CN1869641A - Detection method of ternary silicide high-temp in-situ oxidation - Google Patents
Detection method of ternary silicide high-temp in-situ oxidation Download PDFInfo
- Publication number
- CN1869641A CN1869641A CN 200610028326 CN200610028326A CN1869641A CN 1869641 A CN1869641 A CN 1869641A CN 200610028326 CN200610028326 CN 200610028326 CN 200610028326 A CN200610028326 A CN 200610028326A CN 1869641 A CN1869641 A CN 1869641A
- Authority
- CN
- China
- Prior art keywords
- sample
- ternary silicide
- ternary
- temp
- oxidation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Landscapes
- Investigating And Analyzing Materials By Characteristic Methods (AREA)
- Sampling And Sample Adjustment (AREA)
Abstract
The invention is a method for detecting ternary silicide high temperature in situ oxidization, belonging to material high-temperature oxidization test field. And the invention hangs ternary silicide sample with round bore and measured surface area through Pt-Rh wire burnt to constant weight, where one end of the Pt-Rh wire connected with the sample extends to the middle position of a high temperature hearth and the other end is outside the hearth and connected with a Ni-Cr wire, which is hung under a cotton line, and the cotton line is fixed on a hook at an electronic balance base, the electronic balance is connected with computer data lines, and the sample is heated in the high temperature furnace, and when the temperature is up to 540 deg.C, the sample starts oxidizing and the sample mass changes and the computer continuously records the sample mass change, and reflects antioxidant property of the sample according to the change. And the method is easy to apply, and the test device is simple, not only able to be used to in situ oxidization but also able to be used to circulating oxidization, and the invention can completely visually and conveniently test high temperature antioxidant ability of ternary silicide.
Description
Technical field
What the present invention relates to is a kind of detection method that is used for material at high temperature oxidation field tests, specifically is a kind of detection method of ternary silicide high-temp in-situ oxidation.
Background technology
Silicide material becomes one of the most promising thermal structure candidate material with its high fusing point, low relatively density, good high temperature creep strength and excellent high-temperature oxidation resistance, the research of the antioxygenic property of ternary silicide material (as Mo-Si-B, Mo-Nb-Si etc.) at present develops rapidly abroad and becomes focus, and result of study is existing to be reported in a large number.For characterizing the high-temperature oxidation resistance of ternary silicide, the temperature generally higher (＞1000 ℃) that experiment is adopted, the detection method that is used for the high-temperature oxidation resistance of ternary silicide material mainly contains: (1) high temperature circulation oxidizing process, sample is exposed to atmospheric environment, furnace temperature reaches in the high temperature furnace of probe temperature, at set intervals, the sample taking-up is weighed, the weight per unit area of gained is depicted as curve over time, promptly get the cyclic oxidation kinetic curve, the high temperature circulation oxidizing process realizes that easily its major defect is the mass change rule in the time of can not reflecting intensification and can not changes by the continuous recording sample mass because testing equipment is simple.(2) high-temp in-situ oxidation method mainly adopts the thermogravimetric technology, comprises temperature program(me) control and register system, high sensitivity electronic balance and automated drafting system; In giving fixed temperature and atmosphere, the mass change of METHOD FOR CONTINUOUS DETERMINATION sample unit area and the funtcional relationship of time, i.e. constant temperature oxidation kinetics curve.The high-temp in-situ oxidation method is restricted owing to the thermogravimetric analyzer that is used for high temperature (＞1000 ℃) costs an arm and a leg.These two kinds of methods can be drawn the oxidation kinetics curve according to the mass change of material in oxidizing process.
Find by prior art documents, N.Nomura etc. are at " Intermetallics " (intermetallic compound, 2003, Vol.11,735～742) in " Microstructure and oxidationresistance of a plasma sprayed Mo-Si-B multiphase alloy coating " (a kind of microstructure and inoxidizability of plasma spraying Mo-S-B heterogeneous alloy coating) paper of delivering on, use thermogravimetric analyzer (model is Netzsch STA409C) to measure under different temperatures coating weight over time, comparative studies the high-temperature oxidation resistance of Mo-Si-B alloy.Consider that Netzsch STA409C thermogravimetric analyzer costs an arm and a leg; And can only do in-situ oxidation with this thermogravimetric analyzer and test, can not be used for epoxidation experiments, when therefore adopting this method to test, be subjected to the influence factor of surveying instrument bigger.
Summary of the invention
The objective of the invention is to overcome the deficiencies in the prior art and limitation, a kind of detection method of ternary silicide high-temp in-situ oxidation is provided, making it pass through continuous recording ternary silicide material weight per unit area under different temperatures changes over time, just can reflect the material at high temperature antioxygenic property according to this variation, that the method has is simple, be applicable to the characteristics of working under the hot conditions.
The present invention is achieved by the following technical solutions, circular hole and the accurately ternary silicide material sample of the meter area platinum-rhodium wire suspension of burning to constant weight will be drilled with, one end of the platinum-rhodium wire that links to each other with sample stretches into the high-temperature burner hearth centre position, the other end of platinum-rhodium wire is in the burner hearth outside and links to each other with nickel filament, nickel filament hangs under the cotton thread, cotton thread is fixed on the hook of electronic balance base, and electronic balance links to each other with data line with computing machine.Sample heats with stove in high temperature furnace, when temperature rose to 540 ℃, sample began oxidation, and the quality of sample changes, the computing machine that links to each other with electronic balance can the continuous recording sample mass change, just can reflect the inoxidizability of sample according to this variation.
Described ternary silicide material sample, the cutting of employing line is 13mm * 4mm * 1.5mm or is the thin slice of φ 9mm * 1.5mm, and the thin slice edge adopts the hole of electric spark drill 0.8mm diameter, and sample is polished, dry up after the cleaning, accurately measure the surface area of sample.
Described platinum-rhodium wire, its diameter are the platinum-rhodium wire of 0.5mm.
Described inoxidizability, expression by the in-situ oxidation kinetic curve, specifically be that the sample mass variation of computer recording is long-pending divided by specimen surface, thereby obtain the mass change funtcional relationship in time of unit area, thereby reflect the inoxidizability of sample.
The invention has the advantages that the limitation that has overcome the existing high-temperature oxydation measuring technology of ternary silicide material.Test method is easily gone, test unit is simple, not only can be used for in-situ oxidation, can also be used for cyclic oxidation and (adopt same test unit, experimental sample does not lie in and hangs on the silk, and be placed directly in the corundum crucible with the burner hearth heating, certain hour takes out back weighing on the pan of a steelyard of balance and can realize cyclic oxidation at interval), have the function of a thing multiple-effect.For ternary silicide investigation of materials unit, adopt the inventive method, not only can overcome the testing tool that some new process equipments bring and require shortcomings such as height, equipment cost height, personnel's technical requirement height, and can utilize more existing measurement of correlation devices, transform a little, very the high-temperature oxidation resistance of the test high-temperature material ternary silicide material of intuitive and convenient.It is lower that the present invention can also be generalized to other oxidation rate, the various materials field that oxidization time is short.
Description of drawings
Fig. 1 embodiment of the invention equipment therefor structural representation;
Fig. 2 .Mo-10Si-14B ternary silicide sample (through 1800 ℃/2h vacuum annealing or V=10mm/h directional solidification) is at 1200 ℃ of continuous oxidation kinetics curves
Fig. 3 .Mo-10Si-14B ternary silicide sample (through 1800 ℃/2h vacuum annealing or V=10mm/h directional solidification) is at 1200 ℃ cyclic oxidation kinetic curves
Fig. 4 .Mo-12.5Si-25B and Mo-14Si-28B ternary silicide sample (through 1800 ℃/2h vacuum annealing) are at 1200 ℃ in-situ oxidation kinetic curves
Fig. 5 .Mo-12.5Si-25B and Mo-14Si-28B ternary silicide sample (through 1800 ℃/2h vacuum annealing) are at 1200 ℃ cyclic oxidation kinetic curves
Embodiment
Below in conjunction with drawings and Examples technical scheme of the present invention is further described.Performing step of the present invention is as follows: (1) sample is prepared: the cutting of ternary silicide material sample line is 13mm * 4mm * 1.5mm or is the thin slice of φ 9mm * 1.5mm, the thin slice edge adopts the hole of electric spark drill 0.8mm diameter, sample is polished, dry up after the cleaning, accurately measure the surface area of sample.(2) preparation of oxidation experiment: sample is suspended on burns below the diameter of constant weight is the platinum-rhodium wire of 0.5mm, adjust the sag of whole silk, allow sample be in the burner hearth medium position.The mercury bulb of adjusting balance mediates it, to balance calibrate, zero clearing.Under the atmospheric environment, start the computer program operation that high temperature furnace allows the record sample mass change simultaneously.(3) adopt the in-situ oxidation kinetic curve to reflect the inoxidizability of sample: the sample mass of computer program recorded is changed divided by specimen surface long-pending, thereby obtain the mass change funtcional relationship in time of unit area.
It is the Mo-Si-B ternary silicide material in-situ oxidation behavior at high temperature of aero-turbine machine blade that application the present invention has examined application prospect, purpose is to change behavior for the weight of Mo-Si-B ternary silicide material in temperature-rise period of checking heterogeneity, and the inoxidizability in the isothermal oxidation process, and contrast with the cyclic oxidation behavior, shown the similarities and differences of cyclic oxidation and in-situ oxidation kinetic curve.
Mo-10Si-14B, Mo-12.5Si-25B and Mo-14Si-28B ternary silicide are by vacuum arc melting+vacuum annealing and directional solidification preparation.Wherein the purity of Mo, Si, B is respectively 99.9%, 99.9999% and 99.9%.Proportion of raw materials is calculated by atomic percent.The button ingot that Mo-10Si-14B is gone out through electric arc melting carries out the vacuum annealing of 1800 ℃/2h and the button ingot is carried out directional solidification (V=10mm/h).Mo-12.5Si-25B and Mo-14Si-28B are carried out the vacuum annealing of 1800 ℃/2h through the button ingot that electric arc melting goes out.The sample that the material of directional solidification is φ 9mm * 1.5mm perpendicular to the cutting of direction of growth line; The line of material cutting that vacuum annealing is obtained is the sample of 13mm * 4mm * 1.5mm.The sample edge adopts the hole of electric spark drill 0.8mm diameter, and the sample that is used for the in-situ oxidation experiment polishes specimen surface with abrasive paper for metallograph, cleans with acetone earlier, uses the alcohol wash specimen surface again, dries with calorifier in air.The sample of the oxidation experiment that is useful on before doing oxidation experiment all with accurately meter area, to be used for the calculating that oxidation weight changes.By experimental provision shown in Figure 1, wherein high temperature resistance furnace 1, sample 2, platinum-rhodium wire 3, angle bar 4, metal stool 5, nickel filament 6, thin cotton thread 7, plastics shockproof sheet 8, electronic balance 9, plexiglass tent 10, data line 11, computing machine 12, the sample that is drilled with circular hole is suspended on burns below the diameter of constant weight is the platinum-rhodium wire of 0.5mm, adjust the sag of whole silk, allow sample be in the burner hearth medium position.The mercury bulb of adjusting balance mediates it, to balance calibrate, zero clearing.Under the atmospheric environment, start the computer program operation that high temperature furnace allows the record sample mass change simultaneously.The mass change of computer recording sample changes drafting in-situ oxidation kinetic curve according to quality.By the in-situ oxidation kinetic curve and with the comparison of cyclic oxidation kinetic curve, just can judge inoxidizability (Fig. 2～Fig. 5) and in the mass change rule at oxidation initial stage and reach the complexity of steady state (SS) of the material of three kinds of compositions.
According to Fig. 2 as can be seen, the Mo-10Si-14B sample is when 1200 ℃ of continuous oxidations, the quality of annealed state sample reduces less than directional solidification attitude sample, and the easier steady state (SS) that reaches mass change of annealed state sample, the annealed state sample reaches steady state (SS) at 2h, the directional solidification sample reaches steady state (SS) behind 3.5h, illustrate that the annealed state sample has better inoxidizability.
According to Fig. 3 as can be seen, the Mo-10Si-14B sample is when 1200 ℃ of cyclic oxidations, the quality of annealed state sample reduces still less than directional solidification attitude sample, the annealed state sample reaches steady state (SS) behind 5h, and the directional solidification sample also fails to reach steady state (SS) within 100h, contrast cyclic oxidation kinetic curve and in-situ oxidation kinetic curve illustrate the easier steady state (SS) that reaches of in-situ oxidation.
According to Fig. 4 as can be seen, when 1200 ℃ of continuous oxidations, the quality of Mo-14Si-28B annealed state sample reduces less than Mo-12.5Si-25B annealed state sample, reach steady state (SS) after the Mo-14Si-28B sample oxidation 5h, reach steady state (SS) behind the Mo-12.5Si-25B sample oxidation 7h, illustrate that the Mo-14Si-28B sample has better inoxidizability than Mo-12.5Si-25B sample.
According to Fig. 5 as can be seen, when 1200 ℃ of cyclic oxidations, the quality of Mo-14Si-28B annealed state sample reduces still less than Mo-12.5Si-25B annealed state sample, and two samples all fail to reach steady state (SS) within 100h.The heating-up time of all in-situ oxidations is 70 minutes, and sample heats up with stove during in-situ oxidation; All cyclic oxidations all are that furnace temperature reaches 1200 ℃ sample put into and take out.
Comprehensive above kinetic curve as can be seen, for all samples, obvious minimizing all takes place in the temperature-rise period quality in the sample that is used for in-situ oxidation, and in-situ oxidation is similar to the sample mass Changing Pattern of cyclic oxidation, and in-situ oxidation is than the easier steady state (SS) that reaches of cyclic oxidation.
Claims (5)
1. the detection method of a ternary silicide high-temp in-situ oxidation, it is characterized in that: the ternary silicide material sample platinum-rhodium wire suspension of burning that will be drilled with circular hole and measure surface area to constant weight, one end of the platinum-rhodium wire that links to each other with sample stretches into the high-temperature burner hearth centre position, the other end of platinum-rhodium wire is in the burner hearth outside and links to each other with nickel filament, nickel filament hangs under the cotton thread, cotton thread is fixed on the hook of electronic balance base, electronic balance links to each other with data line with computing machine, sample heats with stove in high temperature furnace, when temperature rises to 540 ℃, sample begins oxidation, the quality of sample changes, the mass change of the computing machine continuous recording sample that links to each other with electronic balance changes the inoxidizability of reflection sample according to this.
2. the detection method of ternary silicide high-temp in-situ oxidation according to claim 1, it is characterized in that, described ternary silicide material sample, the cutting of employing line is 13mm * 4mm * 1.5mm or is the thin slice of φ 9mm * 1.5mm, the thin slice edge adopts the hole of electric spark drill 0.8mm diameter, with the sample polishing, dry up after the cleaning, measure the surface area of sample.
3. according to the detection method of claim 1 or 2 described ternary silicide high-temp in-situ oxidations, it is characterized in that described ternary silicide material sample is selected Mo-Si-B ternary silicide material for use.
4. the detection method of ternary silicide high-temp in-situ oxidation according to claim 1 is characterized in that, described platinum-rhodium wire, its diameter are the platinum-rhodium wire of 0.5mm.
5. the detection method of ternary silicide high-temp in-situ oxidation according to claim 1, it is characterized in that, described inoxidizability, expression by the in-situ oxidation kinetic curve, specifically be that the sample mass variation of computer recording is long-pending divided by specimen surface, thereby obtain the mass change funtcional relationship in time of unit area, thereby reflect the inoxidizability of sample.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100283260A CN100489487C (en) | 2006-06-29 | 2006-06-29 | Ternary silicide high-temperature in-situ oxidation detection method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100283260A CN100489487C (en) | 2006-06-29 | 2006-06-29 | Ternary silicide high-temperature in-situ oxidation detection method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1869641A true CN1869641A (en) | 2006-11-29 |
| CN100489487C CN100489487C (en) | 2009-05-20 |
Family
ID=37443363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100283260A Expired - Fee Related CN100489487C (en) | 2006-06-29 | 2006-06-29 | Ternary silicide high-temperature in-situ oxidation detection method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100489487C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102095480A (en) * | 2010-11-30 | 2011-06-15 | 大连理工大学 | Heating real-time weighting device of high-temperature material |
| CN104048894A (en) * | 2013-03-15 | 2014-09-17 | 宝山钢铁股份有限公司 | Method and device for detecting high temperature dry and wet atmosphere oxidation resistant capacity of graphite roller sleeve |
| CN108918319A (en) * | 2018-05-11 | 2018-11-30 | 东北大学 | A kind of device and method for probing into metallurgical slag Yu experiment crucible material reaction mechanism |
| CN115356232A (en) * | 2022-08-23 | 2022-11-18 | 哈尔滨工业大学 | Method for accurately testing oxidation threshold temperature of titanium alloy and composite material in situ |
-
2006
- 2006-06-29 CN CNB2006100283260A patent/CN100489487C/en not_active Expired - Fee Related
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102095480A (en) * | 2010-11-30 | 2011-06-15 | 大连理工大学 | Heating real-time weighting device of high-temperature material |
| CN102095480B (en) * | 2010-11-30 | 2012-06-13 | 大连理工大学 | Heating real-time weighting device of high-temperature material |
| CN104048894A (en) * | 2013-03-15 | 2014-09-17 | 宝山钢铁股份有限公司 | Method and device for detecting high temperature dry and wet atmosphere oxidation resistant capacity of graphite roller sleeve |
| CN104048894B (en) * | 2013-03-15 | 2017-05-31 | 宝山钢铁股份有限公司 | The detection method and device of graphite roller set resistance high temperature dry and wet ambient oxidation ability |
| CN108918319A (en) * | 2018-05-11 | 2018-11-30 | 东北大学 | A kind of device and method for probing into metallurgical slag Yu experiment crucible material reaction mechanism |
| CN115356232A (en) * | 2022-08-23 | 2022-11-18 | 哈尔滨工业大学 | Method for accurately testing oxidation threshold temperature of titanium alloy and composite material in situ |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100489487C (en) | 2009-05-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5792660B2 (en) | Thermal analyzer | |
| CN100489487C (en) | Ternary silicide high-temperature in-situ oxidation detection method | |
| CN109520856A (en) | A kind of small sample On Creep Crack Growth test method | |
| CN110132750A (en) | A kind of impression test device and test method | |
| CN201653844U (en) | Thermal barrier coating high-temperature oxidation resistant performance test device | |
| CN103645199A (en) | In-situ double-axis tilting nanoindenter for transmission electron microscope | |
| CN108490237A (en) | A kind of device and method of potable metal pipeline thermoelectric gesture nondestructive measurement | |
| CN102944490B (en) | High-temperature rigidity measuring method based on electrified heating | |
| CN215768347U (en) | Thermal extension test device | |
| CN201429579Y (en) | Glass transition temperature measuring device | |
| CN107561315B (en) | The test device and method of microcosmic olefin hydrogen and hydrogen segregation activation energy in a kind of metal | |
| CN209231078U (en) | A kind of miniature on-line heating device in situ | |
| CN203534987U (en) | In-situ biaxial tilting nanoindentor used for transmission electron microscope (TEM) | |
| CN203455295U (en) | Phase-transition temperature tester | |
| Saxena et al. | Fatigue crack growth testing | |
| CN104535410A (en) | Temperature compensation method used for compact tension sample high temperature crack expansion test | |
| CN111579384A (en) | High temperature environment metal material tensile test system | |
| CN104076065A (en) | Online detection device for variation of metal melt structure caused by ultrasonic preprocessing | |
| CN211043216U (en) | Multi-temperature-zone multifunctional high-temperature atmosphere tube furnace | |
| CN1344952A (en) | Heatable sample platform for scanning probe microscope | |
| CN103983657B (en) | A kind of quenching oil cooling rate decline rapid simulation method | |
| CN2443365Y (en) | Sample table capable of rising temp for scanning probe microscope | |
| JP3883724B2 (en) | Thermomechanical measuring apparatus and method | |
| CN105136102A (en) | Metal material deformation amount test box and detection method thereof | |
| CN101788281A (en) | Measuring method of amorphous alloy free volume |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090520 Termination date: 20140629 |
|
| EXPY | Termination of patent right or utility model |