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Database: 365,228(8 Aug 2026)
gas chromatography method introduction analysis method method applicable scenarios key parameters mechanical oscillation gravimetric method result calculation specification headspace method calculation formula gas concentration secondary equilibrium method grading suspended object management system electronic plug gauges scopethis specification
GB/T 17623-2017 in English

GB/T 17623-2017 in English

SUPERSEDED

Determination 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
  • Delivery:Within 1 day
Price(USD): $344.00
$334.00
Standard No: GB/T 17623-2017
Document status: SUPERSEDED
Superseded by: GB/T 17623-2026 Determination of componental contents of gases dissolved in insulating oil by gas chromatography method
Superseded on: 2026-08-01
Title in English: Determination of componental contents of gases dissolvedin insulating oil by gas chromatography method
Title in Chinese: 绝缘油中溶解气体组分含量的气相色谱测定法
Language: English
File Format: Electronic (PDF)
Delivery: Within 1 day
Issued on: 2017-05-12
Implemented on: 2017-12-01
Superseding: GB/T 17623-1998 Determination of componental contents of gases dissolved in insulating oil by gas chromatography method
ICS Classification: 27.100-Power stations in general
Chinese Classification: F24-Electric power testing technique
Professional Classification: GB-National Standard
Related Keywords: gas chromatography method introduction analysis
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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 Dimensions1998 Edition2017 Edition
Instrument ConfigurationOnly variable-diameter piston pump is specifiedAutomatic headspace sampler is added (5.1.3)
Chromatographic Process3 basic processesCapillary column process is added (No. 4 in Table 1)
Stationary Phase Type5 conventional stationary phasesMixed stationary phases and capillary columns are added (Table 2)
Calculation methodSingle vacuum degassing formulaAdd 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:

  1. PLOT/Q column for separation of hydrocarbon gases (30m×0.53mm)
  2. 5A molecular sieve column for separation of H2/O2/N2
  3. 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×(Āiis)×(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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