Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Thermoplastics chemistry

However, the majority of sandwich panels now utilise a honeycomb core rather than either balsa wood or plastic foam the adhesive can be based on either thermosetting or thermoplastic chemistries. The three basic components used in honeycomb sandwich construction are discussed below. [Pg.248]

Cross-linking of a polymer elevates and extends the mbbery plateau little effect on T is noted until extensive cross-linking has been introduced (23,25,28). A cross-link joins more than two primary polymer chains together. In practice, cross-linking of acryflc polymers is used to decrease thermoplasticity and solubility and increase resilience. In some instances cross-linking moieties are used in reactions of a polymer with a substrate (20). The chemistry of cross-linking is described in references 11 and 29—38. [Pg.163]

Toughening of BMIs with thermoplastics is a promising approach however, more information is required about the toughening mechanism involved in order to select the most promising polymers in terms of backbone chemistry, molecular weight, and reactive groups. [Pg.32]

Thermoplastic composites can be classified according to use, cost, performance, or processing methods. In the following discussion of the chemistry of the resin systems utilized in composites, three classes are considered ... [Pg.35]

Block copolymer chemistry and architecture is well described in polymer textbooks and monographs [40]. The block copolymers of PSA interest consist of anionically polymerized styrene-isoprene or styrene-butadiene diblocks usually terminating with a second styrene block to form an SIS or SBS triblock, or terminating at a central nucleus to form a radial or star polymer (SI) . Representative structures are shown in Fig. 5. For most PSA formulations the softer SIS is preferred over SBS. In many respects, SIS may be treated as a thermoplastic, thermoprocessible natural rubber with a somewhat higher modulus due to filler effect of the polystyrene fraction. Two longer reviews [41,42] of styrenic block copolymer PSAs have been published. [Pg.479]

This chapter discusses synthetic polymers based primarily on monomers produced from petroleum chemicals. The first section covers the synthesis of thermoplastics and engineering resins. The second part reviews thermosetting plastics and their uses. The third part discusses the chemistry of synthetic rubbers, including a brief review on thermoplastic elastomers, which are generally not used for tire production but to make other rubber products. The last section addresses synthetic fibers. [Pg.324]

Sanding is carried out at this stage and, after clean-up, the final colour or top-coat is applied. There is some variation in the resin chemistry used. Alkyds crosslinked with melamine-formaldehyde are widely used for non-metallic pigmentation. Metallics are usually based on acrylics for better durability. The acrylic may be thermoset with melamine-formaldehyde or a thermoplastic lacquer (plasticised copolymer of methyl methacrylate). A thickness of about 50ftm is applied and stoved for 20 min at 130°C (lacquers receive a bake-sand-bake process for a smoother appearance). [Pg.627]

The chemistry of synthetic polymers is similar to the chemistry of small molecules with the same functional groups, but the physical properties of polymers are greatly affected by size. Polymers can be classified by physical property into four groups thermoplastics, fibers, elastomers, and thermosetting resins. The properties of each group can be accounted for by the structure, the degree of crystallinity, and the amount of cross-Jinking they contain. [Pg.1220]

Recent work has focused on a variety of thermoplastic elastomers and modified thermoplastic polyimides based on the aminopropyl end functionality present in suitably equilibrated polydimethylsiloxanes. Characteristic of these are the urea linked materials described in references 22-25. The chemistry is summarized in Scheme 7. A characteristic stress-strain curve and dynamic mechanical behavior for the urea linked systems in provided in Figures 3 and 4. It was of interest to note that the ultimate properties of the soluble, processible, urea linked copolymers were equivalent to some of the best silica reinforced, chemically crosslinked, silicone rubber... [Pg.186]

Morita, M., Shigematsu, M. and Sakata, I. (1987). An improvement of the thermoplasticity and the solvent-solubility of cyanoethylated wood by halogen treatment. Cellulose Chemistry and Technology, 21(3), 255-265. [Pg.217]

Thermosets cure into nonmelting, insoluble polymers. Frequently, the curing needs heat, pressure, or catalyst to proceed. Often the final cure, which is nothing more than completion of the cross-linking, takes place in the fabrication or molding operations. The chemistry is about the same as you saw in the thermoplastics, but there are more reactive sites per monomer. (They are polyfunctional.) Consequently, more three-dimensional cross-linking takes place. [Pg.327]

Polypropylene fibers. A small part of the total fibers market (and therefore at the tail end of this section on fibers) is fiber grade polypropylene. The chemistry for polypropylene fibers is the same as for thermoplastics. The spinning mechanics are the same as that for nylon. Polypropylene fibers are particularly resistant to abrasion and chemicals, and they are lightweight. However, they dont take colors very well, and the materials have low softening points and low resilience (they wrinkle). The major applications for polypropylene fibers are carpet-face fiber and backing (because its tough) and rope (because it is strong and floats in water). [Pg.373]

Rubber Chemistry and Technology 65,No.5,Nov./Dec.l992,p.932-55 INFLUENCE OF COMPOSITION AND PROCESSING HISTORY ON THE CELLULAR MORPHOLOGY OF THE FOAMED OI.EFINIC THERMOPLASTIC ELASTOMERS Dutta A Cakmak M Akron,University... [Pg.106]


See other pages where Thermoplastics chemistry is mentioned: [Pg.495]    [Pg.31]    [Pg.495]    [Pg.31]    [Pg.302]    [Pg.41]    [Pg.41]    [Pg.407]    [Pg.5]    [Pg.35]    [Pg.36]    [Pg.38]    [Pg.525]    [Pg.310]    [Pg.411]    [Pg.711]    [Pg.102]    [Pg.169]    [Pg.241]    [Pg.7]    [Pg.75]    [Pg.149]    [Pg.6]    [Pg.109]    [Pg.399]    [Pg.407]    [Pg.1101]    [Pg.234]    [Pg.486]    [Pg.18]    [Pg.189]    [Pg.694]    [Pg.8]    [Pg.125]    [Pg.555]    [Pg.80]    [Pg.212]    [Pg.103]    [Pg.3]   


SEARCH



© 2024 chempedia.info