2011
DOI: 10.1016/j.reactfunctpolym.2011.07.002
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Synthesis and characterization of sulfonated telechelic bisphenol A polycarbonate ionomers

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Cited by 21 publications
(16 citation statements)
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“…In this way a d-spacing of 31 Å has been obtained Figure 3. We have previously reported [39] that the one-pot reaction of BMSC, BPA and SBENa does not produce telechelic ionomers since the reaction mixture remains opaque and the SBENa can be mainly recovered unreacted at the end of the polymerization process. In order to improve the reaction of BMSC with BPA we have adopted an approach similar to that used for telechelic PBT synthesis.…”
Section: Resultsmentioning
confidence: 99%
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“…In this way a d-spacing of 31 Å has been obtained Figure 3. We have previously reported [39] that the one-pot reaction of BMSC, BPA and SBENa does not produce telechelic ionomers since the reaction mixture remains opaque and the SBENa can be mainly recovered unreacted at the end of the polymerization process. In order to improve the reaction of BMSC with BPA we have adopted an approach similar to that used for telechelic PBT synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…For this reason, BPA and 3% by mol of SBENa have been pre-reacted for 90 minutes at 210°C before the addition of BMSC. According to our previous work [39] a mixture of tetramethylammonium hydroxide and NaOH has been used as catalyst. The clay (3 wt% respect to the polymer) modified with a 1,3-di-hexadecylimidazolium salt (D-2AI) was added at the beginning of the pre-step.…”
Section: Resultsmentioning
confidence: 99%
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“…Moreover, since the diphenyl carbonate can react with both phthalic acids and resorcinol, two parallel reaction pathways can occur in this case. Therefore, the study of the reaction mechanism is crucial in order to obtain a polymer with the desired end-groups composition and properties [26][27][28][29][30].…”
Section: Introductionmentioning
confidence: 99%