Polyurethane Styrene butadiene rubber

Order-disorder transitions and spinodals were computed for linear multi block copolymers with differing sequence distributions by Fredrickson et al. (1992). This type of copolymer includes polyurethanes, styrene-butadiene rubber, high impact polystyrene (HIPS) and acrylonitrile-butadiene-styrene (ABS) block copolymers. Thus the theory is applicable to a broad range of industrial thermoplastic elastomers and polyurethanes. The parameter... 

Poly(ethylene terephtlhalate) Phenol-formaldehyde Polyimide Polyisobutylene Poly(methyl methacrylate), acrylic Poly-4-methylpentene-1 Polyoxymethylene polyformaldehyde, acetal Polypropylene Polyphenylene ether Polyphenylene oxide Poly(phenylene sulphide) Poly(phenylene sulphone) Polystyrene Polysulfone Polytetrafluoroethylene Polyurethane Poly(vinyl acetate) Poly(vinyl alcohol) Poly(vinyl butyral) Poly(vinyl chloride) Poly(vinylidene chloride) Poly(vinylidene fluoride) Poly(vinyl formal) Polyvinylcarbazole Styrene Acrylonitrile Styrene butadiene rubber Styrene-butadiene-styrene Urea-formaldehyde Unsaturated polyester... 

Polystyrene (PS) The volume of expanded polystyrene produced probably exceeds the volume production of all other plastics (excluding the polyurethanes) put together. At least half the weight of polystyrene produced is in the form of high impact polystyrene (HIPS)—a complex blend containing styrene-butadiene rubber or polybutadiene. 

Peel Strength Values of Vulcanized Styrene-Butadiene Rubber (SBR) Rubber/Polyurethane Adhesive/Leather Joints... 

FIGURE 27.2 T-peel sfrength values of sulfuric acid-treated styrene-butadiene rubber (SBR)/polyurethane adhesive joints as a function of the immersion time in sulfuric acid. A = adhesion failure R = cohesion failure in the rubber. (From Cepeda-Jimenez, C.M., Pastor-Bias, M.M., Ferrandiz-Gomez, T.P., and Martm-Martmez, J.M., J. Adhes., 73, 135, 2000.)... 

FIGURE 27.9 T-peel strength values of styrene-butadiene rubber (SBS) treated with chloramine T aqueous solutions with different pH/waterbome polyurethane adhesive/roughened leather joints, as a function of the pH value of the chloramine T aqueous solutions. A adhesion failure to the rubber, M cohesive failure in tbe rubber. (From Navarro-Banon, M.V., Pastor-Bias, M.M., and Martm-Martinez, J.M., Proceedings of the 27th Adhesion Society, Wilmington, NC.)... 

Femandez-Garcfa J.C., Orgiles-Barcelo, and A.C., Martm-Martmez J.M., 1991, Halogenation of styrene-butadiene rubber to improve its adhesion to polyurethanes, J. Adhes. Sci Technol, 5, 1065-1080. Oldfield D. and Symes T.E.F., 1983, Surface modification of elastomers for bonding, J. Adhes., 16, 77-96. Pastor-Bias M.M., Ferrandiz-Gomez T.P., and Martm-Martmez J.M., 2000, Chlorination of vulcanized styrene-butadiene rubber using solutions of trichloroisocyanuric acid in different solvents, J. Adhes. Sci. Technol, 14, 561-581. 

In 1994, the worldwide consumption of rubber was approximately 14.5 million tons a year, of which about 40% consisted of natural rubber. Natural rubber is produced as latex by tropical rubber trees (Hevea brasiliensis). It is processed locally and therefore the quality of natural rubber fluctuates remarkably [ 140]. Due to increasing demand for rubbers, combined with a decreasing production capacity in Asia and a vast increase in labor costs, the price of natural rubber is still rising sharply. In 1990-1994, the average price of natural rubber was about 0.38 /lb, while in 1996 it was already over 0.80 /lb. The remaining 60% of the articles were manufactured from synthetic petroleum-based rubbers such as isoprene rubber, styrene-butadiene rubber, chloroprene rubber and polyurethanes. The quality of synthetic rubbers is constant, and their price varies between 2 and 5 US per kilogram [137-140]. 

Ethylene-propylene rubber Fluoro-rubber Hypalon Natural rubber Neoprene rubber Nitrile rubber Polysulphide rubber Polyurethane rubber Silicone rubber Styrene-butadiene rubber (SBR)... 

Other reported TG-MS applications concern polybutadiene [153], styrene-butadiene rubbers [153], gums [14], polyisoprenes [52], polyurethanes [144, 146, 147, 166], ABS [144], chlorosulphonated polyethylene elastomer [169, 170] and elastomer blends (NBR/SBR/ BR) [13]. Table 1.5 summarises the use of advanced TG-MS systems in elastomer analysis. 

Styrene is the monomer for polystyrene and styrene-butadiene rubber. Propylene oxide is mainly used for the manufacture of propylene glycol and polyurethanes. 

Technology for preparing nanocomposites directly via compounding has been investigated by Vaia, Ishii, and Giannelis. Industrial R D efforts have focused on process technology (e.g., melt or monomer exfoliation processes), as there are a number of polymers (e.g., polyolefins) that do not lend themselves to a monomer process. Nanocomposites with a variety of polymers, including polyacrylates or methacrylates, polystyrene, styrene-butadiene rubber, epoxy, polyester, and polyurethane, are amenable to the monomer process. The enhancement of mechanical properties, gas permeability resistance, and heat endurance are the primary objectives for the application of PCN, and their success will establish PCNs as a major commercial product. 

Elastomers include natural rubber (polyisoprene), synthetic polyisoprene, styrene-butadiene rubbers, butyl rubber (isobutylene-isoprene), polybutadiene, ethylene-propylene-diene (EPDM), neoprene (polychloroprene), acrylonitrile-butadiene rubbers, polysulfide rubbers, polyurethane rubbers, crosslinked polyethylene rubber and polynorbomene rubbers. Typically in elastomer mixing the elastomer is mixed with other additives such as carbon black, fillers, oils/plasticizers and accelerators/antioxidants. 

There are two classes of polyolefin blends elastomeric polyolefin blends also called polyolefin elastomers (POE) and nonelastomeric polyolefin blends. Elastomeric polyolefin blends are a subclass of thermoplastic elastomers (TPEs). In general, TPEs are rubbery materials that are processable as thermoplastics but exhibit properties similar to those of vulcanized rubbers at usage temperatures (19). In TPEs, the rubbery components may constitute the major phase. However, TPEs include many other base resins, which are not polyolefins, such as polyurethanes, copolyamides, copolyesters, styrenics, and so on. TPEs are now the third largest synthetic elastomer in total volume produced worldwide after styrene-butadiene rubber (SBR) and butadiene mbber (BR). 

Polymer characterization is an important use of NIR spectrometry. Polymers can be made either from a single monomer, as is polyethylene, or from mixtures of monomers, as are styrene-butadiene rubber from styrene and butadiene and nylon 6-6, made from hexamethylenediamine and adipic acid. An important parameter of such copolymers is the relative amount of each present. This can be determined by NIR for polymers with the appropriate functional groups. Styrene content in a styrene-butadiene copolymer can be measured using the aromatic and aliphatic C—H bands. Nylon can be characterized by the NH band from the amine monomer and the C=0 band from the carboxylic acid monomer. Nitrogen-containing polymers such as nylons, polyurethanes, and urea formaldehyde resins can be measured by using the NH bands. Block copolymers, which are typically made of a soft block of polyester and a hard block containing aromatics, for example, polystyrene, have been analyzed by NIR. These analyses have utilized the... 

The efficacy of polyurethane and styrene butadiene rubber (SBR) as binders for ground rubber prepared from waste tires was compared to a formulation of a compound developed without binder. Without binder, the effect of both sulfur and accelerator content on tensile properties are studied, as well as the effect of ageing on these properties [29]. The suggested uses of the unbound product include rubber blocks, and ballast mats for railway applications. 

Besides melt intercalation, described above, in situ intercalative polymerization of E-caprolactone (e-CL) has also been used [231] to prepare polycaprolactone (PCL)-based nanocomposites. The in situ intercalative polymerization, or monomer exfoliation, method was pioneered by Toyota Motor Company to create nylon-6/clay nanocomposites. The method involves in-reactor processing of e-CL and MMT, which has been ion-exchanged with the hydrochloride salt of aminolauric acid (12-aminodecanoic acid). Nanocomposite materials from polymers such as polystyrene, polyacrylates or methacrylates, styrene-butadiene rubber, polyester, polyurethane, and epoxy are amenable to the monomer approach. 

World rubber usage of around 25.8 million metric tons is split between natural rubber, which constitutes about 43% of global consumption, and synthetic rubber, of which styrene-butadiene rubber (SBR) accounts for 21%. The balance of synthetic rubbers (36%) consists of polybutadiene rubber (BR) and a range of specialty polymers such as polyurethanes, halogenated polymers, silicones, and acrylates. Traditionally, the growth of synthetic and natural rubber consumption is virtually in line with the change in gross domestic product of, collectively. North America, Europe, Japan, China, and India. 

E/TFE = ethylene/tetrafluoroethylene, E/CTFE = ethylene/chlorotrifluoroethylene, EPE = oxide, E/VAL = ethylene/vinyl alcohol, FEP = tetrafluoroethylene/hexafluoropropylene, FU = furan, pA = polyamide, PCTFE = polychlorotrifluoroethyl-ene, HDPE = high-density polyethylene, PF = propylene formaldehyde, PFA = perfluoro alkoxyalkane, PP = polypropylene, PTFE = polytetrafluoroethylene, PUR = polyurethane, PVC = polyvinyl chloride, PVDF = polyvinylidene fluoride, UP = unsaturated polyester, UP-GF = fiberglass-reinforced unsaturated polyester, VE-GF = fiberglass-reinforced vinyl ester, FU-GF = fiberglass-reinforced furane, EP-GF = fiberglass-reinforced ester, CR = chloroprene rubber, CSM = chlo-rosulfonyl polyethylene, FPM = vinylidene fluoride/hexafluoropropylene copolymer, HR = isobutane-isoprene rubber, NBR = nitrile-butadiene rubber, NR = natural rubber, SBR = styrene-butadiene rubber. 

In the present paper an attempt was made to prepare cementitious (lightweight if possible) mortars by adding styrene butadiene rubber (SBR) or polyurethane (PU) waste particles to the mixtures. Mortars were characterized from mechanical and thermal points of view. 

As aggregate fractions, quartz sand (0-5 mm), styrene butadiene rubber (SBR) waste particles (0-12 mm) or polyurethane (PU) waste particles (0-12 mm) were used. Their bulk specific gravities were 2640 kg/m, 550 kg/m and 500 kg/m respectively and their gradations are shown in Fig. 1. 

Mortar Mixture Proportions. Mortar mixture proportions as well as the values of consistency of fresh mortars obtained by means of flow table (according to UNI EN 1015-3) are presented in Table 1. The water to cement ratio and the cement to sand ratio were kept equal to 0.60 and 1 3 (by weight) respectively. Styrene butadiene rubber (SBR) or polyurethane (PU) waste particles were alternatively added to the mixtures at a dosage of either 10% or 30% by volume of aggregate. 

Polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), polystyrene (PS), polymethylmethacrylate (PMMA) Ethylene-tetratluoro-ethylene (ETFE), tetrafluoroethylene/ hexafluoropropylene (THV), polyethylene (PE), polypropylene (PP) Epoxy resin (EP), polyester resin (UP), phenol resin (PF), resorcin resin (RF), polyurethane (PUR) Styrene-butadiene-rubber (SBR), polybutadiene-rubber (BR), ethylene-propylene-diene-rubber (EPDM)... 

Matty polymers may be used for produetion of wire and cable. These include polyethylene, crosslinked polyethylene, chlorosnlfonated polyethylene, ethylene-propylene rubber, polyvinylchloride, bntyl robber, styrene bntadiene rubber, silicone rubber, natural robber, polyisoprene robber, polyurethane, nitrile butadiene rubber, polychloroprene, polysulfone, thermoplastie elastomers, polyimide, and polyamides. Selection of polymer(s) depends on projected conditions of service such as temperature, presence of corrosive liquids, surrounding temperature, quality of insulation, etc. 

The category of elastomers includes a wide range of products, such as natural rubber (NR), styrene-butadiene rubber (SBR), styrene-butadiene-styrene copolymer (SBS known as thermoplastic rubber), styrene-isoprene-styrene copolymer (SIS), polyurethane rubber, polyether-polyester copolymer, olefinic copolymers, ethylene-propylene rubber (EPR) and so on (see also Table 3.16). 

The elastomeric group of adhesives is based on natural rubber latex and its derivatives or totally synthetic rubber known as SBR (styrene butadiene rubber). There is now a wide range of synthetic rubber adhesives based upon SBR including nitrile and butyl rubber. Another elastomeric adhesive is the versatile polyurethane rubber group. 

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