Reactive adhesion promoters

A similar mechanism acts in the case of reactive adhesion promoters such as polyurethanes. Here water is a factor, as well as surface functional groups of fillers. The adhesion promoter is exhausted within the bulk of organic material (coating, adhesive, etc.) and unable to perform the task. 

Ricobond. [Ricon Resins] Reactive adhesive promoter for compounding with elastomers. 

To an experienced operator trained in the handling of industrial chemicals, the dimers present Httle cause for concern in handling or storage. The finished polymer coating presents even less of a health problem contact with the reactive monomer is unlikely. In the ancillary operations, such as cleaning or adhesion promotion, the operator must observe suitable precautions. Before using the process chemicals, operators must read and understand the current Material Safety Data Sheets, which are available from the manufacturers. 

Urethane sealants have good inherent adhesion to most substrates, but silane adhesion promoters are often used to improve this adhesion. Epoxy-, amino-, and mercapto-functional silanes are the most common because of their dual reactive nature. The silane end can react with surface hydroxyls the epoxy, amino, or mercapto end can react with the isocyanate. 

Adhesion promoting silanes are often added to improve adhesion to various substrates. As is the case with urethane sealants, silanes with a dual-reactive nature are typically used. Examples of such silanes are mercapto- and epoxy-functional silanes. Organic titanates may also be used. 

The chemical bonding theory of adhesion applied to silicones involves the formation of covalent bonds across an interface. This mechanism strongly depends on both the reactivity of the selected silicone cure system and the presence of reactive groups on the surface of the substrate. Some of the reactive groups that can be present in a silicone system have been discussed in Section 3.1. The silicone adhesive can be formulated so that there is an excess of these reactive groups, which can react with the substrate to form covalent bonds. It is also possible to enhance chemical bonding through the use of adhesion promoters or chemical modification of the substrate surface. 

Control of fiber friction is essential to the processing of fibers, and it is sometimes desirable to modify fiber surfaces for particular end-uses. Most fiber friction modifications are accomplished by coating the fibers with lubricants or finishes. In most cases, these are temporary treatments that are removed in final processing steps before sale of the finished good. In some cases, a more permanent treatment is desired, and chemical reactions are performed to attach different species to the fiber surface, e.g. siliconized slick finishes or rubber adhesion promoters. Polyester s lack of chemical bonding sites can be modified by surface treatments that generate free radicals, such as with corrosive chemicals (e.g. acrylic acid) or by ionic bombardment with plasma treatments. The broken molecular bonds produce more polar sites, thus providing increased surface wettability and reactivity. 

Under optimum conditions, hydrolysis is rapid, and precedes slower condensation reactions. However, the silanol groups formed in hydrolysis are very reactive, and condensation can be a significant factor even in dilute aqueous solutions. Understanding the kinetics of the hydrolysis and condensation reactions for a specific silane in solution is important because its effectiveness as an adhesion promoter is influenced by the extent of condensation, which, in turn, affects the structure of the interphase in composites. 

Because of this reactivity, primer solutions are formulated as very dilute (typically 0.1 vol %) solutions and used quickly. In industry, however, it is usually not practical to make a fresh APS solution for each application. Therefore, there is some concern as to how oligomerization will affect the adhesion promoting efficiency of such primer solutions over a typical 8-hour shift. 

In 1987 he was promoted to distinguished member of the technical staff and technical manager. His efforts broadened to include projects on polymer-surface interactions adhesion promotion corrosion protection chemical vapor deposition and thin film growth optical fiber coating synthesis, structure, and reactivity of model organic surfaces and time-resolved surface vibrational spectroscopy. 

Abstract The formation of stable metal/polymer joints is an enormous challenge in material sciences. Good adhesion requires an interphase which is able to specifically interact with the metal substrate as well as with the second component. Furthermore, the interphase should compensate thermally generated mechanical tensions between the two adhering components. It will be shown that statistic copolymers of poly(vinyl formamide) and poly(vinyl amine) (PVFA-co-PVAm) are potential candidates for adhesion promoters. The polyelectrolyte character of the copolymers allows to apply them from its aqueous solutions. The primary amino groups exhibit the copolymers as highly reactive to metal surfaces as well as to the second joint partner. The... 

There are a number of silane adhesion promoters available, and they differ in the nature of their reactivity to the resin or adhesive. Silanes may be produced with amine, epoxy, mercaptan, and other functionalities. Some examples are given in Table 10.1. 

Some highly reactive low-molecular-weight silanes are used as adhesion promoters or coupling agents, and chlorosilanes are used as intermediates. They will be reviewed in turn. 

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