Vanillin based polymers: V. Poly(hydrovanilloin–urethane)

2021 ◽  
pp. 204124792198989
Author(s):  
Ananda S Amarasekara ◽  
Rocio Garcia-Obregon

Renewable resources based hydrovanilloin [1,2- bis(4-hydroxy-3-methoxyphenyl)-1,2-ethanediol] was synthesized in 86% yield by electrochemical dimerization of vanillin in aqueous NaOH. This symmetrical bis-phenol monomer was then used for the preparation of urethane polymers by two different methods. In the first method a 1:2 mole ratio mixture of hydrovanilloin and diisocyanate was polymerized in DMF using 1,4-diazabicyclo[2,2,2]octane as the catalyst at 60°C, for 1 h to give poly(hydrovanilloin–urethane)s. In the second method diisocyanates were first reacted with polyethylene glycol-400 to give pre-polymers. Then prepolymers were reacted with equivalent amount of hydrovanilloin at 60°C for 4 days to produce poly(hydrovanilloin-ethylene glycol-urethane)s. The first method resulted hard poly(hydrovanilloin–urethane)s showing Tg values in the range of 121–172°C. The second method yielded softer poly(hydrovanilloin-ethylene glycol-urethane)s and these polymers failed to show distinct glass transition temperatures in the DSC analysis. However, poly(hydrovanilloin-ethylene glycol-urethane)s showed better thermal stabilities than polymers without polyethylene glycol units.

2014 ◽  
Vol 2014 ◽  
pp. 1-7
Author(s):  
Esmael Rostami ◽  
Maryam Bagherzadeh ◽  
Tahereh Alinassab ◽  
Maryam Mohammadpour ◽  
Masume Zangooei ◽  
...  

We report the synthesis of new polyamides containing 2,6-bis(2-thio-2-(4-carboxyphenyl)-1-oxo)pyridine subunit, under microwave irradiation using Yamasaki phosphorylation method. The solubility, thermal behavior, and viscosity of polyamides were evaluated. The structures of polymers have been characterized using IR and 1H NMR spectroscopy. These polyamides showed good solubility, viscosity, high thermal stability, and glass transition temperatures. Their viscosities and glass transition temperatures are in the range of 0.63–0.88 and 223–295°C, respectively. Thermal stabilities for 10% weight loss (T10) are 137–173°C and for 50% weight loss (T50) are in the range of 483–523°C. The study of surface morphology showed particle and amorphous structures.


1997 ◽  
Vol 9 (3) ◽  
pp. 323-332
Author(s):  
H G Boston ◽  
V Sreenivasulu Reddy ◽  
P E Cassidy ◽  
J W Fitch ◽  
Diane Stoakley ◽  
...  

A series of new fluorinated, high-temperature polymers has been prepared from 1, 1, - bis( p-carboxyphenyl)-2, 2, 2-trifluoroethanol (3FOH). This diacid was synthesized by oxidation of 1, 1-di( p-tolyl)-2, 2, 2-trifluoroethanol, which was obtained from p-bromotoluene and ethyl trifluoroacetate. The 3FOH was also reacted with dimethyl sulphate to yield 1-methoxy-1, 1- bis( p-carboxyphenyl)-2, 2, 2-trifluoroethane (3FM), and with SOCl2 to produce 1-chloro-1, 1- bis( p-chloroformylphenyl)-2, 2, 2-trifluoroethane (3FCl). These two diacids, as the acid chlorides, were polymerized with six aromatic and four aliphatic diamines to produce polyamides which had viscosities ranging from 0.32 to 1.52 dl g−1, thermal stabilities up to 518 °C in nitrogen and glass transition temperatures from 165 °C to 337 °C. The dielectric constants of these polyamides ranged from 2.64 to 2.99. The 3FM- and 3FCl-containing polyamides were compared with the 6F (hexafluoroisopropylidene) analogues and found to be somewhat less thermally stable and had equal or lower Tgs.


2021 ◽  
Author(s):  
Minjie Shen ◽  
Srikanth Vijjamarri ◽  
Hongda Cao ◽  
Karla Solis ◽  
Megan L. Robertson

Spiro polycycloacetals were synthesized from vanillin and syringaldehyde, along with high-performance co-monomers, exhibiting high glass transition temperatures and thermal stabilities, and rapid rates of hydrolysis in acidic solutions.


2011 ◽  
Vol 217-218 ◽  
pp. 1606-1610
Author(s):  
Dong Jiang ◽  
Xiao Ran Zhang ◽  
Yan Mei Ma ◽  
Cheng You Ma

A series of random polysulfone/polyethersulfone (PSF/PES) copolymers were synthesized by the polycondensation of 4, 4'-isopropylidendiphenol, 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-dichlorodiphenyl sulfone in the presence of K2CO3. We obtained a series of copolymers by changing the molar ratio of 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-isopropylidendiphenol (it was marked as the ratio of S:A). The copolymers have the similar solubility with polyethersulfone. They also have high glass transition temperatures (Tg: 199°C~229°C) and 5% weight loss temperatures (4, 4'-isopropylidendiphenol: 4, 4΄-dihyolroxy diphenyl sulfone=1:1, Td5=497°C). At the same time the elongation at break is much higher than that of PES, while the tensile strength is a little lower than that of PES.


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