Living Polymer Chains with Predictable Molecular Weight and Dispersity via Carbanionic Polymerization in Continuous Flow: Mixing Rate as a Key Parameter

2016 ◽  
Vol 49 (14) ◽  
pp. 5043-5050 ◽  
Author(s):  
Jan Morsbach ◽  
Axel H. E. Müller ◽  
Elena Berger-Nicoletti ◽  
Holger Frey
Keyword(s):  
Molecular Weight ◽  
Continuous Flow ◽  
Polymer Chains ◽  
Mixing Rate ◽  
Flow Mixing ◽  
Key Parameter

scholarly journals Water vapor induced self-assembly of islands/honeycomb structure by secondary phase separation in polystyrene solution with bimodal molecular weight distribution

2021 ◽  
Author(s):  
Maciej Łojkowski ◽  
Adrian Chlanda ◽  
Emilia Choińska ◽  
Wojciech Swieszkowski
Keyword(s):  
Molecular Weight ◽  
Phase Separation ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Self Assembly ◽  
Secondary Phase ◽  
Honeycomb Structure ◽  
Polymer Chains ◽  
Molecular Weights ◽  
Secondary Phase Separation

<p>The formation of complex structures in thin films is of interest in many fields. Segregation of polymer chains of different molecular weights is a well-known process. However, here, polystyrene with bimodal molecular weight distribution, but no additional chemical modification was used. It was proven that at certain conditions, the phase separation occurred between two fractions of bimodal polystyrene/methyl ethyl ketone solution. The films were prepared by spin-coating, and the segregation between polystyrene phases was investigated by force spectroscopy. Next, water vapour induced secondary phase separation was investigated. The introduction of moist airflow induced the self-assembly of the lower molecular weight into islands and the heavier fraction into a honeycomb. As a result, an easy, fast, and effective method of obtaining island/honeycomb morphologies was demonstrated. The possible mechanisms of the formation of such structures were discussed.</p>

scholarly journals Effect of Structure of Polymers Grafted from Graphene Oxide on the Compatibility of Particles with a Silicone-Based Environment and the Stimuli-Responsive Capabilities of Their Composites

Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 591 ◽  
Author(s):  
Monika Zygo ◽  
Miroslav Mrlik ◽  
Marketa Ilcikova ◽  
Martina Hrabalikova ◽  
Josef Osicka ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Graphene Oxide ◽  
Radical Polymerization ◽  
Polymer Brushes ◽  
Silicone Oil ◽  
Polymer Chains ◽  
Butyl Methacrylate ◽  
Raman Shift ◽  
Stimuli Responsive ◽  
Grafted Polymer

This study reports the utilization of controlled radical polymerization as a tool for controlling the stimuli-responsive capabilities of graphene oxide (GO) based hybrid systems. Various polymer brushes with controlled molecular weight and narrow molecular weight distribution were grafted from the GO surface by surface-initiated atom transfer radical polymerization (SI-ATRP). The modification of GO with poly(n-butyl methacrylate) (PBMA), poly(glycidyl methacrylate) (PGMA), poly(trimethylsilyloxyethyl methacrylate) (PHEMATMS) and poly(methyl methacrylate) (PMMA) was confirmed by thermogravimetric analysis (TGA) coupled with online Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Various grafting densities of GO-based materials were investigated, and conductivity was elucidated using a four-point probe method. Raman shift and XPS were used to confirm the reduction of surface properties of the GO particles during SI-ATRP. The contact angle measurements indicated the changes in the compatibility of GOs with silicone oil, depending on the structure of the grafted polymer chains. The compatibility of the GOs with poly(dimethylsiloxane) was also investigated using steady shear rheology. The tunability of the electrorheological, as well as the photo-actuation capability, was investigated. It was shown that in addition to the modification of conductivity, the dipole moment of the pendant groups of the grafted polymer chains also plays an important role in the electrorheological (ER) performance. The compatibility of the particles with the polymer matrix, and thus proper particles dispersibility, is the most important factor for the photo-actuation efficiency. The plasticizing effect of the GO-polymer hybrid filler also has a crucial impact on the matrix stiffness and thus the ability to reversibly respond to the external light stimulation.

Adsorption of monodisperse polybutadienes on carbon black, 3 Displacement of pre-adsorbed molecules by the same polymer. Conformational and molecular weight effects

e-Polymers ◽  
2005 ◽  
Vol 5 (1) ◽  
Author(s):  
Kathy Vuillaume ◽  
Bassel Haidar ◽  
Alain Vidal
Keyword(s):  
Molecular Weight ◽  
Driving Force ◽  
Polymer Concentration ◽  
Gel Permeation Chromatography ◽  
Polymer Chains ◽  
Gel Permeation ◽  
Conformational Factor ◽  
Before And After ◽  
Displacement Processes

AbstractDisplacement of pre-adsorbed macromolecules by the same polymer, polybutadiene, of the same or of different molecular weight was studied in solution and in the bulk. The effect of polymer concentration on pre-adsorption and displacement processes was determined. Displacement was investigated by gel permeation chromatography and by determination of the amount of bound polymer before and after displacement. A conformational factor was established as a major driving force - besides molecular weight - in the displacement process. Polymer chains adsorbed in flat conformation had the highest adsorption stability and could not be displaced by any other molecular weight of the same polymer.

Tomography images to analyze the deformation of the cavern in the continuous-flow mixing of non-Newtonian fluids

AIChE Journal ◽  
2013 ◽  
Vol 60 (1) ◽  
pp. 315-331 ◽  
Author(s):  
Dineshkumar Patel ◽  
Farhad Ein-Mozaffari ◽  
Mehrab Mehrvar
Keyword(s):  
Continuous Flow ◽  
Newtonian Fluids ◽  
Flow Mixing

Ozonolytic Degradation of Interpolymers of Natural Rubber with Methyl Methacrylate and Styrene

1958 ◽  
Vol 31 (1) ◽  
pp. 82-85
Author(s):  
D. Barnard
Keyword(s):  
Molecular Weight ◽  
Carbon Black ◽  
Natural Rubber ◽  
Accurate Determination ◽  
Synthetic Polymers ◽  
Polymer Chains ◽  
Low Molecular Weight ◽  
Rubber Content ◽  
Tert Butyl Hydroperoxide

Abstract The preparation of graft and block interpolymers of natural rubber and synthetic polymers has made it desirable that the number and size of polymer chains attached to rubber be readily determinate. The degradation of unsaturated polymers with tert-butyl hydroperoxide in the presence of osmium tet oxide has been used for the determination of free polystyrene in SBR and carbon black in several elastomers, and has recently been applied to the present problem. The accurate determination of the rubber content of interpolymers by quantitative ozonolysis essentially according to the method of Boer and Kooyman suggested that this might be made the basis of isolation of the attached polymer, the rubber being degraded into fragments of low molecular weight, from which the polymer could be separated by conventional techniques. The method should be applicable to any interpolymer, or mixture, of a polyunsaturated and a saturated polymer and is illustrated with reference to interpolymers of natural rubber (NR)-polymethyl methacrylate (PMM) and NR-polystyrene (PS).

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