Method for the non-destructive testing of a casing

• US 10,458,906 B2
• Filed: 01/30/2018
• Issued: 10/29/2019
• Est. Priority Date: 01/31/2017
• Status: Active Grant

• Current Assignee: Safran Aircraft Engine Company
• Original Assignee: Safran Aircraft Engine Company
• Inventors: Romero, Jean-Louis, Mainczyk, Angelique Melody Marine Alexia, Martin, Geoffrey
• Primary Examiner(s): Gunberg, Edwin C
• Assistant Examiner(s): Faye, Mamadou
• Application Number:
  US15/883,387
• Publication Number:
  US 20180217057A1
• Time in Patent Office: 637 Days
• CPC Class Codes: G01J 2003/2859 Peak detecting in spectrum
• CPC Class Codes: G01J 3/4338 Frequency modulated spectrometry
• CPC Class Codes: G01M 99/002 Thermal testing flaw detection G01N25/72
• CPC Class Codes: G01N 2021/8427 Coatings
• CPC Class Codes: G01N 2021/8472 Investigation of composite materials
• CPC Class Codes: G01N 21/3563 for analysing solids; Preparation of samples therefor
• CPC Class Codes: G01N 21/8422 Investigating thin films, e.g. matrix isolation method

Abstract

A method for the non-destructive testing of the heating of a part made from polymer material, the method comprising the following steps: a) carrying out a measurement by infrared spectroscopy on a part to be tested and extracting therefrom at least one of absorbance values and transmittance values according to a spatial frequency; and b) from the measurement of at least one of absorbance and transmittance, determining the period of time during which said region of the part to be tested has been subjected to a given heating temperature and determining said heating temperature, using a reference database comprising at least one of absorbance measurements and transmittance measurements, the measurements established over a plurality of reference samples made from polymer material that have been subjected to a given temperature during a given period of time.

Claims

1. A method for non-destructive testing of a heating of a part made from polymer material, the method comprising:

a) carrying out a measurement by infrared spectroscopy at a region of said part to be tested and extracting therefrom test values comprising at least one selected from the group of absorbance values and transmittance values according to a spatial frequency;

b) from test values, determining an interval of spatial frequencies relating to an oxidation of a polymer of said region of the part; and

c) from the test values in said interval of spatial frequencies, determining a period of time during which said region of the part to be tested has been subjected to a given heating temperature and determining said given heating temperature, using a reference database comprising sample values including at least one selected from the group of absorbance measurements and transmittance measurements, the sample values established over a plurality of reference samples made from polymer material that have been subjected to a given temperature during a given period of time, both the given temperature and the given period of time varying among the plurality of reference samples so as to cover a plurality of periods of time and a plurality of temperatures.

2. The method of claim 1, further comprising:

identifying, in the interval of spatial frequencies, a first peak for the part to be tested, an amplitude of which depends on a state of oxidation of the polymer of said region of the part to be tested and determining an amplitude value of the first peak,

performing step c) by comparing the amplitude value of the first peak of the part to be tested with amplitude values of first reference peaks situated in a spatial frequency interval relating to the oxidation of the polymer on said reference samples and contained in the reference database.

3. The method of claim 2, further comprising:

from test values, identifying a second peak for the part to be tested, an amplitude of which is independent of the state of oxidation of the polymer of said region of the part to be tested, and determining an amplitude value of the second peak,

calculating a ratio R of the amplitude value of the first peak obtained on the part to be tested to the amplitude value of the second peak obtained on the part to be tested,

performing step c) by comparing said ratio obtained for said region of the part with reference ratios R_i,j for said reference samples and contained in the reference database, each reference ratio R_i,j for a given sample being calculated by dividing an amplitude value of a first reference peak by an amplitude value of a second reference peak, the amplitude of which is independent of the state of oxidation of the polymer of said given sample.

4. The method of claim 3, wherein the amplitude value of the first peak of the part to be tested and the amplitude value of the second peak of the part to be tested are each, prior to a determination of a ratio in question, corrected by a variation in non-specific absorption that is a function of an emission wavelength of an infrared spectrometer used to carry out the measurement of the region of the part to be tested.

5. The method of claim 4, wherein the second peak of the part to be tested is chosen so as to be positioned relative to the first peak of the part to be tested so that the variation in non-specific absorbance between the first peak and the second peak is substantially linear.

6. The method of claim 5, wherein the first peak of the part to be tested and the second peak of the part to be tested are situated in a spatial frequency interval of less than 500 cm⁻

1, wherein near ends of the spatial frequency interval there are determined two absorbance measurements solely relating to non-specific absorption and from which there is determined the linear variation in non-specific absorption as a function of the spatial frequency in order to make the non-specific absorption variation correction.

7. The method of claim 1, wherein the polymer material comprises reinforcement fibres.