Polybutadiene-vinyl .styrene

PS (polystyrene), PVC [poly(vinyl chloride)], PC (bisphenol A polycarbonate) PMMA [poly (methyl methacrylate)], PB (polybutadiene), SAN (styrene-acrylonitrile copolymer),NBR (acrylonitrile-butadiene rubber), PPE (polyphenylene ether), SBR (styrene-butadiene rubber)... 

Takeuchi, Y. Yoshimura, Y. Ohshima, N. Sakakibara, M. High Vinyl Polybutadiene or Styrene-Butadiene Copolymer. U.S. Patent 4,397,994, Aug 9, 1983 Japan Synthetic Rubber. 

These properties determine how carbon black will be distributed within the blend. These properties are not those of the filler but are the essential properties of the matrix. The matrix thus has strong influence on particle distribution. SEM studies showed that high vinyl polybutadiene and styrene-butadiene copolymers had morphologically identical carbon black distribution. However, their mechanical properties were very different. NMR analysis indicated that the difference in mechanical behavior is related to the interaction and more precisely to the molecular motions in rubbery matrix. 

HIPS) is produced commercially by the emulsion polymerization of styrene monomer containing dispersed particles of polybutadiene or styrene-butadiene (SBR) latex. The resulting product consists of a glassy polystyrene matrix in which small domains of polybutadiene are dispersed. The impact strength of HIPS depends on the size, concentration, and distribution of the polybutadiene particles. It is influenced by the stereochemistry of polybutadiene, with low vinyl contents and 36% d5-l,4-polybutadiene providing optimal properties. Copolymers of styrene and maleic anhydride exhibit improved heat distortion temperature, while its copolymer with acrylonitrile, SAN — typically 76% styrene, 24% acrylonitrile — shows enhanced strength and chemical resistance. The improvement in the properties of polystyrene in the form of acrylonitrile-butadiene-styrene terpolymer (ABS) is discussed in Section VILA. 

More recently, lightly crosslinked, suspension-sized particles have been evaluated. Chemically, networks based on polybutadiene, poly-styrene, or poly(vinyl chloride) have been suggested. These particles are swellable in the unsaturated polyester-styrene mix, but are substantially insoluble in it. On curing the polyester, an IPN is formed. 

Various workers have discussed aspects other than those mentioned above in studies of the viscoelastic properties of polymers. These include PVOH [62], hydroxy-terminated polybutadiene [63], styrene-butadiene and neoprene-type blends [64], and polyamidoimides [65]. Other aspects of viscoelasticity that have been studied include relaxation phenomena in PP [66] and methylmethacrylate-N-methyl glutarimide copolymers [67], shear flow of high-density polyethylene [68], Tg of PMMA and its copolymers with N-substituted maleimide [69] and ethylene-vinyl acetate copolymers [70], and creep behaviour of poly(p-phenylene terephthalate) [71] and PE [72]. 

More recent studies include the use of near-IR spectroscopy to determine cis 1,4, trans 1,4 and 1.2 butadiene units in polybutadiene and styrene butadiene copolymers [12] and Fourier transform Raman spectroscopy to determine cis 1,4, trans 1,4 and vinyl 1,2 contents of polybutadienes [13-15]. 

Polybutadiene/ high vinyl Styrene-butadiene copolymer Butyl rubber- ... 

Styrene-butadiene by NIR. Polybutadiene and styrene-butadiene copolymer are used extensively in the tire and rubber industries. As mentioned earlier in this chapter, there are various stereoisomers associated with the polymerization of butadiene cis-, trans-, and vinyl, and their relative amounts appreciably affect the polymer properties. NMR and infrared spectroscopy can accurately determine the microstructure and composition of these materials. These methods usually require extensive sample preparation and usually, dissolving the polymer in a solvent or pressing the polymer into a thin film. 

Scanning electrochemical microscopy (SECM) has been applied to polymethylmethacrylate, polystyrene and polyethylene glycol. Surface enhanced infrared reflection microscopy was applied to polyacrylonitrile, polybutadiene and styrene resins whilst Fourier transform infrared spectroscopy was applied to polyimides. Finally, nuclear magnetic resonance spectroscopy has been applied to the examination of the surfaces of films of polyethylene, Suryln and ethylene-vinyl acetate copolymer. ... 

It is possible by this technique to quantify small amounts of 1,2-vinyl, and the absence of trans 1,4 units. Other workers who have investigated the applications of NMR spectroscopy to the analysis of unsaturation in polybutadiene and styrene-butadiene copolymers include Carlson and Altenau [28], Carlson and co-workers [26], Binder [27], Braun and Canji [29, 30], Hast and Deur-Siftar [31], Silas and co-workers [32], Cornell and Koenig [21], Neto and Di Lauro [33], Clark and Chen [34] and Harwood and Richey [35]. 

Figure 9.17 Plot of log [i ]M versus retention volume for various polymers, showing how different systems are represented by a single calibration curve when data are represented in this manner. The polymers used include linear and branched polystyrene, poly(methyl methacrylate), poly(vinyl chloride), poly(phenyl siloxane), polybutadiene, and branched, block, and graft copolymers of styrene and methyl methacrylate. [From Z. Grubisec, P. Rempp, and H. Benoit, Polym. Lett. 5 753 (1967), used with permission of Wiley.]...

Fig. 15. Oxygen permeability versus 1/specific free volume at 25 °C (30). 1. Polybutadiene 2. polyethylene (density 0.922) 3. polycarbonate 4. polystyrene 5. styrene-acrylonitrile 6. poly(ethylene terephthalate) 7. acrylonitrile barrier polymer 8. poly(methyl methacrylate) 9. poly(vinyl chloride) 10. acrylonitrile barrier polymer 11. vinyUdene chloride copolymer 12. polymethacrylonitrile and 13. polyacrylonitrile. See Table 1 for unit conversions.

In the mid-1970s there was a short period during which styrene was in very short supply. This led to the development of what were known as high-vinyl polybutadienes which contained pendent vinyl groups as a result of 1,2-polymer-isation mechanisms. These rubbers had properties similar to those of SBR and could replace the latter should it become economically desirable. 

NR, styrene-butadiene mbber (SBR), polybutadiene rubber, nitrile mbber, acrylic copolymer, ethylene-vinyl acetate (EVA) copolymer, and A-B-A type block copolymer with conjugated dienes have been used to prepare pressure-sensitive adhesives by EB radiation [116-126]. It is not necessary to heat up the sample to join the elastomeric joints. This has only been possible due to cross-linking procedure by EB irradiation [127]. Polyfunctional acrylates, tackifier resin, and other additives have also been used to improve adhesive properties. Sasaki et al. [128] have studied the EB radiation-curable pressure-sensitive adhesives from dimer acid-based polyester urethane diacrylate with various methacrylate monomers. Acrylamide has been polymerized in the intercalation space of montmorillonite using an EB. The polymerization condition has been studied using a statistical method. The product shows a good water adsorption and retention capacity [129]. 

The yield of cross-linking depends on the microstructure of polybutadiene and purity of the polymer as well as on whether it is irradiated in air or in vacuum. The cross-link yield, G(X), has been calculated to be lowest for trans and highest for vinyl isomer [339]. The introduction of styrene into the butadiene chain leads to a greater reduction in the yield of cross-linking, than the physical blends of polybutadiene and polystyrene [340]. This is due to the intra- and probably also intermolecular energy transfer from the butadiene to the styrene constituent and to the radiation stability of the latter unit. 

Block copolymers of polystyrene with rubbery polymers are made by polymerizing styrene in the presence of an unsaturated rubber such as 1,4 polybutadiene or polystyrene co-butadiene. Some of the growing polystyrene chains incorporate vinyl groups from the rubbers to create block copolymers of the type shown in Fig. 21.4. The combination of incompatible hard polystyrene blocks and soft rubber blocks creates a material in which the different molecular blocks segregate into discrete phases. The chemical composition and lengths of the block controls the phase morphology. When polystyrene dominates, the rubber particles form... 

The polybutadienes prepared with these barium t-butoxide-hydroxide/BuLi catalysts are sufficiently stereoregular to undergo crystallization, as measured by DTA ( 8). Since these polymers have a low vinyl content (7%), they also have a low gl ass transition temperature. At a trans-1,4 content of 79%, the Tg is -91°C and multiple endothermic transitions occur at 4°, 20°, and 35°C. However, in copolymers of butadiene (equivalent trans content) and styrene (9 wt.7. styrene), the endothermic transitions are decreased to -4° and 25°C. Relative to the polybutadiene, the glass transition temperature for the copolymer is increased to -82°C. The strain induced crystallization behavior for a SBR of similar structure will be discussed after the introduction of the following new and advanced synthetic rubber. 

Grafting of styrene (ST) onto polybutadiene (PB) can occur in two ways Via a chain-transfer reaction with an allylic hydrogen of the 1,4- and the 1,2-units (Case 1) via copolymerization with C=C-double bounds of polybutadiene, in particular with the vinyl groups of the 1,2-units (Case 2) ... 

Homopolymers of polybutadiene can consist of three basic isomeric forms (czs-1,4, trans-1,4, and 1,2 vinyl), and these can be present in different sequential order. Copolymers may obtain a variety of co-monomers, such as styrene, acrylonitrile, etc. Depending on their distribution in the chain, random copolymers or block copolymers of different types and perfection can be produced. There are many synthetic elastomers based on butadiene available commercially. 

The last property is related to the processing of the rubber in the tire making equipment. By using organo-lithium compound in this case, it was possible to maintain a vinyl content not greater than 18, but to produce a polybutadiene styrene copolymer that has random block styrene and without the use of polar modifiers, which normally will increase the 1,2 content. This copolymer, when compounded in the tread recipe, as shown in the Table XVI, gave properties that are actually equivalent to that of emulsion SBR and in some cases even better. This is particularly true in the properties of the Young modulus index, which showed between -38 to -54 C the Stanley London Skid Resistant, in which the control is 100, shows that 110-115 was obtained. 

Butadiene is used primarily in the production of synthetic rubbers, including styrene-butadiene rubber (SBR), polybutadiene nibber (BR), styrene-butadiene latex (SBL), chloroprene rubber (CR) and nitrile rubber (NR). Important plastics containing butadiene as a monomeric component are shock-resistant polystyrene, a two-phase system consisting of polystyrene and polybutadiene ABS polymers consisting of acrylonitrile, butadiene and styrene and a copolymer of methyl methacrylate, butadiene and styrene (MBS), which is used as a modifier for poly(vinyl chloride). It is also used as an intermediate in the production of chloroprene, adiponitrile and other basic petrochemicals. The worldwide use pattern for butadiene in 1981 was as follows (%) SBR + SBL, 56 BR, 22 CR, 6 NR, 4 ABS, 4 hexamethylenediamine, 4 other, 4. The use pattern for butadiene in the United States in 1995 was (%) SBR, 31 BR, 24 SBL, 13 CR, 4 ABS, 5 NR, 2 adiponitrile, 12 and other, 9 (Anon., 1996b). 

HMX HMX HMX HMX HMX HMX HMX HMX HMX HMX HMX HMX HNS NTO NTO/HMX NTO/HMX NTO/HMX PETN PETN PETN PETN PETN PETN PETN PETN PETN PETN RDX RDX RDX RDX RDX RDX RDX RDX RDX RDX RDX RDX RDX TATB/HMX Cariflex (thermoplastic elastomer) Hydroxy-terminated polybutadiene (polyurethane) Hydroxy-terminated polyester Kraton (block copolymer of styrene and ethylene-butylene) Nylon (polyamide) Polyester resin-styrene Polyethylene Polyurethane Poly(vinyl) alcohol Poly(vinyl) butyral resin Teflon (polytetrafluoroethylene) Viton (fluoroelastomer) Teflon (polytetrafluoroethylene) Cariflex (block copolymer of butadiene-styrene) Cariflex (block copolymer of butadiene-styrene) Estane (polyester polyurethane copolymer) Hytemp (thermoplastic elastomer) Butyl rubber with acetyl tributylcitrate Epoxy resin-diethylenetriamine Kraton (block copolymer of styrene and ethylene-butylene) Latex with bis-(2-ethylhexyl adipate) Nylon (polyamide) Polyester and styrene copolymer Poly(ethyl acrylate) with dibutyl phthalate Silicone rubber Viton (fluoroelastomer) Teflon (polytetrafluoroethylene) Epoxy ether Exon (polychlorotrifluoroethylene/vinylidine chloride) Hydroxy-terminated polybutadiene (polyurethane) Kel-F (polychlorotrifluoroethylene) Nylon (polyamide) Nylon and aluminium Nitro-fluoroalkyl epoxides Polyacrylate and paraffin Polyamide resin Polyisobutylene/Teflon (polytetrafluoroethylene) Polyester Polystyrene Teflon (polytetrafluoroethylene) Kraton (block copolymer of styrene and ethylene-butylene)... 

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