Surface treatment rubber

It should not be forgotten that a poor mould design will lead to a poor bond, irrespective of the surface treatment Rubber to metal bonding processii effects. 

Pastor-Sempere N., Eemandez-Garcfa J.C., Orgiles-Barcelo A.C., Pastor-Bias M.M., Martfn-Martfnez J.M., and Dillard J.G., 1998, Surface treatment of styrene-butadiene rubber with carboxylic acid, in First International Congress on Adhesion Science and Technology, W.J. van Ooij and H.R. Anderson Jr. (Eds), Utrecht, VSP, 461 94. 

Xu, Z.N., Losur, S., and Gardner, S.D., Epoxy resin filled with tire rubber particles modified by plasma surface treatment, J. Adv. Mater., 30, 11, 1998. 

Cellulose fibres produced from hardwoods, with various chemical surface treatments to ensure that they are compatible with rubbers, can be used to produce high modulus vulcanisates. The bond between rubber and fibres is created during vulcanisation. These fibres can be used to reinforce extruded hoses gaining orientation in the direction of flow. There is a range of fibres available which are compatible with different rubber types. 

Incorporated in plasticized PVC, P.B.15, like other phthalocyanine pigments, is usually entirely fast to migration. Moreover, it provides excellent lightfastness. P.B.15 also finds use in various types of PUR foam materials as well as in rubber. Its redder and frequently cleaner shade compared to corresponding stabilized types makes it an equally useful pigment for other media. This applies especially for water-based systems. Textile printing, paper mass coloration, paper surface treatment, and paper pulp are areas of application as suitable for the use of P.B.15 as office articles, including colored pencils, blackboard chalks for schools, and water colors. 

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. 

The dynamic response of polydimethylsiloxane (PDMS) reinforced with fused silica with and without surface treatment has been discussed in terms of interactions between the filler and polymer [54]. Since bound rubber measurements showed that PDMS chains were strongly attached to the silica surface, agglomeration due to direct contact between silica aggregates was considered an unlikely explanation for the marked increase in storage modulus seen with increasing filler content at low strains. Instead three types of flller-polymer-flller association were proposed which would cause agglomeration, as depicted in Fig. 15. 

Phosphoric acid is used as an intermediate in the production of animal feed supplements, water treatment chemicals, metal surface treatments, etching agent, and personal care products such as toothpaste. It is used as a catalyst in the petroleum and polymer industry. Phosphoric acid is used in food as a preservative, an acidulant, and flavor enhancer it acidifies carbonated drinks such as Coca Cola and Pepsi, giving them a tangy flavor. Phosphoric acid is used as a rust remover and metal cleaner. Naval Jelly is approximately 25% phosphoric acid. Other uses for phosphoric acid include opacity control in glass production, textile dyeing, rubber latex coagulation, and dental cements. 

Another attempt by Tricas et al. to modify the surface of carbon black was by the plasma polymerization of acrylic acid [34]. Treatment with acrylic acid made carbon black hydrophilic. Plasma-coated carbon black was mixed with natural rubber and showed increased filler-filler interaction. The bound rubber content was reduced after the surface treatment of the filler. The authors also concluded that the surface of the carbon black was completely covered by the plasma polymer film, preventing the carbon black surface from playing any role in the polymer matrix. 

In the past, BCME was used for crosslinking of cellulose, preparation of styrene and other polymers, surface treatment of vulcanized rubber to increase adhesion, and in the manufacture of flameretardant fabrics (EPA 1980a). These applications have been discontinued, and no uses of BCME other than as a nonisolated intermediate were identified. 

Presently DOE is funding Air Products Chemical Company for the development of a fluorine surface treatment of tire rubber (crumb rubber) to modify its adhesion properties. This modified rubber could be used in making polymers such as polyurethane and epoxies. The tire rubber might also be used in certain plastics such as polystyrene and PVC, and in rubber products (68). 

Surface treatments consist of washing with solvent, abrading, or, in the most demanding applications, cyclizing with acid. The most common elastomers to be bonded in this way include nitrile, neoprene, urethane, natural rubber, SBR, and butyl rubber. It is more difficult to achieve good bonds with silicones, fluorocarbons, chlorosulfonated polyethylene, and polyacrylate. 

A wide variety of special durable surface treatments have been used on manufactured fibers. These include treatments for imparting such characteristics as soil resistance, antistatic behavior, and wearer comfort through moisture wicking and transport. Fiber finishes also have been used successfully in promoting adhesion between two materials, as, for example, between polyester tire cord and rubber, and between glass fiber and polyester resin. 

The hydrophobicity of the surface prevents the wetting by tear and tends to expose dry surface of a contact lens. Therefore, rapid dehydration of the corneal tissues could occur, which could cause the damage of corneal epithelium. However, this explanation seems to be oversimplified in light of the adsorption of protein, which makes a hydrophobic surface wettable by tear fluid, as described in Chapter 26. Moreover, the highly hydrophobic surface characteristic of silicone rubber tends to encourage the deposition of protein and mucus of the tear on the surface of the lens. Lipids and lipid-soluble materials follow the same track and eventually penetrate into the bulk phase of the contact lens. Because of these undesirable factors, the use of silicone contact lenses of various chemical compositions and with surface treatments has not been successful but rather disastrous because of the interfacial characteristics of silicone contact lens on the cornea, which cannot be oflfset by these efforts. It indicates that more profound surface modification to cope with the problems rather than mere surface treatment is needed in capitalizing on the advantageous bulk properties of silicone polymers. 

Smith, E.J. Coatings and surface treatments for rubber closures for parenterals. PDA Annual Meeting Washington, DC, 1999. 

This equation was used to estimate the interfacial adhesion in comparison with the acid-base properties of glass fibers in LDPE. The effect of surface treatment of glass beads on their interfacial adhesion to PET was also estimated from a mechanical property measurement. A mathematical model describing the adsorption of polymers on filler surfaces related coupling density to the average area available for coupling between rubber and filler surface. ... 

Silicones pure silicon, fumed silica, silanes, silicone resins and rubbers Materials advanced ceramics, boron compounds, surface treatments and silicon carbide. 

---