides analyzer (hereinafter. the instrument) in the constitution. the host (including flow control devices, air pump, Detectors, etc.), of NO2 converter, the sampling tube (dust containing means and heating means), windpipe, desiccant cooling device or the like.
7.1.2 Requirements
(1) has a display sampling flow;
(2) shows the absolute value of error. <=5% (concentration 8 sampling locations and sampling point Setting the sampling location and sampling point comply with HJ/T 76, HJ/T 373 and GB/T 16157 of. Sampling tube distal end of the instrument as much as possible by Exhaust near the center position.
9 Analysis step
9.1 Scale calibration
NO standard gas measuring instrument in accordance with this standard 9.2 steps, if the error is shown in line with Article 7.1.2 (2) requirements, the instrument is available.
Otherwise, the need to calibrate.
The calibration method.
(1) bag method. first with gas flowmeter calibration instrument sample flow. Standard clean gas collection bag after filling emptied repeatedly Three times, and then filled with reserve. Press the instrument calibration procedures specified in the instructions for calibration.
(2) cylinder method. with a valve, adjustable rotameter and airway standard sampling tube connected to the gas cylinder and open the cylinder Gas valves, regulators rotameter to a predetermined flow rate instrument, the instrument passed into the intake port. Note that each connection can not leak.
Press the instrument calibration procedures specified in the instructions for calibration.
9.2 Determination
9.2.1 Zero calibration
(1) according to the instrument manual, the instrument is properly connected host, sampling tube (including dust means and heating means), windpipe, dehumidification Cooling means, and other means.
(2) the heating device, desiccant cooling devices and other devices powered on, reaching instrument conditions specified in the instructions.
(3) power on the host to clean ambient air or nitrogen gas is zero, the instrument zero calibration.
9.2.2 Sample Determination
The sampling tube into the flue sampling point, sample flow to the instrument specified continuous automatic sampling, sample tube cleaning exhaust gas, the exhaust gas extraction Measured can be recorded after instrument readings stable readings recorded at least once every minute monitoring results.
9.3 Determination of the end
After the measurement, the sampling tube in clean ambient air or high purity nitrogen, showing the value of the instrument back to zero after the shutdown.
9.4 NO2 to NO conversion rate determination method
A certain concentration of NO2 standard gas into the converter before entering the measuring instrument to measure the concentration ratio results and the standard gas is NO2 to NO conversion.
10 Results Calculation and representation
10.1 Calculation Results
NOx concentration equal to the concentration of NO and NO2 converted to NO concentration sum, calculated as NO2 standard state's (273K, Concentration 101.325kPa) under.
rho NO x -/
46rho NO x
22.4
Where. rho NO x-- under standard conditions dry exhaust gas NOx concentration, mg/m3;
rho NO x-- dry NOx in the exhaust gas volume concentration, µmol/mol.
10.2 NO2 to NO conversion efficiency is calculated
E NO 2 -/
rho d
rho s
x 100% ( 2 )
Where. E NO 2-- NO2 to NO conversion efficiency,%;
rho d-- Direct Determination of the concentration of the standard gas, µmol/mol mode;
rho s-- NO2 concentration of the standard gas, µmol/mol.
10.3 The results are shown the results of the concentration of nitrogen oxides retain only integer bit, when the calculated concentration higher result, retained four significant digits.
11 Precision and accuracy
The precision and accuracy of measurement of NO NO2 concentrations are counted.
The precision of the method 11.1 Six laboratories in a power plant emissions of NO concentration were measured simultaneously. One of the units in the exhaust gas concentration of 588mg/m3 ~ 609mg/m3, average of 592mg/m3; another unit in the exhaust gas concentration 187mg/m3 ~ 201mg/m3, average of 195mg/m3.
Laboratory relative standard deviations were. 2.5% to 3.6%, 1.4% ~ 4.2%;
Interlaboratory relative standard deviations were. 1.4%, 2.4%;
Repeatability limit. 55mg/m3,17mg/m3;
Reproducibility limit. 7.4mg/m3,12mg/m3.
6 laboratory levels of 100mg/m3,396mg/NO standard gas m3,1.02 × 103mg/m3 were measured.
Laboratory relative standard deviations were. 0 to 1.0%, from 0 to 0.6%, from 0 to 0.4%;
Interlaboratory relative standard deviations were. 1.9%, 1.2%, 0.4%;
Repeatability limit. 2.1mg/m3,3.7mg/m3,5.1mg/m3;
Reproducibility limit. 4.9mg/m3,12mg/m3,9.6mg/m3.
Accuracy of the method 11.2 6 laboratory standard levels of NO gas 100mg/m3,396mg/m3,1019mg/m3 were measured.
Relative error. 0.3% to 3.4% - 0.8% to 2.0%, from 0.4% to 1.4%;
The final value of the relative error. 1.2% ± 2.7%, 0.4% ± 2.2%, 0.8% ± 0.7%.
12 Quality Assurance and Quality Control
12.1 Instruments and some auxiliary equipment such as a barometer, thermometer must be approved by the relevant units certified by metrological verification, and in the test validity Within limits.
12.2 instrument should be more than the ability to resist negative pressure flue negative pressure to prevent the instrument sampling flow is reduced, resulting in low or measurement results can not be measured.
The components of the instrument should be connected firmly 12.3, measured before and after the screening equipment shall be in accordance with the requirements of air tightness, can be blocking tight inlet, if the instrument Sample flow rate indication to zero in 2min, showed air-tightness.
Determination of zero gas and NO standard gas before the 12.4 measured according to the standard 9.2 step, the Department calculated indication error measurement and inspection equipment System deviation, if the indication error and/or system deviation does not comply with Article 7.1.2 (2) and (3) requirements should find out the reasons and make the appropriate repair dimension Protection, until only after the conduct of monitoring to meet the requirements.
Determination of the standard zero gas and NO gas was measured according to the standard after 12.5 9.2 step, the Department calculated indication error measurement and inspection equipment System deviation. If the indication error and systematic bias in line with Article 7.1.2 (2) and (3) requirements, determines whether the measurement results of this sample is valid; otherwise, the contractor the measurement results once the final version of the sample is invalid.
Zero drift 12.6 measured at least once a month before and after the span drift checks. Zero drift, span drift absolute value should be small to 3% CS (when calibrated span <=200µmol/mol, less than 5.0% CS). Otherwise, it is timely for instrument calibration and maintenance.
12.7 Determination completed before the shutdown, according to the requirements of the specification through the instrument into the ambient air or high purity nitrogen flushed clean instruments.
12.8 at least once every six months with a low (Appendix A (Informative) Measured before and after the performance of the instrument Checklist Laboratory name Location Determination Equipment manufacturing plant as the model, serial number principle of calibrated span (CS) (µmol/mol, mg/m3) gas flow rate (L/min) Ambient temperature (oC) ambient pressure (kPa) relative humidity (RH%) Standard gas production unit measured pollutant name Testers Determination Date The date
Table A-1 shows error
After the measurement before the standard gas measurement Name Concentration/A rated value/A i mean/A (avg) i Indication error /% ( A (avg) i - A )/A Found/A i mean/A (avg) i Indication error /% ( A (avg) i - A )/A NO
NOTE. To determine the value A i refers to standard gas measurement results in direct measurement mode is obtained
Table A-2 system deviation
After the measurement before the standard gas measurement Name concentration measurement value of the system deviation ( B (avg) - A (avg) )/C.S.
Measured value system deviation ( B (avg) - A (avg) )/C.S. A A (avg) B B (avg) A A (avg) B B (avg) Zero gas NO Note. A measured value of 1 means the standard gas measurement results in direct measurement mode; 2 measured values B refers to the measurement result in the system standard gas measurement mode.
Table A-3 zero drift and span drift
Standard gas
Date Time
Zero drift Span drift Zero drift absolutely zero reading error calibration Range delta Z C.S.
Standard gas
reading
Span drift
Absolute error
calibration
Range
delta S
Name Concentration
Starting
finally
deltaZ = Zi -Z0
Starting
finally
deltaS = Si -S0
NOTE. Starting expressed measured before, after the final determination indicates.
Table A-4 NO2 to NO conversion efficiency
Standard gas measurement results Name Concentration/A rated value/A i mean/A (avg) i conversion efficiency /% (A (avg) i/A) NO2
NOTE. To determine the value A i mean NO2 standard gas is converted to NO after the reduction, under the direct measurement mode to get the NO measurement results.
......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 8 pages — is available in the English PDF.
Referenced standards
Normative references
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