Structural Characterization of Segmented Polyurethanes by Small Angle Neutron Scattering

2001 ◽  
Vol 710 ◽  
Author(s):  
Loren I. Espada ◽  
Joseph T. Mang ◽  
E. Bruce Orler ◽  
Debra A. Wrobleski ◽  
David A. Langlois ◽  
...  

ABSTRACTThe beneficial mechanical properties of segmented polyurethanes derive from microphase separation of immiscible hard and soft segment-rich domains at room temperature. We are interested in the structure of the domains, how these are affected by hydrolytic aging, and how the structure is modified by low molecular weight plasticizers. To assessed the distribution of the plasticizer in polyurethane, we did small-angle neutron scattering measurements on mixtures of 23% hard segment poly(esterurethane) with different amounts of either non-deuterated or deuterated plasticizer. We analyzed the results using a simple model in which the contrast, Δρ = ρH Š ρ, between the hard and soft segment-rich domains is varied by the amount of deuterated or hydrogenated plasticizer, using the fact that I(Q) ∼ Δρ2. The result demonstrated that the plasticizer is largely associated with the soft segment rich domains. The structure of PESU with the chain extender of the hard segment was assessed after aging under hydrolytic conditions. The results show that the microphase structure coarsens and segregates and that the hard and soft segments segregated as a result of the loss of constraints from hydrolytic soft segment chain scission. The results on plasticizer distribution and the effects of hydrolytic aging give insight on the loss of mechanical properties that occur in each case.

2001 ◽  
Vol 707 ◽  
Author(s):  
Loren I. Espada ◽  
Joseph T. Mang ◽  
E. Bruce Orler ◽  
Debra A. Wrobleski ◽  
David A. Langlois ◽  
...  

ABSTRACTThe beneficial mechanical properties of segmented polyurethanes derive from microphase separation of immiscible hard and soft segment-rich domains at room temperature. We are interested in the structure of the domains, how these are affected by hydrolytic aging, and how the structure is modified by low molecular weight plasticizers. To assessed the distribution of the plasticizer in polyurethane, we did small-angle neutron scattering measurements on mixtures of 23% hard segment poly(esterurethane) with different amounts of either non-deuterated or deuterated plasticizer. We analyzed the results using a simple model in which the contrast, Δ=H-, between the hard and soft segment-rich domains is varied by the amount of deuterated or hydrogenated plasticizer, using the fact that I(Q) ∼ Δ2. The result demonstrated that the plasticizer is largely associated with the soft segment rich domains. The structure of PESU with the chain extender of the hard segment was assessed after aging under hydrolytic conditions. The results show that the microphase structure coarsens and segregates and that the hard and soft segments segregated as a result of the loss of constraints from hydrolytic soft segment chain scission. The results on plasticizer distribution and the effects of hydrolytic aging give insight on the loss of mechanical properties that occur in each case.


Membranes ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 48 ◽  
Author(s):  
Vitaliy Pipich ◽  
Marcel Dickmann ◽  
Henrich Frielinghaus ◽  
Roni Kasher ◽  
Christoph Hugenschmidt ◽  
...  

The morphology of thin film composite (TFC) membranes used in reverse osmosis (RO) and nanofiltration (NF) water treatment was explored with small-angle neutron scattering (SANS) and positron-annihilation lifetime spectroscopy (PALS). The combination of both methods allowed the characterization of the bulk porous structure from a few Å to µm in radius. PALS shows pores of ~4.5 Å average radius in a surface layer of about 4 μm thickness, which become ~40% smaller at the free surface of the membranes. This observation may correlate with the glass state of the involved polymer. Pores of similar size appear in SANS as closely packed pores of ~6 Å radius distributed with an average distance of ~30 Å. The main effort of SANS was the characterization of the morphology of the porous polysulfone support layer as well as the fibers of the nonwoven fabric layer. Contrast variation using the media H2O/D2O and supercritical CO2 and CD4 identified the polymers of the support layers as well as internal heterogeneities.


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