An Experimental Thermally Deposited Coating for Improved Bonding to Glass-fiber Posts.

G. R. Reis, F. P. Silva, A. Oliveira-Ogliari, A. Faria-E-Silva, R. Moraes, V. R. Novais, M. Menezes
{"title":"An Experimental Thermally Deposited Coating for Improved Bonding to Glass-fiber Posts.","authors":"G. R. Reis, F. P. Silva, A. Oliveira-Ogliari, A. Faria-E-Silva, R. Moraes, V. R. Novais, M. Menezes","doi":"10.3290/j.jad.a37725","DOIUrl":null,"url":null,"abstract":"PURPOSE To determine whether an experimental thermally deposited siloxane-methacrylate coating for use in industrial scale applications would improve the bond strength of resin-based materials to glass fiber posts (GFPs) without affecting their mechanical properties. MATERIALS AND METHODS An experimental 5% (w/v) solution of methacryloxypropyltrimethoxysilane was prepared. Two types of GFPs (Exacto, Angelus; White Post DC, FGM) were divided into the following groups: S: silane; SA: silane and adhesive; HS: 35% H₂O₂ and silane; HSA: 35% H₂O₂, silane and adhesive; Exp: siloxane-methacrylate coating (Si-O) via post immersion in experimental solution followed by heating; Exp-S: silane after Si-O treatment; Exp-A: adhesive after Si-O treatment; and Exp-SA: silane and adhesive after Si-O treatment. The posts were positioned in a mold to allow insertion of a dual-curing resin core, serially sectioned into beams, and subjected to microtensile bond strength (μTSB) testing. The three-point bending test and SEM/EDX analysis were used to assess the mechanical and surface properties of untreated GFPs that were etched with H₂O₂ or treated with Si-O. RESULTS Surface treatments affected the μTSB only for the Exacto GFPs. The highest μTBS (MPa) was observed in Exp-S and Exp-SA groups, whereas H₂O₂ etching resulted in intermediate values. The mechanical properties were not affected by surface treatments. Exacto GFPs had significantly higher flexural strength (σf) and flexural modulus (Ef) than did the White Post DC GFPs, but the latter were significantly stiffer (S) than Exacto, regardless of the surface treatment tested. H₂O₂ promoted morphological changes in post surfaces. The experimental treatment promoted deposition of Si onto the post surface, improving bond strengths of Exacto posts. CONCLUSION The proposed novel coating technique is a viable procedure for fiber post manufacturers to improve the μTSB of resin-based materials.","PeriodicalId":94234,"journal":{"name":"The journal of adhesive dentistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journal of adhesive dentistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3290/j.jad.a37725","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

PURPOSE To determine whether an experimental thermally deposited siloxane-methacrylate coating for use in industrial scale applications would improve the bond strength of resin-based materials to glass fiber posts (GFPs) without affecting their mechanical properties. MATERIALS AND METHODS An experimental 5% (w/v) solution of methacryloxypropyltrimethoxysilane was prepared. Two types of GFPs (Exacto, Angelus; White Post DC, FGM) were divided into the following groups: S: silane; SA: silane and adhesive; HS: 35% H₂O₂ and silane; HSA: 35% H₂O₂, silane and adhesive; Exp: siloxane-methacrylate coating (Si-O) via post immersion in experimental solution followed by heating; Exp-S: silane after Si-O treatment; Exp-A: adhesive after Si-O treatment; and Exp-SA: silane and adhesive after Si-O treatment. The posts were positioned in a mold to allow insertion of a dual-curing resin core, serially sectioned into beams, and subjected to microtensile bond strength (μTSB) testing. The three-point bending test and SEM/EDX analysis were used to assess the mechanical and surface properties of untreated GFPs that were etched with H₂O₂ or treated with Si-O. RESULTS Surface treatments affected the μTSB only for the Exacto GFPs. The highest μTBS (MPa) was observed in Exp-S and Exp-SA groups, whereas H₂O₂ etching resulted in intermediate values. The mechanical properties were not affected by surface treatments. Exacto GFPs had significantly higher flexural strength (σf) and flexural modulus (Ef) than did the White Post DC GFPs, but the latter were significantly stiffer (S) than Exacto, regardless of the surface treatment tested. H₂O₂ promoted morphological changes in post surfaces. The experimental treatment promoted deposition of Si onto the post surface, improving bond strengths of Exacto posts. CONCLUSION The proposed novel coating technique is a viable procedure for fiber post manufacturers to improve the μTSB of resin-based materials.
一种改进玻璃纤维桩粘接的实验热沉积涂层。
目的确定用于工业规模应用的实验性热沉积硅氧烷-甲基丙烯酸酯涂层是否能提高树脂基材料与玻璃纤维桩(gfp)的结合强度而不影响其机械性能。材料与方法制备了5% (w/v)的甲基丙烯氧基丙基三甲氧基硅烷实验溶液。两种类型的gfp (Exacto, Angelus;白柱DC,女性生殖器切割)分为以下组:S:硅烷;SA:硅烷和胶粘剂;HS: 35% h2o2和硅烷;HSA: 35% H₂O₂,硅烷和粘合剂;实验:硅氧烷-甲基丙烯酸酯涂层(Si-O)后浸在实验溶液中加热;Exp-S: Si-O处理后的硅烷;Exp-A: Si-O处理后的胶粘剂;Exp-SA: Si-O处理后的硅烷和胶粘剂。这些桩被放置在一个模具中,允许插入双固化树脂芯,连续分割成梁,并进行微拉伸粘结强度(μTSB)测试。采用三点弯曲试验和SEM/EDX分析来评估未经处理的GFPs的力学和表面性能,这些GFPs分别用h2o蚀刻或Si-O处理。结果表面处理仅对Exacto gfp的μTSB有影响。Exp-S组和Exp-SA组的μTBS (MPa)最高,而H₂O₂腐蚀的μTBS (MPa)为中间值。表面处理对材料的力学性能没有影响。Exacto gfp的抗弯强度(σf)和抗弯模量(Ef)显著高于White Post DC gfp,但后者的刚度(S)显著高于Exacto。H₂O₂促进了桩表面的形态变化。实验处理促进了硅在柱表面的沉积,提高了Exacto柱的结合强度。结论本文提出的新型涂层技术是提高树脂基材料μTSB的可行方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信