Polymeric materials polyesters

About 2 X 10 Ib/year of 1 2 epoxypropane is produced in the United States as an intermediate in the preparation of various polymeric materials including polyurethane plastics and foams and polyester resins A large fraction of the 1 2 epoxypropane is made from propene by way of its chlorohydrm... 

Thermosetting Reactive Polymers. Materials used as thermosetting polymers include reactive monomers such as urea—formaldehyde, phenoHcs, polyesters, epoxides, and vinyls, which form a polymerized material when mixed with a catalyst. The treated waste forms a sponge-like material which traps the soHd particles, but not the Hquid fraction the waste must usually be dried and placed in containers for disposal. Because the urea—formaldehyde catalysts are strongly acidic, urea-based materials are generally not suitable for metals that can leach in the untrapped Hquid fractions. Thermosetting processes have greater utiHty for radioactive materials and acid wastes. 

Paraplex. A trademark for a group of alkyd type polymeric materials known as polyester resins. These resins are primarily long chain polybasic acids esterified with polyhydric alcohols such as glycol sebacate, glycerol, or ethylene glycol. Some are oil-modified while others are unmodified polyesters... 

Divinyl esters reported first by us are efficient monomers for polyester production under mild reaction conditions. In the lipase PF-catalyzed polymerization of divinyl adipate and 1,4-butanediol in diisopropyl ether at 45°C, a polyester with molecular weight of 6.7 x 10 was formed, whereas adipic acid and diethyl adipate did not afford the polymeric materials under similar reaction conditions (Scheme 3). 

Strictly speaking, the term polyester ought to refer to a chemical compound containing many ester groups in each molecule. In practice, however, it usually refers to polymeric materials containing ester groups as major structural components of the main chains of the macromolecules of which the polymer is composed, and this is the sense in which it is used here. The term is not now usually applied to polymers that contain ester groups attached to the main chain either directly, as in cellulose triacetate, poly(vinyl acetate) or poly(methyl acrylate), or within short side-chains. 

Hult A, Malmstrom E, Johansson M (1996) Hyperhranched aliphatic polyesters. In Salamone JC (ed) The polymeric materials encyclopedia synthesis, properties and applications. CRC Press, Boca Raton, Florida... 

This method exclusively yields macrocyclic polyesters without any competition with linear polymers. Furthermore, the coordination-insertion ROP process can take part in a more global construction set, ultimately leading to the development of new polymeric materials with versatile and original properties. Note that other types of efficient coordination initiators, i.e., rare earth and yttrium alkoxides, are more and more studied in the framework of the controlled ROP of lactones and (di)lactones [126-129]. These polymerizations are usually characterized by very fast kinetics so as one can expect to (co)polymerize monomers known for their poor reactivity with more conventional systems. Those initiators should extend the control that chemists have already got over the structure of aliphatic polyesters and should therefore allow us to reach again new molecular architectures. It is also important to insist on the very promising enzyme-catalyzed ROP of (di)lactones which will more likely pave the way to a new kind of macromolecular control [6,130-132]. 

Due to the importance of polymer chemistry for the chemical industry, considerable effort has been devoted to the smdy of the effects of light on polymeric materials. The photochemistry of polymers is complex. However, it is well established that PFR occurs in some aromatic polyesters [211-222] and polyamides [223,224]. This process can take place either in the main chain of the polyester or in the pendant groups. 

The concept of using group I metal initiators was applied in order to minimize the toxicity generated by heavy metal residues in the end product PLAs when using metals like aluminum, tin, and lanthanides as initiators. In recent years, dinuclear lithium and macro-aggregates with phenolate ligands have attracted substantial interest, mainly due to uncommon strucmral feamres and their ability to catalyze formation of polyester and various other polymeric materials via ROP [28]. A series of lithium complexes supported with 2, 2-ethylidene-bis (4, 6-di-tert-butylphenol) (EDBP-H2) 2-6, (Scheme 6) are excellent initiators for the ROP of L-lactide in CH2CI2 at 0 °C and 25 °C [33-35]. In this case, the PDIs of the obtained PLAs were quite narrow (1.04—1.14) and a Unear relationship between and the monomer-to-initiator ratio ([M]o/[I]o) existed at 0 °C. Dimeric complexes 4 and 6 were the... 

Wallace Carothers and coworkers at DuPont synthesized aliphatic polyesters in the 1930s [Furukawa, 1998 Hounshell and Smith, 1988]. These had melting points below 100°C, which made them unsuitable for firber use. Carothers then turned successfully to polyamides, based on the theoretical consideration that amides melt higher than esters. Polyamides were the first synthetic fibers to be produced commercially. The polyester and polyamide research at DuPont had a major impact on all of polymer science. Carothers laid the foundation for much of our understanding of how to synthesize polymeric materials. Out of that work came other discoveries in the late 1930s, including neoprene, an elastomer produced from chloro-prene, and Teflon, produced from tetrafluoroethylene. The initial commercial application for nylon 6/6 was women s hosiery, but this was short-lived with the intrusion of World War II. The entire nylon 6/6 production was allocated to the war effort in applications for parachutes, tire cord, sewing thread, and rope. The civilian applications for nylon products burst forth and expanded rapidly after the war. 

Various a-methylenemacrolides were enzymatically polymerized to polyesters having polymerizable methacrylic methylene groups in the main chain (Fig. 3, left). The free-radical polymerization of these materials produced crosslinked polymer gels [10, 12]. A different chemoenzymatic approach to crosslinked polymers was recently introduced by van der Meulen et al. for novel biomedical materials [11]. Unsaturated macrolactones like globalide and ambrettolide were polymerized by enzymatic ROP. The clear advantage of the enzymatic process is that polymerizations of macrolactones occur very fast as compared to the chemically catalyzed reactions [13]. Thermal crosslinking of the unsaturated polymers in the melt yielded insoluble and fully amorphous materials (Fig. 3, right). 

Plastics are by far the largest group of polymeric materials being processed by electron beam irradiation. Cross-linking of polyolefins, PVC, polyesters, polyurethanes, fluoropolymers, and fiber-reinforced composites is a common practice. 

Among various rubbery polymeric materials, a special polyester resin has been developed as a binder in view of its curing at ambient temperature, low viscosity (as a result of addition of vinyl monomers) without appreciable sedimentation of explosives. In addition, polyester resin has the greatest advantage of having an oxygen moiety in the skeleton which increases oxygen balance of the final sheet,... 

Figure 15 shows the results of threshold energy measurements on a series of 60 nm thick DIP films fabricated with different polymeric materials, each containing 20 weight percent Polyester Yellow. The solid line, about which the data points are scattered, corresponds to the variation of the... 

Amino-1,2,4-thiadiazoles79 and their 3-alkoxy-, 3-alkylmercapto-, and 3-dialkylamino derivatives84 have been claimed to be useful intermediates in the manufacture of dyes,84 pharmaceuticals,84 and materials valuable in pest control.79 Mono-azo dyes derived from diazotized 5-amino-l,2,4-thiadiazoles and coupling components of the benzene series are especially suitable for dyeing polymeric materials such as acetate rayon, polyamides, polyurethanes, polyesters, and... 

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