The Phase Behavior of a Hydrogen Bonding Molecular Composite

1993 ◽  
Vol 305 ◽  
Author(s):  
M. D. Dadmun ◽  
C. C. Han
Keyword(s):  
Hydrogen Bonding ◽  
Glass Transition ◽  
Light Scattering ◽  
Binary System ◽  
Phase Behavior ◽  
Optical Microscopy ◽  
Spinodal Decomposition ◽  
Random Copolymer ◽  
Nucleation And Growth ◽  
Ordering Transition

AbstractThe phase behavior of a blend containing poly(hydroxypropyl L-glutamine) (PHOPG), a rod-like polypeptide, and a coil-like random copolymer with 1.5% hydrogen bonding monomer is studied using light scattering, DSC, and optical microscopy. The results show that this system has an LCST. The phase behavior of this binary system is complicated by a glass transition and an ordering transition. Evidence is also observed of a possible change in phase demixing process, from nucleation and growth to spinodal decomposition, for a 50/50 blend with a change in temperature.

scholarly journals Quadruple Hydrogen Bond-Containing A-AB-A Triblock Copolymers: Probing the Influence of Hydrogen Bonding in the Central Block

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4705
Author(s):  
Boer Liu ◽  
Xi Chen ◽  
Glenn A. Spiering ◽  
Robert B. Moore ◽  
Timothy E. Long
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
Microphase Separation ◽  
Triblock Copolymers ◽  
Random Copolymer ◽  
Thermomechanical Properties ◽  
Structure Property ◽  
Scanning Calorimetry ◽  
Central Block ◽  
Quadruple Hydrogen Bonding

This work reveals the influence of pendant hydrogen bonding strength and distribution on self-assembly and the resulting thermomechanical properties of A-AB-A triblock copolymers. Reversible addition-fragmentation chain transfer polymerization afforded a library of A-AB-A acrylic triblock copolymers, wherein the A unit contained cytosine acrylate (CyA) or post-functionalized ureido cytosine acrylate (UCyA) and the B unit consisted of n-butyl acrylate (nBA). Differential scanning calorimetry revealed two glass transition temperatures, suggesting microphase-separation in the A-AB-A triblock copolymers. Thermomechanical and morphological analysis revealed the effects of hydrogen bonding distribution and strength on the self-assembly and microphase-separated morphology. Dynamic mechanical analysis showed multiple tan delta (δ) transitions that correlated to chain relaxation and hydrogen bonding dissociation, further confirming the microphase-separated structure. In addition, UCyA triblock copolymers possessed an extended modulus plateau versus temperature compared to the CyA analogs due to the stronger association of quadruple hydrogen bonding. CyA triblock copolymers exhibited a cylindrical microphase-separated morphology according to small-angle X-ray scattering. In contrast, UCyA triblock copolymers lacked long-range ordering due to hydrogen bonding induced phase mixing. The incorporation of UCyA into the soft central block resulted in improved tensile strength, extensibility, and toughness compared to the AB random copolymer and A-B-A triblock copolymer comparisons. This study provides insight into the structure-property relationships of A-AB-A supramolecular triblock copolymers that result from tunable association strengths.

scholarly journals Influence of size polydispersity on magnetic field tunable structures in magnetic nanofluids containing superparamagnetic nanoparticles.

2021 ◽  
Author(s):  
Dillip Kumar Mohapatra ◽  
Philip James Camp ◽  
John Philip
Keyword(s):  
Magnetic Field ◽  
Particle Size ◽  
Light Scattering ◽  
Optical Microscopy ◽  
Brownian Dynamics ◽  
Phase Contrast ◽  
Superparamagnetic Nanoparticles ◽  
Magnetic Nanofluids ◽  
Dynamics Simulations ◽  
Brownian Dynamics Simulations

We probe the influence of particle size polydispersity on field-induced structures and structural transitions in magnetic fluids (ferrofluids) using phase contrast optical microscopy, light scattering and Brownian dynamics simulations. Three...

Viscoelastic Behavior of Segmented Elastomers

1967 ◽  
Vol 40 (4) ◽  
pp. 1105-1110 ◽  
Author(s):  
Stuart L. Cooper ◽  
Arthur V. Tobolsky
Keyword(s):  
Hydrogen Bonding ◽  
Glass Transition ◽  
High Temperature ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Viscoelastic Behavior ◽  
Temperature Transition ◽  
Hydrogen Bonding Interactions ◽  
Structural Nature ◽  
Hard Segments

Abstract Viscoelastic behavior of linear segmented elastomers was examined. The unusual properties found in spandex systems are also observable in hydrocarbon block co-polymers, indicating that hydrogen bonding interactions are perhaps not essential. Low temperature properties of segmented systems are governed by the structural nature of the associated flexible segments, which determines the value of the major glass transition temperature (Tg). It appears that an association of the hard segments provides a broad temperature range of enhanced rubbery modulus. This occurs between the major Tg and a secondary high temperature transition.

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