Prepolymer polyols

Another important feature of these polyols is their narrow MWD. Low polydispersity results in lower viscosities in both the polyol and isocyanate-terminated prepolymers. Polyol MWD has a significant effect on the mechanical and dynamic properties of polyurethane and polyurethane/urea systems. Broad-MWD polyols such as PTMEG or polyester polyols contain significant amounts of hard-segment diol, which limits their softness. Acclaim polyols contain no hard-segment diol and thus have inherent superior properties in soft systems. They can be made to approximate broad-MWD polyols such as PTMEG by incorporation of a low MW glycol. 

Some commercial polyurethane elastomers are in fact segmented copolymers prepared by reaction of a diisocyanate with a prepolymer polyol (hydroxyl group functionality 2) and a short-chain diol (e.g. butan-l,4-diol)... 

In more recent years, molded flexible foam products are becoming more popular. The bulk of the molded flexible urethane foam is employed in the transportation industry, where it is highly suitable for the manufacture of seat cushions, back cushions, and bucket-seat padding. TDI prepolymers were used in flexible foam mol ding ia conjunction with polyether polyols. The introduction of organotin catalysts and efficient siHcone surfactants faciHtates one-shot foam mol ding, which is the most economical production method. 

Semiflexible molded polyurethane foams are used in other automotive appHcations, such as instmment panels, dashboards, arm rests, head rests, door liners, and vibrational control devices. An important property of semiflexible foam is low resiHency and low elasticity, which results in a slow rate of recovery after deflection. The isocyanate used in the manufacture of semiflexible foams is PMDI, sometimes used in combination with TDI or TDI prepolymers. Both polyester as well as polyether polyols are used in the production of these water-blown foams. Sometimes integral skin molded foams are produced. 

Polyurethane adhesives are known for excellent adhesion, flexibihty, toughness, high cohesive strength, and fast cure rates. Polyurethane adhesives rely on the curing of multifunctional isocyanate-terrninated prepolymers with moisture or on the reaction with the substrate, eg, wood and ceUulosic fibers. Two-component adhesives consist of an isocyanate prepolymer, which is cured with low equivalent weight diols, polyols, diamines, or polyamines. Such systems can be used neat or as solution. The two components are kept separately before apphcation. Two-component polyurethane systems are also used as hot-melt adhesives. 

Polyurethane sealant formulations use TDI or MDI prepolymers made from polyether polyols. The sealants contain 30—50% of the prepolymer the remainder consists of pigments, fiUers, plastici2ers, adhesion promoters, and other additives. The curing of the sealant is conducted with atmospheric moisture. One-component windshield sealants utili2e diethyl malonate-blocked MDI prepolymers (46). Several polyurethane hybrid systems, containing epoxies, siUcones, or polysulfide, are also used. 

Polyurethane foams may be rigid, semi-rigid or flexible. They may be made from polyesters, polyethers or natural polyols such as castor oil (which contains approximately three hydroxyl groups in each molecule). Three general processes are available known as one-shot, prepolymer or quasi-prepolymer processes. These variations lead to 27 basic types of product or process, all of which have been used commercially. This section deals only with flexible foams (which are made only from polyesters and polyethers). Since prepolymers and... 

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. 

The first urethane reaction in Fig. 1 is used in two major ways in adhesives. In one case, a two-component adhesive usually employs a polyol and polyisocyanate with catalyst. This can react at room temperature to form the polyurethane. The second use of this reaction is to make an isocyanate-terminated prepolymer. Reacting a stoichiometric excess of isocyanate with polyol can produce an isocyanate-terminated prepolymer. A prepolymer is often made with an NCO/OH ratio of 2.0, as shown below, but the isocyanate ratio can range from 1.4 to over 8.0, depending upon the application ... 

The isocyanurate reaction can be both beneficial and troublesome. It can be the bane of production engineers. Low levels of alkaline impurities present in urethane raw materials such as polyols, tackifiers, etc., can cause problems in prepolymer production, resulting in high viscosity products at levels of 5 ppm or less. At higher levels of alkaline impurities, more serious problems can occur, including poor shelf life, poor caulkability, or poor sag resistance. At levels of 15 ppm or higher, the alkalinity can cause an isocyanurate reaction in a prepolymer that can result in a gelled reactor. 

Blocked isocyanate, for our purposes, will refer to the reaction product of a diisocyanate or isocyanate-terminated prepolymer in which the isocyanate functionality has been reacted with a blocking agent . Once blocked , the diisocyanate can be added to polyols or certain chain extenders, and these materials will not react at room temperature. The concept is shown in the sixth item of Fig. 1. An adhesive formulated with a blocked isocyanate is basically a two-component adhesive that does not react until heated to the activation temperature. When an adhesive is made with a blocked isocyanate together with hydroxyl-containing curatives, the adhesive has a good long shelf life at room temperature. However, once heated... 

Most moisture-curing liquid adhesives utilize poly(oxypropylene) (PPG) polyols, as shown above. These raw materials produce among the lowest-viscosity prepolymers but may not have sufficient modulus at higher temperatures for some applications. A certain percentage of polyester polyols may also be utilized to boost performance, but these may cause a large increase in viscosity, and so they are more often used in conjunction with polyether polyols to provide a high-performance adhesive with workable viscosities. Poly(butadiene) polyols may be utilized for specific adhesion characteristics. 

Liquid MDI prepolymer — 2.0 functionality, equivalent wt = 182 Polyol component ... 

Liquid polyester MDI prepolymer, 9% NCO Liquid polymeric MDI, 2.2 functionality Polyol component ... 

Synthesis MDI prepolymer with 1000 MW polyester polyol, NCO/OH = 2.0, chain-extended with 1,4-butandiol, acid number of polyester 0.6. 

Polyol Prepolymers Containing High Energy Oxidizing Groups , Qrtrly Prog Rept 1, Contract AF 04(611)-5690, Shell Development Co, Emeryville (1960)... 

Hawley, Glossary of Chemical Terms , Van-Nostrand-Reinhold,NY (1976), 217 Addnl Refs 1) K.S. Warren, Study Nitrates of Polyhydric Alcohols as Explosives , PATR 1103 (1941) la) D.B. Bright et al, Development of Polyol Prepolymers Containing High Energy Oxidizing Groups , Report No S-13843, Contract AF 04(611>5690, Shed Devel Co, Emeryville (1961) (limited distribution) 2) A.D. McElroy, Basic Approach to Incorporation of NP Propellants , Rept No RPL TDR 6448, Contract AF 04(611)-9059, Callery Chem Co, Phlla (1964) 3)... 

There are many situations where isocyanates are derivatized before use, such as when MDI or TDI are reacted with high-molecular-weight, difunctional polyols to form low-NCO prepolymers used to make cast elastomers by the prepolymer method (Section 4.3.2.1). Because of their molecular weight, prepolymers can be of much higher viscosity than the starting isocyanates, and some are solid at room... 

There is another method, called the quasi-prepolymer technique, which is similar to the full-prepolymer process but utilizes prereacted isocyanates in the 10-20% NCO range. This eases processing compared to full-prepolymer systems, requiring lower temperatures and volume ratios typically from 4 1 to nearly 1 1 (polyol to isocyanate). 

Example 11. One-Component, Moisture-Cure Polyurethane Sealant. This example is of a low-hardness, high-elongation, moisture-curable polyurethane sealant. The material is based on a low-%NCO prepolymer made from 4,4 -MDI and a low-unsaturation (low-monol-content) Acclaim polyol from Bayer. It is adapted from (a) J. Lear et al., Adhesives Age, February 1999, pp. 18-23 and (b) B. Lawrey, et al., presented at UTECH 2000, The Hague, The Netherlands, March 30, 2000, Crain Communications London, 2000. 

Ultralow-monol polyols, 223 Ultrapek, 327, 328 Ultraviolet (UV) radiation, 209 Ultraviolet spectroscopy, 490 Unimolecular micelle, 58 United States, phenolic production in, 375 Unsaturated maleate/O-phthalate/ 1,2-propanediol polyester prepolymer, 101-102 Unsaturated polyester resins (UPRs), 19, 29-30, 58-59... 

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