ASTM E1251-07 PDF

ASTM E – Download as PDF File .pdf), Text File .txt) or read online. Standards. This test method is under the jurisdiction of ASTM Committee E01 on For E – 07 in Spectrochemical Analysis calculations are used to correct for both. Designation: E – 07 Standard Test Method for Analysis of Other forms may 1 This test method is under the jurisdiction of ASTM.

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NOTE 5β€”To achieve the best analytical results, both reference materials and sample specimen should have fresh surfaces.

What is most accurate “referee” method for composition analysis of aluminum alloys?

Enter your account email address to request a password reset: Dear All, I am looking for an authentic statement or any references which can be utilised when there will be any dispute among any analytical findings of the elemental contents of any alloy.

These materials should also possess a metallurgical condition that is similar to the material s that are being analyzed. The actual appearance of a burn will vary with source conditions and alloy. If the instrument is newly installed, give e1251-7 unit sufficient time to stabilize asfm its new environment before proceeding with a drift correction.

If the factors are calculated manually, see Practice E for details. Ken Vlach, Thank you so much for your answer.

Are you sure you want to empty the cart? All connections must be leak-free. Overlapping the burns may adversely affect precision and accuracy. See Practice E for details.

Optionally, the purchaser may also choose to specify that the instrument come completely pre-calibrated for all alloys and all intended analytical tasks.

What is most accurate “referee” method for composition analysis of aluminum alloys?

Last previous edition approved in as E β€” The atsm covered in the scope of this method are listed in the table below. He passed away May 14, It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Whenever standardants are replaced, appropriate procedures must be followed to reference the intensities obtained from the new standardant to the intensities obtained from the standardant being replaced.


Active view current version of standard. Adtm manufacturers may provide for the top plate to be liquid cooled to minimize sample heat-up during the excitation cycle. Samples and reference materials should be sparked atsm 7 to 10 mm from their outer edge.

Bad burns can be caused by an air leak between the sample and the top plate, a poor quality sample, poor quality argon and various other reasons. The excitation chamber will contain a mounting clamp to hold the counter electrode. The argon gas source can be from high-purity compressed gas cylinders, a cryogenic-type cylinder that contains liquid argon or possibly from a central supply liquid only. The counter electrode should be made from thoriated tungsten or silver and have a pointed end.

This standard does not purport to address all of the safety concerns, if any, associated with its use. The exhaust can then be vented into an efficient hood system. The radiant energies of the selected analytical lines and the internal standard line s are converted into electrical signals by either photomultiplier tubes PMTs or a suitable solid state detector.


The elements covered in the scope of this method are listed in the asttm below. Summary of Test Method 4. The aluminum specimen to be analyzed may be in the form of a chill cast disk, casting, foil, sheet, plate, extrusion or some other wrought form or shape. If you like to setup a quick demo, let us know at e1521-07 madcad. All information presented is for general reference and does not represent a professional opinion nor the policy of an author’s employer.


For optimum usefulness, several of the calibrants should have concentrations for the xstm elements that vary over the expected ranges in the specimen to be analyzed. For each specification, measurable elemental ranges, analytical procedures and referenced specifications can be viewed at www.

The concentration ranges given in the above scope were established through cooperative testing ILS of selected reference materials.

Your comments will receive careful consideration at a meeting of the responsible technical committee, which you may attend. Check for clerical errors, elemental interferences or biases if results do not compare favorably. This shall be done by a trained expert initially and as often as necessary thereafter to assure proper alignment.

For best performance it is strongly recommended that the counter electrode be cleaned after every burn. They may be used if the lowest concentration of the element being determined is within ten times the detection limit of that element.

The gas shall be delivered by a? Procedure for Analyzing Specimens Remember, the instrument must be pro? The gap distance between the specimen surface and the tip of the counter electrode is speci? First use a fast, multi-element analysis technique to identify elements possibly out-of-spec. E251-07 many instances a manufacturer asmt offer speci?

Register for a trial account. Therefore, the instrument shall be designed with an internal exhaust system that is equipped with its own set of? The concentration ranges given in the above scope were established through cooperative testing ILS of selected reference materials.

The excitation chamber will also be constructed so that it is?