Phase Transition Behavior of Main Chain Nematic Liquid-Crystalline Polymers Based on 2-methyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone and 2-tert-butyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone

2012 ◽  
Vol 1403 ◽  
Author(s):  
Christain Melchert ◽  
M. Behl ◽  
A. Lendlein

ABSTRACTThe control of phase transition behavior in liquid crystalline polymers could enable potential application in the field of actuators and sensors by enabling a higher actuator performance of liquid crystalline elastomers (LCE). In this context the phase transition behavior of siloxane based liquid crystalline copolymers synthesized from 1,1,3,3-tetramethyldisiloxane, 2-methyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone (M-MeHq), and 2-tert-butyl-1,4-bis[4-(4-pentenyloxy)benzoyl]hydroquinone (M-tBHq) was explored. The selected monomers provided different thermal stabilities of the nematic phase, while the non-flexible siloxane spacer suppressed a smectic phase. The mesogenic properties were studied by means of differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and wide angle X-ray scattering (WAXS). With increasing fraction of M-MeHq the nematic phase of the copolymer was stabilized and a tailoring of relatively low TNI was achieved.

2017 ◽  
Vol 41 (14) ◽  
pp. 6514-6522 ◽  
Author(s):  
Yuki Arakawa ◽  
Yukito Sasaki ◽  
Kazunobu Igawa ◽  
Hideto Tsuji

A novel class of hydrogen bonding liquid crystalline benzoic acids with alkylthio groups was established and their phase transition behavior was investigated in detail.


e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
R. N. Jana ◽  
H. Bhunia ◽  
C. Im

AbstractPhase transition behavior of silicone based liquid crystalline (LC) polymers with variable isotropic transition temperatures (Ti), synthesized from poly(methyl hydrosiloxane), 10-undecenoic acid based crosslinking agent and cholesterol based side chain mesogen, was studied by differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and X-ray diffraction (XRD) measurements. The chemical structure of the mesogenic monomer and the LC polymers were confirmed by Fourier transform infra-red (FT-IR) spectroscopy and 1HNMR spectroscopy. DSC studies showed that the glass transition temperatures (Tg) and Ti of the LC polymers decreased with increasing proportion of mesogenic crosslinking agent at its low proportion and at its higher proportion Ti disappeared completely indicating that the polymeric chains had less chance to orient in the network structure. The results were consistent with the XRD and POM studies.


RSC Advances ◽  
2021 ◽  
Vol 11 (63) ◽  
pp. 39813-39820
Author(s):  
Cong Luo ◽  
Jingke Pei ◽  
Wenyue Zhuo ◽  
Yanhua Niu ◽  
Guangxian Li

The deformation mechanism and phase transition behavior of polytetrafluoroethylene (PTFE) under stretching conditions (25, 50, 100 °C) were investigated by using differential scanning calorimetry (DSC), small angle X-ray scattering (SAXS), and X-ray diffraction (XRD).


2019 ◽  
Vol 10 (8) ◽  
pp. 1725
Author(s):  
Raffaella Aversa ◽  
Relly Victoria Virgil Petrescu ◽  
Antonio Apicella ◽  
Florian Ion Tiberiu Petrescu

A method for PET mechanical properties enhancement by reactive blending with HBA/HNA Liquid Crystalline Polymers for in situ highly fibrillar composites preparation is presented. LCP/PET blends were reactively extruded in presence of Pyromellitic Di-Anhydride (PMDA) and then characterized by Differential Scanning Calorimetry, Thermally Stimulated Currents and tensile mechanical properties. Moderate amounts of LCP in the PET (0.5 and 5%) and small amounts of thermo-active and reactive compatibilizer in the blend (0.3%) were found to significantly improve LCP melt dispersion, melts shear transfer and LCP fibril formation and adhesion. An unexpected improvement was probably due to the presence of two distinct phases’ supra-molecular structures involving PET-LCP and PMDA.


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