Natural rubber compounds solution

Figure 20 GC chromatogram of the dichloromethane partition solution from the distilled water extract of the natural rubber compound NR2 (24 h at 40°C).

Under Behavior Towards Metals and Other Substances. AN very definitely attacks shellac, baked oils and natural rubber compounds if applied as a coating. The only materials that we know of which can be used as coatings for AN and AN solutions are certain polyvinyl chloride coatings and a number of epoxy resins. The Ordnance Department used acid-proof black paint, shellac, baked oil and rubber paints. All were quite unsuccessful over long periods of time... 

The original compound, maleimide (2,5-dioxo-A -pyrroline), is synthesized by the cyclo-condensation of ammonia and maleic acid. Similarly, primary amine is added to maleic anhydride, followed by cyclocondensation, to form N-substituted maleimide (Fig. 2). This reaction is applied to the preparation of bis-maleimides (BMl) [1]. At first, BMI was used as a crosslinking agent for natural rubber (NR). An o-dichlorobenzene solution of NR was crosslinked by BMI at I08-150°C in the presence of peroxides. The radicals generated from peroxides react with the double bonds of both BMI and NR [ 1 ]. 

In the past chemical cure linings have been employed on a wide scale. These linings, usually based on natural rubber or acrylonitrile-butadiene rubber consist of a standard lining compound with a chemical activator such as dibenzylamine incorporated in the formulation. Prior to the application of the lining to the substrate, the individual sheets of rubber are dipped or brush coated with carbon disulphide or a solution of a xanthogen disulphide in a solvent. The carbon disulphide or xanthogen disulphide permeates the rubber and combines with the dibenzylamine to form an ultra-fast dithiocar-bamate accelerator in situ, and thus the rubber rapidly vulcanises at ambient temperature. 

There were essentially three reasons for this opposition. Firstly, many macromolecular compounds in solution behave as colloids. Hence they were assumed to be identical with the then known inorganic colloids. This in turn implied that they were not macromolecular at all, but were actually composed of small molecules bound together by ill-defined secondary forces. Such thinking led the German chemist C. D. Harries to pursue the search for the rubber molecule in the early years of the twentieth century. He used various mild degradations of natural rubber, which he believed would destroy the colloidal character of the material and yield its constituent molecules, which were assumed to be fairly small. He was, of course, unsuccessful. 

The information on physical properties of radiation cross-linking of polybutadiene rubber and butadiene copolymers was obtained in a fashion similar to that for NR, namely, by stress-strain measurements. From Table 5.6, it is evident that the dose required for a full cure of these elastomers is lower than that for natural rubber. The addition of prorads allows further reduction of the cure dose with the actual value depending on the microstructure and macrostructure of the polymer and also on the type and concentration of the compounding ingredients, such as oils, processing aids, and antioxidants in the compound. For example, solution-polymerized polybutadiene rubber usually requires lower doses than emulsion-polymerized rubber because it contains smaller amount of impurities than the latter. Since the yield of scission G(S) is relatively small, particularly when oxygen is excluded, tensile... 

The new absorptions in the spectra of crosslinked rubber are assigned on the basis of 13C solution NMR chemical shifts for a variety of model compounds, such as pentenes and mono-, di- and tri-sulfidic compounds, by using the 13C chemical shift substituent effect. From the calculated values for particular structural units, the experimental spectra of a sulfur vulcanized natural rubber 194,195,106), natural rubber cured by accelerated sulfur vulcanization 197 y-irradiation crosslinked natural rubber198 and peroxide crosslinked natural rubber and cis-polybutadiene 193 1991 are assigned. 

Another addition to polymers with main-chain unsaturation is the Prins reaction between ethylenic hydrocarbons and compounds containing aldehydic carbonyl groups. Kirchof in 1923, described the reaction of natural rubber in benzene solution with aqueous formaldehyde in the presence of concentrated sulfuric acid. The general reaction of an aldehyde, RCHO, with a polyisoprene in the presence of an inorganic or organic acid or an anhydrous metal salt, is represented by... 

Neoprene is also available in a variety of forms. In addition to a neoprene latex that is similar to natural rubber latex, neoprene is produced in a "fluid" form as either a compounded latex dispersion or a solvent solution. Once these materials have solidified or cured, they have the same physical and chemical properties as the solid or cellular forms. 

Thermoplastic rubber is a relatively new class of polymer. It has the solubility and thermoplasticity of polystyrene, while at ambient temperatures it has the toughness and resilience of vulcanized natural rubber or polybutadiene. These rubbers are actually block copolymers. The simplest form consists of a rubbery mid-block with two plastic end blocks (A-B-A), as shown in Figure 5.7. Examples of commercial products are Kraton and Solprene . These materials are often compounded with plasticizers to decrease hardness and modulus, eliminate drawing, enhance pressure-sensitive tack, improve low-temperature flexibility, reduce melt and solution viscosity, decrease cohesive strength or increase plasticity if desired, and substantially lower material costs. Low levels of thermoplastic rubbers are sometimes added to other rubber adhesives. These materials are used as components in the following applications PSAs, hot-melt adhesives, heat-activated-assembly adhesives, contact adhesives, reactive contact adhesives, building construction adhesives, sealants, and binders. Two common varieties of thermoplastic rubber adhesives are styrene-butadiene-styrene (S-B-S) and styrene-isoprene-styrene (S-I-S). ... 

NR composites and nanocomposites can be fabricated by three main techniques, namely latex compounding, solution mixing and melt blending. A variety of nanofillers, such as carbon black, silica, carbon nanotubes, graphene, calcium carbonate, organomodified clay, reclaimed rubber powder, recycled poly(ethylene terephthalate) powder, cellulose whiskers, starch nanocrystals, etc. have been used to reinforce NR composites and nanocomposites over the past two decades. In this chapter, we discuss the preparation and properties of NR composites and nanocomposites from the viewpoint of nanofillers. We divide nanofillers into four different types conventional fillers, natural fillers, metal or compound fillers and hybrid fillers, and the following discussion is based on this classification. 

Manufacture and compounding The majority of organic solvent-based adhesives are based on rubbery polymers, the main ones being natural rubber, polychloroprene, butadiene-acrylonitrile, styrene-butadiene and polyisobutylene. Traditionally, the rubber was placed in a heavy-duty mixer and solvent was added slowly till a smooth solution was formed. In some cases, the rubber was milled beforehand to reduce viscosity and produce smoother solutions. Nowadays, it is possible to obtain some grades of material that only require stirring in a comparatively simple chums. 

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