GlasspodlJ., ‘Prospects for polyols for the European polyurethane industry’, ‘U’ Tech ‘86, The Hague, 18-20 March 1986
2.
Proceedings of the Polyurethane Industry's International Conference, The Hague, The Netherlands, 18-20 March 1986
3.
HepburnC, Proceedings of the Conference ‘Polyurethanes in the Service of Man’, Plastics and Rubber Institute, 14 October 1987. Paper titled: Structure Property Relationships in Transparent Polyurethane Elastomers
4.
BASF's copolyester range
5.
Liquiflex trade name of Petroflex
6.
KirklandC, ‘Is Polyurea the key to automated RIM processing’, Plastics Technology, 32, 3, March 1986, p. 33–83
7.
SyedE.J., MuysJ., KuijpersK.G.Y.A., ‘Novel high performance polyurethane elastomers’, Conference papers of the Polyurethane Industry's International Conference, The Hague, The Netherlands, 18-20 March 1986, pp. 86–89.
8.
IPDI-BF 1540, Huls
9.
BarikaniM. and HepburnC, ‘Isocyanurate Crosslinking as a Means of Producing Thermally Stable PU Elastomers’, Cell. Polymers, Vol. 5, 1986, p. 169–185
10.
Ethacure 300. This is the trade name of the Ethyl Corporation, USA
11.
Polacure is the trade name of the Polaroid Corporation, USA
12.
AlveyF.B., J. of Appl. Polym. Sci., 13, 1969, p. 1473. Also RybnyC.B., FazioC.A., ShadidiJ.K., TrehellisJ.C. and VonaJ.A., J. of Paint Technology, 46, 596, 60, 1974
13.
CohenS.G., PavolaA. and ParsonsG.H.Jr., Chem. Rev., 73, 1973, p. 141
14.
BartholomewR.F., DavidsonR.S., LambrethP.F., McKellarJ.F. and TurnerP.H., J. Chem. Soc., Perkin II, 1972, p. 5.77
15.
‘Witcoflex Staycool’ coating of Baxenden Chemical Co. and The Shirley Research Institute
16.
LehahM.D. and CooperS.L., ‘Polyurethanes in Medicine’, Press CRC, 1986
Millathane Series of TSE, Urethane Division, Petersburg, Ma. 33714, USA; also Notedome Ltd., Coventry, UK
21.
SeefriedC.G., KoleskeJ.V. and CritchfieldF.E., ‘Thermoplastic Urethane Elastomers I: Effect of soft segment variations’, J. Appl. Polym. Sci., 19, 1975, p. 2493; ditto, II: Effect of hard segment content, p. 2503; ditto, III: Effect of isocyanate structure, p. 3185
22.
ZdrahalaR.J., ., ‘Polyester based thermoplastic polyurethanes, I: Effect of hard segment content’, J. Appl. Polym. Sci., 24, 1979, p. 2041
23.
AbouzahrS., WilkesG.L. and OphirZ.H., ‘Structure property behaviour of segmented polyether/MDI/butane diol based urethanes: Effect of composition ratio’, Polymer, 23, 1982, p. 1077
24.
PechholdF. and PruckmayrG., ‘PTME ether glycol: Effect of concentration, molecular weight and molecular weight distribution on properties of MDI/BDO based polyurethanes’, Rubber Chem. and Technol., 55, 1982, p. 76
25.
MinouraY.., ‘Crosslinking and mechanical properties of liquid rubber. Part I: Curative effect of aliphatic diols’, J. Appl. Polym. Sci., 22, 1978, p. 1817; ditto, Part II: Curative effect of aromatic diols, 22, 1978, p. 3101; ditto Part III: Curative effect of aralkyl and alicyclic diols., 23, 1979, p. 1137
26.
DearcoveT.J., CampbellG.A. and AtkinsR.P., ‘Optimising the properties of isocyanate terminated polyurethane prepolymers by SDE’, J. Appl. Polym. Sci., 22, 1978, p. 927
27.
GoodmanJ., ‘Heterochain block copolymers’, Chapter 5 in Developments in Block Copolymers -1. (Ed. Goodman, I.), Elsevier Applied Science, 1985
28.
SpeckhardT.A., ‘Properties of polyiso-butylene polyurethane block copolymers: 2. Macroglycol produced by the Inifer technique’, Polymer, 26, 1955, p. 55
29.
ByrneC.A., ‘Preparation and properties of polyurethane and poly(urethane urea) elastomers from methylene bis 4-cyclohexyl-isocyanate’. Org. Coat. Appl. Polym. Sci. Proc. 47, 1982, p. 49
GuiseG.B. and SmithG.C., ‘Properties of some cast polyurethane rubbers prepared from polycaprolactone polyols and diiso-cyanate’, J. Appl. Polym. Sci., 25, 1980, p. 149
32.
Van BogartJ.W.C., GibsonP.E. and CooperS.L., ‘Structure-property relationships in polycaprolactone polyurethanes’, J. Polym. Sci., Polym. Phys., 21, 1983, p. 65
33.
WrightJ., ‘The development of transparent thermoplastic polyurethane block copolymers’, PERME Report TR7 (November 1977)
34.
RobertsD., ‘The development of transparent polyurethane block copolymers resistant to ballistic impact’, PERME Report TR76, Part 2 (November 1977)
35.
SungC.S. and SchneiderN.S., ‘Structure property relationships of polyurethanes based on TDF, Polymer Alloys (Ed. KlempnerD. and FrischK.C.), Wiley, 1982
36.
AitkenR.R. and JeffsG.H.F., ‘Thermoplastic polyurethane elastomers based on aliphatic diisocyanates: thermal transitions’, Polymer, 18, 1977, p. 197
37.
CunliffeA.V., ., ‘The kinetics of the reaction of isophorone diisocyanate with mono alcohols’, Polymer, 26, 1985, p. 301
38.
ByrneC.A., MackD.P. and CleavesM.A., ‘Aliphatic polyurethane elastomers from the geometric isomers of methylene bis(4-cyclo-hexyl-isocyanate)’, Am. Chem. Soc. Polym Prep., 50, 1983, p. 63
39.
SyedE.A., ‘The synthesis and properties of some transparent polyurethanes’, PhThesis D, Loughborough University of Technology, 1982
40.
Van BogartJ.W.C.., ‘Morphology and properties of short segment block copolymers’, J. Macromol. Sci. Phys., 187, No. 2, 1980 p. 267
41.
Van BogartJ.W.C., ‘PropertiesofMDIand H12MDI based polycaprolactone polyurethanes’, Org. Coat. Plast. Chem., 40, 1979 p. 647
42.
WongS.W.., ‘Reactivity studies and cast elastomers based on trans-cyclohexane 1,4-diisocyanate and 1,6-phenylene diisocyanate’, Org. Coatings Plast. Chem., 43, 1980, p. 926
43.
DeluccaJ.J. and PetrieS., ‘Effects of processing on the optical properties of a transparent polyurethane’, Conf. Plastics Engineering Today for Tomorrow's World, ANTEC ‘83, 41st Annual Conference (SPE), Chicago 2-5 May 1983, pp. 730–733.
44.
Trade literature concerning the FOMBLIN Z range of perfluoropolyethers of Montefluos Spa Division of Montedison, Milan, Italy