Chemical cross-linking, mechanism

No polymer is ever 100% crystalline at best, patches of crystallinity are present in an otherwise amorphous matrix. In some ways, the presence of these domains of crystallinity is equivalent to cross-links, since different chains loop in and out of the same crystal. Although there are similarities in the mechanical behavior of chemically cross-linked and partially crystalline polymers, a significant difference is that the former are irreversibly bonded while the latter are reversible through changes of temperature. Materials in which chemical cross-linking is responsible for the mechanical properties are called thermosetting those in which this kind of physical cross-linking operates, thermoplastic. 

Rocket Propellants. SoHd rocket propellants are mostly based on chemically cross-linked polymeric elastomers to provide the mechanical properties required in launchings and the environmental conditions experienced in storage, shipment, and handling (see Elastomers, synthetic). Double-and triple-based nitrocellulose propellants are also employed as rocket propellants. 

Radiation cross-linking of polyethylene requires considerably less overall energy and less space, and is faster, more efficient, and environmentally more acceptable. Chemically cross-linked PE contains chemicals, which are by-products of the curing system. These often have adverse effects on the dielectric properties and, in some cases, are simply not acceptable. The disadvantage of electron beam cross-linking is a more or less nonuniform dose distribution. This can happen particularly in thicker objects due to intrinsic dose-depth profiles of electron beams. Another problem can be a nonuniformity of rotation of cylindrical objects as they traverse a scanned electron beam. However, the mechanical properties often depend on the mean cross-link density. ... 

When materials are processed using the cross- linking reaction by GA, and especially when the construction of new functions is attempted, the effects of this chemical reaction on the properties of the resultant materials should be kept in mind. Based upon the cross-linking mechanism discussed above, the following effects are expected. 

Isocyanates also can react with each other to produce carbodiimides with the loss of carbon dioxide. This reaction requires high temperatures unless catalyzed by specific phosphorus compounds. Formation of carbodiimides normally is not an important cross-linking mechanism in polyurethane adhesives. However, carbodiimides are sold by Dow Chemicals (Ucarlnk ), Nisshinbo Industries (Carbodilite ), and Stahl USA (XR-2569). They have been recommended as water scavengers, crosslinkers, and stabilizers for carboxyl functional polyurethanes. The carbodiimide can react with water to give a urea, which still can react with additional isocyanate to produce a biuret. 

Immobilization by chemical cross-linking without the addition of an inert carrier or matrix can provide the means to stabilize and reuse a biocatalyst without dilution of volumetric activity. A major deficiency in all of the aforementioned immobilization methods is that a substantial amount of a catalytically inert carrier or matrix is used to bind or contain the biocatalyst. In many cases, the amount of carrier is two orders of magnitude higher than the protein catalyst. Unfortunately, direct cross-linking of the enzyme, followed by precipitation of an amorphous solid often results in low activity and poor mechanically properties and so this method is not often used. Recently, however, cross-linked enzyme crystals have been reported to give many of the desirable properties of immobilized enzymes without the need for a support material (Sect. 6.4.1). 

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