Fabrication of High Dielectric Materials Through Selective Insertion of Functionalized Reduced Graphene Oxide on Hard Segment of Thermoplastic Polyurethane

The presence of microcapacitors near percolatrion threshold determines dielectric permittivity of a material. Motivated by this concept, we focused our work by preferentially allocating functionalized reduced graphene oxide (FRGO) in hard segment (disperse phase) of Thermoplastic polyurethane (TPU) by solution blending method and characterized. Morphological studies of TPU/FRGO nanocomposites established homogeneous dispersion of FRGO throughout the TPU matrix. It is noted that TPU/FRGO (1 phr) nanocomposites exhibit maximum increase in tensile strength (33%) and elongation at break (10%). Thermogravimetric analysis (TGA) showed maximum enhancement in onset of decomposition temperature (~6 °C) in 2 phr FRGO loaded TPU. Differential scanning calorimetry (DSC) analysis showed maximum reduction (~2 °C) in glass transition temperature (Tg) of soft segment of TPU followed by maximum improvements in melting temperature (~4 °C) as well as crystallization temperature (~22 °C) of hard segment compared to neat TPU. Further, a significantly high value of dielectric permittivity (401) is achieved in 1.5 phr loaded FRGO at 100 Hz due to the formation of significantly higher number of microcapacitors near the percolation threshold. It is anticipated that such thermally stable and mechanically strong high dielectric TPU/FRGO nanocomposites can find applications in the field of electronic devices.

Investigating Physio-Thermo-Mechanical Properties of Polyurethane and Thermoplastics Nanocomposite in Various Applications

The effect of the soft and hard polyurethane (PU) segments caused by the hydrogen link in phase-separation kinetics was studied to investigate the morphological annealing of PU and thermoplastic polyurethane (TPU). The significance of the segmented PUs is to achieve enough stability for further applications in biomedical and environmental fields. In addition, other research focuses on widening the plastic features and adjusting the PU–polyimide ratio to create elastomer of the poly(urethane-imide). Regarding TPU- and PU-nanocomposite, numerous studies investigated the incorporation of inorganic nanofillers such as carbon or clay to incorporating TPU-nanocomposite in several applications. Additionally, the complete exfoliation was observed up to 5% and 3% of TPU–clay modified with 12 amino lauric acid and benzidine, respectively. PU-nanocomposite of 5 wt.% Cloisite®30B showed an increase in modulus and tensile strength by 110% and 160%, respectively. However, the nanocomposite PU-0.5 wt.% Carbone Nanotubes (CNTs) show an increase in the tensile modulus by 30% to 90% for blown and flat films, respectively. Coating PU influences stress-strain behavior because of the interaction between the soft segment and physical crosslinkers. The thermophysical properties of the TPU matrix have shown two glass transition temperatures (Tg’s) corresponding to the soft and the hard segment. Adding a small amount of tethered clay shifts Tg for both segments by 44 °C and 13 °C, respectively, while adding clay from 1 to 5 wt.% results in increasing the thermal stability of TPU composite from 12 to 34 °C, respectively. The differential scanning calorimetry (DSC) was used to investigate the phase structure of PU dispersion, showing an increase in thermal stability, solubility, and flexibility. Regarding the electrical properties, the maximum piezoresistivity (10 S/m) of 7.4 wt.% MWCNT was enhanced by 92.92%. The chemical structure of the PU–CNT composite has shown a degree of agglomeration under disruption of the sp2 carbon structure. However, with extended graphene loading to 5.7 wt.%, piezoresistivity could hit 10-1 S/m, less than 100 times that of PU. In addition to electrical properties, the acoustic behavior of MWCNT (0.35 wt.%)/SiO2 (0.2 wt.%)/PU has shown sound absorption of 80 dB compared to the PU foam sample. Other nanofillers, such as SiO2, TiO2, ZnO, Al2O3, were studied showing an improvement in the thermal stability of the polymer and enhancing scratch and abrasion resistance.

Polyurethane-urea-amide-based triblock copolymer contains functionalized polystyrene: Synthesis, characterization and solvent resistivity study

Synthesized polystyrene (PSt) with a molecular weight of 2100 g/mol, hexamethylene diisocyanate (HMDI), 6-hexylamino benzamide (6B), and N1-(6-aminohexyl)-N4-(6-benzoylaminohexyl)terephthalamide (6T6B) are used to make a copolymer of thermoplastic elastomers. The prepared polymers’ inherent viscosity results (0.4–1.1 dL/g) support the polymer’s high mass. The presence of a monodentate urea group in the polymer chain is confirmed by FT-IR tests. The temperature dependence of FT-IR confirms that the synthesized copolymer has a space length dependent reversible crystallinity. Data from differential scanning calorimetry (DSC) also shows that the hard segment crystallization is strong and reversible in nature. The XRD results show that the polymer is semi-crystalline. The TGA analysis confirmed that the synthesized copolymers are thermally stable up to 290°C. The presence of hydrogen bonds in polymer chains is thermally reversible. The polymer’s solvent resistivity is excellent due to its high crystallinity.

Polyimide-Based Membrane Materials for CO2 Separation: A Comparison of Segmented and Aromatic (Co)polyimides

A series of new poly(ethylene oxide) (PEO)-based copolyimides varying in hard segment structure are reported in this work as CO2 selective separation membranes. Their structural diversity was achieved by using different aromatic dianhydrides (4,4′-oxydiphthalic anhydride (ODPA), 4,4’-(hexafluoroisopropylidene)diphthalic anhydride (6FDA)) and diamines (4,4′-oxydianiline (ODA), 4,4′-(4,4′-isopropylidene-diphenyl-1,1′- diyldioxy)dianiline (IPrDA), 2,3,5,6-tetramethyl-1,4-phenylenediamine (4MPD)), while keeping the content of PEO (2000 g/mol) constant (around 50%). To get a better insight into the effects of hard segment structure on gas transport properties, a series of aromatic polyimides with the same chemistry was also studied. Both series of polymers were characterized by 1HNMR, FTIR, WAXD, DSC, TGA, and AFM. Permeabilities for pure He, O2, N2, and CO2 were determined at 6 bar and at 30 °C, and for CO2 for pressures ranging from 1 to 10 bar. The results show that OPDA-ODA-PEO is the most permeable copolyimide, with CO2 permeability of 52 Barrer and CO2/N2 selectivity of 63, in contrast to its fully aromatic analogue, which was the least permeable among polyimides. 6FDA-4MPD-PEO ranks second, with a two times lower CO2 permeability and slightly lower selectivity, although 6FDA-4MPD was over 900 times more permeable than OPDA-ODA. As an explanation, partial filling of hard domain free voids by PEO segments and imperfect phase separation were proposed.

Polyurethane cationomers containing fluorinated soft segments with hydrophobic properties

The synthesis of ecological waterborne polyurethane cationomers containing fluorinated polyol (0–20 wt.%) was successfully performed. FTIR and NMR analysis results confirmed the structure of the obtained polyurethane cationomers and incorporation of fluorinated component into the polyurethane chains. Average molar mass and phase structure of the obtained PU thin films were determined based on GPC, FTIR, WAXD and SEM-EDX results. The obtained cationomers have linear structures with clearly visible microphase separation of soft and hard segment domains; the presence of fluorinated polyol changes the strength of hydrogen bonds and in consequence degree of phase separation. The activation energy of glass transition was calculated based on multi-frequency DSC data. It has been shown that the presence of soft fluorinated segments in the cationomer structure strongly influences the hydrophobic, thermal and mechanical properties of the obtained films.

Hardness Modulated Thermoplastic Poly(ether ester) Elastomers for the Automobile Weather-Strip Application

As a means of developing new material for automobile weather-stripping and seal parts replacing the conventional ethylene propylene diene monomer rubber/polypropylene vulcanizate, a series of poly(ether ester) elastomers are synthesized. The hardness is modulated by controlling chain extender composition after fixing the hard segment to soft segment ratio. Targeted hardness is achieved by partly substituting conventional chain extender 1,4-butandiol for soybean oil-originated fatty acid amide diol that bears a long chain branch. The crystallinity and phase separation behavior resultant elastomer are also tunable simply by modulating chain extender composition and hard to soft segment ratio.