用二氧化钛纳米结构对氧化锆材料进行表面处理,以替代传统的气载粒子表面磨削法

Constantino Fernandes-Neto , Erika Bronze-Uhle , Leonardo Francisco Gonçalves Dias , Fabio Antonio Piola Rizzante , Paulo Noronha Lisboa-Filho , Adilson Yoshio Furuse
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引用次数: 0

摘要

氧化锆已成为间接修复体的热门选择;然而,这种材料的粘附性仍然是一项挑战。本研究旨在评估经过实验性表面处理的四方Y-TZP和立方Y-PSZ氧化锆的表面特征和粘接强度。研究人员制备了 Y-TZP (T) 和 Y-PSZ (P) 试样并将其分为几组:Tf-A)用 3-(氨基丙基)三甲氧基硅烷 (APTMS) 功能化的二氧化钛薄膜;Tf)二氧化钛薄膜;MNt-A)用 APTMS 手工涂覆二氧化钛纳米管;MNt)手工涂覆二氧化钛纳米管;VNt-A)用 APTMS 真空涂覆二氧化钛纳米管;VNt)真空涂覆二氧化钛纳米管;C)用 Al2O3 喷砂进行对照。利用 X 射线光电子能谱(XPS)和扫描电子显微镜(SEM)对其进行了表征。粘接强度通过微剪切粘接强度 (µSBS) 进行评估。数据分析采用双向方差分析和 Tukey's HSD 检验(α = 0.05)。XPS 显示了元素 O 1 s、Ti 2p 和 Zr 3d 5/2 的信号。此外,T-Tf-A/P-Tf-A 经二氧化钛和 APTMS 处理后,高分辨率显示了 Ti-O-Si 和 Zr-O-Si 键合。扫描电子显微镜(SEM)显示 T-Tf/T-Tf-A/P-Tf/P-Tf-A 形成了均匀的薄膜,所有纳米管组都形成了团簇。Y-TZP 和 Y-PSZ 的对照组显示出清晰的表面。除了 T-MNt-A/T-VNt-A/P-MNt-A/P-VNt-A 的平均 µSBS 值最低、试验前失效率最高外,其他试验性表面处理与对照组的 µSBS 值没有差异。使用二氧化钛纳米结构进行表面处理可有效改变两种受评估氧化锆材料的表面,提供强共价键、改变表面拓扑结构,以及与传统喷砂方案相当的剪切结合强度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surface treatments with TiO2 nanostructures for bonding to zirconia materials as an alternative to conventional airborne-particle abrasion of the surface

Zirconia has become a popular choice for indirect restorations; however, adhesion to this material remains a challenge. The present study aimed to evaluate surface characteristics and bond strength to tetragonal Y-TZP and cubic Y-PSZ zirconia submitted to experimental surface treatments. Specimens of Y-TZP (T) and Y-PSZ (P) were prepared and divided into groups: Tf-A) thin TiO2 film functionalized with 3-(aminopropyl)trimethoxysilane (APTMS); Tf) thin TiO2 film; MNt-A) manual application of TiO2 nanotubes with APTMS; MNt) manual application of TiO2 nanotubes; VNt-A) vacuum application of TiO2 nanotubes with APTMS; VNt) vacuum application of TiO2 nanotubes; C) control with Al2O3 sandblasting. Characterization with x-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) was done. Bond strength was evaluated by microshear bond strength (µSBS). Data were analyzed by two-way ANOVA and Tukey’s HSD tests (α = 0.05). XPS showed signals for elements O 1 s, Ti 2p, and Zr 3d 5/2. In addition, high-resolution demonstrated Ti-O-Si and Zr-O-Si bonding for treatments with TiO2 and APTMS for T-Tf-A/P-Tf-A. SEM presented a homogeneous film for T-Tf/T-Tf-A/P-Tf/P-Tf-A and cluster formations for all nanotube groups. Control groups for both Y-TZP and Y-PSZ showed clear surfaces. No differences of µSBS were seen between experimental surface treatments and the controls, except for T-MNt-A/T-VNt-A/P-MNt-A/P-VNt-A, which showed the lowest mean µSBS and highest incidence of pre-test failures. Surface treatments with TiO2 nanostructures were effective in modifying the surface of both zirconia materials evaluated, providing strong covalent bonds, changes to the surface topology, and shear bond strength comparable to conventional sandblasting protocols.

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