Butyl rubber blends

Figure 6 Dependence of Izod impact strength on the DMAE concentration in 80 20 PS-bromo butyl rubber blends. Source Ref. 53.

Maziad, N. A., Hassan, M. M., Study of some properties of waste LDPE/waste butyl rubber blends using different compatibUizing agents and gamma irradiation. Journal of Applied Polymer Science 2007,106(6), 4157-4163. 

With bromobutyl/butyl rubber blends, elastomer structures are essentially the same, but the different reactive functionalities provide different vulcanization chemistry. Since bromobutyl rubber has greater cure reactivity, accelerators that will over-cure the bromobutyl rubber phase should be avoided. Briefly... 

So, a top quality tyre, as required for high speed litxury vehicles, is constructed of three different kinds of rubber in the sidewall (often polybutadiene blends), carcase (natural rubber) and tread (often butyl rubber blends). For a less expensive tyre, constructed totally of natural rubber, a similar (though lesser) effect can be achieved by using more flexible, lightly vulcanised, rubber in the sidewall and higher modulus, more extensively vulcanised, and so more tightly cross-linked, rubber in the tread. 

CHEMICAL RESISTANCE OF 30 VISTALON 6505/70 BUTYL RUBBER BLEND COMPOUND... 

An adhesive consisting of an epoxy resin, a medium high acrylonitrile rubber, and Pb, Cu, Ni, Pd or Co compound fillers was used to bond EPDM vulcanizates. Peel strengths of 22.5 kg/20 mm after a 1 hour at 100 C cure were obtained. Another adhesive composition involving a blend of carboxylated nitrile rubber, epoxy resin and a reactive metal filler has been described for bonding EPDM vulcanizates or EPDM rubber-nitrile or butyl rubber blends. 

Shield and co-workers [37] also used Py-GC-MS to estimate the composition of styrene-butyl rubber/Neoprene butyl rubber blends. Py-GC-MS products that were characteristic of each polymer were identified. The Py-GC-MS peak areas were used to determine the blend composition and this was in agreement with results obtained by TGA. 

In addition to compatibility studies, DSC is often used to characterise the properties of a blend. For example. Van dyke etal [66] have used it to investigate a number of variables (e.g. rubber type, rubber content and degree of cure) on the properties of polyamide 12/butyl rubber blends. More examples of the application of DSC to the characterisation of blends are given in Section 6.4.3. 

Van Dyke ID, Gnatowski M, Koutsandreas A, Burczyk A. Effect of butyl rubber type on properties of polyamide and butyl rubber blends. / Appl Polym Sci 2004 93(3) 1423-1435. 

As mentioned in Section 8.1.1, ethylene-propylene elastomers are currently used in compounds for tyre sidewalls. In this application also ternary blends have been used, including halogenated butyl rubber.With regard to EPDM and butyl rubber blends, there are no covulcanisation problems because both have a similar level of unsaturation. 

In the early stages of development of polypropylene rubbers, particularly butyl rubber, were used to reduce the brittleness of polypropylene. Their use declined for some years with the development of the polypropylene copolymers but interest was greatly renewed in the 1970s. This interest has been centred largely around the ethylene-propylene rubbers which are reasonably compatible in all proportions with polypropylene. At first the main interest was with blends in which the rubber content exceeded 50% of the blend and such materials have been designated as thermoplastic polyolefin elastomers (discussed in Section 11.9.1). There is also increasing interest in compounds with less than 50% rubber, often referred to as elastomer-modified thermoplastics. It is of interest to note... 

Chlorobutyl rubber is prepared by chlorination of butyl rubber (chlorine content is about 1 wt%). This is a substitution reaction produced at the allylic position, so little carbon-carbon double unsaturation is lost. Therefore, chlorobutyl rubber has enhanced reactivity of the carbon-carbon double bonds and supplies additional reactive sites for cross-linking. Furthermore, enhanced adhesion is obtained to polar substrates and it can be blended with other, more unsaturated elastomers. 

Several partially cross-linked butyl rubbers are commercially available. The more tightly cross-linked grades are designed for butyl tapes. On the other hand, various depolymerized butyl rubbers and butyl/plasticizers blends are also available. 

Cohesive strength of these adhesives can be modified by blending butyl rubber and polyisobutylene. Higher strength is obtained by using high molecular weight PIB or butyl rubber. On the other hand, blends of butyl rubber or PIB with chlorinated butyl rubber show improved cure properties. 

Rubber blends with cure rate mismatch is a burning issue for elastomer sandwich products. For example, in a conveyor belt composite structure there is always a combination of two to three special purpose rubbers and, depending on the rubber composition, the curatives are different. Hence, those composite rubber formulations need special processing and formulation to avoid a gross dissimilarity in their cure rate. Recent research in this area indicated that the modification of one or more rubbers with the same cure sites would be a possible solution. Thus, chlorosulfonated polyethylene (CSP) rubber was modified in laboratory scale with 10 wt% of 93% active meta-phenylene bismaleimide (BMI) and 0.5 wt% of dimethyl-di-(/ r/-butyl-peroxy) hexane (catalyst). Mixing was carried out in an oil heated Banbury-type mixer at 150-160°C. The addition of a catalyst was very critical. After 2 min high-shear dispersive melt mix-... 

TPEs from blends of rubber and plastics constitute an important category of TPEs. These can be prepared either by the melt mixing of plastics and rubbers in an internal mixer or by solvent casting from a suitable solvent. The commonly used plastics and rubbers include polypropylene (PP), polyethylene (PE), polystyrene (PS), nylon, ethylene propylene diene monomer rubber (EPDM), natural rubber (NR), butyl rubber, nitrile rubber, etc. TPEs from blends of rubbers and plastics have certain typical advantages over the other TPEs. In this case, the required properties can easily be achieved by the proper selection of rubbers and plastics and by the proper change in their ratios. The overall performance of the resultant TPEs can be improved by changing the phase structure and crystallinity of plastics and also by the proper incorporation of suitable fillers, crosslinkers, and interfacial agents. 

Park et al. [20] reported on the synthesis of poly-(chloroprene-co-isobutyl methacrylate) and its compati-bilizing effect in immiscible polychloroprene-poly(iso-butyl methacrylate) blends. A copolymer of chloroprene rubber (CR) and isobutyl methacrylate (iBMA) poly[CP-Co-(BMA)] and a graft copolymer of iBMA and poly-chloroprene [poly(CR-g-iBMA)] were prepared for comparison. Blends of CR and PiBMA are prepared by the solution casting technique using THF as the solvent. The morphology and glass-transition temperature behavior indicated that the blend is an immiscible one. It was found that both the copolymers can improve the miscibility, but the efficiency is higher in poly(CR-Co-iBMA) than in poly(CR-g-iBMA),... 

Plastics, such as PE, PP, polystyrene (PS), polyester, and nylon, etc., and elastomers such as natural rubber, EPDM, butyl rubber, NR, and styrene butadiene rubber (SBR), etc., are usually used as blend components in making thermoplastic elastomers. Such blends have certain advantages over the other type of TPEs. The desired properties are achieved by suitable elasto-mers/plastic selection and their proportion in the blend. 

It is possible to distinguish between SBR and butyl rubber (BR), NR and isoprene rubber (IR) in a vulcan-izate by enthalpy determination. In plastic-elastomer blends, the existence of high Tg and low Tg components eases the problems of experimental differentiation by different types of thermal methods. For a compatible blend, even though the component polymers have different Tg values, sometimes a single Tg is observed, which may be verified with the help of the following equation ... 

The reactive extrusion of polypropylene-natural rubber blends in the presence of a peroxide (1,3-bis(/-butyl per-oxy benzene) and a coagent (trimethylol propane triacrylate) was reported by Yoon et al. [64]. The effect of the concentration of the peroxide and the coagent was evaiuated in terms of thermal, morphological, melt, and mechanical properties. The low shear viscosity of the blends increased with the increase in peroxide content initially, and beyond 0.02 phr the viscosity decreased with peroxide content (Fig. 9). The melt viscosity increased with coagent concentration at a fixed peroxide content. The morphology of the samples indicated a decrease in domain size of the dispersed NR phase with a lower content of the peroxide, while at a higher content the domain size increases. The reduction in domain size... 

Generally, systems developed in the USA favour a combination of polyethylene with either butyl-rubber or hot-applied mastic adhesives, the latter consisting of a blend of rubber, asphalt and high molecular weight resins. In European and Far East coating plants, epoxy type primers and hard ethylene copolymer adhesives have been successfully employed. 

Halogenated butyl rubber, 4 436 annual capacity, 4 451t blends with brominated... 

Figure 10 shows a spectrum of butyl rubber gum stock obtained on the solid at 80°C using normal pulsed FT techniques. Clearly it could be identified as a component in fabricated materials by direct nmr spectral analysis. Figure 11 shows spectra obtained from various portions of typical rubber products. These samples were cut from the rubber product, placed in an nmr tube without solvent, and spectra obtained at an elevated temperature. The data show how polyisoprene, a polyisoprene/polybutadiene blend and a polyisobutylene/polyisoprene/polybutadiene rubber blend are quickly identified in the materials. Figure 11a shows processing oil was present, and which was confirmed by solvent extraction. 

The carcass requires better flexing properties than the tread and is a blend of natural rubber and SBR, but at least 60% of natural rubber. The sidewalls have a lower percentage of natural rubber, from 0-50%. The liner is made of butyl rubber because of its extreme impermeability to air. 

More than 800 million pounds of EPM and EPDM polymers were produced in the United States in 2001. Their volume ranks these materials fourth behind styrene-1,3-butadiene copolymers, poly( 1,4-butadiene), and butyl rubber as synthetic rubbers. EPM and EPDM polymers have good chemical resistance, especially toward ozone. They are very cost-effective products since physical properties are retained when blended with large amounts of fillers and oil. Applications include automobile radiator hose, weather stripping, and roofing membrane. 

CA 67, 433(1967) (A description of several nonrupturing detonating cords is given. As an example, one of them is prepd by inserting a blend of PETN 85 with equal parts mixt of butyl rubber terpene resin 15% into an elastometric polyurethane sheath. 

Berlin and coworkers (5,56) desired to obtain a material with an increased mechanical strength. They carried out a plasticization of bulk ami emulsion polystyrene molecular weight 80000 and 200000 respectively at 150-160° C, with polyisobutylene, butyl rubber, polychloroprene, polybutadiene, styrene rubber (SKS-30) and nitrile rubber (SKN 18 and SKN 40). The best results were obtained with the blends polystyrene-styrene rubber and polystyrene-nitrile rubber. An increase of rubber content above 20-25% was not useful, as the strength properties were lowered. An increase in the content of the polar comonomer, acrylonitrile, prevents the reaction with polystyrene and decreases the probability of macroradical combination. This feature lowers the strength, see Fig. 14. It was also observed that certain dyes acts as macroradical acceptors, due to the mobile atoms of hydrogen of halogens in the dye, AX ... 

Butyl and Halobutyl Rubber. Butyl mbber is made by the polymerization of isobutylene a small amount of isoprene is added to provide sites for curing. It is designated HR because of these monomers. Halogenation of butyl mbber with bromine or chlorine increases the reaction rate for vulcanization and laminates or blends of halobutyl are feasible for production of mbber goods. It is estimated that of the 100 million kg of butyl (HR) and halobutyl (HIIR) mbber in North America, over 90% is used in tire applications. The halogenated polymer is used in the innerliner of tubeless tires. Butyl mbber is used to make innertubes and curing bladders. The two major suppliers of butyl and halobutyl polymers in North America are Exxon and Bayer (see ELASTOLffiRS, synthetic-butyl rubber). 

Other thermoplastic elastomer combinations, in which the elastomer phase may or may not be cross-linked, include blends of polypropylene with nitrile (30,31), butyl (33), and natural (34) rubbers, blends of PVC with nitrile mbber (35,36), and blends of halogenated polyolefins with ethylene interpolymers (29). Collectively, thermoplastic elastomers of this type are referred to herein as hard polymer/elastomer combinations. Some of the more important examples of the various types are shown in Table 3. 

S—EB—S (compounds) polyurethane/elastomer block copolymers polyester/elastomer block copolymers polyamide/elastomer block copolymers polyetherimide/polysiloxane block copolymers polypropylene/EPDM or EPR blends polypropylene/EPDM dynamic vulcanizates polypropylene/butyl rubber dynamic vulcanizates polypropylene/natural rubber dynamic vulcanizates polypropylene/nitrile rubber dynamic vulcanizates PVC/ nitrile rubber blends... 

Although two dissimilar elastomers—e.g., chlorinated butyl rubber and polybutadiene—may crosslink when in contact with one another, does bonding exist between the two interfaces Based upon thermodynamic theory as well as microscopic observations, we know that two such elastomers are not molecularly dispersed in a blend, so the diagnostic problem is one of considering two dispersed phases. 

PVC can be blended with numerous other polymers to give it better processability and impact resistance. For the manufacture of food contact materials the following polymerizates and/or polymer mixtures from polymers manufactured from the above mentioned starting materials can be used Chlorinated polyolefins blends of styrene and graft copolymers and mixtures of polystyrene with polymerisate blends butadiene-acrylonitrile-copolymer blends (hard rubber) blends of ethylene and propylene, butylene, vinyl ester, and unsaturated aliphatic acids as well as salts and esters plasticizerfrec blends of methacrylic acid esters and acrylic acid esters with monofunctional saturated alcohols (Ci-C18) as well as blends of the esters of methacrylic acid butadiene and styrene as well as polymer blends of acrylic acid butyl ester and vinylpyrrolidone polyurethane manufactured from 1,6-hexamethylene diisocyanate, 1.4-butandiol and aliphatic polyesters from adipic acid and glycols. 

Although most efforts have been devoted to the use of carbon nanotubes in glassy polymers, some studies have reported strong reinforcing effects of CNTs in elastomeric matrices such as butyl (23), natural (17,24-27) and styrene-butadiene rubbers (28-31) as well as styrene-butadiene and butadiene rubber blends (32). 

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