Thermally stable PSA film with reduced adhesion after thermal and UV treatment

IF 6.5 2区 材料科学 Q1 CHEMISTRY, APPLIED Progress in Organic Coatings Pub Date : 2024-11-22 DOI:10.1016/j.porgcoat.2024.108950
Yooseon Hong , Hyung Jun Kim , Subin Park , Hyun Jae Park , Minwook Jeon , Jihye Shim , Cheol-Hee Ahn
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Abstract

Acrylic pressure-sensitive adhesives (PSAs), commonly used for their low glass transition temperature (Tg), often exhibit poor heat resistance. This poses challenges in high-temperature applications in semiconductor processing and enhancing the heat resistance of PSAs has been achieved through chemical crosslinking. In this study, PSAs were developed that maintains adhesion during thermal treatment and reduces adhesion after photo treatment, allowing easy separation from silicon wafers. The PSAs was synthesized by copolymerization of 2-ethylhexyl acrylate (2-EHA), acrylonitrile (AN), and 4-hydroxybutyl acrylate (4-HBA) with final composition ratios of 72.6, 12.3, and 15.1 mol% respectively. Hexamethylene diisocyanate (HDI) and 2-isocyanatoethyl methacrylate (MOI) were attached to the hydroxyl group of 4-HBA to control the degree of crosslinking. Corona-treated polyethylene naphthalate (PEN) was used as a base film, which was suitable for processing at high-temperatures of approximately 250 °C. The peel strength of PSAs decreased from 9.64 N/in. to 6.75 N/in. after thermal treatment. This decrease is attributed to increased crosslinking density through AN cyclization during the thermal treatment unlike conventional PSA which is inseparable after thermal treatment. After photo treatment, peel strength decreased from 6.75 N/in. to 3.62 N/in., indicating additional crosslinking due to intermolecular reactions of the methacrylate groups in MOI. The increase in crosslinking density was verified through gel fraction analysis, which showed a rise from 65.2 %, as prepared, up to 97.6 % after thermal and photo treatment. Trimethylolpropane triacrylate (TMPTA) was used to form additionally crosslinked networks during photo treatment. The final gel fraction increased with the TMPTA content, rising from 97.6 % without TMPTA to 99.1 % with 20 wt% TMPTA. The peel strength also decreased down to 1.50 N/in. with 20 wt% TMPTA with only 0.85 % residue. These results provide valuable insights for engineering PSAs with controlled adhesion characteristics, thereby enabling the development of advanced PSAs suited for semiconductor industry applications.

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热稳定性 PSA 薄膜,经热处理和紫外线处理后粘附性降低
丙烯酸压敏粘合剂(PSA)因其玻璃化转变温度(Tg)较低而常用,但其耐热性通常较差。这给半导体加工中的高温应用带来了挑战,而通过化学交联可以提高压敏胶的耐热性。本研究开发的 PSAs 在热处理过程中可保持粘附性,在光处理后可降低粘附性,从而易于从硅晶片上分离。PSAs 是由 2-乙基己基丙烯酸酯(2-EHA)、丙烯腈(AN)和 4-羟基丁基丙烯酸酯(4-HBA)共聚合合成的,最终成分比分别为 72.6、12.3 和 15.1 摩尔%。在 4-HBA 的羟基上连接了六亚甲基二异氰酸酯 (HDI) 和甲基丙烯酸异氰酸乙酯 (MOI),以控制交联度。电晕处理过的聚萘二甲酸乙二醇酯 (PEN) 用作基膜,适合在约 250 °C 的高温下加工。热处理后,PSA 的剥离强度从 9.64 牛顿/英寸降至 6.75 牛顿/英寸。这一下降归因于热处理过程中 AN 环化增加了交联密度,而传统 PSA 在热处理后是不可分割的。光照处理后,剥离强度从 6.75 N/in. 下降到 3.62 N/in.,这表明 MOI 中的甲基丙烯酸酯基团发生了分子间反应,产生了额外的交联。凝胶馏分分析表明,交联密度的增加从制备时的 65.2% 增加到热处理和光处理后的 97.6%。在光处理过程中,使用三羟甲基丙烷三丙烯酸酯(TMPTA)形成额外的交联网络。最终的凝胶成分随着 TMPTA 含量的增加而增加,从未含 TMPTA 时的 97.6% 增加到含 20 wt% TMPTA 时的 99.1%。当 TMPTA 含量为 20 wt%、残留量仅为 0.85 % 时,剥离强度也降至 1.50 N/in。这些结果为设计具有可控粘附特性的 PSAs 提供了宝贵的见解,从而有助于开发适合半导体工业应用的先进 PSAs。
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来源期刊
Progress in Organic Coatings
Progress in Organic Coatings 工程技术-材料科学:膜
CiteScore
11.40
自引率
15.20%
发文量
577
审稿时长
48 days
期刊介绍: The aim of this international journal is to analyse and publicise the progress and current state of knowledge in the field of organic coatings and related materials. The Editors and the Editorial Board members will solicit both review and research papers from academic and industrial scientists who are actively engaged in research and development or, in the case of review papers, have extensive experience in the subject to be reviewed. Unsolicited manuscripts will be accepted if they meet the journal''s requirements. The journal publishes papers dealing with such subjects as: • Chemical, physical and technological properties of organic coatings and related materials • Problems and methods of preparation, manufacture and application of these materials • Performance, testing and analysis.
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