Root Cause Analysis of Edge Yellowing in PVB Laminated Glass

Yellowing of the Polyvinyl butyral resin (PVB) at the edges of laminated glass is a rare but important quality issue. You usually see it as two yellow spots about 5 cm wide along the edges. Since this tends to happen often, many customers have complained, leading to some losses for the company. This study investigates the cause by checking the production steps, running tests, and using a microscope to pinpoint the issue and find a solution.

 

 

Cause Analysis
Making laminated glass involves several steps: cutting, edging, lamination, autoclave treatment, and finally packaging, storing, and transporting. We've noticed that the yellowing mainly occurs where the glass vials touch the rack base, specifically in a 5 cm area. This yellowing doesn't appear right after autoclaving; it tends to show up during packaging and storage. Here are a few initial ideas about what might be causing it:

  1. Local PVB Aging Due to High Temperature: We tried using glass on a new rack that had a trimmed rubber base and deeper grooves, and there was no yellowing after a day. So, that's not the problem.

  2. Plastic Film Aging Contaminating PVB: We tried switching the film with adhesive tape, but there was still yellowing, which means the film isn’t the main culprit.

  3. Migration of Yellowing from Rubber Material: Seeing that putting glass on a clean rack stopped it from turning yellow makes it pretty clear that the old rubber parts are the cause of the discoloration.

 

Testing and Mechanism Study
We used FTIR and GC-MS to check out the yellowed PVB(Resin B-05SY & PVB SD-2)and rubber materials. The findings included:

  • There weren't any major differences in the composition of PVB or rubber.

  • C-MS detected extra organic compounds in the yellowed PVB, which are rubber additives. These substances migrated to the PVB due to a blooming effect from the EPDM rubber, causing the yellow spots.

Optimization Solutions
Based on our findings, we suggest three solutions:

  1. Prevent Blooming Migration: Add an inorganic barrier between the glass and rubber.

  2. Maintain Rubber Base: Trim aged surfaces periodically.

Conclusion

Identifying the issue has been really beneficial. This approach could also help address yellowing problems in other materials, like Ethylene Vinyl Acetate (EVA), which might spark some useful ideas for related issues.

 

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Is Your AlN Resistant to Hydrolysis?

AlN ceramics exhibit excellent insulation, high thermal conductivity, superior high-temperature resistance, corrosion resistance, and a thermal expansion coefficient that matches silicon, making them an ideal heat dissipation and packaging material for new-generation large-scale integrated circuits, semiconductor module circuits, and high-power devices. However, AlN powder—the raw material for producing high temperature AlN ceramics—is highly susceptible to hydrolysis. This not only complicates its transportation and storage but, more critically, reduces its nitrogen content after hydrolysis, significantly degrading the performance of the final AlN ceramics. Additionally, the hydrolytic instability of AlN powder hinders the development of water-based forming processes for industrial AlN ceramic products.

 

AlN powder

 

Thus, the hydrolytic sensitivity of AlN powder has become the primary obstacle to its widespread application. Overcoming this issue and improving the powder’s hydrolysis resistance to make it suitable for water-based wet forming has become a key research focus in the field of AlN ceramics in recent years.

 

Hydrolysis Mechanism

The conditions and products of AlN powder hydrolysis vary slightly among different studies. Some researchers suggest that the powder first reacts with water to form amorphous AlOOH and ammonia gas. The ammonia then reacts with water to produce OH⁻, increasing the solution's pH. Under certain temperature and acidity conditions, AlOOH further reacts with water to form Al(OH)₃.

 

Hydrolysis mechanism

 

How to Determine if AlN Has Hydrolyzed?

Since hydrolysis generates ammonia gas, which ionizes into NH₄⁺ and OH⁻ in water, the pH of the solution changes, making pH a key indicator of hydrolysis extent.

Additionally, XRD can be used for phase analysis before and after hydrolysis to qualitatively identify new phases and assess hydrolysis products/degree. SEM reveals morphological changes in AlN particles, providing qualitative insights into hydrolysis progression. TEM, beyond morphology analysis,can examine the crystal structure of hydrolysis products. Since hydrolysis consumes AlN powder (via ammonia release), measuring the powder’s mass loss before and after hydrolysis is another critical metric.

How to Mitigate AlN Hydrolysis?

Hydrolysis suppression typically involves coating AlN particles with a protective layer—via chemical bonding or physical adsorption—to isolate them from water.

Key methods include:

1. AlN Surface Modification——Surface Chemical Modification

This approach chemically reacts AlN particles with modifiers to form a passivation layer, enhancing surface properties.

Techniques include:

①Coupling agent modification

②Graft copolymerization modification

③Surface oxidation modification

④Surfactant modification

 

AlN powder

 

2. AlN Surface Treatment——Surface Physical Coating Treatment

(1) Liquid-Phase Coating

Modifiers are added to an AlN powder suspension, forming a coating via mechanical stirring. The coating adheres through adsorption or van der Waals forces, without chemical reactions.

(2) Vapor Deposition Coating

Utilizing the sublimation of materials (e.g., SiO), which are heated to deposit onto AlN particles, improving hydrolysis resistance. For example, SiO powder is sublimed in an Al₂O₃ crucible containing AlN powder, carbon felt, and graphite plates, forming a protective layer.

Alternatively, strong acid modifiers can be mixed with AlN powder via mechanical ball milling. This method avoids high temperatures, offers good reproducibility, and significantly enhances hydrolysis resistance while improving dispersion and stability in water—beneficial for preparing high-solid-content AlN ceramic slurries.

 

AlN ceramics

 

Summary

While all methods improve AlN powder’s hydrolysis resistance, each has limitations.

For instance:

Ceramic-grade AlN powder requires high purity. Silicon-based coatings (e.g., from silane) may introduce impurities during sintering, reducing thermal conductivity. Here, organic acids or thermal oxidation are preferred.

Thermal interface materials (TIMs) demand compatibility with silicone oils/gels for high filler loading and uniformity,Silane-based treatments are more suitable.

Combining multiple modification methods may yield superior results.

 

AlN products

 

About Xiamen Juci Technology Co., Ltd.

Xiamen Juci Technology Co., Ltd. is a high-tech enterprise specializing in the research, development, production, and sales of high-performance AlN materials. As a leading AlN powder suppliers, the company is committed to providing high-quality aluminum nitride series products and solutions for industries such as electronics, semiconductors, and aerospace.Xiamen Juci Technology Co., Ltd. can effectively address the hydrolysis problem of AlN. With exceptional quality and service, Xiamen Juci has earned widespread trust from global customers.

 

Media Contact:
Xiamen Juci Technology Co., Ltd.

Phone: +86 592 7080230
Email: miki_huang@chinajuci.com

Website: www.jucialnglobal.com

 

Applications of N-Phenylmaleimide in Heat-Resistant Polymer Composites

In advanced materials engineering, N‑phenylmaleimide (N‑PMI) manuafctured by Yangchen Tech has emerged as a high‑performance monomer for imparting exceptional heat resistance, dimensional stability, and mechanical robustness to a wide range of polymer composites. By introducing a rigid five‑membered maleimide ring with a phenyl substituent, N‑PMI elevates thermal decomposition thresholds, raises Vicat softening points, and improves tensile and flexural properties across ABS, PVC, Nylon 6, epoxy, and polyimide systems. 

 

N‑phenylmaleimide

 

Why choose N‑Phenylmaleimide?

N‑Phenylmaleimide features a planar cyclic imide core that resists chain scission at elevated temperatures, pushing onset decomposition temperatures 20–30 °C higher than conventional styrenic copolymers . Its phenyl ring further imparts steric hindrance, reducing segmental mobility and boosting glass transition temperatures (Tg) by up to 15 °C in polymer blends .

 

Specification

 

Appearance Melting point  Purity Solubility
Yellow crystalline powder or flakes 85-90℃ >99% Soluble in organic solvents

 

Basic Information

 

 

Chemical Structure N-phenylmaleimide
Chemical Formula C10H7NO2
CAS No. 941-69-5
Molecular Weight 173.16
Packing Type Paper bag (20 kg)
Properties Yellow crystalline powder or needles

 

Core Applications in Polymer Composites