CN107741449A - The test device of Martensite Volume Fraction in austenitic stainless steel - Google Patents
The test device of Martensite Volume Fraction in austenitic stainless steel Download PDFInfo
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Abstract
The present invention relates to technical field of metallographic detection, it is desirable to provide the test device of Martensite Volume Fraction in a kind of austenitic stainless steel.In the device, hydrogen cylinder group and argon bottle group are respectively connected to Pneumatic booster pump；Pneumatic booster pump is connected to experimental enviroment case by gas circuit pipeline, and surge tank, mass spectrograph, vacuum system are set on gas circuit pipeline；Experimental enviroment case is made up of the end cap and casing on top, and both are achieved a fixed connection with fastening bolt；Casing has hollow inner chamber, and its outside is provided with heat exchange jacket；End cap is provided with the end cap through hole of insertion, and the end of gas circuit pipeline connects with end cap through hole；Sample mount is housed in the cavity of casing, heating component is set on the platform of sample mount, the upper surface of heating component is used to place sample.Martensite Volume Fraction overall in austenitic stainless steel can be accurately measured using test device proposed by the invention, it is more accurate compared to the measurement data that the existing method of testing present invention obtains, it can more reflect the truth of sample.
Description
Technical field
The invention belongs to technical field of metallographic detection, Martensite Volume Fraction in more particularly to a kind of austenitic stainless steel
Test device.
Background technology
Austenitic stainless steel is widely used in modern industry because of its good corrosion resistance and mechanical characteristic.Austenite
During processing and manufacturing because of plastic deformation martensitic traoformation would generally occur for stainless steel.Due to martensite and austenite phase
After mechanical characteristic, the difference of corrosion resistance cause martensitic traoformation to occur, the performance of austenitic stainless steel also changes.For
The performance of control austenitic stainless steel, the volume fraction for grasping its internal martensite are particularly important.It is difficult to understand that measure is commonly used at present
The method of Martensite Volume Fraction is divided into three classes in family name's body stainless steel, and one kind is to make martensite and austenite using the method for corrosion
Different colors, then the volume fraction by the area statistics approximate estimation martensite to respective color region are showed, it is this kind of
Method is easily introduced human error, and test zone selection is random big, and test accuracy is low；It is another kind of be based on X-ray diffraction or
The means of testing of the technologies such as EBSD, although this kind of technology can be to institute's test zone surface or the martensite of near surface
Volume fraction is relatively accurately determined, but the martensitic volume point that its test result can not be inside accurate characterization sample
Number situation, test result have very big one-sidedness；In addition, can be to the martensite in sample using equipment such as ferrite measuring instruments
Content is estimated, but such method belongs to indirectly testing means, not only needs other direct means of testing to carry out data scaling,
And the precision of test is relatively low.
The content of the invention
The technical problem to be solved in the present invention is overcome the shortcomings of in currently existing technology, proposes a kind of austenite stainless
The test device of Martensite Volume Fraction in steel.
To solve technical problem, solution of the invention is：
Martensite Volume Fraction test device in a kind of austenitic stainless steel is provided, including carries the hydrogen for the hydrogen that is for experiment
Bottle group and the argon bottle group for providing substitution gas；Hydrogen cylinder group and argon bottle group are respectively connected to the entrance of Pneumatic booster pump
End；Pneumatic booster pump is also connected to experimental enviroment case by gas circuit pipeline, and surge tank, Flow-rate adjustment are provided with gas circuit pipeline
Valve, mass spectrograph, vacuum system and atmospheric valve；
The experimental enviroment case is made up of the end cap on top and the casing of bottom, and both realize fixed connect with fastening bolt
Connect；Casing has hollow inner chamber, and its outside is provided with heat exchange jacket；Heat exchange jacket has heating agent outlet and heating agent entrance, respectively
Heat-exchange system is connected to by pipeline；End cap is provided with the end cap through hole of insertion, and the end of gas circuit pipeline connects with end cap through hole；
Sample mount is housed in the cavity of casing, heating component is set on the platform of sample mount, the upper surface of heating component is used to put
Put sample；
The device also includes a control system, and Pneumatic booster pump, heat-exchange system and vacuum are respectively connected to by signal wire
The power end of system；Temperature measuring probe is provided with heat exchange jacket, control system is connected to by signal wire.
The O-ring of the alloy material for sealing is provided with the present invention, at the connecting portion between end cap and casing.
In the present invention, the sample mount is quartz material, and sample mount hangs on below end cap or is fixedly supported on
On bottom half or its inwall.
In the present invention, the cabinet wall surface has the glass-lined coating that thickness is not less than 10mm.
When device of the present invention is applied to Martensite Volume Fraction test in austenitic stainless steel, following step is specifically included
Suddenly：
(1) sample to be tested is placed in the heating component of sample mount, tightening fastening bolt makes end cap closed with casing
Engagement；
(2) air in experimental enviroment case and connected gas circuit pipeline is extracted out using vacuum system, until system vacuum reaches
To setting value；Hydrogen is carried out using Pneumatic booster pump to experimental enviroment case to fill, until Hydrogen Vapor Pressure reaches in experimental enviroment case
20~30MPa, and stably some fixed value P in section；
(3) heat-exchange system is controlled, the heating agent in heat exchange jacket is warming up to 250~350 DEG C, and stably certain in section
Individual fixed value T1；The temperature is kept to be no less than 72 hours, carrying out heat to sample to be tested is flushed with hydrogen；
(4) heat-exchange system is controlled, the heat medium temperature in heat exchange jacket is dropped to -50 with the speed not less than 50 DEG C/min
~-100 DEG C, and stably some fixed value T in section2；Cooling while, open atmospheric valve release experimental enviroment case with
And the hydrogen in surge tank, at least 3 times displacements are carried out to system using argon gas after the completion of releasing；Atmospheric valve is then shut off, to being
System vacuumizes；Reach 1.0 × 10 in vacuum-6Below Pa and heat medium temperature are stable in T2Afterwards, mass spectrograph is started to experimental enviroment
The real-time content of hydrogen in case in atmosphere is monitored；
(5) run heating component and be warming up to 500 DEG C with constant heating rate, and keeping temperature was more than 30 minutes；
The real-time content of hydrogen in atmosphere in experimental enviroment case is monitored all the time during this, and makes the heat in heat exchange jacket
Matchmaker's temperature is maintained at T2, stop mass spectrograph monitoring after 30 minutes, pass through the real-time content of the hydrogen for monitoring mass spectrograph
Data versus time is integrated, and the total volume Q of hydrogen in sample to be tested is calculated1；
(6) heating component, mass spectrograph and vacuum system are closed successively, are set heat-exchange system, are made the heating agent in heat exchange jacket
Temperature is finally reached room temperature；
(7) end cap and casing are separated, takes out sample to be tested；Load and the sample to be tested same material trade mark, same shape chi
Very little pure austenite standard specimen, the operation of step (1) to (6) is repeated, obtain hydrogen of the standard specimen in step (5) and release
Put total amount Q2；
During this step operation, temperature T when should be flushed with hydrogen experimental enviroment case pressure value P, heat in testing twice1With
Temperature T when discharging hydrogen2Numerical value be consistent；
(9) basis tests the data measured twice, and the volume fraction for calculating martensite in sample to be tested is：
(Q2-Q1)/Q2, %.
In the present invention, the heating-up temperature of heating component is not less than 500 DEG C, and the rate of heat addition is not less than 30 DEG C/min；Heat exchange system
- 100 DEG C of heat-exchange temperature scope~350 DEG C of system.
As preferable scheme, heretofore described end cap and casing are anti-hydrogen embrittlement A286 alloy material systems of good performance
Into.Mass spectrograph is triple quadrupole bar mass spectrum, 0~50amu of its mass number scope.Vacuum system is by oil-sealed rotary pump and molecular pump structure
Into the flow of vacuum system should can cause the vacuum in experimental enviroment case to reach 1.0 × 10-6Pa and following.Surge tank by
Anti-hydrogen embrittlement austenitic stainless steel S31603 manufactures of good performance, its design pressure are not less than 70MPa.Sample is shaped as pros
Shape thin slice, thickness are 0.5~1mm, and sample length is not less than 10mm.
Inventive principle describes：
The present invention determines Martensite Volume Fraction using the difference of hydrogen solubility in austenite and martensite two-phase.Ovshinsky
The solubility of hydrogen is about 1,000 times of hydrogen solubility in martensite or so in body, therefore, for one piece of austenite containing martensite
For stainless steel, it is carried out after being flushed with hydrogen processing, determine sample in hydrogen total content be austenite in sample volume fraction, and
The hydrogen content dissolved in martensite can be ignored, and the hydrogen content according to sample can calculate after obtaining the volume fraction of austenite
The volume fraction of martensite.
Based on above-mentioned principle, HTHP first is carried out to sample to be tested and is flushed with hydrogen processing (due to hydrogen in austenite under normal temperature
Diffusion coefficient is especially low, and the method that is flushed with hydrogen of unique feasible is flushed with hydrogen for HTHP), until hydrogen reaches saturation in the sample, then
The hydrogen content in sample, the method that hydrogen content measure uses the hydrogen desorption that heated up in vacuum are determined at once；Again to one piece with it is to be tested
The sample same material trade mark, the pure austenite standard specimen of same geomery be flushed with hydrogen processing, in same testing standard sample
Hydrogen content, martensite in sample to be tested can be calculated by the contrast to hydrogen content in sample to be tested and standard specimen
Volume fraction.
Compared with prior art, the beneficial effects of the present invention are：
Tested, can be obtained exactly overall in austenitic stainless steel using test device proposed by the invention
Martensite Volume Fraction, compared to being only capable of realizing to specimen surface or near surface Martensite Volume Fraction in existing method of testing
Determination techniques, the measurement data that the present invention obtains is more accurate, can more reflect the truth of sample.
Brief description of the drawings
Fig. 1 is the general arrangement schematic diagram of the present invention；
Fig. 2 is the experimental enviroment case and its cut-away view of the present invention.
In figure：Hydrogen cylinder group 1, Pneumatic booster pump 2, surge tank 3, flow control valve 4, atmospheric valve 5, vacuum system 6, mass spectrum
Instrument valve 7, mass spectrograph 8, experimental enviroment case 9, heat-exchange system 10, control system 11, argon bottle group 12, fastening bolt 13, end cap
14th, O-ring 15, sample mount 16, heat exchange jacket 17, Heating medium 18, casing 19, glass-lined coating 20, heating agent outlet 21, heating
Component 22, sample 23, end cap through hole 24.
Embodiment
Martensite Volume Fraction test device is as shown in figure 1, including carrying in a kind of austenitic stainless steel in the present embodiment
Be for experiment the hydrogen cylinder group 1 of hydrogen, and the argon bottle group 12 replaced for hydrogen in system.Hydrogen cylinder group 1 and argon bottle
The outlet of group 12 is connected to Pneumatic booster pump 2, and the outlet of Pneumatic booster pump 2 is connected to surge tank 3.Surge tank 3 is by resistant to hydrogen
Crisp austenitic stainless steel S31603 manufactures of good performance, its design pressure are not less than 70MPa.In order to be controlled to gas flow
Make, flow control valve 4 is provided with the export pipeline of surge tank 3.The gas for flowing through flow control valve 4 is sent to experimental enviroment all the way
Case 9, another way are connected to atmospheric valve 5.Vacuum system is additionally provided with pipeline between flow control valve 4 and experimental enviroment case 9
System 6, mass spectrograph valve 7 and mass spectrograph 8.Wherein vacuum system 6 is made up of oil-sealed rotary pump and molecular pump, the stream of vacuum system 6
Amount can cause the vacuum in experimental enviroment case 9 to reach 1.0 × 10-6Pa and following.Mass spectrograph 8 is triple quadrupole bar mass spectrum,
Its mass number 0~50amu of scope, the main hydrogen content in the environment of vacuum in monitoring test environmental cabinet 9 of mass spectrograph 8.Change
The heat exchange jacket 17 in the outside of 10 joint test environmental cabinet of hot systems 9, to realize the regulation and control to the temperature of experimental enviroment case 9, heat exchange system
The heat-exchange temperature scope of system 10 is -100 DEG C~350 DEG C, and whole system is monitored and controlled by control system 11.
As shown in Fig. 2 the main body of experimental enviroment case 9 is made up of end cap 14 and casing 19, end cap 14 and casing 19 are by anti-hydrogen embrittlement
A286 alloys steel making of good performance, above-mentioned two parts are attached by fastening bolt 13, and connecting portion is provided with and is used for
The O-ring 15 of sealing, O-ring 15 are manufactured using high-temperature alloy.End cap 14 is provided with end cap through hole 24, and end cap through hole 24 is used for
The disengaging of gas and the monitoring of gas concentration in experimental enviroment case 9.The lower end of end cap 14 connects sample mount 16, and sample mount 16 is adopted
Manufactured with the quartz for not absorbing hydrogen, heating component 22 and sample 23 are sequentially placed in sample mount 16.The heating of heating component 22
Temperature is not less than 500 DEG C, and the rate of heat addition be not less than 30 DEG C/min, and sample 23 is shaped as square sheets, thickness for 0.5~
1mm, sample length are not less than 10mm.The inner surface setting glass-lined coating 20 of casing 19 to avoid the absorption to hydrogen, glass-lined coating 20
Thickness is not less than 10mm, and the outside of casing 19 sets heat exchange jacket 17, is arranged with Heating medium 18 on heat exchange jacket 17 and heating agent goes out
Mouth 21.
The method tested using Martensite Volume Fraction test device in the austenitic stainless steel is described as follows：
(1) end cap 14 and casing 19 are separated first, after having installed sample to be tested 23, with the tight engagement end cap of fastening bolt 13
14 and casing 19；
(2) residual air in experimental enviroment case 9 and subsidiary pipeline is taken out using the oil-sealed rotary pump of vacuum system 6, directly
Vacuum closes vacuum system 6 after reaching setting value in system.Height is carried out to experimental enviroment case 9 using Pneumatic booster pump 2
Pressure hydrogen fills, until Hydrogen Vapor Pressure reaches some fixed value P in 20~30MPa sections in experimental enviroment case 9；
(3) design temperature for adjusting heat-exchange system 10 is some fixed value T in 250~350 DEG C of sections1, then keep
The temperature was not less than 72 hours and then realization is flushed with hydrogen to the heat of sample to be tested 23, and disclosure satisfy that hydrogen content reaches full in sample 23
With；
(4) setting heat-exchange system 10 is cooled to some in -50~-100 DEG C of sections with the speed not less than 50 DEG C/min
Fixed value T2, then temperature keep it is constant.While cooling, open atmospheric valve 5 and release experimental enviroment case 9 and surge tank 3
Interior high pressure hydrogen, at least 3 times displacements are carried out to the hydrogen in system using argon bottle group 12 after the completion of releasing.Close atmospheric valve
5, vacuum system 6 is then opened, when the vacuum in experimental enviroment case 9 reaches 1.0 × 10-6Below Pa and heat-exchange system 10 temperature
Degree is stable in T2Afterwards, mass spectrograph valve 7 is opened, and it is real-time to the hydrogen in atmosphere in experimental enviroment case 9 to start mass spectrograph 8
Content is monitored；
(5) run heating component 22 and it is warming up to 500 DEG C with constant heating rate, kept for 500 DEG C more than 30 points
Clock；The real-time content of hydrogen in atmosphere in experimental enviroment case 9 is monitored all the time in this process, and makes heat exchange jacket
Heat medium temperature in 17 is maintained at T2, stop the monitoring of mass spectrograph 8 after 30 minutes, pass through monitor mass spectrograph 8
The real-time content data of hydrogen integrates the total volume Q that hydrogen in sample to be tested 23 can be calculated to the time1。
(6) heating component 22, mass spectrograph 8, mass spectrograph valve 7, vacuum system 6, the temperature of setting heat-exchange system 10 are closed successively
Spend for room temperature, until temperature reaches room temperature in experimental enviroment case 9
(7) separate end cap 14 and casing 19, installing it is good with the same material trade mark of sample to be tested 23, same geomery it is pure
Austenite standard specimen, then with the tight engagement end cap 14 of fastening bolt 13 and casing 19.Repeat above-mentioned HTHP be flushed with hydrogen and
The process of hydrogen is put in heating, obtains the releasing total amount Q of hydrogen in standard specimen2, P, T in testing twice should be kept in the process1With
T2It is constant；The volume fraction of martensite is (Q in sample to be tested 232-Q1)/Q2%.
As described above, what the present invention can be dissolved by contrasting sample to be tested and standard specimen under the conditions of identical is flushed with hydrogen
The amount of hydrogen calculates the volume fraction of martensite in sample to be tested, can be with using test device proposed by the present invention and method of testing
Martensite Volume Fraction overall in one block of austenitic stainless steel is more accurately obtained, and is only capable of realizing in non-existing method of testing
To the measure of specimen surface or near surface Martensite Volume Fraction；Being flushed with hydrogen for sample 23 is determined same with hydrogen content in the present invention
Completed in experimental enviroment case 9, reduce the release of hydrogen in sample 23 in charged and discharged interval procedure to greatest extent, improved
The reliability of test；The inner surface of experimental enviroment case 9 and sample mount 16 are manufactured using the glass-lined coating 20 or quartz for not inhaling hydrogen,
Above-mentioned material is not inhaling hydrogen, hydrogen is not put during hydrogen is put during being flushed with hydrogen, thus avoid the shadow to hydrogen content test result
Ring, and in hydrogen content test process, using the local heating sample 23 of heating component 22, and simultaneously using the cooling examination of heat-exchange system 10
Environmental cabinet 9 is tested, reduces the release of hydrogen in other components of non-sample to greatest extent, improves the reliability of test.
It is described above, only it is the case study on implementation of the present invention, any formal limitation not is done to the present invention,
Although the present invention is disclosed as above with preferable case study on implementation, but is not limited to the present invention, any to be familiar with this professional skill
Art personnel, without departing from the scope of the present invention, when structure and technology contents using the disclosure above make it is some
Change or change and turn into the equivalence enforcement case of equivalent variations.
Every content without departing from technical solution of the present invention, the technical spirit according to the present invention are made to above case study on implementation
Any simple modification, equivalent change and modification, still fall within the range of technical solution of the present invention.
Claims (4)
1. the test device of Martensite Volume Fraction in a kind of austenitic stainless steel, including put forward the hydrogen cylinder group for the hydrogen that is for experiment
With the argon bottle group for providing substitution gas；Characterized in that, hydrogen cylinder group and argon bottle group are respectively connected to Pneumatic booster pump
Arrival end；Pneumatic booster pump is also connected to experimental enviroment case by gas circuit pipeline, and surge tank, flow are provided with gas circuit pipeline
Regulating valve, mass spectrograph, vacuum system and atmospheric valve；
The experimental enviroment case is made up of the end cap on top and the casing of bottom, and both are achieved a fixed connection with fastening bolt；Case
Body has hollow inner chamber, and its outside is provided with heat exchange jacket；Heat exchange jacket has heating agent outlet and heating agent entrance, passes through pipe respectively
Road is connected to heat-exchange system；End cap is provided with the end cap through hole of insertion, and the end of gas circuit pipeline connects with end cap through hole；In casing
Cavity in sample mount is housed, set heating component on the platform of sample mount, the upper surface of heating component is used to place sample；
The device also includes a control system, and Pneumatic booster pump, heat-exchange system and vacuum system are respectively connected to by signal wire
Power end；Temperature measuring probe is provided with heat exchange jacket, control system is connected to by signal wire.
2. device according to claim 1, it is characterised in that be provided with and be used at the connecting portion between end cap and casing
The O-ring of the alloy material of sealing.
3. device according to claim 1, it is characterised in that the sample mount is quartz material, and sample mount is hung
Below end cap or it is fixedly supported on bottom half or its inwall.
4. device according to claim 1, it is characterised in that the cabinet wall surface has thickness not less than 10mm's
Glass-lined coating.
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| CN201710829158.3A CN107741449B (en) | 2017-09-14 | 2017-09-14 | testing device for martensite volume fraction in austenitic stainless steel |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113804854A (en) * | 2021-09-13 | 2021-12-17 | 浙江大学 | Device and method for testing gas component distribution in hydrogen-doped natural gas |
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| EP0114688A2 (en) * | 1983-01-22 | 1984-08-01 | Nippon Steel Corporation | Sampler and an apparatus for hydrogen determination in molten metal |
| CN101443469A (en) * | 2007-01-31 | 2009-05-27 | 独立行政法人产业技术综合研究所 | Austenitic stainless steel and process for removing hydrogentherefrom |
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| CN113804854A (en) * | 2021-09-13 | 2021-12-17 | 浙江大学 | Device and method for testing gas component distribution in hydrogen-doped natural gas |
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| CN107741449B (en) | 2019-12-13 |
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