http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Hall, Ryan,Kang, Beom-Goo,Lee, Sanghoon,Chang, Taihyun,Venerus, David C.,Hadjichristidis, Nikos,Mays, Jimmy,Larson, Ronald G. American Chemical Society 2019 Macromolecules Vol.52 No.4
<P>We determine experimentally the “dilution exponent” α for entangled polymers from the scaling of terminal crossover frequency with entanglement density from the linear rheology of three 1,4-polybutadiene star polymers that are blended with low-molecular-weight, unentangled linear 1,4-polybutadiene at various star volume fractions, ϕ<SUB><I>s</I></SUB>. Assuming that the rheology of monodisperse stars depends solely on the plateau modulus <I>G</I><SUB><I>N</I></SUB>(ϕ<SUB>s</SUB>) ∝ ϕ<SUB><I>s</I></SUB><SUP>1+α</SUP>, the number of entanglements per chain <I>M</I><SUB><I>e</I></SUB>(ϕ<SUB><I>s</I></SUB>) ∝ ϕ<SUB><I>s</I></SUB><SUP>-α</SUP>, and the tube-segment frictional Rouse time τ<SUB><I>e</I></SUB>(ϕ<SUB><I>s</I></SUB>) ∝ ϕ<SUB><I>s</I></SUB><SUP>-2α</SUP>, we show that only an α = 1 scaling superposes the <I>M</I><SUB><I>e</I></SUB>(ϕ<SUB><I>s</I></SUB>) dependence of the terminal crossover frequency ω<SUB><I>x</I>,<I>t</I></SUB> of the blends with those of pure stars, not α = 4/3. This is the first determination of α for star polymers that does not rely on any particular tube model implementation. We also show that a generalized tube model, the “Hierarchical model”, using the “Das” parameter set with α = 1 reasonably predicts the rheological data of the melts and blends featured in this paper.</P> [FIG OMISSION]</BR>
Architectural Dispersity in Model Branched Polymers: Analysis and Rheological Consequences
Snijkers, Frank,van Ruymbeke, Evelyne,Kim, Paul,Lee, Hyojoon,Nikopoulou, Anastasia,Chang, Taihyun,Hadjichristidis, Nikos,Pathak, Jai,Vlassopoulos, Dimitris American Chemical Society 2011 Macromolecules Vol.44 No.21
<P>We combine state-of-the-art synthetic, chromatographic, rheological, and modeling techniques in order to address the role of architectural polydispersity in the rheology of model branched polymers. This synergy is shown to be imperative in the field and leads to several important results. Even the best available synthesis is prone to “contamination” by side-products. The exact targeted macromolecular structure can be analyzed experimentally and statistically and eventually fractionated. Temperature-gradient interaction chromatography proves to be an indispensible tool in this process. All techniques are sensitive to the various macromolecular structures, but in different ways. In particular, the presence of side-products may or may not influence the linear rheology, due to competing contributions of the different relaxation processes involved, reflecting different structures at different fractions. Hence, combination of all these techniques is the key for fully decoding the architectural composition of branched polymers and its influence on rheology.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/mamobx/2011/mamobx.2011.44.issue-21/ma2013805/production/images/medium/ma-2011-013805_0019.gif'></P>
Hall, Ryan,Desai, Priyanka S.,Kang, Beom-Goo,Huang, Qifan,Lee, Sanghoon,Chang, Taihyun,Venerus, David C.,Mays, Jimmy,Ntetsikas, Konstantinos,Polymeropoulos, George,Hadjichristidis, Nikos,Larson, Ronal American Chemical Society 2019 Macromolecules Vol.52 No.20
<P>We blend newly synthesized nearly monodisperse four-arm star 1,4-polybutadienes with various well-entangled linear polymers, confirming the conclusions in Desai et al. [<I>Macromolecules</I>201649 (13)49644977] that advanced tube models, namely, the hierarchical 3.0 and branch-on-branch models [Wang, Z.; <I>J. Rheol.</I>201054 (2)223260], fail to predict the linear rheological data when the pure linear polymers have shorter relaxation times, but within 3-4 orders of magnitude of the star polymer. However, when the linear polymer has a longer relaxation time than the star, our new work, surprisingly, finds that non-monotonic dependence of terminal relaxation behavior on composition is both observed experimentally and captured by the models. Combined with previous data from the literature, we present results from over 50 1,4-polybutadiene star-linear blends, suitable for thorough testing of rheological models of entangled polymers.</P> [FIG OMISSION]</BR>