CN104049055B - Power equipment oil dissolved gas chromatographic peak area computing method - Google Patents

Power equipment oil dissolved gas chromatographic peak area computing method Download PDF

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CN104049055B
CN104049055B CN201410245425.9A CN201410245425A CN104049055B CN 104049055 B CN104049055 B CN 104049055B CN 201410245425 A CN201410245425 A CN 201410245425A CN 104049055 B CN104049055 B CN 104049055B
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chromatographic
value
curve
object gas
chromatogram
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CN104049055A (en
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李昌
夏湘洪
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Suzhou Chint Enterprise Development Co.,Ltd.
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SHANGHAI SUNRISE POWER TECHNOLOGY Co Ltd
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Abstract

A kind of power equipment oil dissolved gas chromatographic peak area computing method, relate to electric device maintenance technical field, and what solve is the technical matters improving computational accuracy.The method first draws the chromatographic curve of Gas in Oil of Transformer, again according to chromatographic peak beginning and ending time point, the smoothingtime length of chromatographic curve, computer chromatography threshold value, cut-off point value and peak maximum height value, and then adopt peak process function to calculate the chromatographic peak area of object gas chromatographic curve.Method provided by the invention, is applicable to the content detecting Gas in Oil of Transformer.

Description

Power equipment oil dissolved gas chromatographic peak area computing method
Technical field
The present invention relates to electric device maintenance technology, particularly relate to a kind of technology of power equipment oil dissolved gas chromatographic peak area computing method.
Background technology
In electric system, insulating material in the oil-filled pipeline of power equipment of normal operation and Electric Power Equipment Insulation oil, can be aging gradually under the effect such as hot, electric, produce multiple inflammable gas, constantly accumulation, convection current, diffusion, dissolving in the fluid of these gases in the oil-filled pipeline of power equipment, until saturated and bubble, gas content in power equipment oil is analyzed, insulation status and the internal electric equipment discharge scenario of power equipment can be identified, effectively can reduce the generation of power equipment accident.
One of power equipment oil dissolved gas detection method of content uses chromatogram, the method that existing employing chromatogram calculates power equipment oil dissolved gas content is: the chromatographic peak area size first being calculated power equipment oil dissolved gas chromatographic curve by the mode of correlation calibration value, then the gas concentration corresponding according to chromatographic peak area draws power equipment oil dissolved gas content.But because initial peak and end peak easily change by the impact of environmental change, thus have influence on the size of peak area, therefore the method for existing computer chromatography peak area also exists the low defect of computational accuracy.
Summary of the invention
For the defect existed in above-mentioned prior art, technical matters to be solved by this invention is to provide the high power equipment oil dissolved gas chromatographic peak area computing method of a kind of computational accuracy.
In order to solve the problems of the technologies described above, a kind of power equipment oil dissolved gas chromatographic peak area computing method provided by the present invention, it is characterized in that, concrete steps are as follows:
1) utilizing chromatograph, take time shaft as abscissa axis, with chromatogram value axle for axis of ordinates, draws the chromatographic curve of each component gas in power equipment oil;
2) choose and need the gas composition of computer chromatography peak area to be object gas, the chromatographic peak start time point of target setting gas chromatogram curve, chromatographic peak stop time point and chromatographic peak smoothingtime length, chromatographic peak start time point is wherein designated as T0, chromatographic peak stop time point is designated as T1, and chromatographic peak smoothingtime length is for being designated as Δ Tc;
3) calculate Chromatogram Baseline starting point chromatogram value and the Chromatogram Baseline cut off chromatogram value of object gas, its computing formula is:
Vs = ( Σ i = T 0 T 0 + ΔTc V i ) / ΔTc ;
Vt = ( Σ i = T 1 T 1 + ΔTc V i ) / ΔTc ;
In formula, Vs is the Chromatogram Baseline starting point chromatogram value of object gas, and Vt is the Chromatogram Baseline cut off chromatogram value of object gas, V ifor object gas chromatographic curve is in the chromatogram value of time point i;
4) in coordinate system belonging to object gas chromatographic curve, draw straight line L, make this straight line L through coordinate points (T0+ Δ Tc/2, Vs), and coordinate points (T1+ Δ Tc/2, Vt);
5) on the segment of curve of object gas chromatographic curve from T0 to T1, choosing the data point maximum with straight line L spacing, is the peak maximum height value of object gas chromatographic curve by the spacing setting between this data point and straight line L;
6) calculate the chromatographic peak area of object gas chromatographic curve, its computing formula is:
S = 2 × Σ i = T 0 T 1 f ( V i ) ;
In formula:
If V i≤ (Vs+Vt+Hmax)/2, then f (V i)=0;
If V i> (Vs+Vt+Hmax)/2, then f (V i)=V i-(Vs+Vt+Hmax)/2;
In formula, S is the chromatographic peak area of object gas chromatographic curve, V ifor object gas chromatographic curve is in the chromatogram value of time point i, Hmax is the peak maximum height value of object gas chromatographic curve.
Further, the value of the chromatographic peak start time point T0 of object gas chromatographic curve is set as: T0=r × Ts;
In formula, Ts is chromatographic object gas chromatographic peak initial time minimum range, and r is safety factor, and the value of r is 0.9.
Further, the value of the chromatographic peak stop time point T1 of object gas chromatographic curve is set as: T1=k × Tm;
In formula, Tm is chromatographic object gas chromatographic peak end time maximum range, and k is safety factor, and the value of k is 0.95.
Further, the value of the chromatographic peak smoothingtime length Δ Tc of object gas chromatographic curve is set as:
ΔTc=(T1-T0)×(k-1)/2。
Power equipment oil dissolved gas chromatographic peak area computing method provided by the invention, baseline threshold value and cut-off point value is calculated according to the chromatographic peak beginning and ending time of the chromatographic curve of oil dissolved gas, and calculate maximum peak height value, finally calculate the chromatographic peak area of oil dissolved gas, the method adopts peak process function, automatically gives up low value point, reduces the calculation level at initial peak and cut-off peak, the impact of environmental change on chromatogram calculated by peak area can be reduced, thus can improve the computational accuracy of chromatographic peak area.
Accompanying drawing explanation
Fig. 1 is the calculation flow chart of embodiment of the present invention power equipment oil dissolved gas chromatographic peak area computing method.
Embodiment
Illustrate below in conjunction with accompanying drawing and be described in further detail embodiments of the invention, but the present embodiment is not limited to the present invention, every employing analog structure of the present invention and similar change thereof, all should list protection scope of the present invention in.
As shown in Figure 1, a kind of power equipment oil dissolved gas chromatographic peak area computing method that the embodiment of the present invention provides, it is characterized in that, concrete steps are as follows:
1) utilizing chromatograph, take time shaft as abscissa axis, with chromatogram value axle for axis of ordinates, draws the chromatographic curve of each component gas in power equipment oil;
2) choose and need the gas composition of computer chromatography peak area to be object gas, the chromatographic peak start time point of target setting gas chromatogram curve, chromatographic peak stop time point and chromatographic peak smoothingtime length, chromatographic peak start time point is wherein designated as T0, chromatographic peak stop time point is designated as T1, and chromatographic peak smoothingtime length is for being designated as Δ Tc;
Wherein, T0=r × Ts, Ts are chromatographic chromatographic peak initial time minimum range, and r is safety factor, and the value of r is generally 0.9;
Wherein, T1=k × Tm, Tm are chromatographic chromatographic peak end time maximum range, and k is safety factor, and the value of k is generally 0.95;
Wherein, Δ Tc=(T1-T0) × (k-1)/2;
3) calculate Chromatogram Baseline starting point chromatogram value and the Chromatogram Baseline cut off chromatogram value of object gas, its computing formula is:
Vs = ( Σ i = T 0 T 0 + ΔTc V i ) / ΔTc ;
Vt = ( Σ i = T 1 T 1 + ΔTc V i ) / ΔTc ;
In formula, Vs is the Chromatogram Baseline starting point chromatogram value of object gas, and Vt is the Chromatogram Baseline cut off chromatogram value of object gas, V ifor object gas chromatographic curve is in the chromatogram value of time point i;
4) in coordinate system belonging to object gas chromatographic curve, draw straight line L, make this straight line L through coordinate points (T0+ Δ Tc/2, Vs), and coordinate points (T1+ Δ Tc/2, Vt);
5) on the segment of curve of object gas chromatographic curve from T0 to T1, choosing the data point maximum with straight line L spacing, is the peak maximum height value of object gas chromatographic curve by the spacing setting between this data point and straight line L;
6) calculate the chromatographic peak area of object gas chromatographic curve, its computing formula is:
S = 2 × Σ i = T 0 T 1 f ( V i ) ;
In formula:
If V i≤ (Vs+Vt+Hmax)/2, then f (V i)=0;
If V i> (Vs+Vt+Hmax)/2, then f (V i)=V i-(Vs+Vt+Hmax)/2;
In formula, S is the chromatographic peak area of object gas chromatographic curve, V ifor object gas chromatographic curve is in the chromatogram value of time point i, Hmax is the peak maximum height value of object gas chromatographic curve.

Claims (3)

1. power equipment oil dissolved gas chromatographic peak area computing method, it is characterized in that, concrete steps are as follows:
1) utilizing chromatograph, take time shaft as abscissa axis, with chromatogram value axle for axis of ordinates, draws the chromatographic curve of each component gas in power equipment oil;
2) choose and need the gas composition of computer chromatography peak area to be object gas, the chromatographic peak start time point of target setting gas chromatogram curve, chromatographic peak stop time point and chromatographic peak smoothingtime length, chromatographic peak start time point is wherein designated as T0, chromatographic peak stop time point is designated as T1, and chromatographic peak smoothingtime length is for being designated as Δ Tc;
The value of time span Δ Tc is set as:
Tc=(T1-T0)×(k-1)/2;
In formula, k is safety factor, and the value of k is 0.95;
3) calculate Chromatogram Baseline starting point chromatogram value and the Chromatogram Baseline cut off chromatogram value of object gas, its computing formula is:
In formula, Vs is the Chromatogram Baseline starting point chromatogram value of object gas, and Vt is the Chromatogram Baseline cut off chromatogram value of object gas, for object gas chromatographic curve is in the chromatogram value of time point i;
4) in coordinate system belonging to object gas chromatographic curve, draw straight line L, make this straight line L through coordinate points (T0+ Δ Tc/2, Vs), and coordinate points (T1+ Δ Tc/2, Vt);
5) on the segment of curve of object gas chromatographic curve from T0 to T1, choosing the data point maximum with straight line L spacing, is the peak maximum height value of object gas chromatographic curve by the spacing setting between this data point and straight line L;
6) calculate the chromatographic peak area of object gas chromatographic curve, its computing formula is:
In formula:
If , then ;
If , then ;
In formula, S is the chromatographic peak area of object gas chromatographic curve, for object gas chromatographic curve is in the chromatogram value of time point i, Hmax is the peak maximum height value of object gas chromatographic curve.
2. power equipment oil dissolved gas chromatographic peak area computing method according to claim 1, is characterized in that, the value of the chromatographic peak start time point T0 of object gas chromatographic curve is set as: T0=r × Ts;
In formula, Ts is chromatographic object gas chromatographic peak initial time minimum range, and r is safety factor, and the value of r is 0.9.
3. power equipment oil dissolved gas chromatographic peak area computing method according to claim 1, it is characterized in that, the value of the chromatographic peak stop time point T1 of object gas chromatographic curve is set as: T1=k × Tm;
In formula, Tm is chromatographic object gas chromatographic peak end time maximum range, and k is safety factor, and the value of k is 0.95.
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JP6610678B2 (en) * 2015-12-03 2019-11-27 株式会社島津製作所 Peak detection method and data processing apparatus
CN110441420B (en) * 2019-08-02 2022-04-22 长园深瑞监测技术有限公司 Method for automatically identifying gas chromatographic peak for on-line monitoring of dissolved gas in oil

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EP0294121A2 (en) * 1987-05-29 1988-12-07 Hewlett-Packard Company Deconvolving chromatographic peaks
CN1712955A (en) * 2004-06-25 2005-12-28 中国科学院大连化学物理研究所 Precisive measurement for parameter of chromatography spike and area of overlapped peak
CN102998404A (en) * 2012-12-05 2013-03-27 上海申瑞继保电气有限公司 Asymmetric chromatographic detection method for multiple component gases in transformer oil
CN103364511A (en) * 2013-07-26 2013-10-23 上海申瑞继保电气有限公司 Peak area calculating method for asymmetric superposition chromatogram of multiple component gases in oil

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JP3496390B2 (en) * 1996-03-28 2004-02-09 東ソー株式会社 Data processing method for glycated hemoglobin measuring device using liquid chromatography
JP2000088833A (en) * 1998-09-10 2000-03-31 Tosoh Corp Analyzing device for chromatogram
FR2911962B1 (en) * 2007-01-30 2012-06-01 Inst Francais Du Petrole METHOD FOR MAKING A QUANTITATIVE ANALYSIS OF A MIXTURE OF MOLECULAR COMPOUNDS BY TWO - DIMENSIONAL GAS PHASE CHROMATOGRAPHY.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0294121A2 (en) * 1987-05-29 1988-12-07 Hewlett-Packard Company Deconvolving chromatographic peaks
CN1712955A (en) * 2004-06-25 2005-12-28 中国科学院大连化学物理研究所 Precisive measurement for parameter of chromatography spike and area of overlapped peak
CN102998404A (en) * 2012-12-05 2013-03-27 上海申瑞继保电气有限公司 Asymmetric chromatographic detection method for multiple component gases in transformer oil
CN103364511A (en) * 2013-07-26 2013-10-23 上海申瑞继保电气有限公司 Peak area calculating method for asymmetric superposition chromatogram of multiple component gases in oil

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Effective date of registration: 20200521

Address after: 215200 south of Lianyang road and east of Chang'an Road, Wujiang Economic and Technological Development Zone, Suzhou City, Jiangsu Province (Science and technology entrepreneurship Park)

Patentee after: Wujiang science and Technology Pioneer Park Management Service Co., Ltd

Address before: 200233, building 14, building 470, No. 4, Guiping Road, Shanghai, Xuhui District

Patentee before: SHANGHAI SUNRISE POWER TECHNOLOGY Co.,Ltd.

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Effective date of registration: 20201102

Address after: No. 599, South Road, Zhenze Town, Wujiang District, Suzhou City, Jiangsu Province 215200

Patentee after: Suzhou Chint Enterprise Development Co.,Ltd.

Address before: 215200 south of Lianyang road and east of Chang'an Road, Wujiang Economic and Technological Development Zone, Suzhou City, Jiangsu Province (Science and technology entrepreneurship Park)

Patentee before: Wujiang science and Technology Pioneer Park Management Service Co.,Ltd.