The effects of catalyst on the molecular weight, chemical structure, and yellowness of isosorbide-based polycarbonate (ISB-PC) in the melt-transesterification and polycondensation stages were investigated. Results showed that the high steric hindrance and intramolecular hydrogen bonding of the endohydroxyl group (endo−OH) of ISB enabled its reactivity to be lower than that of the exohydroxyl group (exo−OH). We also found that the reactivity of endo− OH with diphenyl carbonate can be preferentially activated by strong electrophilic catalysts, and that the configuration of the ISB-PC chain strongly depended on the reactivity balance between endo−OH and exo−OH. Various catalysts with different coordinate capacities, acidity coefficients, and radius of metal ion were further tested. Catalysts with a calcium or zinc ion showed a higher reactivity of endo−OH than exo−OH, resulting in a high glass-transition temperature of ISB-PCs. Results suggested as well that the thermal stability of ISB-PC may be correlated to the amount of OH groups at the chain ends, whereas its yellowness mainly arose from 1,4-sorbitan due to the hydrolysis of ISB.
Isosorbide polycarbonate (ISB-PC) was prepared by melt transesterification and polycondensation reaction by employing ISB and diphenyl carbonate (DPC) as monomers.
Microwave curing technology has been widely used in resin and its composite materials. In order to study its effect for curing unsaturated polyester resin (UPR) composites containing calcium carbonate (CaCO3) filler, this paper first investigated the influence of microwave power and microwave irradiation time on the curing characteristics of UPR. Then, CaCO3 particles were added to the UPR to investigate the microwave curing effect of the UPR composites containing the CaCO3. The results showed that microwave irradiation could heat the UPR sample evenly, and rapidly cause the chain growth reaction, thus greatly shortening the curing time. The curing degree and products of the samples after microwave curing were consistent with that of the thermal curing. The addition of CaCO3 particles could increase the heating rate of the UPR composites, which would accelerate the curing rate of the UPR. However, higher microwave power could lead to pore defects inside the UPR composites with higher CaCO3 content, resulting in a lower strength. Thus, the compactness of the samples should be improved by reducing the microwave power and prolonging the microwave treatment time.
In this study, we investigated the influence of the small molecule 4,4 0 -thiobis(6-tert-butyl-m-methyl phenol) (AO300) on the miscibility of poly(isosorbide-co-1,4-cyclohexanedimethanol carbonate) (IcC-PC) with bisphenol A polycarbonate (BPA-PC) through the formation of hydrogen-bonding networks. Differential scanning calorimetry and morphological observation revealed that the initially, immiscible BPA-PC/IcC-PC blends become miscible through the addition of small molecules. Fourier transform infrared spectroscopy confirmed that intermolecular hydrogen bonds formed between the hydroxyl groups of AO300 and the carbonyl groups of the studied polycarbonates. These polycarbonates exhibited different hydrogen-bonding behaviors and various degrees of glasstransition temperature composition dependence. Dynamic mechanical analysis demonstrated that AO300 played an antiplasticization role in the BPA-PC/IcC-PC blends with improved storage moduli. To our knowledge, this article is the first to describe the miscibility of isosorbide-based polycarbonate with BPA-PC.
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