Nanoindentation of Amorphous and Nanostructured Polymers

2003 ◽  
Vol 778 ◽  
Author(s):  
Kyle C. Maner ◽  
Matthew R. Begley ◽  
Marcel Utz

AbstractWe present a detailed nanoindentation study of micron-scale thin films of polystyrene (PS), poly(phenylene oxide) (PPO), poly(methyl methacrylate) (PMMA), a metal-centered PMMA-Ruthenium block copolymer, and a PS-poly(ethylene-propylene) (PS-PEP) block copolymer with lamellar morphology. The results show that size-dependence is most readily noticeable for the lamellar PS-PEP film, indicating that the nanoidentation approach has sufficient sensitivity to capture scale dependence on scales in the range of tens of nanometers. The less pronounced scale-dependence (or lack thereof) in the other films is discussed in the context of identifying the physical length-scale of elementary processes of plastic deformation. The results indicate that the upper limit on the size of plastic shear zones in amorphous polymers is approximately 1200-9600 nm3 (i.e. a sphere with a diameter in the range of 20-40 nm).

2007 ◽  
Vol 40 (7) ◽  
pp. 2532-2538 ◽  
Author(s):  
Christophe Sinturel ◽  
Marylène Vayer ◽  
René Erre ◽  
Heinz Amenitsch

2002 ◽  
Vol 734 ◽  
Author(s):  
Janet Ho ◽  
Leon Govaert ◽  
Marcel Utz

ABSTRACTThe shear activation volumes of miscible polystyrene-poly(2,6-dimethyl-1,4-phenylene oxide) (PS-PPO) blends at different PS-PPO ratios were determined experimentally by both plane strain and uniaxial compression at constant strain rates. We find that the same correlation between the shear activation volume and the entanglement density ρe holds for the blend as well as for various pure glassy polymers: . Since the shear activation volume is closely related to the size of the plastic shear zones, this correlation suggests that the cooperativity of the elementary processes of plastic deformation in glassy polymers scales with the entanglement density.


2015 ◽  
Vol 16 (12) ◽  
pp. 3731-3739 ◽  
Author(s):  
Alicja Matuszewska ◽  
Mariusz Uchman ◽  
Agnieszka Adamczyk-Woźniak ◽  
Andrzej Sporzyński ◽  
Stergios Pispas ◽  
...  

2015 ◽  
Vol 47 (5) ◽  
pp. 408-412 ◽  
Author(s):  
Eisuke Baba ◽  
Toshiaki Yatsunami ◽  
Takuya Yamamoto ◽  
Yasuyuki Tezuka

2018 ◽  
Vol 47 (3) ◽  
pp. 426-432 ◽  
Author(s):  
Sivan Yogev ◽  
Ayelet Shabtay-Orbach ◽  
Abraham Nyska ◽  
Boaz Mizrahi

Thermoresponsive materials have the ability to respond to a small change in temperature—a property that makes them useful in a wide range of applications and medical devices. Although very promising, there is only little conclusive data about the cytotoxicity and tissue toxicity of these materials. This work studied the biocompatibility of three Food and Drug Administration approved thermoresponsive polymers: poly( N-isopropyl acrylamide), poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) tri-block copolymer, and poly(lactic acid-co-glycolic acid) and poly(ethylene glycol) tri-block copolymer. Fibroblast NIH 3T3 and HaCaT keratinocyte cells were used for the cytotoxicity testing and a mouse model for the in vivo evaluation. In vivo results generally showed similar trends as the results seen in vitro, with all tested materials presenting a satisfactory biocompatibility in vivo. pNIPAM, however, showed the highest toxicity both in vitro and in vivo, which was explained by the release of harmful monomers and impurities. More data focusing on the biocompatibility of novel thermoresponsive biomaterials will facilitate the use of existing and future medical devices.


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