Application Note | Polymer Deformation

Heat-Deformed Polymer Morphology Using 3D Profilometry

Quantifying a Heat-Induced Hole and Rim by Subtracting Before and After 3D Scans

Heat-deformed polymer surface

Research & Experimental Testing

Craig Leising & Duanjie Li

Visual Design & Editorial

Andrew Shore

Introduction

Surface deformation of materials induced by environmental elements such as temperature, humidity and corrosion is vital to its service quality and functionality. Accurate 3D polymer morphology measurement allows quantifying the physical deformations of the surface form, roughness, volume/area, etc. Surfaces prone to deformation due to contact wear, high heat and others need regular inspection to ensure performance reliability.

Importance of 3D Non-Contact Profilometry for Morphology Analysis

Unlike other techniques such as touch probes or interferometry, the NANOVEA 3D Non-Contact Profilometer, using axial chromatism, can measure nearly any surface with nano through macro range. No sample surface preparation is needed for surface profile measurement of any material, including transparent, opaque, specular, diffusive, polished and rough, etc. The non-contact technique makes it possible to precisely scan samples with complex shape and soft texture. The NANOVEA Non-Contact Profilometer provides an ideal, broad and user friendly tool to maximize surface studies.

ℹ️ Learn more about surface profiling lab services.

Measurement Objective

In this application, the NANOVEA ST400 Profilometer is used to measure the surface morphology of a polymer sample before and after heat deformation. The deformation will be characterized by the relative volume change and flatness as defined by ISO 12781.

NANOVEA ST400 Standard

Optical 3D Profilometer

NANOVEA ST400 modular optical profilometer for non-contact 3D surface measurement
Optical sensor of the profilometer above a dark polymer sample
Fig. 1: Optical sensor scanning on the polymer sample.

Results and Discussion

Fig. 2 displays the 3D view of the polymer sample surface before and after the heat deformation, providing users a straightforward tool to directly observe the sample from different angles. Table 1 compares the Roughness and Flatness values of the polymer surface before and after heat deformation. The surface morphology has been substantially changed by the heating process, forming a hole in the center of the sample. It leads to increased Roughness, Sa, from 1.17 to 74 µm, as well as increased Flatness, FLTt, from 3.8 to 502 µm.

Flat 3D surface of the polymer before heating
(a) Polymer surface before heat deformation.
3D surface of the polymer after heating with a deep central hole
(b) Polymer surface after heat deformation.

Fig. 2: The 3D morphology of the polymer surface before and after heat deformation.

ParameterBeforeAfter
Sa (µm)1.1774
Sq (µm)1.5297.8
Sp (µm)22.3149
Sv (µm)18.7364
Sz (µm)41513
Ssk0.248−1.49
Sku4.65.49
FLTt (µm)3.8502

Table 1: Roughness (ISO 25178) and flatness (ISO 12781) of the polymer surface before and after heat deformation.

Fig. 3 shows the deformed surface subtracted from the original surface with the mean plane of the original surface at zero, illustrating the local height difference between the surface before and after deformation. As the hole forms and grows during heat deformation in the center of the sample, the surface surrounding the hole slightly rises at the same time. This leads to drastic change in the height, both positive and negative, from the original surface. The relative volume calculations by the analysis software show that the volume of the center hole is 12.68 mm³, and the peak volume at the edge of the hole is 3.582 mm³.

3D map of the height difference between the deformed and original surfaces, showing the hole and the raised rim
Fig. 3: The 3D view of the deformed surface subtracted from the original surface.

Conclusion

In this application, we have shown that the NANOVEA 3D Non-Contact Profilometer characterizes the surface morphology of heat deformed polymer. The subtraction of the deformed surface from the original one provides a useful tool to precisely pinpoint the area where shape change occurs, as well as to quantify the volume of such change. Surface deformation of materials may have critical effect on its service quality and functionality. The NANOVEA Non-Contact Profilometer provides an ideal tool for surface deformation inspection.

The data shown here represents only a portion of the calculations available in the analysis software. NANOVEA Profilometers measure virtually any surface in fields including Semiconductor, Microelectronics, Solar, Fiber Optics, Automotive, Aerospace, Metallurgy, Machining, Coatings, Pharmaceutical, Biomedical, Environmental and many others.

Frequently Asked Questions About Measuring Heat Deformation

How is surface deformation quantified?

By scanning the same surface before and after exposure and comparing roughness, flatness and volume; subtracting the two scans shows exactly where the shape changed and by how much.

What happened to the polymer when heated?

A hole formed in the center of the sample while the surrounding surface rose slightly; Sa increased from 1.17 to 74 µm and the flatness deviation FLTt from 3.8 to 502 µm.

How large was the deformation in volume?

The relative volume calculation gave 12.68 mm³ for the center hole and 3.582 mm³ for the raised peak at its edge.

Why use a non-contact profilometer for soft or deformed parts?

Axial chromatism measures nano to macro heights on any material with no surface preparation, and without touching the sample, so complex shapes and soft textures can be scanned precisely.

Which standard defines the flatness value?

ISO 12781; FLTt is the peak-to-valley flatness deviation of the surface.

Which instrument was used?

The NANOVEA ST400 3D non-contact profilometer.

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