scholarly journals Variation of the Hydrodynamic Polymer Layer Thickness on Solid Surfaces with Molecular Weight and Concentration

1995 ◽  
Vol 12 (3) ◽  
pp. 259-265 ◽  
Author(s):  
S. Millot ◽  
J.L. Loubet ◽  
J.M. Georges

An extensive study on the determination of the 'hydrodynamic' layer thickness of polymer solutions and melt polymers was conducted with a surface force apparatus. For different concentrations and polymer molecular weights, a 'hydrodynamic layer' of fluid was detected on each solid surface which did not contribute to the flow. These thicknesses, denoted as LH, are compared to the characteristic polymer dimensions and the hydrodynamic (RH) and gyration (Rg) radii. It appears that in contrast to the molecular weight, polymer concentration has little effect on the relative hydrodynamic layer thickness (LH/2RH, LH/2Rg). Indeed, this ratio indicates that two coils of low molecular weight and one coil of high molecular weight are 'immobile' on the solid surfaces. The mechanism responsible could be entanglement of the free (unattached) chains in the bulk with immobilized chains on the surface.

2004 ◽  
Author(s):  
Kalonji K. Kabanemi ◽  
Jean-Franc¸ois He´tu ◽  
Samira H. Sammoun

An experimental investigation of the flow behavior of dilute, semi-dilute and concentrated polymer solutions has been carried out to gain a better understanding of the underlying mechanisms leading to the occurrence of instabilities at the advancing flow front during the filling of a mold cavity. Experiments were performed using various mass concentrations of low and high molecular weight polyacrylamide polymers in corn syrup and water. This paper reports a new type of elastic fingering instabilities at the advancing flow front that has been observed only in semi-dilute polymer solutions of high molecular weight polymers. These flow front elastic instabilities seem to arise as a result of a mixture of widely separated high molecular weight polymer molecules and low molecular weight solvent molecules, which gives rise to a largely non-uniform polydisperse solution, with respect to all the kinds of molecules in the resulting mixture (solvent molecules and polymer molecules). The occurrence of these instabilities appears to be independent of the injection flow rate and the cavity thickness. Moreover, these instabilities do not manifest themselves in dilute or concentrated regimes, where respectively, polymer molecules and solvent molecules are minor perturbation of the resulting solution. In those regimes, smooth flow fronts are confirmed from our experiments. Based on these findings, the experimental investigations have been extended to polymer melts. Different mixtures of polycarbonate melts of widely separated molecular weights (low and high molecular weights) were first prepared. The effect of the large polydispersity of the resulting mixtures on the flow front behavior was subsequently studied. The same instabilities at the flow front were observed only in the experiments where a very small amount of high molecular weight polycarbonate polymer has been mixed to a low molecular weight polycarbonate melt (oligomers).


2005 ◽  
Vol 51 ◽  
pp. 9-14
Author(s):  
Snezhana Palchevska ◽  
Velibor Tasik ◽  
Petar Korneti ◽  
Georgi Shestakov ◽  
Svetlana Tsekovska

The pattern of urinary proteins in healthy full-term neonates was examined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), coupled with determination of few parameters related to urinary protein excretion. Twenty healthy full-term neonates were included in the investigation. Five urine samples from each subject were collected on days 3, 7, 14, 21 and 28 after birth. Determination of total proteins was performed using turbidimetric method with sulfosalicylic acid. Urinary creatinine concentration was determined by Jaffe method. Urinary proteins were separated by horizontal gradient SDS-PAGE according to Görg. The highest values for total urinary proteins and for protein/creatinine ratio were detected in urine samples excreted on days 3 and 7 after birth. Three types of SDS-PAG electrophoretic profiles were observed. The first type of electrophoretic profile was characterized by the presence of proteins of mixed glomerular and tubular origin with molecular weights from 10 to 160 kDa. Typical for the second type of electrophoretic profile was the presence of two faint fractions with molecular weights of 78 and 90 kDa and several intensive low molecular weight fractions (14-67 kDa). In the third type of electrophoretic profile only low molecular weight proteins (10-67 kDa) were detected in all five urine samples. These findings express the transitory immaturity of the glomerular filter and tubular protein reabsorbing system of the newborn kidney. Apparently, the tubular protein handling normalizes later than the glomerular filtration of proteins.


2020 ◽  
Vol 18 (1) ◽  
pp. 75-92
Author(s):  
Lizcano Nino J.C ◽  
Ferreira Vitor Hugo de Sousa ◽  
Moreno Rosangela B. Z. L

Polymer Flooding has become one of the most implemented EOR techniques, due to three factors: First, Polymer flooding has expanded the range of the screening criteria parameters. Second, this EOR method is more effective than water injection, while handling water management issues in high water-cut reservoirs. Nevertheless, polymer retention can turn a viable technical project into an uneconomical one. Polymer loss due to retention is an inevitable phenomenon, which happens during injection processes. The development of experimental analysis aiming to minimize or reduce polymer loss from the displacing fluid bank is beneficial to broaden the application of this CEOR method. This experimental work evaluated the injection schemes aiming to reduce polymer retention in porous media. The approach consisted of injecting less-concentrated polymer banks followed for the main polymer bank designed for mobility control. An experimental methodology to quantify polymer retention due to each injected polymer bank, cumulative polymer retention, resistance factor, residual resistance factor and inaccessible pore volume (IPV) was developed. The measurement process was based on the injection of 20 PV polymer banks at a constant flow rate of 1ml/min at 25°C, separated by 30 PV brine banks. Two HPAM with molecular weights of 6-8 million and 20 million Daltons using 350mD and 5000 mD sandstone cores were tested, respectively. The HPAM solutions considering a Colombian field (0.7% NaCl) and seawater (3.5% TDS) salinities were prepared. All rock samples were previously submitted to the injection of 50 PV for preventing fines migration. Two injection schemes with variable polymer concentrations were performed: The first one in which the polymer concentration increased in each successive bank, and the second one in which the concentration decreased. HPAM concentration solutions from 50 ppm to 2000 ppm were sequentially used in both injection schemes. By comparing the results of these two schemes, the effect of the injection of the less-concentrated polymer solutions was evaluated. For the increasing concentration experiments, cumulative retention values of 175.7 μg/g and 58.9 μg/g were calculated for the low-molecular weight polymer and the high-molecular weight polymer, respectively. While comparing with decreasing concentration experiments, for the high-molecular weight HPAM a 19% of retention reduction was evidenced, but no retention reduction was observed for the low-molecular weight one. The results indicate that different retention mechanisms are strongly dependents on the absolute permeability of the samples. Additionally, IPV values of 0.5 PV and 0.25 PV were calculated using low and high permeability samples, respectively. There was no linear relation between the absolute permeability reduction and the polymer concentration of the first bank injected into the sample. The novelty of this work is to use sacrificial banks of less-concentrated HPAM solutions as a reducing retention agent for the polymer bank designed for mobility control.


Author(s):  
Renata Czechowska-Biskup ◽  
Radosław A. Wach ◽  
Janusz M. Rosiak ◽  
Piotr Ulański

The aim of this publication is to facilitate the estimation of chitosan molecular weight (MW) in laboratories with no access to sophisticated analytical instruments, by applying the easily accessible and economical capillary viscometry. The procedure of viscosity-average molecular weight (Mv) determination is described in details. The examples provided encompass testing of the experimental procedure for determination of the Mv of chitosan with a low-molecular weight of 7.7 kDa and 88 kDa, after verification with a high-molecular weight polymer (477 kDa). The experimental work demonstrated the importance of the initial concentration of low-MW chitosan for the accurate determination of intrinsic viscosity and, as a consequence, the viscosity-average molecular weight.


2013 ◽  
Vol 734-737 ◽  
pp. 2549-2552
Author(s):  
Jiu Zhou Sun ◽  
Chang Bin Wang ◽  
Liang Kan ◽  
Ze Hua Wang

The laboratory evaluation studied the matching relationship between different concentration polymer solution and the formation permeability,and also the matching relationship between different molecular weight polymer solution and the formation permeability. The influences on the solution viscoelasticity,which were caused by the polymer concentration and the molecular weights,were analysed by the laboratory evaluation tests on the viscoelasticity of the polymer solution.


Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3321
Author(s):  
Katarzyna Kurpet ◽  
Rafał Głowacki ◽  
Grażyna Chwatko

Biothiols are extremely powerful antioxidants that protect cells against the effects of oxidative stress. They are also considered relevant disease biomarkers, specifically risk factors for cardiovascular disease. In this paper, a new procedure for the simultaneous determination of human serum albumin and low-molecular-weight thiols in plasma is described. The method is based on the pre-column derivatization of analytes with a thiol-specific fluorescence labeling reagent, monobromobimane, followed by separation and quantification through reversed-phase high-performance liquid chromatography with fluorescence detection (excitation, 378 nm; emission, 492 nm). Prior to the derivatization step, the oxidized thiols are converted to their reduced forms by reductive cleavage with sodium borohydride. Linearity in the detector response for total thiols was observed in the following ranges: 1.76–30.0 mg mL−1 for human serum albumin, 0.29–5.0 nmol mL−1 for α-lipoic acid, 1.16–35 nmol mL−1 for glutathione, 9.83–450.0 nmol mL−1 for cysteine, 0.55–40.0 nmol mL−1 for homocysteine, 0.34–50.0 nmol mL−1 for N-acetyl-L-cysteine, and 1.45–45.0 nmol mL−1 for cysteinylglycine. Recovery values of 85.16–119.48% were recorded for all the analytes. The developed method is sensitive, repeatable, and linear within the expected ranges of total thiols. The devised procedure can be applied to plasma samples to monitor biochemical processes in various pathophysiological states.


2021 ◽  
Vol 22 (14) ◽  
pp. 7709
Author(s):  
Kyoungwon Cho ◽  
You-Ran Jang ◽  
Sun-Hyung Lim ◽  
Susan B. Altenbach ◽  
Yong Q. Gu ◽  
...  

The low-molecular weight glutenin subunit (LMW-GS) composition of wheat (Triticum aestivum) flour has important effects on end-use quality. However, assessing the contributions of each LMW-GS to flour quality remains challenging because of the complex LMW-GS composition and allelic variation among wheat cultivars. Therefore, accurate and reliable determination of LMW-GS alleles in germplasm remains an important challenge for wheat breeding. In this study, we used an optimized reversed-phase HPLC method and proteomics approach comprising 2-D gels coupled with liquid chromatography–tandem mass spectrometry (MS/MS) to discriminate individual LMW-GSs corresponding to alleles encoded by the Glu-A3, Glu-B3, and Glu-D3 loci in the ‘Aroona’ cultivar and 12 ‘Aroona’ near-isogenic lines (ARILs), which contain unique LMW-GS alleles in the same genetic background. The LMW-GS separation patterns for ‘Aroona’ and ARILs on chromatograms and 2-D gels were consistent with those from a set of 10 standard wheat cultivars for Glu-3. Furthermore, 12 previously uncharacterized spots in ‘Aroona’ and ARILs were excised from 2-D gels, digested with chymotrypsin, and subjected to MS/MS. We identified their gene haplotypes and created a 2-D gel map of LMW-GS alleles in the germplasm for breeding and screening for desirable LMW-GS alleles for wheat quality improvement.


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