The Influential Factors of Property on Polyether-Polyol Type Polyurethane Elastomer

2013 ◽  
Vol 704 ◽  
pp. 289-293 ◽  
Author(s):  
Fu Chun Xie ◽  
Fu Quan Guo

Polyurethane (PU) elastomers based on all kinds of polyether-polygol, diisocyanate and chain extender were prepared by two-step processes;the different influential factors of polyurethane elastomer were discussed in detail. The results showed that when the molecular weight of polyether-polygol increased, the hardnesstensile strength and tear resistance of polyurethane elastomer decreased, but the elongation at break increased;the property of polyurethane elastomer increased with the increasing perecentage of hard segment phase;R numerical value (-NCO/-OH) was controlled between 1.01 and 1.03;the shorter chain-extender had excellent microphase separation and mechanical properties;With the amount of 1, 4-butadiene alcohol (BDO) incrasing, the performance of polyurethane elastomer becomes well,but when the amount of 1, 4-butadiene alcohol comes to a point it appears reverse.

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 212
Author(s):  
Natascha Riehle ◽  
Kiriaki Athanasopulu ◽  
Larysa Kutuzova ◽  
Tobias Götz ◽  
Andreas Kandelbauer ◽  
...  

The effect of hard segment content and diisocyanate structure on the transparency and mechanical properties of soft poly(dimethylsiloxane) (PDMS)-based urea elastomers (PSUs) was investigated. A series of PSU elastomers were synthesized from an aminopropyl-terminated PDMS (M¯n: 16,300 g·mol−1), which was prepared by ring chain equilibration of the monomers octamethylcyclotetrasiloxane (D4) and 1,3-bis(3-aminopropyl)-tetramethyldisiloxane (APTMDS). The hard segments (HSs) comprised diisocyanates of different symmetry, i.e., 4,4′-methylenebis(cyclohexyl isocyanate) (H12MDI), 4,4′-methylenebis(phenyl isocyanate) (MDI), isophorone diisocyanate (IPDI), and trans-1,4-cyclohexane diisocyanate (CHDI). The HS contents of the PSU elastomers based on H12MDI and IPDI were systematically varied between 5% and 20% by increasing the ratio of the diisocyanate and the chain extender APTMDS. PSU copolymers of very low urea HS contents (1.0–1.6%) were prepared without the chain extender. All PSU elastomers and copolymers exhibited good elastomeric properties and displayed elongation at break values between 600% and 1100%. The PSUs with HS contents below 10% were transparent and became increasingly translucent at HS contents of 15% and higher. The Young’s modulus (YM) and ultimate tensile strength values of the elastomers increased linearly with increasing HS content. The YM values differed significantly among the PSU copolymers depending on the symmetry of the diisocyanate. The softest elastomer was that based on the asymmetric IPDI. The elastomers synthesized from H12MDI and MDI both exhibited an intermediate YM, while the stiffest elastomer, i.e., that comprising the symmetric CHDI, had a YM three-times higher than that prepared with IPDI. The PSUs were subjected to load–unload cycles at 100% and 300% strain to study the influence of HS morphology on 10-cycle hysteresis behavior. At 100% strain, the first-cycle hysteresis values of the IPDI- and H12MDI-based elastomers first decreased to a minimum of approximately 9–10% at an HS content of 10% and increased again to 22–28% at an HS content of 20%. A similar, though less pronounced, trend was observed at 300% strain. First-cycle hysteresis among the PSU copolymers at 100% strain was lowest in the case of CHDI and highest in the IPDI-based elastomer. However, this effect was reversed at 300% strain, with CHDI displaying the highest hysteresis in the first cycle. In vitro cytotoxicity tests performed using HaCaT cells did not show any adverse effects, revealing their potential suitability for biomedical applications.


2011 ◽  
Vol 197-198 ◽  
pp. 1294-1298
Author(s):  
Ping Lu ◽  
Wei Bo Huang ◽  
Xue Qiang Ma ◽  
Xu Dong Liu

New polyaspartic ester (PAE) chain extender named PAE-f was prepared via two steps of Michael addition reactions:(1) Michael addition reaction between 4,4’-methylenebis(2-methyl cyclohexyl amine) (Laromin C260) and excessive dialkyl maleates(DEF); (2) The Michael addition reaction of the residual dialkyl maleates of step (1) with polyester polyamine Jeffamine D230. The two-steps method proposed could reduce the reaction time in comparison with the current one step Michael addition reaction method, thus satisfying the industrialized production. New PAE based polyureas were synthesized by reacting the PAE-f chain extender with aliphatic polyisocyanates 4,4’-diisocyanato dicyclohexylmethane (H12MDI) / polyester polyamine Jeffamine D2000 prepolymer at room temperature. FT-IR and GPC were employed to characterize the new PAE prepared, and the morphology, molecular weight distribution and mechanical properties of the prepared PAE based polyureas were investigated by means of FT-IR and GPC. The FT-IR results indicated that the hydrogen bonding degree of amidogen groups in hard segments of the prepared polyureas were high, the length of hydrogen bonding were 0.305nm~0.306nm. The GPC experimental results show that the weight average molecular weight of the PAE-f based polyureas were 4.95×104~6.05×104,Mw/Mn were 1.65~1.97, the molecular weight distribution were relatively narrow. The mechanical properties demonstrated that the tensile strength were 14.7~22.5MPa, Elongation at break were 306~511%, Yang’s modulus were 67~127MPa, Shore A hardness were 64~83. The mechanical properties confirmed that the polyureas based on PAE-f were kinds of elastomeric materials with satisfied flexibility, strength, module and hardness.


2004 ◽  
Vol 77 (2) ◽  
pp. 380-390
Author(s):  
Wonmun Choi ◽  
Tomoyuki Matsumura

Abstract The reactions of dichloroalkanes and sodium tetra-sulfide (Na2S4) were carried out in a mixture of water and toluene to produce corresponding cyclic polysulfides and polysulfide polymer. The low molecular weights of cyclic sulfides were obtained by the reaction at 90 °C, while the high molecular weight of polysulfide polymer was obtained by the reaction at 50 °C. GPC chromatograms and Mass spectra revealed that the structures of cyclic polysulfide were 1:1, 2:2, and 3:3 adducts of dichloroalkane and sodium tetra-sulfide. The mechanical properties of vulcanized NR at 148 °C with cyclic sulfides were similar to that with sulfur. However, both tensile strength and elongation at break of vulcanized NR at 170 °C with cyclic sulfides are much higher than that with sulfur. The aging properties of vulcanized NR at 148 °C or 170 °C with cyclic polysulfides indicate better stability.


2012 ◽  
Vol 512-515 ◽  
pp. 2127-2130
Author(s):  
Li Huo ◽  
Cai Xia Dong

The mechanical properties were investigated of a series of PA-PEG thermalplastic elastomer based on PA1010 and polytetramethylene glycol (PEG) with varying hard and soft segment content. Dynamic mechanical measurements of these polymers have carried out over a wide range of temperatures. The block copolymers exhibit three peaks, designated as α, β and γ in the tanδ-temperature curve. The α transition shifts to higher temperature with increasing hard block molecular weight. However, at a constant hard molecular weight, the α transition shifts to higher temperature and the damping increases on increasing the soft segment molecular weight. DMA results show that the block copolymers exhibit a microphase separation structure and both soft and hard segments were found to be crystallizable. The degree of phase separation increases with increasing hard block molecular weight.


2020 ◽  
Vol 986 ◽  
pp. 18-23
Author(s):  
Patcharapon Somdee ◽  
Timea Lassu-Kuknyo ◽  
Csaba Konya ◽  
Tamás Szabó ◽  
Kálmán Marossy

The effect of monoethylene glycol (mEG) acting as chain extender in polypropylene glycol (PPG-4000) and 4,4ʹ-diphenylmethane diisocyanate (MDI) reaction was investigated. Polyurethane elastomers (PUR) were changed from flexible to rigid materials by varying the mEG content. Results show that Shore A and D hardness values trend to increase with increasing mEG content. It appears that increasing the chain extender content increases the hard segment content in the polyurethane structure. Moreover, increasing the mEG content increases Young’s modulus and the tensile strength of PUR, while elongation at break decreases. The chemical structure of the hard segment of PUR was characterized by Infrared (IR) spectroscopy. IR spectra exhibited the bands typical for PUR consisting of –NH, CH2– and C=O groups. The spectra reveal a few interactions between the polymeric chains that appear to be responsible for the shift of transmittance peak and decrease of some peak intensity. This may be due to the hard segment aggregating more to form domains in the PUR when mEG content was increased.


2020 ◽  
Vol 1001 ◽  
pp. 16-21
Author(s):  
Ju Jie Sun ◽  
Hai Rui Wang ◽  
Lan Cao ◽  
Tridib K. Sinha

Chain extender plays a significant role in enhancing the final mechanical properties of thermoplastic polyurethane (TPUs) derived from polytetra methylene etherglycol (PTMG) and 4,4-diphenylmethane diisocyanate (MDI). In this research we focused on the effect that mixed chain extender of ethylene glycol (EG) and 1,4-butanediol (BDO) used has on the phase behavior and morphology of high hard block content TPUs. DSC, FTIR, and mechanical testing were mainly used to characterize the morphology and properties of the TPUs materials. Through this work we were able to show that mixed ratio of different chain extenders had dramatic effects on the properties of the TPUs. After mixing EG and BDO, the degree of hydrogen bonding, melting temperature, tensile strength, tear strength, and hardness of TPUs are all reduced, the glass transition temperature is increased. when the mixing ratio is 1: 1 , the elongation at break is increased to 672% . However, when the mixing ratio is n (EG): n (BDO) = 1: 2, the tensile strength is increased to 29.2 MPa, and the elongation at break is reduced to 353%.


2011 ◽  
Vol 183-185 ◽  
pp. 1611-1615 ◽  
Author(s):  
Jian Hua Wang ◽  
Shuen Liang ◽  
Yan Yan Wang ◽  
Chun Rong Tian ◽  
Xiu Li Zhao

Polyurethane (PU) with mixed poly(ethylene glycol) / poly(ε-caprolactone) (PEG/PCL) soft segments is a representatively kind of degradable polyurethane material. Polyurethane foams (PUF) with mixed PEG/PCL soft segments were synthesized by using one pot method, and their mechanical and dynamic mechanical properties were investigated. Influences of PEG/PCL weight ratio and molecular weight of soft segments on PUF's mechanical and dynamic mechanical properties were studied. The results showed that: with increasing content of PCL, PUF's tensile strength, elongation at break, stress at certain tensile/compressive strain and storage modulus increased gradually; with increasing molecular weight of soft segment, PUF's elongation at break increased, but tensile strength, stress at certain tensile/compressive strain and storage modulus all decreased accordingly; glass transition temperature (Tg) of PUF with various soft segments decreased according to the following sequence: PEG-400, PCL-210N, PEG-1000 and PTMG1000; loss factor of PUF with PEG/PCL mixed soft segments was higher than that of PUF with individual PEG or PCL soft segments.


RSC Advances ◽  
2014 ◽  
Vol 4 (46) ◽  
pp. 24095-24102 ◽  
Author(s):  
Chao Deng ◽  
Yulin Cui ◽  
Tingting Zhao ◽  
Mei Tan ◽  
He Huang ◽  
...  

Polyurethane–urea supramolecular hydrogel with excellent mechanical and processible properties is developed. The mechanical properties including shear modulus, elongation at break, tensile strength and compression stress can be adjusted by altering the diisocyanate content.


2013 ◽  
Vol 830 ◽  
pp. 172-175
Author(s):  
Cheng Zhi Chuai ◽  
Zhi Zhang

Ethylene glycol (EG) and polyethylene glycol (PEG) were added as plasticizers to improve the processing performance of cellulose acetate (CA). The CA with 30% plasticizers were melted by HAAKE at 200 °C. The effects of EG and PEG (degree of polymerization in 200-800) on rheological properties and mechanical properties of CA were investigated. The results show that the plasticizing time, equilibrium torque and melt viscosity of the plasticizing system increase with the increase of PEG molecular weight, while the processing performance decreased. The tensile strength of the system decrease as the PEG molecular weight increased. The plasticizing system which contents 30% PEG-200(degree of polymerization is 200) shows the maximum elongation at break. The minimum values appeared in both flexural strength and flexural modulus in the CA/PEG-200 system.


2021 ◽  
pp. 089270572110514
Author(s):  
Jing Sun ◽  
Anrong Huang ◽  
Shanshan Luo ◽  
Min Shi ◽  
Jiling Song ◽  
...  

Biodegradable poly(butylene adipate-co-terephthalate)/poly(lactic acid) (PBAT/PLA) composites were prepared by melt blending, and chain extender was used to improve the compatibility of PBAT/PLA blends through the chemical reaction. The influence of PLA and chain extender contents on mechanical properties, morphology, and rheological properties of PBAT/PLA composites was systematically investigated. The results revealed that the Young’s modulus and stress values gradually increased under the same strain, whereas the elongation at break decreased with the increase of chain extender content for PBAT/PLA (80/20) composites. Noteworthy, the presence of chain extender improves the interfacial compatibility between PLA and PBAT phases. At the chain extender content of 0.4, 0.6, and 0.8 wt.%, the extensional viscosity of the composites exhibited an increasing trend, whereas an obvious strain-hardening phenomenon emerged in the uniaxial extensional curves.


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