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PubMed1986

Inflammation spurts: the role of ground substance viscosity.

A cyclical phenomenon of spurting polymorphonuclear leukocytes occurs in a number of skin diseases. The phenomenon is easy to observe because the polymorphonuclear leukocytes move into the epidermis and away from the vascular area. It is proposed that repeated spurting of polymorphonuclear leukocytes may be a broad biologic phenomenon. Edema appears essential to initiate the phenomenon by diluting the tissue fluids. The chemicals released by inflammation decrease ground substance viscosity and therefore interfere with dilution of tissue fluids. This stops the mediation of inflammation. The polymorphonuclear leukocytes also release connective tissue activating peptides which lead to increased glycosaminoglycans production and stimulate fibroblast to proliferate. The tissue activating peptides thus restore the viscosity of the ground substance and the cycle can be repeated. What we interpret as chronic inflammation could be the result of this repeated spurting phenomenon.

Humans↗
PubMed1991

A quartz crystal viscosity sensor for monitoring coagulation reaction and its application to a multichannel coagulation detector.

A quartz crystal viscosity sensor was applied to a coagulation reaction monitoring system. The system consists of 16 oscillating circuits, a channel selector, a frequency counter, a temperature controller and a microcomputer. The system is named the Quartz Chemical Analyzer (QCA). AT-cut quartz crystals (9 MHz) were used as viscosity detectors and were attached to a cell in order to expose only one side of the quartz plate. The system was applied to the detection of the blood coagulation factors VIII (F VIII) and IX (F IX). The activity of these factors was assayed by a single-stage method. A linear relationship was obtained in a double-logarithmic diagram of concentration versus coagulation time with respect to F VIII and F IX in the range 0.05-0.4 unit cm-3 and 0.025-0.2 unit cm-3, respectively.

Biosensing Techniques↗
PubMed2005

Interfacial rheology of adsorbed layers with surface reaction: on the origin of the dilatational surface viscosity.

A theoretical study of the phenomena, occurring in an adsorbed layer, subject to small dilatational perturbations was carried out. Two main processes, provoked by the perturbations (surface reaction and surfactant transport onto the surface) were considered. The reaction was described by means of the reaction coordinate. The derived general rheological equation for insoluble surfactants, gave as limiting cases Voight and Maxwell type equations for fast and slow reactions, respectively. Expressions for all characteristics of the process (surface elasticity, reaction elasticity, reaction relaxation time and dilatational surface viscosity) were obtained. The obtained generalized rheological equation for reactions involving soluble surfactants is a dynamic analog of Gibbs adsorption isotherms for a multi-component system with surface reaction, since similarly to Gibbs equation it relates the surface stress only to surface variables. It gives as limiting cases generalized forms for soluble surfactants of Voight and Maxwell equations. All new rheological equations were analyzed for deformations with constant rate and periodic oscillations and they were applied to three simple surface reactions (monomolecular with one product, dimerization and association). The mass transfer was analyzed initially in the absence of surface reaction. In this system the surface stress is purely elastic, but it was shown that if the adsorption perturbation is small, regardless of the type of surface perturbation and the mechanism of adsorption, the process of mass transport always obeys a Maxwell type rheological equation. For all considered processes surface viscosities were defined, but they were called "apparent", because they stem from diffusion, rather than from interaction between the surfactant molecules and they depend not only on surface parameters, but also on the geometry of the system. The often used in the literature correlations between the lifetime of emulsions and foams and the imaginary elasticity were analyzed. It was shown that this approach lacks serious scientific foundations and could lead to erroneous conclusions. Finally, the problem for the coupling of the surfactant diffusion with the chemical reaction was analyzed and it was demonstrated on a simple example how it could be tackled.

Adsorption↗
PubMed2004

Analysis of the electrophoretic mobility and viscosity of dilute Ludox solutions in terms of a spherical gel layer model.

A spherical gel layer model of colloidal particles is used to analyze the electrophoretic mobility and viscosity of a dilute suspension of the silica sol, Ludox, reported previously by Laven and Stein (J. Laven, H.N. Stein, J. Colloid Interface Sci. 238 (2001) 8-15). The colloid is modeled as a sphere with a solid inner core surrounded by a diffuse gel layer of uniform thickness and comprising a specific fraction, f, of the colloidal particle's mass. The gel layer is accessible to solvent and ions, but the gel layer retards the flow of solvent, which is assumed to obey the Brinkman equation. The colloidal charge is assumed to be spherically symmetric, but its disposition on the surface of the core particle and gel layer (alpha = fraction of charge in the gel layer) is left as an adjustable parameter. Experiments at pH 5.7 and 8.7 over a KCl concentration range of 0.3 to 80 mM are examined. At high salt and/or low pH, the thickness of the gel layer is estimated to be 1.0 to 1.6 nm depending on the assumed fraction of silica present in the gel layer. At low salt (0.3 mM) and high pH, where the net absolute charge of Ludox is large, the thickness of the gel layer is estimated to be 3.7 to 4.1 nm. Thus, the thickness of the gel layer appears to increase with decreasing salt at high pH. The net charge required to simultaneously match experimental and model mobilities and viscosities is sensitive to the choice of f and alpha. Nonetheless, for reasonable choices of these parameters (f = 0.13 and alpha approximately equal to 1.0), the estimated net absolute charges of Ludox from present modeling are in good agreement with the titration charges of Bolt (G.H. Bolt, J. Phys. Chem. 61 (1957) 1166-1169), and Milonjic (S.K. Milonjic, Colloids Surf. 23 (1987) 301-311) over the entire salt concentration range at pH 8.7. At pH 5.7, however, the estimated net absolute charge from current modeling exceeds the Bolt values by about 50%.

Journal Article↗
PubMed2005

Size and shape of soil humic acids estimated by viscosity and molecular weight.

Ultrafiltration fractions of three soil humic acids were characterized by viscometry and high performance size-exclusion chromatography (HPSEC) in order to estimate shapes and hydrodynamic sizes. Intrinsic viscosities under given solute/solvent/temperature conditions were obtained by extrapolating the concentration dependence of reduced viscosities to zero concentration. Molecular mass (weight average molecular weight (M (w)) and number average molecular weight (M (n))) and hydrodynamic radius (R(H)) were determined by HPSEC using pullulan as calibrant. Values of M (w) and M (n) ranged from 15 to 118 x 10(3) and from 9 to 50 x 10(3) (g mol(-1)), respectively. Polydispersity, as indicated by M (w)/M (n), increased with increasing filter size from 1.5 to 2.4. The hydrodynamic radii (R(H)) ranged between 2.2 and 6.4 nm. For each humic acid, M (w) and [eta] were related. Mark-Houwink coefficients calculated on the basis of the M (w)-[eta] relationships suggested restricted flexible chains for two of the humic acids and a branched structure for the third humic acid. Those structures probably behave as hydrated sphere colloids in a good solvent. Hydrodynamic radii of fractions calculated from [eta] using Einstein's equation, which is applicable to hydrated sphere colloids, ranged from 2.2 to 7.1 nm. These dimensions are fit to the size of nanospaces on and between clay minerals and micropores in soil particle aggregates. On the other hand, the good agreement of R(H) values obtained by applying Einstein's equation with those directly determined by HPSEC suggests that pullulan is a suitable calibrant for estimation of molecular mass and size of humic acids by HPSEC.

Journal Article↗
PubMed2005

Study on hydration layers near nanoscale silica dispersed in aqueous solutions through viscosity measurement.

On the basis of the Einstein theory of viscosity of dispersion, a parameter, termed as solvation factor, is presented to evaluate the solvation degree of nanoscale particles dispersed in a liquid in this work. The value of the parameter is obtained through the measurements of relative viscosity of the dispersions as a function of the volume fraction of dry particles. The solvation factor has been used to study the hydration layers near nanoscale silica particles dispersed in water and aqueous electrolyte (NaCl and CaCl2) solutions in this work. The experimental results have shown that a strong hydration indeed applied to the silica surfaces in aqueous solutions, leaving a large volume of hydration layers on the surfaces. Also, it has been found that the hydration of the nanoscale silica particles could be greatly enhanced if they were dispersed in aqueous NaCl or CaCl2 solutions, which might be attributed to that the hydrated cations (Na+ or Ca2+) bind onto the silica/ water interface and thus increase the volume of the hydration layers.

Journal Article↗
PubMed2006

Effect of ionic surfactants on bauxite residues suspensions viscosity.

Measurement of the rheological property of bauxite residue sample received from an Australian alumina refinery, treated with a number of cationic and anionic surfactant in laboratory has been carried out using a Brookfield viscometer for the assessment of the effect of surfactants on the residue viscosity. Sodium laurate, prepared with an excess of sodium hydroxide, was found to be effective while direct addition of anionic surfactants (lauric acid and sodium laureth sulphate) and cationic (cetyl trimethyl ammonium bromide) produce only moderate effect on the red mud suspension apparent viscosity at 65 degrees C. The experimental data appear to confirm the crucial role of the cation sodium in the process of adsorption of anionic surfactants on the flocculated red mud particles.

Journal Article↗
PubMed2006

Effect of time on tensile bond strength of resin cement bonded to dentine and low-viscosity composite.

OBJECTIVES: The purpose of this study was to evaluate the tensile bond strength (TBS) of Panavia F resin cement (PF) applied on dentine pre-treated with ED Primer (ED) and Clearfil Liner Bond 2V (CLB) coated with a layer of low-viscosity composite Protect Liner F (PLF) at 10 min, 24 h and 12 months after curing. METHODS: The labial surfaces of 60 bovine lower incisors were ground to obtain a flat dentine surface, allowing a demarcation of a 4.0 mm-diameter area with adhesive tape. The teeth were randomly divided in six groups; ED was applied in groups A I, A II and A III and CLB was applied, followed by PLF, in groups B I, B II and B III. A resin composite rod with a wire loop was luted directly to the prepared surface of each group with PF. The specimens of groups A I and B I were submitted to TBS test after 10 min. Groups A II and B II were submitted to TBS test after 24 h storage and groups A III and B III were submitted to TBS test after 12 months storage. Each specimen was inspected by SEM and classified according to the failure mode. Additionally, two representative specimens of each failure mode were sectioned for a composite/dentine interface SEM evaluation. RESULTS: No significant statistical differences were observed among the groups at 10 min and 24 h. Groups A III and B III presented the lowest TBS values (p<0.05) after 12 months storage. PF on resin-coated dentin (PLF) showed the highest TBS values and was statistically different to PF on dentine for all the groups. The fracture pattern was generally cohesive on the adhesive/hybrid layer for groups A I, A II and A III and cohesive on composite resin for B I, B II and B III. SIGNIFICANCE: The use of a less hydrophilic self-etching system to pre-treat dentine, coating with a low-viscosity composite layer prior luting with resin cement, may provide a protection of the hybridised complex, allowing a dentine seal during the 12 months storage period.

Acrylic Resins↗
PubMed1990

Mapping of fluorescence anisotropy in living cells by ratio imaging. Application to cytoplasmic viscosity.

Steady-state and time-resolved fluorescence properties of probes incorporated into living cells give information about the microenvironment near the probe. We have extended studies of spatially averaged fluorescence anisotropy (r) by using an epifluorescence microscope, equipped with excitation and emission polarizers and an image analysis system, to map r of nonoriented fluorophores incorporated into cultured cells. With this imaging system, r for reflected light or glycogen scattering solutions was greater than 0.98. Measurement of r over the range 0.01-0.35 for fluorophores in bulk solution and in thin capillary tubes placed side-by-side gave values equivalent to r measured by cuvette fluorometry. Cytoplasmic viscosity (eta) in Madin-Darby canine kidney (MDCK) cells and Swiss 3T3 fibroblasts was examined from anisotropy images and time-resolved fluorescence decay of the cytoplasmic probes 2,7-bis-carboxyethyl-5 (and 6)-carboxy-fluorescein (BCECF) and indo-1. Nanosecond lifetimes and anisotropy decay were measured using a pulsed light source and gated detector interfaced to the epifluorescence microscope. Anisotropy images of BCECF in MDCK cells revealed two distinct regions of r: one from the cytoplasm (r = 0.144 +/- 0.008) and a second appearing at late times from the interstitial region (r = 0.08 +/- 0.03), representing BCECF trapped beneath the tight junctions. Anisotropy values, taken together with intracellular life-times and the calibration between r and eta/tau f for water/glycerol mixtures, gave eta values of 10-13 cP at 23 degrees C. These values assume little fluorophore binding to intracellular components and are therefore upper limits to cytoplasmic viscosity. These data establish a new methodology to map anisotropy in intact cells to examine the role of fluidity in cellular physiology.

Animals↗
PubMed2000

Mobile-phase-viscosity dependence on DNA separation in slalom chromatography.

Slalom chromatography (SC) is an alternative chromatographic procedure for the separation of relatively large double-stranded DNA molecules and is based on a new principle. The retardation of the DNA fragments from the cleavage of the Lambda DNA by the KpnI restriction enzyme was studied using an acetonitrile-phosphate buffer as a mobile phase with various concentrations of viscosity modifier (i.e. glycerol) and a C1 column as a stationary phase. The DNA molecule retention was accurately described over the glycerol concentration range using a model previously established. It was shown that the eluent viscosity increase enhanced the slalom chromatographic capacity to separate the DNA fragments. A connection between SC and 'hydrodynamic chromatography' processes was predicted to link the two processes in a global separation mechanism based on a non-equilibrium principle.

Chromatography, Liquid↗
PubMed2003

Viscosity function in polymer-modified asphalts.

Asphalt is a multidisperse micellar system with rheological behavior resembling that of a low-molecular-weight polymer. Nowadays, asphalt is frequently modified by blending it with various polymers. Such modified asphalt has rheological properties that differ from the properties of the base asphalt. It is quite common to study asphalt in dynamic experiments. Such studies, however useful, cannot reveal all characteristic features of polymer-modified asphalts. Asphalt modification by polymers is strongly manifested in the region of transitions from a viscoelastic fluid to the Newtonian fluid. The viscosity study in this region can reveal behavior characteristic of the used polymer modifier, thus complementing the dynamic studies of these materials. The viscosity of base asphalt modified by styrene-butadiene-styrene and by ethylene-vinyl acetate polymers (in several concentrations) is studied and discussed in this note.

Journal Article↗
PubMed2003

The importance of temperature and viscosity effects for surfactant adsorption measurements made using the electrochemical quartz crystal microbalance.

The measurement of adsorbed surfactant is important to fields such as corrosion inhibition, metal cleaning, and separation technologies. The electrochemical quartz crystal microbalance (EQCM) is an important tool that can be used to measure adsorbed surfactant. However, such measurements are subject to significant temperature and viscosity effects that must be appropriately considered. This paper discusses the effect of temperature and viscosity on EQCM measurements in solution environments and the ability of the EQCM to measure surfactant adsorption.

Journal Article↗
PubMed1999

Apparent digestibility and glycaemic responses to an experimental induced viscosity dietary fibre incorporated into an enteral formula fed to dogs cannulated in the ileum.

The purpose of this study was to evaluate the apparent digestibility and postprandial glycaemic responses of ileal-cannulated dogs when fed an experimental induced viscosity dietary fibre (IVF) incorporated into a liquid enteral formula. Dietary treatments were: (1) control; (2) Glucerna; (3) Glytrol; (4) IVF; and (5) Jevity. Diets varied in concentrations of crude protein (CP), fat, starch and total dietary fibre (TDF). Dry matter and starch intakes by dogs fed the Glucerna and Glytrol treatments were lower (P<0.05) than for those consuming the other diets. However, daily intakes of CP and fat followed a reverse trend. Digestibility of nutrients at the ileum was high (>80%) for all dietary treatments. Mineral absorption proximal to the ileum and from the total tract was not significantly different among treatments. Mean incremental area under the serum glucose response curves for dogs fed Glytrol, Glucerna, and IVF treatments were lower (P<0.05) than the control treatment. Induced viscosity fibre appears to have no negative effects on nutrient digestion throughout the gastrointestinal tract. Its ability to moderate serum glucose concentrations would make it a potentially good choice for a diabetic liquid formula.

Animals↗
PubMed2000

Measurement of the viscosity of irradiated silicone using a differential viscometer

High-energy electron (2.0 MV) and gamma irradiation (60Co) has been used to modify polymeric silicone fluids of initial viscosities in the range, 90-700 cSt. Doses of electron and gamma radiation were delivered at rates of 0.246 kGy s(-1) and 15 kGy h(-1), respectively, exposure times being adjusted to ensure energy deposition in the range 30-360 kGy. Measurements were made using a differential viscometer based on a Bose Institute design. In line with expectation, samples of greater initial molecular weight (and hence greater viscosity), were observed to be more susceptible to radiation induced cross-linking than those of lower molecular weight. The role of dose rate and oxygen diffusion in determining the extent of change is discussed.

Journal Article↗
PubMed2000

Fluid viscosity of Aureobasidium pullulans cultures obtained at two different initial pH values.

Aureobasidium pullulans IAM 5060 grown in media with initial pHs of 6 and 7 differed in its production of exopolysaccharides (EPS). Under the latter condition, EPS of a high molecular weight was produced in an especially large amount. The viscosity of the culture broths and the EPS solutions obtained by removing the microbial cells exhibited a marked non-Newtonian and complex behavior depending on the measurement method. The nature of the viscosity of the fluids is explained by means of several structural models of their constitutive particles.

Journal Article↗
PubMed2003

Viscosity as an experimental tool in studying the mechanism of stereoselective and product-selective chemical transformations through frictional impositions.

In the present Account, we examine the viscosity dependence as a function of temperature, pressure, and solvent polarity for the double inversion in the photolytic azoalkane denitrogenation, the thermal isomerization of housanes, and stereochemical memory versus Curtin-Hammett behavior in radical-cation rearrangements. The analysis of these stereoselective and product-selective viscosity studies in terms of the simple free-volume model demonstrates the utility of frictional effects for the elucidation of complex reaction mechanisms in molecular transformations.

Journal Article↗
PubMedDate not supplied

Prediction of surface tension, viscosity, and thermal conductivity for common organic solvents using quantitative structure-property relationships.

Predictive models for the surface tension, viscosity, and thermal conductivity of 213 common organic solvents are reported. The models are derived from numerical descriptors which encode information about the topology, geometry, and electronics of each compound in the data set. Multiple linear regression and computational neural networks are used to train and evaluate models based on statistical indices and overall root-mean-square error. Eight-descriptor models were developed for both surface tension and viscosity, while a nine-descriptor model was developed for thermal conductivity. In addition, a single nine-descriptor model was developed for prediction of all three properties. The results of this study compare favorably to previously reported prediction methods for these three properties.

Journal Article↗
PubMed2004

Phosphazene-based ionic liquids: synthesis, temperature-dependent viscosity, and effect as additives in water lubrication of silicon nitride ceramics.

Phosphazene rings with (dimethylamino)ethoxy (1, 2), pyridylmethoxy (3), or (dimethylamino)propoxy (4) chains were synthesized and quaternized at the substitutent nitrogen by treatment with methyl iodide at 35 degrees C over 3-6 h to give polyiodo salts, 5-8. Subsequent metathesis with LiN(SO(2)CF(3))(2) or NaBF(4) gave the respective ionic salts, 9-13. The amide salts, 9-12, were viscous liquids with pour points at 55-100 degrees C, and the tetrafluoroborate salt, 13, was a solid, mp 168 degrees C. The compositions of 2 and 5-13 were confirmed by elemental analysis and spectroscopic methods. Compounds 1, 2, and 4 were viscous liquids (d(25) = 1.67 g cm(-3); eta(25) = 0.76-1.56 mPa s(-1) ) with pour points at approximately 15 degrees C. The solid polyquaternary salts, 5-8, melted at 130-194 degrees C. The ionic liquids, 9-12, had an average density of approximately 1.73 g cm(-3) at 25 degrees C, and viscosities (25 degrees C) ranged between 68.3 and 139.2 mPa s(-1). A plot of the viscosities of 9-12 vs temperature revealed an almost linear correlation between 55 and 120 degrees C. Friction and wear properties of water with 0.25 wt % of 9-12 as boundary lubricant additives were evaluated on Si(3)N(4)/Si(3)N(4) ceramic interfaces. The most significant observation is that they caused a decrease in the running-in period.

Journal Article↗