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Localization of Spiropyran Activation

机译:螺芦山激活的本地化

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摘要

Functionalization of planar and curved glass surfaces with spiropyran (SP) molecules and localized UV-induced activation of the mechanophore are demonstrated. Fluorescence spectra of UV-irradiated SP-functionalized surfaces reveal that increases in surface roughness or curvature produce more efficient conversion of the mechanophore to the open merocyanine (MC) form. Further, force-induced activation of the mechanophore is achieved at curved glass-polymer interfaces and not planar interfaces. Minimal fluorescence signal from UV-irradiated SP-functionalized planar glass surfaces precluded mechanical activation testing. Curved glass-polymer interfaces are prepared by SP functionalization of E-glass fibers, which are subsequently embedded in a poly(methyl methacrylate) (PMMA) matrix. Mechanical activation is induced through shear loading by a single fiber microbond testing protocol. In situ detection of SP activation at the interface is monitored by fluorescence spectroscopy. The fluorescence increase during interfacial testing suggests that attachment of the interfacial SP molecule to both fiber surface and polymer matrix is present and able to achieve significant activation of SP at the fiber-polymer matrix interface. Unlike previous studies for bulk polymers, SP activation is detected at relatively low levels of applied shear stress. By linking SP at the glass-polymer interface and transferring load directly to that interface, a more efficient mechanism for eliciting the SP response is achieved.
机译:对螺吡喃(SP)分子(SP)分子的平面和弯曲玻璃表面的官能化进行了说明和局部紫外诱导的机械机械的活化。 UV辐照的SP官能化表面的荧光光谱揭示了表面粗糙度或曲率的增加会产生更有效的机械转化为开放的新硅晶(MC)形式。此外,在弯曲的玻璃 - 聚合物界面处实现力诱导的机械的活化,而不是平面界面。来自紫外线照射的SP官能化平面玻璃表面的最小荧光信号排除了机械活化测试。通过E-玻璃纤维的SP官能化制备弯曲的玻璃 - 聚合物界面,随后将其嵌入聚(甲基丙烯酸甲酯)(PMMA)基质中。通过单纤维微胶体测试协议通过剪切载荷诱导机械激活。以荧光光谱监测界面处的SP激活的原位检测。界面检测期间的荧光增加表明,存在界面SP分子与纤维表面和聚合物基质的附着,并且能够在纤维 - 聚合物基质界面处实现SP的显着激活。与以前的散装聚合物的研究不同,在相对较低的施加剪切应力下检测SP激活。通过将SP连接在玻璃聚合物界面上并直接将负载转移到该界面,实现了更有效的引出SP响应的机制。

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