Molecular design and stabilization mechanism of acrylonitrile bipolymer. Issue 6 (21st February 2013)
- Record Type:
- Journal Article
- Title:
- Molecular design and stabilization mechanism of acrylonitrile bipolymer. Issue 6 (21st February 2013)
- Main Title:
- Molecular design and stabilization mechanism of acrylonitrile bipolymer
- Authors:
- Ju, Anqi
Guang, Shanyi
Xu, Hongyao - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In order to replace terpolymer with bipolymer, a bifunctional comonomer 3‐aminocarbonyl‐3‐butenoic acid methyl ester (ABM) was synthesized for preparing poly(acrylonitrile‐<italic>co</italic>‐3‐aminocarbonyl‐3‐butenoic acid methyl ester) [P(AN‐<italic>co</italic>‐ABM)] bipolymers as carbon fiber precursor. The structure and stabilization of P(AN‐<italic>co</italic>‐ABM) bipolymers were characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, and differential scanning calorimetry. The monomer reactivity ratios were calculated by the Fineman‐Ross and Kelen‐Tüdõs methods, and the results show that ABM displays higher reactivity than acrylonitrile. Two parameters <italic>E</italic><sub><italic>s</italic></sub> = <italic>A</italic><sub>1618cm</sub><sup>‐1</sup>/<italic>A</italic><sub>2244cm</sub><sup>‐1</sup> and <italic>SI</italic> = (<italic>I</italic><sub>0</sub> ‐ <italic>I</italic><sub><italic>s</italic></sub>)/<italic>I</italic><sub>0</sub> were defined to evaluate the extent of stabilization, and the activation energy (<italic>E</italic><sub><italic>a</italic></sub>) of the stabilization reactions were calculated by Kissinger and Ozawa methods. The results show that the P(AN‐<italic>co</italic>‐ABM) bipolymers exhibit significantly improved stabilization performance when compared with polyacrylonitrile (PAN) homopolymer, such as lower cyclization temperature, lower<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In order to replace terpolymer with bipolymer, a bifunctional comonomer 3‐aminocarbonyl‐3‐butenoic acid methyl ester (ABM) was synthesized for preparing poly(acrylonitrile‐<italic>co</italic>‐3‐aminocarbonyl‐3‐butenoic acid methyl ester) [P(AN‐<italic>co</italic>‐ABM)] bipolymers as carbon fiber precursor. The structure and stabilization of P(AN‐<italic>co</italic>‐ABM) bipolymers were characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, and differential scanning calorimetry. The monomer reactivity ratios were calculated by the Fineman‐Ross and Kelen‐Tüdõs methods, and the results show that ABM displays higher reactivity than acrylonitrile. Two parameters <italic>E</italic><sub><italic>s</italic></sub> = <italic>A</italic><sub>1618cm</sub><sup>‐1</sup>/<italic>A</italic><sub>2244cm</sub><sup>‐1</sup> and <italic>SI</italic> = (<italic>I</italic><sub>0</sub> ‐ <italic>I</italic><sub><italic>s</italic></sub>)/<italic>I</italic><sub>0</sub> were defined to evaluate the extent of stabilization, and the activation energy (<italic>E</italic><sub><italic>a</italic></sub>) of the stabilization reactions were calculated by Kissinger and Ozawa methods. The results show that the P(AN‐<italic>co</italic>‐ABM) bipolymers exhibit significantly improved stabilization performance when compared with polyacrylonitrile (PAN) homopolymer, such as lower cyclization temperature, lower <italic>E</italic><sub>a</sub>, and larger extent of stabilization under the same conditions. Simultaneously, the rheological analysis shows that P(AN‐<italic>co</italic>‐ABM) possesses better spinnability than PAN. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013</p> </abstract> … (more)
- Is Part Of:
- Journal of applied polymer science. Volume 129:Issue 6(2013:Sep. 15)
- Journal:
- Journal of applied polymer science
- Issue:
- Volume 129:Issue 6(2013:Sep. 15)
- Issue Display:
- Volume 129, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 129
- Issue:
- 6
- Issue Sort Value:
- 2013-0129-0006-0000
- Page Start:
- 3255
- Page End:
- 3264
- Publication Date:
- 2013-02-21
- 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.38812 ↗
- 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:
- 3664.xml