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Butadiene-nitrile rubber

XNBR carboxylic-nitrile butadiene rubber (carboxynitrile rabber)... [Pg.948]

Acrylonitrile-butadiene rubber (also called nitrile or nitrile butadiene rubber) was commercially available in 1936 under the name Buna-N. It was obtained by emulsion polymerization of acrylonitrile and butadiene. During World War II, NBR was used to replace natural rubber. After World War II, NBR was still used due to its excellent properties, such as high oil and plasticizer resistance, excellent heat resistance, good adhesion to metallic substrates, and good compatibility with several compounding ingredients. [Pg.587]

Several other examples of modified mobile phases are given in Figs. 13.58 and 13.59 using 90/5/5 TEIF/MeOH/ACN and 95/5 chloroform/w-butylamine for the SEC analysis of poloxamer and nitrile-butadiene rubber samples, respectively. [Pg.386]

The hydrogenation of unsaturated polymers and copolymers in the presence of a catalyst offers a potentially useful method for improving and optimizing the mechanical and chemical resistance properties of diene type polymers and copolymers. Several studies have been published describing results of physical and chemical testing of saturated diene polymers such as polybutadiene and nitrile-butadiene rubber (1-5). These reports indicate that one of the ways to overcome the weaknesses of diene polymers, especially nitrile-butadiene rubber vulcanizate, is by the hydrogenation of carbon-carbon double bonds without the transformation of other functional unsaturation such as nitrile or styrene. [Pg.394]

The residual carbon-carbon double bond in nitrile butadiene rubber (NBR) can be catalytically hydrogenated to yield its tougher and more stable derivative, hydrogenated nitrile butadiene rubber (HNBR).2 This class of specialty elastomer was developed to expand the range of operating environments possible for nitrile butadiene rubber NBR in environments that expose the rubber to chemical and thermal attack. [Pg.125]

Crabtree s catalyst is an efficient catalyst precursor for the selective hydrogenation of olefin resident within nitrile butadiene rubber (NBR). Its activity is favorably comparable to those of other catalyst systems used for this process. Under the conditions studied the process is essentially first order with respect to [Ir] and hydrogen pressure, implying that the active complex is mononuclear. Nitrile reduces the catalyst activity, by coordination to the metal center. At higher reaction pressures a tendency towards zero order behavior with respect to catalyst concentration was noted. This indicated the likelihood of further complexity in the system which can lead to possible formation of a multinuclear complex that causes loss of catalyst activity. [Pg.134]

Abbreviation for nitrile-butadiene rubber. See Nitrile Rubber. [Pg.42]

Nitrile rubber is also known as nitrile-butadiene rubber (NBR), government rubber nitrile (GRN), and Buna N. [Pg.1332]

Diene polymers refer to polymers synthesized from monomers that contain two carbon-carbon double bonds (i.e., diene monomers). Butadiene and isoprene are typical diene monomers (see Scheme 19.1). Butadiene monomers can link to each other in three ways to produce ds-1,4-polybutadiene, trans-l,4-polybutadi-ene and 1,2-polybutadiene, while isoprene monomers can link to each other in four ways. These dienes are the fundamental monomers which are used to synthesize most synthetic rubbers. Typical diene polymers include polyisoprene, polybutadiene and polychloroprene. Diene-based polymers usually refer to diene polymers as well as to those copolymers of which at least one monomer is a diene. They include various copolymers of diene monomers with other monomers, such as poly(butadiene-styrene) and nitrile butadiene rubbers. Except for natural polyisoprene, which is derived from the sap of the rubber tree, Hevea brasiliensis, all other diene-based polymers are prepared synthetically by polymerization methods. [Pg.547]

Scheme 19.3 Michael-type addition mechanism for nitrile butadiene rubber (NBR) crosslinking [71]. Scheme 19.3 Michael-type addition mechanism for nitrile butadiene rubber (NBR) crosslinking [71].
Table 19.3 Typical reaction conditions for the hydrogenation of polybutadiene (PB), styrene-butadiene diblock copolymer (SB), styrene-butadiene-styrene triblock copolymer (SBS) and nitrile butadiene rubber (NBR). Table 19.3 Typical reaction conditions for the hydrogenation of polybutadiene (PB), styrene-butadiene diblock copolymer (SB), styrene-butadiene-styrene triblock copolymer (SBS) and nitrile butadiene rubber (NBR).
Scheme 19.5 Mechanism of nitrile butadiene rubber (NBR) hydrogenation catalyzed by Ru(CH=CH(Ph))CI(CO)(PCy3)2. Scheme 19.5 Mechanism of nitrile butadiene rubber (NBR) hydrogenation catalyzed by Ru(CH=CH(Ph))CI(CO)(PCy3)2.
Fig. 19.1 Schematic process for the production of hydrogenated nitrile butadiene rubber (HNBR). Fig. 19.1 Schematic process for the production of hydrogenated nitrile butadiene rubber (HNBR).
The hydrogenation in a liquid-liquid system with ionic liquids as the catalyst phase was also applied to the hydrogenation of polymers. The first studies were presented by the group of Rosso et al. [91], who investigated the rhodium-catalyzed hydrogenation of polybutadiene (PBD), nitrile-butadiene rubber (NBR) and styrene-butadiene rubber (SBR) in a [BMIM][BF4]/toluene and a [BMIM][BF4]/tolu-ene/water system. The activity of the catalyst followed the trend PBD>NBR> SBR, which is the same order as the solubility of the polymers in the ionic liquid. The values in percentage total hydrogenation after 4 h reaction time were 94% for PBD and 43% for NBR, and after a reaction time of 3 h was 19% for SBR. [Pg.1400]

Figure 7. Cure curves of vulcanization process of modeling unfilled elastomeric compositions on the basis of nitrile-butadiene rubber at 155°C with various vulcanization systems. Figure 7. Cure curves of vulcanization process of modeling unfilled elastomeric compositions on the basis of nitrile-butadiene rubber at 155°C with various vulcanization systems.
Plant 000033 produces three types of emulsion crumb rubber in varying quantities. Styrene butadiene rubber (SBR) forms the bulk of production, at nearly 3.7 X lO kkg/year (8.2 X lO lb/year), with nitrile butadiene rubber (NBR) and polybutadiene rubber (PBR) making up the remainder of production [4.5 x 10 kkg/year (1.0 x lO lb/year) and... [Pg.566]

Polymer International 51,No.7, July 2002, p.601-6 PHYSICAL STUDIES OF FOAMED REINFORCED RUBBER COMPOSITES. PART I. MECHANICAL PROPERTIES OF FOAMED ETHYLENE-PROPYLENE-DIENE TERPOLYMER AND NITRILE-BUTADIENE RUBBER COMPOSITES... [Pg.36]

Wang S, Huang Y, Cong G (1997) Study on nitrile-butadiene rubber/poly(propylene carbonate) elastomer as coupling agent of poly(vinyl chloride)/poly(propylene carbonate) blends I. Effect on mechanical properties of blends. J Appl Polym Sci 63 1107-1 111... [Pg.47]

Nitrile rubber polymers, having lower molecular weight have been prepared by metathesis of nitrile butadiene rubber with ruthenium indenylidene complexes [65]. [Pg.273]

Choudhury et al. [36] in their work on hydrogenated nitrile butadiene rubber (HNBR)-nanoclay systems showed the thermodynamic aspects of nanocomposite formation using the mean-field-lattice-based description of polymer melt intercalation, which was first proposed by Vaia and Giannelis [37]. Briefly, the free... [Pg.8]


See other pages where Butadiene-nitrile rubber is mentioned: [Pg.677]    [Pg.948]    [Pg.401]    [Pg.303]    [Pg.464]    [Pg.322]    [Pg.350]    [Pg.125]    [Pg.69]    [Pg.579]    [Pg.1336]    [Pg.1355]    [Pg.1417]    [Pg.624]    [Pg.200]    [Pg.200]    [Pg.136]    [Pg.9]    [Pg.15]    [Pg.120]    [Pg.333]    [Pg.97]    [Pg.677]    [Pg.594]    [Pg.57]   
See also in sourсe #XX -- [ Pg.1400 ]

See also in sourсe #XX -- [ Pg.395 ]

See also in sourсe #XX -- [ Pg.604 ]

See also in sourсe #XX -- [ Pg.49 , Pg.50 ]




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Butadiene-nitrile

Nitrile rubber

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