scholarly journals Oligomeric epoxide–amine adducts based on 2-amino-N-isopropylacetamide and α-amino-ε-caprolactam: Solubility in presence of cyclodextrin and curing properties

2013 ◽  
Vol 9 ◽  
pp. 2803-2811 ◽  
Author(s):  
Julian Fischer ◽  
Helmut Ritter

2-Amino-N-isopropylacetamide and α-amino-ε-caprolactam were reacted with glycerol diglycidyl ether to give novel oligomeric thermoresponsive epoxide–amine adducts. These oligomers exhibit a lower critical solution temperature (LCST) behavior in water. The solubility properties were influenced with randomly methylated β-cyclodextrin (RAMEB-CD) and the curing properties of the amine–epoxide mixtures were analyzed by oscillatory rheology and differential scanning calorimetry, whereby significant differences in setting time, viscosity, and stiffness were observed.

1999 ◽  
Vol 72 (4) ◽  
pp. 580-586 ◽  
Author(s):  
Ramanan Krishnamoorti

Abstract Thermodynamic interactions and phase behavior in binary blends of model mixed microstructure polybutadienes with model 1,4-polyisoprene were studied using small angle neutron scattering and differential scanning calorimetry (DSC). The microstructure of the polybutadiene ranged from 8% 1,2 (92% 1,4) to 90% 1,2 (10% 1,4) units, while the polyisoprene contained 93% 1,4 and 7% 3,4 units. The blends of protonated polybutadienes (HPB) with deuterated 1,4 polyisoprene (DPI) exhibited lower critical solution temperature (LCST) behavior when the polybutadiene contained 38 mol % or more of 1,2 units. Below this 1,2 content of the polybutadiene, all HPB/DPI blends were found to be phase separated at all temperatures above 25 °C. The DSC measurements revealed that other than a blend containing 8% 1,2-polybutadiene and (protonated) 1,4 polyisoprene, all other blends were single phase at room temperature. These results are understood in the context of previous work performed by Han and coworkers on deuterated polybutadiene-protonated polyisoprene blends.


2014 ◽  
Vol 10 ◽  
pp. 1951-1958 ◽  
Author(s):  
Alexander Burkhart ◽  
Helmut Ritter

The monomer 2-methacrylamido-caprolactam (4) was synthesized from methacryloyl chloride (3) and racemic α-amino-ε-caprolactam (2). Copolymerization of 4 with N,N-dimethylacrylamide (5) was carried out by a free-radical mechanism using 2,2’-azobis(2-methylpropionitrile) (AIBN) as an initiator. The new copolymers show a lower critical solution temperature (LCST) in water and an upper critical solution temperature (UCST) in ethanol, 1-propanol, and 1-butanol. The solubility properties of the copolymers can be influenced significantly by the addition of randomly methylated β-cyclodextrin (CD). The complexation of the copolymers with CD, was confirmed by the use of ROESY-NMR-spectroscopy.


2021 ◽  
Vol 5 (9) ◽  
pp. 250
Author(s):  
Natalia V. Bornosuz ◽  
Roman F. Korotkov ◽  
Vyacheslav V. Shutov ◽  
Igor S. Sirotin ◽  
Irina Yu. Gorbunova

The influence of epoxy active diluents, 1,4-butanediol diglycidyl ether (BD) and furfuryl glycidyl ether (FUR), in the mixtures with benzoxazine monomer based on bisphenol A, formaldehyde and m-toluidine (BA-mt), on the properties of a matrix was disclosed in this work. Resins were modified to achieve good tackiness at room temperature and reduced viscosity. The influence of mono- and difunctional modifiers on the process of curing was studied by way of differential scanning calorimetry and oscillatory rheology. The addition of BD and FUR shifted the curing peak to higher temperatures and significantly reduced viscosity. Preferable tackiness at ambient temperature was achieved with 10 phr of epoxy components in mixtures. However, cured blends with difunctional epoxy BD had an advantage over monofunctional FUR in enhanced tensile strength with remaining glass transition temperature at the level of neat benzoxazine (217 °C).


2014 ◽  
Vol 1622 ◽  
pp. 25-30 ◽  
Author(s):  
Sanket A. Deshmukh ◽  
Ganesh Kamath ◽  
Derrick C. Mancini ◽  
Subramanian K.R.S. Sankaranarayanan

ABSTRACTPoly(N-isopropylacrylamide) (PNIPAM) is a thermo-sensitive polymer that exhibits a lower critical solution temperature (LCST) around 305 K. Below the LCST, PNIPAM is soluble in water and above this temperature polymer chains collapse prior to aggregation. In the presence of methanol, electron paramagnetic resonance (EPR) spectroscopy suggests that, LCST of PNIPAM is depressed up to certain mole fraction of methanol (0.35 mole fraction) and it is speculated that addition of methanol affects the PNIPAM-water interactions. Above 0.35 mole fraction of methanol, LCST gets elevated to temperatures above ∼305 K (32°C) and cannot be detected up to 373 K (100 °C). The atomistic origin of this co-solvency effect on the LCST behavior is not completely understood. In the present study, we have used molecular dynamics (MD) simulations to investigate the effect of methanol-water mixtures on conformational transitions and the LCST of PNIPAM. We employ two different force fields i.e. polymer consistent force-field (PCFF) and CHARMM to study solvation dynamics and the PNIPAM LCST phase transition in various methanol-water mixture compositions (0.018, 0.09, 0.27, 0.5, and 0.98 mole fractions). Simulations are conducted at fully atomistic level for three different temperatures (260, 278, and 310 K) and radius of gyration (Rg) of PNIPAM chains was computed for determination of LCST behavior of PNIPAM.


2019 ◽  
Vol 10 (2) ◽  
pp. 260-266 ◽  
Author(s):  
Jin-Jin Li ◽  
Yin-Ning Zhou ◽  
Zheng-Hong Luo ◽  
Shiping Zhu

A polyelectrolyte-containing copolymer with a CO2/N2-switchable cloud point, resulting from the gas-induced alternation of hydrophilicity, was prepared.


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