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Cyanuric special

G. D. Nelson, SmmmingPoolDisinfection with Chlorinated Cyanurates, Special Report 6862, Monsanto Co., St. Louis, Mo., Mar. 8, 1969. [Pg.459]

DPTS-di-pentamethylene thiuram tetrasulfide TDD-thiodiazoIe derivative NC-fatty acid amide amine B-18-special curative DOTG-dior-tho-tolyl guanidine peroxide 14/40-dicumyI peroxide TAC-triallyl cyanurate. [Pg.466]

This approach mimics familiar biological self-assembly phenomena such as protein folding [ 192], protein aggregation [ 192] and nucleotide pairing [ 188]. It incorporates features described in each of the above strategies (i.e., I—III), to give specialized nanoscopic structures, that can be precisely designed, usually with excellent control over CMDPs. Recent examples include so called structure directed synthesis by Stoddart [3a] (see Chapter 1 of this book) to produce toroidal bis-bipyridinium cyclophanes that are reminiscent of a molecular abacus , melamine-cyanuric acid lattices by Whitesides [193] and unique helical structures based on coordination of bipyridyl units to copper (II) ions by Lehn [194],... [Pg.304]

The occurrence of these reactions is restricted to the amorphous phase. Therefore, the photo-cross-linking process has to be performed at temperatures exceeding the crystalline melting point in the case of highly crystalline polymers such as polyethylene. The cross-linking efficiency can be strongly enhanced by the addition of small amounts of multifunctional compounds such as triallyl cyanurate, TAG (see Chart 7.9), or by the incorporation of special diene moieties into copolymers such as ethylene propylene diene copolymers (EPDM elastomers) [33]. [Pg.191]

Styrene is the most common monomer used in crosslinking unsaturated polyesters. When special properties are required, other monomers like methyl methacrylate may be employed. Sometimes this is done in combination with styrene. Diallyl phthalate and triallyl cyanurate form better heat-resistant products. [Pg.294]

Another special feature connected with the 1,3,5-triazine moiety is spontaneous formation of a long-lived glassy state, by bisarylamino-1,3,5-triazines. A wide series of differently substituted derivatives 49 was synthesized by nucleophilic substitution of chlorine atoms in cyanuric chloride 20 with methylamine in the first step and then two equivalents of substituted aniline in the second step (13NJC3881). [Pg.458]

Styrene is the most widely used cross-linking monomer, being preferred because of its compatibility, low viscosity, ease of use and low price. Other materials are sometimes employed when special properties are required. For example, methyl methacrylate is used, often in conjunction with styrene, for the preparation of translucent sheeting. Diallyl phthalate (X) and triallyl cyanurate (XI) are used for heat resistant products. Partially polymerized diallyl phthalate (solid) is used as the cross-linking agent in moulding powders (the so-called alkyd polyester moulding powders) based on linear unsaturated polyesters. [Pg.207]

Cyanuric chloride can be reacted with various amines to give substituted melamines used in speciality amino resin production. [Pg.3]


See other pages where Cyanuric special is mentioned: [Pg.156]    [Pg.53]    [Pg.749]    [Pg.578]    [Pg.306]    [Pg.740]    [Pg.104]    [Pg.672]    [Pg.282]    [Pg.51]    [Pg.160]    [Pg.1355]    [Pg.1597]    [Pg.23]    [Pg.306]    [Pg.316]    [Pg.618]    [Pg.626]    [Pg.133]   


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