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Highly cross-linked

Epoxy novolac resins are produced by glycidation of the low-molecular-weight reaction products of phenol (or cresol) with formaldehyde. Highly cross-linked systems are formed that have superior performance at elevated temperatures. [Pg.1015]

Polymerization. In the absence of inhibitors, acrolein polymerizes readily in the presence of anionic, cationic, or free-radical agents. The resulting polymer is an insoluble, highly cross-linked soHd with no known commercial use. [Pg.128]

Elastomeric Modified Adhesives. The major characteristic of the resins discussed above is that after cure, or after polymerization, they are extremely brittie. Thus, the utility of unmodified common resins as stmctural adhesives would be very limited. Eor highly cross-linked resin systems to be usehil stmctural adhesives, they have to be modified to ensure fracture resistance. Modification can be effected by the addition of an elastomer which is soluble within the cross-linked resin. Modification of a cross-linked resin in this fashion generally decreases the glass-transition temperature but increases the resin dexibiUty, and thus increases the fracture resistance of the cured adhesive. Recendy, stmctural adhesives have been modified by elastomers which are soluble within the uncured stmctural adhesive, but then phase separate during the cure to form a two-phase system. The matrix properties are mosdy retained the glass-transition temperature is only moderately affected by the presence of the elastomer, yet the fracture resistance is substantially improved. [Pg.233]

Membranes made by interfacial polymerization have a dense, highly cross-linked interfacial polymer layer formed on the surface of the support membrane at the interface of the two solutions. A less cross-linked, more permeable hydrogel layer forms under this surface layer and fills the pores of the support membrane. Because the dense cross-linked polymer layer can only form at the interface, it is extremely thin, on the order of 0.1 p.m or less, and the permeation flux is high. Because the polymer is highly cross-linked, its selectivity is also high. The first reverse osmosis membranes made this way were 5—10 times less salt-permeable than the best membranes with comparable water fluxes made by other techniques. [Pg.68]

A unique feature of in situ encapsulation technology is that polymerization occurs ia the aqueous phase thereby produciag a condensation product that deposits on the surface of the dispersed core material where polymerization continues. This ultimately produces a water-iasoluble, highly cross-linked polymer capsule shell. The polymerization chemistry occurs entirely on the aqueous phase side of the iaterface, so reactive agents do not have to be dissolved ia the core material. The process has been commercialized and produces a range of commercial capsules. [Pg.321]

LDPE homopolymers in the 0.2—150 melt index or 100, 000 20,000 mPa s(= cP) viscosity range. Specialty polymers such as greases and waxes or highly cross-linked polymers are not included. [Pg.371]

In recent years, synthetic polymeric pigments have been promoted as fillers for paper. Pigments that ate based on polystyrene [9003-53-6] latexes and on highly cross-linked urea—formaldehyde resins have been evaluated for this appHcation. These synthetic pigments are less dense than mineral fillers and could be used to produce lightweight grades of paper, but their use has been limited in the United States. [Pg.21]

The ultraphosphates are situated between P O q and the metaphosphates. These comparatively Htde-known, highly cross-linked polymers contain at least some of the phosphoms atoms as triply coimected branching points. This stmctural feature is quite unstable toward hydrolysis. Ultraphosphates undergo rapid decomposition upon dissolution. In amorphous ultraphosphates, the cross-linking is presumably scattered randomly throughout the stmctural matrix in contrast, crystalline ultraphosphates have a regular pattern. [Pg.324]

Fig. 4. MiceUular gelation mechanism. A shows micelle nuclei, highly cross-linked B, boundary where micelle growth terminates in styrene block polymers. Fig. 4. MiceUular gelation mechanism. A shows micelle nuclei, highly cross-linked B, boundary where micelle growth terminates in styrene block polymers.
Highly cross-linked polyol polytitanates can be prepared by reaction of a tetraaLkyl titanate with a polyol, such as pentaerythritol, followed by removal of the by-product alcohol (77). The isolated soHds are high activity catalysts suitable for use in the preparation of plasticizers by esterification and/or transesterification reactions. The insoluble nature of these complexes faciUtates their... [Pg.145]

The resins used are highly cross-linked organic polymers with acidic functional groups. The most common of the resins used are sulfonated copolymers of styrene and divinylben2ene (see Ion exchange). [Pg.280]

Wool, as a keratin, is a highly cross-linked, insoluble proteinaceous fiber, and few animals have developed the specialized digestive systems that aUow them to derive nutrition from the potential protein resource. In nature, these few keratin-digesting animals, principally the larvae of clothes moths and carpet beetles, perform a useful function in scavenging the keratinous parts of dead animals and animal debris (fur, skin, beak, claw, feathers) that ate inaccessible to other animals. It is only when these keratin-digesting animals attack processed wool goods that they are classified as pests. Very often they enter domestic or industrial huildings from natural habitats such as birds nests. [Pg.349]

Bismaleimides are best defined as low molecular weight, at least diftinctional monomers or prepolymers, or mixtures thereof, that carry maleimide terminations (Eig. 3). Such maleimide end groups can undergo homopolymerization and a wide range of copolymerizations to form a highly cross-linked network. These cure reactions can be effected by the appHcation of heat and, if required, ia the presence of a suitable catalyst. The first patent for cross-linked resias obtained through the homopolymerization or copolymerization of BMI was granted to Rhc ne Poulenc, Erance, ia 1968 (13). Shordy after, a series of patents was issued on poly(amino bismaleimides) (14), which are synthesized from bismaleimide and aromatic diamines. [Pg.23]

Three different covalent cure systems are commonly used sulfur-based or sulfur donor, peroxide, and maleimide. These systems rely on a cross-linking agent and one or more accelerators to develop high cross-link density. [Pg.493]

In the maleimide cure, the cross-linking agent is -y -phenjlenedimaleimide [3006-93-7] HVA-2. This system has two significant advantages Htharge is not required for high cross-link density and low compression set may be obtained. The accelerators are weak bases, ie,... [Pg.493]

Figure 9.1. Schemalic illuslralion of dependence of Ihe modulus of a polymer on a variety of factors. A is an amorphous polymer of moderate molecular weight whereas B is of such a high molecular weight that entanglements inhibit flow. Similar effects are shown in C and D, where the polymer is respectively lightly and highly cross-linked. In E and F the polymer is capable of crystallisation, F being more highly crystalline than E... Figure 9.1. Schemalic illuslralion of dependence of Ihe modulus of a polymer on a variety of factors. A is an amorphous polymer of moderate molecular weight whereas B is of such a high molecular weight that entanglements inhibit flow. Similar effects are shown in C and D, where the polymer is respectively lightly and highly cross-linked. In E and F the polymer is capable of crystallisation, F being more highly crystalline than E...
As will be seen from curves A, B and C of Figure 9.1, the softening point of an amorphous polymer, i.e. the temperature at which the modulus drops catastrophically, is closely associated with the T. (Such softening does not of course occur in highly cross-linked polymers, as in type D, unless degradation also takes place.)... [Pg.188]

Because of the high cross-link density of polyisocyanurates as prepared above, the resultant foams are brittle, so that there has been a move towards polyisocyanurate-polyurethane combinations. For example, isocyanurate-con-taining polyurethane foams have been prepared by trimerisation isocyanate-tipped TDI-based prepolymers. The isocyanurate trimerising reaction has also been carried out in the presence of polyols of molecular weight less than 300 to give foams by both one-shot and prepolymer methods. [Pg.807]

The maximal flow rates and operational pressures that can be used with Sephadex G types depend primarily on the concentration of dextran and the degree of cross-linking used to stabilize the particle. Sephadex G-10, G-15, G-25, and G-50 are quite highly cross-linked, and the first three types are consid-... [Pg.39]


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Cross-Linking at High Polymer Content

Cross-linked high-amylose starch

Cross-linked high-density polyethylene

HIGHLY CROSS-LINKED POLYMERS

High-temperature polymers cross-linked organic

Highly cross-linked UHMWPE

Highly cross-linked network

Highly cross-linked network chain entanglement

Highly cross-linked polystyrene

Highly cross-linked resins

Matrix highly cross-linked

Polyester resin highly cross-linked networks

Simple Fractionations Employing Highly Cross-Linked Gels

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