Influence of trisilanol isooctyl POSS content on the structure, morphology and rheological properties of thermoplastic polyurethane (TPU)

2020 ◽  
Vol 40 (9) ◽  
pp. 727-735
Author(s):  
Rudinei Fiorio ◽  
Chaitanya Danda ◽  
João Maia

AbstractIn this study, thermoplastic polyurethanes (TPUs) containing trisilanol isooctyl polyhedral oligomeric silsesquioxane (POSS), a reactive nanofiller, were synthesized and characterized rheologically and morphologically, and the effects of POSS content on the melt thermal stability of the TPUs are investigated. Samples containing 0, 0.23, 0.57, 1.14, and 2.23% (w/w) POSS were synthesized by reactive extrusion and characterized by Fourier transform infrared spectroscopy (FTIR), oscillatory and extensional rheometry, atomic force microscopy (AFM), and small- and wide-angle X-ray scattering (SAXS and WAXS, respectively). The rheological properties of molten TPU are time-dependent and the melt thermal stability of the TPU is maximal at 1.14% of POSS. The addition of 0.23 and 0.57% POSS promotes strain-hardening at low extensional strain rates (0.01 and 0.10 s−1), not affecting the extensional characteristics at higher strain rates. The addition of increasing amounts of POSS leads to the formation of POSS-rich clusters well dispersed in the TPU matrix. SAXS and WAXS results show that the POSS domains are amorphous and that POSS does not modify the crystalline structure of TPU. Therefore, this work indicates that synthesizing TPU in the presence of trisilanol isooctyl POSS can increase the melt thermal stability of the polymer, facilitating its processing.

2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Alaaddin Cerit ◽  
Mustafa Esen Marti ◽  
Ulku Soydal ◽  
Suheyla Kocaman ◽  
Gulnare Ahmetli

Epoxy resin (ER) was modified with four different epoxide compounds, 4,5-epoxy-4-methyl-pentane-2-on (EMP), 3-phenyl-1,2-epoxypropane (PhEP), 1-chloro-2,3-epoxy-5-(chloromethyl)-5-hexene (CEH), and a fatty acid glycidyl ester (FAGE), to improve its chemical and physical properties. The effects of the addition and amount of these modifiers on mechanical, thermal, and coating properties were investigated. Atomic force microscopy was used to observe the changes obtained with the modification. The influence of the modifying agents on the curing process was monitored through FTIR spectroscopy. The curing degrees of ER and modified ERs (M-ERs) were found to be over 91%. The results showed that tensile strength of ER improved till 30% (wt.) with addition of the modifier content. Modification with EMP and PhEP remarkably enhanced the thermal stability of ER to be highly resistant to the corrosive media.


2017 ◽  
Vol 41 (22) ◽  
pp. 13287-13292 ◽  
Author(s):  
Karolina Wenelska ◽  
Ewa Mijowska

In this work, exfoliated molybdenum disulfide (MoS2) modified by a metal oxide (MoS2/MxOy) was prepared by a hydrothermal method and characterized by atomic force microscopy (AFM), Raman spectroscopy and transmission electron microscopy (TEM).


2020 ◽  
Vol 299 ◽  
pp. 281-286 ◽  
Author(s):  
D.I. Tishkevich ◽  
A.I. Vorobjova ◽  
A.V. Trukhanov

Through-pores alumina membranes of 50 μm thickness and 70 × 70 mm size have been fabricated to deposit Ni nanowires by electrochemical processing. Due to highly ordered microstructure of the membranes, the pores were filled by nanowires almost to 100%. The membrane nanowires composite morphology, structure and thermodynamic characteristics have been studied by scanning electron microscopy, atomic-force microscopy, X-ray diffraction and differential thermal analysis. The thermal stability of Ni nanowires into porous alumina template and whole composite was determined.


Polymers ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 16 ◽  
Author(s):  
Joanna Brzeska ◽  
Agnieszka Tercjak ◽  
Wanda Sikorska ◽  
Marek Kowalczuk ◽  
Maria Rutkowska

The aim of this study is the analyze the structure of branched polyurethanes based on synthetic poly([R,S]-3-hydroxybutyrate) and their blends with biopolymers and montmorillonite. The properties which would predict the potential susceptibility of these materials to degradation are also estimated. Fourier-transform infrared spectroscopy with attenuated total reflection analysis shows that poly([d,l]-lactide) is on the surfaces of polyurethanes, whereas chitosan and starch are included inside the blend network. Atomic force microscopy images have shown that the surfaces of investigated samples are heterogenous with the formation of spherulites in case of pure polyurethanes. The presence of biopolymers in the blend reduced the crystallinity of polyurethanes. Thermal stability of blends of polyurethanes with poly([d,l]-lactide) and polysaccharides decreased in comparison to pure polyurethanes. Although the tensile strength is reduced after the blending of polyurethanes with biopolymers, the elongation at break increased, especially in the case of polyurethane/poly([d,l]-lactide) blends. The presence of polysaccharides in the obtained blends caused the significant reduction of contact angle after one minute from water drop immersion. This hydrophilizing effect is the highest when montmorillonite has been incorporated into the chitosan blend. The estimated properties of the obtained materials suggest their potential sensitivity on environmental conditions.


2010 ◽  
Vol 445 ◽  
pp. 160-163
Author(s):  
Shigeki Sawamura ◽  
Naonori Sakamoto ◽  
De Sheng Fu ◽  
Kazuo Shinozaki ◽  
Hisao Suzuki ◽  
...  

Thermal stability of bottom electrode thin films (La0.5Sr0.5)CoO3 (LSCO) and (La0.6Sr0.4)MnO3 (LSMO) were investigated. The crystallization and surface morphology of the heterostructure were characterized using x-ray diffraction and atomic force microscopy. Resistivity of the LSCO thin film was 25 cm. However, the resistivity of LSCO thin film increases sharply with annealing temperature. The LSMO thin film has high resistivity (100 mcm). The film does not decompose after thermal processing at 900 °C. To confirm thermal stability, we examined the effect of post annealing at various temperatures on the morphology and resistivity. Results showed that LSMO has higher thermal stability than that of LSCO.


2020 ◽  
Vol 12 (3) ◽  
pp. 319-325
Author(s):  
Seong Baek Yang ◽  
Sung Min Park ◽  
Dong Jun Kwon ◽  
Jae-Cheon Shin ◽  
Yeasmin Sabina ◽  
...  

A novel PVA/clay (MMT) film is prepared for the first time based on the saponification of the PVAc/MMT film in the presence of heterogeneous conditions. With the help of optical microscopy, the characteristics and surface morphology of the saponified PVA/MMT film is confirmed. It is found to contain black MMT nanoparticles in PVAc films as the content of MMT increased. According to atomic force microscopy results, PVAc/MMT films shows unexpected surface roughness owing to the slow progress of the saponification reaction in the presence of MMT contents in the PVAc matrix. The thermal stability of the PVA/MMT film is measured using thermal gravimetric analyses. The results indicate that thermal stability increases significantly when the MMT concentration increases. The entire structure of the PVA/MMT nanocomposite has been elucidated using XRD. To prove the differences between the PVAc/MMT and the PVA/MMT films, XRD measurements and Fourier transform Infrared spectroscopy analyses are utilized.


2014 ◽  
Vol 627 ◽  
pp. 12-17
Author(s):  
Britto Satheesh ◽  
Kim Yeow Tshai ◽  
Nick Warrior

This paper investigates the effects of polysaccharide additive agent on the morphological and thermal properties of thermosetting polymer. The weight percentage (wt%) of Diglycidyl Ether of Bisphenol A (DGEBA) epoxy resin to Hexamethylenediamine (HMDA) hardener were kept constant while a varyingwt% of chitosan, ranging from 0 to 10wt% was introduced. The chitosan filled epoxy hardener mixture was allowed to cure at 40°C for a period of 12 hours. Dynamic Scanning Calorimetry (DSC) and Thermal Gravimetric Analysis (TGA) were conducted on the specimens to analyse the effects of chitosan loading on thermal stability and transition temperature while Atomic Force Microscopy (AFM) was used to investigate the changes to its morphological property. At chitosan loading of 2.5wt% and below, good dispersion of the additive was observed. Apparent agglomeration and phase separation were formed when chitosan content increases above 7.5wt%. The formation of bulky chitosan agglomeration was found capable of enhancing the thermal stability of the thermoset polymer. The diamine acted as the co-reactants with DGEBA as well as spacer which decrease the effect of material brittleness due to addition of chitosan.


Sign in / Sign up

Export Citation Format

Share Document