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Polyurethane hysteresis

Almost all IDA derived chain extenders are made through ortho-alkylation. Diethyltoluenediamine (DE I DA) (C H gN2) (53), with a market of about 33,000 t, is the most common. Many uses for /-B I DA have been cited (1,12). Both DE I DA and /-B I DA are especially useful in RIM appHcations (49,53—55). Di(methylthio)-TDA, made by dithioalkylation of TDA, is used in cast urethanes and with other TDI prepolymers (56). Styrenic alkylation products of TDA are said to be useful, eg, as in the formation of novel polyurethane—polyurea polymers (57,58). Progress in understanding aromatic diamine stmcture—activity relationships for polyurethane chain extenders should allow progress in developing new materials (59). Chlorinated IDA is used in polyurethane—polyurea polymers of low hysteresis (48) and in reinforced polyurethane tires (60). The chloro-TDA is made by hydrolysis of chloro-TDI, derived from TDA (61). [Pg.239]

Abrasion-resistant duties may involve abrasion in an aqueous phase or abrasion by dry particulate materials. The selection of the polyurethane type is most important to obtain the best results. Polyester-based polyurethanes perform best in dry abrasion due to their low hysteresis properties and excellent resistance to cut initiation and propagation. However, polyester polyurethanes are susceptible to hydrolytic degradation, and therefore polyether polyurethanes are normally used for aqueous abrasion duties. [Pg.941]

Short fiber reinforcement of TPEs has recently opened up a new era in the field of polymer technology. Vajrasthira et al. [22] studied the fiber-matrix interactions in short aramid fiber-reinforced thermoplastic polyurethane (TPU) composites. Campbell and Goettler [23] reported the reinforcement of TPE matrix by Santoweb fibers, whereas Akhtar et al. [24] reported the reinforcement of a TPE matrix by short silk fiber. The reinforcement of thermoplastic co-polyester and TPU by short aramid fiber was reported by Watson and Prances [25]. Roy and coworkers [26-28] studied the rheological, hysteresis, mechanical, and dynamic mechanical behavior of short carbon fiber-filled styrene-isoprene-styrene (SIS) block copolymers and TPEs derived from NR and high-density polyethylene (HOPE) blends. [Pg.353]

FIGURE 3.2 Hysteresis of polyurethane foam under compression. [Pg.58]

The shorter the linear diol chains, the better the compression set and the higher the melt temperature of the polyurethane elastomer. The hysteresis curve shows the least retained energy, thus giving a lower heat buildup under load. These desirable properties can be achieved more readily by the diols ranked in the following series ... [Pg.22]

There are a number of other physical properties that are very important to the optimum performance of polyurethane other than the normally quoted ones in trade literature. These include temperature, dynamic, and hysteresis properties. [Pg.117]

The hysteresis property of any polyurethane is composed of two components, namely the spring and the viscous component. The viscous component is responsible for the absorption of the force and the conversion of the energy into heat. Any deflections must be within the limits where Hookes Law is obeyed (i.e., only 1 to 10%). The ratio between the forced and natural frequencies needs to be determined. The natural frequency is a function of the static deflection of the system. The damping ratio of the polyurethane also must be known. This can vary from 0.05 for highly resilient materials to 0.15 for low-resiliency materials. To obtain damping, the forced-to-natural damping frequency ratio must be greater than 1.4. [Pg.158]

Hygroscopic Hysteresis hydroxyl content of 1.0 g of polyol. A material that absorbs moisture readily. The ability of polyurethane to absorb and dissipate energy due to successive deformation and relaxation. A measurement of the area between the deformation and relaxation stress-strain curves. [Pg.220]

Three-component IPNs prepared from polyurethane, epoxy, and unsaturated polyester resin resulted in even broader tan 5 values when compared to two component (PU/E) IPN elastomers. Furthermore, the tan S values for the three component IPN systems were still high after the transitions were apparently complete, which is of enormous significance in sound energy absorption applications. IPN foams prepared by using PU/E (two-component) showed excellent energy absorbing abilities. This was reflected in rebound, hysteresis, and sound absorption studies. [Pg.263]

Foams made from the two-component IPNs showed a significant Increase in energy absorbing ability as compared to the 100% polyurethane foams. This is indicated by increased sound absorption. Increased hysteresis, and decreased rebound. [Pg.298]

Two procedures described in BS4443, Part 2, 1988 [48] are suitable in particular for latex, PVC, and polyurethane foams. One is faster to carry out and can be used as a quality control method (Procedure A). Procedure B can be used to determine the load to give indentations of 25, 40, and 65% deflections and hence the sag factor can be determined. In addition, by measuring the load for specified indentations of the foam on loading (as with Procedure B), followed by measuring the indentations on unloading, a measure of the foam hysteresis can be determined. Hysteresis is a measurement of the energy absorbed by a foam when subjected to a deformation. [Pg.391]

Placed on the body, pressure sensors are able to detect some movement. Dunne et al. (2005) prototyped a sleeveless sensing shirt with six pressure sensors made of Ppy-coated polyurethane foam. The foam exhibits a piezo-resistive behaviour in response to changes in pressure. The shirt was found to be able to detect shoulder and neck movements and shoulder-blade pressure. However, issues around ageing of the sensor and hysteresis still need to be resolved. [Pg.185]

The adhesion of particles by such mechanisms is vitally important in Pharmaceuticals, xerography, semiconductors, printing, and agriculture. Many articles are written on these topics each year. A particular contribution has been made by Rimai, Demejo and Bowen in understanding the adhesion of toner particles which must transfer from a photoconductor to a receiva-. JKR behavior was observed for glass spheres on polyurethane, as shown in Fig. 9.22. Curious effects of large deformation, engulfment and hysteresis were seen. This hysteresis is to be considered next. [Pg.199]

Superhydrophobicity, polyurethane, contact angle hysteresis, surface reorganization... [Pg.139]

It has been demonstrated in this study that by incorporating silica particles, a partially fluorinated polyurethane film can be turned superhydrophobic, despite a large water contact angle hysteresis (sticky superhydrophobic behavior). One major cause for the large CAH is the surface reorganization of the fluorinated polyurethane film upon contact with water. A long PDMS chain can be used to effectively suppress the surface reorganization upon contact with water. [Pg.150]

Hysteresis, which is characteristic of most polyurethanes, has been attributed to a number of factors including nonafline deformation, plastic deformation of the hard... [Pg.116]

A series of studies was also made by us, of the PUs cyclic stress-strain response. The range of structures achieved by us was widened by inclusion of DBDI, as a diisocyanate with a very strong tendency to packing due to its constitutional mobility. A systematic investigation (as shown in Table 4.5), was made of the effects of varying HS and SS chemistry, crosslinking and preparation procedures, on the hysteresis behaviour and Mullins effect of melt-cast polyurethane elastomers. The... [Pg.119]

The book covers aspects from the morphology to mechanical aspects focused on the elasticity and inelasticity of amorphous to crystalline polyurethane elastomers, in relation to their sensitivity to chemical and physical structure. In such polymers, resilience of the material is an important attribute. In many applications they are in commercial competition with other, relatively soft, elastomeric materials. The choice of material for any given application then hinges on a spectrum of key properties offered by relatively soft polymers—stiffness and strain recovery characterizing their elasticity, but also inelastic effects such as hysteresis and stress relaxation. In these respects the mechanical properties of polyurethane elastomers are similar to those of other elastomers. [Pg.268]

Note 15 was a soft, transparent, very flexible polyurethane with high hysteresis and set. [Pg.271]


See other pages where Polyurethane hysteresis is mentioned: [Pg.368]    [Pg.799]    [Pg.96]    [Pg.100]    [Pg.205]    [Pg.554]    [Pg.143]    [Pg.368]    [Pg.119]    [Pg.28]    [Pg.799]    [Pg.239]    [Pg.392]    [Pg.287]    [Pg.627]    [Pg.138]    [Pg.179]    [Pg.188]    [Pg.416]    [Pg.132]    [Pg.331]    [Pg.594]    [Pg.139]    [Pg.782]    [Pg.114]    [Pg.119]    [Pg.129]    [Pg.206]    [Pg.270]    [Pg.104]   
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Hysteresis

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