Al-2.4 Adhesion Promoter

2021 ◽  
Author(s):  
Richard G. Jones ◽  
Christopher K. Ober ◽  
Teruaki Hayakawa ◽  
Christine K. Luscombe ◽  
Natalie Stingelin
Keyword(s):  
2011 ◽  
Vol 39 (1) ◽  
pp. 20-43 ◽  
Author(s):  
A. Ashirgade ◽  
P. B. Harakuni ◽  
W. J. Vanooij

Abstract Adhesion between rubber compound and brass-plated steel tire cord is crucial in governing the overall performance of tires. The rubber-brass interfacial adhesion is influenced by the chemical composition and thickness of the interfacial layer. It has been shown that the interfacial layer consists mainly of sulfides and oxides of copper and zinc. This paper discusses the effect of changes in the chemical composition and the structure of the interfacial layers due to addition of adhesion promoter resins. Grazing incidence x-ray diffraction (GIXRD) experiments were run on sulfidized polished brass coupons previously bonded to five experimental rubber compounds. It was confirmed that heat and humidity conditions lead to physical and chemical changes of the rubber-steel tire cord interfacial layer, closely related to the degree of rubber-brass adhesion. Morphological transformation of the interfacial layer led to loss of adhesion after aging. The adhesion promoter resins inhibit unfavorable morphological changes in the interfacial layer, thus stabilizing it during aging and prolonging failure. Tire cord adhesion tests illustrated that the one-component resins improved adhesion after aging using a rubber compound with lower cobalt loading. Based on the acquired diffraction profiles, these resins were also found to impede crystallization of the sulfide layer after aging, leading to improved adhesion. Secondary ion mass spectrometry depth profiles and scanning electron microscopy micrographs strongly corroborated the findings from GIXRD. This interfacial analysis adds valuable information to our understanding of the complex nature of the rubber-brass bonding mechanism.


1999 ◽  
Vol 565 ◽  
Author(s):  
N. Ariel ◽  
M. Eizenberg ◽  
E. Y. Tzou

AbstractIn order to achieve better performance of devices, the interconnects RC delay time, the limiting factor of the device speed today, must be reduced. This calls for a new interconnect stack: lower resistivity Copper and low k materials (k<3) as dielectrics.Fluorinated amorphous carbon (a-F:C) prepared by HDP- CVD is an attractive candidate as a low-k material. In this work we have studied the film, its stability and its interface with Copper metallization. The high density plasma CVD process resulted in a film which contains C and F at a ratio of 1:0.6 as determined by Nuclear Reactions Analysis. XPS analysis of the Cls transition indicated four types of bonds: C-C, C-CF, CF, and CF2. X-ray diffraction as well as high resolution TEM analyses proved that the film was amorphous at least up to 500°C anneal. For various applications, the advantage of adding a thin bi-layer of a-SiC/SiOx for adhesion promotion purposes was demonstrated. In addition, the interface of a-F:C and the adhesion promoter layer with Ta, TaN and Cu was studied. No interdiffusion was observed by SIMS after 400°C annealing. 500°C annealing caused F outdiffusion from the film and Cu diffusion into the adhesion promoter layer.


2017 ◽  
Vol 22 (1) ◽  
pp. 1-7
Author(s):  
Vikas Garg ◽  
Yuvika Mittal ◽  
Shefally Garg ◽  
Munish Goel ◽  
Sanjeev Soni ◽  
...  

2020 ◽  
Author(s):  
Mohammad Hossein Mazaheri Kouhani ◽  
Alexander Istomin ◽  
Proyag Datta ◽  
Neil H. Talbot

Advances in neural prosthetic technologies demand ever increasing novelty in material composition to enhance the mechanical and electrochemical properties of existing microelectrode arrays. Conductive polymers present advantages such as mechanical flexibility, outstanding biocompatibility, remarkable electrical properties and, most of all, cellular agreement. However, for long-term chronic applications, they fall short in their electrochemical endurance and mechanical adhesion to their substrate materials. Multiple electrochemical approaches have been investigated to improve the adherence of Poly(3,4-ethylenedioxythiophene) (PEDOT) to underlying metallic thin films. In this work, an electrochemical treatment of diazonium salt on platinum microelectrodes is incorporated as an electrochemical adhesion promoter for PEDOT and it is further combined with using the highly microporous geometry of Platinum Grey (Pt-Grey); a technology developed by Second Sight Medical Products Inc (SSMP). The intertwined mechanical integration of Pt-Grey and PEDOT molecules together with the covalent binding agency of diazonium salt demostrate a composite coating technology with long-term stability of more than 452 days while providing >70× enhancement to the interfacial capacitive impedance.


BioResources ◽  
2017 ◽  
Vol 12 (4) ◽  
pp. 8134-8159
Author(s):  
Rico John ◽  
Katja Trommler ◽  
Katja Schreiter ◽  
Carolin Siegel ◽  
Frank Simon ◽  
...  

Wood veneer/biopolyethylene (bio-PE) biocomposite materials were produced by using poly(N-vinylformamide-co-vinylamine) (PVFA-co-PVAm) copolymers as a phase-mediating reagent. In a preliminary step, PVFA-co-PVAm was adsorbed onto the wood veneer component from aqueous solution. In its adsorbed form, it served as an adhesion promoter and improved the compatibility between both the highly polar wood veneer and weakly polar bio-PE surface. Structural parameters and their effect on the adsorption process, such as the degree of hydrolysis (DH) of poly(N-vinylformamide) (PVFA) (30, 50, and > 90%), the molecular weight of PVFA-co-PVAm (Mw 10,000, 45,000, or 340,000 g/mol), and the pH value (4, 7, and 11) influenced the resulting wetting behavior of the PVFA-co-PVAm-modified wood veneer surface. Thus, the hydrophobizing effect of the PVFA-co-PVAm was clearly detectable because the contact angle with water was considerably increased up to 116° by adsorption of PVFA-co-PVAm 9095 at pH 11. The adsorbed amount of PVFA-co-PVAm was determined by energy-dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS). The PVFA-co-PVAm-coated wood veneers were consolidated with bio-PE in a hot press process. The modified composite materials showed remarkably improved Young’s moduli (552 MPa) and tensile strengths (4.5 MPa) compared to former composite materials produced without PVFA-co-PVAm modification.


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