Araştırma Makalesi

Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties

Cilt: 15 Sayı: 4 30 Aralık 2019
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Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties

Öz

Azobenzene polymers have great potential and impact on fundamental and applied research. However little is known about their thermal stability and degradation behaviours. Herein, nine conjugated main chain azobenzene polymers were synthesized using the nitroamine derivatives of some diphenylene compounds such as 4-amino-4′-nitrobiphenyl 1, 4-amino-4′-nitrobiphenyl ether 2 and 4-amino-4′-nitrobiphenyl sulfide 3, and comonomers triphenylamine A, N-methyldiphenyl amine B and triphenylphosphine C via diazo coupling reaction. These heteroatom containing polymers were characterized by 1H- and 31P-NMR, FTIR, UV–Vis and Raman spectroscopy. The thermal stability and degradation behaviour of these polymers were studied by means of TGA technique. Electronic spectra of the polymers recorded in DMF showed two strong maxima at ca. 280 and 380 nm. They were resistant to heat up to 270 °C and, produced 41-61% char under a nitrogen atmosphere at 800 °C. UL 94 burning tests performed for TPU Ravathane® (TPE-U) with added azobenzene polymer revealed that these polymers could be used as an intumescent reactive flame retardant additive, particularly for polyurethanes and elastomers, due to their high char yield at relatively high temperatures (e.g 800 °C). The carbonized materials were further characterized by XRD and SEM/EDX. 



Anahtar Kelimeler

Kaynakça

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Ayrıntılar

Birincil Dil

İngilizce

Konular

Mühendislik

Bölüm

Araştırma Makalesi

Yazarlar

Zeynep Bilen Bu kişi benim

Erhan Budak Bu kişi benim

Ozdemir Ozarslan Bu kişi benim

Yayımlanma Tarihi

30 Aralık 2019

Gönderilme Tarihi

23 Temmuz 2018

Kabul Tarihi

18 Aralık 2019

Yayımlandığı Sayı

Yıl 2019 Cilt: 15 Sayı: 4

Kaynak Göster

APA
Bayazit, M. K., Bilen, Z., Budak, E., & Ozarslan, O. (2019). Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar University Journal of Science, 15(4), 329-336. https://doi.org/10.18466/cbayarfbe.446974
AMA
1.Bayazit MK, Bilen Z, Budak E, Ozarslan O. Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar University Journal of Science. 2019;15(4):329-336. doi:10.18466/cbayarfbe.446974
Chicago
Bayazit, Mustafa Kemal, Zeynep Bilen, Erhan Budak, ve Ozdemir Ozarslan. 2019. “Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties”. Celal Bayar University Journal of Science 15 (4): 329-36. https://doi.org/10.18466/cbayarfbe.446974.
EndNote
Bayazit MK, Bilen Z, Budak E, Ozarslan O (01 Aralık 2019) Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar University Journal of Science 15 4 329–336.
IEEE
[1]M. K. Bayazit, Z. Bilen, E. Budak, ve O. Ozarslan, “Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties”, Celal Bayar University Journal of Science, c. 15, sy 4, ss. 329–336, Ara. 2019, doi: 10.18466/cbayarfbe.446974.
ISNAD
Bayazit, Mustafa Kemal - Bilen, Zeynep - Budak, Erhan - Ozarslan, Ozdemir. “Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties”. Celal Bayar University Journal of Science 15/4 (01 Aralık 2019): 329-336. https://doi.org/10.18466/cbayarfbe.446974.
JAMA
1.Bayazit MK, Bilen Z, Budak E, Ozarslan O. Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar University Journal of Science. 2019;15:329–336.
MLA
Bayazit, Mustafa Kemal, vd. “Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties”. Celal Bayar University Journal of Science, c. 15, sy 4, Aralık 2019, ss. 329-36, doi:10.18466/cbayarfbe.446974.
Vancouver
1.Mustafa Kemal Bayazit, Zeynep Bilen, Erhan Budak, Ozdemir Ozarslan. Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar University Journal of Science. 01 Aralık 2019;15(4):329-36. doi:10.18466/cbayarfbe.446974