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Parylene C has been widely used in the fields of microelectromechanical systems (MEMS) and electronic device encapsulation because of its unique properties, such as biocompatibility and conformal coverage. However, its poor adhesion and low thermal stability limit its use in a wider range of applications. This study proposes a novel method for improving the thermal stability and enhancing the adhesion between Parylene and Si by copolymerizing Parylene C with Parylene F. The successful preparation of Parylene copolymer films containing different ratios of Parylene C and Parylene F was confirmed using Fourier-transform infrared spectroscopy and surface energy calculations. The proposed method resulted in the copolymer film having an adhesion 10.4 times stronger than that of the Parylene C homopolymer film. Furthermore, the friction coefficients and cell culture capability of the Parylene copolymer films were tested. The results indicated no degradation compared with the Parylene C homopolymer film. This copolymerization method significantly expands the applications of Parylene materials.
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Many aquatic creatures in nature have non-cooperative surface scaling abilities using suction organs; micro-/nano-scale structures found in different parts of the organs play an important role in this mechanism. Synthetic bioinspired suction devices have been developed, but the mechanisms of bioinspired suction system need further investigation. This paper presents the development of a synthetic adhesive disc inspired by the hillstream loach. The microscopic structures involved in adhesion of the hillstream loach were investigated. Bioinspired suction discs were designed with single-level or hierarchical micropatterned margins. Micro three-dimensional (3D) printing and micro electromechanical system (MEMs) technology were utilized in the fabrication of the discs, and the adhesion performance was tested on substrates with different roughness values. The engaging and disengaging processes of the margin were simulated by carrying out a peeling test on a submerged substrate. The interactions between the liquid film and the microstructures were observed using fluorescence microscopy. The enhanced adhesion forces due to the synergy of the hierarchically micro-patterned margin and the disc cavity were duplicated in the synthetic adhesion system.
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We found that continuous films of gold (Au) on oxidized silicon (SiO2) substrates, upon treatment with ultraviolet (UV)-ozone, exhibit strong adhesion to the SiO2 support. Importantly, the enhancement is independent of micro- or nanostructuring of such nanometer-thick films. Deposition of a second Au layer on top of the pretreated Au layer makes the adhesion stable for at least 5 months in environmental air. Using this treatment method enables us to large-scale fabricate various SiO2-supported Au structures at various thicknesses with dimensions spanning from a few hundreds of nanometers to a few micrometers, without the use of additional adhesion layers. We explain the observed adhesion improvement as polarization-induced increased strength of Auδ-Siδ+ bonds at the Au-SiO2 interface due to the formation of a gold oxide monolayer on the Au surface by the UV-ozone treatment. Our simple and enabling method thus provides opportunities for patterning Au micro/nanostructures on SiO2 substrates without an intermediate metallic adhesion layer, which is critical for biosensing and nanophotonic applications.
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PURPOSE: To investigate the use of a cold atmospheric plasma (CAP) source in a clinically realistic endodontic procedure to enhance the bond strength of a dental adhesive in root canal restoration. MATERIALS AND METHODS: CAP was generated by a handheld DBD-jet prototype specifically designed for biomedical applications. Extracted monoradicular teeth were standardized through crown sectioning and root canal shaping before being embedded in epoxy resin cylinders using a custom molding procedure designed to ensure the accurate alignment of the specimens. Afterwards, the dentin surface was conditioned according to different protocols including (or not, in controls) chelating agents (EDTA or IP6) and CAP treatment (180 s). Then a self-etch adhesive was applied, followed by a luting material to seal the root canal. Both materials were light cured. Tooth sections were obtained from coronal and middle portions of the root canal, and the push-out test was used to evaluate the bond strength between the adhesive and dentin. RESULTS: Push-out results demonstrated that plasma treatment greatly improved (> twofold) the mechanical properties of the adhesive-dentin interface along the whole length of the root canal. Contact angle measurements and SEM analyses showed that plasma treatment facilitated adhesive permeation into dentinal tubules, hence enhancing the effects of the bonding procedure. CONCLUSIONS: Although investigations on long-term bond stability after CAP treatment and clinical studies are required, the present study indicates that CAP devices may be useful in clinical endodontic treatment.
Asunto(s)
Recubrimiento Dental Adhesivo , Gases em Plasma , Técnica de Perno Muñón , Cementos Dentales , Cavidad Pulpar , Dentina , Recubrimientos Dentinarios , Ensayo de Materiales , Cementos de Resina , Preparación del Conducto RadicularRESUMEN
We study the adhesion of a surface with a 'dimple' which shows a mechanism for a bi-stable adhesive system in surfaces with spaced patterns of depressions, leading to adhesion enhancement, high dissipation and hysteresis. Recent studies were limited mainly to the very short range of adhesion (the so-called JKR regime), while we generalize the study to a Maugis cohesive model. A 'generalized Tabor parameter', given by the ratio of theoretical strength to elastic modulus, multiplied by the ratio of dimple width to depth has been found. It is shown that bistability disappears for generalized Tabor parameter less than about 2. Introduction of the theoretical strength is needed to have significant results when the system has gone in full contact, unless one postulates alternative limits to full contact, such as air entrapment, contaminants or fine scale roughness. Simple equations are obtained for the pull-off and for the full contact pressure in the entire set of the two governing dimensionless parameters. A qualitative comparison with results of recent experiments with nanopatterned bioinspired dry adhesives is attempted in light of the present model.
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Modelos TeóricosRESUMEN
An approach to polymer surface modification using self-assembled layers (SALs) of functional alkoxysilanes has been developed in order to improve the printability of silver nanoparticle inks and enhance adhesion between the metal conducting layer and the flexible polymer substrate. The SALs have been fully characterized by AFM, XPS, and WCA, and the resulting printability, adhesion, and electrical conductivity of the screen-printed metal contacts have been estimated by cross-cut tape test and 4-point probe measurements. It was shown that (3-mercaptopropyl)trimethoxysilane SALs enable significant adhesion improvements for both aqueous- and organic-based silver inks, approaching nearly 100% for PEN and PDMS substrates while exhibiting relatively low sheet resistance up to 0.1 Ω/sq. It was demonstrated that SALs containing functional -SH or -NH2 end groups offer the opportunity to increase the affinity of the polymer substrates to silver inks and thus to achieve efficient patterning of highly conductive structures on flexible and stretchable substrates.