GB/T 17623-2017 in English
SUPERSEDEDDetermination of componental contents of gases dissolvedin insulating oil by gas chromatography method
- Issued on:2017-05-12
- Implemented on:2017-12-01
- File Format:PDF
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《GB/T 17623-2017绝缘油中溶解气体组分含量的气相色谱测定法》由TC322(全国电气化学标准化技术委员会)归口,主管部门为中国电力企业联合会。
Introduction
Analysis of the core content of the standard
This standard specifies the method and process for determining the content of dissolved gas components in insulating oil (including H2, CH4, C2H6, C2H4, C2H2, CO, CO2, O2 and N2, etc.) by gas chromatography. It is suitable for fault diagnosis of oil-filled equipment such as transformers.
Technology Evolution and Standard Update
| Improvement Dimensions | 1998 Edition | 2017 Edition |
|---|---|---|
| Instrument Configuration | Only variable-diameter piston pump is specified | Automatic headspace sampler is added (5.1.3) |
| Chromatographic Process | 3 basic processes | Capillary column process is added (No. 4 in Table 1) |
| Stationary Phase Type | 5 conventional stationary phases | Mixed stationary phases and capillary columns are added (Table 2) |
| Calculation method | Single vacuum degassing formula | Add headspace method calculation formula (8.3.1) |
Key instrument configuration requirements
Gas chromatographRequired configuration:
- Dual detector system (TCD+FID)
- Nickel catalytic converter (CO/CO2 conversion)
- Minimum detection sensitivity must meet the requirements of Table 3 (such as H2≤2μL/L)
Degassing deviceOptional:
- Constant temperature oscillator (275±5 times/min)
- Vacuum degassing device (efficiency ≥ 90%)
- Automatic headspace sampler (with pressure regulation)
Analysis of key points of operation
Sample collection
Fully sealed sampling according to GB/T 7597. Transportation must be protected from light and shock. It is recommended to use a 100mL gas-tight syringe (5.4)
Selection of degassing method
| Method | Applicable scenarios | Key parameters |
|---|---|---|
| Mechanical oscillation method | Conventional analysis | Oscillation at 50℃ for 20min, gas-oil ratio 1:4 |
| Vacuum degassing method | Arbitration test | Toepler pump is required (Appendix A) |
| Automatic headspace method | Batch detection | 70kPa pressure balance (Table 4) |
Chromatographic analysis conditions
Recommended process:
- PLOT/Q column for separation of hydrocarbon gases (30m×0.53mm)
- 5A molecular sieve column for separation of H2/O2/N2
- Carrier gas flow rate 12mL/min (N2 or Ar)
Result calculation specification
Headspace method calculation formula
Gas concentration in oil Xi = 0.929×(P/101.3)×Cis×(Āi/Āis)×(Ki+Vg'/Vl')
Wherein, the value of Ki can be found in Table 5 (e.g., Ki of C2H2=1.02)
Precision control
- Repeatability: when the concentration is >10μL/L, the difference is <10% of the mean value
- Reproducibility: between-laboratory deviation is <15%
Implementation suggestions
Quality control measures
- Verify the recovery rate with standard oil samples every month (Appendix B)
- The secondary equilibrium method is used for unknown oil types (Appendix F)
- Acetone detection requires a DB-WAX capillary column (Appendix G)
Equipment Selection Guide
Preferred choice:
- Chromatograph with automatic valve switching (Table 1 Process 3)
- Vacuum device with degassing efficiency ≥ 95%
- Glass syringe calibrated by gravimetric method

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