Structural effects of diacidic and glycolic moieties on physicochemical properties of aromatic polyesterdiols from glycolysis/esterification of poly(ethylene terephthalate) wastes
M. Billiau-loreau et al., Structural effects of diacidic and glycolic moieties on physicochemical properties of aromatic polyesterdiols from glycolysis/esterification of poly(ethylene terephthalate) wastes, POLYMER, 43(1), 2002, pp. 21-28
Useful polyols for rigid polyurethane foam manufacture may be obtained by g
lycolysis of post-consuming poly(ethylene terephthalate) (PET) wastes. The
physicochemical properties of about 100 polyesterdiols were measured, the p
olyol molecular structure being built on three diacidic moieties and three
glycolic moieties in various proportions. Viscosity, foaming agent compatib
ility and storage stability are the most relevant physicochemical propertie
s.
Statistical analysis was made over more than 50 polyols. Molar ratios of th
e constitutive moieties to terephthalic residue were taken as composition p
arameter. From a Principal Component Analysis (PCA) it was found that 141b
compatibility is of opposite viscosity and independent of polyol storage st
ability, the properties being governed essentially by the glycolic moieties
. Multiple regressions gave prediction equations for viscosity and 141b com
patibility as a function of moieties amounts.
The own effect of each structural unit was also investigated through some m
ore homogeneous panels of polyols. Lack of storage stability appears when t
he proportions of constitutive PET units in glycolic and acidic moieties ov
ercome critical values. The viscosity of the polyols. increases greatly wit
h decreasing hydroxyl value or increasing the proportion of aromatic diacid
ic residues. (C) 2001 Elsevier Science Ltd. All rights reserved.