Natural rubber elastomeric nature

Spandex fibres have replaced natural rubber elastomeric fibres in various... 

Spandex fibres have replaced natural rubber elastomeric fibres in various applications such as foundation garments on account of their greater strength, improved ageing characteristics and easier dyeability. They are also used in stretch fabrics. 

Compatibility and Corrosion. Gas turbine fuels must be compatible with the elastomeric materials and metals used in fuel systems. Elastomers are used for O-rings, seals, and hoses as well as pump parts and tank coatings. Polymers tend to swell and to improve their sealing abiUty when in contact with aromatics, but degree of swell is a function of both elastomer-type and aromatic molecular weight. Rubbers can also be attacked by peroxides that form in fuels that are not properly inhibited (see Elastomers, synthetic Rubber, natural). 

Non-elastomeric chemical derivatives of natural rubber are discussed in Chapter 30 in which chemically related naturally occurring materials such as gutta percha and balata are briefly considered. 

The chemistry and technology of natural rubber were considered briefly in Chapter 11. In this chapter some non-elastomeric derivatives will be reviewed. 

The aim of this chapter is to describe the micro-mechanical processes that occur close to an interface during adhesive or cohesive failure of polymers. Emphasis will be placed on both the nature of the processes that occur and the micromechanical models that have been proposed to describe these processes. The main concern will be processes that occur at size scales ranging from nanometres (molecular dimensions) to a few micrometres. Failure is most commonly controlled by mechanical process that occur within this size range as it is these small scale processes that apply stress on the chain and cause the chain scission or pull-out that is often the basic process of fracture. The situation for elastomeric adhesives on substrates such as skin, glassy polymers or steel is different and will not be considered here but is described in a chapter on tack . Multiphase materials, such as rubber-toughened or semi-crystalline polymers, will not be considered much here as they show a whole range of different micro-mechanical processes initiated by the modulus mismatch between the phases. 

Rubber base adhesives, also called elastomeric adhesives, are widely used in industrial and household applications. In fact, about one-third of the adhesives used in the World are made from natural or synthetic rubbers. Some of the elastomeric adhesive systems showing industrial importance in recent years are the following ... 

Some rubber base adhesives need vulcanization to produce adequate ultimate strength. The adhesion is mainly due to chemical interactions at the interface. Other rubber base adhesives (contact adhesives) do not necessarily need vulcanization but rather adequate formulation to produce adhesive joints, mainly with porous substrates. In this case, the mechanism of diffusion dominates their adhesion properties. Consequently, the properties of the elastomeric adhesives depend on both the variety of intrinsic properties in natural and synthetic elastomers, and the modifying additives which may be incorporated into the adhesive formulation (tackifiers, reinforcing resins, fillers, plasticizers, curing agents, etc.). 

The first elastomeric adhesive was prepared at the end of the 18th Century and consisted of naphtha solutions of natural rubber. This kind of adhesive is currently... 

The chemical nature and molecular weight of the rubber will greatly determine the properties of elastomeric adhesives. However, some common characteristics can be found in most of the rubber base adhesives. The elastomeric adhesives show the following specific features in assembly operations. 

In general, the reaction mechanism of elastomeric polymers with vulcanisation reagents is slow. Therefore, it is natural to add special accelerators to rubber compounds to speed the reaction. Accelerators are usually organic compounds such as amines, aldehyde-amines, thiazoles, thiurams or dithio-carbamates, either on their own or in various combinations. 

Latex Also called emulsion. It is an aqueous dispersion of natural or synthetic elastomeric rubbers and plastics (dispersions of plastic particles in water). 

Polymers containing each of these configurations are known, the most common being the cis- A and the 1,4-isomers. The first of these, poly(c/ -l,4-isoprene), is the macromolecular constituent of natural rubber the second is the material known as gutta percha. The latter, unlike natural rubber, has no elastomeric properties, but has a leathery texture. It has been used for diverse applications such as golf-ball covers and as an insulating material for the trans-Atlantic cables of the late nineteenth century. 

Chattopadhyay S., Chaki T.K., and Bhowmick A.K., New thermoplastic elastomers from poly(ethyle-neoctene) (engage), poly(ethylene-vinyl acetate) and low-density polyethylene by electron beam technology structural characterization and mechanical properties. Rubber Chem. TechnoL, 74, 815, 2001. Roy Choudhury N. and Dutta N.K., Thermoplastic elastomeric natural rubber-polypropylene blends with reference to interaction between the components. Advances in Polymer Blends and Alloys Technology, Vol. 5 (K. Finlayson, ed.), Technomic Publishers, Pensylvania, 1994, 161. 

Roy Choudhury N., De P.P., and Bhowmick A.K., Thermoplastic elastomeric natural rubber-polyolefin blends. Thermoplastic Elastomers from Rubber Plastic Blend (De S.K. and Bhowmick A.K., eds.), Ellis Horwood, London, 1990, 11. 

Roy Choudhury N. and Bhowmick A.K., Compatibilization of natural rubber-polyolefin thermoplastic elastomeric blends by phase modification, J. Appl. Polym. Sci., 30, 1091, 1989. 

Choudhury N.R., Chaki T.K., Dutta A., and Bhowmick A.K. Thermal, x-ray and d3mamic mechanical properties of thermoplastic elastomeric natural rubber-polyethylene blends. Polymer, 30, 2047, 1989. Marasch M.J., TPU s Growth from versatility, 53rd Annual Tech. Conference, Antech 95 4088, Boston, May 7-11, 1995. 

Most polystyrene products are not homopolystyrene since the latter is relatively brittle with low impact and solvent resistance (Secs. 3-14b, 6-la). Various combinations of copolymerization and blending are used to improve the properties of polystyrene [Moore, 1989]. Copolymerization of styrene with 1,3-butadiene imparts sufficient flexibility to yield elastomeric products [styrene-1,3-butadiene rubbers (SBR)]. Most SBR rubbers (trade names Buna, GR-S, Philprene) are about 25% styrene-75% 1,3-butadiene copolymer produced by emulsion polymerization some are produced by anionic polymerization. About 2 billion pounds per year are produced in the United States. SBR is similar to natural rubber in tensile strength, has somewhat better ozone resistance and weatherability but has poorer resilience and greater heat buildup. SBR can be blended with oil (referred to as oil-extended SBR) to lower raw material costs without excessive loss of physical properties. SBR is also blended with other polymers to combine properties. The major use for SBR is in tires. Other uses include belting, hose, molded and extruded goods, flooring, shoe soles, coated fabrics, and electrical insulation. 

Certain elastomeric materials used as gaskets, seals, and hoses can be degraded by aromatic fuel components. Elastomers such as natural rubber, neoprene, Buna-N, and ethylene-propylene will all swell in the presence of aromatic fuel components. 

The solubility of gases in elastomeric membranes is related to the molecular weight of the diffusate molecule. Thus the ratio of the diffusion of oxygen to that of nitrogen differs in natural rubber and in ethylcellulose. 

The testing procedure of properties of elastomeric vulcanizates after immersion in organic liquids is common for both natural and synthetic rubbers. ASTM D171-66 [7] used for this purpose serves as a method for estimating the comparative ability of rubbers to withstand the effects of liquids by examination of the material after removal from the liquid. However proper testing of the physical properties on swollen rubber poses many problems. 

If solid polymer objects are fluorinated or polymer particles much larger than 100 mesh are used, only surface conversion to fluorocarbon results. Penetration of fluorine and conversion of the hydrocarbon to fluorocarbon to depths of at least 0.1 mm is a result routinely obtained and this assures nearly complete conversion of finely powdered polymers. These fluorocarbon coatings appear to have a number of potentially useful applications ranging from increasing the thermal stability of the surface and increasing the resistance of polymer surfaces to solvents and corrosive chemicals, to improving friction and wear properties of polymer surfaces. It is also possible to fluorinate polymers and polymer surfaces partially to produce a number of unusual surface effects. The fluorination process can be used for the fluorination of natural rubber and other elastomeric surfaces to improve frictional characteristics and increase resistance to chemical attack. 

Because of the nonuniform nature of the fibers studied, this work was necessarily empirical in nature. Its main purpose is to illustrate the unique properties and property trends of these elastomeric composites in comparison with conventional rubber compounds. 

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