4.7 Article

Surface modification of acrylonitrile-butadiene-styrene (ABS) with heterogeneous photocatalysis (TiO2) for the substitution of the etching stage in the electroless process

Journal

SURFACE & COATINGS TECHNOLOGY
Volume 206, Issue 6, Pages 1410-1415

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.surfcoat.2011.09.005

Keywords

Electroless; ABS; Hexavalent chromium; Photocatalysis

Funding

  1. CONACYT [67134]

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The acrylonitrile-butadiene-styrene (ABS) is the most commonly used copolymer in industry for metallizing. The process in solution used for depositing metallic films on non-conductive substrates is known as electroless, which is an autocatalytic procedure. However, the sulfo-chromic admixture used to modify the ABS surface, in the first step of this process, is not environmentally suitable due to the use of Cr (VI), and its utilization implies a risk of severe damage to living beings. For this reason, a study of an alternative surface treatment with substantially lower levels concerning environmental impact is presented in this work, which is based on a photocatalytic reaction that is initiated on the copolymer surface by TiO2 nanoparticles (30 nm), as a suspension, under UV exposure. After surface conditioning with the photocatalytic treatment was conducted, the substrates were metallized in two different ways: electroless process or dynamic chemical process (DCP), with a subsequent conventional electrolytic deposit. The DCP does not need a surface activation with palladium ions, unlike electroless process, which simplified the procedure by reducing directly both, the effluents and the costs. The prepared substrates were characterized using: scanning electron microscopy (SEM), atomic force microscopy (AFM), atomic force acoustic microscopy (AFAM), mechanic profilometry, optical interference profilometry, profilometry by AFM, and a cross cut tape test. The results obtained with the proposed pre-treatment stage are shown and compared with those obtained in the conventional electroless process. (C) 2011 Elsevier B.V. All rights reserved.

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