Assessing effects of (3-aminopropyl)trimethoxysilane self-assembled layers on surface characteristics of organosilane-grafted moisture-crosslinked polyethylene substrate: A comparative study between chemical vapor deposition and plasma-facilitated in situ grafting methods

接触角 硅烷 润湿 材料科学 硅氧烷 化学工程 聚乙烯 嫁接 单层 化学气相沉积 高分子化学 X射线光电子能谱 表面改性 基质(水族馆) 傅里叶变换红外光谱 复合材料 纳米技术 聚合物 地质学 工程类 海洋学
作者
Navid Mostofi Sarkari,Öznur Doğan,Erhan Bat,Mohsen Mohseni,Morteza Ebrahimi
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:497: 143751-143751 被引量:34
标识
DOI:10.1016/j.apsusc.2019.143751
摘要

Abstract Silane coupling agents can act as bonding intermediates at the interface of two dissimilar materials by altering surface properties. In this study, (3-aminopropyl)trimethoxysilane (APTMS) was used as a silane precursor for vapor-phase deposition on organosilane-grafted moisture-crosslinked polyethylene (Si-XLPE) substrate. Chemical vapor deposition (CVD) and plasma-facilitated in situ grafting methods (grafting-from and grafting-onto) were employed to graft APTMS, and the consequent effects on surface of Si-XLPE were evaluated. In-depth analysis was done to determine the assembly behavior of the fabricated APTMS layers and their influences on the surface properties. Characterizations were based on the assessment of surface chemistry (by XPS, EDX, and ATR-FTIR), morphology (by AFM and FESEM), and wettability (by contact angle measurement). The results showed that APTMS molecules inclined to form multilayer structures instead of monolayers. Height of the formed layers ranged approximately 5–30 nm. Also, it was deduced that crosslinking of deposited layers happened through different siloxane configurations in siloxane polyhedral networks on the surface. The arrangement of APTMS molecules led to the creation of hydrophobic surfaces (water contact angle ≥100°) implying prevailing attachment of APTMS molecules from amino groups to the substrates. Findings confirmed that the plasma grafting-from approach possessed the highest APTMS attachment efficiency.

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