Scaling equation for viscosity of polydimethylsiloxane in ethyl acetate: From dilute to concentrated solutions

被引:6
|
作者
Agasty, Airit [1 ,2 ]
Wisniewska, Agnieszka [1 ]
Kalwarczyk, Tomasz [1 ]
Koynov, Kaloian [2 ]
Holyst, Robert [1 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
[2] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
基金
欧盟地平线“2020”;
关键词
Rheology; PDMS; DLS; STIFF-CHAIN POLYMERS; LIGHT-SCATTERING; MOLECULAR-WEIGHT; COMPLEX LIQUIDS; SEMIDILUTE; DIFFUSION; SOLVENT; DEPENDENCE; DYNAMICS; FLOW;
D O I
10.1016/j.polymer.2020.122779
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Rheology of polymer solutions suffers from lack of universal model of viscosity applicable across wide range of concentrations. Here we build such a model on the basis of measured viscosity of polydimethylosiloxane (PDMS) in ethyl acetate in a wide range of polymer concentrations: from dilute up to highly concentrated solutions. The relationship between viscosity and different polymer parameters in solution such as coil size, correlation length xi, monomer-solvent and monomer-monomer interaction parameter were established experimentally as a function of concentrations [from 0.001 g/cm(3) to 8.000 g/cm(3)], temperature [in a range 283-303 K] and molecular masses [9-139 kg/mol]. Entanglement onset at the crossover from dilute to semi-dilute solution as well as the solvent-monomer contact reduction at the crossover from semi-dilute to concentrated regime are captured by the model. This model is in accordance with the Eyring rate theory for activated processes.
引用
收藏
页数:7
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