Impact of amine additives on the mechanical properties of hydrogen bonding π-conjugated polymers

Polymer ◽  
2020 ◽  
Vol 204 ◽  
pp. 122856 ◽  
Author(s):  
Shekhar Shinde ◽  
Nagarjuna Gavvalapalli
2020 ◽  
Vol 7 (21) ◽  
pp. 4197-4221 ◽  
Author(s):  
Francisco Colmenero ◽  
Jakub Plášil ◽  
Jiří Sejkora

The structure, hydrogen bonding, X-ray diffraction pattern and mechanical properties of six important uranyl carbonate minerals, roubaultite, fontanite, sharpite, widenmannite, grimselite and čejkaite, are determined using first principles methods.


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.


2015 ◽  
Vol 48 (20) ◽  
pp. 7670-7680 ◽  
Author(s):  
Joshua D. Monk ◽  
Eric W. Bucholz ◽  
Tane Boghozian ◽  
Shantanu Deshpande ◽  
Jay Schieber ◽  
...  

2021 ◽  
Author(s):  
Ming Yan ◽  
Junfeng Shi ◽  
Song Tang ◽  
Guohang Zhou ◽  
Jiexiang Zeng ◽  
...  

The SA/PAA-VSNP fiber was obtained using dynamic wet spinning through dynamic hydrogen bonding in the double network structure.


Author(s):  
Eul-Yong Shin ◽  
Sungmin Park ◽  
Hyungju Ahn ◽  
Hyunjung Jin ◽  
In Soo Kim ◽  
...  

PTO2-urea10 which forms intermolecular hydrogen bonding maintained its TFT mobility well due to improved crystallinity when PTO2-urea10 TFT was stretched despite damage to polymer films.


2020 ◽  
Vol 81 ◽  
pp. 106279 ◽  
Author(s):  
Jyotishkumar Parameswaranpillai ◽  
M.R. Sanjay ◽  
Suchart Siengchin ◽  
Sisanth Krishnan Sidhardhan ◽  
Seno Jose ◽  
...  

ACS Nano ◽  
2012 ◽  
Vol 6 (3) ◽  
pp. 2008-2019 ◽  
Author(s):  
Owen C. Compton ◽  
Steven W. Cranford ◽  
Karl W. Putz ◽  
Zhi An ◽  
L. Catherine Brinson ◽  
...  

2014 ◽  
Vol 29 (5) ◽  
pp. 654-661 ◽  
Author(s):  
Luiz A Kanis ◽  
Ellen L Marques ◽  
Karine M Zepon ◽  
Jefferson R Pereira ◽  
Saulo Pamato ◽  
...  

This study reports the results of the characterization of cellulose acetate butyrate and polycaprolactone-triol blends in terms of miscibility, swelling capacity, mechanical properties, and inflammatory response in vivo. The cellulose acetate butyrate film was opaque and rigid, with glass transition ( T g) at 134℃ and melting temperature of 156℃. The cellulose acetate butyrate/polycaprolactone-triol films were transparent up to a polycaprolactone-triol content of 60%. T g of the cellulose acetate butyrate films decreased monotonically as polycaprolactone-triol was added to the blend, thus indicating miscibility. FTIR spectroscopy revealed a decrease in intramolecular hydrogen bonding in polycaprolactone-triol, whereas no hydrogen bonding was observed between cellulose acetate butyrate and –OH from polycaprolactone-triol. The increase in polycaprolactone-triol content in the blend decreased the water uptake. An increase in polycaprolactone-triol content decreased the modulus of elasticity and increased the elongation at break. A cellulose acetate butyrate/polycaprolactone-triol 70/30 blend implanted in rats showed only an acute inflammatory response 7 days after surgery. No change in inflammation mediators was observed.


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