scholarly journals Synthesis, characterization and properties of phthalonitrile-etherified resole resin

e-Polymers ◽  
2020 ◽  
Vol 20 (1) ◽  
pp. 500-509
Author(s):  
Dayong Zhang ◽  
Xiaohui Liu ◽  
Xuefeng Bai ◽  
Yinyin Zhang ◽  
Gang Wang ◽  
...  

AbstractA new type of phthalonitrile-etherified resole resin (PNR) was synthesized from resole resin and 4-nitrophthalonitrile. The differential scanning calorimetry results showed that the curing temperature of PNR is lower than that of phthalonitrile resin. Excellent thermal stability and bonding properties were obtained after curing at 220°C. TGA showed that in air, the temperature of 5% weight loss (T5%) of the cured PNR was 446°C, approximately 41°C higher than that of resole resin (RS), and the char yield at 800°C increased from 4% for RS to 33% for PNR. The shear strengths of PNR at room temperature and high temperature were increased by 8% and 133%, respectively, over those of RS, and after aging at 350°C for 2 h, these values were increased by 262% and 198%, respectively, over those of RS. Its excellent curing behavior, heat resistance and high bonding strength show that PNR can be used as a high temperature-resistant adhesive.

2017 ◽  
Vol 737 ◽  
pp. 294-298 ◽  
Author(s):  
Sukantika Manatsittipan ◽  
Kamontip Kuttiyawong ◽  
Sunan Tiptipakorn

In this study, the biodegradability and the thermal properties of PBS and levan were prepared in the internal mixer with levan contents of 0, 0.5, and 1 wt%. The results from Differential Scanning Calorimetry (DSC) present that the melting temperature of PBS was slightly decreased with increasing levan contents. That means there was no significant effect of levan on melting behavior of the composites at the added content. From the TGA thermograms, it could be seen that there was no significant effect on the thermal stability when adding levan. The degradation temperature at 5% weight loss for all composites were in the rage of 377-379 oC. Furthermore, char yields for all contents were closed to zero. Moreover, the water absorption of PBS/Levan composites was increased with levan content. The biodegradation was observed after 4-day burial period; the holes from degradation were larger with levan contents.


2017 ◽  
Vol 30 (9) ◽  
pp. 1094-1100 ◽  
Author(s):  
Zhao Juan ◽  
Qing Ning ◽  
Jiang Shaohua ◽  
Wu Suping

A novel carborane-containing epoxy resin was prepared via the curing reaction between epoxy resin (E51) and 1,2-bis(4-aminophthalimide)dimethyl-1,2-dicarba-closododecaborane (4-AP CBR). According to the nonisothermal differential scanning calorimetry method and the T-β extrapolation method, the curing temperatures of the 4-AP CBR/E51 system were theoretically determined. The cured carboranyl epoxy resin was analyzed by thermogravimetric analysis (TGA), which revealed that the resin had excellent thermal stability and thermal oxidative stability. The results of TGA indicated that the initial decomposition temperature of the resin was exceeding 400°C and the char yield at 800°C was around 60% both under nitrogen and in air atmosphere.


2015 ◽  
Vol 19 (4) ◽  
pp. 1411-1414 ◽  
Author(s):  
Ming-Li Jiao ◽  
Kai Yang ◽  
Jian Cao ◽  
Hong-Yan Liu ◽  
Qin Qi ◽  
...  

High-ortho boron-containing phenolic fibers were prepared, and cured in a solution of formaldehyde and hydrochloric acids. The resulted fibers were heattreated in N2 at tiered temperature. Differential scanning calorimetry and thermogravimetric analysis were employed to characterize thermal performance. The results show that the addition of boron in the precursor resin can increase the peak of curing temperature and thermal stability.


2018 ◽  
Vol 51 (1) ◽  
pp. 52-63
Author(s):  
J Dhanalakshmi ◽  
CT Vijayakumar

Bispropargyl ether (BPE) of bisphenol-A was prepared. It was blended with 4,4’-bismaleimido diphenyl methane (BMI, 0.5:0.5 mol). The copper sulphate pentahydrate (CuSO4·5H2O) was blended (1% w/w) separately with pure BPE and BPE-BMI blend and the materials were thermally cured. The structural characterization of the materials was done using a Fourier-transform infrared spectrophotometer. The curing behaviour of the materials was investigated using differential scanning calorimetry. The presence of copper salt in BPE shifted the curing temperature to lower temperature region. The presence of copper salt in BPE-BMI blend also decreased the curing onset temperature by approximately 15°C. The thermal property of the polymers was investigated using thermogravimetry. The incorporation of copper salt in BPE-BMI blend led to polymer with increased thermal stability.


2016 ◽  
Vol 29 (1) ◽  
pp. 13-25 ◽  
Author(s):  
Liping Sheng ◽  
Jingcheng Zeng ◽  
Suli Xing ◽  
Changping Yin ◽  
Jinshui Yang ◽  
...  

To maintain outstanding thermal stability, amino- and hydroxyl-containing phthalonitrile monomers, 4-(4-aminophenoxy)-phthalonitrile (APN) and 4-(4-hydroxyphenoxy)-phthalonitrile (HPN) were selected and synthesized. Their structures were confirmed by proton nuclear magnetic resonance spectroscopy. Their curing polymers were characterized by Fourier transform infrared spectroscopy. The self-catalytic curing behaviors of the monomers were investigated by differential scanning calorimetry (DSC) at different heating rates. From the results, APN exhibits a higher curing temperature, while HPN exhibits a longer curing time. Then, mixtures of these monomers were investigated by DSC. The result shows that the 50/50 mixture exhibits different autocatalytic behaviors: the curing temperature is lower than that of APN and the curing time of the mixture is shorter than that of HPN. Furthermore, thermogravimetric analysis shows that the polymer from the mixture exhibits higher temperature of 5% weight loss ( T5%) and char yield value at 800°C than those of the polymers from each monomer. All these results indicate that the new mixture resin exhibits improved processability with excellent thermal stability, attributed to the synergistic effect between similar monomers; the synergistic effect optimizes the cure reaction kinetics and promotes cross-linking reactions, thereby producing an excellent resin; this approach is a new method for improving the processability without sacrificing thermal stability.


2012 ◽  
Vol 554-556 ◽  
pp. 258-262
Author(s):  
Jiao Jiao Shang ◽  
Jian Wu Lan ◽  
Shao Jian Lin ◽  
Si Chen ◽  
Ya Ni Li

A new poly(ester-imide-ether) (PEIE) was prepared by melt polymerization from 1,4-butanediol(BD), polytetrahydrofuran diol (PTMG) and a novel imide dicarboxylic acid monomer which was synthesized from 3,3',4,4'-biphenyltetracarboxylic di-anhydride(BPDA) and glycine acid(GLY). The structure, thermal behaviour and elastic recovery of polymer were characterized by FT-IR. thermogravimetric analysis (TGA), differential scanning calorimetry thermograms (DSC) and laboratory stretching machine. The results showed this polymer has excellent thermal stability, 5 % weight loss temperature was at 354°C. Meanwhile, the DSC curve showed that glass-transition temperature and crystallization temperature of the polymer were at -30 °C and 160 °C, respectively. The excellent elastic recovery was still displayed at low temperature.


2019 ◽  
Author(s):  
Andreas Boelke ◽  
Yulia A. Vlasenko ◽  
Mekhman S. Yusubov ◽  
Boris Nachtsheim ◽  
Pavel Postnikov

<p>The thermal stability of pseudocyclic and cyclic <i>N</i>-heterocycle-stabilized (hydroxy)aryl- and mesityl(aryl)-l<sup>3</sup>-iodanes (NHIs) through thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) is investigated. NHIs bearing <i>N</i>-heterocycles with a high N/C-ratio such as triazoles show among the lowest descomposition temperatures and the highest decomposition energies. A comparison of NHIs with known (pseudo)cyclic benziodoxolones is made and we further correlated their thermal stability with reactivity in a model oxygenation. </p>


2020 ◽  
pp. 095400832097759
Author(s):  
Ke Li ◽  
Hua Yin ◽  
Kun Yang ◽  
Pei Dai ◽  
Ling Han ◽  
...  

Designing novel low-melting, high-rigidity phthalonitrile resin is of great significance in the current context of development. In this study, rigid spirocycle acetal structure was introduced into phthalonitrile to reduce the melting point and maintain their thermal stability. The chemical structure of resins was confirmed by nuclear magnetic resonance (NMR) spectrometry, matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry and Fourier-transform infrared (FTIR) spectroscopy. The curing behaviors were studied by differential scanning calorimetry (DSC). Thermal stability and mechanical properties of the cured resins were investigated by dynamic mechanical thermal analysis (DMTA) and thermogravimetric analysis (TGA). The processability was studied by rheological analysis. The results indicated the three monomers had a low melting temperature, wide processing windows and low viscosities. These polymers did not exhibit Tg from room temperature to 400°C, exhibited superb dynamic mechanical property and thermal stability.


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