scholarly journals Experiment for Visualization of Polymer Chains in High-Polymer Aqueous Solutions under Shear Flow Regions.

1996 ◽  
Vol 39 (1) ◽  
pp. 112-118
Author(s):  
Hirofumi MIYAMOTO
2013 ◽  
Vol 1 (36) ◽  
pp. 5747 ◽  
Author(s):  
Lei Fang ◽  
Peng Liu ◽  
Benjamin R. Sveinbjornsson ◽  
Sule Atahan-Evrenk ◽  
Koen Vandewal ◽  
...  
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2019 ◽  
Vol 20 (18) ◽  
pp. 4604 ◽  
Author(s):  
Ihsan ◽  
Nargis ◽  
Koyama

A series of N-substituted poly(Gly–alter–Val) peptides were successfully synthesized for the systematic evaluation of the micellization behavior of alternating peptides. Three-component polymerization employing an aldehyde, a primary ammonium chloride, and potassium isocyanoacetate afforded four alternating peptides in excellent yields. We investigated the dependence of the hydrophilic–lipophilic balance of alternating peptides on the micellization behavior. All the aqueous solutions of alternating peptides exhibited upper critical solution temperature (UCST) behaviors, strongly indicating that the alternating binary pattern would mainly contribute to the UCST behaviors. The cloud points of alternating peptides shifted to higher temperatures as the side chains became more hydrophilic, which is opposite to the trend of typical surfactants. Such unusual micellization behaviors appeared to be dependent on the quasi-stable structure of single polymer chains formed in water.


2015 ◽  
Vol 777 ◽  
pp. 327-363 ◽  
Author(s):  
Jacob Page ◽  
Tamer A. Zaki

The viscoelastic analogue to the Newtonian Orr amplification mechanism is examined using linear theory. A weak, two-dimensional Gaussian vortex is superposed onto a uniform viscoelastic shear flow. Whilst in the Newtonian solution the spanwise vorticity perturbations are simply advected, the viscoelastic behaviour is markedly different. When the polymer relaxation rate is much slower than the rate of deformation by the shear, the vortex splits into a new pair of co-rotating but counter-propagating vortices. Furthermore, the disturbance exhibits a significant amplification in its spanwise vorticity as it is tilted forward by the shear. Asymptotic solutions for an Oldroyd-B fluid in the limits of high and low elasticity isolate and explain these two effects. The splitting of the vortex is a manifestation of vorticity wave propagation along the tensioned mean-flow streamlines, while the spanwise vorticity growth is driven by the amplification of a polymer torque perturbation. The analysis explicitly demonstrates that the polymer torque amplifies as the disturbance becomes aligned with the shear. This behaviour is opposite to the Orr mechanism for energy amplification in Newtonian flows, and is therefore labelled a ‘reverse-Orr’ mechanism. Numerical evaluations of vortex evolutions using the more realistic FENE-P model, which takes into account the finite extensibility of the polymer chains, show the same qualitative behaviour. However, a new form of stress perturbation is established in regions where the polymer is significantly stretched, and results in an earlier onset of decay.


1964 ◽  
Vol 42 (3) ◽  
pp. 522-531 ◽  
Author(s):  
C. H. Chou ◽  
H. H. G. Jellinek

The photolysis of polymethacrylic acid was studied in aqueous solutions as a function of pH, polymer concentration, polymer chain length, and small additions of electrolytes in the absence of oxygen with light of wavelength 2537 Å. The random chain scission constants decrease with increasing pH values. Small variations in polymer chain length and concentration and electrolyte concentration have no effect on the photolysis. Changes in the ultraviolet spectra with irradiation time are more pronounced at low pH values than higher ones. It is shown that the decrease in susceptibility to photolysis with increasing degree of ionization of the acid is not proportional to the decrease or increase of the number of COOH or COO− groups respectively. It is rather due to the same causes—that is changes in ionic atmosphere— which make the polymer chains uncoil with increasing ionization.


Background: Anthracene is an organic compound and environmentally resistant pollutant that causes severe damage to human health due to toxic and carcinogenic properties. The present study aimed to investigate the efficiency of magnetic dendrimer nano-adsorbent for the removal of anthracene from aqueous solutions. Methods: In this study, the synthesized iron oxide nanoparticles were modified by dendrimer polymer chains and 4-aminophenol ligand. The Fourier-transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy were conducted to examine the nano-absorbent properties. Different operational parameters in the adsorption process in batch and laboratory conditions were also studied, and the adsorbent reusability was correspondingly examined in this study. The residual concentration of anthracene in aqueous solution was determined and reported by a spectrophotometer. Findings: Optimization results showed that the maximum adsorbent capacity under optimum conditions (pH=7, 20 mg/L anthracene concentration, 0.5 g/L adsorbent dosage, and 30 min contact time) was equal to 83 mg/g. The experimental data fitted with different isotherm models showed that the equilibrium data were well described by the Langmuir model. In this study, the adsorption process overlapped more with the pseudo-second-order kinetics model. Conclusion: The obtained results indicated that the synthesized nanostructured adsorbent has a high adsorption capacity with high recovery and is efficient enough to remove anthracene from aqueous solutions.


Author(s):  
J.P. Armistead ◽  
R.R. Price ◽  
O.-K. Kim ◽  
L.-S. Choi

Small amounts (less than 30 ppm) of polymer dissolved in solution may significantly reduce the work required to pump fluids through a pipe at a given rate. In other words, the drag of the solution along the pipe walls is reduced. Drag reduction by polymers has been well characterized, however the molecular origin of the phenomena is not fully understood. Polymers that exhibit drag reduction characteristics typically have high molecular weight, have predominantly linear, flexible chains, and have an expanded molecular configuration in solution.Work in this laboratory has focused on the drag reduction behavior of poly(acrylic acid), PAA, in recent years. This polymer is one of the most shear stable water-soluble polymers and due to the ionic groups in the polymer chain its conformation in solution changes with pH and ionic strength. In a recent work, PAA solutions of 18 ppm, pH=8.1, showed an initial drag reduction of over thirty-five percent in rotating disc experiments. Over four minutes of shearing the drag reduction decreased to ten percent. This was surprising because of the known shear stability of PAA. When the sheared solution was left undisturbed for two weeks, it did not recover its drag reduction performance. However, the addition of NaCl to the solution during the shearing immediately restored drag reduction to its initial level. It was hypothesized that the shear flow induced interchain association that was possibly stabilized by hydrogen bonding and that the addition of the NaCl caused dissociation and drag reduction recovery. In additional work, fluorescence probe studies showed that shear flow induced local chain rigidity in the originally flexible polymer chains. In this study, the drag reduction experiments were repeated and the configurations of the sheared and unsheared polymer chains were viewed using electron microscopy.


2021 ◽  
pp. 118326
Author(s):  
Alexander L. Kwiatkowski ◽  
Vyacheslav S. Molchanov ◽  
Alexander I. Kuklin ◽  
Anton S. Orekhov ◽  
Natalia A. Arkharova ◽  
...  

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