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Cross-linking bonding

Well, that is the case at the low temperature, when the rubber has a proper modulus of a few GPa. As the rubber warms up to room temperature, the Van der Waals bonds melt. (In fact, the stiffness of the bond is proportional to its melting point that is why diamond, which has the highest melting point of any material, also has the highest modulus.) The rubber remains solid because of the cross-links which form a sort of skeleton but when you load it, the chains now slide over each other in places where there are no cross-linking bonds. This, of course, gives extra strain, and the modulus goes down (remember, E = [Pg.61]

The above results proved the potential viability of the adsorbed hydrophilic macromolecules as bonded phases in chromatography of biopolymers but it must be admitted that additional crosslinking of previously adsorbed macromolecules is usually needed in order to obtain stable composites. The cross-linked bonded polymeric phases, however, may suffer from the restricted flexibility of the chain segment and their steric repellency may be diminished. Moreover, the conformational adaptivity of cross-linked chains for binding with solutes is poorer than that of grafted or chemically bound macromolecules. [Pg.147]

Masuho, Y., Kishida, K., Saito, M., Umemoto, N., and Hara, T. (1982) Importance of the antigen-binding valency and the nature of the cross-linking bond in ricin A-chain conjugates with antibody. J. Biochem. (Tokyo) 91, 1583. [Pg.1092]

You 11 recall that thermosets are polymAs that have lots of cross-linking. The molecules are three-dimensional, rather than two. More importantly, once the cross-linking bonds are in place, the polymer becomes rigid and hard. Put another way, once the thermoset occurs, it is irreversibly set. That s the difference between thermosets and thermoplastics. The latter can be remolded and reshaped the former cannot. When you sweep up the scrap material around the molding/extruding machines that handle thermosets, you throw it away. [Pg.360]

This technique is not so easily extended to nonoxides. Sulphur, for example, does not form the cross-linking bonds needed to form the sol-gel as readily as does oxygen. However, a related method has been used, albeit to a very small extent, to form CdS films. It is based on the thermal decomposition (at ca. 300°C) of a Cd-thiourea complex, which is formed as a film by slowly withdrawing the substrate from a methanolic solution of a Cd salt and thiourea [196]. [Pg.82]

Cross-linking—bonds created between the polymer chains... [Pg.16]

The waste material must be polar so that the microwave energy will generate the heat necessary to devulcanize. Microwave energy between 915 and 2450 MHz and between 41 and 177W/hr/lb is sufficient to sever all cross-link bonds but insufficient to sever polymer chain degradation. The cost of devulcanized... [Pg.2694]

In some cases, purification of unknown target molecules is facilitated by the ability to cleave the cross-linking bonds after isolation of the complex. For instance, a protein modified near its binding site with a photoreactive heterobifunctional cross-linker can be incubated with its receptor or specific binding molecule, a covalent linkage then can be formed by photolyzing, and the complex can be analyzed by subsequent cleavage of the cross-link. [Pg.292]

All penicillins kill growing bacteria by preventing normal development of their cell walls. Unlike our cells and those of other mammals, bacteria rely on a rigid cell wall. The rigidity is maintained by cross-linking bonds between... [Pg.429]


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See also in sourсe #XX -- [ Pg.134 ]




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Bond crossing

Cross-linked polymers hydrogen bonding

Cross-linking bonds

Cross-linking bonds

Double bond cross-linking

Internal bond cross-linking agents

Polymer cross-linking, hydrogen-bonded

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