Solution, natural rubber

Gutta pereha has a lower water absorption than natural rubber and is a good dielectric. It is dissolved by carbon disulphide, chloroform and benzene but alkaline solutions and dilute acids do not affect it. It is destroyed by nitric acid and charred by warm concentrated sulphuric acid but resists hydrofluric acid. 

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 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 ]. 

Standard-grade PSAs are usually made from styrene-butadiene rubber (SBR), natural rubber, or blends thereof in solution. In addition to rubbers, polyacrylates, polymethylacrylates, polyfvinyl ethers), polychloroprene, and polyisobutenes are often components of the system ([198], pp. 25-39). These are often modified with phenolic resins, or resins based on rosin esters, coumarones, or hydrocarbons. Phenolic resins improve temperature resistance, solvent resistance, and cohesive strength of PSA ([196], pp. 276-278). Antioxidants and tackifiers are also essential components. Sometimes the tackifier will be a lower molecular weight component of the high polymer system. The phenolic resins may be standard resoles, alkyl phenolics, or terpene-phenolic systems ([198], pp. 25-39 and 80-81). Pressure-sensitive dispersions are normally comprised of special acrylic ester copolymers with resin modifiers. The high polymer base used determines adhesive and cohesive properties of the PSA. 

Chemical Reactivity - Reactivity with Water Reacts slowly to form flammable hydrogen gas, which can accumulate in closed area Reactivity with Common Materials Corrosive to natural rubber, some synthetic rubbers, some greases and some lubricants Stability During Transport Stable Neutralizing Agents for Acids and Caustics Flush with 3% aqueous ammonia solution, then with water. Methyl alcohol may also be used Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. 

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. 

Handbook of elastomers , A.K. Bhowmick and H.L. Stephens Marcel Dekker (1988) Series Plastics Engineering, Volume 19 ISBN 0824778006. This handbook systematically addresses the manufacturing techniques, properties, processing, and applications of rubbers and rubber-like materials. The Handbook of Elastomers provides authoritative information on natural rubbers, synthetic rubbers, liquid rubbers, powdered rubbers, rubber blends, thermoplastic elastomers, and rubber-based composites— offering solutions to many practical problems encountered with rubber materials. 

Many authors studying the formation of ECC from melts and solutions suggested that preliminary unfolding and extension of macromolecules occurs. Keller and Maehin25 have shown that in all known cases (including such extreme variants as the crystallization of natural rubber under extension and a polyethylene melt under flow) the same initial process of linear nucleation occurs and fibrillar structures is formed by the macromolecu-lar chains oriented parallel to the fibrillar axes27. ... 

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. 

Polysaccharides such as starch and cellulose have been used as reinforcing agents in natural rubber. Both solution blending and dry mixing methods have been employed for the development of biocomposites and the performance compared with the composites obtained using carbon black. Dry mixing method is more economically viable and environment friendly. 

FIGURE 3.12 Morphology of mbber-silica hybrid composites synthesized from solution process using different solvents (a) and (b) are the scanning electron microscopic (SEM) pictures of acrylic rubber (ACM)-silica hybrid composites prepared from THF (T) and ethyl acetate (EAc) (E) and (c) and (d) are the transmission electron microscopic (TEM) pictures of epoxidized natural rubber (ENR)-siUca hybrid composites synthesized from THF and chloroform (CH). (From Bandyopadhyay, A., De Sarkar, M., and Bhowmick, A.K., J. Appl. Polym. Sci., 95, 1418, 2005 and Bandyopadhyay, A., De Sarkar, M., and Bhowmick, A.K., J. Mater. Sci., 40, 53, 2005. Courtesy of Wiley InterScience and Springer, respectively.)... 

FIGURE 33.8 Strain dependence of G for oil extended solution SBR (OESSBR)/BR and natural rubber (NR) filled with a variety of fillers. 

Gee ° has applied this method to the determination of the interaction parameters xi for natural rubber in various solvents. Several rubber vulcanizates were used. The effective value of VelV for each was determined by measuring its extension under a fixed load when swollen in petroleum ether. Samples were then swollen to equilibrium in other solvents, and xi was calculated from the swelling ratio in each. The mean values of xi for the several vulcanizates in each solvent are presented in Table XXXVI, where they are compared with the xi s calculated (Eq. XII-30) from vapor pressure measurements on solutions of unvulcanized rubber in some of the same solvents. The agreement is by no means spectacular, though perhaps no worse than the experimental error in the vapor pressure method. 

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).

Figure 5.9 GALDI mass spectrum of natural rubber (from toluene/THF solution) on silver doped graphite matrix. The signal spacing of 68 Da corresponds to the isoprene monomer...

Conversion of a liquid into vapour, without necessarily raising the temperature to the boiling point of the liquid solutions are concentrated by evaporating off the solvent. One method of concentrating natural rubber latex is by the controlled evaporation of the liquid in which the rubber particles are dispersed. 

An aqueous colloid/emulsion of rubber particles can be up to 65% solids content generally low viscosity compared to polymer solutions. Only rubbers produced by emulsion polymerisation or natural rubber can be found in this form. 

A test which is claimed to be a more reliable guide to the condition of a natural rubber latex than the KOH number. The test is performed by steam distillation of the latex and titration of the distillate with standard alkali solution. The VFA number is a measure of the state of degradation of the latex. 

When the USA and Germany were cut off from the supplies of natural rubber during the Second World War both countries sought to produce a synthetic alternative SBR was the result, and at one stage it was the most commonly used synthetic rubber. It can be produced by both emulsion and solution polymerisation techniques, with the emulsion grades being the most widely used. Emulsion polymerisation yields a random copolymer, but the temperature of the polymerisation reaction also controls the resultant properties obtained. Cold polymerisation yields polymers with superior properties to the hot polymerised types. 

P.B1.25 is very fast in application it is fast to fats, oils, soap, and paraffin, which makes it a suitable candidate for packaging inks. Its lightfastness, however, is not excellent. In natural rubber, P.B1.25 tolerates curing very well, and it bleeds neither into the rubber nor into the fabric backing (Sec. 1.8.3.6). In rubber, the pigment is fast to cold and hot water, to soap, soda, and alkali solutions, and to acetic acid. 

When we compared the viscosities of solutions of natural rubber and of guttapercha and of other elastomers and later of polyethylene vs.(poly)cis-butadiene, with such bulk properties as moduli, densities, X-ray structures, and adhesiveness, we were greatly helped in understanding these behavioral differences by the studies of Wood (6) on the temperature and stress dependent, melting and freezing,hysteresis of natural rubber, and by the work of Treloar (7) and of Flory (8) on the elasticity and crystallinity of elastomers on stretching. Molecular symmetry and stiffness among closely similar chemical structures, as they affect the enthalpy, the entropy, and phase transitions (perhaps best expressed by AHm and by Clapeyron s... 

M. A. Lopez-Manchado, B. Herrero, M. Arroyo, Organoday-natural rubber nanocomposites synthesized by mechanical and solution mixing methods, Polym Int, vol. 53, pp. 766-1772, 2004. 

Solution polymerization is bulk polymerization in which excess monomer serves as the solvent. Solution polymerization, used at approximately 13 plants, is a newer, less conventional process than emulsion polymerization for the commercial production of crumb mbber. Polymerization generally proceeds by ionic mechanisms. This system permits the use of stereospecific catalysts of the Ziegler-Natta or alkyl lithium types which make it possible to polymerize monomers into a cis structure characteristic that is very similar to that of natural rubber. This cis structure yields a rubbery product, as opposed to a trans stmcture which produces a rigid product similar to plastics. 

The small peak at 1.25 ppm is representative of an impurity(ies) that was not removed during the extraction process. Further purification from an ethanolic solution reduces the impurity(ies) to an insignificant level. These peak positions are in excellent agreement with literature values for natural rubber (Hevea). 

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