Balata rubber

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. 

An alternative source of the frani-1,4-polyisoprene is balata, obtained from Mimosups balata, occurring in Venezuela, Barbados and Guyana. The latex is thin and may be tapped in the same way as natural rubber. 

The infrared spectra of hevea (natural rubber), balata (or guttapercha), the latter both in the crystalline (a) and the amorphous forms, and of synthetic polyisoprene are compared in Fig. 32. The hevea and balata (amorphous) spectra offer calibrations for cfs-1,4 and irans-1,4 structures, respectively, in the synthetic polymer. Owing to the presence of the methyl substituent, however, the spectral difference between the as and trans forms is slight both absorb at about 840... 

The hard thermoplastic hydrocarbon obtained from the latex of Mimusops globosa. Balata has the same molecular formula as natural rubber (C5H8)n but has the tram polyisoprene structure whereas natural rubber has c/ s-structure. 

A class of hydrocarbons occurring in many essential oils of plants. They can be regarded as low-molecular weight polymers of isoprene (C5I I8)n. Dipentene is a terpene, while natural rubber, gutta percha and balata have been termed polyterpenes. 

Before 1800 Cotton, flax, wool, and silk fibers bitumens caulking materials glass and hydraulic cements leather and cellulose sheet (paper) natural rubber Hevea brasiliensis), gutta percha, balata, and shellac 1839 Vulcanization of rubber (Charles Goodyear)... 

Natural rubber (Hevea brasiliensis) is as-poly-2-methyl-1,4-butadiene, and gutta-percha (Palaquium oblongi/olium) and balata (Minusops globosa) are polymers of isoprene (2-methyl-1,4-butadiene) with trans configurations. Neoprene is a polymer of 2-chloro-1,3-butadiene (chloroprene). 

Natuial rubber (Hevea) Natsyn 2200° Kuraray TP-301d Natural balata... 

Cis-1,4 polyisoprene (natural rubber or synthetic isoprene rubber) and trans-1,4 polyisoprene (balata or guttah-percha) show strongly different properties. 

Some of the polybutadienes obtained with transition metal-based coordination catalysts have practical significance the most important is cA-1,4-polybutadiene, which exhibits excellent elastomeric properties. As regards isoprene polymers, two highly stereoregular polyisoprenes, a cA-1,4 polymer (very similar to natural rubber) and a trans- 1,4-polymer (of equal structure to that of gutta percha or balata) have been obtained with coordination catalysts. Various polymers of mixed 3,4 structure, amorphous by X-ray, were also obtained [7]. 

By contrast, cis- 1,4-polyisoprene is produced in limited amounts, since it is not price competitive with natural rubber (owing to the relatively high costs of manufacturing the isoprene monomer). The same applies to trans- 1,4-polyisoprene, which is more expensive than its natural counterparts gutta percha and balata. 

The polymer in natural rubber (from the Hevea bmsiliensis tree) is pure cis polyisoprene gutta percha and balata are composed of the trans isomer. 

Related Calculations. This procedure is valid for conveyors using rubber belts reinforced with cotton duck, open-mesh fabric, cords, or steel wires. It is also valid for stitched-canvas belts, balata belts, and flat-steel belts. The required horsepower input includes any power absorbed by idler pulleys. 

Polymers with unsaturated carbon chain backbone form another important class of macromolecules, many of the compounds from this class having properties of elastomers. The most common polymers from this class are obtained from 1,3-butadiene, 2-methyl-1,3-butadiene (isoprene) and their derivatives. Natural rubber, which is poly(c/s-isoprene), as well as the natural polymers gutta-percha and balata also have an unsaturated carbon chain backbone. For many practical applications, the polymers from this class are subject to a process known as vulcanization, which consists of a reaction with sulfur or S2CI2, and leads to the formation of bridges between the molecular chains of the polymer. This process significantly improves certain physical properties of practical interest. A separate subclass of polymers with unsaturated carbon chain backbone is formed by polyacetylene. 

Polyisoprene (R = CH3) with a c/s-1,4 configuration is common in nature in different species of piants and is known as natural rubber. Trans-polyisoprene is found in two naturai resins known as gutta-percha and balata. Natural or synthetic polyisoprenes, as well as polybutadiene, are among the most common elastomers with many practical uses. Other elastomers with extensive practical applications are copolymers, many of them using butadiene or isoprene in the starting monomer mixture. 

Balata tree, Mimusops Balata, have achieved economic importance or are considered as resources for natural mbber as a renewable polymer. Chemically, natural rubbers are polyterpenes consisting of 1,4-c -(mbber) or 1,4-frans-(gutta-percha, balata) polyisoprene, generated by enzymatically catalyzed biosynthetic polymerization of isoprene, and stabilized by phospholipids. 

Natural rubber is 1,4-polyisoprene and the polymer configuration is cis at each double bond in the chain, as shown , in (XI). Consequently, the polymer molecule has a bent and less symmetrical structure. Natural rubber does not crystallize at room temperature and is amorphous and elastomeric. Balata (guttapercha) is also... 

The high-impact PS, HIPS, has been known since 1911 [Matthews, 1911, 1913]. In the USA, Ostromislensky [1924, 1926-28] patented copolymerization of styrene with rubber, balata or other elastic and plastic gum . Production of HIPS, Victron , by the Naugatuck Chemical started in 1925, but soon it was discontinued. 

Solution Balata is the name of the rubber grown in South America. Its chemical name is poly-trans-risoprene and the... 

However, the excellent cold properties of the lithium polymer can be explained on the basis of microstructure in Table II. It seems reasonable to assume that of the three possible microstructures the 1,2 structure is the least desirable for low temperature flexibility followed by the frans-1,4 structure, with the cis-1,4 structure the most desirable. A comparison of the low temperature flexibility of balata (or gutta-percha) vs. Hevea rubber would indicate a preference for the cis-1,4 structure over the trans-1,4 structure, although these natural products are polyisoprenes rather than polybutadienes. In the case of the 1,2 structure, it is generally assumed that the prevalence of this structure in sodium-catalyzed polybutadiene, or butadiene copolymers, accounts for its poor cold properties however, the occurrence of a natural or synthetic product with an entirely 1,2 structure would help to confirm this more definitely. The relative predominance of any single structure is another important consideration in the performance of a rubber at low temperatures because a polymer with a large percentage of one structure would be more likely to crystallize at a low temperature. 

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