scholarly journals Relationships between chemical structures of soft segments and fiber mechanical properties of segmented polyurethanes.

1988 ◽  
Vol 45 (10) ◽  
pp. 795-802 ◽  
Author(s):  
Seiichi YAMASHIRO
Keyword(s):  
Mechanical Properties ◽  
Chemical Structures ◽  
Soft Segments ◽  
Segmented Polyurethanes

Study of the Effect of Soft-Segment Length and Concentration on Properties of Polyetherurethanes. II. The Effect on Mechanical Properties

1985 ◽  
Vol 58 (4) ◽  
pp. 701-712 ◽  
Author(s):  
Zoran S. Petrović ◽  
Jaroslava Budinski-Simendić
Keyword(s):  
Mechanical Properties ◽  
Chain Length ◽  
Plastic Flow ◽  
Soft Segment ◽  
Maximum Strength ◽  
Segment Length ◽  
Elongation At Break ◽  
Mechanical Methods ◽  
Soft Segments ◽  
Segmented Polyurethanes

Abstract Three series of segmented polyurethanes with different soft segment lengths and concentrations were examined by TMA, DMA, and mechanical methods. Maximum tensile strengths were obtained when ssc was 40–50%, which was explained by a specific interlocking morphology. No significant effect of soft-segment chain length on maximum strength was found, but higher values were found in the C series when ssc was 60%. Elongation at break increases linearly with ssc but indications that shorter soft segments produce higher extensions was attributed to plastic flow. TMA showed that Tg was independent of ssc in the C and, to a degree, in the B series, while temperature of α-transition in DMA was independent of ssc only in the C series at ssc above 50%.

scholarly journals Thermal and mechanical properties of linear segmented polyurethanes with butadiene soft segments

1981 ◽  
Vol 21 (11) ◽  
pp. 668-674 ◽  
Author(s):  
C. M. Brunette ◽  
S. L. Hsu ◽  
M. Rossman ◽  
W. J. MacKnight ◽  
N. S. Schneider
Keyword(s):  
Mechanical Properties ◽  
Thermal And Mechanical Properties ◽  
Soft Segments ◽  
Segmented Polyurethanes

scholarly journals Studies on the Modification of Commercial Bisphenol-A-Based Epoxy Resin Using Different Multifunctional Epoxy Systems

2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Bisphenol A ◽  
Epoxy Resin ◽  
Tensile Fracture ◽  
Chemical Structures ◽  
Amino Phenol ◽  
Epoxy Systems

The tensile fracture mechanics and thermo-mechanical properties of mixtures composed of two kinds of epoxy resins of different chemical structures and functional groups were studied. The base resin was a bi-functional epoxy resin based on diglycidyl ether of bisphenol-A (DGEBA) and the other resins were (a) distilled triglycidylether of meta-amino phenol (b) 1, 6–naphthalene di epoxy and (c) fluorene di epoxy. This research shows that a small number of multifunctional epoxy systems, both di- and tri-functional, can significantly increase tensile strength (14%) over neat DGEBA while having no negative impact on other mechanical properties including glass transition temperature and elastic modulus. In fact, when compared to unmodified DGEBA, the tri-functional epoxy shows a slight increase (5%) in glass transition temperature at 10 wt.% concentration. The enhanced crosslinking of DGEBA (90 wt.%)/distilled triglycidylether of meta-amino phenol (10 wt.%) blends may be the possible reason for the improved glass transition. Finally, the influence of strain rate, temperature and moisture were investigated for both the neat DGEBA and the best performing modified system. The neat DGEBA was steadily outperformed by its modified counterpart in every condition.

scholarly journals Sulfonated Binaphthyl-Containing Poly(arylene ether ketone)s with Rigid Backbone and Excellent Film-Forming Capability for Proton Exchange Membranes

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1287 ◽  
Author(s):  
Wenmeng Zhang ◽  
Shaoyun Chen ◽  
Dongyang Chen ◽  
Zhuoliang Ye
Keyword(s):  
Mechanical Properties ◽  
Proton Conductivity ◽  
Proton Exchange Membrane ◽  
Proton Exchange ◽  
Thermal Stabilities ◽  
Chemical Structures ◽  
Arylene Ether ◽  
Film Forming ◽  
Ether Ketone ◽  
Microscopic Morphology

Sterically hindered (S)-1,1′-binaphthyl-2,2′-diol had been successfully copolymerized with 4,4′-sulfonyldiphenol and 4,4′-difluorobenzophenone to yield fibrous poly(arylene ether ketone)s (PAEKs) containing various amounts of binaphthyl unit, which was then selectively and efficiently sulfonated using ClSO3H to yield sulfonated poly(arylene ether ketone)s (SPAEKs) with ion exchange capacities (IECs) ranging from 1.40 to 1.89 mmol·g−1. The chemical structures of the polymers were confirmed by 2D 1H–1H COSY NMR and FT-IR. The thermal properties, water uptake, swelling ratio, proton conductivity, oxidative stability and mechanical properties of SPAEKs were investigated in detail. It was found that the conjugated but non-coplanar structure of binaphthyl unit endorsed excellent solubility and film-forming capability to SPAEKs. The SPAEK-50 with an IEC of 1.89 mmol·g−1 exhibited a proton conductivity of 102 mS·cm−1 at 30 °C, much higher than that of the state-of-the-art Nafion N212 membrane and those of many previously reported aromatic analogs, which may be attributed to the likely large intrinsic free volume of SPAEKs created by the highly twisted chain structures and the desirable microscopic morphology. Along with the remarkable water affinity, thermal stabilities and mechanical properties, the SPAEKs were demonstrated to be promising proton exchange membrane (PEM) candidates for potential membrane separations.

The effect of plasticization on the properties of poly(urethaneureas) based on oligoether diols, 2,4-toluenediisocyanate, and aromatic diamines

2018 ◽  
Vol 51 (4) ◽  
pp. 337-358 ◽  
Author(s):  
Vasiliy Tereshatov ◽  
Marina Makarova ◽  
Valeriy Senichev ◽  
Zhanna Vnutskikh ◽  
Tamara Oshchepkova ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Polymer Matrix ◽  
Arctic Climate ◽  
The Arctic ◽  
Aromatic Diamines ◽  
Plasticization Effect ◽  
Soft Segments ◽  
Potential Applications ◽  
Partial Crystallization ◽  
First Time

Segmented poly(urethaneureas) (SPUUs) modified with low glass transition temperature chemically inert liquids are of interest due to their controllable properties and potential applications under various environmental conditions. Investigation into the influence of plasticizers on the properties of SPUUs based on oligotetramethyleneoxide diol (polytetramethyleneoxide), oligopropyleneoxide diol (polypropyleneoxide), 2,4-toluenediisocyanate, Ethacure-300, and methylene-bis- o-chloroaniline was conducted. Partial crystallization of polytetramethyleneoxide segments was identified during cooling of some SPUU samples plasticized by di-(2-ethylhexyl)sebacate (DEHS) and tributyl phosphate. Polypropyleneoxide segments did not crystallize under the same conditions. A low crystallization temperature for the amorphous component of the polymer matrix in SPUU (−100°C to 103°C) was attained at a molecular mass ( Mn) of soft segments equal to 2000 g mol−1 and a DEHS concentration equal to 40–45%. A relationship between the mechanical properties of plasticized SPUU, microphase segregation, and dilution of the polymer matrix was found. For the first time, the effect of dilution with plasticizer on the strength of elastomers was considered. The plasticization effect on the mechanical properties of SPUU was investigated in the temperature diapason from 50°C to −70°C. The results of these investigations can be used in various technologies including the design of SPUUs with high elastic properties at temperatures as low as −70°C, typical of extreme conditions of the Arctic climate.

Rheology of Block Copolymers

2007 ◽  
Author(s):  
Chang Dae Han
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Block Copolymers ◽  
Small Angle ◽  
Volume Fraction ◽  
Synthesis Methods ◽  
Chemical Structures ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Molecular Weight Form

Block copolymer consists of two or more long blocks with dissimilar chemical structures which are chemically connected. There are different architectures of block copolymers, namely, AB-type diblock, ABA-type triblock, ABC-type triblock, and AmBn radial or star-shaped block copolymers, as shown schematically in Figure 8.1. The majority of block copolymers has long been synthesized by sequential anionic polymerization, which gives rise to narrow molecular weight distribution, although other synthesis methods (e.g., cationic polymerization, atom transfer radical polymerization) have also been developed in the more recent past. Owing to immiscibility between the constituent blocks, block copolymers above a certain threshold molecular weight form microdomains (10–50 nm in size), the structure of which depends primarily on block composition (or block length ratio). The presence of microdomains confers unique mechanical properties to block copolymers. There are many papers that have dealt with the synthesis and physical/mechanical properties of block copolymers, too many to cite them all here. There are monographs describing the synthesis and physical properties of block copolymers (Aggarwal 1970; Burke and Weiss 1973; Hamley 1998; Holden et al. 1996; Hsieh and Quirk 1996; Noshay and McGrath 1977). Figure 8.2 shows schematically four types of equilibrium microdomain structures observed in block copolymers. Referring to Figure 8.2, it is well established (Helfand and Wasserman 1982; Leibler 1980) that in microphase-separated block copolymers, spherical microdomains are observed when the volume fraction f of one of the blocks is less than approximately 0.15, hexagonally packed cylindrical microdomains are observed when the value of f is between approximately 0.15 and 0.44, and lamellar microdomains are observed when the value of f is between approximately 0.44 and 0.50. Some investigators have observed ordered bicontinuous double-diamonds (OBDD) (Thomas et al. 1986; Hasegawa et al. 1987) or bicontinuous gyroids (Hajduk et al. 1994) at a very narrow range of f (say, between approximately 0.35 and 0.40) for certain block copolymers. Figure 8.2 shows only one half of the symmetricity about f = 0.5. Transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS), and small-angle neutron scattering (SANS) have long been used to investigate the types of microdomain structures in block copolymers.

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