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JJG 695-2019 related PDF English

JJG 695-2019 (JJG695-2019) & related versions
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JJG 695-2019English329 Add to Cart 3 days Sulfur Hydrogen Gas Detectors JJG 695-2019 Valid JJG 695-2019
JJG 695-2003English170 Add to Cart 0-9 seconds. Auto delivery. Verification Regulation of Sulfur Hydrogen Gas Detectors JJG 695-2003 Obsolete JJG 695-2003
JJG 695-1990English519 Add to Cart 4 days Regulation of Verification for Hydrogen Sulfide Gas Analyzer JJG 695-1990 Obsolete JJG 695-1990



JJG 695-2019: PDF in English
JJG 695-2003 NATIONAL METROLOGY & CALIBRATION REGULATION OF THE PEOPLE’S REPUBLIC OF CHINA Replacing JJG 695-1990 Sulfur hydrogen gas detectors ISSUED ON: SEPTEMBER 23, 2003 IMPLEMENTED ON: MARCH 23, 2004 Issued by: General Administration of Quality Supervision, Inspection and Quarantine of PRC Table of Contents 1 Scope ... 4  2 Overview ... 4  3 Metrological performance requirements ... 4  3.1 Indication error ... 4  3.2 Repeatability ... 4  3.3 Response time ... 4  3.4 Drift ... 5  3.5 Alarm setting error ... 5  4 General technical requirements ... 5  4.1 Appearance ... 5  4.2 Insulation resistance ... 6  4.3 Dielectric strength ... 6  5 Control of measuring instrument ... 6  5.1 Verification conditions ... 6  5.2 Verification items ... 7  5.3 Verification method ... 7  5.4 Processing of verification result ... 10  5.5 Verification period ... 11  Appendix A Verification record format of hydrogen sulfide gas detector ... 12  Appendix B Format of verification certificate (inner page) ... 14  Appendix C Format of verification result notice (inner page) ... 15  Verification regulation of sulfur hydrogen gas detectors 1 Scope This regulation applies to the first verification, subsequent verification and in- use inspection of hydrogen sulfide gas detectors. 2 Overview The hydrogen sulfide gas detector (hereinafter referred to as the instrument) mainly comprises an electrochemical sensor or an optical sensor, as well as an electronic component and a display portion. The sensor converts hydrogen sulfide gas in the environment into an electrical signal and displays it in a concentration (molar fraction). The instrument is divided into diffused type and pumped type. 3 Metrological performance requirements 3.1 Indication error The indication error of the instrument is as shown in Table 1. Table 1 Hydrogen sulfide gas detector Measuring range Limit of indication error Molar fraction X (H2S): ≤ 100 x 10-6 ± 5 x 10-6 Molar fraction X (H2S): > 100 x 10-6 ± 5%FS 3.2 Repeatability The relative standard deviation shall be not more than 2%. 3.3 Response time For diffused-type instrument, it is not more than 60 s; for pumped-type instrument, it is not more than 30 s. observe whether the instrument has alarm sound and whether the alarm light flashes, check the alarm set point of the instrument. 4.2 Insulation resistance For instruments which use 220V AC, the phase-to-ground insulation resistance of the power supply is not less than 40 MΩ. 4.3 Dielectric strength For instruments which use 220V AC, the insulation strength of the phase- connected line to ground of the power supply shall be able to withstand the AC voltage of 1500V, 50Hz, for a test duration of 1 min, without breakdown and arcing. 5 Control of measuring instrument Instrument control includes first verification, subsequent verification, in-use inspection. 5.1 Verification conditions 5.1.1 Environmental conditions for verification 5.1.1.1 Ambient temperature: 0 ~ 40 °C (fluctuation ≤ 5 °C) 5.1.1.2 Relative humidity: ≤ 85% 5.1.2 Equipment for verification 5.1.2.1 Gas reference material The hydrogen sulfide standard gas which has a concentration of 20%, 50%, 80% of the full scale and 1.5 times the alarm set point is used, which have an uncertainty of not more than 2% (k = 3). 5.1.2.2 Zero calibration gas High-purity nitrogen or clean air. 5.1.2.3 Flowmeter (0 ~ 1) L/min, the accuracy level is not less than level 4. for 1 min, the current is 5 mA. Then the voltage is smoothly lowered to 0 V. The instrument shall not have breakdown and arcing during the whole test. 5.3.4 Indication error After preheating and stabilization, the instrument uses the zero gas and a standard gas with a concentration of about 80% of the upper limit of the measurement range. After calibrating the zero point and the indication value of the instrument, within the measurement range, respectively lead in the standard gas which has a concentration of about 20% and 50%, respectively, of the upper limit of measurement range (if the instrument has two measuring ranges, it shall lead in at least one standard gas within the low measuring range). Record the actual reading after leading in the gas. Repeat the above procedures for 3 times. Use the formula (1) or (2) to calculate the indication error of each verification point: Where: - The average of the readings; As - Standard value; R - Measuring range. When the instrument's range is > 100 × 10-6, it is calculated by formula (1), take the Δe of the maximum absolute value as the indication error of the instrument. When the instrument's range is ≤ 100 × 10-6, it is calculated by formula (2), take the Δe of the maximum absolute value as the indication error of the instrument. 5.3.5 Repeatability After the instrument is stabilized by preheating and its zero point calibrated by the zero point standard gas, lead in the standard gas which has a concentration of about 50% of the measuring range. After the reading is stable, record the measured value. Repeat the above measuring procedure for 6 times. Respectively record the reading Ai. The repeatability is indicated by the relative standard deviation Δc. Use the formula (3) to calculate the repeatability of the instrument: When the instrument's range is > 100 × 10-6, it is calculated by formula (4), take the Δzi of the maximum absolute value as the zero drift of the instrument. When the instrument's range is ≤ 100 × 10-6, it is calculated by formula (5), take the Δzi of the maximum absolute value as the zero drift of the instrument. Calculate the indication drift according to formula (6) or (7): When the instrument's range is > 100 × 10-6, it is calculated by formula (6), take the Δsi of the maximum absolute value as the indication drift of the instrument. When the instrument's range is ≤ 100 × 10-6, it is calculated by formula (7), take the Δsi of the maximum absolute value as the indication drift of the instrument. 5.3.8 Measurement of alarm error After the instrument is stabilized by preheating, use the zero point gas and the standard gas which has a concentration of about 80% of the upper limit of the measuring range, to calibrate the zero point and the indication value of the instrument. Then lead in the standard gas which has a concentration about 1.5 times the alarm set point (As). Record the actual alarm concentration (Ai) of the instrument. Remove the standard gas. Lead in the zero point gas to zero the instrument. Repeat the above procedures for 3 times. Use the formula (8) to calculate the alarm set error of the instrument: Take the ΔAi of the maximum absolute value as the alarm set error of the instrument. 5.4 Processing of verification result The instruments as verified and qualified according to the requirements of this regulation will be issued a verification certificate. The instrument failing to pass the verification will be issued a verification result notice, on which the unqualified items are indicated. ......

BASIC DATA
Standard ID JJG 695-2019 (JJG695-2019)
Description (Translated English) Sulfur Hydrogen Gas Detectors
Sector / Industry Metrology & Measurement Industry Standard
Classification of Chinese Standard A61
Classification of International Standard 17.020
Word Count Estimation 14,152
Date of Issue 2019
Date of Implementation 2020-03-27
Drafting Organization Shanghai Institute of Metrology and Testing Technology, China Institute of Testing Technology
Administrative Organization National Technical Committee on Environmental Stoichiometry
Issuing agency(ies) State Administration for Market Regulation