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      Highly Efficient Rubber-to-Stainless Steel Bonding by Nanometer-Thin Cross-linked Polymer Brushes

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          Abstract

          Stainless steel (SS) surfaces were grafted with poly(glycidyl methacrylate) (PGMA) brushes that were post-modified using allylamine, diallylamine, and propylamine as reagents. Likewise, poly[2-(diethylamino)ethyl methacrylate] brushes were synthesized. All samples were compression molded with uncured ethylene-propylene-diene M-class rubber and dicumyl peroxide and vulcanized for 12 min at 170 °C. The efficiency of the novel bonding solution was evaluated through peel experiments. Two parameters, the fracture toughness ( ) and the cohesive-to-adhesive fracture ratio ( A r), were calculated to evaluate the strength and the performance of the coupling, respectively. For the nanometer-thin PGMA films modified with allylamine, in particular, full cohesive fracture was obtained. The obtained values of (15.4 ± 1.1 N mm –1) and A r (1.00 ± 0.01) matched those obtained for a micrometer-thick commercial bonding agent. Cross-linking of polymer brushes by intermolecular reactions by the primary amines proved to have a significant impact on the type of fracture (cohesive/adhesive) and the performance of the adhesives.

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          Most cited references34

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          Diminishing catalyst concentration in atom transfer radical polymerization with reducing agents.

          The concept of initiators for continuous activator regeneration (ICAR) in atom transfer radical polymerization (ATRP) is introduced, whereby a constant source of organic free radicals works to regenerate the Cu(I) activator, which is otherwise consumed in termination reactions when used at very low concentrations. With this technique, controlled synthesis of polystyrene and poly(methyl methacrylate) (Mw/Mn < 1.2) can be implemented with catalyst concentrations between 10 and 50 ppm, where its removal or recycling would be unwarranted for many applications. Additionally, various organic reducing agents (derivatives of hydrazine and phenol) are used to continuously regenerate the Cu(I) activator in activators regenerated by electron transfer (ARGET) ATRP. Controlled polymer synthesis of acrylates (Mw/Mn < 1.2) is realized with catalyst concentrations as low as 50 ppm. The rational selection of suitable Cu complexing ligands {tris[2-(dimethylamino)ethyl]amine (Me6TREN) and tris[(2-pyridyl)methyl]amine (TPMA)} is discussed in regards to specific side reactions in each technique (i.e., complex dissociation, acid evolution, and reducing agent complexation). Additionally, mechanistic studies and kinetic modeling are used to optimize each system. The performance of the selected catalysts/reducing agents in homo and block (co)polymerizations is evaluated.
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            Fracture mechanics and the adherence of viscoelastic bodies

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              Efficient synthesis of multifunctional polymers via thiol–epoxy “click” chemistry

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                17 December 2018
                31 December 2018
                : 3
                : 12
                : 17511-17519
                Affiliations
                [1] Interdisciplinary Nanoscience Center (iNANO) and §Carbon Dioxide Activation Center (CADIAC), Aarhus University , Gustav Wieds Vej 14, Aarhus C DK-8000, Denmark
                []Department of Chemistry, Aarhus University , Langelandsgade 140, Aarhus C DK-8000, Denmark
                []Department of Engineering, Aarhus University , Hangøvej 2, Aarhus N DK-8200, Denmark
                []Department of Engineering, Aarhus University , Inge Lehmanns Gade 10, Aarhus DK-8000, Denmark
                []Radisurf ApS , Arresøvej 5B, Risskov DK-8240, Denmark
                Author notes
                Article
                10.1021/acsomega.8b02312
                6643628
                12f5277b-2eca-4a33-aaef-42829ed4f8b9
                Copyright © 2018 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 07 September 2018
                : 23 November 2018
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                ao-2018-02312w

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