Typical Defects of UV 3C Coatings (9)


During the application of UV‑3C coatings, curing shrinkage patterns represent a particularly distinctive type of surface defect. They arise when the coating film develops uneven shrinkage during UV curing, resulting in textured surface irregularities. Unlike leveling issues such as orange peel or craters, these defects stem from volumetric changes that occur during the coating’s curing reaction. In high‑end electronic products like smartphones and laptops, the presence of shrinkage patterns can directly compromise the product’s aesthetic quality and may adversely affect the long‑term durability of the coating.

I. Manifestations of Curing Shrinkage Cracks

Curing shrinkage cracks manifest as fine, dense, thread-like patterns on the coating surface, with their orientation often correlating to the stress distribution within the coating. These patterns may appear linear, reticular, or irregularly distributed. Unlike the uneven, raised‑and‑recessed texture of orange peel, shrinkage cracks tend to be more pronounced, resembling fine, linear striations—sometimes even mimicking the crack‑like morphology of a dried riverbed.

Shrinkage marks are typically shallow in depth but become clearly visible under certain lighting angles. In light-colored coatings, the shadows of shrinkage marks are more pronounced; in dark-colored coatings, they may appear as subtle differences in gloss. Unlike cracking, shrinkage marks do not penetrate the full thickness of the coating and are generally confined to the surface or near-surface region.

II. Mechanism of Polymerization Shrinkage

The curing process of UV coatings is essentially a polymerization reaction. Under UV irradiation, monomers and oligomers in the liquid coating undergo crosslinking polymerization, reducing the intermolecular distance from the van der Waals range to the covalent bond length and resulting in a decrease in the overall volume of the system—this phenomenon is known as polymerization shrinkage.

The volumetric shrinkage rates vary among different resin systems. Acrylate systems generally exhibit higher shrinkage than epoxy systems. As crosslink density increases, the number of reactive functional groups per unit volume rises, leading to a greater theoretical shrinkage. The types and proportions of monomers and oligomers in a coating formulation directly influence the extent of volumetric shrinkage during curing.

III. Stress Concentration Caused by Non-Uniform Shrinkage

The formation of shrinkage cracks is not solely due to shrinkage itself, but rather to its non-uniformity. When different regions of the coating exhibit varying degrees of shrinkage, stress concentrations develop at the interfaces between these regions, giving rise to visible surface textures.

Non-uniform shrinkage may stem from variations in coating thickness. In areas with thicker coatings, the degree of shrinkage exceeds that in thinner regions, leading to a stress gradient at the interface and the formation of surface texture. Microscopic irregularities on the substrate surface can also result in differential shrinkage behavior across different coating zones. Differences in the substrate’s affinity for the coating and variations in the curing rates among distinct regions can further compromise the uniformity of shrinkage.

IV. The Effect of Exposure Energy on Contracture Lines

Exposure energy is a critical factor influencing the formation of shrinkage cracks. The energy of UV irradiation directly affects both the rate and extent of the curing reaction. At higher energy levels, the polymerization rate accelerates, causing the coating to undergo most of its shrinkage within a short time; this leads to the concentrated release of shrinkage stresses, thereby facilitating the development of shrinkage cracks.

At lower energy levels, the polymerization rate is slower, allowing the coating more time to relieve shrinkage stresses through molecular chain mobility, thereby reducing the likelihood of surface cracking. However, excessively low energy can lead to incomplete curing; thus, optimizing the curing conditions requires balancing the risk of cracking with the desired degree of cure.

V. The Relationship Between Coating Thickness and Shrinkage Cracks

The influence of coating thickness on shrinkage cracking manifests in two ways. First, thicker coatings exhibit greater shrinkage and higher internal stress accumulation, thereby increasing the risk of shrinkage cracks. Second, during curing, the disparity in cure progression between the surface and the substrate becomes more pronounced: the surface cures and shrinks earlier, while the substrate cures and shrinks later. This differential shrinkage between the two layers gives rise to surface texture.

Thin coatings exhibit less shrinkage, resulting in lower shrinkage stresses and a reduced likelihood of cracking. However, excessively thin coatings may compromise protective performance. The uniformity of coating thickness is equally critical; areas with significant thickness variations are more prone to uneven shrinkage.

VI. The Impact of Shrinkage Marks on Product Performance

The impact of shrinkage marks on appearance quality is readily apparent: they compromise the smoothness and uniform gloss of the coating surface, making it difficult for products to meet high‑quality aesthetic standards. In high‑end electronic devices, the presence of shrinkage marks may result in the product being deemed non‑conforming.

The impact of shrinkage cracks on the long-term performance of coatings also warrants close attention. Shrinkage‑crack regions serve as stress concentration points and may, over prolonged service, become initiation sites for cracking. Under conditions of thermal cycling or mechanical impact, stress relief in these areas can manifest as coating cracking or delamination. Moreover, the presence of shrinkage cracks indicates an uneven internal stress state within the coating, which can compromise its overall durability.

VII. Conclusion

Cure‑shrinkage cracks are a distinctive surface defect in UV‑curable 3C coatings, arising from non‑uniform polymerization shrinkage. Fundamentally, they result from the combined effects of volumetric shrinkage during curing and an uneven distribution of internal stresses within the coating. Polymerization shrinkage is an intrinsic characteristic of UV curing, while non‑uniform shrinkage stems from factors such as variations in coating thickness, differences in substrate condition, and curing parameters. Exposure energy and coating thickness directly influence the severity of these cracks. Beyond compromising the aesthetic quality of the product, cure‑shrinkage cracks can also adversely affect the long‑term durability of the coating. A thorough understanding of the manifestations and underlying causes of cure‑shrinkage cracks is essential for their identification and analysis.

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Bosheng Related Product Recommendations – 3C Coatings

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B-102

Bisphenol A epoxy acrylate

High hardness, high gloss, chemical resistance, contains 15% TMPTA.

B-151

Modified epoxy acrylate

Low halogen, yellowing-resistant, excellent plating performance, and strong adhesion.

B-165

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Good flexibility and strong adhesion

B-216

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Fast curing, high fullness, and excellent toughness.

B-368

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Good toughness, excellent leveling, excellent bend resistance, and excellent heat resistance.

B-574C

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Low viscosity, low odor, excellent wettability, suitable for LED UV.

B-601

Aromatic polyurethane acrylate

High hardness, scratch resistance, chemical resistance, and excellent cost-effectiveness.

B-6019

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Good leveling, excellent wettability, resistant to boiling water, and superior color dispersion.

B-609

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Fast curing, high hardness, scratch resistance, and chemical resistance.

B-615A

Aliphatic polyurethane acrylate

Fast curing, excellent toughness, wear resistance, and chemical resistance.

B-619W

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Fast curing, high hardness, excellent toughness, wear resistance, and chemical resistance.

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B-572

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Low viscosity, low odor, excellent wettability, suitable for LED UV.

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Low viscosity, chemical resistance, environmental resistance, and dual photothermal curing.

B-6263

Special functional group acrylate

Fast curing, high build, boil-resistant, and excellent toughness.

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Low viscosity, solvent resistance, chemical resistance, and steel-wool resistance.

B-919B

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Fast curing, high hardness, excellent toughness, and superior chemical and wear resistance.

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Aliphatic polyurethane acrylate

Low viscosity, yellowing resistance, chemical resistance, and steel-wool resistance.

B-916

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Low viscosity, solvent resistance, chemical resistance, and steel-wool resistance.

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Fast curing, high hardness, excellent toughness, and superior chemical and wear resistance.

Oil-resistant pen

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B-868

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Good leveling, smooth finish, fast curing, and stain resistance.

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Yellowing-resistant, excellent wettability, low viscosity, fast curing

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Self-initiated photopolymerization performance

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B-151

Modified epoxy acrylate

Low halogen, yellowing-resistant, excellent plating performance, and strong adhesion.

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B-296

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Fast curing, chemical resistance, yellowing resistance, impact resistance

B-431

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Yellowing-resistant, excellent wettability, low viscosity, fast curing

Monomer Recommendation

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BM3231 (TMPTA)

Trimethylolpropane triacrylate

High crosslink density, high hardness, high gloss, and excellent wear resistance.

BM3235 (PET3A)

Pentaerythritol triacrylate

Fast curing, high crosslink density, high hardness, and chemical resistance.

BM3380 (3EO-TMPTA)

Pentaerythritol triacrylate

More flexible and less irritating than TMPTA.

BM4241 (DiTMPTA-80)

Bis(2,3-dihydroxypropyl) tetraacrylate

High crosslink density, high hardness, chemical and wear resistance, and water resistance.

BM4242 (Di-TMPTA)

Bis-trimethylolpropane tetraacrylate

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BM6261 (DPHA-80)

Dipentaerythritol hexaacrylate

High crosslink density, high hardness, chemical and wear resistance, and water resistance.

BM6263 (DPHA-90)

Dipentaerythritol hexaacrylate

High crosslink density, high hardness, chemical and wear resistance, and water resistance.

 

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