A replacement mill liner arrives with a material certificate. A handheld analyzer identifies chromium and molybdenum, and its screen displays a familiar alloy family. The casting appears to match the purchase order.
Is that enough to release it for installation?
Not necessarily. If the instrument is a conventional handheld X-ray fluorescence analyzer, it has not directly measured carbon. Carbon can be one of the most important elements controlling the hardness, heat-treatment response and fracture behavior of a cast-steel wear component.
This distinction matters for mining, cement and aggregate equipment. A liner, crusher component, liner bolt or other alloy part may contain the expected chromium and molybdenum while having an unsuitable carbon content, incorrect heat treatment or inadequate mechanical properties.
Positive material identification, commonly called PMI, is valuable. However, an alloy-identification result must be interpreted within the capabilities of the instrument and the requirements of the material specification.
This guide compares handheld XRF, spark optical emission spectrometry and combustion analysis. It explains what each method can establish, what it cannot establish, and how purchasers can specify a practical chemical-verification plan for cast-steel components.
Carbon is a nonmetallic element, but its influence on steel can be greater than that of several deliberately added metals.
In suitable alloy systems, carbon affects:
The correct carbon content depends on the complete alloy and its intended microstructure. A higher carbon result is not automatically better for a wear component.
A heavily impacted liner may require a different balance of hardness and toughness from a component exposed mainly to sliding abrasion. The carbon requirement must therefore be evaluated together with chromium, molybdenum, manganese, nickel, heat treatment and service conditions.
A chemical certificate showing chromium and molybdenum alone cannot establish this balance.
Even when carbon is within specification, a casting may have unsuitable properties because of:
Chemical verification confirms composition at the sampled location. It does not independently confirm casting soundness, heat-treatment quality or fitness for service.
X-ray fluorescence uses an X-ray source to excite the material. The instrument measures characteristic fluorescence emitted by detectable elements and uses the resulting spectrum to estimate composition.
Conventional handheld XRF instruments are useful for identifying many alloying elements, including chromium, nickel and molybdenum. Depending on the instrument, calibration and operating conditions, they may also measure elements such as manganese, copper, cobalt, tungsten and certain lighter elements.
Their portability makes them useful for incoming inspection, material sorting and checking individual components against alloy-family expectations.
However, conventional handheld XRF does not directly measure carbon.
If a material grade is distinguished primarily by carbon content, an XRF grade match cannot confirm that distinction. The displayed grade name is an interpretation based on measured elements and the instrument’s grade library.
A grade-identification function typically compares measured composition with stored limits or reference patterns.
Its reliability depends on:
Two steels may have similar chromium, nickel and molybdenum contents but different carbon requirements. The instrument may identify their common family without resolving the carbon-based difference.
The inspector should therefore review the elemental results and method limitations, not just the suggested grade name.
Spark optical emission spectrometry, or spark OES, uses an electrical discharge to excite a small area of the metal surface. The emitted light is separated and analyzed to determine elemental composition.
With appropriate instrument configuration, calibration, sample preparation and operating conditions, spark OES can measure carbon and other elements important to steel specifications.
ASTM E415 provides a method for analyzing carbon and low-alloy steel by spark atomic emission spectrometry. Its scope includes defined ranges for alloying and residual elements.
The existence of a standard does not mean every instrument can analyze every casting grade under that standard. The laboratory must confirm that the specimen and required composition ranges fall within the method’s validated scope.
Bench instruments normally analyze prepared samples under controlled laboratory conditions. Mobile spark OES can support testing of suitable components at other locations, but it still requires the correct instrument configuration and a suitable prepared surface.
Practical considerations include:
A specification should identify the required result and accepted method. It should not assume that all equipment described as a “spectrometer" has the same capabilities.
Combustion analysis is another established approach for determining carbon and sulfur.
A prepared sample is combusted under controlled conditions, and the resulting gases are analyzed. The procedure requires suitable sampling, sample mass, calibration and quality-control practices.
ASTM E1019 covers methods for determining carbon, sulfur, nitrogen and oxygen in specified metallic materials using combustion and inert-gas-fusion techniques. The applicable procedure must be selected for the element and material being tested.
Combustion analysis is particularly useful when carbon or sulfur needs an agreed laboratory confirmation. It does not provide a complete chromium–nickel–molybdenum analysis from the same carbon/sulfur measurement.
For some orders, spark OES provides routine composition verification while combustion analysis supplies an agreed confirmation of carbon or sulfur. Whether both are necessary depends on the specification, risk and analytical requirements.
| Inspection method | Main practical use | Carbon measurement | Important limitation |
|---|---|---|---|
| Conventional handheld XRF | Alloy-family identification, sorting and checking detectable alloying elements | Does not directly measure carbon | A grade match cannot establish a carbon-based grade distinction |
| Spark OES | Multi-element chemical analysis of suitably prepared metal | Yes, with an appropriate instrument, calibration and procedure | Results depend on material scope, surface preparation and analytical control |
| Combustion carbon/sulfur analysis | Laboratory determination of carbon and sulfur | Yes, under the applicable procedure | Does not replace full multi-element alloy analysis |
| Hardness testing | Checking resistance to indentation and heat-treatment consistency | No | Hardness cannot uniquely identify alloy composition |
| Metallographic examination | Evaluating microstructure and certain defects or inclusions | Not a substitute for bulk chemical analysis | A small examined area may not represent the whole casting |
| Mechanical testing | Determining specified tensile, impact or other properties | No | Results depend on sampling, specimen geometry and test conditions |
These methods answer different questions. A reliable inspection plan combines the methods needed for the actual purchase specification instead of treating one test as a universal substitute.
The table below summarizes general metallurgical roles. It is not a grade specification or a recommendation to change an existing alloy.
| Element | General role in cast steel | Why purchasers should verify it |
|---|---|---|
| Carbon, C | Influences hardness potential, carbide formation and the strength–ductility balance | A chromium or molybdenum match does not establish the required carbon level |
| Chromium, Cr | Influences hardenability and carbide behavior | Incorrect chromium can change transformation and wear response |
| Molybdenum, Mo | Influences hardenability and resistance to temper softening | An incorrect level may change heavy-section response or the intended property balance |
| Nickel, Ni | Can support toughness and hardenability in suitable steel systems | Similar-looking components may contain different nickel levels |
| Manganese, Mn | Influences hardenability and sulfur-related metallurgy | It must be evaluated as part of the complete alloy |
| Silicon, Si | Used in deoxidation and influences matrix behavior | Excess or deficiency may indicate an incorrect heat or composition |
| Sulfur, S | Commonly controlled because of sulfide-related effects | Acceptable major alloying elements do not guarantee suitable sulfur |
| Phosphorus, P | Commonly controlled because of segregation and embrittlement concerns | It may influence toughness without a clear hardness warning |
The appropriate carbon range must come from the specified grade or an approved custom composition. It should never be inferred from a handheld analyzer’s chromium and molybdenum results.
A handheld XRF result can support identification of the chromium–molybdenum alloy family. It cannot establish carbon content or confirm that the liner received the required heat treatment.
For a Cr-Mo liner, a practical verification package may include:
For product context, see our Cr-Mo alloy-steel SAG mill liner page.
Some grade distinctions depend on carbon limits even when the major alloying elements are similar.
If the acceptance requirement depends on carbon, use a carbon-capable method. Do not accept a grade-library identification as proof of an element that was not measured.
Also avoid substituting a wrought-grade designation for a casting-grade designation simply because their names or major alloying elements appear similar.
High-chromium white iron requires verification of carbon as well as chromium and other specified elements.
However, ASTM E415 is a carbon- and low-alloy-steel method. It should not automatically be applied to high-chromium white iron merely because both are iron-based materials.
The laboratory should select and validate an analytical procedure appropriate to the material, its composition and its metallurgical condition.
A reading on weld metal, hardfacing, plating or a contaminated surface may not represent the underlying casting.
Before testing, determine whether the measurement location is:
The test location must match the question being asked.
A technically capable instrument can still produce an unrepresentative result on an unsuitable surface.
Paint, rust, scale, oil, plating and embedded abrasive material can interfere with testing. Rough surfaces can also prevent correct probe contact or sealing.
For spark OES, sample preparation should follow the qualified procedure. Important considerations include:
ASTM E415 notes that improved performance is expected when reference materials and specimens have similar composition and metallurgical condition. Analytical preparation therefore deserves the same attention as instrument selection. See the ASTM E415 method scope.
Do not specify an arbitrary grinding depth for every casting. The required preparation depends on surface condition, manufacturing history and the accepted procedure.
A result can be analytically correct for the tested sample while being insufficient to characterize the whole component or shipment.
This distinction is particularly important for large castings.
A heat-analysis sample supports verification of the melt associated with production. It should be linked to the casting through a traceable heat identification.
A certificate without a reliable relationship to the delivered component provides limited assurance.
Product analysis is performed on material taken from a casting or another agreed product location.
The purchase specification should define:
Castings can contain composition variation associated with solidification. One measurement does not map the entire casting.
Where local variation is a concern, the engineer and laboratory should agree on a sampling plan. Taking many readings without a defined plan does not necessarily produce a more representative conclusion.
ISO 4990 addresses general technical delivery requirements for steel, nickel and cobalt alloy castings, including sample and test-piece selection. The applicable material or product specification remains important when defining acceptance.
A report stating only “PMI passed" leaves important questions unanswered.
| Report item | Why it matters |
|---|---|
| Part number and drawing revision | Connects the test to the correct component |
| Heat number and casting identification | Supports traceability |
| Specified material grade | Establishes the acceptance basis |
| Test method | Identifies what the measurement can establish |
| Instrument identification | Connects results to controlled equipment |
| Calibration or verification reference | Supports confidence in the measurement |
| Surface condition and preparation | Helps determine whether parent metal was tested |
| Test location | Makes the result reproducible and auditable |
| Reported elemental values | Allows comparison with the actual specification |
| Unmeasured required elements | Prevents an incomplete analysis from appearing complete |
| Acceptance limits | Shows the basis for the decision |
| Operator and test date | Supports accountability and record control |
A value that was not measured should be identified as unmeasured. It should not be displayed as zero, assumed compliant or silently omitted where the element is necessary for acceptance.
Confirm the drawing revision, material grade, required chemistry, heat-treatment condition and inspection requirements.
Identify which elements are essential to distinguish the specified material from plausible alternatives.
Compare the casting markings with the packing list, material certificate and heat-treatment records.
If identification is missing or inconsistent, resolve it before relying on analytical results.
Where appropriate, use handheld XRF to check detectable alloying elements and identify obvious material mix-ups.
Record the elemental results and any unresolved grade ambiguity.
If carbon is needed for grade confirmation or acceptance, obtain a result from an appropriate carbon-capable method.
Do not infer carbon from hardness, appearance or a grade-library match.
Determine whether sulfur, phosphorus, silicon or other specified elements have been adequately measured by the accepted procedure.
Instrument capability must be confirmed for the required material and concentration range.
Check hardness, impact, tensile or other required results. Confirm that test pieces and production castings have the agreed relationship.
If a result falls outside the acceptance criteria, follow the agreed procedure for retesting, investigation or disposition.
Do not average unrelated readings to make a nonconforming result appear acceptable.
Hardness is affected by composition, microstructure and processing.
The same steel can have very different hardness values in annealed, normalized, quenched or tempered conditions. Different alloys can also exhibit similar hardness.
Therefore, hardness cannot uniquely establish:
Hardness remains valuable when used for its intended purpose. A hardness map can reveal variation across a casting and help investigate heat-treatment consistency.
For background on how liner geometry and material interact in service, see What Is a SAG Mill Liner and How Does It Work?.
XRF and spark OES use different physical principles and have different capabilities. Identify the actual method in the inspection plan.
A library match is useful supporting information. It should not replace comparison of measured values with specified limits.
A reading from a weld repair, coating or contaminated region may answer a different question from the one intended.
A method intended for carbon and low-alloy steel should not be assumed suitable for every high-alloy steel, white iron or nonferrous casting.
Correct chemistry does not establish that the component has the right shape, heat treatment, toughness or defect acceptance level.
If carbon is required but not measured, the report should make that gap visible.
When requesting cast-steel components, include the following information.
Discuss these requirements before production. Adding an inspection requirement after casting and heat treatment can create sampling difficulties or make the original qualification plan unsuitable.
Handheld XRF equipment produces ionizing radiation and must be operated by trained personnel under applicable radiation-safety requirements and manufacturer instructions.
Spark OES creates an electrical discharge and leaves a small surface mark. Its use requires suitable equipment, surface preparation and site controls. It should not be used in a potentially flammable atmosphere without the necessary assessment and authorization.
Sampling, grinding and cutting introduce additional hazards. Never prepare or test a component while it is moving, inadequately supported or connected to uncontrolled equipment.
The inspection plan should be approved by personnel responsible for material acceptance. This article does not replace the governing material standard, a qualified laboratory procedure or equipment-specific engineering review.
No. A conventional handheld XRF analyzer does not directly measure carbon. Use a suitable carbon-capable analytical method when carbon is required for acceptance.
No. It supports identification based on the measured elements. Unmeasured elements, heat treatment, mechanical properties and casting soundness require separate consideration.
Not automatically. Its suitability depends on the alloy, analytical range, instrument, sample geometry, preparation and required accuracy. The laboratory should select a validated method.
A carbon/sulfur combustion result does not provide a complete chromium–molybdenum analysis. Additional elemental analysis is required.
Not without engineering and specification review. Similar major alloying elements do not make product standards or processing requirements interchangeable.
Not necessarily. Inspection frequency should follow the purchase specification, applicable standard and risk-based acceptance plan. Define the requirements before manufacture.
Handheld XRF is useful for alloy identification and checking detectable alloying elements. Its carbon limitation becomes important when accepting cast-steel mill liners and other components whose properties depend strongly on carbon.
A complete verification plan should connect:
For Cr-Mo cast steel, confirming chromium and molybdenum is only part of the material-verification process. Carbon, residual elements, microstructure and processing must also match the agreed requirements.
Send EB China the component drawing, operating conditions and inspection specification for review. Manufacturing scope, analytical methods and acceptance criteria should be confirmed before quotation and production.
View Cr-Mo Alloy-Steel SAG Mill Liners
Review Quality-Control Information
Send Drawings and Inspection Requirements for Quote
Email: cast@ebcastings.com
Explore drawing-based component enquiries related to this material or fixture discussion.
A replacement mill liner arrives with a material certificate. A handheld analyzer identifies chromium and molybdenum, and its screen displays a familiar alloy family. The casting appears to match the purchase order.
Is that enough to release it for installation?
Not necessarily. If the instrument is a conventional handheld X-ray fluorescence analyzer, it has not directly measured carbon. Carbon can be one of the most important elements controlling the hardness, heat-treatment response and fracture behavior of a cast-steel wear component.
This distinction matters for mining, cement and aggregate equipment. A liner, crusher component, liner bolt or other alloy part may contain the expected chromium and molybdenum while having an unsuitable carbon content, incorrect heat treatment or inadequate mechanical properties.
Positive material identification, commonly called PMI, is valuable. However, an alloy-identification result must be interpreted within the capabilities of the instrument and the requirements of the material specification.
This guide compares handheld XRF, spark optical emission spectrometry and combustion analysis. It explains what each method can establish, what it cannot establish, and how purchasers can specify a practical chemical-verification plan for cast-steel components.
Carbon is a nonmetallic element, but its influence on steel can be greater than that of several deliberately added metals.
In suitable alloy systems, carbon affects:
The correct carbon content depends on the complete alloy and its intended microstructure. A higher carbon result is not automatically better for a wear component.
A heavily impacted liner may require a different balance of hardness and toughness from a component exposed mainly to sliding abrasion. The carbon requirement must therefore be evaluated together with chromium, molybdenum, manganese, nickel, heat treatment and service conditions.
A chemical certificate showing chromium and molybdenum alone cannot establish this balance.
Even when carbon is within specification, a casting may have unsuitable properties because of:
Chemical verification confirms composition at the sampled location. It does not independently confirm casting soundness, heat-treatment quality or fitness for service.
X-ray fluorescence uses an X-ray source to excite the material. The instrument measures characteristic fluorescence emitted by detectable elements and uses the resulting spectrum to estimate composition.
Conventional handheld XRF instruments are useful for identifying many alloying elements, including chromium, nickel and molybdenum. Depending on the instrument, calibration and operating conditions, they may also measure elements such as manganese, copper, cobalt, tungsten and certain lighter elements.
Their portability makes them useful for incoming inspection, material sorting and checking individual components against alloy-family expectations.
However, conventional handheld XRF does not directly measure carbon.
If a material grade is distinguished primarily by carbon content, an XRF grade match cannot confirm that distinction. The displayed grade name is an interpretation based on measured elements and the instrument’s grade library.
A grade-identification function typically compares measured composition with stored limits or reference patterns.
Its reliability depends on:
Two steels may have similar chromium, nickel and molybdenum contents but different carbon requirements. The instrument may identify their common family without resolving the carbon-based difference.
The inspector should therefore review the elemental results and method limitations, not just the suggested grade name.
Spark optical emission spectrometry, or spark OES, uses an electrical discharge to excite a small area of the metal surface. The emitted light is separated and analyzed to determine elemental composition.
With appropriate instrument configuration, calibration, sample preparation and operating conditions, spark OES can measure carbon and other elements important to steel specifications.
ASTM E415 provides a method for analyzing carbon and low-alloy steel by spark atomic emission spectrometry. Its scope includes defined ranges for alloying and residual elements.
The existence of a standard does not mean every instrument can analyze every casting grade under that standard. The laboratory must confirm that the specimen and required composition ranges fall within the method’s validated scope.
Bench instruments normally analyze prepared samples under controlled laboratory conditions. Mobile spark OES can support testing of suitable components at other locations, but it still requires the correct instrument configuration and a suitable prepared surface.
Practical considerations include:
A specification should identify the required result and accepted method. It should not assume that all equipment described as a “spectrometer" has the same capabilities.
Combustion analysis is another established approach for determining carbon and sulfur.
A prepared sample is combusted under controlled conditions, and the resulting gases are analyzed. The procedure requires suitable sampling, sample mass, calibration and quality-control practices.
ASTM E1019 covers methods for determining carbon, sulfur, nitrogen and oxygen in specified metallic materials using combustion and inert-gas-fusion techniques. The applicable procedure must be selected for the element and material being tested.
Combustion analysis is particularly useful when carbon or sulfur needs an agreed laboratory confirmation. It does not provide a complete chromium–nickel–molybdenum analysis from the same carbon/sulfur measurement.
For some orders, spark OES provides routine composition verification while combustion analysis supplies an agreed confirmation of carbon or sulfur. Whether both are necessary depends on the specification, risk and analytical requirements.
| Inspection method | Main practical use | Carbon measurement | Important limitation |
|---|---|---|---|
| Conventional handheld XRF | Alloy-family identification, sorting and checking detectable alloying elements | Does not directly measure carbon | A grade match cannot establish a carbon-based grade distinction |
| Spark OES | Multi-element chemical analysis of suitably prepared metal | Yes, with an appropriate instrument, calibration and procedure | Results depend on material scope, surface preparation and analytical control |
| Combustion carbon/sulfur analysis | Laboratory determination of carbon and sulfur | Yes, under the applicable procedure | Does not replace full multi-element alloy analysis |
| Hardness testing | Checking resistance to indentation and heat-treatment consistency | No | Hardness cannot uniquely identify alloy composition |
| Metallographic examination | Evaluating microstructure and certain defects or inclusions | Not a substitute for bulk chemical analysis | A small examined area may not represent the whole casting |
| Mechanical testing | Determining specified tensile, impact or other properties | No | Results depend on sampling, specimen geometry and test conditions |
These methods answer different questions. A reliable inspection plan combines the methods needed for the actual purchase specification instead of treating one test as a universal substitute.
The table below summarizes general metallurgical roles. It is not a grade specification or a recommendation to change an existing alloy.
| Element | General role in cast steel | Why purchasers should verify it |
|---|---|---|
| Carbon, C | Influences hardness potential, carbide formation and the strength–ductility balance | A chromium or molybdenum match does not establish the required carbon level |
| Chromium, Cr | Influences hardenability and carbide behavior | Incorrect chromium can change transformation and wear response |
| Molybdenum, Mo | Influences hardenability and resistance to temper softening | An incorrect level may change heavy-section response or the intended property balance |
| Nickel, Ni | Can support toughness and hardenability in suitable steel systems | Similar-looking components may contain different nickel levels |
| Manganese, Mn | Influences hardenability and sulfur-related metallurgy | It must be evaluated as part of the complete alloy |
| Silicon, Si | Used in deoxidation and influences matrix behavior | Excess or deficiency may indicate an incorrect heat or composition |
| Sulfur, S | Commonly controlled because of sulfide-related effects | Acceptable major alloying elements do not guarantee suitable sulfur |
| Phosphorus, P | Commonly controlled because of segregation and embrittlement concerns | It may influence toughness without a clear hardness warning |
The appropriate carbon range must come from the specified grade or an approved custom composition. It should never be inferred from a handheld analyzer’s chromium and molybdenum results.
A handheld XRF result can support identification of the chromium–molybdenum alloy family. It cannot establish carbon content or confirm that the liner received the required heat treatment.
For a Cr-Mo liner, a practical verification package may include:
For product context, see our Cr-Mo alloy-steel SAG mill liner page.
Some grade distinctions depend on carbon limits even when the major alloying elements are similar.
If the acceptance requirement depends on carbon, use a carbon-capable method. Do not accept a grade-library identification as proof of an element that was not measured.
Also avoid substituting a wrought-grade designation for a casting-grade designation simply because their names or major alloying elements appear similar.
High-chromium white iron requires verification of carbon as well as chromium and other specified elements.
However, ASTM E415 is a carbon- and low-alloy-steel method. It should not automatically be applied to high-chromium white iron merely because both are iron-based materials.
The laboratory should select and validate an analytical procedure appropriate to the material, its composition and its metallurgical condition.
A reading on weld metal, hardfacing, plating or a contaminated surface may not represent the underlying casting.
Before testing, determine whether the measurement location is:
The test location must match the question being asked.
A technically capable instrument can still produce an unrepresentative result on an unsuitable surface.
Paint, rust, scale, oil, plating and embedded abrasive material can interfere with testing. Rough surfaces can also prevent correct probe contact or sealing.
For spark OES, sample preparation should follow the qualified procedure. Important considerations include:
ASTM E415 notes that improved performance is expected when reference materials and specimens have similar composition and metallurgical condition. Analytical preparation therefore deserves the same attention as instrument selection. See the ASTM E415 method scope.
Do not specify an arbitrary grinding depth for every casting. The required preparation depends on surface condition, manufacturing history and the accepted procedure.
A result can be analytically correct for the tested sample while being insufficient to characterize the whole component or shipment.
This distinction is particularly important for large castings.
A heat-analysis sample supports verification of the melt associated with production. It should be linked to the casting through a traceable heat identification.
A certificate without a reliable relationship to the delivered component provides limited assurance.
Product analysis is performed on material taken from a casting or another agreed product location.
The purchase specification should define:
Castings can contain composition variation associated with solidification. One measurement does not map the entire casting.
Where local variation is a concern, the engineer and laboratory should agree on a sampling plan. Taking many readings without a defined plan does not necessarily produce a more representative conclusion.
ISO 4990 addresses general technical delivery requirements for steel, nickel and cobalt alloy castings, including sample and test-piece selection. The applicable material or product specification remains important when defining acceptance.
A report stating only “PMI passed" leaves important questions unanswered.
| Report item | Why it matters |
|---|---|
| Part number and drawing revision | Connects the test to the correct component |
| Heat number and casting identification | Supports traceability |
| Specified material grade | Establishes the acceptance basis |
| Test method | Identifies what the measurement can establish |
| Instrument identification | Connects results to controlled equipment |
| Calibration or verification reference | Supports confidence in the measurement |
| Surface condition and preparation | Helps determine whether parent metal was tested |
| Test location | Makes the result reproducible and auditable |
| Reported elemental values | Allows comparison with the actual specification |
| Unmeasured required elements | Prevents an incomplete analysis from appearing complete |
| Acceptance limits | Shows the basis for the decision |
| Operator and test date | Supports accountability and record control |
A value that was not measured should be identified as unmeasured. It should not be displayed as zero, assumed compliant or silently omitted where the element is necessary for acceptance.
Confirm the drawing revision, material grade, required chemistry, heat-treatment condition and inspection requirements.
Identify which elements are essential to distinguish the specified material from plausible alternatives.
Compare the casting markings with the packing list, material certificate and heat-treatment records.
If identification is missing or inconsistent, resolve it before relying on analytical results.
Where appropriate, use handheld XRF to check detectable alloying elements and identify obvious material mix-ups.
Record the elemental results and any unresolved grade ambiguity.
If carbon is needed for grade confirmation or acceptance, obtain a result from an appropriate carbon-capable method.
Do not infer carbon from hardness, appearance or a grade-library match.
Determine whether sulfur, phosphorus, silicon or other specified elements have been adequately measured by the accepted procedure.
Instrument capability must be confirmed for the required material and concentration range.
Check hardness, impact, tensile or other required results. Confirm that test pieces and production castings have the agreed relationship.
If a result falls outside the acceptance criteria, follow the agreed procedure for retesting, investigation or disposition.
Do not average unrelated readings to make a nonconforming result appear acceptable.
Hardness is affected by composition, microstructure and processing.
The same steel can have very different hardness values in annealed, normalized, quenched or tempered conditions. Different alloys can also exhibit similar hardness.
Therefore, hardness cannot uniquely establish:
Hardness remains valuable when used for its intended purpose. A hardness map can reveal variation across a casting and help investigate heat-treatment consistency.
For background on how liner geometry and material interact in service, see What Is a SAG Mill Liner and How Does It Work?.
XRF and spark OES use different physical principles and have different capabilities. Identify the actual method in the inspection plan.
A library match is useful supporting information. It should not replace comparison of measured values with specified limits.
A reading from a weld repair, coating or contaminated region may answer a different question from the one intended.
A method intended for carbon and low-alloy steel should not be assumed suitable for every high-alloy steel, white iron or nonferrous casting.
Correct chemistry does not establish that the component has the right shape, heat treatment, toughness or defect acceptance level.
If carbon is required but not measured, the report should make that gap visible.
When requesting cast-steel components, include the following information.
Discuss these requirements before production. Adding an inspection requirement after casting and heat treatment can create sampling difficulties or make the original qualification plan unsuitable.
Handheld XRF equipment produces ionizing radiation and must be operated by trained personnel under applicable radiation-safety requirements and manufacturer instructions.
Spark OES creates an electrical discharge and leaves a small surface mark. Its use requires suitable equipment, surface preparation and site controls. It should not be used in a potentially flammable atmosphere without the necessary assessment and authorization.
Sampling, grinding and cutting introduce additional hazards. Never prepare or test a component while it is moving, inadequately supported or connected to uncontrolled equipment.
The inspection plan should be approved by personnel responsible for material acceptance. This article does not replace the governing material standard, a qualified laboratory procedure or equipment-specific engineering review.
No. A conventional handheld XRF analyzer does not directly measure carbon. Use a suitable carbon-capable analytical method when carbon is required for acceptance.
No. It supports identification based on the measured elements. Unmeasured elements, heat treatment, mechanical properties and casting soundness require separate consideration.
Not automatically. Its suitability depends on the alloy, analytical range, instrument, sample geometry, preparation and required accuracy. The laboratory should select a validated method.
A carbon/sulfur combustion result does not provide a complete chromium–molybdenum analysis. Additional elemental analysis is required.
Not without engineering and specification review. Similar major alloying elements do not make product standards or processing requirements interchangeable.
Not necessarily. Inspection frequency should follow the purchase specification, applicable standard and risk-based acceptance plan. Define the requirements before manufacture.
Handheld XRF is useful for alloy identification and checking detectable alloying elements. Its carbon limitation becomes important when accepting cast-steel mill liners and other components whose properties depend strongly on carbon.
A complete verification plan should connect:
For Cr-Mo cast steel, confirming chromium and molybdenum is only part of the material-verification process. Carbon, residual elements, microstructure and processing must also match the agreed requirements.
Send EB China the component drawing, operating conditions and inspection specification for review. Manufacturing scope, analytical methods and acceptance criteria should be confirmed before quotation and production.
View Cr-Mo Alloy-Steel SAG Mill Liners
Review Quality-Control Information
Send Drawings and Inspection Requirements for Quote
Email: cast@ebcastings.com
Explore drawing-based component enquiries related to this material or fixture discussion.