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Diene rubbers nitrile rubber

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. [Pg.634]

Because of the diene component, nitrile rubbers can be vulcanized with sulfur. A conventional curing system consists of 2.5 parts sulfur, 5.0 parts zinc oxide, 2.0 parts stearic acid, and 0.6 parts N-t-butylbenzothiazole-2-sulfenamide (TBBS) per 100 parts polymer. [Pg.413]

A very wide range of copolymers has been prepared in which a diene, particularly 1,3-butadiene, is the principal comonomer. Only a very small number have achieved commercial significance but one, styrene-butadiene rubber (SBR) has become the world s leading rubber in terms of tonnage consumption. Another, acrylonitrile-butadiene rubber (nitrile rubber, NBR) has been an important oil resistant rubber for some 40 years. It is these two rubbers which form the main subject matter of this chapter which also includes brief notes on two lesser known copolymers, butadiene-vinyl pyridine and butadiene-vinyl isopropyl ketone polymers and on novel alternating copolymers. [Pg.135]

MAJOR POLYMER APPLICATIONS ethylene propylene diene copolymer, nitrile rubber, polyethylene, polyimide, polyoxymethylene, polyvinylaloohol ... [Pg.22]

At one time butadiene-acrylonitrile copolymers (nitrile rubbers) were the most important impact modifiers. Today they have been largely replaced by acrylonitrile-butadiene-styrene (ABS) graft terpolymers, methacrylate-buta-diene-styrene (MBS) terpolymers, chlorinated polyethylene, EVA-PVC graft polymers and some poly acrylates. [Pg.341]

Chemistry of NBR. Nitrile rubbers are copolymers of a diene and a vinyl-unsaturated nitrile. The chemical structure of NBR is given in Fig. 5. [Pg.587]

Hydroformylation of nitrile rubber is another chemical modification that can incorporate a reactive aldehyde group into the diene part and further open up new synthetic routes to the formation of novel nitrile elastomers with a saturated backbone containing carboxyl or hydroxyl functionalities. [Pg.567]

ATBN - amine terminated nitrile rubber X - Flory Huggins interaction parameter CPE - carboxylated polyethylene d - width at half height of the copolymer profile given by Kuhn statistical segment length DMAE - dimethyl amino ethanol r - interfacial tension reduction d - particle size reduction DSC - differential scanning calorimetry EMA - ethylene methyl acrylate copolymer ENR - epoxidized natural rubber EOR - ethylene olefin rubber EPDM - ethylene propylene diene monomer EPM - ethylene propylene monomer rubber EPR - ethylene propylene rubber EPR-g-SA - succinic anhydride grafted ethylene propylene rubber... [Pg.682]

In one of the first reports on fiber reinforcement of rubber, natural rubber (NR) was used by Collier [9] as the rubber matrix, which was reinforced using short cotton fibers. Some of the most commonly used rubber matrices for fiber reinforcement are NR, ethylene-propylene-diene monomer (EPDM) rubber, styrene-butadiene rubber (SBR), polychloroprene rubber, and nitrile rubber [10-13]. These rubbers were reinforced using short and long fibers including jute, silk, and rayon [14—16]. [Pg.353]

The accelerated sulfur vulcanization of general-purpose diene rubbers (e.g., NR, styrene-butadiene rubber [SBR], and butadiene rubber [BR]) by sulfur in the presence of organic accelerators and other rubbers, which are vulcanized by closely related technology (e.g., ethylene-propylene-diene monomer [EPDM] mbber, butyl rubber [HR], halobutyl mbber [XIIR], nitrile rubber [NBR]) comprises more than 90% of all vulcanizations. [Pg.416]

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]. [Pg.866]

The ductility of GRT-polyethylene blends drastically decreases at ground rubber concentration in excess of 5%. The inclusion of hnely ground nitrile rubber from waste printing rollers into polyvinyl chloride (PVC) caused an increase in the impact properties of the thermoplastic matrix [76]. Addition of rubber powder that is physically modihed by ultrasonic treatment leads to PP-waste ethylene-propylene-diene monomer (EPDM) powder blends with improved morphology and mechanical properties [77]. [Pg.1050]

The isoprene units in the copolymer impart the ability to crosslink the product. Polystyrene is far too rigid to be used as an elastomer but styrene copolymers with 1,3-butadiene (SBR rubber) are quite flexible and rubbery. Polyethylene is a crystalline plastic while ethylene-propylene copolymers and terpolymers of ethylene, propylene and diene (e.g., dicyclopentadiene, hexa-1,4-diene, 2-ethylidenenorborn-5-ene) are elastomers (EPR and EPDM rubbers). Nitrile or NBR rubber is a copolymer of acrylonitrile and 1,3-butadiene. Vinylidene fluoride-chlorotrifluoroethylene and olefin-acrylic ester copolymers and 1,3-butadiene-styrene-vinyl pyridine terpolymer are examples of specialty elastomers. [Pg.20]

A gas, CH2CHCHCH2 (buta-1,3-diene), used in the manufacture of polybutadiene rubber and as one of the copolymers in the manufacture of styrene-butadiene and nitrile rubbers. [Pg.15]

Ethylene-propylene-diene monomer Butyl rubber d Nitrile rubber ... [Pg.220]

Several polymers based on 1,3-dienes are used as elastomers. These include styrene-1,3-butadiene (SBR), styrene-1,3-butadiene terpolymer with an unsaturated carboxylic acid (carboxylated SBR), acrylonitrile-1,3-butadiene (NBR or nitrile rubber) (Secs. 6-8a, 6-8e), isobutylene-isoprene (butyl rubber) (Sec. 5-2i-l), and block copolymers of isoprene or... [Pg.699]

Elastomers, synthetic -acrylic elastomers [ELASTOMERS, SYNTHETIC - ACRYLIC ELASTOMERS] (Vol 8) -butyl rubber [ELASTOMERS, SYNTHETIC - BUTYL RUBBER] (Vol 8) -chlorosulfonated polyethylene [ELASTOMERS, SYNTHETIC - CHLOROSULFONATED POLYETHYLENE] (Vol 8) -ethylene-acrylic elastomers [ELASTOMERS, SYNTHETIC - ETHYLENE-ACRYLIC ELASTOMERS] (Vol 8) -ethylene-propylene-diene rubber [ELASTOMERS,SYNTHETTC - ETHYLENE-PROPYLENE-DIENE RUBBER] (Vol 8) -fluorocarbon elastomers [ELASTOMERS, SYNTHETIC - FLUOROCARBON ELASTOMERS] (Vol 8) -nitrile rubber [ELASTOMERS, SYNTHETIC - NITRILE RUBBER] (Vol 8) -phosphazenes [ELASTOMERS, SYNTHETIC - PHOSPHAZENES] (Vol 8) -polybutadiene [ELASTOMERS, SYNTHETIC - POLYBUTADIENE] (Vol 8) -polychloroprene [ELASTOMERS, SYNTHETIC - POLYCHLOROPRENE] (Vol 8) -polyethers (ELASTOMERS, SYNTHETIC - POLYETHERS] (Vol 8) -polyisoprene [ELASTOMERSSYNTHETTC - POLYISOPRENE] (Vol 9) -survey [ELASTOMERS, SYNTHETIC - SURVEY] (Vol 8)... [Pg.354]

RUBBER (Synthetic). Any of a group of manufactured elastomers that approximate one or more of the properties of natural rubber. Some of these aie sodium polysulfide ( Thiokol ). polychloiopiene (neoprene), butadiene-styrene copolymers (SBR), acrylonitrilebutadiene copolymers (nitril rubber), ethvlenepropylene-diene (EPDM) rubbers, synthetic poly-isoprene ( Coral, Natsyn ), butyl rubber (copolymer of isobutylene and isoprene), polyacrylonitrile ( Hycar ). silicone (polysiloranei. epichlorohy-drin, polyurethane ( Vulkollan ). [Pg.1452]

Solid-state 13C NMR has been used to identify elastomers in binary blends of chloroprene (CR) and NR, CR and CSM, NR and CSM, and SBR and acrylonitrile-butadiene rubber (NBR). The type of NBR can be determined by identifying the sequences of acrylonitrile and butadiene. The tertiary blend of NR/SBR/BR was also studied [49]. High-temperature 13C solid-state NMR identified ethylene-propylene diene terpolymer (EPDM) and fluoro and nitrile rubbers [50]. [Pg.340]

Wettability of Elastomers and Copolymers. The wettability of elastomers (37, 38) in terms of critical surface tension was reported previously. The elastomers commonly used for the reinforcement of brittle polymers are polybutadiene, styrene-butadiene random and block copolymers, and butadiene-acrylonitrile rubber. Critical surface tensions for several typical elastomers are 31 dyne/cm. for "Diene rubber, 33 dyne/cm. for both GR-S1006 rubber and styrene-butadiene block copolymer (25 75) and 37 dyne/cm. for butadiene-acrylonitrile rubber, ( Paracril BJLT nitrile rubber). The copolymerization of butadiene with a relatively polar monomer—e.g., styrene or acrylonitrile—generally results in an increase in critical surface tension. The increase in polarity is also reflected in the increase in the solubility parameter (34,39, 40) and in the increase of glass temperature (40). We also noted a similar increase in critical surface tensions of styrene-acrylonitrile copolymers with the... [Pg.103]

During the last 15 years several companies have developed hydrogenated grades of nitrile rubber to both improve its thermal stability and solvent resistance. Although the hydrogenation of a poly diene backbone was done as early as the 1920s, real commercial products with acrylonitrile were not introduced until the mid-1980s.59... [Pg.708]

Note Parts by weight of typical rubber. a Ethylene-propylene diene monomer. b Nitrile rubber. [Pg.69]

The longer the polymer chain is, the better is the resistance to compression set because of the improved ability to store energy. In Figure 8.3, the sealing compounds are NBR (nitrile rubber), EPDM (ethylene-propylene diene rubber), FVMQ (fluoro-vinyl-methyl [fluorosilicone]), VMQ (vinyl-methyl silicone), FKM (fluroelastomers), and FFKM (perfluoroelastomers). [Pg.113]


See other pages where Diene rubbers nitrile rubber is mentioned: [Pg.59]    [Pg.452]    [Pg.235]    [Pg.70]    [Pg.284]    [Pg.580]    [Pg.556]    [Pg.558]    [Pg.568]    [Pg.312]    [Pg.464]    [Pg.777]    [Pg.738]    [Pg.240]    [Pg.132]    [Pg.314]    [Pg.655]    [Pg.472]    [Pg.284]    [Pg.96]    [Pg.240]   
See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.88 ]




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Diene rubbers

Diene-unsaturated nitrile rubber

Dienes nitrile rubber)

Nitrile rubber

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