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热固性二甲基丙烯酸酯聚合物的表面溶解和酯交换反应由二甲基丙烯酸酯胶粘剂树脂和有机催化剂-醇溶液完成。

Surface dissolution and transesterification of thermoset dimethacrylate polymer by dimethacrylate adhesive resin and organic catalyst-alcohol solution.

机构信息

Dental Biomaterial Research Chair, Dental Health Department, College of Applied Medical Sciences, King Saud University, Riyadh 11433, Saudi Arabia.

Institute of Dentistry, Department of Biomaterials Science, University of Turku, FI-20520 Turku, Finland.

出版信息

Dent Mater. 2020 May;36(5):698-709. doi: 10.1016/j.dental.2020.03.005. Epub 2020 Apr 6.

Abstract

OBJECTIVES

To evaluate transesterification based dissolution of dimethacrylate and epoxy polymers, the former containing ester groups. Polymer substrates were treated with an adhesive resin (Stick™ Resin) and an organic catalyst-alcohol solution (ethylene glycol and triazabicyclodecene). The surface was chemically and nanomechanically analyzed with Fourier Transform-Infrared (FTIR) spectroscopy, surface profile peak (R) and nanohardness and modulus of elasticity.

METHODS

A total of 100 specimens each of light-cured dimethacrylate polymer and heat-cured diepoxy polymer were prepared. 20 specimens were randomly selected and used as control group (0s). The remaining specimens were randomly divided into 40 each for treatment with an Stick™ resin and ethylene glycol+triazabicyclodecene. Within each group the 40 specimens were randomly subdivided into 20 each for treatment at 5min and 24h, with 10 specimens for FTIR and nanohardness and modulus of elasticity, and the other 10 for SEM and surface R analyses.

RESULTS

Dimethacrylate polymer showed a reduction in the nanohardness and modulus of elasticity, R values and SEM also showed significant topographical changes after being treated with either Stick™ resin or ethylene glycol+triazabicyclodecene, whereas epoxy resin substrate did not. FTIR analyses affirmed changes in the intensity of ester groups.

SIGNIFICANCE

Ester group containing dimethacrylate polymer showed a reduction in NMP within 5min of exposure to the treatment agents with softening by solution ethylene glycol+triazabicyclodecene associated to the reduction of ester groups in the polymer structure by transesterification. Epoxy polymer without ester groups was not affected by surface softening with treatment agents. Adhesive resin caused surface swelling.

摘要

目的

评估基于酯交换的二甲基丙烯酸酯和环氧树脂的溶解,前者含有酯基。将聚合物基底用胶粘剂树脂(StickTM 树脂)和有机催化剂-醇溶液(乙二醇和三唑并[1,5-A]嘧啶)处理。用傅里叶变换红外光谱(FTIR)、表面轮廓峰(R)和纳米硬度和弹性模量对表面进行化学和纳米力学分析。

方法

制备了每组各 100 个光固化二甲基丙烯酸酯聚合物和热固化双环氧聚合物的样本。随机选择 20 个样本作为对照组(0s)。其余样本随机分为 40 个样本,分别用 StickTM 树脂和乙二醇+三唑并[1,5-A]嘧啶处理。在每组内,40 个样本随机分为每组 20 个,分别在 5 分钟和 24 小时进行处理,其中 10 个样本用于 FTIR 和纳米硬度和弹性模量分析,另外 10 个样本用于 SEM 和表面 R 分析。

结果

二甲基丙烯酸酯聚合物的纳米硬度和弹性模量、R 值和 SEM 均显示出明显的形貌变化,在用 StickTM 树脂或乙二醇+三唑并[1,5-A]嘧啶处理后,而环氧基底没有。FTIR 分析证实了酯基团强度的变化。

意义

含有酯基的二甲基丙烯酸酯聚合物在暴露于处理剂 5 分钟内表现出 NMP 的减少,通过酯交换使聚合物结构中的酯基团减少而软化,并用乙二醇+三唑并[1,5-A]嘧啶溶液软化。不含酯基的环氧聚合物不受处理剂表面软化的影响。胶粘剂树脂导致表面肿胀。

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