Structural characterization of nylon 7 by solid-state nuclear magnetic resonance, differential scanning calorimetry and attenuated total reflectance Fourier transform infra-red spectroscopy

Polymer ◽  
1994 ◽  
Vol 35 (1) ◽  
pp. 66-74 ◽  
Author(s):  
C JOHNSON
2008 ◽  
Vol 33 (4) ◽  
pp. 61-68 ◽  
Author(s):  
C. T. de Carvalho ◽  
A. B. Siqueira ◽  
E. Y. Ionashiro ◽  
M. Pivatto ◽  
M. Ionashiro

The 2-methoxycinnamylidenepyruvic acid (2-MeO-HCP) was synthesized and characterized for nuclear magnetic resonance (¹H and 13C NMR), mass spectrometry (MS), Infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). The application of DSC for purity determination is well documented in literature and is used in the analysis of pure organic compounds. The molecular geometry and vibrational frequencies of 2-MeO-HCP have been calculated.


2021 ◽  
Vol 17 (2) ◽  
pp. 177
Author(s):  
Edi Pramono ◽  
Rosid Eka Mustofa ◽  
Ozi Adi Saputra ◽  
Yulianto Adi Nugroho ◽  
Deana Wahyunigrum ◽  
...  

<p>Kajian struktur dan degradasi termal pada membran hibrida poliviniliden fluorida (PVDF)/lempung bentonit (BNT) telah dilakukan. Penelitian ini bertujuan mengetahui pengaruh penambahan BNT terhadap pembentukan fasa PVDF dan sifat termalnya. Membran hibrida PVDF/lempung BNT dibuat dengan metode inversi fasa. Membran yang dihasilkan dikarakterisasi dengan <em>attenuated total reflectance fourier transform infrared</em> (ATR-FTIR), <em>x-ray diffraction</em> (XRD), dan <em>differential scanning calorimetry</em> (DSC). Hasil penelitian menunjukkan membran PVDF/BNT memiliki struktur polimorf PVDF fasa α dan β yang terkonfirmasi dari data FTIR dan XRD. Data DSC menunjukkan penurunan nilai titik leleh (Tm) dengan penambahan BNT, dan dengan rentang suhu pelelehan yang lebih kecil. Kristalisasi PVDF terjadi secara isothermal dan adanya BNT menghasilkan titik kristalisasi (Tc) pada suhu yang lebih tinggi dibandingkan membran PVDF murni. Analisis termal dengan DSC memberikan informasi komprehensif pelelehan dan kristalisasi dari polimorf PVDF pada matriks membran.</p><p id="docs-internal-guid-c92edf53-7fff-cf03-76f3-f207f37c74f5" style="line-height: 1.2; text-align: justify; margin-top: 6pt; margin-bottom: 6pt;" dir="ltr"><strong>Effect of Bentonite toward Polymorph Phase Formation and Thermal Properties of Polyvinylidene Fluoride/Bentonite Hybrid Membranes. </strong>The study of the structure and thermal properties of PVDF/bentonite (BNT) hybrid membranes has been carried out. This study aims to determine the effect of BNT addition on the phase formation and thermal properties of the PVDF. In this study, PVDF/BNT hybrid membranes were prepared through the phase inversion method. The resulting membrane was characterized by Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR), x-ray diffraction (XRD), and differential scanning calorimetry (DSC). The results showed that the PVDF/BNT membrane has a PVDF polymorph structure with α and β phases confirmed by FTIR and XRD data. The DSC data showed that the addition of BNT decrease of the melting point (Tm) and with a smaller melting temperature range. PVDF polymorph crystallization occurs isothermally and the presence of BNT produces a crystallization point (Tc) at a higher temperature than pristine PVDF membrane. Thermal analysis with DSC provides comprehensive information on melting and crystallization of PVDF polymorphs in the membrane matrix.</p>


2015 ◽  
Vol 2 (1) ◽  
pp. 13-20 ◽  
Author(s):  
Syed Nasir Abbas Bukhari ◽  
Ng Shin Hwei ◽  
Ibrahim Jantan

Current analytical techniques for characterizing solid-state pharmaceuticals include powder x-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, Raman spectroscopy, electron microscopy and nuclear magnetic resonance. Powder x-ray diffraction and differential scanning calorimetry are mainstream techniques but they lack spatial resolution. Scanning electron microscopy and micro-Raman spectroscopy provide good chemical and optical characterization but they are not capable of analysing very small nanoparticles. Transmission electron microscopy and nano-thermal analysis can provide explicit characterization of nanoparticles but they are invasive. Nuclear magnetic resonance offers good spatial resolution but its use is mainly limited by poor sensitivity and high costs. In view of the many challenges posed by existing methods, new and novel techniques are being continually researched and developed to cater to the growing number of solid formulations in the pipeline and in the market. Some of the recent advances attained in the solid-state analysis of pharmaceutical are summarized in this review article.


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