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Structure urethanes

Two-component urethane adhesives 7.1. Structural urethane adhesives... [Pg.795]

Baydur, Rigid structural urethane foam system, Bayer Corp., Polymers Div. [Pg.894]

A mid-to-high modulus structural urethane which is more cost-effective than 5315. [Pg.150]

A hybrid structural urethane that can be utilized to enhance the surface quality of a FRP polyester composite. It may be sprayed between a conventional gelcoat or urethane gelcoat and the FRP polyester. [Pg.297]

Lord 7660 A one part, cross-linking structural urethane adhesive for composites, applied by brush or spray and offering a working time of 30 - 60 minutes. [Pg.325]

Tetradecyltrimethylammonium bromide Poly(oxyethylene) (20) sorbitan monolaurate Wurtzite structure Urethane-methacrylate macromer Ultraviolet... [Pg.225]

Baydur Rigid structural urethane foam, Bayer... [Pg.547]

The molar excess of di-isocyanate is about 30% so that the number of polyesters joined together is only about 2-3 and the resulting unit has isocyanate end groups. A typical structure, with P for polyester groups, U for urethane and I for isocyanates would be... [Pg.785]

In most cases, the allophanate reaction is an undesirable side reaction that can cause problems, such as high-viscosity urethane prepolymers, lower pot lives of curing hot-melt adhesives, or poor shelf lives of certain urethane adhesives. The allophanate reaction may, however, produce some benefits in urethane structural adhesives, e.g., additional crosslinking, additional modulus, and resistance to creep. The same may be said about the biuret reaction, i.e., the reaction product of a substituted urea linkage with isocyanate. The allophanate and biuret linkages are not usually as thermally stable as urethane linkages [8]. [Pg.764]

Modified MDI s Urethane-modified 2.0 Clear, light yellow Flexible, 2-K structural adhesive... [Pg.768]

Urethane structural adhesives have a morphology that is inverse to the toughened epoxy just described. The urethanes have a rubber continuous phase, with glass transition temperatures of approximately —50°C. This phase is referred to as the .soft segment . Often, a discontinuous plastic phase forms within the soft segment, and that plastic phase may even be partially crystalline. This is referred to as the hard segment . A representation of the morphology is shown in Fig. 3 [34]. [Pg.773]

Windshield sealants comprise some of the most significant applications of one-component urethane adhesives. Several years ago, the requirements for these sealants were increased. In an accidental rollover, in certain automobiles, the windshield becomes a structural part of the car. Therefore, the windshield adhesive, which holds the windshield in place, must have structural strength. An example of a one-component windshield sealant is shown below [48] ... [Pg.784]

The two-component urethane structural adhesives are among the most difficult to characterize, simply because of the widely varying properties that are possible. These adhesives may be rigid plastics similar in modulus to standard epoxy adhesives, with glass transition temperatures of the cured adhesive being approximately 60°C. [Pg.795]

Methacrylates and acrylates are readily synthesized from low-cost commercially available resins and (meth)acrylate intermediates or (meth)acrylic acid [19]. A wide range of structural backbones are available, including epoxies, urethanes. [Pg.1020]

Ultraviolet absorptions ofvinylogous lactams were found by MOLCAO calculations and compared with experimental values (663). Infrared spectroscopic studies of vinylogous amides (664) and some fifty vinylogous urethanes (665) allowed configurational and structural assignments. The effect of enamine-imine equilibrium in a series of benzophenone derivatives was established (666) and the effect of structure on enamine basicity studied (667). [Pg.344]

Works on the oxidation of uric acid has unequivocally established the triazine structure > ° (9) of oxonic acid. This is further confirmed by the straightforward synthesis described by Piskala and Gut. ° The reaction of biuret (11) with potassium ethyloxalate yielded a potassium salt (24), that with ethyl oxamate, the amide of oxonic acid (25). Both these compounds were converted to 5-azauracil. An analogous reaction with diethyloxalate which should produce an ester of oxonic acid resulted in a mixture of urethane and parabanic acid, however. [Pg.200]

The structural effect of alkyl groups such as methyl, ethyl, and -butyl on the Rp is small. Alkyl 4-methyl-phenylcarbamate can be chosen as a model compound for the hard segment of poly(ether-urethane) (PEU). This group can initiate grafting reaction with Ce(IV) ion and the grafting site was proposed at the hard segment of PEU [3,15] as shown in Scheme (1). [Pg.542]

From these, prepolymers are prepared where the diisocyanates may be completely reacted as in the case of the urethane oils which resemble the oil-modified alkyds but have urethane (—NHCOO—) links in place of the ester (—COO—) links of the alkyds, or where one only of the isocyanate groups is combined, leaving the other to participate in crosslinking reactions. Such a reactive prepolymer is the biuret that may be prepared from hexamethylene diisocyanate, has the following structure ... [Pg.680]

Unsaturation, degree of. 174 Upfield, (NMR), 445 Uracil, structure of, 1101 Urea, from ammonium cyanate, 2 Urethane, 1214 Uric acid, pKa of, 778... [Pg.1317]

One of the major drawbacks to many promising copolymers is their unsatisfactory electrochemical stability. Carbonyl groups which feature in many of the back-bone/chain linking groups are likely to cause stability concerns. Likewise, urethane, alcohol, and siloxane functions are sensitive to lithium metal. With this in mind, a recent trend has been to find synthetic routes to amorphous structures with... [Pg.505]

With diblock copolymers, similar behavior is also observed. One component is enriched at the surface and depending on miscibility and composition a surface-induced ordered lamellar structure normal to the surface may be formed. Recent investigations include poly (urethanes) [111], poly(methoxy poly (ethyleneglycol) methacrylate)/PS [112] and PS/PMMA [113, 114]. In particular the last case has been extensively studied by various techniques including XPS, SIMS, NR and optical interferometry. PS is enriched at the surface depending on blockcopolymer composition and temperature. A well ordered lamellar structure normal to the surface is found under favourable conditions. Another example is shown in Fig. 6 where the enrichment of poly(paramethylstyrene), PMS(H), in a thin film of a di-... [Pg.381]

An in-depth understanding of structure-property relationships is perhaps the most important concern for the urethane formulation chemist. Material design objectives often go far beyond physical property requirements and may also include considerations like processing characteristics (i.e., compatibility, reactivity,... [Pg.208]


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See also in sourсe #XX -- [ Pg.229 ]




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