polymer fluids
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2022 ◽  
pp. 128203
Author(s):  
Yinuo Li ◽  
Tingting Wei ◽  
Long Chen ◽  
Kaixiang Wang ◽  
Yulin Shi

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Saiful I. Tamim ◽  
Joshua B. Bostwick

AbstractA soft viscoelastic drop has dynamics governed by the balance between surface tension, viscosity, and elasticity, with the material rheology often being frequency dependent, which are utilized in bioprinting technologies for tissue engineering and drop-deposition processes for splash suppression. We study the free and forced oscillations of a soft viscoelastic drop deriving (1) the dispersion relationship for free oscillations, and (2) the frequency response for forced oscillations, of a soft material with arbitrary rheology. We then restrict our analysis to the classical cases of a Kelvin–Voigt and Maxwell model, which are relevant to soft gels and polymer fluids, respectively. We compute the complex frequencies, which are characterized by an oscillation frequency and decay rate, as they depend upon the dimensionless elastocapillary and Deborah numbers and map the boundary between regions of underdamped and overdamped motions. We conclude by illustrating how our theoretical predictions for the frequency-response diagram could be used in conjunction with drop-oscillation experiments as a “drop vibration rheometer”, suggesting future experiments using either ultrasonic levitation or a microgravity environment.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jin Huang ◽  
Yichao Xu ◽  
Shuanhu Qi ◽  
Jiajia Zhou ◽  
Wei Shi ◽  
...  

AbstractEnergy-dissipation elastomers relying on their viscoelastic behavior of chain segments in the glass transition region can effectively suppress vibrations and noises in various fields, yet the operating frequency of those elastomers is difficult to control precisely and its range is narrow. Here, we report a synergistic strategy for constructing polymer-fluid-gels that provide controllable ultrahigh energy dissipation over a broad frequency range, which is difficult by traditional means. This is realized by precisely tailoring the relaxation of confined polymer fluids in the elastic networks. The symbiosis of this combination involves: elastic networks forming an elastic matrix that displays reversible deformation and polymer fluids reptating back and forth to dissipate mechanical energy. Using prototypical poly (n-butyl acrylate) elastomers, we demonstrate that the polymer-fluid-gels exhibit a controllable ultrahigh energy-dissipation property (loss factor larger than 0.5) with a broad frequency range (10−2 ~ 108 Hz). Energy absorption of the polymer-fluid-gels is over 200 times higher than that of commercial damping materials under the same dynamic stress. Moreover, their modulus is quasi-stable in the operating frequency range.


AIP Advances ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 095013
Author(s):  
Jin Su ◽  
Cuihong Hou ◽  
Yingcang Ma ◽  
Yaowu Wang

2020 ◽  
Vol 9 (7) ◽  
pp. 924-928 ◽  
Author(s):  
Marion Grzelka ◽  
Iurii Antoniuk ◽  
Eric Drockenmuller ◽  
Alexis Chennevière ◽  
Liliane Léger ◽  
...  
Keyword(s):  

Géotechnique ◽  
2020 ◽  
pp. 1-10
Author(s):  
John O. Ejezie ◽  
Stephan A. Jefferis ◽  
Carlos Lam ◽  
Majid Sedighi ◽  
Syed M. Ahmad
Keyword(s):  

Author(s):  
William R. Suarez-Fernandez ◽  
Giuseppe Scionti ◽  
Juan D. G. Duran ◽  
Andrey Yu. Zubarev ◽  
Modesto T. Lopez-Lopez

Even in the absence of cross-linking, at large enough concentration, long polymer strands have a strong influence on the rheology of aqueous systems. In this work, we show that solutions of medium molecular weight (120 000–190 000 g mol −1 ) alginate polymer retained a liquid-like behaviour even for concentrations as large as 20% w/v. On the contrary, solutions of alginate polymer of larger (and also polydisperse) molecular weight (up to 600 000 g mol −1 ) presented a gel-like behaviour already at concentrations of 7% w/v. We dispersed micrometre-sized iron particles at a concentration of 5% v/v in these solutions, which resulted in either stable magnetic fluids or gels, depending on the type of alginate polymer employed (medium or large molecular weight, respectively). These magneto-polymer composites presented a shear-thinning behaviour that allowed injection through a syringe and recovery of the original properties afterwards. More interestingly, application of a magnetic field resulted in the formation of particle clusters elongated along the field direction. The presence of these clusters intensely affected the rheology of the systems, allowing a reversible control of their stiffness. We finally developed theoretical modelling for the prediction of the magnetic-sensitive rheological properties of these magneto-polymer colloids. This article is part of the theme issue ‘Patterns in soft and biological matters'.


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