Degradable polyurethane with poly(2-ethyl-2-oxazoline) brushes for protein resistance

RSC Advances ◽  
2016 ◽  
Vol 6 (74) ◽  
pp. 69930-69938 ◽  
Author(s):  
Jinxian Yang ◽  
Lianwei Li ◽  
Chunfeng Ma ◽  
Xiaodong Ye
Keyword(s):  
Chain Length ◽  
Soft Segment ◽  
Protein Resistance ◽  
Graft Density

The effects of chain length and graft density of poly(2-ethyl-2-oxazoline) on the protein resistance of degradable polyurethane-graft-poly(2-ethyl-2-oxazoline) with PCL as the soft segment have been investigated.

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.

Hydrolytic stability of aliphatic poly(carbonate-urea-urethane)s: Influence of hydrocarbon chain length in soft segment

2019 ◽  
Vol 161 ◽  
pp. 283-297 ◽  
Author(s):  
Magdalena Mazurek-Budzyńska ◽  
Marc Behl ◽  
Muhammad Y. Razzaq ◽  
Ulrich Nöchel ◽  
Gabriel Rokicki ◽  
...  
Keyword(s):  
Chain Length ◽  
Soft Segment ◽  
Hydrolytic Stability ◽  
Hydrocarbon Chain ◽  
Hydrocarbon Chain Length ◽  
Poly Carbonate

Study of the Effect of Soft-Segment Length and Concentration on Properties of Polyetherurethanes. II. The Effect on Mechanical Properties

1985 ◽  
Vol 58 (4) ◽  
pp. 701-712 ◽  
Author(s):  
Zoran S. Petrović ◽  
Jaroslava Budinski-Simendić
Keyword(s):  
Mechanical Properties ◽  
Chain Length ◽  
Plastic Flow ◽  
Soft Segment ◽  
Maximum Strength ◽  
Segment Length ◽  
Elongation At Break ◽  
Mechanical Methods ◽  
Soft Segments ◽  
Segmented Polyurethanes

Abstract Three series of segmented polyurethanes with different soft segment lengths and concentrations were examined by TMA, DMA, and mechanical methods. Maximum tensile strengths were obtained when ssc was 40–50%, which was explained by a specific interlocking morphology. No significant effect of soft-segment chain length on maximum strength was found, but higher values were found in the C series when ssc was 60%. Elongation at break increases linearly with ssc but indications that shorter soft segments produce higher extensions was attributed to plastic flow. TMA showed that Tg was independent of ssc in the C and, to a degree, in the B series, while temperature of α-transition in DMA was independent of ssc only in the C series at ssc above 50%.

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