A high temperature polymer of phthalonitrile‐substituted phosphazene with low melting point and good thermal stability. Issue 39 (3rd July 2015)
- Record Type:
- Journal Article
- Title:
- A high temperature polymer of phthalonitrile‐substituted phosphazene with low melting point and good thermal stability. Issue 39 (3rd July 2015)
- Main Title:
- A high temperature polymer of phthalonitrile‐substituted phosphazene with low melting point and good thermal stability
- Authors:
- Zhao, Fenghua
Liu, Ruojin
Yu, Xiaoyan
Naito, Kimiyoshi
Qu, Xiongwei
Zhang, Qingxin - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>A phthalonitrile‐substituted phosphonitrilic monomer has been synthesized from phosphonitrilic chloride trimer and then polymerized with addition of 4‐(hydroxylphenoxy)phthalonitrile (HPPN). The chemical structures of the phosphonitrilic monomer and polymer were characterized by Fourier Transform Infrared spectroscopy (FT‐IR) and proton Nuclear Magnetic Resonance spectroscopy (<sup>1</sup>H NMR). Curing behaviors and thermal stabilities of the polymer were investigated through differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Analysis showed that the monomer has large processing temperature window and good thermal stability. Apparent activation energy, initial curing temperature (<italic>T</italic><sub>i</sub>), curing temperature (<italic>T</italic><sub>p</sub>), and termination curing temperature (<italic>T</italic><sub>f)</sub> of the phosphonitrilic polymer were explored. Dynamic mechanical analysis (DMA), glass transition temperature (<italic>T</italic><sub>g</sub>) were studied, and limiting oxygen index (LOI) were estimated from the van Krevelen equation, which indicates the polymer process high modulus and good flame retardance. Micro‐scale combustion calorimetry (MCC) was also used for evaluating the flammability of the polymers. Postcuring effects were explored, showing excellent thermal and mechanical properties with postcuring. © 2015 Wiley Periodicals, Inc. J. Appl. Polym.<abstract abstract-type="main"> <title>ABSTRACT</title> <p>A phthalonitrile‐substituted phosphonitrilic monomer has been synthesized from phosphonitrilic chloride trimer and then polymerized with addition of 4‐(hydroxylphenoxy)phthalonitrile (HPPN). The chemical structures of the phosphonitrilic monomer and polymer were characterized by Fourier Transform Infrared spectroscopy (FT‐IR) and proton Nuclear Magnetic Resonance spectroscopy (<sup>1</sup>H NMR). Curing behaviors and thermal stabilities of the polymer were investigated through differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Analysis showed that the monomer has large processing temperature window and good thermal stability. Apparent activation energy, initial curing temperature (<italic>T</italic><sub>i</sub>), curing temperature (<italic>T</italic><sub>p</sub>), and termination curing temperature (<italic>T</italic><sub>f)</sub> of the phosphonitrilic polymer were explored. Dynamic mechanical analysis (DMA), glass transition temperature (<italic>T</italic><sub>g</sub>) were studied, and limiting oxygen index (LOI) were estimated from the van Krevelen equation, which indicates the polymer process high modulus and good flame retardance. Micro‐scale combustion calorimetry (MCC) was also used for evaluating the flammability of the polymers. Postcuring effects were explored, showing excellent thermal and mechanical properties with postcuring. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. <bold>2015</bold>, <italic>132</italic>, 42606.</p> </abstract> … (more)
- Is Part Of:
- Journal of applied polymer science. Volume 132:Issue 39(2015)
- Journal:
- Journal of applied polymer science
- Issue:
- Volume 132:Issue 39(2015)
- Issue Display:
- Volume 132, Issue 39 (2015)
- Year:
- 2015
- Volume:
- 132
- Issue:
- 39
- Issue Sort Value:
- 2015-0132-0039-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2015-07-03
- Subjects:
- Polymers -- Periodicals
Polymerization -- Periodicals
668.9 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4628 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/app.42606 ↗
- Languages:
- English
- ISSNs:
- 0021-8995
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4946.600000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3922.xml