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Journal articles on the topic 'PVME'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Robles-Hernández, Beatriz, Marina González-Burgos, José Pomposo, Juan Colmenero, and Ángel Alegría. "Glass-Transition Dynamics of Mixtures of Linear Poly(vinyl methyl ether) with Single-Chain Polymer Nanoparticles: Evidence of a New Type of Nanocomposite Materials." Polymers 11, no. 3 (March 21, 2019): 533. http://dx.doi.org/10.3390/polym11030533.

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Single-chain polymer nanoparticles (SCNPs) obtained through chain collapse by intramolecular cross-linking are attracting increasing interest as components of all-polymer nanocomposites, among other applications. We present a dielectric relaxation study on the dynamics of mixtures of poly(vinyl methyl ether) (PVME) and polystyrene (PS)-based SCNPs with various compositions. Analogous dielectric measurements on a miscible blend of PVME with the linear precursor chains of the SCNPs are taken as reference for this study. Both systems present completely different behaviors: While the blend with the linear precursor presents dynamics very similar to that reported for PVME/PS miscible blends, in the PVME/SCNP mixtures there are an appreciable amount of PVME segments that are barely affected by the presence of SCNPs, which nearly vanishes only for mixtures with high SCNP content. Interestingly, in the frame of a simple two-phase system, our findings point towards the existence of a SCNP-rich phase with a constant PVME fraction, regardless of the overall concentration of the mixture. Moreover, the dynamics of the PVME segments in this SCNP-rich phase display an extreme dynamic heterogeneity, a signature of constraint effects.

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2

Xavier, Priti, Keerthi M. Nair, Lasitha K., and Suryasarathi Bose. "Is kinetic polymer arrest very specific to multiwalled carbon nanotubes?" Physical Chemistry Chemical Physics 18, no. 42 (2016): 29226–38. http://dx.doi.org/10.1039/c6cp04303h.

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3

BarNir, Anat. "Pre-venture managerial experience and new venture innovation." Management Decision 52, no. 10 (November 11, 2014): 1981–2001. http://dx.doi.org/10.1108/md-03-2014-0158.

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Purpose – The purpose of this paper is to explore direct and indirect effects of pre-venture managerial experience (PVME) on new venture innovation. Using opportunity-costs framework, the following questions are explored: does the entrepreneur's PVME directly affect the extent of innovation in the new venture? What is the role of expectation for high returns in the relationship between PVME and innovation? What is the role of expectation for high returns in the relationship between PVME and innovation? Is there a relationship between abilities and expectancies and does it affect innovation? Design/methodology/approach – Data were obtained from the Panel Study of Entrepreneurial Dynamics II, which is a national database of individuals in various stages of starting a business. Overall sample consisted of 982 nascent entrepreneurs. Statistical methods explored a multiple serial mediation model using OLS regressions supplemented by analyses based on bootstrapping for assessment of indirect effects. Findings – PVME effect on innovation is associated with abilities and financial motives, supporting a partial serial multiple mediation model in which PVME affects innovation indirectly through abilities and where abilities affect innovation directly as well as indirectly through expectations. Results also suggest a suppression effect and a possible negative effect of PVME. Originality/value – Abilities facilitate innovation, which has implications for policy makers who aim to enhance innovations, for investors in assessing potential of innovations, and for entrepreneurs who aim at improving innovation. Shedding light on the mechanism by which prior experience affects innovation, including the role of financial expectations and how abilities possibly negate negative effects associated with experience improve the understanding of and ability to enhance innovation and improve new venture competitive stand.

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4

Kuang, Chen, Sahar Qavi, and Reza Foudazi. "Double-stage phase separation in dynamically asymmetric ternary polymer blends." RSC Advances 6, no. 94 (2016): 92104–14. http://dx.doi.org/10.1039/c6ra17274a.

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In this work, the phase separation behavior of ternary blends of polystyrene/poly(vinyl methyl ether)/polyisoprene, PS/PVME/PI, and polystyrene/poly(vinyl methyl ether)/poly(ethyl methacrylate), PS/PVME/PEMA are investigated.

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5

Kar, Goutam Prasanna, Avanish Bharati, Priti Xavier, Giridhar Madras, and Suryasarathi Bose. "The key role of polymer grafted nanoparticles in the phase miscibility of an LCST mixture." Physical Chemistry Chemical Physics 17, no. 2 (2015): 868–77. http://dx.doi.org/10.1039/c4cp02925a.

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A lower graft density leads to entropic penalty, further facilitating PS-g-nAg particles to localize in the PVME phase of the blends. Further, the PS-g-nAg particles delayed the demixing temperature by 18 °C in PS-Br–PVME blends.

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6

Ruiz de Luzuriaga, Alaitz, Hans Grande, and Jose A. Pomposo. "A Theoretical Investigation of Polymer-Nanoparticles as Miscibility Improvers in All-Polymer Nanocomposites." Journal of Nano Research 2 (August 2008): 105–14. http://dx.doi.org/10.4028/www.scientific.net/jnanor.2.105.

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The miscibility behaviour of polymer-nanoparticle / linear-polymer blends (all-polymer nanocomposites) has been investigated using an incompressible mean-field theoretical model that accounts for combinatorial, temperature-dependent exchange interaction energy and nanoparticle-driven effects. The theory is employed to predict the phase diagram of poly(styrene)-nanoparticle (PS-np) / linear-poly(vinyl methyl ether) (PVME) nanocomposites from room temperature to 675 K. Complete miscibility is predicted for PS-nanoparticles with radius < 6 nm blended with PVME (molecular weight 62 500 g/mol, nanoparticle volume fraction 20 %). The effect of PVME molecular weight and blend composition on the miscibility diagram is also addressed. When compared to the well-known experimental phase diagram of linear-PS / PVME blends displaying lower critical solution temperature (LCST) behaviour, the miscibility improving effect of sub-10 nm PS-nanoparticles is clearly highlighted. In terms of the model, this favourable nanoscale effect arises mainly from the reduced stretching induced by the sub-10 nm nanoparticles and the increased exothermic contacts when compared to nanoparticles with sizes > 10 nm.

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7

Yurekli, Koray, Alamgir Karim, Eric J. Amis, and Ramanan Krishnamoorti. "Phase Behavior of PS−PVME Nanocomposites." Macromolecules 37, no. 2 (January 2004): 507–15. http://dx.doi.org/10.1021/ma0302098.

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8

Madkour, Sherif, Paulina Szymoniak, Jörg Radnik, and Andreas Schönhals. "Unraveling the Dynamics of Nanoscopically Confined PVME in Thin Films of a Miscible PVME/PS Blend." ACS Applied Materials & Interfaces 9, no. 42 (October 16, 2017): 37289–99. http://dx.doi.org/10.1021/acsami.7b10572.

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9

NEMOTO, Norio, Takeshi YAMAMURA, and Kunihiro OSAKI. "Diffusion of PS in PS-PVME Mixtures." Nihon Reoroji Gakkaishi(Journal of the Society of Rheology, Japan) 20, no. 1 (1992): 25–28. http://dx.doi.org/10.1678/rheology1973.20.1_25.

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10

Koizumi, Satoshi, and Jun-ichi Suzuki. "Three-dimensional small-angle neutron scattering of shear-induced phase separation in a dynamically asymmetric polymer mixture." Journal of Applied Crystallography 39, no. 6 (November 10, 2006): 878–88. http://dx.doi.org/10.1107/s0021889806039082.

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A polymer mixture of polystyrene (PS)/poly(vinyl methyl ether) (PVME) has been investigated by using a three-dimensional small-angle neutron scattering (3D-SANS) method. PS and PVME exhibit a large difference in the glass transition temperatureTg. Therefore, dynamical asymmetry is strongly enhanced in an intermediate temperature region between theTgvalues of neat PS and PVME. In the intermediate temperature region, a shear deformation was imposed on the polymer mixture to enhance the concentration fluctuations,i.e.shear-induced phase separation. By rotating the film specimen, which was rapidly quenched after deformation, 3D-SANS due to shear-induced phase separation was observed successfully. In theqx=qyplane of the sample coordinate system, whereqis a component of scattering vectorq, it was possible to observe SANS of `double-lobe' shape, with the minor axes of the lobes inclined towardsqx=qy, whereqx,qyandqz, denote the shear, velocity gradient and vorticity directions in reciprocal space, respectively. Abnormal `butterfly' scattering was observed in a section cut through the 3D-SANS in theqxqzplane. The 3D-SANS thus obtained is discussed in comparison with a model of dynamical coupling between stress and diffusion.

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11

Zhang, Li, Nan Wang, Yaping Zheng, and Wenjing Yao. "Phase separation in PVME-H2O transparent system." Procedia Engineering 27 (2012): 1508–17. http://dx.doi.org/10.1016/j.proeng.2011.12.615.

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12

Nemoto, Norio, Takeshi Yamamura, and Kunihiro Osaki. "Diffusion of PS in PS‐PVME mixtures." Journal of Rheology 37, no. 3 (May 1993): 550. http://dx.doi.org/10.1122/1.550411.

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13

Schneider, Hans Adam, and Bernhard Leikauf. "Glass-transition temperatures of PVME - PS blends." Thermochimica Acta 114, no. 1 (April 1987): 165–70. http://dx.doi.org/10.1016/0040-6031(87)80256-3.

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14

Nikulova, Uliana V., and Anatoly E. Chalykh. "Phase Equilibrium and Interdiffusion in Poly(Vinyl Methyl Ether)-Water System." Polymers 12, no. 11 (October 22, 2020): 2445. http://dx.doi.org/10.3390/polym12112445.

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The phase state diagram of the poly(vinyl methyl ether)-water system in a wide concentration range was obtained by the optical interferometry method. It was shown that this system was characterized by a complicated phase equilibrium with two lower critical solution temperatures, one of which was located in the concentrated region at 21 °C, and the other one in the region of a dilute solution at 31 °C. In the framework of the Flory–Huggins theory, pair interaction parameters were calculated for different parts of the binodal curves, and an attempt was made to reverse simulate the diagram in different conditions. It was suggested that the unusual character of the diagram was associated with the formation of a complicated complex between PVME and water in the middle region of the compositions. Concentration profiles for different temperatures were constructed. For the first time for this system, the numerical values of the diffusion coefficients of poly(vinyl methyl ether) (PVME) into water and water in PVME were obtained. Concentration and temperature dependences of diffusion coefficients were constructed and analyzed. The kinetics of water sorption in PVME was plotted, the clustering integral was calculated, and the approximate number of molecules in a water cluster was estimated. It was shown that in the dilute solution region upon passing through the binodal curve, the interphase disappeared immediately, and the remaining fluctuation of the concentration decreased in size with time. The kinetics of this process was estimated from the change in the size of such a particle.

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15

Daivis, P. J., and D. N. Pinder. "Dynamic light scattering experiments on poly(vinyl methyl ether) (PVME)-polystyrene-toluene and PVME-polystyrene-carbon tetrachloride solutions." Macromolecules 26, no. 13 (June 1993): 3381–90. http://dx.doi.org/10.1021/ma00065a023.

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16

Xia, Tian, Yajiang Huang, Xiaolian Jiang, Youbing Li, Xuanlun Wang, and Guangxian Li. "Phase morphology map in LCST-type polymer blends with dynamical asymmetry under different quench depths." RSC Adv. 4, no. 63 (2014): 33431–34. http://dx.doi.org/10.1039/c4ra05478d.

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17

YANG, YULIANG, HONGDONG ZHANG, and FENG QIU. "STRAIN FIELD INDUCED ANISOTROPIC PHASE SEPARATION OF POLYMER BLENDS." International Journal of Modern Physics B 17, no. 01n02 (January 20, 2003): 77–82. http://dx.doi.org/10.1142/s0217979203017114.

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Using a small angle light scattering (SALS) technique, we investigated the anisotropic SALS patterns formed in a phase separating polystyrene (PS) and poly (vinyl methyl ether) (PVME) blend under strain fields. We have found that, in addition to the interfacial relaxations, the stretching of the polymer chains plays an important role in the phase separation of the PS/PVME blend under a strain field. Two novel scattering patterns and the strain induced slowing down of the phase separation dynamics are observed. The experimental results are compared to a theoretical calculation based on a time-dependent Ginzburg-Landau equation incorporated with the chain stretching effect.

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18

El-Mabrouk, Khalil, Sébastien Vaudreuil, Abderrahim Zeghloul, and Mosto Bousmina. "Effect of Shear on Phase-Separation in Polystyrene/Poly(vinyl methyl ether)/Organoclay Nanocomposites." Journal of Nanoscience and Nanotechnology 8, no. 4 (April 1, 2008): 1895–900. http://dx.doi.org/10.1166/jnn.2008.0191895.

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Blends of polystyrene (PS)/poly(vinyl methyl ether) (PVME) modified with two types of organoclay were prepared by solution casting from toluene. The effect of clay addition on the phase separating morphology of PS/PVME blend with critical composition (25/75) was examined both under quiescent conditions and under shear flow. The variation in critical temperature of phase separation was assessed by rheology, small angle laser light scattering (SALLS) and by on-line laser light transmission during shearing at fixed shear rate during heating. Transmission electron microscopy and X-ray diffraction analyses were used to examine the state of delamination and distribution of clay nanoparticles with the blend matrix.

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19

Torres-Figueroa, Ana V., Cinthia J. Pérez-Martínez, J. Carmelo Encinas, Silvia Burruel-Ibarra, María I. Silvas-García, Alejandro M. García Alegría, and Teresa del Castillo-Castro. "Thermosensitive Bioadhesive Hydrogels Based on Poly(N-isopropylacrilamide) and Poly(methyl vinyl ether-alt-maleic anhydride) for the Controlled Release of Metronidazole in the Vaginal Environment." Pharmaceutics 13, no. 8 (August 17, 2021): 1284. http://dx.doi.org/10.3390/pharmaceutics13081284.

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The development of thermosensitive bioadhesive hydrogels as multifunctional platforms for the controlled delivery of microbicides is a valuable contribution for the in situ treatment of vagina infections. In this work, novel semi-interpenetrating network (s-IPN) hydrogels were prepared by the entrapment of linear poly(methyl vinyl ether-alt-maleic anhydride) (PVME-MA) chains within crosslinked 3D structures of poly(N-isopropylacrylamide) (PNIPAAm). The multifunctional platforms were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermal techniques, rheological analysis, swelling kinetic measurements, and bioadhesion tests on porcine skin. The hydrogels exhibited an interconnected porous structure with defined boundaries. An elastic, solid-like behavior was predominant in all formulations. The swelling kinetics were strongly dependent on temperature (25 °C and 37 °C) and pH (7.4 and 4.5) conditions. The s-IPN with the highest content of PVME-MA displayed a significantly higher detachment force (0.413 ± 0.014 N) than the rest of the systems. The metronidazole loading in the s-IPN improved its bioadhesiveness. In vitro experiments showed a sustained release of the antibiotic molecules from the s-IPN up to 48 h (94%) in a medium simulating vaginal fluid, at 37 °C. The thermosensitive and bioadhesive PNIPAAm/PVME-MA systems showed a promising performance for the controlled release of metronidazole in the vaginal environment.

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20

Hess, D. B., and S. J. Muller. "Secondary effects of antioxidant on PS/PVME blends." Polymer 43, no. 4 (February 2002): 1567–70. http://dx.doi.org/10.1016/s0032-3861(01)00704-2.

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21

Capponi, Sara, Fernando Alvarez, and Dušan Račko. "Free Volume in a PVME Polymer–Water Solution." Macromolecules 53, no. 12 (June 3, 2020): 4770–82. http://dx.doi.org/10.1021/acs.macromol.0c00472.

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22

Khalesi Moghaddam, Razie, Fatemeh Goharpey, and Jafar Khademzadeh Yeganeh. "Interplay between phase separation and dewetting in PS/PVME thin films: effect of temperature." Soft Matter 14, no. 32 (2018): 6684–95. http://dx.doi.org/10.1039/c8sm00445e.

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23

Chaykar, Ashkan Shoja, Fatemeh Goharpey, and Jafar Khademzadeh Yeganeh. "Volume phase transition of electron beam cross-linked thermo-responsive PVME nanogels in the presence and absence of nanoparticles: with a view toward rheology and interactions." RSC Advances 6, no. 12 (2016): 9693–708. http://dx.doi.org/10.1039/c5ra21021f.

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We investigate the effect of nanoparticles and radiation dose on interactions in the PVME-based nanogel system and its phase behavior (swelling/deswelling behavior and phase separation mechanism) by rheological and FTIR measurements.

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24

Xavier, Priti, and Suryasarathi Bose. "Mapping the intriguing transient morphologies and the demixing behavior in PS/PVME blends in the presence of rod-like nanoparticles." Physical Chemistry Chemical Physics 17, no. 22 (2015): 14972–85. http://dx.doi.org/10.1039/c5cp01865j.

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The demixing behavior, transient morphologies and mechanism of phase separation in PS/PVME blends were greatly altered in the presence of a very low concentration of rod-like particles (multiwall carbon nanotubes, MWNTs).

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25

Pathak, Binita, Goutam Prasanna Kar, Suryasarathi Bose, and Saptarshi Basu. "Phase separation and physico-chemical processes at microscopic and macroscopic levels in MWCNT laden polymer blends using a unique droplet based architecture." Physical Chemistry Chemical Physics 19, no. 36 (2017): 24961–70. http://dx.doi.org/10.1039/c7cp03621c.

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We propose a unique contact-free droplet based architecture to alter the phase separation behavior in binary polymer solution (PS/PVME in toluene) by tuning the external heating rate and concentration of added MWCNT particles.

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26

Peng, Yong-jin, Yu-ling Liu, Jun-hua Hao, Rong-chun Zhang, and Ping-chuan Sun. "Phase structure and dynamics of polystyrene/poly(vinyl methyl ether) blend studied using solid-state NMR." RSC Advances 7, no. 89 (2017): 56311–16. http://dx.doi.org/10.1039/c7ra12287j.

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In this work, solid-state ¹H NMR experiments were conducted to fully characterize the dynamic characteristics of a polystyrene/poly(vinyl methyl ether) blend with a mass ratio of 3 : 1 (PS/PVME 75/25).

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27

Pastorczak, M., M. Kozanecki, and J. Ulanski. "Water–Polymer interactions in PVME hydrogels – Raman spectroscopy studies." Polymer 50, no. 19 (September 2009): 4535–42. http://dx.doi.org/10.1016/j.polymer.2009.07.048.

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28

Valiquette, Dominic, and Christian Pellerin. "Miscible and Core−Sheath PS/PVME Fibers by Electrospinning." Macromolecules 44, no. 8 (April 26, 2011): 2838–43. http://dx.doi.org/10.1021/ma102121t.

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29

El-Mabrouk, Khalil, Mohamed Belaiche, and Mosto Bousmina. "Phase separation in PS/PVME thin and thick films." Journal of Colloid and Interface Science 306, no. 2 (February 2007): 354–67. http://dx.doi.org/10.1016/j.jcis.2006.10.051.

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30

Loozen, Els, Kurt Van Durme, Erik Nies, Bruno Van Mele, and Hugo Berghmans. "The anomalous melting behavior of water in aqueous PVME solutions." Polymer 47, no. 20 (September 2006): 7034–42. http://dx.doi.org/10.1016/j.polymer.2006.08.003.

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31

Yang, Kun, Qi Yang, Guangxian Li, Yajie Sun, and Yimin Mao. "Phase behavior of near-critical PVME/SAN blend in film." Materials Letters 60, no. 5 (March 2006): 589–93. http://dx.doi.org/10.1016/j.matlet.2005.09.045.

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32

Lee, Hwan-Koo, Chang-Kwon Kang, and Wang-Cheol Zin. "Miscibility in blends of PVME with styrene-based block copolymers." Polymer 38, no. 7 (March 1997): 1595–600. http://dx.doi.org/10.1016/s0032-3861(96)00690-8.

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33

Radusch, Hans-Joachim, Ngo Trinh Tung, and Christian Wohlfarth. "Zum thermodynamischen verhalten von polystyrol (PS)/poly(vinylmethylether) (PVME)-blends." Angewandte Makromolekulare Chemie 235, no. 1 (February 1996): 175–91. http://dx.doi.org/10.1002/apmc.1996.052350115.

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34

Bernaschi, M., and G. Richelli. "Development and Results of PVMe on the IBM 9076 SP1." Journal of Parallel and Distributed Computing 29, no. 1 (August 1995): 75–83. http://dx.doi.org/10.1006/jpdc.1995.1107.

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35

Alegría, A., I. Tellería, and J. Colmenero. "Miscibility and dielectric α-relaxation of PECH/PVME polymer blends." Journal of Non-Crystalline Solids 172-174 (September 1994): 961–65. http://dx.doi.org/10.1016/0022-3093(94)90606-8.

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36

Li, Xue, Zhe Wang, Liang Cui, Rubo Xing, Yanchun Han, and Lijia An. "Phase separation of PS/PVME blend films induced by capillary force." Surface Science 571, no. 1-3 (November 2004): 12–20. http://dx.doi.org/10.1016/j.susc.2004.07.052.

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37

Xia, Tian, Yajiang Huang, Xiaojuan Peng, and Guangxian Li. "Morphological Transition Induced by Nanoparticles in Dynamically Asymmetric PS/PVME Blends." Macromolecular Chemistry and Physics 211, no. 20 (October 7, 2010): 2240–47. http://dx.doi.org/10.1002/macp.201000237.

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38

Malekzadeh, Elham, and Bi-min Zhang Newby. "Thermoresponsive Poly(vinyl methyl ether) (PVME) Retained by 3-Aminopropyltriethoxysilane (APTES) Network." ACS Biomaterials Science & Engineering 6, no. 12 (November 10, 2020): 7051–60. http://dx.doi.org/10.1021/acsbiomaterials.0c01376.

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39

Cox, B. Dwain, Melvin A. Park, R. Gene Kaercher, and Emile A. Schweikert. "Analysis of polystyrene/PVME blends by coincidence counting time-of-flight mass spectrometry." Analytical Chemistry 64, no. 8 (April 15, 1992): 843–47. http://dx.doi.org/10.1021/ac00032a005.

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40

Xavier, Priti, Avanish Bharati, Giridhar Madras, and Suryasarathi Bose. "An unusual demixing behavior in PS–PVME blends in the presence of nanoparticles." Phys. Chem. Chem. Phys. 16, no. 39 (August 14, 2014): 21300–21309. http://dx.doi.org/10.1039/c4cp02485k.

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41

Yurekli, Koray, Alamgir Karim, Eric J. Amis, and Ramanan Krishnamoorti. "Influence of Layered Silicates on the Phase-Separated Morphology of PS−PVME Blends." Macromolecules 36, no. 19 (September 2003): 7256–67. http://dx.doi.org/10.1021/ma020755l.

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42

Cendoya, I., A. Alegría, J. M. Alberdi, J. Colmenero, H. Grimm, D. Richter, and B. Frick. "Effect of Blending on the PVME Dynamics. A Dielectric, NMR, and QENS Investigation." Macromolecules 32, no. 12 (June 1999): 4065–78. http://dx.doi.org/10.1021/ma9819539.

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43

Alegría, A., I. Cendoya, J. Colmenero, J. M. Alberdi, and B. Frick. "QENS investigation of the segmental dynamics of a PVME/dPS miscible polymer blend." Physica B: Condensed Matter 234-236 (June 1997): 442–44. http://dx.doi.org/10.1016/s0921-4526(97)89260-5.

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44

Xavier, Priti, and Suryasarathi Bose. "Non-equilibrium segmental dynamics driven by multiwall carbon nanotubes in PS/PVME blends." Physical Chemistry Chemical Physics 16, no. 20 (2014): 9309. http://dx.doi.org/10.1039/c4cp00832d.

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45

Lenz, Sebastian, Sebastian K. Nett, Mine Memesa, Robert F. Roskamp, Andreas Timmann, Stephan V. Roth, Rüdiger Berger, and Jochen S. Gutmann. "Thermal Response of Surface Grafted Two-Dimensional Polystyrene (PS)/Polyvinylmethylether (PVME) Blend Films." Macromolecules 43, no. 2 (January 26, 2010): 1108–16. http://dx.doi.org/10.1021/ma9021696.

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46

El Mabrouk, Khalil, and Mosto Bousmina. "Effect of molecular weight and shear on phase diagram of PS/PVME blend." Rheologica Acta 45, no. 6 (April 8, 2006): 959–69. http://dx.doi.org/10.1007/s00397-006-0091-5.

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47

Chahid, A., J. Colmenero, and A. Alegría. "Fast dynamics below and around the glass transition in a sidegroup polymer (PVME)." Physica A: Statistical Mechanics and its Applications 201, no. 1-3 (December 1993): 101–5. http://dx.doi.org/10.1016/0378-4371(93)90405-s.

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48

Digar, M., and Ten-Chin Wen. "Role of PVME on the ionic conductivity and morphology of a TPU based electrolyte." Polymer 42, no. 1 (January 2001): 71–81. http://dx.doi.org/10.1016/s0032-3861(00)00322-0.

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49

Huang, He, Chang‐Jun Wang, and Yong‐Jin Peng. "On the Dynamic Mechanical Behavior and Importance of Weak Interactions in PS/PVME Blends." ChemistrySelect 5, no. 46 (December 10, 2020): 14592–95. http://dx.doi.org/10.1002/slct.202004062.

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50

Madkour, Sherif, Paulina Szymoniak, Andreas Hertwig, Mojdeh Heidari, Regine von Klitzing, Simone Napolitano, Michele Sferrazza, and Andreas Schönhals. "Decoupling of Dynamic and Thermal Glass Transition in Thin Films of a PVME/PS Blend." ACS Macro Letters 6, no. 10 (October 2, 2017): 1156–61. http://dx.doi.org/10.1021/acsmacrolett.7b00625.

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