Microphase separation and crystallization behaviors of bi-phased triblock terpolymers with a competitively dissolved middle block

Polymer ◽  
2017 ◽  
Vol 117 ◽  
pp. 140-149 ◽  
Author(s):  
Rui-Yang Wang ◽  
Xiang-Yue Wang ◽  
Bin Fan ◽  
Jun-Ting Xu ◽  
Zhi-Qiang Fan
Keyword(s):  
Microphase Separation ◽  
Crystallization Behaviors ◽  
Triblock Terpolymers

Synthesis and Microphase Separation of Linear Triblock Terpolymers of Polystyrene, High 1,4-Polybutadiene, and High 3,4-Polyisoprene

2002 ◽  
Vol 35 (10) ◽  
pp. 4030-4035 ◽  
Author(s):  
Apostolos Avgeropoulos ◽  
Stella Paraskeva ◽  
Nikos Hadjichristidis ◽  
Edwin L. Thomas
Keyword(s):  
Microphase Separation ◽  
Triblock Terpolymers

Role of the segment distribution in the microphase separation of acrylic diblock and triblock terpolymers

Polymer ◽  
2014 ◽  
Vol 55 (16) ◽  
pp. 4206-4215 ◽  
Author(s):  
James A. Bergman ◽  
Eric W. Cochran ◽  
Jennifer M. Heinen
Keyword(s):  
Microphase Separation ◽  
Segment Distribution ◽  
Triblock Terpolymers

Morphological studies of linear (AB)n multiblock copolymers and their blends

1992 ◽  
Vol 50 (1) ◽  
pp. 384-385
Author(s):  
Richard J. Spontak ◽  
Steven D. Smith ◽  
Arman Ashraf
Keyword(s):  
Electron Microscopy ◽  
Microphase Separation ◽  
Multiblock Copolymers ◽  
First Order ◽  
Morphological Studies ◽  
Transmission Electron ◽  
First Order Phase Transition ◽  
Covalently Bonded ◽  
Total Molecular Weight ◽  
First Order Phase

Block copolymers are composed of sequences of dissimilar chemical moieties covalently bonded together. If the block lengths of each component are sufficiently long and the blocks are thermodynamically incompatible, these materials are capable of undergoing microphase separation, a weak first-order phase transition which results in the formation of an ordered microstructural network. Most efforts designed to elucidate the phase and configurational behavior in these copolymers have focused on the simple AB and ABA designs. Few studies have thus far targeted the perfectly-alternating multiblock (AB)n architecture. In this work, two series of neat (AB)n copolymers have been synthesized from styrene and isoprene monomers at a composition of 50 wt% polystyrene (PS). In Set I, the total molecular weight is held constant while the number of AB block pairs (n) is increased from one to four (which results in shorter blocks). Set II consists of materials in which the block lengths are held constant and n is varied again from one to four (which results in longer chains). Transmission electron microscopy (TEM) has been employed here to investigate the morphologies and phase behavior of these materials and their blends.

Crystallization behaviors of ultrathin Al-doped HfO 2 amorphous films grown by atomic layer deposition

2017 ◽  
Vol 26 (2) ◽  
pp. 027701 ◽  
Author(s):  
Xue-Li Ma ◽  
Hong Yang ◽  
Jin-Juan Xiang ◽  
Xiao-Lei Wang ◽  
Wen-Wu Wang ◽  
...  
Keyword(s):  
Atomic Layer Deposition ◽  
Atomic Layer ◽  
Amorphous Films ◽  
Crystallization Behaviors ◽  
Layer Deposition

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 Impact of Macrodiols on the Morphological Behavior of H12MDI/HDO-Based Polyurethane Elastomer

Polymers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 2060
Author(s):  
Shazia Naheed ◽  
Mohammad Zuber ◽  
Mahwish Salman ◽  
Nasir Rasool ◽  
Zumaira Siddique ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Contact Angle ◽  
Chain Length ◽  
Microphase Separation ◽  
Soft Segment ◽  
Group Identification ◽  
Degree Of Crystallinity ◽  
Polyurethane Elastomers ◽  
Hard Segments ◽  
Morphological Behavior

In this study, we evaluated the morphological behavior of polyurethane elastomers (PUEs) by modifying the soft segment chain length. This was achieved by increasing the soft segment molecular weight (Mn = 400–4000 gmol−1). In this regard, polycaprolactone diol (PCL) was selected as the soft segment, and 4,4′-cyclohexamethylene diisocyanate (H12MDI) and 1,6-hexanediol (HDO) were chosen as the hard segments. The films were prepared by curing polymer on Teflon surfaces. Fourier transform infrared spectroscopy (FTIR) was utilized for functional group identification in the prepared elastomers. FTIR peaks indicated the disappearance of −NCO and −OH groups and the formation of urethane (NHCOO) groups. The morphological behavior of the synthesized polymer samples was also elucidated using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. The AFM and SEM results indicated that the extent of microphase separation was enhanced by an increase in the molecular weight of PCL. The phase separation and degree of crystallinity of the soft and hard segments were described using X-ray diffraction (XRD). It was observed that the degree of crystallinity of the synthesized polymers increased with an increase in the soft segment’s chain length. To evaluate hydrophilicity/hydrophobicity, the contact angle was measured. A gradual increase in the contact angle with distilled water and diiodomethane (38.6°–54.9°) test liquids was observed. Moreover, the decrease in surface energy (46.95–24.45 mN/m) was also found to be inconsistent by increasing the molecular weight of polyols.

Flexible coatings with microphase separation structure attained by copolymers and ultra-fine nanoparticles for endurable antifouling

2021 ◽  
Vol 82 ◽  
pp. 179-186
Author(s):  
Zhuo Chen ◽  
Shun Chen ◽  
Yufei Xiong ◽  
Yuping Yang ◽  
Yang Zhang ◽  
...  
Keyword(s):  
Microphase Separation
Sign in / Sign up

Export Citation Format

Share Document