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Release Agents Polymers

DiBenedetto, L. J., and Huang, S. J., 1989, Biodegradable Hydroxylated Polymers as Controlled Release Agents. Polym. Prepr. 30(1) 453. [Pg.222]

Release agents function by either lessening intermolecular interactions between the two surfaces in contact or preventing such close contact. Thus, they can be low surface-tension materials based on aUphatic hydrocarbon, fluorocarbon groups, or particulate soHds. The principal categories of material used are waxes, fatty acid metal soaps, other long-chain alkyl derivatives, polymers, and fluorinated compounds. [Pg.99]

SuppHers of release agents vary from large, basic polymer producers to small, regional formulators and distributors. Examples from among the hundreds of such suppHers include the following ... [Pg.99]

Because plastics are almost invariably modified with one or more additives, there are three components of chemical analysis the high molecular weight portion, ie, the polymer the additives, ie, plasticizer and mold-release agent and the residuals remaining from the polymerization process. The high... [Pg.525]

Vinyl acetate polymers have long been used as chewing gum bases. They have been studied as controUed release agents for programmed administration of dmgs and as a base for antifouling marine paints (166,167). [Pg.471]

None of the polymers from unbranched olefins, other than ethylene, propylene or but-1-ene, has yet become important as a plastics material although some of them are of interest both as adhesives and release agents. One limitation of a... [Pg.273]

Phosphoranyl radicals can be involved [77] in RAFT processes [78] (reversible addition fragmentation transfer) used to control free radical polymerizations [79]. We have shown [77] that tetrathiophosphoric acid esters are able to afford controlled/living polymerizations when they are used as RAFT agents. This result can be explained by addition of polymer radicals to the P=S bond followed by the selective p-fragmentation of the ensuing phosphoranyl radicals to release the polymer chain and to regenerate the RAFT agent (Scheme 41). [Pg.66]

SEC has sometimes been used with off-line IR spectroscopy for the detection of polymer additives, such as dioctylphthalate, as well as on-line [39]. Dissolutions of PVC/DEHP and of PC/pentaerythritoltetrastearate (release agent) were analysed by SEC-FTIR using the thermospray/moving belt/DRIFT interface [40]. The detection limits of the method were in the 100 ng range, depending on the IR sensitivity and volatility of the solutes. This is not extremely sensitive. [Pg.695]

After cooling, the final part is removed and the mold is recharged with resin. Since the mold surfaces are often complex, processors commonly apply mold release agents to allow the part to demold. Mold release agents are lubricants that coat the metal surface with a waxy material preventing the polymer from adhering to the mold s surface. Examples of mold release agents include silicone sprays or olefin based waxes. [Pg.265]

Early soil-release agents, applied particularly to resin-finished cellulosic goods, were water-soluble polymers, many being related to thickeners (section 10.8) such as starch, hydroxypropyl starch, sodium carboxymethylcellulose, methylcellulose, hydroxyethyl-cellulose, alginates, poly(vinyl alcohol) and poly(vinylpyrrolidone). These functioned essentially as temporary barriers and preferential reservoirs for soil, which was thus easily removed along with the finish in subsequent washing, when they then helped to minimise... [Pg.266]

Essentially nonionic soil-release agents comprise polyesters, polyamides, polyurethanes, polyepoxides and polyacetals. These have been used mainly on polyester and polyester/ cellulosic fabrics, either crosslinked to effect insolubilisation (if necessary) or by surface adsorption at relatively low temperature. Polyester soil-release finishes have been most important, particularly for polyester fibres and their blends with cellulosic fibres. These finishes, however, have much lower relative molecular mass (1000 to 100 000) than polyester fibres and hence contain a greater proportion of hydrophilic hydroxy groups. They have been particularly useful for application in laundering processes. These essentially nonionic polymers may be given anionic character by copolymerising with, for example, the carboxylated polymers mentioned earlier these hybrid types are generally applied with durable press finishes. [Pg.267]

Other Applications. Thus far the phosphazene fluoroelastomers (PNF) and aryloxyphosphazene elastomers (APN) have moved to the commercial stage. In addition to elastomers, phosphazenes are being investigated as fluids, resins and plastics. Other areas which hold promise include fire resistant paints (55), fiber blends and additives, agrichemicals and herbicides, drug release agents and electrically conducting polymers (6). [Pg.238]

Union Carbide (34) and in particular Dow adopted the continuous mass polymerization process. Credit goes to Dow (35) for improving the old BASF process in such a way that good quality impact-resistant polystyrenes became accessible. The result was that impact-resistant polystyrene outstripped unmodified crystal polystyrene. Today, some 60% of polystyrene is of the impact-resistant type. The technical improvement involved numerous details it was necessary to learn how to handle highly viscous polymer melts, how to construct reactors for optimum removal of the reaction heat, how to remove residual monomer and solvents, and how to convey and meter melts and mix them with auxiliaries (antioxidants, antistatics, mold-release agents and colorants). All this was necessary to obtain not only an efficiently operating process but also uniform quality products differentiated to meet the requirements of various fields of application. In the meantime this process has attained technical maturity over the years it has been modified a number of times (Shell in 1966 (36), BASF in 1968 (37), Granada Plastics in 1970 (38) and Monsanto in 1975 (39)) but the basic concept has been retained. [Pg.271]

Uses. A monomer widely used in the production of polymers and copolymers for manufacturing textiles, latex paints, paper coatings, dirt release agents, and specialty plastics... [Pg.307]

Generally, polymer latexes used as cement modifiers are not toxic, are safe materials to handle and require no special precautions. However, because they have an excellent adhesion to various materials, even to metals, all the equipment and tools such as mixers, trowels, and vibrators should be washed down or cleaned immediately with water after use. For concrete requiring formwork, it is advisable to use the most effective mold-release agents, e.g., silicone wax or grease [87, 96]. [Pg.355]


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