Extended polyethers

A synthetic variant is to react firstly the polyether with a small quantity of TDI. The resultant extended polyether, containing urethane groups, participates together with urea groups in polycondensation reactions with aqueous formaldehyde. Thus a true nonaqueous dispersant is formed in situ, with an aminoplast block and a polyether block, which probably assures the efficient stabilisation of the resulting aminoplast dispersion. 

Cai, G., Guo, S. and Yang, L., Thermosets from water-extended polyether-ester emulsions, US Patent 5 633 315, 1997. 

The polyurethane-urea dispersions which are obtained employing these shear-force dispersant methods generally have particle sizes from 0-7 to 3 //m and, from crosslinked particles, films are formed only at temperatures exceeding 100 C. Small amounts of solvent may be added to the prepolymer to improve dispersion and remain in the dispersion, since their removal would impair stability. Best results are obtained with diamine-extended polyether-isocyanate prepolymers. The choice of suitable dispersants is of considerable importance. 

Examples of polymers which form anisotropic polymer melts iaclude petroleum pitches, polyesters, polyethers, polyphosphaziaes, a-poly- -xyljlene, and polysdoxanes. Synthesis goals iaclude the iacorporation of a Hquid crystal-like entity iato the maia chaia of the polymer to iacrease the strength and thermal stabiHty of the materials that are formed from the Hquid crystal precursor, the locking ia of Hquid crystalline properties of the fluid iato the soHd phase, and the production of extended chain polymers that are soluble ia organic solvents rather than sulfuric acid. 

In addition, polyester polyols are made by the reaction of caprolactone with diols. Poly(caprolactone diols) are used in the manufacture of thermoplastic polyurethane elastomers with improved hydrolytic stabiHty (22). The hydrolytic stabiHty of the poly(caprolactone diol)-derived TPUs is comparable to TPUs based on the more expensive long-chain diol adipates (23). Polyether/polyester polyol hybrids are synthesized from low molecular weight polyester diols, which are extended with propylene oxide. 

To improve the rheological properties and extend the very short working time, a simple polyester is kicluded as thinner. Mixing is easy, and dimensional change ki ak is less than 0.1% over several hours. Elastic recovery and reproduction of detail are exceUent. The elastomeric cycHc imine impression materials have a higher modulus of elasticity than the condensation siHcone or polysulfide mbbers, and are more difficult to remove from the mouth. The materials have relatively low tear strength and an equUibrium water sorption of 14% thus, polyether impression materials tear readily. Because of thek poor dimensional stabUity ki water, they should be stored ki a dry environment. 

All these elastomers, especially poly(ethylene- (9-butylene) and poly(ethylene- (9-propylene), are nonpolar. The corresponding block copolymers can thus be compounded with hydrocarbon-based extending oils, but do not have much oil resistance. Conversely, block copolymers with polar polyester or polyether elastomer segments have Htde affinity for such hydrocarbon oils and so have better oil resistance. 

More recently, storage systems based on MDI have become available which pose less of a health hazard than MDI/MOCA systems. Both polyethers and polyesters are used, with glycols being the usual chain extenders. 

Recently, the above mentioned model reaction has been extended to polycondensation reactions for synthesis of polyethers and polysulfides [7,81]. In recent reports crown ether catalysts have mostly been used in the reaction of a bifunctional nucleophile with a bifunctional electrophile, as well as in the monomer species carrying both types of functional groups [7]. Table 5 describes the syntheses of aromatic polyethers by the nucleophilic displacement polymerization using PTC. 

TPU is usually made from hydroxyl-terminated polyether or polyester diols, diisocyanates, and bifunctional chain extenders. Since the composition, the synthetic method, molecular weight, and its distribution are all changeable, there are numerous types of TPUs available, and their prices and properties vary significantly. 

Note Glass filler can considerably extend the performance of the above polymers. PEI = polyetherimide PES = polyether sulfone PPS = polyphenylene sulfide PSF = polysulfone PC = polycarbonate. 

A liquid oil, an emulsifier, and a friction modifier, which includes certain polyether compounds, can be added to a drilling fluid consisting of a water-in-oil emulsion formed from a brine [1155]. The friction modifier serves to decrease the coefficient of friction of the well drilling fluid. Decreasing the coefficient of friction lowers the force required to turn the drill bit in the hole. Gravitational forces increase the coefficient of friction in deviated-, horizontal-, and extended-reach wells. 

Isolated unperturbed polyoxyethylene chains have been simulated on the 2nnd lattice [154], The literature contains RIS models for a large number of polyethers [124], and it is likely that most of these chains could be mapped onto the 2nnd lattice with little difficulty. It is also likely that the work on PP [156,158] can be extended to other vinyl polymers, such as poly(vinyl chloride). This capability should permit the construction and complete equilibration of amorphous poly(vinyl chloride) cells larger than those described to date. They may be large enough to address issues arising from the weak crystallization reported for these systems [174]. 

The hot curing process normally uses polyether diol precursors with molecular weights of 3,000 to 5,000 g/mole. We can control the stiffness of the foam by adjusting the average number of isocyanate groups on the chain extender molecules. The higher the functionality of the isocyanate molecules, the more crosslinked, and hence stiffer, will be the product. 

Impetus was given to work in the field of selective cation complex-ation by the observation of Moore and Pressman (5) in 1964 that the macrocyclic antibiotic valinomycin is capable of actively transporting K+ across mitochondrial membranes. This observation has been confirmed and extended to numerous macrocyclic compounds. There is now an extensive literature on the selective complexation and transport of alkali metal ions by various macrocyclic compounds (e.g., valinomycin, mo-nactin, etc.) (2). From solution spectral (6) and crystal X-ray (7) studies we know that in these complexes the alkali metal cation is situated in the center of the inwardly oriented oxygen donor atoms. Similar results are found from X-ray studies of cyclic polyether complexes of alkali metal ions (8) and barium ion (9). These metal macrocyclic compound systems are especially noteworthy since they involve some of the few cases where alkali metal ions participate in complex ion formation in aqueous solution. 

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