2016
DOI: 10.1080/15685551.2015.1136531
|View full text |Cite
|
Sign up to set email alerts
|

Copolyethersulfones of 1,4:3,6-dianhydrohexitols and bisphenol A

Abstract: International audienc

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
5
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
6

Relationship

2
4

Authors

Journals

citations
Cited by 7 publications
(6 citation statements)
references
References 23 publications
1
5
0
Order By: Relevance
“…From the results given in Figure S3, we can observe that polymers based on isosorbide (P1 and P2) showed higher Tg values, compared to those obtained from bisphenol A (P3 and P4). In a previous work, we have obtained similar behavior for poly(ether-sulfone) from isosorbide and bisphenol A [42]. Not a big difference on Tg values was observed between oxide or sulfide functions.…”
Section: Ref Polymer Yield A) (%)supporting
confidence: 65%
“…From the results given in Figure S3, we can observe that polymers based on isosorbide (P1 and P2) showed higher Tg values, compared to those obtained from bisphenol A (P3 and P4). In a previous work, we have obtained similar behavior for poly(ether-sulfone) from isosorbide and bisphenol A [42]. Not a big difference on Tg values was observed between oxide or sulfide functions.…”
Section: Ref Polymer Yield A) (%)supporting
confidence: 65%
“…In addition, isohexides have been used as bifunctional monomers for the synthesis of polycarbonate, polyester, polyurethane, and polyether through step-growth polymerization. The incorporation of isohexides into polymer backbones can result in achieving favorable properties, including high thermal stability, high glass transition temperature ( T g ), and improved optical transparency and activity [ 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 ]. Furthermore, Mitsubishi has commercialized isosorbide-based polycarbonate under the brand name of Durabio ® , which has already found applications in automobile and electronic industries [ 13 , 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…The high T g values ranging from 144 to 180°C (Table 7) for these polymers, depending on the structure of the diol and fluorinated components in chains. The bio‐based PEPTs (P2 and P4) exhibit higher Tg compared to those of the petro‐based polymers (P1 and P3), as previous work revealed, 66,67,51 because of the high rigidity promoted by the combined presence of 1,2,3‐triazole and dianhydrohexitol heterocyclic moieties. The T g values of PEPTs derived from monomer (7) (P3, 178°C) are higher than those of PEPTs based on monomer (6) (P1, 144°C) due to the presence of inter and intra‐chains hydrogen bonding between hydroxyl groups that can decrease the flexibility of the polymer chains with increasing in their T g .…”
Section: Resultsmentioning
confidence: 86%