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Polydienes applications

Polydienes. Polydienes that are modifled with organosilicons have been described and find application as antifoaming and/or deaeration agents for oil field treating of crude oil [170]. [Pg.323]

The low temperature ene reaction of triazolinediones with polydienes occur under heterogeneous conditions to yield hydrophilic surfaces, especially after neutralization of the resulting pendant urazole groups. Permanent hydrophilic surfaces can be obtained when (TD)2DPM is used. The use of the other RTDs tested results in surfaces that lose their hydrophilicity within 5-20 days. In applications such as improving the adhesion of rubber to other substrates, these reagents are probably sufficient (18). However, when more permanent hydrophilic surfaces are desired a bis-triazolinedione such as (TD)2DPM would be required. [Pg.227]

Comparison of chemiluminescence isothermal runs with oxygen uptake and DSC measurements has been at the centre of interest since practical industrial applications of the chemiluminescence method were attempted. It is a fact that the best comparison may be achieved when studying polymers that give a distinct induction time of oxidation typical for autoaccelerating curves of a stepwise developing oxidation. This is the particular case of polyolefins, polydienes and polyamides. The theoretical justification for the search of a mutual relationship between the oxidation runs found by the various methods follows directly from the kinetic analysis of the Bolland-Gee scheme of polymer oxidation. [Pg.476]

These products find use in specialty applications requiring better thermal stability than available in the sulfur vulcanized elastomers. Other processes are also used to crosslink polydiene rubbers (Secs. 9-2c and 9-2d). [Pg.742]

As a result of its saturated polymer backbone, EPDM is more resistant to oxygen, ozone, UV and heat than the low-cost commodity polydiene rubbers, such as natural rubber (NR), polybutadiene rubber (BR) and styrene-butadiene rubber (SBR). Therefore, the main use of EPD(M) is in outdoor applications, such as automotive sealing systems, window seals and roof sheeting, and in under-the-hood applications, such as coolant hoses. The main drawback of EPDM is its poor resistance to swelling in apolar fluids such as oil, making it inferior to high-performance elastomers, such as fluoro, acrylate and silicone elastomers in that respect. Over the last decade thermoplastic vulcanisates, produced via dynamic vulcanisation of blends of polypropylene (PP) and EPDM, have been commercialised, combining thermoplastic processability with rubber elasticity [8, 9]. [Pg.208]

T T omogeneous catalysis is of major importance in polymer chemistry - - and technology—e.g., in producing vinyl polymers, polydienes, and polycondensation polymers. It permits precise control of all reactants, usually eliminates the necessity of removing catalyst residues from the product, and allows the use of relatively simple apparatus. On the other hand, polymerizations in homogeneous media, especially bulk polymerizations of vinyl monomers, are sometimes so vigorous that proper heat removal may not be eflFected on a large scale. This drawback has limited some of the possible industrial applications (34). [Pg.233]

The interest in the reaction of ozone with polydienes is mainly due to the problems of ozone degradation of mbber materials [1-4] and the application of this reaction to the elucidation of the stmctures of elastomers [5-8], It is also associated with the possibilities of preparing bifunctional oligomers by partial ozonolysis of some unsaturated pol5miers [9-12], Usually, the interpretation of experimental results are based on a simplified scheme of Criegee s mechanism of C=C-double bond ozonolysis, explaining only the formation of the basic product, ozonides [13, 14],... [Pg.280]

The application of these procedures to 1,3-dienes has presented problems. The rates of polymerization were observed to decrease and then stop due to a buildup of excess free nitroxide (Keoshkerian et al., 1998). An effective procedure for the controlled polymerization of isoprene at 145°C involved the addition of a reducing sugar such as glucose in the presence of sodium bicarbonate to react with the excess nitroxide (Keoshkerian et al., 1998). After 4 h, polyisoprene with M = 21,000 and My,/M = 1.33 was obtained in 25% yield. The reaction of TEMPO-terminated polystyrene with either butadiene or isoprene resulted in the formation of the corresponding diblock copolymers that were characterized by NMR and SEC (Georges et al., 1998). No evidence for either polystyrene or polydiene homopolymers was reported. [Pg.41]

Polydienes are amongst the largest worldwide produced and manufactured classes of polymers. This is because of their elastomeric properties, which make them suitable for many applications as synthetic rubbers. ... [Pg.447]

Micellization of polydiene copolymers was examined by Petrak and co-workers [ 165] in the case of PEO-PI-PEO for the development of controlled drug release systems. This interest in biomedical applications was also the starting point for extensive studies on micellar systems obtained with PEO-poly(amino acid) [166, 167], PEO-polyesters block copolymers [168, 169] and PEO-poly (ethylacrylate) [170]. PEO-poly(methylidene malonate), also designated by PEO-PMM 212, of the following structure were developed in our group ... [Pg.200]

Historically, adhesives have been produced from natural products, such as bones or starch. In the last 20 years, many synthetic adhesives have found important applications not only in furniture production but also in the manufacturing of cars, airplanes, microelectronic devices, and even in medical technologies. Typical synthetic adhesives are reactive polymers like polyurethanes, polydienes, polyamides, or polyacrylates. [Pg.506]

The systems made up of epoxidized polydienes and vinylic monomers (e.g., styrene) with mixtures of (especially unsaturated) anhydrides react in ionic catalysis or with radicalic initiators, yielding solid products with various applications. Mixed with other unsaturated polymers, epoxidized polydienes can become solid materials in the presence of radicalic initiators or can participate in sulfur vulcanization of rubber mixtures. [Pg.208]

A simple procedure for modifying epoxidized polydienes is their controlled hydrolysis. Thus, hydrophilic products can be produced with applications in the fibers industry [216] ... [Pg.208]

Besides the mechanistic interest of the problem, it can be realized iitmediately that these controls might have important consequences in terms of applications. The random product is a perfectly amori bous (no melting point) 1.4 polydiene of very low Tg (-IQQ C), while the stereoblock polymer is in fact, v ben the mean D.P.of the blocks is high enough, a thermoplastic elastomer made in one step from one very usual monomer. [Pg.144]


See other pages where Polydienes applications is mentioned: [Pg.395]    [Pg.272]    [Pg.190]    [Pg.357]    [Pg.27]    [Pg.220]    [Pg.178]    [Pg.123]    [Pg.156]    [Pg.51]    [Pg.82]    [Pg.103]    [Pg.161]    [Pg.391]    [Pg.291]    [Pg.52]    [Pg.350]    [Pg.4]    [Pg.679]    [Pg.53]    [Pg.493]    [Pg.53]    [Pg.81]    [Pg.902]    [Pg.30]    [Pg.108]    [Pg.29]    [Pg.124]    [Pg.20]    [Pg.52]    [Pg.38]    [Pg.67]    [Pg.219]   
See also in sourсe #XX -- [ Pg.493 ]




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